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Microbiology Lab Notes

Jayla Williams Microbiology English 74 cards

Cards in this deck (74)

  1. 1Chemically defined mediumthe composition and amount of each ingredient is known.
  2. 2Chemicaly undefined mediumThe composition and amount of each ingredient is not known.
  3. 3Enriched MediumAdditional nutrient added for encouraging the growth of fastidious MO's
  4. 4Differental MediumDifferentales between Mo's based on ability to conduct a metabolic process
  5. 5Selective Medium contains ingredientsthat select for a particular type or group of Mo's
  6. 6Maintence Mediumallows for maintaining organisms for a long period of time
  7. 7Agarcomposed of polysaccharide isolated from red algae
  8. 8Agar-melts at 100*c and solidifies at 45*c
    -most Mo's are unable to utilize agar as a carbon and energy source
    -Utilized to convert medium to solid medium
  9. 9AutoclaveA fancy, expensive pres
  10. 10Aseptic Techniquethe process of handling sterile material in a manner that prevents contamination
  11. 11ContaminationA situation where unwanted Mo's end up in sterile materials or cultures due to the lack of proper aseptic technique
  12. 12Why do we flame a loopto prevent contamination
  13. 13Why do we write on bottom of the plateThats where the media is
  14. 14Why do we incubate media upside down?To prevent contamination
    To prevent condensation
  15. 15Purpose of a streak plateIsolate pure culture
    Determine if a culture is pure
  16. 16How do you know if you have a pure culture on a plateSame characteristics (color, size)
  17. 17Non pathogenic Mo'sdosent cause disease
  18. 18Pathogenic Mo'scause disease
  19. 19Opprotunistic Mo'sneeds help getting in
  20. 20Udipodisfound everywhere
  21. 21Hostwho has disease
  22. 22Reservoirwhere does the pathogen survive grow reproduce and spread from
  23. 23Aerotoleranceindicates the ability or inability of Mo to grow in the presence of oxygen
  24. 24Obligate aerobesorganisms that has to have oxygen to grow
    (grows faster in aerobic in conditions)
  25. 25Faculative Anaerobesgrows in the presence with oxygen or without
    ( grows faster in aerobic conditions)
  26. 26Aerotolerantgrows in the presence of oxygen or without
    ( grows at the same rate in conditions)
  27. 27Obligate Anaerobecannot grow with oxygen
  28. 28Microaerophilesreduced rate of oxygen
  29. 29Capnophilesneeds carbon dioxide
  30. 30Fluid Thioglycollate Mediumcontains yeast extract glucose casein
  31. 31Agarslows down the diffusion of oxygen into a medium
  32. 32Yeast Extractprovides vitiamin and minerals for bacterial growth
  33. 33Glucose and Caseinserve as carbon and energy sources
  34. 34Sodium Thioglycollate and L cystinereduces free oxygen to water making oxygen available
  35. 35Methelyene Blue Indicatoris blue when oxidized (presence of oxygen) and colorless when reduced ( absence of oxygen)
    color- aerobic
    colorless- anaerobic
  36. 36Cardinal TemperaturesMinimum, optimum, maximum
  37. 37Psychrophilesgrows 0 to 20 *c
  38. 38Mesophilesgrow 20 to 40 *c
  39. 39Thermophiles (obligate and facultative)grow 45 to 70 *c
  40. 40Extreme Thermophilesgrow 70 to 100 *c
  41. 41Hyperthermophilesgrows 100 to 150* c
  42. 42pHmeasure of hydrogen ion concentration
    Increase H solution becomes more acidic and ph goes down
    Increase H solution becomes more basic and ph goes up
    Mo's pH ranges 0.5 to 12.0
  43. 43Acidophilesbetween 0.5 to 6.0
  44. 44Neutrophilesbetween 6.0 to 7.5
  45. 45Alkaliphilesbetween 7.5 to 12
  46. 46Osmotic/ Osmosiswater active ( solute present)
    movement of a solvent from high concentration to low concentration until equlibrium is reached
  47. 47Lysisrupture of cells
  48. 48Plasmolysisshrinkage of cells
  49. 49Hypertonicsolutions
  50. 50Halophilessalt loving Mo's
    .5% to 3%
  51. 51Moderate halophilesgrows at a concentration greater than 3% Nacl
  52. 52Extreme HalophilesExtreme Halophiles
  53. 53Turbiditymeasure of cloudness in water or growth in a halophile
  54. 54substage condensercondenses the beam of light onto the specimen
  55. 55Iris diaphramcontrols light intensity of beam on a specimen
  56. 56Stageflat surface on which microscope slide rests
  57. 57Mechanical Stageallows movement of slide in all directions allows minute movement of slide
  58. 58Objective Lensesmagnifies specimen and produces the real image
    (4x) scanning 10x (low power) 40x ( high dry) 100x (oil immersion)
  59. 59Revolving nose pieceenables moving different objectives lenses into position
  60. 60Ocular Lensestwo ocular lenses ( binocular)
  61. 61Turret and Set screwallows loosening and rotation of oculars and locking of turnet in position
  62. 62Fine Focus and Course Knobsfocus adjustment
    Large Knob- coarse focus
    Small Knob- fine focus
  63. 63Total Magnificationocular power times objective power
    4x=40
    10x=100
    40x=400
    100x=1000
  64. 64Resolution or Resolving Powerthe ability of the objective lenses to distinguish two points as clear and specific distance apart
    RP= .5 timess lambda / N.A
    .5 is constant
  65. 65Resolving PowerRP= .5 timess lambda / N.A
    .5 is constant
  66. 66How to improve resolving ituse shorter wavelength of light to improve resolution of microscope
    use immersion oil with 100x to change index refraction
  67. 67Name of microscopecompound microscope or compound bright microscope
  68. 68Problems that can arise that affects ones use of microscopefield of view is dark
    -check to see that light is on
  69. 69Basic Stainstain the bacterial cells ( have negative charge) but does not stain the slide ( has positive charge)
    Positevly charged dyes
  70. 70Acidic StainStain background ( has positive charge) but do not stain the bacterial cells (have negative charge)
  71. 71Simple Stainuses only one dye
    Procedure is used to determine size of cells morphology of cells and arrangement of cells
  72. 72Differntal Stain 2 or more dyespurple in color ( crystal violet)
    Iodine ( Grams Iodine)
    Decolorization ( 95% ethanol)
    Saphrine ( Secondary)
  73. 73Differental Staining4 stages
    primary, mordant, decolorization, counterstain
  74. 74DecolorizationSmear thickness
    too thick of a smear can lead to erroneous results.
    Too thin of a smear can result in immediate decolorization of Gram positive bacteria

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Description
Microbiology Flashcards on Microbiology Lab Notes , created by Jayla Williams on 24/09/2019.
Created by
Jayla Williams · Sep 2019
Updated
Sep 25, 2019
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