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影响大肠杆菌中酰基转移酶酰基选择性的因素。

Factors affecting the acyl selectivities of acyltransferases in Escherichia coli.

作者信息

Okuyama H, Yamada K, Ikezawa H, Wakil S J

出版信息

J Biol Chem. 1976 Apr 25;251(8):2487-92.

PMID:770468
Abstract

In Escherichia coli the synthesis of phosphatidic acid from glycerophosphate involves first the intermediate formation of 1-acyl glycerophosphate. This reaction is catalyzed by the membrane-bound acyl-CoA(acyl-ACP):glycerophosphate acyltransferase. The 1-acylglycerophosphate is then converted to phosphatidic acid by acyl-CoA(acyl-ACP):1-acylglycerophosphate acyltransferase (Okuyama, H., and Wakil, S.J. (1973) J. Biol. Chem. 248, 5197-5205). In vitro both acyltransferases utilize various saturated and unsaturated acyl-CoAs at comparable rates, resulting in the incorporation of both saturated and unsaturated fatty acids into position 1 as well as position 2 of the glycerophosphate moiety. Thus, the specificities of acyltransferase systems as compared with regard to the maximal velocities for various acyl-AoAs, do not explain the positional distribution of the individual fatty acid in phospholipid molecules. The selectivities of the acyltransferases for acyl-CoAs are variable depending upon the acceptor concentration. In the presence of both palmitoyl-CoA and oleoyl-CoA and at low concentrations of the acceptors comparable to those found in vivo, the acylation at position 1 of glycerophosphate by acyl-CoA:glycerophosphate acyltransferase showed higher preference for palmitate, whereas the acylation at position 2 by acyl-CoA:1-acylglycerophosphate acyltransferase showed higher selectivity for oleate. In the presence of saturating amounts of the acceptors, the acylation at position 1 or position 2 was less selective for the acyl-CoAs. The ratios of saturated acyl-CoA to unsaturated acyl-CoA also affect the ratios of the fatty acids incorporated in vitro into positions 1 and 2 of phosphatidic acid; relatively more palmitate was incorporated when the proportion of palmitoyl-CoA among the acyl donors was higher and vice versa. Thus, highly selective positioning of various acyl-CoAs observed at lower concentrations of the acceptors in phosphatidic acid synthesis in vitro helps to explain the selective distribution of saturated and unsaturated fatty acids at positions 1 and 2 of glycerophospholipids in the membranes. Another factor, the availability of acyl donors, affects the proportions of different molecular species of phosphatidic acid, which at least partly explains the variability of molecular species of phospholipids found in vivo.

摘要

在大肠杆菌中,由甘油磷酸合成磷脂酸首先涉及中间产物1-酰基甘油磷酸的形成。该反应由膜结合的酰基辅酶A(酰基-ACP):甘油磷酸酰基转移酶催化。然后,1-酰基甘油磷酸通过酰基辅酶A(酰基-ACP):1-酰基甘油磷酸酰基转移酶转化为磷脂酸(奥库亚马,H.,和瓦基尔,S.J.(1973年)《生物化学杂志》248,5197 - 5205)。在体外,两种酰基转移酶以相当的速率利用各种饱和和不饱和酰基辅酶A,导致饱和脂肪酸和不饱和脂肪酸同时掺入甘油磷酸部分的1位以及2位。因此,与各种酰基辅酶A的最大速度相比,酰基转移酶系统的特异性并不能解释磷脂分子中单个脂肪酸的位置分布。酰基转移酶对酰基辅酶A的选择性因受体浓度而异。在同时存在棕榈酰辅酶A和油酰辅酶A且受体浓度与体内发现的浓度相当低的情况下,酰基辅酶A:甘油磷酸酰基转移酶对甘油磷酸1位的酰化对棕榈酸表现出更高的偏好,而酰基辅酶A:1-酰基甘油磷酸酰基转移酶对2位的酰化对油酸表现出更高的选择性。在受体饱和量存在的情况下,1位或2位的酰化对酰基辅酶A的选择性较低。饱和酰基辅酶A与不饱和酰基辅酶A的比例也影响体外掺入磷脂酸1位和2位的脂肪酸比例;当酰基供体中棕榈酰辅酶A的比例较高时,相对更多的棕榈酸被掺入,反之亦然。因此,在体外磷脂酸合成中较低受体浓度下观察到的各种酰基辅酶A的高度选择性定位有助于解释膜中甘油磷脂1位和2位饱和脂肪酸和不饱和脂肪酸的选择性分布。另一个因素,酰基供体的可用性,影响磷脂酸不同分子种类的比例,这至少部分解释了体内发现的磷脂分子种类的变异性。

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