Cloning, expression and characterization of a fast self-sufficient P450: CYP102A5 from Bacillus cereus

• Published in: Archives of biochemistry and biophysics 2007-12, Vol.468 (1), p.32-43
• Main Authors: Chowdhary, Puneet K., Alemseghed, Mussie, Haines, Donovan C.
• Format: Article
• Language: English
• Subjects: Anthrax; Bacillus cereus; Bacillus cereus - enzymology; Bacillus cereus - genetics; Cloning, Molecular; CYP102A1; CYP102A5; Cytochrome P-450 Enzyme System - chemistry; Cytochrome P-450 Enzyme System - genetics; Cytochrome P450; Cytochrome P450 reductase; Enzyme Activation; Enzyme Stability; Enzymology; Escherichia coli - enzymology; Escherichia coli - genetics; Fatty acid metabolism; Recombinant Proteins - chemistry; Recombinant Proteins - genetics; Substrate Specificity
• ISSN: 0003-9861; 1096-0384
• DOI: 10.1016/j.abb.2007.09.010

CYP102s represent a family of natural self-sufficient fusions of cytochrome P450 and cytochrome P450 reductase found in some bacteria. One member of this family, named CYP102A1 or more traditionally P450BM-3, has been widely studied as a model of human P450 cytochromes. Remarkable detail of P450 structure and function has been revealed using this highly efficient enzyme. The recent rapid expansion of microbial genome sequences has revealed many relatives of CYP102A1, but to date only two from Bacillus subtilis have been characterized. We report here the cloning and expression of CYP102A5, a new member of this family that is very closely related to CYP102A4 from Bacillus anthracis. Characterization of the substrate specificity of CYP102A5 shows that it, like the other CYP102s, will metabolize saturated and unsaturated fatty acids as well as N-acylamino acids. CYP102A5 catalyzes very fast substrate oxidation, showing one of the highest turnover rates for any P450 monooxygenase studied so far. It does so with more specificity than other CYP102s, yielding primarily ω-1 and ω-2 hydroxylated products. Measurement of the rate of electron transfer through the reductase domain reveals that it is significantly faster in CYP102A5 than in CYP102A1, providing a likely explanation for the increased monooxygenation rate. The availability of this new, very fast fusion P450 will provide a great tool for comparative structure–function studies between CYP102A5 and the other characterized CYP102s.