One-step construction of a food-grade expression system based on the URA3 gene in Kluyveromyces lactis

IF 1.8 4区 生物学 Q3 GENETICS & HEREDITY Plasmid Pub Date : 2021-07-01 DOI:10.1016/j.plasmid.2021.102577
Zhicheng Liang , Mulan Deng , Zhi Zhang , Meirong Li , SuJin Zhou , ZhengGang Zhao , YunPing Mu , LiNa Wang , Chengyun Ning , Allan Zijian Zhao , Fanghong Li
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Abstract

Proteins from food-grade expression systems can be used in food products and medical applications. Herein, we describe a one-step method of constructing an expression vector in Kluyveromyces lactis by combining a URA3-deficient strain and a plasmid vector with no drug-resistant selection. Adjacent DNA elements of the vector were assembled in a targeted manner through a reaction with a special recombinase to form a plasmid vector using a one-step reaction. The unnecessary fragments containing the pUC origin and the ampicillin resistance gene were removed, and the vector was isolated and purified before transformation. A single transformation of the vector can produce a URA3-deficient strain. PCR assay, sequencing, and western blot analysis all indicated that the method of vector construction and target protein expression (mCherry and human serum albumin) were successful. This method may potentially be applied to any species containing the URA3 gene; this system has the potential to become a safe and powerful tool for promoting protein expression in food-safe species.

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乳酸菌URA3基因一步法食品级表达体系的构建
来自食品级表达系统的蛋白质可用于食品和医疗应用。在此,我们描述了一种将ura3缺陷菌株与无耐药选择的质粒载体结合在一起,一步构建乳酸克卢维酵母表达载体的方法。通过与特殊的重组酶反应,以靶向方式组装载体的邻近DNA元件,形成质粒载体,采用一步反应。去除含有pUC来源和氨苄西林耐药基因的多余片段,分离纯化转化前的载体。载体的一次转化可以产生缺乏ura3的菌株。PCR、测序和western blot分析均表明载体构建和靶蛋白(mCherry和人血清白蛋白)表达方法是成功的。该方法可能适用于任何含有URA3基因的物种;该系统有可能成为促进食品安全物种中蛋白质表达的安全而有力的工具。
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来源期刊
Plasmid
Plasmid 生物-遗传学
CiteScore
4.70
自引率
3.80%
发文量
21
审稿时长
53 days
期刊介绍: Plasmid publishes original research on genetic elements in all kingdoms of life with emphasis on maintenance, transmission and evolution of extrachromosomal elements. Objects of interest include plasmids, bacteriophages, mobile genetic elements, organelle DNA, and genomic and pathogenicity islands.
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