Coleman R A, Haynes E B
J Biol Chem. 1984 Jul 25;259(14):8934-8.
Hepatic monoacylglycerol acyltransferase activity is 700-fold higher during the suckling period than in the adult rat. Specific activity in total particulate preparations rose from 9.4 nmol/min/mg before birth to a peak of 78 nmol/min/mg on the 6th to 8th postnatal days. Monoacylglycerol acyltransferase activity fell sharply after day 8 and was 1.6 and 0.1 nmol/min/mg on day 28 and in adult rats, respectively. The activity had a pH optimum at 8.0 and was activated by albumin and by phospholipids. With [3H]palmitoyl-CoA and sn-2-monooleoylglycerol, more than 96% of the products were di- and triacylglycerols. More than 92% of the diacylglycerol product was the 1,2 isomer. The activity was stable at 43 degrees C for 50 min. Thermal inactivation showed t 1/2 values of 8 min and 4.5 min at 53.5 and 55 degrees C, respectively. In suckling rats, monoacylglycerol acyltransferase activities in liver and intestinal mucosa were 150- to 800-fold higher than in other tissues. Monoacylglycerol acyltransferase activity was 12.5-fold greater with palmitoyl-CoA than with octanoyl-CoA. Acetyl-CoA was not a substrate. The sn-2-monoacylglycerols were strongly preferred over the sn-1 isomers. No direct relationship was noted between 2-monoacylglycerol chain length and apparent Km value. The presence of high levels of monoacylglycerol acyltransferase activity in suckling rat liver suggests that the monoacylglycerol pathway functions as a major route of hepatic glycerolipid synthesis during the suckling period but not in adult animals.
哺乳期肝单酰甘油酰基转移酶活性比成年大鼠高700倍。全颗粒制剂中的比活性从出生前的9.4 nmol/分钟/毫克升至出生后第6至8天的峰值78 nmol/分钟/毫克。单酰甘油酰基转移酶活性在第8天后急剧下降,在第28天和成年大鼠中分别为1.6和0.1 nmol/分钟/毫克。该活性的最适pH为8.0,可被白蛋白和磷脂激活。以[3H]棕榈酰辅酶A和sn-2-单油酰甘油为底物时,超过96%的产物为二酰甘油和三酰甘油。超过92%的二酰甘油产物为1,2-异构体。该活性在43℃下50分钟内稳定。热失活显示在53.5℃和55℃下的t1/2值分别为8分钟和4.5分钟。在哺乳期大鼠中,肝脏和肠黏膜中的单酰甘油酰基转移酶活性比其他组织高150至800倍。单酰甘油酰基转移酶对棕榈酰辅酶A的活性比对辛酰辅酶A的活性高12.5倍。乙酰辅酶A不是底物。sn-2-单酰甘油比sn-1异构体更受青睐。未发现2-单酰甘油链长与表观Km值之间存在直接关系。哺乳期大鼠肝脏中高水平的单酰甘油酰基转移酶活性表明,单酰甘油途径在哺乳期是肝脏甘油olipid合成的主要途径,但在成年动物中不是。