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鉴定酵母法呢基二磷酸合酶催化活性所必需的赖氨酸残基。

Identification of a lysine residue important for the catalytic activity of yeast farnesyl diphosphate synthase.

机构信息

Laboratoire Métabolisme Secondaire de la Vigne, Univ. Strasbourg, INRA, Inst. Natl. Recherche Agron., Métab. Second. Vigne, Unit Mixte Recherche Santé Vigne and Qual. Vins, Colmar, France.

出版信息

Protein J. 2011 Jun;30(5):334-9. doi: 10.1007/s10930-011-9336-y.

Abstract

The Saccharomyces cerevisiae ERG20 gene (encoding farnesyl diphosphate synthase) has been subjected to a set of mutations at the catalytic site, at position K254 to determine the in vivo impact. The mutated strains have been shown to exhibit various growth rates, sterol profiles and monoterpenol producing capacities. The results obtained suggest that K at position 254 helps to stabilize one of the three Mg(2+) forming a bridge between the enzyme and DMAPP, and demonstrate that destabilizing two of the three Mg(2+) ions, by introducing a double mutation at positions K197 and K254, results in a loss of FPPS activity and a lethal phenotype.

摘要

酿酒酵母 ERG20 基因(编码法呢基二磷酸合酶)在催化位点 K254 处发生了一组突变,以确定体内影响。已显示突变株具有不同的生长速率、固醇谱和单萜醇产生能力。所得结果表明,位置 254 的 K 有助于稳定三个 Mg(2+)之一,该 Mg(2+)在酶和 DMAPP 之间形成桥接,并且证明通过在位置 K197 和 K254 引入双突变破坏三个 Mg(2+)离子中的两个,会导致 FPPS 活性丧失和致死表型。

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