Bioenergetics
INTRODUCTION TO BIOCHEMISTRY
Course: BIOCHEMISTRY CHEM 2713
Instructor: Dr. Amitabh Jha
ENERGY AND BIOENERGETICS
Overview
The topic covers aspects such as:
- The energetics of life
- Laws of Thermodynamics
- Relationships between:
- Free energy
- Equilibrium states
- Reactants and products
- Free energy in biological systems
ENERGY IN LIVING CELLS
Characteristics of Living Cells
Living cells are dynamic structures that perform vital activities:
- Growth
- Movement
- Synthesis of complex macromolecules
- Shuttle substances in/out and between membrane-bound compartmentsAll these activities REQUIRE ENERGY.
Energy Source
Energy from the Sun is absorbed by plants in chloroplasts through photosynthesis, where:
- Plants use solar energy to convert carbon dioxide (CO₂) and water (H₂O) into energy-rich sugar molecules (e.g., Glucose).
- The overall process can be summarized as:
These sugars can subsequently be utilized by animals for energy production through cellular respiration, primarily in the mitochondria, leading to the production of adenosine triphosphate (ATP).
- ATP acts as the energy currency for cellular processes.
BIOENERGETICS
Definition: Bioenergetics describes how organisms capture, transform, store, and utilize energy.
Key questions in bioenergetics include:
- How much food must an animal consume daily to maintain health?
- Why does the brain consume energy even while resting?
- Importance of electrolyte balance in cells.
THERMODYNAMICS
Key Concepts in Thermodynamics
Energy:
- Defined as the capacity to do work.
- Fundamental to all physical and biological processes; in living organisms, work is powered by ATP.Thermodynamics:
- The study of energy transformations accompanying physical and chemical changes.Bioenergetics:
- A special branch focused on biological systems, as illustrated by Einstein's equation:
Factors Affecting Biochemical Reactions
Important factors include:
- Enthalpy (H): Total heat content of a system.
- Entropy (S): Measure of disorder within a system.
- Free Energy (G): Energy available to perform work.Reactions in laboratories reach equilibrium, whereas reactions in living organisms do not reach equilibrium until death occurs.
LAWS OF THERMODYNAMICS
First Law of Thermodynamics
States that energy can be neither created nor destroyed; it only changes forms.
Key Formula:
where:
- = change in internal energy
- = heat exchanged
- = work doneIn a closed system, like the universe, total energy remains constant.
Enthalpy and Heat Exchange
Enthalpy (H) is related to internal energy by:
Changes in enthalpy (ΔH) are critical:
- If riangle H < 0, reaction is exothermic (releases heat). - If riangle H > 0, reaction is endothermic (absorbs heat).At constant temperature, isothermic reactions yield:
Enthalpy of a reaction can be calculated as:
Standard enthalpy change at given conditions is indicated as .
Second Law of Thermodynamics
States that:
- Physical or chemical changes that release energy tend to be spontaneous.
- Non-spontaneous reactions need a continuous energy supply.
- All spontaneous processes lead to increased disorder or entropy in a system.The essential takeaway is that natural processes tend to increase disorder.
Entropy and Spontaneity
For spontaneous processes, the universal entropy change is positive:
Living systems manage internal order but increase the entropy of their surroundings; e.g., animals converting consumed food into disordered waste products (CO₂, H₂O, and heat).
Free Energy and Spontaneity
Gibbs free energy (ΔG) helps predict the spontaneity of reactions:
- ext{If } riangle G < 0: reaction is spontaneous and exergonic. - ext{If } riangle G > 0: reaction is non-spontaneous and endergonic.
- : system is at equilibrium.The Gibbs Free Energy Equation is expressed as:
STANDARD FREE ENERGY CHANGES
Standard free energy (ΔG°) is defined under specific conditions:
- 25°C, 1 atm pressure, and 1.0 M concentration of solutes.Its relationship with the equilibrium constant (K_eq) is represented as:
where
- R = universal gas constant
- T = absolute temperatureMost biochemical reactions occur at or near pH 7, which modifies the considerations for 1.0 M solute concentration to 1.0 M standard variable ().
COUPLED REACTIONS
Many reactions with a positive ΔG°′ (endergonic) can be coupled to drive the spontaneity of reactions:
- The principle of free energy being additive allows coupled reactions to proceed.
- If the net ΔG°′ becomes sufficiently negative, the overall process can be considered exergonic.
Example of Coupled Reaction
Conversion of glucose-6-phosphate to fructose-1,6-bisphosphate involves steps with:
- An endergonic step with ΔG°′ = +1.7 kJ/mol (not favorable by itself).
- An exergonic step with ΔG°′ = -14.2 kJ/mol (favorable due to ATP cleavage).Cumulatively the overall coupled reaction yields a ΔG°′ of -12.5 kJ/mol, indicating that the full process will proceed under standard conditions.
THE HYDROPHOBIC EFFECT
Understanding Aggregation
Spontaneous aggregation of non-polar substances can be understood through thermodynamic principles:
- Aggregation reduces surface area contact with water, thereby increasing overall entropy.
- The overall free energy is negative, which promotes spontaneity in the process.The exclusion of water plays a crucial role in biological processes such as membrane formation and protein folding.