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新型重组大肠杆菌生产 1,3-丙二醇,该菌含有致病菌基因。

1,3-Propanediol production by new recombinant Escherichia coli containing genes from pathogenic bacteria.

机构信息

Poznań University of Life Sciences, Department of Biochemistry and Biotechnology, Dojazd 11, 60-632 Poznań, Poland.

Poznań University of Life Sciences, Department of Biochemistry and Biotechnology, Dojazd 11, 60-632 Poznań, Poland.

出版信息

Microbiol Res. 2015 Feb;171:1-7. doi: 10.1016/j.micres.2014.12.007. Epub 2014 Dec 23.

Abstract

1,3-Propanediol (1,3-PDO) is an organic compound, which is a valuable intermediate product, widely used as a monomer for synthesizing biodegradable polymers, increasing their strength; as well as an ingredient of textile, cosmetic and medical products. 1,3-PDO is mostly synthesized chemically. Global companies have developed technologies for 1,3-PDO synthesis from petroleum products such as acrolein and ethylene oxide. A potentially viable alternative is offered by biotechnological processes using microorganisms capable of synthesizing 1,3-PDO from renewable substrates (waste glycerol, a by-product of biofuel production, or glucose). In the present study, genes from Citrobacter freundii and Klebsiella pneumoniae were introduced into Escherichia coli bacteria to enable the synthesis of 1,3-PDO from waste glycerol. These strains belong to the best 1,3-PDO producers, but they are pathogenic, which restricts their application in industrial processes. The present study involved the construction of two gene expression constructs, containing a total of six heterologous glycerol catabolism pathway genes from C. freundii ATCC 8090 and K. pneumoniae ATCC 700721. Heterologous genes encoding glycerol dehydratase (dhaBCE) and the glycerol dehydratase reactivation factor (dhaF, dhaG) from C. freundii and gene encoding 1,3-PDO oxidoreductase (dhaT) from K. pneumoniae were expressed in E. coli under the control of the T7lac promoter. An RT-PCR analysis and overexpression confirmed that 1,3-PDO synthesis pathway genes were expressed on the RNA and protein levels. In batch fermentation, recombinant E. coli bacteria used 32.6gl(-1) of glycerol to produce 10.6 gl(-1) of 1,3-PDO, attaining the efficiency of 0.4 (mol₁,₃-PDO molglycerol(-1)). The recombinant E. coli created is capable of metabolizing glycerol to produce 1,3-PDO, and the efficiency achieved provides a significant research potential of the bacterium. In the face of shortage of fossil fuel supplies and climate warming there is an increasing industrial need to exchange the chemical way of chemicals synthesis for biotechnological - more ecological manner. The 1,3-PDO production from glycerol is an desirable alternative to the traditional production from non-renewable resources. This work is a part of project, which opens a way to development of innovative "green chemistry" and new perspectives to chemical industry.

摘要

1,3-丙二醇(1,3-PDO)是一种有机化合物,是一种有价值的中间产物,广泛用作合成可生物降解聚合物的单体,以提高其强度;也可用作纺织、化妆品和医疗产品的成分。1,3-PDO 主要通过化学方法合成。全球公司已经开发出了从丙烯醛和环氧乙烷等石油产品合成 1,3-PDO 的技术。利用能够从可再生基质(生物燃料生产的副产物废甘油或葡萄糖)合成 1,3-PDO 的微生物的生物技术工艺提供了一种潜在可行的替代方案。在本研究中,将柠檬酸杆菌和肺炎克雷伯氏菌的基因引入到大肠杆菌中,使大肠杆菌能够利用废甘油合成 1,3-PDO。这些菌株属于最好的 1,3-PDO 生产者,但它们是病原体,这限制了它们在工业过程中的应用。本研究涉及构建两个基因表达构建体,其中包含来自柠檬酸杆菌 ATCC 8090 和肺炎克雷伯氏菌 ATCC 700721 的总共六个异源甘油分解代谢途径基因。来自柠檬酸杆菌的异源基因编码甘油脱水酶(dhaBCE)和甘油脱水酶再激活因子(dhaF、dhaG)以及来自肺炎克雷伯氏菌的基因编码 1,3-PDO 氧化还原酶(dhaT)在 T7lac 启动子的控制下在大肠杆菌中表达。RT-PCR 分析和过表达证实,1,3-PDO 合成途径基因在 RNA 和蛋白质水平上均有表达。在分批发酵中,重组大肠杆菌利用 32.6gl(-1)的甘油生产了 10.6 gl(-1)的 1,3-PDO,效率达到 0.4(mol₁,₃-PDO molglycerol(-1))。所创建的重组大肠杆菌能够代谢甘油生产 1,3-PDO,并且实现的效率提供了该细菌的显著研究潜力。在面临化石燃料供应短缺和气候变暖的情况下,工业界越来越需要用生物技术(更生态的方式)取代化学合成的化学方法。从甘油生产 1,3-PDO 是传统的从不可再生资源生产 1,3-PDO 的替代方法。这项工作是项目的一部分,为开发创新的“绿色化学”开辟了道路,并为化学工业带来了新的视角。

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