Literature DB >> 12576596

Characterization of a nitrate-respiring bacterial community using the nitrate reductase gene (narG) as a functional marker.

Lisa G Gregory1, Philip L Bond, David J Richardson, Stephen Spiro.   

Abstract

Bacterial cultures capable of reducing nitrate to nitrite, or of complete denitrification, were established from 5, 10, 15 and 20 cm depths of a freshwater sediment. Taxonomic analysis of the 56 isolates using 16S rRNA gene sequences revealed an unexpected species richness, which included representatives of the gamma-Proteobacteria, Bacillus spp., Staphylococcus spp. and members of the Actinobacteria. Gram-positive species tended to predominate in the lower depths of the sediment, where there was evidence of active sulphate respiration. Sequences (from the narG gene) potentially encoding the catalytic subunit of the membrane-associated nitrate reductase were successfully amplified from 46 of the isolates, using a nested PCR with four degenerate primers. NarG sequences clustered into three major groupings that were supported by alternative phylogenetic analyses. The NarG sequences from Gram-positive isolates (according to rRNA gene phylogeny) clustered together within sequences from the low-G+C Gram-positive bacteria. However, this cluster also included two sequences from members of the genus Pseudomonas. Another group contained mostly NarG sequences from the Proteobacteria (according to rRNA gene phylogeny), but also included five sequences from Gram-positive species. The third group of NarG sequences contained three sequences from Gram-positive species. Thus, the NarG-derived phylogeny is not entirely consistent with 16S rRNA-based taxonomy, precluding the use of the narG gene as a taxonomically useful tool for the characterization of nitrate-respiring bacteria. Total DNA was also extracted from the four depth intervals of the sediment sample and used in similar narG amplifications. Most sequences amplified directly from environmental DNA clustered in the Gram-negative group, and none was in the predominantly Gram-positive group. The study also revealed a degree of spatial organization of a nitrate-respiring community in terms of both microbiology and narG sequences.

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Year:  2003        PMID: 12576596     DOI: 10.1099/mic.0.25849-0

Source DB:  PubMed          Journal:  Microbiology (Reading)        ISSN: 1350-0872            Impact factor:   2.777


  18 in total

1.  Coupling of functional gene diversity and geochemical data from environmental samples.

Authors:  A V Palumbo; J C Schryver; M W Fields; C E Bagwell; J-Z Zhou; T Yan; X Liu; C C Brandt
Journal:  Appl Environ Microbiol       Date:  2004-11       Impact factor: 4.792

2.  Comparative analysis of bacterial diversity in freshwater sediment of a shallow eutrophic lake by molecular and improved cultivation-based techniques.

Authors:  Hideyuki Tamaki; Yuji Sekiguchi; Satoshi Hanada; Kazunori Nakamura; Nakao Nomura; Masatoshi Matsumura; Yoichi Kamagata
Journal:  Appl Environ Microbiol       Date:  2005-04       Impact factor: 4.792

3.  Resolution of distinct membrane-bound enzymes from Enterobacter cloacae SLD1a-1 that are responsible for selective reduction of nitrate and selenate oxyanions.

Authors:  Helen Ridley; Carys A Watts; David J Richardson; Clive S Butler
Journal:  Appl Environ Microbiol       Date:  2006-08       Impact factor: 4.792

4.  Diversity and abundance of nitrate reductase genes (narG and napA), nitrite reductase genes (nirS and nrfA), and their transcripts in estuarine sediments.

Authors:  Cindy J Smith; David B Nedwell; Liang F Dong; A Mark Osborn
Journal:  Appl Environ Microbiol       Date:  2007-03-30       Impact factor: 4.792

5.  Genome-derived criteria for assigning environmental narG and nosZ sequences to operational taxonomic units of nitrate reducers.

Authors:  Katharina Palmer; Harold L Drake; Marcus A Horn
Journal:  Appl Environ Microbiol       Date:  2009-06-05       Impact factor: 4.792

6.  Respiratory and dissimilatory nitrate-reducing communities from an extreme saline alkaline soil of the former lake Texcoco (Mexico).

Authors:  Rocio J Alcántara-Hernández; César Valenzuela-Encinas; Rodolfo Marsch; Luc Dendooven
Journal:  Extremophiles       Date:  2008-12-03       Impact factor: 2.395

Review 7.  Relationships between protein-encoding gene abundance and corresponding process are commonly assumed yet rarely observed.

Authors:  Jennifer D Rocca; Edward K Hall; Jay T Lennon; Sarah E Evans; Mark P Waldrop; James B Cotner; Diana R Nemergut; Emily B Graham; Matthew D Wallenstein
Journal:  ISME J       Date:  2014-12-23       Impact factor: 10.302

8.  Frequency and diversity of nitrate reductase genes among nitrate-dissimilating Pseudomonas in the rhizosphere of perennial grasses grown in field conditions.

Authors:  L Roussel-Delif; S Tarnawski; J Hamelin; L Philippot; M Aragno; N Fromin
Journal:  Microb Ecol       Date:  2005-01-11       Impact factor: 4.552

9.  Potentially Mobile Denitrification Genes Identified in Azospirillum sp. Strain TSH58.

Authors:  Jeonghwan Jang; Yoriko Sakai; Keishi Senoo; Satoshi Ishii
Journal:  Appl Environ Microbiol       Date:  2019-01-09       Impact factor: 4.792

10.  Bacterial Populations Associated with Smokeless Tobacco Products.

Authors:  Jing Han; Yasser M Sanad; Joanna Deck; John B Sutherland; Zhong Li; Matthew J Walters; Norma Duran; Matthew R Holman; Steven L Foley
Journal:  Appl Environ Microbiol       Date:  2016-09-30       Impact factor: 4.792

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