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深渊霉素 A:20 年回顾

Abyssomicins-A 20-Year Retrospective View.

机构信息

Department of Microbiology/Biotechnology, Interfaculty Institute of Microbiology and Infection Medicine Tübingen (IMIT), University of Tuebingen, Auf der Morgenstelle 28, D-72076 Tübingen, Germany.

出版信息

Mar Drugs. 2021 May 24;19(6):299. doi: 10.3390/md19060299.

Abstract

Abyssomicins represent a new family of polycyclic macrolactones. The first described compounds of the abyssomicin family were abyssomicin B, C, atrop-C, and D, produced by the marine actinomycete strain AB-18-032, which was isolated from a sediment collected in the Sea of Japan. Among the described abyssomicins, only abyssomicin C and atrop-abyssomicin C show a high antibiotic activity against Gram-positive bacteria, including multi-resistant and vancomycin-resistant strains. The inhibitory activity is caused by a selective inhibition of the enzyme 4-amino-4-deoxychorismate synthase, which catalyzes the transformation of chorismate to para-aminobenzoic acid, an intermediate in the folic acid pathway.

摘要

深渊霉素代表了一类新型的多环大环内酯。深渊霉素家族的首批被描述的化合物是深渊霉素 B、C、atrop-C 和 D,由海洋放线菌菌株 AB-18-032 产生,该菌株是从日本海采集的沉积物中分离出来的。在所描述的深渊霉素中,只有深渊霉素 C 和 atrop-abyssomicin C 对革兰氏阳性菌具有较高的抗生素活性,包括多耐药和万古霉素耐药菌株。这种抑制活性是由于对酶 4-氨基-4-脱氧胆酸合酶的选择性抑制所致,该酶催化分支酸转化为对氨基苯甲酸,这是叶酸途径中的一个中间产物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0349/8225091/5d4e5fd49928/marinedrugs-19-00299-g001.jpg

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