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Comparison of six commercial kits to extract bacterial chromosome and plasmid DNA for MiSeq sequencing

We compared commercial kits for extraction of genomic DNA from the Gram-negative bacterium Klebsiella pneumoniae for subsequent Miseq sequencing. Purification of DNA was based on matrix binding (silica or anion exchange resin) or differential precipitation (salting out), respectively. The choice of...

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Autores principales: Becker, Laura, Steglich, Matthias, Fuchs, Stephan, Werner, Guido, Nübel, Ulrich
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4911584/
https://www.ncbi.nlm.nih.gov/pubmed/27312200
http://dx.doi.org/10.1038/srep28063
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author Becker, Laura
Steglich, Matthias
Fuchs, Stephan
Werner, Guido
Nübel, Ulrich
author_facet Becker, Laura
Steglich, Matthias
Fuchs, Stephan
Werner, Guido
Nübel, Ulrich
author_sort Becker, Laura
collection PubMed
description We compared commercial kits for extraction of genomic DNA from the Gram-negative bacterium Klebsiella pneumoniae for subsequent Miseq sequencing. Purification of DNA was based on matrix binding (silica or anion exchange resin) or differential precipitation (salting out), respectively. The choice of extraction kit had little effect on sequencing quality and coverage across drastically different replicons, except for an apparent depletion of small plasmids (<5 kb) during precipitation-based extractions. Sequencing coverage provided copy-number estimates for small plasmids that were consistently higher than those from quantitative real-time PCR.
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spelling pubmed-49115842016-06-17 Comparison of six commercial kits to extract bacterial chromosome and plasmid DNA for MiSeq sequencing Becker, Laura Steglich, Matthias Fuchs, Stephan Werner, Guido Nübel, Ulrich Sci Rep Article We compared commercial kits for extraction of genomic DNA from the Gram-negative bacterium Klebsiella pneumoniae for subsequent Miseq sequencing. Purification of DNA was based on matrix binding (silica or anion exchange resin) or differential precipitation (salting out), respectively. The choice of extraction kit had little effect on sequencing quality and coverage across drastically different replicons, except for an apparent depletion of small plasmids (<5 kb) during precipitation-based extractions. Sequencing coverage provided copy-number estimates for small plasmids that were consistently higher than those from quantitative real-time PCR. Nature Publishing Group 2016-06-17 /pmc/articles/PMC4911584/ /pubmed/27312200 http://dx.doi.org/10.1038/srep28063 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Becker, Laura
Steglich, Matthias
Fuchs, Stephan
Werner, Guido
Nübel, Ulrich
Comparison of six commercial kits to extract bacterial chromosome and plasmid DNA for MiSeq sequencing
title Comparison of six commercial kits to extract bacterial chromosome and plasmid DNA for MiSeq sequencing
title_full Comparison of six commercial kits to extract bacterial chromosome and plasmid DNA for MiSeq sequencing
title_fullStr Comparison of six commercial kits to extract bacterial chromosome and plasmid DNA for MiSeq sequencing
title_full_unstemmed Comparison of six commercial kits to extract bacterial chromosome and plasmid DNA for MiSeq sequencing
title_short Comparison of six commercial kits to extract bacterial chromosome and plasmid DNA for MiSeq sequencing
title_sort comparison of six commercial kits to extract bacterial chromosome and plasmid dna for miseq sequencing
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4911584/
https://www.ncbi.nlm.nih.gov/pubmed/27312200
http://dx.doi.org/10.1038/srep28063
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