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CHAPTER 21 Lipid Biosynthesis . Biosynthesis of fatty acids and eicosanoids Biosynthesis of isoprenes and cholesterol Cholesterol regulation Biosynthesis of triacylglycerols, and membrane lipids. Key topics : . Lipids Fulfill a Variety of Biological Functions. Storage of energy
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CHAPTER 21Lipid Biosynthesis • Biosynthesis of fatty acids and eicosanoids • Biosynthesis of isoprenes and cholesterol • Cholesterol regulation • Biosynthesis of triacylglycerols, and membrane lipids Key topics:
Lipids Fulfill a Variety of Biological Functions • Storage of energy • Constituents of cellular membranes • Anchors for membrane proteins • Cofactors for enzymes • Signaling molecules • Pigments • Detergents • Transporters • Antioxidants
Catabolism and Anabolic of Fatty Acids Proceed via Different Pathways • Catabolism of fatty acids • produced acetyl-CoA • reducing power to NADH • location: mitochondria • Anabolism of fatty acids • requires malonyl-CoA and acetyl-CoA • reducing power from NADPH • location: cytosol in animals, chloroplast in plants
Overview of Fatty Acid Synthesis • Fatty acids are built in several passes processing one acetate unit at a time • Acetate from activated malonate in the form of malonyl-CoA • In each pass involves reduction of a carbonyl carbon to a methylene carbon
Synthesis of Malonyl-CoA (1) • The three-carbon precursor for fatty acid synthesis is made from acetyl-CoA and CO2 • The reaction is catalyzed by acetyl-CoA carboxylase (ACC) • ACC is a bifunctional enzyme • Biotin carboxylase • Transcarboxylase • ACC contains biotin, nature’s carrier of CO2 • Biotin shuttles between the two active sites
Synthesis of Malonyl-CoA (2) • Bicarbonate reacts with the terminal phosphate of ATP to give carbamoyl phosphate • Biotin carries out a nucleophilic attack to carbamoyl phosphate • The product is a good donor of a carboxylate group
Synthesis of Malonyl-CoA (3) • The arm swing moves carboxybiotin to the transcarboxylase site • Terminal methyl of acetyl-CoA probably deprotonates to give a resonance-stabilized carbanion • The carbanion picks up the carboxylate moiety from biotin
Fatty Acid Synthesis • Overall goal is to attach a two-carbon acetate unit from malonyl-CoA to a growing chain and then reduce it • Reaction involves cycles of four enzyme-catalyzed steps • Condensation of the growing chain with activated acetate • Reduction of carbonyl to hydroxyl • Dehydration of alcohol to trans-alkene • Reduction of alkene to alkane • The growing chain is initially attached to the enzyme via a thioester linkage • During condensation, the growing chain is transferred to the acyl carrier protein • After the second reduction step, the elongated chain is transferred back to fatty acid synthase
Acyl Carrier Protein • Contains a covalently attached prothetic group 4’-phospho-pantethiene • The acyl carrier protein delivers acetate (in the first step) or malonate (in all the next steps) to the fatty acid synthase • The acyl carrier protein shuttles the growing chain from one active site to another during the four-step reaction
Charging the Acyl Carrier Protein and Fatty Acid Synthase • Two thiols participate in the fatty acid synthesis • Thiol from 4-phosphopantethine in acyl carrier protein • Thiol from cysteine in fatty acid synthase • Both thiols must be charged for the condensation reaction to occur • In the first step, acetyl from acetyl-CoA is transferred to acyl carrier protein • Acyl carrier protein passes this acetate to fatty acid synthase • Acyl carrier protein is then re-charged with malonyl from malonyl-CoA
Assimilation of Two-Carbon UnitsCondensation and First Reduction • 1 Condensation of an activated acyl group • 2 the β-keto group is reduced to an alcohol
Assimilation of Two-Carbon UnitsDehydration and Second Reduction • 3 elimination of H2O creates a double bond, and • 4 the double bond is reduced
Enzymatic Activities in Fatty Acid Synthase • Condensation with acetate • -ketoacyl-ACP synthase (KS) • Reduction of carbonyl to hydroxyl • -ketoacyl-ACP reductase (KR) • Dehydration of alcohol to alkene • -hydroxyacyl-ACP dehydratase (DH) • Reduction of alkene to alkane • enoyl-ACP reductase (ER) • Chain transfer • Malonyl/acetyl-CoA ACP transferase
C16, C18 and of Un-saturated Fatty Acids • Animals can readily introduce one double bond to palmitate and stearate • Vertebrates cannot introduce additional double bonds between C10 and methyl-terminal • We must obtain linoleate and -linolenate with diet; these are essential fatty acids • Plants, algae, and some insects synthesize linoleate from oleate
PC-Oleate Acts as A Substrate for Plant Desaturases • Oleic and Linoleic Acids are essential Fatty acids
Vertebrate Fatty Acyl Desaturase • Non-Heme Iron -- Mixed Function Oxidase • O2 accepts four electrons from two substrates • Two electrons come from saturated fatty acid • Two electrons come from ferrous state of Cytochrome b5
Oxidases, Monooxygenase, Dioxygenase • Molecular oxygen can serve as an electron acceptor • Oxidases do not incorporate oxygen atoms into the organic product • Oxygen atoms usually end up in hydrogen peroxide • Often use flavin as redox cofactors • Monooxygenases incorporate one of the oxygen atoms into the product • The other oxygen ends up in water • Often use iron as redox cofactor • Cytochrome P450 • Dioxygenases incorporate both oxygen atoms into the organic product
Eicosanoids - Signalling functions • Prostaglandins • Gastric Mucin (Cox-1) • Inflammation, Pain Fever (Cox-2) • Thromboxanes • Blood Clotting • Leukotrienes • Signal through G-protein Coupled receptors • Asthma and Bronchodilation
Synthesis of Eicosanoids • Cyclooxygenase is a target for many anti-inflammatory drugs
Biosynthesis of Cholesterol • Summary 1. Acetyl CoA => Mevalonate 2. Mevalonate => Isoprenes 3. 6 isoprenes => squalene 4. Squalene to lanosterol
1. Formation of Mevalonate • HMG-CoA reductase is a target for some cardiovascular drugs
Formation of Activated Isoprene • Pyrophosphate is a good leaving group in these nucleophilic substitution reactions
Cholesteryl esters. Esters more hydrophobic for storage and transport
Sterol regulatory element-binding proteins (SREBPs) released in response to membrane sterol content