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甜菜(Beta vulgaris L.)叶片GOGAT与GS协同变化分析

Synergetic analysis of GOGAT and GS in sugar beet (Beta vulgaris L.) leaves

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GS/GOGAT循环是甜菜氮素同化主要途径。甜菜幼苗在氮素诱导下,通过使用不同浓度重氮乙酰丝氨酸处理,并在处理后2、6、9、12和24 h分别取样,利用qRT-PCR技术检测幼苗GS1、GS2及GOGAT的mRNA表达水平,同时测定GOGAT和GS酶活性,分析GOGAT与GS协同变化作用。结果表明,重氮乙酰丝氨酸处理后,GOGAT酶活性在6 h时开始被抑制。GS活性在9 h时开始被抑制;GOGAT的mRNA表达量于6 h时开始下调, GS1的mRNA表达量在2 h时开始下调,而GS2的mRNA表达量于9 h时开始下调,甜菜叶片NH4+的同化以GS2/GOGAT为主。
GS/GOGAT cycle is the main assimilation ways in sugar beet. This study is based on nitrogen induction of sugar beet seedings. We processed sugar beet seedings with ranges of azaserine concentrations at different time, and quantified the GS1, GS2 and GOGAT mRNA expression level using qRT-PCR method. Simultaneously GOGAT and GS enzyme activity was also determined, further to elaborate the synegy changes of two enzymes. The results showed that after azaserine treatment of sugar beet leaves, GOGAT activity began to be inhibited at 6 h, GS activity began to be inhibited at 9 h. In addition, GOGAT mRNA expression level started to decrease at 6 h, GS1 mRNA expression level began to drop at 2 h, and GS2 mRNA expression levels started to decrease at 9 h, indicated GS2/GOGAT cycle was the main synergy way in sugar beet seedlings.

sugar beetglutamate synthaseglutamine synthetasegene expression

李彩凤、徐影、郭剑、陈明、桑丽敏、刘磊、王玉波、马凤鸣

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东北农业大学农学院,哈尔滨 150030

甜菜 谷氨酸合成酶 谷氨酰胺合成酶 基因表达

国家自然科学基金国家甜菜现代产业技术体系建设项目

31171493CARS-210306-04

2015

东北农业大学学报
东北农业大学

东北农业大学学报

CSTPCDCSCD北大核心
影响因子:0.752
ISSN:1005-9369
年,卷(期):2015.(4)
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