Model Answer / Key
(a) Features of a mitochondrion and their roles in cellular respiration:
(i) Folded inner membrane (Cristae): Provides a vast surface area for the attachment of electron transport chain (ETC) protein complexes, electron carriers (cytochromes), and stalked particles (ATP synthase/F0-F1 ATPases), maximizing oxidative phosphorylation and ATP generation.
(ii) Matrix: Contains a concentrated aqueous mixture of soluble respiratory enzymes (e.g., citrate synthase, dehydrogenase) required for the Krebs cycle (TCA cycle) and beta-oxidation of fatty acids, as well as NAD+ and FAD coenzymes to accept hydrogen atoms.
(iii) Circular DNA (mtDNA): Encodes essential mitochondrial respiratory proteins and enzyme subunits (including components of the electron transport chain and ATP synthase), enabling the mitochondrion to synthesize its own respiratory machinery semi-autonomously and replicate when metabolic demands increase.
(iv) Ribosomes (70S Ribosomes): Translate mitochondrial mRNA into polypeptide chains and structural enzymes within the organelle, allowing direct local protein synthesis without total reliance on the cell's nucleus and cytoplasm.
(b) Importance of the specified organelles (two points each):
(i) Microtubules:
1. Spindle Apparatus Formation: Form the spindle fibers during mitosis and meiosis that attach to kinetochores and ensure precise segregation of sister chromatids and homologous chromosomes.
2. Cytoskeletal Support and Motility: Maintain eukaryotic cell shape, act as intracellular tracks for organelle and vesicle transport (via motor proteins kinesin and dynein), and form the 9+2 structural core (axoneme) of cilia and flagella for cellular movement.
(ii) Golgi body:
1. Modification and Sorting: Chemically modifies proteins and lipids received from the rough and smooth endoplasmic reticulum (e.g., glycosylation to form glycoproteins and glycolipids) and packages them for targeted delivery.
2. Secretion and Lysosome Formation: Packages secretory products into vesicles for exocytosis across the cell membrane, synthesizes plant cell wall pectins, and forms primary lysosomes packed with acid hydrolases.
(iii) Lysosomes:
1. Heterophagy and Autophagy: Fuse with phagocytic vacuoles to digest engulfed pathogens (e.g., bacteria in macrophages) and degrade worn-out intracellular organelles to recycle vital macromolecular constituents.
2. Autolysis (Programmed Cell Death): Release hydrolytic enzymes to break down the entire cell during metamorphosis, developmental tissue resorption (such as tadpole tail regression), or removal of damaged/senescent cells.
Examiner's Explanation
This question evaluates understanding of mitochondrial ultrastructure in relation to biochemical energetics, alongside the physiological roles of microtubules, Golgi apparatus, and lysosomes.
Mark Allocation Criteria
- Part (a)(i): Folded inner membrane surface area for ETC and ATP synthase explained (1 mark)
- Part (a)(ii): Matrix role as enzyme site for Krebs cycle and beta-oxidation explained (1 mark)
- Part (a)(iii): Circular DNA role in semi-autonomous replication and respiratory protein coding (1 mark)
- Part (a)(iv): 70S Ribosomes role in local translation of mitochondrial proteins (1 mark)
- Part (b)(i): Microtubules - 2 valid functions (spindle fibers, motility/transport) (2 marks)
- Part (b)(ii): Golgi body - 2 valid functions (protein packaging/modification, lysosome synthesis) (2 marks)
- Part (b)(iii): Lysosomes - 2 valid functions (pathogen digestion/autophagy, autolysis) (2 marks)