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源自一株分离菌的铝霉素生物合成基因簇的醌类化合物抗菌活性的表征

Characterization of the Antibacterial Activity of Quinone-Based Compounds Originating from the Alnumycin Biosynthetic Gene Cluster of a Isolate.

作者信息

Sagurna Leonie, Heinrich Sascha, Kaufmann Lara-Sophie, Rückert-Reed Christian, Busche Tobias, Wolf Alexander, Eickhoff Jan, Klebl Bert, Kalinowski Jörn, Bandow Julia E

机构信息

Applied Microbiology, Faculty of Biology and Biotechnology, Ruhr University Bochum, 44780 Bochum, Germany.

Technology Platform Genomics, Center for Biotechnology, Bielefeld University, 33594 Bielefeld, Germany.

出版信息

Antibiotics (Basel). 2023 Jun 28;12(7):1116. doi: 10.3390/antibiotics12071116.

Abstract

Bacteria of the genus produce various specialized metabolites. Single biosynthetic gene clusters (BGCs) can give rise to different products that can vary in terms of their biological activities. For example, for alnumycin and the shunt product K115, antimicrobial activity was described, while no antimicrobial activity was detected for the shunt product 1,6-dihydro 8-propylanthraquinone. To investigate the antibacterial activity of 1,6-dihydro 8-propylanthraquinone, we produced alnumycin and 1,6-dihydro 8-propylanthraquinone from a isolate containing the alnumycin BGC. The strain was cultivated in liquid glycerol-nitrate-casein medium (GN), and both compounds were isolated using an activity and mass spectrometry-guided purification. The structures were validated via nuclear magnetic resonance (NMR) spectroscopy. A minimal inhibitory concentration (MIC) test revealed that 1,6-dihydro 8-propylanthraquinone exhibits antimicrobial activity against Δ, , an type strain, and a vancomycin intermediate-resistance strain (VISA). Activity of 1,6-dihydro 8-propylanthraquinone against Δ was approximately 10-fold higher than that of alnumycin. We were unable to confirm gyrase inhibition for either compound and believe that the modes of action of both compounds are worth reinvestigating.

摘要

属的细菌产生各种特殊代谢产物。单个生物合成基因簇(BGCs)可产生不同的产物,其生物活性可能各不相同。例如,对于铝霉素和分流产物K115,已描述了其抗菌活性,而对于分流产物1,6 - 二氢 - 8 - 丙基蒽醌未检测到抗菌活性。为了研究1,6 - 二氢 - 8 - 丙基蒽醌的抗菌活性,我们从一个含有铝霉素BGC的分离株中生产了铝霉素和1,6 - 二氢 - 8 - 丙基蒽醌。该菌株在液体甘油 - 硝酸盐 - 酪蛋白培养基(GN)中培养,两种化合物均通过活性和质谱引导的纯化方法进行分离。通过核磁共振(NMR)光谱对结构进行了验证。最低抑菌浓度(MIC)测试表明,1,6 - 二氢 - 8 - 丙基蒽醌对Δ、、一种型菌株和一株万古霉素中介耐药菌株(VISA)具有抗菌活性。1,6 - 二氢 - 8 - 丙基蒽醌对Δ的活性比铝霉素高约10倍。我们无法证实这两种化合物对gyrase的抑制作用,并且认为这两种化合物的作用方式值得重新研究。

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