BackMicrobial Metabolism, Genetics, Growth Control, and Pathogenesis Study Guide Unit 2
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Microbial Metabolism
Metabolism, Anabolism, and Catabolism
Metabolism refers to all chemical reactions occurring within a cell, encompassing both energy-producing and energy-consuming processes.
Anabolism: The synthesis of complex molecules from simpler ones; requires energy (endothermic).
Catabolism: The breakdown of complex molecules into simpler ones; releases energy (exothermic).
Endothermic Reaction: Absorbs energy from surroundings (e.g., photosynthesis).
Exothermic Reaction: Releases energy (e.g., cellular respiration).
Example: Glucose breakdown in glycolysis is catabolic and exothermic.
Enzymes and Coenzymes
Enzymes are biological catalysts that speed up metabolic reactions without being consumed.
Characteristics: Specificity, efficiency, sensitivity to temperature and pH.
Coenzymes: Organic molecules (often vitamins) that assist enzymes (e.g., NAD, FAD).
Example: NAD acts as an electron carrier in cellular respiration.
Electron and Hydrogen Carriers
Electron carriers are molecules that transport electrons during metabolic reactions.
NAD (Nicotinamide adenine dinucleotide): Accepts electrons and hydrogen.
FAD (Flavin adenine dinucleotide): Accepts electrons and hydrogen.
Coenzyme A: Transfers acetyl groups in metabolism.
Aerobic Respiration
Aerobic respiration is the process by which cells convert glucose and oxygen into energy, carbon dioxide, and water.
General Balanced Equation:
Final Hydrogen and Electron Acceptor: Oxygen (O2).
Glycolysis
Glycolysis is the first step in cellular respiration, breaking down glucose into pyruvate.
Location: Cytoplasm of the cell.
Activation Energy: 2 ATP molecules are invested to start glycolysis.
Example: Glucose (6C) → 2 Pyruvate (3C each).
Krebs Cycle (Citric Acid Cycle)
The Krebs cycle further oxidizes pyruvate, generating electron carriers and ATP.
ATP Yield: Each NADH2 yields 3 ATP; each FADH2 yields 2 ATP.
Example: For each glucose, the cycle produces multiple NADH and FADH2.
Electron Transport System (ETS)
The ETS is the final stage of aerobic respiration, generating most ATP.
Location in Bacteria: Cell membrane.
ATP Generation: Most ATP is produced here via oxidative phosphorylation.
Fermentation and Anaerobic Respiration
Fermentation and anaerobic respiration occur in the absence of oxygen.
Fermentation: Organic molecules are the final electron acceptors (e.g., pyruvate).
Anaerobic Respiration: Inorganic molecules (e.g., nitrate, sulfate) are final electron acceptors.
Difference: Fermentation does not use ETS; anaerobic respiration does.
Microbial Genetics
Genome, Genes, Genotype, and Phenotype
The genome is the complete set of genetic material in an organism.
Gene: Segment of DNA coding for a protein or trait.
Genotype: Genetic makeup of an organism.
Phenotype: Observable traits resulting from genotype.
DNA Structure and Replication
DNA is a double helix with antiparallel strands; replication is semi-conservative.
Antiparallel Arrangement: Strands run in opposite directions (5' to 3' and 3' to 5').
Primer: RNA primer initiates replication; later removed by enzymes.
Mutation: Change in DNA sequence.
RNA Structure and Function
RNA is single-stranded and comes in several forms, each with specific functions.
mRNA: Messenger RNA; carries genetic code from DNA to ribosome.
tRNA: Transfer RNA; brings amino acids to ribosome.
rRNA: Ribosomal RNA; forms part of ribosome structure.
Transcription and Translation
Transcription is the synthesis of RNA from DNA; translation is the synthesis of protein from RNA.
Transcription: DNA → RNA.
Translation: RNA → Protein.
RNA Pairing and Codons
RNA pairs with DNA during transcription and with itself in secondary structures.
RNA-DNA Pairing: A-U, T-A, C-G, G-C.
Codon: Three-base sequence in mRNA coding for an amino acid.
Anticodon: Three-base sequence in tRNA complementary to codon.
Horizontal Gene Transfer in Bacteria
Bacteria can exchange genetic material through several mechanisms.
Transformation: Uptake of naked DNA from environment.
Conjugation: Transfer of DNA via direct cell-to-cell contact (pilus).
Genetic Engineering: Manipulation of genes for desired traits.
Microbial Growth Control
Definitions of Control Methods
Various terms describe methods to control microbial growth.
Antisepsis: Removal of pathogens from living tissue.
Degermation: Mechanical removal of microbes from skin.
Disinfection: Removal of pathogens from inanimate objects.
Sterilization: Complete destruction of all microbial life.
Sanitation: Reduction of microbial population to safe levels.
Microbial Resistance
Microbes vary in their resistance to control methods.
Easiest to Eliminate: Enveloped viruses, vegetative bacteria.
Hardest to Eliminate: Bacterial endospores, prions.
Factors Influencing Antimicrobial Effectiveness
Number of microbes
Type of microbe
Environment (organic matter, temperature, biofilms)
Time of exposure
Physical Agents of Control
Physical methods are used to control microbial growth.
Heat: Sterilization (autoclaving), pasteurization.
Filtration: Removal of microbes from liquids or air.
Radiation: UV, ionizing radiation for sterilization.
Chemical Agents of Control
Chemical methods are used for disinfection and antisepsis.
Alcohols: Disinfect surfaces, skin.
Halogens: Chlorine, iodine for water and surfaces.
Phenolics: Disinfectants for surfaces.
Quaternary Ammonium Compounds: Used in sanitation.
Pathogenesis and Epidemiology
The Microbiome
The microbiome is the collection of microorganisms living in and on the human body.
Origin: Acquired at birth and from environment.
Colonization, Infection, and Disease
Microbes interact with hosts in various ways.
Colonization: Establishment of microbes without causing disease.
Infection: Invasion and multiplication of microbes in host.
Disease: Disruption of normal host function due to infection.
Steps in Causing Disease
Pathogenesis involves several steps.
Entry into host
Attachment to host tissues
Survival and multiplication
Causing damage (toxins, immune response)
Exotoxin: Secreted proteins causing damage (e.g., tetanus toxin).
Endotoxin: Lipid A component of Gram-negative bacteria released upon cell death.
Signs vs. Symptoms
Sign: Objective evidence of disease (e.g., fever).
Symptom: Subjective experience (e.g., pain).
Patterns of Transmission
Communicable diseases can be transmitted in various ways.
Direct contact
Indirect contact (fomites)
Vehicle transmission (water, food)
Vector transmission (insects)
Koch’s Postulates
Koch’s Postulates are criteria to establish a microbe as the cause of a disease.
Microbe must be found in all cases of disease.
Microbe must be isolated and grown in pure culture.
Pure culture must cause disease in healthy host.
Microbe must be re-isolated from experimentally infected host.
Morbidity vs. Mortality
Morbidity: Incidence of disease.
Mortality: Incidence of death.
Key Epidemiological Terms
Term | Definition |
|---|---|
Reservoir | Source of pathogen (e.g., humans, animals, environment) |
Nosocomial | Hospital-acquired infection |
Fomite | Inanimate object transmitting disease |
Vehicle | Non-living carrier (e.g., water, food) |
Vector | Living carrier (e.g., mosquito) |
Communicable | Transmissible from person to person |
Contagious | Highly transmissible |