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阿奇霉素和红霉素对流感嗜血杆菌细胞中50S核糖体亚基组装的抑制作用。

Inhibition of 50S ribosomal subunit assembly in Haemophilus influenzae cells by azithromycin and erythromycin.

作者信息

Champney W Scott, Miller Mindy

机构信息

Department of Biochemistry and Molecular Biology, J.H. Quillen College of Medicine, East Tennessee State University, Johnson City, TN 37614, USA.

出版信息

Curr Microbiol. 2002 Jun;44(6):418-24. doi: 10.1007/s00284-001-0016-6.

Abstract

Azithromycin is an important antibiotic for the treatment of several different Gram-positive and Gram-negative bacterial infections. Erythromycin and clarithromycin are less useful antibiotics against Gram-negative infections. This difference in inhibitory activity was explored by comparing the effects of azithromycin and erythromycin on cellular functions in Haemophilus influenzae cells. Effects of both antibiotics on translation, cell viability, and growth rates have been measured. An IC(50) of 0.4 microg/ml was found for the effects of azithromycin on each of these processes. For erythromycin, an IC(50) of 1.5 microg/ml was observed, indicating a fourfold lower sensitivity of the organisms to this compound. The features of a second target for macrolide antibiotic inhibition in H. influenzae cells have also been examined. Inhibition of the synthesis of the large 50S ribosomal subunit was measured. Subunit formation was prevented in a concentration dependent fashion, with azithromycin showing a ninefold greater effect on this process compared with erythromycin. Synthesis of the 30S ribosomal subunit was not effected. Pulse and chase labeling kinetics confirmed the slower synthesis rate of the 50S particle in the presence of each antibiotic. The results are discussed in terms of the stronger effect of azithromycin on ribosome biosynthesis in this organism.

摘要

阿奇霉素是治疗多种不同革兰氏阳性和革兰氏阴性细菌感染的重要抗生素。红霉素和克拉霉素对革兰氏阴性感染的抗菌作用较弱。通过比较阿奇霉素和红霉素对流感嗜血杆菌细胞功能的影响,探讨了它们在抑制活性上的差异。测定了这两种抗生素对翻译、细胞活力和生长速率的影响。发现阿奇霉素对这些过程的半数抑制浓度(IC50)为0.4微克/毫升。对于红霉素,观察到的IC50为1.5微克/毫升,表明该微生物对这种化合物的敏感性低四倍。还研究了流感嗜血杆菌细胞中大环内酯类抗生素抑制的第二个靶点的特征。测定了50S大亚基核糖体合成的抑制情况。亚基形成受到浓度依赖性抑制,与红霉素相比,阿奇霉素对该过程的影响大九倍。30S核糖体亚基的合成未受影响。脉冲追踪标记动力学证实了在每种抗生素存在下50S颗粒的合成速率较慢。根据阿奇霉素对该生物体核糖体生物合成的更强作用对结果进行了讨论。

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