Molecular analysis of a sulphate-reducing consortium used to treat metal-containing effluents

Biometals. 2006 Dec;19(6):601-9. doi: 10.1007/s10534-006-0006-z. Epub 2006 Aug 31.

Abstract

A sulphate-reducing consortium used in a bioprocess to remove toxic metals from solution as insoluble sulphides, was characterised using molecular (PCR-based) and traditional culturing techniques. After prolonged cultivation under anoxic biofilm-forming conditions, the mixed culture contained a low diversity of sulphate-reducing bacteria, dominated by one strain closely related to Desulfomicrobium norvegicum, identified by three independent PCR-based analyses. The genetic targets used were the 16S rRNA gene, the 16S-23S rRNA gene intergenic spacer region and the disulfite reductase (dsr) gene, which is conserved amongst all known sulphate-reducing bacteria. This organism was also isolated by conventional anaerobic techniques, confirming its presence in the mixed culture. A surprising diversity of other non-sulphate-reducing facultative and obligate anaerobes were detected, supporting a model of the symbiotic/commensal nature of carbon and energy fluxes in such a mixed culture while suggesting the physiological capacity for a wide range of biotransformations by this stable microbial consortium.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacteria / genetics*
  • Bacteria / metabolism
  • Biodegradation, Environmental
  • Bioreactors / microbiology
  • Deltaproteobacteria / genetics
  • Deltaproteobacteria / isolation & purification
  • Deltaproteobacteria / metabolism
  • Metals / metabolism*
  • Phylogeny
  • Polymerase Chain Reaction
  • RNA, Ribosomal, 16S / genetics
  • Sulfates / metabolism*
  • Symbiosis
  • Water Microbiology
  • Water Pollutants, Chemical / metabolism*

Substances

  • Metals
  • RNA, Ribosomal, 16S
  • Sulfates
  • Water Pollutants, Chemical