Divalent metal addition restores sulfide-inhibited N(2)O reduction in Pseudomonas aeruginosa

Nitric Oxide. 2010 Sep 15;23(2):101-5. doi: 10.1016/j.niox.2010.04.005. Epub 2010 Apr 21.

Abstract

Hydrogen sulfide (H(2)S) inhibits the last step of the denitrification process, i.e. the reduction of nitrous oxide (N(2)O) to dinitrogen gas (N(2)), both in natural environments (marine sediments) and industrial processes (activated sludge, methanogenic sludge, BioDeNOx process). In a previously published study, we showed that the inhibitory effect of sulfide to N(2)O reduction in mixed microbial communities is reversible and can be counteracted by dosing trace amounts of copper. It remained, however, unclear if this was due to copper sulfide precipitation or a retrofitting of the copper containing N(2)O-reductase (N(2)OR). The present study aimed to elucidate the mechanism of the restoration of sulfide-inhibited N(2)O reducing activity by metal addition to a pure Pseudomonas aeruginosa culture. This was done by using other metals (zinc, cobalt and iron) in comparison with copper. Zinc and cobalt clearly alleviated the sulfide inhibition of N(2)OR to the same extent as copper and the activity restoration was extremely fast (within 15 min, Fig. 3) for zinc, cobalt and copper. This suggests that the alleviation of the inhibitory effect of sulfide is due to metal sulfide precipitation and thus not exclusively limited to Cu. This work also underlines the importance of metal speciation: supply of iron did not restore the N(2)OR activity because it was precipitated by the phosphates present in the medium and thus could not precipitate the sulfide.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cations, Divalent / pharmacology
  • Cobalt / pharmacology
  • Copper / pharmacology
  • Hydrogen Sulfide / metabolism*
  • Metals, Heavy / pharmacology*
  • Nitrates / chemistry
  • Nitrates / metabolism
  • Nitrous Oxide / chemistry*
  • Nitrous Oxide / metabolism*
  • Oxidation-Reduction / drug effects
  • Oxidoreductases / antagonists & inhibitors
  • Oxidoreductases / metabolism
  • Phosphates / chemistry
  • Phosphates / metabolism
  • Pseudomonas aeruginosa / drug effects*
  • Pseudomonas aeruginosa / growth & development
  • Pseudomonas aeruginosa / metabolism*
  • Time Factors
  • Zinc / pharmacology

Substances

  • Cations, Divalent
  • Metals, Heavy
  • Nitrates
  • Phosphates
  • Cobalt
  • Copper
  • Oxidoreductases
  • nitrous oxide reductase
  • Zinc
  • Nitrous Oxide
  • Hydrogen Sulfide