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36 Cards in this Set
- Front
- Back
What are the 4 fates of UDP-Glucose?
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1) UDP-Glucuronic Acid
2) Glycogen 3) Glycoproteins, Polysaccharides, Gal Metab. 4) Glucose 1 P |
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What is the net anaerobic glucose reaction?
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Glucose + 2P + 2ADP --> 2 Lactate + 2ATP + 2H20
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What is the net aerobic glycolysis reaction?
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Glucose + 2P + 2ADP +2NAD --> 2 Pyruvate +2ATP +2NADH + 2H+ +2H20
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What is the investment phase of glycolysis?
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Glucose --> G6P (requires ATP) --> F6P --> F1,6BP (requires ATP)
-need to put in 2 ATP |
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Why do we use F16BP instead of G16BP?
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Because we want to get symmetric products (two 3 carbon molecules)
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What is the second phase of glycolysis? How much ATP does it produce?
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G3P & DHAP --> 13BPG --> 3PG (generates ATP) --> 2PG --> P-enolpyruvate --> Pyruvate (generates ATP)
-4 ATP made |
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Red cells lack _______, so they depend on ______ for ATP production?
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-mitochondria
-glycolysis |
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A woman with unstable red blood cells & anemia has a problem with what?
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glycolysis
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How does glycolysis provide energy for exercise?
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-starts with ATP already present --> uses anaerobic glycolysis (2 mins) --> uses aerobic glycolysis + TCA
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What are the 3 fates of G6P?
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1) Pentose 5-Phosphate (nucleotides & NADPH)
2) Pyruvate (can go to lactate) 3) Glycogen |
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Dihydroxyacetone phosphate provides intermediates for ________ synthesis
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lipid
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Dihydroxyacetone phosphate can be converted to phosphatidic acid which is a precursor to ______ & ______
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-triacylglycerol
-phospholipids |
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1,3 BPG generates _________, which regulates hemoglobin. Which enzyme does this conversion?
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-2,3 BPG
-bisphosphoglycerate mutase |
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We can generate ______ from 3 phosphoglycerate?
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Serine (amino acids)
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What does G3P dehydrogenase catalyze? What does it require?
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-G3P --> 1,3BPG
-requires P & NAD+ |
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What does arsenic do?
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Targets G3P dehydrogenase and pretends to be phosphate
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How do we regenerate NAD+ back from G3P dehydrogenase reaction under anaerobic conditions?
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-Conversion of Pyruvate --> Lactate by LDH
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G3P dehydrogenase shows ______ cooperativity. What does this mean?
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-negative
-means enzyme is less sensitive to changes in substrate concentration --> always wants to do glycolysis |
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What do oxidizing reactions use ____ and reduce it to _____ to oxidize the substrate
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NAD+
NADH |
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Is there more NAD+ or NADH in the cell?
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NAD+ because that is the form it gets used
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Pellagra
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-Selective deficiency of niacin (nicotinic acid)
-NAD formed from niacin (member of VItamin B familiy) -D cubed --> Dimentia, Dirreah, Dermetitis |
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The regulation of glycolysis occurs at steps that are far from _______
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equilibrium
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Which enzymes are regulated (irreversible) in glycolysis & what regulates them?
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1) hexokinase (neg: G6P)
2) PFK-1 (pos: AMP, neg: ATP & citrate) 3) Pyruvate Kinase (pos: F16BP) |
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What is the key regulatory enzyme/step in glycolysis?
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F6P --> F16BP by PFK-1
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Under resting conditions, PFK-1 is strongly _________
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inhibited
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Rate of PFK-1 is determined by amount of ___________ (pos. regulator), especially in liver
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Fructose-2,6-Bisphosphate
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Fructose-2,6-Bisphosphate is made from ________ by ________
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-F6P
-PFK-II |
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Which phosphatases change F26BP & F16BP back to F6P?
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-Phosphatase I & Phosphatase II
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How is PFK2 regulated by insulin?
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-when PFK2 phosphorylated it goes from kinase --> phosphatase which changes F26BP --> F6P: TURNS OFF PK1
-Insulin activates phosphatase to take phosphate off of PFK2 --> turns it back into kinase --> makes F6P into F26BP: TURNS ON PFK1 |
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Deficiencies in glycolysis mainly affect _____ & _______
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-red cells
-skeletal muscle |
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Pyruvate can be made into lactate, go into TCA or be made into _______
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amino acids
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2-Deoxyglucose affects _________ by generating neg. feedback inhibition
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hexokinase
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Fluroide inhibits _______
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Enolase
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________ is the most common enzyme defect in glycolysis
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Pyruvate Kinase
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How come pyruvate kinase can be defective in red blood cells & normal in other tissues?
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-PK comes in 4 isoenzymes: M1, M2, L & R
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Patient has defect in Muscle PFK1, why do they not have anemia?
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Because there are 3 PFK enzymes --> Red cells have mix of the 3, so they're ok
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