首页 | 本学科首页   官方微博 | 高级检索  
     检索      

转甜菜碱醛脱氢酶基因宁夏粳稻幼苗生理研究
引用本文:周晓燕,甘晓燕,石磊,宋玉霞.转甜菜碱醛脱氢酶基因宁夏粳稻幼苗生理研究[J].中国农学通报,2012,28(6):35-38.
作者姓名:周晓燕  甘晓燕  石磊  宋玉霞
作者单位:1. 宁夏农业生物技术重点实验室,银川750002;宁夏大学生命科学学院,银川750021
2. 宁夏农业生物技术重点实验室,银川,750002
基金项目:宁夏回族自治区科技攻关宁陕合作项目“抗旱耐盐碱基因克隆、功能分析及应用研究”
摘    要:为了提高植物耐盐性,充分利用盐碱地,通过采用农杆菌介导法将超旱生耐盐植物梭梭(Haloxylon ammodendron)的甜菜碱醛脱氢酶基因(HaBADH)转入宁夏粳稻,对其阳性植株幼苗进行耐盐性方面的相关生理研究。结果表明,在高浓度NaCl(5.0,7.0 g/L)胁迫下,与对照相比,转HaBADH基因粳稻幼苗的超氧化物歧化酶(SOD)、过氧化物酶(POD)、过氧化氢酶(CAT)的活性显著提高;丙二醛(MDA)的含量显著降低。说明转入HaBADH基因提高了粳稻对盐胁迫的耐受性。

关 键 词:银杏  银杏  FLS  基因  FLS  基因启动子  生物信息学  
收稿时间:2011/9/21 0:00:00
修稿时间:2011/11/22 0:00:00

Study on the Physiology of Transgenic Japonica Rice in Ningxia Seedlings with Gene of Betaine Aldehyde
Zhou Xiaoyan , Gan Xiaoyan , Shi Lei , Song Yuxia.Study on the Physiology of Transgenic Japonica Rice in Ningxia Seedlings with Gene of Betaine Aldehyde[J].Chinese Agricultural Science Bulletin,2012,28(6):35-38.
Authors:Zhou Xiaoyan  Gan Xiaoyan  Shi Lei  Song Yuxia
Institution:1(1Ningxia Academy of Agriculture and Forestry Sciences,Yinchuan 750002;2College of Life Science,Ningxia University,Yinchuan 750021)
Abstract:In order to improve plant salt tolerance,full use of saline-alkali soil,through the use of Agrobacterium tumefaciens ultra xeric salt-tolerant plants Haloxylon(Haloxylon ammodendron) of betaine aldehyde dehydrogenase gene(HaBADH) into Japonica rice of Ningxia,its positive seedings to salt tolerance in plants related to physiological research.The results showed that high concentrations of NaCl(5.0,7.0 g/L) stress,compared with the control,transfer HaBADH gene rice seedings superoxide dismutase(SOD),peroxidase(POD),catalase(CAT) activity was significantly increased;malondialdehyde(MDA) levels were significantly reduced.The results showed that,transfer HaBADH gene could increase Japonica rice of Ningxia tolerance to salt stress.
Keywords:Betaine aldehydede hydrogenase(BADH)  rice  transformation  salt tolerance
本文献已被 CNKI 维普 万方数据 等数据库收录!
点击此处可从《中国农学通报》浏览原始摘要信息
点击此处可从《中国农学通报》下载免费的PDF全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号