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Fatty acyl groups

HisN03,(CH3)3N + -CH2 CH0H CH2C00-. Isolated from skeletal muscle. It acts as a carrier for ethanoyl groups and fatty acyl groups across the mitochondrial membrane during the biosynthesis or oxidation of fatty acids. [Pg.84]

Another microbial polysaccharide-based emulsifier is Hposan, produced by the yeast Candida lipolytica when grown on hydrocarbons (223). Liposan is apparentiy induced by certain water-immiscible hydrocarbons. It is composed of approximately 83% polysaccharide and 17% protein (224). The polysaccharide portion consists of D-glucose, D-galactose, 2-amino-2-deoxy-D-galactose, and D-galacturonic acid. The presence of fatty acyl groups has not been demonstrated the protein portion may confer some hydrophobic properties on the complex. [Pg.298]

Carnitine Carries Fatty Acyl Groups Across the Inner Mitochondrial Membrane... [Pg.782]

Figure 3. Mitochondrial fatty acid oxidation. Long-chain fatty acids are converted to their CoA-esters as described in the text, and their fatty-acyl-groups transferred to CoA in the matrix by the concerted action of CPT 1, the acylcarnitine/carnitine exchange carrier and CPT (A) as described in the text. Medium-chain and short-chain fatty acids (Cg or less) diffuse directly into the matrix where they are converted to their acyl-CoA esters by a acyl-CoA synthase. The mechanism of p-oxidation is shown below (B). Each cycle of P-oxidation removes -CH2-CH2- as an acetyl unit until the fatty acids are completely converted to acetyl-CoA. The enzymes catalyzing each stage of P-oxidation have different but overlapping specificities. In muscle mitochondria, most acetyl-CoA is oxidized to CO2 and H2O by the citrate cycle (Figure 4) some is converted to acylcamitine by carnitine acetyltransferase (associated with the inner face of the inner membrane) and exported from the matrix. Some acetyl-CoA (if in excess) is hydrolyzed to acetate and CoASH by acetyl-CoA hydrolase in the matrix. Enzymes ... Figure 3. Mitochondrial fatty acid oxidation. Long-chain fatty acids are converted to their CoA-esters as described in the text, and their fatty-acyl-groups transferred to CoA in the matrix by the concerted action of CPT 1, the acylcarnitine/carnitine exchange carrier and CPT (A) as described in the text. Medium-chain and short-chain fatty acids (Cg or less) diffuse directly into the matrix where they are converted to their acyl-CoA esters by a acyl-CoA synthase. The mechanism of p-oxidation is shown below (B). Each cycle of P-oxidation removes -CH2-CH2- as an acetyl unit until the fatty acids are completely converted to acetyl-CoA. The enzymes catalyzing each stage of P-oxidation have different but overlapping specificities. In muscle mitochondria, most acetyl-CoA is oxidized to CO2 and H2O by the citrate cycle (Figure 4) some is converted to acylcamitine by carnitine acetyltransferase (associated with the inner face of the inner membrane) and exported from the matrix. Some acetyl-CoA (if in excess) is hydrolyzed to acetate and CoASH by acetyl-CoA hydrolase in the matrix. Enzymes ...
Subbanagounder, G., Leitinger, N., Schwenke, D.C., Wong, J.W., Lee, H.R., Watson, A.D., FauU, K.F., Fogelman, A.M., and Berliner, J.A., 2000, Determination of bioactivity of oxidized phospholipids Specific oxidized fatty acyl groups at the sn-2 position, Arterioscler. Thromb. Vase. Biol. 20 2248-2254. [Pg.95]

This enzyme catalyzes the reaction of an acyl-CoA derivative with l-acyl-vn-glycerol 3-phosphate to generate coenzyme A and l,2-diacyl-5 n-glycerol 3-phosphate. The animal enzyme is reported to be specific for the transfer of unsaturated fatty acyl groups. Interestingly, the acyl-[acyl-carrier-protein] can also act as an acyl donor. [Pg.30]

SCHEME 6. In vivo oxidation of cholesterol (R = H) and other Upids (R = fatty acyl group) under the influence of UV radiation, by two different paths... [Pg.682]

Biological membranes are constructed of lipid bilayers 3 nm (30 A) thick, with proteins protruding on each side. The hydrocarbon core of the membrane, made up of the —CH2— and —CH3 of the fatty acyl groups, is about as nonpolar as decane, and liposomes formed in the laboratory from pure lipids are essentially impermeable to polar solutes, as are biological membranes (although the latter, as we shall see, are permeable to solutes for which they have specific transporters). [Pg.373]

In the third and final step of the carnitine shuttle, the fatty acyl group is enzymatically transferred from carnitine to intramitochondrial coenzyme A by carnitine acyltransferase II. This isozyme, located on the inner face of the inner mitochondrial membrane, regenerates fatty acyl-CoA and releases it, along with free carnitine, into the matrix (Fig. 17-6). Carnitine reenters the intermembrane space via the acyl-camitine/car-nitine transporter. [Pg.636]

The first steps of glycerophospholipid synthesis are shared with the pathway to triacylglycerols (Fig. 21-17) two fatty acyl groups are esterified to C-l and C-2 of L-glycerol 3-phosphate to form phosphatidic acid. Commonly but not invariably, the fatty acid at C-l is saturated and that at C-2 is unsaturated. A second route to phosphatidic acid is the phosphorylation of a diacyl-glycerol by a specific kinase. [Pg.809]


See other pages where Fatty acyl groups is mentioned: [Pg.298]    [Pg.124]    [Pg.148]    [Pg.279]    [Pg.783]    [Pg.821]    [Pg.330]    [Pg.330]    [Pg.53]    [Pg.15]    [Pg.343]    [Pg.41]    [Pg.240]    [Pg.295]    [Pg.475]    [Pg.533]    [Pg.554]    [Pg.613]    [Pg.684]    [Pg.684]    [Pg.684]    [Pg.684]    [Pg.684]    [Pg.109]    [Pg.613]    [Pg.684]    [Pg.684]    [Pg.684]    [Pg.684]    [Pg.684]    [Pg.375]    [Pg.381]    [Pg.383]    [Pg.631]    [Pg.642]    [Pg.789]    [Pg.805]    [Pg.813]    [Pg.814]   
See also in sourсe #XX -- [ Pg.109 ]




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Acyl group

Acyl group acylation

Fatty acyl

Fatty acylation

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