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作 者:雷明娜 李晶 LEI Mingna;LI Jing(College of Bioscience and Resource Environment/Key Laboratory of Urban Agriculture(North China),Ministry of Agriculture and Rural Affairs,Beijing University of Agriculture,Beijing 102206,China)
机构地区:[1]北京农学院生物与资源环境学院/农业农村部华北都市农业重点实验室,北京102206
出 处:《北京农学院学报》2023年第1期1-6,共6页Journal of Beijing University of Agriculture
基 金:北京市教委科研计划一般项目(KM201910020014);北京农学院青年科学基金(SXQN201802)。
摘 要:【目的】为探究拟南芥小热休克蛋白HSP17.4与过氧化氢酶2的关系。【方法】构建带有组氨酸标签的小热休克蛋白HSP17.4的原核蛋白表达载体,将小热休克蛋白HSP17.4与过氧化氢酶2的重组蛋白诱导表达后进行体外免疫共沉淀试验,并利用过氧化氢酶活性试剂盒检测过氧化氢酶活力。【结果】成功构建了带有组氨酸标签的小热休克蛋白HSP17.4的蛋白表达载体,并通过体外免疫共沉淀试验发现带有组氨酸标签的小热休克蛋白HSP17.4能够将无纯化标签的过氧化氢酶2成功纯化出来,过氧化氢酶活性检测表明小热休克蛋白HSP17.4可以显著增强过氧化氢酶2活性。【结论】本研究证明小热休克蛋白HSP17.4与过氧化氢酶2存在相互作用,并且小热休克蛋白HSP17.4激活过氧化氢酶2酶活性,为进一步研究小热休克蛋白HSP17.4通过调控过氧化氢酶2参与非生物胁迫响应奠定基础。[Objective]To explore the relationship between Arabidopsis small heat shock protein HSP17.4 and catalase CAT2. [Method]The His-HSP17.4 prokaryotic protein expression vector was constructed, and the recombinant protein of HSP17.4 and CAT2 was induced and expressed. Subsequently, the pull-down assay was carried out in vitro, and the catalase activity was tested by catalase activity kit. [Result]The expression vector of His-HSP17.4 was successfully constructed. The result of pull-down assay showed that His-HSP17.4 could successfully purify the CAT2 without purification tag. Catalase activity assay showed that the small heat shock protein HSP17.4 significantly enhanced CAT2 activity. [Conclusion]This study proves that small heat shock protein HSP17.4 interacts with CAT2 and activates CAT2, which lays a foundation for further research on the role of small heat shock protein HSP17.4 in abiotic stress response through regulating CAT2 activity.
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