Aerobic Plate Count, Gram Stain, and Isolation - PowerPoint PPT Presentation

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Aerobic Plate Count, Gram Stain, and Isolation

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Title: Aerobic Plate Count, Gram Stain, and Isolation


1
Aerobic Plate Count, Gram Stain, and Isolation
  • Food Microbiology Laboratory

2
Aerobic Plate Count
  • Provides general estimate of live, aerobic,
    bacteria
  • Excludes
  • Obligate Anaerobes
  • Microaerophiles

3
Plate Counts
  • Assumption
  • Each colonies arises from a single bacterial cell
  • Bacteria like to clump together so some
    colonies may arise from more than one cell
  • Report as
  • Colony Forming Unit (CFU)/gram or ml
  • NOT at total bacteria

4
APC Results
  • Evaluate Sanitation of Product
  • Predict Shelf-life
  • Safety Indicator
  • Monitor Environment

5
Limitations of APC
  • Only aerobic organisms are counted
  • Bacteria Type not known
  • Media may not support growth of certain bacteria
  • Eye strain/Human Error
  • Hard to Distinguish Between food particles and
    bacteria
  • Dont Use on Fermented Foods
  • Colonies may be too small to see

6
Types of Samples
  • Liquid
  • Non-viscous Liquids can be measured with pipet
  • Viscous liquids should be weighed
  • Solid
  • Aseptically weigh Sample
  • Sponge/Swab
  • Collect sample by swabbing a defined area
  • Environmental and Container
  • Rinse inside of Containers
  • Open Plate to Collect Air Samples
  • RODAC Plates

7
Protocol for Plate Counts
  • Prepare a Sample Homogenate
  • 110 dilution
  • 1 part sample to 10 parts total volume
  • Blend in Blender or Stomacher for 2 min.

90 ml of diluent
10 g/ml sample
110 Dilution 10-1
8
Formula
  • 10 ml/g sample, want 1100 dilution
  • 100 10 90 ml of diluent needed
  • Start with Different Sample Sizes
  • 50 g sample
  • Must have 500 g total volume for 110
  • 500 50 450 ml diluent needed
  • 95 ml sample
  • Must have 950 total volume for 110
  • 950 95 855 ml of diluent

9
Plate Count Protocol
  • Prepare Serial Dilutions
  • Dilute to a level where you will get countable
    colonies on plates
  • Use a NEW STERILE PIPET between each dilution
  • Place pipet tip down in pipet tanks
  • Shake each dilution bottle 25 times in a 90
    degree arc within 7 seconds.
  • Phosphate Buffer or Peptone Buffer to Dilute

10
Dilutions
Dilution Blanks Containing 90 ml Diluent
Sample Homogenate
10 ml
10 ml
10 ml
10 ml
10-2
10-3
10-4
10-5
10-1
(1100)
(11000)
(1100000)
(110)
(110000)
11
Plating
Put 1 ml of Each Dilution into Empty Petri-Dish
10-4
10-5
10-2
10-3
10-1
1 ml
1 ml
1 ml
1 ml
1 ml
1 ml
1 ml
1 ml
1 ml
1 ml
12
APC Protocol
  • Add 18-20 ml of tempered (45-50 F), molten plate
    count agar to the petri dish.
  • Agar MUST be tempered or the bacteria will be
    killed by heat
  • Standard Methods or Plate Count Agar
  • Swirl 10 times in each direction
  • Allow to Solidify
  • Incubate inverted at 35-37 C for 48 hours

13
Sterilization
  • Equipment and Media MUST be Sterile
  • Hot Air Sterilization
  • 170 C for 1 hour
  • Equipment Temperature
  • Put in oven for 2 hours
  • Wrap in paper, foil, etc.
  • Steam Sterilization
  • 121 C for 15 min. MUST have 15 psi pressure
  • Liquid Media or Equipment
  • Dont Put Lids on tightly

14
Counting Plates
  • Only count plates with 25-250 colonies
  • More than 250
  • Too Numerous To Count TNTC
  • Less than 25
  • Too Few to Count - TFTC

15
Counting Plates
Plate 110 1100 11000 110000 1100000
1 TNTC1 TNTC TNTC 200 222
2 TNTC TNTC TNTC 150 10
Average - - - 175 -
1 Too Numerous to Count 2 Too Few to Count
  • Average two countable plates and Multiply by
    Dilution Factor
  • Count is 175 x 104
  • Must Convert to TWO Significant Digits
  • 1.8 x 106 cfu/ml or g


16
Counting - Examples
Plate 10-1 10-2 10-3 10-4
1 TNTC 300 150 10
2 TNTC 200 100 20
Average - 250 125 TFTC
Use ALL FOUR even though 300 is outside range.
If ONE PLATE is in RANGE, use BOTH for
Average. 250 x 102 2.5 x 104 125 x 103 1.3
x 105 AVERAGE 7.8 x 104 cfu/g or ml
17
Counting Examples
Plate 10-1 10-2 10-3 10-4
1 TNTC TNTC TNTC 300
2 TNTC TNTC TNTC 400
Average - - - 350
All Dilutions are outside Range so we MUST use
counts Outside range 350 x 104 3.5 x 106
cfu/ml or g Use an when using dilutions
outside countable ranges This means it is an
ESTIMATED count
18
Counting Examples
Plate 10-1 10-2 10-3
1 TNTC 300 10
2 TNTC 400 5
Average - 250 125
If Both Dilutions are outside Range, use the
Higher Dilution (LOWER COUNTS) 7.5 x 103 cfu/ml
or g
19
Overloaded Plates
  • Use Highest Dilution and Use Grid on Colony
    Counter
  • 1 Grid 1 cm2
  • A standard Plastic Plate has 56 cm2 surface area
  • If lt10 colonies/cm2, count 12 squares (6
    consecutive horizontally and 6 consecutive
    vertically)
  • Total and Divide by 12 (average). Multiply by 56
    to get total colonies on plate. Report as
    Estimate
  • If gt10 colonies/cm2
  • Count 4 squares, average and multiply by 56

20
APC Variations
  • Psychrotrophic
  • Incubate at 5-7 C for 10 days
  • Use Pre-poured Plates
  • Thermoduric
  • Hold 5 ml liquid sample or 110 diluent of solid
    sample in 60-80 C water bath for 30 min
  • Cool on ice for 10 min
  • Plate and incubate

21
Dilution Variations
99 ml Dilution Blanks
1 ml
1 ml
1 ml
10-7
10-3
10-5
10-1
0.1 ml
1 ml
1 ml
0.1 ml
0.1 ml
1 ml
1 ml
0.1 ml
-7
-5
-3
-1
-8
-6
-4
-2
CAN NOT use with petri-film
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