lab exam 1-6

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33 Terms

1
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What is the lab benches dissinfected with before and after each lab?

10% bleach

2
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Where should culture tubes never be placed?

Never placed in the lab bench drawers

3
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What should prepared slides and microscope objective lens be cleaned with?

Lens paper moistened with 5% Windex after oil immersion use

4
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Where are staining solutions poured?

Into the chemical waste container

5
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How is the total magnification of a compound microscope calculated?

multiplying the magnification of the ocular lens (eyepiece) by the magnification of the active objective lens

6
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Low power TM

100x

7
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High power TM

400x

8
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Oil immersion TM

1000x

9
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Lab 1 and 2 was on?

Suvery of microorganisms

10
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What was used in Labs 1 and 2 Suvery of Microorganisms?

Bacteria, cyanobacteria, fungi, algae, protozoa

11
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Labs 3 and 4 were on?

Cytological techniques

12
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What are the 7 cytological techniques?

Negative stain, smear prep, simple stain, gram stain, acid-fast stain, spore stain, capsule stain

13
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What were the five prepared slides used within lab 3 and 4?

bacterial flagella, bacterial spores, capsule stain, acid-fast stain, and metachromatic granules

14
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What technique has to be maintained for all procedures in the cytological techniques?

Aseptic/sterile technique has to be maintained for all procedures of these lab exercises

15
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When water is mentioned as an ingredient, what is used for all procedures?

Sterile DI H20 is used for all procedures where water is mentioned as an ingredient

16
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What organisms were used for smear preparation?

liquid and solid media of b. megaterium, s epidermidis, e.coli

17
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In simple and acid-fast stain, what are the smears stained with?

methylene blue (Loeffler’s)

18
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What are smears stained with in gram stain?

Crystal violet

19
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What are stains dried with after being stained?

Bibulous paper

20
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What are smears in spore stain stained with?

5% malachite green

21
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What is lab 6?

Enumeration of microorganisms

22
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What are the 3 techniques of enumeration of microorganisms?

Direct count with hemocytometer, viable count (plate count), turbidity study with spectrophotometer (growth determination by optical density)

23
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What organism was used for the direct count by hemacytometer?

pure yeast (saccharomyces cerevisiae)

24
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How do you calculate the actual cell number per ml?

Total cell count per 5 boxes x 5 × 10^4 = cells per ml of solution

25
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What is the cell number per ml equal to?

The cell number per ml is equal to total cell number in 25 larger boxes x 10^4

26
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What organisms are used in the viable count - plate count?

pure yeast (saccharomyces cerevisiae)

27
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What is viable count measured by?

CFUs (colony forming units) per ml

28
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What are colony forming units?

cells that are viable, capable of reproduction and colony formation

29
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What does viable count =?

Viable count (cell number/ml) = the plate count x dilution factors

30
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To determine percent viability from a CFU count, what calculation is used?

Colony count/cells per ml plated x 100% = percent viability

31
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What is the other equation to determine percent viability from CFU count?

viability = viable count / direct count x 100%

32
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What organisms were used in the turbidity study?

yeast (saccharomyces cerevisia)

33
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What is optical density measurement?

measured as % absorbance