Rotman B
J Supramol Struct. 1977;7(1):29-35. doi: 10.1002/jss.400070104.
Strains of Escherichia coli K12 were constructed for the specific purpose of evaluating the inducibility of the influx mechanism controlled by the lacY gene. These strains are heteromerodiploids characterized by a high and relatively constant level of beta-D-galactosidase which is not affected significantly by induction of the Lac operon. These properties were obtained by introducing episomal lacI+,Oc,Z+,Y-genes into the cells. In these merodiploids the rate of o-nitrophenyl-beta-D-galactopyranoside (ONPG) hydrolysis of extracted cells is 50-times that of intact cells. This difference indicates that the rate limiting step in the ONPG hydrolysis by intact cells is influx. Using a set of merodiploids with and without the LacY transport system, we were able to demonstrate a specific induction of ONPG influx. However, the increase in influx due to induction was only 3.5-fold as compared to the 40-fold increase observed when the LacY permease was measured by intracellular accumulation of [14C]TMG.
构建大肠杆菌K12菌株的特定目的是评估由lacY基因控制的流入机制的可诱导性。这些菌株是异源二倍体,其特征在于β-D-半乳糖苷酶水平高且相对恒定,不受Lac操纵子诱导的显著影响。这些特性是通过将附加体质lacI +、Oc、Z +、Y-基因导入细胞而获得的。在这些部分二倍体中,提取细胞的邻硝基苯基-β-D-吡喃半乳糖苷(ONPG)水解速率是完整细胞的50倍。这种差异表明完整细胞进行ONPG水解的限速步骤是流入。使用一组具有和不具有LacY转运系统的部分二倍体,我们能够证明ONPG流入的特异性诱导。然而,与通过[14C]TMG的细胞内积累测量LacY通透酶时观察到的40倍增加相比,诱导引起的流入增加仅为3.5倍。