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. 1979 Jun;43(2):260–296. doi: 10.1128/mr.43.2.260-296.1979

Methanogens: reevaluation of a unique biological group.

W E Balch, G E Fox, L J Magrum, C R Woese, R S Wolfe
PMCID: PMC281474  PMID: 390357

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Almassy R. J., Dickerson R. E. Pseudomonas cytochrome c551 at 2.0 A resolution: enlargement of the cytochrome c family. Proc Natl Acad Sci U S A. 1978 Jun;75(6):2674–2678. doi: 10.1073/pnas.75.6.2674. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Aranki A., Freter R. Use of anaerobic glove boxes for the cultivation of strictly anaerobic bacteria. Am J Clin Nutr. 1972 Dec;25(12):1329–1334. doi: 10.1093/ajcn/25.12.1329. [DOI] [PubMed] [Google Scholar]
  3. Balch W. E., Magrum L. J., Fox G. E., Wolfe R. S., Woese C. R. An ancient divergence among the bacteria. J Mol Evol. 1977 Aug 5;9(4):305–311. doi: 10.1007/BF01796092. [DOI] [PubMed] [Google Scholar]
  4. Balch W. E., Wolfe R. S. New approach to the cultivation of methanogenic bacteria: 2-mercaptoethanesulfonic acid (HS-CoM)-dependent growth of Methanobacterium ruminantium in a pressureized atmosphere. Appl Environ Microbiol. 1976 Dec;32(6):781–791. doi: 10.1128/aem.32.6.781-791.1976. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Balch W. E., Wolfe R. S. Specificity and biological distribution of coenzyme M (2-mercaptoethanesulfonic acid). J Bacteriol. 1979 Jan;137(1):256–263. doi: 10.1128/jb.137.1.256-263.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Balch W. E., Wolfe R. S. Transport of coenzyme M (2-mercaptoethanesulfonic acid) in Methanobacterium ruminantium. J Bacteriol. 1979 Jan;137(1):264–273. doi: 10.1128/jb.137.1.264-273.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Bellemare G., Vigne R., Jordan B. R. Interaction between Escherichia coli ribosomal proteins and 5S RNA molecules: recognition of prokaryotic 5S RNAs and rejection of eukaryotic 5S RNAs. Biochimie. 1973;55(1):29–35. doi: 10.1016/s0300-9084(73)80233-0. [DOI] [PubMed] [Google Scholar]
  8. Best A. N. Composition and Characterization of tRNA from Methanococcus vannielii. J Bacteriol. 1978 Jan;133(1):240–250. doi: 10.1128/jb.133.1.240-250.1978. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Bonen L., Doolittle W. F. On the prokaryotic nature of red algal chloroplasts. Proc Natl Acad Sci U S A. 1975 Jun;72(6):2310–2314. doi: 10.1073/pnas.72.6.2310. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Bonen L., Doolittle W. F. Partial sequences of 16S rRNA and the phylogeny of blue-green algae and chloroplasts. Nature. 1976 Jun 24;261(5562):669–673. doi: 10.1038/261669a0. [DOI] [PubMed] [Google Scholar]
  11. Bonen L., Doolittle W. F. Ribosomal RNA homologies and the evolution of the filamentous blue-green bacteria. J Mol Evol. 1978 Feb 21;10(4):283–291. doi: 10.1007/BF01734218. [DOI] [PubMed] [Google Scholar]
  12. Bryant M. P. Commentary on the Hungate technique for culture of anaerobic bacteria. Am J Clin Nutr. 1972 Dec;25(12):1324–1328. doi: 10.1093/ajcn/25.12.1324. [DOI] [PubMed] [Google Scholar]
  13. Bryant M. P., McBride B. C., Wolfe R. S. Hydrogen-oxidizing methane bacteria. I. Cultivation and methanogenesis. J Bacteriol. 1968 Mar;95(3):1118–1123. doi: 10.1128/jb.95.3.1118-1123.1968. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Bryant M. P., Wolin E. A., Wolin M. J., Wolfe R. S. Methanobacillus omelianskii, a symbiotic association of two species of bacteria. Arch Mikrobiol. 1967;59(1):20–31. doi: 10.1007/BF00406313. [DOI] [PubMed] [Google Scholar]
  15. Daniels L., Fuchs G., Thauer R. K., Zeikus J. G. Carbon monoxide oxidation by methanogenic bacteria. J Bacteriol. 1977 Oct;132(1):118–126. doi: 10.1128/jb.132.1.118-126.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Daniels L., Zeikus J. G. One-carbon metabolism in methanogenic bacteria: analysis of short-term fixation products of 14CO2 and 14CH3OH incorporated into whole cells. J Bacteriol. 1978 Oct;136(1):75–84. doi: 10.1128/jb.136.1.75-84.1978. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Doddema H. J., Vogels G. D. Improved identification of methanogenic bacteria by fluorescence microscopy. Appl Environ Microbiol. 1978 Nov;36(5):752–754. doi: 10.1128/aem.36.5.752-754.1978. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Edwards T., McBride B. C. New method for the isolation and identification of methanogenic bacteria. Appl Microbiol. 1975 Apr;29(4):540–545. doi: 10.1128/am.29.4.540-545.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Eirich L. D., Vogels G. D., Wolfe R. S. Proposed structure for coenzyme F420 from Methanobacterium. Biochemistry. 1978 Oct 31;17(22):4583–4593. doi: 10.1021/bi00615a002. [DOI] [PubMed] [Google Scholar]
  20. Ferry J. G., Wolfe R. S. Nutritional and biochemical characterization of Methanospirillum hungatii. Appl Environ Microbiol. 1977 Oct;34(4):371–376. doi: 10.1128/aem.34.4.371-376.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Fox G. E., Magrum L. J., Balch W. E., Wolfe R. S., Woese C. R. Classification of methanogenic bacteria by 16S ribosomal RNA characterization. Proc Natl Acad Sci U S A. 1977 Oct;74(10):4537–4541. doi: 10.1073/pnas.74.10.4537. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Fox G. E., Woese C. R. 5S RNA secondary structure. Nature. 1975 Aug 7;256(5517):505–507. doi: 10.1038/256505a0. [DOI] [PubMed] [Google Scholar]
  23. 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]
  24. Fuchs G., Stupperich E., Thauer R. K. Acetate assimilation and the synthesis of alanine, aspartate and glutamate in Methanobacterium thermoautotrophicum. Arch Microbiol. 1978 Apr 27;117(1):61–66. doi: 10.1007/BF00689352. [DOI] [PubMed] [Google Scholar]
  25. Gunsalus R. P., Romesser J. A., Wolfe R. S. Preparation of coenzyme M analogues and their activity in the methyl coenzyme M reductase system of Methanobacterium thermoautotrophicum. Biochemistry. 1978 Jun 13;17(12):2374–2377. doi: 10.1021/bi00605a019. [DOI] [PubMed] [Google Scholar]
  26. Gunsalus R. P., Wolfe R. S. Stimulation of CO2 reduction to methane by methylcoenzyme M in extracts Methanobacterium. Biochem Biophys Res Commun. 1977 Jun 6;76(3):790–795. doi: 10.1016/0006-291x(77)91570-4. [DOI] [PubMed] [Google Scholar]
  27. HUNGATE R. E. The anaerobic mesophilic cellulolytic bacteria. Bacteriol Rev. 1950 Mar;14(1):1–49. doi: 10.1128/br.14.1.1-49.1950. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Hippe H., Caspari D., Fiebig K., Gottschalk G. Utilization of trimethylamine and other N-methyl compounds for growth and methane formation by Methanosarcina barkeri. Proc Natl Acad Sci U S A. 1979 Jan;76(1):494–498. doi: 10.1073/pnas.76.1.494. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Holdeman L. V., Moore W. E. Roll-tube techniques for anaerobic bacteria. Am J Clin Nutr. 1972 Dec;25(12):1314–1317. doi: 10.1093/ajcn/25.12.1314. [DOI] [PubMed] [Google Scholar]
  30. Jones J. B., Bowers B., Stadtman T. C. Methanococcus vannielii: ultrastructure and sensitivity to detergents and antibiotics. J Bacteriol. 1977 Jun;130(3):1357–1363. doi: 10.1128/jb.130.3.1357-1363.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Jones J. B., Stadtman T. C. Methanococcus vannielii: culture and effects of selenium and tungsten on growth. J Bacteriol. 1977 Jun;130(3):1404–1406. doi: 10.1128/jb.130.3.1404-1406.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. Kandler O., Hippe H. Lack of peptidoglycan in the cell walls of Methanosarcina barkeri. Arch Microbiol. 1977 May 13;113(1-2):57–60. doi: 10.1007/BF00428580. [DOI] [PubMed] [Google Scholar]
  33. Kandler O., König H. Chemical composition of the peptidoglycan-free cell walls of methanogenic bacteria. Arch Microbiol. 1978 Aug 1;118(2):141–152. doi: 10.1007/BF00415722. [DOI] [PubMed] [Google Scholar]
  34. Langenberg K. F., Bryant M. P., Wolfe R. S. Hydrogen-oxidizing methane bacteria. II. Electron microscopy. J Bacteriol. 1968 Mar;95(3):1124–1129. doi: 10.1128/jb.95.3.1124-1129.1968. [DOI] [PMC free article] [PubMed] [Google Scholar]
  35. MYLROIE R. L., HUNGATE R. E. Experiments on the methane bacteria in sludge. Can J Microbiol. 1954 Aug;1(1):55–64. doi: 10.1139/m55-008. [DOI] [PubMed] [Google Scholar]
  36. Macy J. M., Snellen J. E., Hungate R. E. Use of syringe methods for anaerobiosis. Am J Clin Nutr. 1972 Dec;25(12):1318–1323. doi: 10.1093/ajcn/25.12.1318. [DOI] [PubMed] [Google Scholar]
  37. Mah R. A., Smith M. R., Baresi L. Studies on an acetate-fermenting strain of Methanosarcina. Appl Environ Microbiol. 1978 Jun;35(6):1174–1184. doi: 10.1128/aem.35.6.1174-1184.1978. [DOI] [PMC free article] [PubMed] [Google Scholar]
  38. Mah R. A., Ward D. M., Baresi L., Glass T. L. Biogenesis of methane. Annu Rev Microbiol. 1977;31:309–341. doi: 10.1146/annurev.mi.31.100177.001521. [DOI] [PubMed] [Google Scholar]
  39. Makula R. A., Singer M. E. Ether-containing lipids of methanogenic bacteria. Biochem Biophys Res Commun. 1978 May 30;82(2):716–722. doi: 10.1016/0006-291x(78)90933-6. [DOI] [PubMed] [Google Scholar]
  40. McBride B. C., Wolfe R. S. A new coenzyme of methyl transfer, coenzyme M. Biochemistry. 1971 Jun 8;10(12):2317–2324. doi: 10.1021/bi00788a022. [DOI] [PubMed] [Google Scholar]
  41. Miller T. L., Wolin M. J. A serum bottle modification of the Hungate technique for cultivating obligate anaerobes. Appl Microbiol. 1974 May;27(5):985–987. doi: 10.1128/am.27.5.985-987.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
  42. Mink R. W., Dugan P. R. Tentative identification of methanogenic bacteria by fluorescence microscopy. Appl Environ Microbiol. 1977 Mar;33(3):713–717. doi: 10.1128/aem.33.3.713-717.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
  43. Mitchell R. M., Loeblich L. A., Klotz L. C., Loeblich A. R., 3rd DNA organization of Methanobacterium thermoautotrophicum. Science. 1979 Jun 8;204(4397):1082–1084. doi: 10.1126/science.377486. [DOI] [PubMed] [Google Scholar]
  44. Nomura M., Traub P., Bechmann H. Hybrid 30S ribosomal particles reconstituted from components of different bacterial origins. Nature. 1968 Aug 24;219(5156):793–799. doi: 10.1038/219793b0. [DOI] [PubMed] [Google Scholar]
  45. Nottingham P. M., Hungate R. E. Isolation of methanogenic bacteria from feces of man. J Bacteriol. 1968 Dec;96(6):2178–2179. doi: 10.1128/jb.96.6.2178-2179.1968. [DOI] [PMC free article] [PubMed] [Google Scholar]
  46. Pantskhava E. S., Pchelkina V. V. Korrinoidnye soedineniia, sinteziruemye vydelennym novym vidom metanobrazuiushchikh bakterii. Dokl Akad Nauk SSSR. 1968 Sep;182(2):457–458. [PubMed] [Google Scholar]
  47. Patel G. B., Roth L. A., van den Berg L., Clark D. S. Characterization of a strain of Methanospirillum hungatti. Can J Microbiol. 1976 Sep;22(9):1404–1410. doi: 10.1139/m76-208. [DOI] [PubMed] [Google Scholar]
  48. Paynter M. J., Hungate R. E. Characterization of Methanobacterium mobilis, sp. n., isolated from the bovine rumen. J Bacteriol. 1968 May;95(5):1943–1951. doi: 10.1128/jb.95.5.1943-1951.1968. [DOI] [PMC free article] [PubMed] [Google Scholar]
  49. Pechman K. J., Woese C. R. Characterization of the primary structural homology between the 16s ribosomal RNAs of Escherichia coli and Bacillus megaterium by oligomer cataloging. J Mol Evol. 1972;1(3):230–240. doi: 10.1007/BF01660242. [DOI] [PubMed] [Google Scholar]
  50. SCHILDKRAUT C. L., MARMUR J., DOTY P. Determination of the base composition of deoxyribonucleic acid from its buoyant density in CsCl. J Mol Biol. 1962 Jun;4:430–443. doi: 10.1016/s0022-2836(62)80100-4. [DOI] [PubMed] [Google Scholar]
  51. SMITH P. H., HUNGATE R. E. Isolation and characterization of Methanobacterium ruminantium n. sp. J Bacteriol. 1958 Jun;75(6):713–718. doi: 10.1128/jb.75.6.713-718.1958. [DOI] [PMC free article] [PubMed] [Google Scholar]
  52. STADTMAN T. C., BARKER H. A. Studies on the methane fermentation. IX. The origin of methane in the acetate and methanol fermentations by methanosarcina. J Bacteriol. 1951 Jan;61(1):81–86. doi: 10.1128/jb.61.1.81-86.1951. [DOI] [PMC free article] [PubMed] [Google Scholar]
  53. STADTMAN T. C., BARKER H. A. Studies on the methane fermentation. X. A new formate-decomposing bacterium, Methanococcus vannielii. J Bacteriol. 1951 Sep;62(3):269–280. doi: 10.1128/jb.62.3.269-280.1951. [DOI] [PMC free article] [PubMed] [Google Scholar]
  54. STANIER R. Y., VAN NIEL C. B. The concept of a bacterium. Arch Mikrobiol. 1962;42:17–35. doi: 10.1007/BF00425185. [DOI] [PubMed] [Google Scholar]
  55. STANIER R. Y. [The place of bacteria in the living world]. Ann Inst Pasteur (Paris) 1961 Sep;101:297–312. [PubMed] [Google Scholar]
  56. Sanger F., Brownlee G. G., Barrell B. G. A two-dimensional fractionation procedure for radioactive nucleotides. J Mol Biol. 1965 Sep;13(2):373–398. doi: 10.1016/s0022-2836(65)80104-8. [DOI] [PubMed] [Google Scholar]
  57. Schwartz R. M., Dayhoff M. O. Origins of prokaryotes, eukaryotes, mitochondria, and chloroplasts. Science. 1978 Jan 27;199(4327):395–403. doi: 10.1126/science.202030. [DOI] [PubMed] [Google Scholar]
  58. Smith M. R., Mah R. A. Growth and methanogenesis by Methanosarcina strain 227 on acetate and methanol. Appl Environ Microbiol. 1978 Dec;36(6):870–879. doi: 10.1128/aem.36.6.870-879.1978. [DOI] [PMC free article] [PubMed] [Google Scholar]
  59. Stanier R. Y., Van Niel C. B. The Main Outlines of Bacterial Classification. J Bacteriol. 1941 Oct;42(4):437–466. doi: 10.1128/jb.42.4.437-466.1941. [DOI] [PMC free article] [PubMed] [Google Scholar]
  60. Steitz J. A. Methanogenic bacteria. Nature. 1978 May 4;273(5657):10–10. doi: 10.1038/273010a0. [DOI] [PubMed] [Google Scholar]
  61. Taylor C. D., McBride B. C., Wolfe R. S., Bryant M. P. Coenzyme M, essential for growth of a rumen strain of Methanobacterium ruminantium. J Bacteriol. 1974 Nov;120(2):974–975. doi: 10.1128/jb.120.2.974-975.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
  62. Taylor C. D., Wolfe R. S. Structure and methylation of coenzyme M(HSCH2CH2SO3). J Biol Chem. 1974 Aug 10;249(15):4879–4885. [PubMed] [Google Scholar]
  63. Taylor G. T., Pirt S. J. Nutrition and factors limiting the growth of a methanogenic bacterium (Methanobacterium thermoautotrophicum). Arch Microbiol. 1977 May 13;113(1-2):17–22. doi: 10.1007/BF00428574. [DOI] [PubMed] [Google Scholar]
  64. Thauer R. K., Jungermann K., Decker K. Energy conservation in chemotrophic anaerobic bacteria. Bacteriol Rev. 1977 Mar;41(1):100–180. doi: 10.1128/br.41.1.100-180.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
  65. Tornabene T. G., Langworthy T. A. Diphytanyl and dibiphytanyl glycerol ether lipids of methanogenic archaebacteria. Science. 1979 Jan 5;203(4375):51–53. doi: 10.1126/science.758677. [DOI] [PubMed] [Google Scholar]
  66. Tornabene T. G., Wolfe R. S., Balch W. E., Holzer G., Fox G. E., Oro J. Phytanyl-glycerol ethers and squalenes in the archaebacterium Methanobacterium thermoautotrophicum. J Mol Evol. 1978 Aug 2;11(3):259–266. doi: 10.1007/BF01734487. [DOI] [PubMed] [Google Scholar]
  67. Tzeng S. F., Wolfe R. S., Bryant M. P. Factor 420-dependent pyridine nucleotide-linked hydrogenase system of Methanobacterium ruminantium. J Bacteriol. 1975 Jan;121(1):184–191. doi: 10.1128/jb.121.1.184-191.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]
  68. Tzing S. F., Bryant M. P., Wolfe R. S. Factor 420-dependent pyridine nucleotide-linked formate metabolism of Methanobacterium ruminantium. J Bacteriol. 1975 Jan;121(1):192–196. doi: 10.1128/jb.121.1.192-196.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]
  69. Uchida T., Bonen L., Schaup H. W., Lewis B. J., Zablen L., Woese C. The use of ribonuclease U2 in RNA sequence determination. Some corrections in the catalog of oligomers produced by ribonuclease T1 digestion of Escherichia coli 16S ribosomal RNA. J Mol Evol. 1974 Feb 28;3(1):63–77. doi: 10.1007/BF01795977. [DOI] [PubMed] [Google Scholar]
  70. 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]
  71. Weimer P. J., Zeikus J. G. Acetate metabolism in Methanosarcina barkeri. Arch Microbiol. 1978 Nov 13;119(2):175–182. doi: 10.1007/BF00964270. [DOI] [PubMed] [Google Scholar]
  72. Weimer P. J., Zeikus J. G. One carbon metabolism in methanogenic bacteria. Cellular characterization and growth of Methanosarcina barkeri. Arch Microbiol. 1978 Oct 4;119(1):49–57. doi: 10.1007/BF00407927. [DOI] [PubMed] [Google Scholar]
  73. Wellinger A., Wuhrmann K. Influence of sulfide compounds on the metabolism of Methanobacterium strain AZ. Arch Microbiol. 1977 Oct 24;115(1):13–17. doi: 10.1007/BF00427839. [DOI] [PubMed] [Google Scholar]
  74. Wilson A. C., Carlson S. S., White T. J. Biochemical evolution. Annu Rev Biochem. 1977;46:573–639. doi: 10.1146/annurev.bi.46.070177.003041. [DOI] [PubMed] [Google Scholar]
  75. Woese C. R., Fox G. E. Phylogenetic structure of the prokaryotic domain: the primary kingdoms. Proc Natl Acad Sci U S A. 1977 Nov;74(11):5088–5090. doi: 10.1073/pnas.74.11.5088. [DOI] [PMC free article] [PubMed] [Google Scholar]
  76. Woese C. R., Magrum L. J., Fox G. E. Archaebacteria. J Mol Evol. 1978 Aug 2;11(3):245–251. doi: 10.1007/BF01734485. [DOI] [PubMed] [Google Scholar]
  77. Woese C. R., Sogin M. L., Bonen L., Stahl D. Sequence studies on 16S ribosomal RNA from a blue-green alga. J Mol Evol. 1975 Mar 24;4(4):307–315. doi: 10.1007/BF01732533. [DOI] [PubMed] [Google Scholar]
  78. Woese C., Sogin M., Stahl D., Lewis B. J., Bonen L. A comparison of the 16S ribosomal RNAs from mesophilic and thermophilic bacilli: some modifications in the Sanger method for RNA sequencing. J Mol Evol. 1976 Apr 9;7(3):197–213. doi: 10.1007/BF01731489. [DOI] [PubMed] [Google Scholar]
  79. Wolfe R. S. Microbial formation of methane. Adv Microb Physiol. 1971;6:107–146. doi: 10.1016/s0065-2911(08)60068-5. [DOI] [PubMed] [Google Scholar]
  80. Wrede P., Erdmann V. A. Activities of B. stearothermophilus 50 S ribosomes reconstituted with prokaryotic and eukaryotic 5 S RNA. FEBS Lett. 1973 Jul 15;33(3):315–319. doi: 10.1016/0014-5793(73)80219-4. [DOI] [PubMed] [Google Scholar]
  81. Zablen L. B., Kissil M. S., Woese C. R., Buetow D. E. Phylogenetic origin of the chloroplast and prokaryotic nature of its ribosomal RNA. Proc Natl Acad Sci U S A. 1975 Jun;72(6):2418–2422. doi: 10.1073/pnas.72.6.2418. [DOI] [PMC free article] [PubMed] [Google Scholar]
  82. Zablen L., Bonen L., Meyer R., Woese C. R. The phylogenetic status of Pasteurella pestis. J Mol Evol. 1975 Mar 24;4(4):347–358. doi: 10.1007/BF01732536. [DOI] [PubMed] [Google Scholar]
  83. Zablen L., Woese C. R. Procaryote phylogeny IV: concerning the phylogenetic status of a photosynthetic bacterium. J Mol Evol. 1975 Jun 9;5(1):25–34. doi: 10.1007/BF01732011. [DOI] [PubMed] [Google Scholar]
  84. Zeikus J. G., Bowen V. G. Comparative ultrastructure of methanogenic bacteria. Can J Microbiol. 1975 Feb;21(2):121–129. doi: 10.1139/m75-019. [DOI] [PubMed] [Google Scholar]
  85. Zeikus J. G., Bowen V. G. Fine structure of Methanospirillum hungatii. J Bacteriol. 1975 Jan;121(1):373–380. doi: 10.1128/jb.121.1.373-380.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]
  86. Zeikus J. G., Fuchs G., Kenealy W., Thauer R. K. Oxidoreductases involved in cell carbon synthesis of Methanobacterium thermoautotrophicum. J Bacteriol. 1977 Nov;132(2):604–613. doi: 10.1128/jb.132.2.604-613.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
  87. Zeikus J. G., Henning D. L. Methanobacterium arbophilicum sp.nov. An obligate anaerobe isolated from wetwood of living trees. Antonie Van Leeuwenhoek. 1975;41(4):543–552. doi: 10.1007/BF02565096. [DOI] [PubMed] [Google Scholar]
  88. Zeikus J. G. The biology of methanogenic bacteria. Bacteriol Rev. 1977 Jun;41(2):514–541. doi: 10.1128/br.41.2.514-541.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
  89. Zeikus J. G., Wolfe R. S. Fine structure of Methanobacterium thermoautotrophicum: effect of growth temperature on morphology and ultrastructure. J Bacteriol. 1973 Jan;113(1):461–467. doi: 10.1128/jb.113.1.461-467.1973. [DOI] [PMC free article] [PubMed] [Google Scholar]
  90. Zeikus J. G., Wolfe R. S. Methanobacterium thermoautotrophicus sp. n., an anaerobic, autotrophic, extreme thermophile. J Bacteriol. 1972 Feb;109(2):707–715. doi: 10.1128/jb.109.2.707-713.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]
  91. Zuckerkandl E., Pauling L. Molecules as documents of evolutionary history. J Theor Biol. 1965 Mar;8(2):357–366. doi: 10.1016/0022-5193(65)90083-4. [DOI] [PubMed] [Google Scholar]

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