Epoxide Hydrolases: Multipotential Biocatalysts

被引:22
作者
Bucko, Marek [1 ]
Kaniakova, Katarina [2 ]
Hronska, Helena [2 ]
Gemeiner, Peter [1 ]
Rosenberg, Michal [2 ]
机构
[1] Slovak Acad Sci, Inst Chem, Ctr Glycom, Dept Glycobiotechnol, Dubravska Cesta 9, Bratislava 84538, Slovakia
[2] Slovak Univ Technol Bratislava, Inst Biotechnol, Fac Chem & Food Technol, Radlinskeho 9, Bratislava 81237, Slovakia
关键词
epoxide hydrolase; epoxides; chiral precursors; biocatalysis; enantioselectivity; enzyme engineering; stabilization; immobilization; enzyme cascade; AGROBACTERIUM-RADIOBACTER AD1; HYDROLYTIC KINETIC RESOLUTION; CIS-EPOXYSUCCINATE HYDROLASE; RACEMIC STYRENE OXIDE; DIRECTED EVOLUTION; MICROBIOLOGICAL TRANSFORMATIONS; CASCADE BIOCATALYSIS; ASPERGILLUS-NIGER; ENZYMATIC TRANSFORMATIONS; ASYMMETRIC HYDROLYSIS;
D O I
10.3390/ijms24087334
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Epoxide hydrolases are attractive and industrially important biocatalysts. They can catalyze the enantioselective hydrolysis of epoxides to the corresponding diols as chiral building blocks for bioactive compounds and drugs. In this review article, we discuss the state of the art and development potential of epoxide hydrolases as biocatalysts based on the most recent approaches and techniques. The review covers new approaches to discover epoxide hydrolases using genome mining and enzyme metagenomics, as well as improving enzyme activity, enantioselectivity, enantioconvergence, and thermostability by directed evolution and a rational design. Further improvements in operational and storage stabilization, reusability, pH stabilization, and thermal stabilization by immobilization techniques are discussed in this study. New possibilities for expanding the synthetic capabilities of epoxide hydrolases by their involvement in non-natural enzyme cascade reactions are described.
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页数:27
相关论文
共 164 条
[1]   Computational Design of Enantiocomplementary Epoxide Hydrolases for Asymmetric Synthesis of Aliphatic and Aromatic Diols [J].
Arabnejad, Hesam ;
Bombino, Elvira ;
Colpa, Dana I. ;
Jekel, Peter A. ;
Trajkovic, Milos ;
Wijma, Hein J. ;
Janssen, Dick B. .
CHEMBIOCHEM, 2020, 21 (13) :1893-1904
[2]   Structure of Rhodococcus erythropolis limonene-1,2-epoxide hydrolase reveals a novel active site [J].
Arand, M ;
Hallberg, BM ;
Zou, JY ;
Bergfors, T ;
Oesch, F ;
van der Werf, MJ ;
de Bont, JAM ;
Jones, TA ;
Mowbray, SL .
EMBO JOURNAL, 2003, 22 (11) :2583-2592
[3]   Epoxide hydrolases: new tools for the synthesis of fine organic chemicals [J].
Archelas, A ;
Furstoss, R .
TRENDS IN BIOTECHNOLOGY, 1998, 16 (03) :108-116
[4]  
Archelas A., 2016, GREEN BIOCATAL, P179, DOI DOI 10.1002/9781118828083
[5]   Recent developments in the asymmetric hydrolytic ring opening of epoxides catalysed by microbial epoxide hydrolase [J].
Bala, Neeraj ;
Chimni, Swapandeep Singh .
TETRAHEDRON-ASYMMETRY, 2010, 21 (24) :2879-2898
[6]   Isolation of the stable strain Labrys sp BK-8 for L(+)-tartaric acid production [J].
Bao, Wenna ;
Pan, Haifeng ;
Zhang, Zhenhong ;
Cheng, Yongqing ;
Xie, Zhipeng ;
Zhang, Jianguo .
JOURNAL OF BIOSCIENCE AND BIOENGINEERING, 2015, 119 (05) :538-542
[7]  
Basheer S.M., 2017, Bioresources and Bioprocess in Biotechnology, P151
[8]   Epoxide hydrolase-catalysed kinetic resolution of a spiroepoxide, a key building block of various 11-heterosteroids [J].
Bottalla, Anne-Lise ;
Ibrahim-Ouali, Malika ;
Santelli, Maurice ;
Furstoss, Roland ;
Archelas, Alain .
ADVANCED SYNTHESIS & CATALYSIS, 2007, 349 (07) :1102-1110
[9]  
BRENDA, US
[10]  
Buchholz K., 2005, Biocatalysts and enzyme technology