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Dr. Cop's Chapter 7

QuestionAnswer
Metabolism: the sum total of the chemical reactions in an organism or cell.
Catabolism: degradative or breakdown reactions; release energy (exergonic); ex: hydrolysis.
Anabolism: biosynthetic or buildup reactions; require energy input (endergonic); ex: dehydration synthesis.
Energy: the capacity to do work: life can't create or destroy it; organisms convert it form one form to another.
Covalent bonds represent a bit of trapped energy. As a result, energy will be given will be given off when covalent bonds are broken and , it will require input of energy to make covalent bonds.
Metabolic activities are never 100% efficient; there is always some wasted energy, usually in the form of heat.
A metabolic pathway is a sequence of enzymatically catalyzed chemical reactions in a cell
In a metabolic pathway, the products of one reaction are the reactants for the next reaction, etc.
Metabolic pathways are determined by enzymes; each reaction will have a specific enzyme
Enzymes are encoded by genes (most are proteins).
Enzymes are Biological catalysts, are specific, and can act fast.
Biological catalysts are specific for a chemical reaction; not used up in that reatcion - makes them efficient.
Most enzymes are proteins.
Ribozymes are RNA molecules with enzymatic activity; some require a cofactor
Aponenzyme is a protein
Cofactor: Nonprotein component.
Coenzyme: organic cofactor
Holoenzyme: Aponezyme plus cofactor
Enzyme inhibitors blocks substrate binding to active site; competitive inhibition.
Allosteric inhibition noncompetitive inhibition.
Oxidation Adds oxygen, removes elections, and removes hydrogen.
Reduction Removes oxygen, adds electrons, and adds hydrogen.
"Redux" reaction is the simultaneous oxidation of one substance and reduction of another.
Oxidation reduces energy content.
Reduction increases energy content.
Microbes are more metabolically diverse than eukaryotes.
Any organism will require a carbon sourse and an energy source.
Many anabolic or biosynthetic pathways are similar; more diversity exists in the reactions used by microbes to acquire the energy that they need.
Energy metabolism in heterotrophs involves: catabolism.
Microbes are divided into categories based on their preferred carbon source and their preffered energy source.
Microbes are divided into these four basic nutritional categories: Chemoheterotrophs, Chemoautotrophs, Photoheterotrophs, and Photoautotrophs.
Chemoheterotrophs('hetero' means 'other'): Energy source: oxidize organic chemical compounds; carbon source: organic compounds; most microbes fall into this category
Chemoautotrophs ('auto' means 'self'): Energy source: oxidize inorganic chemical compounds; carbon source: Co2; only some bacteria and archaea are in this category.
Photoautotrophs: Energy source: light; carbon source: CO2; includes only bacteria and those eucaryotes that contain chloroplasts.
Photoheterotrophs: Energy source: light; carbon source: organic compounds; some bacteria and some algae are in this category.
Microbial metabolism is also categorized on the basis of its relationship to oxygen.
Aerobes: organisms that have adapted to growth in the presence of air (which is about 20% oxygen).
Anaerobes: organisms that have no protective mechanisms against the toxic effects of oxygen; live in habitats from wich oxygen is excluded.
Metabolism of aerobes: oxygenic, photosynthesis, anoxygenic, and photosynthesis.
Metabolism of anaerobes: Fermentation, anaerobic respiration, anoxygenic, and phothsynthesis.
Many microbes can switch from one category to another, depending on the conditions. Many chemoheterotrophs use aerobic respiration when oxygen is present and fermentation (or anaerobic respiration) when it is absent or aerobically as chemoheterotrophes using aerobic respiration
Bacteria can grow anerobically in the light, using anoxygenic photosynthesis, or aerobically as chemoheterotrophs using aerobic respiration.
The term facultative is used to designate organisms that can use two or more modes of metabolism ("take it or leave it").
The opposite of facultative is obligate ("have to").
Centeral metabolism: interconverts a small number of small organic compounds needed for biosynthesis; many of same reactions used in energy metabolism as well; such pathways are called amphibolic.
The pathways of centeral metabolism, biosynthesis, and macromolecule assembly are nearly identical in all organisms.
The commonality of central metabolism, biosynthesis, and macromolecule assembly, often termed unity of biochemistry, is powerful evidence for the descent of all life on earth from a single common ancestor.
Oxoglutarate dehydrogenase is found principally in aerobic chemoheterotrophs; allows them to have a complete Krebs cycle.
Chemoheterotrophs normally use the same organic compound for both biosysthesis and respiration; ex: glucose.
Macromolecules are hydrolyzed by extracellular enzymes.
The first step in the degradation of most organic matter is hydrolysis to monomers.
Eucaryotic microbes do this within phagolysosomes during intracellular digestion: the monomers are taken into the cytosol by permeases in the phagolysosome membrane.
Procaryotes hydrolyze macromolecules by secreting extracellular hydrolases; the monomers are taken up by active transport.
Most solute uptake by procaryotes is by active transport.
The procaryote's low-nutrient environments force them to use active transport by high-affinity prmeases to concentrate the compounds they take up.
The use of permeases maintains habitats so deficient in nutrients.
In most habitats, nearly all of the available soluble nutrients have been assimilated into microbial cells or oxidizzed to CO2 (very competitive environments).
In many bacteria, sugar uptake is by a phosphotransferase system.
Adding phosphorus to something: changes it.
Cells interconvert two forms of energy: an ionic potential and high energy compounds like ATP.
Ionic potential refers to a significant concentration gradient for an ion between two locations (often H+ and often across a membrane); movement of the ions is a useable form of energy.
All cells need chemical energy in the form of ATP, GTP, UTP, PEP (phosphoenolpyruvate), and some others.
ATP is used in most energy-requiring reactions of biosynthesis.
GTP and UTP are frequently used in macromolecular assembly reactions.
PEP is used in many transport reactions.
Prokaryotes will demonstrate greater diversity in forms of energy used.
The chemiosmotic potential that releases energy during ionic movement is due to the exterior of the cell being more acidic and more positively charged relative to the interior fo the cell.
A chemiosmotic potential can be made in two ways: Interconversion of membrane potential and chemical energy.
How do cells generate ATP Substrate level phosphorylation, oxidative phosphorylation, and photophosphorylation. (part of photosynthesis).
Phosphorylation refers to adding a phosphate ion to another compound; commonly adding phosphate to ADP to make ATP again.
Energy catabolism is converting covalent chemical bond energy into usable from - like ATP.
Energy catabolism is the breaking down (primarily by oxidation) of "food fuels" to simpler compounds, releasing energy.
"Food fuels" are compounds that contain calories (a unit for measuring energy); includes carbs, lipids, and proteins; usually begin with carbs since glucose is common energy source usable by most organisms.
The breakdown of carbohydrates to release energy may involve three metabolic pathways: Glycolysis, Kreb's cycle, and electron transport chain.
Glycolysis the oxidation of glucose to pyruvic acid produces ATP and NADH2.
Glycolysis acts in these ways - in cytoplasm- 10 reactions -to lop off the glucose half- specific enzyme for each - rxns are fast & easy- anaerobic- 'old' pathway- products are: 2 pyruvic acid 2 ATP (net) 2 NADH2
Although it is an oxidation, glycolysis does not use oxygen (is anaerobic).
Fermentation is a mode of chemotrophic energy metabolism in which most or all of the ATP is made by substrate-level phosphorylation.
Last action of fermentation is substreate action of phosphorolation.
Fermentation produces end products at the same average redox level as the substrates.
Some fermentations do not involve redox reactions.
The chemistry is such that a substrate-level phosphorylation can occur without any oxidation of the organic substrate.
Many different kinds of compounds can be fermented - commonly involves carbs, especially sugars; amino acids also can be fermented and other organic compounds.
Sugars might derive from polysaccharides like starch and amino acids from protien breakdown.
Individual microbes are generally limited in their fermentation capabiity but, recall that pure cultures do not occur in nature - mixed cultures do, so overall a mixture of fermenting organisms can result in substantial breakdown of biomass.
Alternatives to glycolysis - Pentose phosphate pathway / shunt: uses pentoses and NADPH2, supplies ribose and deoxyribose, supplies reduced NADP needed for lipid synthesis, and operates with glycolysis.
Respiration is a type of chemotrophic energy metabolism isn which most or all of the ATP is made by chemiosmotic means.
In aerobic respiration, oxygen is used as food fuels are completely oxidized to carbon dioxide and water.
Many covalent bonds are broken in aerobic respiration so much energy is released.
Some of theis energy is 'trapped' in the ATP molecule.
Glycolysis is the first pathway in aerobic repiration.
The 'additional rxns' of fermentation are not done, instead pyruvic acid enters the Kreb's cycle.
Reactions of the electron transport chain (ETC) will complete the process.
Most oxidations of woganic compounds reduce NAD+.
Every oxidation must be accompanied by a simultaneous reduction.
Electrons removed from one compound (oxidation) must be added to another (reduction).
Most of the soluble oxidation reaction of metabolism use the same electron acceptor: NAD
Some reduced NAD was produced in glycolysis but much more will be produced in the next pathway - the Kreb's cycle.
In eukaryotes, the Kreb's cycle takes place in the matrix of the mitochondria (inside the inner membrane).
Kreb's cycle begins with the pyruvic acid produced in glycolysis.
Pyruvic acid (from glycolysis is oxidized and decarboyxlated.
Oxidation of acetyl CoA produces NADH2 and FADH2.
Kreb's cycle is 8 reactions that to in a circle; twice per glucose
In eukaryotes, takes place in matrix of mitochondria.
The Electron transport chain is a series of carrier molecules that are, in turn, reduced and then oxidized as electrons are passed down the chain.
Energy released can be used to produce ATP by chemiosmosis.
In ETC, a series of carrier molecules generally are embedded in a membrane; in eukaryotes - the inner membrane of the mitochondria (there is also an ETC in the thylakoid membranes in chloroplasts in photosynthetic eukaryotes).
ETC is blocked by cyanide.
The electron transport system consists of two or three separate complexes of protein.
Each of the proteins of the electron transport system has prosthetic groups that are responsible for carrying the electrons.
The most common prosthetic groups are hemes and iron-sulfur centers.
One or another quinone mediates transfer from the dehydrogenase complex to the cytochrome b/c complex.
A small, soluble cytochrome normally mediates transfer of electrons from the cytochrome b/c complex to the oxidase.
Pathway for eukaryote and prokaryote glycolysis cytoplasm.
Pathway for eukaryote and prokaryote intermediate step cytoplasm.
Pathway for Kreb's cycle in eukaryote mitochondrial matrix
Pathway for Kreb's cycle in prokaryote cytoplasm.
Pathway for ETC in eukaryote mitochondrial inner membrane
Pathway for ETC in prokaryote plasma membrane.
Total possible 38 ATP per glucose.
Fermentation produced 2 ATP per glucose.
Aerobic respiration is more efficient.
Fermentation is only used by some microbes (doesn't produce enough ATP to support a large, multicellular eukaryote. organism).
Aerobic respiration only traps 43% of the bond energy from glucose in ATP - remainder is heat.
Some microbes can use something other than oxygen as the terminal electron acceptor; this is called anaerobic respiration.
Alternate oxidases are used for different electron acceptors.
Many prokaryotes are able to use nitrate or nitrite in the absence of oxygen.
Nitrate respiration is when the nitrate is reduced to the nitrite or ammonia.
When the nitrate is reduced to the gaseous end-product N2, the process is called denitrification.
Dead fish smell is trimethylamine.
NH3= ammonia
Fatty acids are made by adding 2-co 'units' together and they are broken down the same way (called beta oxidation).
Protein catabolism= deamination, decarboxylation, dehydrogenation->organic acid,->Kreb's cycle.
80-90% of alcohol is metabolized in the liver.
Remainder of alcolol is excreted thru the lungs, kidneys, and skin.
The average person can metabolize 18g/hour.
3 metabolic pathways can metabolize alcohol: dehydrogenase (cytoplasm), MEOS (microsomal ethanol-oxidizing system)with H2O2 in proxisomes.
Acetaldehyde is toxic in cells.
Acetaledhyde is changed to acetate in the mitochondria.
MEOS also yeilds zero free radicals.
When MEOS enzymes are increased, it often alters metabolism of drugs, toxins, vitamins A&D, and carcinogens.
MEOS enzymes will first work on alcohol - then will work on medications.
Alcoloh preferentially ties up NAD (among other things, can decrease gluconeogenesis->hypoglycemia and increase uric acid (gout).
Inorganic= non-carbon.
Chemoautotrophic respiration= rock eaters
Chemoautotrophs oxidize inorganic electorn donors for energy.
As autotrophs, they need a reductant for CO2 fixation.
Chemoautotroph's inorganic electron donor has to do 2 things: provide electrons fro energy-yeilding electron transport and provide electrons for CO2 reduction.
Oxidation of inorganic electron donors usually occurs in the periplasm.
A majority of chemoautotrophic substrates are oxidized by enzymes in the perilasm that pass electrons to quinone or cytochrome c.
Reverse electron transport is necessary for chemoautotrophs to generate reductant.
Chemoautotrophic respiration is ver inefficient for 2 related reasons: electrons enter the electron transport chain at the level of quinone or cytochrome c, few protons are pumped per pair of electrons, and much of the ^p is expended on generating reductant rather than ATP.
Anaerobic chemoautotrophic respirations commonly use H2 as electron donor.
Methanogenesis pumps ions without a cytochrome-based electron transport system.
Methanogenesis is the other major strictly anaerobic chemoautotrophic respiration.
Methanogenesis is unique to the archaea and is the principal consumer of hydrogen in anaerobic soils, fresh water sediments, and the animal intestinal tract.
Created by: czmamasan
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