首页> 外文期刊>Molecular Biology Reports >Cloning and characterization of ribulose-1,5-bisphosphate carboxylase/oxygenase small subunit (RbcS) cDNA from green microalga Ankistrodesmus convolutus
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Cloning and characterization of ribulose-1,5-bisphosphate carboxylase/oxygenase small subunit (RbcS) cDNA from green microalga Ankistrodesmus convolutus

机译:绿色微藻卷积弧菌核糖-1,5-双磷酸羧化酶/加氧酶小亚基(RbcS)cDNA的克隆与鉴定

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An initial study on gene cloning and characterization of unicellular green microalga Ankistrodesmus convolutus was carried out to isolate and characterize the full-length cDNA of ribulose-1,5-bisphosphate carboxylase/oxygenase small subunit (RbcS) as a first step towards elucidating the structure of A. convolutus RbcS gene. The full-length of A. convolutus RbcS cDNA (AcRbcS) contained 28 bp of 5′ untranslated region (UTR), 225 bp of 3′ non-coding region, and an open reading frame of 165 amino acids consisting of a chloroplast transit peptide with 24 amino acids and a mature protein of 141 amino acids. The amino acid sequence has high identity to those of other green algae RbcS genes. The AcRbcS contained a few conserved domains including protein kinase C phosphorylation site, tyrosine kinase phosphorylation site and N-myristoylation sites. The AcRbcS was successfully expressed in Escherichia coli and a ~21 kDa of anticipated protein band was observed on SDS-PAGE. From the phylogenetic analysis of RbcS protein sequences, it was found that the RbcS of A. convolutus has closer genetic relationship with green microalgae species compared to those of green seaweed and green macroalgae species. Southern hybridization analysis revealed that the AcRbcS is a member of a small multigene family comprising of two to six members in A. convolutus genome. Under different illumination conditions, RT-PCR analysis showed that AcRbcS transcription was reduced in the dark, and drastically recovered in the light condition. Results presented in this paper established a good foundation for further study on the photosynthetic process of A. convolutus and other green algae species where little information is known on Rubisco small subunit.
机译:初步研究了单细胞绿色微藻盘旋菌的基因克隆和鉴定,以分离和鉴定核糖-1,5-双磷酸羧化酶/加氧酶小亚基(RbcS)的全长cDNA,这是阐明结构的第一步卷积曲霉RbcS基因的克隆卷积曲霉RbcS cDNA(AcRbcS)的全长包含28 bp的5'非翻译区(UTR),225 bp的3'非编码区和一个由叶绿体转运肽组成的165个氨基酸的开放阅读框具有24个氨基酸和141个氨基酸的成熟蛋白。该氨基酸序列与其他绿藻RbcS基因具有高度同一性。 AcRbcS包含几个保守域,包括蛋白激酶C磷酸化位点,酪氨酸激酶磷酸化位点和N-肉豆蔻酰基化位点。 AcRbcS在大肠杆菌中成功表达,在SDS-PAGE上观察到约21 kDa的预期蛋白条带。通过对RbcS蛋白序列的系统发育分析,发现卷积曲霉的RbcS与绿色微藻物种相比,与绿色海藻和绿色大型藻物种具有更紧密的遗传关系。 Southern杂交分析表明,AcRbcS是一个小的多基因家族成员,由卷积曲霉基因组中的两个到六个成员组成。在不同的光照条件下,RT-PCR分析表明AcRbcS转录在黑暗中减少,而在光照条件下则大幅度恢复。本文介绍的结果为进一步研究卷积曲霉和其他绿藻物种的光合作用奠定了良好的基础,而关于卷柏小亚基的信息很少。

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