Detection of genes for periplasmic nitrate reductase in nitrate respiring bacteria and in community DNA


Flanagan D., Gregory L., Carter J., Karakas-Sen A., Richardson D., Spiro S.

FEMS MICROBIOLOGY LETTERS, vol.177, no.2, pp.263-270, 1999 (Peer-Reviewed Journal) identifier identifier identifier

  • Publication Type: Article / Article
  • Volume: 177 Issue: 2
  • Publication Date: 1999
  • Doi Number: 10.1016/s0378-1097(99)00324-9
  • Journal Name: FEMS MICROBIOLOGY LETTERS
  • Journal Indexes: Science Citation Index Expanded, Scopus
  • Page Numbers: pp.263-270

Abstract

A nested PCR primed by four degenerate oligonucleotides was developed for the specific amplification of sequences from the napA gene encoding the periplasmic nitrate reductase. This approach was used to amplify fragments of the napA gene from 10 Pseudomonas species and one Moraxella sp., previously shown to be able to express the periplasmic nitrate reductase activity, from Rhodobacter capsulatus and from community DNA extracted from a fresh-water sediment. Amino acid sequences encoded by the napA fragments were compared to one another;md to the corresponding regions of related enzymes. This comparison indicates that the amplification protocol is specific for its intended target. The napA sequences amplified from community DNA were tightly clustered, which may indicate a degree of homogeneity in the sediment community. All tested Gram-negative strains capable of aerobic nitrate respiration were found to have periplasmic nitrate reductase genes. However, some strains which have and express the genes are incapable of aerobic nitrate respiration. The PCR primers and amplification protocols described will be useful in future studies of nitrate respiring populations. (C) 1999 Federation of European Microbiological Societies. Published by Elsevier Science B.V. All rights reserved.