Fatty acids 3-hydroxy

Diarrhea is a common problem that is usually self-limiting and of short duration. Increased accumulations of small intestinal and colonic contents are known to be responsible for producing diarrhea. The former may be caused by increased intestinal secretion which may be enterotoxin-induced, eg, cholera and E. col] or hormone and dmg-induced, eg, caffeine, prostaglandins, and laxatives decreased intestinal absorption because of decreased mucosal surface area, mucosal disease, eg, tropical spme, or osmotic deficiency, eg, disaccharidase or lactase deficiency and rapid transit of contents. An increased accumulation of colonic content may be linked to increased colonic secretion owing to hydroxy fatty acid or bile acids, and exudation, eg, inflammatory bowel disease or amebiasis decreased colonic absorption caused by decreased surface area, mucosal disease, and osmotic factors and rapid transit, eg, irritable bowel syndrome. [Pg.202]

Dehydration. Dehydration of hydroxy fatty acids is quite common. Other compounds undergo the same reaction, eg, elymoclavine [548-43-6] to agroclavine [548-42-5] chanoclavine [2390-99-0] and other compounds and <7j -terpin hydrate [2541-01-63] to a-terpineol [98-55-5] (19). [Pg.313]

Ozyessigsaure, /. hydroxyacetic acid. Oxyfettsaure,/. hydroxy fatty acid, ozygenieren, v.t. oxygenate, oxygenize, Ozygenierung, /. oxygenation. [Pg.330]

Water repellant To impart water-resistant properties, particularly in greases Aliphatic amines, hydroxy fatty acids and some organic silicone polymers... [Pg.450]

The cell walls of mycobacteria contain three structures peptidoglycan, an arabinogalactan polysaccharide and long chain hydroxy fatty acids (mycolic acids) which are all covalently linked. Additional non-covalently attached lipid components found in the wall include glycolipids, various phospholipids and waxes. The lipid-rich nature of the mycobacterial wall is responsible for the characteristic acid-fastness on staining and serves as a penetration barrier to many antibiotics. Isoniazid and ethambutol have long been known as specific antimycobacterial agents but their mechanisms of action have only recently become more clearly understood. [Pg.168]

Suzuki T, K Tanaka, I Matsubara, S Kinoshita (1969) Trehalose lipid and alpha-branched-beta-hydroxy fatty acid formed by bacteria grown on -alkanes. Agric Biol Chem 33 1619-1627. [Pg.239]

Camp, R.D., Mallet, A.L, Woolard, P.M., Brain, S.D., Kobza-Black, A. and Greaves, M.W. (1983). The identification of hydroxy fatty acids in psoriatic skin. Prostaglandins, 26, 431-447. [Pg.121]

Free radicals are by-products of prostaglandin metabolism and may even regulate the activity of the arachidonate pathway. Arachidonic acid, released from lipids as a result of activation of phospholipases by tissue injury or by hormones, may be metabolized by the prostaglandin or leu-kotriene pathways. The peroxidase-catalysed conversion of prostaglandin G2 to prostaglandin H2 (unstable prostanoids) and the mechanism of hydroperoxy fatty acid to the hydroxy fatty acid conversion both yield oxygen radicals, which can be detected by e.s.r. (Rice-Evans et al., 1991). [Pg.193]

A. Fox. R. M. T. Rosario, and L. Larsson, Monitoring of bacterial sugars and hydroxy fatty acids in dust from air conditions by gas chromatography-mass spectrometry. Appl. Environ. Microbiol.. 59 4354 (1993). [Pg.405]

At the end of the reaction, hydroperoxide can be easily recovered in the aqueous phase (98-99%) after its separation from the organic phase and precipitation of the enzymes. The hydroperoxides obtained are highly reactive molecules [109]. They are intermediate compounds in the lipoxygenase pathway in plants, precursors for the synthesis of hydroxy-fatty acids (i.e., ( + )-coriolic acid [38,110], and regulators of the prostaglandins biosynthesis [111-113]. [Pg.579]

Szponar, B. Krasnik, L. Hryniewiecki, T. Gamian, A. Larsson, L. Distribution of 3-hydroxy fatty acids in tissues after intra-peritoneal injection of endotoxin. Clin. Chem. 2003,49,1149-1153. [Pg.35]

The affinity of the PHA polymerase that performs the polymerization reaction differs clearly for the various 3-hydroxy fatty acids. Based on the composition data of PHA synthesized from alkanes or fatty acids it is clear that the 3-hydroxy fatty acids with chain lengths of 8,9, or 10 carbon atoms are preferred. The affinity of the polymerase decreases for 3-hydroxy fatty acids with longer or shorter chains. [Pg.163]

As mentioned in the introduction, 3-hydroxy fatty acids with functional groups can also be incorporated in poly(3HAMCL). Table 2 illustrates this with many examples of alkenes, 3-hydroxyalkenoic acids, and substituted 3-hy-droxyalkanoic acids that are readily integrated in poly(3HAMCL). Long chain fatty acids have also been used successfully as substrates for poly(3HAMCL) production. De Waard et al. [44] used oleic acid and linoleic acid to produce... [Pg.163]

Prostaglandins and Hydroxy-Fatty Acids 2.3.1 Terpios zeteki... [Pg.128]

Figure 8.9 Total ion current chromatograms of (a) acidic and (b) neutral fractions of the sample collected from the Palaeolithic flint flake, taOHCx y are hydroxy fatty acids of chain length x with the hydroxy group at position cu and with y double bonds a,uidiCx y are a, uj dicarboxylic fatty acids of chain length x and with y double bonds...

$Figure 8.9 Total ion current chromatograms of (a) acidic and (b) neutral fractions of the sample collected from the Palaeolithic flint flake, taOHCx y are hydroxy fatty acids of chain length x with the hydroxy group at position cu and with y double bonds a,uidiCx y are a, uj dicarboxylic fatty acids of chain length x and with y double bonds...$

The aliphatic components of SOM, derived from various sources, tend to persist in soil (Almendros et al. 1998 Lichtfouse et al. 1998a Lichtfouse et al. 1998b Mosle et al. 1999 Poirier et al. 2000). The principal source of aliphatic materials in soil is plant cuticular materials, especially cutin, an insoluble polyester of cross-linked hydroxy-fatty acids and hydroxy epoxy-fatty acids (Kolattukudy 2001). Some plant cuticles also contain an acid and base hydrolysis-resistant biopolymer, comprised of aliphatic chains attached to aromatic cores known as cutan (Tegelaar et al. 1989 McKinney et al. 1996 Chefetz 2003 Sachleben et al. 2004). [Pg.129]

In plant tissues, various enzymes convert the hydroperoxides produced by LOX to other products, some of which are important as flavor compounds. These enzymes include hydroperoxide lyase, which catalyzes the formation of aldehydes and oxo acids hydroperoxide-dependent peroxygenase and epoxygenase, which catalyze the formation of epoxy and hydroxy fatty acids, and hydroperoxide isomerase, which catalyzes the formation of epoxyhydroxy fatty acids and trihydroxy fatty acids. LOX produces flavor volatiles similar to those produced during autoxidation, although the relative proportions of the products may vary widely, depending on the specificity of the enzyme and the reaction conditions. [Pg.122]

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