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Literature summary for 2.4.1.309 extracted from

  • Yi, W.; Zhu, L.; Guo, H.; Li, M.; Li, J.; Wang, P.G.
    Formation of a new O-polysaccharide in Escherichia coli O86 via disruption of a glycosyltransferase gene involved in O-unit assembly (2006), Carbohydr. Res., 341, 2254-2260.
    View publication on PubMed
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Natural Substrates/ Products (Substrates)

Natural Substrates Organism Comment (Nat. Sub.) Natural Products Comment (Nat. Pro.) Rev. Reac.
additional information Escherichia coli the enzyme is involved in the the biosynthesis of the O-polysaccharide repeating unit of Escherichia coli serotype O86 ?
-
 ?
additional information Escherichia coli O86 the enzyme is involved in the the biosynthesis of the O-polysaccharide repeating unit of Escherichia coli serotype O86 ?
-
 ?

Organism

Organism UniProt Comment Textmining
Escherichia coli
-
-
-
Escherichia coli O86
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-
-

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
additional information the enzyme is involved in the the biosynthesis of the O-polysaccharide repeating unit of Escherichia coli serotype O86 Escherichia coli ?
-
 ?
additional information the enzyme is involved in the the biosynthesis of the O-polysaccharide repeating unit of Escherichia coli serotype O86 Escherichia coli O86 ?
-
 ?

Synonyms

Synonyms Comment Organism
WbnI
-
 Escherichia coli

General Information

General Information Comment Organism
malfunction wbnI gene is replaced by a chloramphenicol acetyltransferase gene using the RED recombination system of phage lambda. Inactivated the wbnI gene shows that the mutant strain produces a different polysaccharide without the a-(1->3)-linked Galp side chain. The yield of the polysaccharide is substantially lower than the one produced by the wild-type strain Escherichia coli