School of Interdisciplinary Bioscience and Bioengineering, Pohang University of Science and Technology (POSTECH), 77 Cheongam-Ro, Nam-Gu, Pohang, Gyeongbuk 37673, Republic of Korea.
School of Chemical and Biological Engineering, Institute of Chemical Process, Seoul National University, 1 Gwanak-Ro, Gwanak-Gu, Seoul 08826, Republic of Korea.
Metab Eng. 2018 May;47:113-120. doi: 10.1016/j.ymben.2018.03.009. Epub 2018 Mar 13.
3-Hydroxypropionic acid (3-HP) is an important platform chemical, and biological production of 3-HP from glycerol as a carbon source using glycerol dehydratase (GDHt) and aldehyde dehydrogenase (ALDH) has been revealed to be effective because it involves a relatively simple metabolic pathway and exhibits higher yield and productivity than other biosynthetic pathways. Despite the successful attempts of 3-HP production from glycerol, the biological process suffers from problems arising from low activity and inactivation of the two enzymes. To apply the directed evolutionary approach to engineer the 3-HP production system, we constructed a synthetic selection device using a 3-HP-responsive transcription factor and developed a selection approach for screening 3-HP-producing microorganisms. The method was applied to an ALDH library, specifically aldehyde-binding site library of alpha-ketoglutaric semialdehyde dehydrogenase (KGSADH). Only two serial cultures resulted in enrichment of strains showing increased 3-HP production, and an isolated KGSADH variant enzyme exhibited a 2.79-fold higher catalytic efficiency toward its aldehyde substrate than the wild-type one. This approach will provide the simple and efficient tool to engineer the pathway enzymes in metabolic engineering.
3-羟基丙酸(3-HP)是一种重要的平台化学品,利用甘油脱水酶(GDHt)和醛脱氢酶(ALDH)从甘油作为碳源生物生产 3-HP 已被证明是有效的,因为它涉及相对简单的代谢途径,并且比其他生物合成途径具有更高的产率和生产力。尽管从甘油生产 3-HP 的生物过程取得了成功,但该生物过程仍存在两个酶活性和失活的问题。为了应用定向进化方法来构建 3-HP 生产系统,我们使用 3-HP 响应转录因子构建了一个合成选择装置,并开发了一种筛选 3-HP 产生微生物的选择方法。该方法应用于 ALDH 文库,特别是α-酮戊二酸半醛脱氢酶(KGSADH)的醛结合位点文库。只有两次连续培养导致了 3-HP 产量增加的菌株的富集,分离出的 KGSADH 变体酶对其醛底物的催化效率比野生型酶高 2.79 倍。该方法将为代谢工程中的途径酶工程提供简单有效的工具。