首页> 外文期刊>Asian Journal of Pharmaceutical and Clinical Research >ISOLATION OF TAXOL PRODUCING FUSICOCCUM SPECIES FROM CURRY LEAF AND ITS RANDOM AMPLIFIED POLYMORPHIC DNA ANALYSIS
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ISOLATION OF TAXOL PRODUCING FUSICOCCUM SPECIES FROM CURRY LEAF AND ITS RANDOM AMPLIFIED POLYMORPHIC DNA ANALYSIS

机译:咖喱叶中产生紫杉醇的镰刀菌属物种的分离及其多态性多态性DNA分析

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Objective: The potential compound of taxol has been used treatment of cancer in the medical field. This study is focused on the extraction of taxol from Fusicoccum sp. Methods: The pathogenic strain was grown in MID medium for the taxol production and extracted from the Fusicoccum culture filtrate and processed to the ultraviolet (UV)-spectroscopy analysis as well as infrared (IR) spectra analysis was done, and the sample was performed to the high-performance column chromatography and further processed to the random amplified polymorphic DNA (RAPD) analysis of specific primer is PGFO1, PGFO2 are performed. Results: UV-visible spectral analysis showed maximum value for 273 nm. The result of IR-spectrum analysis to find out the functional groups present in sample and characteristic peak to conform the existences of OH group. The presence of taxol was confirmed using column chromatography. An analysis of taxol production was on the external standard of authentic taxol. The column chromatography process shows the amount of taxol production by Fusicoccum spp. 325 μg/L. RAPD analysis indicates the genetic relation among all isolates of fungus was analyzed by two random primers PGF01 and PGF02. Conclusion: The present investigation revealed that the taxol production from biological source was a significant effect, and the presence of taxol amount is analysis in Fusicoccum sp. 325 μg/L. The RAPD analysis of genetic stability of in vitro grown fungus and genotypic with two different primers shows that five fungus species with corresponding primer efficiency was amplified.
机译:目的:紫杉醇的潜在化合物已在医学领域用于治疗癌症。这项研究的重点是从镰刀菌中提取紫杉醇。方法:将病原菌在MID培养基中生长以生产紫杉醇,并从镰刀菌培养滤液中提取,然后进行紫外(UV)光谱分析和红外(IR)光谱分析,并进行样品分析。高性能柱色谱法,然后进一步处理,以随机扩增多态性DNA(RAPD)分析特异性引物是PGFO1,PGFO2。结果:紫外可见光谱分析显示最大值为273 nm。红外光谱分析的结果是找出样品中存在的官能团和特征峰,以证实OH基团的存在。使用柱色谱法确认紫杉醇的存在。紫杉醇产量的分析是基于真实紫杉醇的外标进行的。柱色谱法显示了镰刀菌产生的紫杉醇的量。 325微克/升RAPD分析表明,通过两个随机引物PGF01和PGF02分析了真菌的所有分离株之间的遗传关系。结论:本研究表明,从生物来源生产紫杉醇具有显着效果,并且分析了镰刀菌属中紫杉醇的存在。 325微克/升用两种不同的引物对真菌和基因型的遗传稳定性进行RAPD分析表明,扩增了5种具有相应引物效率的真菌。

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