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Applied and Environmental Microbiology, November 2006, p. 6902-6906, Vol. 72, No. 11
0099-2240/06/$08.00+0 doi:10.1128/AEM.00849-06
Copyright © 2006, American Society for Microbiology. All Rights Reserved.
Department of Biotechnology Engineering,1 National Institute for Biotechnology in the Negev, Ben-Gurion University of the Negev, P.O. Box 653, Be'er-Sheva 84105, Israel2
Received 11 April 2006/ Accepted 23 August 2006
To overcome the shortcomings of universal 16S rRNA gene primers 8F and 907R when studying the diversity of complex microbial communities, the 3' termini of both primers were replaced with inosine. A comparison of the clone libraries derived using both primer sets showed seven bacterial phyla amplified by the altered primer set (8F-I/907R-I) whereas the original set amplified sequences belonging almost exclusively to Proteobacteria (95.8%). Sequences belonging to Firmicutes (42.6%) and Thermotogae (9.3%) were more abundant in a library obtained by using 8F-I/907R-I at a PCR annealing temperature of 54°C, while Proteobacteria sequences were more frequent (62.7%) in a library obtained at 50°C, somewhat resembling the result obtained using the original primer set. The increased diversity revealed by using primers 8F-I/907R-I confirms the usefulness of primers with inosine at the 3' termini in studying the microbial diversity of environmental samples.
Published ahead of print on 1 September 2006.
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