State Key Laboratory of Chemical Resource Engineering, Beijing University of Chemical Technology, Beijing 100029, China; Beijing Advanced Innovation Center for Soft Matter Science and Engineering, Beijing University of Chemical Technology, Beijing 100029, China.
BiotecEra Inc., Athens, GA 30602, USA.
Metab Eng. 2017 Jul;42:59-65. doi: 10.1016/j.ymben.2017.05.006. Epub 2017 Jun 3.
Acyl-CoAs are essential intermediates in the biosynthetic pathways of a number of industrially and pharmaceutically important molecules. When these pathways are reconstituted in a heterologous microbial host for metabolic engineering purposes, the acyl-CoAs may be subject to undesirable hydrolysis by the host's native thioesterases, resulting in a waste of cellular energy and decreased intermediate availability, thus impairing bioconversion efficiency. 4-hydroxycoumarin (4HC) is a direct synthetic precursor to the commonly used oral anticoagulants (e.g. warfarin) and rodenticides. In our previous study, we have established an artificial pathway for 4HC biosynthesis in Escherichia coli, which involves the thioester intermediate salicoyl-CoA. Here, we utilized the 4HC pathway as a demonstration to examine the negative effect of salicoyl-CoA degradaton, identify and inactivate the responsible thioesterase, and eventually improve the 4HC production. We screened a total of 16 E. coli thioesterases and tested their hydrolytic activity towards salicoyl-CoA in vitro. Among all the tested candidate enzymes, YdiI was found to be the dominant contributor to the salicoyl-CoA degradation in E. coli. Remarkably, the ydiI knockout strain carrying the 4HC pathway exhibited an up to 300% increase in 4HC production. An optimized 4HC pathway construct introduced in the ydiI knockout strain led to the accumulation of 935mg/L of 4HC in shake flasks, which is about 1.5 folds higher than the wild-type strain. This study demonstrates a systematic strategy to alleviate the undesirable hydrolysis of thioester intermediates, allowing production enhancement for other biosynthetic pathways with similar issues.
酰基辅酶 A 是许多工业和制药领域重要分子的生物合成途径中的重要中间体。当这些途径在异源微生物宿主中被重新构建以进行代谢工程时,酰基辅酶 A 可能会被宿主自身的天然硫酯酶水解,导致细胞能量浪费和中间产物可用性降低,从而降低生物转化效率。4-羟基香豆素 (4HC) 是常用口服抗凝剂(如华法林)和杀鼠剂的直接合成前体。在我们之前的研究中,我们已经在大肠杆菌中建立了 4HC 生物合成的人工途径,该途径涉及硫酯中间体水杨酰辅酶 A。在这里,我们利用 4HC 途径作为一个范例,来检验水杨酰辅酶 A 降解的负面影响,鉴定并失活负责的硫酯酶,最终提高 4HC 的产量。我们筛选了总共 16 种大肠杆菌硫酯酶,并测试了它们在体外对水杨酰辅酶 A 的水解活性。在所有测试的候选酶中,YdiI 被发现是大肠杆菌中水杨酰辅酶 A 降解的主要贡献者。值得注意的是,携带 4HC 途径的 ydiI 敲除菌株的 4HC 产量增加了 300%。在 ydiI 敲除菌株中引入优化的 4HC 途径构建体,导致摇瓶中 4HC 的积累达到 935mg/L,比野生型菌株高 1.5 倍左右。这项研究展示了一种系统的策略,可以减轻硫酯中间体的不良水解,从而为其他具有类似问题的生物合成途径的生产增强提供了可能。