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Microbial 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

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