Borum P R, Monty K J
J Bacteriol. 1976 Jan;125(1):94-101. doi: 10.1128/jb.125.1.94-101.1976.
The cysB region in Salmonella typhimurium regulates in a positive manner the noncontiguous structural genes for the enzymes responsible for sulfate reduction in cysteine biosynthesis. We treated three cysB mutants with chemical mutagens and selected 81 secondary mutants in which the inability to utilize sulfate was suppressed. Growth experiments on the suppressed mutants showed that the original loss of sulfate utilization had been corrected to varying degrees and that portions of the pathway had been established in abnormal relationship to one another. Sixty of the suppressed mutations were mapped via transductional analysis, and each was very closely linked to the original cysB mutation. We demonstrated that the cysB product functions in the regulation of the cysteine biosynthetic enzymes during both logarithmic growth and stationary phase. Mutation can alter the regulatory response of one enzyme in either an upward or downward direction while the regulation of other enzymes in the pathway remains unchanged. These data are consistent with the idea of a multivalent or multisite regulator molecule.
鼠伤寒沙门氏菌中的cysB区域以正向方式调节参与半胱氨酸生物合成中负责硫酸盐还原的酶的不连续结构基因。我们用化学诱变剂处理了三个cysB突变体,并筛选出81个抑制了无法利用硫酸盐能力的二级突变体。对这些抑制突变体的生长实验表明,最初无法利用硫酸盐的情况已得到不同程度的纠正,并且该途径的各部分之间已建立起异常的相互关系。通过转导分析对60个抑制突变进行了定位,每个突变都与原始的cysB突变紧密连锁。我们证明,cysB产物在对数生长期和稳定期均参与半胱氨酸生物合成酶的调节。突变可以使一种酶的调节反应在向上或向下的方向上发生改变,而该途径中其他酶的调节则保持不变。这些数据与多价或多位点调节分子的观点一致。