Test 1

Here is a study guide for Chapters 2 through 5, combining high-yield test concepts, detailed mechanisms, and core definitions to ensure full preparation for exams.


Chapter 2: The Chemistry of Life1. Major Chemical Elements & Atomic Structure

  • Six Major Elements of Life: Oxygen, carbon, hydrogen, nitrogen, calcium, and phosphorus make up 98.5%98.5\% of body mass.


  • Valence Electrons: Electrons in the outermost shell that determine chemical bonding properties and reactivity.


  • Free Radicals & Antioxidants:



    • Free Radicals: Particles with an unpaired electron, making them highly reactive and destructive to cellular structures (cause oxidative stress).


    • Antioxidants: Neutralize free radicals (e.g., Superoxide Dismutase [SOD], Vitamin C, Vitamin E).


2. Chemical Bonds & Reactions

  • Types of Bonds:



    • Ionic Bond: Attraction between oppositely charged ions (cation ++ and anion −-); easily dissociate in water.


    • Covalent Bond: Sharing of electron pairs; nonpolar covalent (equal sharing, hydrophobic) vs. polar covalent (unequal sharing, hydrophilic).


    • Hydrogen Bond: Weak attraction between a partially positive hydrogen atom and a partially negative oxygen or nitrogen atom; responsible for water's properties and protein 3D structure.


    • Van der Waals Forces: Very weak, brief attractions between neutral atoms due to random electron fluctuations.


  • Electrolytes: Ionized salts in solution capable of conducting electricity; critical for muscle contraction, nerve signaling, and osmotic balance.


  • Reaction Types:



    • Decomposition (Catabolism): AB→A+B\text{AB} \rightarrow \text{A} + \text{B} (exergonic, releases energy).


    • Synthesis (Anabolism): A+B→AB\text{A} + \text{B} \rightarrow \text{AB} (endergonic, requires energy).


    • Exchange: AB+CD→AD+CB\text{AB} + \text{CD} \rightarrow \text{AD} + \text{CB}.


    • Oxidation-Reduction (Redox): Oxidation is electron loss (exergonic); Reduction is electron gain (endergonic).


3. Solutions, pH, & Biological Macromolecules

  • Liquid Mixtures:



    • Solution: Solute <1 nm< 1\text{ nm}; clear; does not separate on standing; passes through membranes.


    • Colloid: Particles 1–100 nm1\text{--}100\text{ nm}; cloudy; does not separate; cannot pass through membranes (e.g., albumin in blood).


    • Suspension: Particles >100 nm> 100\text{ nm}; opaque; settles out on standing (e.g., blood cells in plasma).


  • pH Scale: Negative logarithm of hydrogen ion concentration (−log⁡[H+]-\log[\text{H}^+]). Neutral = 7; Acidic <7< 7; Basic >7> 7. Buffers resist pH changes.


  • Macromolecules:



    • Carbohydrates: Monosaccharides (glucose, fructose), Disaccharides (sucrose, lactose), Polysaccharides (glycogen = animal energy storage; starch = plant storage; cellulose = indigestible fiber).


    • Lipids: Hydrophobic molecules.



      • Triglycerides: Glycerol ++ 3 fatty acids (energy storage, thermal insulation).


      • Phospholipids: Amphipathic (hydrophilic phosphate head ++ 2 hydrophobic fatty acid tails); basic unit of cell membranes.


      • Steroids: 4-ring carbon backbone derived from cholesterol (precursor to steroid hormones like estrogen, testosterone, cortisol).


    • Proteins: Polymers of 20 amino acids joined by peptide bonds.



      • Structures: Primary (amino acid sequence), Secondary (α\alpha-helix, β\beta-sheet via hydrogen bonds), Tertiary (3D folding via disulfide bonds/hydrophobic interactions), Quaternary (association of multiple polypeptide chains).


      • Denaturation: Irreversible destruction of protein structure caused by heat or extreme pH.


    • Enzymes: Biological catalysts; lower activation energy to accelerate reactions. Bind specific substrates at an active site.


    • Nucleotides: Composed of a sugar, phosphate, and nitrogenous base. ATP (Adenosine Triphosphate) stores energy in high-energy phosphate bonds.


Chapter 3: Cellular Form and Function1. Plasma Membrane & Structure

  • Fluid Mosaic Model: Consists of phospholipids (75%75\%), cholesterol (20%20\%, regulates membrane fluidity), and glycolipids/glycoproteins (5%5\%, form the glycocalyx for cell recognition).


  • Membrane Proteins:



    • Transmembrane Proteins: Pass completely through the membrane (e.g., channels, pumps, receptors).


    • Peripheral Proteins: Adhere to one surface of the membrane.


  • Cell Extensions:



    • Microvilli: Non-motile; expand cell surface area for absorption (e.g., intestinal epithelium).


    • Cilia: Motile projections with a 9+29+2 microtubule array (axoneme); move mucus/materials across surfaces.


    • Flagella: Long, single projection used for cell motility (sperm).


2. Transport Mechanisms (High Exam Weight)

  • Passive Transport (No ATP required):



    • Filtration: Hydrostatic pressure forces fluid and small solutes through structural gaps.


    • Simple Diffusion: Net movement of particles from high to low concentration.


    • Osmosis: Net movement of water through a selectively permeable membrane toward higher solute concentration via aquaporins.


  • Tonicity:



    • Hypotonic Solution: Lower solute concentration than cytoplasm →\rightarrow water enters cell →\rightarrow cell swells and undergoes lysis.


    • Hypertonic Solution: Higher solute concentration than cytoplasm →\rightarrow water leaves cell →\rightarrow cell shrivels (crenation).


    • Isotonic Solution: Equal solute concentration →\rightarrow no net water movement.


  • Carrier-Mediated Transport:



    • Facilitated Diffusion: Passive transport using a protein carrier down a concentration gradient.


    • Primary Active Transport: Carrier uses ATP directly to move solutes against their gradient (e.g., Na+–K+\text{Na}^+\text{--K}^+ Pump moves 3 Na+3\text{ Na}^+ OUT for every 2 K+2\text{ K}^+ IN).


    • Secondary Active Transport: Carrier moves a solute against its gradient by pairing it with another solute moving down its gradient (e.g., SGLT glucose transporter).


    • Carrier Types: Uniport (1 solute), Symport (2 solutes, same direction), Antiport (2 solutes, opposite directions).


  • Vesicular Transport (Uses ATP):



    • Endocytosis: Phagocytosis ("cell eating"), Pinocytosis ("cell drinking"), Receptor-Mediated Endocytosis (selective uptake using clathrin-coated pits).


    • Exocytosis: Secretion of intracellular contents out of the cell.


3. Organelles & Cytoskeleton

  • Nucleus: Double-membrane nuclear envelope with nuclear pores; contains nucleoli where ribosomes are assembled.


  • Endoplasmic Reticulum (ER):



    • Rough ER: Parallel cisternae covered in ribosomes; synthesizes membrane and secreted proteins.


    • Smooth ER: Tubular cisternae without ribosomes; synthesizes lipids, detoxifies drugs, and stores calcium (Ca2+\text{Ca}^{2+}).


  • Ribosomes: Protein synthesis engines; unattached in cytosol or bound to Rough ER.


  • Golgi Complex: Receives newly synthesized proteins from Rough ER; modifies, packages, and routes them into vesicles.


  • Lysosomes: Vesicles containing digestive enzymes for autophagy (recycling damaged organelles) and autolysis (programmed cell destruction).


  • Peroxisomes: Oxidize fatty acids and toxic chemicals; produce hydrogen peroxide (H2O2\text{H}_2\text{O}_2) as a byproduct and neutralize it via catalase.


  • Mitochondria: Double-membrane organelle with internal folds (cristae); main site of ATP production via aerobic respiration.


  • Cytoskeleton: Microfilaments (actin), Intermediate Filaments (keratin), Microtubules (tubulin).


Chapter 4: Genes and Cellular Function1. Molecular Genetics: DNA & RNA Structure

  • DNA Structure: Polymer of nucleotides (Deoxyribose sugar ++ Phosphate group ++ Nitrogenous base).



    • Base Pairing Rules: Adenine (A) pairs with Thymine (T) via 2 hydrogen bonds; Guanine (G) pairs with Cytosine (C) via 3 hydrogen bonds.


    • Chromatin: DNA wrapped around histone proteins; repeating units are called nucleosomes.


  • RNA Structure: Single-stranded; Ribose sugar; Uracil (U) replaces Thymine (T).


2. Protein Synthesis (Transcription & Translation)

  • Genetic Code: Codons are 3-base sequences on mRNA. Start Codon: AUG (Methionine). Stop Codons: UAG, UGA, UAA.


  • Transcription (Nucleus): RNA Polymerase reads DNA template strand to build pre-mRNA.



    • Splicing: Introns (non-coding sequences) are removed; Exons (coding sequences) are spliced together.


    • Alternative Splicing: Allows a single gene to encode multiple distinct protein variants.


  • Translation (Cytoplasm): Ribosome reads mRNA codons. Transfer RNA (tRNA) carries matching amino acids via its anticodon.


  • Protein Folding & Processing: Chaperone proteins assist in folding. Rough ER modifies proteins →\rightarrow Transport vesicles →\rightarrow Golgi complex →\rightarrow Secretory vesicles/lysosomes.


3. DNA Replication & The Cell Cycle

  • Semiconservative Replication: Each original DNA strand serves as a template for a new strand.



    • DNA Helicase: Unzips the double helix.


    • DNA Polymerase: Synthesizes new complementary DNA strands.


  • Cell Cycle Phases:



    • Interphase:



      • G1G_1 (First Gap): Cell growth, protein synthesis, normal metabolic functions.


      • SS (Synthesis): Replication of genomic DNA.


      • G2G_2 (Second Gap): Final preparation for cell division, centriole replication.


      • G0G_0 Phase: Non-dividing resting state.


    • Mitosis (Nuclear Division):



      • Prophase: Chromosomes condense; nuclear envelope breaks down; mitotic spindle forms.


      • Metaphase: Chromosomes line up along the equatorial plate.


      • Anaphase: Sister chromatids separate and move to opposite poles.


      • Telophase: Chromatids uncoil; new nuclear envelopes reform.


    • Cytokinesis: Cytoplasmic division via an actin cleavage furrow.


4. Inheritance & Cancer Concepts

  • Chromosomes: Somatic cells are diploid (2n=462n = 46 chromosomes); Gametes are haploid (n=23n = 23chromosomes).


  • Inheritance Patterns:



    • Alleles: Dominant (masks recessive allele) vs. Recessive.


    • Codominance: Both alleles fully expressed (e.g., ABO blood group IAIBI^A I^B).


    • Incomplete Dominance: Intermediate phenotype expressed.


    • Polygenic Inheritance: Multiple genes dictate one trait (e.g., skin color, height).


    • Pleiotropy: Single gene affects multiple un-related traits (e.g., Sickle-cell anemia).


  • Cancer Genetics:



    • Proto-oncogenes: Normal genes coding for cell growth signals; mutated form becomes an oncogene (causes uncontrolled growth).


    • Tumor-Suppressor Genes: Genes that inhibit cell division or repair DNA damage (e.g., p53p53); inactivation leads to cancer.


Chapter 5: The Human Tissues1. Primary Germ Layers & Classification

  • Four Primary Tissue Classes: Epithelial, Connective, Nervous, Muscular.


  • Embryonic Germ Layers:



    • Ectoderm: Gives rise to nervous system and epidermis.


    • Mesoderm: Forms mesenchyme →\rightarrow muscle, bone, blood, cartilage.


    • Endoderm: Gives rise to inner mucous membrane lining of digestive and respiratory tracts.


2. Epithelial Tissue (Avascular, High Cellularity)

  • Simple Epithelia (Single layer):



    • Simple Squamous: Rapid diffusion/filtration (alveoli, glomeruli, endothelium).


    • Simple Cuboidal: Secretion and absorption (kidney tubules, liver).


    • Simple Columnar: Absorption; features goblet cells (mucus) and microvilli (GI tract).


    • Pseudostratified Columnar: Looks layered but all cells touch basement membrane; ciliated with goblet cells (respiratory tract).


  • Stratified Epithelia (Multiple layers):



    • Keratinized Stratified Squamous: Dead surface layer containing keratin; resists abrasion and water loss (epidermis).


    • Nonkeratinized Stratified Squamous: Moist surface layer; resists abrasion (esophagus, vagina).


    • Stratified Cuboidal: Secretion (sweat gland ducts).


    • Urothelium (Transitional): Stretches to accommodate fluid volume (urinary bladder, ureters).


3. Connective Tissue (Cells + Extracellular Matrix)

  • Fibrous CT Components:



    • Cells: Fibroblasts (produce matrix/fibers), Macrophages (phagocytosis), Leukocytes, Plasma cells (antibodies), Mast cells (histamine/heparin), Adipocytes.


    • Fibers: Collagenous (tough, flexible, white), Reticular (thin, branching framework), Elastic (stretch and recoil).


  • Types of Connective Tissue:



    • Loose CT: Areolar (underlies almost all epithelia), Reticular (structural mesh of spleen and lymph nodes).


    • Dense CT: Dense Regular (parallel collagen fibers; tendons and ligaments), Dense Irregular(randomly arranged fibers; dermis and organ capsules).


    • Adipose Tissue: White fat (energy storage, thermal insulation, cushioning) vs. Brown fat (heat generation via uncoupled respiration in infants).


    • Cartilage: Avascular; matrix rich in chondroitin sulfate; cells called chondrocytes inside spaces called lacunae.



      • Hyaline Cartilage: Smooth, glossy; clear matrix (articular joints, trachea).


      • Elastic Cartilage: Rich in elastic fibers (external ear, epiglottis).


      • Fibrocartilage: Coarse collagen bundles; absorbs shock (intervertebral discs, pubic symphysis).


    • Bone (Osseous Tissue): Calcified matrix containing osteocytes in lacunae; organized into osteonsin compact bone.


    • Blood: Liquid matrix (plasma) with formed elements (erythrocytes, leukocytes, platelets).


4. Nervous & Muscular Tissues (Excitable Tissues)

  • Nervous Tissue: Specialized for fast electrical signaling.



    • Neurons: Consist of a soma (cell body), dendrites (input signals), and axon (output signal).


    • Neuroglia: Supporting glial cells that protect and assist neurons.


  • Muscular Tissue: Specialized for contraction and movement.



    • Skeletal Muscle: Long cylindrical fibers, striated, multinucleated, voluntary.


    • Cardiac Muscle: Short branched cells (cardiomyocytes), striated, single nucleus, involuntary, joined by intercalated discs (gap junctions ++ desmosomes).


    • Smooth Muscle: Fusiform cells, non-striated, single nucleus, involuntary (walls of digestive tract, blood vessels).


5. Junctions, Glands, & Tissue Alterations

  • Intercellular Junctions:



    • Tight Junctions: Continuous outer seal blocking substances from passing between cells (epithelia).


    • Desmosomes: Patch-like structural rivets that prevent cells from pulling apart under mechanical stress. Hemidesmosomes anchor cells to basement membrane.


    • Gap Junctions: Ring of transmembrane proteins (connexons) surrounding a central pore; allows direct passage of ions and small solutes between cells.


  • Glands:



    • Exocrine (maintain a duct to a surface) vs. Endocrine (ductless; secrete hormones directly into bloodstream).


    • Secretion Types: Merocrine/Eccrine (exocytosis, e.g., sweat glands), Apocrine (fatty droplet buds off, e.g., mammary glands), Holocrine (entire cell disintegrates, e.g., sebaceous glands).


  • Tissue Growth, Modification, & Death:



    • Hyperplasia: Tissue growth via cell multiplication.


    • Hypertrophy: Tissue growth via enlargement of existing cells.


    • Metaplasia: Transformation of one mature tissue type into another (e.g., pseudostratified respiratory epithelium changing to stratified squamous in smokers).


    • Regeneration (replaces damaged tissue with same functional cell type) vs. Fibrosis (replaces damaged tissue with scar tissue/collagen).


    • Necrosis (pathological cell death due to injury/toxins) vs. Apoptosis (programmed, orderly cell suicide).