与gramicidin S相关的环十肽类抗生素的分离。

IF 1.6 3区 化学 Q3 CHEMISTRY, APPLIED
Alexander S Tikhomirov, Svetlana E Solov'eva, Tatiana S Shkuratova, Natalya M Malyutina, Daria V Andreeva, George V Zatonsky, Natalia E Grammatikova, Andrey E Shchekotikhin
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引用次数: 0

摘要

天然产物仍是开发抗菌剂的重要来源。在这项研究中,我们分离并评估了短芽孢杆菌var. G-B R+产生的gramicidin S (GS)抗生素复合物的主要生物学特性。利用高效液相色谱技术,我们获得了高纯度的GS及其5种主要相关成分的样品。分离的化合物结构被指定为GS同源物,具有几个氨基酸残基取代,其中两个以前没有描述过。新环十肽的抗菌活性接近GS,而五个分离的化合物中有两个显示出高达4倍的溶血降低。GS同源物与亲本抗生素的圆二色光谱显示出相同的β-结构构象。综上所述,本研究表明,分析抗生素复合物的次要成分可能导致发现具有更好疗效或有利治疗效果的新抗菌化合物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Isolation of cyclic decapeptide antibiotics related to gramicidin S.

Natural products remain to be an important source for the development of antibacterial agents. In this study, we isolated and evaluated the key biological properties of minor components of the gramicidin S (GS) antibiotic complex produced by Bacillus brevis var. G-B R+. Using HPLC techniques, we obtained highly pure samples of GS and its five major related components in individual form. Structures of isolated compounds were assigned as GS homologues, featuring several amino acid residue substitutions, two of which are previously undescribed. Antibacterial activity of new cyclic decapeptides was close to GS, while two of five isolated compounds demonstrated up to 4 times reduced haemolysis. Circular dichroism spectra of GS homologues and the parental antibiotic exhibited the same β-structure conformation. Taken together, this study demonstrates that analysis of minor components of antibiotic complexes could result in the discovery of new antibacterial compounds with better efficacy or favourable therapeutic profile.

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来源期刊
Natural Product Research
Natural Product Research 化学-医药化学
CiteScore
5.10
自引率
9.10%
发文量
605
审稿时长
2.1 months
期刊介绍: The aim of Natural Product Research is to publish important contributions in the field of natural product chemistry. The journal covers all aspects of research in the chemistry and biochemistry of naturally occurring compounds. The communications include coverage of work on natural substances of land and sea and of plants, microbes and animals. Discussions of structure elucidation, synthesis and experimental biosynthesis of natural products as well as developments of methods in these areas are welcomed in the journal. Finally, research papers in fields on the chemistry-biology boundary, eg. fermentation chemistry, plant tissue culture investigations etc., are accepted into the journal. Natural Product Research issues will be subtitled either ""Part A - Synthesis and Structure"" or ""Part B - Bioactive Natural Products"". for details on this , see the forthcoming articles section. All manuscript submissions are subject to initial appraisal by the Editor, and, if found suitable for further consideration, to peer review by independent, anonymous expert referees. All peer review is single blind and submission is online via ScholarOne Manuscripts.
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