NHM MP Staff Nurse-2022
Biochemistry & Nutrition
Medium

Beta oxidation of fatty acids takes place at

Appeared in: NHM MP Staff Nurse-2022

Explanation

  • Beta-oxidation is the catabolic process where fatty acids are broken down to produce acetyl-CoA, NADH, and FADH₂.
  • This process occurs in two main cellular locations depending on the length of the fatty acid chain.
  • Mitochondria are the primary site for the oxidation of short, medium, and long-chain fatty acids, which constitute the majority of dietary fats.
  • Peroxisomes are responsible for the initial oxidation of very-long-chain fatty acids (VLCFAs) and branched-chain fatty acids.
  • The shortened fatty acids from peroxisomes are then transferred to mitochondria for complete oxidation. Therefore, both organelles are involved.

Why Other Options Were Wrong

  • Option A: This option is incomplete. While peroxisomes are a site for beta-oxidation, they are specialized for very-long-chain fatty acids and are not the sole location for this metabolic process.
  • Option B: This option is incomplete. Although mitochondria are the primary site for the beta-oxidation of most common fatty acids, they cannot process very-long-chain fatty acids without initial breakdown in the peroxisomes.
  • Option D: Liposomes are not cellular organelles involved in metabolism. They are artificially created lipid vesicles used primarily for drug delivery systems.

Related Visual

Visual explanation — Related Visual
Clinical Relevance
  • Nursing practice connection: This is primarily an exam-oriented knowledge point with limited direct bedside application, so retain Cellular location of fatty acid beta-oxidation as background academic context rather than a clinical decision trigger.
  • Understanding the dual locations of beta-oxidation is crucial for diagnosing certain genetic metabolic disorders.
  • Defects in mitochondrial beta-oxidation, such as Medium-Chain Acyl-CoA Dehydrogenase (MCAD) deficiency, can lead to hypoglycemia, lethargy, and coma, especially during fasting. It is a cause of Sudden Infant Death Syndrome (SIDS).
  • Disorders of peroxisomal function, like Zellweger syndrome, result in the accumulation of very-long-chain fatty acids in tissues, leading to severe neurological damage, liver dysfunction, and early death.
How to Approach the Question
  • First, identify the core concept of the question, which is the cellular location of 'beta-oxidation of fatty acids'.
  • Recall the major metabolic pathways related to lipids and the organelles involved. Remember that mitochondria are the 'powerhouses' of the cell and are central to energy production.
  • Consider if there are any exceptions or special cases. While mitochondria handle most fatty acids, recall that very-long-chain fatty acids require a special initial processing step.
  • Evaluate the options based on this knowledge. 'Peroxisome' and 'Mitochondria' are both involved, making them individually incomplete.
  • Select the option that encompasses all correct locations. 'Mitochondria and peroxisome' is the most comprehensive and accurate choice.
  • Eliminate options that are clearly incorrect, such as 'Liposomes', which are not metabolic organelles.
Concept Tested & Keywords
  • Concept Tested: Cellular location of fatty acid beta-oxidation
  • Stem keywords: Beta oxidation, fatty acids
  • Lead-in keywords: takes place at

Question ID

QoI51dJcug_slFGN76vmKU

Reference Book

E6 Harper's Illustrated Biochemistry2023 (pp 26-793 of 813) pp. 204-206, 202-204

Practise the full NHM MP Staff Nurse-2022

Attempt every question from this paper in a timed mock, then review the full solution for each one.

More Lipids Questions

More NHM MP Staff Nurse-2022 Questions