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工程化丁酸梭菌从头生物合成丁酸丁酯。

De novo biosynthesis of butyl butyrate in engineered Clostridium tyrobutyricum.

机构信息

School of Biology and Biological Engineering, South China University of Technology, Guangzhou, 510006, China.

School of Biology and Biological Engineering, South China University of Technology, Guangzhou, 510006, China; Guangdong Provincial Key Laboratory of Fermentation and Enzyme Engineering, South China University of Technology, Guangzhou, 510006, China.

出版信息

Metab Eng. 2023 May;77:64-75. doi: 10.1016/j.ymben.2023.03.009. Epub 2023 Mar 21.

DOI:10.1016/j.ymben.2023.03.009
PMID:36948242
Abstract

Butyl butyrate has broad applications in foods, cosmetics, solvents, and biofuels. Microbial synthesis of bio-based butyl butyrate has been regarded as a promising approach recently. Herein, we engineered Clostridium tyrobutyricum ATCC 25755 to achieve de novo biosynthesis of butyl butyrate from fermentable sugars. Through introducing the butanol synthetic pathway (enzyme AdhE2), screening alcohol acyltransferases (AATs), adjusting transcription of VAAT and adhE2 (i.e., optimizing promoter), and efficient supplying butyryl-CoA, an excellent engineered strain, named MUV3, was obtained with ability to produce 4.58 g/L butyl butyrate at 25 °C with glucose in serum bottles. More NADH is needed for butyl butyrate synthesis, thus mannitol (the more reduced substrate) was employed to produce butyl butyrate. Ultimately, 62.59 g/L butyl butyrate with a selectivity of 95.97%, and a yield of 0.21 mol/mol was obtained under mannitol with fed-batch fermentation in a 5 L bioreactor, which is the highest butyl butyrate titer reported so far. Altogether, this study presents an anaerobic fermentative platform for de novo biosynthesis of butyl butyrate in one step, which lays the foundation for butyl butyrate biosynthesis from renewable biomass feedstocks.

摘要

丁酸丁酯在食品、化妆品、溶剂和生物燃料中有广泛的应用。微生物合成生物基丁酸丁酯最近被认为是一种很有前途的方法。在此,我们通过引入丁醇合成途径(酶 AdhE2)、筛选醇酰基转移酶(AATs)、调整 VAAT 和 adhE2 的转录(即优化启动子)以及高效供应丁酰辅酶 A,将 Clostridium tyrobutyricum ATCC 25755 工程化为能够从头生物合成丁酸丁酯的工程菌株。在血清瓶中以葡萄糖为原料,在 25°C 下,该工程菌 MUV3 能够生产 4.58 g/L 的丁酸丁酯。由于丁酸丁酯合成需要更多的 NADH,因此采用甘露醇(更还原的底物)来生产丁酸丁酯。最终,在 5 L 生物反应器中,通过甘露醇补料分批发酵,获得了 62.59 g/L 的丁酸丁酯,选择性为 95.97%,摩尔收率为 0.21 mol/mol,这是迄今为止报道的丁酸丁酯最高浓度。总之,该研究提供了一个在厌氧发酵条件下一步法从头生物合成丁酸丁酯的平台,为利用可再生生物质原料合成丁酸丁酯奠定了基础。

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