Lecture 16B Flashcards

(70 cards)

1
Q

The end a free anomeric carbon is the ____.

A

Reducing End

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2
Q

Polymeric form of glucose that is found in special granules primarily in the liver and skeletal muscles of mammals.

A

Glycogen

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3
Q

May represent up to 10% f the weight of the liver and 1-2% of the weight of skeletal muscle.

A

Glycogen

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4
Q

True-False; Storage of glycogen reduces the concentration of glucose from 400 mM to 0.01uM

A

True

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5
Q

____ glycogen can be exhausted in less than an hour during a vigorous workout;
____ glycogen can last 12-24 hours.

A

Muscle

Liver

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6
Q

Glycogen Breakdown requires which 3 enzymes?

A

Glycogen Phosphorylase
Glycogen Debranching Enzyme
Phosphoglucomutase

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7
Q

Which enzyme removes glucose residues from the non-reducing ends of glycogen via attack by inorganic phosphate?

A

Glycogen Phosphorylase

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8
Q

Which enzyme produces Glucose-1-phosphate?

A

Glycogen Phosphorylase

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9
Q

Energy of the glycosidic bond is preserved by the formation of a

A

Phosphodiester Bond

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10
Q

Why does direct production of G6P not occur?

A

It would not result in hydrolysis of a glucose residue from the glycogen chain and it is energetically unfavorable.

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11
Q

Glycogen residues are removed from glycogen by

A

Glycogen phosphorylase

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12
Q

Pyridoxal phosphate is a cofactor with which enzyme?

A

Glycogen Phosphorylase

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13
Q

Glycogen Phosphorylase works on _____ ends until it reaches four residues from an (__ ->__) branch point.

A

non-reducing

alpha 1->6

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14
Q

Transfers a block of 3 residues to the non-reducing end of the chain.

A

Debranching enzyme

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15
Q

Cleaves the single remaining alpha 1->6 linked glucose

A

Debranching Enzyme

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16
Q

Glucose 1- Phosphate is converted to G6P by

A

Phosphoglucomutase

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17
Q

This enzyme first generates G16P then G6P in a freely reversible reaction

A

Phosphoglucomutase

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18
Q

Phosphoglucomutase acts on which Amino Acid Residue?

A

Serine

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19
Q

G6P enters glycolysis in order to produce for muscle contraction in which organ?

A

Muscle

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20
Q

G6P is dephosphorylated by G6Phosphatase to produce glucose which is then exported to the blood stream. Which organ does this happen in?

A

Endoplasmic Reticulum

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21
Q

What leads to glycogen storage disease?

A

Genetic defects is G6Pase or T1 (specific transporter)

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22
Q

G6P is dephosphorylated in the ___ for transport out of the ____.

A

liver

liver

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23
Q

G6P is transported into the liver via and out of the liver by.

A

T1 (into liver)

T2 (out of liver)

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24
Q

What is the T3 transporter used for?

A

Phosphate out of the liver

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25
Many anabolic reactions involving sugars require them to be activated. Most often this requires attachment to ___.
UDP
26
Is the formation of UDP reversible or irreversible?
Irreversible; due to subsequent hydrolysis of PPi
27
What is the good leaving group, making nucleophilic reactions very favorable?
Nucleotidyl Group
28
___ is the starting point for glycogen synthesis.
G6P
29
G6P is then converted to ___ by ___.
G1P | Phosphoglucomutase
30
___ converts G1P + UTP -> UDP-glucose and PPi
UDP-glucose pyrophosphorylase
31
Glycogen synthase requires a primer of at least 8 glucose residues joined in a
alpha 1 -> 4 linkage
32
Glycogen Synthesis primer is supplied by
Glycogenin
33
Glycogen covalently attaches a glucose residue to
Tyr-194 residue
34
Glycogenin then forms a tight complex with glycogen synthase and the nascent chain is extended by up to 7 more residues by _____.
Glycogenin
35
Glycogen synthase begins to extend the chain, eventually disassociating from ____.
Glycogenin
36
Glycogenin remans buried within the glycogen molecule, covalently attached to the ______.
single reducing end
37
Branches are formed by ____ enzyme, which transfers 6 or 7 glucose residues from the nonreducing end of a glycogen chain containing at least 11 glucose residues to a C6 hydroxyl group of an interior residue.
Glycogen-Branching Enzyme
38
Glycogen regulations occurs primarily through which 2 enzymes?
Glycogen Phosphorylase/Glycogen Synthase
39
This enzyme is regulated allosterically and hormonally. It exists in 2 interconvertible forms.
Glycogen Phosphorylase
40
What is the inactive form of Phosphorylase?
Phosphorylase B
41
How is Phosphorylase converted to the active form?
Phosphorylase A; phosphorylation
42
How is phosphorylation regulated?
Hormonally
43
Glucose is an ____ inhibitor of the liver enzyme.
Allosteric
44
Phosphorylase B predominates in ____, but epinephrine triggers phosphorylation to the a state.
resting muscle
45
Phosphorylation state of glycogen phosphorylase is controlled by
Phosphorylase B Kinase
46
Phosphorylase B Kinase is controlled by _____ or ___- via signaling cascade involving the 2nd msgr cAMP.
Glucagon | Epinephrine
47
The enzyme cascade induced by cAMP allows for tremendous amplification of the
initial signal
48
_____ converts phosphorylase a to the inactive b form once the extracellular signal is removed.
Phosphoryla a phosphatase (pp1)
49
Which 2 allosteric activators contribute to glucose release.
Ca -> activates phosphorylase b by promoting conversion to the a form AMP -> acts as an allosteric activator to the a form
50
Active form of glycogen synthase is ___.
unphosphorylated
51
Dephosphorylation is catalyzed by _______, which is part of the glycogen particle.
Phosphorylation phosphatase-1
52
Which 2 enzymes are regulated by phosphorylation-dephosphorylation cycle and are never fully active simultaneously.
Glycogen Synthase | Phosphoprotein phosphatase-1
53
Phosphorylation states are regulated by the hormones ___ and ___.
insulin | glucagon
54
Insulin is released by the ___ and influences glucagon synthase and breakdown via a signaling cascade that involves numerous phosphorylation events.
Pancreas
55
Insulin increases glucose into the
Muscle
56
Insulin stimulates the activity of muscle
Hexokinase
57
Insulin activates
Glycogen Synthase
58
Increased hexokinase activity enables activation of
Glucose
59
Glycogen synthase makes glycogen for
energy storage
60
What is the well fed state?
High blood glucose
61
During the well fed state, what hormone is released? and and what is inactivated and what is activated
Insulin Inactivated -> GSK3 Activated -> PP1 (Glycogen synthase)
62
What transporters are used during the well fed state?
GLUT2; increase in glucose concentration activates hexokinase, making G6P for glycogen synthesis
63
During the fasting state, which hormone is activated?
Glucagon
64
Which enzymes are activated and inactivated during the well-fed state?
Activated -> PKA and Glycogen Phosphorylase Inactivated ->Glycogen Synthase
65
What is the end result in a fasting state?
Increase blood glucose levels via Glucagon; | Activate glycogen phosphorylase and inactivate glycogen synthase
66
Gluconeogenesis is also activated during which state? fasting or well fed?
Fasting
67
Gluconeogenesis is also activated by a decrease in
F26BP
68
Glycolysis is inactivated by inactivation of
Pyruvate Kinase
69
Control of carb metabolism in the liver vs. the muscle; | What is the difference?
In the liver, Glucose 6P goes to the blood glucose; Pyruvate always goes to Glucose 6P In the muscle, Glycogen -> Glucose 6P -> Pyruvate
70
In which organ system does G6P get converted to Pyruvate?
Muscle