Carb, lipids and amino acid metabolism W1 Flashcards

1
Q

What are the four stages of biochemical energy production?

A

Stage one = the process of digestion changes large complex molecules into small, simple ones

Stage two = small molecules from digestion are degraded to smaller units primarily the two carbon acetal group that becomes part of acetylCoA

Stage three = acetylCoA is oxidised to produce carbon dioxide and reduced coat enzymes in the citric acid cycle

Stage four = NADH and FADH facilitate ATP production through the electron transport chain and oxidative phosphorylation

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

When ingested what do fats turn into?

A

Fatty acids and glycerol

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

When ingested what do you carbohydrates turn into?

A

Glucose and other sugars

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

What do proteins turn into when ingested?

A

Amino acids

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

What is metabolism?

A

The total of all the biochemical reactions within a living organism

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

What is catabolism?

A

Where large biochemical molecules are broken down into smaller ones

Produces energy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

What is anabolism

A

We are small biochemical molecules are joined together to form larger ones

Consumes energy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

What is NAD +?

A

Nicotinamide Adine dinucleotide

It is a redox cofactor which accepts or donate H+

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

What can NADH do?

A

It can reduce things, i.e. to NAD+

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

What is FAD

A

Flavin adenine dinucleotide

It is also a redox factor

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

What is COA?

A

Coenzyme A

It is an acyl-carrier

Contains a thioether functional group which looks like an Esther, but with a sulphur atom instead

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

What happens when blood glucose is oxidated and what happens when it is store?

A

When oxidation occurs blood glucose becomes energy (ATP)

When storage occurs blood glucose is stored as glycogen

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

What is glycogenesis?

A

biochemical process of synthesizing glycogen from glucose

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

What is glycogenolysis?

A

breakdown of glycogen into glucose-1-phosphate (G1P) and free glucose,

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

What is glycolysis?

A

is the metabolic pathway that breaks down glucose (a 6-carbon sugar) into pyruvate (a 3-carbon compound), generating ATP and NADH in the process

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

What is gluconeogenesis?

A

metabolic process by which the body creates glucose from non-carbohydrate sources, mainly during periods of fasting, starvation, or intense exercise

17
Q

Briefly explain the citric acid cycle

A

oxidizes acetyl-CoA (from carbohydrates, fats, or proteins) into carbon dioxide, producing NADH, FADH₂, and GTP (or ATP). It takes place in the mitochondrial matrix.

18
Q

Briefly explained the digestion of glucose before the citric acid cycle

A

Glucose (6C) is broken down into two molecules of pyruvate (3C)

This produces 2xATP and 2xNADH

Pyruvate dehydrogenase complex convert pyruvate to acetal-coA

This releases 1xCO2 and 1xNADH

Acetyl coA now enters the citric acid cycle

19
Q

What is the electron transport chain?

A

A series of biochemical reactions in which electrons and hydrogen atoms from NADH and FADH are passed to intermediate carriers and then ultimately react with molecular oxygen water

For every two electrons pass through the chain, 10 H + ions are pumped from the matrix into the inter membrane space and this result in a buildup of H + in the into membrane space

20
Q

What is oxidative phosphorylation?

A

The biochemical process by which ATP is synthesised from ADP at the end of the electron transport chain

The buildup of H plus in the into membrane space generates an electrochemical gradient and the flow of proteins from this space back into the matrix is accompanied by the formation of ATP

21
Q

B-oxidation of fatty acid

A

Pathway that degrade fatty acids to acetalCoA by removing two carbon atoms at a time

FADH and NADH are also produced

22
Q

What is more energy rate a sugar or a fat?

23
Q

What what does skeletal muscle use in active and resting state?

A

Glucose inactive and fatty acid in resting

24
Q

What does cardiac muscle use as fuel?

A

Fatty acids first but may use ketone bodies, glucose and lactate

25
What does liver use as a fuel?
Fatty acids first but may use ketone bodies, glucose and lactate
26
What does the brain use as a fuel?
Glucose and keto bodies since fatty acids cannot cross the blood brain barrier
27
What is lipogenesis?
process of synthesizing fatty acids (and eventually fats like triglycerides) from excess glucose or other carbon sources.
28
Why amino acid and nitrogen metabolism is important
because it helps the body manage protein turnover, energy production, and the safe handling of nitrogen, which can be toxic if not properly managed. - amino acids are the building block of proteins - When needed amino acids can be broke down for energy - Some amino acids can be converted to glucose - Amino acids contain nitrogen which isn’t stored in the body like carbs or fats and excess nitrogen from amino acid breakdown is converted to ammonia which is toxic
29
What is transamination mechanism?
key reaction in amino acid metabolism, where the amino group (–NH₂) from an amino acid is transferred to a keto acid, forming a new amino acid and a new keto acid.
30
Every molecule in glycolysis
- Glucose - Glucose-6-phosphate - Fructose-6-phosphate - Fructose-1, 6-bi-phosphate - Dihydroxyacetone-phosphate - Glyceraldehyde-3-phosphate - 1,3-biphosphoglycerate - 3-phosphoglycerate - 2-phosphoglycerate - Pyruvate