Transcript Chapter 3
Microscopy and cellular morphology Applications of Light Microscopy • Observe less detailed features of intact cell than advanced microscopy (i.e. electron and laser) • Shape, presence of flagella, diagnostic stain, arrangement of cells, some large internal features • <1000X magnification • Brightfield – Stained cells or cells with color/contrast – External features Path of Light: Brightfield • Illuminator – Filter for shorter λ; blue light • Condenser – Focuses light into specimen • Diaphragm (iris) – Controls amount of light to specimen • Specimen on slide – Diffracts light as it passes throughimage produced • Objective lenses at nosepiece – Magnifies image 10, 40, or 100 times – Image inverted • Head with prism – Direct light path into ocular lens – Ocular lens magnifies image 10X – Image path sent to eye Magnification Versus Resolution • Magnification = increase in apparent size – Objective and ocular lenses • Resolution = clarity – Ability to see 2 nearby objects as distinct objects – Resolving power depends on numerical aperture of lens • Ability to gather light; increase aperture and increase resolution of lens • Increase magnification must increase aperture; aperture limit • Highest resolution possible is 0.2μm with 100X lens – Steps you can take to increase resolution • GET MORE LIGHT TO LENS! • Oil immersion with 100X lens – Same refractive index as glass; prevents loss of light to air • • • • Small wavelength light (blue light) Adjust diaphragm and condenser as you increase magnification Course focus and fine focus to focus image Clean lenses and slide Microscopy • Field of vision – Smaller at higher powers; must CENTER object or you will lose it at higher power – Mechanical stage adjuster!!! • Parfocal – Focus under low power then move to high power immediately; don’t move focus in between; then fine focus after you get to high power. • Contrast versus resolution. – you need light to increase resolution, but too much light can decrease contrast; must find a happy medium. • What happens if I go from low power to high power and the cells disappear? – – – – – Field of vision narrowed—center specimen Not enough light—open diaphragm Slightly out of focus—use fine focus Resolution not optimal—clean lenses or slide, use oil if using 100X lens, open diaphragm, The lens is not clicked all the way in place—make sure it clicks Cellular Morphology • Prokaryotes – – – – – Rods (strep or single arrangement) Cocci (staph, strep or single arrangement) Spirillum No nuclei present. Must have cells under oil immersion to see any detail. • Eukaryotes – Cells larger than prokaryotes – Can’t always see nucleus – Fungi • Molds versus single celled fungi • Yeast – Candida albicans; vaginal yeast infection and thrush – Saccharomyces cerevisiae; bakers yeast; brewing yeast Cellular Morphology Continued • More Eukaryotes – Fungi • Molds – – – – Filamentous due to hyphae; multicellular Penicillium » Yes it makes penicillin; grows on bread Aspergillus, » Some produce aflotoxins (pathogenic) Rhizopus » Classic bread mold and house mold • Yeast – – Algae • • – Have pigments associated with them; single cell Dinoflagellate called Peridinium Protozoa • • • – Saccharomyces (bread and beer yeast) or Candida albicans (yeast infections) Single cell Trypanosoma gambiensae Causes Sleeping Sickness; nervous disorders; central Africa; tsetse flies Helminth • • • Multi cell Schistosoma mansonni Causes schistosomiasis