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谷氨酰胺合成酶基因GS1和GS2在转基因水稻植株中的高效表达提高了耐缺氮能力。

Highly effective expression of glutamine synthetase genes GS1 and GS2 in transgenic rice plants increases nitrogen-deficiency tolerance.

作者信息

Sun Hui, Huang Qi-Man, Su Jin

机构信息

Biotechnology Research Institute, Chinese Academy of Agricultural Sciences, Beijing 100081, China.

出版信息

Zhi Wu Sheng Li Yu Fen Zi Sheng Wu Xue Xue Bao. 2005 Oct;31(5):492-8.

Abstract

Glutamine synthetase (GS, EC6.3.1.2) is a key enzyme in ammonia assimilation both in plants and in Gram-negative microorganisms. It plays an important role in efficient use of nitrogen sources and nitrogen metabolism in organisms. Two groups of GS isoenzymes, plastidic (GS2) and cytosolic (GS1), have been identified in higher plants. A plant constitutive expression vector p2GS harboring GS1 and GS2 under the control of rice actin 1 (Act1) and maize ubiquitin (Ubi) promoters was constructed for the first time in a single plasmid, and 3 rounds of ligation and transformation were performed. There has been no report about studies on rice transformation with the two GS enzymes (GS1 and GS2). The p2GS thus constructed was introduced into rice var. Zhonghua 10 by Agrobacterium-mediated transfer method, and transgenic plants with resistance to hygromycin (Hyg) were obtained. Results of PCR and Southern blot analysis showed that the foreign genes have been integrated into the rice genome. The transcription of GS1-GS2 genes in the transformants was also confirmed by Northern blot analysis. The transgenic rice plants thus obtained can grow well in an MS medium in which the nitrogen source was replaced by (NH(4))(2)SO(4) 0.7 mmol/L, and fresh weight of the transformants was significantly higher than the control rice plants. The result suggests that expression of p2GS makes the transgenic rice plants tolerant to nitrogen-deficiency.

摘要

谷氨酰胺合成酶(GS,EC6.3.1.2)是植物和革兰氏阴性微生物中氨同化的关键酶。它在生物体有效利用氮源和氮代谢中发挥着重要作用。在高等植物中已鉴定出两组GS同工酶,即质体(GS2)和胞质(GS1)。首次在单个质粒中构建了一个植物组成型表达载体p2GS,其在水稻肌动蛋白1(Act1)和玉米泛素(Ubi)启动子的控制下携带GS1和GS2,并进行了三轮连接和转化。关于用两种GS酶(GS1和GS2)转化水稻的研究尚无报道。将如此构建的p2GS通过农杆菌介导的转化方法导入水稻品种中花10,获得了对潮霉素(Hyg)具有抗性的转基因植株。PCR和Southern杂交分析结果表明外源基因已整合到水稻基因组中。Northern杂交分析也证实了转化体中GS1 - GS2基因的转录。如此获得的转基因水稻植株能够在以0.7 mmol/L硫酸铵((NH(4))(2)SO(4))替代氮源的MS培养基中良好生长,且转化体的鲜重显著高于对照水稻植株。结果表明p2GS的表达使转基因水稻植株耐受缺氮。

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