摘要
根据酵母整合质粒的设计要求,PCR扩增特定的2.2kbrDNA片段,并以此替换酿酒酵母(Saccharomycescerevisiae)整合载体YIp5的URA3片段;在此基础上,引入G418抗性基因KanMX和酵母磷酸甘油激酶(phosphoglyceratekinase,PGK)组成型强启动子和终止子序列(PGKpt),构建适合酿酒酵母工业菌株高拷贝整合表达载体pYMIKP.以细菌木糖异构酶(xyloseisomerase,XI)基因xylA为目标基因,通过载体pYMIKP引入到酵母工业菌株NAN27中.酵母转化子在非选择培养条件下,连续生长50世代质粒稳定性为99.72%.目标基因高拷贝重组菌的木糖异构酶比酶活是对照菌株的67.2倍,达到0.672Umg蛋白,实现了外源基因在酿酒酵母工业菌株中的稳定高效表达.
Based on the YIp5 (yeast integration vector), construction of the multi-copy integration vector pYMIKP was investigated by using a 2.2 kb designed rDNA fragment from Saccharomyces cerevisiae to replace the original URA3 gene for targeted homologous recombination. The G418 resistance gene KanMX was used as the dominant selection marker, and yeast phosphoglyceric kinase (PGK) constitutive promoter and terminator (PGKp-t) were used for expression control element in the pYMIKP respectively. The plasmid carrying xylA gene was transformed and the xylA gene was integrated into genome rDNA locus of S. cerevisiae NAN-27 by using the pYMIKP. The xylose isomerase XI specific activity of recombinant strain XH34 is 0.672 U/mg protein, which is 67.2 times as much as the parent strain. The integrants are mitotically stable for 50 generations under the non-selective pressure condition.
出处
《山东大学学报（理学版）》
CAS
CSCD
北大核心
2005年第3期105-109,共5页
Journal of Shandong University(Natural Science)
基金
国家自然科学基金委员会
中国节能投资公司联合研究基金资助项目(50273019)
国家重点基础研究发展计划(973计划)资助项目(2004CB719702)
关键词
RDNA
显性选择标记
多拷贝整合
ribosomal DNA
dominant selectable marker
multi-copy integration
