Gibrat R, Grouzis J P, Rigaud J, Galtier N, Grignon C
Biochimie et Physiologie Végétales, INRA (CNRS URA 198), ENSAM, Montpellier, France.
Biochim Biophys Acta. 1989 Feb 13;979(1):46-52. doi: 10.1016/0005-2736(89)90521-x.
The microelectrophoretic mobility of corn root plasma membranes and the inhibition of the Mg+2-ATPase by vanadate were investigated under different ionic conditions. The Mg2+-ATPase was uncompetitively inhibited and a 10-fold variation of the apparent inhibition constant was observed, depending on the addition of K+ and Mg2+. The determination of the zeta potential indicated that a 5-fold decrease of the apparent inhibition constant was due to aspecific electrostatic interactions of the vanadate anion and the negative charge of the membrane. The screening and masking effects of 6 mM free Mg2+ totally abolished electrostatic interactions and allowed the direct determination of the intrinsic vanadate inhibition constant (KIi). On the other hand, a specific, non-electrostatic, effect of K+ caused a 2-fold decrease of the inhibition constant in addition to the electrostatic effect. Finally, the electrostatic analysis indicates that the Mg2+-ATPase is inhibited by the monomeric bivalent anion HVO4(2-).
在不同离子条件下,研究了玉米根质膜的微电泳迁移率以及钒酸盐对Mg+2-ATP酶的抑制作用。Mg2+-ATP酶受到非竞争性抑制,根据K+和Mg2+的添加情况,表观抑制常数出现了10倍的变化。ζ电位的测定表明,表观抑制常数降低5倍是由于钒酸根阴离子与膜的负电荷之间的非特异性静电相互作用。6 mM游离Mg2+的屏蔽和掩蔽作用完全消除了静电相互作用,并使得能够直接测定钒酸盐的内在抑制常数(KIi)。另一方面,K+的特异性非静电作用除了静电效应外,还使抑制常数降低了2倍。最后,静电分析表明,Mg2+-ATP酶受到二价阴离子单体HVO4(2-)的抑制。