Unit 2 Lab Exam Flashcards

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1
Q

What does sterile mean

A

lacking ALL life forms

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2
Q

Define a pure culture

A

a growth of microorganisms that contain only one specific kind (strain) of microbe

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3
Q

What is the most common way to obtain pure cultures

A

streaking a culture of microbes for single colonies on a solid medium (agar plate)

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4
Q

How much should we turn the bunsen burner for gas flow

A

1-half of a turn

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5
Q

When should we take the wire out of the flame for sterlization

A

when it turns orange

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6
Q

How long should we let the flamed wire cool before use

A

10-15 seconds–do not wave it around

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7
Q

When re sterilizing the wire which direction should we move

A

towards the tip so that the inoculum doesn’t spatter and create aerosol of viable cells

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8
Q

Do we hold the tube containing the inoculum source and the tube with the recipient medium in the same or different hands for a tube to tube transfer

A

same

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9
Q

How should the plugs or caps be removed for tube to tube transfer

A

with the last two fingers of the hand holding the needle or loop, leaving the thumb and index finger free to hold and manipulate the loop with the middle finger as a guide

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10
Q

With a plate to tube transfer should both be handled at the same time

A

no

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11
Q

For a plate to tube transfer where do we want to place the inoculum in the tube? How do we mix it?

A

rub the wire on the moistened side of the tube just above fluid level and slant it to wash the inoculum down; do not rattle the wire against the sides of the tubes to shake it into broth

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12
Q

What is the streaking plate method used for

A

mechanically diluting a concentrated sample of microorganisms to a small, scattered population of cells over the surface of the solid medium

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13
Q

What is the primary purpose of plating

A

obtain well-isolated colonies on a large part of the plate surface

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14
Q

What must be done to the wire when streaking a plate

A

re sterilize the loop with the flame between each streak

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15
Q

How big should our first phase of the streak be

A

1/4th of the plate

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16
Q

How big should our second phase of the streak be

A

1/2 of the plate

17
Q

________ _________ are essential in pure culture techniques

A

isolated colonies

18
Q

What does colony formation result from

A

growth and replication of a cell that can use the medium as a source of nutrients and that can tolerate the physical conditions present

19
Q

After streaking a plate, the cell should multiply and result in

A

resulting, during incubation, a colony of identical cells

20
Q

Define colony

A

visible (to the naked eye) mass of millions of cells that arose from a common source

21
Q

What do we use when we consider the common origin for the cells of a colony

A

CFU–colony forming unit

22
Q

Define a spore

A

dormant type of cell whose main advantage is being able to withstand harsh environmental conditions

23
Q

When will a spore become a vegetative cell again

A

when growth conditions return

24
Q

Spores qualify as colony forming units T/F

A

True

25
Q

What type of growth is the first streaking of a streak plate

A

confluent growth

26
Q

What are the three reasons that we should treat all cultures as pathogenic

A
  1. cultures may have been contaminated
  2. they may contain unknown environmental microbes
  3. microbes may have acquired virulence by mutation or natural transformation
27
Q

What is Nutrient broth medium for

A

organisms that are not nutritionally fastidious

28
Q

Glucose is added to NB for what

A

to allow fermentation under the low oxygen conditions by incubating the tubes in non shaking incubator

29
Q

What is the purpose of sterlizing between streaks

A

to ensure that we will eventually dilute the culture to have isolated colonies in the last streaking quadrant

30
Q

Streaking a plate will check ______ among colonies

A

uniformity

31
Q

Cloudiness =

A

turbidity

32
Q

Can you tell if you aseptic technique in the tube transfers are only the desired microbes

A

no, we can’t be certain because it could have been contaminated during the incovulation procedure