Suppr超能文献

抑制细胞外麻风分枝杆菌中酚糖脂-I的合成作为抗菌活性的指标。

Inhibition of phenolic glycolipid-I synthesis in extracellular Mycobacterium leprae as an indicator of antimicrobial activity.

作者信息

Harris E B, Franzblau S G, Hastings R C

机构信息

Biochemistry Research Department, GWL Hansen's Disease Center, Carville, Louisiana 70721.

出版信息

Int J Lepr Other Mycobact Dis. 1988 Dec;56(4):588-91.

PMID:3065422
Abstract

The effects of 22 antimicrobial agents on the incorporation of [U14C] palmitic acid ([U14C] PA) into the unique phenolic glycolipid-I (PGL-I) antigen of Mycobacterium leprae were studied. Nude-mouse-propagated M. leprae were incubated in a modified Dubos medium in the presence of antimicrobial agents for 4 days. [U14C] PA was then added and incubation was continued for 8 days. The antileprosy agents dapsone, rifampin, and clofazimine (2 micrograms/ml each) caused a significant reduction in [U14C] PA incorporation into PGL-I. Among other agents, the most active were erythromycin, chloramphenicol, and cerulenin. Low concentrations of ethionamide, tetracycline, and minocycline stimulated label incorporation. This system may prove useful in the evaluation of antileprosy agents.

摘要

研究了22种抗菌剂对[U14C]棕榈酸([U14C]PA)掺入麻风分枝杆菌独特的酚糖脂-I(PGL-I)抗原的影响。将裸鼠繁殖的麻风分枝杆菌在改良的杜博斯培养基中与抗菌剂一起孵育4天。然后加入[U14C]PA并继续孵育8天。抗麻风病药物氨苯砜、利福平和氯法齐明(各2微克/毫升)使[U14C]PA掺入PGL-I的量显著减少。在其他药物中,最有效的是红霉素、氯霉素和浅蓝菌素。低浓度的乙硫异烟胺、四环素和米诺环素刺激标记物掺入。该系统可能在抗麻风病药物的评估中证明有用。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验