Argaud D, Lange A J, Becker T C, Okar D A, el-Maghrabi M R, Newgard C B, Pilkis S J
Department of Physiology and Biophysics, SUNY at Stony Brook 11794, USA.
J Biol Chem. 1995 Oct 13;270(41):24229-36. doi: 10.1074/jbc.270.41.24229.
6-Phosphofructo-2-kinase/fructose-2,6-bisphosphatase has been postulated to be a metabolic signaling enzyme, which acts as a switch between glycolysis and gluconeogenesis in mammalian liver by regulating the level of fructose 2,6-bisphosphate. The effect of overexpressing the bifunctional enzyme was studied in FAO cells transduced with recombinant adenoviral constructs of either the wild-type enzyme or a double mutant that has no bisphosphatase activity or protein kinase phosphorylation site. With both constructs, the mRNA and protein were overexpressed by 150- and 40-fold, respectively. Addition of cAMP to cells overexpressing the wild-type enzyme increased the S0.5 for fructose 6-phosphate of the kinase by 1.5-fold but had no effect on the overexpressed double mutant. When the wild-type enzyme was overexpressed, there was a decrease in fructose 2,6-bisphosphate levels, even though 6-phosphofructo-2-kinase maximal activity increased more than 22-fold and was in excess of fructose-2,6-bisphosphatase maximal activity. The kinase:bisphosphatase maximal activity ratio was decreased, indicating that the overexpressed enzyme was phosphorylated by cAMP-dependent protein kinase. Overexpression of the double mutant resulted in a 28-fold increase in kinase maximal activity and a 3-4-fold increase in fructose 2,6-bisphosphate levels. Overexpression of this form inhibited the rate of glucose production from dihydroxyacetone by 90% and stimulated the rate of lactate plus pyruvate production by 200%. In contrast, overexpression of the wild-type enzyme enhanced glucose production and inhibited lactate plus pyruvate production. These results provide direct support for fructose 2,6-bisphosphate as a regulator of gluconeogenic/glycolytic pathway flux and suggest that regulation of bifunctional enzyme activities by covalent modification is more important than the amount of the protein.
6-磷酸果糖-2-激酶/果糖-2,6-二磷酸酶被认为是一种代谢信号酶,它通过调节果糖2,6-二磷酸的水平,在哺乳动物肝脏中充当糖酵解和糖异生之间的开关。在用野生型酶或无双磷酸酶活性或蛋白激酶磷酸化位点的双突变体重组腺病毒构建体转导的FAO细胞中,研究了过表达双功能酶的效果。使用这两种构建体时,mRNA和蛋白质分别过表达了150倍和40倍。向过表达野生型酶的细胞中添加cAMP,使激酶对6-磷酸果糖的S0.5增加了1.5倍,但对过表达的双突变体没有影响。当野生型酶过表达时,尽管6-磷酸果糖-2-激酶的最大活性增加了22倍以上且超过了果糖-2,6-二磷酸酶的最大活性,但果糖2,6-二磷酸水平仍下降。激酶:双磷酸酶的最大活性比降低,表明过表达的酶被cAMP依赖性蛋白激酶磷酸化。双突变体的过表达导致激酶最大活性增加28倍,果糖2,6-二磷酸水平增加3-4倍。这种形式的过表达使二羟基丙酮的葡萄糖生成速率降低了90%,并使乳酸加丙酮酸的生成速率提高了200%。相反,野生型酶的过表达增强了葡萄糖生成并抑制了乳酸加丙酮酸的生成。这些结果为果糖2,6-二磷酸作为糖异生/糖酵解途径通量调节剂提供了直接支持,并表明通过共价修饰调节双功能酶活性比蛋白质的量更重要。