Moreno F, Fernandez T, Fernandez R, Herrero P
Eur J Biochem. 1986 Dec 15;161(3):565-9. doi: 10.1111/j.1432-1033.1986.tb10479.x.
Hexokinase PII is not inhibited by high Mg-ATP concentrations if the Mg2+-free ATP is kept at low levels (0.01 mM) in the assay mixture. Hexokinase PI activity is not affected either by Mg2+-free ATP nor by free Mg2+ in the assay mixture. Thus, hexokinase PI and PII activities appear not to be regulated by substrate inhibition as proposed previously [Kopetzki, E. & Entian, K. D. (1985) Eur. J. Biochem. 146, 657-662]. However, the level of Mg2+-free ATP in the hexokinase PII assay mixture strongly affects the enzyme activity by decreasing the Vmax and increasing the Km value for Mg-ATP from 0.15 mM to 5.0 mM. The physiological role of this inhibition, which has not been described previously, was investigated by determining the cytosolic ATP and Mg2+ concentrations in yeast cells grown under derepressing and repressing conditions. Derepression is accompanied by an important loss of Mg2+ from the cells, maintaining the ATP concentration constant. This produces an increase of Mg2+-free ATP in the cytosol from 0.01 mM to 0.1 mM. This free ATP concentration would lead to a maximal inhibition of hexokinase PII.
如果在测定混合物中使无镁ATP保持在低水平(0.01 mM),己糖激酶PII不会受到高浓度Mg-ATP的抑制。己糖激酶PI的活性既不受测定混合物中无镁ATP的影响,也不受游离镁离子的影响。因此,如先前所述[Kopetzki, E. & Entian, K. D. (1985) Eur. J. Biochem. 146, 657 - 662],己糖激酶PI和PII的活性似乎不受底物抑制的调节。然而,己糖激酶PII测定混合物中无镁ATP的水平通过降低Vmax并将Mg-ATP的Km值从0.15 mM增加到5.0 mM,强烈影响酶活性。通过测定在去阻遏和阻遏条件下生长的酵母细胞中的胞质ATP和镁离子浓度,研究了这种先前未描述的抑制作用的生理作用。去阻遏伴随着细胞中镁离子的大量流失,同时ATP浓度保持恒定。这使得胞质中无镁ATP的浓度从0.01 mM增加到0.1 mM。这种游离ATP浓度将导致己糖激酶PII受到最大程度的抑制。