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J Biotechnol ; 131(2): 205-8, 2007 Aug 31.
Article in English | MEDLINE | ID: mdl-17655961

ABSTRACT

A steroid 15beta-hydroxylating whole-cell solvent tolerant biocatalyst was constructed by expressing the Bacillus megaterium steroid hydroxylase CYP106A2 in the solvent tolerant Pseudomonas putida S12. Testosterone hydroxylation was improved by a factor 16 by co-expressing Fer, a putative Fe-S protein from Bacillus subtilis. In addition, the specificity for 15beta-hydroxylation was improved by mutating threonine residue 248 of CYP106A2 into valine. These new insights provide the basis for an optimized whole-cell steroid-hydroxylating biocatalyst that can be applied with an organic solvent phase.


Subject(s)
Bacterial Proteins/genetics , Bacterial Proteins/metabolism , Cytochrome P-450 Enzyme System/genetics , Cytochrome P-450 Enzyme System/metabolism , Pseudomonas putida/genetics , Solvents/pharmacology , Testosterone/metabolism , Gene Expression Regulation, Bacterial , Hydroxylation , Models, Biological , Mutagenesis, Site-Directed , Organisms, Genetically Modified , Substrate Specificity
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