首页> 外文期刊>Journal of crop science and Biotechnology >Evaluating Genetic Biodiversity of Parkia biglobosa (Jacq.) R. Br. Ex Don (African Locust Bean) Accessions from Nigeria Using Seed Protein Electrophoresis
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Evaluating Genetic Biodiversity of Parkia biglobosa (Jacq.) R. Br. Ex Don (African Locust Bean) Accessions from Nigeria Using Seed Protein Electrophoresis

机译:评估Parkia Biglobosa的遗传生物多样性(JACQ。)R.Br。 前唐(非洲蝗虫)从尼日利亚使用种子蛋白电泳来加入

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摘要

Thirty-four accessions of African locust bean (Parkia biglobosa) collected from different localities across Nigeria were screened for variability in seed storage proteins. Globulin, albumin, and vicilin fractions were investigated by means of sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) and native PAGE. Both methods of analysis revealed a substantial degree of heterogeneity in the protein fractions. However, native PAGE produced fewer protein bands and profiles than SDS-PAGE.Although accessions exhibited significant similarity in their polypeptide profiles, differences in migration rate and staining intensities as well as presence / absence of specific bands accounted for variations obtained in the accessions examined. The absence of 10 kDa albumin subunit was specific to accessions 24, 25, 26, and 29 while the presence of 30.4 kDa vicilin was unique to accessions 5, 6, and 7. One major cluster of globulin band between two polypeptides 42.7 - 50 kDa, and two minor bands 31.4 and 16.2 kDa were observed. Protein fraction profiles were in most cases not similar among the accessions collected from same agroecological zone. This suggests that gene flow between the different zones must have occurred due to movement of germplasmand exchange of genetic material among farmers and markets. Groupings based on cluster analysis and polypeptide patterns agree and confirm the presence of duplicates within the accessions studied.
机译:在尼日利亚跨尼日利亚的不同地区收集的非洲蝗虫(Parkia Biglobosa)的三十四次加入用于种子储存蛋白的可变性。通过十二烷基硫酸钠聚丙烯酰胺凝胶电泳(SDS-PAGE)和天然页面来研究球蛋白,白蛋白和维生素级分。两种分析方法揭示了蛋白质级分中的相当程度的异质性。然而,本机页面产生的蛋白质条带和配置文件比SDS-PAGE。虽然载体在其多肽曲线中表现出显着相似性,但迁移率和染色强度的差异以及特定条带的存在/不存在占所检查中获得的变化。没有10kDa白蛋白亚基的载体24,25,26和29种,而30.4kDa vicilin的存在对于探剂5,6和7.两种多肽之间的一组聚球蛋白带簇是独特的.2.7-50kDa观察到两个小条带31.4和16.2 kda。蛋白质馏分曲线在来自相同生态区收集的释放中的大多数情况下不相似。这表明,由于农民和市场之间的种质和遗传物质交换的运动,必须发生不同区域之间的基因流。基于聚类分析和多肽模式的分组同意并确认所研究的载体内的重复情况。

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