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伊祖米诺利德——一种由小单孢菌产生的新型β-内酰胺酶抑制剂。II.生物学特性。

Izumenolide-a novel beta-lactamase inhibitor produced by Micromonospora. II. Biological properties.

作者信息

Bush K, Bonner D P, Sykes R B

出版信息

J Antibiot (Tokyo). 1980 Nov;33(11):1262-9. doi: 10.7164/antibiotics.33.1262.

Abstract

Izumenolide is a potent inhibitor of beta-lactamases, especially from Gram-negative bacteria. The I50 value of 0.01 microgram/ml for TEM-2 beta-lactamase, after 10 min preincubation, corresponds to a ratio of 7.6 moles inhibitor per mole of enzyme. The initial inhibitory reaction with TEM-2 beta-lactamase exhibits mixed reaction kinetics, suggesting a possible overlapping binding site with the active center. Tem-2 beta-lactamase is irreversible inactivated by izumenolide in a biphasic reaction. Carbenicillin offers partial protection against inactivation. Izumenolide exhibits limited antibiotic activity against some Gram-negative bacteria. Against beta-lactamase producing bacteria izumenolide provides protection to ampicillin and cephaloridine but the protection is limited due to permeability problems associated with izumenolide entry into the cells.

摘要

伊祖梅诺利德是一种强效的β-内酰胺酶抑制剂,对革兰氏阴性菌产生的β-内酰胺酶尤其有效。在预孵育10分钟后,对TEM-2β-内酰胺酶的I50值为0.01微克/毫升,这相当于每摩尔酶有7.6摩尔抑制剂。与TEM-2β-内酰胺酶的初始抑制反应表现出混合反应动力学,表明其与活性中心可能存在重叠的结合位点。伊祖梅诺利德在双相反应中使Tem-2β-内酰胺酶发生不可逆失活。羧苄青霉素对失活有部分保护作用。伊祖梅诺利德对一些革兰氏阴性菌表现出有限的抗菌活性。对于产β-内酰胺酶的细菌,伊祖梅诺利德可为氨苄西林和头孢菌素提供保护,但由于伊祖梅诺利德进入细胞存在通透性问题,这种保护作用有限。

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