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首页> 外文期刊>Indian journal of pharmaceutical sciences. >Purification, Fractionation and Characterization of Anthocyanin from in vitro Culture of Bridelia retusa (L.) Spreng
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Purification, Fractionation and Characterization of Anthocyanin from in vitro Culture of Bridelia retusa (L.) Spreng

机译:来自Bridelia Retusa(L.)Speng的体外培养的花青素的纯化,分馏和表征

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摘要

Bridelia retusa is traditionally used as an astringent and for treating rheumatic pains. Present study revealed that 2,4-dichlorophenoxyacetic acid alone or in combination with kinetin-fortified Murashige and Skoog medium showed good response in terms of callus from leaf explants of B. retusa. Growth hormones, pH, light, and carbon source influenced secondary metabolic pathways. The highest callus induction was 98.9 % with N6-benzyladenine (2.5 mg/l) and 2,4-dichlorophenoxyacetic acid (2 mg/l). The optimal fresh and dry weights of the calli were 1.9 +/- 0.04 and 0.45 +/- 0.03 g, respectively. The calli incubated in light on Murashige and Skoog medium with 4 % glucose containing benzyladenine (2.5 mg/l) and 2,4-dichlorophenoxyacetic acid (2 mg/l) at pH 3.5 yielded 2.8 mg/g of anthocyanins. Murashige and Skoog medium with glucose was optimal compared to sucrose for anthocyanin synthesis. Addition of kinetin inhibited anthocyanin accumulation. Pigmented calli transferred to half strength Murashige and Skoog medium with NH+/NO3 (1: 4 ratio), 70 g/l sucrose and supplementation with benzyladenine and 2,4-dichlorophenoxyacetic acid produced remarkable biomass production with anthocyanin synthesis when compared with the initial culture conditions. Suspension cultures of Murashige and Skoog medium containing 2,4-dichlorophenoxyacetic acid (2.5 mg/l) and benzyladenine (2 mg/l) at pH 5.0 induced anthocyanin synthesis into the medium with pH 4.44.6. HCl-water and HCl-ethanol extractions for 90 min was attempted to obtain the maximum amount of anthocyanin content. Temperature factors and pH against anthocyanin extraction and stability was analyzed. Enhancement in the degradation rate constant with a corresponding decline in the t(1/2) values was seen with the increasing temperature at pH 1 and 4. Fractionation of anthocyanin was carried by high performance liquid chromatography coupled mass spectrometry revealed 09 fractions comprising acylated cyanidins and two peonidins. The major compounds were cyanidin 3-p-coumaroyl and feruloyl diglucoside-5-glucosides. Thus, the calli from leaf explants could be a good source for anthocyanin synthesis.
机译:Bridelia Retusa传统上用作涩味和治疗风湿疼痛。目前的研究表明,单独的2,4-二氯苯酸乙酸单独或与Kinetin-Figtified Murashige和Skoog培养基的组合表现出良好的愈伤组织从B. Retusa的叶子外植物的愈伤组织。生长激素,pH,光和碳源影响二次代谢途径。最高的愈伤组织诱导为98.9%,N6-苄基腺嘌呤(2.5mg / L)和2,4-二氯苯乙酸(2mg / L)。 Calli的最佳新鲜和干重分别为1.9 +/- 0.04和0.45 +/- 0.03g。在Murashige和Skoog培养基上孵育的愈伤组织在Murashige和Skoog培养基中,在pH 3.5的苄基腺嘌呤(2.5mg / L)和2,4-二氯苯甲酸乙酸(2mg / L)的4%葡萄糖产生2.8mg / g的花青素。与花青素合成的蔗糖相比,Murashige和Skoog培养基是最佳的。添加导素抑制花青素积累。用NH + / NO3(1:4比例),70克/升蔗糖和2,4-二氯苯乙烯酸的补充剂转移到半强度Murashige和Skoog培养基,并与初始培养相比,用青霉素合成产生显着的生物质生产。状况。 Murashige和Skoog培养基的悬浮培养物在pH 5.0诱导pH5.0的pH5.0诱导培养型培养基中的2,4-二氯苯乙烯酸(2.5mg / L)和苄基腺嘌呤(2mg / L)。 HCl-水和HCl-乙醇提取90分钟,以获得最大量的花青素含量。分析了温度因子和对抗青少年素提取和稳定性的pH。在pH 1和4的升高温度下观察到具有相应的T(1/2)值下降的降解速率恒定的增强,并且通过高效液相色谱偶联质谱法携带花青素的分馏显示了包含酰化Cyanidins的09级分和两个peonidins。主要化合物是Cyanidin 3-P-Coumaroyl和Foruloyl碳粉酰胺-5-葡糖苷。因此,来自叶片外植体的愈伤组织可能是花青素合成的好来源。

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