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光照和不同形态氮营养盐供应对坛紫菜硝酸还原酶活性的影响 被引量:6
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作者 徐智广 邹定辉 +2 位作者 张鑫 刘树霞 高坤山 《水产学报》 CAS CSCD 北大核心 2007年第1期90-96,共7页
为了探讨光照、NO3--N和NH4+-N对坛紫菜(Porphyra haitanensis)硝酸还原酶活性(NRA)的影响,在光照和黑暗条件下分别对坛紫菜叶状体进行氮(N)饥饿→氮(N)加富和N加富→N饥饿处理,并测定NRA的变化。结果表明:在N饥饿→N加富过程中,光照下... 为了探讨光照、NO3--N和NH4+-N对坛紫菜(Porphyra haitanensis)硝酸还原酶活性(NRA)的影响,在光照和黑暗条件下分别对坛紫菜叶状体进行氮(N)饥饿→氮(N)加富和N加富→N饥饿处理,并测定NRA的变化。结果表明:在N饥饿→N加富过程中,光照下NRA比黑暗中要高;NO3--N的加富能提高NRA,且在光照下比黑暗中NRA达到最大值的时间要短;而NH4+-N与NO3--N共同对N饥饿藻体加富时NRA没有明显变化,并与NH4+-N单独加富无显著差异。另外,对于N加富→N饥饿的处理,在光照下NO3--N加富和NH4+-N与NO3--N共同加富的NR都能在N饥饿处理后的一段时间内维持较高的活性。这些结果说明:光照和硝酸盐对NRA起正调节作用,而铵盐对NRA起负调节作用,但NRA与体外硝酸盐浓度并不成直接的正相关关系。 展开更多
关键词 坛紫菜 硝酸还原酶活性 氮饥饿 氮加富 光照 营养盐
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氮磷饥饿诱导的水稻糖转运体基因的cDNA克隆和鉴定(英文) 被引量:2
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作者 陈青爽 黄帼 +3 位作者 易可可 王小兵 刘非燕 吴平 《植物生理与分子生物学学报》 CAS CSCD 2002年第3期227-234,共8页
运用快速扣除杂交 (RaSH)方法构建了水稻氮饥饿诱导的cDNA文库。从该文库获得了一个cDNA克隆OsNSI1 (Oryzasativanitrogenstarva tion inducible 1 )。该全长cDNA编码 5 77个氨基酸 ,蛋白分子量为 6 1 .2kD。推测得出的氨基酸序列与其... 运用快速扣除杂交 (RaSH)方法构建了水稻氮饥饿诱导的cDNA文库。从该文库获得了一个cDNA克隆OsNSI1 (Oryzasativanitrogenstarva tion inducible 1 )。该全长cDNA编码 5 77个氨基酸 ,蛋白分子量为 6 1 .2kD。推测得出的氨基酸序列与其他物种的糖转运体有很高的同源性。水合性分析表明OsNSI1包含有 1 2个跨膜区域和一个中心亲水环。这些数据提示OsNSI1是一个糖转运体蛋白。Southern印迹分析表明OsNSI1是一个单拷贝基因。Northern印迹分析表明OsNSI1主要在叶及根中表达 ,氮。 展开更多
关键词 氮磷饥饿 诱导 水稻 糖转运体基因 CDnA克隆 鉴定
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TaARR1, a cytokinin response regulator gene in Triticum aestivum, is essential in plant N starvation tolerance via regulating the N acquisition and N assimilation 被引量:4
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作者 YANG Meng-ya CHEN Jia-qi +2 位作者 TIAN He-yang NI Chen-yang XIAO Kai 《Journal of Integrative Agriculture》 SCIE CAS CSCD 2019年第12期2691-2702,共12页
Plant N starvation response is closely associated with the N signaling components that involve transduction of the low-N cues. In this study, we functionally characterized Ta ARR1, a cytokinin(CK) response regulator g... Plant N starvation response is closely associated with the N signaling components that involve transduction of the low-N cues. In this study, we functionally characterized Ta ARR1, a cytokinin(CK) response regulator gene in Triticum aestivum, in mediating the N starvation adaptation in plants. Ta ARR1 harbors two conserved domains specified by plant ARR family members;subcellular localization analysis indicated its target onto nucleus after endoplasmic reticulum assortment. Ta ARR1 displayed modified expression upon the N starvation stressor, showing upregulated expression in roots and leaves over a 27-h N starvation treatment and whose induced transcripts were gradually recovered along with progression of the N recovery treatment. The tobacco lines overexpressing Ta ARR1 displayed improved low-N stress tolerance, displaying enlarged phenotype, increased biomass and N accumulation, and enhanced glutamine synthetase(GS) activities compared with wild type(WT) following the N starvation treatment. Expression analysis on genes encoding the nitrate transporter(NRT) and GS proteins in Nicotiana tabacum revealed that Nt NRT2.2 and Nt GS3 are upregulated in expression in the N-deprived transgenic lines, whose expression patterns were contrasted to other above family genes that were unaltered on transcripts between the transgenic lines and WT. Transgene analysis validated the function of Nt NRT2.2 and Nt GS3 in regulating N accumulation, GS activity, growth traits, and N use efficiency in plants. These results suggested the internal connection between the Ta ARR1-mediated N starvation tolerance and the modified transcription of distinct N acquisitionand assimilation-associated genes. Our investigation together indicates that Ta ARR1 is essential in plant N starvation adaptation due to the gene function in transcriptionally regulating distinct NRT and GS genes that affect plant N uptake and assimilation under the N starvation condition. 展开更多
关键词 wheat(Triticum AESTIVUM L.) CYTOKInIn response regulator GEnE expression n starvation functional characterization
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