Chapter 2 - Microscopy Preparation and Culturing Flashcards
1 focusing lens
simple
use visible light to illuminate specimens, glass lenses to focus; have light pass through specimen
light microscopes
2 focusing lenses form image
compound
two lenses of compound
objective, ocular
the ability to distinguish two close, adjacent objects as separate and distinct
resolution
resolution is determine by the blank of light used and the lenses used
wavelength
shorter wavelength = blank resolution
greater
produces a dark image against a brighter background
bright field microscope
these microscopes stay in focus when objective lens is changed
parfocal
adding this to slide will increase resolution on the highest power lens
oil
produces a bright image of the object against a dark background
dark field microscope
dark field microscope is good to observe blank of eukaryotes
internal structures
dark field microscope was used to identify Treponema pallidum which causes blank
syphilis
converts slight differences in refractive index and cell density into easily detected variations in light intensity
phase contrast microscope
phase contrast microscope can be used to study blank organisms
living
used to visualize specimens that fluoresce after exposure specimen to uv, violet or blue light
fluorescence microscope
some cells fluoresce naturally called blank
autofluorescence
creates image by detecting differences in refractive indices and thickness of different parts of specimen
differential interference contrast microscope
creates sharp, composite 3d image of specimens by using laser beam, aperture
confocal microscopes
drop of liquid with living organisms and unstained
wet mount
dye added to wet mount; stains living organisms; may eventually kill microorganism
vital stains
staining improves blank which results in a better final image
contrast
kills microorganisms, preserves internal and external structures and adheres them to the slide
fixation
any distortion in the true morphology of the microorganism due to the technique
artifact
artifact that is with the Bunsen burner
heat fixation
blank fixation is more expensive, more time consuming, less artifacts, and used with larger, more delicate organisms
chemical
stains are blank compounds or salts that have different affinities for specific cellular materials
organic
coloring ion in staining
chromophore
chromophore cation; binds to cells; most dyes
basic
dye that is chromophore anion; repelled by cells; stains background
acidic
one dye; few steps; all stained the same
simple
2 or more dyes; several steps
differential staining
two types of differential stains
gram, acid-fast
differential stain is used to detect presence or absence of blank
structures
mostly widely used differential staining procedure
gram staining
gram staining divides bacteria into these two groups
gram positive, gram negative
acid fast staining is useful for staining member of the genus blank
Mycobacterium
Mycobacterium have a high blank content in cell walls
lipid
heated, double staining technique where bacterial endospore is one color and vegetative cell is a different color
endospore staining
capsules may be colorless against a stained background in this stain
negative stain
uses electrons instead of light as the illuminating beam
electron microscopy
electron beam makes blank
illumination
magnets act as blank in electron microscopy
lenses
beam of electrons pass through specimen and electromagnets function as lenses in this
transmission electron microscope
heavy metals do not penetrate the specimen but render dark background used for study of viruses and bacteria
negative staining
blank are used for staining in electron microscopes
metals
rapid freezing technique provides way to preserve native state of structures examined in vacuum
electron cryotomography
scanning tunneling microscope that can magnify blank million times and view blank
100, atoms, scanning probe microscopy
to grow microorganisms; the liquid or solid substance containing growing microorganisms
culture
the nutrient material used to culture microbes
medium
2 or more species grown together
mixed culture
only 1 species being grown
pure culture
free of all viable microbes
sterile
adding microorganisms to culture media
inoculation
any unwanted microbe in the medium
contaminant
anything done to minimize contamination
asceptic techniques