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新进化酶的调控。III. 在选择增强乳糖酶活性过程中ebg阻遏物的进化。

Regulation of newly evolved enzymes. III Evolution of the ebg repressor during selection for enhanced lactase activity.

作者信息

Hall B G, Clarke N D

出版信息

Genetics. 1977 Feb;85(2):193-201. doi: 10.1093/genetics/85.2.193.

Abstract

The evolution of lactose utilization by lacZ deletion strains of E. coli occurs via mutations in the ebg genes. We show that one kind of mutation in the regulatory gene ebgR results in a repressor which retains the ability to repress synthesis of ebg enzymes, but which permits 4.5-fold more ebg enzyme synthesis during lactose induction than does the wild-type repressor. A comparison between the growth rate of various ebg+ strains on lactose and the amount of ebg enzyme synthesized by these strains shows that the rate of enzyme synthesis permitted by the wild-type repressor is insufficient for growth on lactose as a sole carbon source by a cell with the most active ebg lactase yet isolated. We conclude, therefore, that the evolution of lactose utilization requires both a structural and a regulatory mutation.

摘要

大肠杆菌lacZ缺失菌株利用乳糖的进化是通过ebg基因的突变发生的。我们发现,调控基因ebgR中的一种突变会产生一种阻遏物,它保留了抑制ebg酶合成的能力,但在乳糖诱导期间允许合成的ebg酶比野生型阻遏物多4.5倍。对各种ebg+菌株在乳糖上的生长速率与这些菌株合成的ebg酶量之间的比较表明,野生型阻遏物允许的酶合成速率不足以使具有迄今分离出的最活跃ebg乳糖酶的细胞以乳糖作为唯一碳源生长。因此,我们得出结论,乳糖利用的进化既需要结构突变也需要调控突变。

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