Study Group Practical 1 Flashcards

(36 cards)

1
Q

Inoculation Temperature

A

37(Degree Sign)C

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2
Q

TSB

A

A nutrient-rich liquid medium used for cultivating bacteria.
B for BROTH

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3
Q

TSA

A

A nutrient-rich solid medium used for growing bacterial cultures.

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4
Q

TSB vs. TSA

A

TSB is liquid, used for growing bacteria in suspension; TSA is solid (contains agar), used for isolating colonies.

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5
Q

Pure Culture

A

A culture containing only one type of microorganism.

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6
Q

Mixed Culture

A

A culture containing two or more types of microorganisms.

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7
Q

Contaminated Culture

A

A culture that contains unintended microorganisms.

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8
Q

BAP

A

A type of enriched agar that contains red blood cells to support growth of fastidious bacteria and to observe hemolysis (breakdown of RBCs).

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9
Q

Fastidious Bacteria

A

Bacteria that require specific nutrients or growth conditions.

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10
Q

Solid Media

A

Culture media that is firm due to the presence of agar, used for isolating colonies.

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11
Q

Semi-Solid Media

A

Culture media with a lower concentration of agar, used to test motility or support microaerophiles.

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12
Q

Petri Plate

A

A shallow, flat, round dish used to hold solid culture media.

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13
Q

Slant

A

A test tube containing solid media that has solidified at an angle, providing a larger surface area for growth.

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14
Q

Deep

A

A test tube containing solid media that is fully solidified vertically, often used for anaerobic or motility tests.

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15
Q

Agar Melting Temperature

A

100(degree sign)C

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16
Q

Agar Holding Temperature

A

50(Degree sign)C

17
Q

Agar Pouring Temperature

A

45(Degree Sign)C

18
Q

Agar Resolidfication Temperature

A

40(Degree Sign)C

19
Q

Problems with pouring agar too cold

A

Lumps will occur in the plate or agar won’t pour

20
Q

Problems with pouring agar to hot

A

Condensation will occur in plate and many bacteria will be killed

21
Q

Why sterilize tubes before and after transfer

A

To prevent contamination from external microbes and ensure aseptic technique.

22
Q

How to sterilize tubes before and after transfer

A

Flame the opening of the tube using a Bunsen burner before and after transferring microorganisms.

23
Q

Why incubate upside down

A

To prevent condensation from dripping on agar surface and to read labels while being able to see organism from top.

24
Q

Asepsis

A

Practice of preventing contamination by microorganisms

25
Where to start flaming loop?
Start at the base of the wire and move toward the tip.
26
Why start loop sterilization at base
Complete sterilization of part of loop being used, not burning yourself. (Don't flame the handle!!)
27
Possible contamination points in lab
Tube openings, loop tips, Petri dish lids, bench surfaces, gloves, and hands.
28
Cover Slip
A small, thin piece of glass placed over a specimen on a slide for microscopy.
29
Slide
flat piece of glass used to hold specimens for microscopic examination.
30
Bunsen Burner
A device that produces a single open flame for sterilization or heating in the lab.
31
Bilbious Paper
Absorbent paper used to blot excess liquid from microscope slides. (Can also be used to dry slides, but pat don't wipe!!)
32
Striker
A tool used to ignite the Bunsen burner safely.
33
Ubiquitous
Present or found everywhere (common in nature).
34
Omnipresent
Present everywhere at the same time
35
Ubiquitous vs. Omnipresent
“Ubiquitous” implies widespread presence; “omnipresent” implies being everywhere simultaneously, often in a figurative or absolute sense.
36
Aseptic Technique
a set of practices in healthcare and other fields designed to prevent contamination by pathogenic microorganisms and reduce the risk of infection.