湖北省自然科学基金(2003ABA118)和国家高技术“863”计划资助项目(2002AA227011).
This work was supported by grants from The National Natural Sciences Foundation of Hubei Province (2003ABA118) and State 863 High Technology R&D Project of China (2002AA227011).
通过分析拟南芥与大豆的羧基转移酶α亚基的cDNA序列,运用RT-PCR、RACE和基因组步行(Genome walking)三种技术进行组合克隆,首次从油菜开花后20~29天的幼胚中,克隆到质体定位的羧基转移酶α亚基的全长cDNA.同源性分析表明,其开放阅读框(ORF)编码的氨基酸序列与拟南芥、大豆的羧基转移酶α亚基的同源性分别为85%、59%.将此cDNA去除叶绿体转运肽编码序列的成熟肽编码序列,克隆到表达载体pHBM625上,蛋白质印迹分析,它在大肠杆菌中成功表达.
By analyzing the cDNA sequences of carboxyltransferase alpha subunits(α-CTs) from Arabidopsis thaliana and Glycine max,and combination RT-PCR, 3′-rapid amplification of cDNA ends (3′-RACE) and Genome walking techniques, the full length cDNA of plastid α-CT from embryos of Brassica napus between 20 and 29 days after flowering was cloned. Homologous analysis showed that the amino acid sequence deduced from it shares 85% and 59% homology with those of α-CT in Arabidopsis thaliana and Glycine max, respectively. The sequence encoding mature peptide that was absent from chloroplast transit peptide has been inserted into expression vector pHBM625 and expressed successfully in Escherichia coli by Western blotting analysis.
武玉永,马立新,蒋思婧.甘蓝型油菜羧基转移酶α亚基全长cDNA的克隆及在大肠杆菌中表达[J].生物化学与生物物理进展,2004,31(9):847-854
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