Previous Article | Next Article ![]()
Appl. Environ. Microbiol., Nov 1995, 4016-4021, Vol 61, No. 11
B Anyango, KJ Wilson, JL Beynon and KE Giller
Rhizobia were isolated from two Kenyan soils with pHs of 4.5 and 6.8 and
characterized on the basis of their host ranges for nodulation and nitrogen
fixation, colony morphologies, restriction fragment fingerprints, and
hybridization with a nifH probe. The populations of rhizobia nodulating
Phaseolus vulgaris in the two soils were similar in numbers and in
effectiveness of N(inf2) fixation but were markedly different in
composition. The population in the Naivasha soil (pH 6.8) was dominated by
isolates specific in host range for nodulation to P. vulgaris; these all
had multiple copies, in most cases four, of the structural nitrogenase gene
nifH. Only one of the isolates from this soil formed effective nodules on
Leucaena leucocephala, and this isolate had only a single copy of nifH. By
contrast, the population in the acid Daka-ini soil (pH 4.5) was composed
largely of broad-host-range isolates which had single copies of nifH. The
isolates from the Daka-ini soil which were specific to P. vulgaris
generally had three copies of nifH, although one isolate had only two
copies. These rhizobial isolates are indigenous to Kenyan soils and yet
have marked similarities to previously described Rhizobium species from
other continents.
Copyright © 1995, American Society for Microbiology
Diversity of Rhizobia Nodulating Phaseolus vulgaris L. in Two Kenyan Soils with Contrasting pHs
Department of Biological Sciences, Wye College, University of London, Wye, Ashford, Kent, TN25 5AH, United Kingdom; Department of Botany, University of Nairobi, Nairobi, Kenya; and Center for the Application of Molecular Biology to International Agriculture, Canberra, Australian Capital Territory 2601, Australia
This article has been cited by other articles:
| J. Bacteriol. | Microbiol. Mol. Biol. Rev. | Eukaryot. Cell | All ASM Journals |
|---|