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Metabolism
set of all chemical reactions used in a living organism to convert food into: energy, molecules body needs, waste products digestion (trypsine) absorption (steroids) transport utilization in cells -energy production -growth and maintenance -other uses of that energy elimination …
Catabolism
reactions that break molecules apart degrade compounds (oxidative process) NAD glucose ----> CO2, H2O, and energy
Anabolism`
reactions that build up compounds biosynthesize compounds (AA + ATP --> ADP + proteins) NADP energy + simple compound ----> complex compound
Metabolism Pathway
A--E1--> B --E2--> C --E3--> D
Pathways
stepwise series of reactions taking in food, breathing food out glucose + 6 O2 ---> 6 CO2 + 6 H2O
Central
very important for energy production interconnected (lipids, nucleotides, etc.)
Energy
oxidize glucose (CO2; burn!) harness energy to make ATP, NADH + H+ and FADH2
ATP
high energy carrying molecule (a lot of negative charges right next to each other) "energy currency" of cell interchangeable in many reactions  rapidly recycled
NADH
electron carrying molecule reduced form equal to 3 ATP
Central Energy Pathways
Goal: oxidize glucose, harness energy to make ATP and high energy molecules (C6H12O6) + 6 O2 ---> 6 CO2 + 6 H2O Includes: glycolysis, TCA cycle, Ox Phos Trend always toward increased oxidation of glucose
Enzymes
globular proteins catalysts for reactions in living things reactant in an enzyme-catalyzed reaction is substrate catalyzes a specific reaction enhancers, not consumed (lower activation energy)
Importance of Enzymes
understanding metabolism measurement of enzymes in body fluids i.e. lactate dehydrogenase - myocardial infarction used as reagents to measure concentrations of other components of body fluids i.e. glucose oxidase (measure glucose in blood and urine)
Dehydrogenases
oxidation-reduction reactions using NAD or FAD as oxidizing agents get 1 NADH i.e. Glyceraldehyde-3-phosophate dehydrogenase
Isomerases
convert a molecule into an isomer i.e. hexosephosphate isomerase
Mutases
move a phosphate ester (functional groups) within a molecule i.e. phosophoglycerate mutase
Kinases
add a phosphate ester to a molecule using ATP (phosphate donor) get 1 ATP i.e. pyruvate kinase, hexokinase
Glycolysis
10 steps glucose ---> 2 Pyretic acid overall: 2 ATP and 2 NADH Anaerobic Reaction in cytoplasm goes to form lactic acid
Aerobic Glycolysis
pyruvic acid is further oxidized can recycle NAD using Ox Phos (requires oxygen) 10 NADH ---> 30 ATP 2 FADH2 ---> 4 ATP ------->TOTAL 38 ATP 4 ATP
TCA Cycle
TOTAL FOR 1 PYRUVATE (15 ATP, *30 ATP) 4 NADH *8 NADH 1 ATP *2 ATP 1 FADH2 *2 FADH2 *need to do this twice for glycolysis
Electron Transport and Oxidative Phosphorylation
Purposes: 1) recycle NADH (reoxidize NAD) 2) recycle FADH2 (reoxidize FAD) 3) while deoxidizing NADH and FADH2, harness the energy to make more ATP takes place in mitochondria Process: 1)electrons are passed from NADH or FADH2 to other molecules down a chain of electors carriers…
Gluconeogenesis
synthesis of glucose from pyruvic acid, lactic acid, or amino acids  very energy favorable reaction replace enzymes, pull off phosphate (phosphotase) amino acids can be used for energy most amino acids are broken down to pyruvic acid or oxaloacetic acid i.e. liver
Pentose Shunt
synthesis of Ribose-5-P and NADPH from Glucose-6-P make ribose for DNA, RNA, and other molecules make NADPH as reducing agent for biosynthesis reactions oxidative----> decarboxylation
Glycogen Synthesis
starts with Glucose-6-P stores glucose in the form of glycogen forward and reverse reaction i.e. liver (stores glucose for keeping blood glucose levels constant) muscles (store glucose for later energy needs)
Glycogenolysis
breaks down glycogen to get stored glucose and use it for energy needs i.e. liver (maintain levels) muscle (use energy, no enzyme because it doesn't need to be modified)
"Glucogenic"
amino acids that can be used to synthesize glucose
Fatty Acid Beta-Oxidation
Fatty acid --B-oxidation---> Acetyl CoA ----> TCA cycle NADH NADH FADH2 FADH2 ATP B a R-CH2-CH2-CH2-CH2-COOH
Fatty Acid Catabolism
takes place in mitochondria CoA carries fat acid chain as it is degraded NADH, FADH2 produced
Fatty Acid Synthesis
takes place in cytoplasm Acyl Carrier Protein (ACP) carries fatty acid chain as it grows NADPH is used
Catabolism of Amino Acids for Energy
1) transaminase reaction 2) a-keto acid feeds into glycolysis or TCA cycle 3) remove amino group from glutamic acid to regenerate a-ketogultaric acid + NH4+ 4) get rid of NH4+ via Urea Cycle
Ketosis
disturbance of metabolism when shortage of carbohydrates and lots of fats are being catabolized: starvation, prolonged fasting, diabetes excess of Acetyl CoA due from B-oxidation of fatty acids shortage of oxaloacetic acid (being used in gluconeogenesis) not all acetyl CoA can feed in…
Ketone Bodies
acetoacetate (3-ketobutanoate) 3-hydroxybutanoate acetone
Glucogenic Amino Acids
amino acids that are broken down to pyruvate, oxaloacetate, or other TCA cycle intermediates
Ketogenic Amino Acids
amino acids that are broken down to Acetyl CoA
Insulin
produced in and secreted from B-ells of pancreas sign of "well-fed state", blood glucose is high signals liver to take up and store glucose
Glucogen
produced in and secreted from the a-cells of pancreas sign that blood glucose is low signals liver to break down glycogen and release glucose to blood stream
Type 1 Diabetes
"insulin dependent" pancreas doesn't produce insulin B-cells of pancreas have been destroyed or made non-functional
Type 2 Diabetes
"insulin independent" deficiency in insulin receptors on liver cells liver doesn't get insulin signal due to lack of insulin receptors
Body Fluids
blood (clinically most important) lymph CSF Urine saliva sweat milk
Hemoglobin
in red blood cells globin folds alpha helices oxygen and CO2 exchange oxygen carrying protein cooperative
Erythrocytes
red blood cells 45% of total blood
Plasma
55% of total blood can be stored frozen whole blood minus "formed elements"
Whole Blood
stored cold, not frozen (would rupture cells) taken directly from patient
Buffy Coat
leukocytes and platelets less than 1% of total blood
Serum
allowed to clot then spun in centrifuge supernatant whole blood minus cells, platelets and clotting proteins
"Formed Elements"
platelets red blood cells (erythrocytes) white blood cells (immune system) components surrounded by lipid bilayer membrane
Small Molecules
nutrients (carbs, lipids, amino acids, glucose) waste products (urea) other organics (hormones, vitamins) metabolic intermediates (lactate)
Electrolytes
Na+ K+ Ca2+ Mg2+ Cl- HCO3- HPO42- ATP pumps organic and inorganic substances
Immunoglobulins
4 polypeptide chains 2 antigen-binding sites quaternary structure
Urea Cycle
NH4+ converted into urea and then secreted starts when ammonium ion, bicarbonate, and ATP react to form carbamoyl phosphate (1 nitrogen ion, other from aspartic acid) transaminase reaction to produce aspartic acid from oxaloacetic acid catabolism of amino acids
"Clotting Cascade"
stop from bleeding punches a hole in membrane of an invading bacterium and kills it
Respiratory Acidosis
caused by hypoventilation CO2 retained so blood becomes more acidic
Respiratory Alkalosis
caused by hyperventilation CO2 lost so blood becomes alkaline
Metabolic Acidosis
too much acid is produced (build up of Acetyl CoA) body tries to lose CO2--> hyperventilation
Metabolic Alkalosis
too much acid lost (prolonged vommitting) body tries to retain CO2---> hypoventilation
Kidneys
get rid of end-products of metabolism (waste products, urea) control concentration of some components of body fluids  -electrolytes (Na+) -H+ (helps control blood pH) -total fluid (water) content and hence osmotic pressure simple dialysis
Milk
produced in mammary tissue of mammals as food for young high levels of protein, carbs, lipids necessary for growth and development
Cerebrospinal Fluid
around most central nervous tissue composition similar to plasma
Lymph
in lymphatic ducts transport of macromolecules (proteins) lipid transport
Digestive Fluids
saliva and bile digestive enzymes, lubricants, detergents, buffers
Globular Proteins in Blood
soluble albumin globulins (antibodies) complement proteins fibrinogen and other clotting proteins lipoproteins enzymes protein hormones
Serum Albumin
binds fatty acids, metal ions, drug molecules regulates osmotic pressure 60% of soluble protein in plasma loss of it can cause edema
Osmotic Pressure
water rushes to the side of the membrane with higher concentration of solutes two substances that are separated
Complete Proteins
help immune system kill invading bacteria way to get rid of bacteria in blood
Fibrinogen and other clotting proteins
inactive enzymes protease if active the blood wouldn't pump produce clotting when circulatory system is broken
Lipoproteins
throughout body transport lipids and cholesterol protein triglycerides (cholesterol) phospholipid
Protein Hormones
insulin human growth hormone follicle stimulating hormone (FSH) present in small amounts (trauma can increase)
Immune System
protects body from infection by recognizing and destroying foreign molecules -cells (various white blood cells) -antibodies (immunoglobins) -complement
Antigen
foreign molecule that IgG "recognizes" anything that isn't cells or your body
Antibody
react with antigenic determinants on B-cell surface crosslink and immobilize antigens water-soluble circulate in blood stream and other body fluids
Cooperative
one of the subunits can help all other subunits bind to oxygen
Complement
series of proteins in blood that take part in killing invading cells use a gradient of H+ ion concentration across membranes to generate ATP

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