Genome Sequence of Thermofilum pendens Reveals an Exceptional Loss of Biosynthetic Pathways without Genome Reduction

Author:

Anderson Iain1,Rodriguez Jason23,Susanti Dwi24,Porat Iris5,Reich Claudia6,Ulrich Luke E.7,Elkins James G.8,Mavromatis Kostas1,Lykidis Athanasios1,Kim Edwin1,Thompson Linda S.19,Nolan Matt1,Land Miriam8,Copeland Alex1,Lapidus Alla1,Lucas Susan1,Detter Chris19,Zhulin Igor B.7,Olsen Gary J.6,Whitman William5,Mukhopadhyay Biswarup23104,Bristow James1,Kyrpides Nikos1

Affiliation:

1. Joint Genome Institute, 2800 Mitchell Drive, Walnut Creek, California 94598

2. Virginia Bioinformatics Institute

3. Departments of Biochemistry

4. Genetics, Bioinformatics and Computational Biology Graduate Program, Virginia Polytechnic Institute and State University, Blacksburg, Virginia 24061

5. Department of Microbiology, University of Georgia, Athens, Georgia 30602

6. Department of Microbiology, University of Illinois, Urbana, Illinois 61801

7. Joint Institute for Computational Sciences, University of Tennessee-Oak Ridge National Laboratory, Oak Ridge, Tennessee 37831

8. Bioscience Division, Oak Ridge National Laboratory, Oak Ridge, Tennessee 37831

9. Bioscience Division, Los Alamos National Laboratory, Los Alamos, New Mexico 87545

10. Biological Sciences

Abstract

ABSTRACT We report the complete genome of Thermofilum pendens , a deeply branching, hyperthermophilic member of the order Thermoproteales in the archaeal kingdom Crenarchaeota. T. pendens is a sulfur-dependent, anaerobic heterotroph isolated from a solfatara in Iceland. It is an extracellular commensal, requiring an extract of Thermoproteus tenax for growth, and the genome sequence reveals that biosynthetic pathways for purines, most amino acids, and most cofactors are absent. In fact, T. pendens has fewer biosynthetic enzymes than obligate intracellular parasites, although it does not display other features that are common among obligate parasites and thus does not appear to be in the process of becoming a parasite. It appears that T. pendens has adapted to life in an environment rich in nutrients. T. pendens was known previously to utilize peptides as an energy source, but the genome revealed a substantial ability to grow on carbohydrates. T. pendens is the first crenarchaeote and only the second archaeon found to have a transporter of the phosphotransferase system. In addition to fermentation, T. pendens may obtain energy from sulfur reduction with hydrogen and formate as electron donors. It may also be capable of sulfur-independent growth on formate with formate hydrogen lyase. Additional novel features are the presence of a monomethylamine:corrinoid methyltransferase, the first time that this enzyme has been found outside the Methanosarcinales , and the presence of a presenilin-related protein. The predicted highly expressed proteins do not include proteins encoded by housekeeping genes and instead include ABC transporters for carbohydrates and peptides and clustered regularly interspaced short palindromic repeat-associated proteins.

Publisher

American Society for Microbiology

Subject

Molecular Biology,Microbiology

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