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Gene products required for surface expression of the capsular form of the group 1 K antigen in Escherichia coli (O9a:K30)
Author(s) -
Drummelsmith Jolyne,
Whitfield Chris
Publication year - 1999
Publication title -
molecular microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.857
H-Index - 247
eISSN - 1365-2958
pISSN - 0950-382X
DOI - 10.1046/j.1365-2958.1999.01277.x
Subject(s) - biology , periplasmic space , escherichia coli , gene , lipid a , bacterial capsule , microbiology and biotechnology , glycosyltransferase , biochemistry , genetics , bacteria , virulence
The group 1 K30 antigen from Escherichia coli (O9a:K30) is present on the cell surface as both a capsular structure composed of high‐molecular‐weight K30 polysaccharide and as short K30 oligosaccharides linked to lipid A‐core in a lipopolysaccharide molecule (K30 LPS ). To determine the molecular processes that are responsible for the two forms of K antigen, the 16 kb chromosomal cps region has been characterized. This region encodes 12 gene products required for the synthesis, polymerization and translocation of the K30 antigen. The gene products include four glycosyltransferases responsible for synthesis of the K30 repeat unit; a PST(1) exporter (Wzx), required to transfer lipid‐linked K30 units across the plasma membrane to the periplasmic space; and a K30‐antigen polymerase (Wzy). These gene products are typical of those seen in O‐antigen biosynthesis gene clusters and they interact with the lipopolysaccharide translocation pathway to express K30 LPS on the cell surface. The same gene products also provide the biosynthetic intermediates for the capsule assembly pathway, although they are not in themselves sufficient for synthesis of the K30 capsule. Three additional genes, wza , wzb and wzc , encode homologues to proteins that are encoded by gene clusters involved in expression of a variety of bacterial exopolysaccharides. Mutant analysis indicates that Wza and Wzc are required for wild‐type surface expression of the capsular structure but are not essential for polymerization and play no role in the translocation of K30 LPS . These surface expression components provide the key feature that distinguishes the assembly systems for O antigens and capsules.