Shimizu R W, Botsford J L
J Gen Microbiol. 1981 Apr;123(2):351-4. doi: 10.1099/00221287-123-2-351.
Strains of Escherichia coli isogenic except for the trpR locus were grown in glucose-limited chemostats. Anthranilate synthase was assayed spectrofluorimetrically to measure trp expression. The specific activity was about ten times greater in the trpR- strain than in the trpR+ strain. In glucose-limited chemostats, the specific activity of anthranilate synthase was independent of growth rate. Both strains produced two to three times more anthranilate synthase in chemostats than in batch culture. The addition of 19 amino acids (not including tryptophan) increased trp expression of anthranilate synthase fivefold in the trpR+ strain.
除trpR基因座外其余基因均同型的大肠杆菌菌株在葡萄糖受限的恒化器中培养。采用荧光分光光度法测定邻氨基苯甲酸合酶以测量色氨酸表达。trpR-菌株中邻氨基苯甲酸合酶的比活性比trpR+菌株高约10倍。在葡萄糖受限的恒化器中,邻氨基苯甲酸合酶的比活性与生长速率无关。两种菌株在恒化器中产生的邻氨基苯甲酸合酶比在分批培养中多两到三倍。添加19种氨基酸(不包括色氨酸)使trpR+菌株中邻氨基苯甲酸合酶的色氨酸表达增加了五倍。