Affiliation:
1. Department of Biology, Marquette University, Milwaukee, Wisconsin,1 and
2. Complex Carbohydrate Research Center, University of Georgia, Athens, Georgia2
Abstract
ABSTRACT
Judged by migration of its lipopolysaccharide (LPS) in gel electrophoresis, the O antigen of
Rhizobium etli
mutant strain CE166 was apparently of normal size. However, its LPS sugar composition and staining of the LPS bands after electrophoresis indicated that the proportion of its LPS molecules that possessed O antigen was only 40% of the wild-type value. Its LPS also differed from the wild type by lacking quinovosamine (2-amino-2,6-dideoxyglucose). Both of these defects were due to a single genetic locus carrying a Tn
5
insertion. The deficiency in O-antigen amount, but not the absence of quinovosamine, was suppressed by transferring into this strain recombinant plasmids that shared a 7.8-kb stretch of the
R. etli
CE3
lps
genetic region α, even though this suppressing DNA did not carry the genetic region mutated in strain CE166. Strain CE166 gave rise to pseudonodules on legume host
Phaseolus vulgaris
, whereas the mutant suppressed by DNA from
lps
region α elicited nitrogen-fixing nodules. However, the nodules in the latter case developed slowly and were widely dispersed. Two other
R. etli
mutants that had one-half or less of the normal amount of O antigen also gave rise to pseudonodules on
P. vulgaris
. The latter strains were mutated in
lps
region α and could be restored to normal LPS content and normal symbiosis by complementation with wild-type DNA from this region. Hence, the symbiotic role of LPS requires near-normal abundance of O antigen and may require a structural feature conferred by quinovosamine.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Cited by
53 articles.
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