为检测α-甘露糖苷酶的表达及其可能的功能,制备了稻瘟病菌一假定α-甘露糖苷酶多克隆抗体,并探索其可能应用。将与-His标签融合的过量表达一假定α-甘露糖苷酶蛋白的稻瘟病菌转化子,在液体完全培养基中培养,收集其上清液,经Ni2+-NTA亲和柱纯化后,得到可溶的融合蛋白α-甘露糖苷酶-His。纯化后的融合蛋白免疫新西兰兔,得到抗α-甘露糖苷酶蛋白的多克隆抗体,ELISA检测结果表明抗体效价达1:51200,特异性高。利用该多克隆抗体以ELISA方法检测并Western验证分析稻瘟病菌30个田间菌株培养液α-甘露糖苷酶的表达量。不同菌株α-甘露糖苷酶表达量有明显差异。进一步分析表明,菌株70-15接种水稻后,不同时期α-甘露糖苷酶的表达量差异明显。菌株间致病型等生物学和生理学差异可能与α-甘露糖苷酶表达的差异有关。
α Magnaporthe oryzae,a polyclonal antibody of a putative α-Mannosidase was prepared.A transformant of Magnaporthe oryzae,overexpressing a putative α-Mannosidase-His tag fusion protein was grown in liquid media.The α-Mannosidase fusion protein was purified by Ni 2 +-NTA affinity chromatography column from culture filtrate.The fusion protein was then injected into and used to immune New Zealand rabbits to produce polyclonal antibody.The titer of this polyclonal antibody was 1:51200 and with good specificity after ELISA analysis.Protein of 30 M.oryzae strains were tested against this antibody using ELISA and Western blotting show that the expression level of the α-Mannosidase appeared to be significantly different among strains as well as infection stages when inoculated with the strain 70-15.The difference expression level of the α-Mannosidase among different strains may be related to the physiological and biological characteristic such as pathogenicity of the fungus.