1. Chapter 20 DNA Transformation A. P. Biology Mr. Knowles Liberty Senior High School

2. pGLO™ Transformation and Purification of Green Fluorescent Protein (GFP)

3. Central Framework of Molecular Biology DNA RNA ProteinTrait

4. The Central Dogma Trait (phenotype)

7. Using GFP as a biological tracer http://www.conncoll.edu/ccacad/zimmer/GFP-ww/prasher.html With permission from Marc Zimmer

8. Links to Real-world GFP is a visual marker Study of biological processes (example: synthesis of proteins) Localization and regulation of gene expression Cell movement Cell fate during development Formation of different organs Screenable marker to identify transgenic organisms Real-World Applications

9. GFP Transformed into Bacteria

10. Applications of GFP

11. GFP in a Plant, Arabadopsis

12. GFP in a Mouse

13. Genetically Engineered Fish

14. Bacterial DNA Plasmid DNA Bacterial cell Genomic DNA

17. What is a plasmid? An extrachromosomal, circular piece of autonomously replicating DNA. Originally evolved by bacteria. May express an antibiotic resistance gene or be modified to express proteins of interest.

18. The Many Faces of Plasmids Scanning electron micrograph of supercoiled plasmid Graphic representation Plasmids act as vectors – carriers for foreign DNA fragments (genes) that have been inserted into them and then propagated. Usually put into cells to make the desired protein.

19. Gene Expression Beta Lactamase –Ampicillin resistance Green Fluorescent Protein (GFP) –Aequorea victoria jellyfish gene araC regulator protein –Regulates GFP transcription p BAD

20. pGLO

21. Bacterial Transformation Beta lactamase (ampicillin resistance) pGLO plasmids Bacterial chromosomal DNA Cell wall GFP Flagellum

22. What is Transformation? Uptake of foreign DNA, often a circular plasmid. May involve bacteria or many eukaryotic types of cells. Process of copying genes of interest and making proteins from them. GFP Beta-lactamase Ampicillin Resistance

23. Transformation Procedure Overview Day 1 Day 2

26. Transcriptional Regulation Lactose operon Arabinose operon pGLO plasmid

27. Transcriptional Regulation BAD araC BAD RNA Polymerase Effector (Arabinose) araC BAD ara Operon RNA Polymerase ZYA ZYA LacI Effector (Lactose) ZYA LacI lac Operon p BAD

28. Gene Regulation RNA Polymerase araC ara GFP Operon GFP Gene araC GFP Gene araC GFP Gene Effector (Arabinose) BAD araC BAD RNA Polymerase Effector (Arabinose) araC BAD ara Operon p BAD

29. Methods of Transformation Electroporation –Electrical shock makes cell membranes permeable to DNA Calcium Chloride/Heat-Shock –Chemically-competent cells uptake DNA after heat shock

30. Transformation Procedure Suspend bacterial colonies in Transformation solution Add pGLO plasmid DNA Place tubes on ice Heat-shock at 42°C and place on ice Incubate with nutrient broth Streak plates

31. Reasons for Performing Each Transformation Step? 1.Transformation solution = CaCI 2 Positive charge of Ca ++ ions shields negative charge of DNA phosphates Ca ++ O CH 2 O PO O O Base CH 2 O P O O O Base OH Sugar O Ca ++

32. Why Perform Each Transformation Step? 2. Incubate on ice slows fluid cell membrane 3. Heat-shock Increases permeability of membranes 4. Nutrient broth incubation Allows beta-lactamase expression Beta-lactamase (ampicillin resistance) Cell wall GFP

33. What is Nutrient Broth? Luria-Bertani (LB) broth Medium that contains nutrients for bacterial growth and gene expression –Carbohydrates –Amino acids –Nucleotides –Salts –Vitamins We will have THREE Types of Agar Plates: -LB only -LB + Amp -LB + Amp + Arabinose

34. Grow? Glow? Follow protocol On which plates will colonies grow ? Which colonies will glow ?

35. Laboratory Quick Guide

36. Volume Measurement

37. Aequorea victoria- a jellyfish