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[硫胺素给药后维生素B1缺乏大鼠肝脏转酮醇酶激活的机制]

[Mechanisms of liver transketolase activation in B1-deficient rats after administration of thiamine].

作者信息

Vinogradov V V, Mandrik K A, Strumilo S A, Matsiuk S K

出版信息

Biokhimiia. 1979 May;44(5):868-75.

PMID:454716
Abstract

Gel filtration and equilibrium dialysis demonstrated that the hyaloplasmic fraction of the liver of B1-deficient rats does not practically bind C-TDP in vitro. An addition of the excess of non-labelled coenzyme does not increase the transketolase activity. The data obtained suggest that transketolase activation in the hyaloplasmic fraction of the liver of B1-deficient rats after administration of thiamine in vivo is due to stimulation of the additional synthesis of the enzyme protein rather than to the saturation of the free apoenzyme with newly-formed TDP. In vivo and in vitro studies suggest that the hyaloplasmic fraction of the liver of B1-deficient rats contains no free apoenzyme of transketolase.

摘要

凝胶过滤和平衡透析表明,维生素B1缺乏大鼠肝脏的透明质部分在体外几乎不结合C-TDP。添加过量的未标记辅酶并不会增加转酮醇酶的活性。所获得的数据表明,维生素B1缺乏大鼠肝脏透明质部分在体内给予硫胺素后转酮醇酶的激活是由于酶蛋白的额外合成受到刺激,而不是游离脱辅基酶被新形成的TDP饱和。体内和体外研究表明,维生素B1缺乏大鼠肝脏的透明质部分不含转酮醇酶的游离脱辅基酶。

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