Downey R J, South P A
Department of Microbiology, Ohio University, Athens 45701.
Can J Microbiol. 1988 Jan;34(1):68-72. doi: 10.1139/m88-012.
The nitrate reductase (NADPH) (EC 1.6.6.3) from Aspergillus nidulans is influenced directly by mutations in the structural gene (niaD) for the major subunit of the enzyme and indirectly by mutation in any of several molybdenum cofactor loci (cnx). The cnxE-14 and the cnxH-3 mutants have been noted to contain the enzyme in two distinct forms following induction with nitrate. With the cnxH-3 as a prototype cnxH mutant, 10 other cnxH were found to be devoid of the assembled (dimeric) form of the enzyme. Two monoclonal antibodies specific for the native enzyme of the wild type (biA-1) recognized an epitope on the enzyme from the cnxE-14 and cnxH-3 mutants that was common to both and another that was unique to the cnxH gene specified protomer. Another monoclonal antibody recognized an epitope that occurs only in the assembled dimerio form of the enzyme from the wild type or the cnxE-14 mutant. The experiments further substantiate the cnxH phenotype as one involving unassembled protomers of the nitrate reductase in Aspergillus.
构巢曲霉的硝酸还原酶(NADPH)(EC 1.6.6.3)直接受该酶大亚基结构基因(niaD)突变的影响,也间接受几个钼辅因子位点(cnx)中任何一个位点突变的影响。已注意到cnxE - 14和cnxH - 3突变体在用硝酸盐诱导后含有两种不同形式的该酶。以cnxH - 3作为典型的cnxH突变体,发现另外10个cnxH突变体缺乏该酶的组装(二聚体)形式。两种针对野生型天然酶的单克隆抗体(biA - 1)识别来自cnxE - 14和cnxH - 3突变体的酶上的一个共同表位以及另一个仅由cnxH基因指定的原体所特有的表位。另一种单克隆抗体识别仅存在于野生型或cnxE - 14突变体的酶的组装二聚体形式中的一个表位。这些实验进一步证实了cnxH表型是构巢曲霉中涉及未组装的硝酸还原酶原体的一种表型。