The Genome of <i>M. acetivorans</i> Reveals Extensive Metabolic and Physiological Diversity

James E. Galagan(Whitehead Institute for Biomedical Research), Chad Nusbaum(Uniformed Services University of the Health Sciences), Alice C. Roy(Whitehead Institute for Biomedical Research), Matthew G. Endrizzi(J. Craig Venter Institute), Pendexter Macdonald(J. Craig Venter Institute), Will FitzHugh(Whitehead Institute for Biomedical Research), Sarah E. Calvo(Whitehead Institute for Biomedical Research), Reinhard Engels(Whitehead Institute for Biomedical Research), Serge Smirnov(Whitehead Institute for Biomedical Research), Deven Atnoor(Massachusetts Institute of Technology), Adam Brown(University of Wisconsin–Madison), Nicole R. Allen(Uniformed Services University of the Health Sciences), Jerome W. Naylor(Whitehead Institute for Biomedical Research), Nicole Stange-Thomann(Whitehead Institute for Biomedical Research), Kurt DeArellano(Whitehead Institute for Biomedical Research), Robin R. Johnson(Massachusetts Institute of Technology), Lauren Linton(Whitehead Institute for Biomedical Research), Paul McEwan(Whitehead Institute for Biomedical Research), Kevin McKernan(Whitehead Institute for Biomedical Research), Jessica A. Talamas(Whitehead Institute for Biomedical Research), Andrea Tirrell(Pennsylvania State University), Wenjuan Ye(Cornell University), Andrew Zimmer(Whitehead Institute for Biomedical Research), Robert D. Barber(University of Wisconsin–Parkside), Isaac Cann(University of Illinois Urbana-Champaign), David E. Graham(Virginia Tech), David A. Grahame(Uniformed Services University of the Health Sciences), Adam M. Guss(University of Illinois Urbana-Champaign), Reiner Hedderich(Max Planck Institute for Terrestrial Microbiology), Cheryl Ingram‐Smith(University of Wisconsin–Madison), H. Craig Kuettner(University of Illinois Urbana-Champaign), Joseph A. Krzycki(Harvard University Press), John A. Leigh(University of Washington), Weixi Li(University of Kentucky), Jinfeng Liu(Columbia University), Biswarup Mukhopadhyay(University of Illinois Urbana-Champaign), John N. Reeve(Clemson University), Kerry S. Smith(Clemson University), Timothy A. Springer(University of Wisconsin–Madison), Lowell Umayam, Owen White, Robert H. White(Virginia Tech), Everly Conway de Macario(University of Wisconsin–Madison), James G. Ferry(Pennsylvania State University), Ken F. Jarrell(University of Wisconsin–Madison), Jing Hua(University of Wisconsin–Madison), Alberto J.L. Macario(New York State Department of Health), Ian T. Paulsen(University of Wisconsin–Madison), Matthew A. Pritchett(Massachusetts Institute of Technology), Kevin R. Sowers(University of Maryland, Baltimore), Ronald V. Swanson, Steven H. Zinder(University of Wisconsin–Madison), Eric S. Lander(University of Wisconsin–Madison), William W. Metcalf(University of Illinois Urbana-Champaign), Bruce W. Birren(Whitehead Institute for Biomedical Research)
Genome Research
April 1, 2002
Cited by 632Open Access
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Abstract

Methanogenesis, the biological production of methane, plays a pivotal role in the global carbon cycle and contributes significantly to global warming. The majority of methane in nature is derived from acetate. Here we report the complete genome sequence of an acetate-utilizing methanogen, Methanosarcina acetivorans C2A. Methanosarcineae are the most metabolically diverse methanogens, thrive in a broad range of environments, and are unique among the Archaea in forming complex multicellular structures. This diversity is reflected in the genome of M. acetivorans. At 5,751,492 base pairs it is by far the largest known archaeal genome. The 4524 open reading frames code for a strikingly wide and unanticipated variety of metabolic and cellular capabilities. The presence of novel methyltransferases indicates the likelihood of undiscovered natural energy sources for methanogenesis, whereas the presence of single-subunit carbon monoxide dehydrogenases raises the possibility of nonmethanogenic growth. Although motility has not been observed in any Methanosarcineae, a flagellin gene cluster and two complete chemotaxis gene clusters were identified. The availability of genetic methods, coupled with its physiological and metabolic diversity, makes M. acetivorans a powerful model organism for the study of archaeal biology. [Sequence, data, annotations and analyses are available at http://www-genome.wi.mit.edu/.]


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