UPSC MainsBOTANY-PAPER-II202415 Marks
Q11.

Describe along with illustrated diagrams the structure and function of mitochondria and endoplasmic reticulum.

How to Approach

This question requires a detailed understanding of two crucial cell organelles: mitochondria and endoplasmic reticulum. The approach should be to first define each organelle, then describe their structure with well-labeled diagrams, and finally explain their functions. A comparative approach highlighting their differences can also be beneficial. Focus on the key features relevant to their roles in cellular processes. The answer should demonstrate a clear grasp of cellular biology.

Model Answer

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Introduction

Cells, the fundamental units of life, rely on specialized structures called organelles to perform specific functions. Among these, mitochondria and the endoplasmic reticulum (ER) are paramount. Mitochondria are often referred to as the "powerhouses of the cell" due to their role in ATP production, while the endoplasmic reticulum is a vast network involved in protein and lipid synthesis, transport, and detoxification. Understanding their structure and function is crucial to comprehending cellular processes and overall organismal physiology. This answer will detail the structure and function of both organelles, supported by illustrative diagrams.

Mitochondria: Structure and Function

Mitochondria are double-membrane bound organelles found in most eukaryotic cells. They are responsible for generating most of the cell’s supply of adenosine triphosphate (ATP), used as a source of chemical energy.

Structure

The structure of a mitochondrion can be described as follows:

  • Outer Membrane: Smooth and permeable to small molecules.
  • Inner Membrane: Highly folded into cristae, increasing surface area for ATP synthesis. Impermeable to most ions and molecules, requiring transport proteins.
  • Intermembrane Space: The space between the outer and inner membranes.
  • Matrix: The space enclosed by the inner membrane, containing enzymes, ribosomes, mitochondrial DNA (mtDNA), and other molecules involved in ATP production.
  • Cristae: Infoldings of the inner membrane, providing a large surface area for the electron transport chain and ATP synthase.
Mitochondria Structure

Function

The primary function of mitochondria is to generate ATP through cellular respiration. This process involves:

  • Glycolysis: Occurs in the cytoplasm, breaking down glucose into pyruvate.
  • Krebs Cycle (Citric Acid Cycle): Occurs in the mitochondrial matrix, oxidizing pyruvate to produce carbon dioxide, ATP, NADH, and FADH2.
  • Electron Transport Chain (ETC): Located on the inner mitochondrial membrane, using NADH and FADH2 to generate a proton gradient.
  • Oxidative Phosphorylation: Uses the proton gradient to drive ATP synthase, producing large amounts of ATP.

Mitochondria also play roles in apoptosis (programmed cell death), calcium signaling, and heat production.

Endoplasmic Reticulum: Structure and Function

The endoplasmic reticulum (ER) is an extensive network of membranes found throughout the cytoplasm of eukaryotic cells. It plays a crucial role in the synthesis, folding, modification, and transport of proteins and lipids.

Structure

The ER exists in two main forms:

  • Rough Endoplasmic Reticulum (RER): Studded with ribosomes, giving it a rough appearance. Involved in protein synthesis and modification.
  • Smooth Endoplasmic Reticulum (SER): Lacks ribosomes. Involved in lipid synthesis, carbohydrate metabolism, and detoxification.
Endoplasmic Reticulum Structure

Function

The functions of the ER are diverse and depend on the cell type:

  • Protein Synthesis and Folding (RER): Ribosomes on the RER synthesize proteins destined for secretion, insertion into membranes, or localization to organelles. The ER also assists in protein folding and quality control.
  • Lipid Synthesis (SER): The SER synthesizes phospholipids, steroids, and other lipids.
  • Carbohydrate Metabolism (SER): The SER is involved in glycogen breakdown in liver cells.
  • Detoxification (SER): The SER detoxifies drugs and poisons, particularly in liver cells.
  • Calcium Storage (SER): The SER stores calcium ions, which are important for muscle contraction and other cellular processes.

Comparative Table: Mitochondria vs. Endoplasmic Reticulum

Feature Mitochondria Endoplasmic Reticulum
Primary Function ATP Production Protein & Lipid Synthesis/Transport
Membrane Structure Double Membrane Single Membrane (network of tubules & sacs)
Ribosomes Absent Present (RER) / Absent (SER)
Location Throughout Cytoplasm Throughout Cytoplasm
Genetic Material mtDNA None

Conclusion

In conclusion, mitochondria and the endoplasmic reticulum are essential organelles with distinct structures and functions. Mitochondria are the powerhouses of the cell, generating ATP through cellular respiration, while the ER is a versatile network involved in protein and lipid synthesis, transport, and detoxification. Their coordinated activities are vital for maintaining cellular homeostasis and supporting life processes. Further research continues to reveal the intricate roles these organelles play in health and disease.

Answer Length

This is a comprehensive model answer for learning purposes and may exceed the word limit. In the exam, always adhere to the prescribed word count.

Additional Resources

Key Definitions

ATP (Adenosine Triphosphate)
ATP is a complex organic chemical that provides energy for many processes occurring in cells, such as muscle contraction, nerve impulse transmission, and chemical synthesis.
Cristae
Cristae are the folds of the inner mitochondrial membrane. These folds increase the surface area available for the electron transport chain and ATP synthase, maximizing ATP production.

Key Statistics

Approximately 90% of the energy used by human cells is generated through mitochondrial oxidative phosphorylation.

Source: Lodish et al., Molecular Cell Biology, 4th edition (2000)

The endoplasmic reticulum occupies more than 10% of the total cell volume in eukaryotic cells.

Source: Alberts et al., Essential Cell Biology, 4th edition (2014)

Examples

Mitochondrial Diseases

Mutations in mitochondrial DNA can lead to a variety of mitochondrial diseases, affecting organs with high energy demands like the brain, heart, and muscles. Examples include Leber's hereditary optic neuropathy and mitochondrial encephalomyopathy.

Frequently Asked Questions

What happens if a cell's mitochondria are damaged?

Damaged mitochondria can lead to reduced ATP production, increased oxidative stress, and ultimately cell death. This can contribute to various diseases, including neurodegenerative disorders and cancer.