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Bioreactor cultivation of Escherichia coli for production of recombinant penicillin G amidase from Alcaligenes faecalis
Authors:Deak Peter M  Lutz-Wahl Sabine  Bothe Harald  Fischer Lutz
Affiliation:(1) Lehrstuhl für Biotechnologie, Institut für Lebensmitteltechnologie, Universität Hohenheim, Emil-Wolff-Straße 14, 70599 Stuttgart, Germany
Abstract:The penicillin G amidase (PGA) from Alcaligenes faecalis, which has interesting properties for use in combinatorial biochemistry, was produced by recombinant expression in Escherichia coli. The corresponding gene was cloned into a multicopy vector under the strict regulatory control of the rhamnose inducible promoter. Cells were grown in a synthetic minimal medium in a bioreactor (5 l working vol.), and production of PGA was induced by repeated addition of the inducer rhamnose, that served also as a carbon source. The fermentation yield was about 4500 units PGA activity per liter of culture medium.
Keywords:Alcaligenes faecalis  fermentation  penicillin G amidase  recombinant protein production  rhamnose inducible promoter
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