Journal of Bacteriology, October 2000, p. 5317-5324, Vol. 182, No. 19
0021-9193/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Department of Biology, Marquette University, Milwaukee, Wisconsin,1 and Complex Carbohydrate Research Center, University of Georgia, Athens, Georgia2
Received 7 April 2000/Accepted 9 July 2000
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 Tn5 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
, 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
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
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.
This article has been cited by other articles:
| Appl. Environ. Microbiol. | Infect. Immun. | Eukaryot. Cell |
|---|---|---|
| Mol. Cell. Biol. | J. Virol. | Microbiol. Mol. Biol. Rev. |
| ALL ASM JOURNALS |