Goto K, Iwatuki Y, Kitano K, Obata T, Hara S
National Research Institute of Brewing, Tokyo, Japan.
Agric Biol Chem. 1990 Apr;54(4):979-84.
The KHR gene cloned from a genomic library was on 4.7-kbp DNA fragment and was inserted into YCpG11 vector (KHR-YCp) and YEp vector (KHP-YEp). Transformants with KHR-YEp could secrete 3-4 times as much killer toxin into the media as the donor strain. The complete nucleotide sequence of the KHR gene was analyzed. It was found that the KHR gene consisted of 888 bp. It was suggested that this protein was processed before being secreted into the media, because its molecular mass presumed from the nucleotide sequence was larger than that of the mature killer toxin.
从基因组文库中克隆出的KHR基因位于4.7千碱基对的DNA片段上,并被插入到YCpG11载体(KHR - YCp)和YEp载体(KHP - YEp)中。带有KHR - YEp的转化体分泌到培养基中的杀伤毒素量是供体菌株的3至4倍。对KHR基因的完整核苷酸序列进行了分析。发现KHR基因由888个碱基对组成。由于根据核苷酸序列推测的该蛋白质分子量大于成熟杀伤毒素的分子量,因此推测该蛋白质在分泌到培养基之前经过了加工处理。