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Methanopyrus kandleri, gen. and sp. nov. represents a novel group of hyperthermophilic methanogens, growing at 110°C

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Abstract

A novel group of hyperthermophilic rod-shaped motile methanogens was isolated from a hydrothermally heated deep sea sediment (Guaymas Basin, Gulf of California) and from a shallow marine hydrothermal system (Kolbeinsey ridge, Iceland). The grew between 84 and 110°C (opt: 98°C) and from 0.2% to 4% NaCl (opt. 2%) and pH 5.5 to 7 (opt: 6.5). The isolates were obligate chemolithoautotrophes using H2/CO2 as energy and carbon sources. In the presence of sulfur, H2S was formed and cells tended to lyse. The cell wall consisted of a new type of pseudomurein containing ornithin in addition to lysine and no N-acetylglucosamine. The pseudomurein layer was covered by a detergent-sensitive protein surface layer. The core lipid consisted exclusively of phytanyl diether. The GC content of the DNA was 60 mol%. By 16S rRNA comparisons the new organisms were not related to any of the three methanogenic lineages. Based on the physiological and molecular properties of the new isolates, we describe here a new genus, which we name Methanopyrus (the “methane fire”). The type species is Methanopyrus kandleri (type strain: AV19; DSM 6324).

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References

  • Balch WE, Wolfe RS (1976) New approach to the cultivation of methanogenic bacteria: 2-mercaptoethanesulfonic acid (HS-CoM)dependent growth of Methanobacterium ruminantium in a pressurized atmosphere. Appl Environ Microbiol 32:781–791

    Google Scholar 

  • Balch WE, Fox GE, Magrum LJ, Woese CR, Wolfe RS (1979) Methanogens: reevaluation of a unique biological group. Microbiol Rev 43:260–296

    Google Scholar 

  • Brenner DJ (1973) Deoxyribonucleic acid reassociation in the taxonomy of enteric bacteria. Int J Syst Bacteriol 43:298–307

    Google Scholar 

  • Burggraf S, Jannasch HW, Nicolaus B, Stetter KO (1990a) Archaeoglobus profundus sp. nov., represents a new species within the sulfate-reducing archaebacteria. System Appl Microbiol 13:24–28

    Google Scholar 

  • Burggraf S, Fricke H, Neuner A, Kristjansson JK, Rouvier P, Mandelco L, Woese CR, Stetter KO (1990b) Methanococcus igneus sp. nov., a novel hyperthermophilic methanogen from a shallow submarine hydrothermal system. Syst Appl Microbiol 13:263–269

    Google Scholar 

  • De Rosa M, Gambacorta A, Nicolaus B, Chappe B, Albrecht P (1983) Isoprenoid ethers: backbone of complex lipids of the archaebacterium Sulfolobus solfataricus. Biochim Biophys Acta 753:249–256

    Google Scholar 

  • Drobner E, Huber H, Wächtershäuser G, Rose D, Stetter KO (1990) Pyrite formation linked with hydrogen evolution under anaerobic conditions. Nature 346:742–744

    Google Scholar 

  • Grunstein M, Hogness DS (1975) Colony hybridization: a method for the isolation of cloned DNAs that contain a specific gene. Proc Natl Acad Sci USA 72:3961–3965

    Google Scholar 

  • Hensel R, König H (1988) Thermoadaption of methanogenic bacteria by intracellular ion concentration. FEMS Microbiol Lett 49:75–79

    Google Scholar 

  • Holt SC, Leadbetter ER (1967) Fine structure of Sporocytophaga myxococcoides. Arch Mikrobiol 57:199–213

    Google Scholar 

  • Huber H, Thomm M, König H, Thies G, Stetter KO (1982) Methanococcus thermolithotrophicus, a novel thermophilic lithotrophic methanogen. Arch Microbiol 132:47–50

    Google Scholar 

  • Huber R, Kurr M, Jannasch HW, Stetter KO (1989a) A novel group of abyssal methanogenic archaebacteria (Methanopyrus) growing at 110°C. Nature 342:833–834

    Google Scholar 

  • Huber R, Woese CR, Langworthy TA, Fricke H, Stetter KO (1989b) Thermosipho africanus gen. nov., represents a new genus of thermophilic eubacteria within the “Thermotogales”. Syst Appl Microbiol 12:32–37

    Google Scholar 

  • Huber R, Woese CR, Langworthy TA, Kristjansson JK, Stetter KO (1990) Fervidobacterium islandicum sp. nov., a new extremely thermophilic eubacterium belonging to the “Thermotogales”. Arch Microbiol 154:105–111

    Google Scholar 

  • Humphries P, McConell DJ, Gordon RL (1973) A procedure for the purification of Escherichia coli deoxyribonucleic acid dependent ribonucleic acid polymerase. Biochem J 133:201–203

    Google Scholar 

  • Jones WJ, Leigh JA, Mayer F, Woese CR, Wolfe RS (1983) Methanococcus jannaschii sp. nov., an extremely thermophilic methanogen from a submarine hydrothermal vent. Arch Microbiol 136:154–261

    Google Scholar 

  • Kandler O, König H (1978) Chemical composition of the peptidogylcan-free cell walls of methanogenic bacteria. Arch Microbiol 118:141–152

    Google Scholar 

  • Kelly RB, Cozzarelli NR, Deutscher MP, Lehmann JR, Kornberg A (1970) Enzymatic synthesis of deoxyribonucleic acid. XXXII. Replication of duplex deoxyribonucleic acid by polymerase at a single strand break. J Biol Chem 245:39–45

    Google Scholar 

  • König H, Kandler O (1979a) The amino acid sequence of the peptide moiety of the pseudomurein of Methanobacterium thermoautotrophicum. Arch Microbiol 121:271–275

    Google Scholar 

  • König H, Kandler O (1979b) N-Acetyltalosaminuronic acid, a constituent of the pseudomurein of the genus Methanobacterium. Arch Microbiol 123:295–299

    Google Scholar 

  • König H, Kralik R, Kandler O (1982) Structure and modifications of pseudomurein of Methanobacteriales. Zentralbl Bakt Hyg I. Abt Orig C 3:179–191

    Google Scholar 

  • König H, Kandler P, Jensen M, Rietschel ETh (1983) The primary structure of the glycan moiety of the pseudomurein from Methanobacterium thermoautotrophicum. Hoppe-Seyler's Z Physiol Chem 364:627–636

    Google Scholar 

  • Laemmli UK (1970) Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature 227:680–685

    Google Scholar 

  • Langworthy TA, Pond JL (1986) Membranes and lipids of thermophiles. In: Brock TD (ed) Thermophiles: general, molecular, and applied microbiology. Wiley, New York, pp 107–135

    Google Scholar 

  • Lauerer G, Kristiansson JK, Langworthy TA, König H, Stetter KO (1986) Methanothermus sociabilis sp. nov., a second species within the Methanothermaceae growing at 97°C. Syst Appl Microbiol 8:100–105

    Google Scholar 

  • Madon J, Zillig W (1983) A form of the DNA-dependent RNA polymerase of Halobacterium halobium, containing an additional component, is able to transcribe native DNA. Eur J Biochem 133:471–474

    Google Scholar 

  • Marmur J, Doty P (1961) Thermal renaturation of deoxyribonucleic acids. J Mol Biol 3:585–594

    Google Scholar 

  • Marmur J, Doty P (1962) Determination of the base composition of deoxyribonucleic acid from its thermal denaturation temperatures. J Mol Biol 5:109–118

    Google Scholar 

  • Meyer SA, Schleifer KH (1978) Deoxyribonucleic acid reassociation in the classification of coagulase-positive staphylococci. Arch Microbiol 117:183–188

    Google Scholar 

  • Mirault ME, Scherrer K (1971) Isolation of preribosomes from Hela cells and their characterization by electrophoresis on uniform and exponential-gradient-polyacrylamide gels. Eur J Biochem 23:372–386

    Google Scholar 

  • Pfennig N, Wagener S (1986) An improved method of preparing wet mounts for photomicrographs of microorganisms. J Microbiol Methods 4:303–306

    Google Scholar 

  • Rudnick HS, Hendrich S, Pilatus U, Blotevogel HK (1990) Phosphate accumulation and the occurrence of polyphosphates and cyclic 2,3-diphosphoglycerate in Methanosarcina frisia. Arch Microbiol 154:584–588

    Google Scholar 

  • Schnabel R, Thomm M, Gerardy-Schahn R, Zillig W, Stetter KO, Huet J (1983) Structural homology between different archaebacterial DNA-dependent RNA polymerases analyzed by immunological comparison of their components. EMBO J 2:751–755

    Google Scholar 

  • Seely RJ, Fahrney DE (1984) The cyclic 2,3-diphosphoglycerate from Methanobacterium thermoautotrophicum is the d-enantiomer. Curr Microbiol 10:85–88

    Google Scholar 

  • Stetter KO (1982) Ultrathin mycelia-forming organisms from submarine vulcanic areas having an optimum growth temperature of 105°C. Nature 300:258–260

    Google Scholar 

  • Stetter KO, König H, Stackebrandt E (1983) Pyrodictium gen. nov., a new genus of submarine disc-shaped sulphur reducing archaebacteria growing optimally at 105°C. Syst Appl Microbiol 4:535–551

    Google Scholar 

  • Stetter KO, Thomm M, Winter J, Wildgruber G, Huber H, Zillig W, Janecovic D, König H, Palm P, Wunderl S (1981) Methanothermus fervidus, sp. nov., a novel extremely thermophilic methanogen isolated from an Icelandic hot spring. Zentralbl Bakt Hyg I Orig C 2:166–178

    Google Scholar 

  • Stetter KO, Fiala G, Huber G, Huber R, Segerer A (1990) Hyperthermophilic microorganisms. FEMS Microbiol Rev 75:117–124

    Google Scholar 

  • Thomm M, Madon J, Stetter KO (1986) DNA-dependent RNA polymerase of the three orders of methanogens. Biol Chem Hoppe-Seyler 367:473–481

    Google Scholar 

  • Towbin H, Staehelin T, Gordon J (1979) Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: Procedure and some applications. Proc Natl Acad Sci USA 76:4350–4354

    Google Scholar 

  • Trincone A, De Rosa M, Gambacorta A, Lanzotti V, Nicolaus B, Harris JE, Grant WD (1988) A simple chromatographic procedure for the detection of cyclized archaebacterial glycerol-bisphytanyl-glycerol tetraether core lipids. J Gen Microbiol 134:3159–3163

    Google Scholar 

  • Woese CR, Kandler O, Wheelis ML (1990) Towards a natural system of organisms: Proposal for the domains Archaea, Bacteria, and Eucarya. Proc Natl Acad Sci USA 87:4576–4579

    Google Scholar 

  • Zeikus JG, Wolfe RS (1972) Methanobacterium thermoautotrophicum sp. nov., an anaerobic, autotrophic, extreme thermophile. J Bacteriol 109:707–713

    Google Scholar 

  • Zillig W, Stetter KO, Wunderl S, Schulz W, Priess H, Scholz J (1980) The “Sulfolobus-Caldariella”-group: Taxonomy on the basis of the structure of DNA-dependent RNA polymerases. Arch Microbiol 125:259–269

    Google Scholar 

  • Zobell CE (1941) Studies on marine bacteria. I. The cultural requirements of heterotrophic aerobes. J Marin Res 4:42–75

    Google Scholar 

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This paper is dedicated to Otto Kandler on the occasion of his 70th birthday

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Kurr, M., Huber, R., König, H. et al. Methanopyrus kandleri, gen. and sp. nov. represents a novel group of hyperthermophilic methanogens, growing at 110°C. Arch. Microbiol. 156, 239–247 (1991). https://doi.org/10.1007/BF00262992

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