Xx. Zhang et al., Genetic diversity among rhizobial isolates from field-grown Astragalus sinicus of southern China, SYST APPL M, 22(2), 1999, pp. 312-320
The genetic diversity among 204 rhizobial isolates from field-grown Astraga
lus sinicus collected from 52 ecological different sites of seven southern
provinces of China was investigated by using rep-PCR fingerprinting with RE
P primers and 16S rDNA PCR-RFLP and sequence analyses. Most isolates (78.4%
) belonged to different 16S rDNA genotypes from that of Mesorhizobium huaku
ii type strain CCBAU2609(T). Rep-PCR fingerprinting analysis of 136 randoml
y chosen isolates categorized 27 REP groups at a similarity level of 60%. G
enetically diverse rhizobial strains could be detected at single site, and
strains with the same genetic type could be found in different geographic l
ocations. Twelve representative strains were selected for identification us
ing 16S and 23S rDNA analyses, which resulted in four 16S and five 23S rDNA
PCR-RFLP genotypes. When both 16S and 23S rDNA PCR-RFLP data were combined
together, seven different genotypes were detected among the 12 representat
ive strains, and no strain shared a genotype with the M. huakuii type strai
n. Both 16S and 23S rRNA genes analyses clustered the 12 representative sta
ins within the Mesorhizobium branch. The 16S rRNA results obtained by PCR-R
FLP were confirmed by sequencing the first 600 bp of the 16S rRNA genes.