戊二酸
生物转化
生物催化
化学
生物反应器
有机化学
己二酸
辅因子
微生物联合体
微生物代谢
组合化学
生物化学
催化作用
酶
微生物
细菌
生物
发酵
离子液体
遗传学
作者
Cong Gao,Jiaping Wang,Liang Guo,Guipeng Hu,Jia Liu,Wei Song,Li Liu,Xiulai Chen
出处
期刊:Chemcatchem
[Wiley]
日期:2021-10-15
卷期号:13 (23): 5047-5055
被引量:6
标识
DOI:10.1002/cctc.202101245
摘要
Abstract Glutaric acid is an important C5 platform compound for the synthesis of nylon polymers. However, its production titer and cost are limited by the need for expensive cofactors addition as well as the difficulty of reusing microbial catalysts. Herein, to address these problems, two regeneration systems each for NAD(P) + and α‐ketoglutaric acid were introduced into a five‐enzyme cadaverine pathway for a whole‐cell biocatalytic approach. We demonstrated the efficient conversion of lysine to glutaric acid in a synthetic microbial consortium manner, producing 73.2 g/L glutaric acid with a 74 % molar yield in a 5‐L bioreactor scale. Moreover, with a colloidal chitin‐based immobilization, the engineered microbial consortium exhibited good stability and reusability in a five‐cycle bioconversion. This study provides an efficient microbial platform for glutaric acid production by developing a cheaper and universal cell immobilization approach.
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