生物转化
皂甙元
代谢工程
合成生物学
化学
生化工程
有机合成
制药工业
生物技术
化学合成
绿色化学
组合化学
有机化学
生物
生物化学
计算生物学
催化作用
反应机理
工程类
医学
病理
酶
体外
替代医学
作者
Jinhui Feng,Qiaqing Wu,Dunming Zhu,Yanhe Ma
出处
期刊:Chemsuschem
[Wiley]
日期:2022-01-28
卷期号:15 (9)
被引量:32
标识
DOI:10.1002/cssc.202102399
摘要
Abstract Steroids have been widely used in birth‐control, prevention, and treatment of various diseases, representing the largest sector after antibiotics in the global pharmaceutical market. The steroidal active pharmaceutical ingredients (APIs) have been produced via partial synthetic processes first mainly from sapogenins, which was converted into 16‐dehydropregnenolone by the famous “Marker Degradation”. Traditional mutation and screening, and process engineering have resulted in the industrial production of 4‐androstene‐3,17‐dione (AD), androst‐1,4‐diene‐3,17‐dione (ADD), 9α‐hydroxy‐androsta‐4‐ene‐3,17‐dione (9α‐OH‐AD), and so on, which serve as the key intermediates for the synthesis of steroidal APIs. Recently, genetic and metabolic engineering have generated highly efficient microbial strains for the production of these precursors, leading to the replacement of sapogenins with phytosterols as the starting materials. Further advances in synthetic biology hold promise in the design and construction of microbial cell factories for the industrial production of steroidal intermediates and/or APIs from simple carbon sources such as glucose. Integration of biotransformation into the synthesis of steroidal APIs can greatly reduce the number of reaction steps, achieve lower waste discharge and higher production efficiency, thus enabling a greener steroidal pharmaceutical industry.
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