Brownlee A G, Arst H N
J Bacteriol. 1983 Sep;155(3):1138-46. doi: 10.1128/jb.155.3.1138-1146.1983.
In Aspergillus nidulans, chlorate strongly inhibited net nitrate uptake, a process separate and distinct from, but dependent upon, the nitrate reductase reaction. Uptake was inhibited by uncouplers, indicating that a proton gradient across the plasma membrane is required. Cyanide, azide, and N-ethylmaleimide were also potent inhibitors of uptake, but these compounds also inhibited nitrate reductase. The net uptake kinetics were problematic, presumably due to the presence of more than one uptake system and the dependence on nitrate reduction, but an apparent Km of 200 microM was estimated. In uptake assays, the crnA1 mutation reduced nitrate uptake severalfold in conidiospores and young mycelia but had no effect in older mycelia. Several growth tests also indicate that crnA1 reduces nitrate uptake. crnA expression was subject to control by the positive-acting regulatory gene areA, mediating nitrogen metabolite repression, but was not under the control of the positive-acting regulatory gene nirA, mediating nitrate induction.
在构巢曲霉中,氯酸盐强烈抑制硝酸盐的净吸收,这一过程与硝酸盐还原酶反应不同且独立,但依赖于该反应。质子载体抑制剂可抑制吸收,这表明跨质膜的质子梯度是必需的。氰化物、叠氮化物和N - 乙基马来酰亚胺也是吸收的有效抑制剂,但这些化合物也抑制硝酸盐还原酶。净吸收动力学存在问题,可能是由于存在多个吸收系统以及对硝酸盐还原的依赖性,但估计其表观Km值为200微摩尔。在吸收试验中,crnA1突变使分生孢子和幼菌丝体中的硝酸盐吸收降低了几倍,但对老菌丝体没有影响。多项生长试验也表明crnA1降低了硝酸盐吸收。crnA的表达受正向作用调节基因areA的控制,介导氮代谢物阻遏,但不受正向作用调节基因nirA的控制,nirA介导硝酸盐诱导。