Chemoenzymatic Synthesis of Steroidal Products: Recent Advances

被引:3
|
作者
Zheng, Mengmeng [1 ,2 ]
Lin, Zhi [1 ,2 ]
Lin, Shuangjun [1 ]
Qu, Xudong [1 ,2 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Life Sci & Biotechnol, State Key Lab Microbial Metab, Shanghai 200240, Peoples R China
[2] Shanghai Jiao Tong Univ, Zhangjiang Inst Adv Study, Shanghai 200240, Peoples R China
基金
中国国家自然科学基金;
关键词
Chemoenzymatic Synthesis; Steroids; Biocatalysis; Regio- and Stereoselective modification; Enzyme cascade; URSODEOXYCHOLIC ACID; 7-BETA-HYDROXYSTEROID DEHYDROGENASE; ENZYMATIC REDUCTION; DIRECTED EVOLUTION; HYDROXYLATION; DEGRADATION; DELTA(1)-DEHYDROGENATION; DEHYDROEPIANDROSTERONE; 19-HYDROXYLATION; 9,11-SECOSTEROL;
D O I
10.1002/ejoc.202301066
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The synthesis of steroidal products has garnered sustained interest due to their versatile bioactivities and physicochemical properties in pharmaceutics. However, the complicated structure of steroids, especially their highly oxygenated skeleton, has presented significant challenges. Benefitted from recent advancements in bioinformatics, genetics, and enzyme engineering, chemoenzymatic strategy combines the flexibility of chemical synthesis with the high regio- and stereo-selectivity of biocatalysis, being an effective approach for the concise synthesis of natural products. In this concept, we review and discuss the recent advances in chemoenzymatic approaches for efficient synthesis of steroids and their analogs, as well as future research opportunities and challenges. This article summarizes the recent breakthroughs in chemoenzymatic synthesis of steroidal products. Integrating steroid hydroxylase, reductase, or dehydrogenase to produce regio- and stereoselective catalysis, enabling the synthetic route more concise, effective and environment-friendly.image
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页数:9
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