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首页> 外文期刊>World Journal of Microbiology and Biotechnology >Influence of Agrobacterium rhizogenes on induction of hairy roots and benzylisoquinoline alkaloids production in Persian poppy (Papaver bracteatum Lindl.): preliminary report
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Influence of Agrobacterium rhizogenes on induction of hairy roots and benzylisoquinoline alkaloids production in Persian poppy (Papaver bracteatum Lindl.): preliminary report

机译:发根农杆菌对波斯罂粟(Papaver bracteatum Lindl。)毛状根诱导和苄基异喹啉生物碱产生的影响:初步报告

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摘要

Persian poppy (Papaver bracteatum Lindl.) is an important medicinal plant and source of the opium alkaloids codeine, morphine and thebaine. Transgenic root cultures of P. bracteatum Lindl. are well-defined model systems to investigate the molecular and metabolic regulation of benzylisoquinoline alkaloid biosynthesis. Agrobacterium rhizogenes was able to produce hairy roots on wounded Persian poppy seedlings. Excised shoots from 7-day-old Persian poppy were co-cultivated with the A. rhizogenes strain R15834 carrying the pBI121 binary vector. All media, except for the co-cultivation medium, included 40 mg l?1 paromomycin to select for pBI121 transformants and 200 mg l?1 cefotaxime to eliminate the Agrobacterium. Eight weeks after infection, paromomycin-resistant roots appeared on 45–50% of explants maintained on hormone-free medium. Isolated hairy roots were propagated in liquid medium containing 1.0 mg l?1 1-naphthaleneacetic acid to promote rapid growth. Also, callus induction and shoot regeneration of transformed Calli in vitro was achieved on B5 medium containing 1.0 mg l?1 1-naphthaleneacetic acid. Detection of the neomycin phosphotransferase gene and GUS histochemical localization confirmed the integrative transformation of root cultures. This is the first study to illustrate useful protocol to introduce foreign genes into transgenic Persian poppy hairy root cultures using A. rhizogenes strain R15834.
机译:波斯罂粟(Papaver bracteatum Lindl。)是重要的药用植物,也是鸦片生物碱可待因,吗啡和蒂巴因的来源。百日草的转基因根培养。是定义明确的模型系统,用于研究苄基异喹啉生物碱生物合成的分子和代谢调控。发根农杆菌能够在受伤的波斯罂粟幼苗上产生毛状根。将来自7天大的波斯罂粟的切下的芽与带有pBI121二元载体的发根农杆菌菌株R15834共培养。除共培养培养基外,所有培养基均包括40 mg l?1 巴龙霉素以选择pBI121转化子,以及200 mg l?1 头孢噻肟以消除农杆菌。感染后八周,在​​不含激素的培养基中外植体的45-50%出现了耐巴龙霉素的根。分离出的毛状根在含有1.0 mg l?1 1-萘乙酸的液体培养基中繁殖,以促进快速生长。此外,在含有1.0 mg l?1 1-萘乙酸的B5培养基上,可以实现对转化愈伤组织的愈伤组织诱导和芽再生。新霉素磷酸转移酶基因的检测和GUS组织化学定位证实了根培养物的整合转化。这是第一个阐明使用外源基因使用发根农杆菌菌株R15834将外源基因引入转基因波斯罂粟毛状根培养物中的有用方案的研究。

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