Metabolism of saccharides - exercise - Vladimíra Kvasnicová Glucose enter the cells by a) free diffusion b) facilitated diffusion c) active transport d) secondary active transport Glucose enter the cells by a) free diffusion b) facilitated diffusion c) active transport d) secondary active transport Insulin-dependent transport of glc into the cell is found in the a) liver b) erytrocyte c) adipose tissue d) muscle Insulin-dependent transport of glc into the cell is found in the a) liver b) erytrocyte c) adipose tissue d) muscle Glucose transport into cells: facilitated diffusion (protein transporter GLUT – various types) ERYTROCYTES NERVOUS TISSUE - insulin-independent transport The figure is found at http://www.kumc.edu/research/medicine/biochemistry/bioc800/car02fra.htm (Jan 2007) HEPATOCYTES - insulin-independent transport The figure is found at http://www.kumc.edu/research/medicine/biochemistry/bioc800/car02fra.htm (Jan 2007) FATTY TISSUE MUSCLES - insulin-DEPENDENT transport insulin increases number of glc transporters The figure is found at http://www.kumc.edu/research/medicine/biochemistry/bioc800/car02fra.htm (Jan 2007) Secondary-active transport of GLC: symport with Na+ - small intestine, kidneys The figure was adopted from Devlin, T. M. (editor): Textbook of Biochemistry with Clinical Correlations, 4th ed. Wiley-Liss, Inc., New York, 1997. ISBN 0-471-15451-2 Glucose from a diet can be used a) as an energy source for cells b) for glycogen synthesis c) for formation of fat (= energy store) d) as a main substrate for production of NADPH Glucose from a diet can be used a) as an energy source for cells b) for glycogen synthesis c) for formation of fat (= energy store) d) as a main substrate for production of NADPH Glc-6-P !!! + NADPH = hepatocyte The figure is found at http://www.kumc.edu/research/medicine/biochemistry/bioc800/car02fra.htm (Jan 2007) Glycolysis (= oxidative cleavage of glucose) a) is located in a mitochondrion b) can proceed under anaerobic conditions as well c) produces 2 moles of pyruvate / 1 mole of Glc d) generates 2 moles of ATP as a net energy acquisition Glycolysis (= oxidative cleavage of glucose) a) is located in a mitochondrion b) can proceed under anaerobic conditions as well c) produces 2 moles of pyruvate / 1 mole of Glc d) generates 2 moles of ATP as a net energy acquisition Products of aerobic glycolysis 2 Products of anaerobic glycolysis 2 NADH was consumed in conversion of pyruvate to lactate The figure is found at http://www.kumc.edu/research/medicine/biochemistry/bioc800/car02fra.htm (Jan 2007) Enzyme hexokinase a) catalyzes esterification of glucose b) has higher affinity to glucose than glucokinase c) phosphorylates fructose as well d) is found in a cytoplasm of many cells Enzyme hexokinase a) catalyzes esterification of glucose b) has higher affinity to glucose than glucokinase c) phosphorylates fructose as well d) is found in a cytoplasm of many cells IRREVERSIBLE REACTION The figure is found at http://www.kumc.edu/research/medicine/biochemistry/bioc800/car02fra.htm (Jan 2007) Km Km The glucokinase has higher value of Kmthan hexokinase glucokinase has lower affinity to glucose (it needs more glucose to reach the reaction velocity of Vmax/2) The figure is found at http://www.kumc.edu/research/medicine/biochemistry/bioc800/car02fra.htm (Jan 2007) Enzyme 6-phosphofructokinase-1 (PFK-1) a) is a main regulatory enzyme of glycolysis b) converts fructose-1,6-bisphosphate to fructose-6-phosphate c) is activated by citrate and ATP/ADP d) is regulated by insulin Enzyme 6-phosphofructokinase-1 (PFK-1) a) is a main regulatory enzyme of glycolysis b) converts fructose-1,6-bisphosphate to fructose-6-phosphate c) is activated by citrate and ATP/ADP d) is regulated by insulin IRREVERSIBLE REACTION The figure is found at http://www.kumc.edu/research/medicine/biochemistry/bioc800/car02fra.htm (Jan 2007) NADH+H+ forming in glycolysis a) is a coenzyme of oxidoreductases b) can be reoxidized back to NAD+ in a conversion of pyruvate to lactate c) can be used in a reduction of malate to oxaloacetate d) is a source of reducing equivalents entering a respiratory chain, but only under aerobic conditions NADH+H+ forming in glycolysis a) is a coenzyme of oxidoreductases b) can be reoxidized back to NAD+ in a conversion of pyruvate to lactate c) can be used in a reduction of malate to oxaloacetate d) is a source of reducing equivalents entering a respiratory chain, but only under aerobic conditions The figure is found at http://www.kumc.edu/research/medicine/biochemistry/bioc800/car02fra.htm (Jan 2007) The figure is found at http://www.kumc.edu/research/medicine/biochemistry/bioc800/car02fra.htm (Jan 2007) Transport of reducing equivalents to mitochondria The figure was adopted from Devlin, T. M. (editor): Textbook of Biochemistry with Clinical Correlations, 4th ed. Wiley-Liss, Inc., New York, 1997. ISBN 0-471-15451-2 MALATE-ASPARTATE SHUTTLE GLYCEROL PHOSPHATE SHUTTLE The figure was adopted from Devlin, T. M. (editor): Textbook of Biochemistry with Clinical Correlations, 4th ed. Wiley-Liss, Inc., New York, 1997. ISBN 0-471-15451-2 2,3-bisphosphoglycerate (2,3-BPG) a) belongs among energy rich compounds b) is formed from glyceraldehyde-3-phosphate by phosphorylation using inorganic phosphate c) can be transformed to 3-phosphoglycerate, ATP is simultaneously formed from ADP d) is formed only in the liver as a shunt of glycolysis 2,3-bisphosphoglycerate (2,3-BPG) a) belongs among energy rich compounds b) is formed from glyceraldehyde-3-phosphate by phosphorylation using inorganic phosphate c) can be transformed to 3-phosphoglycerate, ATP is simultaneously formed from ADP d) is formed only in the liver as a shunt of glycolysis 2,3-BPG shunt IN ERYTROCYTES: 2,3-BPG affinity of Hb to O2 The figure was adopted from Devlin, T. M. (editor): Textbook of Biochemistry with Clinical Correlations, 4th ed. Wiley-Liss, Inc., New York, 1997. ISBN 0-471-15451-2 ATP is formed in the reactions of glycolysis a) phosphoenolpyruvate (PEPA) → pyruvate b) glucose → glucose-6-phosphate c) fructose-1,6-bisphosphate → fructose-6-phosphate d) glyceraldehyde-3-phosphate → 1,3-bisphosphoglycerate ATP is formed in the reactions of glycolysis a) phosphoenolpyruvate (PEPA) → pyruvate b) glucose → glucose-6-phosphate c) fructose-1,6-bisphosphate → fructose-6-phosphate ATP is consumed = not energy-rich comp. d) glyceraldehyde-3-phosphate → 1,3-bisphosphoglycerate IRREVERSIBLE REACTION = substrate level phosphorylation (ATP formation using energy released from cleavage of an energy rich compound = macroergic compound) The figure is found at http://www.kumc.edu/research/medicine/biochemistry/bioc800/car02fra.htm (Jan 2007) Pi + = substrate level phosphorylation The figure is found at http://www.kumc.edu/research/medicine/biochemistry/bioc800/car02fra.htm (Jan 2007) Pyruvate can be transformed by a) carboxylation to acetyl-CoA b) reduction to lactate c) oxidative decarboxylation to oxaloacetate d) transamination to aspatate Pyruvate can be transformed by a) carboxylation to acetyl-CoA b) reduction to lactate c) oxidative decarboxylation to oxaloacetate d) transamination to aspatate = transamination = carboxylation = reduction = oxidative decarboxylation The figure is found at http://www.kumc.edu/research/medicine/biochemistry/bioc800/car02fra.htm (Jan 2007) Choose correct statements about regulation of glycolysis a) it is activated by insulin b) it is activated by glucagon c) regulatory enzymes of glycolysis are kinases d) pH inhibits glycolysis Choose correct statements about regulation of glycolysis a) it is activated by insulin b) it is activated by glucagon c) regulatory enzymes of glycolysis are kinases d) pH inhibits glycolysis Regulation of glycolysis regulatory enzyme activation inhibition glucose-6-phosphate hexokinase glucokinase insulin (induction) fructose-1-phosphate (liver) 6-phosphofructo1-kinase (PFK-1) ATP / AMP fructose-6-phosphate ATP / AMP fructose-2,6-bisphosphate citrate ( if insulin / glucagon) acidic pH insulin (induction) main regulatory enzyme (key enzyme) pyruvate kinase insulin (induction) glukagon (repression, fructose-1,6-bisphosphate inhibition by phosphorylation) ATP / AMP (feed foreward regulation) acetyl-CoA Enzymes of gluconeogenesis (= synthesis of glucose „de novo“) a) are found in a cytoplasm only b) are active mainly in a brain and erytrocytes c) are completely the same as enzymes of glycolysis (catalyze oposite reactions of glycolysis) d) are not found in the liver Enzymes of gluconeogenesis (= synthesis of glucose „de novo“) a) are found in a cytoplasm only b) are active mainly in a brain and erytrocytes c) are completely the same as enzymes of glycolysis (they catalyze oposite reactions of glycolysis) d) are not found in the liver gluconeogenesis proceeds only in the liver and the kidneys in mitochondria only The figure is found at http://www.kumc.edu/research/medicine/biochemistry/bioc800/car02fra.htm (lJan 2007) Gluconeogenesis The figure is found at http://www.kumc.edu/research/medicine/biochemistry/bioc800/car02fra.htm (Jan 2007) Choose substrates of gluconeogenesis a) acetyl-CoA b) pyruvate c) glycerol d) lactate Choose substrates of gluconeogenesis a) acetyl-CoA b) pyruvate c) glycerol d) lactate it can not be converted to pyruvate Cori cycle and muscle The figure was adopted from Devlin, T. M. (editor): Textbook of Biochemistry with Clinical Correlations, 4th ed. Wiley-Liss, Inc., New York, 1997. ISBN 0-471-15451-2 Glucose-alanine cycle The figure was adopted from Devlin, T. M. (editor): Textbook of Biochemistry with Clinical Correlations, 4th ed. Wiley-Liss, Inc., New York, 1997. ISBN 0-471-15451-2 = tuk The figure was adopted from Devlin, T. M. (editor): Textbook of Biochemistry with Clinical Correlations, 4th ed. Wiley-Liss, Inc., New York, 1997. ISBN 0-471-15451-2 Choose enzymes of gluconeogenesis a) pyruvate kinase b) PEP carboxykinase c) pyruvate carboxylase d) pyruvate dehydrogenase Choose enzymes of gluconeogenesis a) pyruvate kinase b) PEP carboxykinase c) pyruvate carboxylase d) pyruvate dehydrogenase Pyruvate DeHydrogenase complex is found in mitochondria (multienzyme complex, PDH) the reaction is IRREVERSIBLE The figure is found at http://faculty.uca.edu/~johnc/pdhrxns.gif (Jan 2006) The reactions participate in gluconeogenesis a) pyruvate + CO2 → oxaloacetate b) pyruvate + ATP → phosphoenolypyruvate c) fructose-1,6-bisphosphate → fructose-6phosphate + ATP d) glucose-6-phosphate → glucose + ATP The reactions participate in gluconeogenesis a) pyruvate + CO2 → oxaloacetate b) pyruvate + ATP → phosphoenolypyruvate c) fructose-1,6-bisphosphate → fructose-6phosphate + ATP d) glucose-6-phosphate → glucose + ATP Gluconeogenesis is a) activated by insulin b) inhibited by citrate c) activated by AMP d) inhibited by glucagon Gluconeogenesis is a) activated by insulin b) inhibited by citrate c) activated by AMP d) inhibited by glucagon the opposite answers are correct Regulation of gluconeogenesis regulatory enzyme activation inhibition pyruvate carboxylase acetyl-Co A cortisol, glucagon (induction) insulin (repression) phosphoenolpyruvate carboxykinase cortisol, glucagon (induction) insulin (repression) fructose-1,6bisphosphatase cortisol, glucagon (induction) AMP / ATP fructose-2,6bisphosphate ( if insulin / glucagon) insulin (repression) glucose-6phosphatase cortisol, glucagon (induction) insulin (repression) Metabolism of glycogen a) is regulated by glycogen synthase and glycogen phosphorylase b) is located in a cytoplasm c) is regulated by insulin d) proceeds on reducing ends of glycogen molecule Metabolism of glycogen a) is regulated by glycogen synthase and glycogen phosphorylase b) is located in a cytoplasm c) is regulated by insulin d) proceeds on reducing ends of glycogen molecule Metabolism of glycogen The figure is found at http://www.kumc.edu/research/medicine/biochemistry/bioc800/car02fra.htm (Jan 2007) During glycogen synthesis (= glycogenesis) a) Glc-6-P is transformed to UDP-6-glc b) glycogen synthase participates in a formation of both (1→4) and (1→6) glycosidic bonds c) a macroergic phosphate is consumed d) is glycogen synthase activated by glucagon During glycogen synthesis (= glycogenesis) a) Glc-6-P is transformed to UDP-6-glc b) glycogen synthase participates in a formation of both (1→4) and (1→6) glycosidic bonds c) a macroergic phosphate is consumed d) is glycogen synthase activated by glucagon The figure is found at http://www.kumc.edu/research/medicine/biochemistry/bioc800/car02fra.htm (Jan 2007) During degradation of glycogen within cells (= glycogenolysis) a) (1→6) glycosidic bonds are split by glycogen phosphorylase b) glucose is transfered to phosphate: glc-1-P is formed as a product of the degradation c) (1→4) bonds are split hydrolytically d) 1 ATP is consumed if 1 glc is released During degradation of glycogen within cells (= glycogenolysis) a) (1→6) glycosidic bonds are split by glycogen phosphorylase b) glucose is transfered to phosphate: glc-1-P is formed as a product of the degradation c) (1→4) bonds are split hydrolytically d) 1 ATP is consumed if 1 glc is released The figure is found at http://www.kumc.edu/research/medicine/biochemistry/bioc800/car02fra.htm (Jan 2007) If glycogenolysis is followed by glycolysis a) the net gain of the anaerobic glycolysis is 3 ATP b) the process is called gluconeogenesis c) both the cytoplasmatic and mitochondrial enzymes participate in the reactions d) oxaloacetate is formed as an intermediate If glycogenolysis is followed by glycolysis a) the net gain of the anaerobic glycolysis is 3 ATP b) the process is called gluconeogenesis c) both the cytoplasmatic and mitochondrial enzymes participate in the reactions d) oxaloacetate is formed as an intermediate glycogen Pi glucose ATP ADP The figure is found at http://www.kumc.edu/research/medicine/biochemistry/bioc800/car02fra.htm (Jan 2007) Regulation of glycogen metabolism regulatory enzyme activation glucagon, glykogen adrenaline phosphorylase (phosphorylation) (glycogen degradation) inhibition ATP / AMP glucose-6-phosphate glucose ATP / AMP Ca2+ (muscle) glykogen synthase (glycogen synthesis) insulin (induction) glucose-6-phosphate glucagon, adrenaline (phosphorylation) Pentose cycle (= Hexose MonoPhosphate Pathway, HMPP) a) is located in a cytoplasm b) includes direct oxidation of glucose monophosphate c) is a shunt of glycolysis (products of HMPP can enter glycolysis) d) produces pentoses Pentose cycle (= Hexose MonoPhosphate Pathway, HMPP) a) is located in a cytoplasm b) includes direct oxidation of glucose monophosphate c) is a shunt of glycolysis (products of HMPP can enter glycolysis) d) produces pentoses The figure is found at http://www.richmond.edu/~jbell2/14F34.JPG (Dec 2006) Choose enzymes of HMPP a) transketolase b) transaminase c) glucose-6-phosphate dyhydrogenase (glc-6-P DH) d) pyruvate carboxylase Choose enzymes of HMPP a) transketolase b) transaminase c) glucose-6-phosphate dyhydrogenase (glc-6-P DH) = regulatory enzyme d) pyruvate carboxylase Pentose cycle a) produces NADPH which can be oxidized in a respiratory chain → energy is produced b) generates saccharides used in a glycoprotein synthesis c) forms ribose-5-phosphate a substrate of nucleic acids synthesis d) forms fru-6-P and glyceraldehyde-3-P which can enter glycolysis or gluconeogenesis Pentose cycle a) produces NADPH which can be oxidized in a respiratory chain → energy is produced b) generates saccharides used in a glycoprotein synthesis c) forms ribose-5-phosphate a substrate of nucleic acids synthesis d) forms fru-6-P and glyceraldehyde-3-P which can enter glycolysis or gluconeogenesis If NADPH accumulates a) oxidative part of HMPP is inhibited b) ribose-5-phosphate can not be synhesized c) glc-6-P dehydrogenase is activated d) the reversible reactions of the HMPP can only proceed If NADPH accumulates a) oxidative part of HMPP is inhibited b) ribose-5-phosphate can not be synhesized c) glc-6-P dehydrogenase is activated d) the reversible reactions of the HMPP can only proceed I R R E V E R S I B L E The figure is found at http://web.indstate.edu/thcme/mwking/pentose-phosphate-pathway.html (Dec 2006) synthesis of nucleotides R E V E R S I B L E intermediates of glycolysis The figure is found at http://web.indstate.edu/thcme/mwking/pentose-phosphate-pathway.html (Dec 2006) Regulation of HMPP • on the level of substrates availability and products consumption NADPH / NADP+ reaction using NADP+ are inhibited by lack of the coenzyme Fructose a) is metabolized mainly in the liver b) can be transformed to fru-6-P by fructokinase c) can be formed from sorbitol as well d) can be transformed to glucose Fructose a) is metabolized mainly in the liver b) can be transformed to fru-6-P by fructokinase c) can be formed from sorbitol as well d) can be transformed to glucose Metabolism of fructose in the liver glycolysis or gluconeogenesis The figure is found at http://web.indstate.edu/thcme/mwking/glycolysis.html (Jan 2007) The figure was adopted from Devlin, T. M. (editor): Textbook of Biochemistry with Clinical Correlations, 4th ed. Wiley-Liss, Inc., New York, 1997. ISBN 0-471-15451-2 When Fru is converted to Fru-1-P a) it can be split by an aldolase to glyceraldehyde and dihydroxyacetone phosphate b) is fructose metabolised in glycolysis faster then glucose c) glyceraldehyde made by spliting of fru-1-P can be converted to glycerol d) glucokinase can be activated by fru-1-P When Fru is converted to Fru-1-P a) it can be split by an aldolase to glyceraldehyde and dihydroxyacetone phosphate b) is fructose metabolised in glycolysis faster then glucose c) glyceraldehyde made by spliting of fru-1-P can be converted to glycerol d) glucokinase can be activated by fru-1-P Glucose can be converted to a) galactose: glc-6-P → gal-6-P b) fructose: glc → glucitol → fru c) glucuronic acid: UDP-glc + 2 NAD+ → UDP-glukuronate + 2 NADH+H+ d) ribose: glc-6-P → → ribulose-5-P → rib-5-P Glucose can be converted to a) galactose: glc-6-P → gal-6-P b) fructose: glc → glucitol → fru c) glucuronic acid: UDP-glc + 2 NAD+ → UDP-glukuronate + 2 NADH+H+ d) ribose: glc-6-P → → ribulose-5-P → rib-5-P Metabolism of galactose epimerization proceeds on the level of UDPderivatives The figure is found at http://web.indstate.edu/thcme/mwking/glycolysis.html (Jan 2007) The figure is found at http://www.kumc.edu/research/medicine/biochemistry/bioc800/car02fra.htm (Jan 2007)