生物化学
焊剂(冶金)
脂肪酸
大肠杆菌
代谢途径
代谢工程
乙酰辅酶A
化学
脂肪酸合成
脂肪酸合酶
NAD+激酶
脱水酶
新陈代谢
酶
有机化学
基因
作者
Xirui Xiao,Xingye Yu,Chaitan Khosla
出处
期刊:Biochemistry
[American Chemical Society]
日期:2013-10-22
卷期号:52 (46): 8304-8312
被引量:31
摘要
The entire fatty acid biosynthetic pathway of Escherichia coli, starting from the acetyl-CoA carboxylase, has been reconstituted in vitro from 14 purified protein components. Radiotracer analysis verified stoichiometric conversion of acetyl-CoA and NAD(P)H to the free fatty acid product, allowing implementation of a facile spectrophotometric assay for kinetic analysis of this multienzyme system. At steady state, a maximal turnover rate of 0.5 s(-1) was achieved. Under optimal turnover conditions, the predominant products were C16 and C18 saturated as well as monounsaturated fatty acids. The reconstituted system allowed us to quantitatively interrogate the factors that influence metabolic flux toward unsaturated versus saturated fatty acids. In particular, the concentrations of the dehydratase FabA and the β-ketoacyl synthase FabB were found to be crucial for controlling this property. Via changes in these variables, the percentage of unsaturated fatty acid produced could be adjusted between 10 and 50% without significantly affecting the maximal turnover rate of the pathway. Our reconstituted system provides a powerful tool for understanding and engineering rate-limiting and regulatory steps in this complex and practically significant metabolic pathway.
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