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Pradimicin-IRD from Amycolatopsis sp. IRD-009 and its antimicrobial and cytotoxic activities

机译:来自amycolatopsis sp的Pradimicin-Ird。 IRD-009及其抗微生物和细胞毒性活动

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摘要

A new polycyclic antibiotic, pradimicin-IRD, was isolated from actinobacteria Amycolatopsis sp. IRD-009 recovered from soil of Brazilian rainforest undergoing restoration area. This molecule is the major compound produced in solid culture media. The new compound was detected by a focused method of precursor ion (high-performance liquid chromatography coupled to tandem mass spectrometer) developed previously to identify unusual aminoglycosyl sugar moieties. The compound was isolated and its structure was, therefore, elucidated by high-resolution mass spectrometry, and 1D and 2D nuclear magnetic resonance experiments. Pradimicin-IRD displayed potential antimicrobial activity against Streptococcus agalactiae (MIC 3.1 mu g/mL), Pseudomonas aeruginosa (MIC 3.1 mu g/mL) and Staphylococcus aureus (MIC 3.1 mu g/mL), and also cytotoxicity against tumour and non-tumour cell lines with IC50 values ranging from 0.8 mu M in HCT-116 colon carcinoma cells to 2.7 mu M in MM 200 melanoma cells. Particularly, these biological properties are described for the first time for this chemical class.
机译:一种新的多环抗生素,Pradimicin-Ird与actinobacteria amycolatopsis sp分离。 IRD-009从巴西雨林的土壤中恢复过恢复区。该分子是固体培养基中产生的主要化合物。通过先前开发的前体离子(高性能液相色谱法偶联至串联质谱仪的高性能液相色谱仪)检测新化合物以鉴定异常的氨基糖基糖部分。分离化合物,因此,通过高分辨率质谱和1D和2D核磁共振实验阐明其结构。 Pradimicin-IRD针对链球菌(MIC3.1μg/ mL),假单胞菌铜绿假单胞菌(MIC3.1μg/ ml)和金黄色葡萄球菌(MIC3.1μg/ ml),以及针对肿瘤和非肿瘤的细胞毒性的潜在抗菌活性具有IC50值的细胞系,在Hct-116结肠癌细胞中的0.8μm,在mm 200黑色素瘤细胞中为2.7μm。特别地,这些生物学性质首次描述了该化学类。

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