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干旱胁迫条件下发菜Ferritin差异表达与基因克隆 被引量:4

Differential Expression and Gene Cloning of Ferritin from Nostoc flagelliformeSubjected to Desiccation
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摘要 发菜(Nostoc flagelliforme)是一种陆生固氮蓝藻,具有强烈的旱生生态适应性。运用双向电泳技术、凝胶图像分析、MALDI-TOF-TOF/MS质谱鉴定和数据库检索,发现发菜Ferritin在干旱胁迫条件下表达量逐渐降低。根据鉴定的Ferritin已知氨基酸序列设计简并性引物克隆该基因,获得了长度为540 bp的DNA,GenBank登陆号为HM854287。序列比较显示该基因具有较高的保守性,蛋白质二级结构主要由α螺旋和随机卷曲构成。RT-PCR分析表明,Ferritin mRNA在干旱胁迫条件下表达量逐渐降低,与Ferritin的表达趋势一致。将Ferritin基因在大肠杆菌中表达,获得符合预期的外源重组蛋白(22.4 kD)。实验结果可为进一步研究发菜耐旱的分子机理及探讨发菜对极端干旱环境的适应和保护机制奠定基础。 Nostoc flagelliforme is a terrestrial nitrogen-fixing cyanobacterium with strong drought adaptability.We performed 2-DE analysis,gel image analysis and MALDI-TOF-TOF/MS to compare and identify differential proteins from N.flagelliforme subjected to desiccation.The results indicated that Ferritin,Dps family protein expression quantum gradually declined under desiccation stress.The Ferritin gene was cloned by designed degeneracy primer based on identified amino acid sequences.A full length of 540 bp DNA was obtained(GenBank access number: HM854287).Homology analysis showed that the N.flagelliforme Ferritin gene had high consensus regions.The secondary structures of Ferritin were made up of α helix and random coil.The RT-PCR showed that mRNA of Ferritin gradually declined under drought stress.The Ferritin gene was expressed in Escherichia coli,and a 22.4 kD heterologous protein was observed.The results laid a foundation for understanding the drought-resistant molecular mechanisms and protection mechanisms of N.flagelliforme in extreme arid environments.
出处 《植物科学学报》 CAS CSCD 北大核心 2012年第1期72-78,共7页 Plant Science Journal
基金 国家自然科学基金资助项目(31060038)
关键词 发菜 FERRITIN 差异表达 基因克隆 RT-PCR 原核表达 Nostoc flagelliforme Ferritin Differential expression Gene cloning RT-PCR Prokaryotic expression
作者简介 梁文裕(1969-),男,博士,教授,主要从事植物资源及植物分子生物学的研究(E-mail:liangwy2009@163.com)。
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