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阴沟肠杆菌的I型β-内酰胺酶与对β-内酰胺类抗生素的耐药性

Type I beta-lactamases of Enterobacter cloacae and resistance to beta-lactam antibiotics.

作者信息

Tejedor-Junco M T, González-Martín M, Lupiola P, González-Lama Z

机构信息

Departamento de Ciencias Clínicas, Microbiología, Universidad de Las Palmas de Gran Canaria, Canary Islands, Spain.

出版信息

Folia Microbiol (Praha). 1998;43(6):683-6. doi: 10.1007/BF02816390.

Abstract

The interaction of type-I beta-lactamases from Enterobacter cloacae with diverse beta-lactam compounds was examined. The ability of penicillin and cefoxitin to induce beta-lactamase production in this strain was assessed. The effect of beta-lactamase inhibitors was measured on beta-lactamase extracts and on intact cells. E. cloacae 78 strain is a stably derepressed mutant showing limited susceptibility to a number of antibiotics except imipenem. Imipenem would therefore be the appropriate choice for therapy of infections caused by stably derepressed mutants of Enterobacter sp. producing type-I beta-lactamases.

摘要

研究了阴沟肠杆菌I型β-内酰胺酶与多种β-内酰胺类化合物的相互作用。评估了青霉素和头孢西丁在该菌株中诱导β-内酰胺酶产生的能力。测定了β-内酰胺酶抑制剂对β-内酰胺酶提取物和完整细胞的作用。阴沟肠杆菌78菌株是一种稳定去阻遏突变体,除亚胺培南外,对多种抗生素敏感性有限。因此,亚胺培南将是治疗由产生I型β-内酰胺酶的阴沟肠杆菌稳定去阻遏突变体引起的感染的合适选择。

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