YPD培养基培养的牛曲霉细胞外滤液对人肿瘤细胞的细胞毒电位

T. B. Alves, G. M. Roberto, M. Brassesco, L. H. S. Guimarães
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引用次数: 0

摘要

不同种类的真菌,特别是曲霉属的真菌,已经被报道为具有生物活性的小分子,包括蛋白质的生产者,更好地了解它们的来源、结构、功能和毒性对它们的生物技术应用至关重要。基于此,我们的目的是评价牛痘芽孢杆菌细胞外滤液的细胞毒活性。将粗滤液置于含有18 kDa蛋白的YPD培养基中,培养120 h后,采用吉姆萨染色法测定其对不同人肿瘤细胞系的细胞毒性。粗过滤液在20µg/mL的浓度下,对ONS-76(髓母细胞瘤)、HT144T(黑色素瘤)、HOS(骨肉瘤)、T98G(胶质母细胞瘤)人肿瘤细胞系和MRC-5(成纤维细胞)人正常细胞抑制作用(从27%到50%)。据此,通过质谱(MS/MS)分析对DEAE-Cellulose程序获得的18 kDa蛋白带和馏分进行了评估,发现存在与其他曲霉物种中描述的α -sarcin, mitogillin和Aspf1核糖素相似的肽。综上所述,含核糖素样蛋白的niveus胞外滤液在体外可抑制人肿瘤细胞株的生长,表明其生物技术潜力,表明其在免疫毒素制备方面的潜在应用前景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cytotoxic Potential from the Extracellular Filtrate from Aspergillus niveus Cultured in YPD Medium against Human Tumor Cells
Different fungal species, especially from the genus Aspergillus, have been reported as producers of small molecules, including proteins, with biological activity and a better understanding of their sources, structure, function and toxicity is essential for their biotechnological applications. According to this, our aim was to evaluate the cytotoxic activity of the extracellular filtrate produced by A. niveus. The crude filtrate obtained in YPD medium containing 18 kDa protein, after cultivation for 120 h, was selected for cytotoxic assay, assessed by Giemsa staining, against different human tumor cell lines. Crude filtrate inhibited (from 27% to 50%) the ONS-76 (medulloblastoma), HT144T (melanoma), HOS (osteosarcoma), T98G (glioblastoma) human tumor cell lines and MRC-5 (fibroblasts) human normal cells, at 20 µg/mL for 72 h treatment. According to this, the 18 kDa protein band and the fractions obtained after DEAE-Cellulose procedure were evaluated through mass spectrometry (MS/MS) analysis, revealing the presence of peptides with similarity to the alpha-sarcin, mitogillin and Aspf1 ribotoxins described for other Aspergillus species. In conclusion, the A. niveus extracellular filtrate containing ribotoxin-like proteins reduced, in vitro, the growth of human tumor cell lines indicating their biotechnological potential, indicating a possible future application in the elaboration of immunotoxins.
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