Gunsalus R P, Miguel A G, Gunsalus G L
J Bacteriol. 1986 Jul;167(1):272-8. doi: 10.1128/jb.167.1.272-278.1986.
A radioimmunoassay for the Trp repressor protein of Escherichia coli was developed with antisera raised against purified Trp repressor protein. This assay was used to directly measure the intracellular Trp repressor content in several E. coli K-12 and B/r strains. Repressor levels varied from 2.5- to 3-fold in response to L-tryptophan concentration in the growth medium (15 to 44 ng of repressor per mg of protein). Neither cell growth rate nor culture age had a significant effect on repressor concentrations within the cell. Addition of L-tryptophan to the growth medium resulted in lowered intracellular levels of Trp repressor. The absolute amounts of native Trp repressor molecules per cell varied between 120 and 375 dimers in the presence and absence of L-tryptophan in the culture medium, respectively. Assuming an intracellular volume of 7.3 microliters/10(10) E. coli cells, the Trp repressor concentration varied from 270 to 850 nM in response to extracellular tryptophan levels. These findings represent the first direct measurements of Trp repressor levels in E. coli and confirm the autoregulatory nature of the trpR gene.
利用针对纯化的色氨酸阻遏蛋白产生的抗血清,开发了一种用于检测大肠杆菌色氨酸阻遏蛋白的放射免疫测定法。该测定法用于直接测量几种大肠杆菌K - 12和B/r菌株细胞内色氨酸阻遏蛋白的含量。阻遏蛋白水平随生长培养基中L - 色氨酸浓度变化2.5至3倍(每毫克蛋白质中阻遏蛋白为15至44纳克)。细胞生长速率和培养时间对细胞内阻遏蛋白浓度均无显著影响。向生长培养基中添加L - 色氨酸会导致细胞内色氨酸阻遏蛋白水平降低。在培养基中存在和不存在L - 色氨酸的情况下,每个细胞中天然色氨酸阻遏蛋白分子的绝对量分别在120至375个二聚体之间变化。假设细胞内体积为7.3微升/10¹⁰个大肠杆菌细胞,色氨酸阻遏蛋白浓度随细胞外色氨酸水平变化在270至850纳摩尔之间。这些发现是对大肠杆菌中色氨酸阻遏蛋白水平的首次直接测量,并证实了trpR基因的自我调节性质。