Literature DB >> 11133483

Microvariation artifacts introduced by PCR and cloning of closely related 16S rRNA gene sequences.

A G Speksnijder1, G A Kowalchuk, S De Jong, E Kline, J R Stephen, H J Laanbroek.   

Abstract

A defined template mixture of seven closely related 16S-rDNA clones was used in a PCR-cloning experiment to assess and track sources of artifactual sequence variation in 16S rDNA clone libraries. At least 14% of the recovered clones contained aberrations. Artifact sources were polymerase errors, a mutational hot spot, and cloning of heteroduplexes and chimeras. These data may partially explain the high degree of microheterogeneity typical of sequence clusters detected in environmental clone libraries.

Mesh:

Substances:

Year:  2001        PMID: 11133483      PMCID: PMC92603          DOI: 10.1128/AEM.67.1.469-472.2001

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


  25 in total

1.  Methyl-directed repair of frameshift heteroduplexes in cell extracts from Escherichia coli.

Authors:  B A Learn; R H Grafstrom
Journal:  J Bacteriol       Date:  1989-12       Impact factor: 3.490

2.  16S ribosomal DNA amplification for phylogenetic study.

Authors:  W G Weisburg; S M Barns; D A Pelletier; D J Lane
Journal:  J Bacteriol       Date:  1991-01       Impact factor: 3.490

3.  PAGE analysis of the heteroduplexes formed between PCR-amplified 16S rRNA genes: estimation of sequence similarity and rDNA complexity.

Authors:  R T Espejo; C G Feijóo; J Romero; M Vásquez
Journal:  Microbiology       Date:  1998-06       Impact factor: 2.777

4.  Frequency of formation of chimeric molecules as a consequence of PCR coamplification of 16S rRNA genes from mixed bacterial genomes.

Authors:  G C Wang; Y Wang
Journal:  Appl Environ Microbiol       Date:  1997-12       Impact factor: 4.792

5.  The frequency of chimeric molecules as a consequence of PCR co-amplification of 16S rRNA genes from different bacterial species.

Authors:  G C Wang; Y Wang
Journal:  Microbiology (Reading)       Date:  1996-05       Impact factor: 2.777

6.  A new computational method for detection of chimeric 16S rRNA artifacts generated by PCR amplification from mixed bacterial populations.

Authors:  G A Komatsoulis; M S Waterman
Journal:  Appl Environ Microbiol       Date:  1997-06       Impact factor: 4.792

7.  Secondary structure within PCR target sequences may facilitate heteroduplex production.

Authors:  E Separovic; S A Nadin-Davis
Journal:  PCR Methods Appl       Date:  1994-02

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

Authors:  J Brosius; T J Dull; D D Sleeter; H F Noller
Journal:  J Mol Biol       Date:  1981-05-15       Impact factor: 5.469

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

Authors:  V Farrelly; F A Rainey; E Stackebrandt
Journal:  Appl Environ Microbiol       Date:  1995-07       Impact factor: 4.792

10.  Recovery of a Nitrosomonas-like 16S rDNA sequence group from freshwater habitats.

Authors:  A G Speksnijder; G A Kowalchuk; K Roest; H J Laanbroek
Journal:  Syst Appl Microbiol       Date:  1998-06       Impact factor: 4.022

View more
  62 in total

1.  Heteroduplexes in mixed-template amplifications: formation, consequence and elimination by 'reconditioning PCR'.

Authors:  Janelle R Thompson; Luisa A Marcelino; Martin F Polz
Journal:  Nucleic Acids Res       Date:  2002-05-01       Impact factor: 16.971

2.  Widespread distribution in polar oceans of a 16S rRNA gene sequence with affinity to Nitrosospira-like ammonia-oxidizing bacteria.

Authors:  James T Hollibaugh; Nasreen Bano; Hugh W Ducklow
Journal:  Appl Environ Microbiol       Date:  2002-03       Impact factor: 4.792

3.  Extensive profiling of a complex microbial community by high-throughput sequencing.

Authors:  Janet E Hill; Robyn P Seipp; Martin Betts; Lindsay Hawkins; Andrew G Van Kessel; William L Crosby; Sean M Hemmingsen
Journal:  Appl Environ Microbiol       Date:  2002-06       Impact factor: 4.792

4.  Community structure of ammonia-oxidizing bacteria within anoxic marine sediments.

Authors:  Thomas E Freitag; James I Prosser
Journal:  Appl Environ Microbiol       Date:  2003-03       Impact factor: 4.792

5.  Modeling bacterial species abundance from small community surveys.

Authors:  R Narang; J Dunbar
Journal:  Microb Ecol       Date:  2003-11-12       Impact factor: 4.552

6.  Cyanobacterial ecotypes in different optical microenvironments of a 68 degrees C hot spring mat community revealed by 16S-23S rRNA internal transcribed spacer region variation.

Authors:  Mike J Ferris; Michael Kühl; Andrea Wieland; David M Ward
Journal:  Appl Environ Microbiol       Date:  2003-05       Impact factor: 4.792

7.  Biodiversity, community structural shifts, and biogeography of prokaryotes within Antarctic continental shelf sediment.

Authors:  John P Bowman; Robert D McCuaig
Journal:  Appl Environ Microbiol       Date:  2003-05       Impact factor: 4.792

8.  Combining culture-dependent and -independent methodologies for estimation of richness of estuarine bacterioplankton consuming riverine dissolved organic matter.

Authors:  Veljo Kisand; Johan Wikner
Journal:  Appl Environ Microbiol       Date:  2003-06       Impact factor: 4.792

9.  Cyanobacterial diversity in natural and artificial microbial mats of Lake Fryxell (McMurdo Dry Valleys, Antarctica): a morphological and molecular approach.

Authors:  Arnaud Taton; Stana Grubisic; Evelyne Brambilla; Rutger De Wit; Annick Wilmotte
Journal:  Appl Environ Microbiol       Date:  2003-09       Impact factor: 4.792

10.  Molecular characterization of a dechlorinating community resulting from in situ biostimulation in a trichloroethene-contaminated deep, fractured basalt aquifer and comparison to a derivative laboratory culture.

Authors:  Tamzen W Macbeth; David E Cummings; Stefan Spring; Lynn M Petzke; Kent S Sorenson
Journal:  Appl Environ Microbiol       Date:  2004-12       Impact factor: 4.792

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.