脂肪酸的代谢3.pptx

Phosphatidic acid in lipid biosynthesis.Phosphatidic acid is the precursor of both triacylglycerols and glycerophospholipids.The mechanisms for head-group attachment in phospholipid synthesis are described later in this section.1.三酰甘油的合成Some of the fatty acids released into the blood are used for energy(in muscle,for example),and some are taken up by the liver and used in triacylglycerolsynthesis.The triacylglycerol formed in the liver is transported in the blood back to adipose tissue,where the fatty acid is released by extracellular lipoprotein lipase,taken up by adipocytes,and reesterifiedThe triacylglycerol cycle.In mammals,triacylglycerol molecules are broken down and resynthesized in a triacylglycerol cycle during starvation.Some of the fatty acids released by lipolysis of triacylglycerol in adipose tissue pass into the bloodstream,and the remainder are used for resynthesis of triacylglycerol.Insulin stimulates conversion of dietary carbohydrates and proteins to fat.Individuals with diabetes mellitus lack insulin;in uncontrolled disease,this results in diminished fatty acid synthesis,and the acetyl-CoA arising from catabolism of carbohydrates and proteins is shunted instead to ketone body production.People in severe ketosis smell of acetone,so the condition is sometimes mistaken for drunkenness.Regulation of triacylglycerol synthesis by insulinGlyceroneogenesis.The pathway is essentially an abbreviated version of gluconeogenesis,from pyruvate to dihydroxyacetonephosphate(DHAP),followed by conversion of DHAP to glycerol 3-phosphate,which is used for the synthesis of triacylglycerol.Regulation of glyceroneogenesis.(a)Glucocorticoid hormones stimulate glyceroneogenesis and gluconeogenesis in the liver,while suppressing glyceroneogenesis in the adipose tissue(by reciprocal regulation of the gene expressing PEP carboxykinase(PEPCK)in the two tissues);this increases the flux through the triacylglycerol cycle.The glycerol freed by the breakdown of triacylglycerol in adipose tissue is released to the blood and transported to the liver,where it is primarily converted to glucose,although some is converted to glycerol 3-phosphate by glycerol kinase.Thiazolidinediones activate a nuclear receptor called peroxisome proliferator-activated receptor (PPAR),which induces the activity of PEP carboxykinase.Therapeutically,thiazolidinediones increase the rate of glyceroneogenesis,thus increasing the resynthesis of triacylglycerol in adipose tissue and reducing the amount of free fatty acid in the blood.(b)A class of drugs called thiazolidinediones are now used to treat type 2 diabetes.In this disease,high levels of free fatty acids in the blood interfere with glucose utilization in muscle and promote insulin resistance.2.真核细胞中磷脂的合成Two general strategies for forming the phosphodiester bond of phospholipids.In both cases,CDP supplies the phosphate group of the phosphodiester bond.Initially,a head group(either serine or glycerol 3-phosphate)is attached via a CDPdiacylglycerolintermediate.For phospholipids other than phosphatidylserine,the head group is further modified,as shown here.In the enzyme names,PG represents phosphatidylglycerol;PS,phosphatidylserine.Origin of the polar head groups of phospholipids in E.coliThese glycero-phospholipids are synthesized using strategy 1.Phospha-tidylglycerol is synthesized as in bacteria.PI represents phospha-tidylinositol.Synthesis of cardiolipin and phosphatidylinositol in eukaryotesThe“salvage”pathway from phosphatidylserine tophosphatidylethanolamine and phosphatidylcholine in yeast.Phosphatidylserine and phosphatidylethanolamine are interconverted by a reversible head-group exchange reaction.In mammals,phosphatidylserine is derived from phosphatidylethanolamine by a reversal of this reaction;adoMet is S-adenosylmethionine;adoHcy,Sadenosylhomocysteine.Pathway for phosphatidylcholine synthesis from choline in mammals.The same strategy shown here(strategy 2)is also used for salvaging ethanolamine in phosphatidylethanolamine synthesis.Summary of the pathways to phosphatidyl-choline andPhosphatidyl-ethanolamine.Conversion of phosphatidyl-ethanolamineto phosphatidyl-choline in mammals takes place only in the liver.真核细胞中磷脂的合成（综合1）真核细胞中磷脂的合成（综合2）哺乳动物磷脂酰胆碱和磷脂酰乙醇氨的相互转化真核细胞中CDP-二酰甘油是合成磷脂酰肌醇，磷脂酰甘油，心磷脂的前体。3.动物细胞中缩醛磷脂的合成血小板活化因子:1-烷基-2-乙酰甘油磷酸胆碱的合成4.鞘脂的生物合成由3-酮鞘氨醇合成酶催化的反应开始3-酮鞘氨醇二氢鞘氨醇N-脂酰二氢鞘氨醇神经酰胺动物细胞中糖基神经酰胺，神经节苷脂和鞘磷脂的由神经酰胺合成。鞘磷脂5.花生四烯酸是合成前列腺素，血拴烷和白三烯的前体。前列腺素内过氧化物合成酶催化PGH2的合成阿斯匹林使环加氧酶失活5.胆固醇的合成甲羟戊酸的合成甲羟戊酸合成的机制HMG-CoA还原酶的活力受合成速度、降解速度及磷酸化和脱磷酸调控。甲羟戊酸到鲨烯的转化Oxidation at C-15 converts retinol to the aldehyde,retinal(c),and further oxidation produces retinoic acid(d),a hormone that regulates gene expression.Retinal combines with the protein opsin to form rhodopsin(not shown),a visual pigment widespread in nature.In the dark,retinal of rhodopsin is in the 11-cis form(c).When a rhodopsin molecule is excited by visible light,the 11-cis-retinal undergoes a series of photochemical reactions that convert it to all-trans-retinal(e),forcing a change in the shape of the entire rhodopsin molecule.This transformation in the rod cell of the vertebrate retina sends an electrical signal to the brain that is the basis of visual transduction.(a)-Carotene is the precursor of vitamin A1.Isoprene structural units are set off by dashed red lines.Cleavage of-carotene yields two molecules of vitamin A1(retinol)(b).Vitamin A1 and its precursor and derivatives由鲨烯转化为胆固醇豆甾醇豆甾醇麦角甾醇麦角甾醇 胆固醇的合成是一个高度耗能的过程，合成一个胆固醇需18个乙酰辅酶A，36个ATP，16个NADPH。能源物质过剩时，胆固醇的合成速度加快，午夜时，合成速度较快，膳食固醇类，特别是植物固醇可抑制胆固醇的合成。Lipoproteins.(a)Structure of a low-density lipoprotein(LDL).Apolipoprotein B-100(apoB-100)is one of the largest single polypeptide chains known,with 4,636 amino acid residues(Mr 513,000).(b)Four classes of lipoproteins,visualized in the electron microscope after negative staining.Clockwise from top left:chylomicrons,50 to 200 nm in diameter;VLDL,28 to 70 nm;HDL,8 to 11 nm;and LDL,20 to 25 nm.脂类是由脂蛋白运输的Lipoproteins and lipid transport.(a)Lipids are transported in the bloodstream as lipoproteins,which exist as several variants that have different functions,different protein and lipid compositions,and thus different densities.Dietary lipids are packaged into chylomicrons;much of their triacylglycerol content is released by lipoprotein lipase to adipose and muscle tissues during transport through capillaries.Chylomicron remnants(containing largely protein and cholesterol)are taken up by the liver.Endogenous lipids and cholesterol from the liver are delivered to adipose and muscle tissue by VLDL.Extraction of lipid from VLDL(along with loss of some apolipoproteins)gradually converts some of it to LDL,which delivers cholesterol to extrahepatic tissues or returns to the liver.The liver takes up LDL,VLDL remnants,and chylomicron remnants by receptor-mediated endocytosis.Excess cholesterol in extrahepatic tissues is transported back to the liver as HDL.In the liver,some cholesterol is converted to bile salts.(b)Blood plasma samples collected after a fast(left)and after a high-fat meal(right).Chylomicrons produced after a fatty meal give the plasma a milky appearance.Reaction catalyzed by lecithin-cholesterol acyl transferase(LCAT).This enzyme is present on the surface of HDL and isstimulated by the HDL component apoA-I.Cholesteryl esters accumulatewithin nascent HDLs,converting them to mature HDLs.载脂蛋白在肝细胞内质网合成，在内质网组装成脂蛋白颗粒，在高尔基体加工，包装成分泌小泡，分泌到肝细胞外。脂蛋白颗粒的胞吞和降解LDL受体的结构SREBP activation.Sterol regulatory element-binding proteins(SREBPs,shown in green)are embedded in the ER when firstsynthesized,in a complex with the protein SREBP cleavage-activating protein(SCAP,red).(N and C represent the amino and carboxyl termini of the proteins.)When bound to SCAP,SREBPs are inactive.When sterol levels decline,the complex migrates to the Golgi complex,and SREBP is cleaved by two different proteases in succession.The liberated amino-terminal domain of SREBP migrates to the nucleus,where it activates transcription of sterol-regulated genes.Regulation of cholesterol formation balances synthesis with dietary uptake.Glucagon promotes phosphorylation(inactivation)of HMG-CoA reductase;insulin promotes dephosphorylation(activation).X represents unidentified metabolites of cholesterol that stimulate proteolysis of HMG-CoA reductase.动脉斑的照片胆酸和胆酸盐的合成降低血清胆固醇的药物7-脱氢酶的混合氧化酶活性固醇类激素的合成孕酮孕烷醇酮睾酮醛固酮雌二醇一种兴奋剂一种兴奋剂基本要求1.掌握饱和脂肪酸的合成途径及调控。（重点）2.熟悉不饱和脂肪酸的合成途径及调控。3.熟悉磷脂、鞘脂类和甾醇的合成途径及调控。