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Journal of Biomolecular Screening
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Protocol for Mutagenesis of Alkene Monooxygenase and Screening for Modified Enantiocomposition of the Epoxypropane Product

Ashlee Perry

Biomedical Research Centre, Sheffield Hallam University, Sheffield, United Kingdom

Thomas J. Smith

Biomedical Research Centre Faculty of Health and Well-Being, Sheffield Hallam University, Howard Street Sheffield, S1 1WB, United Kingdom t.j.smith{at}shu.ac.uk

Alkene monooxygenase (AMO) from Rhodococcus rhodochrous B-276 is a 3-component enzyme system encoded by the 4-gene operon amoABCD, which catalyzes the stereoselective epoxidation of aliphatic alkenes yielding primarily the R enantiomer. With propene as the substrate, wild-type AMO yields R-epoxypropane with an enantiomeric excess (e.e.) of 83%. The presumed site of alkene oxidation is a dinuclear iron center situated within the large subunit of the epoxygenase component, AmoC. Substantial problems with the expression of recombinant AMO were previously overcome. In this study, the authors have further developed this expression system to allow amoC to be subjected to mutagenesis by means of error-prone PCR, with the aim of developing a system that could be used to manipulate the enantioselectivity of the enzyme. The mutants were screened for altered stereoselectivity in the propene/epoxypropane reaction by a whole-cell assay, solvent extraction, and chiral gas chromatography analysis protocol that is suitable for scale up to several thousand mutants and that is estimated to detect differences in e.e. of as little as 5%.

Key Words: alkene monooxygenase • epoxygenase • directed evolution • propene • epoxypropene

This version was published on August 1, 2006

Journal of Biomolecular Screening, Vol. 11, No. 5, 553-556 (2006)
DOI: 10.1177/1087057106287930
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