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![Page 1: Instructor: Mykhaylo Korda Offices: 378 Clippinger; Telephone: 517-2944 E-Mail: kordam@ohio.edukordam@ohio.edu Office Hours: 11:10-12:00 MWF in Clippinger.](https://reader036.fdocuments.in/reader036/viewer/2022062519/5697c0131a28abf838cccc60/html5/thumbnails/1.jpg)
Instructor: Mykhaylo Korda
Offices: 378 Clippinger;
Telephone: 517-2944
E-Mail: [email protected]
Office Hours: 11:10-12:00 MWF in Clippinger 378 or by appointment
Lectures: 8:10-9:00 am MWF in Clip
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Introduction to Introduction to MetabolismMetabolism
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•Metabolism - the entire network of chemical reactions carried out by living cells. Metabolism also includes coordination, regulation and energy requirement.
•Metabolites - small molecule intermediates in the degradation and synthesis of polymers
Most organism use the same general pathway for extraction and utilization of energy.
All living organisms are divided into two major classes:
Autotrophs – can use atmospheric carbon dioxide as a sole source of carbon for the synthesis of macromolecules. Autotrophs use the sun energy for biosynthetic purposes. Heterotrophs – obtain energy by ingesting complex carbon-containing compounds.
Heterotrophs are divided into aerobs and anaerobs.
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Common features of organisms
1. Organisms or cells maintain specific internal concentrations of inorganic ions, metabolites and enzymes
2. Organisms extract energy from external sources to drive energy-consuming reactions
3. Organisms grow and reproduce according to instructions encoded in the genetic material
4. Organisms respond to environmental influences
5. Cells are not static, and cell components are continually synthesized and degraded (i.e. undergo turnover)
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(a) Linear (b) Cyclic
(c) Spiral pathway (fatty acid biosynthesis)
A sequence of reactions that has a specific purpose (for instance: degradation of glucose, synthesis of fatty acids) is called metabolic pathway.
Metabolic pathway may be:
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Catabolic reactions - degrade molecules to create smaller molecules and energy Anabolic reactions - synthesize molecules for cell maintenance, growth and reproduction
Metabolic pathways can be grouped into two paths – catabolism and anabolism
Catabolism is characterized by oxidation reactions and by release of free energy which is transformed to ATP. Anabolism is characterized by reduction reactions and by utilization of energy accumulated in ATP molecules.Catabolism and anabolism are tightly linked together by their coordinated energy requirements: catabolic processes release the energy from food and collect it in the ATP; anabolic processes use the free energy stored in ATP to perform work.
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Anabolism and catabolism are coupled by energy
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•Multiple-step pathways permit control of energy input and output
•Catabolic multi-step pathways provide energy in smaller stepwise amounts
•Each enzyme in a multi-step pathway usually catalyzes only one single step in the pathway
•Control points occur in multistep pathways
Metabolism Proceeds by Discrete Steps Single-step vs multi-
step pathways
A multistep enzyme pathway releases energy in smaller amounts that can be used by the cell
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•Metabolism is highly regulated to permit organisms to respond to changing conditions
•Most pathways are irreversible
•Flux - flow of material through a metabolic pathway which depends upon:
(1) Supply of substrates(2) Removal of products(3) Pathway enzyme activities
Metabolic Pathways Are Regulated
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Levels of Metabolism Regulation
1.Nervous system.2.Endocrine system.3.Interaction between organs.4.Cell (membrane) level.5.Molecular level
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• Product of a pathway controls the rate of its own synthesis by inhibiting an early step (usually the first “committed” step (unique to the pathway)
Feedback inhibition
• Metabolite early in the pathway activates an enzyme further down the pathway
Feed-forward activation
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•Interconvertible enzyme activity can be rapidly and reversibly altered by covalent modification
•Protein kinases phosphorylate enzymes (+ ATP)
•Protein phosphatases remove phosphoryl groups
Covalent modification for enzyme regulation
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Regulatory role of a protein kinase, amplification by a signaling
cascadeThe initial signal may be amplified by the “cascade” nature of this signaling
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Stages of metabolismCatabolismStage I. Breakdown of macromolecules
(proteins, carbohydrates and lipids to respective building blocks.
Stage II. Amino acids, fatty acids and glucose are oxidized to common metabolite (acetyl CoA)
Stage III. Acetyl CoA is oxidized in citric acid cycle to CO2 and water. As result reduced cofactor, NADH2 and FADH2, are formed which give up their electrons. Electrons are transported via the tissue respiration chain and released energy is coupled directly to ATP synthesis.
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Glycerol
Catabolism
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Catabolism is characterized by convergence of three major routs toward a final common pathway.
Different proteins, fats and carbohydrates enter the same pathway – tricarboxylic acid cycle.
Anabolism can also be divided into stages, however the anabolic pathways are characterized by divergence.
Monosaccharide synthesis begin with CO2, oxaloacetate, pyruvate or lactate. Amino acids are synthesized from acetyl CoA, pyruvate or keto acids of Krebs cycle. Fatty acids are constructed from acetyl CoA.
On the next stage monosaccharides, amino acids and fatty acids are used for the synthesis of polysaccharides, proteins and fats.
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•Compartmentation of metabolic processes permits:
- separate pools of metabolites within a cell
- simultaneous operation of opposing metabolic paths
- high local concentrations of metabolites
•Example: fatty acid synthesis enzymes (cytosol), fatty acid breakdown enzymes (mitochondria)
Compartmentation of Metabolic Processes in Cell
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Compartmentation of metabolic processes
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Interorgan Metabolism
Cells from different tissues are distinguished by their complement of enzymes (for example: liver – biosynthesis of urea; pancreas – biosynthesis of proteolytic enzymes etc.).
Some pathways involve reactions in several tissues (synthesis of creatin in kidney and liver). This require the transport of metabolites between tissues.
The division of labor between tissues allows site-specific regulation of metabolic processes.
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The chemistry of metabolism
There are about 3000 reactions in human cell.
All these reactions are divided into six categories:
1. Oxidation-reduction reactions
2. Group transfer reactions
3. Hydrolysis reactions
4. Nonhydrolytic cleavage reactions
5. Isomerization and rearrangement reactions
6. Bond formation reactions using energy from ATP
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1. Oxidation-reduction reactions
-oxidases - peroxidases - dehydrogenases -oxigenases
Oxidation-reduction reactions are those in which electrons are transferred from one molecule or atom to another
Enzymes: oxidoreductases
Coenzymes: NAD+, NADP+, FAD+, FMN+
Example:
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2. Group transfer reactionsTransfer of a chemical functional group from one molecule to another (intermolecular) or group transfer within a single molecule (intramolecular)
Enzymes: transferases
Examples:
Phosphorylation Acylation Glycosylation
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3. Hydrolysis reactions•Water is used to split the single molecule into
two molecules
- esterases - peptidases - glycosidases
Enzymes: hydrolases
Example:
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4. Nonhydrolytic cleavage reactions
•Split or lysis of a substrate, generating a double bond in a nonhydrolytic (without water), nonoxidative elimination
Example:
Enzymes: lyases
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5. Isomerization and rearrangement reactions
Two kinds of chemical transformation:
1. Intramolecular hydrogen atom shifts changing the location of a double bond. 2. Intramolecular rearrangment of functional groups.Enzymes: isomerases
Example:
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•Ligation, or joining of two substrates
•Require chemical energy (e.g. ATP)
6. Bond formation reactions using energy from ATP
Enzymes: ligases (synthetases)
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•Add labeled substrate to tissues, cells, and follow emergence of intermediates. Use sensitive isotopic tracers (3H, 14C etc)
•Verify pathway steps in vitro by using isolated enzymes and substrates
•Study of the mutations in genes associated with the production of defective enzymes
•Use metabolic inhibitors to identify individual steps and sequence of enzymes in a pathway
Experimental Methods for Studying Metabolism