Magill C W, Sweeney H, Woodward V W
J Bacteriol. 1972 Apr;110(1):313-20. doi: 10.1128/jb.110.1.313-320.1972.
Kinetic parameters for three systems of active histidine uptake by germinated conidia of Neurospora crassa have been measured. Each system appears to follow typical Michaelis-Menten kinetics when studied separately from the other systems. Under the conditions studied, the general amino acid transport system was found to account for the major portion of histidine uptake from low concentrations. Three types of transport mutants with altered growth inhibition patterns were selected in a histidine auxotroph. Growth of one mutant, type bas(a), could be inhibited by the addition of methionine to a histidine-supplemented medium, and another type, neu(a), could be inhibited by the addition of arginine. These mutants were shown to be lacking active histidine uptake by the basic amino acid and neutral amino acid transport systems, respectively. Another type of double mutant (his-3, neu(r)) could be inhibited only by the addition of very high concentrations of methionine in the presence of arginine and histidine, and the mutation appeared to have altered the specificity of the neutral amino acid permease.
已测定了粗糙脉孢菌萌发分生孢子的三种活性组氨酸摄取系统的动力学参数。当与其他系统分开研究时,每个系统似乎都遵循典型的米氏动力学。在所研究的条件下,发现一般氨基酸转运系统在低浓度时占组氨酸摄取的主要部分。在组氨酸营养缺陷型中选择了三种具有改变的生长抑制模式的转运突变体。一种突变体bas(a)型,在补充组氨酸的培养基中添加蛋氨酸可抑制其生长,另一种neu(a)型,添加精氨酸可抑制其生长。这些突变体分别被证明缺乏通过碱性氨基酸和中性氨基酸转运系统的活性组氨酸摄取。另一种双突变体(his-3, neu(r))仅在存在精氨酸和组氨酸的情况下添加非常高浓度的蛋氨酸时才会受到抑制,并且该突变似乎改变了中性氨基酸通透酶的特异性。