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Competitive Medical MCQs – Up To Date Vitamins ( Biochemistry ) MCQs

Competitive Medical MCQs – Up To Date Vitamins ( Biochemistry ) MCQs

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Latest Medical MCQs

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Latest Vitamins ( Biochemistry ) Mcqs

The most occurred mcqs of Vitamins ( Biochemistry ) in past papers. Past papers of Vitamins ( Biochemistry ) Mcqs. Past papers of Vitamins ( Biochemistry ) Mcqs . Mcqs are the necessary part of any competitive / job related exams. The Mcqs having specific numbers in any written test. It is therefore everyone have to learn / remember the related Vitamins ( Biochemistry ) Mcqs. The Important series of Vitamins ( Biochemistry ) Mcqs are given below:

Which of the following combination is correct ?

A. Biotin-CO2
B. Thiamine – Acyl CoA
C. ATP-Hydrogen
D. All of the above

In the body, metabolism of 10 g of protein would produce approximately____________?

A. 410 Kcal
B. 41 Kcal
C. 1 Kcal
D. 4100 Kcal

Alkaptonuria an inherited metabolic disorder is due to the deficiency of____________?

A. Homogentisate oxidase
B. Pheylalanine hydroxylase
C. Cystathionase
D. Tyrosine transaminase

Colloidal osmotic pressure of plasma is by___________?

A. Albumin
B. Globulin
C. Fibrinogen
D. Prothrombin

The daily requirement of protein for the adults is_________________?

A. 120 gms
B. 60 gms
C. 6 gms
D. 250 gms

The fastest moving fraction of protein in serum When subjected to paper electrophoresis is_____________?

A. Albumin
B. Beta Globulin
C. Alpha 1 globulin
D. Gamma Globulin

Most common non protein nitrogenous fraction of blood_____________?

A. Uric acid
B. Urea
C. Urobilinogen
D. Creatinin

Proteins are linear polymers of amino acids, They fold into compact structures Sometimes these folded structures associate to form homo or hetero dimers Which one of the following refers to this associated form ?

A. Molecular aggregation
B. Denatured state
C. Precipitation
D. Quaternary structure

The protein rich in basic amino acids, which functions in the packaging of DNA is chromosomes is______________?

A. Histone
B. Fibrinogen
C. Hyaluronic acid binding protein
D. Collagen

Which of the following is not a post transcriptional modification of RNA ?

A. 5′ capping
B. Splicing
C. 3′ polyadenylation
D. Glycosylation

Thyroxine and catecholamines are derived from_____________?

A. Tyrosine
B. Alanine
C. Tryptophan
D. Leucine

In Hartnup’s disease _______ is excreted in the urine?

A. Glutamine
B. Ornithine
C. Tryptophan
D. Phenylalanine

Which of the following is not a part of hemoglobin molecule___________?

A. Vinyl groups
B. Pyrrole rings
C. Histidine
D. Ferric ions

Proteins are absorbed from GIT as_____________?

A. Amino acids
B. Peptones
C. Peptides
D. All of the above

Which of the following is a precursor of protoporphyrin_______________?

A. Leucine
B. Alanine
C. Histidine
D. Glycine

Cytochromes are_____________?

A. Riboflavin containing nucleotides
B. Pyridine nucleotides
C. Metal containing flavoproteins
D. Iron-porphyrin proteins

Heme in haemoglobin is____________?

A. Surrounded by non polar environment
B. Between Helix C and D
C. Bonded to E7 histidine
D. Protoporophyrin IX

Which of the following is correct about breakdown of hemoglobin (Hb)_____________?

A. Heme→Hb→Biliverdin→Urobilinogen
B. Hb→Heme→bilirubin→Urobilinogen
C. Hb→Heme→Bilverdin→Uro bilinogen
D. Hb→Heme→bilirubin→Urobilinogen→Biliverdin

Creatine is formed metabolically from______________?

A. Phenylalanine
B. Arginine
C. Tryptophan
D. Histidine

Major source of ammonia in the kidney is___________?

A. Aspartate
B. Urea Aspartate
C. Glutamine
D. Glutamate

Key enzyme in urea synthesis is____________?

A. Arginase
B. Carbamyl synthetase
C. Urease
D. Ornithine

Ammonia is detoxified in liver to form____________?

A. Glutamine
B. Uric acid
C. Creatinine
D. Urea

A small Ca+2 binding protein that modifies the activity of many enzymes and other proteins in response to changes of Ca+2 concentration is known as______________?

A. Collagen
B. Calmodulin
C. Cycline
D. Kinesin

Decarboxylation of which of the following amino acids results in formation of a vasodilator ?

A. Arginine
B. Valine
C. Histidine
D. Glutamic acid

A mutation that converts an amino acid codon to a stop codon is a_____________?

A. Nonsense mutation
B. Silent mutation
C. Transversion
D. Frame shift mutation

Histidine is converted to histamine by_____________?

A. Hydroxylation
B. Transamination
C. Decarboxylation
D. Reduction

ALbumin is synthesized by_____________?

A. Liver
B. Muscle
C. Kidney
D. Spleen

Which of the following amino acids is quickly converted to tyrosine ?

A. Glycine
B. Arginine
C. Phenylalanine
D. Leucine

Synthesis of protein occurs on__________________?

A. Nucleus
B. Poly ribosomes
C. Mitochondria
D. Golgi bodies

Which of the following is present in the plasma but absent in the serum ?

A. Globulin
B. Albumin
C. Lecithin
D. Firbinogen

The amino acid, which is used is the estimation of collagen is_____________?

A. Hydroxyproline
B. Lysine
C. Proline
D. Glycine

The amino acid from which niacin is synthesized is______________?

A. Theronine
B. Tyrosine
C. Tryptophan
D. Histidine

Hydroxylation of proline require the following except____________?

A. O2
B. Fe+2
C. Ascorbic acid
D. Succinate

The process by which a base sequence of messenger RNA is synthesized (by a RNA polymerase) on a template of complementary DNA is called______________?

A. Transcription
B. Translation
C. Transduction
D. Translocation

The major fuel for the brain after several weeds of starvation______________?

A. Fatty acid
B. Glucose
C. Beta hydroxy butyrate
D. Glycerol

Carbohydrate MCQs ( Biochemistry )

Non essential amino acids are not_____________?

A. Forming part of the proteins
B. Used by the body
C. Required in the diet
D. Absorbed in the intestines

The following is false about tryptophan_____________?

A. Non-essential amino acid
B. Involved in niacin synthesis
C. Involved in serotonin synthesis
D. Involved in melatonin in synthesis

Which of the following amino acid is involved in gluconeogenesis______________?

A. Valine
B. Glycine
C. Cysteline
D. All of the above

Glycine is present in____________?

A. Glutathione
B. Hemoglobin
C. Purines
D. Creatine
E. All of the above

Quaternary structure of protein is_____________?

A. The arrangement sequence of amino acids in the polypeptide chain
B. Inter relation of amino acids in 2 polypeptide chains
C. Inter relation between amino acids in a single polypeptide chain
D. The inter relation and arrangement of polypeptides in a protein with more than 2 polypeptide chains

Which of the following is a derived a derived protein_____________?

A. Prolamines
B. Peptones
C. Protamines
D. Lactalbumin

All are genetic amino acid deficiency disease except___________?

A. Alkaptonuria
B. Phenyl ketonuria
C. Homocystinuria
D. 6alactosemia

Mannose 6 phosphate containing freshly synthesized proteins are directed to_____________?

A. Mitochondria
B. Lysosomes
C. Nucleus
D. Golgi apparatus

Glutamine replaced by valine in sckle cell anaemia is characterized________________?

A. Degradation of beta chain
B. Missense mutation of beta chain
C. Non Sense mutation of beta chain
D. Deletion of beta chain

All are true about glutathione except ?

A. It conjugates xenobiotics
B. It converts hemoglobin to methemoglobin
C. It is a tripetide
D. It scavenges free radicals and superoxide ions

The class of amino acids that contains only non essential amino acids is_______________?

A. Acidic
B. Aromatic
C. Basic
D. Branched chain

The nitrogen content in 50 gm of a typical dietary protein is most likely to be_____________?

A. 10 gm
B. 8 gm
C. 5 gm
D. 16 gm

The number of essential amino acid are______________?

A. 12
B. 8
C. 6
D. 16

The amino acid residue having animino side chain is____________?

A. Tyrosine
B. Histidine
C. Lysine
D. Proline

The primary role of chaperones is to help in______________?

A. Protein degradation
B. Protein synthesis
C. Protein denaturation
D. Protein folding

Argentaffinoma is characterized by excess excretion of_____________?

A. 5- Hydroxy indole acetate
B. Phenyl lactate
C. 3- Hydroxy phenyl pyruvate
D. Phenyl acetate

Urea is formed in_____________?

A. Kidney
B. Brain
C. Liver
D. Intestine

The following is not a carrier protein________________?

A. Transferrin
B. Cerruloplasmin
C. Transcobalamine
D. Haptoglobulin

False statement about haemoglobin structure________________?

A. Hb has 2 polypeptide chains
B. Hb structurally similar to myoglobin
C. Iron is present in ferrous state
D. Ferrous ions are in porphyrin rings

At PH 7 the binding of 2,3 DPG to hemoglobin occurs at which site ?

A. Carboxy terminal
B. Sulphydryl group
C. Amino terminal
D. Histidine

Iron is complexed in haemoglobin to_______________?

A. Isoleucine
B. Histidine
C. Leucine
D. Valine

Urea is produced by the enzyme_____________?

A. Uricase
B. Urease
C. Arginase
D. Glutaminase

Urinary protein is detected by______________?

A. Hay’s test
B. Barfoed test
C. Boiling test
D. Ehrlich’s test

Which is the by product of the urea cycle_______________?

A. Succinate
B. Aspartate
C. Ornithine
D. Fumarate

Amino acids excreted in the urine in cystinosis______________?

A. Ornithine
B. Cystine
C. Arginine
D. Lysine
E. All of the above

Albinism is a genetic disease that results in incomplete metabolism of______________?

A. Cystine
B. Histidine
C. Tyrosine
D. Alanine

All of the following are globular proteins except_______________?

A. Albumin
B. Prolamines
C. Globulin
D. Myosin

Which one of the following amino acids is purely ketogenic ?

A. Phenylalanine
B. Proline
C. Isoleucine
D. Leucine

Collagen is rich in_____________?

A. Alanine and glycine
B. Glutamate and glycine
C. Proline and glycine
D. Glutamate and proline

Digestion of proteins is initiated by________________?

A. Sucrase
B. Amylase
C. Chymotrypsin
D. Pepsin

The nitrogen of the body is supplied by______________?

A. Glucose
B. Proteins
C. Triacyl glycerol
D. Lipids

Alkaptonuria, an inherited metabolic disorder of L0tyrosine metabolism is due to lack of_____________?

A. Tyrosine transaminase
B. Parahydroxy phenyl pyruvate Hydroxylase
C. Homogentisate oxidase
D. Tyrosine oxidase

One of the following is not an amino acid______________?

A. Hydroxy proline
B. Glycine
C. Glutamic acid
D. Choline

Precursor of melanin is________________?

A. Tryptophan
B. Phenylalanine
C. Tyrosine
D. Methionine

The reducing end of glutathione, the amino acid is_________________?

A. Glycine
B. Lycie
C. Leucine
D. Valine

Following are the essential amino acid______________?

A. Phenylalanine, Tryptophan lysine
B. Phenylalanine, Valine, Glycine
C. Phenylalanine, Arginine Methinonine
D. Histidine, Glutamine, Valine

The process of transfer of information from the RNA to the proteins is called______________?

A. Transcription
B. Translation
C. Mutation
D. Conjugation

Following is non-essential amino acid_______________?

A. Tryptophan
B. Proline
C. Phenylalanine
D. Threonine

One of the following is nonessential amino acid______________?

A. Tyrosine
B. Methionine
C. Valine
D. Cystine

Aromatic ring is present in_____________?

A. Glycine
B. Arginine
C. Phenylalanine
D. Phenylalanine, Glycine

In maple syrup urine disease the amino acids excreted in the urine are______________?

A. Isoleucine
B. Leucine
C. Valine
D. All of the above

Indole ring is present in______________?

A. Tryptophan
B. Methionine
C. Valine
D. Histidine

Biuret test is confirmatory test for_______________?

A. Protein
B. Carbohydrate
C. Fat
D. None of the above

Albumins and globulins are ________ proteins?

A. Simple
B. Prolamines
C. Peptones
D. Lactalbumin

Tertiary structure of protein is maintained by all except______________?

A. Hydrophobic
B. H2 bond
C. Ionic bond
D. Disulphide bond
E. None of the above

Competitive Medical MCQs – Up To Date Vitamins ( Biochemistry ) MCQs