Applied and Environmental Microbiology, October 2001, p. 4495-4503, Vol. 67, No. 10
0099-2240/01/$04.00+0 DOI: 10.1128/AEM.67.10.4495-4503.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Environmental Sciences Division, Oak Ridge National Laboratory, Oak Ridge, Tennessee 38831,1 and Center for Microbial Ecology, Michigan State University, East Lansing, Michigan 488242
Received 27 March 2001/Accepted 11 July 2001
Recovery of mRNA from environmental samples for measurement of in
situ metabolic activities is a significant challenge. A robust,
simple, rapid, and effective method was developed for simultaneous
recovery of both RNA and DNA from soils of diverse composition by
adapting our previous grinding-based cell lysis method (Zhou et al.,
Appl. Environ. Microbiol. 62:316-322, 1996) for DNA extraction. One of
the key differences is that the samples are ground in a denaturing
solution at a temperature below 0°C to inactivate nuclease activity.
Two different methods were evaluated for separating RNA from DNA. Among
the methods examined for RNA purification, anion exchange resin
gave the best results in terms of RNA integrity, yield, and purity.
With the optimized protocol, intact RNA and high-molecular-weight DNA
were simultaneously recovered from 19 soil and stream sediment samples
of diverse composition. The RNA yield from these samples ranged from
1.4 to 56 µg g of soil
1 dry weight), whereas the DNA
yield ranged from 23 to 435 µg g
1. In addition, studies
with the same soil sample showed that the DNA yield was, on average,
40% higher than that in our previous procedure and 68%
higher than that in a commercial bead milling method. For the majority
of the samples, the DNA and RNA recovered were of sufficient purity for
nuclease digestion, microarray hybridization, and PCR or reverse
transcription-PCR amplification.
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