Immobilisation of cells and enzymes can be a convenient and rapid way for t
esting and transforming substances. Cytochromes P450 may be useful in numer
ous biotransformations of varied lipophilic substrates, performing both reg
io- and stereo-specific monooxygenation reactions. However, one limitation
of their use in vitro is the requirement of cofactor for the supply of elec
trons in the catalytic cycle. Here we report CYP105D1 from Streptomyces gri
seus expressed in Escherichia coli can be immobilised from cell-free extrac
ts using DE52, that the immobilised protein is active in bioconversions and
that a requirement for cofactor can be sustained by a recycling system for
NADH regeneration. (C) 2000 Academic Press.