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共生梭菌谷氨酸脱氢酶突变亚基的1:5杂种在氨基酸特异性上存在差异的变构行为。

Allosteric behaviour of 1:5 hybrids of mutant subunits of Clostridium symbiosum glutamate dehydrogenase differing in their amino acid specificity.

作者信息

Goyal A, Wang X G, Engel P C

机构信息

Department of Biochemistry and Conway Institute of Biomolecular and Biomedical Research, University College Dublin, Belfield, Dublin 4, Ireland.

出版信息

Biochem J. 2001 Dec 15;360(Pt 3):651-6. doi: 10.1042/0264-6021:3600651.

Abstract

Hybrid hexamers were made by refolding mixtures of two mutant forms of clostridial glutamate dehydrogenase. Mutant Cys320Ser (C320S) has a similar activity to the wild-type enzyme, but is unreactive with Ellman's reagent, 5,5'-dithiobis(2-nitrobenzoate) (DTNB). The triple mutant Lys89Leu/Ala163Gly/Ser380Ala (K89L/A163G/S380A), active with norleucine but not glutamate, is inactivated by DTNB, since the amino acid residue at position 320 is a cysteine residue. The chosen ratio favoured 1:5 hybrids of the triple mutant and C320S. The renatured mixture was treated with DTNB and separated on an NAD(+)-agarose column to which only C320S subunits bind tightly. Fractions were monitored for glutamate and norleucine activity and for releasable thionitrobenzoate to establish subunit stoichiometry. A fraction highly enriched in the 1:5 hybrid was identified. Homohexamers (C320S with 40 mM glutamate and 1 mM NAD(+) at pH 8.8, or K89L/A163G/S380A with 70 mM norleucine and 1 mM NAD(+) at pH 8.5) showed allosteric activation; succinate activated C320S approx. 50-fold (EC(50)=70 mM, h=2.4), and glutarate gave approx. 30-fold activation (EC(50)=35 mM, h=2.3). For the triple mutant, corresponding values were 80 mM and 2.2 for succinate, and 75 mM and 1.7 for glutarate, but maximal activation was only about 2-fold. In the 1:5 hybrid, with only one norleucine-active subunit per hexamer, responses to glutarate and succinate were still co-operative, and activation was more extensive than in the triple mutant homohexamer. A single norleucine-active subunit can thus respond co-operatively to a substrate analogue at the other five inactive sites. On the other hand, similar hyperbolic dependence on the norleucine concentration for the hybrid and the triple mutant homohexamer reflected the inability of C320S subunits to bind norleucine. With glutamate at pH 8.8, an h value of 3.6 was obtained for the 1:5 hybrid, in contrast with an h value of 5.2 for the C320S homohexamer. The "foreign" subunit evidently impedes inter-subunit communication to some extent.

摘要

通过重折叠两种梭菌谷氨酸脱氢酶突变形式的混合物制备了杂合六聚体。突变体Cys320Ser(C320S)具有与野生型酶相似的活性,但与埃尔曼试剂5,5'-二硫代双(2-硝基苯甲酸)(DTNB)无反应。三重突变体Lys89Leu/Ala163Gly/Ser380Ala(K89L/A163G/S380A)对正亮氨酸有活性但对谷氨酸无活性,由于320位的氨基酸残基是半胱氨酸残基,所以它会被DTNB灭活。选择的比例有利于三重突变体与C320S形成1:5的杂合体。将复性后的混合物用DTNB处理,并在NAD(+) -琼脂糖柱上进行分离,只有C320S亚基能紧密结合到该柱上。监测各馏分的谷氨酸和正亮氨酸活性以及可释放的硫代硝基苯甲酸,以确定亚基化学计量。鉴定出了高度富集1:5杂合体的馏分。同型六聚体(pH 8.8时含40 mM谷氨酸和1 mM NAD(+)的C320S,或pH 8.5时含70 mM正亮氨酸和1 mM NAD(+)的K89L/A163G/S380A)表现出别构激活;琥珀酸激活C320S约50倍(EC(50)=70 mM,h=2.4),戊二酸给出约30倍的激活(EC(50)=35 mM,h=2.3)。对于三重突变体,琥珀酸的相应值为80 mM和2.2,戊二酸为75 mM和1.7,但最大激活仅约为2倍。在1:5杂合体中,每个六聚体只有一个对正亮氨酸有活性的亚基,对戊二酸和琥珀酸的反应仍然是协同的,并且激活比三重突变体同型六聚体更广泛。因此,单个对正亮氨酸有活性的亚基可以在其他五个无活性位点对底物类似物做出协同反应。另一方面,杂合体和三重突变体同型六聚体对正亮氨酸浓度的类似双曲线依赖性反映了C320S亚基无法结合正亮氨酸。在pH 8.8时用谷氨酸处理,1:5杂合体的h值为3.6,而C320S同型六聚体的h值为5.2。“外来”亚基显然在一定程度上阻碍了亚基间的通讯。

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