Norton S J, Talesa V, Yuan W J, Principato G B
Department of Biochemistry, University of North Texas, Denton.
Biochem Int. 1990 Nov;22(3):411-8.
Glyoxalase I and glyoxalase II from the outer green rind of Aloe vera leaves were purified by (matrix) affinity ligand-enzyme binding methods. The purified enzymes exhibited single protein bands on SDS-PAGE electrophoresis, with MW values of approximately 44,000 and 27,000 for glyoxalase I and glyoxalase II, respectively. The glyoxalase I is a basic protein (pI 7.8), while the glyoxalase II (3 protein bands) is acidic (pI 4.7, 4.8 [prevalent form], and 5.0). The kinetic constants, Km and Vmax, and Ki values for certain inhibitors are reported for both glyoxalase I and glyoxalase II. The glyoxalase enzymes from Aloe vera were compared with reported animal and plant glyoxalases.
采用(基质)亲和配体-酶结合法从库拉索芦荟叶片的外层绿色外皮中纯化出乙二醛酶I和乙二醛酶II。纯化后的酶在SDS-PAGE电泳上呈现单一条带,乙二醛酶I和乙二醛酶II的分子量分别约为44,000和27,000。乙二醛酶I是一种碱性蛋白(pI 7.8),而乙二醛酶II(3条蛋白带)是酸性的(pI 4.7、4.8[主要形式]和5.0)。报告了乙二醛酶I和乙二醛酶II的动力学常数Km和Vmax以及某些抑制剂的Ki值。将库拉索芦荟的乙二醛酶与已报道的动植物乙二醛酶进行了比较。