- Research article
- Open Access
Sequence-based identification of inositol monophosphatase-like histidinol-phosphate phosphatases (HisN) in Corynebacterium glutamicum, Actinobacteria, and beyond
BMC Microbiology volume 17, Article number: 161 (2017)
The eighth step of l-histidine biosynthesis is carried out by an enzyme called histidinol-phosphate phosphatase (HolPase). Three unrelated HolPase families are known so far. Two of them are well studied: HAD-type HolPases known from Gammaproteobacteria like Escherichia coli or Salmonella enterica and PHP-type HolPases known from yeast and Firmicutes like Bacillus subtilis. However, the third family of HolPases, the inositol monophosphatase (IMPase)-like HolPases, present in Actinobacteria like Corynebacterium glutamicum (HisN) and plants, are poorly characterized. Moreover, there exist several IMPase-like proteins in bacteria (e.g. CysQ, ImpA, and SuhB) which are very similar to HisN but most likely do not participate in l-histidine biosynthesis.
Deletion of hisN, the gene encoding the IMPase-like HolPase in C. glutamicum, does not result in complete l-histidine auxotrophy. Out of four hisN homologs present in the genome of C. glutamicum (impA, suhB, cysQ, and cg0911), only cg0911 encodes an enzyme with HolPase activity. The enzymatic properties of HisN and Cg0911 were determined, delivering the first available kinetic data for IMPase-like HolPases.
Additionally, we analyzed the amino acid sequences of potential HisN, ImpA, SuhB, CysQ and Cg0911 orthologs from bacteria and identified six conserved sequence motifs for each group of orthologs. Mutational studies confirmed the importance of a highly conserved aspartate residue accompanied by several aromatic amino acid residues present in motif 5 for HolPase activity. Several bacterial proteins containing all identified HolPase motifs, but showing only moderate sequence similarity to HisN from C. glutamicum, were experimentally confirmed as IMPase-like HolPases, demonstrating the value of the identified motifs. Based on the confirmed IMPase-like HolPases two profile Hidden Markov Models (HMMs) were build using an iterative approach. These HMMs allow the fast, reliable detection and differentiation of the two paralog groups from each other and other IMPases.
The kinetic data obtained for HisN from C. glutamicum, as an example for an IMPase-like HolPases, shows remarkable differences in enzyme properties as compared to HAD- or PHP-type HolPases. The six sequence motifs and the HMMs presented in this study can be used to reliably differentiate between IMPase-like HolPases and IMPase-like proteins with no such activity, with the potential to enhance current and future genome annotations. A phylogenetic analysis reveals that IMPase-like HolPases are not only present in Actinobacteria and plant but can be found in further bacterial phyla, including, among others, Proteobacteria, Chlorobi and Planctomycetes.
The gram-positive soil-bacterium Corynebacterium glutamicum, a member of the order Corynebacteriales within the taxonomical class Actinobacteria , plays an important role in industrial amino acid fermentation, with annual production scales of more than 2.5 and 1.5 million tons l-glutamate and l-lysine, respectively . Strains for the production of further amino acids including l-alanine, l-isoleucine, l-phenylalanine, l-serine, l-tryptophan, and l-valine are available . It is obvious that the in-depth understanding of the amino acid biosynthesis pathways and their regulation in this organism is necessary not only for further improvement of existing production strains, but also facilitates the development of new production strains, like for the production of l-histidine .
The entire l-histidine biosynthesis pathway is present in C. glutamicum and has been reviewed recently . So far, all organisms known to synthesize l-histidine, including archaea, bacteria, yeast, and plants, use the same pathway for the biosynthesis. Although there are differences in gene organization, including several gene fusion events, most of the enzymes seem to have a common ancestor [5, 6]. One interesting exception is the histidinol-phosphate phosphatase (HolPase) [EC 220.127.116.11] catalyzing the eighth step of l-histidine biosynthesis, the dephosphorylation of l-histidinol-phosphate (HolP) to l-histidinol. Three unrelated HolPase families are known so far. C. glutamicum possesses a HolPase belonging to the family of inositol monophosphatase (IMPase)-like proteins, a subgroup of the FIG (FBPase/IMPase/GlpX-like domain) superfamily encoded by hisN [7, 8]. IMPase-like HolPases are a characteristic of the Actinobacteria and genera possessing a HisN homolog can be found in almost all taxonomical orders of this bacterial class . Additionally, IMPase-like HolPases have been discovered in plants . Functional characterizations of IMPase-like HolPases have been conducted in C. glutamicum , Streptomyces coelicolor , and Arabidopsis thaliana . The HolPase activity of the HisN homolog in Mycobacterium tuberculosis (gene Rv3137) is supported at least indirectly, since it is not possible to delete this gene if a l-histidine free medium is used during the required selection steps .
Outside the Actinobacteria, there exist at least two further major classes of HolPases. The first class belongs to the HAD (Haloacid dehalogenase-like hydrolase) superfamily of proteins. The HAD-type HolPase activity is in general present on a bifunctional His(NB) enzyme that catalyzes the eighth and additionally the sixth step of l-histidine biosynthesis, the dehydration of imidazole glycerol-phosphate (IGP) . The two activities are independent of each other with the HolPase and IGP dehydratase activities being found in the N-terminal and C-terminal domain of the bifunctional protein, respectively . Bifunctional HAD-type HolPases are in general only found in Gammaproteobacteria , and have been extensively studied in Salmonella enterica serovar Typhimurium [14, 15] and Escherichia coli . A monofunctional HAD-type HolPase has been discovered in the archaeon Thermococcus onnurieneus few years ago and homologs can be found in further archaeal genomes . The second class of HolPases belongs to the PHP (polymerase and HolPase) subfamily of the metallo-dependent hydrolase (MDH) superfamily of proteins. The PHP-type HolPases are monofunctional and can be found in yeasts and in different bacterial lineages . Examples for organisms with a well-studied PHP-type HolPase are Saccharomyces cerevisiae [17, 18], Bacillus subtilis , and Lactococcus lactis .
Our special interest in the corynebacterial HolPase arises from the observation that deletion of hisN in C. glutamicum results in pronounced l-histidine bradytrophy instead of complete auxotrophy . A similar observation has been previously made with HolPase mutants of S. cerevisiae, resulting in the discovery of a second phosphatase with HolPase side activity . Four HisN paralogs are encoded in the genome of C. glutamicum (Cg0911, SuhB, ImpA, and CysQ) [7, 21] and are therefore interesting candidates for alternative HolPases. The present study pursued three different aims: 1) The identification of an alternative HolPase in C. glutamicum; 2) The determination of the kinetic parameters of HisN in C. glutamicum, since up to our knowledge no such data has been reported for any IMPase-like HolPase so far; 3) The identification of one or more sequence motifs to reliably discriminate between IMPase-like HolPases and other IMPase-like proteins with no such activity.
Genetic study on hisN and its four paralogs
During our previous investigation of different l-histidine gene deletion mutants of C. glutamicum , we observed that deletion of hisN, encoding the IMPase-like HolPase, does not result in l-histidine auxotrophy, but only in a pronounced bradytrophy of the mutant. Therefore, we started a closer investigation of the 8th step of l-histidine biosynthesis in C. glutamicum in general and the ΔhisN mutant in particular.
Growth of the ΔhisN mutant was visible after several days of incubation on minimal medium plates without l-histidine. Addition of l-histidine abolished the observed growth defect completely (Fig. 1). The residual growth of the ΔhisN mutant was not specific to one single mutant, but was observed with every confirmed hisN deletion mutant constructed during this study and was also confirmed for an independently constructed ΔhisN strain  that slightly differed in the extend of the hisN deletion (data not shown). The genome of C. glutamicum contains four genes encoding putative HisN paralogs that have been already recognized in the original publication describing the HolPase activity of the hisN gene product . All of them are grouped into the FIG superfamily of proteins according to their conserved domains and most of them are annotated as putative IMPases or fructose-1,6-bisphosphatases (Table 1). The degree of sequence similarity between HisN and one of its four putative paralogs is comparable in every case (24-26% identity, 37-41% similarity) with CysQ being least similar. In addition, all putative paralogs share the same degree of similarity if compared one to another. Since the four paralogs have so far not been analyzed for their function in C. glutamicum, we hypothesized that one of them might be responsible for the residual growth of the ΔhisN mutant.
Moreover, two of the putative hisN paralogs, namely cg0911 and impA, form operons with other l-histidine biosynthesis genes. The cg0911 gene is transcribed together with hisN and impA is part of the larger hisHA-impA-hisFI-cg2294 transcription unit .
In order to test if any of the four putative hisN paralogs encodes a gene with HolPase activity, the genes were cloned into the constitutive shuttle expression vector pZMP (approximately 15 copies per cell, tac promoter). Sequencing of the inserts revealed that the cg0911 gene sequence from the C. glutamicum wild type strain used in this study is identical to that presented in the C. glutamicum ATCC 13032 reference sequence BA000036.3  and has two single nucleotide polyphormisms as compared to reference sequence BX927147.1  (one silent mutation and one resulting in a G50R mutation). The resulting plasmids were isolated from E. coli and subsequently transferred into the C. glutamicum ΔhisN strain. Since it was not possible to obtain an error free impA insert in E. coli (i.e. frame shift or promoter mutations; data not shown) the pZMP::impA assembly mix was directly used for transformation of C. glutamicum ΔhisN resulting in the correct ΔhisN pZMP::impA mutant (checked by sequencing of the impA insert and the promoter region). A comparative growth test was conducted on minimal medium plates to check if one of the genes is able to complement the ΔhisN growth defect in trans (Fig. 1).
Expression of impA, suhB or cysQ did not improve the growth of the ΔhisN strain on minimal medium. Beside the complementation by hisN itself, a complementation of the ΔhisN growth defect was only observed with cg0911. However, growth of the ΔhisN pZMP::cg0911 strain was slower compared to the WT. Single colonies of this strain appeared 24 h later on the plates and remained smaller in size, even if the incubation was prolonged (data not shown). Supplementation with l-histidine resulted in the same growth phenotype of all tested mutants and did not differ from the WT. These results suggest that cg0911 is encoding an enzyme with weak HolPase activity.
To obtain further insight into the function of the different hisN paralogs, deletion mutants were constructed. Each paralog was separately deleted in the WT. In addition, a ΔhisN Δcg0911 double mutant and a quintuple mutant, lacking hisN and all its paralogs, were generated. Growth of the different mutants was again monitored on minimal medium plates (Fig. 2).
The single deletion of one of the hisN paralogs in the WT had no effect on growth of the mutants. Unexpectedly, we did not observe a further reduction of growth of the ΔhisN Δcg0911 double or the ΔhisN Δcg0911 ΔimpA ΔsuhB ΔcysQ quintuple mutant as compared to the ΔhisN single mutant. Supplementation with l-histidine resulted in the same growth of all mutants. None of the hisN paralogs was needed for normal growth of C. glutamicum under the tested conditions. Moreover, although the complementation assay clearly demonstrated HolPase activity of the cg0911 gene product in vivo if expressed on a multiple copy plasmid, this activity does not account for l-histidine biosynthesis in a measurable degree if present in single copy under control of the native promotor.
Enzymatic characterization of HisN and Cg0911
To the best of our knowledge, no kinetic data is available on the HolPase activity of HisN from C. glutamicum or any other organism possessing an IMPase-like HolPase. HolPase activity of the IMPase-like HolPases from A. thaliana and S. coelicolor has been deduced from complementation studies, and only the general phosphatase activity using the substrate para-nitrophenylphosphate (pNPP) has been demonstrated in vitro for the latter [9, 10]. Therefore, we determined the kinetic parameters of an IMPase-like HolPase with its natural substrate HolP using HisN Cg as an example and comparing it to the HolPase activity of Cg0911, the second IMPase-like protein in C. glutamicum possessing HolPase activity.
Both proteins were heterologously expressed in E. coli and purified tag-free using the commercial IMPACT™ system. Purity and molecular weight of the purified proteins were estimated by one-dimensional SDS-PAGE (Additional file 1: Figure S1) and identity was confirmed by MALDI-TOF-MS analysis (data not shown). The activity of HisN and Cg0911 was assayed by the release of inorganic phosphate (Pi) from HolP as described in Materials and Methods.
So far, all studied HolPases of the PHP- or HAD-type were shown to be dependent on divalent metal ions [13, 16, 20, 23]. The same holds true for eukaryotic and bacterial IMPases [11, 24, 25]. Therefore, in a first step, we evaluated the metal ion preference of HisN and Cg0911 as examples of IMPase-like HolPases (Fig. 3).
Both enzymes were inactive if metal ions were omitted from the reaction mixture. Presence of 10 mM EDTA also resulted in no activity (data not shown). In the presence of 5 mM Mg2+, Mn2+, or Co2+, release of Pi was detected. HisN showed a clear preference towards Mg2+ (100% activity) over Co2+ (20% activity) and Mn2+ (11% activity). The metal ion preference of Cg0911 was less pronounced. The enzyme still exhibited 78% of its maximal activity in the presence of Mn2+ and 47% in the presence of Co2+. No release of Pi from HolP was detectable in the presence of Zn2+, Cu2+, Ca2+, Fe2+, or Ni2+ with either enzyme.
Next, activity of HisN and Cg0911 was assayed in response to the pH of the reaction buffer (Fig. 4a). The buffering substances were adapted to the intended pH values. HisN exhibited maximal activity at pH 7.35. HisN activity decreases almost uniformly beyond the optimal pH, with no activity present at around pH 6 and reduced to 10% at around pH 10. The pH profile of Cg0911 was shifted to the alkaline conditions by 0.5 to 1 pH units. Maximal Cg0911 activity was observed at around pH 8 and was only little reduced at pH 7.35, followed by a sharp loss in activity towards more acidic conditions. The drop in activity towards more alkaline conditions was less pronounced and the enzyme exhibited still 30% of its activity at around pH 10. Since both HisN and Cg0911 were highly active at pH = 7.35, and this pH value corresponded well to the internal pH value of 7.5 ± 0.5 in C. glutamicum , a pH of 7.35 was kept constant during all further measurements.
The activity of HisN and Cg0911 was determined in a temperature range from 20 to 50 °C (Fig. 4b). Maximal HisN activity was reached at 35–40 °C. No activity was observed at 50 °C, indicating heat denaturation of the protein. The HolPase activity of Cg0911 was even more heat sensitive. Maximal Cg0911 activity was reached at 30 °C and less than 5% of this activity remained at 40 °C. To retain comparability between the two enzymes, all following measurements were conducted at 30 °C, since both enzymes were active at this temperature and it reflects the optimal growth temperature of C. glutamicum.
The turnover number (kcat) of HisN and Cg0911 in the presence of Mg2+, as well as the HolP and Mg2+-concentrations necessary for half maximal enzyme activity (Km values for HolP and Mg2+) were determined (Table 2). The parameters were obtained by non-linear curve fitting of the data points to the Hill-equation .
HisN was very specific towards HolP with a Km value of about 25 μM. The kcat value was around 1 s−1 resulting in a catalytic efficiency of the enzyme of 4.41 × 104 s−1 M-1. The Hill coefficient of HisN regarding HolP was around 1.5 indicating only a little cooperative effect.
The HolPase activity of Cg0911 was almost 80-times lower compared to HisN and the Km value for HolP was around 650 μM, resulting in a catalytic efficiency of 1.98 × 101 s−1 M−1. The Hill coefficient of around 1.8 hints to some cooperative effect of HolP on Cg0911 HolPase activity. The kinetic parameters for Cg0911 indicate that HolP is not the preferred substrate of this protein and the ability to hydrolyze HolP might reflect only a side activity of the enzyme.
We also tested the affinity of the two enzymes towards bivalent magnesium ions. The Km values for Mg2+ were about 650 μM and 5000 μM for HisN and Cg0911, respectively. They were about 30-times and 10-times higher compared to the Km values for HolP, respectively. The Hill coefficients regarding Mg2+ were around 2.4 for HisN and around 3.0 for Cg0911, indicating pronounced cooperativity of both enzymes in respect to the metal ion. This assumption is reinforced by the observation that no HisN or Cg0911 activity was measurable at Mg2+ concentrations ≤ 100 μM or ≤ 625 μM, respectively (data not shown).
Neither HisN nor Cg0911 showed any phosphatase activity against the general phosphatase substrate para-nitrophenyl phosphate (data not shown). The ability to hydrolyze other natural phosphatase substrates was not tested.
Finally, the potential inhibition of HisN and Cg0911 by l-histidine or the two direct reaction products l-histidinol and Pi was examined. No inhibitory effect of l-histidine was observed with concentrations up to 60 mM l-histidine (data not shown). A different effect of the addition of Pi and l-histidinol to the reaction mixture was observed for HisN and Cg0911. While HisN was not inhibited by Pi up to a concentration of 250 μM (higher concentrations were not tested for HisN), activity of Cg0911 decreased to 40% at 375 μM Pi (Fig. 4c). Unfortunately, it was not possible to test the effect of higher Pi concentrations, since the addition of external Pi interferes with the detection of Pi released during hydrolysis of HolP. It cannot be excluded, that HisN is inhibited by Pi concentrations > 250 μM.
HolPase activity of HisN was also not affected by the presence of l-histidinol (Fig. 4d). The enzyme was fully active up to 20 mM l-histidinol. The slight reduction to 80% activity at 40 mM most likely reflects a pH artifact, since HisN activity is optimal at pH 7.35 and rising l-histidinol concentrations cause a drop in pH even in 1 M TEA buffer (pH 7.5 and pH 7.0 at 0 mM and 200 mM l-histidinol, respectively; estimated with pH indicator stripes at RT).
Surprisingly, we observed a stimulating effect of l-histidinol on the HolPase activity of Cg0911. The activity increased almost five-fold at l-histidinol concentrations ≥ 10 mM. Half maximal stimulation was reached at 0.86 ± 0.06 mM l-histidinol. Since no release of Pi was detectable if the substrate HolP was omitted from the assay (data not shown), any contamination of the l-histidinol reagent with Pi or other phosphorous substances can be excluded. It appears therefore, that Cg0911 is positively feedback regulated by l-histidinol.
Identification of sequence motifs for the discrimination of IMPase-like HolPases from other IMPase-like proteins in C. glutamicum and other bacteria
The presence of several IMPase-like proteins in one species (e.g. five in C. glutamicum) complicates the discrimination between an IMPase-like HolPase and IMPase-like proteins with different substrate specificities. Within the class Actinobacteria, it is rather easy to identify the HolPases due to a much higher sequence similarity to HisN Cg than to the other IMPase-like proteins. However, this becomes more difficult in other bacterial phyla or even in different kingdoms. Therefore, we were interested in the identification of amino acid motifs that allow the unambiguous discrimination of IMPase-like HolPases purely based on the protein sequence.
For each of the five IMPase-like proteins in C. glutamicum (HisN, Cg0911, SuhB, ImpA, and CysQ) we performed a multiple sequence alignment of potential orthologs from a wide range of bacteria to identify highly conserved amino acid residues. The comparison of the highly conserved residues in each group of orthologs allowed the determination of six amino acid motifs distributed over the entire protein sequence that can be used for the discrimination of HisN orthologs from other IMPase-like proteins. Orthologs were identified by a BlastP search using the respective protein sequence from C. glutamicum as query. A BlastP score ≥ 125 was set as cut-off for identification. This cut-off was chosen, because it was sufficient to reliably distinguish between HisN and the other IMPase-like proteins in C. glutamicum, M. tuberculosis, and S. coelicolor (data not shown). With very few exceptions, maximum one (HisN, SuhB, and CysQ) or three sequences (Cg0911 and ImpA) per genus were randomly chosen for the multiple sequence alignment (see Additional file 2 for a complete list of used sequences).
Since we were most interested in motifs for the identification of IMPase-like HolPase, only the HisN motifs will be described in detail below.
Motif 1 consist of a strictly conserved lysine (Lys36), a highly conserved aspartate (Asp38), a threonine or serine at position 40, followed by a highly conserved proline (Pro41), a strictly conserved valine (Val42) and threonine or serine at position 43. An aspartate at position 46 is strictly conserved in all analyzed IMPase-like proteins and can be used for positioning of motif 1. Interestingly, motif 1 is completely absent in some of the HisN orthologs (11 out of 147 analyzed sequences mostly from Alpha- or Gammaproteobacteria). However, a different conserved motif is present in these cases consisting of lysine at position 34 or 35, an aromatic amino acid at position 40 and aspartate at position 41 followed by valine (Val42) and threonine (Thr43) (not shown).
Motif 2 consist of a highly conserved glycine (Gly68) followed by two strictly conserved glutamate residues (Glu69 and Glu70). Motif 2 is very similar in all analyzed groups of orthologs, with the exception of CysQ, where the conserved glycine is replaced by a strictly conserved serine (Ser64) and preceded by a highly conserved leucine (Leu63). Therefore, motif 2 is most suitable for the discrimination of HisN homologs from CysQ orthologs.
Motif 3 contains four of the active site key residues typical of all IMPase-like proteins (HisN Cg : Asp85, Ile87, Asp88, and Thr90) [28, 29]. But not only these four residues are strongly conserved in HisN and the other IMPase-like proteins, but all residues ranging from positions 82 to 90. Therefore motif 3 is most suited for the identification of IMPase-like proteins in general. Striking differences between the different ortholog-groups within motif 3 appear only at position 91. There is a preference for a lysine at this position in HisN orthologs.
A highly conserved motif 4 is only present in CysQ orthologs. However, there exists a motif 4 in HisN orthologs, too. It consist of a moderately conserved arginine (Arg95), a strongly conserved glycine (Gly96) and proline (Pro98), followed by an aromatic amino acid at position 100, a strongly conserved threonine (Thr102) and a strongly conserved leucine (Leu103). Especially the combination of the aromatic amino acid at position 100 followed by Thr102 and Leu103 is very typical of HisN orthologs.
Motif 5 is the most characteristic motif of HisN orthologs. It consists of a highly conserved arginine (Arg187; replaced by Val or Leu in many alphaproteobacteria), a highly conserved glycine (Gly190) and an almost strictly conserved aspartate (Asp191). Only in some sequences of Gammaproteobacteria Asp191 is replaced with glutamate. Neither aspartate nor glutamate was found at this position in any other of the analyzed IMPase-like protein sequences. Moreover, several aromatic amino acids are present in motif 5 of HisN orthologs. One of these aromatic amino acids is present at position 188 or more likely 189, with the respective other position being occupied by a small residue (mostly glycine or alanine). Two more aromatic residues are usually present at position 193 and 195. Especially in actinobacterial HisN orthologs, there is also an additional aromatic amino acid at position 192. Whereas usually only phenylalanine, tyrosine or tryptophan residues are present at positions 188, 189, 192 and 193 the aromatic amino acid histidine might be present at position 195. No aromatic amino acids are present at the positions 192–195 in the corresponding motifs of the other IMPase-like proteins. Therefore, this motif is very specific for HisN orthologs. Next to the already described characteristics, the HisN-specific motif 5 is lacking a highly conserved aspartate followed by a leucine residue that are present in Cg0911, SuhB and ImpA orthologs (Asp203 and Leu204 in SuhB Cg ). A specific motif 5 can also be identified in the other analyzed groups of IMPase-like proteins. Two consecutive arginine residues (Arg195 and Arg196 in SuhB Cg ), followed by the sequence GSAAL, are very typical of SuhB orthologs. On the other hand, two arginine residues interspaced by a non-conserved amino acid (Arg179 and Arg181 in ImpA Cg ) are very typical of ImpA orthologs.
The last motif, motif 6, is very similar in all analyzed IMPase-like ortholog groups. It contains the strictly conserved aspartate residue (Asp215) involved in coordination of the metal ions in the active site [28, 29]. Most interesting for discrimination between HisN and the other groups is position 219. Whereas a very highly conserved glycine (Cg0911, SuhB or ImpA) or a proline (CysQ) is usually present at this position in the other groups of orthologs, no glycine was present at position 219 in any of the analyzed HisN orthologs.
Although we included only sequences of bacterial IMPase-like HolPases in our motif search, all six identified HolPase motifs can also be found in the protein sequence of HISN7 from the plant A. thaliana (Additional file 1: Figure S2). HISN7 At has been previously experimentally confirmed as IMPase-like HolPase , despite its low overall sequence similarity to HisN Cg (24% identity, 36% similarity, BlastP-score: 103 bits).
Identification of IMPase-like HolPases based on the described sequence motifs and experimental validation of HolPase activity by complementation experiments
In order to prove the value of the identified HolPase motifs, different potential HisN orthologs were tested for their ability to complement a C. glutamicum ΔhisN strain, thus demonstrating HolPase activity of the respective gene products (Table 3). The potential HolPase genes from the actinobacterium Dietzia sp. strain Chol2 (genome announcement in preparation; preliminary locus tag Dietzia_sp.-Draft_1801, here referred to as hisN Dz ) and the alphaproteobacterium Zymomonas mobilis ZM4 (; locus tag ZMO_RS06805, here referred to as hisN Zm ) were chosen, because the HolPase motifs are conserved in the respective gene products despite a relatively low overall sequence similarity to HisN Cg .
In addition, we investigated potential HisN orthologs from Actinoplanes utahensis NRRL 12052 . This actinobacterium possesses two genes encoding IMPase-like proteins that are most similar to HisN Cg . The first gene product (locus tag MB27_13025, referred to as HisN Au ) is characterized by a high sequence similarity to HisN Cg and the presence of all six HolPase motifs. The second gene product (locus tag KHD72131.1, for convenience reasons referred to as HisN2 Au ) is also more similar to HisN Cg then to another IMPase-like proteins in C. glutamicum and five of the six identified motifs are at least moderately conserved. However, motif 5 is absent in this protein (Table 3, Additional file 1: Figure S3).
The above described genes were cloned into the constitutive pZMP vector and tested for their ability to complement the l-histidine bradytrophic growth phenotype of the C. glutamicum ΔhisN mutant. As expected, hisN Dz , hisN Zm , and hisN Au were able to fully complement the C. glutamicum ΔhisN mutant (data not shown). In contrast, the expression of hisN2 Au failed to complement the C. glutamicum ΔhisN mutant, even though the overall similarity of the gene product to HisN Cg is higher than that of HisN Dz and HisN Zm . These results underline the importance of the motif 5 (Fig. 5) for HolPase activity of IMPase-like proteins.
Our continuing analyses revealed that many IMPase-like proteins within NCBI’s non-redundant protein database are either not classified in more detail (mostly only as IMPases or IMPase-like proteins) or are even wrongly classified. Some examples of misclassified IMPases are given in Table 4. By comparing the amino acid sequence of these IMPase-like proteins to the five IMPase-like proteins in C. glutamicum and by checking for the presence of the expected motifs, we were able to assign a more accurate function to these proteins.
This list demonstrates that many IMPase-like HolPases are not recognized as such in the databases (class 1). By checking for the presence of the HolPase motifs it is possible to accurately classify even those HisN homologs that show only a moderate overall similarity to HisN Cg (BlastP score < 125 bits). On the other hand, there are also many examples of IMPase-like proteins that have been wrongly annotated as HolPases. Two classes can be distinguished here. The first class (class 2) consists of proteins which indeed are most similar to HisN Cg , however the overall sequence similarity is rather low (BlastP scores usually < 125 bits). Most importantly, HolPase motif 5 is missing in these proteins. Next to the two examples given in Table 4, HisN2 Au (Table 3) also belongs to this class 2 of misclassified proteins. Since hisN2 Au was unable to complement the C. glutamicum ΔhisN strain, all HisN homologs belonging to class 2 most likely do not exhibit HolPase activity. Their substrate specificity remains to be elucidated. The second class of wrongly annotated HolPases (class 3) includes sequences which have been simply misclassified. They exhibit a comparably low sequence similarity to HisN Cg (BlastP scores usually < 100 bits), are indeed more similar to SuhB Cg , and possess the motifs typical of SuhB orthologs.
Survey of the crystal structure of HisN Zm focusing on the conserved HolPase motifs
To get a better understanding of the putative function of some of the conserved residues within the six detected HolPase motifs, we had a closer look on the IMPase-like HolPase from Z. mobilis (HisN Zm ). HisN Zm is only moderately similar to HisN Cg but all HolPase motifs are present (Additional file 1: Figure S2) and we were able to experimentally verify its HolPase activity (see above). The crystal structure of this protein has been solved recently by Hwang et al. in 2014. Up to date, it represents the only solved crystal structure of an IMPase-like HolPase. There is evidence from the crystal structure as well as from gel filtration experiments that native HisN Zm is a homodimer . Notably, Hwang et al. did not recognize HisN Zm , which they refer to as CbbF, being a HolPase. The protein has been crystallized by Hwang and coworkers in its apo form without metal ions, which are needed for enzymatic activity, or any substrate . However, the crystal structure contains a sulfate ion at the position which most likely resembles the binding site of the substrate’s phosphate group .
We examined the localization of the highly conserved residues of the six HolPase motifs in the HisN Zm crystal structure and investigated their putative interactions with other residues. Fig. 6 shows a part of the HisN Zm homodimer, centered on one of the two identical supposed active sites depicted as space-filling model (a) and as ribbon diagram with stick representation of selected residues (b).
Many of the highly conserved residues within the HolPase motifs are located close to the active center as indicated by the location of the sulfate ion. This sulfate ion is forming hydrogen bonds with Asp86, Asp89, Gly90, Thr91 (corresponding to position 85, 88, 89 and 90 of the HisN-specific motif 3; Fig. 5) and Asp210 (motif 6; position 215). A part of these residues, as well as Ile88 (motif 3; position 87) and Glu70 (motif 2; position 69), are supposed to be involved in coordination of three catalytic Mg2+ ions according to the known structures of different IMPases [28, 29].
The side chains of most of the highly conserved residues of motif 1 (Lys37, Asp39, Ser41, Val43 and Thr44; corresponding to positions 36, 38, 40, 42, and 43 in Fig. 5) point to the side of the enzyme where the active site is located. This part of the enzyme (residues 29–41) has been recognized as a mobile catalytic loop in different IMPases-like proteins which changes its spatial position in response to binding of metal ions or the substrate . Therefore, these residues might play a crucial role in recognition of the substrate HolP.
Several of the conserved aromatic amino acids within the different motifs seem to play an important role for the formation of the tertiary and quaternary structure of HisN Zm and IMPase-like HolPases in general. For example, Phe94, corresponding to the conserved aromatic amino acid at position 93 in the HisN-specific motif 3 (Fig. 5), has hydrophobic interactions with nine other amino acids (including residues from the motifs 1, 3 and 4). Two of these interactions are additionally stabilized by aromatic-aromatic interactions. All these interactions connect the α-helices 1, 2, and 3 with the active site key residue Ile88 and thereby contribute to the formation of the active site. A similar structural function might be attributed to some of the conserved branched chain amino acids. Leu214, for instance, which is very typical of IMPase-like HolPases (motif 6, position 219), has hydrophobic interactions with the likewise conserved Leu103 (motif 4, position 103) and three additional residues. One of the residues interacting with Leu214 is Tyr190, one of the aromatic amino acids highly conserved within motif 5 of IMPase-like HolPases (motif 5, position 195). Therefore, this aromatic amino acid might primarily have a structural function. However, Tyr190 is the only of the typically three conserved aromatic amino acids within motif 5 that is at least partially exposed to the surface and located close to the supposed substrate binding site (Fig. 6a). It is therefore possible that Tyr190 is additionally involved in substrate recognition, possibly by aromatic interaction with the likewise aromatic substrate HolP. The two other highly conserved aromatic amino acids within motif 5 of IMPase-like HolPases correspond to Tyr188 (motif 5, position 193) and Leu183 (motif 5, position 188) in HisN Zm . The side chains of both residues are located on the “back side” of the enzyme and distant from the active site. Leu183 is interacting with several other hydrophobic amino acids from the second subunit of the HisN Zm homodimer (among others with Leu183 itself). Tyr188 has some intramolecular hydrophobic and aromatic interactions stabilizing the tertiary structure, but it additionally forms a hydrogen bond with Arg29 from the second subunit. An important role of Leu183 and Tyr188 might therefore be the stabilization of the quaternary structure of the HisN Zm homodimer.
Most important, the analysis of the HisN Zm crystal structure suggest a direct involvement of Asp186 (motif 5, position 191) in substrate recognition. The Asp186 side chain is accessible to the solvent, points towards the supposed substrate binding site (Fig. 6a), and there is no indication that the carboxylic group is involved in the formation of any H-bonds or salt bridges. Consequently, Asp186 would be available for interaction with the substrate HolP, for instance by the formation of H-bonds between the amino group of HolP and the carboxylic group of the aspartate. This is in good agreement with our observation that replacement of the conserved Asp191 in HisN Cg with alanine, serine, or asparagine, but not glutamate, results in a considerably reduced ability of the gene products to complement a hisN deletion in C. glutamicum (Additional file 1: Figure S4). However, since there is no crystal structure available of any IMPase-like HolPase in complex with catalytic metal ions and the substrate HolP or at least the products l-histidinol or Pi, any interaction between HolP and Asp186 (and possibly Tyr190) remains speculative.
Distribution of HisN and Cg0911 orthologs within bacteria
The presence of an IMPase-like HolPases has so far only been experimentally proven in C. glutamicum and S. coelicolor [7, 10], but there is evidence, that this type of HolPase is a general feature of the Actinobacteria . According to this assumption, we were able to prove the in vivo HolPase activity of HisN homologs in the actinobacterial genera Actinoplanes and Dietzia in the present study. However, the recent identification of the IMPase-like HolPase in the plant Arabidopsis thaliana , the results of our extensive Blast-analysis in order to identify the HolPase motifs, and finally our experimental confirmation of a functional IMPase-like HolPase in the alphaproteobacterium Z. mobilis suggests that this type of HolPases might be more widespread than initially assumed. Therefore, we systematically examined the distribution of HisN orthologs within the bacterial kingdom and additionally extended the analysis to Cg0911 orthologs. The results are depicted in Fig. 7.
In this analysis, HisN and Cg0911 homologs were identified by a protein Blast search (BlastP) within NCBI’s non-redundant protein sequences database. A BlastP score ≥ 125 was set as cut-off for identification. This cut-off was chosen, because it was sufficient to reliably distinguish between HisN, Cg0911, and the other IMPase-like homologs ImpA, SuhB, and CysQ in C. glutamicum, M. tuberculosis, and S. coelicolor (data not shown). In addition, all putative HisN orthologs were checked for the presence of the HisN-specific motif 5. A HisN or Cg0911 ortholog was regarded a general feature of the genus if it was present in at least one species belonging to this genus. It was regarded a general feature of the family, if it was present in at least three or half of all genera, and the same criteria applied to the higher taxonomic levels.
According to this analysis, HisN orthologs are a general feature of all orders of the class Actinobacteria (BlastP scores > 250 bits). The only exception are the Kineosporiales, however this is most likely attributed to the lack of sequence data for some of the genera. Indeed, HisN orthologs are present in Kineococcus and Angustibacter. HisN orthologs with an unusually low similarity to HisN Cg within the class Actinobacteria are present within the Dietziaceae (BlastP scores ≤ 108 bits). However, despite the overall low sequence similarity we could identify all HolPase motifs (alternative motif 1) in all potential HisN orthologs within Dietziaceae. Additionally we proved the in vivo HolPase activity of the HisN homolog from Dietzia sp. strain Chol2 (see above). A BlastP query revealed highest sequence similarity of these HisN orthologs to HisN orthologs from different species of the order Rhizobiales (max. BlastP score: 210 bits), indicating a recent horizontal gene transfer event.
Although widely distributed within the class Actinobacteria, HisN orthologs are not generally present in all classes of the phylum Actinobacteria. They can be identified in Acidimicrobiia (genus Ilumatobacter; max. BlastP score: 179 bits), Nitriliruptoria (genus Nitriliruptor; max. BlastP score: 174 bits), and Rubrobacteria (genus Rubrobacter, max. BlastP score: 123 bits), however with considerably lower BlastP scores as compared to the class Actinobacteria. In contrast, no HisN orthologs were identified in the classes Coriobacteriia and Thermoleophilia, despite the availability of complete genome sequences.
IMPase-like HolPases were also identified outside the phylum Actinobacteria. The presence of HisN orthologs seems to be a general feature of the phyla Chlorobi (green sulfur bacteria), Fibrobacteres (cellulose-degrading bacteria), and Nitrospinae (marine nitrite oxidizing bacteria). It is also generally found in the class Chloroflexia within the phylum Chloroflexi (green non-sulfur bacteria) and the class Planctomycetia within the phylum Planctomycetes (aquatic bacteria). The HisN orthologs from Planctomycetaceae exhibit particularly high similarity to HisN Cg (BlastP scores: 162–194 bits). HisN orthologs were also identified in some members of the family Chitinophagaceae, phylum Bacteroidetes, and the order Spirochaetales, phylum Spirochaetes.
We also identified HisN orthologs within the phylum Proteobacteria, with the exception of Epsilonproteobacteria. They are generally present in the alphaproteobacterial order Rhizobiales, in the deltaproteobacterial order Myxococcales, and in the betaproteobacterial family Burkholderiaceae. Interestingly, HisN orthologs are also present in many Gammaproteobacteria, which are known for the presence of a bifunctional HAD-type HolPase . Five families with a general occurrence of HisN orthologs were observed. In three of them, the Thiotrichaceae, Sinobacteraceae, and Ectothiorhodospiracea, our analysis did not reveal the additional presence of a bifunctional HAD-type HolPase. In the other two, Enterobacteriaceae and Xanthomonadaceae, a bifunctional His(NB) homolog was identified in all genera with a putative HisN ortholog. However, in the case of Enterobacteriaceae, HisN orthologs are present in less than 15% of all genera listed in NCBI taxonomy (11 of 76, including “candidatus” genera). No HisN orthologs were identified in Escherichia and Salmonella, two genera from Enterobacteriaceae with a well characterized HAD-type HolPase [13,14,15].
Within the phylum Firmicutes, HisN orthologs were only identified in two single species, namely Bacillus sp. EGD-AK10 (draft; AVPM00000000.1) and Dehalobacter sp. FTH1 (draft; AQYY00000000.1). This might be attributed to a recent horizontal gene transfer, according to sequence similarity most likely from an actinobacterial species from the orders Micrococcales and Propionibacteriales, respectively. Apart from that, no HisN orthologs were identified in any other member of the Firmicutes, which is in accordance with the supposed presence of a PHP-type HolPase in this phylum , which was positively spot-checked during our analysis using the HisJ protein sequence of B. subtilis.
Unlike the HisN orthologs, which are spread throughout various bacterial phyla, Cg0911 orthologs are restricted to a few actinobacterial genera (Fig. 7). They can be generally found in the families Corynebacteriaceae, both in Corynebacterium and Turicella, Dietziaceae, Nakamurellaceae, Micrococcaceae, and Intersporangiaceae, but their presence is not restricted to these families. Interestingly, only a Cg0911 but not a HisN ortholog was identified in Kytococcus for which at least one complete genome is available (CP001686.1). In those species that contain both orthologs and where genome data was available (finished and draft genomes), we checked for the gene organization. In C. glutamicum the cg0911 gene is directly followed by hisN and the two genes form an operon . The same organization in such a cg0911-hisN homolog tandem was also found in almost all other available Corynebacterium genomes with very few exceptions (data not shown). The cg0911-hisN homolog tandem was also present in Turicella otitidis (draft; CAJZ00000000.1), however not in any other genus possessing both homologs, and can be therefore considered a characteristic of Corynebacteriaceae only.
In order to validate the BlastP results, the tool jackhmmer was used to create and refine HMMs based on all functionally validated orthologs of HisN (HisN Cg , HisN Au , HisN Dz , and HisN Zm ) respectively Cg0911 Cg using a E-value cutoff of 1e-65. In both cases the results corroborate the BlastP results. In addition, the searches with the HisN HMM revealed HisN to be generally present in the alphaproteobacterial orders Rhodobacterales, Rhodospirillales, Caulobacterales, and Sphingomonadales. Additionally, HisN orthologs were identified in several species within the phyla Cyanobacteria and Verrucomicrobia. While below the BlastP cutoff, motif 5 (as well as the others) was found to be present in 1687 out of 1695 sequences identified by the HMM, with the exeption of several sequences from "Candidatus Curtissbacterium" species and a few others (close to the gathering threshold). The HMMs obtained after the final iteration can be found in Additional file 3 (HisN) and Additional file 4 (Cg0911) and can be used for an easy classification of these two groups in the future.
Of the four genes encoding HisN paralogs within the genome of C. glutamicum (namely cg0911, impA, suhB, and cysQ) only cg0911 is capable of at least partially complementing the growth defect of the ΔhisN strain in l-histidine free medium in vivo. The results with the purified Cg0911 enzyme confirmed its HolPase activity also in vitro. However, the very low catalytic efficiency kcat/Km of only 1.98 × 101 s−1 M−1 indicates, that the HolPase activity of Cg0911 might represent only a side activity of this enzyme. The actual substrate of Cg0911 remains to be elucidated. Known substrates of other IMPase-like proteins are, e.g., inositol-1-P, inositol-2-P, inositol-3-P, glucitol-6-P, glycerol-2-P, 2’-AMP, and l-galactose-1-phosphate [25, 34, 35].
Particular surprising was the fact that impA does not encode a protein with HolPase activity. This gene is part of an operon with other l-histidine biosynthesis genes in C. glutamicum  and a similar gene arrangement is also observed in many other species of different genera including Corynebacterium, Dietzia, Gordonia, Mycobacterium, and Nocardia (data not shown). The substrate of ImpA remains to be elucidated, but its involvement in mycobacterial cell wall biosynthesis is discussed .
The concurrent deletion of hisN and all its four paralogs in the C. glutamicum quintuple mutant demonstrates two things: Firstly, the absence of all five IMPase-like proteins does not result in complete l-histidine auxotrophy. Thus, at least one additional protein with HolPase activity must exist in C. glutamicum. Such an alternative non-IMPase-like HolPase has been identified in S. coelicolor , however a homolog is not present in C. glutamicum (data not shown). A HolPase side activity has been demonstrated for alkaline phosphatases in S. cerevisiae  and Neurospora crassa  and has also been reported in E. coli . Such a side activity might also be present in C. glutamicum. Eventually, one should also consider the possibility of non-enzymatic dephosphorylation of HolP within the cell.
Secondly, the activity of all this five IMPase-like proteins is totally dispensable for growth of C. glutamicum on minimal medium under the tested conditions. IMPases are thought to synthesize myo-inositol from IMP. Myo-inositol is supposed to be mainly used for the synthesis of the coryne- and mycobacterial cell envelope phospholipids phosphatidylinositol and phosphatidylinositol dimannoside [11, 36, 39,40,41]. The results of the C. glutamicum quintuple mutant suggest that the two phospholipids mentioned above are dispensable for C. glutamicum or that myo-inositol synthesis is carried out by a yet unknown enzyme. The IMPase-like proteins might be additionally involved in other reactions than the synthesis of myo-inositol. A high in vitro activity with the substrates sorbitol-6-phosphate, next to IMP itself, has been demonstrated for SuhB from M. tuberculosis . CysQ from M. tuberculosis exhibits a more than tenfold higher turnover number with the substrate 3′-phosphoadenosine-5′-phosphate (PAP) as compared to IMP and accepts also 3'-phosphoadenoside-5'-phosphosulfate (PAPS) as a substrate . Therefore, it has been suggested that CysQ primarily functions as regulator of the sulfur assimilation in M. tuberculosis . Based on high sequence similarity of CysQ Mt to CysQ Cg (47% identity, 58% similarity) the same enzyme function can be assumed. However, since C. glutamicum uses a PAPS independent sulfur assimilation route , the function of CysQ Cg remains uncertain.
Our results with the purified HisN prove the in vitro HolPase activity of an IMPase-like HolPase (Table 2) for the first time. The catalytic efficiency kcat/Km of 4.41 × 104 s−1 M−1 is four orders of magnitude lower compared to that of the HAD-type HolPase from E. coli  or T. onnurineus , but it is in good agreement with the values of several PHP-type HolPases . The kcat of HisN fits very well to the kcat reported for HisG Cg , the ATP-PR transferase catalyzing the first step of l-histidine biosynthesis in C. glutamicum , demonstrating an equal catalytic rate for at least two of the nine enzymes involved in l-histidine biosynthesis.
The low kcat of HisN Cg , especially as compared to that of the HolPase from E. coli, might be partially compensated for by the high affinity of the enzyme to its substrate. The Km-value of HisN Cg for HolP of only roughly 25 μM is the lowest value reported for any HolPase so far. The absence of inhibition of HisN Cg by l-histidine and l-histidinol reflects another strategy to deal with the low turnover number. A resistance to inhibition by l-histidine and l-histidinol can also by observed with the PHP-type HolPase of S. cerevisiae (Ki for l-histidinol: 5–10 mM ), which, based on kinetic data of other PHP-type HolPases , have a rather low kcat. HAD-type HolPases on the other hand exhibit a high kcat and are strongly inhibited by these two substances (e.g. Ki for l-histidinol = 52 μM in S. enterica) . HisN Cg is also not inhibited by Pi at least not up to a concentration of 250 μM Pi (a concentration that cannot be easily exceeded with the applied HolPase activity assay). However it was demonstrated for the HAD-type HolPase from S. enterica that it is not affected by Pi up to a concentration of 25 mM Pi .
Both HisN Cg and Cg0911 are strictly dependent on addition of bivalent metal ions to the reaction buffer for HolPase activity, with Mg2+ being the preferred ion and reduced activity with Mn2+ and Co2+ (Fig. 3). This is in accordance with results from a general study on IMPases in Mycobacterium smegmatis. This study demonstrated that IMPase activity is maximal with Mg2+, is inhibited by Zn2+ , and about 25% of activity can be obtained with Mn2+ . The need for metal ion addition to the in vitro assay has also been observed for HAD-type HolPases that exhibit a binuclear metal cluster in the active center [13, 16]. In contrast to HisN Cg and Cg0911, some HAD-type HolPases are also active with Zn2+, Cu2+ or Ni2+ [13, 16]. Interestingly, PHP-type HolPases, although exhibiting a trinuclear metal cluster in the active center, do not rely on addition of external metal ions for activity [20, 23]. This suggests a very tight binding of the metal ions in the metal cluster, resulting in a retention during the protein purification process. In contrast, binding of metal ions in the active site of HAD-type and IMPase-like HolPases seems to be much weaker, resulting in the need of metal ion addition after the protein purification process. This weak binding is supported by the relatively high Km values of Mg2+ for HisN and Cg0911 (Table 2) and actinobacterial IMPases in general .
The tertiary structure of IMPase-like HolPases, as shown using the example of HisN Zm , is very similar to that of various mammalian IMPases (data not shown) including the IMPases of Homo sapiens  and Bos taurus . Three Mg2+ ions have been identified in the active site of these two intensively investigated proteins coordinated by five highly conserved amino acid residues [24, 28, 29]. These five residues are conserved in HisN Zm , HisN Cg , and all analyzed HisN orthologs. It is therefore very likely that the proposed three-metal mechanism for hydrolysis of inositol monophosphate in eukaryotic IMPases might be also employed for hydrolysis of HolP in IMPase-like HolPases. In that case, binding of the second Mg2+ ion would be cooperative , fitting well to the determined Hill-coefficients of 2.5-3 that indicate a cooperative effect of Mg2+ on the HolPase activity of HisN Cg and Cg0911.
The optimal pH for the HolPase activity of HisN Cg (pH ~7.5) and Cg0911 (pH ~8) reflects the internal pH of C. glutamicum (7.5 ± 0.5 ). The unusually high optimal pH for HisG activity of around 10  is therefore no general attribute of enzymes involved in l-histidine biosynthesis in C. glutamicum. Moreover, the pH optima of Cg0911 and HisN Cg differ significantly from the pH optima of HAD- or PHP-type HolPases. HolPases of the PHP-family are most active at pH 8.5-9 [18, 20]. In contrast, HolPases from the HAD-family exhibit their maximal activity at a slightly acidic pH [14, 16].
Overall, there are significant differences in regard to Km-values, turnover numbers, inhibition behavior, metal ion preference and pH-optima between HisN Cg (as one example of an IMPase-like HolPase) and HolPases of the HAD- or PHP-type. Therefore, IMPase-like HolPases do not only differ in protein sequence and tertiary structure from the two other HolPase families, but their differing enzymatic properties might reflect an adaptation to their host organism.
There are also interesting differences in some aspects of HolPase activity between HisN Cg and Cg0911. Next to the very obvious differences in kcat and Km, the two enzymes also differ in their pH and temperature profiles. The HolPase activity of Cg0911 does not account significantly for the in vivo l-histidine biosynthesis in C. glutamicum under the tested conditions. However, since the catalytic properties of HisN Cg and Cg0911 are not identical, their might exist some growth conditions, where the HolPase activity of Cg0911 becomes relevant for the cell, for instance under alkaline stress conditions.
The most interesting observation concerning Cg0911 is the almost five-fold stimulation of HolPase activity by l-histidinol. This kind of a positive feedback by the direct reaction product on enzyme activity has been recently described for the RelA protein of E. coli, which synthesizes guanosine tetraphosphate (ppGpp) during the stringent response and is activated by ppGpp via positive allosteric feedback regulation .
The analysis of 165 potential bacterial HisN orthologs resulted in the formulation of six sequence motifs (Fig. 5) that can be used for the discrimination of IMPase-like HolPases from other IMPase-like proteins. This is of special interest, since there exist several IMPase-like protein families in bacteria (five are present in C. glutamicum) and there are substantial differences in their substrate specificity. The preferred substrates of the ImpA and Cg0911 orthologs still remain to be elucidated. However, at least in Actinobacteria, IMP is supposed to be the main substrate of SuhB orthologs , PAP and PAPS that of CysQ orthologs  and HolP that of HisN orthologs. The different substrate specificities illustrate that each of these IMPase-like proteins is involved in very different metabolic processes and underlines the need to clearly distinguish between the different paralogs. The motifs presented in this study ideally serve this purpose. Moreover, they can also be used for the identification of IMPase-like HolPases in plants.
Within the Actinobacteria, it is rather easy to distinguish the different IMPase-like proteins by comparing the amino acid sequences to the corresponding orthologs in C. glutamicum. However, since the amino acid sequences of all IMPase-like proteins share a big degree of similarity (approximately 20-30% sequence identity between the different IMPase-like proteins in C. glutamicum), it gets harder to classify IMPase-like proteins in more distantly related bacteria based on the overall sequence similarity alone. The motifs described in the present study are therefore of great help in assigning a specific function to a not yet characterized IMPase-like protein. We demonstrated this by proving HolPase activity of HisN orthologs from the genera Dietzia and Zymomonas that are only moderately similar to HisN Cg but possess the expected motifs. We could also demonstrate that a potential HisN Cg homolog from A. utahensis, with rather high overall sequence similarity but entirely lacking the HolPase motif 5, is not a functional HolPase.
The last result underlines the importance of motif 5 for HolPase activity of HisN orthologs. The detailed examination of the recently solved structure of the IMPase-like HolPase from Z. mobilis, suggests that the carboxylic group of the aspartate present in HolPase motif 5 might be involved in substrate recognition. A similar function might be also attributed to at least one of the aromatic amino acids present in motif 5 (Fig. 5: HisN motif 5, position 195). However, since no IMPase-like HolPase has been crystallized in the presence of the substrate HolP or the products l-histidinol and Pi, any interaction of the conserved residues with the substrates or the products remains speculative.
The application of the here presented motifs for the classification of IMPase-like proteins can help to improve the annotation of IMPase-like proteins. If a suspected HisN ortholog exhibits all HolPase motifs, and especially motif 5, it is very likely that this protein is a HolPase. Vice versa, if the motifs typical of one of the over IMPase-like proteins are identified in a suspected HisN ortholog, it is very likely that this protein is exactly this IMPase-like protein and not a HolPase. Consideration of the overall sequence similarity to HisN Cg is not sufficient to identify IMPase-like HolPase. HisN Zm is only moderately similar to HisN Cg (BlastP score: 101 bits) but possesses all HolPase motifs and we were able to experimentally prove its HolPase activity. In contrast, the SuhB ortholog from Sediminibacterium salmoneum has an overall equal degree of similarity to HisN Cg (BlastP score: 102 bits) but it is very unlikely a HolPase, since all the HolPase motifs are absent. This demonstrates the benefit of the presented motifs for the functional classification of IMPase-like proteins. The HMMs supplied as Additional file 3 (HisN) and Additional file 4 (Cg0911) should greatly facilitate the correct classification of IMPase-like HolPases.
Our analysis of the distribution of HisN homologs within the bacterial kingdom revealed, that IMPase-like HolPases are not restricted to the phylum Actinobacteria (Fig. 7). They appear to be generally present in different phyla like Chlorobi, Fibrobacteres and Nitrospinae. However, HolPase activity of these potential HisN orthologs has not been demonstrated so far. Interestingly, we also detected many putative IMPase-like HolPases in Gammaproteobacteria. This is surprising as many gammaproteobacteria are known to possess a bifunctional HAD-type HolPase homologous to the His(NB) protein from E. coli . In those gammaproteobacterial families where we did not detect such an additional His(NB) homolog, it is likely that the IMPase-like proteins are the main HolPases. In contrast, the role of the putative HisN orthologs within those gammaproteobacterial families with concurrent occurrence of His(NB) and HisN homologs is less evident. It is possible, that these genera simply possess two different HolPases or that the HisN homologs from these families do not possess HolPase activity. It is also possible that a second, yet unknown activity of HisN orthologs is required in these genera. It has been demonstrated for the IMPase-like HolPase HISN7 from A. thaliana, that it additionally catalyzes the dephosphorylation of d-inositol-1-phosphate, d-inositol-3-phosphate, and l-galactose-1-phosphate .
Since we used a rather restrictive cut-off for the identification of HisN orthologs (BlastP score ≥ 125 bits with HisN Cg as query), Fig. 7 does not give the exhaustive picture of the distribution of IMPase-like HolPases within bacteria. Indeed, the HMM for HisN reveals additional species that possess such an ortholog, however with a BlastP score below the cut-off.
The distribution of Cg0911 orthologs is restricted to the four actinobacterial orders Corynebacteriales, Frankiales, Micrococcales, and Propionibacteriales and even within these orders only a few genera possess such a homolog. We identified only a Cg0911 ortholog but no HisN ortholog in Kytococcus. It is possible, that Cg0911 is the main HolPase in Kytococcus, since presence of other his genes indicates the general possibility of l-histidine biosynthesis (data not shown).
The occurrence of the genes encoding HisN and Cg0911 orthologs as a tandem within Corynebacteriaceae implies a recent gene duplication event. However, HisN and Cg0911 share only the same degree of similarity as do HisN or Cg0911 with one of the three other paralogs in C. glutamicum (Table 1). This indicates that all five paralogs evolved more or less simultaneously and are not a result of a recent duplication event. Although we currently do not know which phosphorylated substance might be the preferred substrate of Cg0911, one could assume that both enzymes are needed in the same context most of the time. However since the genes encoding HisN and Cg0911 orthologs are not clustered in all other genera besides Corynebacterium and Turicella, this clustering might be simply a result of chance or indicate a special, yet unknown function of Cg0911 orthologs in Corynebacteriaceae.
Here, using the example of the histidinol-phosphate phosphatase HisN from C. glutamicum, we present for the first time kinetic data on an IMPase-like HolPases with its natural substrate l-histidinol-phosphate. Based on this data, IMPase-like HolPases show remarkable differences in enzyme properties as compared with HAD- or PHP-type HolPases. Moreover, six sequence motifs have been presented in this study that can be used to reliably differentiate between IMPase-like HolPases and IMPase-like proteins with no such activity (like SuhB or CysQ), with the potential to enhance current and future genome annotations. A phylogenetic analysis reveals that IMPase-like HolPases are not only present in Actinobacteria and plants but can be found in further bacterial phyla, including Chlorobi, Fibrobacteres, and Proteobacteria.
Bacterial strains and cultivation conditions
All strains and plasmids used in this study are given in Additional file 1: Table S1 and Table S2, respectively. Escherichia coli DH5α MCR  was used for general cloning works and plasmid maintenance. E. coli ER2566 (New England Biolabs, Ipswich, MA) was used for heterologous gene expression in the context of protein purification. E. coli strains were grown in lysogeny broth (LB) Lennox medium. Solid medium contained 1.7% agar. Kanamycin (50 μg ml−1) and ampicillin (200 μg ml−1) were added where appropriate. E. coli strains were incubated at 37 °C if not stated otherwise.
Corynebacterium glutamicum ATCC 13032 [47, 48] and all thereof derived mutants (this work) were incubated at 30 °C. Caso broth (Carl Roth, Karlsruhe, Germany) or MM1 minimal medium was used for solid cultivations, supplemented with 1.7% agar. Nalidixic acid (50 μg ml−1), kanamycin (25 μg ml−1), l-histidine (100 μM), and sucrose (10%) were added where appropriate. The MM1 minimal medium (MMYE medium without yeast extract ) was constituted as follows: glucose (20 g l−1), (NH4)2SO4 (10 g l−1), urea (3 g l−1), K2HPO4 ∙ 3 H2O (1.3 g l−1), MgSO4 ∙ 7 H2O (400 mg l−1), thiamine (500 μg l−1), biotin (50 μg l−1), FeSO4 ∙ 7 H2O (2 mg l−1), MnSO4 ∙ 7 H2O (2 mg l−1), NaCl (50 mg l−1).
Recombinant DNA work
A complete list of primers used in this study is given in Additional file 1: Table S3. Phusion high-fidelity DNA polymerase (Thermo Scientific, Dreieich, Germany) was used to amplify DNA fragments for cloning or for sequencing. To improve the amplification of GC-rich DNA from Dietzia and A. utahensis the GC-buffer provided by the supplier was used and dimethyl sulfoxide (DMSO) was added to the PCR mixture to a final concentration of 8.3%. Plasmids were constructed in two different ways: In the first method, vector and insert were cut with restriction enzymes and joined by a DNA ligase according to standard cloning procedures . Restriction sites needed for cloning of the insert were included in the 5’ overhang of the primers used for the amplification. All restriction and DNA-modifying enzymes were purchased from Thermo Scientific. In the second method, vector and insert were assembled in an isothermal enzymatic reaction by taking advantage of complementary DNA sequences at the end of the DNA fragments as described by Gibson (2011) . For this purpose, vector DNA was linearized in a PCR reaction using the KOD hot start DNA polymerase (Novagen, San Diego, CA). Overlapping DNA-sequences (20–30 bp) were generated by including sequences complementary to the ends of the linearized vector within the 5’ ends of the primers used for amplification of the insert. Specific mutations in an insert were introduced by including the desired mutation in the primers used for amplification of the DNA. All plasmids were constructed and propagated in E. coli prior to transfer to C. glutamicum.
Competent E. coli cells were prepared according to an optimized CaCl2 method and transformed with plasmid DNA by applying a heat-pulse . Competent C. glutamicum cells were prepared as described previously and transformed with plasmid DNA via electroporation  at 2.5 kV, 200 Ω and 25 μF.
Gene deletion in C. glutamicum
Gene deletion in C. glutamicum relied on homologues recombination and a double cross-over event using the non-replicating pK18mobsacB vector  as described before . The genomic regions flanking the deletion of interest were amplified from genomic DNA of the C. glutamicum wild type. These fragments (approximately 500 bp) were either fused via the gene splicing by overlap extension (gene SOEing) technique [56, 57] and used for ligation into the pK18mobsacB vector or they were directly used for the isothermal enzymatic assembly with the vector (Gibson assembly, ). The deletion plasmids constructed in either way were used for transformation of C. glutamicum. After selection for the double cross-over event, desired deletions were confirmed by PCR using primers binding to genomic sequences up- and down-stream of the deletion and that were not part of deletion plasmid. All deletion mutants generated in this study are listed in Additional file 1: Table S1.
C. glutamicum ΔhisN complementation experiments
The constitutive expression vector pZMP  was used for expression of putative HolPase genes in the C. glutamicum (plasmids listed in Additional file 1: Table S2). A SD-sequence exactly matching the 3’ end of the 16S-rRNA in C. glutamicum was included within the 5’ extension of the primers used for gene amplification. Gene expression from pZMP is under control of the tac promoter. Approximately 15 copies of the plasmid are present per C. glutamicum cell (unpublished observation). The DNA sequence of the inserts was confirmed by sequencing. Plasmid DNA was isolated from E. coli and used for transformation of C. glutamicum ΔhisN. Successful transformants were identified by selection for the plasmid-encoded kanamycin resistance. Presence of the insert was additionally confirmed by amplification of the insert using vector-specific primers and comparing the size of the PCR product with the expectation.
The C. glutamicum ΔhisN complementation experiments were conducted on MM1 minimal medium plates either supplemented or unsupplemented with l-histidine. The different mutants were diluted in liquid MM1 medium and drops containing the same amount of cells were applied to the plates. The plates were incubated for several days at 30 °C and pictures were taken in 24 h intervals. The ability of a putative HolPase gene to complement the genomic hisN deletion of C. glutamicum was assessed by comparing the growth of the expression mutants to the C. glutamicum ΔhisN or wild type strain.
Purification of the HisN Cg and Cg0911 enzymes
The commercial IMPACTTM system (New England Biolabs, Ipswich, MA) was used for the tag-free purification of HisN and Cg0911 according to the manufacturer’s instructions. In this system, a self-cleavable intein tag is translationally fused to the protein of interest. The tag binds specifically to chitin beads and its self cleavage activity is induced by thiol reagents, allowing the elution of unmodified protein.
The coding DNA sequences (CDS) of hisN Cg and cg0911 were amplified from genomic DNA without the start and stop codon (the start codon ATG is present on the vector) and inserted into the pXTB1 (New England Biolabs) vector by isothermal enzymatic assembly. This resulted in the translational fusion of the intein tag to the C-terminus of HisN Cg and Cg0911, respectively. The inserts were sequenced to exclude undesired mutations. The plasmids were transferred to E. coli ER2566 for heterologous gene expression. Details regarding cultivation, induction of protein expression, cell lyses, protein purification, concentration, and quality control have been described previously . Diverging from this description, column and cleavage buffers used during affinity purification and on column cleavage contained 20 mM TRIS as buffering substance instead of Na2HPO4. Additionally, a different storage buffer was used (10 mM NaCl, 20 mM TRIS, pH 7.5). The purified proteins were mixed with glycerol (final concentration: 50% (w/v)) and stored at -80 °C.
HolPase activity assay
HolPase activity can be assayed by the release of inorganic phosphate (Pi) from the substrate HolP. However, conditions needed for the colorimetric detection of Pi are not compatible with the standard conditions for enzymatic catalysis. Therefore, catalysis and Pi detection had to be separated.
The reaction conditions for the catalysis step of the HolPase activity were based on the conditions described for the HolPase of S. enterica . If not stated otherwise, reactions were conducted in 1.5 ml polypropylene microcentrifuge tubes in a water bath tempered to 30 °C. The standard reaction volume was 100 μl. 80 μl of reaction buffer (100 mM triethanolamine (TEA), pH 7.5 at 22 °C (corresponding to pH 7.35 at 30 °C)) were supplemented with MgSO4 resulting in the desired final metal ion concentration (5 mM in standard settings) and were mixed with 10 μl protein solution (freshly diluted with reaction buffer to 0.1 μg μl−1 (HisN) or 1 μg μl−1 (Cg0911), respectively) and preincubated for 10 min. The reaction was started by addition of 10 μl HolP solution (5 mM; HolP purchased from Paragos, Herdecke, Germany). Samples (30 μl) were taken in appropriate time intervals (e.g. after 1, 2, and 3 min). The reaction was stopped by immediately mixing the withdrawn sample with 30 μl of ice-cold EDTA solution (20 mM). Each enzymatic reaction was performed in at least three replicates.
Some modifications of the catalytic part of the assay were made to access individual enzyme parameters. (1) Temperature optimum: Variation of incubation temperature from 20 °C to 50 °C. The pH of the reaction buffer was adjusted to be 7.35 at every tested temperature. (2) pH-optimum: The pH of the reaction buffer was varied (pH 6–10). The buffer substances (always 100 mM) were changed according to their optimal buffering range (pH 6 [22 °C]/5.98 [30 °C]: 2-(N-morpholino)ethanesulfonic acid (MES); pH 7/6.90: 3-(N-morpholino)propanesulfonic acid (MOPS); pH 8/7.94: 4-(2-hydroxyethyl)-1-piperazineethanesulfonic acid (HEPES); pH 9/8.83: 2-(cyclohexylamino)ethanesulfonic acid (CHES); pH 10/9.83: CHES). (3) Metal ion preference: The metal salts CaCl2, CoCl2, CuSO4, FeSO4, MnSO4, NiCl2, or ZnCl2 (5 mM final concentration) were used instead of MgSO4. (4) Determination of Km and kcat: The HolP concentration was kept constant at 500 μM in the measurements for the determination of the Km value for Mg2+. At least nine different Mg2+ concentrations were tested ranging from 312.5 μM to 5 mM (HisN Cg ) or from 312.5 μM to 10 mM (Cg0911). The Mg2+ concentration was kept constant at 5 mM for the determination of the Km value for HolP. At least seven different HolP concentrations were tested ranging from 17.5 μM to 200 μM (HisN Cg ) or from 125 μM to 1 mM (Cg0911). Every concentration was tested in at least six replicates.
The detection of released Pi was based on the complex formation of malachite green with phosphomolybdate under acidic conditions . The method was adopted for measurement in transparent flat bottom 96-well plates in an Infinite M200 plate reader (Tecan, Männedorf, Switzerland). 90 μl H2O, 20 μl reagent A (1.75% (w/v) ammonium heptamolybdate tetrahydrate in 6.3 N sulfuric acid), and 10 μl of a Pi-containing sample were mixed directly in a 96-well plate and incubated at RT for 10 min. Then, 20 μl of reagent C (0.35% (w/v) polyvinyl alcohol (MW ≈ 30 kDa, fully hydrolyzed), 0.035% (w/v) malachite green) were added. The mixture was incubated for additional 45 min at RT. The absorption at 610 nm was measured three times in 3 min intervals. Every Pi containing sample was measured in three technical replicates. Samples with known Pi concentrations (0.1 - 3.13 mM KH2PO4) were used to record a calibration curve. Linearity of the measurement was ensured in the range from 0.07 - 0.85 absorption units at 610 nm.
The enzyme activity corresponds to the slope of the linear regression curve through the data points in a plot of released Pi against the time. Values for Km, kcat and the Hill-coefficients were determined by non-linear curve fitting of the data points in a plot of enzyme activity against the varied substrate concentration to the Hill equation  using OriginPro9.0 (function “Hill”; Origin Lab Corporation, Northampton, MA). The molecular masses of HisN Cg (27893.16 g mol−1) and Cg0911 (30695.27 g mol−1) were used for the calculation of the turnover numbers (kcat) and were based on the pure amino acid sequence of the monomers.
The online BlastP suite of the National Center for Biotechnology Information (NCBI) was used for the identification of homologous protein sequences. If not stated otherwise, NCBI’s non-redundant (nr) protein sequence database was queried using the default parameters .
The online tool Emboss Needle, provided by the European Bioinformatics Institute (EMBL-EBI, ), was used in its default settings in order to determine the degree of identity [%] and similarity [%] between two homologous proteins (pairwise sequence alignment). Multiple sequence alignments were conducted with EMBL-EBI’s online tool Clustal Omega in the default settings .
The jackhmmr tool was used online on the HMMER webserver, provided by the European Bioinformatics Institute (EMBL-EBI, ), to create HMMs for HisN and Cg0911. The UniProt RefProt database was used for an iterative search with either a multiple alignment of all validated HisN orthologs (HisN Cg , HisN Au , HisN Dz , and HisN Zm ) or the single Cg0911 sequence, respectively. Significance E-value cutoffs for sequence andd hit were set to 1e-65 and the the search was iterated until no new hits were found.
The graphical representations of amino acid motifs were created with the online tool WebLogo . The homologous sequences used for these logos were identified by a BlastP search and aligned using Clustal Omega. The multiple alignments were improved manually if appropriate (local rearrangement of gaps or removal of whole sequences from the alignment).
The Ccp4mg molecular-graphics software (version 2.10.5) was used for visualization and analysis of protein structures . Additionally, the online Protein Interactions Calculator (PIC) was used to determine intra- and intermolecular interaction within the protein structures including hydrogen bonds, salt bridges, hydrophobic interactions, as well as aromatic interactions .
Gao B, Gupta RS. Phylogenetic framework and molecular signatures for the main clades of the phylum Actinobacteria. Microbiol Mol Biol Rev. 2012;76:66–112.
Becker J, Wittmann C. Systems and synthetic metabolic engineering for amino acid production – the heartbeat of industrial strain development. Curr Opin Biotechnol. 2011;23:1–9.
Becker J, Wittmann C. Bio-based production of chemicals, materials and fuels – Corynebacterium glutamicum as versatile cell factory. Curr Opin Biotechnol. 2012;23:631–40.
Kulis-Horn RK, Persicke M, Kalinowski J. Corynebacterium glutamicum ATP-phosphoribosyl transferases suitable for l-histidine production – Strategies for the elimination of feedback inhibition. J Biotechnol. 2015;206:26–37.
Kulis-Horn RK, Persicke M, Kalinowski J. Histidine biosynthesis, its regulation and biotechnological application in Corynebacterium glutamicum. Microb Biotechnol. 2014;7:5–25.
Alifano P, Fani R, Lió P, Lazcano A, Bazzicalupo M, Carlomagno MS, Bruni CB. Histidine biosynthetic pathway and genes. structure, regulation, and evolution. Microbiol Rev. 1996;60:44–69.
Mormann S, Lömker A, Rückert C, Gaigalat L, Tauch A, Pühler A, Kalinowski J. Random mutagenesis in Corynebacterium glutamicum ATCC 13032 using an IS6100-based transposon vector identified the last unknown gene in the histidine biosynthesis pathway. BMC Genomics. 2006;7:205.
Marchler-Bauer A, Zheng C, Chitsaz F, Derbyshire MK, Geer LY, Geer RC, Gonzales NR, Gwadz M, Hurwitz DI, Lanczycki CJ, Lu F, Lu S, Marchler GH, Song JS, Thanki N, Yamashita RA, Zhang D, Bryant SH. CDD: conserved domains and protein three-dimensional structure. Nucleic Acids Res. 2012;41:D348.
Petersen LN, Marineo S, Mandala S, Davids F, Sewell BT, Ingle RA. The missing link in plant histidine biosynthesis: Arabidopsis myoinositol monophosphatase-like2 encodes a functional histidinol-phosphate phosphatase. Plant Physiol. 2010;152:1186–96.
Marineo S, Cusimano MG, Limauro D, Coticchio G, Puglia AM. The histidinol phosphate phosphatase involved in histidine biosynthetic pathway is encoded by SCO5208 (hisN) in Streptomyces coelicolor A3(2). Curr Microbiol. 2008;56:6–13.
Movahedzadeh F, Wheeler PR, Dinadayala P, Av-Gay Y, Parish T, Daffé M, Stoker NG. Inositol monophosphate phosphatase genes of Mycobacterium tuberculosis. BMC Microbiol. 2010;10:50.
Brilli M, Fani R. Molecular evolution of hisB genes. J Mol Evol. 2004;58:225–37.
Rangarajan ES, Proteau A, Wagner J, Hung M, Matte A, Cygler M. Structural snapshots of Escherichia coli histidinol phosphate phosphatase along the reaction pathway. J Biol Chem. 2006;281:37930–41.
Brady DR, Houston LL. Some properties of the catalytic sites of imidazoleglycerol phosphate dehydratase-histidinol phosphate phosphatase, a bifunctional enzyme from Salmonella typhimurium. J Biol Chem. 1973;248:2588–92.
Staples MA, Houston LL. Purification of the bifunctional enzyme, imidazoleglycerolphosphate dehydratase-histidinol phosphatase, of Salmonella typhimurium. Biochim Biophys Acta. 1980;613:210–9.
Lee HS, Cho Y, Lee J, Kang SG. Novel monofunctional histidinol-phosphate phosphatase of the DDDD superfamily of phosphohydrolases. J Bacteriol. 2008;190:2629–32.
Gorman JA, Hu AS. The separation and partial characterization of l-histidinol phosphatase and an alkaline phosphatase of Saccharomyces cerevisiae. J Biol Chem. 1969;244:1645–50.
Millay Jr RH, Houston LL. Purification and properties of yeast histidinol phosphate phosphatase. Biochemistry. 1973;12:2591–6.
le Coq D, Fillinger S, Aymerich S. Histidinol phosphate phosphatase, catalyzing the penultimate step of the histidine biosynthesis pathway, is encoded by ytvP (hisJ) in Bacillus subtilis. J Bacteriol. 1999;181:3277–80.
Ghodge SV, Fedorov AA, Fedorov EV, Hillerich B, Seidel R, Almo SC, Raushel FM. Structural and mechanistic characterization of l-histidinol phosphate phosphatase from the polymerase and histidinol phosphatase family of proteins. Biochemistry. 2013;52:1101–12.
Kalinowski J, Bathe B, Bartels D, Bischoff N, Bott M, Burkovski A, Dusch N, Eggeling L, Eikmanns BJ, Gaigalat L, Goesmann A, Hartmann M, Huthmacher K, Krämer R, Linke B, McHardy AC, Meyer F, Möckel B, Pfefferle W, Pühler A, Rey DA, Rückert C, Rupp O, Sahm H, Wendisch VF, Wiegräbe I, Tauch A. The complete Corynebacterium glutamicum ATCC 13032 genome sequence and its impact on the production of l-aspartate-derived amino acids and vitamins. J Biotechnol. 2003;104:5–25.
Ikeda M, Nakagawa S. The Corynebacterium glutamicum genome. features and impacts on biotechnological processes. Appl Microbiol Biotechnol. 2003;62:99–109.
Omi R, Goto M, Miyahara I, Manzoku M, Ebihara A, Hirotsu K. Crystal structure of monofunctional histidinol phosphate phosphatase from Thermus thermophilus HB8. Biochemistry. 2007;46:12618–27.
Strasser F, Pelton PD, Ganzhorn AJ. Kinetic characterization of enzyme forms involved in metal ion activation and inhibition of myo-inositol monophosphatase. Biochem J. 1995;307(Pt 2):585–93.
Nigou J, Dover LG, Besra GS. Purification and biochemical characterization of Mycobacterium tuberculosis SuhB, an inositol monophosphatase involved in inositol biosynthesis. Biochemistry. 2002;41:4392–8.
Follmann M, Ochrombel I, Krämer R, Trötschel C, Poetsch A, Rückert C, Hüser A, Persicke M, Seiferling D, Kalinowski J, Marin K. Functional genomics of pH homeostasis in Corynebacterium glutamicum revealed novel links between pH response, oxidative stress, iron homeostasis and methionine synthesis. BMC Genomics. 2009;10:621.
Weiss JN. The Hill equation revisited: uses and misuses. FASEB J. 1997;11:835–41.
Gill R, Mohammed F, Badyal R, Coates L, Erskine P, Thompson D, Cooper J, Gore M, Wood S. High-resolution structure of myo-inositol monophosphatase, the putative target of lithium therapy. Acta Crystallogr D Biol Crystallogr. 2005;61:545–55.
Singh N, Halliday AC, Knight M, Lack NA, Lowe E, Churchill GC. Cloning, expression, purification, crystallization and X-ray analysis of inositol monophosphatase from Mus musculus and Homo sapiens. Acta Crystallogr F Struct Biol Cryst Commun. 2012;68:1149–52.
Seo J, Chong H, Park HS, Yoon K, Jung C, Kim JJ, Hong JH, Kim H, Kim J, Kil J, Park CJ, Oh H, Lee J, Jin S, Um H, Lee H, Oh S, Kim JY, Kang HL, Lee SY, Lee KJ, Kang HS. The genome sequence of the ethanologenic bacterium Zymomonas mobilis ZM4. Nat Biotechnol. 2005;23:63–8.
Velasco-Bucheli R, del Cerro C, Hormigo D, Acebal C, Arroyo M, García JL, de La Mata I. Draft genome sequence of Actinoplanes utahensis NRRL 12052, a microorganism involved in industrial production of pharmaceutical intermediates. Genome Announc. 2015;3:e01411–14.
Hwang H, Park S, Kim J. Crystal structure of cbbF from Zymomonas mobilis and its functional implication. Biochem Biophys Res Commun. 2014;445:78–83.
Stieglitz KA, Johnson KA, Yang H, Roberts MF, Seaton BA, Head JF, Stec B. Crystal structure of a dual activity IMPase/FBPase (AF2372) from Archaeoglobus fulgidus. The story of a mobile loop. J Biol Chem. 2002;277:22863–74.
Nigou J, Besra GS. Characterization and regulation of inositol monophosphatase activity in Mycobacterium smegmatis. Biochem J. 2002;361:385–90.
Torabinejad J, Donahue JL, Gunesekera BN, Allen-Daniels MJ, Gillaspy GE. VTC4 Is a bifunctional enzyme that affects myoinositol and ascorbate biosynthesis in plants. Plant Physiol. 2009;150:951–61.
Parish T, Liu J, Nikaido H, Stoker NG. A Mycobacterium smegmatis mutant with a defective inositol monophosphate phosphatase gene homolog has altered cell envelope permeability. J Bacteriol. 1997;179:7827–33.
Morales A, Nozawa S, Thedei Jr G, Maccheroni Jr W, Rossi A. Properties of a constitutive alkaline phosphatase from strain 74A of the mold Neurospora crassa. Braz J Med Biol Res. 2000;33:905–12.
Garen A, Levinthal C. A fine-structure genetic and chemical study of the enzyme alkaline phosphatase of E. coli I. Purification and characterization of alkaline phosphatase. Biochim Biophys Acta. 1960;38:470–83.
Dinev Z, Gannon CT, Egan C, Watt JA, McConville MJ, Williams SJ. Galactose-derived phosphonate analogues as potential inhibitors of phosphatidylinositol biosynthesis in mycobacteria. Org Biomol Chem. 2007;5:952.
Jackson M, Crick DC, Brennan PJ. Phosphatidylinositol is an essential phospholipid of mycobacteria. J Biol Chem. 2000;275:30092–9.
Burkovski A. Cell envelope of Corynebacteria: Structure and influence on pathogenicity. ISRN Microbiol. 2013;2013:1–11.
Hatzios SK, Iavarone AT, Bertozzi CR. Rv2131c from Mycobacterium tuberculosis is a CysQ 3′-phosphoadenosine-5′-phosphatase. Biochemistry. 2008;47:5823–31.
Lee H. Sulfur metabolism and its regulation. In: Eggeling L, Bott M, editors. Handbook of Corynebacterium glutamicum. Boca Raton: Taylor & Francis; 2005. p. 351–76.
Zhang Y, Shang X, Deng A, Chai X, Lai S, Zhang G, Wen T. Genetic and biochemical characterization of Corynebacterium glutamicum ATP phosphoribosyltransferase and its three mutants resistant to feedback inhibition by histidine. Biochimie. 2012;94:829–38.
Shyp V, Tankov S, Ermakov A, Kudrin P, English BP, Ehrenberg M, Tenson T, Elf J, Hauryliuk V. Positive allosteric feedback regulation of the stringent response enzyme RelA by its product. EMBO Rep. 2012;13:835–9.
Grant SGN, Jessee J, Bloom FR, Hanahan D. Differential plasmid rescue from transgenic mouse DNAs into Escherichia coli methylation-restriction mutants. Proc Natl Acad Sci U S A. 1990;87:4645–9.
Kinoshita S, Nakayama S, Akita S. Taxonomic study of glutamic acid accumulating bacteria, Micrococcus glutamicus, nov. sp. Bull Agr Chem Soc Jpn. 1958;22:176–85.
Abe S, Takayama K, Kinoshita S. Taxonomical studies on glutamic acid-producing bacteria. J Gen Appl Microbiol. 1967;13:279–301.
Katsumata R, Ozaki A, Oka T, Furuya A. Protoplast transformation of glutamate-producing bacteria with plasmid DNA. J Bacteriol. 1984;159:306–11.
Holert J, Yücel O, Suvekbala V, Kulić Ž, Möller H, Philipp B. Evidence of distinct pathways for bacterial degradation of the steroid compound cholate suggests the potential for metabolic interactions by interspecies cross-feeding. Environ Microbiol. 2014;16:1424–40.
Schrimpf G. Gentechnische Methoden: Eine Sammlung von Arbeitsanleitungen für das molekularbiologische Labor. 3rd ed. Heidelberg: Spektrum Akad. Verl; 2002.
Gibson DG. Enzymatic assembly of overlapping DNA fragments. Methods Enzymol. 2011;498:349–61.
Inoue H, Nojima H, Okayama H. High efficiency transformation of Escherichia coli with plasmids. Gene. 1990;96:23–8.
Tauch A, Kirchner O, Löffler B, Götker S, Pühler A, Kalinowski J. Efficient electrotransformation of Corynebacterium diphtheriae with a mini-replicon derived from the Corynebacterium glutamicum plasmid pGA1. Curr Microbiol. 2002;45:362–7.
Schäfer A, Tauch A, Jäger W, Kalinowski J, Thierbach G, Pühler A. Small mobilizable multi-purpose cloning vectors derived from the Escherichia coli plasmids pK18 and pK19. Selection of defined deletions in the chromosome of Corynebacterium glutamicum. Gene. 1994;145:69–73.
Vallejo AN, Pogulis RJ, Pease LR. In vitro synthesis of novel genes. Mutagenesis and recombination by PCR. PCR Method Appl. 1994;4:S123–30.
Wehmeier L, Schäfer A, Burkovski A, Krämer R, Mechold U, Malke H, Pühler A, Kalinowski J. The role of the Corynebacterium glutamicum rel gene in (p)ppGpp metabolism. Microbiology. 1998;144:1853–62.
Walter F, Grenz S, Ortseifen V, Persicke M, Kalinowski J. Corynebacterium glutamicum ggtB encodes a functional γ-glutamyl transpeptidase with γ-glutamyl dipeptide synthetic and hydrolytic activity. J Biotechnol. 2015;232:99–109.
Martin RG, Berberich MA, Ames BN, Davis WW, Goldberger RF, Yourno JD.  Enzymes and intermediates of histidine biosynthesis in Salmonella typhimurium. In: Tabor H, Tabor CW, editors. Methods in enzymology, Metabolism of amino acids and amines part B. New York: Academic; 1971. p. 3–44.
van Veldhoven PP, Mannaerts GP. Inorganic and organic phosphate measurements in the nanomolar range. Anal Biochem. 1987;161:45–8.
Camacho C, Coulouris G, Avagyan V, Ma N, Papadopoulos J, Bealer K, Madden TL. BLAST+: architecture and applications. BMC Bioinf. 2009;10:421.
Li W, Cowley A, Uludag M, Gur T, McWilliam H, Squizzato S, Park YM, Buso N, Lopez R. The EMBL-EBI bioinformatics web and programmatic tools framework. Nucleic Acids Res. 2015;43:W580–4.
Finn RD, Clements J, Arndt W, Miller BL, Wheeler TJ, Schreiber F, Bateman A, Eddy SR. HMMER web server: 2015 update. Nucleic Acids Res. 2015;43:W30–8.
Crooks GE, Hon G, Chandonia J, Brenner SE. WebLogo: a sequence logo generator. Genome Res. 2004;14:1188–90.
McNicholas S, Potterton E, Wilson KS, Noble MEM. Presenting your structures: the CCP4mg molecular-graphics software. Acta Crystallogr D Biol Crystallogr. 2011;67:386–94.
Tina KG, Bhadra R, Srinivasan N. PIC: Protein interactions calculator. Nucleic Acids Res. 2007;35:W473.
R. K. Kulis-Horn was supported by a CLIB-GC (Graduate Cluster Industrial Biotechnology) Phd grant co-funded by the Ministry of Innovation, Science and Research of the federal state of North Rhine-Westphalia (MIWF). This work was part of the SysEnCor research project (grant 0315598E) funded by the German Federal Ministry of Education and Research (BMBF). Besides financing the funding body played no role, active or passive, in study design, data collection and interpretation, and manuscript writing.
Availability of data and materials
The datasets used and/or analyzed during the current study are included in this published article and its supplementary information files.
Ethics approval and consent to participate
Consent for publication
The authors declare that they have no competing interest.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Supplementary Figures and Tables. The supplementary figures comprise the SDS-PAGE of purified HisN Cg and Cg0911, several alignments of IMPase-like proteins in C. glutamicum and other species, and the complementation assay for various hisN Cg gene mutants. Furthermore, supplementary tables carry the used strains, plasmids and primers. (DOCX 200 kb)
Data collection for motif analysis. This data collection contains all sequence data of IMPase-like proteins belonging to the group Cg0911, CysQ, HisN, ImpA, and SuhB used for motif analysis. Furthermore, HisN orthologues not used for the motif analysis were listed. (DOCX 120 kb)
HisN-HMM. Hidden Markov model of 1681 HisN sequences based on an iterative approach using Jackhmmer. (HMM 121 kb)
Cg0911-HMM. Hidden Markov model of 103 Cg0911 sequences based on an iterative approach using Jackhmmer. (HMM 131 kb)
About this article
Cite this article
Kulis-Horn, R.K., Rückert, C., Kalinowski, J. et al. Sequence-based identification of inositol monophosphatase-like histidinol-phosphate phosphatases (HisN) in Corynebacterium glutamicum, Actinobacteria, and beyond. BMC Microbiol 17, 161 (2017). https://doi.org/10.1186/s12866-017-1069-4
- Histidinol-phosphate phosphatase (HolPase)
- Inositol monophosphatase (IMPase)-like
- Corynebacterium glutamicum
- Kinetic data
- Sequence motifs
- Phylogenetic analysis