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首页> 外文期刊>Breeding science >Characterization of HMW-GS and evaluation of their diversity in morphologically elite synthetic hexaploid wheats.
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Characterization of HMW-GS and evaluation of their diversity in morphologically elite synthetic hexaploid wheats.

机译:HMW-GS的特性及其在形态上优异的合成六倍体小麦中的多样性评估。

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摘要

High molecular weight glutenin subunit composition and variation in 95 Elite-1 synthetic hexaploid (SH) wheats (Triticum turgidum/Aegilops tauschii; 2n=6x=42; AABBDD) were determined by sodium dodecyl sulphate polyacrylamide gel electrophoresis method (SDS-PAGE). Twenty two different alleles at Glu-1 loci in SHs were observed. Forty four different patterns of HMW-GS in synthetics were found. This higher HMW glutenin composition was due to higher proportion of D-genome encoded subunits in these SHs. 8% urea/SDS-PAGE better discriminated subunit 2* than 12% gels. However 12% urea/SDS-PAGE allowed differentiated mobility of Glu-Dt1 subunits. Genetic variability at Glu-Dt1 locus was greater than Glu-A1 and Glu-B1 loci. The relative high frequency of superior alleles, Glu-B1b and Glu-Dt1d indicated the superior bread making quality attributes embedded in these synthetic hexaploid wheats. Of the 95 Elite-1 SHs 27.1% possessed superior alleles at Glu-A1 and 51% had superior alleles at Glu-B1 locus. At Glu-Dt1 frequency of inferior allele 1Dx2+1Dy12 was very low (5.26%) and nine different rare alleles along with the higher frequency (22.1%) of D-genome encoded subunit, 1Dx5+1Dy10, were observed. These superior alleles shall form the priority selective sieve for their usage in wheat improvement efforts.
机译:用十二烷基硫酸钠聚丙烯酰胺凝胶电泳法(SDS-PAGE)测定95个Elite-1合成六倍体(SH)小麦(Triticum turgidum / Aegilops tauschii; 2n = 6x = 42; AABBDD)中的高分子量谷蛋白亚基组成和变异。观察到SH中Glu-1基因座的22个不同等位基因。在合成物中发现了44种不同的HMW-GS模式。较高的HMW谷蛋白成分是由于这些SH中较高比例的D基因组编码的亚基。与12%的凝胶相比,8%的尿素/ SDS-PAGE更好地区分了亚基2 *。但是12%的尿素/ SDS-PAGE可以使Glu-D t 1个亚基具有不同的迁移率。 Glu-D t 1基因座的遗传变异性大于Glu-A1和Glu-B1基因座。优良等位基因Glu-B1b和Glu-D t 1d的相对高频率表明这些合成六倍体小麦具有较高的面包制作品质属性。在95个Elite-1 SHs中,有27.1%在Glu-A1处具有优势等位基因,而51%在Glu-B1位置处具有优势等位基因。在Glu-D t 1时,下等位基因1Dx2 + 1Dy12的频率非常低(5.26%),并且有9个不同的稀有等位基因以及D基因组编码的亚基1Dx5 +的较高频率(22.1%)观察到1Dy10。这些上等位基因应构成优先选择筛,用于小麦改良工作。

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