首页> 外文期刊>Journal of Applied Phycology >Cloning and expression of a gene coding for the major light-harvesting chlorophyll a/b protein of photosystem II in the green alga Dunaliella salina.
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Cloning and expression of a gene coding for the major light-harvesting chlorophyll a/b protein of photosystem II in the green alga Dunaliella salina.

机译:绿藻杜氏盐藻中编码光系统II主要光捕获叶绿素a / b蛋白的基因的克隆和表达。

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摘要

Genes encoding proteins of the major light-harvesting complex of photosystem II (LHCII) in higher plants are well studied. However, little is known about the corresponding genes in the green alga Dunaliella salina, although this knowledge might provide valuable information about the respective roles of each LHCII protein at the molecular level under extreme environmental conditions. Here, we describe an additional LhcII gene from D. salina. An LhcII cDNA cloned by screening a D. salina cDNA library contains an open reading frame encoding a protein of 261 amino acids with a calculated molecular mass of 27.8 kDa. The deduced amino acid sequence shows high homology with other LHCII proteins. Genomic DNA-obtained by PCR using a specific primer set corresponding to the 5' and 3' untranslated regions-was used to determine the intron-exon structure. Short-term changes in mRNA levels after a shift from low-light to high-light or dark conditions were analyzed by real-time quantitative PCR, and indicated that this gene expresses different mRNA levels under different light conditions.
机译:对高等植物中光系统II主要光捕获复合体(LHCII)的蛋白质编码基因进行了深入研究。然而,尽管在极端环境条件下,这种知识可能提供有关每种LHCII蛋白在分子水平上的各自作用的有价值的信息,但对绿藻杜氏盐藻中相应基因的了解却很少。在这里,我们描述了来自D. salina的另一个LhcII基因。通过筛选D. salina cDNA文库而克隆的LhcII cDNA包含一个开放阅读框,其编码261个氨基酸的蛋白质,计算的分子量为27.8 kDa。推导的氨基酸序列与其他LHCII蛋白具有高度同源性。通过使用对应于5'和3'非翻译区的特异性引物组通过PCR获得的基因组DNA被用于确定内含子-外显子结构。通过实时定量PCR分析了从弱光条件转换为强光条件或黑暗条件后mRNA水平的短期变化,表明该基因在不同光照条件下表达不同的mRNA水平。

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