Zone of Inhibition Area around antibiotic disk with no bacterial growth. Bacteriocidal – no bacteria living in ZOI. Bacteriostatic – bacteria are not reproducing.

Slides:



Advertisements
Similar presentations
Module based on a kit from Bio-Rad Laboratories, Inc. Thank you to :
Advertisements

Bacteria Transformation!
Lab 5/5a Transformation of E. coli with a Recombinant Plasmid
Griffith ’ s Mysterious Transformation Experiment.
Chapter 20 DNA Transformation A. P. Biology Mr. Knowles Liberty Senior High School.
PGLO™ Transformation. Central Framework of Molecular Biology DNA RNA ProteinTrait.
pGLO Transformation LAB AP LAB 6 BIO-RAD lab book pGLO ori bla GFP araC.
Modeling Transformation What does each step do?. Transformation Procedure.
Transformation of Escherichia coli
PGLO™ & GFP.
Bacterial Transformation
Lab Exam 2 Overview. Bacterial Transformation To impart new phenotype by adding expressible genes Why use bacteria? – Rapid growth – Plasmids as vectors.
AP Bio Lab 8: Transformation We will start on TUESDAY!
Genetic transformation of E. coli bacteria
GFP Transformation Lab Images taken without permission from
Plasmid DNA Restriction Enzymes “cut” Plasmid DNA Piece of DNA is Removed New Piece (gene) of DNA is “stitched” to Plasmid DNA New DNA (gene)
Biotechnology and Bacterial Transformation
Biotechnology Explorer Program Serious About Science Education.
PGLO™ Transformation and Purification of Green Fluorescent Protein (GFP)
Learning Targets “I Can...” -Explain what it means for a gene to be expressed. -Explain the role of plasmids. -Define bacteria “transformation.” -Insert.
Mrs. Stewart Medical Interventions Central Magnet School
Bacterial Transformation Lab “pGLO”
Learning Targets “I Can...” -Explain what it means for a gene to be expressed. -Explain the role of plasmids. -Insert a plasmid into bacteria to observe.
Bacterial Transformation
Introduction to pGLO lab Bacteria Transformation Please take these notes carefully. You do not need to write anything in RED.
GFP Transformation Lab Images taken without permission from
Bacteria Bacteria – single-celled organisms that are prokaryotic (no true nucleus)
BRIDGES  DNA ➔ RNA ➔ PROTEIN ➔ TRAIT Genotype Phenotype.
PGLO ™ & GFP. Central Framework of Molecular Biology DNA RNA ProteinTrait.
Genetic Engineering. What is genetic engineering? Definition: process of changing an organism’s genetic material to produce a new and useful result This.
Genetic Engineering BSC 1010L Transformation of E. coli with Jellyfish GFP.
Transforming E. coli with a Recombinant Plasmid. What is biotechnology? Employs use of living organisms in technology and medicine Modifying living organisms.
Bacterial Transformation
Bacterial Transformation Lab “pGLO”
In the pGLO lab, we will: Use recombinant DNA Genetically engineer E. coli bacteria by inserting a plasmid Plate and grow bacteria Determine if the proteins.
Transport Nucleus Cytoplasm Protein gene DNA mRNA The Cell:
In the pGLO lab, we will: Use recombinant DNA Genetically engineer E. coli bacteria by inserting a plasmid Plate and grow bacteria Determine if the proteins.
Bacterial Transformation What is transformation? Changing the genes and phenotype of a bacteria by uptake of foreign/new DNA Let’s review bacterial DNA.
PGLO Transformation LAB AP LAB 6 BIO-RAD lab book pGLO ori bla GFP araC.
Transformation MISS : SALSABEEL H. AL- JOUJOU.
Bacterial Transformation Green Fluorescent Protein.
Bacterial Transformation. Chromosome? A long piece of DNA with many pieces of information on it, each piece is a set of directions for making a protein.
GFP Transformation Lab
Transformation of Bacteria
Transformation of Escherichia coli
pGLO™ Transformation and Purification of
pGLO™ Transformation and Purification of
pGLO Transformation LAB AP BIO LAB 6
Methods of transformation
Pre-Lab: pGLO Bacterial Transformation
pGLO Transformation LAB AP Investigation 8
Bacterial Transformation Lab “pGLO”
Lab 8 Warm-Up What are plasmids?
Biorad pGlo-Biotechnology
PGLO Lab Purpose: To transform E. coli bacteria by adding plasmids that allow the bacteria to glow green under UV light in the presence of arabinose sugar.
PGLO Transformation.
Lab 8 Warm-Up What are plasmids?
Accelerated Biology Transformation Lab
Transport Nucleus Cytoplasm Protein gene DNA mRNA The Cell:
Bacterial Transformation
Introduction to the pGLO Lab
pGLO Transformation LAB AP LAB 6
Transformation of Escherichia coli
Bacterial Transformation Lab “pGLO”
Modeling Transformation
Transformation of Escherichia coli
Transformation of Escherichia coli
GFP Transformation Lab
Transformation of Escherichia coli
Presentation transcript:

Zone of Inhibition Area around antibiotic disk with no bacterial growth. Bacteriocidal – no bacteria living in ZOI. Bacteriostatic – bacteria are not reproducing in ZOI. Note the lawn of bacteria.

Bacteria and Antibiotics Bacteria – single-celled organisms that are prokaryotic (no true nucleus)

Bacteria and Antibiotics Bacteria are often used in Biotech to study genes. Why use bacteria? Simple to grow Grow rapidly 24 hours 37 0 C

Bacteria and Antibiotics To grow bacteria, need: 1.Correct nutrients – LB agar (solid) or LB broth (liquid). 2. Correct temperature – 37 0 C. 3. Can divide every 20 minutes.

1.Takes time to adjust n 3. Run out of nutrients

Bacteria and Antibiotics Antibiotics – any chemical which prevent bacteria from growing. 1.Bacteriocidal- kills bacteria. 2. Bacteriostatic- prevents bacteria from reproducing. Originals are not dead!

Sterile Technique Preventing contamination: - of you by experiment. - of experiment by you. Ex. Gloves, keeping lids closed, alcohol, flame.

Transformation Changing an organism’s traits by adding a new gene. Why bacteria? Simple organisms with few genes. One change in genotype will probably lead to change in phenotype.

Ways to get DNA into a cell: Electroporation Using electricity to poke holes in cell membrane; DNA rushes into cell.

Ways to get DNA into a cell: Virus Infection -Remove disease causing genes from virus. -Insert gene of interest. -Virus “infects” cell with new gene.

Ways to get DNA into a cell: Gene Gun -DNA attached to gold pellet. -Pellet fired into cell. -Typically used with plants. Why? Gene Gun Animation

Ways to get DNA into a cell: Heat Shock Using heat to open pores in cell membrane. (see sketch on board).

Transformation Efficiency # of bacterial cells on plate # bacterial cells possible on plate For heat shock, this number is <0.01%

How do you know which cells have been transformed? Selectable marker – gene which gives an obvious phenotype to transformed cell and allows only transformed cells to survive. Ex. Antibiotic resistance genes

What DNA will we transform into cells? pVIB luciferase – gene encoding bioluminescence amp r = ampicillin-resistance gene – beta- galactasidase which breaks down cell wall Any bacteria with this gene can grow in presence of ampicillin (antibiotic)

What DNA will we transform into cells? pGREEN GFP – Green Fluorescent Protein Also amp r

What DNA will we transform into cells? pUWL500 luciferase and amp r

What DNA will we transform into cells? pGEM3z- Just amp r

What type of bacterial cells are we going to transform? E. Coli that are “competent”. Competent – ready to be transformed.

How are we going to make competent cells? Treat cells with CaCl 2 In solution CaCl 2  Ca Cl - Positively charged Ca 2+ coats negatively charged pores. DNA can move into cell. Heat Shock Animation