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Glucose central molecule in metabolism
Glucose = central metabolite and primary energy source for most cells.
Plants store glucose as
Starch (amylose and amylopectin).
Animals store glucose as
Glycogen, mainly in liver and skeletal muscle.
The main energy-carrying molecules produced in metabolism are
ATP and NADH.
Each metabolic step is catalyzed by
A specific enzyme.
Regulation of metabolism primarily occurs by
Controlling enzyme activity, often through allosteric regulation.
Glycolysis converts
1 Glucose → 2 Pyruvate.
Net yield of ATP per glucose molecule in glycolysis is
2 ATP.
Glycolysis occurs in the
Cytoplasm (cytosol).
The first five reactions of glycolysis are known as the
Energy investment phase.
The second half of glycolysis is the
Energy payoff phase.
The enzyme that catalyzes the first step of glycolysis is
Hexokinase.
The reaction catalyzed by hexokinase uses which energy source
ATP.
The product of the hexokinase reaction is
Glucose-6-phosphate (G6P).
The phosphoglucose isomerase reaction converts b
Glucose-6-phosphate → Fructose-6-phosphate (F6P). b
The key regulatory enzyme of glycolysis is
Phosphofructokinase-1 (PFK-1).
PFK-1 is activated by
ADP and Fructose-2,6-bisphosphate.
PFK-1 is inhibited by
Phosphoenolpyruvate (PEP) and Citrate.
The aldolase reaction splits fructose-1,6-bisphosphate into
Glyceraldehyde-3-phosphate (G3P) and Dihydroxyacetone phosphate (DHAP).
The triose phosphate isomerase reaction interconverts
DHAP ↔ G3P.
The byproduct methylglyoxal, formed from enediol intermediate, is
Toxic byproduct formed nonenzymatically from triose phosphates.
GAPDH uses which cofactor
NAD⁺ (reduced to NADH).
The GAPDH reaction is inhibited by
Arsenate (AsO₄³⁻).
The enolase enzyme is inhibited by
Fluoride (F⁻) and inorganic phosphate (Pi).
The product of the enolase reaction is
Phosphoenolpyruvate (PEP).
The pyruvate kinase reaction produces
Pyruvate and ATP.
3 irreversible steps in glycolysis catalyzed by
Hexokinase, Phosphofructokinase-1 (PFK-1), Pyruvate kinase.
Pyruvate kinase is activated by
Fructose-1,6-bisphosphate (feed-forward activation).
The net yield of glycolysis per glucose is
2 ATP, 2 NADH, and 2 Pyruvate.
Under anaerobic conditions in muscle, pyruvate is converted to
Lactate.
In yeast, pyruvate is converted to
Ethanol.
Glycolysis and gluconeogenesis are coordinated to prevent
Futile cycling and ATP waste.
The fate of pyruvate depends on
Oxygen availability, cell type, and energy needs.
Lactate dehydrogenase is required to
oxidize nadh to nad+
In yeast, pyruvate is converted to ethanol through
(1) Pyruvate → Acetaldehyde (pyruvate decarboxylase); (2) Acetaldehyde → Ethanol (alcohol dehydrogenase).
Coenzyme A is essential for pyruvate decarboxylation because it
Carries and activates the acetyl group.
Pyruvate carboxylase requires which cofactor
Biotin (Vitamin B₇).
Gluconeogenesis is activated when
Glycogen stores are depleted.
The conversion of pyruvate to PEP requires
Pyruvate carboxylase and PEP carboxykinase (PEPCK); consumes ATP and GTP.
Which molecules can serve as gluconeogenic precursors
Pyruvate, lactate, glycerol, and glucogenic amino acids (all except leucine and lysine).
Fatty acids are generally
Not gluconeogenic (cannot form oxaloacetate).
Glycogen synthesis begins with 9
Glucose-6-phosphate, converted to Glucose-1-phosphate. 9
UDP-glucose is formed from
Glucose-1-phosphate + UTP.
The enzyme forming UDP-glucose is
UDP-glucose pyrophosphorylase.
Glycogen synthase forms which type of linkage
α(1→4) glycosidic linkages.
Glycogen phosphorylase catalyzes
Glycogen breakdown (phosphorolysis).
The product of glycogenolysis is
Glucose-1-phosphate.
In the liver, glucose-6-phosphatase converts G6P into
Free glucose.
Glycogen metabolism is regulated by
Hormones (insulin, glucagon, epinephrine).
The PPP uses which substrate
Glucose-6-phosphate (G6P).
The PPP primarily produces
Ribose-5-phosphate and NADPH.
The oxidative phase of the PPP produces
2 NADPH and CO₂.
The key enzyme in the oxidative phase is
Glucose-6-phosphate dehydrogenase (G6PD).
The two major enzymes of the non-oxidative phase are
Transketolase and Transaldolase.
The PPP does not produce o
ATP. o
The PPP is activated when
NADP⁺ levels are high (when NADPH is low).
The PPP is inhibited by
NADPH (feedback inhibition).
Pyruvate links glycolysis with
TCA cycle, gluconeogenesis, fatty acid synthesis, and amino acid synthesis.
Simultaneous glycolysis and gluconeogenesis would
Waste ATP and cause a net energy loss.
The liver supplies glucose to other tissues via
Glucose-6-phosphatase hydrolyzing G6P → free glucose for release into blood.
The PPP supports biosynthesis of
fatty acids and nucleotides
Red blood cells rely on glycolysis because they
Lack mitochondria and depend solely on glycolysis for ATP.
Hexokinase deficiency causes
Reduced glycolysis and less 2,3-BPG, decreasing oxygen delivery to tissues.
Fructose intolerance is due to a deficiency in
Fructose-1-phosphate aldolase, causing phosphate trapping and ATP depletion