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首页> 外文期刊>Industrial Crops and Products >Isolation and optimization of plumbagin production in root callus of Plumbago zeylanica L. augmented with chitosan and yeast extract
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Isolation and optimization of plumbagin production in root callus of Plumbago zeylanica L. augmented with chitosan and yeast extract

机译:用壳聚糖和酵母提取物中肠球菌愈伤组愈伤组织的分离与优化。用壳聚糖和酵母提取物

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Chitrak (Plumbago zeylanica L.), a renowned traditional medicinal plant, is being exploited extensively for its roots which are employed in the preparations of many important herbal products (e.g. Dashmularisht, Chitrakadivati) possessing anticancer, anti-atherogenic, cardiotonic, hepatoprotective and neuroprotective properties. P. zeylanica roots, being the major source of plumbagin, were used for its isolation. Plumbagin isolation from in vivo roots was done employing column chromatography and thin layer chromatography (TLC) using a hexane: ethyl acetate (70:30) mobile phase. A total of 65 fractions were obtained which pooled down to 8 (F1-F8) based on their similar Rf values. Of the 8 fractions, F2 gave a single spot corresponding to that of the standard plumbagin which subsequently was validated and confirmed through H-1-NMR and FT-IR. For elicitation to increase plumbagin, in vitro root callus initially raised on Murashige and Skoog medium + 5 mu M TDZ was augmented with different concentrations of precursors (sodium acetate, L-tyrosine), biotic (chitosan, proline, lysine, salicylic acid, yeast extract) and abiotic [Pb(NO3)(2), CdCl2] elicitors either alone or in combinations. The optimum increase of up to 2.07 and 2.64-folds in plumbagin was seen when callus cultures were fed individually with sodium acetate (1 mg/L) and L-tyrosine (25 mg/L), respectively. Similarly, chitosan and yeast extract when used alone, the plumbagin content was enhanced 4.58-fold at 50 mg/L and 6.50-fold at 100 mg/L, respectively. However, an enormous increase of 12.08-fold plumbagin content occurred when a combination of 50 mg/L chitosan + 100 mg/L yeast extract was used. A combination of salicylic acid (25 mu M) and yeast extract (100 mg/L) also enhanced plumbagin content up to 8.23-fold. Thus, this is our first report of scaling up to 12.08-fold plumbagin content using simple and cost effective elicitors.
机译:Chitrak(Plumbago Zeylanica L.)是一位着名的传统药用植物,正在广泛利用它的根源,这些植物是在许多重要的草药产品(例如Dashmularisht,Chitrakadivati)的制剂中,具有抗癌,抗动脉粥样硬化,肝脏保护和神经保护作用特性。 P. Zeylanica Roots,是肠球素的主要来源,用于其分离。使用己烷:乙酸乙酯(70:30)流动相,采用柱色谱和薄层色谱(TLC)从体内根部分离使用柱色谱和薄层色谱(TLC)。获得总基于其相似的RF值汇集到8(F1-F8)的65个级分。在8个级分中,F2给出了对应于标准铅素蛋白的单点,随后通过H-1-NMR和FT-IR确认。对于诱导增加肠果,最初在Murashige和Skoog培养基上提高的体外根愈伤组织+ 5亩M TDZ以不同浓度的前体(醋酸钠,L-酪氨酸),生物(壳聚糖,脯氨酸,赖氨酸,水杨酸,酵母)增强提取)和非生物[Pb(NO 3)(2),CDCL2]诱导单独或组合。当愈伤组织培养物用醋酸钠(1mg / L)和L-酪氨酸(25mg / L)单独进料时,观察到肠道素高达2.07和2.64倍的最佳增加。类似地,壳聚糖和酵母提取物单独使用,分别以50mg / L和6.50倍的50mg / L增强4.58倍和6.50倍。然而,当使用50mg / L壳聚糖+ 100mg / L酵母提取物时,发生巨大增加12.08倍的肠果含量。水杨酸(25μm)和酵母提取物(100 mg / L)的组合也增强了肠果含量高达8.23倍。因此,这是我们使用简单且具有成本效益的Elicitors缩放高达12.08倍的朱敏素内容的第一个报告。

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