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首页> 外文期刊>Plant Molecular Biology >Rubisco activase transcript (rca) abundance increases when the marine unicellular green alga Chlorococcum littorale is grown under high-CO sub(2) stress
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Rubisco activase transcript (rca) abundance increases when the marine unicellular green alga Chlorococcum littorale is grown under high-CO sub(2) stress

机译:在高CO sub(2)胁迫下生长海洋单细胞绿藻Chlorococcum littorale时,Rubisco激活酶转录物(rca)的丰度增加

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摘要

cDNA and the corresponding genomic DNA region encoding Rubisco activase were isolated from the unicellular green alga Chlorococcum littorale. The deduced amino acid sequence encoded by the cDNA was 403 amino acids long and exhibited important homology with those of other known Rubisco activases. Its N-terminal sequence was similar to the chloroplastic transit peptides in Chlamydomonas reinhardtii. The mature protein had a predicted molecular mass of 42 kDa. Five introns were located inside the genomic gene encoding Rubisco activase (rca). Genomic Southern blots indicated that two copies of the rca gene were present in the genome of C. littorale. The level of rca messenger RNA increased when cells of C. littorale were subjected to high-CO sub(2) stress (i.e. grown under at least 20% CO sub(2)). Hsp70 heat-shock protein was also induced under high-CO sub(2) conditions and, as expected, was also induced at 35 degree C. The rca gene, in contrast, was not induced at 35 degree C, indicating that this gene was induced in response to the high CO sub(2) concentration and not to general stress. A search of the promoter-binding proteins by a gel retardation assay showed that, under the high-CO sub(2) conditions, a protein(s) which was probably an activator of the rca transcription was synthesized.
机译:从单细胞绿藻Chlorococcum littorale中分离出cDNA和编码Rubisco激活酶的相应基因组DNA区域。 cDNA编码的推导氨基酸序列长403个氨基酸,与其他已知的Rubisco活化酶具有重要的同源性。它的N端序列类似于莱茵衣藻中的叶绿体转运肽。成熟蛋白的预测分子量为42 kDa。五个内含子位于编码Rubisco激活酶(rca)的基因组基因内。基因组Southern印迹表明,在滨海假丝酵母的基因组中存在两个拷贝的rca基因。当滨海假丝酵母的细胞受到高CO sub(2)胁迫(即在至少20%CO sub(2)下生长)时,rca信使RNA的水平增加。 Hsp70热休克蛋白也在高CO sub(2)条件下诱导,并且正如预期的那样,也在35摄氏度下诱导。相反,rca基因在35摄氏度下未诱导,表明该基因是诱导响应高CO sub(2)浓度而不是一般压力。通过凝胶阻滞分析对启动子结合蛋白的搜索显示,在高CO sub(2)条件下,合成了可能是rca转录激活因子的蛋白。

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