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通过代谢工程改造高赖氨酸生产菌用于从头合成赖氨酸衍生化合物。

Metabolic Engineering of High L-Lysine-Producing for de Novo Production of L-Lysine-Derived Compounds.

机构信息

State Key Laboratory of Biobased Material and Green Papermaking (LBMP), Qilu University of Technology, Jinan, Shandong 250353, Republic of China.

School of Bioengineering, Qilu University of Technology (Shandong Academy of Sciences), Jinan 250353, Republic of China.

出版信息

ACS Synth Biol. 2024 Sep 20;13(9):2948-2959. doi: 10.1021/acssynbio.4c00356. Epub 2024 Aug 19.

Abstract

5-Aminovalerate (5-AVA), 5-hydroxyvalerate (5-HV), and 1,5-pentanediol (1,5-PDO) are l-lysine derivatives with extensive applications in the production of materials such as polyesters, polyurethane, plasticizers, inks, and coatings. However, their large-scale production is limited by the lack of efficient synthetic pathways. Here, we aimed to construct multiple synthetic pathways by screening the key enzymes involved in the synthesis of these compounds in . The engineered pathway utilizing RaiP demonstrated a superior catalytic efficiency. The LER strain that overexpressed only successfully synthesized 9.70 g/L 5-HV and 8.31 g/L 5-AVA, whereas the strain LERGY that overexpressed , and accumulated 9.72 g/L 5-HV and 7.95 g/L 5-AVA from 20 g/L glucose. The introduction of exogenous transaminases and dehydrogenases enhanced cell growth and fermentation efficiency with respect to 5-HV synthesis, albeit without significantly impacting the yield. Strain LE05, incorporating only two exogenous enzymes, RaiP and CaR, produced 1.87 g/L 1,5-PDO, 3.85 g/L 5-HV, and 4.78 g/L 5-hydroxyglutaraldehyde from 20 g/L glucose after 6 days. The strain LE02G, fortified with transaminase, dehydrogenase, and NADPH regeneration system, accumulated 7.82 g/L 1,5-PDO, whereas the -knock out LE02G2 synthesized 10.98 g/L 1,5-PDO from 50 g/L glucose in fed-batch fermentation after 6 days, yielding 0.22 g/g glucose (0.37 mol/mol). Introducing the NADPH regeneration pathway and deleting the NADPH-consuming pathways increased the 1,5-PDO yield and decreased the precursor concentration. The proposed pathways and engineering strategies presented in this study can prove instrumental in developing biological routes for the practical production of 5-AVA, 5-HV, and 1,5-PDO.

摘要

5-氨基戊酸(5-AVA)、5-羟基戊酸(5-HV)和 1,5-戊二醇(1,5-PDO)是赖氨酸的衍生物,广泛应用于聚酯、聚氨酯、增塑剂、油墨和涂料等材料的生产。然而,由于缺乏有效的合成途径,其大规模生产受到限制。在这里,我们旨在通过筛选这些化合物合成中涉及的关键酶,构建多种合成途径。利用 RaiP 构建的工程途径表现出较高的催化效率。仅过表达 的 LER 菌株成功合成了 9.70 g/L 的 5-HV 和 8.31 g/L 的 5-AVA,而同时过表达 、 和 的 LERGY 菌株则从 20 g/L 葡萄糖中积累了 9.72 g/L 的 5-HV 和 7.95 g/L 的 5-AVA。引入外源转氨酶和脱氢酶可以提高 5-HV 合成的细胞生长和发酵效率,尽管对产率没有显著影响。仅包含两个外源酶 RaiP 和 CaR 的菌株 LE05 在 6 天后从 20 g/L 葡萄糖中生产了 1.87 g/L 的 1,5-PDO、3.85 g/L 的 5-HV 和 4.78 g/L 的 5-羟基戊二醛。强化了转氨酶、脱氢酶和 NADPH 再生系统的菌株 LE02G 积累了 7.82 g/L 的 1,5-PDO,而 -敲除的 LE02G2 在补料分批发酵 6 天后从 50 g/L 葡萄糖中合成了 10.98 g/L 的 1,5-PDO,产率为 0.22 g/g 葡萄糖(0.37 mol/mol)。引入 NADPH 再生途径并删除 NADPH 消耗途径可以提高 1,5-PDO 的产量并降低前体浓度。本研究提出的途径和工程策略可为实用生产 5-AVA、5-HV 和 1,5-PDO 的生物途径的开发提供依据。

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