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Efficient Screening of a Novel Antimicrobial Peptide from Jatropha curcas by Cell Membrane Affinity Chromatography

机译:细胞膜亲和色谱法从麻风树中高效筛选新型抗菌肽

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摘要

A novel method named cell membrane affinity chromatography was used to screen antimicrobial peptides from Jatropha curcas. A cationic antimicrobial peptide (KVFLGLK, )Cpep7) was successfully isolated and identified. Antimicrobial assays indicated that JCpep7 was active against the tested microorganisms (Salmonella typhimurium ATCC .50013, Shigella dysenteriae ATCC 51302, Pseudomonas aeruginosa ATCC 27553, Staphylococcus aureus ATCC 25923, Bacillus subtilis ATCC 23631, and Streptococcus pneumoniae ATCC 49619) with minimal inhibitory concentration (MIC) values ranging from 24 to 64 μg/mL. The antimicrobial mechanisms based on Fourier transform infrared (FTIR) spectroscopy and transmission electron microscopy (TEM) techniques showed that JCpep7 killed microbes principally via breaking of their cell walls and membranes, followed by cell lysis. The results indicated that cell membrane affinity chromatography could be a promising approach for high-throughput screening of antimicrobial peptides from J. curcas.
机译:一种名为细胞膜亲和层析的新方法被用来筛选麻疯树的抗菌肽。阳离子抗菌肽(KVFLGLK,)Cpep7)已成功分离和鉴定。抗菌试验表明,JCpep7对被测微生物具有活性(鼠伤寒沙门氏菌ATCC .50013,痢疾志贺氏菌ATCC 51302,铜绿假单胞菌ATCC 27553,金黄色葡萄球菌ATCC 25923,枯草芽孢杆菌ATCC 23631和链霉菌最小浓度49MIC) )值范围从24到64μg/ mL。基于傅立叶变换红外(FTIR)光谱和透射电子显微镜(TEM)技术的抗菌机制表明,JCpep7主要通过破坏细胞壁和细胞膜,然后裂解细胞来杀死微生物。结果表明,细胞膜亲和层析可能是一种有前途的高通量筛选麻疯树抗菌肽的方法。

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