Abstract
A novel expression vector (pLR) driven by hup promoter and Bifidobacterium beta-galactosidase signal peptide was constructed. The pLR vector was used for the expression of the optimized human IL-10 synthetic gene in Escherichia coli and Bifidobacterium longum. In both microorganisms, rhIL-10 was in a soluble form in total extract cells. The recombinant hIL-10 was partially processed in E. coli, whereas in Bifidobacterium all rhIL-10 was found in the mature form.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Base Sequence
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Bifidobacterium / metabolism*
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Biotechnology / methods*
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Codon
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Escherichia coli / metabolism*
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Gene Expression Regulation
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Genetic Vectors
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Humans
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Interleukin-10 / chemistry
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Interleukin-10 / metabolism
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Interleukin-10 / physiology*
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Molecular Sequence Data
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Plasmids / metabolism
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Promoter Regions, Genetic
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Recombinant Proteins / chemistry
Substances
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Codon
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Recombinant Proteins
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Interleukin-10