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. 1992 Oct;174(20):6688–6693. doi: 10.1128/jb.174.20.6688-6693.1992

Biosynthetic pathways of the osmolytes N epsilon-acetyl-beta-lysine, beta-glutamine, and betaine in Methanohalophilus strain FDF1 suggested by nuclear magnetic resonance analyses.

M F Roberts 1, M C Lai 1, R P Gunsalus 1
PMCID: PMC207655  PMID: 1400220

Abstract

Methanohalophilus strain FDF1 synthesizes beta-glutamine, betaine, and N epsilon-acetyl-beta-lysine as osmoprotective agents when the cells are grown in high external concentrations of NaCl. Nuclear magnetic resonance spectroscopic analyses of 13CH3OH-12CO2 label incorporation by the cells provide information on the biosynthetic pathways of these organic osmolytes. The labeling studies indicate that Methanohalophilus strain FDF1 produces glutamate and beta-glutamine via a partial oxidative Krebs pathway. 13C labeling of betaine is consistent with methylation of glycine generated from serine (via serine hydroxymethyltransferase). The labeling pattern for N epsilon-acetyl-beta-lysine is consistent with the synthesis of its precursor alpha-lysine occurring by the diaminopimelate pathway in these cells.

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Selected References

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  1. Baraniak J., Moss M. L., Frey P. A. Lysine 2,3-aminomutase. Support for a mechanism of hydrogen transfer involving S-adenosylmethionine. J Biol Chem. 1989 Jan 25;264(3):1357–1360. [PubMed] [Google Scholar]
  2. Edmunds H. N., Barker H. A. Aerobic metabolism of L- -lysine in a Pseudomonas. Coenzyme A-dependent acetylation of L- -lysine. Arch Biochem Biophys. 1973 Jan;154(1):460–470. doi: 10.1016/0003-9861(73)90079-9. [DOI] [PubMed] [Google Scholar]
  3. Ekiel I., Smith I. C., Sprott G. D. Biosynthetic pathways in Methanospirillum hungatei as determined by 13C nuclear magnetic resonance. J Bacteriol. 1983 Oct;156(1):316–326. doi: 10.1128/jb.156.1.316-326.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Evans J. N., Tolman C. J., Kanodia S., Roberts M. F. 2,3-Cyclopyrophosphoglycerate in methanogens: evidence by 13C NMR spectroscopy for a role in carbohydrate metabolism. Biochemistry. 1985 Oct 8;24(21):5693–5698. doi: 10.1021/bi00342a001. [DOI] [PubMed] [Google Scholar]
  5. Fuchs G., Stupperich E. Evidence for an incomplete reductive carboxylic acid cycle in Methanobacterium thermoautotrophicum. Arch Microbiol. 1978 Jul;118(1):121–125. doi: 10.1007/BF00406084. [DOI] [PubMed] [Google Scholar]
  6. Hanson A. D., May A. M., Grumet R., Bode J., Jamieson G. C., Rhodes D. Betaine synthesis in chenopods: Localization in chloroplasts. Proc Natl Acad Sci U S A. 1985 Jun;82(11):3678–3682. doi: 10.1073/pnas.82.11.3678. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. KHEDOURI E., MEISTER A. SYNTHESIS OF D-BETA-GLUTAMINE FROM BETA-GLUTAMIC ACID BY GLUTAMINE SYNTHETASE. J Biol Chem. 1965 Aug;240:3357–3360. [PubMed] [Google Scholar]
  8. Lai M. C., Sowers K. R., Robertson D. E., Roberts M. F., Gunsalus R. P. Distribution of compatible solutes in the halophilic methanogenic archaebacteria. J Bacteriol. 1991 Sep;173(17):5352–5358. doi: 10.1128/jb.173.17.5352-5358.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Mathrani I. M., Boone D. R. Isolation and characterization of a moderately halophilic methanogen from a solar saltern. Appl Environ Microbiol. 1985 Jul;50(1):140–143. doi: 10.1128/aem.50.1.140-143.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Robertson D. E., Lai M. C., Gunsalus R. P., Roberts M. F. Composition, Variation, and Dynamics of Major Osmotic Solutes in Methanohalophilus Strain FDF1. Appl Environ Microbiol. 1992 Aug;58(8):2438–2443. doi: 10.1128/aem.58.8.2438-2443.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Robertson D. E., Lesage S., Roberts M. F. Beta-aminoglutaric acid is a major soluble component of Methanococcus thermolithotrophicus. Biochim Biophys Acta. 1989 Sep 15;992(3):320–326. doi: 10.1016/0304-4165(89)90091-3. [DOI] [PubMed] [Google Scholar]
  12. Robertson D. E., Noll D., Roberts M. F. Free amino acid dynamics in marine methanogens. beta-Amino acids as compatible solutes. J Biol Chem. 1992 Jul 25;267(21):14893–14901. [PubMed] [Google Scholar]
  13. Robertson D. E., Noll D., Roberts M. F., Menaia J. A., Boone D. R. Detection of the osmoregulator betaine in methanogens. Appl Environ Microbiol. 1990 Feb;56(2):563–565. doi: 10.1128/aem.56.2.563-565.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Robertson D. E., Roberts M. F., Belay N., Stetter K. O., Boone D. R. Occurrence of beta-glutamate, a novel osmolyte, in marine methanogenic bacteria. Appl Environ Microbiol. 1990 May;56(5):1504–1508. doi: 10.1128/aem.56.5.1504-1508.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Robertson D. E., Roberts M. F. Organic osmolytes in methanogenic archaebacteria. Biofactors. 1991 Jan;3(1):1–9. [PubMed] [Google Scholar]
  16. Sowers K. R., Robertson D. E., Noll D., Gunsalus R. P., Roberts M. F. N epsilon-acetyl-beta-lysine: an osmolyte synthesized by methanogenic archaebacteria. Proc Natl Acad Sci U S A. 1990 Dec;87(23):9083–9087. doi: 10.1073/pnas.87.23.9083. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Sprott G. D., Usher J. R. The electrochemical proton gradient and phenylalanine transport in Escherichia coli irradiated with near-ultraviolet light. Can J Microbiol. 1977 Dec;23(12):1683–1688. doi: 10.1139/m77-242. [DOI] [PubMed] [Google Scholar]
  18. Weimer P. J., Zeikus J. G. Acetate assimilation pathway of Methanosarcina barkeri. J Bacteriol. 1979 Jan;137(1):332–339. doi: 10.1128/jb.137.1.332-339.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]

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