Chapter 21 Lipid Metabolism Mary K. Campbell Shawn O. Farrell Paul D. Adams University of Arkansas.
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Transcript of Chapter 21 Lipid Metabolism Mary K. Campbell Shawn O. Farrell Paul D. Adams University of Arkansas.
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Chapter 21Lipid Metabolism
Mary K. CampbellShawn O. Farrellhttp://academic.cengage.com/chemistry/campbell
Paul D. Adams • University of Arkansas
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Generation and Storage of Energy
• The oxidation of fatty acids (FA)in triacylglycerols is the _________________________________ for most organisms• Their carbon chains are in a highly reduced form• The energy yield per gram of fatty acid oxidized is greater
than that per gram of carbohydrate oxidized
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Catabolism of Lipids
• ____________ catalyze hydrolysis of bonds between fatty acid and the rest of triacylglycerols
• __________________ catalyze hydrolysis of bonds between fatty acid and the rest of phosphoacylglycerols
• May have multiple sites of action
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Fatty Acid Activation
• Fatty acid oxidation begins with ____________• A thioester bond is formed between the carboxyl
group of the FA and the thiol of CoA-SH
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The Role of Carnitine in Acyl-CoA Transfer
• The acyl-CoA crosses the ____________ mitochondrial membrane, but not the ____________ membrane
• The acyl group is then transferred to carnitine, carried across the inner mitochondrial membrane, and transferred to mitochondrial CoA-SH
• Carnitine Palmitoyltransferase (CPT-1) has specificity for acyl groups between 14 and 18 carbons long
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The Role of Carnitine in Acyl-CoA Transfer
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-Oxidation
• -Oxidation:-Oxidation: a series of reactions that cleaves carbon atoms __________ at a time from the carboxyl end of a fatty acid
• The complete cycle of one -oxidation requires four enzymes• Reaction 1: Oxidation of the , carbon-carbon single
bond to a carbon-carbon double bond• Reaction 2: Hydration of the carbon-carbon double
bond• Reaction 3: Oxidation of the -hydroxyl group to a
carbonyl group• Reaction 4: Cleavage of the carbon chain by a
reverse Claisen reaction
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-Oxidation
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Summary
• Fatty acids are activated and transported to the mitochondrial matrix for further catabolism
• The breakdown of fatty acids takes place in the mitochondrial matrix and proceeds by successive removal of two-carbon units as acetyl-CoA
• Each cleavage of a two-carbon moiety requires a four-step reaction sequences called -oxidation
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Energy Yield from FA Oxidation
• The energy released by the oxidation of acetyl-CoA formed by -oxidation of FA can drive ___ synthesis
• ____________ cycles of -oxidation are required for the oxidation of stearic acid to acetyl-CoA
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Energy Yield from FA Oxidation
• The overall equation for oxidation of stearic acid can be obtained by adding the equations for -oxidation, the ______________________, and ___________________________________
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Energy Yield from FA Oxidation
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Summary
• The complete oxidation of FA by the citric acid cycle and the electron transport chain releases large amounts of energy
• When we include the reoxidation of NADH and FADH2 from -oxidation and the citric acid cycle, we obtain a net yield of 120 ATP for a single molecule of stearic acid
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Catabolism of Odd-Numbered FA
• Odd-numbered FA are not frequently encountered, but do also undergo -oxidation
• The last -oxidation cycle of a fatty acid with an odd number of carbons gives
_______________
_______________
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Oxidation of an Unsaturated FA
• A cis-trans isomerization is needed to convert unsaturated FA to acetyl-CoA
• This enzyme is known as an ______________
• Oxidation of unsaturated FA does not generate as much ATP relative to saturated FA with the same # of carbons
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Oxidation of an Unsaturated FA
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Summary
• FA with odd number of carbons produce propionyl-CoA in the last step of the oxidation
• Propionyl-CoA can be converted to succinyl-CoA, which plays a role in the citric acid cycle
• The oxidation of unsaturated FA requires enzymes that catalyze isomerization around the double bonds so that oxidation can proceed
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Ketone Bodies
• Formation of ketone bodies occurs when the amount of acetyl-CoA produced is excessive compared to the amount of oxaloacetate available to react with it• Intake high in _______ and low in ______________ • Diabetes not suitably controlled• Starvation
• Ketone bodies Ketone bodies areare: acetone, -hydroxybutyrate, and acetoacetate• Formed principally in ___________ mitochondria• Can be used as a fuel in most tissues and organs
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Ketone Bodies
Summary:
• If an organism has an excess of acetyl-CoA, it produces ketone bodies.
• This situation can arise from an excessive intake of fats compared to carbohydrates, or from diabetes.
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Fatty Acid Biosynthesis
• Biosynthesis is not exact reversal of oxidation
• Biosynthetic reactions occur in the ___________
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Fatty Acid Biosynthesis
• Carboxylation of acetyl-CoA occurs in the cytosol• Catalyzed by acetyl-CoA carboxylase• ___________ is the carrier of the carboxyl group• Malonyl-CoA is key intermediate that is produced
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Biosynthesis of Palmitate
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Sites of Fatty Acid Metabolism in an Animal Cell
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Summary
• Acetyl-CoA is transported to the cytosol and converted to malonyl-CoA• The biosynthesis of FA proceeds by the addition of 2-carbon units to the
hydrocarbon chain. • The process is catalyzed by the fatty-acid synthase complex
Comparison of FA Degradation and Biosynthesis
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Triacylglycerol Biosynthesis
Lipids such as triacylglycerols, phosphoacylglycerols, and steroids are derived ___________
__________________
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Biosynthesis of Phosphoacylglycerols
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Biosynthesis of Sphingosine/Ceramide
Requires starting materials _______________and serine
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Cholesterol Biosynthesis
• All carbon atoms of cholesterol and steroids synthesized from it are derived from the two-carbon acetyl group of ___________________
• Involves many reaction steps
• Involvement of ___________ units are key to the biosynthesis of steroids and other biomolecules known as ________
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Overall View of Cholesterol Biosynthesis
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Cholesterol Biosynthesis
• Synthesis begins with the condensation of 2 molecules of __________________
• Next, condensation with a 3RD molecule of __________
• The formation of mevalonate is completed by reduction of the thioester to a 1° alcohol
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Mevalonate to Squalene
• The pyrophosphosphorylation of the 1° alcohol of mevalonate (two moles of ATP) is followed by phosphorylation of the 3° alcohol (one mole of ATP), then the concerted decarboxylation and -elimination of phosphate ion gives ______________________ ______________________
• Then there is an enzyme-catalyzed isomerization of the carbon-carbon double bond that gives dimethylallyl pyrophosphate
• Dimethylallyl pyrophosphate is then converted to isopentyl pyrophosphate, which is followed by H+ loss to give farnesyl pyrophosphate
• The joining together of two units of farnesyl pyrophosphate (C15) units by a 2-electron oxidation gives ___________ (C30)
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The Conversion of Mevalonate to Squalene
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Squalene to Cholesterol
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Cholesterol as a Precursor
Cholesterol is the precursor for a number of ______________________
______________________
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Role of Cholesterol in Heart Disease
• Lipids are transported in the blood stream by ______________________
• Cholesterol and its fatty acid esters are packaged into several classes of lipoproteins for transport
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The LDL Particle
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The Fate of Cholesterol
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Summary
• The biosynthesis of cholesterol proceeds by the condensation of five-carbon isoprenoid units
• Isoprenoid units in turn are derived from the reaction of three acetyl-CoA units
• Once cholesterol is formed, it serves as a precursor for other steroids
• Cholesterol must be packaged for transport in the bloodstream. Some of these forms of cholesterol play a role in heart disease