Hsieh B, Tolbert N E
J Biol Chem. 1976 Jul 25;251(14):4408-15.
An aminotransferase was isolated from peroxisomes that had been separated by isopycnic centrifugation of homogenates from rat liver or kidney. The enzyme was located only in the peroxisomes and in the soluble fraction, presumably from broken peroxisomes. Within the peroxisomes, this aminotransferase was in the soluble matrix. This specific aminotransferase was not found in spinach leaves. The enzyme was relatively specific for glyoxylate as the amino group acceptor. L-Leucine and L-phenylalanine were the preferred amino donors; other amino acids were less efficiently utilized. Rates were 181 nmol X min-1 of peroxisomal protein with leucine, and 134 with phenylalanine. The rate with serine was only 28% as fast and there was no reaction with glutamate. The reactions were essentially irreversible. Treatment of peroxisomes with 0.04% Triton X-100 increased enzyme activity 80%. The enzyme in the peroxisomes was stable at 50 degrees. The enzyme was purified 100-fold. Activities with leucine, phenylalanine, and histidine could not be separated by gel filtration and DEAE-cellulose chromatography. Its molecular weight was estimated to be 72,000. Reaction kinetics were ping-pong. The Km (glyoxylate) was 0.5 mM with leucine and 0.67 mM with phenylalanine. Km (leucine) was 2.5 mM and Km (phenylalanine) was 2.8 mM. Substrate inhibition occurred at over 4 mM glyoxylate but did not occur with the amino donors. pH optima were 8.5 for leucine and phenylalanine and 6.2 for histidine. There was no requirement for exogenous pyridoxal phosphate, but activity was inhibited by phenylhydrazine and isonicotinic acid hydrazide. The glyoxylate aminotransferase developed postnatally and increased with age until rats were 40 days old. There was more activity in female than male rats. About 50% of the activity disappeared if rats were starved overnight. Clofibrate treatment of male rats increased this enzyme activity in isolated peroxisomes. Rats on a high casein diet had slightly higher enzyme activity.
一种转氨酶是从过氧化物酶体中分离出来的,这些过氧化物酶体是通过对大鼠肝脏或肾脏匀浆进行等密度离心分离得到的。该酶仅存在于过氧化物酶体和可溶部分中,推测可溶部分来自破碎的过氧化物酶体。在过氧化物酶体内,这种转氨酶存在于可溶基质中。菠菜叶中未发现这种特异性转氨酶。该酶相对特异性地以乙醛酸作为氨基受体。L-亮氨酸和L-苯丙氨酸是优选的氨基供体;其他氨基酸的利用效率较低。以亮氨酸为底物时过氧化物酶体蛋白的反应速率为181 nmol·min⁻¹,以苯丙氨酸为底物时为134 nmol·min⁻¹。以丝氨酸为底物时反应速率仅为其28%,与谷氨酸不发生反应。这些反应基本上是不可逆的。用0.04% Triton X-100处理过氧化物酶体可使酶活性提高80%。过氧化物酶体中的酶在50℃时稳定。该酶被纯化了100倍。用凝胶过滤和DEAE-纤维素色谱法无法分离亮氨酸、苯丙氨酸和组氨酸的活性。其分子量估计为72,000。反应动力学为乒乓机制。以亮氨酸为底物时Km(乙醛酸)为0.5 mM,以苯丙氨酸为底物时为0.67 mM。Km(亮氨酸)为2.5 mM,Km(苯丙氨酸)为2.8 mM。当乙醛酸浓度超过4 mM时会发生底物抑制,但氨基供体不会出现这种情况。以亮氨酸和苯丙氨酸为底物时最适pH为8.5,以组氨酸为底物时为6.2。不需要外源磷酸吡哆醛,但苯肼和异烟肼会抑制其活性。乙醛酸转氨酶在出生后发育,并随着年龄增长而增加,直到大鼠4日龄。雌性大鼠中的活性高于雄性大鼠。如果大鼠禁食过夜,约50%的活性会消失。用氯贝丁酯处理雄性大鼠可增加分离出的过氧化物酶体中的这种酶活性。高酪蛋白饮食的大鼠酶活性略高。