拟肽
铜绿假单胞菌
抗生素
微生物学
生物发生
细菌外膜
生物
假单胞菌
革兰氏阴性菌
细菌
细菌细胞结构
脂多糖
化学
肽
生物化学
遗传学
大肠杆菌
基因
免疫学
作者
Nityakalyani Srinivas,Peter Jetter,Bernhard J. Ueberbacher,Martina Werneburg,Katja Zerbe,Jessica Steinmann,Benjamin van der Meijden,Francesca Bernardini,Alexander Lederer,Ricardo L. A. Dias,Pauline E. Misson,Heiko Henze,Jürg Zumbrunn,Frank O. Gombert,Daniel Obrecht,Peter Hunziker,Stefan Schauer,Urs Ziegler,Andres Käch,Leo Eberl,Katharina Riedel,Steven J. DeMarco,John A. Robinson
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2010-02-18
卷期号:327 (5968): 1010-1013
被引量:504
标识
DOI:10.1126/science.1182749
摘要
Killing Pseudomonas Gram-negative Pseudomonas bacteria are opportunistic pathogens, and drug-resistant strains present a serious health problem. Srinivas et al. (p. 1010 ) synthesized a family of peptidomimetic antibiotics that is active only against Pseudomonas . These antibiotics do not lyse the cell membrane, but instead target an essential outer membrane protein, LptD, which plays a role in the assembly of lipopolysaccharide in the outer cell membrane. Activity in a mouse infection model suggests that the antibiotics might have therapeutic potential. In addition, LptD is widely distributed in gram-negative bacteria and so its validation as a target has the potential to drive development of antibiotics with a broader spectrum of activity against gram-negative pathogens.
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