Literature DB >> 16903836

Coexpression of all constituents of the cholesterol hydroxylase/lyase system in Escherichia coli cells.

T V Shashkova1, V N Luzikov, L A Novikova.   

Abstract

Using the pTrc99A/P450scc vector, a plasmid was constructed in which cDNAs for cytochrome P450scc, adrenodoxin reductase, and adrenodoxin are situated in a single expression cassette. This plasmid was shown to direct the synthesis of all the above proteins in Escherichia coli. Their localization in the E. coli cells and stoichiometry were determined. Cell homogenates exhibited cholesterol hydroxylase/lyase activity, due to catalytically active forms of all three proteins. Thus, the full set of constituents of the mammalian cholesterol hydroxylase/lyase system was shown to be synthesized in bacterial cells for the first time.

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Year:  2006        PMID: 16903836     DOI: 10.1134/s0006297906070145

Source DB:  PubMed          Journal:  Biochemistry (Mosc)        ISSN: 0006-2979            Impact factor:   2.487


  2 in total

1.  Expression of Cholesterol Hydroxylase/Lyase System Proteins in Yeast S. cerevisiae Cells as a Self-Processing Polyprotein.

Authors:  Vera S Efimova; Ludmila V Isaeva; Desislava S Makeeva; Mikhail A Rubtsov; Ludmila A Novikova
Journal:  Mol Biotechnol       Date:  2017-10       Impact factor: 2.695

2.  Analysis of In Vivo Activity of the Bovine Cholesterol Hydroxylase/Lyase System Proteins Expressed in Escherichia coli.

Authors:  V S Efimova; L V Isaeva; M A Rubtsov; L A Novikova
Journal:  Mol Biotechnol       Date:  2019-04       Impact factor: 2.695

  2 in total

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