Metabolism 1 & 2 Flashcards

1
Q

Four fates of acetyl coA

A

Lipogenesis
Cholesterol synthesis
Formation of ketone bodies
TCA cycle

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2
Q

What type of reaction is the TCA cycle?

A

Combustion reaction: produces H20, CO2, and ATP

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3
Q

Where does beta-oxidation take place?

A

In the mitochondria

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4
Q

What structures have the highest stores of glycogen?

A

Liver, heart/skeletal muscle

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5
Q

How does amino acid metabolism lead to TCA cycle propagation?

A

Proteins can be broken down either to acetyl coA or to an intermediate in the TCA cycle

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6
Q

Driving force for the coordination of metabolism

A

To provide the brain with glucose. (That and ketone bodies [during starvation] are the only source of fuel for the brain)

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7
Q

Hydration status in stored macromolecules

A

Proteins and carbohydrates are stored in a hydrated state; lipids are stored in an anhydrous state

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8
Q

Ratio of pancreatic amylase release to the amount of starch intake

A

There is a large excess of the enzyme released relative to the amount ingested

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9
Q

Relative amounts of sucrase and lactase

A

Sucrase is generally in great excess; lactase is less abundant

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10
Q

Products of bacterial breakdown of lactose left in the lumen

A

Lactic acid, methane, carbon dioxide, and hydrogen gas

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11
Q

How many mutations of the LCT gene have been identified?

A

9

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12
Q

Lactose anaphylaxis

A

Milk-induced allergic reaction in response to alpha S1 casein

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13
Q

Secondary lactose intolerance

A

Present in children who have recently had gastroenteritis that caused damage to the epithelial lining of the gut; once the epithelial lining is healed, the symptoms resolve

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14
Q

What long-term effects does insulin have on metabolism?

A

Glycolysis and glycogen synthesis

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15
Q

Net products of glycolysis

A

2 pyruvate, 2 ATP, 2 NADH, and 2 water

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16
Q

Daily glucose usage in the brain vs muscle

A

120 g vs 40 g

17
Q

Where are the only glucagon receptors located?

A

On the liver

18
Q

Fate of lysed glycogen in the liver

A

Once the glycogen is cleaved into G6P, the liver does not use it

19
Q

Products of the pentose phosphate pathway

A

NADPH and ribose-5-phosphate

20
Q

Red blood cell metabolism

A

They lack a nucleus and mitochondria, so they depend 100% on glycolysis

21
Q

Function of GLUT2 having lower affinity for glucose

A

All the other GLUT transporters are saturated at normal concentrations of glucose; this allows GLUT2 to be the “override” transporter that is present for excess glucose after a carbohydrate-rich meal

22
Q

Functional components of GLUT transporters

A

12 membrane-spanning helices with intracellular loop between 6th and 7th helices

23
Q

How much of glucose is metabolized in an insulin-independent manner?

24
Q

Three mechanisms of regulation of regulatory enzymes in glycolysis

A

Allosteric in/activation, covalent modifications, and regulation of enzyme synthesis

25
Three regulated enzymes in glycolysis
Hexokinase/glucokinase PFK-1 Pyruvate kinase
26
Glycolysis produces energy in the form of ___
NADH and ATP
27
What can pyruvate be used for in the presence of sufficient energy?
Can be used in protein synthesis
28
Significance of first phosphorylation step
Once glucose is phosphorylated, it is trapped inside the cell and will continue metabolism in one way or another
29
Most highly regulated step of the glycoloysis pathway
Aldolase A (splits F16BP into dihydroxyacetone phosphate and glyceraldehyde 3 P)
30
Deficiency of any of the glycolytic enzymes
Red blood cells become swollen and they burst, causing hemolytic anemia
31
Substrate-level phosphorylation during glycolysis
Occurs during the step where 13BPG is converted to 3PG by phosphoglycerate kinase
32
Glycolytic enzymes producing ATP
Pyruvate kinase and phosphoglycerate kinase
33
Three stages of glycolysis
Stage 1: prepping stage Stage 2: splitting stage Stage 3: oxidoreduction/phosphorylation stage
34
Allosteric regulation
Activates or inhibits enzyme activity; products of the enzyme will allosterically inhibit the enzymes in glycolysis, whereas substrates will activate them. Transient and easily reversible.
35
Covalent modification
In/activation of an enzyme based on phosporylation
36
Enzyme synthesis based on translation stability
Long-term control of enzyme activity