Cell-density-dependent sensitivity of a mer-lux bioassay

Appl Environ Microbiol. 1997 Aug;63(8):3291-3. doi: 10.1128/aem.63.8.3291-3293.1997.

Abstract

The sensitivity of a previously described assay (O. Selifonova, R. Burlage, and T. Barkay, Appl. Environ. Microbiol. 59:3083-3090, 1993) for the detection of bioavailable inorganic mercury (Hg2+) by the activation of a mer-lux fusion was increased from nanomolar to picomolar concentrations by reducing biomass in the assays from 10(7) to 10(5) cells ml-1. The increase in sensitivity was due to a reduction in the number of cellular binding sites that may compete with the regulatory protein, MerR, for binding of the inducer, Hg2+. These results show that (i) the sensitivity of the mer-lux assay is sufficient for the detection of Hg2+ in most contaminated natural waters and (ii) mer-specified reactions, Hg2+ reduction and methylmercury degradation, can be induced in natural waters and may participate in the geochemical cycling of mercury.

MeSH terms

  • Bacterial Proteins / genetics*
  • Biological Assay / methods*
  • Biomass
  • DNA-Binding Proteins / genetics*
  • Escherichia coli / genetics*
  • Escherichia coli / metabolism*
  • Mercury / metabolism
  • Methylmercury Compounds / metabolism
  • Repressor Proteins*
  • Sensitivity and Specificity
  • Trans-Activators*
  • Water Microbiology

Substances

  • Bacterial Proteins
  • DNA-Binding Proteins
  • MerR protein, Bacteria
  • Methylmercury Compounds
  • Repressor Proteins
  • Trans-Activators
  • LuxR autoinducer binding proteins
  • Mercury