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转羧酶的缔合-解离

Association-dissociation of transcarboxylase.

作者信息

Poto E M, Wood H G

出版信息

Biochemistry. 1977 May 3;16(9):1949-55. doi: 10.1021/bi00628a030.

Abstract

Transcarboxylase consists of a central subunit to which two sets of three subunits each are attached at opposite faces. Evidence obtained by various ultracentrifugal techniques has shown that there is an equilibrium between active forms of the enzyme with six, five, four, three, two, and one subunits attached to the central subunit. Since each attached subunit contains two biotins, the biotin content of these forms varies from 12 to 2. By reactive enzyme sedimentation at pH 5.5, it has been shown that the largest form of the enzyme (with 12 biotins and a molecular weight of 1.2 X 10(6) is active and that at pH 6.8 this form of the enzyme dissociates to an enzymatically active form containing three attached subunits. This result is in accord with previous observations (Wood, H.G., Chiao, J.P., and Poto, E.M.(1977), J Biol. Chem. 252, 1490; Wrigley, N.G., Chiao, J.P., and Wood, H.G. (1977), J Biol. Chem. 252, 1500) which showed that dissociation of three of the six attache subunits occurs preferentially from one face of the central subunit and that the remaining three attached subunits are quite firmly bound to the second face of the central subunit. Multiple peaks are obtained in sedimentation velocity experiments at 60 000 rpm because the rate of sedimentation outstrips the rate of equilibration of the different forms of transcarboxylase, whereas at 30 000 rpm a single peak of the multiple form of the enzyme is observed, since equilibration of the different forms keeps abreast of the sedimentation. The rate and extent of dissociation are increased by increase in temperature. It has been shown by centrifugation under oil that the association-dissociation of the large form of the enzymes with six, five, and four attached subunits is not affected by hydrostatic pressure. In contrast, the association-dissociation of the enzyme with three and two attached subunits appears to be affected by pressure. The accumulated results indicate that the native form of the enzyme in the cytosol of the cell consists of a series of enzymatically active forms with one to six attached subunits. The predominant forms in the cytosol will depend on the concentration of the constituent subunits, the pH, the concentration of ions (particularly divalent anions), and the temperature.

摘要

转羧酶由一个中央亚基组成,在其相对的两个面上各连接有两组,每组三个亚基。通过各种超速离心技术获得的证据表明,在与中央亚基相连的亚基数为六个、五个、四个、三个、两个和一个的酶的活性形式之间存在平衡。由于每个连接的亚基含有两个生物素,这些形式的生物素含量从12到2不等。通过在pH 5.5下进行活性酶沉降实验表明,酶的最大形式(含有12个生物素,分子量为1.2×10⁶)具有活性,并且在pH 6.8时,这种酶形式会解离为含有三个连接亚基的酶活性形式。这一结果与先前的观察结果一致(伍德,H.G.,焦,J.P.,和波托,E.M.(1977年),《生物化学杂志》252,1490;里格利,N.G.,焦,J.P.,和伍德,H.G.(1977年),《生物化学杂志》252,1500),这些观察结果表明,六个连接亚基中的三个优先从中央亚基的一个面解离,而其余三个连接亚基则相当牢固地结合在中央亚基的第二个面上。在60000转/分钟的沉降速度实验中会出现多个峰,因为沉降速度超过了转羧酶不同形式的平衡速度,而在30000转/分钟时,观察到酶的多种形式的单一峰,因为不同形式的平衡与沉降同步。解离的速率和程度会随着温度的升高而增加。通过油下离心表明,与六个、五个和四个连接亚基相连的酶的大形式的缔合-解离不受静水压力的影响。相反,与三个和两个连接亚基相连的酶的缔合-解离似乎受压力影响。累积的结果表明,细胞胞质溶胶中酶的天然形式由一系列具有一到六个连接亚基的酶活性形式组成。胞质溶胶中的主要形式将取决于组成亚基的浓度、pH值、离子浓度(特别是二价阴离子)和温度。

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