首页> 外文期刊>Tropical Journal of Pharmaceutical Research >Enhancement of Diosgenin Production in Plantlet and Cell Cultures of Dioscorea zingiberensis by Palmarumycin C13 from the Endophytic fungus, Berkleasmium sp. Dzf12
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Enhancement of Diosgenin Production in Plantlet and Cell Cultures of Dioscorea zingiberensis by Palmarumycin C13 from the Endophytic fungus, Berkleasmium sp. Dzf12

机译:内生真菌Berkleasmium sp。的Palmarumycin C13增强了黄薯薯os和细胞培养物中薯os皂甙元的生产。 Dzf12

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Purpose: To study the effect of palmarumycin C13, an elicitor from the endophytic fungus Berkleasmium sp. Dzf12, on growth and diosgenin production in plantlet or cell cultures of its host plant, Dioscorea zingiberensis . Methods: Palmarumycin C13 was isolated from the ethyl acetate extract of the endophytic fungus Berkleasmium sp. Dzf12 using a combination of high-speed counter-current chromatography (HSCCC), Sephadex LH-20 chromatography and preparative high performance liquid chromatography (HPLC). The biomass of the plantlet and cell cultures of D. zingiberensis as well as their diosgenin content and yield were analyzed after treatment with palmarumycin C13. Results: Optimal elicitation of diosgenin production by palmarumycin C13 in D. zingiberensis plantlet and cell cultures was achieved when palmarumycin C13 was added to the medium at a concentration of 60 mg/L (for plantlet culture) at the beginning of culturing or 10 mg/L (for cell culture) on day 25 after inoculation. By using these optimal concentrations, the diosgenin yield of the cultured plantlets reached its maximum of 6.44 mg/L, that is, > 1.4-fold increase, while diosgenin yield of the cultured cells reached a maximum of 10.73 mg/L, which is an > 8.0-fold increase. Conclusion: Addition of palmarumycin C13 from the endophytic fungus, Berkleasmium sp. Dzf12, is a potentially effective strategy for enhancing diosgenin production in D. zingiberensis plantlet and cell cultures.
机译:目的:研究内生真菌Berkleasmium sp。的引发剂palumarumycin C 13 的作用。 Dzf12,关于其寄主植物Dioscorea zingiberensis的苗或细胞培养物中的生长和薯os皂苷元的生产。方法:从内生真菌Berkleasmium sp。的乙酸乙酯提取物中分离出Palmarumycin C 13 。 Dzf12结合使用了高速逆流色谱(HSCCC),Sephadex LH-20色谱和制备型高效液相色谱(HPLC)。用棕榈茶霉素C 13 处理后,分析了金缕梅植物幼苗和细胞培养物中的生物量以及薯os皂苷元含量和产量。结果:以60 mg的浓度向培养基中添加棕榈棕霉素C 13 可最佳诱导姜黄D. singiberensis苗和细胞培养物中薯gen皂苷元的产生。培养开始时为/ L(用于苗培养)或接种后第25天为10 mg / L(用于细胞培养)。通过使用这些最佳浓度,培养的苗中薯gen皂苷元的产量达到最大值6.44 mg / L,即增加> 1.4倍,而培养细胞的薯in皂苷元的产量达到最大值10.73 mg / L,这是> 8.0倍增加。结论:从内生真菌Berkleasmium sp。中添加了棕榈金霉素C 13 。 Dzf12是提高姜黄D. zingiberensis苗和细胞培养物中薯os皂苷元产量的潜在有效策略。

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