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Expression of the legume symbiotic lectin genes psl and gs52 promotes rhizobial colonization of roots in rice

机译:豆科植物共生凝集素基因psl和gs52的表达促进了水稻根的根瘤菌定殖

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摘要

Transgenic rice (Oryza sativa L. cv. Murasaki) carrying genes encoding pea (Pisum sativum) lectin (PSL) or wild-soybean (Glycine soja) lectin-nucleotide phosphohydrolase (GS52) were inoculated with Rhizobium leguminosarum bv. viciae or Bradyrhizobium japonicum USDA110, respectively, as well as with Rhizobium sp. NGR234, and root colonization was assessed in comparison to comparably inoculated control plants. The data showed that expression of PSL and GS52 significantly promoted rhizobial colonization of root epidermal cells including root hairs in rice. In addition, in the case of R. leguminosarum bv. viciae and B. japonicum USDA110 colonization of the psl and gs52 transgenic rice plants, respectively, the bacterial cells were found to preferentially home towards and aggregate maximally at the root hair tip regions rather than on the root hair "stalks". The above data suggest that the lectins PSL and GS52, which participate in rhizobial recognition by root epidermal cells in pea and soybean, respectively, are also able to facilitate rhizobial attachment and colonization of the epidermal cells in rice roots. Moreover, aggregation of R. leguminosarum bv. viciae and B. japonicum USDA110 cells preferentially at root hair tip regions suggest that similar to legumes, the PSL and GS52 lectins are targeted to the root hair tips in transgenic rice, enabling higher bacterial attachment/colonization at the tip region. Rhizobial colonization at root hair tips in the psl and gs52 rice plants frequently led to the localized dissolution of the cell wall creating perforations at the tip region. It is likely that the presence of lectins, such as PSL and GS52 leads to structural modifications in cell wall organization of the root hair/epidermal cells, making them prone to localized dissolution by the hydrolytic activity of compatible rhizobia to permit invasion of the root cells. © 2005 Elsevier Ireland Ltd. All rights reserved.
机译:用豆根瘤菌接种携带编码豌豆(Pisum sativum)凝集素(PSL)或野生大豆(甘氨酸大豆)凝集素核苷酸磷酸水解酶(GS52)的基因的转基因水稻(Oryza sativa L. cv。Murasaki)。蚕豆或日本根瘤菌USDA110,以及与根瘤菌(Rhizobium sp。)与同等接种的对照植物相比,评估了NGR234和根定植。数据表明,PSL和GS52的表达显着促进了水稻根系表皮细胞(包括根毛)的根瘤菌定植。另外,在豆科植物R. leguminosarum bv的情况下。分别在psl和gs52转基因水稻植株的蚕豆和日本芽孢杆菌USDA110上定殖,发现细菌细胞优先向根毛尖端区域迁移并最大程度地聚集,而不是在根毛“茎”上聚集。上述数据表明,凝集素PSL和GS52分别通过豌豆和大豆中的根表皮细胞参与根瘤菌识别,也能够促进水稻根中表皮细胞的根瘤菌附着和定植。此外,豆科植物R. leguminosarum bv的聚集。蚕豆和日本芽孢杆菌USDA110细胞优先位于根毛尖端区域,这表明与豆类相似,PSL和GS52凝集素也靶向转基因水稻的根毛尖端,从而在尖端区域具有更高的细菌附着/定殖能力。在psl和gs52水稻植株根毛尖的根瘤菌定植经常导致细胞壁的局部溶解,在尖端区域产生穿孔。凝集素(如PSL和GS52)的存在可能导致根毛/表皮细胞的细胞壁组织结构发生结构性修饰,使其易于因相容性根瘤菌的水解活性而发生局部溶解,从而允许根细胞入侵。 ©2005爱思唯尔爱尔兰有限公司。保留所有权利。

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