Carbohydrate Metabolism Flashcards

(72 cards)

1
Q

Enzyme that breaks down amylose and amylopctin

A

Amylase

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2
Q

Amylase will breakdown amylose and amylopectin into?

A

Dextrin and maltose

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3
Q

% of starch broken down in the mouth

A

5%

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4
Q

mixture of partially digested food and digestive
juices

A

Chyme

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5
Q

breaks down dextrin into shorter carbohydrate
chain.

A

Pancreatic Amylase

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6
Q

what enzymes?
1. Sucrose → Glucose + Fructose
2. Maltose → Glucose + Glucose
3. Lactose → Glucose + Galactose

A
  1. Sucrase
  2. Maltase
  3. Lactase
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7
Q

Once broken down into monosaccharides, compounds
are ready to enter bloodstream via facilitated diffusion &
active transport
1. _____→ fructose
2._____→ glucose and galactose

A
  1. Facilitated Diffusion
  2. Active Transport
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8
Q

First organ to receive monosaccharides:

A

Liver

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9
Q

Liver converts galactose to?

A

Glucose

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10
Q

Liver Stores glucose as?

A

glycogen

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11
Q

two metabolic pathways of glucose?

A

Glycolysis & pentose phosphate pathway

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12
Q

the process of storing excess glucose
from the bloodstream into the liver and muscles (anabolic)

A

Glycogenesis

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13
Q

the process of utilizing the stored
glucose, in response to demand for glucose in certain
tissues (catabolic)

A

Glycogenolysis

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14
Q

sourcing carbohydrate from noncarbohydrate compounds by a series of metabolic
pathways; the process that transforms non-carbohydrate
substrates (such as lactate, amino acids, and glycerol) into glucose

A

Gluconeogenisis

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15
Q

First stage of glucose metabolism.

A

GLYCOLYSIS

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16
Q

glycolysis takes place where?

A

cytoplasm/cytosol

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17
Q

two phases of glycolysis

A
  1. phosphorylation/priming phase
  2. energy yielding phase
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18
Q

conversion of two molecules glyceraldehyde-3-
phosphate; 2 ATPs are used to prime these reactions

A

phosphorylation of
glucose/Priming phase

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19
Q

Formation of
glyceraldehyde-3-phosphate to pyruvate and coupled
formation of 4 molecules of ATP

A

ENERGY-YIELDING Phase

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20
Q

In all these reactions, the conversion of glucose to product is

A

Oxidation Reaction

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21
Q

when NAD+ is converted to NADH.

reduction or oxidation?

A

reduction

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22
Q

Net Reaction: of glycolysis

A

Glucose + 2ADP + 2Pi → 2 Pyruvate + 2 ATP

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23
Q

5 steps of priming phase:

A

Phosphorylation
Isomerization
Phosphorylation
Cleavage
Isomerization

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24
Q

5 steps of energy yielding phase

A

Oxidation (and phosphorylation)
Transfer of a phosphate group
Isomerization
Dehydration
Transfer of phosphate group

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25
reaction involved in step 1: phosphorylation
Glucose + ATP → Glucose-6-phosphate + ADP
26
reaction involved in step 2: isomerization
Glucose-6-phosphate → Fructose-6-phosphate
27
reaction involved in step 3: Phosphorylation
Fructose-6-phosphate + ATP → Fructose-1,6-bisphosphate + ADP
28
reaction involved in step 4: cleavage
Fructose-1,6-bisphosphate → Glyceraldehyde-3-phosphate + Dihydroxyacetone phosphate
29
reaction involved in step 5: isomerization
Dihydroxyacetone phosphate → Glyceraldehyde-3-phosphate
30
reaction invloved in step 6: oxidation
Glyceraldehyde-3-phosphate + NAD+ + Pi → NADH + 1,3-bisphosphoglycerate + H+
31
reaction involved in step 7: transfer of phosphate group
1,3-bisphosphoglycerate + ADP → 3-phosphoglycerate + ATP
32
reaction involved in step 8: isomerization
3-phosphoglycerate → 2-phosphoglycerate
33
reaction involved in step 9: Dehydration
2-phosphoglycerate → phosphoenolpyruvate + H2O
34
reaction involved in step 10: Transfer of phosphate group
Phosphoenolpyruvate + ADP → Pyruvate + ATP
35
enzymes involved in glycolysis
Hexokinase/Glucokinase Glucose phosphate isomerase Phosphofructokinase Aldolase Triose phosphate isomerase Glyceraldehyde-3-P dehydrogenase Phosphoglycerate kinase Phosphoglyceromutase Enolase Pyruvate Kinase
36
an NADH-linked dehydrogenase that catalyzes the conversion of pyruvate to lactate
Lactate dehydrogenase
37
Glucokinase: is found where?
liver
38
what is hexokinase?
general enzyme that attaches phosphate to any hexose molecule
39
Possible Fates of Pyruvate in Glycolysis:
Aerobic metabolism: pyruvate loses CO2 then forms acetyl-CoA Anaerobic metabolism: Pyruvate becomes acetaldehyde Fermentation: Acetaldehyde is reduced to ethanol Anaerobic glycolysis: Pyruvate is reduced to lactic acid
40
pathway of glucose metabolism that is not for the production of energy.
Pentose-Phosphate Pathway
41
Important for the production of pentoses
Pentose-Phosphate Pathway
42
important for the production of nicotinamide adenine dinucleotide phosphate (NADPH),
Pentose-Phosphate Pathway
43
what is nicotinamide adenine dinucleotide phosphate (NADPH)
a coenzyme critical in the biosynthesis of lipids.
44
what First reaction of Pentose-Phosphate Pathway and its enzyme?
(Glucose-6-phosphate to 6-Phosphogluconate) enzyme: Glucose-6-phosphate dehydrogenase
45
2nd reaction of (PPT) and its enzyme?
(6-Phosphogluconate to Ribulose-5-phosphate) enzyme: 6-phosphogluconate dehydrogenase
46
the first and 2nd reactions of PPT are? oxidative or nonoxidative?
oxidative
47
the remaning reactions of PPT are? oxidative or non oxidative?
nonoxidative
48
two different reactions in which ribulose-5-phosphate isomerizes are catalyzed by?
phosphopentose-3-epimerase and phosphopentose isomerase
49
in the reaction that is catalyzed by phosphopentose-3-epimerase; what is produced?
xylulose-5- phosphate,
50
in the reaction that is catalyzed phosphopentose isomerase; what is produced?
ribose-5-phosphate.
51
it is a necessary building block for the synthesis of nucleic acids (DNA or RNA) and coenzymes such as NADH.
ribose-5-phosphate.
52
In PPT what are the Two enzymes that are responsible for the re shuffling of the carbon atoms of sugars such as ribose-5-phosphate and xylulose-5- phosphate in the remainder of the pathway, which consists of three reactions.
tansketolase and transaldolase
53
Formation of glycogen from excessive glucose in the bloodstream
GLYCOGENESIS
54
Glycogen synthesis is primed by
glycogenin
55
Glucose-6-phosphate reacts with UTP to yield?
UDP-glucose
56
Continuous addition of UDPG to a growing chain. Each step involves formation of a new
α(1→4) glycosidic linkage.
57
At about 8th residue during glycogenisis what takes over in catalyzing the synthesis of glycogen
glycogen synthase
58
At about 12th residue, a _______ catalyzes the attachment of a glucose oligosaccharide through an α(1→6) glycosidic linkage.
branching enzyme
59
the Release of liver glycogen store is triggered by low blood glucose levels.
Glycogenolysis
60
In the first reaction, each glucose residue cleaved from glycogen reacts with phosphate to give? what is the enzyme?
glucose-1-phosphate. enzyme: Glycogen phosphorylase
61
In the second reaction, glucose-1-phosphate is isomerized to give? what is the enzyme?
glucose-6-phosphate enzyme: Phosphoglucomutase
62
Not the reverse of glycolysis
GLUCONEOGENESIS
63
it is an important intermediate between citric acid cycle (Krebs cycle) and gluconeogenesis
Oxaloacetate
64
reversible reactions that differs glycolysis and gluconeogenisis
1. Production of pyruvate from phophoenolpyruvate 2. Production of fructose-1,6-bisphosphate from fructose-6-phosphate 3. Production of glucose-6-phosphate from glucose
65
Why must oxaloacetate be converted to malate?
because oxaloacetate cannot leave the mitochondrion.
66
before leaving the mitochondrion oxaloacetate reduces to?
malate
67
Fructose, upon reaching the liver, undergoes
fructolysis.
68
Galactose, on the other hand, undergoes _____ to become glucose-6-phosphate
leloir pathway
69
Condition in which blood glucose levels are too high due to absence (or low levels) of insulin or insensitivity to the hormone.
Diabetes Mellitus
70
Inherited disorder that prevents the processing of galactose, resulting to the build-up of the compound and can cause serious complications in the body.
Galactosemia
71
Aka Von Gierke’s disease, it affects the ability of the body to release glucose from glycogen stores, with affected people prone to hypoglycemia.
Type I Glycogen Storage Disorder
72
Rare, inherited, and often fatal disorder that disables heart and skeletal muscles caused by mutations in the gene that produce acid alpha glucosidase, an enzyme similar to a debranching enzyme, but in muscle cells.
Pompe Disease