PUTIDAREDOXIN REDUCTASE-PUTIDAREDOXIN-CYTOCHROME P450(CAM) TRIPLE FUSION PROTEIN - CONSTRUCTION OF A SELF-SUFFICIENT ESCHERICHIA-COLI CATALYTIC-SYSTEM

Fusion proteins of cytochrome P450(cam) with putidaredoxin (Pd) and pu tidaredoxin reductase (PdR), the two proteins required to transfer ele ctrons from NADH to P450(cam), were constructed by fusing cDNAs encodi ng the three proteins in the expression vector pCWori(+). Several fusi on proteins, in which the order of the three protein domains and the l inkers between them were varied, were expressed in Escherichia coli, p urified, and characterized, The highest activity (k(cat) = 30 min(-1)) was obtained with a PdR-Pd-P450(cam) construct in which the peptides TDGTASS and PLEL were used, respectively, to Link the PdR to the Pd an d the Pd to the P450(cam) domains, Oxygen and NADH consumption is tigh tly coupled to substrate oxidation in the fusion proteins, The rate-li miting step in the catalytic turnover of these fusion proteins is elec tron transfer from Pd to P450(cam). This is indicated by high rates of electron transfer from the PdR and Pd domains to exogenous electron a ccepters, by an increase in the activity of the P450(cam) domain upon addition of exogenous Pd, and by the high activity of wild-type P450(c am) when incubated with a PdR-Pd fusion protein. E. cold cells express ing the PdR-Pd-P450(cam) fusion protein efficiently oxidize camphor to 5-exo-hydroxycamphor and 5-oxocamphor. E. coli cells expressing the t riple fusion protein thus constitute the first heterologous self-suffi cient catalytic system for the oxidation of camphor and other substrat es by P450(cam).