Biochemistry: Catabolism and Anabolism

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Questions and Answers

What is the role of reducing equivalents in cellular metabolism?

  • They release energy through electron transfers. (correct)
  • They provide structural integrity to cells.
  • They are responsible for DNA replication.
  • They store energy for future use.

How do enzyme inhibitors affect enzymatic function?

  • They change the temperature to improve reaction rates.
  • They increase the activation energy required.
  • They bind to the active site and prevent substrate binding. (correct)
  • They enhance substrate concentration in the reaction.

What distinguishes fermentation from glycolysis?

  • Fermentation occurs exclusively in prokaryotes.
  • Fermentation requires oxygen to proceed.
  • Fermentation produces more energy than glycolysis.
  • Fermentation does not generate energy directly. (correct)

What occurrence is primarily responsible for denaturing enzymes?

<p>Extreme pH levels. (B)</p> Signup and view all the answers

In the context of cellular respiration, what is substrate-level phosphorylation?

<p>ATP generation directly from a metabolic pathway. (A)</p> Signup and view all the answers

What describes the growth characteristics of obligate anaerobes?

<p>They cannot survive in the presence of oxygen. (A)</p> Signup and view all the answers

Which process is critical for ATP synthesis during oxidative phosphorylation?

<p>Electron transport chain utilizing reduced electron carriers. (C)</p> Signup and view all the answers

What characterizes the four stages of microbial growth?

<p>Variation in nutrient availability and waste levels. (B)</p> Signup and view all the answers

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Study Notes

Catabolism vs Anabolism & Exergonic vs Endergonic Reactions

  • Catabolism: The breakdown of complex molecules into simpler ones, releasing energy.
  • Anabolism: The synthesis of complex molecules from simpler ones, requiring energy.
  • Exergonic Reaction: Releases energy, often as heat, and has a negative change in free energy (ΔG).
  • Endergonic Reaction: Requires energy to proceed, has a positive change in free energy (ΔG).

Reducing Equivalents, ATP & Energy Transfer

  • Reducing Equivalents: Electron carriers like NADH and FADH2 carry electrons and release energy when transferring them to other molecules.
  • ATP Hydrolysis: Breaking the phosphate bonds in ATP releases energy, which can be used to power endergonic reactions (coupled reaction).

Enzyme Function

  • Enzyme: A biological catalyst that speeds up chemical reactions without being consumed.
  • Enzyme Substrate: The specific molecule that an enzyme acts upon.
  • Active Site: The region on the enzyme where the substrate binds.
  • Activation Energy: The minimum energy required for a reaction to occur. Enzymes lower the activation energy, making reactions happen faster.

Apoenzymes & Cofactors

  • Apoenzyme: The protein component of an enzyme.
  • Cofactor: A non-protein molecule required for enzyme activity, can be metal ions or organic coenzymes.

Enzyme Inhibition

  • Enzyme Inhibitors: Molecules that block enzymatic function, preventing the enzyme from binding to its substrate.
  • Competitive Inhibition: The inhibitor binds to the active site, preventing the substrate from binding.
  • Non-competitive Inhibition: The inhibitor binds to a different site on the enzyme, changing its shape and preventing substrate binding.
  • Antimicrobial Treatments: Block the activity of essential enzymes in pathogens, inhibiting their growth and survival.

Temperature & pH Effects on Enzymes

  • Temperature: Extreme temperatures can denature the enzyme, altering its shape and preventing function. Optimal temperature for each enzyme varies.
  • pH: Enzymes have optimal pH ranges. Changes outside this can affect their activity and lead to denaturation.

Cellular Respiration Overview

  • Cellular Respiration: The process of converting glucose into ATP, the cell's energy currency.
  • Glycolysis: Breakdown of glucose into pyruvate, occurs in the cytoplasm, generates ATP and reducing equivalents.
  • Krebs Cycle (Citric Acid Cycle): Further breakdown of pyruvate, generates ATP and reducing equivalents, occurs in the mitochondria.
  • Electron Transport Chain: Utilizes reducing equivalents from glycolysis and the Krebs Cycle to generate ATP through oxidative phosphorylation, occurs in the mitochondrial membrane.
  • Substrate-Level Phosphorylation: ATP is produced directly from a metabolic reaction, occurs in glycolysis and the Krebs Cycle, less efficient than oxidative phosphorylation.

ATP Synthesis & Oxidative Phosphorylation

  • Oxidative Phosphorylation: Uses the energy from the electron transport chain to generate ATP, the primary method of ATP production.
  • Net ATP Production: Cellular respiration produces approximately 38 ATP molecules per glucose molecule. Glycolysis alone produces much less.

Fermentation

  • Fermentation: Generates ATP through glycolysis, but lacks a final electron acceptor for the electron transport chain, leading to the production of byproducts like lactic acid or ethanol.
  • Final Electron Acceptor: Oxygen is the usual final electron acceptor in cellular respiration, but some organisms can use other molecules like nitrates or sulfates.
  • Industrial & Food Production: Fermentation is used in the production of various food products like yogurt, cheese, bread, wine, and beer.

Prokaryotic Binary Fission vs Eukaryotic Mitosis

  • Prokaryotic Binary Fission: A single-celled organism divides into two identical cells.
  • Eukaryotic Mitosis: Nuclear division in eukaryotic cells, followed by cytokinesis (cell division).

Microbial Growth

  • Logarithmic (Exponential) Growth: Under ideal conditions, microbial populations increase rapidly and exponentially.

Microbial Growth Stages

  • Lag Phase: Initial period with slow or no growth, microorganisms adjust to the new environment.
  • Log Phase: Rapid growth, with a steady increase in microbial population.
  • Stationary Phase: Growth rate plateaus, the number of new cells equals the number of dying cells due to limited resources.
  • Death Phase: Nutrient depletion and waste accumulation lead to a decline in the microbial population.

Biofilm Formation

  • Biofilm Formation: Microorganisms adhere to a surface, forming a structured community encased in a matrix of extracellular polymers.
  • Clinical Environments: Biofilms in hospitals and medical devices can cause infections, making treatment challenging due to their resistance to antibiotics.

Oxygen Tolerance of Microorganisms

  • Obligate Aerobes: Require oxygen for growth, have enzymes to detoxify reactive oxygen species (ROS).
  • Obligate Anaerobes: Cannot grow in the presence of oxygen, lack enzymes to detoxify ROS, oxygen is toxic.
  • Facultative Anaerobes: Can grow with or without oxygen, prefer oxygen for efficient energy production.
  • Aerotolerant Anaerobes: Can tolerate oxygen but don't use it for growth, have mechanisms to detoxify ROS
  • Microaerophiles: Require low oxygen levels, grow in the upper layers of liquid thioglycolate broth.
  • ROS: Reactive oxygen species are toxic byproducts of oxygen metabolism, damage cells.
  • Enzymes: Catalase and superoxide dismutase are enzymes used to detoxify ROS.

Temperature & Microbial Growth

  • Optimal Growth Temperature: The temperature at which an organism grows most rapidly.
  • Below Optimal Temperature: Growth slows down, enzymes work less efficiently.
  • Above Optimal Temperature: Enzymes denature, leading to cell death.

Microorganisms in Extreme Environments

  • Thermophiles: Grow at high temperatures.
  • Psychrophiles: Grow at low temperatures.
  • Acidophiles: Grow at low pH (acidic).
  • Alkalophiles: Grow at high pH (alkaline).
  • Halophiles: Thrive in high salt concentrations.
  • Barophiles: Adapt to high pressure.

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