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WorksheetsBiochem Block 4 – Worksheet Questions (Extracted)
Total questions: 80
Worksheet time: 3600secs
A 45-year-old female presents with dry mouth and difficulty swallowing. Biopsy shows lymphocytic infiltration of salivary glands. Which condition is most likely?
Sialolithiasis
Xerostomia
Achlorhydria
Gastritis
A patient with chronic gastritis is found to have no hydrochloric acid in their gastric juice (achlorhydria). This condition would most significantly impair the activation of which enzyme?
Salivary amylase
Trypsinogen
Pepsinogen
Lingual lipase
A 50-year-old male with a history of alcohol abuse presents with severe epigastric pain radiating to the back. Serum amylase and lipase are elevated. What is the diagnosis?
Cholelithiasis
Acute pancreatitis
Gastric ulcer
Lactose intolerance
A child with foul-smelling, fatty stools (steatorrhea) and recurrent respiratory infections is diagnosed with cystic fibrosis. The primary biochemical defect involves which of the following?
Sodium channels
Chloride channels (CFTR)
Bicarbonate secretion
Potassium pumps
During the secretion of HCl in parietal cells, which ion is pumped into the gastric lumen in exchange for potassium (K+)?
Na+
Cl−
H+
HCO3−
A patient presents with right upper quadrant pain after fatty meals. An ultrasound reveals gallstones. This condition (cholelithiasis) is often due to an imbalance in the concentration of which substances?
Bile salts and cholesterol
Bilirubin and albumin
Pepsin and gastrin
Amylase and lipase
Which enzyme in the succus entericus is responsible for activating pancreatic zymogens by converting trypsinogen to trypsin?
Aminopeptidase
Lactase
Enteropeptidase
Maltase
A 20-year-old student experiences bloating, gas, and diarrhea after consuming dairy products. The deficiency of which enzyme is responsible?
Sucrase
Lactase
Isomaltase
Maltase
Which glucose transporter (GLUT) is insulin-dependent and found primarily in muscle and adipose tissue?
GLUT-1
GLUT-2
GLUT-3
GLUT-4
The SGLT-1 transporter moves glucose into intestinal mucosal cells against a concentration gradient using the energy from which source?
ATP hydrolysis directly
Sodium (Na+) gradient
Potassium (K+) gradient
Facilitated diffusion
In aerobic glycolysis, the net yield of ATP per molecule of glucose is:
2 ATP
5 or 7 ATP (depending on shuttle)
30 or 32 ATP
38 ATP
A patient presents with chronic hemolytic anemia. Biochemical analysis shows a deficiency in a glycolytic enzyme that converts phosphoenolpyruvate to pyruvate. Which enzyme is deficient?
Hexokinase
Phosphofructokinase-1
Pyruvate kinase
Aldolase
Which hormone increases during fasting to stimulate glycogenolysis and gluconeogenesis?
Insulin
Glucagon
Growth hormone
Thyroxine
The rate-limiting enzyme of glycolysis is:
Glucokinase
Phosphofructokinase-1 (PFK-1)
Pyruvate kinase
Enolase
In anaerobic conditions (like exercising muscle), pyruvate is reduced to lactate by NADH. This reaction is essential to regenerate which molecule?
FAD
NAD+
ATP
Glucose
Which complex is responsible for the oxidative decarboxylation of pyruvate to acetyl-CoA?
Pyruvate carboxylase
Pyruvate dehydrogenase complex
Lactate dehydrogenase
Succinate dehydrogenase
How many molecules of NADH are produced during one turn of the TCA (Krebs) cycle?
1
2
3
4
The conversion of pyruvate to oxaloacetate in gluconeogenesis requires which cofactor?
Thiamine (B1)
Biotin (B7)
Niacin (B3)
Pyridoxine (B6)
The Cori cycle involves the transport of lactate from muscle to the liver, where it is converted back to which compound?
Alanine
Glycogen
Glucose
Pyruvate
Which substrate provides the carbon skeleton for glucose synthesis during prolonged starvation via the glucose–alanine cycle?
Fatty acids
Muscle protein (alanine)
Acetyl-CoA
Lactate only
Which enzyme in the TCA cycle is also a part of the electron transport chain (Complex II)?
Citrate synthase
Isocitrate dehydrogenase
Succinate dehydrogenase
Malate dehydrogenase
Fluoroacetate is a potent inhibitor of the TCA cycle. It inhibits which enzyme?
Aconitase
Fumarase
Alpha-ketoglutarate dehydrogenase
Malate dehydrogenase
High levels of acetyl-CoA act as an allosteric activator for which gluconeogenic enzyme?
PEP carboxykinase (PEPCK)
Pyruvate carboxylase
Fructose 1,6-bisphosphatase
Glucose 6-phosphatase
Arsenic poisoning affects the pyruvate dehydrogenase complex and alpha-ketoglutarate dehydrogenase by binding to which cofactor?
Thiamine pyrophosphate (TPP)
Lipoic acid
FAD
NAD+
A 6-month-old infant presents with hepatomegaly and severe fasting hypoglycemia. A liver biopsy shows an inability to dephosphorylate glucose-6-phosphate (Von Gierke's disease). This is glycogen storage disease (GSD) type:
I
II
III
V
Which glycogen storage disease is characterized by painful muscle cramps during exercise and the absence of muscle phosphorylase (McArdle’s disease)?
Type I
Type II
Type IV
Type V
The primary purpose of the hexose monophosphate (HMP) shunt is to produce:
ATP and NADH
NADPH and pentose sugars
Glucose and fructose
Lactate and pyruvate
A patient with G6PD deficiency develops hemolytic anemia after taking primaquine (an antimalarial). This occurs because red blood cells cannot maintain adequate levels of which molecule?
Oxidized glutathione
Reduced glutathione
ATP
Oxygen
Which enzyme in the HMP shunt requires thiamine pyrophosphate (TPP) and is used clinically to assess thiamine status?
Glucose-6-phosphate dehydrogenase
Transketolase
Transaldolase
Lactonase
Which pathway is responsible for the formation of cataracts in diabetic patients due to accumulation of sorbitol?
Glycolysis
Polyol (sorbitol) pathway
Uronic acid pathway
Glycogenesis
In the uronic acid pathway, humans cannot synthesize vitamin C (ascorbic acid) because they lack which enzyme?
Uronic acid reductase
L-gulonolactone oxidase
Xylitol dehydrogenase
Glucuronidase
Glycogenolysis in the liver is stimulated by glucagon via which second messenger?
cAMP
IP3
Ca2+
cGMP
Chronic ethanol consumption leads to a high NADH/NAD+ ratio. This favors the conversion of pyruvate to:
Glucose
Oxaloacetate
Lactate
Acetyl-CoA
Fatty liver (steatosis) in alcoholics occurs because high NADH inhibits:
Fatty acid synthesis
Beta-oxidation of fatty acids
Glycolysis
Protein synthesis
The component of the electron transport chain that is a mobile electron carrier between Complex III and IV is:
Ubiquinone (CoQ)
Cytochrome c
FMN
Cytochrome a3
Cyanide and carbon monoxide (CO) inhibit the electron transport chain by binding to:
Complex I
Complex II
Complex III
Complex IV (Cytochrome oxidase)
An uncoupler like 2,4-dinitrophenol (DNP) causes:
Inhibition of electron flow
Decreased oxygen consumption
Increased heat production and decreased ATP synthesis
Inhibition of Complex V only
Oligomycin inhibits ATP synthesis by:
Dissipating the proton gradient
Blocking the F_o pore of ATP synthase (Complex V)
Inhibiting Complex III
Binding to cytochrome c
Which shuttle system for reducing equivalents yields more ATP (approximately 2.5 per NADH)?
Glycerol 3-phosphate shuttle
Malate-aspartate shuttle
Citrate-malate shuttle
Lactate-pyruvate shuttle
The chemiosmotic hypothesis states that ATP is produced as H+ ions flow from the:
Matrix to intermembrane space
Intermembrane space to matrix
Cytosol to matrix
Inner membrane to outer membrane
A child presents with edema, thinned hair, and a "flaky paint" dermatosis, despite having a relatively normal caloric intake but very low protein. This is:
Marasmus
Kwashiorkor
Scurvy
Rickets
A 1-year-old child appears "skin and bones" with severe muscle wasting and no edema. This is characteristic of:
Kwashiorkor
Marasmus
Cachexia
Obesity
A BMI (Body Mass Index) of 32 kg/m2 is classified as:
Overweight
Obese (Class I)
Morbidly obese
Underweight
Which type of obesity is associated with a higher risk of metabolic syndrome and cardiovascular disease?
Gynoid (lower body)
Android (upper body/central)
Peripheral
Subcutaneous
Basal metabolic rate (BMR) is generally higher in:
Females than males
Older adults than children
People with higher lean muscle mass
Hypothyroid patients
What is the energy content of 1 gram of alcohol?
4 kcal
7 kcal
9 kcal
0 kcal
A patient with gluten enteropathy (celiac disease) must avoid:
Milk
Wheat, barley, and rye
Fructose
Meat
During pregnancy, the daily caloric requirement typically increases by approximately how many kcal in the second trimester?
100 kcal
340 kcal
1000 kcal
No increase is needed
Dietary fiber is recommended in patients with hemorrhoids because it:
Increases cholesterol excretion
Softens stools and reduces straining
Slows glucose absorption
Increases BMR
Which of the following is a macronutrient?
Vitamin A
Iron
Fat
Zinc
The committed step in purine synthesis is catalyzed by:
PRPP synthetase
PRPP glutamyl amidotransferase
Xanthine oxidase
HGPRT
The parent purine nucleotide from which both AMP and GMP are derived is:
XMP
IMP
OMP
TMP
A 5-year-old boy shows self-mutilation (biting lips/fingers), hyperuricemia, and intellectual disability. He likely lacks which enzyme?
Adenosine deaminase
HGPRT (Lesch-Nyhan syndrome)
Xanthine oxidase
APRT
Severe Combined Immunodeficiency (SCID) is most commonly associated with a deficiency in:
HGPRT
Adenosine deaminase (ADA)
UMP synthase
Ribonucleotide reductase
Gout is caused by the accumulation of crystals of:
Calcium oxalate
Monosodium urate
Cholesterol
Urea
Allopurinol treats gout by inhibiting which enzyme?
PRPP synthetase
Xanthine oxidase
HGPRT
Adenosine deaminase
Orotic aciduria (Type I) results from a deficiency in UMP synthase. It is characterized by megaloblastic anemia and is a disorder of:
Purine synthesis
Pyrimidine synthesis
Urea cycle
HMP shunt
The drug methotrexate inhibits which enzyme, thereby reducing the availability of THF for nucleotide synthesis?
Dihydrofolate reductase
Thymidylate synthase
Xanthine oxidase
Ribonucleotide reductase
5-Fluorouracil (5-FU) is a pyrimidine analog that primarily inhibits:
Ribonucleotide reductase
Thymidylate synthase
PRPP amidotransferase
Dihydrofolate reductase
Which enzyme reduces ribose to deoxyribose for DNA synthesis and is inhibited by hydroxyurea?
PRPP synthetase
Ribonucleotide reductase
DNA polymerase
Dihydrofolate reductase
CPS-II (Carbamoyl Phosphate Synthetase II) is involved in pyrimidine synthesis and is located in the:
Mitochondria
Cytosol
Nucleus
Lysosome
Mycophenolic acid acts as an immunosuppressant by inhibiting the synthesis of:
AMP
GMP
CTP
UTP
A patient with uncontrolled diabetes mellitus presents with Kussmaul breathing and a blood pH of 7.25. This is:
Metabolic alkalosis
Metabolic acidosis
Respiratory acidosis
Respiratory alkalosis
The primary compensatory mechanism for metabolic acidosis is:
Renal excretion of bicarbonate
Hyperventilation to blow off carbon dioxide
Hypoventilation
Increased ammonium production in the liver
Which of the following causes respiratory acidosis?
High altitude
Anxiety attack
Chronic obstructive pulmonary disease (COPD)
Excessive vomiting
A patient with severe prolonged vomiting is likely to develop:
Metabolic acidosis
Metabolic alkalosis
Respiratory acidosis
Respiratory alkalosis
The anion gap is calculated as:
[Na+] − ([Cl−] + [HCO3−])
[Na+] + [K+]
[Cl−] − [HCO3−]
[HCO3−] − [H+]
In a patient with alkalosis, the decrease in ionized calcium levels can lead to:
Hypertension
Tetany (increased neuromuscular excitability)
Jaundice
Diarrhea
Hyperventilation due to a panic attack leads to which acid–base disturbance?
Metabolic acidosis
Respiratory acidosis
Respiratory alkalosis
Metabolic alkalosis
The normal ratio of bicarbonate to dissolved carbon dioxide in blood at pH 7.4 is:
10:1
20:1
1:20
1:1
A chronic alcoholic presents with hypoglycemia. The high NADH/NAD+ ratio inhibits gluconeogenesis by pushing which reaction toward the product?
Pyruvate → Lactate
Glucose → Glucose-6-phosphate
Alanine → Pyruvate
PEP → Pyruvate
A patient has pCO2 = 60 mmHg (normal ≈ 40) and pH = 7.2. This is:
Metabolic acidosis
Respiratory acidosis
Metabolic alkalosis
Respiratory alkalosis
In the malate–aspartate shuttle, which amino acid is used to transport nitrogen back to the cytosol?
Glutamate
Aspartate
Alanine
Glycine
Which enzyme deficiency causes a "mousy odor" to urine and intellectual disability?
Tyrosinase
Phenylalanine hydroxylase (PKU)
Lactase
Arginase
A patient is diagnosed with high-altitude sickness. The body compensates for the resulting respiratory alkalosis by:
Increasing carbon dioxide retention
Excreting bicarbonate in urine
Producing more lactic acid
Decreasing respiratory rate
Which of the following is an inhibitor of Complex I of the electron transport chain?
Rotenone
Antimycin A
Azide
Malonate
A patient with a high-protein diet will have increased activity of which cycle to dispose of nitrogen?
TCA cycle
Urea cycle
Cori cycle
Glucose–alanine cycle
Glucose-6-phosphate dehydrogenase (G6PD) deficiency follows what inheritance pattern?
Autosomal dominant
Autosomal recessive
X-linked recessive
Mitochondrial
What is the effect of insulin on glycogen synthase?
Inhibits it by phosphorylation
Activates it by dephosphorylation
Has no effect
Degrades it
In pyruvate dehydrogenase (PDH) deficiency, the buildup of pyruvate leads to its conversion into:
Ethanol
Lactate (causing lactic acidosis)
Glucose
Fatty acids
