Lecture Overview: How chemoorganotrophic microbes obtain energy from organic molecules.
Key Processes: Glycolysis, citric acid cycle, fermentation, aerobic and anaerobic respiration.
Important Concepts: Proton motive force and ATP synthase.
Textbook Reference: Chapter 3.6-3.10
Energy Sources:
Chemicals:
Organic: glucose, acetate
Inorganic: Fe2+, NH4+
Types of Chemoorganotrophs:
Chemoorganotrophs
Chemolithotrophs
Phototrophs
Reactions:
Glucose + 6 O2 -> 6 CO2 + 6 H2O
H2S + 2 O2 -> S° + H2O
How Biology Generates ATP:
Substrate-level phosphorylation:
ATP produced directly in metabolic reactions from exergonic reactions.
Oxidative phosphorylation:
Energy from electron transfer creates proton motive force to synthesize ATP.
Photophosphorylation:
Light energy captures protons to generate ATP.
Chemoorganotrophs prefer glucose as an energy source, undergoing a sequence of oxidation reactions.
Other organic compounds, including various sugars, can also be used to generate energy.
Process Overview:
Glucose is broken down into two pyruvate molecules through multiple steps.
Important metabolic pathway found in all life domains; provides energy quickly and feeds into the citric acid cycle.
Oxygen Requirement:
Does not require O2, can proceed to respiration or fermentation.
Overall Reaction:
Input: Glucose + 2 NAD+ + 2 Pi + 2 ADP
Output: 2 pyruvate + 2 NADH + 2 ATP + 2 H+ + 2 H2O
Substrate-level phosphorylation: Produces 2 ATP per glucose.
Redox Balance:
Generates NADH with no electron acceptor available to regenerate NAD+; resolved via fermentation or respiration.
Also known as Kreb’s cycle; begins with conversion of pyruvate to acetyl-CoA.
Utilizes a variety of organic compounds (e.g., lipids, amino acids) alongside sugars.
Provides key intermediates for anabolic reactions and serves as a metabolic hub.
Occurs in mitochondria in eukaryotes.
Overall Reaction:
Input: Acetyl-CoA + 2 NAD+ + NADP+ + FAD + Pi + ADP + 2 H2O
Output: 2 CO2 + CoA + 2 NADH + NADPH + FADH2 + ATP + 2 H+
Generates ATP and reducing power (NADH/FADH2) for electron transport chain.
Located in cytoplasmic membrane (inner mitochondrial membrane for eukaryotes).
Restores redox balance and generates proton motive force for ATP production.
Electrons pass through a series of carriers towards terminal acceptors (O2 for aerobic respiration).
Types:
Iron-sulfur proteins: Metal cofactors facilitating electron transfer.
Quinones: Non-protein molecules transport electrons between carriers.
Cytochromes: Proteins with heme groups facilitating high-potential electron transfers.
Converts proton motive force into mechanical energy to synthesize ATP from ADP.
Approximately 3.3 protons translocated generates 1 ATP.
Can function reversibly to maintain PMF in certain organisms.
Preferential use of glucose (catabolite repression) but can utilize different organic molecules (fatty acids, amino acids).
Multiple terminal electron acceptors available for respiration (nitrate, sulfate).
E. coli as a facultative anaerobe:
Capable of aerobic respiration, anaerobic respiration, and fermentation.
Adapts electron transport chain based on oxygen availability.
Definition: Chemotrophic metabolism without external electron acceptors (anaerobic).
Uses substrate-level phosphorylation to generate ATP; maintains redox balance through fermentation products.
Glucose converted to 2 pyruvate, then to 2 lactate with net gain of 2 ATP.
Regenerates NAD+ allowing continued glucose breakdown.
Produces 2 pyruvate, decarboxylated to 2 acetaldehyde and then to ethanol, with CO2 released.
Widely used by certain yeast (e.g., Saccharomyces cerevisiae) in food/beverage fermentation.
Microbes can ferment various organic compounds, not just glucose.
Generates energy-rich compounds for ATP, allowing redox balance and diverse metabolic adaptations.
Lactic Acid Fermentation:
Net: 2 ATP from glucose.
Aerobic Respiration:
Net: Up to 38 ATP from complete oxidation of glucose.