Microbiology
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Microbiology 149 (2003), 2529-2537; DOI  10.1099/mic.0.26351-0
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Salmassi, T. M.
Right arrow Articles by Leadbetter, J. R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Salmassi, T. M.
Right arrow Articles by Leadbetter, J. R.
Agricola
Right arrow Articles by Salmassi, T. M.
Right arrow Articles by Leadbetter, J. R.
Microbiology 149 (2003), 2529-2537; DOI  10.1099/mic.0.26351-0
© 2003 Society for General Microbiology

Analysis of genes of tetrahydrofolate-dependent metabolism from cultivated spirochaetes and the gut community of the termite Zootermopsis angusticollis

Tina M. Salmassi{dagger} and Jared R. Leadbetter

Environmental Science and Engineering, M/C 138-78, California Institute of Technology, Pasadena, CA 91125, USA

Correspondence
Jared R. Leadbetter
jleadbetter{at}caltech.edu

The hindguts of wood-feeding termites are the sites of intense, CO2-reductive acetogenesis. This activity profoundly influences host nutrition and methane emissions. Homoacetogens previously isolated from diverse termites comprised novel taxa belonging to two distinct bacterial phyla, Firmicutes and Spirochaetes. Little else is known about either the diversity or abundance of homoacetogenic species present in any given termite or the genetic details underlying CO2-reductive acetogenesis by Spirochaetes. A key enzyme of CO2-reductive acetogenesis is formyltetrahydrofolate synthetase (FTHFS). A previously designed primer set was used to amplify FTHFS genes from three isolated termite-gut spirochaetes. Sequencing DNA flanking the FTHFS gene of Treponema strain ZAS-2 revealed genes encoding two acetogenesis-related enzymes, methenyltetrahydrofolate cyclohydrolase and methylenetetrahydrofolate dehydrogenase. Although termite-gut spirochaetes are only distantly related to clostridia at the ribosomal level, their tetrahydrofolate-dependent enzymes appear to be closely related. In contrast, homologous proteins identified in the non-homoacetogenic oral spirochaete Treponema denticola were only distantly related to those from clostridia and the termite-gut treponemes. Having demonstrated their utility with spirochaete pure cultures, the FTHFS primers were used to construct a 91-clone library from the termite-gut community DNA. From this, 19 DNA and eight amino acid FTHFS types were identified. Over 75 % of the retrieved clones formed a novel, coherent cluster with the FTHFS homologues obtained from the termite-gut treponemes. Thus, FTHFS gene diversity in the gut of the termite Zootermopsis angusticollis appears to be dominated by spirochaetes. The homoacetogenic capacity of termite-gut spirochaetes may have been acquired via lateral gene transfer from clostridia.


Abbreviations: FTHFS, formyltetrahydrofolate synthetase; MTHFC, methenyltetrahydrofolate cyclohydrolase; MTHFD, methylenetetrahydrofolate dehydrogenase; THF, tetrahydrofolate

The nucleotide and deduced amino acid sequences for the FTHFS genes recovered from pure cultures and environmental samples during the course of this study can be found in GenBank under accession numbers AY162294AY162314, AY162316 and AY254548.

{dagger}Present address: Faculty for Biological Sciences, BS 344, California State University, Los Angeles, Los Angeles, CA 90032-4226, USA.




This article has been cited by other articles:


Home page
ScienceHome page
E. A. Ottesen, J. W. Hong, S. R. Quake, and J. R. Leadbetter
Microfluidic Digital PCR Enables Multigene Analysis of Individual Environmental Bacteria
Science, December 1, 2006; 314(5804): 1464 - 1467.
[Abstract] [Full Text] [PDF]


Home page
Appl. Environ. Microbiol.Home page
J. R. Graber and J. A. Breznak
Folate Cross-Feeding Supports Symbiotic Homoacetogenic Spirochetes
Appl. Envir. Microbiol., April 1, 2005; 71(4): 1883 - 1889.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
INT J SYST EVOL MICROBIOL MICROBIOLOGY J GEN VIROL
J MED MICROBIOL ALL SGM JOURNALS
Copyright © 2003 Society for General Microbiology.