ROLE OF LIPIDS IN HEME SYNTHESIS

被引:14
作者
YONEYAMA, Y
SAWADA, H
TAKESHITA, M
SUGITA, Y
机构
[1] Department of Biochemistry, School of Medicine, University of Kanazawa, Kanazawa, Ishikawa
关键词
D O I
10.1007/BF02531000
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
The effect of lipids on protoheme ferrolyase, which combines ferrous iron with protoporphyrin, was investigated. The enzyme extracted with 1% Na cholate from acetone-dried powder of chicken erythrocyte stroma showed high enzymic activity, while that extracted with 0.4 M KCl showed little activity. The former contained lipids, the main components of which were lecithin and phosphatidylethanolamine, whereas the latter contained little lipid. Crude lipids of several sources restored the enzyme activity of 0.4 M KCl extracts. The activating effects of purified lipids, especially phospholipids which showed the strongest activation, were further examined. Phospholipids were divided into three groups: the choline-containing group, lecithin and sphingomyelin, was inhibitory or slightly accelerative on heme synthesis; the acidic phospholipids, namely phosphatidylethanolamine, cardiolipin, phosphatidic acid and phosphatidylinositol, were strong activators and the intensity of activation was in the order of the acidity of the phospholipids; and the lysophospholipids, namely lysolecithin, lysophosphatidylethanolamine and sphingosylphosphorylcholine, activated the heme synthesis most effectively. In the presence of cholate, choline-containing lipids were highly effective, while acidic phospholipids were inhibitory and lysophospholipids were neutral. Palmitic acid showed slight stimulative effect. Tripalmitin was neutral or inhibitory. Anionic, cationic and neutral synthetic detergents were slightly stimulative in low concentration and inhibitory in high concentration. An activation mechanism of phospholipids was proposed in which the hydrophilic anionic part of lipid in the lipoprotein enzyme molecule attracts ferrous iron. After being stripped of solvation water, the ferrous iron is transferred to the hydrophobic part of the enzyme molecule to be inserted into porphyrin. © 1969 American Oil Chemists' Society.
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页码:321 / &
相关论文
共 17 条
[1]   RELATION BETWEEN THE ACTIVITY OF A LECITHINASE AND THE ELECTROPHORETIC CHARGE OF THE SUBSTRATE [J].
BANGHAM, AD ;
DAWSON, RMC .
BIOCHEMICAL JOURNAL, 1959, 72 :486-492
[2]   CONTROL OF LECITHINASE ACTIVITY BY THE ELECTROPHORETIC CHARGE ON ITS SUBSTRATE SURFACE [J].
BANGHAM, AD ;
DAWSON, RMC .
NATURE, 1958, 182 (4645) :1292-1293
[3]  
BYRNE WL, 1967, OCT P ROL LIP ENZYM
[4]  
COHEN M, 1963, J BIOL CHEM, V238, P879
[5]  
FISUSUS WG, 1966, J BIOL CHEM, V241, P3324
[6]  
GRINSTEIN M, 1947, J BIOL CHEM, V167, P515
[7]   HYDROLYSIS OF LECITHIN BY PLANT PLASTID ENZYMES [J].
KATES, M .
CANADIAN JOURNAL OF BIOCHEMISTRY AND PHYSIOLOGY, 1955, 33 (04) :575-589
[8]   PHOSPHOLIPIDS .3. CHROMATOGRAPHIC SEPARATION OF GLYCEROPHOSPHOLIPIDS [J].
LEA, CH ;
RHODES, DN ;
STOLL, RD .
BIOCHEMICAL JOURNAL, 1955, 60 (1-4) :353-363
[9]  
MATSUMOTO M, 1961, J BIOCHEM-TOKYO, V49, P32
[10]   EFFECT OF LIPIDS AND ORGANIC SOLVENTS ON ENZYMIC FORMATION OF ZINC PROTOPORPHYRIN AND HAEM [J].
MAZANOWSKA, AM ;
NEUBERGER, A ;
TAIT, GH .
BIOCHEMICAL JOURNAL, 1966, 98 (01) :117-+