Gardiol A, Arias A, Cerveñansky C, Gaggero C, Martínez-Drets G
J Bacteriol. 1980 Oct;144(1):12-6. doi: 10.1128/jb.144.1.12-16.1980.
A double mutant strain (UR3) of Rhizobium meliloti L5-30 was isolated from a phosphoglucose isomerase mutant (UR1) on the basis of its resistance to fructose inhibition when grown on fructose-rich medium. UR3 lacked both phosphoglucose isomerase and fructokinase activity. A mutant strain (UR4) lacking only the fructokinase activity was derived from UR3; it grew on the same carbon sources as the parent strain, but not on fructose, mannitol, or sorbitol. A spontaneous revertant (UR5) of normal growth phenotype contained fructokinase activity. A fructose transport system was found in L5-30, UR4, and UR5 grown in arabinose-fructose minimal medium. No fructose uptake activity was detected when L5-30 and UR5 were grown on arabinose minimal medium, but this activity was present in strain UR4. Free fructose was concentrated intracellularly by UR4 > 200-fold above the external level. A partial transformation of fructose into mannitol and sorbitol was detected by enzymatic analysis of the uptake products. Polyol dehydrogenase activity was detected in UR4 grown in arabinose-fructose minimal medium. The induction pattern of polyol dehydrogenase activities in this strain might be due to slight intracellular fructose accumulation.
从磷酸葡萄糖异构酶突变体(UR1)中分离出苜蓿根瘤菌L5 - 30的双突变菌株(UR3),其依据是在富含果糖的培养基上生长时对果糖抑制具有抗性。UR3既缺乏磷酸葡萄糖异构酶活性,也缺乏果糖激酶活性。仅缺乏果糖激酶活性的突变菌株(UR4)由UR3衍生而来;它能在与亲本菌株相同的碳源上生长,但不能在果糖、甘露醇或山梨醇上生长。具有正常生长表型的自发回复突变体(UR5)含有果糖激酶活性。在阿拉伯糖 - 果糖基本培养基中生长的L5 - 30、UR4和UR5中发现了一种果糖转运系统。当L5 - 30和UR5在阿拉伯糖基本培养基上生长时,未检测到果糖摄取活性,但该活性存在于UR4菌株中。UR4将细胞内的游离果糖浓缩至胞外水平的200倍以上。通过对摄取产物的酶分析检测到果糖部分转化为甘露醇和山梨醇。在阿拉伯糖 - 果糖基本培养基中生长的UR4中检测到多元醇脱氢酶活性。该菌株中多元醇脱氢酶活性的诱导模式可能是由于细胞内果糖的轻微积累。