Department of Chemistry, Brown University , Box H, Providence, Rhode Island 02912-9108, United States.
Department of Molecular Biology, Cell Biology and Biochemistry, Brown University , Providence, Rhode Island 02912, United States.
J Am Chem Soc. 2016 Sep 28;138(38):12678-89. doi: 10.1021/jacs.6b08610. Epub 2016 Sep 16.
The final step in the biosynthesis of the sesquiterpenoid antibiotic pentalenolactone (1) is the highly unusual cytochrome P450-catalyzed, oxidative rearrangement of pentalenolactone F (2), involving the transient generation and rearrangement of a neopentyl cation. In Streptomyces arenae this reaction is catalyzed by CYP161C2 (PntM), with highly conserved orthologs being present in at least 10 other Actinomycetes. Crystal structures of substrate-free PntM, as well as PntM with bound substrate 2, product 1, and substrate analogue 6,7-dihydropentalenolactone F (7) revealed interactions of bound ligand with three residues, F232, M77, and M81 that are unique to PntM and its orthologs and absent from essentially all other P450s. Site-directed mutagenesis, ligand-binding measurements, steady-state kinetics, and reaction product profiles established there is no special stabilization of reactive cationic intermediates by these side chains. Reduced substrate analogue 7 did not undergo either oxidative rearrangement or simple hydroxylation, suggesting that the C1 carbocation is not anchimerically stabilized by the 6,7-double bond of 2. The crystal structures also revealed plausible proton relay networks likely involved in the generation of the key characteristic P450 oxidizing species, Compound I, and in mediating stereospecific deprotonation of H-3re of the substrate. We conclude that the unusual carbocation intermediate results from outer shell electron transfer from the transiently generated C1 radical to the tightly paired heme-•Fe(3+)-OH radical species. The oxidative electron transfer is kinetically dominant as a result of the unusually strong steric barrier to oxygen rebound to the neopentyl center C-1si, which is flanked on each neighboring carbon by syn-axial substituents.
倍半萜类抗生素戊烯内酯(1)生物合成的最后一步是细胞色素 P450 催化的、戊烯内酯 F(2)的氧化重排,涉及新戊基阳离子的瞬时生成和重排。在链霉菌 arenae 中,该反应由 CYP161C2(PntM)催化,至少在其他 10 种放线菌中存在高度保守的同源物。无底物的 PntM 以及与底物 2、产物 1 和底物类似物 6,7-二氢戊烯内酯 F(7)结合的 PntM 的晶体结构揭示了结合配体与三个残基 F232、M77 和 M81 的相互作用,这些残基是 PntM 及其同源物所特有的,而基本上不存在于所有其他 P450 中。定点突变、配体结合测量、稳态动力学和反应产物谱确定,这些侧链不会对反应性正碳离子中间体进行特殊稳定化。还原的底物类似物 7 既没有发生氧化重排也没有简单的羟化,这表明 C1 碳正离子不是通过 2 的 6,7-双键进行的内酰基稳定。晶体结构还揭示了合理的质子传递网络,可能涉及关键特征 P450 氧化物种复合物 I 的生成,以及介导底物 H-3re 的立体特异性去质子化。我们得出结论,不寻常的碳正离子中间体是由于瞬态生成的 C1 自由基向紧密配对的血红素•Fe(3+)-OH 自由基物种的外层电子转移所致。由于氧向新戊基中心 C-1si 回弹的非同寻常强空间位阻,导致氧化电子转移在动力学上占主导地位,而 C-1si 被相邻碳原子上的顺式轴向取代基包围。