What is fatty acid oxidation

    • [DOC File]Open.Michigan

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      biochemistry Fatty Acid Oxidation Disorders. 750 (4) Fatty Acid Oxidation Disorders. Carnitine Deficiency1. Primary Generalized Carnitine Deficiency (carnitine transport defect)1. Primary Muscle Carnitine Deficiency2. Secondary Carnitine Deficiency2. …

      fatty acid oxidation pathway


    • [DOCX File]Title

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      26.2 Fatty acid oxidation. What does a fatty acid look like. Has an even number of C’s, can have C=C. Fatty acid oxidation takes place in the mitochondria near the Krebs cycle etc., makes it v. efficient. I. Step One - Fatty acid must be activated, it is relatively inert - Activated by removing –OH, subst. with CoA (uses up eff. 2 ATP)

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    • [DOC File]Chapter 1 – name

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      The follow-up has been refined as the amino acid disorders, fatty acid oxidation disorders, organic acid disorder and isolated analyte elevations have been fully incorporated into the Patient Care module. This makes the day to day tasks more precise, so training now …

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    • [DOCX File]Medium Chain Acyl CoA Dehydrogenase Deficiency

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      1. With respect to amino acid metabolism, A. it ends with oxidation of short chain fatty acids in peroxisomes. B. oxidation of saturated fatty acids involves . cis. intermediates. C. enoyl-CoA isomerase is not needed for oxidation of saturated fatty . acids. D. ketone body synthesis uses the last enzyme of fatty acid synthesis. 2.

      complete oxidation of fatty acids


    • [DOC File]CHAPTER 26: Lipid Metabolism

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      Long-chain fatty acid oxidation disorders (FAODs) are a group of rare inherited inborn errors of metabolism. Individuals with long-chain FAODs are unable to use dietary fat (long chain fat) for energy. The inability to break down fats for energy and the buildup of fatty acids causes serious health problems.

      fatty acid oxidation defect


    • [DOCX File]D. ketone body synthesis uses the last enzyme of fatty ...

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      34. Fatty acid oxidation results in the direct production of. a. ketones. b. fructose. c. pyruvate. d. acetyl CoA. 35. Production of excessive amounts of acetyl CoA molecules leads to the synthesis of. a. fatty acids only. b. fatty acids and glucose only. c. fatty acids and fructose only. d. fatty …

      fatty acid oxidation disease


    • [DOC File]The Center for Inherited Disorders of Energy Metabolism ...

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      Beta-oxidation is the initial phase of fatty acid oxidation. This occurs in the mitochondria. There are quite a few reactions, but the result is that the fatty acid chains are broken into two-carbon acetic acid fragments, and coenzymes are reduced.

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    • Understanding Fatty Acid Oxidation & Your Energy Levels / N…

      Fatty acids are the second major source of fuel used by cardiac and skeletal muscles; because carbons are completely reduced, oxidation of the carbons releases lots of energy. Carbohydrates are partially oxidized – i.e. have –OH groups – so their oxidation yields less energy than B-oxidation of fatty acids.

      fatty acid beta oxidation


    • [DOC File]Learning Objective: Energy Metabolism

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      1.MCAD is an aberration of fatty acid oxidation (Fig. 1). Although fatty acid oxidation (FAO) is a normal physiological process, the activity of this pathway is greatly increased in a starved state, in diabetes and during periods of strenuous exercise. The process is described as follows: a.Fatty acids (FA) are mobilized from the adipose tissue ...

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    • [DOC File]Nutricia North America

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      Fatty Acid Oxidation: Defects of fatty acid oxidation may be suspected in non-ketotic fasting hypoglycemia associated with dicarboxylic aciduria or in unexplained cardiomyopathy or rhabdomyolysis. Certain defects (e.g.: medium-chain acyl-CoA dehydrogenase deficiency) in many cases (but not all) can be diagnosed directly by DNA mutational analysis.

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