Tsay S S, Brown K K, Gaudy E T
J Bacteriol. 1971 Oct;108(1):82-8. doi: 10.1128/jb.108.1.82-88.1971.
In Pseudomonas aeruginosa, the transport of glycerol was shown to be genetically controlled and to be dependent on induction by glycerol. Accumulation of (14)C-glycerol was almost completely absent in uninduced cells and in a transport-negative mutant. Kinetic studies with induced cells suggested that glycerol may be transported by two systems with different affinities for glycerol. Osmotically shocked cells did not transport glycerol, and the supernatant fluid from shocked cells contained glycerol-binding activity demonstrable by equilibrium dialysis. The binding protein was not glycerol kinase. Binding activity was absent in shock fluids from the transport-negative mutant and from uninduced cells. The glycerol-binding protein was partially purified by precipitation with ammonium sulfate. Mild heat treatment completely eliminated the binding activity of shock fluid and of the partially purified protein. Sodium azide and N-ethylmaleimide inhibited both transport by whole cells and binding of glycerol by shock fluid. It is concluded that transport of glycerol by P. aeruginosa involves a binding protein responsible for recognition of glycerol and may occur by facilitated diffusion or active transport. A requirement for energy has not been demonstrated.
在铜绿假单胞菌中,甘油的转运显示受基因控制且依赖于甘油诱导。在未诱导的细胞和转运阴性突变体中,几乎完全不存在(14)C-甘油的积累。对诱导细胞的动力学研究表明,甘油可能通过两种对甘油具有不同亲和力的系统进行转运。经渗透压休克处理的细胞不转运甘油,且休克细胞的上清液含有可通过平衡透析证明的甘油结合活性。该结合蛋白不是甘油激酶。在转运阴性突变体和未诱导细胞的休克液中不存在结合活性。通过硫酸铵沉淀对甘油结合蛋白进行了部分纯化。温和的热处理完全消除了休克液和部分纯化蛋白的结合活性。叠氮化钠和N-乙基马来酰亚胺既抑制全细胞的转运,也抑制休克液对甘油的结合。得出的结论是,铜绿假单胞菌对甘油的转运涉及一种负责识别甘油的结合蛋白,可能通过易化扩散或主动转运发生。尚未证明对能量有需求。