MBOD Block 4 Week 2 Flashcards

(392 cards)

2
Q

<p>What are the fuels for the energy reserves of humans?</p>

A

<p>TAG, Protein, Glycogen, Glucose</p>

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2
Q

<p>What are the fuels for the energy reserves of humans?</p>

A

<p>TAG, Protein, Glycogen, Glucose</p>

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3
Q

<p>Which tissues house the energy reserves of humans?</p>

A

<p>Adipose, Muscle, Liver, Body fluids</p>

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3
Q

<p>Which tissues house the energy reserves of humans?</p>

A

<p>Adipose, Muscle, Liver, Body fluids</p>

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4
Q

<p>Which tissues has the most energy reserves?</p>

A

<p>Adipose</p>

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4
Q

<p>Which tissues has the most energy reserves?</p>

A

<p>Adipose</p>

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5
Q

<p>What are the anabolic pathways?</p>

A

<p>Gluconeogenesis, Glycogenesis, Protein Synthesis, Lipogenesis</p>

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5
Q

<p>What are the anabolic pathways?</p>

A

<p>Gluconeogenesis, Glycogenesis, Protein Synthesis, Lipogenesis</p>

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6
Q

<p>What are the substrates involved in gluconeogenesis?</p>

A

<p>Lactate, alanine, glycerol</p>

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6
Q

<p>What are the substrates involved in gluconeogenesis?</p>

A

<p>Lactate, alanine, glycerol</p>

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7
Q

<p>What is the end product of gluconeogenesis?</p>

A

<p>Glucose</p>

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7
Q

<p>What is the end product of gluconeogenesis?</p>

A

<p>Glucose</p>

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8
Q

<p>What are the substrates involved in glycogenesis?</p>

A

<p>Glc-1-P, Glc</p>

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8
Q

<p>What are the substrates involved in glycogenesis?</p>

A

<p>Glc-1-P, Glc</p>

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9
Q

<p>What is the end product of glycogenesis?</p>

A

<p>Glycogen</p>

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9
Q

<p>What is the end product of glycogenesis?</p>

A

<p>Glycogen</p>

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10
Q

<p>What are the substrates involved in protein synthesis?</p>

A

<p>Amino acids</p>

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10
Q

<p>What are the substrates involved in protein synthesis?</p>

A

<p>Amino acids</p>

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11
Q

<p>What is the end product of protein synthesis?</p>

A

<p>Proteins</p>

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11
Q

<p>What is the end product of protein synthesis?</p>

A

<p>Proteins</p>

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12
Q

<p>What are the substrates involved in lipogenesis?</p>

A

<p>Glc, glycerol, acetyl-CoA</p>

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12
Q

<p>What are the substrates involved in lipogenesis?</p>

A

<p>Glc, glycerol, acetyl-CoA</p>

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13
Q

<p>What are the end products of lipogenesis?</p>

A

<p>Fatty acids, TAG</p>

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13
Q

<p>What are the end products of lipogenesis?</p>

A

<p>Fatty acids, TAG</p>

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14

What are the catabolic pathways?

Glycolysis, CAC + ETC, Glycogenolysis, Proteolysis, Lipolysis, P-gluconate pathway

14

What are the catabolic pathways?

Glycolysis, CAC + ETC, Glycogenolysis, Proteolysis, Lipolysis, P-gluconate pathway

15

What is the substrate involved in glycolysis?

Glucose

15

What is the substrate involved in glycolysis?

Glucose

16

What is the end product of glycolysis?

Pyruvate, ATP

16

What is the end product of glycolysis?

Pyruvate, ATP

17

What substrates are involved in CAC + ETC?

Acetyl CoA, OAA

17

What substrates are involved in CAC + ETC?

Acetyl CoA, OAA

18

What are the end products of CAC + ETC?

NADH, ATP, CO2

18

What are the end products of CAC + ETC?

NADH, ATP, CO2

19

What is the substrate involved in glycogenolysis?

Glycogen

19

What is the substrate involved in glycogenolysis?

Glycogen

20

What are the end products of glycogenolysis?

Glc-1-P, Glc

20

What are the end products of glycogenolysis?

Glc-1-P, Glc

21

What is the substrate involved in proteolysis?

Proteins

21

What is the substrate involved in proteolysis?

Proteins

22

What are the end products of lipolysis?

Acetyl CoA, glycerol

22

What are the end products of lipolysis?

Acetyl CoA, glycerol

23

What is the substrate involved in the P-gluconate Pathway?

Glc-6-P

23

What is the substrate involved in the P-gluconate Pathway?

Glc-6-P

24

What are the end products of the P-gluconate Pathway?

pentoses, CO2, NADPH (->FA)

24

What are the end products of the P-gluconate Pathway?

pentoses, CO2, NADPH (->FA)

25

What happens to the blood glucose in the fed state?

It increases

25

What happens to the blood glucose in the fed state?

It increases

26

What are the stages of the Feed-Fast Cycle?

Fed state; Post-prandial state; Post-absorptive state; Basal state; Fasting state; Starved state

26

What are the stages of the Feed-Fast Cycle?

Fed state; Post-prandial state; Post-absorptive state; Basal state; Fasting state; Starved state

27

After how many hours does the Post-prandial state occur?

~2hrs

27

After how many hours does the Post-prandial state occur?

~2hrs

28

After how many hours does the Post-absorptive state occur?

~6-8hrs

28

After how many hours does the Post-absorptive state occur?

~6-8hrs

29

Which state occurs after ~12 hours?

Basal state (Early fasting state)

29

Which state occurs after ~12 hours?

Basal state (Early fasting state)

30

After how many hours does the Fasting state occur?

24-72 hrs

30

After how many hours does the Fasting state occur?

24-72 hrs

31

Which state occurs after ~72 hours?

Starved state

31

Which state occurs after ~72 hours?

Starved state

32

What are the fates of fuels in the fed state?

Storage, synthesis, oxidation

32

What are the fates of fuels in the fed state?

Storage, synthesis, oxidation

33

What occurs in muscle metabolism during the resting state?

Synthesis of glycogen and protein.

33

What occurs in muscle metabolism during the resting state?

Synthesis of glycogen and protein.

34

What occurs in muscle metabolism during exerise?

Use glycogen, make lactate if O2 is limiting.

34

What occurs in muscle metabolism during exerise?

Use glycogen, make lactate if O2 is limiting.

35

What happens to the levels of Glucose, Insulin, and glucagon in the blood during the basal state?`

Glucose and insulin decreases; glucagon increases

35

What happens to the levels of Glucose, Insulin, and glucagon in the blood during the basal state?`

Glucose and insulin decreases; glucagon increases

36

What is used as an alternate fuel in the basal state?

Ketone bodies

36

What is used as an alternate fuel in the basal state?

Ketone bodies

37

Where are ketones formed?

In the liver

37

Where are ketones formed?

In the liver

38

What happens to the levels of Insulin and glucagon in the blood during the fed state?`

Insulin increases; Glucagon decreases

38

What happens to the levels of Insulin and glucagon in the blood during the fed state?`

Insulin increases; Glucagon decreases

39

What happens to the levels of Glucose, Insulin, and glucagon in the blood during the starved state?`

Glucose and insulin decreases; glucagon increases

39

What happens to the levels of Glucose, Insulin, and glucagon in the blood during the starved state?`

Glucose and insulin decreases; glucagon increases

40

What processes does insulin cause an increase in?

Glu uptake, Glc utilization, Protein syn, Lipogenesis, glycogenesis

40

What processes does insulin cause an increase in?

Glu uptake, Glc utilization, Protein syn, Lipogenesis, glycogenesis

41

What processes does insulin cause an decrease in?

Lipolysis, Glc output, gluconeogenesis, glycogenolysis, ketogenesis

41

What processes does insulin cause an decrease in?

Lipolysis, Glc output, gluconeogenesis, glycogenolysis, ketogenesis

42

What processes does glucagon cause an increase in?

Lipolysis, Glc output, gluconeogenesis, glycogenolysis, ketogenesis

42

What processes does glucagon cause an increase in?

Lipolysis, Glc output, gluconeogenesis, glycogenolysis, ketogenesis

43

What processes does glucagon cause an decrease in?

Glycogenesis

43

What processes does glucagon cause an decrease in?

Glycogenesis

45

What is the branch point for several metabolic pathways?

Glu-6-Phosphate

45

What is the branch point for several metabolic pathways?

Glu-6-Phosphate

46

Why can glucose not diffuse across the hydrophobic phospholipid bilayer of the cell membrane?

It is polar

46

Why can glucose not diffuse across the hydrophobic phospholipid bilayer of the cell membrane?

It is polar

47

How does glucose get across the membrane?

It binds to transport proteins that bind glucose on one side of the membrane and release it on the opposite side.

47

How does glucose get across the membrane?

It binds to transport proteins that bind glucose on one side of the membrane and release it on the opposite side.

48

What are the two types of transport proteins in intestinal epithelial cells?

Na+ dependent glucose transporter; Facilitative glucose transporter

48

What are the two types of transport proteins in intestinal epithelial cells?

Na+ dependent glucose transporter; Facilitative glucose transporter

49

Where do the Na+ dependent glucose transporters reside?

On the lumenal side of absorptive epithelial cells

49

Where do the Na+ dependent glucose transporters reside?

On the lumenal side of absorptive epithelial cells

50

What is the role of Na+K+ATPase?

Keeps intracellular Na+ low

50

What is the role of Na+K+ATPase?

Keeps intracellular Na+ low

51

T/F Glucose transport goes from low to high conc. in Na+ transport

TRUE

51

T/F Glucose transport goes from low to high conc. in Na+ transport

TRUE

52

T/F Na+ transport goes from high to low conc.

TRUE

52

T/F Na+ transport goes from high to low conc.

TRUE

53

T/F Facilitative Glucose Transporters move glucose from high conc to low conc w/o the expenditure of energy.

TRUE

53

T/F Facilitative Glucose Transporters move glucose from high conc to low conc w/o the expenditure of energy.

TRUE

54

Where are the amino and carboxy-terminal residues of the facilitative glucose transporters located?

In the cytoplasm.

54

Where are the amino and carboxy-terminal residues of the facilitative glucose transporters located?

In the cytoplasm.

55

How many glucose transport proteins are in the family of Facilitative glucose transporters?

Five

55

How many glucose transport proteins are in the family of Facilitative glucose transporters?

Five

56

What is the Km of GLUT 1?

1 mM

56

What is the Km of GLUT 1?

1 mM

57

What is the tissue location of GLUT2?

Liver and pancreatic B cells

57

What is the tissue location of GLUT2?

Liver and pancreatic B cells

58

What is the Km of GLUT2?

15-20mM

58

What is the Km of GLUT2?

15-20mM

59

What is the role of GLUT2?

Plays a role in the regulation of insulin in the the pancreas; Removes excess glucose from the blood in the liver.

59

What is the role of GLUT2?

Plays a role in the regulation of insulin in the the pancreas; Removes excess glucose from the blood in the liver.

60

What is the tissue location of GLUT4?

Muscle and fat cells

60

What is the tissue location of GLUT4?

Muscle and fat cells

61

What is the Km of GLUT4?

5mM

61

What is the Km of GLUT4?

5mM

62

What is the role of GLUT4?

The amount in muscle plasma membrane increases with endurance training.

62

What is the role of GLUT4?

The amount in muscle plasma membrane increases with endurance training.

63

What is the tissue location of GLUT5?

Small intestine

63

What is the tissue location of GLUT5?

Small intestine

64

What is the role of GLUT5?

Primarily a fructose transporter

64

What is the role of GLUT5?

Primarily a fructose transporter

65

How does glucose bin to the transport protein in facilitative glucose transport?

Via interactions with its hydroxyl groups

65

How does glucose bin to the transport protein in facilitative glucose transport?

Via interactions with its hydroxyl groups

66

What happens to the transport protein in facilitative Glucose transport when glucose is transported?

It undergoes a conformational change.

66

What happens to the transport protein in facilitative Glucose transport when glucose is transported?

It undergoes a conformational change.

67

What happped to the transport protein as glucose is released to the other side of the membrane?

It closes

67

What happped to the transport protein as glucose is released to the other side of the membrane?

It closes

68

What does the type of GLUT expressed by the cells reflect?

The function of glucose metabolism in that tissue.

68

What does the type of GLUT expressed by the cells reflect?

The function of glucose metabolism in that tissue.

69

Which GLUT is expressed on the surface of a red blood cell?

GLUT1

69

Which GLUT is expressed on the surface of a red blood cell?

GLUT1

70

What stimulates the recruitment of GLUT4 to the membrane to increase glucose transport?

Insulin

70

What stimulates the recruitment of GLUT4 to the membrane to increase glucose transport?

Insulin

71

What is an important function of the liver?

To maintain blood glucose levels

71

What is an important function of the liver?

To maintain blood glucose levels

72

What is the role of GLUT2 in the pancreas?

Stimulates glucose uptake in pancreatic B-cells

72

What is the role of GLUT2 in the pancreas?

Stimulates glucose uptake in pancreatic B-cells

73

What does an elevated ATP/ADP ratio result in?

An increase in cytosolic Ca++

73

What does an elevated ATP/ADP ratio result in?

An increase in cytosolic Ca++

74

What does an increase in cytosolic Ca++ cause?

It triggers the fusion of insulin-containing vesicles with the plasma membrant releasing insulin.

74

What does an increase in cytosolic Ca++ cause?

It triggers the fusion of insulin-containing vesicles with the plasma membrant releasing insulin.

75

What are some of the symptoms of decreased supply of glucose to the brain?

Lightheadedness, dizziness, coma

75

What are some of the symptoms of decreased supply of glucose to the brain?

Lightheadedness, dizziness, coma

76

What is the decreased supply of glucose to the brain due to?

A slow rate of glucose transport through the blood brain barrier.

76

What is the decreased supply of glucose to the brain due to?

A slow rate of glucose transport through the blood brain barrier.

77

What are the characteristics of the Neural Blood-Brain barrier?

1. Tight junctions between endothelial cells; 2. Narrow intercellular space; 3. Lack of pinocytosis; 4. Continuous basement membrane; 5. Glucose transporters in both membranes.

77

What are the characteristics of the Neural Blood-Brain barrier?

1. Tight junctions between endothelial cells; 2. Narrow intercellular space; 3. Lack of pinocytosis; 4. Continuous basement membrane; 5. Glucose transporters in both membranes.

78

What phosphorylates glucose once it enters a cell?

Hexokinase (HK)

78

What phosphorylates glucose once it enters a cell?

Hexokinase (HK)

79

What are the different metabolic pathways that glucose-6-phosphate can enter?

Glycolysis; Pentose Phosphate pathway; Glycogen Synthesis

79

What are the different metabolic pathways that glucose-6-phosphate can enter?

Glycolysis; Pentose Phosphate pathway; Glycogen Synthesis

80

What are the functions of glucose phosphorylation?

Controls the amount of glc taken up by cells; activates glc for further metabolism; keeps glc within cell; determines the direction of glc metabolism

80

What are the functions of glucose phosphorylation?

Controls the amount of glc taken up by cells; activates glc for further metabolism; keeps glc within cell; determines the direction of glc metabolism

81

What enzyme converts glucose-6-phosphate back to glucose?

Glucose-6-phosphatase

81

What enzyme converts glucose-6-phosphate back to glucose?

Glucose-6-phosphatase

82

What catalyzes the first step in glucose metabolism?

Hexokinase (HK)

82

What catalyzes the first step in glucose metabolism?

Hexokinase (HK)

83

What is the first step in glucose metabolism?

The transfer of phosphate from ATP to glucose resulting in glucose-6-phosphate

83

What is the first step in glucose metabolism?

The transfer of phosphate from ATP to glucose resulting in glucose-6-phosphate

84

What is HK IV also called?

Glucokinase (GK)

84

What is HK IV also called?

Glucokinase (GK)

85

What tissues are GK distributed in?

Liver, B-cells of pancreas

85

What tissues are GK distributed in?

Liver, B-cells of pancreas

86

What is the Km for HK?

~0.1mM or lower

86

What is the Km for HK?

~0.1mM or lower

87

What is the KM for GK?

10-20mM

87

What is the KM for GK?

10-20mM

88

What is HK inhibited by?

Glu-6-Phosphate

88

What is HK inhibited by?

Glu-6-Phosphate

89

What is GK induced by?

Insulin

89

What is GK induced by?

Insulin

90

Where is glucose-6-phosphatase found?

In the liver and kidney

90

Where is glucose-6-phosphatase found?

In the liver and kidney

92

What is the function of glycolysis?

Oxidation of glucose to generate ATP and lactate under anaerobic conditions via oxygen-independent substrate level phosphorylation

92

What is the function of glycolysis?

Oxidation of glucose to generate ATP and lactate under anaerobic conditions via oxygen-independent substrate level phosphorylation

93

What is pyruvate further oxidized by?

The PDH complex, the citric acid cycle and the ETC and oxidation phosphorylation

93

What is pyruvate further oxidized by?

The PDH complex, the citric acid cycle and the ETC and oxidation phosphorylation

94

Where are the glycolytic enzymes found?

In the cytosol

94

Where are the glycolytic enzymes found?

In the cytosol

95

T/F Glycolysis is oxygen independent

TRUE

95

T/F Glycolysis is oxygen independent

TRUE

96

What does the metabolism of the products depend on?

The availability of oxygen

96

What does the metabolism of the products depend on?

The availability of oxygen

97

What happens to pyruvate under aerobic conditions?

It is completely oxidized and electrons from glycolytic NADH enter the mitochondria for ATP generation.

97

What happens to pyruvate under aerobic conditions?

It is completely oxidized and electrons from glycolytic NADH enter the mitochondria for ATP generation.

98

What happens to pyruvate under anaerobic conditions?

Pyruvate and NADH are used to form lactate via the LDH reaction.

98

What happens to pyruvate under anaerobic conditions?

Pyruvate and NADH are used to form lactate via the LDH reaction.

99

What is the significance of the LDH reaction?

NAD+ is regenerated for glycolysis.

99

What is the significance of the LDH reaction?

NAD+ is regenerated for glycolysis.

100

How many ATPs are formed per glucose oxidized to pyruvate?

2

100

How many ATPs are formed per glucose oxidized to pyruvate?

2

101

What are the shuttles that transfer electrons from glycolytic formed NADH into the mitochondria?

Malate shuttle and glycerol phosphate shuttle

101

What are the shuttles that transfer electrons from glycolytic formed NADH into the mitochondria?

Malate shuttle and glycerol phosphate shuttle

102

What does the energy utilizing phase involve?

Phosphorylation of glucose by HK or GK and PFK-1 to form fru-1,6-bisphosphate

102

What does the energy utilizing phase involve?

Phosphorylation of glucose by HK or GK and PFK-1 to form fru-1,6-bisphosphate

103

How many ATPs are required for the energy-utilizing phase?

2

103

How many ATPs are required for the energy-utilizing phase?

2

104

What does the energy-generating phase involve?

Clevage by aldolase; oxidation by glyceraldehyde-3-P dehydrogenase with NADH formation; and synthesis of ATP

104

What does the energy-generating phase involve?

Clevage by aldolase; oxidation by glyceraldehyde-3-P dehydrogenase with NADH formation; and synthesis of ATP

105

How many moles of ATP are produced from the energy-generating phase?

4

105

How many moles of ATP are produced from the energy-generating phase?

4

106

how many substrate-level phosphorylation reactions occur during the energy-generating phase?

2

106

how many substrate-level phosphorylation reactions occur during the energy-generating phase?

2

107

What sugars other than glucose can feed carbons into the glycolytic pathway?

fructose, galactose, mannose, pentose sugars, glycerol

107

What sugars other than glucose can feed carbons into the glycolytic pathway?

fructose, galactose, mannose, pentose sugars, glycerol

108

T/F GK has a high specificity for glucose.

TRUE

108

T/F GK has a high specificity for glucose.

TRUE

109

What is phosphofructokinase inhibited by?

ATP and citrate

109

What is phosphofructokinase inhibited by?

ATP and citrate

110

What is phosphofructokinase activated by?

AMP and Fru-2,6-bisphosphate

110

What is phosphofructokinase activated by?

AMP and Fru-2,6-bisphosphate

111

What is an important regulator of glycolysis and gluconeogenesis?

Fru-2-6-bisphosphate

111

What is an important regulator of glycolysis and gluconeogenesis?

Fru-2-6-bisphosphate

112

What lowers the concentration of fru-2,6-bisphosphate?

Glucagon acting through cAMP

112

What lowers the concentration of fru-2,6-bisphosphate?

Glucagon acting through cAMP

113

T/F The conc of Fru-2,6-bisphosphate is high in the fed state and low in the fasting state.

TRUE

113

T/F The conc of Fru-2,6-bisphosphate is high in the fed state and low in the fasting state.

TRUE

114

What does the low conc of fru-2,6-bisphosphate cause?

It decreases glycolysis and increases gluconeogenesis

114

What does the low conc of fru-2,6-bisphosphate cause?

It decreases glycolysis and increases gluconeogenesis

115

What is pyruvate kinase inhibited by?

ATP and alanine

115

What is pyruvate kinase inhibited by?

ATP and alanine

116

What is pyruvate kinase activated by?

Fru-1,6-P2

116

What is pyruvate kinase activated by?

Fru-1,6-P2

117

What inactivates pyruvate kinase?

It being phosphorylated by glucagon via protein kinase A; promoting gluconeogenesis

117

What inactivates pyruvate kinase?

It being phosphorylated by glucagon via protein kinase A; promoting gluconeogenesis

118

What does the alanine inhibition of hepatic PK promote?

Gluconeogenesis

118

What does the alanine inhibition of hepatic PK promote?

Gluconeogenesis

119

How many moles of ATP are formed for each mole of NADH oxidized?

2.5

119

How many moles of ATP are formed for each mole of NADH oxidized?

2.5

120

How many moles of ATP are formed for each mole of FADH2 oxidized?

1.5

120

How many moles of ATP are formed for each mole of FADH2 oxidized?

1.5

121

What compound dereases the affinity of hemoglobin for oxygen?

2,3-BPG

121

What compound dereases the affinity of hemoglobin for oxygen?

2,3-BPG

122

Where in 2,3-BPG found in high concentration?

RBC

122

Where in 2,3-BPG found in high concentration?

RBC

123

What is lost when 2,3-BpG is synthesized?

An ATP

123

What is lost when 2,3-BpG is synthesized?

An ATP

124

What can 2,3-BPG be converted to that will re-enter the glycolytic pathway?

3-phosphoglycerate

124

What can 2,3-BPG be converted to that will re-enter the glycolytic pathway?

3-phosphoglycerate

125

What is substrate level phosphorylation?

The creation of a high-energy phosphate bond in a metabolite by a mechanism other than electron flow in the mitochondria membrane.

125

What is substrate level phosphorylation?

The creation of a high-energy phosphate bond in a metabolite by a mechanism other than electron flow in the mitochondria membrane.

126

What is AST?

Aspartate amino transferase; intracellular enzymes in amion acid and carbohydrate metabolism.

126

What is AST?

Aspartate amino transferase; intracellular enzymes in amion acid and carbohydrate metabolism.

127

What is an end-product of anaerobic glycolysis?

Lactate

127

What is an end-product of anaerobic glycolysis?

Lactate

128

What is lactate produced by?

Erythrocytes and by skeletal muscle after exercise.

128

What is lactate produced by?

Erythrocytes and by skeletal muscle after exercise.

129

What is lactate normally metabolized by?

Liver and cardiac muscle

129

What is lactate normally metabolized by?

Liver and cardiac muscle

130

Under what conditions will lactate increase?

If there is poor delivery of oxygen to tissues and the oxygen levels are insufficient to support normal aerobic oxidation of glucose.

130

Under what conditions will lactate increase?

If there is poor delivery of oxygen to tissues and the oxygen levels are insufficient to support normal aerobic oxidation of glucose.

131

What does lactate production form?

Hydrogen ions

131

What does lactate production form?

Hydrogen ions

132

What does excess production of lactate result in?

lactate acidosis

132

What does excess production of lactate result in?

lactate acidosis

133

What does tissue hypoxia result in?

Increased lactate production through increased NADH levels; Type A lactic acidosis

133

What does tissue hypoxia result in?

Increased lactate production through increased NADH levels; Type A lactic acidosis

134

What is Type B lactic acidosis?

Lactate accumulation in the blood in the absence of tissue hypoxia; severe hepatic failure

134

What is Type B lactic acidosis?

Lactate accumulation in the blood in the absence of tissue hypoxia; severe hepatic failure

135

What does alcohol ingestion do?

Increases NADH levels; resulting in conversion of pyruvate to lactate.

135

What does alcohol ingestion do?

Increases NADH levels; resulting in conversion of pyruvate to lactate.

136

What decreases the activity of the pyruvate dehydrogenase complex, causing pyruvate to accumulate and form lactate?

Thiamine deficiency (common in alcoholics)

136

What decreases the activity of the pyruvate dehydrogenase complex, causing pyruvate to accumulate and form lactate?

Thiamine deficiency (common in alcoholics)

137

What is the anion gap?

The difference between the commonly measured serum anions and cations; around 12-18 mEq/L

137

What is the anion gap?

The difference between the commonly measured serum anions and cations; around 12-18 mEq/L

138

What are the disorders associated with glycolysis?

Red cell glycolytic deficiencies; pyruvate dehydrogenase deficiency; PFK-1 deficiency

138

What are the disorders associated with glycolysis?

Red cell glycolytic deficiencies; pyruvate dehydrogenase deficiency; PFK-1 deficiency

139

What are hemolytic anemias caused by?

Deficiencies of RBC glycolytic enzymes such as hexokinase, gluc-6-phosphate isomerase, aldolase, triose phosphatte dehydrogenase, enolase, and pyruvate kinase; results in a deficiency of ATP

139

What are hemolytic anemias caused by?

Deficiencies of RBC glycolytic enzymes such as hexokinase, gluc-6-phosphate isomerase, aldolase, triose phosphatte dehydrogenase, enolase, and pyruvate kinase; results in a deficiency of ATP

140

What does pyruvate dehydrogenase deficiency cause?

Accumulation of pyruvate and lactate; resulting in lactic acidosis

140

What does pyruvate dehydrogenase deficiency cause?

Accumulation of pyruvate and lactate; resulting in lactic acidosis

141

What is muscle PFK-1 deficiency classified as?

A glycogen storage disease

141

What is muscle PFK-1 deficiency classified as?

A glycogen storage disease

142

Which vitamins and coenzymes are involved in glycolysis?

Thiamine (B1), Riboflavin (B2), Niacin (nicotinic acid), Pantothenic acid (B5), Pyridoxine (B6)

142

Which vitamins and coenzymes are involved in glycolysis?

Thiamine (B1), Riboflavin (B2), Niacin (nicotinic acid), Pantothenic acid (B5), Pyridoxine (B6)

143

What is the coenzyme for Thiamine?

Thiamine pyrophosphate (TPP)

143

What is the coenzyme for Thiamine?

Thiamine pyrophosphate (TPP)

144

What is the role of Thiamine?

Required for the complete oxidation of glucose via the PDH complex and the citric acid cycle.

144

What is the role of Thiamine?

Required for the complete oxidation of glucose via the PDH complex and the citric acid cycle.

145

What are the coenzymes for Riboflavin?

FAD and FADH2; FMN and FMNH2

145

What are the coenzymes for Riboflavin?

FAD and FADH2; FMN and FMNH2

146

What is the role of Riboflavin?

Required for the complete oxidation of glucose via pyruvate by the PDH complex and the citric acid cycle. Used in the glycerol-phosphate shuttle.

146

What is the role of Riboflavin?

Required for the complete oxidation of glucose via pyruvate by the PDH complex and the citric acid cycle. Used in the glycerol-phosphate shuttle.

147

What are the coenzymes for Niacin?

NAD+, NADH, NADP+, NADPH

147

What are the coenzymes for Niacin?

NAD+, NADH, NADP+, NADPH

148

What is the role of Niacin?

Required cofactor in oxidation-reduction reactions. Used in the Malate Shuttle, LDH reaction, PDH complex, and citric acid cycle.

148

What is the role of Niacin?

Required cofactor in oxidation-reduction reactions. Used in the Malate Shuttle, LDH reaction, PDH complex, and citric acid cycle.

149

What is the coenzyme for Pantothenic acid?

Coenzyme A

149

What is the coenzyme for Pantothenic acid?

Coenzyme A

150

What is the role of Pantothenic acid?

Required for the complete oxidation of glucose via pyruvate by the PDH complex and the citric acid cycle. Involved in most reactions involving acyl group transfer and metabolism

150

What is the role of Pantothenic acid?

Required for the complete oxidation of glucose via pyruvate by the PDH complex and the citric acid cycle. Involved in most reactions involving acyl group transfer and metabolism

151

What is the coenzyme for Pyridoine?

Pyridoxal phosphate (PLP)

151

What is the coenzyme for Pyridoine?

Pyridoxal phosphate (PLP)

152

What is the role of Pyridoxine?

Used in transaminations.

152

What is the role of Pyridoxine?

Used in transaminations.

153

What is the principle pathway by which every cell generates ATP from glucose?

Glycolysis

153

What is the principle pathway by which every cell generates ATP from glucose?

Glycolysis

154

T/F Glycolysis occurs under both aerobic and anaerobic conditions.

TRUE

154

T/F Glycolysis occurs under both aerobic and anaerobic conditions.

TRUE

155

What is the subcellular localization of glycolysis?

Cytosol

155

What is the subcellular localization of glycolysis?

Cytosol

156

What does glycolysis begin with?

Either glucose or glycogen

156

What does glycolysis begin with?

Either glucose or glycogen

157

What are the two phases of glycolysis?

Preparative phase; ATP-generating phase

157

What are the two phases of glycolysis?

Preparative phase; ATP-generating phase

158

How many NADHs are generated in the ATP-generating phase?

2

158

How many NADHs are generated in the ATP-generating phase?

2

159

What are the regulated steps of glycolysis?

Glucose ->G-6-P (HK); Fru-6-phos->Fru-1,6-bisphos (phosphofructokinase-1)

159

What are the regulated steps of glycolysis?

Glucose ->G-6-P (HK); Fru-6-phos->Fru-1,6-bisphos (phosphofructokinase-1)

160

How many triose phosphates are generated in the preparative phase of glycolysis?

2

160

How many triose phosphates are generated in the preparative phase of glycolysis?

2

161

What is lactate oxidized back to?

Pyruvate

161

What is lactate oxidized back to?

Pyruvate

162

What is pyruvate used to synthesize?

Glucose

162

What is pyruvate used to synthesize?

Glucose

163

Under aerobic conditions what is pyruvate completely oxidized to?

CO2 by pyruvate dehydrogenase and the TCA cycle in the mitochondria.

163

Under aerobic conditions what is pyruvate completely oxidized to?

CO2 by pyruvate dehydrogenase and the TCA cycle in the mitochondria.

164

Where does the oxidation of cytosolic NADH back to NAD+ occur?

In the mitochondria via the electron transport chain.

164

Where does the oxidation of cytosolic NADH back to NAD+ occur?

In the mitochondria via the electron transport chain.

165

T/F the mitochondrial inner membrane is impermeable to NADH

TRUE

165

T/F the mitochondrial inner membrane is impermeable to NADH

TRUE

166

What is the enzyme that works in the glycerol-3-phosphate shuttle?

glycerol 3-P dehydrogenase

166

What is the enzyme that works in the glycerol-3-phosphate shuttle?

glycerol 3-P dehydrogenase

167

What precursors for bioshythetic pathways does glycolysis provide?

Five-carbon sugars; 2,3-bis phosphoglycerate; serine; alanine; Glutamate; Fatta acids; Glycerol-P

167

What precursors for bioshythetic pathways does glycolysis provide?

Five-carbon sugars; 2,3-bis phosphoglycerate; serine; alanine; Glutamate; Fatta acids; Glycerol-P

168

What are the major requlatory enzymes of glycolysis?

Hexokinase, Phosphofructokinase; Pyruvate kinase; Pyruvate dehydrogenase

168

What are the major requlatory enzymes of glycolysis?

Hexokinase, Phosphofructokinase; Pyruvate kinase; Pyruvate dehydrogenase

169

How does ATP serve as an inhibitor of PFK-1?

ATP binds to the substrate binding site as well as the inhibitory site.

169

How does ATP serve as an inhibitor of PFK-1?

ATP binds to the substrate binding site as well as the inhibitory site.

170

How does citrate serve as an inhibitor of PFK-1?

It is a sign that the citric acid cycle is saturated and glycolysis is not needed.

170

How does citrate serve as an inhibitor of PFK-1?

It is a sign that the citric acid cycle is saturated and glycolysis is not needed.

171

How does AMP serve as an activator of PFK-1?

It binds to the activator site and increase of PFK-1 for F-6-P.

171

How does AMP serve as an activator of PFK-1?

It binds to the activator site and increase of PFK-1 for F-6-P.

172

What is the most potent activator of PFK-1?

Fructose 2,6 bis-phosphate.

172

What is the most potent activator of PFK-1?

Fructose 2,6 bis-phosphate.

173

What does F-2,6-P do?

Binds to PFK-1 and removes the inhibitory effect of ATP and turns glycolysis ON.

173

What does F-2,6-P do?

Binds to PFK-1 and removes the inhibitory effect of ATP and turns glycolysis ON.

174

What is pyruvate dehydrogenase regulated by?

The rate of ATP utilization

174

What is pyruvate dehydrogenase regulated by?

The rate of ATP utilization

176

What must all carbs be digested to in order to be metabolized?

Monosaccharides

176

What must all carbs be digested to in order to be metabolized?

Monosaccharides

177

What are the major dietary carbohydrates?

Starch, sucrose, lactose

177

What are the major dietary carbohydrates?

Starch, sucrose, lactose

178

What is starch composed of?

Amylose and amylopectin

178

What is starch composed of?

Amylose and amylopectin

179

What is amylose?

Unbranched chains composed of glucose residues linked alpha-1,4-

179

What is amylose?

Unbranched chains composed of glucose residues linked alpha-1,4-

180

What is amylopectin?

Alpha-1,4- linked chains with alpha 1-6-linked branches.

180

What is amylopectin?

Alpha-1,4- linked chains with alpha 1-6-linked branches.

181

What is sucrose made up of?

Glucose and Fructose

181

What is sucrose made up of?

Glucose and Fructose

182

What is lactose made up of?

Galactose and Glucose

182

What is lactose made up of?

Galactose and Glucose

183

What are the two types of amylase?

Salivary and pancreatic

183

What are the two types of amylase?

Salivary and pancreatic

184

Where does pancreatic amylase work?

In the lumen of the intestine

184

Where does pancreatic amylase work?

In the lumen of the intestine

185

How do salivary and pancreatic amylases begin the process of digestion of polysaccarides?

By hydrolyzing starch and glycogen.

185

How do salivary and pancreatic amylases begin the process of digestion of polysaccarides?

By hydrolyzing starch and glycogen.

186

What linkages does amylase hydrolyze?

Alpha-1,4-glycosidic linkages forming maltose, maltotriose, glucose, and limit dextrins

186

What linkages does amylase hydrolyze?

Alpha-1,4-glycosidic linkages forming maltose, maltotriose, glucose, and limit dextrins

187

Where are disaccharidases located?

In the intestinal villa

187

Where are disaccharidases located?

In the intestinal villa

188

What is the role of the glucoamylase complex?

Cleaves glucose from the nonreducing end of oligosaccharides, and cleaves maltose and isomaltase.

188

What is the role of the glucoamylase complex?

Cleaves glucose from the nonreducing end of oligosaccharides, and cleaves maltose and isomaltase.

189

How much of the total intestinal maltase activity does the glucoamylase complex have?

20%

189

How much of the total intestinal maltase activity does the glucoamylase complex have?

20%

190

How much of the total intestinal isomaltase activity does the glucoamylase complex have?

10%

190

How much of the total intestinal isomaltase activity does the glucoamylase complex have?

10%

191

What is the role of the sucrase-isomaltase complex?

Cleaves alpha-1,4-, and alpha-1,6-linkages.

191

What is the role of the sucrase-isomaltase complex?

Cleaves alpha-1,4-, and alpha-1,6-linkages.

192

How much of the total intestinal maltase activity does the Sucrase-isomaltase complex have?

80%

192

How much of the total intestinal maltase activity does the Sucrase-isomaltase complex have?

80%

193

How much of the total intestinal isomaltase activity does the sucrase-isomaltase complex have?

>90%

193

How much of the total intestinal isomaltase activity does the sucrase-isomaltase complex have?

>90%

194

Which end does glucoamylase work first?

The non-reducing end

194

Which end does glucoamylase work first?

The non-reducing end

195

What does lactase do?

Hydrolyzes the beta-1,4-linkages found in lactose, and in some complex lipids.

195

What does lactase do?

Hydrolyzes the beta-1,4-linkages found in lactose, and in some complex lipids.

196

What does trehalase do?

Hydrolyzes the alpha-1,1,-linkage found in trehalose

196

What does trehalase do?

Hydrolyzes the alpha-1,1,-linkage found in trehalose

197

What is trehalose?

A disaccharide composed of 2 glucose residues linked alpha-1,1-)

197

What is trehalose?

A disaccharide composed of 2 glucose residues linked alpha-1,1-)

198

What is the activity of maltase?

Hydrolyzes alpha-1,4,-glycosidic linkages; cleaves maltose

198

What is the activity of maltase?

Hydrolyzes alpha-1,4,-glycosidic linkages; cleaves maltose

199

What is the activity of Isomaltase?

Hydrolyzes alpha-1,6,-glycosidic linkages; cleaves isomaltose

199

What is the activity of Isomaltase?

Hydrolyzes alpha-1,6,-glycosidic linkages; cleaves isomaltose

200

What is the activty of sucrase?

Hydrolyzes B-1,4 gylcosidis linkages; hydrolyze lactose to Glc and Gal

200

What is the activty of sucrase?

Hydrolyzes B-1,4 gylcosidis linkages; hydrolyze lactose to Glc and Gal