首页> 外国专利> METHOD FOR PREPARING ACANTHOPANAX SENTICOSUS TISSUE CULTURE PRODUCT CONTAINING ELEUTHEROSIDES AND OTHER PHYSIOLOGICALLY ACTIVE SUBSTANCE

METHOD FOR PREPARING ACANTHOPANAX SENTICOSUS TISSUE CULTURE PRODUCT CONTAINING ELEUTHEROSIDES AND OTHER PHYSIOLOGICALLY ACTIVE SUBSTANCE

机译:制备含有辣椒苷和其他生理活性物质的刺五加组织培养产品的方法

摘要

PURPOSE:To massively produce an Acanthopanax senticosus tissue cultured product containing physiologically active substances in the same amounts as the natural Acanthopanax senticosus by culturing a callus derived from the plant tissue of the Acanthopanax senticosus in a medium containing ammonium sulfate. CONSTITUTION:The plant tissue of Acanthopanax senticosus is sterilized with an alcohol, antiformin, etc., embedded aseptically in a nutritive agar medium containing auxin and cytokinin and subsequently cultured at 23-27 deg.C in a dark state. A callus is generated from the small piece of the tissue and subcultured in the same medium until the growth of a size larger 3-4 times than the original size for 4 weeks. The calluses are subsequently cultured in a medium containing ammonium sulfate preferably in an amount of 100-200mg/l, such as Gamborg B-5 medium at 23-27 deg.C to produce the Acanthopanax senticosus tissue cultured product containing eleutherosides and physiologically active substances such as isofraxidin and chlorogenic acid in the same or more amounts as the natural Acanthopanax senticosus.
机译:目的:通过在含有硫酸铵的培养基中培养源自刺五加植物组织的愈伤组织,以大量生产含有与天然刺五加相同数量的生理活性物质的刺五加组织培养产品。组成:刺五加的植物组织用酒精,抗福尔马林等消毒,无菌包埋在含有生长素和细胞分裂素的营养琼脂培养基中,然后在黑暗状态下于23-27℃培养。从一小块组织中产生愈伤组织,并在相同的培养基中进行继代培养,直到4周内生长出比原始大小大3-4倍的大小。随后将愈伤组织在含有硫酸铵(优选量为100-200mg / l)的培养基中进行培养,例如Gamborg B-5培养基,温度为23-27℃,以生产出含有五倍子苷和生理活性物质的刺五加组织培养产品。例如异氟昔丁和绿原酸的含量与天然刺五加相同或更多。

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