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Vejovine, a new antibiotic from the scorpion venom of Vaejovis mexicanus

机译:Vejovine,一种来自墨西哥Vaejovis蝎毒的新型抗生素

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Multidrug resistant bacterial infections are one of the most important health problems in recent years. Resistance to conventional antibiotics limits the therapeutic options causing increase rate in morbid-mortality in hospitals. Therefore, new antibacterial agents with new bacterial targets have been searched and found in many different sources, including scorpion venom and scorpion hemolymph. Here, we report a new anti-microbial peptide named Vejovine. This peptide was isolated from the venom of the Mexican scorpion Vaejovis mexicanus by two steps of reversed phase high performance liquid chromatography (RP-HPLC). It is composed of 47 amino acid residues with no cysteine residues in its sequence, with a molecular weight of 4873aaDa. The chemical synthesis of Vejovine was performed by the solid phase method of Merrifield, using fluoren-9-ylmethoxycarbonyl (Fmoc)-amino acids. Both the native and synthetic peptides were shown to have essentially the same activity. Vejovine inhibits growth of clinical isolates of Gram-negative multidrug resistant (Pseudomonas aeruginosa, Klebsiella pneumoniae, Escherichia coli, Enterobacter cloacae and Acinetobacter baumanii) causing nosocomial infections with a minimum inhibitory concentration (MIC) of 4.4aaI14M up to 50aaI14M. This peptide has also hemolytic activity against human erythrocytes with a HC50 value of 100aaI14M. A cDNA library of the venomous gland of this scorpion provided material for cloning the gene encoding Vejovine. This peptide is a new type of antibiotic, showing less than 50% similarity to other known scorpion peptides. Vejovine is a candidate to be used as a leading compound for future development of an effective peptide against multidrug resistant bacteria.
机译:耐多药细菌感染是近年来最重要的健康问题之一。对常规抗生素的耐药性限制了治疗选择,导致医院病死率上升。因此,已经在包括蝎毒和蝎血淋巴在内的许多不同来源中搜索并发现了具有新细菌靶标的新型抗菌剂。在这里,我们报告了一种名为Vejovine的新型抗微生物肽。通过两步反相高效液相色谱(RP-HPLC)从墨西哥蝎Vaejovis mexicanus的毒液中分离出该肽。它由47个氨基酸残基组成,序列中没有半胱氨酸残基,分子量为4873aaDa。 Vejovine的化学合成是通过Merrifield的固相方法,使用芴9-基甲氧基羰基(Fmoc)-氨基酸进行的。天然肽和合成肽均显示具有基本相同的活性。 Vejovine抑制引起革兰氏阴性多重耐药的临床分离株(铜绿假单胞菌,肺炎克雷伯菌,大肠杆菌,阴沟肠杆菌和鲍曼不动杆菌)的生长,引起医院感染,最低抑菌浓度(MIC)为4.4aaI14M,最高50aaI14M。该肽还具有针对人红细胞的溶血活性,HC50值为100aaI14M。该蝎子有毒腺的cDNA文库为克隆编码Vejovine的基因提供了材料。这种肽是一种新型的抗生素,与其他已知的蝎子肽的相似性不到50%。 Vejovine是候选化合物,可作为未来开发抗多药耐药细菌的有效肽的主导化合物。

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