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干旱胁迫条件下发菜Ferritin差异表达与基因克隆
引用本文:梁文裕,焦广飞,周有文,张亚萍,陈伟.干旱胁迫条件下发菜Ferritin差异表达与基因克隆[J].武汉植物学研究,2012,30(1):72-78.
作者姓名:梁文裕  焦广飞  周有文  张亚萍  陈伟
作者单位:1. 宁夏大学生命科学学院,银川,750021
2. 福建农林大学生命科学学院,福州,350002
基金项目:国家自然科学基金资助项目(31060038)
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.

关 键 词:发菜  Ferritin  差异表达  基因克隆  RT-PCR  原核表达

Differential Expression and Gene Cloning of Ferritin from Nostoc flagelliforme Subjected to Desiccation
LIANG Wen-Yu , JIAO Guang-Fei , ZHOU You-Wen , ZHANG Ya-Ping , CHEN Wei.Differential Expression and Gene Cloning of Ferritin from Nostoc flagelliforme Subjected to Desiccation[J].Journal of Wuhan Botanical Research,2012,30(1):72-78.
Authors:LIANG Wen-Yu  JIAO Guang-Fei  ZHOU You-Wen  ZHANG Ya-Ping  CHEN Wei
Institution:1.School of Life Sciences,Ningxia University,Yinchuan 750021,China; 2.College of Life Sciences,Fujian Agriculture and Forestry University,Fuzhou 350002,China)
Abstract: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.
Keywords:Nostoc flagelliforme  Ferritin  Differential expression  Gene cloning  RT-PCR  Prokaryotic expression
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