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Edited by Brenda Holmes MSN/Ed, RN Associate Professor South Arkansas Community College
Chapter  4 Cellular Metabolism Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display.
Metabolic processes  – all chemical reactions that occur in the body  There are two (2) types of metabolic reactions: Anabolism Larger molecules are made from smaller ones Requires energy Catabolism Larger molecules are broken down into smaller ones Releases energy
Consists of two processes: Anabolism Catabolism
Anabolism  provides the materials needed for cellular growth and repair  Dehydration synthesis  Type of anabolic process Used to make polysaccharides, triglycerides, and proteins Produces water CH 2 OH H H OH O H OH Monosaccharide + H HO H OH H H OH O H OH Monosaccharide H HO H OH H H OH O H OH Disaccharide H 2 O Water + H HO H H H OH O H OH H O H OH Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. CH 2 OH CH 2 OH CH 2 OH
Amino acid N H H C C H R Dipeptide molecule + + Peptide  bond Amino acid N H H C C H H H R H O N H H C C H R H O N H C C OH R H O O N H H C C H R N H C C OH R H O O Water Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. O O H 2 O H C H Glycerol 3 fatty acid molecules + OH HO H C OH HO H C C C C OH HO H O O C C C O O O H C H Fat molecule (triglyceride) + H C H C O O O H 3 water molecules (CH 2 ) 14  CH 3 (CH 2 ) 14  CH 3 (CH 2 ) 14  CH 3 (CH 2 ) 14  CH 3 (CH 2 ) 14  CH 3 (CH 2 ) 14  CH 3 H 2 O H 2 O H 2 O Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. O
Catabolism  breaks down larger molecules into smaller ones Hydrolysis A catabolic process Used to decompose carbohydrates, lipids, and proteins Water is used to split the substances Reverse of dehydration synthesis CH 2 OH H H OH O H OH Monosaccharide + H HO H OH H H OH O H OH Monosaccharide H HO H OH H H OH O H OH Disaccharide H 2 O Water + H HO H H H OH O H OH H O H OH Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. CH 2 OH CH 2 OH CH 2 OH
Amino acid N H H C C H R Dipeptide molecule + + Peptide  bond Amino acid N H H C C H H H R H O N H H C C H R H O N H C C OH R H O O N H H C C H R N H C C OH R H O O Water Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. O O H 2 O H C H Glycerol 3 fatty acid molecules + OH HO H C OH HO H C C C C OH HO H O O C C C O O O H C H Fat molecule (triglyceride) + H C H C O O O H 3 water molecules (CH 2 ) 14  CH 3 (CH 2 ) 14  CH 3 (CH 2 ) 14  CH 3 (CH 2 ) 14  CH 3 (CH 2 ) 14  CH 3 (CH 2 ) 14  CH 3 H 2 O H 2 O H 2 O Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. O
Enzymes Control rates of metabolic reactions Lower activation energy needed to start reactions Most are globular proteins with specific shapes Not consumed in chemical reactions Substrate specific Shape of active site determines substrate Product molecule Active site (a) (b) (c) Substrate molecules Unaltered enzyme molecule Enzyme-substrate complex Enzyme molecule Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display.
Metabolic pathways Series of enzyme-controlled reactions leading to formation of a product Each new substrate is the product of the previous reaction Enzyme names commonly: Reflect the substrate Have the suffix – ase Examples: sucrase, lactase, protease, lipase Substrate 1 Enzyme A Substrate 2 Enzyme B Substrate 3 Enzyme C Substrate 4 Enzyme D Product Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display.
Cofactors  Make some enzymes active Non-protein component Ions or coenzymes Coenzymes Organic molecules that act as cofactors Vitamins
Factors that alter enzymes : Heat Radiation Electricity Chemicals Changes in pH
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Limited number of regulatory enzymes Negative feedback Inhibition Substrate 1 Substrate 2 Enzyme B Substrate 3 Enzyme C Substrate 4 Enzyme D Product Rate-limiting Enzyme A Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display.
Energy  is the capacity to change something; it is the ability to do work  Common forms of energy: Heat Light Sound Electrical energy Mechanical energy Chemical energy
Each ATP molecule has three parts: An adenine molecule A ribose molecule Three phosphate molecules in a chain Third phosphate attached by high-energy bond When the bond is broken, energy is transferred   When the bond is broken, ATP becomes ADP ADP becomes ATP through phosphorylation Phosphorylation requires energy release from cellular respiration Energy transferred and utilized by metabolic reactions when phosphate bond is broken Energy transferred from cellular respiration used to reattach phosphate P P P P P P P Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display.
Chemical bonds are broken to release energy We burn glucose in a process called  oxidation
Occurs in a series of reactions: Glycolysis Citric acid cycle  (aka TCA or Kreb’s Cycle) Electron transport system
Produces: Carbon dioxide Water ATP (chemical energy) Heat Includes: Anaerobic reactions (without O 2 ) - produce little ATP Aerobic reactions (requires O 2 ) - produce most ATP
Series of ten reactions Breaks down glucose into 2 pyruvic acid molecules Occurs in cytosol Anaerobic phase of cellular respiration Yields two ATP molecules per glucose molecule Summarized by three main phases or events: Phosphorylation Splitting Production of NADH and ATP
Event 1 -  Phosphorylation Two phosphates added to glucose Requires ATP Event 2 –  Splitting (cleavage) 6-carbon glucose split into two 3-carbon molecules Phase 1 priming Phase 2 cleavage Phase 3 oxidation and formation of ATP and release of high energy electrons 2 ADP 2  NADH + H + 2 NAD + 2  NADH + H + 2 NAD + P ATP P P P Glyceraldehyde phosphate Glucose Dihydroxyacetone phosphate 2 4 ADP ATP 4 Fructose-1,6-diphosphate O 2 2 Pyruvic acid 2 Lactic acid To citric acid cycle and electron transport chain (aerobic pathway) Carbon atom Phosphate P P Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. O 2
Event 3 –  Production of NADH and ATP  Hydrogen atoms are released Hydrogen atoms bind to NAD +  to produce NADH NADH delivers hydrogen atoms to electron transport system if oxygen is available ADP is phosphorylated to become ATP Two molecules of pyruvic acid are produced Two molecules of ATP are generated Phase 1 priming Phase 2 cleavage Phase 3 oxidation and formation of ATP and release of high energy electrons 2 ADP 2  NADH + H + 2 NAD + 2  NADH + H + 2 NAD + P ATP P P P Glyceraldehyde phosphate Glucose Dihydroxyacetone phosphate 2 4 ADP ATP 4 Fructose-1,6-diphosphate O 2 2 Pyruvic acid 2 Lactic acid To citric acid cycle and electron transport chain (aerobic pathway) Carbon atom Phosphate P P Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. O 2
If oxygen is  not  available: Electron transport system cannot accept new electrons from NADH Pyruvic acid is converted to lactic acid Glycolysis is inhibited ATP production is less than in aerobic reactions Phase 1 priming Phase 2 cleavage Phase 3 oxidation and formation of ATP and release of high energy electrons 2 ADP 2  NADH + H + 2 NAD + 2  NADH + H + 2 NAD + P ATP P P P Glyceraldehyde phosphate Glucose Dihydroxyacetone phosphate 2 4 ADP ATP 4 Fructose-1,6-diphosphate O 2 2 Pyruvic acid 2 Lactic acid To citric acid cycle and electron transport chain (aerobic pathway) Carbon atom Phosphate P P Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. O 2
If oxygen  is  available:  Pyruvic acid is used to produce acetyl CoA Citric acid cycle begins Electron transport system functions Carbon dioxide and water are formed 34 molecules of ATP are produced per each glucose molecule ATP 2 ATP 2 Glucose Pyruvic acid Pyruvic acid Acetyl CoA CO 2 2 CO 2 Citric acid O 2 H 2 O 2e – + 2H + Electron transport chain ATP 32-34 Cytosol Mitochondrion High energy electrons (e – ) and hydrogen ions (H + ) High energy electrons (e – ) and hydrogen ions (h + ) Oxaloacetic acid High energy electrons (e – ) and hydrogen ions (H + ) Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display.
Begins when acetyl CoA combines with oxaloacetic acid to produce citric acid Citric acid is changed into oxaloacetic acid through a series of reactions Cycle repeats as long as pyruvic acid and oxygen are available For each citric acid molecule:  One ATP is produced Eight hydrogen atoms are transferred to NAD +  and FAD Two CO 2  produced Citric acid cycle ADP + ATP Pyruvic acid from glycolysis Citric acid (start molecule) Acetyl CoA (replenish molecule) Acetic acid Oxaloacetic acid (finish molecule) Isocitric acid CO 2 CO 2 CO 2 Succinyl-CoA Succinic acid FAD FADH 2 Fumaric acid Malic acid Cytosol Mitochondrion NADH + H + NAD + NADH + H + NAD + NADH + H + NAD + CoA CoA CoA CoA P NADH + H + NAD + P CoA Carbon atom Phosphate Coenzyme A -Ketoglutaric acid Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display.
ATP ADP + ATP synthase Electron transport chain Energy P 2H + + 2e – 2e – 2H + NADH + H + NAD + 2H + + 2e – FADH 2 FAD O 2 H 2 O Energy Energy Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. NADH and FADH2 carry electrons to the ETS ETS is a series of electron carriers located in cristae of mitochondria Energy from electrons transferred to ATP synthase ATP synthase catalyzes the phosphorylation of ADP to ATP Water is formed
Glycolysis Cytosol Mitochondrion A T P 2 Glucose High-energy electrons (e – ) High-energy electrons (e – ) High-energy electrons (e – ) 2e – and 2H + A T P 2 H 2 O O 2 A T P 32–34 CO 2 Pyruvic acid Pyruvic acid 2 CO 2 Acetyl Co A Citric acid Oxaloacetic acid 1 3 4 2 Glycolysis The 6-carbon sugar glucose is broken down in the cytosol into two 3-carbon pyruvic acid molecules with a net gain of 2 ATP and release of high-energy electrons. Citric Acid Cycle The 3-carbon pyruvic acids generated by glycolysis enter the mitochondria. Each loses a carbon (generating CO 2  and is combined with a coenzyme to form a 2-carbon acetyl coenzyme A (acetyl CoA). More high-energy  electrons are released. Each acetyl CoA combines with a 4-carbon oxaloacetic acid to form the 6-carbon citric acid, for which the cycle is named. For each citric acid, a series of reactions  removes 2 carbons (generating 2 CO 2 ’s), synthesizes 1 ATP, and releases more high-energy electrons. The figure shows 2  ATP, resulting directly from 2 turns of the cycle per glucose molecule that enters glycolysis. Electron Transport Chain The high-energy electrons still contain most of the chemical energy of the original glucose molecule. Special carrier molecules bring the high-energy electrons to a series of enzymes that convert much of the remaining  energy to more ATP molecules. The other products are heat and water. The function of oxygen as the final electron acceptor in this last step is why the overall process is called aerobic respiration. Electron transport chain Citric acid cycle Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display.
Carbohydrate molecules from foods can enter: Catabolic pathways for energy production Anabolic pathways for storage
Excess glucose stored as:  Glycogen (primarily by liver and muscle cells) Fat Converted to amino acids Hydrolysis Monosaccharides Energy + CO 2  + H 2 O Glycogen or Fat Amino acids Carbohydrates from foods Catabolic pathways Anabolic pathways Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display.
High energy electrons carried by NADH and FADH 2 Breakdown of simple molecules to acetyl coenzyme A accompanied by production of limited ATP and high energy electrons H 2 O 2e –  and 2H + Waste products – NH 2 CO 2 CO 2 Citric acid cycle Electron transport chain Amino acids Acetyl coenzyme A Simple sugars (glucose) Glycerol Fatty acids Proteins (egg white) Carbohydrates (toast, hashbrowns) Food Fats (butter) Pyruvic acid ATP ATP Breakdown of large macromolecules to simple molecules Glycolysis 1 2 3 ATP Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. © Royalty Free/CORBIS.  ½ O 2 High energy electrons carried by NADH and FADH 2 Complete oxidation of acetyl coenzyme A to H 2 O and CO 2  produces high energy electrons (carried by NADH and FADH 2 ), which yield much ATP via the electron transport chain Breakdown of simple molecules to acetyl coenzyme A accompanied by production of limited ATP and high energy electrons H 2 O 2e –  and 2H + Waste products – NH 2 CO 2 CO 2 Citric acid cycle Electron transport chain Amino acids Acetyl coenzyme A Simple sugars (glucose) Glycerol Fatty acids Proteins (egg white) Carbohydrates (toast, hashbrowns) Food Fats (butter) Pyruvic acid ATP ATP Breakdown of large macromolecules to simple molecules Glycolysis 1 2 3 ATP © Royalty Free/CORBIS.  ½ O 2
Instruction of cells to synthesize proteins comes from a nucleic acid, DNA
Gene  – segment of DNA that codes for one protein Genetic information  – instructs cells how to construct proteins; stored in DNA Genome  – complete set of genes Genetic Code  – method used to translate a sequence of nucleotides of DNA into a sequence of amino acids
DNA Profiling Frees A Prisoner
Two polynucleotide chains Hydrogen bonds hold nitrogenous bases together Bases pair specifically (A-T and C-G) Forms a helix DNA wrapped about histones forms chromosomes G C G G A T C C A P G C P T P P C G P G P C P A P P P Thymine (T) Cytosine (C) Adenine (A) Guanine (G) Nucleotide strand Globular histone proteins Metaphase chromosome Segment of DNA molecule Chromatin (a) Hydrogen bonds (b) (c) Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display.
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Hydrogen bonds break between bases Double strands unwind and pull apart New nucleotides pair with exposed bases Controlled by DNA polymerase Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. C C A T C C G G C C G C G A A T T C G C A T Newly formed DNA molecules Region of replication Original DNA molecule G G G G G G G G G C C C C C G A A A T T A A T T T T T A A A T A A T
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Nucleic Acid Amplification
Specification of the correct sequence of amino acids in a polypeptide chain Each amino acid is represented by a triplet code
Transfer RNA (tRNA) : Carries amino acids to mRNA Carries anticodon to mRNA Translates  a codon of mRNA into an amino acid Ribosomal RNA (rRNA): Provides structure and enzyme activity for ribosomes Messenger RNA (mRNA): Making of mRNA (copying of DNA) is  transcription
Messenger RNA   (mRNA) : Delivers genetic information from nucleus to the cytoplasm Single polynucleotide chain Formed beside a strand of DNA RNA nucleotides are complementary to DNA nucleotides (exception – no thymine in RNA; replaced with uracil) Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. DNA RNA S G S C S S S S C G T A S S S S G C A U Direction of “reading” code P P P P P P P P P P
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Messenger RNA 1 DNA information is copied, or transcribed, into mRNA following complementary base pairing 2 mRNA leaves the nucleus and attaches to a ribosome 3 Translation begins as tRNA anticodons recognize complementary mRNA codons, thus bringing the correct amino acids into position on the growing polypeptide chain 4 As the ribosome moves along the mRNA, more amino acids are added 5 At the end of the mRNA, the ribosome releases the new protein 6 Amino acids attached to tRNA Polypeptide chain Cytoplasm DNA double helix DNA strands pulled apart Transcription (in nucleus) Translation (in cytoplasm) Nucleus C Codon 1 Codon 2 Codon 3 Codon 4 Codon 5 Codon 6 Codon 7 G G G G G A A A U U C C C C C C G G G A Methionine Glycine Amino acids represented Serine Alanine Threonine Alanine Glycine DNA strand Messenger RNA A T A A T T T A T A T A T A T A T U A U A U A G C C G C G C G C G C G C G C G G C C G C C G U A C G C G G G G G G G G G G C C C C C C C C C C A A A A A T T A A T A T A T A T C G G C G C G C T A T A T A C G A T G C T A C G T A C G C G G C A T T A C G G C T T G C G C G C G C G C G C G C G C G Nuclear pore tRNA molecules can pick up another molecule of the same amino acid and be reused Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. G C C G A G G C U C T C C G A G
Next amino acid Anticodon Codons Growing polypeptide chain 1 1 2 2 3 3 4 4 5 5 6 6 7 C U G G Ribosome 1 1 2 2 3 3 7 4 4 5 5 6 7 C C C G U C U G C G U Next amino acid Anticodon Codons 1 1 2 2 3 3 4 4 5 5 6 6 7 Peptide bond C U G C G U C C G C G U 6 Messenger RNA Transfer RNA Next amino acid 1 1 2 2 3 3 4 4 5 5 6 7 6 7 U C G G A A A A A A G G G G G G G G C C C C C C C U U U C G G A A A A A A G G G G G G G G C C C C C C C U U U C G G A A A A A A G G G G G G G G C C C C C C C U U U C G G A A A A A A G G G G G G G G C C C C C C C U U The transfer RNA molecule for the last amino acid added holds the growing polypeptide chain and is attached to its complementary codon on mRNA. A second tRNA binds complementarily to the next codon, and in doing so brings the next amino acid into position on the ribosome. A peptide bond forms, linking the new amino acid to the growing polypeptide chain. The tRNA molecule that brought the last amino acid to the ribosome is released to the cytoplasm, and will be used again. The ribosome moves to a new position at the next codon on mRNA. A A new tRNA complementary to the next codon on mRNA brings the next amino acid to be added to the growing polypeptide chain. 2 1 3 4 Messenger RNA Transfer RNA Next amino acid Transfer RNA Messenger RNA Transfer RNA Growing polypeptide chain Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display.
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MicroRNAs and RNA Interference
Only about 1/10 th  of one percent of the human genome differs from person to person
Mutations  – change in genetic information Result when: Extra bases are added or deleted Bases are changed May or may not change the protein  Code for glutamic acid Mutation Direction of “reading” code Code for valine (a) (b) S S S C T A P P P S S S C T T P P P Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display.
Repair enzymes  correct the mutations
Occurs from inheriting a mutation that then alters an enzyme This creates a block in an otherwise normal biochemical pathway
The Human Metabolome
Important Points in Chapter 4: Outcomes to be Assessed 4.1: Introduction Define metabolism. Explain why protein synthesis is important. 4.2: Metabolic Processes Compare and contrast anabolism and catabolism. Define dehydration synthesis and hydrolysis. 4.3: Control of Metabolic Reactions Describe how enzymes control metabolic reactions. List the basic steps of an enzyme-catalyzed reaction. Define active site.
Important Points in Chapter 4: Outcomes to be Assessed Define a rate-limiting enzyme and indicate why it is important in a metabolic pathway. 4.4: Energy for Metabolic Reactions Explain how ATP stores chemical energy and makes it available to a cell. State the importance of the oxidation of glucose. 4.5: Cellular Respiration Describe how the reactions and pathways of glycolysis, the citric acid cycle, and the electron transport chain capture the energy in nutrient molecules. Discuss how glucose is stored, rather than broken down.
Important Points in Chapter 4: Outcomes to be Assessed 4.6: Nucleic Acids and Protein Synthesis Define gene and genome. Describe the structure of DNA, including the role of complementary base pairing. Describe how DNA molecules replicate. Define genetic code. Compare DNA and RNA. Explain how nucleic acid molecules (DNA and RNA) carry genetic information. Define transcription and translation. Describe the steps of protein synthesis.
Important Points in Chapter 4: Outcomes to be Assessed 4.7: Changes in Genetic Information Compare and contrast mutations and SNPs. Explain how a mutation can cause a disease. Explain two ways that mutations originate. List three types of genetic changes. Discuss two ways that DNA is protected against mutation.
Quiz 4 Complete Quiz 4 now! Read Chapter 5.

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Chapt04 Holes Lecture Animation[1]

  • 1. Edited by Brenda Holmes MSN/Ed, RN Associate Professor South Arkansas Community College
  • 2. Chapter 4 Cellular Metabolism Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display.
  • 3. Metabolic processes – all chemical reactions that occur in the body There are two (2) types of metabolic reactions: Anabolism Larger molecules are made from smaller ones Requires energy Catabolism Larger molecules are broken down into smaller ones Releases energy
  • 4. Consists of two processes: Anabolism Catabolism
  • 5. Anabolism provides the materials needed for cellular growth and repair Dehydration synthesis Type of anabolic process Used to make polysaccharides, triglycerides, and proteins Produces water CH 2 OH H H OH O H OH Monosaccharide + H HO H OH H H OH O H OH Monosaccharide H HO H OH H H OH O H OH Disaccharide H 2 O Water + H HO H H H OH O H OH H O H OH Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. CH 2 OH CH 2 OH CH 2 OH
  • 6. Amino acid N H H C C H R Dipeptide molecule + + Peptide bond Amino acid N H H C C H H H R H O N H H C C H R H O N H C C OH R H O O N H H C C H R N H C C OH R H O O Water Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. O O H 2 O H C H Glycerol 3 fatty acid molecules + OH HO H C OH HO H C C C C OH HO H O O C C C O O O H C H Fat molecule (triglyceride) + H C H C O O O H 3 water molecules (CH 2 ) 14 CH 3 (CH 2 ) 14 CH 3 (CH 2 ) 14 CH 3 (CH 2 ) 14 CH 3 (CH 2 ) 14 CH 3 (CH 2 ) 14 CH 3 H 2 O H 2 O H 2 O Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. O
  • 7. Catabolism breaks down larger molecules into smaller ones Hydrolysis A catabolic process Used to decompose carbohydrates, lipids, and proteins Water is used to split the substances Reverse of dehydration synthesis CH 2 OH H H OH O H OH Monosaccharide + H HO H OH H H OH O H OH Monosaccharide H HO H OH H H OH O H OH Disaccharide H 2 O Water + H HO H H H OH O H OH H O H OH Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. CH 2 OH CH 2 OH CH 2 OH
  • 8. Amino acid N H H C C H R Dipeptide molecule + + Peptide bond Amino acid N H H C C H H H R H O N H H C C H R H O N H C C OH R H O O N H H C C H R N H C C OH R H O O Water Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. O O H 2 O H C H Glycerol 3 fatty acid molecules + OH HO H C OH HO H C C C C OH HO H O O C C C O O O H C H Fat molecule (triglyceride) + H C H C O O O H 3 water molecules (CH 2 ) 14 CH 3 (CH 2 ) 14 CH 3 (CH 2 ) 14 CH 3 (CH 2 ) 14 CH 3 (CH 2 ) 14 CH 3 (CH 2 ) 14 CH 3 H 2 O H 2 O H 2 O Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. O
  • 9. Enzymes Control rates of metabolic reactions Lower activation energy needed to start reactions Most are globular proteins with specific shapes Not consumed in chemical reactions Substrate specific Shape of active site determines substrate Product molecule Active site (a) (b) (c) Substrate molecules Unaltered enzyme molecule Enzyme-substrate complex Enzyme molecule Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display.
  • 10. Metabolic pathways Series of enzyme-controlled reactions leading to formation of a product Each new substrate is the product of the previous reaction Enzyme names commonly: Reflect the substrate Have the suffix – ase Examples: sucrase, lactase, protease, lipase Substrate 1 Enzyme A Substrate 2 Enzyme B Substrate 3 Enzyme C Substrate 4 Enzyme D Product Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display.
  • 11. Cofactors Make some enzymes active Non-protein component Ions or coenzymes Coenzymes Organic molecules that act as cofactors Vitamins
  • 12. Factors that alter enzymes : Heat Radiation Electricity Chemicals Changes in pH
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  • 14. Limited number of regulatory enzymes Negative feedback Inhibition Substrate 1 Substrate 2 Enzyme B Substrate 3 Enzyme C Substrate 4 Enzyme D Product Rate-limiting Enzyme A Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display.
  • 15. Energy is the capacity to change something; it is the ability to do work Common forms of energy: Heat Light Sound Electrical energy Mechanical energy Chemical energy
  • 16. Each ATP molecule has three parts: An adenine molecule A ribose molecule Three phosphate molecules in a chain Third phosphate attached by high-energy bond When the bond is broken, energy is transferred When the bond is broken, ATP becomes ADP ADP becomes ATP through phosphorylation Phosphorylation requires energy release from cellular respiration Energy transferred and utilized by metabolic reactions when phosphate bond is broken Energy transferred from cellular respiration used to reattach phosphate P P P P P P P Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display.
  • 17. Chemical bonds are broken to release energy We burn glucose in a process called oxidation
  • 18. Occurs in a series of reactions: Glycolysis Citric acid cycle (aka TCA or Kreb’s Cycle) Electron transport system
  • 19. Produces: Carbon dioxide Water ATP (chemical energy) Heat Includes: Anaerobic reactions (without O 2 ) - produce little ATP Aerobic reactions (requires O 2 ) - produce most ATP
  • 20. Series of ten reactions Breaks down glucose into 2 pyruvic acid molecules Occurs in cytosol Anaerobic phase of cellular respiration Yields two ATP molecules per glucose molecule Summarized by three main phases or events: Phosphorylation Splitting Production of NADH and ATP
  • 21. Event 1 - Phosphorylation Two phosphates added to glucose Requires ATP Event 2 – Splitting (cleavage) 6-carbon glucose split into two 3-carbon molecules Phase 1 priming Phase 2 cleavage Phase 3 oxidation and formation of ATP and release of high energy electrons 2 ADP 2 NADH + H + 2 NAD + 2 NADH + H + 2 NAD + P ATP P P P Glyceraldehyde phosphate Glucose Dihydroxyacetone phosphate 2 4 ADP ATP 4 Fructose-1,6-diphosphate O 2 2 Pyruvic acid 2 Lactic acid To citric acid cycle and electron transport chain (aerobic pathway) Carbon atom Phosphate P P Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. O 2
  • 22. Event 3 – Production of NADH and ATP Hydrogen atoms are released Hydrogen atoms bind to NAD + to produce NADH NADH delivers hydrogen atoms to electron transport system if oxygen is available ADP is phosphorylated to become ATP Two molecules of pyruvic acid are produced Two molecules of ATP are generated Phase 1 priming Phase 2 cleavage Phase 3 oxidation and formation of ATP and release of high energy electrons 2 ADP 2 NADH + H + 2 NAD + 2 NADH + H + 2 NAD + P ATP P P P Glyceraldehyde phosphate Glucose Dihydroxyacetone phosphate 2 4 ADP ATP 4 Fructose-1,6-diphosphate O 2 2 Pyruvic acid 2 Lactic acid To citric acid cycle and electron transport chain (aerobic pathway) Carbon atom Phosphate P P Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. O 2
  • 23. If oxygen is not available: Electron transport system cannot accept new electrons from NADH Pyruvic acid is converted to lactic acid Glycolysis is inhibited ATP production is less than in aerobic reactions Phase 1 priming Phase 2 cleavage Phase 3 oxidation and formation of ATP and release of high energy electrons 2 ADP 2 NADH + H + 2 NAD + 2 NADH + H + 2 NAD + P ATP P P P Glyceraldehyde phosphate Glucose Dihydroxyacetone phosphate 2 4 ADP ATP 4 Fructose-1,6-diphosphate O 2 2 Pyruvic acid 2 Lactic acid To citric acid cycle and electron transport chain (aerobic pathway) Carbon atom Phosphate P P Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. O 2
  • 24. If oxygen is available: Pyruvic acid is used to produce acetyl CoA Citric acid cycle begins Electron transport system functions Carbon dioxide and water are formed 34 molecules of ATP are produced per each glucose molecule ATP 2 ATP 2 Glucose Pyruvic acid Pyruvic acid Acetyl CoA CO 2 2 CO 2 Citric acid O 2 H 2 O 2e – + 2H + Electron transport chain ATP 32-34 Cytosol Mitochondrion High energy electrons (e – ) and hydrogen ions (H + ) High energy electrons (e – ) and hydrogen ions (h + ) Oxaloacetic acid High energy electrons (e – ) and hydrogen ions (H + ) Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display.
  • 25. Begins when acetyl CoA combines with oxaloacetic acid to produce citric acid Citric acid is changed into oxaloacetic acid through a series of reactions Cycle repeats as long as pyruvic acid and oxygen are available For each citric acid molecule: One ATP is produced Eight hydrogen atoms are transferred to NAD + and FAD Two CO 2 produced Citric acid cycle ADP + ATP Pyruvic acid from glycolysis Citric acid (start molecule) Acetyl CoA (replenish molecule) Acetic acid Oxaloacetic acid (finish molecule) Isocitric acid CO 2 CO 2 CO 2 Succinyl-CoA Succinic acid FAD FADH 2 Fumaric acid Malic acid Cytosol Mitochondrion NADH + H + NAD + NADH + H + NAD + NADH + H + NAD + CoA CoA CoA CoA P NADH + H + NAD + P CoA Carbon atom Phosphate Coenzyme A -Ketoglutaric acid Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display.
  • 26. ATP ADP + ATP synthase Electron transport chain Energy P 2H + + 2e – 2e – 2H + NADH + H + NAD + 2H + + 2e – FADH 2 FAD O 2 H 2 O Energy Energy Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. NADH and FADH2 carry electrons to the ETS ETS is a series of electron carriers located in cristae of mitochondria Energy from electrons transferred to ATP synthase ATP synthase catalyzes the phosphorylation of ADP to ATP Water is formed
  • 27. Glycolysis Cytosol Mitochondrion A T P 2 Glucose High-energy electrons (e – ) High-energy electrons (e – ) High-energy electrons (e – ) 2e – and 2H + A T P 2 H 2 O O 2 A T P 32–34 CO 2 Pyruvic acid Pyruvic acid 2 CO 2 Acetyl Co A Citric acid Oxaloacetic acid 1 3 4 2 Glycolysis The 6-carbon sugar glucose is broken down in the cytosol into two 3-carbon pyruvic acid molecules with a net gain of 2 ATP and release of high-energy electrons. Citric Acid Cycle The 3-carbon pyruvic acids generated by glycolysis enter the mitochondria. Each loses a carbon (generating CO 2 and is combined with a coenzyme to form a 2-carbon acetyl coenzyme A (acetyl CoA). More high-energy electrons are released. Each acetyl CoA combines with a 4-carbon oxaloacetic acid to form the 6-carbon citric acid, for which the cycle is named. For each citric acid, a series of reactions removes 2 carbons (generating 2 CO 2 ’s), synthesizes 1 ATP, and releases more high-energy electrons. The figure shows 2 ATP, resulting directly from 2 turns of the cycle per glucose molecule that enters glycolysis. Electron Transport Chain The high-energy electrons still contain most of the chemical energy of the original glucose molecule. Special carrier molecules bring the high-energy electrons to a series of enzymes that convert much of the remaining energy to more ATP molecules. The other products are heat and water. The function of oxygen as the final electron acceptor in this last step is why the overall process is called aerobic respiration. Electron transport chain Citric acid cycle Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display.
  • 28. Carbohydrate molecules from foods can enter: Catabolic pathways for energy production Anabolic pathways for storage
  • 29. Excess glucose stored as: Glycogen (primarily by liver and muscle cells) Fat Converted to amino acids Hydrolysis Monosaccharides Energy + CO 2 + H 2 O Glycogen or Fat Amino acids Carbohydrates from foods Catabolic pathways Anabolic pathways Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display.
  • 30. High energy electrons carried by NADH and FADH 2 Breakdown of simple molecules to acetyl coenzyme A accompanied by production of limited ATP and high energy electrons H 2 O 2e – and 2H + Waste products – NH 2 CO 2 CO 2 Citric acid cycle Electron transport chain Amino acids Acetyl coenzyme A Simple sugars (glucose) Glycerol Fatty acids Proteins (egg white) Carbohydrates (toast, hashbrowns) Food Fats (butter) Pyruvic acid ATP ATP Breakdown of large macromolecules to simple molecules Glycolysis 1 2 3 ATP Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. © Royalty Free/CORBIS. ½ O 2 High energy electrons carried by NADH and FADH 2 Complete oxidation of acetyl coenzyme A to H 2 O and CO 2 produces high energy electrons (carried by NADH and FADH 2 ), which yield much ATP via the electron transport chain Breakdown of simple molecules to acetyl coenzyme A accompanied by production of limited ATP and high energy electrons H 2 O 2e – and 2H + Waste products – NH 2 CO 2 CO 2 Citric acid cycle Electron transport chain Amino acids Acetyl coenzyme A Simple sugars (glucose) Glycerol Fatty acids Proteins (egg white) Carbohydrates (toast, hashbrowns) Food Fats (butter) Pyruvic acid ATP ATP Breakdown of large macromolecules to simple molecules Glycolysis 1 2 3 ATP © Royalty Free/CORBIS. ½ O 2
  • 31. Instruction of cells to synthesize proteins comes from a nucleic acid, DNA
  • 32. Gene – segment of DNA that codes for one protein Genetic information – instructs cells how to construct proteins; stored in DNA Genome – complete set of genes Genetic Code – method used to translate a sequence of nucleotides of DNA into a sequence of amino acids
  • 33. DNA Profiling Frees A Prisoner
  • 34. Two polynucleotide chains Hydrogen bonds hold nitrogenous bases together Bases pair specifically (A-T and C-G) Forms a helix DNA wrapped about histones forms chromosomes G C G G A T C C A P G C P T P P C G P G P C P A P P P Thymine (T) Cytosine (C) Adenine (A) Guanine (G) Nucleotide strand Globular histone proteins Metaphase chromosome Segment of DNA molecule Chromatin (a) Hydrogen bonds (b) (c) Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display.
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  • 36. Hydrogen bonds break between bases Double strands unwind and pull apart New nucleotides pair with exposed bases Controlled by DNA polymerase Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. C C A T C C G G C C G C G A A T T C G C A T Newly formed DNA molecules Region of replication Original DNA molecule G G G G G G G G G C C C C C G A A A T T A A T T T T T A A A T A A T
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  • 39. Specification of the correct sequence of amino acids in a polypeptide chain Each amino acid is represented by a triplet code
  • 40. Transfer RNA (tRNA) : Carries amino acids to mRNA Carries anticodon to mRNA Translates a codon of mRNA into an amino acid Ribosomal RNA (rRNA): Provides structure and enzyme activity for ribosomes Messenger RNA (mRNA): Making of mRNA (copying of DNA) is transcription
  • 41. Messenger RNA (mRNA) : Delivers genetic information from nucleus to the cytoplasm Single polynucleotide chain Formed beside a strand of DNA RNA nucleotides are complementary to DNA nucleotides (exception – no thymine in RNA; replaced with uracil) Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. DNA RNA S G S C S S S S C G T A S S S S G C A U Direction of “reading” code P P P P P P P P P P
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  • 43. Please note that due to differing operating systems, some animations will not appear until the presentation is viewed in Presentation Mode (Slide Show view). You may see blank slides in the “Normal” or “Slide Sorter” views. All animations will appear after viewing in Presentation Mode and playing each animation. Most animations will require the latest version of the Flash Player, which is available at http://get.adobe.com/flashplayer.
  • 44. Messenger RNA 1 DNA information is copied, or transcribed, into mRNA following complementary base pairing 2 mRNA leaves the nucleus and attaches to a ribosome 3 Translation begins as tRNA anticodons recognize complementary mRNA codons, thus bringing the correct amino acids into position on the growing polypeptide chain 4 As the ribosome moves along the mRNA, more amino acids are added 5 At the end of the mRNA, the ribosome releases the new protein 6 Amino acids attached to tRNA Polypeptide chain Cytoplasm DNA double helix DNA strands pulled apart Transcription (in nucleus) Translation (in cytoplasm) Nucleus C Codon 1 Codon 2 Codon 3 Codon 4 Codon 5 Codon 6 Codon 7 G G G G G A A A U U C C C C C C G G G A Methionine Glycine Amino acids represented Serine Alanine Threonine Alanine Glycine DNA strand Messenger RNA A T A A T T T A T A T A T A T A T U A U A U A G C C G C G C G C G C G C G C G G C C G C C G U A C G C G G G G G G G G G G C C C C C C C C C C A A A A A T T A A T A T A T A T C G G C G C G C T A T A T A C G A T G C T A C G T A C G C G G C A T T A C G G C T T G C G C G C G C G C G C G C G C G Nuclear pore tRNA molecules can pick up another molecule of the same amino acid and be reused Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. G C C G A G G C U C T C C G A G
  • 45. Next amino acid Anticodon Codons Growing polypeptide chain 1 1 2 2 3 3 4 4 5 5 6 6 7 C U G G Ribosome 1 1 2 2 3 3 7 4 4 5 5 6 7 C C C G U C U G C G U Next amino acid Anticodon Codons 1 1 2 2 3 3 4 4 5 5 6 6 7 Peptide bond C U G C G U C C G C G U 6 Messenger RNA Transfer RNA Next amino acid 1 1 2 2 3 3 4 4 5 5 6 7 6 7 U C G G A A A A A A G G G G G G G G C C C C C C C U U U C G G A A A A A A G G G G G G G G C C C C C C C U U U C G G A A A A A A G G G G G G G G C C C C C C C U U U C G G A A A A A A G G G G G G G G C C C C C C C U U The transfer RNA molecule for the last amino acid added holds the growing polypeptide chain and is attached to its complementary codon on mRNA. A second tRNA binds complementarily to the next codon, and in doing so brings the next amino acid into position on the ribosome. A peptide bond forms, linking the new amino acid to the growing polypeptide chain. The tRNA molecule that brought the last amino acid to the ribosome is released to the cytoplasm, and will be used again. The ribosome moves to a new position at the next codon on mRNA. A A new tRNA complementary to the next codon on mRNA brings the next amino acid to be added to the growing polypeptide chain. 2 1 3 4 Messenger RNA Transfer RNA Next amino acid Transfer RNA Messenger RNA Transfer RNA Growing polypeptide chain Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display.
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  • 47. MicroRNAs and RNA Interference
  • 48. Only about 1/10 th of one percent of the human genome differs from person to person
  • 49. Mutations – change in genetic information Result when: Extra bases are added or deleted Bases are changed May or may not change the protein Code for glutamic acid Mutation Direction of “reading” code Code for valine (a) (b) S S S C T A P P P S S S C T T P P P Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display.
  • 50. Repair enzymes correct the mutations
  • 51. Occurs from inheriting a mutation that then alters an enzyme This creates a block in an otherwise normal biochemical pathway
  • 53. Important Points in Chapter 4: Outcomes to be Assessed 4.1: Introduction Define metabolism. Explain why protein synthesis is important. 4.2: Metabolic Processes Compare and contrast anabolism and catabolism. Define dehydration synthesis and hydrolysis. 4.3: Control of Metabolic Reactions Describe how enzymes control metabolic reactions. List the basic steps of an enzyme-catalyzed reaction. Define active site.
  • 54. Important Points in Chapter 4: Outcomes to be Assessed Define a rate-limiting enzyme and indicate why it is important in a metabolic pathway. 4.4: Energy for Metabolic Reactions Explain how ATP stores chemical energy and makes it available to a cell. State the importance of the oxidation of glucose. 4.5: Cellular Respiration Describe how the reactions and pathways of glycolysis, the citric acid cycle, and the electron transport chain capture the energy in nutrient molecules. Discuss how glucose is stored, rather than broken down.
  • 55. Important Points in Chapter 4: Outcomes to be Assessed 4.6: Nucleic Acids and Protein Synthesis Define gene and genome. Describe the structure of DNA, including the role of complementary base pairing. Describe how DNA molecules replicate. Define genetic code. Compare DNA and RNA. Explain how nucleic acid molecules (DNA and RNA) carry genetic information. Define transcription and translation. Describe the steps of protein synthesis.
  • 56. Important Points in Chapter 4: Outcomes to be Assessed 4.7: Changes in Genetic Information Compare and contrast mutations and SNPs. Explain how a mutation can cause a disease. Explain two ways that mutations originate. List three types of genetic changes. Discuss two ways that DNA is protected against mutation.
  • 57. Quiz 4 Complete Quiz 4 now! Read Chapter 5.