首页|红色荧光蛋白基因银耳表达载体的构建及表达鉴定

红色荧光蛋白基因银耳表达载体的构建及表达鉴定

扫码查看
以pET-28a-RFP质粒为模板,PCR扩增红色荧光蛋白(red fluorescent protein,RFP)基因,并克隆到真核表达载体pTE11上,置于RP27启动子调控之下,成功构建表达载体pTE 11-RFP.采用PEG介导转化法,将pTE 11-RFP转入银耳芽孢中.提取转化子基因组DNA,RFP基因特异性引物扩增获得与目的基因大小一致的特异条带;日光下肉眼观察转化子略显红色,荧光显微镜观察有明显的红色荧光.以上结果证明RFP基因已成功转入银耳芽孢并进行表达,RP27启动子可以调控外源基因RFP在银耳芽孢中的正确表达,为进一步研究外源基因在银耳芽孢生物反应器中的高效表达奠定了一定的基础.
Construction of Plasmid Vector and Expression Identification of RFP Gene in Tremella fuciformis
The RFP (red fluorescent protein) gene was obtained by polymerase chain reaction (PCR) in which plasmid pET-28a-RFP was used as a template, and cloned into pTE11 vector under the control of RP27 promoter.The recombinant plasmid pTE11-RFP was successfully constructed as confirmed by enzymatic digestion and DNA sequencing.The PEG mediated transformation method was performed to transfer plasmid DNA of pTE11-RFP into yeast-like conidia of Tremellafuciformis.The expected amplified bands appeared when the chromosomal DNA of the transformants was used as the templates for the PCR with the RFP-specific primers.The colonies showed pink in tube and distinct red fluorescence could be observed from the colonies of YLCs by fluorescence microscopy.These results indicated that RFP gene was integrated into the genome of T.fuciformis and was expressed successfully by the regulation of RP27 promoter which laid the foundation for foreign gene expression in YLCs of Tremella fuciformis.

Tremella fuciformisRFP geneExpression vector

阮玲云、翁彩红、陈世友、陈文星、赖春芬、艾柳英、胡开辉、孙淑静

展开 >

福建农林大学生命科学学院,福建福州 350002

银耳芽孢 红色荧光蛋白基因 表达载体

福建省发改委农业五新工程项目福建省自然科学基金杰出青年项目福建农林大学校杰出青年人才项目国家自然科学基金青年项目教育部博士点基金

闽发改委投资[2012]931号2014J06010xjq2012093120166920103515120015

2015

热带作物学报
中国热带作物学会

热带作物学报

CSTPCDCSCD北大核心
影响因子:0.807
ISSN:1000-2561
年,卷(期):2015.36(10)
  • 4
  • 16