Literature DB >> 9922239

Assembly of the K40 antigen in Escherichia coli: identification of a novel enzyme responsible for addition of L-serine residues to the glycan backbone and its requirement for K40 polymerization.

P A Amor1, J A Yethon, M A Monteiro, C Whitfield.   

Abstract

Escherichia coli O8:K40 coexpresses two distinct lipopolysaccharide (LPS) structures on its surface. The O8 polysaccharide is a mannose homopolymer with a trisaccharide repeat unit and is synthesized by an ABC-2 transport-dependent pathway. The K40LPS backbone structure is composed of a trisaccharide repeating unit of N-acetylglucosamine (GlcNAc) and glucuronic acid (GlcA) and has an uncommon substitution, an L-serine moiety attached to glucuronic acid. The gene cluster responsible for synthesis of the K40 polysaccharide has previously been cloned and sequenced and was found to contain six open reading frames (ORFs) (P. A. Amor and C. Whitfield, Mol. Microbiol. 26:145-161, 1997). Here, we demonstrate that insertional inactivation of orf1 results in the accumulation of a semirough (SR)-K40LPS form which retains reactivity with specific polyclonal serum in Western immunoblots. Structural and compositional analysis of the SR-K40LPS reveals that it comprises a single K40 repeat unit attached to lipid A core. The lack of polymerization of the K40 polysaccharide indicates that orf1 encodes the K40 polymerase (Wzy) and that assembly of the K40 polysaccharide occurs via a Wzy-dependent pathway (in contrast to that of the O8 polysaccharide). Inactivation of orf3 also results in the accumulation of an SR-LPS form which fails to react with specific polyclonal K40 serum in Western immunoblots. Methylation linkage analysis and fast atom bombardment-mass spectrometry of this SR-LPS reveals that the biological repeat unit of the K40 polysaccharide is GlcNAc-GlcA-GlcNAc. Additionally, this structure lacks the L-serine substitution of GlcA. These results show that (i) orf3 encodes the enzyme responsible for the addition of the L-serine residue to the K40 backbone and (ii) substitution of individual K40 repeats with L-serine is essential for their recognition and polymerization into the K40 polysaccharide by Wzy.

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Year:  1999        PMID: 9922239      PMCID: PMC93442     

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  38 in total

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Journal:  J Bacteriol       Date:  1989-09       Impact factor: 3.490

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6.  Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications.

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Journal:  Proc Natl Acad Sci U S A       Date:  1979-09       Impact factor: 11.205

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Authors:  K Jann; T Dengler; B Jann
Journal:  Zentralbl Bakteriol       Date:  1992-01

8.  The structure of Proteus mirabilis O3 O-specific polysaccharide containing N-(2-hydroxyethyl)-D-alanine.

Authors:  E V Vinogradov; W Kaca; A S Shashkov; D Krajewska-Pietrasik; A Rozalski; Y A Knirel; N K Kochetkov
Journal:  Eur J Biochem       Date:  1990-03-30

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Authors:  J Binotto; P R MacLachlan; K E Sanderson
Journal:  Can J Microbiol       Date:  1991-06       Impact factor: 2.419

10.  Structure of Proteus mirabilis O27 O-specific polysaccharide containing amino acids and phosphoethanolamine.

Authors:  E V Vinogradov; D Krajewska-Pietrasik; W Kaca; A S Shashkov; Y A Knirel; N K Kochetkov
Journal:  Eur J Biochem       Date:  1989-11-20
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4.  Identification of a Wzy polymerase required for group IV capsular polysaccharide and lipopolysaccharide biosynthesis in Vibrio vulnificus.

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5.  MoeH5: a natural glycorandomizer from the moenomycin biosynthetic pathway.

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  5 in total

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