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作 者:刘维振[1,2] 陈华民[2] 于清[2] 田芳[2] 唐嘉义[1] 何晨阳[2]
机构地区:[1]云南农业大学植物保护学院云南省植物病理重点实验室,昆明650201 [2]中国农业科学院植物保护研究所,植物病虫害生物学国家重点实验室,北京100193
出 处:《植物病理学报》2015年第2期151-157,共7页Acta Phytopathologica Sinica
基 金:国家“863”计划项目(2012AA101504);国家“973”计划项目(2011CB100700)
摘 要:为揭示来源于番茄细菌性斑点病菌(Xanthomonas campestris pv.vesicatoria,Xcv)菌株XV18鞭毛素(FliCxcv)作为一种病原相关分子模式(PAMP)诱导水稻免疫反应的功能,本研究对FliCxcv编码基因flicxcv进行了基因克隆、序列分析、原核表达、蛋白纯化和诱导活性测定。结果表明,通过PCR特异性扩增,从Xcv菌株XV18中克隆了1 200bp的fliCxcv基因片段,其序列与GenBank中己测序菌株的完全一致。在大肠杆菌中对该基因全长、N端和C端截短序列进行了原核表达,并获得了纯化的FliCxcv全长及其截短蛋白。将纯化蛋白浸润接种到水稻品种日本晴叶片组织,发现FliCxcv全长及其截短蛋白均能诱导水稻叶片细胞死亡、H2O2产生以及防卫基因(OsPAL和OsPR1b)表达等免疫反应,但诱导活性存在差异。因此,本研究验证了FliCxcv具有激发水稻细胞免疫反应的PAMP功能,为水稻免疫诱导制剂的研发提供了材料。To elucidate whether the flagellin (FliCxcv) from Xanthomonas campestris pv. vesicatoria (Xcv) act as a PAMP to induce PTI (PAMP-triggered-immunity) in rice, the gene cloning, sequence analysis, prokaryotic expression, protein purification and PAMP activity assay of FliCxcv and truncated proteins were performed in this study. The results show that the fliCxcv gene was cloned through PCR specific amplication from the genomic DNA of Xcv strain XV18, the sequence of which is identical to that of the sequenced strain in the GenBank. Moreover, the full-length, N- and C-terminal domains were expressed in Escherichia coli respectively and purified to get FliCxcv and truncated proteins FliCxcv-N and FliCxcv-C. The immunity responses including hypersensitive cell death, H2O2production and expression of defense-related genes, such as OsPAL and OsPRlb were observed in rice leave tissues infiltrated by these purified proteins. These results suggested that Xcv flagellin was an effective PAMP to elicit PTI in rice, which can be used for the development of novel inducing agent of rice disease resistance.
关 键 词:番茄细菌性斑点病菌 鞭毛素 病原相关分子模式 水稻 免疫反应
分 类 号:S432.42[农业科学—植物病理学]
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