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水稻质体葡萄糖-6-磷酸脱氢酶基因的克隆与表达研究
引用本文:侯夫云,黄骥,陆驹飞,王州飞,张红生.水稻质体葡萄糖-6-磷酸脱氢酶基因的克隆与表达研究[J].遗传学报,2006,33(5):441-448.
作者姓名:侯夫云  黄骥  陆驹飞  王州飞  张红生
作者单位:1. 山东省农科院
2. 南京农业大学作物遗传与种质创新国家重点实验室,南京,210095
3. 扬州大学农学院,扬州,225009
基金项目:This work was supported by the National Transgenic Plant Research Program in China (No.JY03A1101), Major Project of Province Key Laboratory of Plant Functional Genome in Yangzhou University (No.KJS03098) and Changjiang Scholars and Innovative Research Team in University(PCSIRT).
摘    要:戊糖磷酸途径是高等植物中重要的代谢途径,主要生理功能是产生NADPH以及供核酸代谢的磷酸戊糖。葡萄糖-6-磷酸脱氢酶(G6PDH)是戊糖磷酸途径的关键酶,广泛存在于高等植物细胞的细胞质和质体中。木研究首次从水稻(Oryza sativa L.)幼苗中分离了核编码的质体G6PDH基因OsG6PDH2,序列分析表明OsG6PDH2编码一个具有588个氨基酸残基的多肽,等电点为8.5,分子量66kDa。OsG6PDH2的N端有1个70个氨基酸的信号肽,推测的裂解位点为Gly55和Val56,表明OsG6PDH2编码产物可能定位于质体。多序列比较的结果表明OsG6PDH2与拟南芥、烟草、马铃薯质体G6PDH的一致性分别达81%、87%、83%。进化关系说明水稻OsG6PDH2与拟南芥(AtG6PDH3)、马铃薯(StG6PDH1)处于高等植物P2型质体G6PDH分支上,暗示了OsG6PDH2可能是一个P2型的质体蛋白。Matinspector程序分析表明,OsG6PDH2在起始密码子上游含有一个bZIP转录因子识别位点、一个ABA应答元件、一个CRT/DRE元件和1个W-box元件。半定量RT-PCR分析表明,OsG6PDH2在水稻根、茎、叶和幼穗组织中都呈低丰度组成型表达,在根部表达较高,在水稻幼苗中的表达显著受暗处理的诱导。将OsG6PDH2的完整开放阅读框构建到大肠杆菌表达载体pET30a(+)中,pET30a(+)-OsG6PDH2在大肠杆菌中得到了有效表达。酶活性测定证明,OsG6PDH2的编码产物具有葡萄糖-6-磷酸脱氢酶的功能。

关 键 词:水稻  葡萄糖-6-磷酸脱氢酶  基因克隆  表达分析
收稿时间:2005-04-23
修稿时间:2005-04-232005-09-13

Isolation and Expression Analysis of Plastidic Glucose-6-phosphate Dehydrogenase Gene from Rice (Oryza sativa L.)
HOU Fu-Yun,HUANG Ji,LU Ju-Fei,WANG Zhou-Fei,ZHANG Hong-Sheng.Isolation and Expression Analysis of Plastidic Glucose-6-phosphate Dehydrogenase Gene from Rice (Oryza sativa L.)[J].Journal of Genetics and Genomics,2006,33(5):441-448.
Authors:HOU Fu-Yun  HUANG Ji  LU Ju-Fei  WANG Zhou-Fei  ZHANG Hong-Sheng
Institution:1. State Key Laboratory of Crop Genetics and Germplasm Enhancement, Nanjing Agricultural University, Nanjing 210095, China; 2. College of Agriculture, Yangzhou University, Yangzhou 225009, China
Abstract:Glucose-6-phosphate dehydrogenase is a rate-limiting enzyme of pentose phosphate pathway, existing in cytosolic and plastidic compartments of higher plants. A novel gene encoding plastidic glucose-6-phosphate dehydrogenase was isolated from rice (Oryza sativa L.) and designated OsG6PDH2 in this article. Through semiquantitative RT-PCR approach it was found that OsG6PDH2 mRNA was weakly expressed in rice leaves, stems, immature spikes or flowered spikes, and a little higher in roots. However, the expression of OsG6PDH2 in rice seedlings was significantly induced by dark treatment. The complete opening read-ing frame (ORF) of OsG6PDH2 was inserted into pET30a (+), and expressed in Escherichia coli strain BL21 (DE3). The enzyme activity assay of transformed bacterial cells indicated that OsG6PDH2 encoding product had a typical function of glu-cose-6-phosphate dehydrogenase.
Keywords:rice  glucose-6-phosphate dehydrogenase  gene cloning  expression analysis
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