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Rapid and Easy High-Molecular-Weight Glutenin Subunit Identification System by Lab-on-a-Chip in Wheat (Triticum aestivum L.)

机译:通过实验室芯片在小麦(Triticum aestivum L.)中快速简便的高分子量谷蛋白亚基鉴定系统

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摘要

Lab-on-a-chip technology is an emerging and convenient system to easily and quickly separate proteins of high molecular weight. The current study established a high-molecular-weight glutenin subunit (HMW-GS) identification system using Lab-on-a-chip for three, six, and three of the allelic variations at the Glu-A1, Glu-B1, and Glu-D1 loci, respectively, which are commonly used in wheat breeding programs. The molecular weight of 1Ax1 and 1Ax2* encoded by Glu-A1 locus were of 200 kDa and 192 kDa and positioned below 1Dx subunits. The HMW-GS encoded by Glu-B1 locus were electrophoresed in the following order below 1Ax1 and 1Ax2*: 1Bx13 ≥ 1Bx7 = 1Bx7OE > 1Bx17 > 1By16 > 1By8 = 1By18 > 1By9. 1Dx2 and Dx5 showed around 4-kDa difference in their molecular weights, with 1Dy10 and 1Dy12 having 11-kDa difference, and were clearly differentiated on Lab-on-a-chip. Additionally, some of the HMW-GS, including 1By8, 1By18, and 1Dy10, having different theoretical molecular weights showed similar electrophoretic mobility patterns on Lab-on-a-chip. The relative protein amount of 1Bx7OE was two-fold higher than that of 1Bx7 or 1Dx5 and, therefore, translated a significant increase in the protein amount in 1Bx7OE. Similarly, the relative protein amounts of 8 & 10 and 10 & 18 were higher than each subunit taken alone. Therefore, this study suggests the established HMW-GS identification system using Lab-on-a-chip as a reliable approach for evaluating HMW-GS for wheat breeding programs.
机译:实验室上的单芯片技术是一个新兴的方便的系统,高分子量的容易且快速地分开的蛋白质。目前的研究确立了高分子量麦谷蛋白亚基(HMW-GS)识别使用Lab-上的单芯片系统为三,六,和三个在GLU-A1,GLU-B1中的等位基因变异的,和Glu -D 1位点,分别,它们通常在小麦育种计划中。 1Ax1和1Ax2 *由GLU-A1基因座编码的分子量分别为200 kDa的和192千道尔顿和位于下方1DX亚基。 1Bx13≥1Bx7 = 1Bx7OE> 1Bx17> 1By16> 1By8 = 1By18> 1By9:所述HMW-GS编码由谷氨酸-B1位点在下面1Ax1和1Ax2 *下列顺序进行电泳。 1Dx2和Dx5的显示周围4- kDa的差在它们的分子量,与1Dy10和1Dy12具有11-kDa的差异,并明确区分在Lab-上的单芯片。此外,一些所述HMW-GS,包括1By8,1By18和1Dy10,具有不同的理论分子量表明在Lab-上的单芯片类似电泳迁移率的模式。 1Bx7OE的相对蛋白量为2倍比1Bx7或1Dx5的更高,因此,在翻译中1Bx7OE蛋白量的显著增加。类似地,相对蛋白量的8 10和10 18比单独采用每个亚基更高。因此,这项研究表明使用Lab-上的单芯片作为评价HMW-GS小麦育种计划的可靠方法的建立HMW-GS识别系统。

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