Biochemistry Flashcards

1
Q

What is glycogenesis?

A

Synthesis of glycogen from glucose

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2
Q

What is glycogenolysis?

A

Breakdown of glycogen to form glucose

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3
Q

Where is glycogen stored in the body?

A

Liver
Muscle cells

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4
Q

When enough glucose is present, glycogen synthesis begins: glucose-6-phosphate is converted to what?

A

Glucose-1-phosphate

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5
Q

What is formed from glucose-1-phosphate in glycogen synthesis?

A

UDP-glucose

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6
Q

What is UDP-glucose?

A

Essentially an active form of glucose

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7
Q

When does glycogenolysis occur?

A

Between meals to maintain blood glucose levels

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8
Q

Which enzyme catalyses glycogenolysis?

A

Glycogen phosphorylase

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9
Q

What are the 2 regulatory actions of glucagon upon glycogenolysis?

A

Stimulates glycogen breakdown
Inhibits glycogen synthase

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10
Q

What is gluconeogenesis? When does it occur?

A

Synthesis of glucose from non-carbohydrate precursors
Occurs when glycogen stores are completely depleted

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11
Q

Where does gluconeogenesis mainly occur?

A

Liver

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12
Q

Which TCA cycle intermediate is needed for gluconeogenesis? Why is it needed?

A

Oxaloacetate (4C)
Accepts acetyl groups from fat breakdown

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13
Q

Describe the Cori Cycle

A

Blood transports lactate to liver
Liver converts lactate to glucose
Glucose is released into blood

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14
Q

What effect do insulin and glucagon have on gluconeogenesis?

A

Insulin inhibits gluconeogenesis
Glucagon stimulates gluconeogenesis

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15
Q

What happens when increased fat intake is not coupled with appropriate energy expenditure?

A

OBESITY
Increase in number and size of adipocytes

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16
Q

Fat provides us with 2x more energy than carbohydrates. True/False?

A

True

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17
Q

What are essential fatty acids?

A

Fatty acids required by, but cannot be synthesised by, the body

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18
Q

What are the main products of lipid digestion?

A

Glycerol
Fatty acids
Monoglycerides

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19
Q

What must happen to long-chain fatty acids to make them transportable?

A

Resynthesised to triglyceride and coated into a chylomicron, which enters the lymph

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20
Q

What happens to chylomicrons at muscle and adipose tissue?

A

Cleaved by lipoprotein lipase into free fatty acids

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21
Q

What happens to free fatty acids at muscle and adipose tissue?

A

Resynthesised into triglyceride or oxidised to provide energy

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22
Q

Where does further oxidation of fatty acid occur?
Why is this a problem for acyl-CoA?

A

Oxidation occurs in the mitochondrial matrix
acyl-CoA is formed in the cytoplasm!

23
Q

What transports acyl-CoA into the mitochondrial matrix?

A

Carnitine shuttle

24
Q

How is acyl-carnitine formed in the cytoplasm?

A

Fatty acids are transferred from acyl-CoA to carnitine to form acyl-carnitine

25
How does acyl-carnitine get across the inner membrane into the matrix? What happens to the carnitine?
Via a transporter Carnitine is cleaved off, leaving acyl group
26
In the matrix, what happens to the free acyl- group?
Combines with CoA again to form acyl-CoA Net effect: acyl-CoA ends up in the matrix!
27
What happens to acyl-CoA in the matrix?
Shortened by 2C to form acetyl-CoA and a new acyl-CoA
28
What are the products of one round of B-oxidation of fatty acid?
1 acetyl-CoA 1 acyl-CoA, shortened by 2C 1 FADH2 1 NADH + H
29
How and where are ketone bodies formed?
Formed from acetyl-CoA during B-oxidation in liver mitochondria
30
What is lipogenesis?
Synthesis of fatty acids
31
Lipogenesis is a reductive process (electrons are required). True/False?
True
32
What transports acetyl-CoA from mitochondrial matrix into cytoplasm?
Citrate
33
What is the vital first step in lipogenesis from acetyl-CoA?
Activation of acetyl-CoA by acetyl-CoA carboxylase into malonyl-CoA
34
Which enzyme catalyses synthesis of long chain fatty acid from malonyl-CoA, acetyl-CoA and NADH?
Fatty acid synthase
35
Which component of fatty acid synthase carries the growing fatty acid chain during synthesis?
Acyl-carrier protein (ACP)
36
When a fatty acid chain length of __C is reached, the fatty acid is released
16C
37
Synthesis of fatty acids is maximal when carbohydrate is scarce. True/False?
False Synthesis occurs when carbohydrate is in plentiful supply + fatty acids are scarce (otherwise lipolysis would occur)
38
Amino acids which are not used for proteins are stored in the liver. True/False?
False Amino acids cannot be stored and are degraded if not used as building blocks
39
Where is the major site of amino acid degradation?
Liver
40
What does amino acid degradation primarily produce?
Ammonia (NH3) and ammonium ions
41
What are the 3 steps by which urea is formed?
Transaminiation De-amination Urea cycle
42
Which organ is albumin secreted from?
Liver
43
Name the main liver-derived plasma proteins (4), in order of increasing molecular weight
Albumin alpha-globulins beta-globulins gamma-globulins
44
What characteristic of plasma proteins enables them to maintain osmotic pressure which increases fluid movement out of the tissues into the blood?
They are insoluble - they do not diffuse into the interstitial fluid and only circulate in the blood
45
List some hydrophobic substances that are carried in the blood by plasma proteins (4)
Steroid hormones Free fatty acids Bilirubin Cholesterol
46
Give 2 examples of alpha-globulin plasma proteins
Ceruloplasmin Retinol-binding protein
47
Give 2 examples of beta-globulin plasma proteins
Transferrin Fibrinogen
48
Transferrin transports Fe2+ (ferrous iron). True/False?
False Transports Fe3+ (ferric iron)
49
What is the most abundant plasma protein in the blood?
Albumin
50
Insulin inhibits production of albumin. True/False?
False Insulin stimulates production of albumin
51
Are albumin levels low or high in liver disease?
Low
52
Iron is transported in the ferrous/ferric state bound to ____, and is stored in the ferrous/ferric state bound to ____
Iron is transported in the ferric state bound to transferrin, and is stored in the ferrous state bound to ferritin
53
Which plasma protein does copper bind to for transport?
Ceruloplasmin
54
Which disease results due to accumulation of copper due to deficiency of ceruloplasmin?
Wilson's disease