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代谢工程大肠杆菌中依赖于丙酰辅酶 A 的 2-羟基丁酸酯含聚羟基烷酸的生物合成。

Propionyl-CoA dependent biosynthesis of 2-hydroxybutyrate containing polyhydroxyalkanoates in metabolically engineered Escherichia coli.

机构信息

Department of Environmental Engineering and Energy-Undergraduate Program, Myongji University, San 38-2, Nam-dong, Cheoin-gu, Yongin-si, Gyeonggido 449-728, Republic of Korea.

出版信息

J Biotechnol. 2013 May 20;165(2):93-8. doi: 10.1016/j.jbiotec.2013.03.005. Epub 2013 Mar 21.

DOI:10.1016/j.jbiotec.2013.03.005
PMID:23524059
Abstract

We have previously reported in vivo biosynthesis of 2-hydroxyacid containing polyesters including polylactic acid (PLA), poly(3-hydroxybutyrate-co-lactate) [P(3HB-co-LA)], and poly(3-hydroxybutyrate-co-2-hydroxybutyrate-co-lactate) [P(3HB-co-2HB-co-LA)] employing metabolically engineered Escherichia coli strains by the introduction of evolved Clostridium propionicum propionyl-CoA transferase (Pct(Cp)) and Pseudomonas sp. MBEL 6-19 polyhydroxyalkanoate (PHA) synthase 1 (PhaC1(Ps6-19)). In this study, we further engineered in vivo PLA biosynthesis system in E. coli to synthesize 2HB-containing PHA, in which propionyl-CoA was used as precursor for 2-ketobutyrate that was converted into 2HB-CoA by the sequential actions of Lactococcus lactis (D)-2-hydroxybutyrate dehydrogenase (PanE) and Pct(Cp) and then 2HB-CoA was polymerized by PhaC1(Ps6-19). The recombinant E. coli XL1-blue expressing the phaC1437 gene, the pct540 gene, and the Ralstonia eutropha prpE gene together with the panE gene could be grown to 0.66 g/L and successfully produced P(70 mol%3HB-co-18 mol%2HB-co-12 mol%LA) up to the PHA content of 66 wt% from 20 g/L of glucose, 2 g/L of 3HB and 1 g/L of sodium propionate. Removal of the prpC gene in the chromosome of E. coli XL1-blue could increase the mole fraction of 2HB in copolymer, but the PHA content was decreased. The metabolic engineering strategy reported here suggests that propionyl-CoA can be successfully used as the precursor to provide PHA synthase with 2HB-CoA for the production of PHAs containing 2HB monomer.

摘要

我们之前曾报道过,通过引入进化的梭菌丙酰辅酶 A 转移酶(Pct(Cp))和假单胞菌 MBEL 6-19 聚羟基烷酸(PHA)合酶 1(PhaC1(Ps6-19)),利用代谢工程大肠杆菌菌株在体内合成含有 2-羟基酸的聚酯,包括聚乳酸(PLA)、聚(3-羟基丁酸酯-co-乳酸)[P(3HB-co-LA)]和聚(3-羟基丁酸酯-co-2-羟基丁酸酯-co-乳酸)[P(3HB-co-2HB-co-LA)]。在这项研究中,我们进一步对大肠杆菌体内 PLA 生物合成系统进行了工程改造,以合成含有 2HB 的 PHA,其中丙酰辅酶 A 用作 2-酮丁酸的前体,2-酮丁酸通过乳酸乳球菌(D)-2-羟基丁酸脱氢酶(PanE)和 PCT(Cp)的连续作用转化为 2HB-CoA,然后 2HB-CoA 由 PhaC1(Ps6-19)聚合。表达 phaC1437 基因、pct540 基因和 Ralstonia eutropha prpE 基因以及 panE 基因的重组大肠杆菌 XL1-blue 可以生长到 0.66 g/L,并成功地从 20 g/L 葡萄糖、2 g/L 3HB 和 1 g/L 丙酸钠生产出 P(70 mol%3HB-co-18 mol%2HB-co-12 mol%LA),PHA 含量达到 66 wt%。在大肠杆菌 XL1-blue 的染色体中去除 prpC 基因可以增加共聚物中 2HB 的摩尔分数,但 PHA 含量会降低。这里报道的代谢工程策略表明,丙酰辅酶 A 可以成功地用作前体,为 PHA 合酶提供 2HB-CoA,用于生产含有 2HB 单体的 PHAs。

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