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吡咯吲哚霉素,由 rugosporus 链霉菌 LL - 42D005 产生的新型抗生素。II. 生物活性。

Pyrroindomycins, novel antibiotics produced by Streptomyces rugosporus LL-42D005. II. Biological activities.

作者信息

Singh M P, Petersen P J, Jacobus N V, Mroczenski-Wildey M J, Maiese W M, Greenstein M, Steinberg D A

机构信息

Natural Products Research Section, American Cyanamid Company, Pearl River, New York 10965.

出版信息

J Antibiot (Tokyo). 1994 Nov;47(11):1258-65. doi: 10.7164/antibiotics.47.1258.

Abstract

The pyrroindomycins, a complex of novel antibiotics identified in fermentation broths of "Streptomyces rugosporus" LL-42D005, demonstrated excellent in vitro activity against Gram-positive bacteria. The semisynthetic diacetyl derivative of pyrroindomycin B (pyrroindomycin B-Ac2) was bactericidal for exponential-phase cells, but not for stationary-phase cells. This compound also exhibited marginal protection against a lethal Staphylococcus aureus challenge in mice. The poor in vivo activity of this antibiotic complex may be related to binding to blood components, as suggested by elevated MICs observed in blood-containing media. Incorporation of radiolabeled precursors into DNA, RNA, and protein was inhibited in an exponential-phase culture of Bacillus subtilis within ten minutes of exposure to pyrroindomycin B-Ac2. Microscopic examinations of drug-treated cells revealed lysis within the same ten minute period. These data are consistent with an effect of pyrroindomycin B-Ac2 on the integrity of the bacterial membrane.

摘要

吡咯吲哚霉素是在“ rugosporus链霉菌”LL - 42D005发酵液中鉴定出的一种新型抗生素复合物,对革兰氏阳性菌具有优异的体外活性。吡咯吲哚霉素B的半合成二乙酰衍生物(吡咯吲哚霉素B - Ac2)对指数生长期的细胞具有杀菌作用,但对稳定期细胞则无此作用。该化合物对小鼠金黄色葡萄球菌致死性攻击也仅表现出微弱的保护作用。这种抗生素复合物较差的体内活性可能与它和血液成分的结合有关,含血培养基中观察到的最低抑菌浓度升高就表明了这一点。在暴露于吡咯吲哚霉素B - Ac2的十分钟内,枯草芽孢杆菌指数生长期培养物中放射性标记前体掺入DNA、RNA和蛋白质的过程受到抑制。对药物处理细胞的显微镜检查显示在相同的十分钟内细胞发生裂解。这些数据与吡咯吲哚霉素B - Ac2对细菌细胞膜完整性的影响一致。

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