Acetone utilization by sulfate-reducing bacteria: draft genome sequence of Desulfococcus biacutus and a proteomic survey of acetone-inducible proteins

BMC Genomics. 2014 Jul 11;15(1):584. doi: 10.1186/1471-2164-15-584.

Abstract

Background: The sulfate-reducing bacterium Desulfococcus biacutus is able to utilize acetone for growth by an inducible degradation pathway that involves a novel activation reaction for acetone with CO as a co-substrate. The mechanism, enzyme(s) and gene(s) involved in this acetone activation reaction are of great interest because they represent a novel and yet undefined type of activation reaction under strictly anoxic conditions.

Results: In this study, a draft genome sequence of D. biacutus was established. Sequencing, assembly and annotation resulted in 159 contigs with 5,242,029 base pairs and 4773 predicted genes; 4708 were predicted protein-encoding genes, and 3520 of these had a functional prediction. Proteins and genes were identified that are specifically induced during growth with acetone. A thiamine diphosphate-requiring enzyme appeared to be highly induced during growth with acetone and is probably involved in the activation reaction. Moreover, a coenzyme B12- dependent enzyme and proteins that are involved in redox reactions were also induced during growth with acetone.

Conclusions: We present for the first time the genome of a sulfate reducer that is able to grow with acetone. The genome information of this organism represents an important tool for the elucidation of a novel reaction mechanism that is employed by a sulfate reducer in acetone activation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetone / metabolism*
  • Bacterial Proteins / genetics*
  • Bacterial Proteins / metabolism
  • Butyric Acid / metabolism
  • Contig Mapping
  • Deltaproteobacteria / genetics*
  • Deltaproteobacteria / metabolism
  • Gene Expression Regulation, Bacterial
  • Genome, Bacterial
  • Molecular Sequence Annotation
  • Proteome / genetics*
  • Proteome / metabolism
  • Sequence Analysis, DNA
  • Transcriptional Activation

Substances

  • Bacterial Proteins
  • Proteome
  • Butyric Acid
  • Acetone