Industrial production of chiral intermediate of cilastatin by nitrile hydratase and amidase catalyzed one-pot, two-step biotransformation

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• 作者：Ren-Chao Zheng^a ; ^b ; Zhong-Yi Yang^c ; ^d ; Cong-Cheng Li^d ; Yu-Guo Zheng^a ; ^b ; ^{zhengyg@zjut.edu.cn" class="auth_mail} ; Yin-Chu Shen^a ; ^b
• 关键词：Nitrile hydratase ; Amidase ; One-pot ; Two-step biotransformation ; (S)-2 ; 2-Dimethylcyclopropanecarboxamide ; Cilastatin
• 刊名：Journal of Molecular Catalysis B: Enzymatic
• 出版年：April, 2014
• 年：2014
• 卷：102
• 期：Complete
• 页码：161-166
• 全文大小：344 K

文摘

An industrial one-pot, two-step bioprocess catalyzed by nitrile hydratase (NHase) and amidase was developed for (S)-2,2-dimethylcyclopropanecarboxamide (1), the key chiral intermediate of cilastatin. The key unit operations of the whole process including fermentative production of enzymes, biotransformation, isolation of product, and recycling of by-product were reported for the first time. The volumetric enzyme activities of NHase and amidase in 1000-L fermentor were enhanced to 351,000 and 5880 U/L, respectively. The two-step, one-pot biotransformation of rac-2,2-dimethylcyclopropanecarbonitrile (2) took full advantage of both enzymes, leading to accumulation of (S)-1 in 47% yield and 99.6% ee. (S)-1 and the by-product (R)-2,2-dimethylcyclopropanecarboxylic acid (3) were obtained with yields of 38% and 45%, respectively, by a novel macroporous resin adsorption chromatography. Moreover, the total yield of (S)-1 was further increased to 53% after one recycling of (R)-3. The new bioprocess dramatically improved process efficiency compared with the chemical route by elimination of six synthetic steps and proved to be a superior and more cost-effective approach towards (S)-1.