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Taxonomic characterization and plant colonizing abilities of some bacteria related to Bacillus amyloliquefaciens and Bacillus subtilis
The phylogenetic relationships of 17 Bacillus strains isolated from plants and soil were determined from partial sequences of genes encoding 16S rRNA, gyraseA ( gyrA) and the cheA histidine kinase. Five strains were closely related to Bacillus subtilis subsp. subtilis, three strains were more closel...
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Published in: | FEMS microbiology ecology 2004-05, Vol.48 (2), p.249-259 |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | The phylogenetic relationships of 17
Bacillus strains isolated from plants and soil were determined from partial sequences of genes encoding 16S rRNA, gyraseA (
gyrA) and the
cheA histidine kinase. Five strains were closely related to
Bacillus subtilis subsp.
subtilis, three strains were more closely related to
B. subtilis subsp.
spizizeni and two strains were identified as
B. mojavensis. The remaining seven strains formed a cluster closely related to, but distinct from,
Bacillus amyloliquefaciens. Some of these strains formed red-pigmented colonies. The abilities of selected strains to survive in the rhizosphere and to colonize plants were studied using oilseed rape (
Brassica napus), barley (
Hordeum vulgare) and thale cress (
Arabidopsis thaliana) as model plants. It was shown by following the titre of bacteria in seedlings and by scanning electron microscopy that survival of
Bacillus cells on the roots of seedlings during the first week after treatment of seeds with spore suspensions was crucial for colonization of the rhizosphere and for biocontrol activity. The group of strains related to
B. amyloliquefaciens were generally better adapted to colonization of the rhizosphere of plants than other members of the
B. subtilis group and could be considered a distinct ecotype of
B. amyloliquefaciens. Bacteria in this taxon could be recognized on the basis of amplification of a PCR product with primers directed to the
tetB(L) locus but no product with primers directed to the α-amylase gene of
B.amyloliquefaciens sensu stricto. |
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ISSN: | 0168-6496 1574-6941 |
DOI: | 10.1016/j.femsec.2004.02.003 |