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首页> 外文期刊>Turkish journal of biology >A preliminary analysis of the gene all0012 of Anabaena PCC 7120
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A preliminary analysis of the gene all0012 of Anabaena PCC 7120

机译:鱼腥藻PCC 7120基因all0012的初步分析

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The genes coding for methyltransferase during the maturation of phycobilisomes in Synechococcus sp. strain PCC 7002 and Synechocystis sp. strain PCC 6803 were indentified and named CpcM. Using bioinformatics methods, it was found that a probable methyltransferase gene denoted all0012, because of its highly similarity, is likely to be the molecule that edits and modifies the β-subunit in Anabaena sp. strain PCC 7120. The present study was intended to analyze the probable functions of gene all0012. After bioinformatic analyses, we constructed an appropriate heterologous all0012 expression carrier and the characteristics of expression were evaluated by SDS-PAGE. Afterwards, a deletion mutant was characterized via a shuttle vector by means of triparental transformation. Intact phycobilisomes were separately isolated from null mutant and wild-type strains and their absorption spectra were compared. To further analyze possible functions of all0012, null alleles of cyanobacteria were cultured in the same specific conditions as the wild type under various intensities of light. The absorbance properties of the null mutant were very similar to those of the wild-type. Meanwhile, a dramatic photosensitization difference was observed under high-level illumination, which is similar to the phenotype of methylationdeficient strains observed in previous research. This study suggests that the gene may play an important role in the methylation of the β-subunit of phycobiliprotein.
机译:Synechococcus sp。藻胆体成熟过程中编码甲基转移酶的基因。菌株PCC 7002和集胞藻(Synechochocystis sp。)确定了菌株PCC 6803,并将其命名为CpcM。使用生物信息学方法,发现一个可能的甲基转移酶基因all0012,由于其高度相似性,很可能是编辑和修饰鱼腥藻β-亚基的分子。菌株PCC7120。本研究旨在分析基因all0012的可能功能。经过生物信息学分析,我们构建了适当的异源all0012表达载体,并通过SDS-PAGE评估了表达特性。之后,通过穿梭载体借助三亲转化来表征缺失突变体。从无效突变株和野生型菌株中分别分离完整的藻胆体,并比较它们的吸收光谱。为了进一步分析all0012的可能功能,在与野生型相同的特定条件下,在各种光照下培养了蓝藻无效等位基因。空突变体的吸收特性与野生型非常相似。同时,在高强度照明下观察到了巨大的光敏性差异,这与先前研究中观察到的甲基化缺陷型菌株的表型相似。这项研究表明该基因可能在藻胆蛋白β亚基的甲基化中起重要作用。

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