首页> 美国卫生研究院文献>The Plant Cell >Inactivation of a Synechocystis sp strain PCC 6803 gene with homology to conserved chloroplast open reading frame 184 increases the photosystem II-to-photosystem I ratio.
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Inactivation of a Synechocystis sp strain PCC 6803 gene with homology to conserved chloroplast open reading frame 184 increases the photosystem II-to-photosystem I ratio.

机译:与保守的叶绿体开放阅读框184具有同源性的集胞藻属菌株PCC 6803基因的失活增加了光系统II与光系统I的比率。

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摘要

A gene of the unicellular cyanobacterium Synechocystis sp strain PCC 6803 that is homologous to the conserved chloroplast open reading frame orf184 has been cloned and sequenced. The nucleotide sequence of the gene predicts a protein of 184 amino acids with a calculated molecular mass of 21.5 kD and two membrane-spanning regions. Amino acid sequence analysis showed 46 to 37% homology of the cyanobacterial orf184 with tobacco orf184, rice orf185, liverwort orf184, and Euglena gracilis orf206 sequences. Two orf184-specific mutants of Synechocystis sp PCC 6803 were constructed by insertion mutagenesis. Cells of mutants showed growth characteristics similar to those of the wild type. Their pigment composition was distinctly different from the wild type, as indicated by an increase in the phycocyanin-to-chlorophyll ratio. In addition, mutants also had a two- to threefold increase in photosynthetic electron transfer rates as well as in photosystem II-to-photosystem I ratio-a phenomenon hitherto not reported for mutants with altered photosynthetic characteristics. The observed alterations in the orf184-specific mutants provide strong evidence for a functional role of the orf184 gene product in photosynthetic processes.
机译:已经克隆并测序了与保守的叶绿体开放阅读框orf184同源的单细胞蓝藻Synechocystis sp菌株PCC 6803的基因。该基因的核苷酸序列可预测184个氨基酸的蛋白质,计算分子量为21.5 kD,具有两个跨膜区域。氨基酸序列分析显示,蓝细菌orf184与烟草orf184,水稻orf185,地艾草orf184和细叶Euglena gracilis orf206序列具有46%到37%的同源性。通过插入诱变构建了两个拟南芥sp PCC 6803的orf184特异性突变体。突变体的细胞显示出与野生型相似的生长特征。藻蓝蛋白与叶绿素比例的增加表明它们的色素组成与野生型明显不同。此外,突变体的光合电子传递速率以及光系统II与光系统I的比率也增加了2到3倍,这是迄今为止尚未报道的光合特性改变的突变体的现象。观察到的orf184特异性突变体的变化为orf184基因产物在光合作用过程中的功能作用提供了有力的证据。

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