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Apple polygalacturonase inhibiting protein1 expressed in transgenic tobacco inhibits polygalacturonases from fungal pathogens of apple and the anthracnose pathogen of lupins

机译:在转基因烟草中表达的苹果多聚半乳糖醛酸酶抑制蛋白1抑制苹果真菌病原体和羽扇豆炭疽病病原体的多聚半乳糖醛酸酶

摘要

Extracts from apple fruit (cultivar “Granny Smith”) inhibited the cell-wall degrading polygalacturonase (PG) activity of Colletotrichum lupini, the causal agent of anthracnose on lupins, as well as Aspergillus niger PG. Southern blot analysis indicated that this cultivar of apple has a small gene family of polygalacturonase inhibiting proteins (pgips), and therefore heterologous expression in transgenic tobacco was used to identify the specific gene product responsible for the inhibitory activity. A previously isolated pgip gene, termed Mdpgip1, was introduced into tobacco (Nicotiana tabacum) by Agrobacterium-mediated transformation. The mature MdPGIP1 protein was purified to apparent homogeneity from tobacco leaves by high salt extraction, clarification by DEAE-Sepharose and cation exchange HPLC. Purified MdPGIP1 inhibited PGs from C. lupini and PGs from two economically important pathogens of apple trees, Botryosphaeria obtusa and Diaporthe ambigua. It did not inhibit the A. niger PG, which was in contrast to the apple fruit extract used in this study. We conclude that there are at least two active PGIPs expressed in apple, which differ in their charge properties and ability to inhibit A. niger PG.
机译:苹果果实(品种“格兰尼·史密斯”(Granny Smith))的提取物抑制了炭疽菌对羽扇豆的致病因子Colletotrichum lupini和黑曲霉PG的细胞壁降解性聚半乳糖醛酸酶(PG)活性。 Southern印迹分析表明,该苹果品种具有小的聚半乳糖醛酸酶抑制蛋白(pgips)基因家族,因此使用转基因烟草中的异源表达来鉴定负责抑制活性的特定基因产物。通过农杆菌介导的转化,将先前分离的pgip基因(称为Mdpgip1)引入烟草(Nicotiana tabacum)中。通过高盐提取,DEAE-Sepharose和阳离子交换HPLC纯化,从烟叶中纯化出成熟的MdPGIP1蛋白,使其具有明显的同质性。纯化的MdPGIP1抑制了卢氏梭菌的PG和苹果树的两种经济上重要的病原体obtrya obtusa和Diaporthe ambigua的PG。它没有抑制黑曲霉PG,这与本研究中使用的苹果果实提取物相反。我们得出的结论是,苹果中至少表达了两种活性PGIP,它们的电荷性质和抑制黑曲霉PG的能力不同。

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