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Identification isolation and N-terminal sequencing of style glycoproteins associated with self-incompatibility in Nicotiana alata.

机译:鉴定分离和N型末端糖蛋白与N型烟草的自交不亲和性的N端测序。

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摘要

S-Gene-associated glycoproteins (S-glycoproteins) from styles of Nicotiana alata, identified by non-equilibrium two-dimensional electrophoresis, were purified by cation exchange fast protein liquid chromatography with yields of 0.5 to 8 micrograms of protein per style, depending on the S-genotype of the plant. The method relies on the highly basic nature of the S-glycoproteins. The elution profiles of the different S-glycoproteins from the fast protein liquid chromatography column were characteristic of each S-glycoprotein, and could be used to establish the S-genotype of plants in outbreeding populations. In all cases, the S-genotype predicted from the style protein profile corresponded to that predicted from DNA gel blot analysis using S-allele-specific DNA probes and to that established by conventional breeding tests. Amino-terminal sequences of five purified S-glycoproteins showed a high degree of homology with the previously published sequences of N. alata and Lycopersicon esculentum S-glycoproteins.
机译:通过非平衡二维电泳鉴定的,来自烟草等类型的S基因相关糖蛋白(S-糖蛋白),通过阳离子交换快速蛋白质液相色谱纯化,每种类型的蛋白质产量为0.5至8微克,具体取决于植物的S基因型。该方法依赖于S-糖蛋白的高度碱性。快速蛋白质液相色谱柱中不同S-糖蛋白的洗脱图谱是每种S-糖蛋白的特征,可用于建立近交群体中植物的S基因型。在所有情况下,从样式蛋白谱预测的S基因型与使用S等位基因特异性DNA探针的DNA凝胶印迹分析预测的基因型相对应,并与常规育种测试确定的基因型相对应。五个纯化的S-糖蛋白的氨基末端序列与先前公布的N. alata和番茄的S-糖蛋白序列具有高度的同源性。

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