| 大型多管水母的绿色荧光蛋白 |
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| 引用本文： | 罗文新,张军,杨海杰,谢小燕,覃映雪,逄淑强,李少菁,夏宁邵.大型多管水母的绿色荧光蛋白[J].海洋学报,2002,24(4):82-91. |
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| 作者姓名： | 罗文新 张军 杨海杰 谢小燕 覃映雪 逄淑强 李少菁 夏宁邵 |
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| 作者单位： | 厦门大学, 细胞生物学与肿瘤细胞工程教育部重点实验室, 福建, 厦门, 361005 |
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| 基金项目： | 国家海洋“86 3”计划领域青年基金资助项目 (819-Q - 0 6 )，国家自然科学基金资助项目 (C0 10 4 0 10 1)，福建省自然科学基金资助项目 (C0 0 10 0 0 1)，国家海洋局海洋生物工程重点实验室开放基金资助项目 (HY970 3) |
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| 摘 要： | 采用PCR扩增和southern杂交筛选相结合的方法,从厦门水域的大型多管水母中分离到了新的绿色荧光蛋白基因gfpxm,并在大肠杆菌中进行了表达.gfpxmDNA序列编码区长为1042bp,包含3个外显子和两个内含子,cDNA编码区全长为717bp.gfpxmcDNA与已知野生型Aeqgfp 10cDNA长度一致,核苷酸同源性为81.9%,推导的氨基酸序列全长为238个氨基酸,与AeqGFP10的氨基酸同源性为83.6%.将gfpxm克隆至pTO-T7表达载体,GFPxm在大肠杆菌BL21中的表达量达菌体总蛋白的50%左右.荧光性质和强度分析结果表明,GFPxm蛋白的激发峰为476nm,发射峰为496nm,荧光量子产率为1. GFPxm蛋白的荧光很稳定,对热、碱性、变性剂和盐等有较强抗性.
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| 关 键 词： | 大型多管水母 绿色荧光蛋白 克隆表达 荧光性质 |
| 文章编号： | 0253-4193(2002)04-0082-10 |
| 收稿时间： | 2001/2/26 0:00:00 |
| 修稿时间： | 2001年2月26日 |
Green fluorescent protein of the jellyfish Aequorea macrodactyla |
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| LUO Wen-xin,ZHANG Jun,YANG Hai-jie,XIE Xiao-yan,QIN Ying-xue,PANG Shu-qiang,LI Shao-jin and XIA Ning-shao.Green fluorescent protein of the jellyfish Aequorea macrodactyla[J].Acta Oceanologica Sinica (in Chinese),2002,24(4):82-91. |
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| Authors: | LUO Wen-xin ZHANG Jun YANG Hai-jie XIE Xiao-yan QIN Ying-xue PANG Shu-qiang LI Shao-jin and XIA Ning-shao |
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| Institution: | Ministry of Education, Cell Biology and Tumor Cell Engineering Laboratory, Xiamen University, Xiamen 361005, China |
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| Abstract: | A new green fluorescent protein gene gfpxm was isolated from jellyfish Aequorea macrodactyla in the coastal region of East China Sea by the method of combination of PCR amplification and southern hybridization analysis. The gfpxm gene contains three extrons and two introns spread over 1 042 bp of genomic DNA, the entire coding region of cDNA is 717 bp, being identical to the wild type gfp Aeqgfp10 cDNA in length. The amino acid sequence of GFPxm deduced from the nucleotide sequence is 238 aa residue, sharing homology of 83 6% with that of AeqGFP10. The entire coding sequence was cloned into the pTO T7 expression vector and expressed in E coli. The expression yield of GFPxm was amounted to 50% of the total protein. Compared with GFP of A victoria, the expressed GFPxm exhibited an excitation peak at a higher wave length of 476nm and an emission peak at a lower wave length 496 nm with a higher quantum yield of 1 0. The fluorescence of GFPxm is significant stable, showing strong resistant to heat, alkaline, denaturants and salts. |
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| Keywords: | Aequorea macrodactyla green fluorescent protein gene cloning and expression fluorescent property |
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