Abstract
A maltose-inducible expression vector in Bacillus subtilis has been developed and characterized. The vector permitted beta-galactosidase expression at a high level (maximum activity, 8.16 U/ml) when induced and its expression was markedly repressed by glucose. Using this vector, we successfully expressed the other two genes, bioA and vgb. This thus provided a potential expression system for cloned genes in B. subtilis.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Bacillus subtilis / genetics*
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Bacillus subtilis / metabolism
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Bacterial Proteins / metabolism
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Enzyme Induction
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Gene Expression Regulation, Bacterial / genetics*
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Genetic Vectors / biosynthesis
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Genetic Vectors / genetics*
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Hemeproteins / metabolism
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Maltose / metabolism
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Operon / genetics*
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Promoter Regions, Genetic
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Transaminases / metabolism
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Transformation, Bacterial
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beta-Galactosidase / metabolism
Substances
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Bacterial Proteins
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Hemeproteins
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Vgb protein, Bacteria
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Maltose
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Transaminases
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BioA protein, bacteria
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beta-Galactosidase