FOM 3.4.2 Flashcards

1
Q

What percent of daily caloric requirement are from carbs?

A

55%

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2
Q

What is some of the substrates for glycolysis?

A

Fructose, galactose, and glucose

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3
Q

What tissue is most dependent on glucose?

A

The brain

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4
Q

What enzymes are responsible for adding and removal of glycogen branches?

A

Branching enzyme and debranching enzyme

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5
Q

What is the first reaction needed before glucose-1-phosphate can enter glycolysis?

A

It needs to be converted into G-6-P by phosphoglucomutase

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6
Q

After G-1-P is released from glycogen and converted to G-6-P what is it converted to by what before being released into the blood?

A

It is converted it free glucose by glucose-6-phosphatase

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7
Q

At what steps in glycolysis is energy input needed to drive it forward?

A

The enzymes that input energy required for glycolysis are hexokinase (step 1) and phosphofructokinase (step 3)

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8
Q

What are the glycolytic reactions that produce ATP?

A

Phosphoglycerate kinase and pyruvate kinase both work and create 2 ATP molecules each.

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9
Q

What is the only reaction that produces NADH from NAD+?

A

Glyceraldehyde-3-phosphate dehydrogenase

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10
Q

What is a common metal cofactor in kinases?

A

Magnesium is a common co-factor because it is a divalent cation that stabilizes the phosphates on ATP.

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11
Q

What is the process by which NAD+ is regenerated in the absence of O2? Can this be a good clinical test?

A

NADH created from the glyceraldehyde 3 phosphate dehydrogenase reaction is then shuttled to react with pyruvate and create lactate. This can be used as a good clinical test because it can measure how well the mitochondria based on the amount of NADH are being used in the ETC.

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12
Q

What is the fate of NADH that is produced from glycolysis?

A

NADH is shuttled through the malate-aspartate shuttle system or the glycerophosphate shuttle.

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13
Q

What is the importance of tightly regulating glycolysis?

A

Both glycolysis and gluconeogenesis are occurring in the cytsoplasm of the cell.

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14
Q

What are the reactions that are thought to be essentially irreversible and how does this relate to their free energies?

A

Hexokinase (reaction 1) has deltaG of 27

Phosphofructokinase (reaction 3) has a deltaG of 26

Pyruvate Kinase (reaction 10) has a deltaG of nearly 14

Because of their large negative Values these reactions are seen as essentially irreversible because it would take a large input of energy to do the reverse reaction.

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15
Q

What is the importance of the reactions with smaller deltaG?

A

Allows the cell to only have to regulate a few enzymes tightly and the rest will drive it forward

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16
Q

What are the important factors of the pentose phosphate pathway?

A

It is the main source of NADPH in the cell and it creates ribose sugars

17
Q

What is the importance of fructose-2,6-bisphosphate?

A

It acts as a main regulatory molecule for glycolysis. It allosterically activates phosphofructokinase (glycolysis enzyme) and allosterically inhibits fructose bisphosphatase (gluconeogenic enzyme).

18
Q

What are the roles of PFK-2 and FBPase-2?

A

These two enzymes control the formation and deformation of F-2,6-BP.

PFK-2 uses ATP and creates it and FBPase2 uses h2o and gets rid of it.

19
Q

What is the fate of glucose in the liver?

A

It is taken to the muscle and turned into alanine via a pyruvate intermediate. The alanine in then shuttled back into the into the liver.

20
Q

What is required for glycogen synthase?

A

Glucose must react with UTP and create UDP glucose. This can then be added to glycogen by glycogen synthase.

21
Q

How can deficiency in erthrocyte pyruvate kinase result in anemia?

A

Red blood cells lack a mitochondria so they rely on glycolysis for the production of their energy. A reduction in the amount of PYK would cause a back up in the other previous reactions. 1,3-BPG could then be changed into 2,3-BPG. Higher levels of this would cause the the release of o2 from the heme.

22
Q

How could a hexokinase deficiency in erythrocytes be disruptive?

A

A hexokinase deficiency would cause not enough 2,3-BPG to be made. Thus the hemoglobin would have an increased affinity for the O2 and not want to release it at the correct time.

23
Q

How can a fructose intolerance be applied to this and what is the mechanism?

A

Due to a hereditary conditiong that alters the function of aldolase F-1-P cannot be turned into glyceraldehyde. This means that there is a buildup of Fru-1P, which cannot do anything in the cell but take up ATP. This means there is a reduced amount of available ATP that is going to actually be helpful, and can lead to problems like what is demonstrated.