Unit 5 Lab Exam Flashcards

(37 cards)

1
Q

The pour plate technique is a common laboratory method used when counting ________ microorganisms

A

living

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2
Q

What type of plate uses the beads to mix

A

spread plate

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3
Q

The beads used in the spread technique are ________; pour about ___-_______ beads

A

sterile; 5-10

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4
Q

how is dilution factor calculated

A

1/ dilution

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5
Q

What is the dilution and dilution factor of the following: you take 1 mL of your sample and mix it with 99 mL of diluent

A

dilution total: 100mL
dilution factor: 1/100mL

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6
Q

What is a straight forward way to count the number of living bacteria in a sample

A

spread a small sample on a petri dish and count the number of colonies through serial dilutions

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7
Q

What is the statistically significant countable number of colonies on a plate

A

30-300 colonies

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8
Q

What is serial dilutions

A

a way of making very large dilutions accurately using small volumes

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9
Q

In microliters what is the range of measurement for the following pipette:

P20 (yellow dot)

A

2 ul - 20ul

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10
Q

In microliters what is the range of measurement for the following pipette:

P200 (yellow dot)

A

20 ul - 200 ul

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11
Q

In microliters what is the range of measurement for the following pipette:

P1000 (blue dot)

A

200ul - 1000 ul

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12
Q

Explain the two stop system

A

Hit resistance to suck up the intended amount and when you push it out do it fully past the resistance

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13
Q

Where do you want to submerge the tip of pipettes

A

just below the meniscus of the liquid to be transferred and slowly aspirate the solution

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14
Q

DO NOT GET ANY LIQUID IN THE _____ OF THE MICROPIPETTE

A

BORE

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15
Q

What two ways can you get liquid into the bore of the pipette

A
  1. tipping it up
  2. having bubbles of the solution that can shoot up into the bore
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16
Q

Spectrophotometer is a machine that has a light source and a detector to measure _________

A

transmittance

17
Q

When one is measuring a cell sample in the spectrophotometer, one is measuring

A

the light scattering or transmission

18
Q

Turbidity is a measurement with the _____________-

A

spectrophotometer

19
Q

What are the two ways we will do viable cell count by plating

A

spread plates with glass beads

pour plates with melted medium

20
Q

(T) aka % transmittance =

A

percent of light that reaches the detector

21
Q

What is optical density (1/T)

A

measure of amount of light scattering

22
Q

_______ OD = more light scattering = ______ cells

23
Q

What is viable count measuring

A

cell’s ability to form a colony

24
Q

To accurately take an absorbance reading, a _______ wavelength of light must be used since samples may scatter or absorb different wavelengths of light differently

25
What is the single wavelength selected by
monochromator
26
What do monochromators do
they break white light into its component wavelengths
27
What is our way of direct counting
petroff-hausser or hemacytometer
28
What is an advantage of viable cell count
it helps us observe the dynamic changes in bacterial growth--live cells
29
Does direct cell counting count both live and dead cells
yes
30
There are _________ cells in a liquid sample than a solid sample
fewer
31
What is the log phase
actively growing phase; this is the period when the microbes are growing and dividing at a steady rate
32
When is the lag phase
right away as the microbes adjust to their environment
33
What is the stationary phase
growth of microbes slows down because nutrients have been exhausted
34
bacteria replicate via
binary fission
35
How do we plot the rate of growth: X axis Y axis
time unit cell number
36
What is growth rate
the number of generations (doubling) per hour
37
What is generation time
time it takes for the population to double