Enhanced Acetate Tolerance and Recombinant Protein Accumulation in Escherichia coli by Transgenic Expression of a Heat Shock Protein from Carrot (Daucus carota L.).

IF 1.6 4区 生物学 Q4 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Minhye Kim, Eunju Im, Yeh Jin Ahn
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引用次数: 1

Abstract

Background: In Escherichia coli (E. coli) culture, acetate accumulates as an undesirable by-product of aerobic fermentation on glucose and inhibits cell growth and recombinant protein production.

Objectives: We examined whether the heterologous expression of a eukaryotic heat shock protein (Hsp) can confer tolerance to acetate in E. coli.

Materials and methods: Transgenic cell lines (TCLs) heterologously expressing a small heat shock protein (sHsp) from carrot (Daucus carota L.), DcHsp17.7, were exposed to heat, sodium acetate, and alkaline conditions. The cell growth and cell viability were examined by measuring O.D.600 and colony-forming units (CFU), respectively. The His-tagged recombinant alcohol dehydrogenase (ADH) gene cloned in a pET11a expression vector was introduced into TCL1 and expressed by isopropyl β-D-1-thiogalactopyranoside treatment. After purifying using Ni-NTA affinity chromatography, its accumulation levels were examined using SDS-PAGE in the presence of acetate.

Results: TCLs constitutively expressing DcHsp17.7 showed improved growth, cell density, and cell viability under the stress conditions of heat, acetate, and alkaline compared to an empty vector control line. In acetate stress conditions, TCL1 accumulated more cellular proteins (approximately 130%) than the control. The recombinant ADH accumulated to a higher level in TCL1 (2.2-fold at 16 °C) than the control. The addition of acetate reduced the recombinant ADH level by 70% in the control when compared with the absence of acetate. In contrast, recombinant ADH accumulation was not affected by acetate in TCL1. In the presence of acetate, TCL1 accumulated 6.4-fold more recombinant ADH than did the control. Furthermore, recombinant ADH produced in TCL1 showed 1.5-fold higher enzyme activity than that produced in the control in the presence or absence of acetate.

Conclusion: Our study showed that heterologously expressed DcHsp17.7 from carrot can alleviate the negative effects of acetate on E. coli.

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转表达胡萝卜热休克蛋白增强大肠杆菌对醋酸盐的耐受性和重组蛋白积累。
背景:在大肠杆菌(E. coli)培养中,醋酸盐作为葡萄糖有氧发酵的不良副产物积累,抑制细胞生长和重组蛋白的生产。目的:我们研究了真核热休克蛋白(Hsp)的异源表达是否能赋予大肠杆菌对醋酸盐的耐受性。材料和方法:将胡萝卜(Daucus carota L.)小热休克蛋白(sHsp) DcHsp17.7转基因细胞株(TCLs)暴露于高温、醋酸钠和碱性条件下。分别测定od值600和菌落形成单位(CFU),检测细胞生长和细胞活力。将在pET11a表达载体上克隆的his标记的重组乙醇脱氢酶(ADH)基因导入TCL1,经异丙基β- d -1-硫代半乳糖苷处理后表达。用Ni-NTA亲和层析纯化后,在乙酸存在下用SDS-PAGE检测其积累水平。结果:与空白载体对照线相比,组成型表达DcHsp17.7的TCLs在高温、醋酸盐和碱性胁迫条件下表现出更好的生长、细胞密度和细胞活力。在醋酸胁迫条件下,TCL1比对照积累了更多的细胞蛋白(约130%)。重组ADH在TCL1中积累的水平高于对照组(16°C时为2.2倍)。与不添加乙酸相比,乙酸的添加使对照组的重组ADH水平降低了70%。相比之下,重组ADH在TCL1中的积累不受乙酸的影响。在乙酸存在的情况下,TCL1积累的重组ADH比对照组多6.4倍。此外,在存在或不存在乙酸的情况下,TCL1中产生的重组ADH的酶活性比对照高1.5倍。结论:本研究表明,从胡萝卜中异源表达DcHsp17.7可以减轻醋酸盐对大肠杆菌的负面影响。
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来源期刊
Iranian Journal of Biotechnology
Iranian Journal of Biotechnology BIOTECHNOLOGY & APPLIED MICROBIOLOGY-
CiteScore
2.60
自引率
7.70%
发文量
20
期刊介绍: Iranian Journal of Biotechnology (IJB) is published quarterly by the National Institute of Genetic Engineering and Biotechnology. IJB publishes original scientific research papers in the broad area of Biotechnology such as, Agriculture, Animal and Marine Sciences, Basic Sciences, Bioinformatics, Biosafety and Bioethics, Environment, Industry and Mining and Medical Sciences.
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