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A Trypsin Inhibitor from Tecoma stans Leaves Inhibits Growth and Promotes ATP Depletion and Lipid Peroxidation in Candida albicans and Candida krusei

机译:一种来自Tecoma stans叶片的胰蛋白酶抑制剂抑制白色念珠菌和克鲁斯念珠菌的生长并促进ATP消耗和脂质过氧化

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摘要

Tecoma stans (yellow elder) has shown medicinal properties and antimicrobial activity. Previous reports on antifungal activity of T. stans preparations and presence of trypsin inhibitor activity from T. stans leaves stimulated the investigation reported here. In this work, we proceeded to the purification and characterization of a trypsin inhibitor (TesTI), which was investigated for anti-Candida activity. Finally, in order to determine the potential of TesTI as a new natural chemotherapeutic product, its cytotoxicity to human peripheral blood mononuclear cells (PBMCs) was evaluated. TesTI was isolated from saline extract by ammonium sulfate fractionation followed by ion exchange and gel filtration chromatographies. Antifungal activity was evaluated by determining the minimal inhibitory (MIC) and fungicide (MFC) concentrations using fungal cultures containing only yeast form or both yeast and hyphal forms. Candida cells treated with TesTI were evaluated for intracellular ATP levels and lipid peroxidation. Cytotoxicity of TesTI to PBMCs was evaluated by MTT assay. TesTI (39.8 kDa, pI 3.41, Ki 43 nM) inhibited similarly the growth of both C. albicans and C. krusei culture types at MIC of 100 μg/mL. The MFCs were 200 μg/mL for C. albicans and C. krusei. Time-response curves revealed that TesTI (at MIC) was more effective at inhibiting the replication of C. albicans cells. At MIC, TesTI promoted reduction of ATP levels and lipid peroxidation in the Candida cells, being not cytotoxic to PBMCs. In conclusion, TesTI is an antifungal agent against C. albicans and C. krusei, without toxicity to human cells.
机译:Tecoma stans(黄色长者)​​已显示出药性和抗菌活性。以前关于T. stans制剂的抗真菌活性的报道以及来自T. stans叶片的胰蛋白酶抑制剂活性的存在刺激了此处报道的研究。在这项工作中,我们进行了胰蛋白酶抑制剂(TesTI)的纯化和表征,该酶已针对抗念珠菌活性进行了研究。最后,为了确定TesTI作为新的天然化学治疗产品的潜力,评估了其对人外周血单核细胞(PBMC)的细胞毒性。通过硫酸铵分级分离,离子交换和凝胶过滤层析从盐提取物中分离出TesTI。通过仅使用酵母形式或酵母和菌丝形式的真菌培养物确定最小抑制(MIC)和杀真菌剂(MFC)的浓度来评估抗真菌活性。评价用TesTI处理的念珠菌细胞的ATP水平和脂质过氧化作用。通过MTT分析评估TesTI对PBMC的细胞毒性。 TesTI(39.8 kDa,pI 3.41,Ki 43 nM)在MIC为100μg/ mL时同样抑制白色念珠菌和克鲁斯梭菌培养物类型的生长。白色念珠菌和克鲁斯梭菌的MFCs为200μg/ mL。时间响应曲线表明,TesTI(在MIC处)在抑制白色念珠菌细胞复制方面更为有效。在MIC,TesTI促进了念珠菌细胞中ATP水平的降低和脂质过氧化作用,对PBMC没有细胞毒性。总之,TesTI是一种针对白色念珠菌和克鲁斯梭菌的抗真菌剂,对人体细胞无毒性。

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