Kocharian Sh M, Melkumian M A
Genetika. 1986 Aug;22(8):2055-65.
Two types of mutants lacking the second purine nucleoside phosphorylase (PNPase 2) activity were isolated using the Escherichia coli K-12 pndR strains with constitutive or inosine-inducible synthesis of the PNPase 2. The mutations of the first type are recessive to the pndR+ allele on the F' episome. They are closely linked to the original pndR+ mutations and therefore affect the pndR gene encoding the activator protein. The mutations of the second type affect the PNPase 2 structural gene (pndA) and are recessive to the pndA+ allele on the F' episome. The nupC-pndR-pndA-ptsH-cysA gene order was established by means of four- and five-factorial transductional crosses.
利用大肠杆菌K-12 pndR菌株,通过组成型或肌苷诱导型合成嘌呤核苷磷酸化酶2(PNPase 2),分离出两种缺乏第二种嘌呤核苷磷酸化酶(PNPase 2)活性的突变体。第一类突变对F'附加体上的pndR +等位基因呈隐性。它们与原始的pndR +突变紧密连锁,因此影响编码激活蛋白的pndR基因。第二类突变影响PNPase 2结构基因(pndA),对F'附加体上的pndA +等位基因呈隐性。通过四因子和五因子转导杂交确定了nupC-pndR-pndA-ptsH-cysA基因顺序。