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在酿酒酵母中高效合成具有酶活性的小牛凝乳酶。

Efficient synthesis of enzymatically active calf chymosin in Saccharomyces cerevisiae.

作者信息

Mellor J, Dobson M J, Roberts N A, Tuite M F, Emtage J S, White S, Lowe P A, Patel T, Kingsman A J, Kingsman S M

出版信息

Gene. 1983 Sep;24(1):1-14. doi: 10.1016/0378-1119(83)90126-9.

Abstract

We have constructed a high-efficiency expression vector to direct the synthesis of heterologous polypeptides in yeast. The vector is termed a sandwich expression vector as the heterologous gene is inserted between the 5' and 3' control regions of the efficiently expressed yeast PGK gene. We have used this vector to direct the expression of three derivatives of the calf chymosin cDNA gene; preprochymosin, prochymosin and chymosin. Prochymosin is synthesised to at least 5% of total yeast-cell protein and furthermore, it can be readily activated to produce an enzyme which has milk-clotting activity.

摘要

我们构建了一种高效表达载体,用于在酵母中指导异源多肽的合成。该载体被称为夹心表达载体,因为异源基因插入到高效表达的酵母磷酸甘油酸激酶(PGK)基因的5'和3'控制区之间。我们已使用该载体指导小牛凝乳酶cDNA基因的三种衍生物的表达:前原凝乳酶、原凝乳酶和凝乳酶。原凝乳酶的合成量至少占酵母细胞总蛋白的5%,此外,它可以很容易地被激活以产生具有凝乳活性的酶。

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