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The process of obtaining transform of yeast strains containing multiple copies of desired stable genetic information inserted in the genome

机译:获得酵母菌株的转化过程,该菌株含有插入基因组中的所需稳定遗传信息的多个副本

摘要

The process of obtaining transform of yeast strains containing multiple copies of desired stable genetic information inserted in the genome. The present application consists in the development of a new process that allows for the genetic transformation of strains of the yeast Saccharomyces spp from the culture collection of lab and yeasts employed in industrial processes.To do so, a genetic transformation vector was constructed that consists of a DNA fragment of double strand containing a yeast gene expression cassette flanked by fragments corresponding to the regions of the transposons franqueadoras Ty1 and Ty2.These DNA fragments are long terminal regions ("long terminal page" - LTR elements) that are called Delta ( sym ) and are present in more than 200 copies in the genome of yeast cells.To construct the new system of transformation, it was important to use, as an example, a gene reporter has confirmed the success of transformation, through the verification of the insertion of the genetic information required in the genome of yeast. To do so, was the chosen cDNA of glicoamilase of aspergilius awamori, building up the vector p Glico sym sym.
机译:获得酵母菌株转化过程的过程,该菌株含有插入基因组中的所需稳定遗传信息的多个副本。本申请包括开发新方法,该方法允许从实验室和工业过程中使用的酵母的培养物集合对酵母酵母属菌株进行遗传转化。为此,构建了由以下组成的遗传转化载体:含有酵母基因表达盒的双链DNA片段,其侧翼是与转座子弗兰克斯杜拉丝Ty1和Ty2区域相对应的片段。这些DNA片段是长末端区域(“长末端页面”-LTR元件),称为Delta ()并以200多个拷贝存在于酵母细胞的基因组中。要构建新的转化系统,重要的是使用一个基因报告子,例如通过验证酵母基因组中所需遗传信息的插入。为此,选择了泡盛曲霉的葡糖酰胺酶的cDNA,建立了载体p Glico sym sym。

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