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溶酶体磷脂酰胆碱:双(单酰甘油)磷酸酯酰基转移酶:对供体sn-1脂肪酸的特异性以及与磷脂酶A1的共纯化

Lysosomal phosphatidylcholine: bis(monoacylglycero)phosphate acyltransferase: specificity for the sn-1 fatty acid of the donor and co-purification with phospholipase A1.

作者信息

Huterer S J, Hostetler K Y, Gardner M F, Wherrett J R

机构信息

Department of Medicine (Neurology), University of Toronto, Ontario, Canada.

出版信息

Biochim Biophys Acta. 1993 Apr 7;1167(2):204-10. doi: 10.1016/0005-2760(93)90163-4.

Abstract

Positional specificities in donor and acceptor phospholipids of the lysosomal phosphatidylcholine: bis(monoacylglycero)phosphate acyltransferase have been determined. Comparison of the transfer of labelled fatty acid from sn-1 [14C]acyl and sn-2 [14C]acylphosphatidylcholines by extracts of rat liver lysosomes revealed that fatty acids in the sn-1 position were exclusively transferred. Degradation of the acylphosphatidylglycerol product by Rhizopus arrhizus lipase, highly specific for fatty acids esterified to sn-1 or sn-3 positions, indicated that sn-1 or sn-3 rather than sn-2 positions had been acylated. Assays of phospholipase A1, phosphatidylcholine: bis(monoacylglycero)phosphate acyltransferase, the conversion of lysophosphatidylglycerol to bis(monoacylglycero)phosphate and phospholipase A2 were performed at various steps in the purification of lysosomal phospholipase A1. After the penultimate step of chromatofocusing, there was a 1086-fold increase of phospholipase A1 specific activity over the homogenate and this was accompanied by a 11 998-fold increase of phosphatidylcholine: bis(monoacylglycero)phosphate acyltransferase specific activity. A second preparation carried through to the final step of gel-filtration retained a similar ratio of acyltransferase activity. On the other hand, specific activities of phospholipase A2 and of the conversion of lysophosphatidylglycerol to bis(monoacylglycero)phosphate increased to the step where enzyme was solubilized from lysosomes, but were lost from later steps. These findings suggest that phosphatidylcholine: bis(monoacylglycero)phosphate acyltransferase is catalyzed by lysosomal phospholipase A1. The site of acylation in the bis(monoacylglycero)phosphate acceptor appears to be either sn-1 or sn-3. Since the lysosomal extracts did not catalyze the transacylation of phosphatidylglycerol, we conclude that the formation of acylphosphatidylglycerol in lysosomes requires the sequential acylation of lysophosphatidylglycerol to form bis(monoacylglycero)phosphate by an unidentified enzymatic mechanism followed by a transacylation of bis(monoacylglycero)phosphate in either sn-1 or sn-3 position to form acylphosphatidylglycerol which is catalyzed by phospholipase A1.

摘要

已确定溶酶体磷脂酰胆碱

双(单酰甘油)磷酸酯酰基转移酶的供体和受体磷脂中的位置特异性。通过大鼠肝脏溶酶体提取物对来自sn-1 [14C]酰基和sn-2 [14C]酰基磷脂酰胆碱的标记脂肪酸转移进行比较,结果显示sn-1位的脂肪酸被专门转移。用对酯化到sn-1或sn-3位的脂肪酸具有高度特异性的米根霉脂肪酶对酰基磷脂酰甘油产物进行降解,表明被酰化的是sn-1或sn-3位而非sn-2位。在溶酶体磷脂酶A1的纯化过程中的不同步骤进行了磷脂酶A1、磷脂酰胆碱:双(单酰甘油)磷酸酯酰基转移酶、溶血磷脂酰甘油向双(单酰甘油)磷酸酯的转化以及磷脂酶A2的测定。在层析聚焦的倒数第二步之后,磷脂酶A1的比活性相对于匀浆增加了1086倍,同时磷脂酰胆碱:双(单酰甘油)磷酸酯酰基转移酶的比活性增加了11998倍。进行到凝胶过滤最后一步的第二种制剂保留了相似的酰基转移酶活性比例。另一方面,磷脂酶A2以及溶血磷脂酰甘油向双(单酰甘油)磷酸酯转化的比活性在酶从溶酶体中溶解的步骤中增加,但在后续步骤中丧失。这些发现表明磷脂酰胆碱:双(单酰甘油)磷酸酯酰基转移酶由溶酶体磷脂酶A1催化。双(单酰甘油)磷酸酯受体中的酰化位点似乎是sn-1或sn-3。由于溶酶体提取物不催化磷脂酰甘油的转酰基作用,我们得出结论,溶酶体中酰基磷脂酰甘油的形成需要通过一种未知的酶促机制将溶血磷脂酰甘油顺序酰化以形成双(单酰甘油)磷酸酯,随后双(单酰甘油)磷酸酯在sn-1或sn-3位进行转酰基作用以形成酰基磷脂酰甘油,这一过程由磷脂酶A1催化。

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