{"title":"Construction of a host-vector system in the osmophilic haploid yeast Zygosaccharomyces rouxii","authors":"Kohei Ushio , Hiroki Tatsumi , Hiroyuki Araki , Akio Toh-e , Yasuji Oshima","doi":"10.1016/0385-6380(88)90079-9","DOIUrl":null,"url":null,"abstract":"<div><p>A host-vector system for <em>Zygosaccharomyces rouxii</em> was developed. Chimeric plasmids useful as the <em>Escherichia coli-Z. rouxii</em> shuttle vector were constructed with a DNA fragment of pBR322, a fragment of pSR1 plasmid of <em>Z. rouxii</em> or the <em>ARS1</em> sequence of <em>Saccharomyces cerevisiae</em>, and a fragment of the <em>LEU2</em> gene of <em>S. cerevisiae</em> or a DNA fragment bearing Tn<em>601</em> which confers G-418 resistance as a selective marker of the plasmid. For the hosts, wild-type strains of <em>Z. rouxii</em> were modified to give improved transformation frequencies or to mark a leucine-auxotrophic mutation which is complementable by the <em>LEU2</em> DNA of <em>S. cerevisiae</em>. Transformation frequencies from several hundred to two thousand transformant clones per μg plasmid DNA samples were obtained.</p></div>","PeriodicalId":15702,"journal":{"name":"Journal of Fermentation Technology","volume":"66 5","pages":"Pages 481-488"},"PeriodicalIF":0.0000,"publicationDate":"1988-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0385-6380(88)90079-9","citationCount":"24","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Fermentation Technology","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/0385638088900799","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 24
Abstract
A host-vector system for Zygosaccharomyces rouxii was developed. Chimeric plasmids useful as the Escherichia coli-Z. rouxii shuttle vector were constructed with a DNA fragment of pBR322, a fragment of pSR1 plasmid of Z. rouxii or the ARS1 sequence of Saccharomyces cerevisiae, and a fragment of the LEU2 gene of S. cerevisiae or a DNA fragment bearing Tn601 which confers G-418 resistance as a selective marker of the plasmid. For the hosts, wild-type strains of Z. rouxii were modified to give improved transformation frequencies or to mark a leucine-auxotrophic mutation which is complementable by the LEU2 DNA of S. cerevisiae. Transformation frequencies from several hundred to two thousand transformant clones per μg plasmid DNA samples were obtained.