Effects of phospholipid headgroup and phase on the activity of diacylglycerol kinase of Escherichia coli

被引:23
作者
Pilot, JD [1 ]
East, JM [1 ]
Lee, AG [1 ]
机构
[1] Univ Southampton, Sch Biol Sci, Div Biochem & Mol Biol, Southampton SO16 7PX, Hants, England
关键词
D O I
10.1021/bi011333r
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
Diacylglycerol kinase (DGK) of Escherichia coli has been reconstituted into a variety of phospholipid bilayers and its activity determined as a function of lipid headgroup structure and phase preference. The anionic phospholipids dioleoylphosphatidic acid, dioleoylphosphatidylserine, and cardiolipin were all found to support activities lower than that supported by dioleoylphosphatidylcholine. In mixtures of dioleoylphosphatidylcholine and 20 mol % anionic phospholipids, the presence of anionic phospholipids all resulted in lower activities than in dioleoylphosphatidylcholine, except for dioleoylphosphatidylglycerol whose presence had little effect on activity. In some cases, the low activity in the presence of anionic phospholipid followed from a decrease in v(max); in some cases, it followed from an increase in the K-m for diacylglycerol, and in the case of dioleoylphosphatidic acid, it followed from both. Activities in mixtures containing 80 mol % dioleoylphosphatidylethanolamine were lower than in dioleoylphosphatidyleholine at temperatures where both lipids adopted a bilayer phase; at higher temperatures where dioleoylphosphatidylethanolamine preferred a hexagonal Hn phase, the differences in activity were greater. These experiments suggest that the presence of lipids preferring a hexagonal Hit phase leads to low activities. Activities of DGK are low in a gel phase lipid.
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页码:14891 / 14897
页数:7
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共 39 条
[1]   Escherichia coli diacylglycerol kinase is an evolutionarily optimized membrane enzyme and catalyzes direct phosphoryl transfer [J].
Badola, P ;
Sanders, CR .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (39) :24176-24182
[2]   LIPID DEPENDENCE OF DIACYLGLYCEROL KINASE FROM ESCHERICHIA-COLI [J].
BOHNENBERGER, E ;
SANDERMANN, H .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1983, 132 (03) :645-650
[3]   Phospholipid-binding protein domains [J].
Bottomley, MJ ;
Salim, K ;
Panayotou, G .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS, 1998, 1436 (1-2) :165-183
[4]   MODULATION OF RHODOPSIN FUNCTION BY PROPERTIES OF THE MEMBRANE BILAYER [J].
BROWN, MF .
CHEMISTRY AND PHYSICS OF LIPIDS, 1994, 73 (1-2) :159-180
[5]   INFLUENCE OF METAL-IONS ON THE PHASE PROPERTIES OF PHOSPHATIDIC-ACID IN COMBINATION WITH NATURAL AND SYNTHETIC PHOSPHATIDYLCHOLINES - AN X-RAY-DIFFRACTION STUDY USING SYNCHROTRON RADIATION [J].
CAFFREY, M ;
FEIGENSON, GW .
BIOCHEMISTRY, 1984, 23 (02) :323-331
[6]   HUMAN-ERYTHROCYTE HEXOSE TRANSPORTER ACTIVITY IS GOVERNED BY BILAYER LIPID-COMPOSITION IN RECONSTITUTED VESICLES [J].
CARRUTHERS, A ;
MELCHIOR, DL .
BIOCHEMISTRY, 1984, 23 (26) :6901-6911
[7]   INFRARED AND P-31-NMR STUDIES OF THE INTERACTION OF MG-2+ WITH PHOSPHATIDYLSERINES - EFFECT OF HYDROCARBON CHAIN UNSATURATION [J].
CASAL, HL ;
MANTSCH, HH ;
HAUSER, H .
BIOCHIMICA ET BIOPHYSICA ACTA, 1989, 982 (02) :228-236
[8]   POLYMORPHIC PHASE BEHAVIOR OF PHOSPHATIDYLETHANOLAMINES OF NATURAL AND SYNTHETIC ORIGIN - P-31 NMR-STUDY [J].
CULLIS, PR ;
DEKRUIJFF, B .
BIOCHIMICA ET BIOPHYSICA ACTA, 1978, 513 (01) :31-42
[9]   Anionic phospholipids decrease the rate of slippage on the Ca2+-ATPase of sarcoplasmic reticulum [J].
Dalton, KA ;
Pilot, JD ;
Mall, S ;
East, JM ;
Lee, AG .
BIOCHEMICAL JOURNAL, 1999, 342 :431-438
[10]   MODIFICATION BY DIACYLGLYCEROL OF THE STRUCTURE AND INTERACTION OF VARIOUS PHOSPHOLIPID-BILAYER MEMBRANES [J].
DAS, S ;
RAND, RP .
BIOCHEMISTRY, 1986, 25 (10) :2882-2889