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磷酸糖与核酮糖-1,5-二磷酸羧化酶催化位点的相互作用。

Interaction of sugar phosphates with the catalytic site of ribulose-1,5-bisphosphate carboxylase.

作者信息

Badger M R, Lorimer G H

出版信息

Biochemistry. 1981 Apr 14;20(8):2219-25. doi: 10.1021/bi00511a023.

Abstract

The activated and catalytically competent form of ribulose-1,5-bisphosphate carboxylase is a ternary complex of enzyme-activator CO2 x Mg. The effectors of NADPH and 6-phosphogluconate promoted activation by formation of a rapid equilibrium quaternary complex of enzyme-activation CO2 x Mg x effector; i.e., the effectors did not activate the enzyme per se but promoted the basic activation process by stabilizing the activated enzyme-activator CO2 x Mg complex. Kinetic and gel filtration studies showed that the effectors stabilized the binding of the activator CO2 and MG2+ (or Mn2+), thereby decreasing the rate of deactivation. Binding studies indicated the presence of one 6-phosphogluconate binding site per protomer. The binding of 6-phosphogluconate and NADPH to the enzyme-activator CO2 x Mg complex was (a) completely prevented when the catalytic site for ribulose bisphosphate was occupied by the transition-state analogue, 2-carboxyarabinitol 1,5-bisphosphate, and (b) competitively diminished in the presence of 3-phosphoglycerate, the product of the carboxylation reaction. NADPH, 6-phosphogluconate, and 3-phosphoglycerate acted as linear competitive inhibitors of carboxylation with respect to ribulose bisphosphate. These results demonstrate that the effectors elicit their response through interaction at the catalytic site for ribulose bisphosphate and that their effect is secondary to the basic CO2-Mg2+-dependent activation reaction. An enzyme molecule cannot be simultaneously catalytically competent (capable of binding and carboxylating ribulose bisphosphate) and activated by an effector, since the latter involves occupancy of the ribulose bisphosphate binding site.

摘要

1,5 - 二磷酸核酮糖羧化酶的活性且具有催化活性的形式是酶 - 激活剂 - CO₂ - Mg的三元复合物。NADPH和6 - 磷酸葡萄糖酸的效应物通过形成酶 - 激活剂 - CO₂ - Mg - 效应物的快速平衡四级复合物来促进激活;即,效应物本身并不激活酶,而是通过稳定激活的酶 - 激活剂 - CO₂ - Mg复合物来促进基本的激活过程。动力学和凝胶过滤研究表明,效应物稳定了激活剂CO₂和Mg²⁺(或Mn²⁺)的结合,从而降低了失活速率。结合研究表明每个原体存在一个6 - 磷酸葡萄糖酸结合位点。当二磷酸核酮糖的催化位点被过渡态类似物2 - 羧基阿拉伯糖醇1,5 - 二磷酸占据时,6 - 磷酸葡萄糖酸和NADPH与酶 - 激活剂 - CO₂ - Mg复合物的结合被(a)完全阻止,并且(b)在羧化反应产物3 - 磷酸甘油酸存在下竞争性减弱。NADPH、6 - 磷酸葡萄糖酸和3 - 磷酸甘油酸作为二磷酸核酮糖羧化作用的线性竞争性抑制剂。这些结果表明,效应物通过在二磷酸核酮糖的催化位点相互作用来引发其反应,并且它们的作用是依赖于CO₂ - Mg²⁺的基本激活反应的次要作用。一个酶分子不能同时具有催化活性(能够结合并羧化二磷酸核酮糖)并被效应物激活,因为后者涉及占据二磷酸核酮糖结合位点。

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