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杜氏盐藻光系统Ⅱ反应中心蛋白D2基因的克隆及序列分析

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刘红涛 宋建伟 臧卫东 鲁照明 王鹏举 薛乐勋

郑州大学医学实验中心,郑州450052

华中师范大学学报:自然科学版
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国际标准刊号:ISSN 1000-1190
国内统一刊号:CN 42-1178

摘  要:

根据莱茵衣藻(Chlamydomonas reinhardtii)、Oryza sativa、Chlorella vulgaris以及Me-sostigma viride等真核生物的psbD基因的氨基酸高度保守序列,设计一对简并引物,利用TRIzol试剂提取杜氏盐藻(Dunaliella salina)细胞的总RNA,通过RT-PCR,得到杜氏盐藻cDNA片段的长度大约为1 000bp.该序列的PCR产物经T-A克隆并测序分析以及测序结果推导成氨基酸序列,Blast同源性分析表明所克隆的基因为杜氏盐藻psbD基因,编码杜氏盐藻光系统Ⅱ反应中心D2蛋白,该序列已递交GenBank(GenBank登录号为:DQ074450).编码的氨基酸序列,同源性依次为:Chlamydomonas reinhardtii92%,Nephroselmis olivacea88%,Pinus thunbergii88%,Am-borella trichopoda88%,Chlorella vulgaris88%.通过密码子偏爱性分析表明,psbD基因存在明显的密码子偏爱性,其(A+T)含量明显高于(G+C)含量.[著者文摘]

绿藻和蓝藻通过两个光系统反应中心,光系统工(Photosystem 工,PS工)和光系统Ⅱ(Photosystem 1,PS 1),执行产氧光合作用.PS Ⅱ由叶绿素P680以及与异二聚体D1和D2相关的许多电子受体组成,D1和D2分别由psbA和psbD基因编码l_lj.PS1I的组成极其复杂,捕光色素蛋白可能以12聚体形式围绕在PS1I光化学反应中心周围,它们吸收光能,并以极高的效率传给光化学反应中心.反应中心色素P680被激发,并发生电荷分离,激发的电子通过电子传递链最后传到黄素蛋白,使NADP+还原形成高能化合物l_2].PS 1I反应中心蛋白不仅提供电荷分离反应的场所,而且会直接影响电子的传递效率,其反应中心蛋白D1和D2蛋白组成异二聚体再与PS 1反应中心色素一叶绿素P680分子结合,共同构成光系统Ⅱ的光化学反应中心.因此D1蛋白和D2蛋白在光合作用中起着十分重要的作用.由于D1蛋白还是除草剂的结合位点,所以在它被确认为反应中心蛋白以前......
Journal of Central China Normal University(Natural Sciences)

分 类 号:

Q785

文献标识码:

A

文章编号:

1000-1190(2007)03-0431-06

相关文章:

参考文献(11篇)  主题相关

[参考文献]

Cloning and analysis of cDNA of photosystem Ⅱ reactor center protein D2 of Dunaliella salina

LIU Hongtao, SONG Jianwei, ZANG Weidong, LU Zhaoming, WANG Pengju, XUE Lexun (Expermental Center for Medicine, Zhengzhou University, Zhengzhou 450052)

Abstract:

One pair of degenerate primers was designed according to conserved motifs ot the psbD (encoding PhotosystemⅡreactor center proteins D2 ) of Chlarnydornonas refnhardtii , Oryza sativa , Chlorella vulgaris and Mesostigrna viride. And a total RNA of Dunaliella salina (D. salina) was extracted with TRIzol reagent. A cDNA fragment, 1000bp in length, from green algal D. salina was obtained through RT-PCR method. The resulting PCR products were cloned into T-vector and screened to determine their sequence. Homologous analysis of the deduced amino acid sequence was performed by BLAST and subsequently compared to that of other species, it is shown that the sequence cloned is a cDNA fragments of psbD from D. salina, the sequence has submitted to GenBank(GenBank accession number: DQ074450). In addition, homology analysis of psbD shows that Dunaliella salina are high identity with the following species: Chlamydornonas reinhardtii 92%, Nephroselrnis olfvacea 88%, Pinus thunbergii 88%, Amborella trichopoda 88%, and Chlorella vulgaris 88%. Also, the analysis of codon bias reveals that the codon usage of psbD gene of D. salina is apparently biased, and the content of (A+T) is obviously higher than that of (G+C), in the meanwhile, the numbers of Lys in the psbD gene is 3, and this property will provide the theoretical basis of isolation, purification and study of the proteins of D2.[著者文摘]

Key words:

Dunaliella salina; D2 proteins; psbD gene; degenerate primer; codon bias

收稿日期: 2007-01-22

基金资助:

国家自然科学基金资助项目(30600006).

作者简介:

通讯联系人.E—mail:xuelx@371.net.

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