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Ammonia production by human faecal bacteria, and the enumeration, isolation and characterization of bacteria capable of growth on peptides and amino acids



The products of protein breakdown in the human colon are considered to be detrimental to gut health. Amino acid catabolism leads to the formation of sulfides, phenolic compounds and amines, which are inflammatory and/or precursors to the formation of carcinogens, including N-nitroso compounds. The aim of this study was to investigate the kinetics of protein breakdown and the bacterial species involved.


Casein, pancreatic casein hydrolysate (mainly short-chain peptides) or amino acids were incubated in vitro with suspensions of faecal bacteria from 3 omnivorous and 3 vegetarian human donors. Results from the two donor groups were similar. Ammonia production was highest from peptides, followed by casein and amino acids, which were similar. The amino acids metabolized most extensively were Asp, Ser, Lys and Glu. Monensin inhibited the rate of ammonia production from amino acids by 60% (P = 0.001), indicating the involvement of Gram-positive bacteria. Enrichment cultures were carried out to investigate if, by analogy with the rumen, there was a significant population of asaccharolytic, obligately amino acid-fermenting bacteria (‘hyper-ammonia-producing’ bacteria; HAP) in the colon. Numbers of bacteria capable of growth on peptides or amino acids alone averaged 3.5% of the total viable count, somewhat higher than the rumen. None of these were HAP, however. The species enriched included Clostridium spp., one of which was C. perfringens, Enterococcus, Shigella and Escherichia coli.


Protein fermentation by human faecal bacteria in the absence of sugars not only leads to the formation of hazardous metabolic products, but also to the possible proliferation of harmful bacteria. The kinetics of protein metabolism were similar to the rumen, but HAP bacteria were not found.


Protein is an abundant substrate for bacterial growth in the human intestine, possibly more so than carbohydrate in the distal colon [1]. Some of the protein may be of dietary origin, but large intestinal fermentation probably depends more on endogenous sources, including mucus and host proteins and bacterial protein resulting from bacterial cell turnover. The metabolism of protein and its peptide and amino acid hydrolysis products by colonic bacteria can lead to the formation of several by-products that may be hazardous to health [2]. N-nitroso compounds are formed from amines and amides, which in turn arise from the metabolism of amino acids; they are heavily implicated in the etiology of colorectal cancer [3]. Hydrogen sulfide is a product of the breakdown of cysteine and methionine; sulfides induce hyperproliferation of crypt cells [4], and predispose to colonic carcinomas [5] and ulcerative colitis [6]. Other potentially toxic products of protein breakdown in the large intestine include phenols, ammonia and indoles [7]. Thus, understanding the processes and bacteria that carry out proteolysis and its subsequent reactions is highly relevant to human gut health.

Proteolytic species from the human colon have been well characterized [1, 8, 9], and some aspects of the metabolism of peptides are known [1, 10]. Bacterial species able to grow on individual amino acids as N and energy source are fairly well understood [11]. They include many of the ‘putrefactive’ Clostridium, Peptostreptococcus and Fusobacterium species [11, 12]. Some evidence that gut bacteria can also use Stickland reactions, which involves the coupled oxidation and reduction of pairs of amino acids to organic acids [13], was obtained by Smith and Macfarlane [1]. However, bacteria able to grow on a mixture of protein breakdown products, although known to be numerous [11], have not been characterized. It is possible that the species that derive energy from protein in the colon are among the most numerous species which, when carbohydrate has been exhausted, switch to amino acids as a substrate for generating metabolic energy. It is also possible, however, that a less numerous, high-activity functional group of deaminative bacteria exists, analogous to the ‘hyper-ammonia-producing’ (HAP) bacteria of the rumen [1418]. These asaccharolytic bacteria generate NH3 at a rate far greater than the most numerous ruminal species, such that, although their population size is small, they may make a significant contribution to overall NH3 production in the rumen of cattle and sheep. Attention has been paid to these bacteria because of their impact on N retention in the animal. If they were to exist in the human colon, they might have a similar significance, except to human health rather than nutrition. They might also be subject to dietary manipulation, as in the rumen [18, 19]. The aim of the present work was therefore to investigate the properties of NH3 production from protein in the colon, and to use methods that revealed the ruminal HAP population to determine if HAP populations also exist in the human colonic microbiota.


Ammonia production in faecal suspensions in vitro

The rate of NH3 production by mixed faecal bacteria depended on the donor and the substrate. Six samples were investigated for their activity with Trypticase, a pancreatic casein hydrolysate containing predominantly peptides, and an amino acid mixture formulated to contain the same amino acid composition (Table 1). There were significant differences (P < 0.001) between production rates on Trypticase and amino acids, and the production rate was decreased by monensin (P < 0.001) but there was no interaction (P = 0.866). Activities were similar in the 3 samples from omnivores and in one sample from a vegetarian, while one vegetarian sample had about half the average activity and the other double the average. The type of subject diet did not affect production rate (P = 0.678). In a different set of samples from donors O1, O2 and V1, the rate of NH3 production from casein was 19% lower than from Trypticase (P = 0.04) and not different from amino acids (P >0.05) (results not shown). Monensin had a greater effect on NH3 production from amino acids (60% inhibition) compared to peptides (Trypticase; 39% inhibition) (Table 1; P = 0.003).

Table 1 Ammonia production from peptides (Trypticase) and amino acids by mixed human faecal bacteria in vitro with and without added 5 μM monensin

Amino acid analysis revealed that total amino acid breakdown was slightly greater with peptides than amino acids, but the effect was not significant (Table 2). No amino acid was degraded completely during the course of the incubations. The order of rates of disappearance of different amino acids was also similar for both substrates, with Glu, Asp, Ser and Lys being most rapidly degraded and the aromatic amino acids, Phe and Tyr, being most resistant to degradation. Tryptophan was not present in the analysis because it was destroyed during the acid hydrolysis method used to hydrolyse samples. Monensin had a major inhibitory effect on the breakdown of amino acids in both substrates, with an inhibition of 61% with amino acids and 48% with Trypticase (Table 2). The effects were different with different amino acids and according to the substrate. The breakdown of free Glu and Ala was completely inhibited, resulting in slight net synthesis, and Pro metabolism decreased by 86%. In contrast, breakdown of Asp in the amino acids mixture was unaffected by monensin, and Arg breakdown was inhibited only by 15% For the most part, monensin inhibited amino acid dissimilation to the same extent, whether present in peptides or amino acids. Again, Glu was an exception, its metabolism being inhibited less when present in peptide form.

Table 2 Amino acid utilization from peptides (Trypticase) and amino acids by mixed human faecal bacteria in vitro with and without added 5 μM monensin

Assessment of population size of bacteria capable of growth on peptides and amino acids

When dilutions of faecal bacteria were inoculated into liquid media in anaerobic culture tubes, both the number of tubes showing growth and the cell density achieved increased with the time of incubation. Numbers on complete medium generally reached a plateau at 2 d, while growth on the other, sugars-free media usually reached a maximum at 4 d, although because a few increases were observed between 4 and 7 d, 7-d values were used to calculate bacterial numbers (Figure 1). Total numbers approached 1010 (g wet wt)-1, while numbers capable of growing on sugar-free media after 7 d were about 108 (g wet wt)-1. Actual counts on Trypticase medium varied from 0.8 × 107 to 3.5 × 108 (g wet wt)-1. Monensin decreased numbers in Trypticase medium by an average of 92% to 105-106 (g wet wt)-1. Amino acid utilizers were on average only slightly (26%) fewer in number than Trypticase utilizers.

Figure 1
figure 1

Most-probable-numbers (MPN) counts of Trypticase and amino acid-utilising bacteria in faeces from human omnivorous (O2 and O3) and vegetarian (V1 and V2) donors. Results are from 7-d counts. Error bars represent 95% confidence levels.

Bacterial isolates

A total of 53 isolates was isolated from the highest dilutions of faecal bacteria from two ominivores and one vegetarian. Twenty-eight survived repeated sub-culture, of which 24 gave full length or near full length 16S rRNA gene sequences (Table 3). The remaining four were identified from partial sequences. None of the isolates was asaccharolytic, growth being increased significantly in all cases by the addition of glucose to the medium. The bacteria enriched from the faecal samples appeared to be different depending on whether the substrate was peptides or amino acids. Shigella spp. and E. coli were more numerous in the amino acids-containing cultures. Other pathogens that were enriched included Enterococcus faecalis, Staphylococcus sp. and Eggerthella lenta.

Table 3 Identity of bacteria isolated from peptides or amino acids enrichments


The measurements made here of rates of NH3 production from different amino acid-containing substrates, the influence of monensin on these rates, and the properties of bacteria isolated on the basis of being able to grow on Trypticase have important implications for understanding the biochemistry and microbial ecology of amino acid metabolism, and therefore the production of potentially hazardous products that can be formed from amino acids and related nitrogenous compounds in the human colon [2]. These results add to the substantial body of knowledge generated by Smith and Macfarlane [1, 811, 20] in the following respects. Ammonia production from peptides and amino acids was compared in diluted fresh samples of faeces in a similar way, with very similar results to earlier studies. However, utilization of individual amino acids from peptides was also compared, using faecal samples from both vegetarians and omnivorous donors. The differences may be explained by different permease mechanisms for peptides and amino acids. The effects of monensin on NH3 production and amino acid dissimilation were shown, providing clues about the biochemistry and microbial ecology of amino acid dissimilation. Finally, the bacteria that were enriched by growth on peptides or amino acids as energy source were isolated and identified based on 16S rRNA gene sequences. Similar methodology in the rumen revealed the HAP population, with significant implications for animal nutrition. The results imply that, unlike in the rumen, there is no significant population of ‘hyper-ammonia-producing’ bacteria [18]. Instead, the species that were enriched by growth on peptides and amino acids in the absence of carbohydrates include several pathogenic species that have important implications for health.

Ammonia production rates from Trypticase were higher than from casein or from a corresponding amino acid mixture. Casein is a protein that is atypically susceptible to proteolytic degradation, so it may be concluded that the first step of protein degradation to NH3 in the intestine, namely proteolysis, would generally be rate-limiting. Smith & Macfarlane [1] also noted that NH3 production was greater from peptides than amino acids, and suggested that amino acid transport in the form of peptides would be more energy-efficient than free amino acids. NH3 production from amino acids was more sensitive to the ionophore, monensin, than from peptides. The greater sensitivity to monensin of amino acid compared to peptide metabolism presumably reflects differences in transport mechanisms into bacteria. Transport of peptides in bacteria occurs predominantly by the ABC superfamily of transporters, which use ATP to drive uptake [21, 22], while amino acid transport is more commonly linked to proton or Na+ gradients [23]. As monensin catalyzes Na+/H+ antiport in susceptible bacteria [24, 25], this ionophore would therefore affect ion-linked amino acid transport more than ATP-linked peptide transport.

Smith & Macfarlane [20] investigated the metabolism of individual amino acids and a few pairs of amino acids in slurries of human faecal bacteria, and found that Ser was much more rapidly degraded than other amino acids. The same authors investigated breakdown of a complete mixture of free amino acids added to a fermenter that had been inoculated with a suspension of human faecal bacteria. Ser was again degraded most rapidly, with Asp close behind, followed by Arg. Glu was lost at less than one-quarter of the rate of Asp. Aromatic amino acids were degraded most slowly. The results of the present study were fairly similar, with the major exceptions of Glu, which was broken down most rapidly of all amino acids, and Lys, which was third or fourth most rapidly degraded amino acid in our studies but among the very lowest in Smith & Macfarlane [1]. While there were differences between methods in the studies, none offers an obvious explanation for these differences. Also, it is not clear whether the routes of metabolism of relatively low concentrations of amino acids in a complete mixture and metabolized by a mixed microbiota would be the same as pure cultures metabolizing the amino acid as a single substrate. This may be particularly relevant to Glu, which can be metabolized either via the methylaspartate pathway in clostridia or the hydroxyglutamate pathway in other species [26, 27], yet, in mixtures of amino acids in a mixed culture with lower concentrations of Glu, Glu is most probably deaminated or transaminated to α-oxoglutarate, which then enters and disperses into central metabolic pathways.

The pattern of utilization of different amino acids was similar whether the amino acids were free or added as peptides. This provides a major contrast to the rumen, where peptide-bound amino acids are metabolized at different rates to free amino acids and in a different order [28, 29]. Peptide uptake can predominate over amino acids in the ruminal bacteria of many animals, depending on the predominant microbiota that is present [30, 31]. The present results with the human microbiota suggest that, at least in the individuals who provided samples here, amino acid utilizing bacteria are more dominant than peptide utilizers. The results with faecal samples from omnivores compared to vegetarians were inconclusive in terms of NH3 production, but the ranking order of dissimilation of different amino acids was similar.

The influence of monensin was different with different amino acids. Pro, Ala and Glu were inhibited most, with Asp and Lys affected only to a minor extent. Once again, the reason for this difference is unclear, but presumably reflects the inhibition of some transport systems and not others, or possibly a differential inhibition of species that metabolize different amino acids [17, 18].

One of the principal aims of this work was to investigate if, by analogy with the rumen, HAP bacteria were present in the human colon. Conditions of low-carbohydrate, high-protein nutrient availability would favour bacteria able to derive energy from amino acids, particularly in the distal colon, but the general procedure of routinely adding sugars to growth media may have concealed these bacteria in culture-based studies. There had been a long-held assumption for the rumen that a large group of bacteria identified many years ago [32] was responsible for ruminal amino acid deamination. Russell and his colleagues at Cornell University challenged this assumption, and isolated less numerous, but much more active, asaccharolytic, obligately peptide-fermenting bacteria, the HAP species [18]. Growth of HAP bacteria was inhibited by monensin, while the more numerous NH3 producers were unaffected, yet NH3 production by the mixed ruminal microbiota was monensin-sensitive. The present paper suggests that the human microbiota has an NH3-producing activity about one-third that of the rumen [17]. Nevertheless, it is clear that a substantial fraction of NH3 production from peptides and amino acids is monensin-sensitive, so the possibility existed that HAP species were present in human colonic digesta.

Bacteria capable of growth on peptides as energy source were variable in number, averaging 3.5% of the total viable count. This proportion is somewhat higher than was found in ruminal digesta [1618]. Actual numbers varied from 0.8 × 107 to 3.5 × 108 (g wet wt)-1, which compares with 1011 per g dry weight on peptone medium measured by Smith & Macfarlane [1]. Numbers capable of growth on amino acids were almost as high as those growing on Trypticase, which is a complete contrast to the rumen, where numbers of amino acids utilizers were two orders of magnitude less than Trypticase utilizers [17]. Thus, the bacterial population capable of using protein breakdown products in the human colon was more numerous than in the rumen, but less active, and differed in its much lower preference for peptides. As with the rumen, >90% of Trypticase utilizers were sensitive to inhibition by monensin, indicating that the bacteria were predominantly Gram-positive [33].

Smith & Macfarlane [1] enumerated amino acid-fermenting colonic bacteria in medium containing peptone, but did not isolate the bacteria concerned, concentrating on bacteria growing on individual or Stickland pairs of amino acids. The latter included mainly Clostridium species, with Peptostreptococcus, Fusobacterium, Actinomyces, Bacteroides, Megasphaera and Propionibacterium all represented. In the present study, the enrichments resulted in the isolation of several groups of bacteria. None was a HAP species, as all fermented glucose. Thus, the microbial ecology of the rumen and the human colon are fundamentally different in this respect. The species were also different to those isolated by Smith & Macfarlane [1]. Clostridium and Bacteroides were similarly predominant, though the species were different. Notably, one of the bacteria enriched was C. perfringens, which is a pathogen in animal species and man [34, 35]. One might conclude, therefore, that individuals consuming a low-carbohydrate, high-protein weight loss diet would be vulnerable to increased numbers of pathogens in the intestine, as well as the better characterized genotoxic and inflammatory products of amino acid catabolism [2].


The metabolism of peptides and amino acids by human faecal bacteria has many parallels with similar metabolism in the rumen, except that the bacteria that grow on these substrates are not specialist asaccharolytic (HAP) species. Instead, they tend to be pathogens. Thus, the implication is that when protein is the main substrate for intestinal bacteria, not only are the products of protein fermentation toxic, the bacteria enriched by these conditions may be harmful.



These experiments were carried out in compliance with the Helsinki Declaration of Ethical Principles for Medical Research Involving Human Subjects ( Ethical approval was granted by the North of Scotland Research Ethics Committee and all subjects provided informed signed consent. Fresh faeces were obtained from three omnivorous (O1 – O3) and three vegetarian (V1 – V3) donors. No specific diets were given. O1 and O2 were 33-year-old females, O3 was a 47-year-old female, V1 and V3 were 56- and 26-year-old males, and V2 was a 43-year-old female. None had received antibiotic therapy for 3 months before samples were given. All samples were used fresh.

Measurement of ammonia production in faecal suspensions in vitro

Faecal samples were diluted 1:10 wet weight in Chen & Russell basal medium [36], the suspension was homogenized in a stomacher, and 10 ml were added, under CO2, to Hungate-type tubes containing 200 mg substrate with or without 10 μl ethanol or 10 μl 5 mM monensin (Sigma, Poole, Dorset, UK) in ethanol. This monensin concentration (5 μM) was based on that used by Chen & Russell [16, 37], which is similar to the estimated monensin concentration in vivo[38]. Tubes were incubated in vitro under CO2 in a water bath at 37°C. Substrates included casein (Sigma), Trypticase® peptone (Becton Dickinson Microbiology Systems, Cockeysville, MD 21030), and an amino acids mixture based on the composition of casein. The amino acids mixture comprised Gibco casein hydrolysate No. 5 (Life Technologies Ltd, Paisley, UK) plus added L-tryptophan (0.87%), L-methionine (0.17%) and L-cysteine (0.14%). One-ml samples were removed at 0, 2, 4, 6 and 8 h into 1.5-ml microcentrifuge tubes containing 0.25 ml 25% TCA. Samples were stored at 4°C, then centrifuged at 27,000 g for 20 min and ammonia was measured on supernatants. Ammonia was determined in the supernatant fluid by an automated phenol-hypochlorite method [39] and protein was determined on the acid precipitate using the Folin reagent [40]. For amino acids analysis, aliquots from the supernatant were dried under vacuum and hydrolysed by a vapour phase method (constant boiling HCl, 110°C, 18 h) and then derivatized with phenylisothionate and analysed by HPLC [41].

Bacterial counts

Samples of faecal suspensions were diluted serially ten-fold under CO2 in a vitamins/minerals medium with no carbohydrate source, based on that described by Chen & Russell [36]. The basal medium contained, per liter, 292 mg of K2HPO4, 292 mg of KH2PO4, 480 mg of Na2SO4, 480 mg of NaCl, 100 mg of MgSO4.7H2O, 55 mg anhydrous CaCl2, 1.0 ml of 0.1% resazurin, 600 mg of cysteine hydrochloride and vitamins and minerals solutions [36]. The medium was adjusted to pH 7.0 before autoclaving. These dilutions were used to inoculate (1%, v/v) Hungate tubes containing four different liquid media: A, complete liquid form of medium M2 [42]; B, basal + 15 g/liter Trypticase® peptone (Becton Dickinson Microbiology Systems, Cockeysville, MD 21030); C, medium B + 5 μM monensin; D, basal + 15 g l-1 Casamino acids (Difco, Becton Dickinson Europe, 38241 Meylan cedex, France). Five tubes were inoculated for each dilution, the gas phase was 100% CO2, and tubes were incubated at 37°C. The optical density at 650 nm was determined periodically using an LKB Novaspec spectrophotometer. Numbers were calculated using most-probable-number tables [43], using a threshold of 0.1 as positive for growth.

Isolation and identification of peptide and amino acid utilisers

Cultures from the highest dilutions in medium B and D were passaged once more in the same medium as before, then streaked on the corresponding agar medium. Individual colonies of different morphology were picked off, transferred to the same medium and incubated at 37°C. The isolation was then repeated. The ability of isolates to use glucose for growth was examined by inoculating the isolates into medium B or D to which 0.1% glucose had been added, and comparing the optical density after 48 h incubation with the corresponding optical density in unmodified medium. DNA was extracted from bacteria grown in both media using QIAmp DNA stool mini kit (Qiagen, Crawley, West Sussex, UK). Sequences of 16S rRNA genes were amplified using universal primers, fD1 and rP2 [44], in a mixture that contained 0.6 μM of each of the primers, 100 μM of each of the dNTPs, 2.5 mM MgCl2 in 1× buffer and 0.025 U/ml Taq polymerase (Bioline Ltd, London, UK). Amplification was carried out using a BioRad Icycler and the following programme: 94°C for 10 min; 35 cycles of 94°C for 1 min, 60°C for 1 min, 72°C for 2 min; then 72°C for 10 min, then 4°C. Amplification was confirmed by agarose gel electrophoresis. PCR products were cleaned up using WizardR SV Gel & PCR Clean-up system (Promega). Sequencing was carried out with fD1 and rP2 primers as before, with 2 further forward (926f, 519f) and 2 reverse primers (926r, 519r) based on Lane et al. [45]. Sequences were assembled with the Lasergene programme [46] and bacteria identified with NCBI Blastn. Where samples did not produce long enough sequences, amplified DNA was cloned into the PCR®2.1-TOPO vector (Invitrogen BV, Leek, the Netherlands). Plasmids were isolated from recombinant colonies using Wizard®Plus SV Miniprep DNA Purification System (Promega). Plasmids were checked for inserts by amplification with M13F and M13R primers followed by agarose gel electrophoresis. Plasmids which contained inserts were sequenced using M13F and M13R primers initially then all 6 primers as used before. Sequences were assembled and identified as before. Full length or near full length 16S rRNA genes sequences have been deposited in the GenBank database, with accession numbers GU968162-GU968185.

Data analysis

Ammonia production rates were analysed by hierarchical Analysis of Variance, with a between and within subject stratum, with factors for diet (omnivore vs vegetarian), medium (Trypticase vs amino acids) and monensin and their interactions.

Production was linear during the incubations and rates of NH3 production were determined by linear regression and compared by ANOVA in Microsoft Excel.



‘Hyper-ammonia-producing’ bacteria.


  1. Smith EA, Macfarlane GT: Enumeration of amino acid fermenting bacteria in the human large intestine: effects of pH and starch on peptide metabolism and dissimilation of amino acids. FEMS Microbiol Ecol. 1998, 25: 355-368. 10.1111/j.1574-6941.1998.tb00487.x.

    Article  CAS  Google Scholar 

  2. Hughes R, Magee EA, Bingham S: Protein degradation in the large intestine: relevance to colorectal cancer. Curr Issues Intest Microbiol. 2000, 1: 51-58.

    PubMed  CAS  Google Scholar 

  3. Gill CIR, Rowland IR: Diet and cancer: assessing the risk. Br J Nutr. 2002, 88: S73-S87. 10.1079/BJN2002632.

    Article  PubMed  CAS  Google Scholar 

  4. Christl SU, Eisner HD, Dusel G, Kasper H, Scheppach W: Antagonistic effects of sulfide and butyrate on proliferation of colonic mucosa; a potential role for these agents in the pathogenesis of ulcerative colitis. Dig Dis Sci. 1996, 41: 2477-2481. 10.1007/BF02100146.

    Article  PubMed  CAS  Google Scholar 

  5. Yamada M, Ohkusa T, Okayasu I: Occurrence of dysplasia and adenocarcinoma after experimental chronic ulcerative colitis in hamsters induced by dextran sulfate sodium. Gut. 1992, 33: 1521-1527. 10.1136/gut.33.11.1521.

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  6. Kitano A, Matsumoto T, Hiki M, Hashimura H, Yoshiyasu K, Okawa K, Kuwajima S, Kobayashi K: Epithelial dysplasia of the rabbit colon induced by degraded carrageenan. Cancer Res. 1986, 46: 1374-1376.

    PubMed  CAS  Google Scholar 

  7. Smith EA, Macfarlane GT: Formation of phenolic and indolic compounds by anaerobic bacteria in the human large intestine. Microb Ecol. 1997, 33: 180-188. 10.1007/s002489900020.

    Article  PubMed  CAS  Google Scholar 

  8. Macfarlane GT, Allison C, Gibson SAW, Cummings JH: Contribution of the microflora to proteolysis in the human large intestine. J Appl Bacteriol. 1988, 64: 37-46. 10.1111/j.1365-2672.1988.tb02427.x.

    Article  PubMed  CAS  Google Scholar 

  9. Macfarlane GT, Macfarlane S, Gibson GR: Synthesis and release of proteases by bacteroides fragilis. Curr Microbiol. 1992, 24: 55-59. 10.1007/BF01570100.

    Article  CAS  Google Scholar 

  10. Macfarlane GT, Allison C: Utilisation of protein by human gut bacteria. FEMS Microbiol Ecol. 1986, 38: 19-24. 10.1111/j.1574-6968.1986.tb01934.x.

    Article  CAS  Google Scholar 

  11. Smith EA, Macfarlane GT: Enumeration of human colonic bacteria producing phenolic and indolic compounds: effects of pH, carbohydrate availability and retention time on dissimilatory aromatic amino acid metabolism. J Appl Bacteriol. 1996, 81: 288-302. 10.1111/j.1365-2672.1996.tb04331.x.

    Article  PubMed  CAS  Google Scholar 

  12. Mead GC: The amino acid fermenting clostridia. J Gen Microbiol. 1971, 67: 47-56.

    Article  PubMed  CAS  Google Scholar 

  13. Nisman B: The stickland reaction. Bacteriol Rev. 1954, 18: 16-42.

    PubMed  CAS  PubMed Central  Google Scholar 

  14. Attwood GT, Klieve AV, Ouwerkerk D, Patel BKC: Ammonia-hyperproducing bacteria from New Zealand ruminants. Appl Environ Microbiol. 1998, 64: 1796-1804.

    PubMed  CAS  PubMed Central  Google Scholar 

  15. Chen G, Russell JB: Fermentation of peptides and amino acids by a monensin-sensitive ruminal peptostreptococcus. Appl Environ Microbiol. 1988, 54: 2742-2749.

    PubMed  CAS  PubMed Central  Google Scholar 

  16. Chen G, Russell JB: More monensin-sensitive, ammonia-producing bacteria from the rumen. Appl Environ Microbiol. 1989, 55: 1052-1057.

    PubMed  CAS  PubMed Central  Google Scholar 

  17. Eschenlauer SC, McKain N, Walker ND, McEwan NR, Newbold CJ, Wallace RJ: Ammonia production by ruminal microorganisms and enumeration, isolation, and characterization of bacteria capable of growth on peptides and amino acids from the sheep rumen. Appl Environ Microbiol. 2002, 68: 4925-4931. 10.1128/AEM.68.10.4925-4931.2002.

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  18. Russell JB, Onodera R, Hino T, et al: Ruminal protein fermentation: new perspectives on previous contradictions. Physiological aspects of digestion and metabolism in ruminants. Edited by: Tsuda T, Sasaki Y. 1991, San Diego: Academic, 681-697.

    Chapter  Google Scholar 

  19. McIntosh FM, Williams P, Losa R, Wallace RJ, Beever DA, Newbold CJ: Effects of essential oils on ruminal microorganisms and their protein metabolism. Appl Environ Microbiol. 2003, 69: 5011-5014. 10.1128/AEM.69.8.5011-5014.2003.

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  20. Smith EA, Macfarlane GT: Dissimilatory amino acid metabolism in human colonic bacteria. Anaerobe. 1997, 3: 327-337. 10.1006/anae.1997.0121.

    Article  PubMed  CAS  Google Scholar 

  21. Payne JW, Smith MW: Peptide transport by microorganisms. Adv Microb Physiol. 1994, 36: 1-80.

    Article  PubMed  CAS  Google Scholar 

  22. Linton KJ, Higgins CF: The Escherichia coli ATP-binding cassette (ABC) proteins. Mol Microbiol. 1998, 28: 5-13.

    Article  PubMed  CAS  Google Scholar 

  23. Martin SA: Nutrient transport by ruminal bacteria - a review. J Anim Sci. 1994, 72: 3019-3031.

    PubMed  CAS  Google Scholar 

  24. Pressman BC: Ionophorous antibiotics as models for biological transport. Fed Proc. 1968, 27: 1283-1288.

    PubMed  CAS  Google Scholar 

  25. Russell JB, Strobel HJ: Mini-review: The effect of ionophores on ruminal fermentation. Appl Environ Microbiol. 1988, 55: 1-6.

    Google Scholar 

  26. Horler DF, Westlake DW, McConnel WB: Conversion of glutamic acid to volatile acids by micrococcus aerogenes. Can J Microbiol. 1966, 12: 47-53. 10.1139/m66-008.

    Article  PubMed  CAS  Google Scholar 

  27. Buckel W: Analysis of the fermentation pathways of clostridia using double labeled glutamate. Arch Microbiol. 1980, 127: 167-169. 10.1007/BF00428021.

    Article  PubMed  CAS  Google Scholar 

  28. Prins RA, Van Gestel JC, Counotte GHM: Degradation of amino acids and peptides by mixed rumen microorganisms. Z Tierphysiol Tierernahr Futtermittelkd. 1979, 42: 333-339. 10.1111/j.1439-0396.1979.tb01226.x.

    Article  PubMed  CAS  Google Scholar 

  29. Wallace RJ: Ruminal microbial metabolism of peptides and amino acids. J Nutr. 1996, 126: 1326S-1334S.

    PubMed  CAS  Google Scholar 

  30. Armstead IP, Ling JR: Variations in the uptake and metabolism of peptides and amino acids by mixed ruminal bacteria in vitro. Appl Environ Microbiol. 1993, 59: 3360-3366.

    PubMed  CAS  PubMed Central  Google Scholar 

  31. Ling JR, Armstead IP: The in vitro uptake and metabolism of peptides and amino acids by five species of rumen bacteria. J Appl Bacteriol. 1995, 78: 116-124. 10.1111/j.1365-2672.1995.tb02831.x.

    Article  PubMed  CAS  Google Scholar 

  32. Bladen HA, Bryant MD, Doetsch RN: A study of bacterial species from the rumen which produce ammonia from protein hydrolyzate. Appl Microbiol. 1961, 9: 175-180.

    PubMed  CAS  PubMed Central  Google Scholar 

  33. Chen M, Wolin MJ: Effect of monensin and lasalocid-sodium on the growth of methanogenic and rumen saccharolytic bacteria. Appl Environ Microbiol. 1979, 38: 72-77.

    PubMed  CAS  PubMed Central  Google Scholar 

  34. McDevitt RM, Brooker JD, Acamovic T, Sparks NHC: Necrotic enteritis; a continuing challenge for the poultry industry. World’s Poultry Sci J. 2006, 62: 221-247. 10.1079/WPS200593.

    Article  Google Scholar 

  35. Macfarlane GT, Gibson GR: Bacterial infections and diarrhea. Human colonic bacteria: role in nutrition, physiology, and pathology. Edited by: Gibson GR, Macfarlane GT. 1995, Boca Raton, Florida: CRC Press, 201-226.

    Google Scholar 

  36. Chen GJ, Russell JB: Transport and deamination of amino acids by a gram-positive, monensin-sensitive ruminal bacterium. Appl Environ Microbiol. 1990, 56: 2186-2192.

    PubMed  CAS  PubMed Central  Google Scholar 

  37. Chen G, Russell JB: Effect of monensin and a protonophore on protein degradation, peptide accumulation and deamination by mixed ruminal microorganisms in vitro. J Anim Sci. 1991, 69: 2196-2203.

    PubMed  CAS  Google Scholar 

  38. Wallace RJ, Czerkawski JW, Breckenridge G: Effect of monensin on the fermentation of basal rations in the rumen simulation technique (rusitec). Br J Nutr. 1981, 46: 131-148. 10.1079/BJN19810016.

    Article  PubMed  CAS  Google Scholar 

  39. Whitehead R, Cooke GH, Chapman BT: Problems associated with the continuous monitoring of ammoniacal nitrogen in river water. Automat Analytic Chem. 1967, 2: 377-380.

    Google Scholar 

  40. Wallace RJ, Broderick GA, Brammall ML: Microbial protein and peptide metabolism in ruminal fluid from faunated and ciliate-free sheep. Br J Nutr. 1987, 58: 87-93. 10.1079/BJN19870072.

    Article  PubMed  CAS  Google Scholar 

  41. Heinrikson RL, Meredith SC: Amino acid analysis by reverse-phase high-performance liquid chromatography: precolumn derivatization with phenylisothiocyanate. Analyt Biochem. 1984, 136: 65-74. 10.1016/0003-2697(84)90307-5.

    Article  PubMed  CAS  Google Scholar 

  42. Hobson PN: Rumen bacteria. Methods in Microbiology. Edited by: Norris JR, Ribbons DW. 1969, London. Academic, 133-139.

    Google Scholar 

  43. Alexander M: Methods of soil analysis, part 2, Agronomy Monograph No. 9. Most probable number method for microbial populations. 1982, 815-820. 2

    Google Scholar 

  44. Weisburg WG, Barns SM, Pelletier DA, Lane DJ: 16S ribosomal DNA amplification for phylogenetic study. J Bacteriol. 1991, 173: 697-703.

    PubMed  CAS  PubMed Central  Google Scholar 

  45. Lane DJ, Pace B, Olsen GJ, Stahl DA, Sogin ML, Pace NR: Rapid determination of 16S ribosomal RNA sequences for phylogenetic analyses. Proc Natl Acad Sci U S A. 1985, 82: 6955-6959. 10.1073/pnas.82.20.6955.

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  46. Burland TG: DNASTAR’s Lasergene sequence analysis software. Meth Mol Biol. 2000, 132: 71-91.

    CAS  Google Scholar 

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The Rowett Institute of Nutrition and Health is funded by the Rural and Environment Science and Analytical Services Division (RESAS) of the Scottish Government. We thank Mrs V. Buchan for amino acid analysis, Ms F. McIntosh and P. Young for help with DNA sequencing, and G. Horgan for statistical analysis. We thank the volunteers for their contribution, without which the project would not have been possible!

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Correspondence to R John Wallace.

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AJR carried out most of the experimental work, organised the volunteers and suggested corrections to the manuscript. NMcK carried out some experimental work, advised on techniques and suggested modifications to the manuscript. RJW initiated the work, designed the experiments and wrote the manuscript. All authors read and approved the final manuscript.

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Richardson, A.J., McKain, N. & Wallace, R.J. Ammonia production by human faecal bacteria, and the enumeration, isolation and characterization of bacteria capable of growth on peptides and amino acids. BMC Microbiol 13, 6 (2013).

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