Takeda S, Tamaki E, Miura K, Kumagai I
Department of Industrial Chemistry, Faculty of Engineering, University of Tokyo, Japan.
Biochem Biophys Res Commun. 1990 Dec 14;173(2):741-7. doi: 10.1016/s0006-291x(05)80098-1.
An expression plasmid for goat alpha-lactalbumin in Saccharomyces cerevisiae, pSKA100, was constructed into a shuttle vector, pYG100, by inserting cDNA which encodes goat pre-alpha-lactalbumin and two-thirds of the 3'-non-coding region. The goat alpha-lactalbumin was expressed under the yeast glyceraldehyde 3-phosphate dehydrogenase (GPD) promoter and terminator of pYG100 and secreted in the growth medium for yeast as a precise mature protein, possessing specific activity essentially the same as that of authentic goat alpha-lactalbumin in lactose synthesis.
通过插入编码山羊前α-乳白蛋白和三分之二3'-非编码区的cDNA,将用于在酿酒酵母中表达山羊α-乳白蛋白的表达质粒pSKA100构建到穿梭载体pYG100中。山羊α-乳白蛋白在pYG100的酵母甘油醛-3-磷酸脱氢酶(GPD)启动子和终止子的控制下表达,并作为一种精确的成熟蛋白分泌到酵母生长培养基中,其比活性与乳糖合成中天然山羊α-乳白蛋白的比活性基本相同。