IGNOU MFN 2 SOLVED ASSIGNMENT

Ques 1.

What are monosaccharides? Explain any two properties of monosaccharides.

Ques 2.

Saponification

Ques 3.

 Rancidity

Ques 4.

What are Eicosonoids? Briefly describe their role in the body.

Ques 5.

Discuss the four basic structural levels of proteins, giving exampls

Ques 6.

 Discuss the properties and importance of following vitamins in our body:

a) Vitamin C

b) Vitamin K

Ques 7.

Explain the mechanism of enzyme action in our body. Enumerate the factors affecting enzyme activity.

Ques 8.

Explain the process of absorption of amino acids and peptides in our body.

Ques 9.

 What is gluconeogenesis? Discuss the four substrates used in gluconeogenesis.

Ques 10.

 What are the components of the electron transport chain? Explain briefly.

Ques 11.

 How cholesterol is metabolized in our body? Explain.

Ques 12.

b) Differentiate between the following sets of terms:

i. LDL and HDL

ii. Ketogenic and Glucogenic amino acid

Ques 13.

 Briefly describe synthesis of Pyrimindine in our body.

Ques 14.

How and where toxic ammonia is converted into urea in our body? Explain briefly.

Ques 15.

Define free radicals. Explain physiological mechanisms to limit free radical damage

Ques 16.

 What is the composition and function of chylomicron?

Ques 17.

 a) Describe functions of following minerals:

i. Calcium

ii. Iron

Ques 18.

b) Briefly enumerate biochemical role of following hormones:

i. Insulin

ii. Glucocorticoids

Ques 19.

 List the common inborn errors due to carbohydrate metabolism. Explain briefly any two of them.

Ques 20.

efine haemoglobinopathies. Elaborate any one in detail.

Ques 21.

 Explain the following in 2-3 sentences. Also give the structure wherever possible.

Ques 22.

Recombinnt DNA

Ques 23.

Mutarotation

Ques 24.

Sterols

Ques 25.

 Zwitterion

Ques 26.

Holoenzyme

Ques 27.

 Competitive inhibition

Ques 28.

Coenzyme A

Ques 29.

Chiral carbon atom

Ques 30.

Micelle

Ques 31.

Glycolysis

Ques 32.

2. Name the defective enzyme in the following diseases:

a) Alcaptonuria

b) Gaucher's disease

c) Homocystinuria

d) Pentosuria

e) Albinism

3. Give the significance/role of following:

a) Conversion of IMP to AMP

b) Vitamin B6 in transamination

c) Oxygen free radicals

d) Phenylalanine hydroxylase

e) Fight or flight response

Ques 33.

What are monosaccharides? Explain any two properties of monosaccharides.

Ques 34.

Saponification

Ques 35.

 Rancidity

Ques 36.

What are Eicosonoids? Briefly describe their role in the body.

Ques 37.

Discuss the four basic structural levels of proteins, giving exampls

Ques 38.

 Discuss the properties and importance of following vitamins in our body:

a) Vitamin C

b) Vitamin K

Ques 39.

Explain the mechanism of enzyme action in our body. Enumerate the factors affecting enzyme activity.

Ques 40.

Explain the process of absorption of amino acids and peptides in our body.

Ques 41.

 What is gluconeogenesis? Discuss the four substrates used in gluconeogenesis.

Ques 42.

 What are the components of the electron transport chain? Explain briefly.

Ques 43.

 How cholesterol is metabolized in our body? Explain.

Ques 44.

b) Differentiate between the following sets of terms:

i. LDL and HDL

ii. Ketogenic and Glucogenic amino acid

Ques 45.

 Briefly describe synthesis of Pyrimindine in our body.

Ques 46.

How and where toxic ammonia is converted into urea in our body? Explain briefly.

Ques 47.

Define free radicals. Explain physiological mechanisms to limit free radical damage

Ques 48.

 What is the composition and function of chylomicron?

Ques 49.

 a) Describe functions of following minerals:

i. Calcium

ii. Iron

Ques 50.

b) Briefly enumerate biochemical role of following hormones:

i. Insulin

ii. Glucocorticoids

Ques 51.

 List the common inborn errors due to carbohydrate metabolism. Explain briefly any two of them.

Ques 52.

efine haemoglobinopathies. Elaborate any one in detail.

Ques 53.

 Explain the following in 2-3 sentences. Also give the structure wherever possible.

Ques 54.

Recombinnt DNA

Ques 55.

Mutarotation

Ques 56.

Sterols

Ques 57.

 Zwitterion

Ques 58.

Holoenzyme

Ques 59.

 Competitive inhibition

Ques 60.

Coenzyme A

Ques 61.

Chiral carbon atom

Ques 62.

Micelle

Ques 63.

Glycolysis

Ques 64.

2. Name the defective enzyme in the following diseases:

a) Alcaptonuria

b) Gaucher's disease

c) Homocystinuria

d) Pentosuria

e) Albinism

3. Give the significance/role of following:

a) Conversion of IMP to AMP

b) Vitamin B6 in transamination

c) Oxygen free radicals

d) Phenylalanine hydroxylase

e) Fight or flight response

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