Discrimination ofRhizobium tropici and R. leguminosarumstrains by PCR‐specific amplification of 16S–23S rDNA spacer region fragments and denaturing gradient gel electrophoresis (DGGE)
Author:
Affiliation:
1. Embrapa Solos, Rio de Janeiro, RJ, Brazil,
2. National Center for Genome Resources, Santa Fe, NM, USA, and 4Research Institute for Plant Protection, Wageningen, The Netherlands
3. Fundação André Tosello, Campinas, SP,
Publisher
Wiley
Subject
Applied Microbiology and Biotechnology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1046/j.1365-2672.1999.00480.x
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3. Denaturing gradient gel electrophoresis profiles of 16S rRNA‐defined populations inhabiting a hot spring microbial mat community.;Ferris M.J.;Applied and Environmental Microbiology,1996
4. New approaches to typing and identification of bacteria using the 16S-23S rDNA spacer region
5. Importance of host plants for detecting the population diversity of Rhizobium leguminosarum biovar viciae in soil
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