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Anaerobic Carbon Monoxide Dehydrogenase Diversity in the Homoacetogenic Hindgut Microbial Communities of Lower Termites and the Wood Roach

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Journal PLoS One
Date 2011 May 5
PMID 21541298
Citations 10
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Abstract

Anaerobic carbon monoxide dehydrogenase (CODH) is a key enzyme in the Wood-Ljungdahl (acetyl-CoA) pathway for acetogenesis performed by homoacetogenic bacteria. Acetate generated by gut bacteria via the acetyl-CoA pathway provides considerable nutrition to wood-feeding dictyopteran insects making CODH important to the obligate mutualism occurring between termites and their hindgut microbiota. To investigate CODH diversity in insect gut communities, we developed the first degenerate primers designed to amplify cooS genes, which encode the catalytic (β) subunit of anaerobic CODH enzyme complexes. These primers target over 68 million combinations of potential forward and reverse cooS primer-binding sequences. We used the primers to identify cooS genes in bacterial isolates from the hindgut of a phylogenetically lower termite and to sample cooS diversity present in a variety of insect hindgut microbial communities including those of three phylogenetically-lower termites, Zootermopsis nevadensis, Reticulitermes hesperus, and Incisitermes minor, a wood-feeding cockroach, Cryptocercus punctulatus, and an omnivorous cockroach, Periplaneta americana. In total, we sequenced and analyzed 151 different cooS genes. These genes encode proteins that group within one of three highly divergent CODH phylogenetic clades. Each insect gut community contained CODH variants from all three of these clades. The patterns of CODH diversity in these communities likely reflect differences in enzyme or physiological function, and suggest that a diversity of microbial species participate in homoacetogenesis in these communities.

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References
1.
Overbeek R, Begley T, Butler R, Choudhuri J, Chuang H, Cohoon M . The subsystems approach to genome annotation and its use in the project to annotate 1000 genomes. Nucleic Acids Res. 2005; 33(17):5691-702. PMC: 1251668. DOI: 10.1093/nar/gki866. View

2.
Ragsdale S . Life with carbon monoxide. Crit Rev Biochem Mol Biol. 2004; 39(3):165-95. DOI: 10.1080/10409230490496577. View

3.
Odelson D, Breznak J . Volatile Fatty Acid production by the hindgut microbiota of xylophagous termites. Appl Environ Microbiol. 1983; 45(5):1602-13. PMC: 242507. DOI: 10.1128/aem.45.5.1602-1613.1983. View

4.
Kane M, Breznak J . Effect of host diet on production of organic acids and methane by cockroach gut bacteria. Appl Environ Microbiol. 1991; 57(9):2628-34. PMC: 183631. DOI: 10.1128/aem.57.9.2628-2634.1991. View

5.
Lilburn T, Kim K, Ostrom N, Byzek K, Leadbetter J, Breznak J . Nitrogen fixation by symbiotic and free-living spirochetes. Science. 2001; 292(5526):2495-8. DOI: 10.1126/science.1060281. View