Biochemistry Flashcards

1
Q

Fat is essential for the absorption of which vitamins?

A

Vitamins A,D,E and K

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2
Q

What is the main storage form of lipids?

A

Triglycerides

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3
Q

Polyunsaturated fats are essential fatty acids - what does this mean?

A

They have more than one double bond and can’t be synthesised by the body, therefore meaning they must be obtained from the diet

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4
Q

What is a chylomicron? What is the purpose of a chylomicron?

A
  • lipoprotein particle
  • triglycerides coated with - phospholipids, cholesterol, and proteins.
  • They are important for the transport of fats around the body
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5
Q

The breakdown of lipids is referred to as ‘lipolysis’. Outline this process

A

*Fatty acids are converted into CoA derivatives (e.g Fatty Acyl CoA) - CYTOPLASM
*The carnitine shuttle transfers Acyl CoA into the mitochondrial matrix
*B oxidation occurs -4 steps-
Acyl CoA goes in, and the products for each cycle = 1 acetyl CoA, 1 FADH2, 1 NADH and H+ and Fattyl acyl CoA (shortened by 2C atoms)

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6
Q

Under what conditions are ketone bodies generated and where does this occur?

A

Fasting conditions

Liver mitochondria

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7
Q

By what process are ketone bodies formed?

A

Ketone bodies are formed from acetyl CoA as a by- product of B-oxidation

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8
Q

Although ketone bodies can cause problems if they accumulate, they are still important - outline some of their uses in the body

A

Energy metabolism for the brain, heart muscle and renal cortex

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9
Q

What can high levels of ketone bodies cause?

A

Fruity breath

Severe acidosis which causes impaired tissue function

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10
Q

What is meant by lipogenesis and where in the body does this occur?

A

The synthesis of lipids - occurs mainly in the liver and usually occurs when there has been excess energy intake

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11
Q

What substance is the major fatty acid precursor used to form all fatty acids?

A

Malonyl- CoA

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12
Q

Acetyl CoA is converted to Malonyl CoA which is the major precursor for fatty acid synthesis. Which enzyme catalyses this conversion?

A

Acetyl CoA Carboxylase

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13
Q

Describe the process of lipogenesis

A

Lipogenesis is the synthesis of lipids.
Firstly Acetyl CoA which is produced in the mitochondrial matrix by B oxidation must be transported to the cytoplasm. Citrate is used to do this. Once in the cytoplasm, Acetyl is converted to Malonyl CoA with he help of the enzyme: acetyl-CoA carboxylase. Malonyl CoA then transfers 2 C atoms to the acetyl CoA to form a fatty acid chain. This is a reductive process for which NADPH is the electron donor.

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14
Q

Lipogenesis will only occur when there is plenty energy available. To control this process, Acetyl CoA can be unregulated or down-regulated to determine whether the process proceeds and fatty acids are synthesised. Which substances affect Acetyl CoA?

A
UPREGULATION 
Insulin 
citrate 
DOWNREGULATION 
Glucagon 
Adrenaline 
Palmitoyl CoA
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15
Q

Triglycerides can be produced by esterifying fatty acids on to glycerol. Production of triglycerides only occurs in the fed state, what substance must be present for the process to proceed?

A

G-3-P from glucose, indicating a fed state

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16
Q

What does the breakdown of amino acids produce? Which of these products can be very toxic to the body if it accumulates?

A

Ammonia

Ammonium ions - toxic at high concentrations

17
Q

The synthesis of urea occurs in 3 main steps. Where in the body does this occur?

A

Occurs in the liver

18
Q

What are the 3 main steps in the synthesis of urea?

A

Transamination
Deamination
Urea cycle

19
Q

What is maple syrup disease?

A

An inherited disorder in which the degradation of valine, isoleucine and leucine are blocked - this can cause mental and physical disorders but can be controlled by diet

20
Q

What is phenylketonuria?

A

An inherited disorder in which degradation of phenylalanine is blocked, causing it to accumulate in body fluids.
Leads to severe mental retardation if untreated. It can however be controlled/ prevented by a low phenylalanine diet.

21
Q

What is alcaptonuria?

A

An inherited disorder in which degradation of phenylalanine and tyrosine is blocked

22
Q

What is glycogenesis?

A

The synthesis of glycogen from glucose

23
Q

What enzymes are involved in glycogenesis?

A
Hexokinase 
Phosphoglucomutase 
UDP-glucose 
Phosphorylase 
Glycogen synthase
24
Q

What is glycogenin and what is its role?

A

Glycogenin is the catalyst at the centre of the glycogen polymer which is the starting point to allow the glycogen polymer to be extended

25
Q

What is glycogenolysis?

A

The breakdown of glycogen to produce glucose

26
Q

What enzymes are involved in glycogenolysis?

A

Glycogen phosphorylase
glucose-6-phosphatase
phosphoclucomutase

27
Q

What is gluconeogenesis?

A

The synthesis of glucose from non-carbohydrate precursors

28
Q

What is glycolysis?

A

The breakdown of glucose