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蓝蝴蝶(Clitoria ternatea L.)毛状根培养:影响转化的农杆菌与植物因素。

Hairy root cultures of butterfly pea (Clitoria ternatea L.): Agrobacterium × plant factors influencing transformation.

机构信息

Plant Cell, Tissue & Organ Culture Facility, Post-Graduate Department of Botany, Utkal University, Bhubaneswar, 751 004, Orissa, India.

出版信息

World J Microbiol Biotechnol. 2012 Feb;28(2):729-39. doi: 10.1007/s11274-011-0869-1. Epub 2011 Sep 4.

Abstract

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 μM) to an OD(660) ≅ 0.6, diluted to a density of 10(9) cells ml(-1), followed by 5-day co-cultivation. Roots were individually cultured in MS0 supplemented with the bacteriostatic antibiotic cefotaxime (500 μg ml(-1)). Rhizoclones were renewed through successive subcultures in MS0 under diffused illumination. The T ( L )-DNA rolB and rolC ORF were detected in rhizoclones through PCR amplification. The T ( R )-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.

摘要

转化生根苗是由根癌农杆菌处理药用重要的双生豆科植物三叶赤车使者的外植体产生的。优化了影响转化事件的几个关键因素。A4T 是使用的菌株中最具传染性的。节间段比叶片更有反应性,室外生长的外植体比体外培养的外植体更喜欢。使用预穿孔的节间段外植体进行浸泡(10 分钟),可获得高达 85.8%的生根频率,将过夜生长的带有乙酰丁香酮(100 μM)的根癌农杆菌悬浮液(OD660 约为 0.6)稀释至 10(9)个细胞/ml(1),然后进行 5 天的共培养。将根单独培养在补充有抑菌抗生素头孢噻肟(500 μg/ml)的 MS0 中。通过在漫射光下在 MS0 中进行连续的继代培养来更新生根苗。通过 PCR 扩增在生根苗中检测到 T(L)-DNA rolB 和 rolC ORF。通过阳性扩增和农杆菌和甘露碱生物合成证实了 T(R)-DNA 基因编码甘露碱合酶(man2),所有选定的转化生根苗均表达了该基因。讨论了这些发现的意义,包括利用这些遗传转化的根培养物可持续生产药用植物化合物,以及为植物保护提供一种手段。

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