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首页> 外文期刊>World Journal of Microbiology & Biotechnology >Hairy root cultures of butterfly pea (Clitoria ternatea L.): Agrobacterium x plant factors influencing transformation.
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Hairy root cultures of butterfly pea (Clitoria ternatea L.): Agrobacterium x plant factors influencing transformation.

机译:蝴蝶豌豆(Clitoria ternatea L.)的毛状根培养物:影响转化的农杆菌x植物因子。

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摘要

Transformed rhizoclones were developed from Agrobacterium-treated explants of the medicinally important twinning legume Clitoria ternatea L. Several key factors influencing transformation events were optimized. A4T was the most infectious among the strains employed. Internode segments were more responsive than leaves, outdoor-grown explants preferred to those from in vitro cultures. High frequency transformation, resulting in up to 85.8% rhizogenesis, was attained using pre-pricked internodal explants for immersion (10 min) in Agrobacterium rhizogenes suspension grown overnight with acetosyringone (100 micro M) to an OD660 identical-to 0.6, diluted to a density of 109 cells ml-1, followed by 5-day co-cultivation. Roots were individually cultured in MS0 supplemented with the bacteriostatic antibiotic cefotaxime (500 micro g ml-1). Rhizoclones were renewed through successive subcultures in MS0 under diffused illumination. The TL-DNA rolB and rolC ORF were detected in rhizoclones through PCR amplification. The TR-DNA gene encoding mannopine synthase (man2) was revealed by positive amplification and opine gene expression substantiated by agropine and mannopine biosynthesis in all selected transformed rhizoclones. The implication of such findings is discussed on the context of utilization of such genetically transformed root cultures towards sustainable production of medicinally useful phytocompounds, besides providing a means for plant conservation.
机译:转化的根瘤菌是由农杆菌处理的药用重要双生豆科植物 Clitoria ternatea L转化而来的。优化了影响转化事件的几个关键因素。在所用菌株中,A4T最具传染性。节间节段比叶子更敏感,而室外种植的外植体更胜于叶子。使用预先刺穿的节间外植体浸泡(10分钟)并用乙酰丁香酮(100 micro M)过夜生长至OD < sub> 660 等于0.6,稀释至10 9 细胞ml -1 的密度,然后进行5天共培养。在补充了抑菌抗生素头孢噻肟(500 micro g ml -1 )的MS0中分别培养根。通过在弥散照明下在MS0中连续传代培养来更新根瘤菌。在根瘤菌中检测到 T L -DNA rol B和 rol C ORF通过PCR扩增。通过阳性扩增和阿片基因表达揭示了编码甘露平合酶( man 2)的 T R -DNA基因在所有选定的转化的根瘤菌中均被农业碱和甘露聚糖的生物合成所证实。除了为植物保护提供手段外,还讨论了利用这些遗传转化的根系培养物以可持续生产可药用的植物化合物的背景,讨论了这些发现的含义。

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