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首页> 外文期刊>Indian Journal of Plant Physiology >Induction of hairy roots and over production of anthraquinones in Oldenlandia umbellata L.: a dye yielding medicinal plant by using wild type Agrobacterium rhizogenes strain
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Induction of hairy roots and over production of anthraquinones in Oldenlandia umbellata L.: a dye yielding medicinal plant by using wild type Agrobacterium rhizogenes strain

机译:诱导毛根部的生产醌类化合物在Oldenlandia umbellata L。:染料利用野生型的药用植物农杆菌属rhizogenes应变

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摘要

Hairy root cultures of Oldenlandia umbellata L. was established by infecting leaf explants with wild type Agrobacterium rhizogenes strain (MTCC 532). Leaf explants were co-cultured with activated bacteria in half strength Murashige and Skoog (MS) basal medium containing 500 mg l"1 ampicillin for the induction of hairy roots. To facilitate effective transfer of T-DNA of Ri plasmid, duration of co-cultivation and concentration of acetosyringone were standardized as 48 h and 200 uM, respectively. Rootswere produced from the infected leaves within 14 days. Fast growing roots (2-3 cm) were excised and sub-cultured in half strength basal MS liquid medium for the development of transgenic lines. Thus ten hairy root lines were raised and superior line L3 was selected on the basis of fresh weight (1.5 g), dry weight (0.26 g) and anthraquinone (AQ) content (10.374 mg g-1 dry wt). Superior line (L3) was further cultured to test stability of AQ production and found that stable production of AQ during five consecutive sub-cultures. High performance liquid chromatographic method was adopted for quantification of purpurin from samples. Hairy roots produced 21.83 mg g-1 purpurin, while roots from wild growing plants produced 6.08 mg g_1 purpurin. Thus purpurin content in hairy roots was about 3.6 times higher than wild growing roots. Further, polymerase chain reaction based amplification using primers specific for genes rolA, rolB, and rolC confirmed the transformation.
机译:毛状根的文化Oldenlandia umbellata L。建立了感染叶外植体野生型土壤杆菌属(MTCC rhizogenes压力532)。激活一半力量Murashige和细菌斯库格(MS)基础培养基含有500毫克l”1氨苄青霉素诱导的多毛的根源。促进有效的国际扶轮本文分别转让质粒,co-cultivation和持续时间浓度acetosyringone标准化分别为48 h和200嗯。从受感染的叶子在14天内。快速增长的根源(2 - 3厘米)被切除亚文化圈一半力量基底女士液体媒介的发展转基因线。因此十毛状根线是和上级行L3选择的基础上鲜重(1.5 g),干重(0.26 g)蒽醌(AQ)内容(10.374毫克努力干wt)。测试AQ的稳定生产和发现在连续5 AQ的稳定生产亚文化群。采用色谱测定方法量化的红紫素样品。根产生21.83毫克g - 1红紫素级,而根源从野生植物生长产生6.08毫克g_1里面红紫素。是野生的约3.6倍增长的根源。使用引物扩增特定的基因劳拉,rolB rolC证实了转换。

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