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Shikimic acid production from Ginkgo biloba via callus culture

机译:Shikimic酸生产从银杏叶通过愈伤组织培养

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Shikimic acid is a very important precursor for industrial synthesis of oseltamivir (Tamiflu~R) which is used for the antiviral treatment. In this study, callus culture of Ginkgo biloba for shikimic acid production was reported. Callus induced from either leaves or nodal stems of sterilized ginkgo was grown on MS medium supplemented with a combination of plant growth regulators as followed: MS+KD, MS+BD, MS+KN and MS+BN for 90 days. Morphological changes, fresh weight and shikimic acid content of callus in each medium were monitored every 30 days. The result showed that callus cultures from each treatment were morphologically different. It is likely due to explant used for callus induction and type of plant growth regulators added into the medium. Browning effect was noticeably detected from 60 days to 90 days. Moreover, fresh weight and shikimic acid content of callus culture depended on cultivation time, cultivation medium and type of explants used for callus induction. Callus induced from nodal stem grown on MS+BN for 30 days offered the highest fresh weight. For shikimic acid production, the most satisfied quantity of shikimic acid was achieved from callus cultured on MS+KN for 30 days by exploiting nodal stem as explant.
机译:Shikimic acid是一种非常重要的奥司他虫(Tamiflu〜R)的工业合成前体,用于抗病毒治疗。在本研究中,报道了Ginkgo Biloba的愈伤组织培养物。从灭菌银杏的任何叶片或节点茎诱导的愈伤组织在补充有植物生长调节剂组合的MS培养基上,如如下所示:MS + Kd,MS + Bd,MS + KN和MS + BN持续90天。每30天监测每种培养基中愈伤组织的形态变化,新鲜重量和Shikimic酸含量。结果表明,来自每种治疗的愈伤组织培养物在形态上不同。它可能是由于用于愈伤组织诱导和植物生长调节剂的植物的外植体。从60天至90天开始褐变效果。此外,愈伤组织培养的新鲜重量和籽酸含量依赖于培养时间,培养培养基和用于愈伤组织诱导的外植体。从Nodal茎诱导的愈伤组织在MS + BN上生长30天,提供了最高的鲜重量。对于Shikimic酸生产,通过剥削节点茎作为外植体,通过在MS + Kn上培养30天的愈伤组织来实现最满意的Shikimic酸。

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