A Rapid and Economical Method for Efficient DNA Extraction from Diverse Soils Suitable for Metagenomic Applications.

A rapid, cost effective method of metagenomic DNA extraction from soil is a useful tool for environmental microbiology. The present work describes an improved method of DNA extraction namely "powdered glass method" from diverse soils. The method involves the use of sterile glass powder for...

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Main Authors: Selvaraju Gayathri Devi, Anwar Aliya Fathima, Sudhakar Radha, Rex Arunraj, Wayne R Curtis, Mohandass Ramya
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2015-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4500551?pdf=render
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spelling doaj-715d2f1898a545ceb0c9a9cbe495c8472020-11-25T01:45:45ZengPublic Library of Science (PLoS)PLoS ONE1932-62032015-01-01107e013244110.1371/journal.pone.0132441A Rapid and Economical Method for Efficient DNA Extraction from Diverse Soils Suitable for Metagenomic Applications.Selvaraju Gayathri DeviAnwar Aliya FathimaSudhakar RadhaRex ArunrajWayne R CurtisMohandass RamyaA rapid, cost effective method of metagenomic DNA extraction from soil is a useful tool for environmental microbiology. The present work describes an improved method of DNA extraction namely "powdered glass method" from diverse soils. The method involves the use of sterile glass powder for cell lysis followed by addition of 1% powdered activated charcoal (PAC) as purifying agent to remove humic substances. The method yielded substantial DNA (5.87 ± 0.04 μg/g of soil) with high purity (A260/280: 1.76 ± 0.05) and reduced humic substances (A340: 0.047 ± 0.03). The quality of the extracted DNA was compared against five different methods based on 16S rDNA PCR amplification, BamHI digestion and validated using quantitative PCR. The digested DNA was used for a metagenomic library construction with the transformation efficiency of 4 X 106 CFU mL-1. Besides providing rapid, efficient and economical extraction of metgenomic DNA from diverse soils, this method's applicability is also demonstrated for cultivated organisms (Gram positive B. subtilis NRRL-B-201, Gram negative E. coli MTCC40, and a microalgae C. sorokiniana UTEX#1666).http://europepmc.org/articles/PMC4500551?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Selvaraju Gayathri Devi
Anwar Aliya Fathima
Sudhakar Radha
Rex Arunraj
Wayne R Curtis
Mohandass Ramya
spellingShingle Selvaraju Gayathri Devi
Anwar Aliya Fathima
Sudhakar Radha
Rex Arunraj
Wayne R Curtis
Mohandass Ramya
A Rapid and Economical Method for Efficient DNA Extraction from Diverse Soils Suitable for Metagenomic Applications.
PLoS ONE
author_facet Selvaraju Gayathri Devi
Anwar Aliya Fathima
Sudhakar Radha
Rex Arunraj
Wayne R Curtis
Mohandass Ramya
author_sort Selvaraju Gayathri Devi
title A Rapid and Economical Method for Efficient DNA Extraction from Diverse Soils Suitable for Metagenomic Applications.
title_short A Rapid and Economical Method for Efficient DNA Extraction from Diverse Soils Suitable for Metagenomic Applications.
title_full A Rapid and Economical Method for Efficient DNA Extraction from Diverse Soils Suitable for Metagenomic Applications.
title_fullStr A Rapid and Economical Method for Efficient DNA Extraction from Diverse Soils Suitable for Metagenomic Applications.
title_full_unstemmed A Rapid and Economical Method for Efficient DNA Extraction from Diverse Soils Suitable for Metagenomic Applications.
title_sort rapid and economical method for efficient dna extraction from diverse soils suitable for metagenomic applications.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2015-01-01
description A rapid, cost effective method of metagenomic DNA extraction from soil is a useful tool for environmental microbiology. The present work describes an improved method of DNA extraction namely "powdered glass method" from diverse soils. The method involves the use of sterile glass powder for cell lysis followed by addition of 1% powdered activated charcoal (PAC) as purifying agent to remove humic substances. The method yielded substantial DNA (5.87 ± 0.04 μg/g of soil) with high purity (A260/280: 1.76 ± 0.05) and reduced humic substances (A340: 0.047 ± 0.03). The quality of the extracted DNA was compared against five different methods based on 16S rDNA PCR amplification, BamHI digestion and validated using quantitative PCR. The digested DNA was used for a metagenomic library construction with the transformation efficiency of 4 X 106 CFU mL-1. Besides providing rapid, efficient and economical extraction of metgenomic DNA from diverse soils, this method's applicability is also demonstrated for cultivated organisms (Gram positive B. subtilis NRRL-B-201, Gram negative E. coli MTCC40, and a microalgae C. sorokiniana UTEX#1666).
url http://europepmc.org/articles/PMC4500551?pdf=render
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