Modulation of Redox Potential and Alteration in Reactivity via the Peroxide Shunt Pathway by Mutation of Cytochrome P450 around the Proximal Heme Ligand

详细信息    查看全文

• 作者：Hirotoshi Matsumura ; Masahiro Wakatabi ; Sayaka Omi ; Akashi Ohtaki ; Nobuhumi Nakamura ; Masafumi Yohda ; Hiroyuki Ohno
• 刊名：Biochemistry
• 出版年：2008
• 出版时间：April 22, 2008
• 年：2008
• 卷：47
• 期：16
• 页码：4834 - 4842
• 全文大小：296K
• 年卷期：v.47,no.16(April 22, 2008)
• ISSN：1520-4995

文摘

In the thermophilic cytochrome P450 from the thermoacidophilic crenarchaeon Sulfolobus tokodaii strain 7 (P450st), a phenylalanine residue at position 310 and an alanine residue at position 320 are located close to the heme thiolate ligand, Cys317. Single site-directed mutants F310A and A320Q and double mutant F310A/A320Q have been constructed. All mutant enzymes as well as wild-type (WT) P450st were expressed at high levels. The substitution of F310 with Ala and of A320 with Gln induced shifts in redox potential and blue shifts in Soret absorption of ferrous−CO forms, while spectral characterization showed that in the resting state, the mutants almost retained the structural integrity of the active site. The redox potential of the heme varied as follows: –481 mV (WT), –477 mV (A320Q), –453 mV (F310A), and –450 mV (F310A/A320Q). The trend in the Soret band of the ferrous−CO form was as follows: 450 nm (WT) < 449 nm (A320Q) < 446 nm (F310A) < 444 nm (F310A/A320Q). These results established that the reduction potential and electron density on the heme iron are modulated by the Phe310 and Ala320 residues in P450st. The electron density on the heme decreases in the following order: WT > A320Q > F310A > F310A/A320Q. The electron density on the heme iron infers an essential role in P450 activity. The decrease in electron density interferes with the formation of a high-valent oxo−ferryl species called Compound I. However, steady-state turnover rates of styrene epoxidation with H₂O₂ show the following trend: WT ≈ A320Q < F310A ≈ F310A/A320Q. The shunt pathway which can provide the two electrons and oxygen required for a P450 reaction instead of NAD(P)H and dioxygen can rule out the first and second heme reduction in the catalytic process. Because the electron density on the heme iron might be deeply involved in the k_cat values in this system, the intermediate Compound 0 which is the precursor species of Compound I mainly appears to participate dominantly in epoxidation with H₂O₂.