NEET-PG 2012 - Biochemistry Practice Questions

Q: Why is oxidized LDL considered more atherogenic?

Is taken up by scavenger receptors. ***Is taken up by scavenger receptors*** - **Oxidized LDL (oxLDL)** is taken up by **scavenger receptors (CD36, SR-A)** on macrophages, which have **no feedback regulation**. - Unlike native LDL receptors that downregulate when cells have sufficient cholesterol, **scavenger receptors continue unlimited uptake**, leading to foam cell formation. - This **unregulated uptake mechanism** is the key reason why oxLDL is **more atherogenic** than native LDL. - The result is lipid-laden macrophages forming **fatty streaks**, the initial lesions of **atherosclerosis**. *Is not recognized by LDL receptors* - While true that oxLDL has **reduced affinity** for native LDL receptors due to oxidative modification, this alone doesn't explain increased atherogenicity. - The critical factor is what happens instead—its uptake via an **alternative, unregulated pathway**. *Accumulates in macrophages* - This is a **consequence** of scavenger receptor uptake, not the primary mechanism. - Foam cell formation occurs **because** of unregulated scavenger receptor uptake, making this a downstream effect. *Promotes inflammation in arterial walls* - OxLDL does promote inflammation through multiple mechanisms (cytokine release, endothelial dysfunction). - However, this is a **secondary effect** that occurs after uptake and accumulation—not the primary reason for atherogenicity.

Q: Which of the following enzymes is not involved in the urea cycle?

CPS-II. ***CPS-II*** - Carbamoyl phosphate synthetase II is involved in **pyrimidine synthesis**, not the urea cycle. - It uses **glutamine** as a nitrogen donor and is located in the **cytosol**. *CPS-I* - Carbamoyl phosphate synthetase I is the **rate-limiting enzyme** of the urea cycle. - It catalyzes the formation of **carbamoyl phosphate** from **ammonia**, CO2, and ATP in the mitochondria. *Arginase* - Arginase is the **final enzyme** in the urea cycle, converting **arginine** to **ornithine** and **urea**. - This reaction occurs in the cytosol and releases urea for excretion. *Argininosuccinate lyase* - Argininosuccinate lyase catalyzes the cleavage of **argininosuccinate** into **fumarate** and **arginine**. - This is a key step in regenerating arginine for the final step of the urea cycle.

Q: Urea & Kreb's cycle are linked at?

Fumarate. ***Fumarate*** - **Fumarate** is a key intermediate produced during the **urea cycle** when argininosuccinate is cleaved into arginine and fumarate. - This fumarate then enters the **Krebs cycle** (citric acid cycle) as an intermediate to be converted into malate and then oxaloacetate, thus linking the two cycles. *Arginine* - **Arginine** is an amino acid that participates in the urea cycle, serving as a precursor for the formation of urea. - While arginine is a part of the urea cycle, it does not directly enter the Krebs cycle or serve as its linking metabolite. *Ornithine* - **Ornithine** is another amino acid central to the urea cycle, being regenerated at the end of the cycle to combine with carbamoyl phosphate. - It is a carrier molecule for the nitrogen atoms, but it does not directly link to the Krebs cycle. *Oxaloacetate* - **Oxaloacetate** is a central intermediate in the Krebs cycle, and it can be a precursor for intermediates in the urea cycle (e.g., through aspartate). - However, it is not the direct molecule that links the two cycles in the direction of the urea cycle feeding into the Krebs cycle.

Q: Which will activate carbamoyl phosphate synthase I?

N-acetyl glutamate. **N-acetyl glutamate** - **N-acetyl glutamate** is an **allosteric activator** of **carbamoyl phosphate synthase I (CPS I)**, which is the mitochondrial enzyme that catalyzes the first committed step of the **urea cycle**. - Its synthesis is stimulated by high levels of **arginine**, linking nitrogen load to urea production. *Acetyl-CoA* - Acetyl-CoA is a common **substrate** and **product** in various metabolic pathways, but it is not a direct activator of CPS I. - It is a precursor for the synthesis of **N-acetyl glutamate**, but does not activate CPS I directly. *Ornithine* - **Ornithine** is a key intermediate of the **urea cycle**, but it does not directly activate CPS I. - It combines with carbamoyl phosphate (the product of CPS I) in the second step of the urea cycle to form citrulline. *ATP* - **ATP** is a **substrate** used by CPS I to provide energy for the synthesis of carbamoyl phosphate. - While essential for the reaction, ATP itself does not act as an allosteric activator of the enzyme.

Q: Ochronosis is due to accumulation of ?

Homogentisic acid. ***Homogentisic acid*** - Ochronosis is a condition caused by the excessive accumulation of **homogentisic acid** in connective tissues. - This accumulation occurs due to a deficiency of the enzyme **homogentisate 1,2-dioxygenase** (HGD), which is responsible for breaking down homogentisic acid in the tyrosine degradation pathway. *Phenylpyruvate* - **Phenylpyruvate** accumulates in **phenylketonuria (PKU)**, a different metabolic disorder where there's a deficiency in phenylalanine hydroxylase. - PKU leads to intellectual disability and other neurological problems, not the characteristic pigmentation and arthritis of ochronosis. *Xanthurenate* - **Xanthurenate** is an abnormal metabolite of tryptophan metabolism that can accumulate in **vitamin B6 deficiency**. - Its accumulation is associated with increased urinary excretion and is not directly implicated in the pathology of ochronosis. *Glyoxylate* - **Glyoxylate** is involved in various metabolic pathways, and its accumulation (or accumulation of its metabolic products like oxalate) is associated with **primary hyperoxaluria**. - Primary hyperoxaluria leads to kidney stones and kidney failure, a condition distinct from ochronosis.

Q: Organ that can utilize glucose, fatty acids and ketone bodies is:

Skeletal muscle. ***Skeletal muscle*** - Skeletal muscle is highly adaptable and can utilize **glucose**, **fatty acids (FAs)**, and **ketone bodies** as fuel sources, especially during prolonged exercise or starvation. - Its metabolic flexibility allows it to switch between these substrates depending on their availability and the body's energy demands. *Liver* - The liver is central to metabolism but primarily **produces ketone bodies** from fatty acids rather than utilizing them as a major fuel source for its own energy needs. - While it uses glucose and FAs, its role in ketone body metabolism is largely synthetic. *Brain* - The brain preferentially uses **glucose** as its primary fuel. - During prolonged starvation, it can adapt to utilize **ketone bodies** as an alternative fuel source, but it does not significantly use fatty acids directly. *RBC* - Red blood cells (RBCs) lack mitochondria and therefore rely exclusively on **anaerobic glycolysis** for energy, metabolizing only **glucose**. - They cannot utilize fatty acids or ketone bodies.

Q: Which of the following is not the source of cytosolic NADPH ?

ATP citrate lyase. ***ATP citrate lyase*** - **ATP citrate lyase** is an enzyme involved in the synthesis of **acetyl-CoA** from citrate in the cytosol, which is then used for **fatty acid synthesis**. It does not generate NADPH. - While the **acetyl-CoA** produced is used in pathways that require NADPH, ATP citrate lyase itself does not directly produce NADPH. *Isocitrate dehydrogenase* - Cytosolic **isocitrate dehydrogenase** catalyzes the oxidative decarboxylation of **isocitrate** to alpha-ketoglutarate, producing **NADPH**. - This reaction is an important source of **cytosolic NADPH**, especially in non-photosynthetic tissues. *Malic enzyme* - **Malic enzyme** catalyzes the oxidative decarboxylation of **malate** to pyruvate, simultaneously reducing **NADP+ to NADPH**. - This enzyme is a significant source of **cytosolic NADPH** in various tissues, contributing to fatty acid synthesis and other reductive processes. *G6PD* - **Glucose-6-phosphate dehydrogenase (G6PD)** is the rate-limiting enzyme in the **pentose phosphate pathway** (PPP). - It catalyzes the first step of the PPP, converting **glucose-6-phosphate** to 6-phosphogluconolactone and producing **NADPH** as a crucial coenzyme.

Q: Which amino acid requires ascorbic acid for its formation in the body?

Hydroxyproline. ***Hydroxyproline*** - **Ascorbic acid (Vitamin C)** is an essential cofactor for **prolyl hydroxylase** and **lysyl hydroxylase** enzymes - These enzymes catalyze the **post-translational hydroxylation** of proline and lysine residues within collagen chains to form hydroxyproline and hydroxylysine - This hydroxylation is crucial for **stabilization of the collagen triple helix** structure - Hydroxyproline is formed by **modification of proline after incorporation into collagen**, not as a free amino acid - **Scurvy** (Vitamin C deficiency) results in defective collagen due to inadequate hydroxyproline formation *Lysine* - Lysine is an **essential amino acid** obtained from diet - Does not require ascorbic acid for its synthesis or formation - While lysine residues in collagen can be hydroxylated (forming hydroxylysine), the question asks about the amino acid whose formation requires Vitamin C *Cysteine* - Cysteine is a **sulfur-containing amino acid** synthesized from methionine via transsulfuration pathway - Its synthesis does not involve ascorbic acid *Proline* - Proline is a **non-essential amino acid** synthesized from glutamate - **Proline synthesis does not require ascorbic acid** - Proline serves as the precursor that gets hydroxylated to hydroxyproline within collagen

Q: Which of the following requires vitamin B12?

Conversion of homocysteine to methionine. ***Homocysteine to methionine*** - The conversion of **homocysteine to methionine** is catalyzed by **methionine synthase**, an enzyme that requires **vitamin B12** (cobalamin) as a cofactor. - **Vitamin B12** facilitates the transfer of a methyl group from **methyltetrahydrofolate** to homocysteine, forming methionine. *Conversion of serine to lysine* - The metabolism of **serine to lysine** involves multiple steps and different enzymes, but it does not directly require **vitamin B12**. - Lysine is an **essential amino acid** and is primarily obtained from dietary sources or synthesized through complex pathways. *Conversion of serine to glycine* - The conversion of **serine to glycine** is catalyzed by **serine hydroxymethyltransferase**, which requires **tetrahydrofolate (THF)** as a cofactor, not vitamin B12. - This reaction generates **5,10-methylenetetrahydrofolate**, an important one-carbon donor. *Conversion of glutamine to glutamate* - The conversion of **glutamine to glutamate** is primarily catalyzed by **glutaminase**, an enzyme that does not require **vitamin B12**. - This reaction involves the removal of an **ammonia group** from glutamine to form glutamate.

Q: Which of the following micronutrient deficiencies can lead to anemia?

Copper. ***Copper*** - **Copper** is essential for **iron metabolism** and red blood cell formation; its deficiency can lead to **sideroblastic anemia** (often with microcytic or normocytic features) that may be accompanied by neutropenia. - Copper is required for **ceruloplasmin** function, which is necessary for iron mobilization from stores and incorporation into hemoglobin. - It also plays a role in the function of **superoxide dismutase** and **cytochrome c oxidase**, enzymes involved in antioxidant defense and energy production. *Molybdenum* - **Molybdenum** is a cofactor for several enzymes, including **xanthine oxidase** and **sulfite oxidase**, crucial for purine metabolism and detoxification. - While essential, its deficiency does not typically lead to **anemia** in humans. *Selenium* - **Selenium** is a component of selenoproteins, such as **glutathione peroxidase**, which protect cells from oxidative damage. - Deficiency is associated with conditions like **Keshan disease** (cardiomyopathy) but not primary anemia. *Fluorine* - **Fluorine** (as fluoride) is primarily known for its role in **bone and tooth mineralization**, protecting against dental caries. - It does not directly participate in **hematopoiesis** or iron metabolism, and its deficiency is not linked to anemia.

Question 1

Why is oxidized LDL considered more atherogenic?

Accepted Answer

Is taken up by scavenger receptors

Answer

Is not recognized by LDL receptors

Answer

Promotes inflammation in arterial walls

Answer

Accumulates in macrophages

Question 2

Which of the following enzymes is not involved in the urea cycle?

Accepted Answer

CPS-II

Answer

Arginase

Answer

Argininosuccinate lyase

Answer

CPS-I

Question 3

Urea & Kreb's cycle are linked at?

Accepted Answer

Fumarate

Answer

Arginine

Answer

Ornithine

Answer

Oxaloacetate

Question 4

Which will activate carbamoyl phosphate synthase I?

Accepted Answer

N-acetyl glutamate

Answer

ATP

Answer

Acetyl-CoA

Answer

Ornithine

Question 5

Ochronosis is due to accumulation of ?

Accepted Answer

Homogentisic acid

Answer

Phenylpyruvate

Answer

Xanthurenate

Answer

Glyoxylate

Question 6

Organ that can utilize glucose, fatty acids and ketone bodies is:

Accepted Answer

Skeletal muscle

Answer

Liver

Answer

Brain

Answer

RBC

Question 7

Which of the following is not the source of cytosolic NADPH ?

Accepted Answer

ATP citrate lyase

Answer

Malic enzyme

Answer

G6PD

Answer

Isocitrate dehydrogenase

Question 8

Which amino acid requires ascorbic acid for its formation in the body?

Accepted Answer

Hydroxyproline

Answer

Lysine

Answer

Cysteine

Answer

Proline

Question 9

Which of the following requires vitamin B12?

Accepted Answer

Conversion of homocysteine to methionine

Answer

Conversion of serine to lysine

Answer

Conversion of serine to glycine

Answer

Conversion of glutamine to glutamate

Question 10

Which of the following micronutrient deficiencies can lead to anemia?

Accepted Answer

Copper

Answer

Molybdenum

Answer

Fluorine

Answer

Selenium

NEET-PG 2012 — Biochemistry