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首页> 外文期刊>Plant Cell, Tissue and Organ Culture: An International Journal on in Vitro Culture of Higher Plants >Metabolic evaluation of cellular differentiation of tobacco leaf explants in response to plant growth regulators in tissue cultures using 1H NMR spectroscopy and multivariate analysis.
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Metabolic evaluation of cellular differentiation of tobacco leaf explants in response to plant growth regulators in tissue cultures using 1H NMR spectroscopy and multivariate analysis.

机译:利用 1 H NMR光谱和多变量分析对组织培养中植物生长调节剂响应的烟叶外植体细胞分化进行代谢评估。

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摘要

To investigate the metabolic changes that precede visible organogenesis in tissue culture, tobacco leaf explants were cultured on media supplemented with various plant growth regulators (PGRs) and analyzed with proton nuclear magnetic resonance (1H NMR) spectroscopy. Principal component analysis (PCA) of 1H NMR spectral data was unable to differentiate between leaf explants cultured with alpha -naphthaleneacetic acid and those cultured with 6-benzyladenine after 4 days of culture; however, a difference was evident after 8 days of culture. A hierarchical dendrogram from PCA analysis could be grouping leaf explants cultured with various auxins separately from those treated by various cytokinins. However, leaf explants cultured with thidiazuron (TDZ) were identified as an outlier group; TDZ appeared to produce pleiotropic metabolic effects that differed from those induced by other PGRs. These results show that dedifferentiation can be initiated by either auxins or cytokinins, which is reflected by similar metabolic changes produced by the two distinct PGRs during the initial incubation period. The subsequent redifferentiation differs according to the PGR treatment, which is reflected by differential metabolic changes, depending on the fate of cells in organogenesis. Glutamine and glutamate levels increased approximately twofold in cytokinin-treated leaf explants compared with auxin-treated explants; however, changes in the levels of sugar compounds did not differ between the two treatments, demonstrating auxin regulation of the carbonitrogen ratio in favor of rooting. Taken together, our results suggest that 1H-NMR spectroscopy combined with multivariate analysis is a promising means for the metabolic evaluation of plant growth and differentiation.
机译:为了研究组织培养中可见器官发生之前的代谢变化,将烟叶外植体培养在添加了多种植物生长调节剂(PGR)的培养基上,并用质子核磁共振波谱( 1 H NMR)进行分析。培养4天后, 1 1H NMR光谱数据的主成分分析(PCA)无法区分使用α-萘乙酸和6-苄基腺嘌呤培养的叶片外植体。但是,培养8天后差异明显。 PCA分析得出的树状图可以将用各种生长素培养的外植体与用各种细胞分裂素处理的外植体分开进行分组。然而,用噻唑隆(TDZ)培养的叶片外植体被确定为一个离群群体。 TDZ似乎产生与其他PGR诱导的多效代谢作用不同。这些结果表明,去分化可以由生长素或细胞分裂素引发,这可以通过初始孵育期间两个不同的PGR产生的相似代谢变化来反映。随后的再分化根据PGR的处理而不同,这取决于器官发生过程中细胞的命运,这由代谢差异的变化反映出来。与用生长素处理的外植体相比,用细胞分裂素处理的叶片外植体中的谷氨酰胺和谷氨酸水平增加了约两倍;然而,两种处理之间糖类化合物含量的变化没有差异,表明生长素调节碳/氮比有利于生根。综上所述,我们的结果表明, 1 H-NMR光谱技术与多变量分析相结合是一种用于植物生长和分化代谢评估的有前途的手段。

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