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Acyl CoA dehydrogenases

FIGURE 21.V The fatty acyl-CoA dehydrogenase reaction, emphasizing that the reaction involves reduction of enzyme-bonnd FAD (indicated by brackets). [Pg.684]

This is a crucial point because (as we will see) proton transport is coupled with ATP synthesis. Oxidation of one FADHg in the electron transport chain results in synthesis of approximately two molecules of ATP, compared with the approximately three ATPs produced by the oxidation of one NADH. Other enzymes can also supply electrons to UQ, including mitochondrial 5w-glyc-erophosphate dehydrogenase, an inner membrane-bound shuttle enzyme, and the fatty acyl-CoA dehydrogenases, three soluble matrix enzymes involved in fatty acid oxidation (Figure 21.7 also see Chapter 24). The path of electrons from succinate to UQ is shown in Figure 21.8. [Pg.684]

FIGURE 24.11 The acyl-CoA dehydrogenase reaction. The two electrons removed in this oxidation reaction are delivered to the electron transport chain in the form of reduced coenzyme Q (UQH9). [Pg.785]

FIGURE 24.12 The mechanism of acyl-CoA dehydrogenase. Removal of a proton from the u-C is followed by hydride transfer from the /3-carbon to FAD. [Pg.785]

FIGURE 24.13 The subunit structure of medium chain acyl-CoA dehydrogenase from pig liver mitochondria. Note the location of the bound FAD (red). (Adapted from Kim, J-T., and Wiz, J., 1988. Structure of the medium-chain acyl-CoA clchyclro-genase from pig liver mitochonciria at 3-A resolution. Proceedings of the National Academy of Sciences, USA 85 6671-668. )... [Pg.785]

A Metabolite of Hypoglycin from Akee Fruit Inhibits Acyl-CoA Dehydrogenase... [Pg.786]

The unripened fruit of the akee tree contains hypoglycin, a rare amino acid (Figure 24.14). Metabolism of hypoglycin yields methylenecydopropylacetyl-CoA (MCPA-CoA). Acyl-CoA dehydrogenase will accept MCPA-CoA as a substrate,... [Pg.786]

FIGURE 24.14 The conversion of hypoglycin from akee fruit to a form that inhibits acyl-CoA dehydrogenase. [Pg.786]

Polyunsaturated fatty acids pose a slightly more complicated situation for the cell. Consider, for example, the case of linoleic acid shown in Figure 24.24. As with oleic acid, /3-oxidation proceeds through three cycles, and enoyl-CoA isomerase converts the cA-A double bond to a trans-b double bond to permit one more round of /3-oxidation. What results this time, however, is a cA-A enoyl-CoA, which is converted normally by acyl-CoA dehydrogenase to a trans-b, cis-b species. This, however, is a poor substrate for the enoyl-CoA hydratase. This problem is solved by 2,4-dienoyl-CoA reductase, the product of which depends on the organism. The mammalian form of this enzyme produces a trans-b enoyl product, as shown in Figure 24.24, which can be converted by an enoyl-CoA isomerase to the trans-b enoyl-CoA, which can then proceed normally through the /3-oxidation pathway. Escherichia coli possesses a... [Pg.794]

FIGURE 24.24 The oxidation pathway for polyunsaturated fatty adds, illustrated for linoleic add. Three cycles of /3-oxidation on linoleoyl-CoA yield the cis-A, d.s-A intermediate, which is converted to a tran.s-A, cis-A intermediate. An additional round of /S-oxi-dation gives d.s-A enoyl-CoA, which is oxidized to the trans-A, d.s-A species by acyl-CoA dehydrogenase. The subsequent action of 2,4-dienoyl-CoA reductase yields the trans-A product, which is converted by enoyl-CoA isomerase to the tran.s-A form. Normal /S-oxida-tion then produces five molecules of acetyl-CoA. [Pg.795]

Step 1 of Figure 29.3 Introduction of a Double Bond The /3-oxidation pathway begins when a fait)7 acid forms a thioester with coenzyme A to give a fatty acyl Co A. Two hydrogen atoms are then removed from C2 and C3 of the fatty acyl CoA by one of a family of acyl-CoA dehydrogenases to yield an a,/3-unsaturated acyl CoA. This kind of oxidation—the introduction of a conjugated double bond into a carbonyl compound—occurs frequently jn biochemical pathways and usually involves the coenzyme flavin adenine dinucleotide (FAD). Reduced FADH2 is the by-product. [Pg.1133]

Enzymes 7,9, and 13 form a trifunctional protein associated with the inner face of the inner mitochondrial membrane. Very-long-chain acyl-CoA dehydrogenase is also associated with other inner mitochondrial membranes while the other enzymes are in the matrix and may be loosely associated with the inner face of the inner membrane. A medium-chain 2-enoyl-CoA hydratase may also be present in the mitochondrial matrix. [Pg.114]

Short-chain acyl-CoA dehydrogenase (SCAD) deficiency has been recorded in only a few patients and these show wide variation in clinical presentation. The defect has been seen in infants with a syndrome of psychomotor retardation and failure to thrive. These infants showed abnormal organic aciduria, and drastically decreased SCAD activity was demonstrable in cultured fibroblasts. Muscle symptoms were only part of a wider syndrome in all infants and children so far reported to have SCAD deficiency, but were the sole presenting feature in two adult patients, in whom lipid storage was demonstrable in skeletal muscle. The gene encoding for human SCAD has been mapped to chromosome 12. [Pg.306]

Daubner SC, G Gadda, Mp Valley, PF Fitzpatrick (2002) Cloning of nitroalkane oxidase from Fusarium oxysporum identifies a new member of the acyl-CoA dehydrogenase superfamily. Proc Natl Acad Sci USA 99 2702-2707. [Pg.587]

Babidge W, Millard S, Roediger W. 1998. Sulfides impair short chain fatty acid -oxidation at acyl-CoA dehydrogenase level in coloncytes Implications for ulcerative colitis. Mol Cell Biochem 181 117-124. [Pg.177]

The oxidation of fatty acids within the Knoop-Lynen cycle occurs in the matrix. The Knoop-Lynen cycle includes four enzymes that act successively on acetyl-CoA. These are acyl-CoA dehydrogenase (FAD-dependent enzyme), enoyl-CoA hydratase, 3-hydroxyacyl-CoA dehydrogenase (NAD-dependent enzyme), and acetyl-CoA acyltrans-ferase. Each turn, or revolution, of the fatty acid spiral produces... [Pg.196]

Fig. 14.1. Role ofthe pyruvate dehydrogenase complex (PDC) during aerobic/ anaerobic transitions in the development of Ascaris suum. PDC, pyruvate dehydrogenase complex AD, acyl CoA dehydrogenase ER, enoyl CoA reductase FR, fumarate reductase SDH, succinate dehydrogenase. Fig. 14.1. Role ofthe pyruvate dehydrogenase complex (PDC) during aerobic/ anaerobic transitions in the development of Ascaris suum. PDC, pyruvate dehydrogenase complex AD, acyl CoA dehydrogenase ER, enoyl CoA reductase FR, fumarate reductase SDH, succinate dehydrogenase.
Very-long-chain acyl-CoA dehydrogenase and trifunctional protein are the two inner membrane-bound... [Pg.699]


See other pages where Acyl CoA dehydrogenases is mentioned: [Pg.681]    [Pg.784]    [Pg.784]    [Pg.787]    [Pg.794]    [Pg.795]    [Pg.1134]    [Pg.607]    [Pg.114]    [Pg.114]    [Pg.114]    [Pg.121]    [Pg.304]    [Pg.306]    [Pg.306]    [Pg.306]    [Pg.307]    [Pg.87]    [Pg.181]    [Pg.183]    [Pg.188]    [Pg.132]    [Pg.197]    [Pg.280]    [Pg.95]    [Pg.42]    [Pg.696]    [Pg.698]    [Pg.701]   
See also in sourсe #XX -- [ Pg.137 ]

See also in sourсe #XX -- [ Pg.445 ]

See also in sourсe #XX -- [ Pg.544 ]




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2-Methyl branched-chain acyl-CoA dehydrogenase

Acyl CoA dehydrogenase and electron-transferring flavoprotein

Acyl dehydrogenase

Acyl-CoA

Acyl-CoA dehydrogenase

Acyl-CoA dehydrogenase

Acyl-CoA dehydrogenase, deficiencies

Acyl-CoA dehydrogenase, in fatty acid

Enzyme acyl-CoA dehydrogenase

Fatty acyl CoA dehydrogenases

Hydroxy-acyl CoA dehydrogenase

Long-chain 3-hydroxy acyl-CoA dehydrogenase

Long-chain 3-hydroxy acyl-CoA dehydrogenase deficiency

Long-chain acyl-CoA dehydrogenase

Long-chain acyl-CoA dehydrogenase LCAD)

Medium-chain acyl-CoA dehydrogenase

Medium-chain acyl-CoA dehydrogenase MCAD) deficiency

Medium-chain acyl-CoA dehydrogenase deficiency

Multiple acyl-CoA dehydrogenase deficiency

Short-chain acyl-CoA dehydrogenase

Short-chain acyl-CoA dehydrogenase SCAD)

Short-chain acyl-CoA dehydrogenase deficiency

Very long-chain acyl-CoA dehydrogenase

Very long-chain acyl-CoA dehydrogenase deficiency

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