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Microbiology Fall 2016 Study Guide Lab Exam 1

1.

What are the standard things you do upon arriving to class each day, before the activity starts?

decontaminate work surface with disinfectant

2.

what are some of the standard things you do before leaving class each day?

decontaminate work surface with disinfectant

3.

what needs to be written on each plate or test tube?

your name, name of organism, and date it was innoculated

4.

where do we dispose of broken glass and old prepared slides?

broken glass container

5.

where do we dispose of old Petri plates?

autoclaveable containers: Sharps container or orange biohazard bag

6.

What are some of the objects that are regularly flamed to avoid contamination with unwanted bacteria?

inoculating loop and top of glass tube

7.

what is the power of the ocular lens?

10x

8.

what is the power of the four objective lenses on our microscope?

4x, 10x, 40x, 100x

9.

what is the equation to calculate total magnification?

ocular lens x objective lense

10.

what is the purpose of immersion oil

to increase the resolving power of a microscope

11.

which objective lens requires immersion oil?

100x

12.

why do we go through the effort of fusing the bacteria of the smear.

to kill the bacteria and to make sure it sticks to the slide, so when we stain, it's there

13.

what are the three things we flamed during the preparation of smear

inoculating loop, top of test tube, and slide to heat fix

14.

why to we flame these objects?

to avoid contamination and to make sure the bacteria stick to the slide

15.

what is a wet mount?

organism on a slide in a drop of liquid, organism is still alive, requires coverslip

16.

what is the advantage of using a wet mount instead of a smear?

the organisms are alive

17.

why do we stain microorganisms?

some are transparent; to be able to see them in contrast

18.

how is a simple stain different from a differential stain?

simple stains color the everything on the slide, differential stains color only certain types of cells

19.

what are the names of the two simple stains we used in our lab?

safranin and methylene blue

20.

when are simple stains used in differential staining protocol?

as a counterstain

21.

what are the four basic steps of a differential stain?

  1. primary stain
  2. mordant
  3. decolorizer
  4. counterstain
22.

For gram staining what is the primary stain ?

crystal violet

23.

For gram staining what is the mordant

gram's iodine

24.

For gram staining what is the decolorizer?

acetone or alcohol

25.

For gram staining what is the counterstain?

safranin

26.

For gram staining which of the chemicals used in the staining procedure that we did in lab does not match the lab book?

alcohol/acetone

27.

what color is gram positive cells at the end of the stain?

purple

28.

what color is the gram negative cells at the end of the stain?

pink

29.

what is the structural difference between gram - and gram + cells?

gram - has two plasma membrane and one thin cell wall

gram + have a thick cell wall

30.

what shape and color is the bacteria of Staphylococcus aureus

cocci, purple

31.

what shape and color is the bacteria of Bacillus brevis

bacili, purple

32.

what shape and color is the bacteria of Escherichia coli

bacili, pink

33.

Gram + and Gram - staining

34.

For spore staining, what is the primary stain?

malachite green

35.

For spore staining, what is the mordant

steam

36.

For spore staining, what is the decolorizer?

water

37.

For spore staining, what was the counterstain ?

safranin

38.

For spore staining, what are the two general of common spore formers?

Bacillus and Clostridium

39.

Where do spore-forming bacteria commonly grow?

survive environmental conditions that are not favorable

40.

what color are the endospore at the end of the stain?

green

41.

Spore staining

42.

why do bacteria form endospore?

spore are produced when conditions become unfavorable

43.

what appear pink at the end of the spore stain?

the vegetative cells

44.

For acid-fast staining what is the primary stain ?

basic fuchsin

45.

For acid-fast staining what is the mordant

steam

46.

For acid-fast staining what is the decolorizer?

acid alcohol

47.

For acid-fast staining what is the counterstain?

methylene blue

48.

For acid-fast staining what chemical was used for the primary stain in our lab ?

carbol fuchsin

49.

What color are the acid fast positive cells at the end of the stain?

metallic shiny red

50.

what is the genus of the organism that was used as a acid-fast negative control?

Staphylococcus

51.

Acid-fast staining

52.

For capsule staining how is the basis of a negative stain different from the other staining protocols ?

The background is dark and the cells are clear.

53.

how is the fixing step for the capsule stain different from the other staining protocols that we performed so far in lab?

it is chemically fixed with acid alcohol. and not heat fixed

54.

For capsule staining what is the primary stain?

congo red stain

55.

For capsule staining what is the purpose of acid alcohol?

fixing the smear on the slide

56.

For capsule staining what is the secondary stain ?

carbol fuchsin

57.

For capsule staining what is the genus of the organism that was used in class for this stain?

Klebsiella

58.

For capsule staining what color is the capsule at the end of the procedure?

mostly clear or colorless

59.

For capsule staining what color is the background?

purple/grey/red

60.

how does the presence of a capsule affect the pathogenicity of a bacterium?

the capsule shield from immune response

61.

Capsule Staining