Lab 1: ubiquity testing, aseptic technique, and bacterial isolation techniques Flashcards

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1
Q

What are the two ways of making microorganisms visible?

A
  1. microscopy in conjugation with staining

2. culturing

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2
Q

_________: when a mass of genetically identical bacteria is produced through the multiplication of a single cell

A

binary fission

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3
Q

______: a group of microbial cells growing on a solid surface that is visible to the naked eye

A

a colony

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4
Q

the cells that make up a colony are therefore considered to be genetically ____ and _________

A

pure and identical

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5
Q

The material that microbiologists use to grow microorganisms is called __________

A

medium

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6
Q

__________ microbes have special nutrient requirements or differentiate one group of microbes from another

A

fastidious

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7
Q

Liquid media is called ______

A

broth

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8
Q

Solid media is called ________

A

agar

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9
Q

________: a thick layer on the surface of a broth

A

pellicle

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10
Q

________: particles that have settled to the bottom of a broth

A

sediment

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11
Q

solid media is then referred to as _________ _________

A

nutrient agar

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12
Q

does agar supply nutrients to microbes?

A

no

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13
Q

__________: microbes are put into the agar when it is semi liquid but not so hot that it kills them

A

pour-plate technique

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14
Q

______ _______: are used when we want a large number of cells for use in a single application

A

broth tubes

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15
Q

a test tube with nutrient agar is called _____ ______ and it is most useful for growing microbes with low or zero O2 requirements deeply within the agar

A

agar deep

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16
Q

An ______ ______ is a test tube of nutrient agar that was allowed to solidify at an angle creating a larger flat surface for growth at the top of the agar

A

agar slant

17
Q

An _______ ______ is a petri plate containing nutrient agar that provides the largest surface area fro growth of microorganisms

A

agar plate

18
Q

_____ cultures: contain only one species of microbe

A

pure

19
Q

_______ ________: sequential transferring a constant volume minimum of three times that results in the decrease of concentration

A

serial dilution

20
Q

how do we calculate the number of viable cells (colony forming units in the original sample)

A

of colonies on the plate X dilution factor / mL of dilution plated