马生军, 王文全. 不同浓度锰处理对甘草 SQS1基因表达及其甘草酸含量影响的分析J. 药学学报, 2015,50(1): 111-117.
引用本文: 马生军, 王文全. 不同浓度锰处理对甘草 SQS1基因表达及其甘草酸含量影响的分析J. 药学学报, 2015,50(1): 111-117.
MA Sheng-jun, WANG Wen-quan. The expression of SQS1 gene and the content of glycyrrhizic acid of Glycyrrhiza uralensis Fisch. in different concentrations of Mn2+J. Acta Pharmaceutica Sinica, 2015,50(1): 111-117.
Citation: MA Sheng-jun, WANG Wen-quan. The expression of SQS1 gene and the content of glycyrrhizic acid of Glycyrrhiza uralensis Fisch. in different concentrations of Mn2+J. Acta Pharmaceutica Sinica, 2015,50(1): 111-117.

不同浓度锰处理对甘草 SQS1基因表达及其甘草酸含量影响的分析

The expression of SQS1 gene and the content of glycyrrhizic acid of Glycyrrhiza uralensis Fisch. in different concentrations of Mn2+

  • 摘要: 以一年生甘草移栽苗为实验材料, 设置5个锰离子浓度水平, 分别为0、1.81、18.1、36.2和54.3 mg·L-1 (MnSO4·H2O), 利用实时荧光定量PCR和高效液相色谱方法对甘草鲨稀合成酶1 (SQS1) 基因相对表达量和甘 草酸含量进行测定, 从而探讨锰处理对甘草 SQS1基因表达量与甘草酸积累的影响。结果表明随着锰处理浓度的增加, 甘草 SQS1基因的相对表达量和甘草酸含量均呈现先升高后下降的趋势, 且两者之间存在极显著正相关 (P < 0.01, r=0.737)。 SQS1基因表达量在18.1 mg·L-1浓度处理时达到最大值为7.90, 分别是对照 (0 mg·L-1)、1.81、36.2和54.3 mg·L-1处理的1.75、1.37、1.37和2.33倍, 且差异极显著 (P < 0.01)。甘草酸含量在1.81和18.1 mg·L-1浓度处理时达到最大值, 且两者之间差异不显著 (P > 0.05), 与其他3个处理间存在极显著差异 (P < 0.01)。本研究说明适量浓度的锰处理对甘草 SQS1基因的表达和甘草酸的积累具有一定的促进作用。

     

    Abstract: The transplants of one-year-old Glycyrrhiza uralensis Fisch. were subjected to five concentrations of MnSO4·H2O (0, 1.81, 18.1, 36.2 and 54.3 mg·L-1) culturing in vermiculite. qRT-PCR and HPLC were respectively used to measure the relative expression of SQS1 gene and the content of glycyrrhizic acid of G.uralensis in different concentrations of MnSO4·H2O. This is to explore discuss the effects of the expression of SQS1 gene and the accumulation of glycyrrhizic acid by Mn treatment. The results showed both the expression of SQS1 gene and the content of glycyrrhzic acid of G. uralensis tended to rise after the fall of the first with the increase of concentration of Mn treatment. And they were of very significant positive correlation (P < 0.01, r=0.737). Relative expression of SQS1 gene reached the highest 7.90 under 18.1 mg·L-1 MnSO4·H2O treatment. It was very significantly different between 18.1 mg·L-1 concentration of MnSO4·H2O treatment and CK (0 mg·L-1), 1.81, 36.2 and 54.3 mg·L-1 (P < 0.01), and 1.75, 1.37, 1.37, 2.33 times respectively. The content of glycyrrhizic acid reached the highest under 1.81 and 18.1 mg·L-1 MnSO4·H2O treatment, and there were not significant difference (P > 0.05). It was very significantly different between them and other concentrations of MnSO4·H2O treatment (P < 0.01). This study suggests the appropriate concentration of Mn treatment could certain promote the expression of SQS1 gene and the accumulation of glycyrrhizic acid of G. uralensis.

     

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