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中国生物工程杂志

CHINA BIOTECHNOLOGY
中国生物工程杂志  2007, Vol. 27 Issue (10): 87-92    
研究报告     
甘蔗全长丙酮酸磷酸二激酶(PPDK)基因的克隆
杨福明 徐德昌 侯爱菊
哈尔滨工业大学食品科学与工程学院 哈尔滨工业大学食品科学与工程学院 哈尔滨工业大学食品科学与工程学院
Cloning for full-length pyruvate orthophosphate dikinase gene of sugarcane
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摘要:

和C3植物相比,C4植物具有明显的生长优势及水分和营养利用率,生物产量也较高。甘蔗是典型的C4作物之一。以甘蔗叶片提取的基因组DNA为模板,以GenBank公布的甘蔗PPDK基因cDNA序列设计引物,进行LA-PCR(Long Acute PCR)扩增。将PCR产物克隆到pMD18-T载体中,转化大肠杆菌JM109,测序,得到了13.5Kb的甘蔗全长PPDK基因序列。为方便后续实验,在引物中引入可利用的XhoI和NotI酶切位点,将全长PPDK基因分两段克隆到pMD18-T Simple载体中,转化大肠杆菌JM109,完成了甘蔗全长丙酮酸磷酸二激酶(PPDK)基因的完整克隆,为将其导入C3作物中奠定了研究基础,实验室保藏菌种。

Abstract:

Compared with C3 plant, C4 plant had evident growth advantage, higher rates of water and nutrition using, and higher bio-yield than C3 plant, Sugarcane was one of the typical C4 plants. DNA was extracted from sugarcane leaves, primers were designed by the cDNA sequence of PPDK gene from GenBank. Then DNA was amplified by LA-PCR(Long Acute PCR) method, ligated into pMD18-T vectors, transformed E.coli. JM109, sequenced. Full-length PPDK gene sequence of sugarcane was obtained, the sequence was 13.5Kb in length. For convenient of the next experiment, two digest sites(XhoI and NotI) were introduced into primers, the full-length PPDK gene was splitted to two parts, each ligated into pMD18-T Simple vectors, transformed E.coli. JM109, whole PPDK gene clone of sugarcane was finished, preparation of transferring it into C3 plant was made. The strains were storaged in our lab.

收稿日期: 2007-06-07 出版日期: 2007-10-25
通讯作者: 徐德昌   
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引用本文:

杨福明,徐德昌,侯爱菊. 甘蔗全长丙酮酸磷酸二激酶(PPDK)基因的克隆[J]. 中国生物工程杂志, 2007, 27(10): 87-92.

. Cloning for full-length pyruvate orthophosphate dikinase gene of sugarcane. China Biotechnology, 2007, 27(10): 87-92.

链接本文:

https://manu60.magtech.com.cn/biotech/CN/        https://manu60.magtech.com.cn/biotech/CN/Y2007/V27/I10/87

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