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利用基因工程大肠杆菌合成 L-5-甲基四氢叶酸。

Biosynthesis of L-5-methyltetrahydrofolate by genetically engineered Escherichia coli.

机构信息

State Key Laboratory of Microbial Technology, Microbial Technology Institute, Shandong University, Qingdao, China.

State Key Laboratory of Microbial Metabolism, School of Life Sciences and Biotechnology, Shanghai Jiao Tong University, Shanghai, China.

出版信息

Microb Biotechnol. 2022 Nov;15(11):2758-2772. doi: 10.1111/1751-7915.14139. Epub 2022 Sep 7.

Abstract

L-5-Methyltetrahydrofolate (L-5-MTHF) is the only biologically active form of folate in the human body. Production of L-5-MTHF by using microbes is an emerging consideration for green synthesis. However, microbes naturally produce only a small amount of L-5-MTHF. Here, Escherichia coli BL21(DE3) was engineered to increase the production of L-5-MTHF by overexpressing the intrinsic genes of dihydrofolate reductase and methylenetetrahydrofolate (methylene-THF) reductase, introducing the genes encoding formate-THF ligase, formyl-THF cyclohydrolase and methylene-THF dehydrogenase from the one-carbon metabolic pathway of Methylobacterium extorquens or Clostridium autoethanogenum and disrupting the gene of methionine synthase involved in the consumption and synthesis inhibition of the target product. Thus, upon its native pathway, an additional pathway for L-5-MTHF synthesis was developed in E. coli, which was further analysed and confirmed by qRT-PCR, enzyme assays and metabolite determination. After optimizing the conditions of induction time, temperature, cell density and concentration of IPTG and supplementing exogenous substances (folic acid, sodium formate and glucose) to the culture, the highest yield of 527.84 μg g of dry cell weight for L-5-MTHF was obtained, which was about 11.8 folds of that of the original strain. This study paves the way for further metabolic engineering to improve the biosynthesis of L-5-MTHF in E. coli.

摘要

L-5-甲基四氢叶酸(L-5-MTHF)是人体内叶酸的唯一具有生物活性的形式。利用微生物生产 L-5-MTHF 是绿色合成的一个新兴考虑因素。然而,微生物自然产生的 L-5-MTHF 量很少。在这里,通过过表达二氢叶酸还原酶和亚甲基四氢叶酸(亚甲基-THF)还原酶的内在基因,引入来自甲基杆菌或产甲烷菌一碳代谢途径的编码甲酸盐-THF 连接酶、甲酰基-THF 环水解酶和亚甲基-THF 脱氢酶的基因,并破坏参与目标产物消耗和合成抑制的蛋氨酸合酶基因,工程改造大肠杆菌 BL21(DE3)以增加 L-5-MTHF 的产量。因此,在其天然途径中,在大肠杆菌中开发了 L-5-MTHF 合成的额外途径,通过 qRT-PCR、酶测定和代谢物测定对其进行了进一步分析和验证。在优化诱导时间、温度、细胞密度和 IPTG 浓度以及向培养物中补充外源物质(叶酸、甲酸钠和葡萄糖)的条件后,获得了 527.84μg g 干细胞重量的 L-5-MTHF 最高产量,约为原始菌株的 11.8 倍。这项研究为进一步的代谢工程铺平了道路,以提高大肠杆菌中 L-5-MTHF 的生物合成。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4bc1/9618320/182b2b824e66/MBT2-15-2758-g003.jpg

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