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Basic Microbiology Lab Test (Theory base)

Total questions: 50

Worksheet time: 17mins

Name
Class
Date
1.

What is the primary purpose of practicing aseptic technique in microbiology?

a)

To speed up experiments

b)

To ensure accuracy in measurements

c)

To prevent contamination

d)

To enhance sample visibility

2.

Which of the following is an essential step in aseptic technique when working with cultures?

a)

Using dirty glassware

b)

Opening culture tubes quickly

c)

Sterilizing equipment before and after use

d)

Leaving the laboratory door open

3.

What should you do if the microscope slide is too bright when observing a specimen?

a)

Increase the light intensity

b)

Close the diaphragm

c)

Use a higher magnification

d)

Remove the specimen

4.

What is the purpose of flaming the mouth of a culture tube before and after use?

a)

To create a cool flame

b)

To provide light in the laboratory

c)

To kill contaminants

d)

To melt the agar

5.

What is the purpose of the coarse adjustment knob on a microscope?

a)

To control the amount of light

b)

To change the objective lens

c)

To focus on the specimen at low power

d)

To fine-tune the focus at high power

6.

Which part of the microscope controls the amount of light passing through the specimen?

a)

Condenser

b)

Objective lens

c)

Diaphragm

d)

Coarse adjustment knob

7.

At what magnification should you start focusing on a specimen using the fine adjustment knob?

a)

4x

b)

10x

c)

40x

d)

100x

8.

What is the purpose of the oil immersion lens in a microscope?

a)

To increase magnification

b)

To improve resolution

c)

To make the specimen visible

d)

To protect the lenses

9.

If the image appears blurry even after using the fine adjustment knob, what should you check first?

a)

The objective lens

b)

The eyepiece

c)

The condenser

d)

The microscope slide

10.

What is the function of the mechanical stage on a microscope?

a)

To adjust the height of the microscope

b)

To control the light intensity

c)

To hold and move the microscope slide

d)

To change the objective lens

11.

Which instrument is commonly used to sterilize microbiological tools such as inoculating loops and needles?

a)

Microcentrifuge

b)

Autoclave

c)

Spectrophotometer

d)

Petri dish

12.

What is the purpose of a laminar flow hood in a microbiology laboratory?

a)

To maintain a sterile environment

b)

To amplify DNA

c)

To refrigerate samples

d)

To visualize bacteria

13.

What is the purpose of a Bunsen burner in a microbiology laboratory?

a)

Separating DNA fragments

b)

Creating a sterile work environment

c)

Measuring temperature

d)

Quantifying microbial biomass

14.

Why is it important to sterilize agar media before use in microbiological experiments?

a)

To enhance flavor

b)

To increase agar concentration

c)

To eliminate contaminants

d)

To speed up microbial growth

15.

Which component of bacterial cells is the primary target for the Gram stain?

a)

Capsule

b)

Cell wall

c)

Flagellum

d)

Cytoplasm

16.

What is the primary purpose of the Gram stain in microbiology?

a)

To identify bacterial species

b)

To determine the shape of bacteria

c)

To assess motility

d)

To visualize cellular structures

17.

Which color do Gram-positive bacteria stain after the Gram staining procedure?

a)

Pink

b)

Purple

c)

Red

d)

Green

18.

What is the decolorizing agent used in the Gram staining process?

a)

Crystal violet

b)

Safranin

c)

Safranin

d)
  • Alcohol or acetone

19.

Which step of the Gram stain procedure is critical for differentiating between Gram-positive and Gram-negative bacteria?

a)

Staining with crystal violet

b)

Application of iodine

c)

Decolorization

d)

Counterstaining with safranin

20.

What is the counterstain used in the Gram staining procedure?

a)

Crystal violet

b)

Iodine

c)

Safranin

d)

Methylene blue

21.

If a Gram-negative bacterium is mistakenly stained as Gram-positive, which step in the procedure is likely to have been mishandled?

a)

Application of crystal violet

b)

Application of iodine

c)

Decolorization

d)

Counterstaining with safranin

22.

Which step in the Gram stain methodology involves flooding the bacterial smear with crystal violet?

a)

Primary staining

b)

Decolorization

c)

Counterstaining

d)

Fixation

23.

If a bacterial smear is over-decolorized during the Gram stain procedure, what is the likely outcome?

a)

Gram-positive cells appear Gram-negative

b)

Gram-negative cells appear Gram-positive

c)

No impact on staining

d)

Improved cell visualization

24.

Which type of microscopy is commonly used to observe bacterial cells after the Gram stain procedure?

a)

Transmission Electron Microscopy (TEM)

b)

Scanning Electron Microscopy (SEM)

c)

Fluorescence Microscopy

d)

Light Microscopy

25.

What bacterial genus is this seen in this picture?

a)

Streptococcus

b)

Staphylococcus

c)

Escherichia

d)

Enterobacteriaceae

26.

What genus of bacteria is seen in this picture?

a)

Streptococcus

b)

Staphylococcus

c)

Escherichia

d)

Enterobacteriaceae

27.

What is the primary purpose of the Striking Plate Method in microbiology?

a)

To visualize bacterial colonies

b)

To sterilize equipment

c)

To isolate DNA

d)

To measure bacterial motility

28.

n the Striking Plate Method, what is commonly used to spread the bacterial sample evenly on the agar surface?

a)

Inoculating loop

b)

Pipette

c)

Microcentrifuge

d)

PCR machine

29.

What type of agar medium is often used in the Striking Plate Method for bacterial culture?

a)

Blood agar

b)

MacConkey agar

c)

Nutrient agar

d)

Selective agar

30.


How is contamination minimized in the Striking Plate Method?

a)

By using the loop at extreme heat while picking up the bacteria from the agar plate

b)

By keep using the loop without re-flaming in between streaks.

c)

By using a flame to sterilize the loop between streaks

d)

By avoiding agar plates

31.

In the Striking Plate Method, what is the purpose of streaking the bacterial sample in a specific pattern on the agar surface?

a)

To create a random pattern

b)

To promote bacterial motility

c)

To isolate individual colonies

d)

To increase contamination

32.

Choose the best streaking agar plate outcome.

a)

A

b)

B

c)

C

d)

Non of the above

33.

You have been tasked with preparing Gram-stained slides for a mixed bacterial culture. Explain how you would differentiate between Gram-positive and Gram-negative bacteria under the microscope and provide reasons for your observations.

a)

Describing the staining process

b)

Identifying bacterial morphologies

c)

Interpreting staining outcomes

d)

Selecting appropriate staining reagents

34.

Imagine you are working in a microbiology lab and need to identify a bacterial species from a patient sample. Describe the specific steps and procedures you would follow to apply the Gram stain technique in this diagnostic process.

a)

Selecting the microscope

b)

Preparing a bacterial smear

c)

Applying crystal violet

d)

Interpreting the staining results

35.

The picture show a Penicillium species. What is A label?

a)

Phialides

b)

Metulea

c)

Conidia

d)

Rami

36.

The picture show a Penicillium species. What is B label?

a)

Phialides

b)

Metulea

c)

Conidia

d)

Stipes

37.

The picture show a Penicillium species. What is C label?

a)

Phialides

b)

Ramuli

c)

Metulea

d)

Stipes

38.

The picture show a Penicillium species. What is D label?

a)

Phialides

b)

Ramuli

c)

Metulea

d)

Stipes

39.

The picture show a Penicillium species. What is F label?

a)

Rami

b)

Ramuli

c)

Metulea

d)

Stipes

40.

The picture show a Penicillium species. What is G label?

a)

Rami

b)

Ramuli

c)

Metulea

d)

Stipes

41.

Which of the following statement is TRUE regarding Gram positive bacteria?

a)

Cell wall have high lipid content

b)

Lipopolysacharides layer is present

c)

crystal violet stain is retained

d)

Have 2 layers of cytoplasmic membrane.

42.

Which of these is a cocci occurring in pairs?

a)

Streptococci

b)

Diplococci

c)

Streptococci

d)

Staphylococci

43.

This media selects for gram-negative organisms and isolates lactose fermenters (pink) and non-lactose fermenters (clear).

a)

choclate agar

b)

Mannitol salt agar

c)

Eosin-methylene blue (EMB) agar

d)

MacConkey agar

44.

This is a general purpose medium that supports the growth of a wide variety of bacteria.

a)

blood agar

b)

nutrient agar

c)

chocolate agar

d)

MacConkey agar

45.

Based on this figure, which of the alphabet is the starting point to culture bacteria and will show discrete colonies?

a)

A : Starting point ; C : Discrete colonies

b)

D : Starting point ; A : Discrete colonies

c)

A : Starting point ; D : Discrete colonies

d)

B : Starting point ; C : Discrete colonies

46.

You are planning to start culturing bacteria. What are the apparatus that are required for the culturing and maintaining bacteria?

a)

Inoculation loop, 37oC and agar

b)

Inoculation loop or needle, 37oC incubator, agar or broth

c)

Inoculation loop or needle, 37oC waterbath, broth

d)

Forceps, 37oC incubator and agar

47.

Mycology is the study of __________.

a)

fungi

b)

bacteria

c)

algae

d)

protozoa

48.
Plates should be incubated
a)
agar side up
b)
agar side down 
c)

Open Lid

d)

Doesn't matter, as long as it is in the oven.

49.

What is the concentration of alcohol used in the lab to disinfect the work bench?

a)

30%

b)

50%

c)

70%

d)

90%

50.

Why is it important that the Petri plates are incubated upside down?

a)

To get dense colonies

b)

To get mat culture

c)

To get colonies with reduced growth

d)

To prevent moisture from condensing onto the agar surface