为了明确缺氮条件下甜菜NR的活性,用活体测定法检测了经缺氮胁迫不同时间后甜菜叶中NR活性.结果表明,随着缺氮处理时间的延长,甜菜叶中的NR活性逐渐降低,在缺氯处理1h后,其活性下降较快.用50mmol/1.KNO3溶液处理的甜菜幼苗总RNA,通过RT—PCR分离得到了硝酸还原酶基因片段,长度为471bp,Blast分析表明,其与Genbank中硝酸还原酶基因部分序列具有高度同源性.
The experiments are conducted to investigate the activity of nitrate reductase in sugar beet (Beta vulgaris L. ) under different time of N - absent treatment. The results show that the activity of NR rapidly decrease in the first 1 h and gradually decrease when the time of N - absent treatment is prolonged. The homolog cDNA with 471 base pairs of nitrate reduetase gene is obtained by RT - PCR from total RNA using Beta vulgaris treated by 50 mmoL/L KNO3 as material. Blast analysis showed high identity to part sequence of Beta vulgaris nitrate reductase gene.