乙醛酸循环
代谢工程
立体专一性
化学合成
生物合成
合成生物学
代谢途径
大肠杆菌
辅酶A
组合化学
脱氢酶
化学
生物
精细化工
辅因子
生物催化
拉伤
苹果酸脱氢酶
酶
生物化学
反应条件
生物转化
生化工程
工业生物技术
作者
Chenkai Cao,Jilong Wang,Mengzhen Nie,Jing Zhao,Yuchen Wang,Kechun Zhang
标识
DOI:10.1016/j.ymben.2025.09.007
摘要
D-Pantothenate (D-PA), a crucial precursor for coenzyme A, is widely used in various industries. Traditional chemical synthesis of D-PA involves toxic inputs, including cyanide, and generates environmental pollution. Total biosynthesis from glucose still has limitation in long reaction time and low titer. To provide a new approach to D-PA, we designed a hybrid pathway. First, we used green chemical method to convert inexpensive glyoxylate and isobutyaldehyde into 2-hydroxy-3-methyl-3-formylbutyric acid (HMFBA). Then we established a biosynthetic pathway to transform HMFBA into D-PA. Specifically, we engineered a malate dehydrogenase to achieve the efficient stereospecific conversion step. Optimization efforts led to a strain producing 116.5 g/L D-PA in 48 h, which is the highest rate and titier reported so far. This new approach offers a potentially economic and high-rate production route of D-PA.
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