ch13 full review bc

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64 Terms

1
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Glucose central molecule in metabolism

Glucose = central metabolite and primary energy source for most cells.

2
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Plants store glucose as

Starch (amylose and amylopectin).

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Animals store glucose as

Glycogen, mainly in liver and skeletal muscle.

4
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The main energy-carrying molecules produced in metabolism are

ATP and NADH.

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Each metabolic step is catalyzed by

A specific enzyme.

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Regulation of metabolism primarily occurs by

Controlling enzyme activity, often through allosteric regulation.

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Glycolysis converts

1 Glucose → 2 Pyruvate.

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Net yield of ATP per glucose molecule in glycolysis is

2 ATP.

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Glycolysis occurs in the

Cytoplasm (cytosol).

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The first five reactions of glycolysis are known as the

Energy investment phase.

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The second half of glycolysis is the

Energy payoff phase.

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The enzyme that catalyzes the first step of glycolysis is

Hexokinase.

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The reaction catalyzed by hexokinase uses which energy source

ATP.

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The product of the hexokinase reaction is

Glucose-6-phosphate (G6P).

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The phosphoglucose isomerase reaction converts b

Glucose-6-phosphate → Fructose-6-phosphate (F6P). b

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The key regulatory enzyme of glycolysis is

Phosphofructokinase-1 (PFK-1).

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PFK-1 is activated by

ADP and Fructose-2,6-bisphosphate.

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PFK-1 is inhibited by

Phosphoenolpyruvate (PEP) and Citrate.

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The aldolase reaction splits fructose-1,6-bisphosphate into

Glyceraldehyde-3-phosphate (G3P) and Dihydroxyacetone phosphate (DHAP).

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The triose phosphate isomerase reaction interconverts

DHAP ↔ G3P.

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The byproduct methylglyoxal, formed from enediol intermediate, is

Toxic byproduct formed nonenzymatically from triose phosphates.

22
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GAPDH uses which cofactor

NAD⁺ (reduced to NADH).

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The GAPDH reaction is inhibited by

Arsenate (AsO₄³⁻).

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The enolase enzyme is inhibited by

Fluoride (F⁻) and inorganic phosphate (Pi).

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The product of the enolase reaction is

Phosphoenolpyruvate (PEP).

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The pyruvate kinase reaction produces

Pyruvate and ATP.

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3 irreversible steps in glycolysis catalyzed by

Hexokinase, Phosphofructokinase-1 (PFK-1), Pyruvate kinase.

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Pyruvate kinase is activated by

Fructose-1,6-bisphosphate (feed-forward activation).

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The net yield of glycolysis per glucose is

2 ATP, 2 NADH, and 2 Pyruvate.

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Under anaerobic conditions in muscle, pyruvate is converted to

Lactate.

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In yeast, pyruvate is converted to

Ethanol.

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Glycolysis and gluconeogenesis are coordinated to prevent

Futile cycling and ATP waste.

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The fate of pyruvate depends on

Oxygen availability, cell type, and energy needs.

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Lactate dehydrogenase is required to

oxidize nadh to nad+

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In yeast, pyruvate is converted to ethanol through

(1) Pyruvate → Acetaldehyde (pyruvate decarboxylase); (2) Acetaldehyde → Ethanol (alcohol dehydrogenase).

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Coenzyme A is essential for pyruvate decarboxylation because it

Carries and activates the acetyl group.

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Pyruvate carboxylase requires which cofactor

Biotin (Vitamin B₇).

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Gluconeogenesis is activated when

Glycogen stores are depleted.

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The conversion of pyruvate to PEP requires

Pyruvate carboxylase and PEP carboxykinase (PEPCK); consumes ATP and GTP.

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Which molecules can serve as gluconeogenic precursors

Pyruvate, lactate, glycerol, and glucogenic amino acids (all except leucine and lysine).

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Fatty acids are generally

Not gluconeogenic (cannot form oxaloacetate).

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Glycogen synthesis begins with 9

Glucose-6-phosphate, converted to Glucose-1-phosphate. 9

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UDP-glucose is formed from

Glucose-1-phosphate + UTP.

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The enzyme forming UDP-glucose is

UDP-glucose pyrophosphorylase.

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Glycogen synthase forms which type of linkage

α(1→4) glycosidic linkages.

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Glycogen phosphorylase catalyzes

Glycogen breakdown (phosphorolysis).

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The product of glycogenolysis is

Glucose-1-phosphate.

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In the liver, glucose-6-phosphatase converts G6P into

Free glucose.

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Glycogen metabolism is regulated by

Hormones (insulin, glucagon, epinephrine).

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The PPP uses which substrate

Glucose-6-phosphate (G6P).

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The PPP primarily produces

Ribose-5-phosphate and NADPH.

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The oxidative phase of the PPP produces

2 NADPH and CO₂.

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The key enzyme in the oxidative phase is

Glucose-6-phosphate dehydrogenase (G6PD).

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The two major enzymes of the non-oxidative phase are

Transketolase and Transaldolase.

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The PPP does not produce o

ATP. o

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The PPP is activated when

NADP⁺ levels are high (when NADPH is low).

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The PPP is inhibited by

NADPH (feedback inhibition).

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Pyruvate links glycolysis with

TCA cycle, gluconeogenesis, fatty acid synthesis, and amino acid synthesis.

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Simultaneous glycolysis and gluconeogenesis would

Waste ATP and cause a net energy loss.

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The liver supplies glucose to other tissues via

Glucose-6-phosphatase hydrolyzing G6P → free glucose for release into blood.

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The PPP supports biosynthesis of

fatty acids and nucleotides

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Red blood cells rely on glycolysis because they

Lack mitochondria and depend solely on glycolysis for ATP.

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Hexokinase deficiency causes

Reduced glycolysis and less 2,3-BPG, decreasing oxygen delivery to tissues.

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Fructose intolerance is due to a deficiency in

Fructose-1-phosphate aldolase, causing phosphate trapping and ATP depletion