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首页> 外文期刊>Journal of natural products >Chaxamycins A-D, bioactive ansamycins from a hyper-arid desert Streptomyces sp.
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Chaxamycins A-D, bioactive ansamycins from a hyper-arid desert Streptomyces sp.

机译:Chaxamycins A-D,来自高干旱沙漠链霉菌sp。的生物活性安沙霉素。

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摘要

Streptomyces sp. strain C34, isolated from soil collected in the Chilean hyper-arid Atacama Desert, was cultured on different media, resulting in the isolation and identification of four new ansamycin-type polyketides. The organism was selected for chemical investigation on the basis of a genome-mining PCR-based experiment targeting the gene encoding rifamycin-specific 3-amino-5-hydroxybenzoic acid synthetase (AHBA). The isolated compounds were structurally characterized using NMR and MS techniques and named chaxamycins A-D (1-4). Compounds 1-4 were tested for their antibacterial activity against Staphylococcus aureus ATCC 25923 and Escherichia coli ATCC 25922 and for their ability to inhibit the intrinsic ATPase activity of the heat shock protein 90 (Hsp90). Chaxamycin D (4), which showed a selective antibacterial activity against S. aureus ATCC 25923, was tested further against a panel of MRSA clinical isolates. In a virtual screening experiment, chaxamycins A-D (1-4) have also been docked into the ATP-binding pocket in the N-terminal domain of the Hsp90, and the observed interactions are discussed.
机译:链霉菌从智利超干旱阿塔卡马沙漠中收集的土壤中分离出的C34菌株在不同培养基上进行培养,从而分离和鉴定了四种新的安沙霉素型聚酮化合物。根据针对编码利福霉素特异性3-氨基-5-羟基苯甲酸合成酶(AHBA)的基因的基于基因组挖掘PCR的实验,选择了该生物进行化学研究。使用NMR和MS技术对分离的化合物进行结构表征,并命名为沙卡霉素A-D(1-4)。测试了化合物1-4对金黄色葡萄球菌ATCC 25923和大肠杆菌ATCC 25922的抗菌活性,以及​​它们抑制热激蛋白90(Hsp90)的固有ATP酶活性的能力。 Chaxamycin D(4)对金黄色葡萄球菌ATCC 25923具有选择性的抗菌活性,还针对一组MRSA临床分离株进行了进一步测试。在虚拟筛选实验中,查卡霉素A-D(1-4)也已停靠在Hsp90 N末端域的ATP结合袋中,并讨论了观察到的相互作用。

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