Affiliation:
1. Department of Pharmacology, Washington University School of Medicine, St. Louis, Missouri
2. Max-Planck-Institut für Immunbiologie, Freiburg, Germany
Abstract
Lüderitz
, O. (Max-Planck-Institut für Immunbiologie, Frieburg, Germany), H. J.
Risse, H. Schulte-Holthausen, J. L. Strominger, I. W. Sutherland, and O. Westphal
. Biochemical studies of the smooth-rough mutation in
Salmonella minnesota
. J. Bacteriol.
89:
343–354. 1965.—A comparative study of the O antigen from the smooth strain of
Salmonella minnesota
and of the two R antigens derived from two rough forms of
S. minnesota
(strains R 60 and R 345) has been carried out. The O-specific polysaccharide of the smooth form is composed of heptose, galactose, glucose, glucosamine, galactosamine, and ketodeoxyoctanoate (KDO). R 60 polysaccharide contains KDO, heptose, galactose, glucose, and glucosamine, whereas the R 345 polysaccharide contains only KDO, heptose, galactose, and glucose. Serologically, R 345 and R 60 polysaccharides belong to serogroups R I and R II, respectively. Enzymatic studies revealed that the acetylgalactosamine-synthesizing enzyme, uridine diphosphate-
N
-acetylglucosamine-4-epimerase, is present in wild-type and R 345 cells but is absent from R 60 cells. Two distinct polysaccharides were obtained from the R 345 cells: a polysaccharide derived from the R antigen (lipopolysaccharide) containing no galactosamine and exerting R specificity, and a soluble polysaccharide containing galactosamine and exerting O specificity. The structure of O and R antigens is discussed, together with the general significance of the results for the biosynthesis of the O antigens of the genus
Salmonella
.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
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