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Saturation of fatty acids

Table II compares the fatty acid composition of MGDG from the thylakoid membranes and the three types of PSII preparations. The PSII membranes and thylakoid membranes were rich in the trienoic acids, 18 3 and 16 3. In PSII core complex, the relative content of trienoic acids was reduced, and that of the saturated acids, 14 0, 16 0 and 18 0, increased. The 16 1(9c) and 18 1 also increased. Such an increase in the saturated and cis-monounsaturated fatty acids and the corresponding decrease in the trienoic acids were the most prominent in the PSII reaction center complex. The sum of saturated acids amounted to 50% of the total fatty acids, whereas the total of trienoic acids was only 29% (Table II). Since the saturation of fatty acids provides more rigid structure of the constituting lipid molecules, the occurrence of saturated fatty acids of lipids in the reaction center complex suggests that they stabilize the conformation of reaction center complex. Table II compares the fatty acid composition of MGDG from the thylakoid membranes and the three types of PSII preparations. The PSII membranes and thylakoid membranes were rich in the trienoic acids, 18 3 and 16 3. In PSII core complex, the relative content of trienoic acids was reduced, and that of the saturated acids, 14 0, 16 0 and 18 0, increased. The 16 1(9c) and 18 1 also increased. Such an increase in the saturated and cis-monounsaturated fatty acids and the corresponding decrease in the trienoic acids were the most prominent in the PSII reaction center complex. The sum of saturated acids amounted to 50% of the total fatty acids, whereas the total of trienoic acids was only 29% (Table II). Since the saturation of fatty acids provides more rigid structure of the constituting lipid molecules, the occurrence of saturated fatty acids of lipids in the reaction center complex suggests that they stabilize the conformation of reaction center complex.
Lawton, C.L., Delargy, H.J., Brockman, J., Smith, F.C. Blundell, J.E. The degree of saturation of fatty acids influences post-ingestive satiety. Br. J. Nutr. 2000, 83 473-482. [Pg.22]

A) Direct Gorribination of Fatty Acids with Alkali.—This method consists in the complete saturation of fatty acids with alkali, and permits of the use of the deglycerised products mentioned in chapter ii., section 2, and of carbonated alkalies or caustic soda or potash. Fatty acids are readily saponified with caustic soda or caustic potash of all strengths. [Pg.45]

The degree of saturation of fatty acids might also be somewhat related to cholesterol absorption, especially in relation to the well known hypocholesterolemic effect of polyunsaturated fatty acids[103, 104]. Human studies, however, showed that polyunsaturated fat feeding caused an increased excretion of both acidic sterols and endogenous neutral sterols but had no apparent effect on cholesterol absorp-tion[105,106]. [Pg.50]

Browning Reactions. The fluorescent components formed in the browning reaction (8) of peroxidized phosphatidylethanolamine are produced mainly by interaction of the amine group of PE and saturated aldehydes produced through the decomposition of fatty acid hydroperoxides. [Pg.99]

There are essentially four steps or unit operations in the manufacture of fatty acids from natural fats and oils (/) batch alkaline hydrolysis or continuous high pressure hydrolysis (2) separation of the fatty acids usually by a continuous solvent crystallisation process or by the hydrophilisation process (J) hydrogenation, which converts unsaturated fatty acids to saturated fatty acids and (4) distillation, which separates components by their boiling points or vapor pressures. A good review of the production of fatty acids has been given (1). [Pg.89]

A purified fatty acid is recommended for the preparation of a pure a-sulfo acid. Purified palmitic acid (m.p. 60.8-61.4°, neutralization equivalent 256.2) is prepared by twice recrystallizing a good commercial grade of palmitic acid from acetone at 0°, using a solvent ratio of 10 ml. to 1 g. However, the reaction may be applied to commercial saturated higher fatty acids, if the iodine number is sufficiently low. The checkers obtained similar results with recrystaUized Neo-Fat 1-56 (Armour and Company, Chicago, 111.) or Eastman white label palmitic acid. [Pg.84]

Natural fats are glycerol esters of fatty acids known as triglycerides. Unsaturated fats are generally liquids (oils) at room temperature, while triglycerides rich in saturated fatty acids are generally solids. View tristearin and triolein. Which one of these is saturated and which is unsaturated Are die double bonds in the unsaturated fat cis or transl... [Pg.157]

Uptake of LCFAs across the lipid-bilayer of most mammalian cells occurs through both a passive diffusion of LCFAs and a protein-mediated LCFA uptake mechanism. At physiological LCFA concentrations (7.5 nM) the protein-mediated, saturable, substrate-specific, and hormonally regulated mechanism of fatty acids accounts for the majority (>90%) of fatty acid uptake by tissues with high LCFA metabolism and storage such as skeletal muscle, adipose tissue, liver,... [Pg.494]

By depolymerizing PET waste with a polyol and subsequently condensing the oligomeric product with a polycarboxylic acid or anhydride, polyester resins are produced which have wide industrial applications. Depending on the polyol and polycarboxylic acid or anhydride used, saturated resins, alkyd resins, or unsaturated resins are obtained. PET wastes have been used for the production of alkyd resins in water thinnable paints. The materials obtained from the reaction of PET with a mixture of fatty acids high in linoleic acid content and trimethylolethane have been used in the preparation of water-dispersible coatings. Products of the depolymerization of PET with trimethylolpropane and pentaerythritol are used in the manufacture of high-solids paints. In the first step, PET is depolymerized with trimethylopropane and pentaerythritol at temperatures of 230-240°C. The final paint compositions contain 30-50% of PET depolymerization products.12... [Pg.530]

The raw materials for the manufacture of soap, the alkali salts of saturated and unsaturated C10-C20 carboxylic acids, are natural fats and fatty oils, especially tallow oil and other animal fats (lard), coconut oil, palm kernel oil, peanut oil, and even olive oil. In addition, the tall oil fatty acids, which are obtained in the kraft pulping process, are used for soap production. A typical formulation of fats for the manufacture of soap contains 80-90% tallow oil and 10-20% coconut oil [2]. For the manufacture of soft soaps, the potassium salts of fatty acids are used, as are linseed oil, soybean oil, and cottonseed oil acids. High-quality soap can only be produced by high-quality fats, independent of the soap being produced by saponification of the natural fat with caustic soda solution or by neutralization of distilled fatty acids, obtained by hydrolysis of fats, with soda or caustic soda solutions. Fatty acids produced by paraffin wax oxidation are of inferior quality due to a high content of unwanted byproducts. Therefore in industrially developed countries these fatty acids are not used for the manufacture of soap. This now seems to be true as well for the developing countries. [Pg.2]

Other lipophilic groups possibly attached to the maleic acid anhydride are alkanolamides of fatty acids. In this case the variations could be chain length and/or saturation grade of the C chain, the type of alkanolamine (most common are isopropanolamine, monoethanolamine, and diglycolamine), or an etho-... [Pg.506]

Tall oil fatty acids consist of resin acids (25% to 30%) and of a mixture of linolic acid, conjugated Cig fatty acids (45% to 65%), oleic acid (25% to 45%), 5,9,12-octadecatrienic acid (5% to 12%), and saturated fatty acids (1% to 3%). Resin acids are abietinic acid, dehydroabietic acid, and others. Properties of fatty acids are shown in Table 6-1. [Pg.89]

The major components have been identified tentatively as phenolic and fatty acids. At this time, seven phenolics have been identified in only four of the fractions. These are shown in Table III. A measure of the magnitude of the confidence level (cc) with a spectrum of standards is given. The first three entries are from the sunflower the last, from the Jerusalem artichoke. In all fractions isolated, both from the sunflower and the Jerusalem artichoke, a homologous series of fatty acids ranging from Cjo to Ci8 have been identified also by GC-MS. Even-chain, Cj6 to Cjs saturated and Cxs mono- and di-unsaturated, predominated. This is not surprising, since fatty acids are major constituents of plant... [Pg.104]

SFC has played an important role in the extraction and isolation of fatty acids [355,356]. Underivatised fatty acids and methyl esters of fatty acids are surprisingly easy to elute using a bonded phase or a silica based packed column and pure C02, probably due to the long hydrocarbon tails on the molecules [357]. On the other hand, most aromatic and polysubstituted acids will not elute. Triglycerides with saturated fatty acids can be analysed faster with pSCF-ELSD than with GC-FID and do not require sample preparation [358]. Using... [Pg.216]

HPLC has also been used for analysing fatty acid mixtures [708] and for the characterisation of fatty acids and their derivatives [709]. Fatty acids are commonly analysed on polymeric RPLC columns. Only multiple unsaturated fatty acids can be detected by UV in HPLC the others require derivatisation into UV-absorbing or fluorescing derivatives. Simultaneous determination of saturated and unsaturated fatty acids (C12-C24) by means of RPLC has been reported [710]. Derivatisation is necessary. [Pg.251]

The preparation of fatty acids substituted within an aliphatic chain is necessary to prepare dermatological pharmaceuticals. The unsaturated acyl fatty acids are the intermediate and can be produced by Kao Corporation starting from low-cost saturated compounds applying whole... [Pg.91]


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Fatty acid saturation

Fatty acids saturated

Saturated acids

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