Banks G R, Shelton P A, Kanuga N, Holden D W, Spanos A
Genetics Division, National Institute for Medical Research, Mill Hill, London, UK.
Gene. 1993 Sep 6;131(1):69-78. doi: 10.1016/0378-1119(93)90670-x.
The nar1 gene was cloned from Ustilago maydis and the 908-amino-acid (aa) sequence of the encoded protein found to have strong identities with other nitrate reductases from fungi and plants. This was especially so in three domains which define enzyme cofactor-binding sites. The gene was isolated alone and in association with the nir1 gene, suggesting that the two genes are closely linked on the chromosome. The phenotype of a strain in which nar1 had been disrupted was consistent with the only role of nar1 being in nitrate reduction. Nitrate ions induced a 90-fold increase in nar1 transcript levels, while ammonium ions repressed transcript levels.
从玉米黑粉菌中克隆出nar1基因,发现其编码的908个氨基酸的蛋白质序列与其他真菌和植物的硝酸还原酶有很强的同源性。在定义酶辅因子结合位点的三个结构域中尤其如此。该基因单独分离出来,也与nir1基因一起分离出来,这表明这两个基因在染色体上紧密相连。nar1基因被破坏的菌株的表型与nar1仅在硝酸盐还原中起作用一致。硝酸根离子使nar1转录水平增加90倍,而铵离子则抑制转录水平。