Literature DB >> 11157271

Quantification of ammonia-oxidizing bacteria in arable soil by real-time PCR.

A Hermansson1, P E Lindgren.   

Abstract

Real-time PCR was used to quantify populations of ammonia-oxidizing bacteria representing the beta subdivision of the class Proteobacteria in samples of arable soil, both nitrogen fertilized and unfertilized, from Mellby, Sweden. Primers and probes targeting a 16S ribosomal DNA region of the ammonia-oxidizing bacteria were designed and used. In the fertilized soil there were approximately 6.2 x 10(7) ammonia-oxidizing bacteria per g of soil, three times more than the number of bacteria in the unfertilized soil. The lytic efficiency of bead beating in these soils was investigated by using populations of free or loosely attached bacteria, bacteria tightly bound to particles, and bacteria in nonfractionated samples. The shapes of the curves generated in these tests showed that the concentration of template DNA released at various times remained constant after 10 to 100 s of bead beating.

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Year:  2001        PMID: 11157271      PMCID: PMC92675          DOI: 10.1128/AEM.67.2.972-976.2001

Source DB:  PubMed          Journal:  Appl Environ Microbiol        ISSN: 0099-2240            Impact factor:   4.792


  24 in total

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Authors: 
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3.  Microscale distribution of populations and activities of Nitrosospira and Nitrospira spp. along a macroscale gradient in a nitrifying bioreactor: quantification by in situ hybridization and the use of microsensors.

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Journal:  Appl Environ Microbiol       Date:  1999-08       Impact factor: 4.792

4.  RFLP of rRNA genes and sequencing of the 16S-23S rDNA intergenic spacer region of ammonia-oxidizing bacteria: a phylogenetic approach.

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5.  Real time quantitative PCR.

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8.  Gene organization and primary structure of a ribosomal RNA operon from Escherichia coli.

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9.  Effect of genome size and rrn gene copy number on PCR amplification of 16S rRNA genes from a mixture of bacterial species.

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10.  Analysis of ammonia-oxidizing bacteria of the beta subdivision of the class Proteobacteria in coastal sand dunes by denaturing gradient gel electrophoresis and sequencing of PCR-amplified 16S ribosomal DNA fragments.

Authors:  G A Kowalchuk; J R Stephen; W De Boer; J I Prosser; T M Embley; J W Woldendorp
Journal:  Appl Environ Microbiol       Date:  1997-04       Impact factor: 4.792

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Review 2.  Detection and quantification of gene expression in environmental bacteriology.

Authors:  Freddie H Sharkey; Ibrahim M Banat; Roger Marchant
Journal:  Appl Environ Microbiol       Date:  2004-07       Impact factor: 4.792

3.  Real-time quantitative PCR for assessment of abundance of Pseudoalteromonas species in marine samples.

Authors:  Torben L Skovhus; Niels B Ramsing; Carola Holmström; Staffan Kjelleberg; Ingela Dahllöf
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4.  Ammonia-oxidizing bacteria respond to multifactorial global change.

Authors:  Hans-Peter Horz; Adrian Barbrook; Christopher B Field; Brendan J M Bohannan
Journal:  Proc Natl Acad Sci U S A       Date:  2004-10-06       Impact factor: 11.205

5.  Use of functional gene expression and respirometry to study wastewater nitrification activity after exposure to low doses of copper.

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7.  Specific detection and real-time PCR quantification of potentially mycophagous bacteria belonging to the genus Collimonas in different soil ecosystems.

Authors:  Sachie Höppener-Ogawa; Johan H J Leveau; Wiecher Smant; Johannes A van Veen; Wietse de Boer
Journal:  Appl Environ Microbiol       Date:  2007-05-04       Impact factor: 4.792

8.  Quantification of key genes steering the microbial nitrogen cycle in the rhizosphere of sorghum cultivars in tropical agroecosystems.

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9.  Quantitative detection of methanotrophs in soil by novel pmoA-targeted real-time PCR assays.

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10.  Autecology of an arsenite chemolithotroph: sulfide constraints on function and distribution in a geothermal spring.

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Journal:  Appl Environ Microbiol       Date:  2007-09-07       Impact factor: 4.792

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