Function and regulation of isoforms of carbon monoxide dehydrogenase/acetyl coenzyme A synthase in Methanosarcina acetivorans

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

  • Nicole Matschiavelli - , TUD Dresden University of Technology, University Hospital Frankfurt (Author)
  • Ellen Oelgeschläger - , University Hospital Frankfurt, Bayer AG (Author)
  • Berardino Cocchiararo - , University Hospital Frankfurt, Senckenberg Gesellschaft für Naturforschung (Author)
  • Johannes Finke - , University Hospital Frankfurt (Author)
  • Michael Rother - , TUD Dresden University of Technology, University Hospital Frankfurt (Author)

Abstract

Conversion of acetate to methane (aceticlastic methanogenesis) is an ecologically important process carried out exclusively by methanogenic archaea. An important enzyme for this process as well as for methanogenic growth on carbon monoxide is the five-subunit archaeal CO dehydrogenase/acetyl coenzyme A (CoA) synthase multienzyme complex (CODH/ACS) catalyzing both CO oxidation/CO2 reduction and cleavage/synthesis of acetyl-CoA. Methanosarcina acetivorans C2A contains two very similar copies of a six-gene operon (cdh genes) encoding two isoforms of CODH/ACS (Cdh1 and Cdh2) and a single CdhA subunit, CdhA3. To address the role of the CODH/ACS system in M. acetivorans, mutational as well as promoter/reporter gene fusion analyses were conducted. Phenotypic characterization of cdh disruption mutants (three single and double mutants, as well as the triple mutant) revealed a strict requirement of either Cdh1 or Cdh2 for acetotrophic or carboxidotrophic growth, as well as for autotrophy, which demonstrated that both isoforms are bona fide CODH/ACS. While expression of the Cdh2-encoding genes was generally higher than that of genes encoding Cdh1, both appeared to be regulated differentially in response to growth phase and to changing substrate conditions. While dispensable for growth, CdhA3 clearly affected expression of cdh1, suggesting that it functions in signal perception and transduction rather than in catabolism. The data obtained argue for a functional hierarchy and regulatory cross talk of the CODH/ACS isoforms.

Details

Original languageEnglish
Pages (from-to)5377-5387
Number of pages11
JournalJournal of bacteriology
Volume194
Issue number19
Publication statusPublished - Oct 2012
Peer-reviewedYes
Externally publishedYes

External IDs

PubMed 22865842

Keywords

ASJC Scopus subject areas