A rationally designed miniature of soluble methane monooxygenase enables rapid and high-yield methanol production in Escherichia coli

被引:3
|
作者
Yu, Yeonhwa [1 ]
Shi, Yongfan [2 ]
Kwon, Young Wan [3 ]
Choi, Yoobin [1 ]
Kim, Yusik [1 ]
Na, Jeong-Geol [2 ]
Huh, June [1 ]
Lee, Jeewon [1 ]
机构
[1] Korea Univ, Dept Chem & Biol Engn, Anam Dong 5-1, Seoul 02841, South Korea
[2] Sogang Univ, Dept Chem & Biomol Engn, Seoul 04107, South Korea
[3] Korea Univ, KU KIST Grad Sch Converging Sci & Technol, Anam Dong 5-1, Seoul 02841, South Korea
基金
新加坡国家研究基金会;
关键词
RECOMBINANT HUMAN H; BIOLOGICAL CONVERSION; DIOXYGEN ACTIVATION; ELECTRON-TRANSFER; CRYSTAL-STRUCTURE; SUBSTRATE ACCESS; HUMAN FERRITIN; ACTIVE-SITE; OXIDATION; BIOCHEMISTRY;
D O I
10.1038/s41467-024-48671-w
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Soluble methane monooxygenase (sMMO) oxidizes a wide range of carbon feedstocks (C1 to C8) directly using intracellular NADH and is a useful means in developing green routes for industrial manufacturing of chemicals. However, the high-throughput biosynthesis of active recombinant sMMO and the ensuing catalytic oxidation have so far been unsuccessful due to the structural and functional complexity of sMMO, comprised of three functionally complementary components, which remains a major challenge for its industrial applications. Here we develop a catalytically active miniature of sMMO (mini-sMMO), with a turnover frequency of 0.32 s(-1), through an optimal reassembly of minimal and modified components of sMMO on catalytically inert and stable apoferritin scaffold. We characterise the molecular characteristics in detail through in silico and experimental analyses and verifications. Notably, in-situ methanol production in a high-cell-density culture of mini-sMMO-expressing recombinant Escherichia coli resulted in higher yield and productivity (similar to 3.0 g/L and 0.11 g/L/h, respectively) compared to traditional methanotrophic production.
引用
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页数:16
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