Kumano Y, Nikawa J
Department of Biochemical Engineering and Science, Faculty of Computer Science and Systems Engineering, Kyushu Institute of Technology, Fukuoka, Japan.
FEMS Microbiol Lett. 1995 Feb 1;126(1):81-4. doi: 10.1111/j.1574-6968.1995.tb07394.x.
The PIS gene for an enzyme phosphatidylinositol synthase having an increased Km for myo-inositol, was isolated from Saccharomyces cerevisiae. The mutant PIS gene contained a CAA codon at position 114 instead of the CAC codon observed in the wild-type gene, resulting in alteration of the amino acid from His to Gln. Oligonucleotide mediated site-directed mutagenesis of PIS at codon 114 revealed that mutant genes with codons for Ala, Thr and Leu could support yeast cell growth in vivo, but those for Asp, Lys and Tyr could not. All mutant enzymes when expressed in Escherichia coli showed greatly reduced in vitro activity.
从酿酒酵母中分离出一种编码磷脂酰肌醇合酶的PIS基因,该酶对肌醇的米氏常数(Km)有所增加。突变的PIS基因在第114位含有CAA密码子,而非野生型基因中的CAC密码子,导致氨基酸从组氨酸变为谷氨酰胺。对PIS基因第114位密码子进行寡核苷酸介导的定点诱变后发现,编码丙氨酸、苏氨酸和亮氨酸的突变基因能够在体内支持酵母细胞生长,而编码天冬氨酸、赖氨酸和酪氨酸的突变基因则不能。所有突变酶在大肠杆菌中表达时,其体外活性都大幅降低。