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Phosphatidate

Lipoproteins. The lipid moiety of lipoproteins is quite variable both qualitatively and quantitatively. The a-lipoprotein of serum contains glyceride, phosphatide and cholesterol to about 30 -40% of the total complex. The -lipoprotein of serum contains some glyceride but the phosphatide and cholesterol account for nearly 75% of the total. [Pg.332]

Triacylglycerols arise not by acylation of glycerol itself but by a sequence of steps m which the first stage is acyl transfer to l glycerol 3 phosphate (from reduction of dihy droxyacetone 3 phosphate formed as described m Section 25 21) The product of this stage IS called a phosphatidic acid... [Pg.1077]

Hydrolysis of the phosphate ester function of the phosphatidic acid gives a diacylglycerol which then reacts with a third acyl coenzyme A molecule to produce a triacylglycerol... [Pg.1078]

Phospholipids. Glycerides esterified by fatty acids at the 1,2 positions and a phosphoric acid residue at the 3 position constitute the class called phosphoHpids (3). In older Hterature and in commercial practice, these materials are described as phosphatides. [Pg.123]

Cmde oils from these processes are often of insufficient quaUty to be used directly, particularly for edible products. Impurities such as pigments, phosphatides, volatile odorous compounds, and certain metals must be removed by further processing. [Pg.124]

Lecithin. Lecithin [8002-43-5] (qv) is a mixture of fat-like compounds that includes phosphatidyl choline, phosphatidyl ethanolamines, inositol phosphatides, and other compounds (37). Commercial lecithin was originally obtained from egg yolks, but is now extracted from soybean oil. Lecithin is used in many products, including margarine, chocolate, ice cream, cake batter, and bread. [Pg.438]

Fig. 1. Chemical stmcture of phosphatidylcholine (PC) (1) and other related phosphohpids. R C O represents fatty acid residues. The choline fragment may be replaced by other moieties such as ethanolamine (2) to give phosphatidylethanolamine (PE), inositol (3) to give phosphatidylinositol (PI), serine (4), or glycerol (5). IfH replaces choline, the compound is phosphatidic acid (6). The corresponding lUPAC-lUB names ate (1), l,2-diacyl-t -glyceto(3)phosphocholine (2), l,2-diacyl-t -glyceto(3)phosphoethanolamine (3), 1,2-diacyl-t -glyceto(3)phosphoinositol (4), 1,2-diacyl-t -glyceto(3)phospho-L-serine and (5), l,2-diacyl-t -glyceto(3)phospho(3)-t -glycetol. Fig. 1. Chemical stmcture of phosphatidylcholine (PC) (1) and other related phosphohpids. R C O represents fatty acid residues. The choline fragment may be replaced by other moieties such as ethanolamine (2) to give phosphatidylethanolamine (PE), inositol (3) to give phosphatidylinositol (PI), serine (4), or glycerol (5). IfH replaces choline, the compound is phosphatidic acid (6). The corresponding lUPAC-lUB names ate (1), l,2-diacyl-t -glyceto(3)phosphocholine (2), l,2-diacyl-t -glyceto(3)phosphoethanolamine (3), 1,2-diacyl-t -glyceto(3)phosphoinositol (4), 1,2-diacyl-t -glyceto(3)phospho-L-serine and (5), l,2-diacyl-t -glyceto(3)phospho(3)-t -glycetol.
The quaHty, ie, level of impurities, of the fats and oils used in the manufacture of soap is important in the production of commercial products. Fats and oils are isolated from various animal and vegetable sources and contain different intrinsic impurities. These impurities may include hydrolysis products of the triglyceride, eg, fatty acid and mono/diglycerides proteinaceous materials and particulate dirt, eg, bone meal and various vitamins, pigments, phosphatides, and sterols, ie, cholesterol and tocopherol as weU as less descript odor and color bodies. These impurities affect the physical properties such as odor and color of the fats and oils and can cause additional degradation of the fats and oils upon storage. For commercial soaps, it is desirable to keep these impurities at the absolute minimum for both storage stabiHty and finished product quaHty considerations. [Pg.150]

In addition to the triglycerides, the four oilseeds also contain phosphatides. For example, soybean oil containing 1.47% phosphatides consists of 48.9% phosphatidylcholine, 27.0% phosphatidylethanolamine, 21.9% phosphatidjlinositol and 2.2% phosphatidic acid (24). Total phosphatides of cottonseed and peanut kernels are estimated to be 1.5—1.9 and 0.8%, respectively (25). [Pg.294]

Apply bands of sample solution, overspray with [35] 12% hydrochlonc acid, leave in an atmosphere of nitrogen for 2 imn and then dry in a stream of nitrogen, then chromatograph The vinyl ether linkages in the phosphatides are hydrolyzed... [Pg.62]

Phosphatidic acids not only are intennediates in the biosynthesis of triacylglycerols but also are biosynthetic precursors of other members of a group of compounds called phosphoglycerides or glycerol phosphatides. Phosphorus-containing derivatives of lipids are known as phospholipids, and phosphoglycerides are one type of phospholipid. [Pg.1078]

FIGURE 8.4 Phosphatidic acid, the parent compound for glycerophospholipids. [Pg.244]

Phosphatidic acid, the parent compound for the glycerol-based phospholipids (Figure 8.4), consists of 5w-glycerol-3-phosphate, with fatty acids esterified at the T and 2-positions. Phosphatidic acid is found in small amounts in most natural systems and is an important intermediate in the biosynthesis of the more common glycerophospholipids (Figure 8.6). In these compounds, a... [Pg.244]

Plasmalogens are ether glycerophospholipids in which the alkyl moiety is d5-a,/3-unsaturated (Figure 8.10). Common plasmalogen head groups include choline, ethanolamine, and serine. These lipids are referred to as phosphati-dal choline, phosphatidal ethanolamine, and phosphatidal serine. [Pg.248]

FIGURE 25.18 Synthesis of glycerolipids in eukaryotes begins with the formation of phosphatidic acid, which may be formed from dihydroxyace-tone phosphate or glycerol as shown. [Pg.820]


See other pages where Phosphatidate is mentioned: [Pg.307]    [Pg.307]    [Pg.307]    [Pg.369]    [Pg.1077]    [Pg.1077]    [Pg.1078]    [Pg.1078]    [Pg.753]    [Pg.124]    [Pg.125]    [Pg.125]    [Pg.125]    [Pg.98]    [Pg.98]    [Pg.99]    [Pg.233]    [Pg.150]    [Pg.302]    [Pg.531]    [Pg.1077]    [Pg.1077]    [Pg.1078]    [Pg.243]    [Pg.244]    [Pg.246]    [Pg.247]    [Pg.270]    [Pg.820]   
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See also in sourсe #XX -- [ Pg.533 , Pg.534 ]

See also in sourсe #XX -- [ Pg.3 , Pg.246 ]

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See also in sourсe #XX -- [ Pg.248 ]

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Acetal phosphatide

Acetal phosphatides

Alkenylacylethanolamine phosphatides

Brain phosphatides

Choline phosphatide, ozonides

Choline-containing phosphatides

Choline-containing phosphatides separation

Cyclic phosphatidic acid

Cytoplasm, phosphatides

DOPC with Phosphatidic Acid under Sink Conditions

Dimyristoyl phosphatidic

Dimyristoyl phosphatidic acid

Effect of Lipotropic Substances on Phosphatide Turnover in Liver

Ethanolamine phosphatide

Ethanolamine phosphatide, ozonides

Ethanolamine phosphatides

Ether phosphatides

Glycerol Ether Phosphatides

Glycerol phosphatides

Glycerolipids phosphatidic acid

Glycerolipids synthesis from phosphatidic acid

Glycerophospholipids phosphatidic acid

Hydrolase phosphatidic acid phospho

Inositol phosphatides formation

Inositols phosphatides

L-a-dimyristoyl phosphatidic acid

Lipid phosphatidic acid

Lipids phosphatides

Magnesium salts of phosphatidic acid

Membrane bound phosphatidate

Metal phosphatidates

Milk, phosphatides

Mixed soybean phosphatides

Monolayers phosphatidic acid

Nonhydratable phosphatides

Origin of Milk Phosphatides

Origin of Phosphatides in Chick Embryo

Origin of Plasma Phosphatides

Passage of Phosphatides into Lymphatic Channels

Phosphate, inorganic Phosphatides

Phosphatidal choline

Phosphatidal derivative

Phosphatidal ethanolamine

Phosphatidate cytidyltransferase

Phosphatidate cytidylyltransferase

Phosphatidate phosphatase

Phosphatidate phosphohydrolase

Phosphatidate structure

Phosphatidate synthesis

Phosphatidate, phosphatidic acid analysis, separation

Phosphatidate, phosphatidic acid biosynthesis

Phosphatidate, phosphatidic acid membrane-bound

Phosphatidate, phosphatidic acid soluble

Phosphatidate, phosphatidic acid turnover

Phosphatidates

Phosphatidates cytidyltransferase

Phosphatidates lysophosphatidate

Phosphatidates phosphatase

Phosphatide

Phosphatide

Phosphatide Formation in Tissue Slices

Phosphatide bases, biosynthesis

Phosphatide cations

Phosphatide combined

Phosphatide deuterium

Phosphatide extraction from liver

Phosphatide group transfer

Phosphatide molecules, origin

Phosphatide plasmalogens

Phosphatide purification

Phosphatide turnover studies

Phosphatide vacuoles

Phosphatide, definition

Phosphatide, phosphatidic acid, phosphatidylcholine, phosphatidylethanolamine

Phosphatide, phosphatidic acid, phosphatidylcholine, phosphatidylethanolamine phosphatidylinositol, phosphatidylserine

Phosphatides

Phosphatides classification

Phosphatides occurrence

Phosphatides structure

Phosphatides table

Phosphatides, biochemistry

Phosphatidic acid

Phosphatidic acid , differences

Phosphatidic acid , metabolic roles

Phosphatidic acid /phosphatidylcholine

Phosphatidic acid /phosphatidylethanolamine

Phosphatidic acid Phosphatidyl choline, 861,

Phosphatidic acid biosynthesis

Phosphatidic acid functional derivatives

Phosphatidic acid glycerolipids from

Phosphatidic acid glycerophospholipids from

Phosphatidic acid kinase

Phosphatidic acid methyl esters

Phosphatidic acid molecular species

Phosphatidic acid pathway

Phosphatidic acid phosphatase

Phosphatidic acid phosphatase and

Phosphatidic acid phosphatidate

Phosphatidic acid products

Phosphatidic acid synthesis

Phosphatidic acid transport protein

Phosphatidic acid, definition

Phosphatidic acid, phospholipids derived

Phosphatidic acid, structure

Phosphatidic acid-cholesterol

Phosphatidic acids, isolation

Phosphatidic acids, isolation cells

Phosphatidic acids, isolation properties

Phosphatidic acids, isolation structure

Phosphatidic add

Phosphatidylcholine phosphatide hydrolase

Phosphatidylglycerol phosphatidic acid

Plasma phosphatides

Platelets and Platelet Phosphatides

Purification of Phosphatides

Reaction with phosphatidic acid

Soluble soya bean phosphatide reversal

Soya bean phosphatide

Soya bean phosphatide mixture

Soya phosphatides

Triacylglycerol phosphatidic acid

Turnover of Phosphatides

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