Skip to Main Content
Have previous year question papers?
BACEBiotility — University of FloridaProfessional CertificationIndustry-Recognized CredentialMultiple Choice

BACE: Biotechnology Skills (Practical) Practice Questions & Answers

Badge: Biotechnology Skills

Type: Practical | Weight: 23% of Exam

This module tests the foundational hands-on skills required in a laboratory setting. Questions often involve procedural ordering and image analysis.

Key Topics:

  • Aseptic Technique: Sterility maintenance and contamination avoidance.
  • Micropipetting: Correct usage of micro/macro pipettes.
  • Solution Prep: pH adjustments, buffers, and serial dilutions.
  • Cell Culture: Streaking plates and maintaining cell lines.

Recommended Resource: Bio-Rad Lab Skills Course

Ready to test yourself?

Take this exam in our timed interactive simulator to track your performance and get detailed analytics.

Which of the following best describes the primary purpose of aseptic technique in a biotechnology laboratory?

  • To ensure all equipment is cleaned with soap and water before use.

  • To prevent contamination of the culture, the environment, and the researcher.

  • To sterilize all solutions using high heat and pressure immediately after use.

  • To increase the growth rate of the bacterial culture being studied.

View Answer & Explanation
Correct Answer: Option B -

To prevent contamination of the culture, the environment, and the researcher.

Explanation:

Aseptic technique is a set of practices used to prevent the introduction of contamination (unwanted microbes) into samples, the sterile field, or the researcher.

What are the standard conditions for sterilizing liquid media in an autoclave?

  • 100°C at 0 psi for 60 minutes

  • 121°C at 15 psi for 15-20 minutes

  • 150°C at 30 psi for 5 minutes

  • 200°C at 10 psi for 45 minutes

View Answer & Explanation
Correct Answer: Option B -

121°C at 15 psi for 15-20 minutes

Explanation:

The standard autoclave cycle for sterilizing liquids is 121°C at 15 psi pressure for approximately 15 to 20 minutes.

When working in a laminar flow hood, where should you perform your work to minimize contamination?

  • At the very front edge of the hood, closest to the user.

  • Outside the hood, transferring items in only when necessary.

  • At least 6 inches inside the hood, in the center of the sterile airflow.

  • Against the back wall of the hood to avoid air turbulence.

View Answer & Explanation
Correct Answer: Option C -

At least 6 inches inside the hood, in the center of the sterile airflow.

Explanation:

Work should be performed at least 6 inches inside the hood to ensure that the air flow is laminar and undisturbed by the turbulence at the front opening or the back obstruction.

Which of the following actions represents a violation of aseptic technique?

  • Flaming the mouth of a glass tube before and after transferring a sample.

  • Placing a sterile cap face-down on the lab bench while pipetting.

  • Holding the test tube at an angle while the cap is removed.

  • Using a fresh, sterile pipette tip for each transfer.

View Answer & Explanation
Correct Answer: Option B -

Placing a sterile cap face-down on the lab bench while pipetting.

Explanation:

Placing a sterile cap face-down on a non-sterile surface (like a lab bench) introduces contamination. Caps should be held in the hand or placed face-up if absolutely necessary, though holding is preferred.

Identify the correct order of steps for aseptically transferring a bacterial culture from a tube to a fresh broth tube.

  • Flame loop \rightarrow Remove cap \rightarrow Flame tube lip \rightarrow Obtain sample \rightarrow Flame tube lip \rightarrow Recap

  • Remove cap \rightarrow Flame loop \rightarrow Obtain sample \rightarrow Flame tube lip \rightarrow Recap

  • Flame tube lip \rightarrow Flame loop \rightarrow Remove cap \rightarrow Obtain sample \rightarrow Recap

  • Obtain sample \rightarrow Flame loop \rightarrow Flame tube lip \rightarrow Remove cap \rightarrow Recap

View Answer & Explanation
Correct Answer: Option A -

Flame loop \rightarrow Remove cap \rightarrow Flame tube lip \rightarrow Obtain sample \rightarrow Flame tube lip \rightarrow Recap

Explanation:

The correct sequence ensures sterility at every exposure point: Sterilize the tool (loop), open the container, sterilize the air-interface (lip), perform transfer, re-sterilize the interface, and close.

What is the function of the Bunsen burner flame during tube-to-tube transfers?

  • To heat the liquid culture to boiling point.

  • To create an updraft that pushes airborne contaminants away from the open tube.

  • To illuminate the workspace.

  • To burn off excess oxygen in the tube.

View Answer & Explanation
Correct Answer: Option B -

To create an updraft that pushes airborne contaminants away from the open tube.

Explanation:

Besides sterilizing loops, the flame heats the air, causing it to rise (convection). This updraft helps prevent airborne dust and microbes from falling into open containers near the flame.

Which Personal Protective Equipment (PPE) is most essential for protecting the sample from contamination by the researcher's skin flora?

  • Safety goggles

  • Gloves

  • Closed-toe shoes

  • Fire extinguisher

View Answer & Explanation
Correct Answer: Option B -

Gloves

Explanation:

Gloves cover the skin of the hands, which sheds skin cells and bacteria, thus protecting the sample from the researcher's flora. Goggles and shoes primarily protect the researcher.

You observe a broth culture that was supposed to be sterile but now appears cloudy (turbid). What is the most likely conclusion?

  • The broth has evaporated.

  • The broth is contaminated with microbial growth.

  • The pH of the broth has spontaneously changed.

  • The broth was over-sterilized.

View Answer & Explanation
Correct Answer: Option B -

The broth is contaminated with microbial growth.

Explanation:

Turbidity (cloudiness) in a liquid medium is a classic visual sign of microbial growth (contamination).

What is the correct method for sterilizing an inoculating loop in a Bunsen burner flame?

  • Pass it quickly through the yellow part of the flame once.

  • Hold it in the blue cone of the flame until it glows red hot along the entire wire.

  • Hold it in the flame for exactly 3 seconds, regardless of color.

  • Dip it in ethanol and then waive it near the flame to dry.

View Answer & Explanation
Correct Answer: Option B -

Hold it in the blue cone of the flame until it glows red hot along the entire wire.

Explanation:

The loop must be heated until it glows red hot to ensure all organic matter and microbes are incinerated. The blue cone is the hottest part of the flame.

Why must you wait for the inoculating loop to cool after flaming before touching a bacterial colony?

  • The hot loop will melt the agar and ruin the plate.

  • The hot loop will kill the bacteria you are trying to pick up.

  • The hot loop will cause the bacteria to mutate.

  • The hot loop will cause aerosols that contaminate the air.

View Answer & Explanation
Correct Answer: Option B -

The hot loop will kill the bacteria you are trying to pick up.

Explanation:

Touching a live culture with a red-hot loop will instantly kill the cells (sizzle sound), resulting in no viable transfer.

More from BACE

Found in Biotechnology Certification

BACE: Technical Skills & Applications

50-question knowledge section covering PCR, Electrophoresis, Immunoassays, and Chromatography.

Practice Now

BACE: Applied Mathematics

30-question calculation section on dilutions, molarity, unit conversions, and standard curves.

Practice Now
ExamOven Logo
ExamOven Support
We typically reply instantly