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.

Highlights

  • Anaerobic carbon monoxide dehydrogenase (CODH) enzymes have been the subject of rigorous biochemical, genetic, and structural investigations

  • Our inventories contain a broad diversity of cooS genes, each of which grouped into one of three distinct phylogenetic clades based on translated amino acid sequences

  • Similar G+C content was observed between cooS genes that belong to different clades but are from the same microbial species

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Summary

Introduction

Anaerobic carbon monoxide dehydrogenase (CODH) enzymes have been the subject of rigorous biochemical, genetic, and structural investigations. Unlike the -named (though non-homologous) aerobic carbon monoxide dehydrogenase (CoxL), anaerobic CODH is a central enzyme in the Wood-Ljungdahl (acetyl-CoA) pathway for acetogenesis. This metabolism is distributed among only a few phyla but is found in bacteria inhabiting many anaerobic environments, both free-living and host-associated [4,5]. Acetogenic bacteria use CODH in conjunction with acetyl-CoA synthetase (ACS) to catalyze the reduction of CO2 to CO through the carbonyl branch of the acetyl-CoA pathway [6,7,8]. Via the CODH/ACS enzyme complex, acetogenic bacteria form acetyl-CoA, which can either be used for energy conservation or generation of cell carbon

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