Mann Laboratory, Department of Vegetable Crops, University of California, Davis, California 95616.
Plant Physiol. 1987 Aug;84(4):993-6. doi: 10.1104/pp.84.4.993.
An anion-sensitive H(+)-translocating ATPase was identified in membrane vesicles isolated from mature green tomato (Lycopersicon esculentum) fruit. The H(+)-ATPase was associated with a low density membrane population having a peak density of 1.11 grams per cubic centimeter, and its activity was inhibited by NO(3) (-), N,N'-dicyclohexylcarbodiimide and diethylstilbestrol but not by vanadate, azide, molybdate, or oligomycin. This H(+)-ATPase has an unusual pH dependence indicating both a slightly acidic and a near neutral peak of activity. Chloride was found to be a potent stimulator of ATPase activity. The K(m) for the H(+)-ATPase was approximately 0.8 millimolar ATP. The characteristics of this H(+)-ATPase are very similar to those described for a number of plant cell tonoplast H(+)-ATPases suggesting that the activity identified in tomato fruit membranes is tonoplast-associated. This report demonstrates the feasibility of isolating tonoplast vesicles from acidic fruit tissues for studies of transport activities associated with fruit development and maturation.
从成熟绿番茄(Lycopersicon esculentum)果实分离的膜囊泡中鉴定出一种阴离子敏感的 H(+)-转运 ATP 酶。该 H(+)-ATP 酶与具有 1.11 克/立方厘米峰值密度的低密度膜群体相关联,其活性受到 NO(3) (-)、N,N'-二环己基碳二亚胺和己烯雌酚的抑制,但不受钒酸盐、叠氮化物、钼酸盐或寡霉素的抑制。这种 H(+)-ATP 酶具有不寻常的 pH 依赖性,表明其活性存在略微酸性和近中性的峰值。氯离子被发现是 ATP 酶活性的有效刺激物。H(+)-ATP 酶的 K(m)约为 0.8 毫摩尔 ATP。该 H(+)-ATP 酶的特性与许多植物细胞质膜 H(+)-ATP 酶的描述非常相似,表明在番茄果实膜中鉴定出的活性与质膜相关。本报告证明了从酸性果实组织中分离质膜囊泡进行与果实发育和成熟相关的运输活性研究的可行性。