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Intra-specific genetic relationship analyses of Elaeagnus angustifolia based on RP-HPLC biochemical markers

机译:基于RP-HPLC生化标志物的沙枣(Elaeagnus angustifolia)种内遗传关系分析

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Elaeagnus angustifolia Linn. has various ecological, medicinal and economical uses. An approach was established using RP-HPLC (reversed-phase high-performance liquid chromatography) to classify and analyse the intra-specific genetic relationships of seventeen populations of E. angustifolia, collected from the Xinjiang areas of China. Chromatograms of alcohol-soluble proteins produced by seventeen populations of E. angustifolia, were compared. Each chromatogram of alcohol-soluble proteins came from a single seed of one wild plant only. The results showed that when using a Waters Delta Pak. C18, 5 microm particle size reversed phase column (150 mm x 3.9 mm), a linear gradient of 25%-60% solvent B with flow rate of 1 ml/min and run time of 67 min, the chromatography yielded optimum separation of E. angustifolia alcohol-soluble proteins. Representative peaks in each population were chosen according to peak area and occurrence in every seed. The converted data on the elution peaks of each population were different and could be used to represent those populations. GSC (genetic similarity coefficients) of 41% to 62% showed a medium degree of genetic diversity among the populations in these eco-areas. Cluster analysis showed that the seventeen populations of E. angustifolia could be divided into six clusters at the GSC=0.535 level and indicated the general and unique biochemical markers of these clusters. We suggest that E. angustifolia distribution in these eco-areas could be classified into six variable species. RP-HPLC was shown to be a rapid, repeatable and reliable method for E. angustifolia classification and identification and for analysis of genetic diversity.
机译:Elaeagnus angustifolia Linn。具有各种生态,医学和经济用途。建立了一种使用RP-HPLC(反相高效液相色谱)对从中国新疆地区收集的17个大肠埃希氏菌种群的种内遗传关系进行分类和分析的方法。比较了十七种E. angustifolia产生的醇溶性蛋白质的色谱图。醇溶性蛋白质的每个色谱图仅来自一种野生植物的单个种子。结果表明,使用沃特世三角洲包装时。 C18,5微米粒径反相柱(150 mm x 3.9 mm),线性梯度为25%-60%的溶剂B,流速为1 ml / min,运行时间为67分钟,色谱法可实现E的最佳分离Angustifolia醇溶性蛋白质。根据峰面积和每个种子中的出现情况选择每个种群中的代表性峰。每个种群的洗脱峰的转换数据是不同的,可以用来代表那些种群。 GSC(遗传相似系数)在41%至62%之间,表明这些生态区人群的遗传多样性处于中等水平。聚类分析表明,在GSC = 0.535的水平上,十七种马鞭草可分为六个簇,表明了这些簇的一般和独特的生化标记。我们建议,在这些生态区中的E. angustifolia分布可分为六个可变物种。 RP-HPLC被证明是一种快速,可重复和可靠的方法,用于安氏小肠埃希菌的分类和鉴定以及遗传多样性的分析。

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