Sugai Yuki, Karasawa Masayuki, Shoji Osami
Department of Chemistry, Graduate School of Science, Nagoya University, Furo-cho, Chikusa-ku, Nagoya, Aichi 464-8602, Japan.
JACS Au. 2025 Jul 29;5(9):4196-4203. doi: 10.1021/jacsau.5c00453. eCollection 2025 Sep 22.
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 . With the most effective decoy molecule -(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 deactivationan advantage over engineered mutants, which often suffer from reduced stability.
我们报道了一种基于诱饵分子的全细胞生物转化系统,该系统利用在[具体宿主]中表达的野生型细胞色素P450BM3实现丙烷直接羟基化为2-丙醇。使用最有效的诱饵分子-(2-环戊基乙基)-脯氨酰-苯丙氨酸(2CPE-Pro-Phe),最终2-丙醇的产生浓度为29 mM,选择性高达99%。使用这种方法实现的催化活性高于使用先前报道的P450BM3突变体所达到的活性,这表明诱饵分子辅助的P450BM3在温和条件下对气态烷烃进行可扩展转化具有潜力。诱饵分子系统能够使用稳定的野生型P450BM3,保持长期活性而不发生失活——这是相对于工程突变体的一个优势,工程突变体常常稳定性降低。