Tsuchiya T, Hasan S M, Raven J
J Bacteriol. 1977 Sep;131(3):848-53. doi: 10.1128/jb.131.3.848-853.1977.
The role of Na+ in glutamate transport was studied in Escherichia coli B, strain 29-78, which possesses a very high activity of glutamate transport (L. Frank and I. Hopkins, J. Bacteriol., 1969). Energy-depleted cells were exposed to radioactive glutamate in the presence of a sodium gradient, a membrane potential, or both. One hundred- to 200-fold accumulation of the amino acid was attained in the presence of both electrical and chemical driving forces for the sodium ion. Somewhat lower accumulation values were obtained when either chemical or electrical driving forces were applied separately. A chemical driving force was produced by the addition of external Na+ to Na+-free cells. A membrane potential was established by a diffusion potential either of H+ in the presence of carbonyl cyanide p-trifluoromethoxyphenylhydrazone or of SCN-. These results support the hypothesis of a Na+-glutamate cotransport. Na+-driven glutamate transport was also observed in wild-type E. coli B but not in a strain of K-12.
在具有非常高的谷氨酸转运活性的大肠杆菌B菌株29 - 78中研究了Na⁺在谷氨酸转运中的作用(L.弗兰克和I.霍普金斯,《细菌学杂志》,1969年)。将能量耗尽的细胞置于存在钠梯度、膜电位或两者皆有的情况下,使其接触放射性谷氨酸。在存在钠离子的电驱动力和化学驱动力的情况下,氨基酸积累了100至200倍。当单独施加化学驱动力或电驱动力时,获得的积累值略低。通过向无钠细胞中添加外部Na⁺产生化学驱动力。通过在羰基氰化物对三氟甲氧基苯腙存在下H⁺的扩散电位或SCN⁻的扩散电位建立膜电位。这些结果支持了Na⁺ - 谷氨酸共转运的假说。在野生型大肠杆菌B中也观察到了Na⁺驱动的谷氨酸转运,但在K - 12菌株中未观察到。