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GmSKP1,a Novel S-phase Kinase-associated Protein 1 in Glycine max,Enhancing Resistance Against Phytophthora sojae Infection
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作者 Ning Bin Li Wei-wei +9 位作者 Liu Xin Ji Wei Wang Yu-hong Zhao Ming he sheng-fu Zhang Chuan-zhong Rong Tian-yu Liu Dong-xue Xu Peng-fei Zhang Shu-zhen 《Journal of Northeast Agricultural University(English Edition)》 CAS 2023年第1期1-12,共12页
Phytophthora root and stem rot of soybean caused by Phytophthora sojae(P.sojae)is a devastating disease that affects soybean[Glycine max(L.)Merr.]all over the world.S-phase kinase-associated protein 1(SKP1)proteins ar... Phytophthora root and stem rot of soybean caused by Phytophthora sojae(P.sojae)is a devastating disease that affects soybean[Glycine max(L.)Merr.]all over the world.S-phase kinase-associated protein 1(SKP1)proteins are key members of the SKP1/Cullin/F-box protein(SCF)ubiquitin ligase complex and play diverse roles in plant biology.However,the role of SKP1 in soybean against the phytopathogenic oomycete P.sojae remains unclear.In this study,a novel member of the soybean SKP1 gene family,GmSKP1 which was significantly induced by P.sojae,was reported.The expression of GmSKP1 was simultaneously induced by methyl jasmonate(MeJA),salicylic acid(SA)and ethylene(ET),which might suggest an important role for GmSKP1 of plant in responses to hormone treatments.Functional analysis using GmSKP1 overexpression lines showed that GmSKP1 enhanced resistance to P.sojae in transgenic soybean plants.Further analyses showed that GmSKP1 interacted with a homeodomain-leucine zipper protein transcription factor(GmHDL56)and a WRKY transcription factor(GmWRKY31),which could positively regulate responses to P.sojae in soybean.Importantly,several pathogenesis-related(PR)genes were constitutively activated,including GmPR1a,GmPR2,GmPR3,GmPR4,GmPR5a and GmPR10,in GmSKP1-OE soybean plants.Taken together,these results suggested that GmSKP1 enhanced resistance to P.sojae in soybean,possibly by activating the defense-related PR genes. 展开更多
关键词 Phytophthora sojae SOYBEAN SKP1 OVEREXPRESSION pathogenesis-related gene
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粒状交联聚丙烯酸钠的制备及其对Pb2+的吸附性能 被引量:4
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作者 毛淑华 贺盛福 +1 位作者 张帆 彭清静 《高校化学工程学报》 EI CAS CSCD 北大核心 2017年第1期243-251,共9页
采用反相悬浮聚合法制备了粒状交联聚丙烯酸钠(gc-PAANa)凝胶,对gc-PAANa凝胶样品进行了SEM、FT-IR和TGA表征及溶胀率测试。将gc-PAANa凝胶用于吸附水溶液中Pb^(2+)的研究,结果表明,在p H=3.0~5.0 gc-PAANa凝胶对Pb^(2+)的吸附具有非常... 采用反相悬浮聚合法制备了粒状交联聚丙烯酸钠(gc-PAANa)凝胶,对gc-PAANa凝胶样品进行了SEM、FT-IR和TGA表征及溶胀率测试。将gc-PAANa凝胶用于吸附水溶液中Pb^(2+)的研究,结果表明,在p H=3.0~5.0 gc-PAANa凝胶对Pb^(2+)的吸附具有非常好的效果。0.02~0.1 mol×L-1 Ca2+/Mg2+的存在对Pb^(2+)的吸附几乎无影响,Pb^(2+)初始浓度对吸附结果影响较大,gc-PAANa凝胶对初始浓度低于350 mg×L-1的Pb^(2+)废水,Pb^(2+)的去除率可达到95%以上。gc-PAANa凝胶对Pb^(2+)的吸附动力学符合准二级模型,吸附等温线符合Langmuir模型,293 K下的最大吸附量为446.98 mg×g-1;吸附热力学分析表明,gc-PAANa凝胶对Pb^(2+)的吸附属于自发的放热反应。XPS分析表明,gc-PAANa凝胶吸附Pb^(2+)的机理属于-COO-与Pb^(2+)的螯合作用。吸附-解吸附循环实验显示,gc-PAANa凝胶处理含Pb^(2+)废水具有很好的重复利用性能。 展开更多
关键词 反相悬浮聚合法 聚丙烯酸钠 凝胶 铅离子 吸附
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