NEET-PG 2012 - Biochemistry Practice Questions

Q: Which of the following is a Fat Soluble vitamin?

Vitamin A. ***Vitamin A*** - **Vitamin A** is one of the four essential **fat-soluble vitamins** (A, D, E, K), meaning it dissolves in fat and is stored in the body's fatty tissues and liver. - Its **absorption** relies on dietary fats and bile salts, distinguishing it from water-soluble vitamins. *Thiamine* - **Thiamine** (Vitamin B1) is a **water-soluble vitamin** that plays a crucial role in metabolism, converting carbohydrates into energy. - It is **not stored** in large amounts in the body and needs to be replenished regularly through diet. *Niacin* - **Niacin** (Vitamin B3) is a **water-soluble vitamin** vital for cellular metabolism, involving in DNA repair and steroid hormone synthesis. - It is readily excreted in urine when consumed in excess and does not accumulate in fatty tissues. *Riboflavin* - **Riboflavin** (Vitamin B2) is a **water-soluble vitamin** essential for energy production, cellular function, and the metabolism of fats, drugs, and steroids. - Like other B vitamins, it has limited storage in the body and is not dissolved in fat.

Q: Pyridoxine deficiency leads to altered metabolism of?

Tryptophan. ***Tryptophan*** - **Pyridoxine (vitamin B6)** is a critical coenzyme in the metabolism of **tryptophan**, particularly in its conversion to **niacin** and serotonin. - A deficiency leads to an accumulation of abnormal tryptophan metabolites, such as **xanthurenic acid**, which can be excreted in the urine. *Phenylalanine* - The metabolism of phenylalanine involves its conversion to tyrosine, a process catalyzed by **phenylalanine hydroxylase**, which does not directly require pyridoxine. - Deficiencies in phenylalanine metabolism often point to issues like **phenylketonuria**. *Methionine* - Methionine metabolism involves a cycle that generates **S-adenosylmethionine (SAM)** and then homocysteine. - While vitamin B6 is involved in the transsulfuration pathway (converting homocysteine to cysteine), its primary direct impact on methionine metabolism itself is less pronounced than on tryptophan. *Tyrosine* - Tyrosine is synthesized from phenylalanine and is a precursor for **catecholamines** and thyroid hormones. - Its metabolism does not directly rely on pyridoxine as a coenzyme in the main initial steps.

Q: The Shine-Dalgarno sequence is primarily associated with which biological process?

Translation. ***Translation*** - The **Shine-Dalgarno sequence** is a **ribosome-binding site** in prokaryotic messenger RNA (mRNA) that helps recruit the ribosome to the mRNA to initiate protein synthesis. - Its interaction with the **16S rRNA** of the small ribosomal subunit positions the start codon (AUG) correctly for **translation initiation**. - This sequence is located approximately **8 base pairs upstream** of the start codon in bacterial mRNA. *Transcription* - **Transcription** is the process of synthesizing RNA from a DNA template. - It involves elements like **promoters** and **enhancers**, not the Shine-Dalgarno sequence. *DNA replication* - **DNA replication** is the process by which DNA makes a copy of itself. - This process involves origins of replication, helicases, and DNA polymerases, with no role for the Shine-Dalgarno sequence. *RNA splicing* - **RNA splicing** is a eukaryotic process that removes introns from pre-mRNA. - The Shine-Dalgarno sequence is found in **prokaryotes**, which lack splicing machinery and introns.

Q: What is the primary function of a primer in DNA replication?

Initiation of DNA replication. ***Initiation of DNA replication*** - DNA polymerase cannot synthesize new DNA strands de novo; it requires a pre-existing 3'-hydroxyl group to begin adding nucleotides. - The **primer**, a short RNA sequence, provides this necessary **3'-hydroxyl group**, allowing DNA polymerase to start synthesizing the new DNA strand. *Transcription* - This process involves synthesizing **RNA from a DNA template**, primarily carried out by **RNA polymerase**. - While primers are involved in DNA synthesis, they do not directly initiate the process of transcription. *Translation* - **Translation** is the process of synthesizing **proteins from mRNA templates** using ribosomes, tRNA, and amino acids. - This process is distinct from DNA synthesis and does not involve primers; its initiation involves start codons and ribosomal subunits. *Termination of DNA replication* - **Termination of DNA replication** occurs when replication forks meet or at specific termination sequences, often with the involvement of specialized proteins. - Primers are involved in the *start* of replication, not its conclusion.

Q: Acute intermittent porphyria is due to deficiency of?

Porphobilinogen deaminase. ***Porphobilinogen deaminase*** - **Acute intermittent porphyria (AIP)** results from a deficiency in **porphobilinogen deaminase** (also known as hydroxymethylbilane synthase). - This enzyme deficiency leads to the accumulation of **aminolevulinic acid (ALA)** and **porphobilinogen (PBG)**, which are neurotoxic and cause the characteristic symptoms of AIP. *Uroporphyrinogen III synthase* - A deficiency in **uroporphyrinogen III synthase** causes **congenital erythropoietic porphyria (Günther disease)**, which is characterized by severe photosensitivity and hemolytic anemia. - This enzyme defect leads to the accumulation of uroporphyrinogen I and coproporphyrinogen I, not the ALA and PBG associated with AIP. *Ferrochelatase* - Deficiency in **ferrochelatase** causes **erythropoietic protoporphyria (EPP)**, which presents with photosensitivity and chronic liver disease due to the accumulation of **protoporphyrin**. - This condition does not cause the acute neurological attacks seen in AIP. *ALA synthase* - **ALA synthase** is the **rate-limiting enzyme** in heme synthesis; while its activity is crucial, a congenital *deficiency* is not the cause of AIP. - Instead, the *upregulation* of ALA synthase activity in AIP (due to the PBG deaminase block) contributes to the accumulation of ALA and PBG.

Q: What is the primary metal ion found in myoglobin?

Iron. ***Iron*** - **Iron** is the central metal ion in the **heme group** of myoglobin. - It is responsible for **binding oxygen** reversibly, which is myoglobin's primary function in muscle tissue. *Copper* - **Copper** is a component of several enzymes, such as **cytochrome c oxidase** and **superoxide dismutase**, but not myoglobin. - It plays a role in **electron transport** and connective tissue formation. *Selenium* - **Selenium** is an essential trace element that functions as a component of **glutathione peroxidase**, an antioxidant enzyme. - It is not found in the structure of myoglobin. *Zinc* - **Zinc** is a critical component of many enzymes, including **carbonic anhydrase** and **DNA polymerase**. - It is involved in **immune function** and wound healing, but not in oxygen transport by myoglobin.

Q: Which of the following is a tripeptide?

Glutathione. ***Glutathione*** - **Glutathione** is a tripeptide composed of three amino acids: **glutamate**, **cysteine**, and **glycine**. - It plays a crucial role as an **antioxidant** in the body, protecting cells from damage by **free radicals**. *Angiotensin* - **Angiotensin** is a peptide hormone that causes **vasoconstriction** and an increase in **blood pressure**. - It is an **oligopeptide** (typically 8-10 amino acids) rather than a tripeptide. *Glucagon* - **Glucagon** is a peptide hormone produced by the **alpha cells** of the pancreas that raises **blood glucose levels**. - It is a **29-amino acid** polypeptide, much larger than a tripeptide. *Oxytocin* - **Oxytocin** is a hormone involved in social bonding and sexual reproduction, best known for its role in **childbirth** and **lactation**. - It is a **nonapeptide**, meaning it consists of nine amino acids.

Q: Which of the following is the shortest peptide?

Angiotensin III. ***Angiotensin III*** - **Angiotensin III** is a **heptapeptide**, meaning it consists of **7 amino acids**. - It is formed by the removal of the N-terminal aspartate from Angiotensin II (8 amino acids), making it the shortest peptide among the options. - It has similar but weaker actions compared to Angiotensin II in regulating blood pressure and aldosterone secretion. *Oxytocin* - **Oxytocin** is a **nonapeptide**, composed of **9 amino acids**. - It plays a role in uterine contractions during labor and milk ejection during lactation. *Vasopressin* - **Vasopressin**, also known as **antidiuretic hormone (ADH)**, is a **nonapeptide** (**9 amino acids**). - Its primary functions are water reabsorption in the kidneys and vasoconstriction. *Angiotensin II* - **Angiotensin II** is an **octapeptide**, containing **8 amino acids**. - It is a potent vasoconstrictor and stimulates aldosterone secretion, playing a key role in blood pressure regulation.

Q: Where does omega oxidation of fatty acids occur?

Endoplasmic Reticulum. ***Endoplasmic Reticulum*** - **Omega oxidation** of fatty acids occurs in the **endoplasmic reticulum (microsomes)** of liver and kidney cells. - This pathway involves **hydroxylation of the terminal omega carbon** by **cytochrome P450 enzymes** located in the smooth ER. - The omega carbon is then oxidized to a **carboxyl group**, forming a **dicarboxylic acid**. - This is a **minor pathway** that becomes important when **beta-oxidation is impaired** or for metabolism of **medium-chain fatty acids**. *Cytosol* - The cytosol is involved in **fatty acid synthesis**, not omega oxidation. - While some later steps of fatty acid metabolism occur in the cytosol, the initial hydroxylation step of omega oxidation requires ER-localized cytochrome P450 enzymes. *Mitochondria* - **Mitochondria** are the primary site for **beta-oxidation** of fatty acids, not omega oxidation. - Beta-oxidation sequentially removes **two-carbon units from the carboxyl end**, which is distinct from omega oxidation. - The dicarboxylic acids produced by omega oxidation may subsequently undergo beta-oxidation in mitochondria. *None of the options* - This option is incorrect because the endoplasmic reticulum is the correct cellular location for omega oxidation. - The ER contains the necessary cytochrome P450 enzymes for the hydroxylation reaction that initiates this pathway.

Q: Which of the following is not affected in Abetalipoproteinemia ?

HDL. ***HDL*** - **Abetalipoproteinemia** is caused by a defect in the **microsomal triglyceride transfer protein (MTP)**, which is essential for the assembly and secretion of **chylomicrons**, **VLDL**, and subsequently **LDL** and **IDL**. - **HDL synthesis** and secretion occur independently of MTP, as nascent HDL particles are formed in the plasma from lipids and apolipoproteins (primarily apoA-I) released from other lipoproteins and cells. *LDL* - **LDL** is critically affected in abetalipoproteinemia because it is a metabolic product of **VLDL**. - Since **VLDL** production is severely impaired due to the MTP defect, there is a profound deficiency of **LDL** in the plasma. *VLDL* - **VLDL** production is severely impaired in abetalipoproteinemia because **microsomal triglyceride transfer protein (MTP)** is required for its assembly and secretion from the liver. - The inability to load triglycerides onto apoB leads to very low or absent plasma **VLDL** levels. *IDL* - **IDL** is an intermediate lipoprotein in the metabolism of **VLDL** to **LDL**. - Given that both **VLDL** and **LDL** are severely deficient in abetalipoproteinemia, **IDL** levels are also consequently very low or absent.

Question 1

Which of the following is a Fat Soluble vitamin?

Accepted Answer

Vitamin A

Answer

Thiamine

Answer

Niacin

Answer

Riboflavin

Question 2

Pyridoxine deficiency leads to altered metabolism of?

Accepted Answer

Tryptophan

Answer

Phenylalanine

Answer

Methionine

Answer

Tyrosine

Question 3

The Shine-Dalgarno sequence is primarily associated with which biological process?

Accepted Answer

Translation

Answer

Transcription

Answer

DNA replication

Answer

RNA splicing

Question 4

What is the primary function of a primer in DNA replication?

Accepted Answer

Initiation of DNA replication

Answer

Transcription

Answer

Translation

Answer

Termination of DNA replication

Question 5

Acute intermittent porphyria is due to deficiency of?

Accepted Answer

Porphobilinogen deaminase

Answer

Uroporphyrinogen III synthase

Answer

Ferrochelatase

Answer

ALA synthase

Question 6

What is the primary metal ion found in myoglobin?

Accepted Answer

Iron

Answer

Copper

Answer

Selenium

Answer

Zinc

Question 7

Which of the following is a tripeptide?

Accepted Answer

Glutathione

Answer

Angiotensin

Answer

Glucagon

Answer

Oxytocin

Question 8

Which of the following is the shortest peptide?

Accepted Answer

Angiotensin III

Answer

Oxytocin

Answer

Vasopressin

Answer

Angiotensin II

Question 9

Where does omega oxidation of fatty acids occur?

Accepted Answer

Endoplasmic Reticulum

Answer

Cytosol

Answer

Mitochondria

Answer

None of the options

Question 10

Which of the following is not affected in Abetalipoproteinemia ?

Accepted Answer

HDL

Answer

LDL

Answer

IDL

Answer

VLDL

NEET-PG 2012 — Biochemistry