Zhicheng Liang , Mulan Deng , Zhi Zhang , Meirong Li , SuJin Zhou , ZhengGang Zhao , YunPing Mu , LiNa Wang , Chengyun Ning , Allan Zijian Zhao , Fanghong Li
{"title":"乳酸菌URA3基因一步法食品级表达体系的构建","authors":"Zhicheng Liang , Mulan Deng , Zhi Zhang , Meirong Li , SuJin Zhou , ZhengGang Zhao , YunPing Mu , LiNa Wang , Chengyun Ning , Allan Zijian Zhao , Fanghong Li","doi":"10.1016/j.plasmid.2021.102577","DOIUrl":null,"url":null,"abstract":"<div><p><span>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 </span><span><em>Kluyveromyces lactis</em></span> by combining a <span><em>URA3</em></span><span>-deficient strain and a plasmid vector<span> with no drug-resistant selection. Adjacent DNA<span> elements of the vector were assembled in a targeted manner through a reaction with a special recombinase<span> 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 </span></span></span></span><em>URA3</em><span>-deficient strain. PCR assay, sequencing, and western blot analysis<span> 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 </span></span><em>URA3</em> gene; this system has the potential to become a safe and powerful tool for promoting protein expression in food-safe species.</p></div>","PeriodicalId":49689,"journal":{"name":"Plasmid","volume":"116 ","pages":"Article 102577"},"PeriodicalIF":1.8000,"publicationDate":"2021-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.plasmid.2021.102577","citationCount":"0","resultStr":"{\"title\":\"One-step construction of a food-grade expression system based on the URA3 gene in Kluyveromyces lactis\",\"authors\":\"Zhicheng Liang , Mulan Deng , Zhi Zhang , Meirong Li , SuJin Zhou , ZhengGang Zhao , YunPing Mu , LiNa Wang , Chengyun Ning , Allan Zijian Zhao , Fanghong Li\",\"doi\":\"10.1016/j.plasmid.2021.102577\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p><span>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 </span><span><em>Kluyveromyces lactis</em></span> by combining a <span><em>URA3</em></span><span>-deficient strain and a plasmid vector<span> with no drug-resistant selection. Adjacent DNA<span> elements of the vector were assembled in a targeted manner through a reaction with a special recombinase<span> 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 </span></span></span></span><em>URA3</em><span>-deficient strain. PCR assay, sequencing, and western blot analysis<span> 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 </span></span><em>URA3</em> gene; this system has the potential to become a safe and powerful tool for promoting protein expression in food-safe species.</p></div>\",\"PeriodicalId\":49689,\"journal\":{\"name\":\"Plasmid\",\"volume\":\"116 \",\"pages\":\"Article 102577\"},\"PeriodicalIF\":1.8000,\"publicationDate\":\"2021-07-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/j.plasmid.2021.102577\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Plasmid\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0147619X2100024X\",\"RegionNum\":4,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"GENETICS & HEREDITY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plasmid","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0147619X2100024X","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"GENETICS & HEREDITY","Score":null,"Total":0}
One-step construction of a food-grade expression system based on the URA3 gene in Kluyveromyces lactis
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.
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.