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利用大肠杆菌全细胞催化生产 1,4-丁二醇。

Production of 1,4-Butanediol from Succinic Acid Using Escherichia Coli Whole-Cell Catalysis.

机构信息

School of Biotechnology and Key Laboratory of Industrial Biotechnology of Ministry of Education, Jiangnan University, Wuxi, 214122.

School of Life Sciences and Health Engineering, Jiangnan University, Wuxi, 214122, China.

出版信息

Chembiochem. 2024 Jun 3;25(11):e202400142. doi: 10.1002/cbic.202400142. Epub 2024 May 14.

Abstract

The widespread attention towards 1,4-butanediol (BDO) as a key chemical raw material stems from its potential in producing biodegradable plastics. However, the efficiency of its biosynthesis via current bioprocesses is limited. In this study, a dual-pathway approach for 1,4-BDO production from succinic acid was developed. Specifically, a double-enzyme catalytic pathway involving carboxylic acid reductase and ethanol dehydrogenase was proposed. Optimization of the expression levels of the pathway enzymes led to a significant 318 % increase in 1,4-BDO titer. Additionally, the rate-limiting enzyme MmCAR was engineered to enhance the k/K values by 50 % and increase 1,4-BDO titer by 46.7 %. To address cofactor supply limitations, an NADPH and ATP cycling system was established, resulting in a 48.9 % increase in 1,4-BDO production. Ultimately, after 48 hours, 1,4-BDO titers reached 201 mg/L and 1555 mg/L in shake flask and 5 L fermenter, respectively. This work represents a significant advancement in 1,4-BDO synthesis from succinic acid, with potential applications in the organic chemical and food industries.

摘要

1,4-丁二醇(BDO)作为一种关键的化学原料,受到了广泛关注,因为它具有生产可生物降解塑料的潜力。然而,目前生物工艺生产 BDO 的效率有限。在这项研究中,开发了一种从琥珀酸生产 1,4-BDO 的双途径方法。具体来说,提出了一种涉及羧酸还原酶和乙醇脱氢酶的双酶催化途径。优化途径酶的表达水平,使 1,4-BDO 产量显著增加了 318%。此外,对限速酶 MmCAR 进行了工程改造,将 k/K 值提高了 50%,并将 1,4-BDO 产量提高了 46.7%。为了解决辅因子供应限制问题,建立了 NADPH 和 ATP 循环系统,使 1,4-BDO 的产量增加了 48.9%。最终,经过 48 小时,摇瓶和 5L 发酵罐中的 1,4-BDO 产量分别达到 201mg/L 和 1555mg/L。这项工作代表了从琥珀酸合成 1,4-BDO 的重大进展,在有机化学和食品工业中有潜在的应用。

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