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The Research on Biotransformation Pathway of Digitoxin by Aspergillus ochraceus and the Analysis of Products Activity

机译:och曲霉生物转化人毒素的途径及产物活性分析

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In order to analyze the biotransformation pathway of digitoxin by Aspergillus ochraceus Rn405, a product-digitoxigenin was used as the substrate to biotransform. The substrate consumption and product synthesis were monitored by HPLC during the bioconversion process. The preliminary results were as follows: Firstly, hydrolysis reaction happened and digitoxin was converted into digitoxigenin; then, with extension of the reaction time, the hydroxyl group was introduced to the C-11 of digitoxigenin by the role of hydroxylase and another product named 11α-hydroxydigitoxigenin was generated in a large amount. The influences of these two products on myocardial apoptosis and their antineoplastic activities were further analyzed. It was found that compared with the substrate digitoxin and reference substance digoxin, the apoptosis effects of digitoxigenin and 11α-hydroxydigitoxigenin on rat myocardial cells remarkably decreased; but no obvious antineoplastic activities on the four tumor cells, including human breast cancer cell MCF-7, rat breast cancer cell 4T1, human cervical cancer cell Hela, and rat melanoma cell B-16 were observed.
机译:为了分析och曲霉Rn405对洋地黄毒苷的生物转化途径,使用产物洋地黄毒苷作为底物进行生物转化。在生物转化过程中,通过HPLC监测底物的消耗和产物的合成。初步结果如下:首先发生水解反应,将洋地黄毒苷转化为洋地黄毒苷。然后,随着反应时间的延长,通过羟化酶的作用将羟基引入到洋地黄毒苷的C-11中,并大量生成了另一种名为11α-羟基洋地黄毒苷的产物。进一步分析了这两种产品对心肌细胞凋亡及其抗肿瘤活性的影响。结果发现,与底物洋地黄毒苷和参考物质地高辛相比,洋地黄毒苷原和11α-羟基洋地黄毒苷对大鼠心肌细胞的凋亡作用明显降低。但未观察到对人乳腺癌细胞MCF-7,大鼠乳腺癌细胞4T1,人宫颈癌Hela和大鼠黑色素瘤细胞B-16这四个肿瘤细胞有明显的抗肿瘤活性。

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