Fu Chun-Xiang, Jin Zhi-Ping, Yang Rui, Wu Feng-Yan, Zhao De-Xiu
Institute of Botany, Chinese Academy of Sciences, Beijing 100093, China.
Sheng Wu Gong Cheng Xue Bao. 2004 May;20(3):366-71.
Hairy root clones of Saussurea involucrata transformed with Agrobacterium rhizogenes strains R1601, R1000, and LBA9402 were established to investigate the flavonoid production. Opine synthesis and PCR analysis confirmed the integration of the T-DNA fragment of Ri plasmid from A. rhizogenes strain R1601 into the transformed root genome. The frequency of hairy root formation from root segments, which were pre-cultured 2 days in N6 solid medium without plant growth regulators, amounted to 100% following infection with R1601 strain of A. rhizogenes. The transformed roots were kept in hormone-free N6 liquid medium in the dark at 25 degrees C, 110r/min and routinely subcultured every 20 - 24 days. One hairy root clone, which grew vigorously with lateral branches, was periodically examined for the ability to produce flavonoid. The maximum of biomass and flavonoid yield achieved 66.7 g/L (fresh weight) and 102.3mg/g dry weight after incubation 20 days. The calli were induced from the hairy root culture in the presence of 0.5mg/L IBA and intact plantlets were regenerated from these calli. The regeneration plantlets from hairy roots, in which the flavonoid content were 53% in that of untransformed plants, weren't different in growth and morphology of the untransformed plantlets. Therefore plant regeneration from hairy roots may be also a means for producing transformed S. involucrata plants. Hairy root cultures of S. involucrata clearly showed higher flavonoid contents compared to the wild plant or the regeneration seedlings. As the wild S. involucrata grows only in special regions with peculiar climate, and cultivation of this species in a normal climate has been unsuccessful so far. The success in obtaining a method for high production of flavonoid might very well be one of the solutions for this problem in the future.
为了研究黄酮类化合物的产生,建立了用发根农杆菌菌株R1601、R1000和LBA9402转化的雪莲毛状根克隆。冠瘿碱合成和PCR分析证实发根农杆菌菌株R1601的Ri质粒的T-DNA片段整合到了转化根基因组中。在不含植物生长调节剂的N6固体培养基中预培养2天的根段,在用发根农杆菌R1601菌株感染后,毛状根形成频率达到100%。将转化根置于不含激素的N6液体培养基中,在25℃、110r/min的黑暗条件下培养,并每隔20 - 24天定期继代培养。对一个生长旺盛且有侧枝的毛状根克隆进行定期检测,以评估其产生黄酮类化合物的能力。培养20天后,生物量和黄酮产量最高分别达到66.7g/L(鲜重)和102.3mg/g干重。在0.5mg/L IBA存在的情况下,从毛状根培养物中诱导出愈伤组织,并从这些愈伤组织中再生出完整植株。来自毛状根的再生植株,其黄酮含量为未转化植株的53%,在生长和形态上与未转化植株没有差异。因此,从毛状根再生植株也可能是生产转化雪莲植株的一种方法。与野生植株或再生幼苗相比,雪莲毛状根培养物中的黄酮含量明显更高。由于野生雪莲仅生长在气候特殊的特定区域,迄今为止,在正常气候条件下种植该物种尚未成功。成功获得一种高产黄酮类化合物的方法很可能是未来解决这一问题的方案之一。