Affiliation:
1. Max Planck Institute for Terrestrial Microbiology, Karl-von-Frisch-Str. 10, D-35043 Marburg, Germany
Abstract
ABSTRACT
Here, we report an efficient method for extracting high-quality mRNA from soil. Key steps in the isolation of total RNA were low-pH extraction (pH 5.0) and Q-Sepharose chromatography. The removal efficiency of humic acids was 94 to 98% for all soils tested. To enrich mRNA, subtractive hybridization of rRNA was most efficient. Subtractive hybridization may be followed by exonuclease treatment if the focus is on the analysis of unprocessed mRNA. The total extraction method can be completed within 8 h, resulting in enriched mRNA ranging from 200 bp to 4 kb in size.
Publisher
American Society for Microbiology
Subject
Ecology,Applied Microbiology and Biotechnology,Food Science,Biotechnology
Reference34 articles.
1. Molecular biology of the cell 1994
2. Andersson, C. R., A. Isaksson, and M. G. Gustafsson. 2006. Bayesian detection of periodic mRNA time profiles without use of training examples. BMC Bioinformatics7:63.
3. mRNA Extraction and Reverse Transcription-PCR Protocol for Detection of
nifH
Gene Expression by
Azotobacter vinelandii
in Soil
4. Celesnik, H., A. Deana, and J. G. Belasco. 2007. Initiation of RNA decay in Escherichia coli by 5′ pyrophosphate removal. Mol. Cell27:79-90.
5. Chen, Y., M. G. Dumont, A. Cébron, and J. C. Murrell. 2007. Identification of active methanotrophs in a landfill cover soil through detection of expression of 16S rRNA and functional genes. Environ. Microbiol.9:2855-2869.
Cited by
93 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献