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CHEM 210 BIOCHEMISTRY MODULE 4 EXAM 2026/2027 UPDATE | Geneva College / Portage Learning | Verified Questions & Revised Answers | Pass Guaranteed - A+ Graded

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Excel on your CHEM 210 Biochemistry Module 4 Exam at Geneva College with this comprehensive 2026/2027 updated resource featuring verified questions and revised correct answers aligned with Portage Learning curriculum standards. This A+ Graded resource for the CHEM 210 Biochemistry Module 4 Examination contains complete exam questions with verified answers and detailed rationales directly aligned with current Geneva College and Portage Learning biochemistry curriculum, module 4 learning objectives, and 2026/2027 academic standards . Featuring complete coverage of amino acid structure and classification, peptide bonds, acid-base chemistry of amino acids, and foundational biochemistry concepts with detailed rationales for every correct and incorrect answer, it provides an authentic replication of the CHEM 210 Module 4 Exam format and biochemistry rigor. With hydrogen bonding, London forces, dipole-dipole interactions, pH calculations, free-energy change (ΔG), enthalpy (ΔH), entropy (ΔS), protein conformation, cofactors, and lipid characteristics plus our Pass Guarantee, this is the definitive tool to earn your A+ on the CHEM 210 Module 4 Exam and successfully complete your biochemistry course with confidence . Download now and pass first try.

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CHEM 210 BIOCHEMISTRY MODULE 4 EXAM 2026/2027
UPDATE | Geneva College / Portage Learning | Verified
Questions & Revised Answers | Pass Guaranteed - A+
Graded

Time Allowed: 90 minutes
Total Points: 100



SECTION A: MULTIPLE CHOICE

(15 questions, 3 points each = 45 points total)

Instructions: Select the best answer for each question. Each question has exactly one
correct answer.



Q1. Which monosaccharide is the primary fuel for the brain under normal physiological
conditions?

A. Fructose

B. Galactose

C. Glucose. [CORRECT]

D. Mannose

Correct Answer: C

Rationale: Glucose is the primary and preferred fuel for the brain under normal
conditions. The brain consumes approximately 120 grams of glucose daily, representing

,about 60% of the body's glucose utilization at rest. While the brain can adapt to use
ketone bodies during prolonged fasting or starvation, glucose remains essential for
optimal neurological function. Fructose (A) is primarily metabolized by the liver and
cannot efficiently cross the blood-brain barrier. Galactose (B) must be converted to
glucose-1-phosphate via the Leloir pathway before systemic utilization. Mannose (D) is
a C-2 epimer of glucose but is not a significant energy source for neural tissue.



Q2. In the glycolytic pathway, which enzyme catalyzes the first committed step and is
the primary regulatory point?

A. Hexokinase

B. Phosphofructokinase-1 (PFK-1). [CORRECT]

C. Pyruvate kinase

D. Glyceraldehyde-3-phosphate dehydrogenase

Correct Answer: B

Rationale: Phosphofructokinase-1 (PFK-1) catalyzes the phosphorylation of
fructose-6-phosphate to fructose-1,6-bisphosphate, representing the first irreversible,
committed step of glycolysis. This reaction is highly exergonic (ΔG°' = -14.2 kJ/mol) and
subject to complex allosteric regulation: activated by AMP and
fructose-2,6-bisphosphate (F2,6BP), inhibited by ATP and citrate. While hexokinase (A)
catalyzes the first step, it is not the committed step (glucose-6-phosphate can enter
glycogen synthesis or PPP). Pyruvate kinase (C) is an important regulatory enzyme but
controls the final step. Glyceraldehyde-3-phosphate dehydrogenase (D) is not a major
regulatory point.

, Q3. A patient with Type 1 Diabetes Mellitus presents with fasting hyperglycemia (320
mg/dL) and glycosuria. Which metabolic consequence results from the absence of
functional insulin signaling?

A. Decreased hepatic gluconeogenesis

B. Increased hepatic gluconeogenesis and decreased peripheral glucose uptake.
[CORRECT]

C. Increased glycogen synthesis in liver and muscle

D. Decreased lipolysis in adipose tissue

Correct Answer: B

Rationale: In Type 1 DM, absolute insulin deficiency leads to: (1) unrestrained hepatic
gluconeogenesis (insulin normally suppresses via decreased FOXO1 activity and
reduced enzyme expression), and (2) failed GLUT4 translocation in muscle/adipose
tissue, preventing glucose uptake. This creates the "starvation in the midst of plenty"
paradox—hyperglycemia with cellular glucose deprivation. Option A is incorrect
(gluconeogenesis increases, not decreases). Option C is incorrect (glycogenolysis
predominates; glycogen synthesis requires active glycogen synthase via
insulin-dependent dephosphorylation). Option D is incorrect (lipolysis increases
dramatically due to uninhibited hormone-sensitive lipase).



Q4. Which intermediate of the pentose phosphate pathway (PPP) provides the carbon
skeleton for nucleotide biosynthesis?

A. Glucose-6-phosphate

B. Ribose-5-phosphate. [CORRECT]

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