Stevens F J, Wu T T
J Gen Microbiol. 1976 Dec;97(2):257-65. doi: 10.1099/00221287-97-2-257.
Escherichia coli K12 cannot grow on D-lyxose, but a mutant was isolated which can utilize D-lyxose as sole source of carbon and energy for growth. D-Lyxose is transported into the bacteria by the D-xylose permease. The mutant constitutively synthesizes a new isomerase which is not inducible in the parent strain under any of the conditions tested. This enzyme, whose native substrate appears to be D-mannose, fortuitously converts D-lyxose into D-xylulose. Its structural gene is located at around 85 min on the E. coli genetic map, away from other known isomerase genes. D-Xylulose is subsequently catabolized by the enzymes of the normal D-xylose metabolic pathway. D-Mannose isomerase was partially purified and some of its properties were examined.
大肠杆菌K12不能利用D-来苏糖生长,但分离出了一个突变体,它能将D-来苏糖作为唯一的碳源和能源用于生长。D-来苏糖通过D-木糖通透酶转运进入细菌。该突变体组成型合成一种新的异构酶,在所测试的任何条件下,亲本菌株中该酶均不可诱导。这种酶的天然底物似乎是D-甘露糖,它偶然地将D-来苏糖转化为D-木酮糖。其结构基因位于大肠杆菌遗传图谱上约85分钟处,远离其他已知的异构酶基因。D-木酮糖随后通过正常的D-木糖代谢途径的酶进行分解代谢。对D-甘露糖异构酶进行了部分纯化,并检测了它的一些特性。