The carbonic anhydrase of Clostridium autoethanogenum represents a new subclass of β-carbonic anhydrases

Appl Microbiol Biotechnol. 2019 Sep;103(17):7275-7286. doi: 10.1007/s00253-019-10015-w. Epub 2019 Jul 25.

Abstract

Carbonic anhydrase catalyses the interconversion of carbon dioxide and water to bicarbonate and protons. It was unknown if the industrial-relevant acetogen Clostridium autoethanogenum possesses these enzymes. We identified two putative carbonic anhydrase genes in its genome, one of the β class and one of the γ class. Carbonic anhydrase activity was found for the purified β class enzyme, but not the γ class candidate. Functional complementation of an Escherichia coli carbonic anhydrase knock-out mutant showed that the β class carbonic anhydrase could complement this activity, but not the γ class candidate gene. Phylogenetic analysis showed that the β class carbonic anhydrase of Clostridium autoethanogenum represents a novel sub-class of β class carbonic anhydrases that form the F-clade. The members of this clade have the shortest primary structure of any known carbonic anhydrase.

Keywords: Carbon dioxide; Carbon monoxide; Carbonic anhydrase; Clostridium autoethanogenum; Enzyme characterisation; Gas fermentation.

MeSH terms

  • Bacterial Proteins / chemistry
  • Bacterial Proteins / genetics
  • Bacterial Proteins / metabolism*
  • Bicarbonates / metabolism
  • Carbon Dioxide / metabolism
  • Carbonic Anhydrases / chemistry
  • Carbonic Anhydrases / genetics
  • Carbonic Anhydrases / metabolism*
  • Catalysis
  • Clostridium / classification
  • Clostridium / enzymology*
  • Clostridium / genetics
  • Escherichia coli / genetics
  • Gene Knockout Techniques
  • Genetic Complementation Test
  • Kinetics
  • Molecular Weight
  • Phylogeny
  • Protein Multimerization

Substances

  • Bacterial Proteins
  • Bicarbonates
  • Carbon Dioxide
  • Carbonic Anhydrases