Bonini Beatriz M, Van Dijck Patrick, Thevelein Johan M
Laboratory of Molecular Cell Biology, Institute of Botany and Microbiology, Katholieke Universiteit Leuven, Kasteelpark Arenberg 31, B-3001 Leuven-Heverlee, Flanders, Belgium.
Biochim Biophys Acta. 2003 Sep 30;1606(1-3):83-93. doi: 10.1016/s0005-2728(03)00086-0.
In the yeast Saccharomyces cerevisiae inactivation of trehalose-6-phosphate (Tre6P) synthase (Tps1) encoded by the TPS1 gene causes a specific growth defect in the presence of glucose in the medium. The growth inhibition is associated with deregulation of the initial part of glycolysis. Sugar phosphates, especially fructose-1,6-bisphosphate (Fru1,6bisP), hyperaccumulate while the levels of ATP, Pi and downstream metabolites are rapidly depleted. This was suggested to be due to the absence of Tre6P inhibition on hexokinase. Here we show that overexpression of Tre6P (as well as glucose-6-phosphate (Glu6P))-insensitive hexokinase from Schizosaccharomyces pombe in a wild-type strain does not affect growth on glucose but still transiently enhances initial sugar phosphate accumulation. We have in addition replaced the three endogenous glucose kinases of S. cerevisiae by the Tre6P-insensitive hexokinase from S. pombe. High hexokinase activity was measured in cell extracts and growth on glucose was somewhat reduced compared to an S. cerevisiae wild-type strain but expression of the Tre6P-insensitive S. pombe hexokinase never caused the typical tps1Delta phenotype. Moreover, deletion of TPS1 in this strain expressing only the Tre6P-insensitive S. pombe hexokinase still resulted in a severe drop in growth capacity on glucose as well as sensitivity to millimolar glucose levels in the presence of excess galactose. In this case, poor growth on glucose was associated with reduced rather than enhanced glucose influx into glycolysis. Initial glucose transport was not affected. Apparently, deletion of TPS1 causes reduced activity of the S. pombe hexokinase in vivo. Our results show that Tre6P inhibition of hexokinase is not the major mechanism by which Tps1 controls the influx of glucose into glycolysis or the capacity to grow on glucose. In addition, they show that a Tre6P-insensitive hexokinase can still be controlled by Tps1 in vivo.
在酿酒酵母中,由TPS1基因编码的海藻糖-6-磷酸(Tre6P)合酶(Tps1)失活会导致在培养基中存在葡萄糖时出现特定的生长缺陷。生长抑制与糖酵解起始部分的失调有关。糖磷酸酯,尤其是果糖-1,6-二磷酸(Fru1,6bisP)过度积累,而ATP、Pi和下游代谢物的水平迅速耗尽。这被认为是由于缺乏Tre6P对己糖激酶的抑制作用。在这里我们表明,在野生型菌株中过表达来自粟酒裂殖酵母的对Tre6P(以及葡萄糖-6-磷酸(Glu6P))不敏感的己糖激酶,不会影响在葡萄糖上的生长,但仍会短暂增强初始糖磷酸酯的积累。此外,我们用来自粟酒裂殖酵母的对Tre6P不敏感的己糖激酶取代了酿酒酵母的三种内源性葡萄糖激酶。在细胞提取物中检测到高己糖激酶活性,与酿酒酵母野生型菌株相比,在葡萄糖上的生长有所降低,但对Tre6P不敏感的粟酒裂殖酵母己糖激酶的表达从未导致典型的tps1Δ表型。此外,在仅表达对Tre6P不敏感的粟酒裂殖酵母己糖激酶的该菌株中删除TPS1,仍然导致在葡萄糖上的生长能力严重下降,以及在存在过量半乳糖的情况下对毫摩尔葡萄糖水平敏感。在这种情况下,在葡萄糖上生长不良与葡萄糖进入糖酵解的通量降低而非增强有关。初始葡萄糖转运不受影响。显然,删除TPS1会导致粟酒裂殖酵母己糖激酶在体内的活性降低。我们的结果表明,Tre6P对己糖激酶的抑制不是Tps1控制葡萄糖进入糖酵解的通量或在葡萄糖上生长能力的主要机制。此外,它们表明对Tre6P不敏感的己糖激酶在体内仍可受Tps1调控。