Hipkin C R, Kau D A, Cannons A C
Biochemistry Research Group, School of Biological Sciences, University of Wales, Swansea, U.K.
Biochem J. 1993 Oct 15;295 ( Pt 2)(Pt 2):611-5. doi: 10.1042/bj2950611.
Synthesis of nitrate reductase protein and increases in nitrate reductase activity occurred in cultures of the yeast Candida nitratophila when they were incubated in medium containing ammonium nitrate. Similar treatment with glutamine plus nitrate resulted in little increase in nitrate reductase activity, in cultures grown previously with reduced nitrogen compounds, and decreases in enzyme activity, in cultures adapted to nitrate. Labelling studies conducted in vivo revealed a rapid cessation of de novo nitrate reductase synthesis when glutamine was supplied to nitrate-adapted cultures in the presence of nitrate. Intracellular glutamine concentrations increased rapidly under these conditions and these cultures exhibited high glutamine: glutamate ratios. As nitrate was taken up in the presence of glutamine in these experiments, it is concluded that the glutamine-stimulated inhibition of nitrate reductase synthesis is a consequence of repression and rapid turnover of nitrate reductase mRNA and not inducer (nitrate) exclusion.
当将硝酸盐还原酶蛋白合成并增加硝酸盐还原酶活性时,嗜硝酸盐假丝酵母在含有硝酸铵的培养基中培养。在先前用还原态氮化合物培养的培养物中,用谷氨酰胺加硝酸盐进行类似处理导致硝酸盐还原酶活性几乎没有增加,而在适应硝酸盐的培养物中酶活性降低。体内标记研究表明,当在硝酸盐存在下向适应硝酸盐的培养物中供应谷氨酰胺时,从头合成硝酸盐还原酶会迅速停止。在这些条件下,细胞内谷氨酰胺浓度迅速增加,并且这些培养物表现出高谷氨酰胺:谷氨酸比率。由于在这些实验中在谷氨酰胺存在下硝酸盐被吸收,因此得出结论,谷氨酰胺刺激的硝酸盐还原酶合成抑制是硝酸盐还原酶mRNA的阻遏和快速周转的结果,而不是诱导剂(硝酸盐)排除的结果。