Abstract
The acetan biosynthetic pathway in Acetobacter xylinum is an ideal model system for engineering novel bacterial polysaccharides. To genetically manipulate this pathway, an Acetobacter strain (CKE5), more susceptible to gene-transfer methodologies, was developed. A new gene, aceP, involved in acetan biosynthesis was identified, sequenced and shown to have homology at the amino acid level with beta-D-glucosyl transferases from a number of different organisms. Disruption of aceP in strain CKE5 confirmed the function assigned above and was used to engineer a novel polysaccharide with a pentasaccharide repeat unit.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Amino Acid Sequence
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Bacterial Proteins / genetics
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Bacterial Proteins / metabolism
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Carbohydrate Sequence
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Genes, Bacterial*
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Gluconacetobacter xylinus / enzymology
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Gluconacetobacter xylinus / genetics
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Gluconacetobacter xylinus / metabolism*
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Glycosyltransferases / genetics*
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Glycosyltransferases / isolation & purification
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Glycosyltransferases / metabolism
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Molecular Sequence Data
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Polysaccharides, Bacterial / biosynthesis*
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Polysaccharides, Bacterial / metabolism
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Sequence Homology, Amino Acid
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Transformation, Bacterial
Substances
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Bacterial Proteins
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Polysaccharides, Bacterial
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acetan
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AceP protein, Acetobacter xylinum
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Glycosyltransferases