Gene Transformation – In Person
Scroll below for In Person Lab unit
Lab Handout for Gene Transformation lab – Part 1
Read along in your Part 1 and Part 2 (see below) lab handouts with the information on this webpage. Fill in and answer all questions accordingly in your lab handout. These will be collected and graded later.
Parts 1 and 2 will cover 2 weeks of lab.
Good background information. Also read the Additional Background Information in your lab handout.
Using Restriction Enzymes and DNA Ligase to make plasmids (1:38)
Stanford Scientists Produce Cancer Drugs from Rare Plants (1:59) by making plasmids and inserting them into more easily grown plants or yeasts.
Funding Basic Science to Revolutionize Medicine (3:59) that show how the focus in research has changed over the past 50 years.
How GFP is used in research (10:03)
Video of BIORAD pGlo Transformation procedure (7:01) – what we will do in lab.
Activity 1: In-Lab discussion with your TA – Important Concepts in the Transformation Procedures:
pGlo Plasmid we will use in lab. Why are these genes important? What do they code for?
DNA transformation using plasmids – animation explaining the steps in our Transformation procedure. It is very important to understand the nature of the bacterial cell wall, why CaCl2 is used, and why the heat shock is important.
Answer the Protocol Discussion questions #1-8.
Measurement marks on disposable plastic pipettes provided in the BIORAD kit:
Activity 3 – Experimental Treatments and Proposed Results
- Fill out the table at the end of this handout to indicate what you think the results would be for each of the 4 agar plates that were inoculated in this procedure. Also fill out the gray boxes for the agar plates that were not inoculated, but still indicate what you’d expect to happen with those nutrient conditions for the bacterial growth plates that did and did not get the plasmid added. Include why you think you’d get these results in ALL the boxes as well.
End of Transformation Part 1 (week 1)
Start of Transformation Part 2 (week 2).
Transformation Efficiency Calculation
Lab Handout for Gene Transformation Calculations – Part 2 In Person lab – read before coming to lab.
Activity 1: Data Collection from Transformation Plates
Your Results: Record your bacterial growth on the different nutrient agar plates under white light and UV light.
- Record your data in Table 1 in your lab handout that corresponds to your assigned Group. Be sure to collect data under both White Light and the UV Light.
- Answer questions #2-6.
Activity 2: Calculating Transformation Efficiency
- Read through the provided information and follow the prompts to calculate the transformation efficiency on your assigned +LB/amp/ara agar plate. Be sure to include the units as you set up each of the equations.
- Transformation Efficiency data from each lab group will be recorded and shared on the class whiteboard.
- Answer all the Discussion Questions at the end of the lab unit.
The Evolution of Bacteria on a Mega-Plate Petri Dish – Natural mutation for antibiotic resistance in bacteria growing on nutrient agar containing an antibiotic.
Molecular Visualization of DNA
0-1:48 = DNA Structure — Also seen in the Mitosis and Meiosis lab
1:48-2:53 = DNA Replication –Can you relate this to DNA synthesis? = S phase that you leaned about in the Mitosis and Meiosis in lecture
2:53-4:48 = Transcription – (you will learn about this and Translation later in lecture)
4:48-6:57 = Translation – (you will learn about this and Translation later in lecture)
6:58-7:47 = Hemoglobin and Sickle Cell Anemia -not narrated
DNA Presentations will be presented live in lab using PowerPoint or Google Slides June 15 in Lab.
To practice your presentations skills, each group of students will receive a DNA Topic and Target Audience to present to the class. These presentations should run 5-10 minutes. Each individual will need to speak and be equal partners in the presentation. All presentations will be recorded so that a self assessment can be done by each students of their own presentation skills. See the links below for more information. This will help you better organize and present your Group Review Paper Presentations the final week of labs.
Each student will use the Peer Evaluation form provided below to evaluate themselves and each person in their group. Submit this on Moodle by the start of the lab the week of your presentation.
DNA Presentation Expectations and Self Assessment – 30 points total
DNA Presentation TA Evaluation Sheet
Peer Evaluation form for DNA Group Presentations
Additional Information on Biotechnology:
Check out the opportunities for undergraduate students! Certificate, Minor, Courses…..(look under Academic Programs)
Link to information on a Minor in the Biotechnology Program at NCSU and Courses in Biotechnology (BIT) at NCSU
Link to the Undergraduate Programs at the BTEC center on Centennial Campus NCSU – where industry and education meet.
At BTEC they use similar transformation procedures to engineer bacteria and yeasts to make (biomanufacturing) chemicals, medicines, vaccines, enzymes, proteins, biofuels…….
Careers in Biotech – nice website. Careers at the Bench and Beyond
Great Short articles related to increasingly important Biotechnology
GFP – Green Fluorescent Protein – Cool Uses
Brianbow – New Resources and Emerging Biological Applications for Multicolor Genetic Labeling and Analysis – Informative and beautiful images!
PCR Animation – a nice simple step by step animation to show how PCR works.
ELISA Anitbody tests – animation that shows the different steps involved in ELISA testing for the presence of antibodies.
Biology of SARS-CoV-2 – nice powerpoint with basic explanations
Ten Years of CRISPR – highlights 7 ways that CRISPR has been used in gene editing