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Cellular Metabolism-Chapter 4
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4.1: Introduction 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
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Metabolic Processes Anabolism-synthesis reactions ex: dehydration synthesis (joining two molecules together by removing water) Catabolism-breakdown reactions ex: hydrolysis (splitting of a molecule by the addition of water)
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Control of reactions in metabolic pathways (series of reactions)
Enzyme-protein catalyst which controls the rate of a reaction by lowering the activation energy (energy needed to start the reaction) Enzymes are needed in small amounts because they can be used over & over. Enzymes are specific (each enzyme catalyzes ONE kind of reaction)
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Each enzymes has an ACTIVE SITE which the substrate (reactant) fits into. The combination is called the ENZYME-SUBSTRATE COMPLEX. The enzyme remains unchanged during the reaction. Enzymes function at specific pH, temp, etc. Enzyme helpers are: coenzymes (molecules such as vitamins) and cofactors (ions such as Ca++)
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4.3: Control of Metabolic Reactions
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 Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. Substrate molecules Product molecule Active site Enzyme molecule Enzyme-substrate complex Unaltered enzyme molecule (a) (b) (c)
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04_04 Enzyme catalyzed reaction
Slide number: 2 Substrate molecule Active site Enzyme molecule Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display.
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04_04 Enzyme catalyzed reaction
Slide number: 3 Enzyme-substrate complex Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display.
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04_04 Enzyme catalyzed reaction
Slide number: 4 Product molecules Unaltered enzyme molecule Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display.
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Control of Metabolic Reactions
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 sucrase, lactase, protease, lipase
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Factors That Alter Enzymes
Heat Radiation Electricity Chemicals Changes in pH
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Animation: How Enzymes Work
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Energy release from breakdown of molecules
OXIDATION Gradual enzyme-controlled breakdown in which much of the chemical energy is captured by energy carrying molecules and transferred to energy-requiring reactions in the cell. The rest is lost as heat. BURNING All of the chemical energy stored in the bonds of the molecule is released as heat and light. Heat and light energy cannot be converted by a cell into other forms.
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ATP-Adenosine Triphosphate-the cell’s energy carrier
ADP + P + energy ATP can give up its energy. ADP can pick up energy.
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4.5: Cellular Respiration
Occurs in a series of reactions: Glycolysis Citric acid cycle (aka TCA or Kreb’s Cycle) Electron transport system
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Cellular Respiration-process by which cells obtain energy from breakdown of foods - 3 stages
C6H12O6 + 6O2 ---> 6CO2 + 6H2O + energy Hydrogen is gradually removed from glucose and carried by H-carriers (NADH and FADH) to the inner membrane of the mitochondrion where hydrogen combines with oxygen to form water.
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Stages of cell respiration
Glycolysis-occurs in the cytoplasm-anaerobic-glucose is split into 2 molecules of pyruvic acid-a little ATP is made-some hydrogen is removed
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If oxygen is present, the pyruvic acid now enters the mitochondrion to continue its breakdown: it changes to Acetyl CoA and enters: Kreb’s (citric acid) cycle-occurs in the mitochondrion-aerobic-the rest of the H’s are removed-some ATP is made-CO2 is released
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Electron Transport-occurs in mitochondrion-aerobic-NADH and FADH release H (H+ and e-) to the inner membrane--H+ passes through and e- flows down a set of proteins within the inner membrane, losing energy which is used to make lots of ATP--then the hydrogen ions combine with the electrons and oxygen to make water.
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4.5: Cellular Respiration
Occurs in a series of reactions: Glycolysis Citric acid cycle (aka TCA or Kreb’s Cycle) Electron transport system
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Cellular Respiration Produces: Carbon dioxide Water
ATP (chemical energy) Heat Includes: Anaerobic reactions (without O2) - produce little ATP Aerobic reactions (requires O2) - produce most ATP
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Glycolysis 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
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Glycolysis Event 1 - Phosphorylation Two phosphates added to glucose
Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. Event 1 - Phosphorylation Two phosphates added to glucose Requires ATP Phase 1 priming Glucose Carbon atom P Phosphate 2 ATP 2 ADP Fructose-1,6-diphosphate P P Phase 2 cleavage Event 2 – Splitting (cleavage) 6-carbon glucose split into two 3-carbon molecules Dihydroxyacetone phosphate Glyceraldehyde phosphate P P Phase 3 oxidation and formation of ATP and release of high energy electrons P 2 NAD+ 4 ADP 2 NADH + H+ 4 ATP 2 Pyruvic acid O2 O2 2 NADH + H+ 2 NAD+ To citric acid cycle and electron transport chain (aerobic pathway) 2 Lactic acid
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Glycolysis 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 Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. Phase 1 priming Glucose Carbon atom P Phosphate 2 ATP 2 ADP Fructose-1,6-diphosphate P P Phase 2 cleavage Dihydroxyacetone phosphate Glyceraldehyde phosphate P P Phase 3 oxidation and formation of ATP and release of high energy electrons P 2 NAD+ 4 ADP 2 NADH + H+ 4 ATP 2 Pyruvic acid O2 O2 2 NADH + H+ 2 NAD+ To citric acid cycle and electron transport chain (aerobic pathway) 2 Lactic acid
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Anaerobic Reactions If oxygen is not available:
Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. 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 Glucose Carbon atom P Phosphate 2 ATP 2 ADP Fructose-1,6-diphosphate P P Phase 2 cleavage Dihydroxyacetone phosphate Glyceraldehyde phosphate P P Phase 3 oxidation and formation of ATP and release of high energy electrons P 2 NAD+ 4 ADP 2 NADH + H+ 4 ATP 2 Pyruvic acid O2 O2 2 NADH + H+ 2 NAD+ To citric acid cycle and electron transport chain (aerobic pathway) 2 Lactic acid
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Aerobic Reactions If oxygen is available:
Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. 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 Glucose High energy electrons (e–) and hydrogen ions (H+) 2 ATP Pyruvic acid Pyruvic acid Cytosol Mitochondrion High energy electrons (e–) and hydrogen ions (h+) CO2 Acetyl CoA Oxaloacetic acid Citric acid High energy electrons (e–) and hydrogen ions (H+) 2 CO 2 2 ATP Electron transport chain 32-34 ATP O 2 2e – + 2H + H 2 O
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Citric Acid Cycle 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 Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. Pyruvic acid from glycolysis Cytosol Carbon atom + P Phosphate NAD CO 2 Mitochondrion CoA Coenzyme A NADH + H + Acetic acid CoA Acetyl CoA (replenish molecule) Oxaloacetic acid Citric acid (finish molecule) (start molecule) NADH + H + CoA NAD + Malic acid Isocitric acid NAD + For each citric acid molecule: One ATP is produced Eight hydrogen atoms are transferred to NAD+ and FAD Two CO2 produced Citric acid cycle CO 2 NADH + H + Fumaric acid -Ketoglutaric acid CO 2 CoA FADH 2 NAD + FAD NADH + H + Succinic acid Succinyl-CoA CoA ADP + P ATP
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Electron Transport System
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 Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. ATP synthase ADP + P ATP Energy NADH + H+ Energy 2H+ + 2e– FADH2 Energy NAD+ 2H+ + 2e– FAD Electron transport chain 2e– 2H+ O 2 H2O
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Summary of Cellular Respiration
Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. Glucose 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. High-energy electrons (e–) 1 Glycolysis 2 A T P Cytosol Pyruvic acid Pyruvic acid Citric Acid Cycle The 3-carbon pyruvic acids generated by glycolysis enter the mitochondria. Each loses a carbon (generating CO2 and is combined with a coenzyme to form a 2-carbon acetyl coenzyme A (acetyl CoA). More high-energy electrons are released. 2 High-energy electrons (e–) CO 2 Acetyl Co A 3 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 CO2’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. Oxaloacetic acid Citric acid Citric acid cycle Mitochondrion High-energy electrons (e–) 2 CO 2 2 A T P 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 4 32–34 A T P 2e – and 2H + O 2 H 2 O
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Nucleic Acids and Protein Synthesis
A gene is a section of DNA which codes for the production of a polypeptide (chain of amino acids) in a cell. There are thousands of genes on a chromosome. Each chromosome is a DNA molecule.
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Genetic Information Genetic information – instructs cells how to construct proteins; stored in DNA Gene – segment of DNA that codes for one protein Genome – complete set of genes Genetic Code – method used to translate a sequence of nucleotides of DNA into a sequence of amino acids
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Deoxyribonucleic Acid (DNA) structure
made of 2 strands of nucleotides which spiral (double helix) Each nucleotide contains: 5-C sugar (deoxyribose), phosphate, and a nitrogenous base (adenine, guanine, cytosine, or thymine) The backbone of each strand is a sugar-phosphate chain The bases of complementary strands hydrogen bond to each other: C-G, A-T
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Animation: DNA Structure
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DNA Replication H-bonds between base pairs break, separating the complementary strands New nucleotides pair with each strand (C-G, A-T), resulting in two identical DNA molecules Semiconservative
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Ribonucleic Acid (RNA)-help DNA in protein production in cell
single strand of nucleotides each nucleotide contains: ribose, phosphate, base (A, G, C, and Uracil instead of Thymine) shorter than DNA different types: mRNA (carries code from DNA to ribosome), tRNA (brings amino acids to ribosome), rRNA (a component of ribosomes)
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Protein Production 1. Transcription-occurs in nucleus as DNA is converted into mRNA 2. Translation/protein synthesis-occurs on the ribosomes in the cytoplasm as amino acids join together
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How can a gene provide a code for amino acid sequence in a polypeptide?
Each group of 3 bases on mRNA (codon) codes for 1 amino acid The base sequence of a gene then determines the amino acid sequence in a polypeptide But proteins are made in the cytoplasm, and DNA is in the nucleus---so mRNA helps by carrying the “code” from DNA to the ribosome
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Transcription a section of DNA opens up (just where the gene coding for the particular protein is) mRNA nucleotides pair up with the DNA bases on one side (template)---uracil is used instead of thymine formed mRNA moves away and DNA closes up mRNA goes through nuclear pore and attaches to a ribosome in the cytoplasm
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Animation: Stages of Transcription
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Translation each tRNA molecule has an attachment point for a specific amino acid each tRNA also has a region of 3 bases called an anticodon which is attracted to complementary mRNA codons as the ribosome moves down the mRNA strand, tRNA’s bringing their aa’s are attracted to the mRNA codons
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as tRNA goes to the mRNA (which is attached to a ribosome), it brings an amino acid with it--these aa’s then combine with each other and the tRNA’s leave this results in a polypeptide chain and the ribosome “lets go”
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Animation: How Translation Works
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animation
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Animation: Protein Synthesis
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Mutation A mutation is any change in the sequence of bases on DNA--could result in a change in the amino acid sequence of a protein
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Nature of Mutations Mutations – change in genetic information
Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. Result when: Extra bases are added or deleted Bases are changed Code for glutamic acid Mutation Code for valine P P T T S S Direction of “reading” code P P T A S S May or may not change the protein P P C C S S (a) (b)
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