作为紫杉醇半合成前体10-去乙酰基紫杉醇III来源的红豆杉的组织培养。

A Zhiri, M Jaziri, Y Guo, R Vanhaelen-Fastré, M Vanhaelen, J Homès, K Yoshimatsu, K Shimomura
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引用次数: 14

摘要

红豆杉愈伤组织的培养。下胚轴和叶片外植体在木本植物培养基上(无激素或添加激素)诱导出缢蛏。在连续黑暗条件下,下胚轴愈伤组织和叶片愈伤组织均可再生不定根。采用兔抗10-琥珀酰-10-去乙酰baccatin III抗体对红豆杉培养物中10-去乙酰baccatin III进行检测和半定量测定。采用薄层色谱(TLC)、高效液相色谱(HPLC)和质谱(CI-MS)等方法证实了愈伤组织提取物中10-去乙酰巴accatin III的存在。在叶源愈伤组织提取物中检测到最高的类杉衍生物当量含量(7.83 mg/100 g干wt.)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Tissue cultures of Taxus baccata as a source of 10-deacetylbaccatin III, a precursor for the hemisynthesis of taxol.

Callus cultures of Taxus baccata L. cv. stricta were induced from hypocotyl and leaf explants on Woody Plant medium (hormone-free or additionated with phytohormones). Under continuous dark condition, adventitious roots were regenerated from hypocotyl- and leaf-derived callus cultures. Antibodies raised in rabbits against 10-succinyl-10-deacetylbaccatin III were used for the detection and the semi-quantitative determination of 10-deacetylbaccatin III in Taxus cultures. The presence of 10-deacetylbaccatin III in callus extracts was confirmed by TLC, HPLC using a photodiode array detector and mass spectrometry (CI-MS). The highest equivalent content of the taxoid derivatives (7.83 mg/100 g dry wt.) was detected in an extract from leaf-derived callus.

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