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Regulation of Multiple Carbon Monoxide Consumption Pathways in Anaerobic Bacteria

Carbon monoxide (CO), well known as a toxic gas, is increasingly recognized as a key metabolite and signaling molecule. Microbial utilization of CO is quite common, evidenced by the rapid escalation in description of new species of CO-utilizing bacteria and archaea. Carbon monoxide dehydrogenase (CO...

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Autores principales: Techtmann, Stephen M., Colman, Albert S., Murphy, Michael B., Schackwitz, Wendy S., Goodwin, Lynne A., Robb, Frank T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Research Foundation 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3135865/
https://www.ncbi.nlm.nih.gov/pubmed/21808633
http://dx.doi.org/10.3389/fmicb.2011.00147
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author Techtmann, Stephen M.
Colman, Albert S.
Murphy, Michael B.
Schackwitz, Wendy S.
Goodwin, Lynne A.
Robb, Frank T.
author_facet Techtmann, Stephen M.
Colman, Albert S.
Murphy, Michael B.
Schackwitz, Wendy S.
Goodwin, Lynne A.
Robb, Frank T.
author_sort Techtmann, Stephen M.
collection PubMed
description Carbon monoxide (CO), well known as a toxic gas, is increasingly recognized as a key metabolite and signaling molecule. Microbial utilization of CO is quite common, evidenced by the rapid escalation in description of new species of CO-utilizing bacteria and archaea. Carbon monoxide dehydrogenase (CODH), the protein complex that enables anaerobic CO-utilization, has been well-characterized from an increasing number of microorganisms, however the regulation of multiple CO-related gene clusters in single isolates remains unexplored. Many species are extraordinarily resistant to high CO concentrations, thriving under pure CO at more than one atmosphere. We hypothesized that, in strains that can grow exclusively on CO, both carbon acquisition via the CODH/acetyl CoA synthase complex and energy conservation via a CODH-linked hydrogenase must be differentially regulated in response to the availability of CO. The CO-sensing transcriptional activator, CooA is present in most CO-oxidizing bacteria. Here we present a genomic and phylogenetic survey of CODH operons and cooA genes found in CooA-containing bacteria. Two distinct groups of CooA homologs were found: one clade (CooA-1) is found in the majority of CooA-containing bacteria, whereas the other clade (CooA-2) is found only in genomes that encode multiple CODH clusters, suggesting that the CooA-2 might be important for cross-regulation of competing CODH operons. Recombinant CooA-1 and CooA-2 regulators from the prototypical CO-utilizing bacterium Carboxydothermus hydrogenoformans were purified, and promoter binding analyses revealed that CooA-1 specifically regulates the hydrogenase-linked CODH, whereas CooA-2 is able to regulate both the hydrogenase-linked CODH and the CODH/ACS operons. These studies point to the ability of dual CooA homologs to partition CO into divergent CO-utilizing pathways resulting in efficient consumption of a single limiting growth substrate available across a wide range of concentrations.
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spelling pubmed-31358652011-08-01 Regulation of Multiple Carbon Monoxide Consumption Pathways in Anaerobic Bacteria Techtmann, Stephen M. Colman, Albert S. Murphy, Michael B. Schackwitz, Wendy S. Goodwin, Lynne A. Robb, Frank T. Front Microbiol Microbiology Carbon monoxide (CO), well known as a toxic gas, is increasingly recognized as a key metabolite and signaling molecule. Microbial utilization of CO is quite common, evidenced by the rapid escalation in description of new species of CO-utilizing bacteria and archaea. Carbon monoxide dehydrogenase (CODH), the protein complex that enables anaerobic CO-utilization, has been well-characterized from an increasing number of microorganisms, however the regulation of multiple CO-related gene clusters in single isolates remains unexplored. Many species are extraordinarily resistant to high CO concentrations, thriving under pure CO at more than one atmosphere. We hypothesized that, in strains that can grow exclusively on CO, both carbon acquisition via the CODH/acetyl CoA synthase complex and energy conservation via a CODH-linked hydrogenase must be differentially regulated in response to the availability of CO. The CO-sensing transcriptional activator, CooA is present in most CO-oxidizing bacteria. Here we present a genomic and phylogenetic survey of CODH operons and cooA genes found in CooA-containing bacteria. Two distinct groups of CooA homologs were found: one clade (CooA-1) is found in the majority of CooA-containing bacteria, whereas the other clade (CooA-2) is found only in genomes that encode multiple CODH clusters, suggesting that the CooA-2 might be important for cross-regulation of competing CODH operons. Recombinant CooA-1 and CooA-2 regulators from the prototypical CO-utilizing bacterium Carboxydothermus hydrogenoformans were purified, and promoter binding analyses revealed that CooA-1 specifically regulates the hydrogenase-linked CODH, whereas CooA-2 is able to regulate both the hydrogenase-linked CODH and the CODH/ACS operons. These studies point to the ability of dual CooA homologs to partition CO into divergent CO-utilizing pathways resulting in efficient consumption of a single limiting growth substrate available across a wide range of concentrations. Frontiers Research Foundation 2011-07-11 /pmc/articles/PMC3135865/ /pubmed/21808633 http://dx.doi.org/10.3389/fmicb.2011.00147 Text en Copyright © 2011 Techtmann, Colman, Murphy, Schackwitz, Goodwin and Robb. http://www.frontiersin.org/licenseagreement This is an open-access article subject to a non-exclusive license between the authors and Frontiers Media SA, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and other Frontiers conditions are complied with.
spellingShingle Microbiology
Techtmann, Stephen M.
Colman, Albert S.
Murphy, Michael B.
Schackwitz, Wendy S.
Goodwin, Lynne A.
Robb, Frank T.
Regulation of Multiple Carbon Monoxide Consumption Pathways in Anaerobic Bacteria
title Regulation of Multiple Carbon Monoxide Consumption Pathways in Anaerobic Bacteria
title_full Regulation of Multiple Carbon Monoxide Consumption Pathways in Anaerobic Bacteria
title_fullStr Regulation of Multiple Carbon Monoxide Consumption Pathways in Anaerobic Bacteria
title_full_unstemmed Regulation of Multiple Carbon Monoxide Consumption Pathways in Anaerobic Bacteria
title_short Regulation of Multiple Carbon Monoxide Consumption Pathways in Anaerobic Bacteria
title_sort regulation of multiple carbon monoxide consumption pathways in anaerobic bacteria
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3135865/
https://www.ncbi.nlm.nih.gov/pubmed/21808633
http://dx.doi.org/10.3389/fmicb.2011.00147
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