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来自链霉菌R61的胞外DD-羧肽酶-转肽酶、底物和β-内酰胺抗生素之间的相互作用。模型的选择。

Interaction between the exocellular DD-carboxypeptidase-transpeptidase from Streptomyces R61, substrate and beta-lactam antibiotics. A choice of models.

作者信息

Frère J M, Ghuysen J M, Perkins H R

出版信息

Eur J Biochem. 1975 Sep 15;57(2):353-9. doi: 10.1111/j.1432-1033.1975.tb02308.x.

Abstract

The interaction between the exocellular DD-carboxypeptidase-transpeptidase of Streptomyces R61 and beta-lactam antibiotics is a multistep process during which a rather stable enzyme - antibiotic complex is formed. This mechanism of interaction is compatible with Lineweaver-Burk plots that are typical of a competitive inhibition of the hydrolysis of the peptide donor by the antibiotic. In fact, however, the same Lineweaver-Burk plots can be obtained on the basis of a non-competitive type of inhibition. At present, a choice between the two models cannot be made.

摘要

链霉菌R61的胞外DD-羧肽酶-转肽酶与β-内酰胺抗生素之间的相互作用是一个多步骤过程,在此过程中会形成一种相当稳定的酶-抗生素复合物。这种相互作用机制与Lineweaver-Burk图相符,该图是抗生素对肽供体水解的竞争性抑制的典型特征。然而,实际上,基于非竞争性抑制类型也可以得到相同的Lineweaver-Burk图。目前,无法在这两种模型之间做出选择。

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