The native molecular size of alkyl-dihydroxyacetonephosphate synthase and dihydroxyacetonephosphate acyltransferase

被引:5
作者
Biermann, J
Schoonderwoerd, K
Hom, ML
Luthjens, LH
Van den Bosch, H
机构
[1] Univ Utrecht, Ctr Biomembranes & Lipid Enzymol, Biomembrane Inst, Dept Biochem Lipids, NL-3584 CH Utrecht, Netherlands
[2] Erasmus Univ, Fac Med & Hlth Sci, Inst Cardiovasc Res, Dept Biochem, NL-3000 DR Rotterdam, Netherlands
[3] Delft Univ Technol, Interfac Reactor Inst, Dept Radiat Chem, NL-2629 JB Delft, Netherlands
来源
BIOCHIMICA ET BIOPHYSICA ACTA-LIPIDS AND LIPID METABOLISM | 1998年 / 1393卷 / 01期
关键词
ether phospholipid; peroxisome; radiation inactivation;
D O I
10.1016/S0005-2760(98)00071-X
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Dihydroxyacetonephosphate acyltransferase (DHAP-acyltransferase) and alkyl-dihydroxyacetonephosphate synthase (alkyl-DHAP synthase) are the first two enzymes involved in the biosynthesis of ether phospholipids. Both peroxisomal enzymes have recently been purified to homogeneity and their molecular weights under denaturing conditions were reported. To determine the in situ functional size of both enzymes, radiation inactivation experiments were performed. Alkyl-DHAP synthase showed single exponential decays, both when enzymatic activity and when immunoreactive protein levels were measured, from which target sizes of 79 +/- 2 kDa and 78 +/- 4 kDa, respectively, were calculated. DHAP-acyltransferase activity increased at lower doses and decayed upon further irradiation with an apparent target size of 62 +/- 7 kDa. We conclude from these data that the functional unit sizes for both enzymes in situ are represented by their single polypeptide chains. (C) 1998 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:137 / 142
页数:6
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