Recyclable Whole-Cell Biotransformation System for the Direct Hydroxylation of Propane Catalyzed by a Robust Intracellular Wild-Type Cytochrome P450BM3 Activated by Decoy Molecules.

IF 8.7 Q1 CHEMISTRY, MULTIDISCIPLINARY
JACS Au Pub Date : 2025-07-29 eCollection Date: 2025-09-22 DOI:10.1021/jacsau.5c00453
Yuki Sugai, Masayuki Karasawa, Osami Shoji
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引用次数: 0

Abstract

We report a decoy molecule-based whole-cell biotransformation system that achieves the direct hydroxylation of propane to 2-propanol using wild-type cytochrome P450BM3 expressed in Escherichia coli. With the most effective decoy molecule N-(2-cyclopentylethyl)-prolyl-phenylalanine (2CPE-Pro-Phe), 2-propanol was produced at a final concentration of 29 mM with a high selectivity of 99%. The catalytic activity achieved using this approach was higher than that achieved using previously reported P450BM3 mutants, demonstrating the potential of decoy molecule-assisted P450BM3 for the scalable conversion of gaseous alkanes under mild conditions. The decoy molecule system enables the use of stable wild-type P450BM3, maintaining long-term activity without deactivationan advantage over engineered mutants, which often suffer from reduced stability.

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可回收的全细胞生物转化系统,用于丙烷的直接羟基化,由诱饵分子激活的细胞内野生型细胞色素P450BM3催化。
我们报道了一个基于诱骗分子的全细胞生物转化系统,该系统利用大肠杆菌中表达的野生型细胞色素P450BM3实现了丙烷直接羟基化为2-丙醇。以N-(2-环戊乙基)-脯氨酸-苯丙氨酸(2CPE-Pro-Phe)为最有效的诱饵分子,最终浓度为29 mM,选择性为99%。使用该方法获得的催化活性高于先前报道的P450BM3突变体所获得的催化活性,证明了诱饵分子辅助P450BM3在温和条件下可扩展转化气态烷烃的潜力。诱骗分子系统能够使用稳定的野生型P450BM3,保持长期活性而不失活这是工程突变体的优势,工程突变体经常遭受稳定性降低的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
9.10
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