Dong J G, Fernández-Maculet J C, Yang S F
Mann Laboratory, Department of Vegetable Crops, University of California, Davis 95616.
Proc Natl Acad Sci U S A. 1992 Oct 15;89(20):9789-93. doi: 10.1073/pnas.89.20.9789.
1-Aminocyclopropane-1-carboxylate (ACC) oxidase catalyzes the oxidation of ACC to ethylene. Following conventional column fractionation, the enzyme was purified 180-fold to near homogeneity with a specific activity of 20 nmol/(mg.min). This purified enzyme preparation migrated as a single protein band with an apparent molecular mass of 35 kDa on SDS/PAGE and 39 kDa on gel filtration. As in vivo, the purified enzyme required CO2 for activity. Removal of CO2 from the reaction mixture completely abolished the enzyme activity, while 0.5% atmospheric CO2 (0.15 mM in the medium) gave half-maximal activity. The purified enzyme displayed an absolute requirement for Fe2+ and ascorbate. The stoichiometry of the enzymatic reaction was determined: ACC + ascorbate + O2-->C2H4 + HCN + CO2 + dehydroascorbate + 2 H2O. A polyclonal antibody was raised against a synthetic tridecapeptide (PDLEEEYRKTMKE) whose sequence was deduced from the apple pAE12 cDNA [Dong, J. G., Olson, D., Silverstone, A. & Yang, S. F. (1992) Plant Physiol. 98, 1530-1531], which is homologous to tomato cDNAs encoding ACC oxidase. On a Western blot, this antibody specifically recognized the purified ACC oxidase protein. The amino acid composition of the purified enzyme agreed well with that deduced from the pAE12 sequence. When the protein was cleaved with CNBr and one of the peptide fragments was isolated and sequenced for 20 cycles, its sequence (KEFAVELEKLAEKLLDLLCE) precisely matched that predicted from pAE12 (residues 115-134). When preclimacteric apple fruit was treated with ethylene, a parallel increase in in vivo and in vitro ACC oxidase activities was observed, and this increase was accompanied by a concomitant increase in the level of pAE12 transcript. These observations support the conclusion that the isolated ACC oxidase protein is encoded by pAE12.
1-氨基环丙烷-1-羧酸(ACC)氧化酶催化ACC氧化生成乙烯。经过常规柱层析分离后,该酶被纯化了180倍,达到近乎纯的状态,比活性为20 nmol/(mg·min)。这种纯化的酶制剂在SDS/PAGE上迁移为一条单一的蛋白带,表观分子量为35 kDa,在凝胶过滤中为39 kDa。与体内情况一样,纯化的酶活性需要CO₂。从反应混合物中去除CO₂会完全消除酶活性,而0.5%的大气CO₂(培养基中为0.15 mM)可产生半数最大活性。纯化的酶对Fe²⁺和抗坏血酸有绝对需求。确定了酶促反应的化学计量:ACC + 抗坏血酸 + O₂→C₂H₄ + HCN + CO₂ + 脱氢抗坏血酸 + 2H₂O。针对一种合成的十三肽(PDLEEEYRKTMKE)制备了多克隆抗体,该十三肽的序列是根据苹果pAE12 cDNA推导出来的[董,J.G.,奥尔森,D.,西尔弗斯通,A. & 杨,S.F.(1992)植物生理学。98,1530 - 1531],它与编码ACC氧化酶的番茄cDNA同源。在蛋白质印迹法中,这种抗体特异性识别纯化的ACC氧化酶蛋白。纯化酶的氨基酸组成与从pAE12序列推导出来的结果非常吻合。当用CNBr切割该蛋白并分离出一个肽片段并进行20个循环的测序时,其序列(KEFAVELEKLAEKLLDLLCE)与从pAE12预测的序列(第115 - 134位残基)精确匹配。当用乙烯处理跃变前的苹果果实,观察到体内和体外ACC氧化酶活性平行增加,并且这种增加伴随着pAE12转录本水平的相应增加。这些观察结果支持这样的结论:分离的ACC氧化酶蛋白由pAE12编码。