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[临床分离的铜绿假单胞菌对氨基糖苷类抗生素的灭活作用]

[Inactivation of aminoglycoside antibiotics by clinically isolated Pseudomonas aeruginosa].

作者信息

Sato K, Kurimoto T, Okachi R

出版信息

Jpn J Antibiot. 1983 Jan;36(1):194-8.

PMID:6405063
Abstract

Minimal inhibitory concentrations (MIC) of micronomicin (MCR) and gentamicin (GM) against clinically isolated Pseudomonas aeruginosa F 4150 were 1.56 mcg/ml and 6.25 mcg/ml, respectively. Sisomicin, dibekacin, amikacin, netilmicin, tobramycin ribostamycin and kanamycin did not inhibit the strain at the concentrations less than 25 mcg/ml. Each aminoglycoside antibiotic was incubated in Tris-HCl buffer solutions (pH 7.8) containing cell free crude enzyme preparations obtained by sonic oscillation of intact cells of P. aeruginosa F 4150, coenzyme A and adenosine-5'-triphosphate. The residual activity at 3 hours of incubation at 37 degrees C was 88% for MCR and 33.6% for GM, while all of the other aminoglycoside antibiotics tested were completely inactivated under this condition.

摘要

小诺米星(MCR)和庆大霉素(GM)对临床分离的铜绿假单胞菌F 4150的最低抑菌浓度(MIC)分别为1.56微克/毫升和6.25微克/毫升。西索米星、地贝卡星、阿米卡星、奈替米星、妥布霉素、核糖霉素和卡那霉素在浓度低于25微克/毫升时均未抑制该菌株。将每种氨基糖苷类抗生素在含有通过对铜绿假单胞菌F 4150完整细胞进行超声振荡获得的无细胞粗酶制剂、辅酶A和腺苷-5'-三磷酸的Tris-HCl缓冲溶液(pH 7.8)中孵育。在37℃孵育3小时时,MCR的残留活性为88%,GM为33.6%,而所有其他测试的氨基糖苷类抗生素在此条件下均完全失活。

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