Industrial Application of 2-Oxoglutarate-Dependent Oxygenases

被引:38
|
作者
Peters, Christin [1 ]
Buller, Rebecca M. [1 ]
机构
[1] Zurich Univ Appl Sci, Inst Chem & Biotechnol, Competence Ctr Biocatalysis, Dept Life Sci & Facil Management, Einsiedlerstr 31, CH-8820 Wadenswil, Switzerland
来源
CATALYSTS | 2019年 / 9卷 / 03期
关键词
2-oxoglutarate-dependent oxygenases; industrial biocatalysis; hydroxylation; alpha-ketoglutarate; amino acid modification; antibiotic synthesis; DEACETOXYCEPHALOSPORIN-C SYNTHASE; L-ISOLEUCINE DIOXYGENASE; L-PIPECOLIC ACID; STREPTOMYCES-CLAVULIGERUS; PROLINE; 3-HYDROXYLASE; CLAVAMINATE SYNTHASE; ESCHERICHIA-COLI; NONHEME IRON; FE(II)/ALPHA-KETOGLUTARATE-DEPENDENT DIOXYGENASE; STEREOSPECIFIC HYDROXYLATION;
D O I
10.3390/catal9030221
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
C-H functionalization is a chemically challenging but highly desirable transformation. 2-oxoglutarate-dependent oxygenases (2OGXs) are remarkably versatile biocatalysts for the activation of C-H bonds. In nature, they have been shown to accept both small and large molecules carrying out a plethora of reactions, including hydroxylations, demethylations, ring formations, rearrangements, desaturations, and halogenations, making them promising candidates for industrial manufacture. In this review, we describe the current status of 2OGX use in biocatalytic applications concentrating on 2OGX-catalyzed oxyfunctionalization of amino acids and synthesis of antibiotics. Looking forward, continued bioinformatic sourcing will help identify additional, practical useful members of this intriguing enzyme family, while enzyme engineering will pave the way to enhance 2OGX reactivity for non-native substrates.
引用
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页数:20
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