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Cloning and structure analysis of hydrogenase gene from Chlamydomonas reinhardtii SE

机译:莱茵衣藻SE中氢化酶基因的克隆与结构分析

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The cDNA of Chlamydomonas reinhardtii SE encoding hydrogenase (HydA2) was obtained from the total RNA of C. reinhardtii SE by RT-PCR. The DNA of hydrogenase was amplified by PCR from the genomic DNA of C. reinhardtii SE. The cDNA and DNA of hydrogenase were sequenced, respectively. The structure of hydrogenase gene was analyzed by biology software. The open reading frame predicts that the hydrogenase is composed of 3584 bp encoding 505 amino acids in length with a predicted M.W. of 53.69 kDa. Ten exons (including 1518 bp) and nine introns (including 2066 bp) have been found in the hydrogenase, and there were two potential N-glycosylate sites, eight protein kinase C phosphorylation site, eight casein kinase Ⅱ phosphorylation site and one sulphorylation in the sequence. The theory pI was 6.15. Total number of negatively charged residues (Asp + Glu) and positively charged residues (Arg + Lys) were 55 and 61, respectively.
机译:通过RT-PCR从莱茵衣藻SE的总RNA中获得了莱茵衣藻SE编码cDNA的酶(HydA2)。通过PCR从莱茵衣藻SE的基因组DNA中扩增出氢化酶的DNA。分别对氢化酶的cDNA和DNA进行测序。用生物学软件分析了氢化酶基因的结构。开放阅读框预测该氢化酶由3584bp组成,其编码505个氨基酸,预测的M.W.为53.69kDa。在氢化酶中发现了10个外显子(包括1518 bp)和9个内含子(包括2066 bp),其中有两个潜在的N-糖基化位点,8个蛋白激酶C磷酸化位点,8个酪蛋白激酶Ⅱ磷酸化位点和一个硫酸化位点。序列。理论pI为6.15。带负电的残基(Asp + Glu)和带正电的残基(Arg + Lys)的总数分别为55和61。

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