Engineered P450 BM3 and cpADH5 coupled cascade reaction for β-oxo fatty acid methyl ester production in whole cells

被引:10
作者
Ensari, Yunus [1 ,2 ]
Santos, Gustavo de Almeida [1 ]
Ruff, Anna Joelle [1 ]
Schwaneberg, Ulrich [1 ,3 ]
机构
[1] Rhein Westfal TH Aachen, Lehrstuhl Biotechnol, Worringerweg 3, D-52074 Aachen, Germany
[2] Kafkas Univ, Fac Engn & Architecture, Dept Bioengn, Kars, Turkey
[3] DWI Leibniz Inst Interakt Mat, Forckenbeckstr 50, D-52056 Aachen, Germany
基金
欧盟地平线“2020”;
关键词
directed evolution; P450; BM3; Alcohol dehydrogenase; whole cell; biocatalysis; fatty acid methyl ester; ALPHA-KETO ACIDS; CYTOCHROME-P450; BM3; DOUBLE OXIDATION; ESCHERICHIA-COLI; HYDROXYLATION; BIOCATALYST; EVOLUTION; ALCOHOLS; CLONING; MONOOXYGENASE;
D O I
10.1016/j.enzmictec.2020.109555
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Hydroxy- or ketone- functionalized fatty acid methyl esters (FAMEs) are important compounds for production of pharmaceuticals, vitamins, cosmetics or dietary supplements. Biocatalysis through enzymatic cascades has drawn attention to the efficient, sustainable, and greener synthetic processes. Furthermore, whole cell catalysts offer important advantages such as cofactor regeneration by cell metabolism, omission of protein purification steps and increased enzyme stability. Here, we report the first whole cell catalysis employing an engineered P450 BM3 variant and cpADH5 coupled cascade reaction for the biosynthesis of hydroxy- and keto-FAMEs. Firstly, P450 BM3 was engineered through the KnowVolution approach yielding P450 BM3 variant YE_M1_2, (R47S/Y51W/T235S/N239R/I401 M) which exhibited boosted performance toward methyl hexanoate. The initial oxidation rate of YE_M1_2 toward methyl hexanoate was determined to be 23-fold higher than the wild type enzyme and a 1.5-fold increase in methyl 3-hydroxyhexanoate production was obtained (YE_M1_2; 2.75 mM and WT; 1.8 mM). Subsequently, the whole cell catalyst for the synthesis of methyl 3-hydroxyhexanoate and methyl 3-oxohexanoate was constructed by combining the engineered P450 BM3 and cpADH5 variants in an artificial operon. A 2.06 mM total product formation was achieved by the whole cell catalyst including co-expressed channel protein, FhuA and co-solvent addition. Moreover, the generated whole cell biocatalyst also accepted methyl valerate, methyl heptanoate as well as methyl octanoate as substrates and yielded omega-1 ketones as the main product.
引用
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页数:10
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