Front Matter

(Tina Sui) #1

12 Phospholipases Used in Lipid


Transformations


Renate Ulbrich-Hofmann

Abbreviations


AOT bis-(2-ethylhexyl)sodium sulfosuccinate

GPI glycosylphosphatidylinositol

HEPES N-(2-hydroxyethyl)-piperazine-N’-ethanesulfonic acid

Lyso-PC lyso-phosphatidylcholine

PC phosphatidylcholine

PE phosphatidylethanolamine

PG phosphatidylglycerol

PI phosphatidylinositol

PLA 1 phospholipase A 1

PLA 2 phospholipase A 2

PLC phospholipase C

PLD phospholipase D

PS phosphatidylserine

SDS sodium dodecylsulfate

Tris tris(hydroxymethyl)aminomethane

12.1 Classificationofphospholipasesandtheirsubstrates


Phospholipases are a group of enzymes whose natural function consists of the hy-

drolysis of phospholipids. This class of compounds represent the main components

of biological membranes. Phospholipids also occur in large amounts in plant seeds

and chicken eggs. Some phospholipid members are biological signal molecules;

phospholipases, therefore, effect the metabolism, construction, and reorganization

of biological membranes, and are involved in signal cascades. The molecular fea-

ture of phospholipids is the diester structure of phosphoric acid in which one alco-

holic moiety (X) is polar and the other (Y) is nonpolar (Figure 1). The third acidic

function of the phosphoric acid is ionized at physiological pH. Most natural phos-

pholipids are glycerophospholipids (phosphatides), where the nonpolar alcoholic

component is a 1,2-diacyl-sn-glycerol (Figure 1). The esterification to phosphoric

acid is insn-3 position of the glycerol moiety. The notationsnrefers to the ‘stereo-

specific numbering’ adopted by IUPAC-IUB (IUPAC-IUB Commission on Bio-

chemical Nomenclature, 1978a,b). As polar alcoholic components, charged or non-

charged compounds such as choline, ethanolamine (both positively charged), serine

(zwitterionic), inositol and glycerol (both noncharged) occur, yielding either neutral

or negatively charged phospholipids. Inositol can be further modified by one or more

Enzymesin LipidModification.Editedby UweT. Bornscheuer
Copyright 2000 Wiley-VCHVerlagGmbH& Co. KGaA,Weinheim.ISBN:3-527-30176-3
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