Skip to main content
  • Research article
  • Open access
  • Published:

The low-affinity phosphate transporter PitA is dispensable for in vitro growth of Mycobacterium smegmatis



Mycobacteria have been shown to contain an apparent redundancy of high-affinity phosphate uptake systems, with two to four copies of such systems encoded in all mycobacterial genomes sequenced to date. In addition, all mycobacteria also contain at least one gene encoding the low-affinity phosphate transporter, Pit. No information is available on a Pit system from a Gram-positive microorganism, and the importance of this system in a background of multiple other phosphate transporters is unclear.


The aim of this study was to determine the physiological role of the PitA phosphate transporter in Mycobacterium smegmatis. Expression of pitA was found to be constitutive under a variety of growth conditions. An unmarked deletion mutant in pitA of M. smegmatis was created. The deletion did not affect in vitro growth or phosphate uptake of M. smegmatis. Expression of the high-affinity transporters, PstSCAB and PhnDCE, was increased in the pitA deletion strain.


PitA is the only low-affinity phosphate transport system annotated in the genome of M. smegmatis. The lack of phenotype of the pitA deletion strain shows that this system is dispensable for in vitro growth of this organism. However, increased expression of the remaining phosphate transporters in the mutant indicates a compensatory mechanism and implies that PitA is indeed used for the uptake of phosphate in M. smegmatis.


Uptake of phosphate by bacteria most commonly occurs via two systems, the low-affinity, constitutively expressed Pit system, and the high-affinity, phosphate-starvation induced Pst system [1, 2]. Pit systems consist of a single membrane protein, encoded by pitA or pitB, and are energized by the proton motive force [2, 3]. Pst systems are multi-subunit ABC transporters, usually encoded by a four-gene operon, pstSCAB [1, 2]. Several bacterial species also contain additional transporters for the uptake of alternative phosphorus-compounds. Examples include the Ptx and Htx systems of Pseudomonas stutzeri, which transport phosphonates, phosphite and hypophosphite [4, 5], and the Phn-system for the uptake of phosphonates in E. coli and several other Gram-negative bacteria [68].

Mycobacteria appear unique in that they contain several copies of high-affinity systems specific for phosphate: In the pathogenic species, such as M. tuberculosis, M. bovis and M. leprae, this is due to duplication of the pst genes [9]. For example, M. tuberculosis contains three different copies of pstS, two copies each of pstC and pstA, and one copy of pstB [10], plus a homologous gene, phoT, which has been shown to fulfill the same function as pstB in M. bovis [11]. Expression of all three copies of pstS under phosphate-limited conditions has been shown for M. bovis BCG [9], although a recent microarray analysis of phosphate-limited M. tuberculosis only found one of the pst-operons to be upregulated [12].

The environmental species M. smegmatis possesses only a single copy of the pst-operon, but it also contains a second operon, phnDCE, which encodes another phosphate-specific high-affinity transporter [13]. Furthermore, a third, as yet unidentified, high-affinity phosphate transport system may be present in M. smegmatis, because a phnD/pstS double deletion mutant still retained phosphate uptake activity with a Km-value of around 90 μM, which is similar to the values of the Pst and Phn systems [13].

Despite this abundance of high-affinity transporters, all mycobacterial genomes available to date also contain a pitA gene, encoding the low-affinity system, with the genome of M. tuberculosis containing a second Pit system, encoded by pitB [14]. The present study was directed at investigating the role of the low-affinity phosphate transporter in a bacterium containing at least two high-affinity systems, using the model of M. smegmatis.

Results and Discussion

PitA is constitutively expressed

Previous studies of Pit systems have focused on Gram-negative bacteria, where pitA expression is independent of phosphate concentrations [1, 15], while pitB of E. coli and the pit-like gene of Sinorhizobium meliloti are repressed at low phosphate concentrations [16, 17]. To study the expression of M. smegmatis pitA, a low-copy number transcriptional pitA-lacZ fusion (pAH1) was introduced into wild-type M. smegmatis. The resulting strain had β-galactosidase activities of about 135 Miller Units (MU), both when grown in ST medium containing 100 mM phosphate and after 2 h starvation in phosphate-free ST medium (Figure 1). Pit systems of Gram-negatives recognize a metal-phosphate complex (MeHPO4) as substrate [18, 19]. It was therefore possible that expression of M. smegmatis pitA was regulated by the availability of such MeHPO4 complexes, free divalent cations (e.g. Mg2+) or pH, as the latter influences the distribution of the different phosphate species in solution [19]. We tested the pitA-lacZ reporter strain after 2 h incubation in Mg2+-free ST medium, exposure to 5 mM EDTA, or incubation in ST medium buffered to pH 4 or pH 9. Under all conditions tested β-galactosidase activities were in the range between 100 MU and 150 MU (Figure 1). No significant differences to the control condition were observed (p > 0.05 in a one-way ANOVA test followed by Dunnett's post-test analysis), suggesting that expression of M. smegmatis pitA was constitutive under all conditions tested.

Figure 1
figure 1

Expression of a transcriptional pitA-lacZ fusion construct in M. smegmatis. Wild-type M. smegmatis harbouring the pitA-lacZ construct pAH1 was grown in ST medium containing 100 mM phosphate (Control), followed by 2 h starvation in phosphate-free (-Pi) or Mg2+-free (-Mg2+) ST medium, or 2 h exposure to 5 mM EDTA (+ EDTA), pH 4 or pH 9. β-Galactosidase (β-Gal) activities were assayed and are expressed in Miller Units (MU). Results are the mean ± standard deviation of three independent experiments.

A pitA deletion mutant has no growth defect in vitro

To determine if pitA played a role in growth and phosphate uptake of M. smegmatis, we next constructed an unmarked pitA deletion strain by an adaptation of the two-step protocol used previously to create a double-kanamycin marked mutant of M. smegmatis [20] (Figure 2). In the first step of mutagenesis, the construct was integrated into the chromosome by growth at 40°C. Southern hybridization analysis showed that correct integration had occurred via a cross-over event in the left flank (Figure 2B). Excision of the plasmid backbone through a second cross-over event was then selected for by growth on 10% sucrose. This second cross-over could lead either to reversion to wild-type or to deletion of the target gene. Nine colonies were screened by Southern hybridization, of which four had reverted back to the wild-type pattern, while five displayed the correct band pattern of a pitA deletion mutant (Figure 2C). One of the latter was chosen for further characterization.

Figure 2
figure 2

Construction of an unmarked pitA deletion mutant of M. smegmatis mc2155. A: Schematic diagram of the two-step approach for deletion of pitA. The knock-out construct consisted of two fragments flanking pitA on the left (LF) and right (RF) in pX33. Integration of the vector (thick grey line) into the chromosome (thin black line) via the left flank (Int LF) or right flank (Int RF) and subsequent deletion of pitA (KO) are shown. Restriction sites of BamHI (B) and fragment sizes as detected in Southern hybridization are indicated. Drawing not to scale. WT, wild-type. B: Southern hybridization analysis of the integration event. BamHI-digests of genomic DNA of wild-type mc2155 (lane 1) and a candidate colony (lane 2) were probed with radiolabeled right flank PCR product of the deletion construct. C: Southern hybridization analysis of pitA deletion. Analysis of wild-type mc2155 (lane 1) and the pitA deletion strain (lane 2) was performed as in panel B. Molecular masses are indicated in kb.

Growth experiments showed no difference between wild-type and pitA mutant in LBT medium or ST medium, either under phosphate-replete conditions (100 μM to 100 mM phosphate) or phosphate-limited conditions (10 μM or 50 μM phosphate) (not shown). This characteristic of the pitA mutant is markedly different from the previously created M. smegmatis mutants in the high-affinity phosphate transporters, which were unable to grow in minimal medium at 10 mM phosphate or below [13]. As mentioned above, Pit systems of Gram-negative bacteria transport a metal-phosphate complex. While no information regarding their substrate is available for Pit systems of Gram-positives, a mutant of Bacillus subtilis carrying an uncharacterized mutation in phosphate uptake was also defective in uptake of metal ions [21], suggesting an interrelation between uptake of phosphate and metals. The biological role of Pit in a bacterium with a plethora of high-affinity phosphate transporters may therefore be in uptake of divalent metal ions. To test this, we performed growth experiments in Mg2+-limited ST medium (2 μM to 2 mM MgCl2), but could not discern a difference between the pitA and wild-type strain (not shown). Because the distribution of MeHPO4 versus free phosphate depends on the medium pH, with MeHPO4 being the predominant species at high pH values [19], it was conceivable that the physiological role of Pit is to act under conditions where most phosphate is present as MeHPO4. To simulate such a condition in vitro, we modified the ST medium to contain a high concentration of MgCl2 (8 mM) and low concentration of phosphate (100 μM) and adjusted the pH to 8.5 (buffered with 100 mM Tricine). No difference was found between the wild-type and pitA mutant strains (not shown). An E. coli pitA mutant displayed increased resistance to toxic divalent cations (Zn2+ and Cd2+), due to reduced uptake of these ions [22]. The M. smegmatis pitA mutant and wild-type strain were therefore grown on solid media (ST agar, 50 mM MES [pH 7], 1 mM phosphate) containing 1-15 mM ZnSO4 or CuSO4. Both strains were able to grow in the presence of 1 mM of either salt, but could not grow at concentrations of 5 mM or higher. Taken together, the data presented here suggest that either PitA of M. smegmatis does not transport MeHPO4, or that one or both of the high-affinity systems also recognize such a complex as substrate. It should be noted that no substrate specificities have been determined to date for a Pst system from a Gram-positive bacterium, or for a Phn system.

The pitAmutant displays no defect in phosphate uptake

We next determined the rates and kinetics of uptake of [33P]ortho-phosphate, to assess whether the pitA deletion strain had a defect in phosphate uptake. To prevent induction of the Pst or Phn systems, cells were grown in LBT medium as described in the methods section. As shown in figure 3, maximum uptake rates were 12.9 ± 1.6 nmol min-1 mg protein-1 for the wild-type, and 9.9 ± 1.0 nmol min-1 mg protein-1 for the pitA strain. Kd values were similar between the strains, with 50.1 ± 26 μM phosphate for the wild-type and 27.9 ± 16.4 μM phosphate for the pitA strain. Slight differences in transport rates at the higher phosphate concentrations were not significant (p > 0.2 in unpaired, two-tailed t-test).

Figure 3
figure 3

Kinetics of phosphate uptake. Initial uptake rates of ortho-phosphate (33P, > 92.5 TBq mmol-1) into LBT-grown whole cells of M. smegmatis mc2155 (solid squares) and the pitA deletion strain (open squares) were measured over 60 s at phosphate concentrations between 25 μM and 500 μM. Rates are expressed as nmol phosphate min-1 mg mycobacterial protein extract-1, and data are shown as the mean ± standard error of the mean from two to five independent measurements per point.

These kinetic parameters suggest that the rates of transport determined are due to activity of the high-affinity systems, because Kd values of phosphate uptake under phosphate-starved (i.e. Pst and Phn systems induced) conditions were found to be between 40 and 90 μM phosphate [13]. The rates of transport in the present study are about ten-fold lower than those in phosphate-starved cells, consistent with the previously described 20-fold lower expression from the pst and phn promoters under these conditions [13]. PitA of M. smegmatis therefore appears to be either not active, or to have a very low activity, which cannot be detected over the background of the high-affinity systems using the assay employed here. Considering the abundance of phosphate transport systems in M. smegmatis, we hypothesized that loss of PitA is easily compensated for by increased use of the Pst and Phn systems.

Deletion of pitAcauses increased expression of the Pst and Phn systems

To address the question whether the pitA deletion mutant employs increased expression of either the Pst or Phn system to compensate for the deletion, we introduced the previously created transcriptional pstS-lacZ (pSG42) and phnD-lacZ (pSG10) fusion constructs [13] into the pitA deletion background. As shown in figure 4, under phosphate-replete conditions the activity of both promoters was increased by about two-fold in the pitA strain. Complementation of the deletion with a single copy of pitA under control of its native promoter restored expression of pstS-lacZ and phnD-lacZ to wild-type levels. No differences between strains were observed in phosphate-starved cells (data not shown). These data imply that PitA is indeed used for phosphate uptake under high phosphate conditions by M. smegmatis, but that loss of this system is easily compensated for by the remaining phosphate transporters.

Figure 4
figure 4

Expression from the pst and phn promoters in the pitA deletion background. Transcriptional phnD-lacZ and pstS-lacZ fusion constructs were introduced into wild-type M. smegmatis (open bars), the pitA deletion strain (black bars) and the pitA complemented strain (hatched bars). β-Galactosidase (β-Gal) activities, expressed as Miller Units (MU), were determined from cultures grown in ST medium with 100 mM phosphate and are shown as the mean ± standard deviation from three independent experiments. Significant differences between samples in one-way ANOVA followed by Bonferroni post-test analyses are indicated by two (p < 0.01) or three (p < 0.001) asterisks.


In summary, we here show that the PitA system of M. smegmatis is constitutively expressed under a variety of growth conditions, and that deletion of the pitA gene does not appear to affect growth or phosphate uptake in vitro. This is presumably due to compensation of the deletion by increased expression of the high-affinity phosphate transport systems, PstSCAB and PhnDCE.

The lack of phenotype of the pitA mutant under the growth conditions tested here, together with the wild-type levels of phosphate uptake in the mutant strain, raises the question as to why mycobacteria still contain this transporter. This point is further emphasized by the presence of a functional pitA gene in M. leprae, whose genome has undergone reductions and decay to the point where the bacterium is unable to replicate outside of its host [23]. The answer may be found in the energetics of transport: Pit systems transport metal-phosphate in symport with protons at a stoichiometry of 1:1 [3], while the Pst and Phn systems are ABC-transporters and thus likely require hydrolysis of two ATP per substrate transported [24]. Uptake of phosphate via the Pit system is therefore energetically less expensive to the cell, and this could be important under conditions where energy is limiting. However, there was no significant difference in the molar growth yield (mg [dry weight] cells/mmol of substrate consumed) between the pitA deletion mutant and the wild-type when grown under carbon limitation in continuous culture at a dilution rate of 0.01 h-1 (doubling-time of 70 h) (our own unpublished results). We therefore hypothesize that a phenotype for a pitA mutant of mycobacteria may well only manifest itself in vivo under conditions where the cell is exposed to multiple limitations (e.g. carbon, energy, oxygen), such as are commonly found in the intraphagosomal environment of the pathogens or the soil habitat of environmental species.


Bacterial strains and growth conditions

All strains and plasmids used in this study are listed in Table 1. Escherichia coli strains were grown in Luria-Bertani (LB) medium at 37°C with agitation (200 rpm). Mycobacterium smegmatis strain mc2155 [25] and derived strains were routinely grown at 37°C, 200 rpm in LB containing 0.05% (w/v) Tween80 (LBT) or in modified Sauton's (ST) medium [13]. Variations of phosphate and MgCl2 concentrations and other modifications of the ST medium are given in the text. Cells to be used as inoculum in phosphate-limited ST medium were washed once in phosphate-free medium prior to use. Starvation experiments in phosphate-free ST medium were carried out as described previously [13]. M. smegmatis transformants were grown at 28°C for propagation of temperature-sensitive vectors and at 40°C for allelic exchange mutagenesis. Selective media contained kanamycin (50 μg ml-1 for E. coli; 20 μg ml-1 for M. smegmatis), gentamycin (20 μg ml-1 for E. coli; 5 μg ml-1 for M. smegmatis) or hygromycin (200 μg ml-1for E. coli; 50 μg ml-1 for M. smegmatis). Solid media contained 1.5% agar. Optical density was measured at 600 nm (OD600) using culture samples diluted in saline to bring OD600 to below 0.5 when measured in cuvettes of 1 cm light path length in a Jenway 6300 spectrophotometer.

Table 1 Bacterial strains, plasmids and primers used in this study

DNA manipulation and cloning of constructs

All molecular biology techniques were carried out according to standard procedures [26]. Restriction or DNA modifying enzymes and other molecular biology reagents were obtained from Roche Diagnostics or New England Biolabs. Genomic DNA of M. smegmatis was isolated as described previously [13]. All primer sequences are listed in Table 1.

To create a transcriptional fusion of the pitA promoter to lacZ, a fragment containing 750 bp of upstream sequence to pitA (MSMEG_1064) was amplified with primers PitA6 and PitA5 and cloned into the BamHI and SphI sites of the low copy-number vector (3-10 copies per cell) pJEM15 [27], resulting in plasmid pAH1. Assays for β-galactosidase activity were carried out as described previously [13]. Cells of M. smegmatis harbouring the empty vector pJEM15 displayed β-galactosidase activities of less than 2 MU. Statistical analysis of reporter-strain experiments after starvation or stress-exposure was performed using one-way ANOVA followed by a Dunnett's post-test comparison of each sample to the control condition. Data from experiments of the phnD-lacZ and pstS-lacZ constructs in various genetic backgrounds were analyzed by one-way ANOVA followed by Bonferroni post-test comparison of all pairs of data-sets. All statistical analyses were performed using GraphPad Prism 4 software.

To create a construct for markerless deletion of pitA, an 833 bp fragment flanking pitA on the left, including 62 bp coding sequence, was amplified with primers PitA1 and PitA2, and a 1022 bp fragment flanking pitA on the right, including 4 bp coding sequence, was amplified with primers PitA3 and PitA4. The two products were fused by PCR-overlap extension [28], cloned into the SpeI site of the pPR23-derived [29] vector pX33 [13], creating pPitAKO, and transformed into M. smegmatis mc2155. Deletion of pitA was carried out using the two-step method for integration and excision of the plasmid as described previously [20]. Correct integration and excision were confirmed by Southern hybridization analysis as described previously [13]. The deletion resulted in loss of 95% of the pitA coding sequence, creating strain NP6

For complementation of the pitA deletion, pitA plus 790 bp upstream DNA was PCR amplified with primers cPitAf and cPitAr and cloned as a HindIII fragment into the integrative E. coli/mycobacteria shuttle vector pUHA267 (AgResearch, Wallaceville), creating plasmid pCPitA. Transformation into the pitA mutant resulted in strain NP13.

Phosphate transport assays

Strains of M. smegmatis were grown to an OD600 of 1 in LBT medium, collected by centrifugation and resuspended to an OD600 between 1.5 and 2 in pre-warmed assay buffer (50 mM MOPS [pH 7.5], 5 mM MgCl2, 0.05% (w/v) Tween80, 0.4% glycerol, 37°C). Initial rates of uptake of [33P]ortho-phosphate (> 92.5 TBq mmol-1; Amersham) were determined over a range of phosphate concentrations between 25 μM and 500 μM as described previously [13].


  1. Wanner BL: Phosphorus Assimilation and Control of the Phosphate Regulon. Escherichia coli and Salmonella: cellular and molecular biology. Edited by: Neidhardt FC, Curtiss R III, Ingraham JL, Lin ECC, Low KB, Magasanik B, Reznikoff WS, Riley M, Schaechter M, Umbarger HE. 1996, Washington, DC: ASM Press, 1: 1357-1381. 2

    Google Scholar 

  2. van Veen HW: Phosphate transport in prokaryotes: molecules, mediators and mechanisms. Antonie Van Leeuwenhoek. 1997, 72 (4): 299-315. 10.1023/A:1000530927928.

    Article  CAS  PubMed  Google Scholar 

  3. van Veen HW, Abee T, Kortstee GJ, Konings WN, Zehnder AJ: Mechanism and energetics of the secondary phosphate transport system of Acinetobacter johnsonii 210A. J Biol Chem. 1993, 268 (26): 19377-19383.

    CAS  PubMed  Google Scholar 

  4. White AK, Metcalf WW: The htx and ptx operons of Pseudomonas stutzeri WM88 are new members of the pho regulon. J Bacteriol. 2004, 186 (17): 5876-5882. 10.1128/JB.186.17.5876-5882.2004.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  5. White AK, Metcalf WW: Two C-P lyase operons in Pseudomonas stutzeri and their roles in the oxidation of phosphonates, phosphite, and hypophosphite. J Bacteriol. 2004, 186 (14): 4730-4739. 10.1128/JB.186.14.4730-4739.2004.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  6. Voegele RT, Bardin S, Finan TM: Characterization of the Rhizobium (Sinorhizobium) meliloti high- and low-affinity phosphate uptake systems. J Bacteriol. 1997, 179 (23): 7226-7232.

    CAS  PubMed Central  PubMed  Google Scholar 

  7. Metcalf WW, Wanner BL: Involvement of the Escherichia coli phn (psiD) gene cluster in assimilation of phosphorus in the form of phosphonates, phosphite, Pi esters, and Pi. J Bacteriol. 1991, 173 (2): 587-600.

    CAS  PubMed Central  PubMed  Google Scholar 

  8. Imazu K, Tanaka S, Kuroda A, Anbe Y, Kato J, Ohtake H: Enhanced utilization of phosphonate and phosphite by Klebsiella aerogenes. Appl Environ Microbiol. 1998, 64 (10): 3754-3758.

    CAS  PubMed Central  PubMed  Google Scholar 

  9. Lefèvre P, Braibant M, de Wit L, Kalai M, Roeper D, Grotzinger J, Delville JP, Peirs P, Ooms J, Huygen K, et al: Three different putative phosphate transport receptors are encoded by the Mycobacterium tuberculosis genome and are present at the surface of Mycobacterium bovis BCG. J Bacteriol. 1997, 179 (9): 2900-2906.

    PubMed Central  PubMed  Google Scholar 

  10. Braibant M, Lefèvre P, de Wit L, Ooms J, Peirs P, Huygen K, Wattiez R, Content J: Identification of a second Mycobacterium tuberculosis gene cluster encoding proteins of an ABC phosphate transporter. FEBS Lett. 1996, 394 (2): 206-212. 10.1016/0014-5793(96)00953-2.

    Article  CAS  PubMed  Google Scholar 

  11. Collins DM, Kawakami RP, Buddle BM, Wards BJ, de Lisle GW: Different susceptibility of two animal species infected with isogenic mutants of Mycobacterium bovis identifies phoT as having roles in tuberculosis virulence and phosphate transport. Microbiology. 2003, 149 (Pt 11): 3203-3212. 10.1099/mic.0.26469-0.

    Article  CAS  PubMed  Google Scholar 

  12. Rifat D, Bishai WR, Karakousis PC: Phosphate Depletion: A Novel Trigger for Mycobacterium tuberculosis Persistence. J Infect Dis. 2009, 200 (7): 1126-1135. 10.1086/605700.

    Article  CAS  PubMed  Google Scholar 

  13. Gebhard S, Tran SL, Cook GM: The Phn system of Mycobacterium smegmatis : a second high-affinity ABC-transporter for phosphate. Microbiology. 2006, 152 (Pt 11): 3453-3465. 10.1099/mic.0.29201-0.

    Article  CAS  PubMed  Google Scholar 

  14. Cole ST, Brosch R, Parkhill J, Garnier T, Churcher C, Harris D, Gordon SV, Eiglmeier K, Gas S, Barry CE, et al: Deciphering the biology of Mycobacterium tuberculosis from the complete genome sequence. Nature. 1998, 393 (6685): 537-544. 10.1038/31159.

    Article  CAS  PubMed  Google Scholar 

  15. Rosenberg H, Gerdes RG, Chegwidden K: Two systems for the uptake of phosphate in Escherichia coli. J Bacteriol. 1977, 131 (2): 505-511.

    CAS  PubMed Central  PubMed  Google Scholar 

  16. Harris RM, Webb DC, Howitt SM, Cox GB: Characterization of PitA and PitB from Escherichia coli. Journal of bacteriology. 2001, 183 (17): 5008-5014. 10.1128/JB.183.17.5008-5014.2001.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  17. Bardin SD, Voegele RT, Finan TM: Phosphate assimilation in Rhizobium (Sinorhizobium) meliloti : identification of a pit-like gene. J Bacteriol. 1998, 180 (16): 4219-4226.

    CAS  PubMed Central  PubMed  Google Scholar 

  18. van Veen HW, Abee T, Kortstee GJ, Konings WN, Zehnder AJ: Translocation of metal phosphate via the phosphate inorganic transport system of Escherichia coli. Biochemistry. 1994, 33 (7): 1766-1770. 10.1021/bi00173a020.

    Article  CAS  PubMed  Google Scholar 

  19. van Veen HW, Abee T, Kortstee GJ, Konings WN, Zehnder AJ: Substrate specificity of the two phosphate transport systems of Acinetobacter johnsonii 210A in relation to phosphate speciation in its aquatic environment. J Biol Chem. 1994, 269 (23): 16212-16216.

    CAS  PubMed  Google Scholar 

  20. Tran SL, Cook GM: The F1Fo-ATP synthase of Mycobacterium smegmatis is essential for growth. J Bacteriol. 2005, 187 (14): 5023-5028.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  21. Kay WW, Ghei OK: Inorganic cation transport and the effects on C4 dicarboxylate transport in Bacillus subtilis. Can J Microbiol. 1981, 27 (11): 1194-1201.

    Article  CAS  PubMed  Google Scholar 

  22. Beard SJ, Hashim R, Wu G, Binet MR, Hughes MN, Poole RK: Evidence for the transport of zinc(II) ions via the pit inorganic phosphate transport system in Escherichia coli. FEMS Microbiol Lett. 2000, 184 (2): 231-235. 10.1111/j.1574-6968.2000.tb09019.x.

    Article  CAS  PubMed  Google Scholar 

  23. Cole ST, Eiglmeier K, Parkhill J, James KD, Thomson NR, Wheeler PR, Honore N, Garnier T, Churcher C, Harris D, et al: Massive gene decay in the leprosy bacillus. Nature. 2001, 409 (6823): 1007-1011. 10.1038/35059006.

    Article  CAS  PubMed  Google Scholar 

  24. Dawson RJ, Hollenstein K, Locher KP: Uptake or extrusion: crystal structures of full ABC transporters suggest a common mechanism. Mol Microbiol. 2007, 65 (2): 250-257. 10.1111/j.1365-2958.2007.05792.x.

    Article  CAS  PubMed  Google Scholar 

  25. Snapper SB, Melton RE, Mustafa S, Kieser T, Jacobs WR: Isolation and characterization of efficient plasmid transformation mutants of Mycobacterium smegmatis. Mol Microbiol. 1990, 4 (11): 1911-1919. 10.1111/j.1365-2958.1990.tb02040.x.

    Article  CAS  PubMed  Google Scholar 

  26. Sambrook J, Fritsch EF, Maniatis T: Molecular cloning: a laboratory manual. 1989, Cold Spring Harbor, N.Y.: Cold Spring Harbor Laboratory Press, 2

    Google Scholar 

  27. Timm J, Lim EM, Gicquel B: Escherichia coli-mycobacteria shuttle vectors for operon and gene fusions to lacZ : the pJEM series. J Bacteriol. 1994, 176 (21): 6749-6753.

    CAS  PubMed Central  PubMed  Google Scholar 

  28. Ho SN, Hunt HD, Horton RM, Pullen JK, Pease LR: Site-directed mutagenesis by overlap extension using the polymerase chain reaction. Gene. 1989, 77 (1): 51-59. 10.1016/0378-1119(89)90358-2.

    Article  CAS  PubMed  Google Scholar 

  29. Pelicic V, Jackson M, Reyrat JM, Jacobs WR, Gicquel B, Guilhot C: Efficient allelic exchange and transposon mutagenesis in Mycobacterium tuberculosis. Proc Natl Acad Sci USA. 1997, 94 (20): 10955-10960. 10.1073/pnas.94.20.10955.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  30. Hanahan D, Jessee J, Bloom FR: Plasmid transformation of Escherichia coli and other bacteria. Methods Enzymol. 1991, 204: 63-113. full_text.

    Article  CAS  PubMed  Google Scholar 

Download references


The authors would like to thank A. Hümpel for cloning of the pitA deletion and promoter fusion constructs.

Author information

Authors and Affiliations


Corresponding author

Correspondence to Susanne Gebhard.

Additional information

Authors' contributions

SG contributed to design of the study, participated in growth experiments, phosphate transport and reporter gene assays and drafted the manuscript. NE carried out the molecular work and participated in all other experimental aspects. GMC contributed to design of the study, participated in phosphate transport assays and helped to draft the manuscript. All authors read and approved the final manuscript.

Authors’ original submitted files for images

Rights and permissions

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Reprints and permissions

About this article

Cite this article

Gebhard, S., Ekanayaka, N. & Cook, G.M. The low-affinity phosphate transporter PitA is dispensable for in vitro growth of Mycobacterium smegmatis. BMC Microbiol 9, 254 (2009).

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: