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通过亲和层析法纯化奇异变形杆菌不稳定原生质球L型的膜结合DD-羧肽酶。青霉素对该酶的非竞争性抑制作用以及酶-抑制剂复合物的低稳定性。

Purification of the membrane-bound DD-carboxypeptidase of the unstable spheroplast L-form of Proteus mirabilis by affinity chromatography. Non-competitive inhibition of the enzyme by penicillins and low stability of the enzyme-inhibitor complex.

作者信息

Martin H H, Schilf W, Maskos C

出版信息

Eur J Biochem. 1976 Dec 11;71(2):585-93. doi: 10.1111/j.1432-1033.1976.tb11149.x.

Abstract

Membrane-bound DD-carboxypeptidase of the unstable L-form of Proteus mirabilis was solubilized by the non-ionic detergent Genapol X-100 and purified to protein homogeneity by affinity chromatography on ampicillin bound to succinyl-aminododecyl-cellulose. The purified enzyme with a molecular weight of 43000 is inhibited non-competitively by penicillin G and carbenicillin, indicating a function of the penicillins as allosteric inhibitors. Sensitivity of the enzyme to penicillins is only moderate with a Ki of 1 muM for penicillin G. Breakdown of.the enzyme-inhibitor complex EI with different penicillins occurs rapidly with reappearance of active DD-carboxypeptidase. The half-life of EI with penicillin G is 5.5 min at 30 degrees C and 3.5 min at 37 degrees C, 10--1000-fold shorter than EI half-lives of DD-carboxypeptidases in several other bacteria. The low stability of the enzyme-inhibitor complex and the moderate penicillin sensitivity appear to be the basis for the continued activity of DD-carboxypeptidase during growth of the L-form and synthesis of peptidoglycan in the presence of high concentrations of penicillin.

摘要

奇异变形杆菌不稳定L型的膜结合DD-羧肽酶可通过非离子型去污剂Genapol X-100溶解,并通过在与琥珀酰-氨基十二烷基纤维素结合的氨苄青霉素上进行亲和层析纯化至蛋白质均一性。纯化后的酶分子量为43000,受青霉素G和羧苄青霉素非竞争性抑制,表明青霉素作为变构抑制剂发挥作用。该酶对青霉素的敏感性中等,青霉素G的Ki为1μM。不同青霉素与酶抑制剂复合物EI的分解迅速,活性DD-羧肽酶重新出现。EI与青霉素G在30℃时的半衰期为5.5分钟,在37℃时为3.5分钟,比其他几种细菌中DD-羧肽酶的EI半衰期短10 - 1000倍。酶抑制剂复合物的低稳定性和对青霉素的中等敏感性似乎是L型生长过程中以及在高浓度青霉素存在下肽聚糖合成过程中DD-羧肽酶持续活性的基础。

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