Exhaustive Review of Microbiology, Metabolism, and Genetics

Biomolecules: Phospholipids, Triglycerides, and Nucleic Acids
  • Phospholipid Structure: Consists of a phosphate group, a head called phosphatide, and two long fatty acid tails.
  • Triglyceride Structure: Comprised of a three-carbon sugar, three fatty acid chains, and a phosphate group.
  • DNA vs. RNA Comparison:
        * Shape: DNA typically exists in a full double-helical shape. RNA is usually single-stranded but can be double-stranded in certain viruses.
        * Nucleotide Bases:
            * DNA contains Adenine, Guanine, Cytosine, and Thymine.
            * RNA contains Adenine, Guanine, Cytosine, and Uracil (Uracil replaces Thymine).
        * Sugars: RNA contains ribose (ribonucleotide), while DNA contains deoxyribose (deoxyribonucleotide). The primary chemical difference is the presence of an oxygen hydroxyl group in ribose.
Metabolism and Enzyme Function
  • Anabolism: The process of building up larger molecules from smaller ones.
  • Catabolism: The process of breaking down larger molecules into smaller ones.
  • Enzymes as Catalysts: Enzymes facilitate metabolic reactions. Without the presence of specific enzymes, these reactions will not occur.
  • Enzyme Mechanism: Typically, two substrates bind into an enzyme to be linked together into a new product (anabolism), or a single product enters the enzyme and is broken apart (catabolism).
The Central Dogma: Transcription and Translation
  • Cellular Components: The process involves the cell wall, cytoplasm, and the nuclear membrane (nuke).
  • Transcription: DNA located inside the nucleus is transcribed into mRNA (messenger RNA) using polymerases.
  • Export and Translation: mRNA exports out of the nucleus to the cytoplasm where translation occurs.
  • Translation Machinery:
        * Ribosomes: These structures hold the machinery together and "read" the mRNA.
        * Codon: The sequence of three bases on the mRNA that codes for a specific amino acid.
        * tRNA (Transfer RNA): Brings individual amino acids to the ribosome. It contains an anticodon (the opposite/complement of the codon) to link with the mRNA.
  • Protein Synthesis: As amino acids link, they form a peptide (short chain). Once the chain is very long, it is called a protein.
  • Protein Structure:
        * Primary Structure: The linear sequence of amino acids.
        * Secondary Structure: Local folding (e.g., alpha helices or beta sheets).
        * Tertiary Structure: The overall three-dimensional shape.
        * Quaternary/Globular Structure: Complex folding that allows for functional sites.
  • Functional Examples:
        * Enzymes: Folded to create specific pockets for substrates to enter and exit after a reaction.
        * Structural Proteins: Examples include actin and myosin in muscle tissues, which are long, sturdy, and tightly bound to provide strength.
Nutrient Acquisition and Redox Reactions
  • Autotrophs: Organisms like plants that make their own food.
  • Heterotrophs: Organisms that must eat other things to obtain nutrients.
  • Redox (Reduction-Oxidation) Reactions: These reactions occur simultaneously; one molecule is oxidized while another is reduced through the transfer of an electron.
  • LEO (Lose Electron = Oxidation): The molecule donating the electron is oxidized.
  • GER (Gain Electron = Reduction): The molecule accepting the electron is reduced.
Cellular Respiration and ATP Production
  • ATP (Adenosine Triphosphate): The essential energy molecule required by all cells. Energy is transferred between bonds and is never destroyed.
  • Glycolysis: The process of breaking down glucose (six carbons) into pyruvate (three carbons).
        * The cell invests 22 ATP units.
        * The process produces 44 ATP units.
        * The net profit is 22 ATP units.
  • The Krebs Cycle (Citric Acid Cycle/Calvin Cycle): Pyruvate is converted into a two-carbon molecule that enters this cycle.
        * Produces water (H2OH_2O) and Carbon Dioxide (CO2CO_2).
        * Involves electron acceptors and receivers, such as the transition from FADFAD to FADH2FADH_2.
  • Mitochondria and the Electron Transport Chain (ETC):
        * The mitochondria are the "powerhouse" of the cell.
        * The ETC pumps electrons through the membrane using a series of catcher/releaser molecules.
        * ATP Synthase: An enzyme/machine pump in the membrane that synthesized ATP using a concentration gradient of hydrogen ions (H+H^+).
        * One glucose molecule can yield approximately 3636 ATP (efficient cells can make up to 3838 ATP).
Microbial Growth and Environmental Conditions
  • Four Phases of Growth:
        * 1. Lag Phase: Cells are adapting to environment, temperature, and climate. They are gathering nutrients and building proteins but not yet multiplying.
        * 2. Log Phase (Exponential Phase): Rapid, exponential growth of the population.
        * 3. Stationary Phase: The rate of death and reproduction are equivalent. Growth levels off.
        * 4. Death Phase: Nutrients run low, and cells die faster than they reproduce.
  • Binary Fission: The method of division for prokaryotes (bacteria).
        * DNA replicates and the cell splits without mitosis.
        * FtsZ (FITC): A protein that forms a ring at the site of division. Preventing this ring prevents cell division, causing cells to grow long and eventually burst.
  • Oxygen Requirements:
        * Obligate Aerobe: Requires oxygen to live.
        * Obligate Anaerobe: Cannot use oxygen; prefers CO2CO_2.
        * Facultative: Can do both but prefers oxygen.
        * Aero-tolerant Anaerobe: Can tolerate oxygen but prefers anaerobic environments.
        * Microaerophile: Requires only a small amount of oxygen; lives just below the surface.
  • Growth Preferences:
        * Halophiles: Like salt (e.g., Staphylococcus likes salt and moisture).
        * Acidophiles: Thrive in acidic environments.
        * Mesophiles: Prefer moderate temperatures (e.g., human body temperature).
        * Extremophiles: Thrive in extreme conditions.
        * Psychrophiles: Prefer cold temperatures.
DNA Structure and Replication
  • Nucleotide Structure: Consists of a phosphate group, a five-carbon sugar, and a nitrogenous base.
  • Phosphodiester Backbone: The structural framework of DNA/RNA.
  • Hydrogen Bonds: Hold the two strands together. They are relatively weak to allow the strands to "unzip" for transcription or replication.
  • Genomes: Prokaryotes usually have one circular DNA chromosome. Eukaryotes have double-stranded linear DNA wrapped around histones to form chromosomes (humans have 2323 pairs).
  • Genotype vs. Phenotype: The genotype (genes) predicts the phenotype (the expressed proteins/traits).
  • Replication Enzymes:
        * Helicase: Unwinds the DNA strands.
        * Gyrase: Reduces torsion/tension from unwinding.
        * Primase: Places primers to start replication.
        * Polymerase: Synthesizes the complementary strand.
        * Ligase: Joins Okazaki fragments on the lagging strand.
  • Directionality: Replication always occurs in the 55' to 33' direction.
  • Types of Replication:
        * Rolling Circle Replication: Used by prokaryotes.
        * Bubble Replication: Used by eukaryotes, forming multiple replication pockets.
Gene Regulation and Molecular Technology
  • Operon: A cluster of genes involved in a single metabolic process, synthesized simultaneously when needed.
        * Repressor Protein: Holds the process in check until needed.
        * Operator: The site where the repressor binds or releases.
  • Molecular Tools:
        * PCR (Polymerase Chain Reaction): Used for diagnosis (pathogen levels) and research (making copies of genes).
        * Arrays: Monitor gene expression (which genes are "turned on" or "off") under specific conditions like drug exposure or temperature changes.
        * Sequencing: Used to track mutations and variants in pathogens (e.g., Hantavirus).
        * CRISPR: A system for gene editing (removing or inserting DNA). This technology raises significant ethical concerns.
Growth Control and Antibiotics
  • Definitions:
        * Bacteriostatic: Slows metabolism to stop growth without killing the bacteria.
        * Bactericidal: Kills the bacteria.
        * Antiseptic: Safe for use on living tissue.
        * Disinfectant: Toxic; used only on inanimate surfaces.
  • Antibiotic Mechanisms of Action:
        1. Inhibition of cell wall synthesis.
        2. Inhibition of DNA synthesis.
        3. Inhibition of protein synthesis.
        4. Inhibition of metabolic pathways.
        5. Disruption of the cell membrane (e.g., Polymyxin B pokes holes in the membrane).
  • Mechanisms of Resistance:
        1. Efflux pumps (pumping the drug out).
        2. Blocking drug entry.
        3. Altering the drug target site.
        4. Target replication/DNA synthesis changes.
  • Types of Resistance:
        * Intrinsic: Natural resistance (e.g., Pseudomonas aeruginosa).
        * Acquired: Gained through incomplete antibiotic courses or mutation.
        * Horizontal Gene Transfer: Movement of resistance genes via plasmids between bacteria.
        * Genetic Drift: Gradual change in a whole group or portion of genes over time.
Pathogenesis and Epidemiology
  • Pathogenesis: The process by which a pathogen causes disease, including entry, invasion, and damage.
  • Stages of Disease Progression: Incubation
    ightarrow Period of Illness (peak)
    ightarrow Convalescence.
  • Virulence Factors: Evasion mechanisms, entry methods, toxins, and capsules (to prevent or survive phagocytosis).
  • Infectious Dose: The number of bacteria or viruses required to cause infection.
  • Epidemiology: Tracking and tracing infections to find the source.
        * John Snow: Known for tracing the cholera pump.
        * Florence Nightingale and Typhoid Mary: Other historical figures in epidemiology.
        * Active Surveillance: Actively seeking data or hunting for cases.
        * Passive Surveillance: Gathering data from patients who voluntarily come into hospitals.
Immunology
  • Innate vs. Adaptive Immunity:
        * Innate: The first line of defense (barriers).
        * Adaptive: Stronger, specific response involving B-cells and T-cells.
  • Bridge Components: Antigen-presenting cells (APCs), macrophages, Natural Killer (NK) cells, cytokines, and complement protein systems.
  • Specific Cell Roles:
        * Cytokines: Signals to produce an activity or bring cells into an area.
        * Chemokines: Siren-like signals that direct cells toward the specific site of infection.
        * Natural Killer (NK) Cells: Kill infected cells by secreting perforins to punch holes in target cell membranes.
        * B-cells: Stimulated by APCs or Helper T-cells to produce antibodies.
        * Helper T-cells: Regulate the adaptive immune process.
Questions & Discussion
  • Student Question: "Is it the shape [that is different between DNA and RNA]?"
  • Instructor Response: Not strictly the shape, but the DNA double helix versus the single-stranded RNA. RNA can be double-stranded in viruses.
  • Student Question: "Wait, there are four bases in DNA… adenine, guanine, cytosine, thymine?"
  • Instructor Response: Yes, and in RNA, Uracil replaces Thymine.
  • Student Question: "Anabolism is building up and catabolism is breaking down?"
  • Instructor Response: Correct.
  • Student Question: "What is the name of the little three bases they're reading?"
  • Instructor Response: It's called a codon.
  • Student Question: "Staph likes what?"
  • Instructor Response: Salt. It likes salt, moisture, and warmth; like ocean water.
  • Student Question: "What does PCR stand for?"
  • Instructor Response: Polymerase Chain Reaction.
  • Student Question: "Who was the person who tracks things?"
  • Instructor Response: John Snow and the pump."