 What is different between these 2 sequences? GGAATTCCTAGCAAT CCTTAAGGATCGTTA CTACGTGAGGAATTC GATGCACTCCTTAAG.

Slides:



Advertisements
Similar presentations
Restriction Enzymes.
Advertisements

Dolly the sheep ( ) 1. Animal and human cloning 2. Gene cloning.
Bacterial Transformation
GENETIC ENGINEERING. MANIPULATING GENES… Can we make our food taste better? Can we make humans live longer? Can we make X-men like mutants?!? Let’s start.
Transgenic Organisms.
Genetic engineering Recombinant DNA technology. Questions: Name 3 things you know about bacteria. What are some characteristics that make bacteria a good.
PRINCIPLES OF BIOTECHNOLOGY
Biotechnology The use of biological processes, organisms, or systems to manufacture products intended to improve the quality of human life.
DNA Technology Chapter 12. Applications of Biotechnology Biotechnology: The use of organisms to perform practical tasks for human use. – DNA Technology:
Recombinant DNA Technology Bacterial Transformation & GFP.
National 5 Biology Course Notes Unit 1 : Cell Biology Part 6 : Genetic Engineering.
Objective: Chapter 13- Biotechnology
Recombinant DNA. Scope Human Genome = 3x10 9 Average Gene = 3x10 4 (1/10 5 ) SNP Mutation (1/10 9 ) Process Cut DNA into pieces Insert DNA into vectors.
Restriction Enzymes Enzymes that CUT
Genetics of Cancer.
Yesterday: Genetic Disorders and Gene Therapy
Molecular Basis for Relationship between Genotype and Phenotype DNA RNA protein genotype function organism phenotype DNA sequence amino acid sequence transcription.
© 2012 Pearson Education, Inc. Lecture by Edward J. Zalisko PowerPoint Lectures for Campbell Biology: Concepts & Connections, Seventh Edition Reece, Taylor,
Restriction Enzymes. Restriction Endonucleases Also called restriction enzymes “molecular scissors” discovered in in bacteria Restriction enzymes is an.
Genetic Technologies Manipulating & Cloning DNA.
NIS - BIOLOGY Lecture 57 – Lecture 58 DNA Technology Ozgur Unal 1.
Uses of DNA technology You will need to convince a grant committee to fund further research into your area of application of DNA technology Read your assigned.
Recombinant DNA. Review Restriction enzymes cut DNA molecules at certain ‘restricted’ points A plasmid is also cut at the same point The ends match up.
Recombinant DNA rDNA. “rDNA” contains DNA from 2 or more different sources contains DNA from 2 or more different sources the DNA has been “spliced” together!
DNA Manipulation Diabetes Genetic Engineering – Animals – Drugs Bacteria Plasmid Biopharming Transgenic Organisms Knockout Mice Cloning.
AP Biology DNA Study Guide. Chapter 16 Molecular Basis of Heredity The structure of DNA The major steps to replication The difference between replication,
Chapter 9 Genetic Engineering. Genetic engineering: moving a gene from one organism to another – Making insulin and other hormones – Improving food –
© SSER Ltd.. Gene Technology or Recombinant DNA Technology is about the manipulation of genes Recombinant DNA Technology involves the isolation of DNA.
Chapter 9: Genetic Engineering
Introduction to Biotechnology ~manipulating and analyzing DNA.
 What is it?  What are they?  What is it?  How does it work?  DNA is isolated  DNA is copied with PCR  Cut with restriction enzymes  Run through.
PHARMACOBIOTECHNOLOGY.  Recombinant DNA (rDNA) is constructed outside the living cell using enzymes called “restriction enzymes” to cut DNA at specific.
BIOTECHNOLOGY.
Biotechnology -- Chap. 16. The use of biological systems for the production of materials (most work is in the field of Genetic Engineering)
GENETIC RECOMBINATION By Dr. Nessrin Ghazi AL-Abdallat Lecturer of Microbiology.
Studying the genomes of organisms GENE TECHNOLOGY.
Genetic Engineering Genetic engineering is also referred to as recombinant DNA technology – new combinations of genetic material are produced by artificially.
8.1 - Manipulating & Cloning DNA
Copyright © 2009 Pearson Education, Inc. Head Tail fiber DNA Tail.
Chapter 20: Part 1 DNA Cloning and Plasmids
A Molecular Toolkit AP Biology Fall The Scissors: Restriction Enzymes  Bacteria possess restriction enzymes whose usual function is to cut apart.
Transformation Lab What are plasmids? Circular sequences of DNA that can be incorporated into a bacterial host genome. What makes them so special?? They.
Genetic Engineering Chapter 13 Test on Friday 03/13/09 Reviewing Content Due 03/12/ and #28.
SBI 4U December 2012 Manipulating & Cloning DNA. Introduction Insulin, diabetes and genetic engineering Genetic engineering: the intentional production.
nome/program.html.
Steps to Recombinant DNA 1) Isolate the foreign DNA fragment 2) Attach DNA fragment to a “vehicle” called a Vector 3) Transfer the vector into a host.
KEY CONCEPT DNA sequences of organisms can be changed.
Aim: What are some applications of Genetic Engineering? Genetic Engineering is a process that is used to the alter the genetic instructions in organisms.
Chapter 9-1: Manipulating DNA Chapter 9.4: Genetic Engineering “Miracles of genetic engineering”
Aim #68: What are some applications of Genetic Engineering? Genetic Engineering is a process that is used to the alter the genetic instructions in organisms.
Restriction enzymes Are found in bacteria and are used to cut up DNA from a virus that might enter and take over the bacteria. They cut at specific sequences.
Topics to be covers Basic features present on plasmids
4/26/2010 BIOTECHNOLOGY.
Aim: What are some applications of Genetic Engineering?
Aim: What are some applications of Genetic Engineering?
Bacterial Transformation
Introduction to Biotechnology
CHAPTER 12 DNA Technology and the Human Genome
Genetic Engineering Insulin production Extra-nutrient foods
Biotechnology: Part 1 DNA Cloning, Restriction Enzymes and Plasmids
Manipulating DNA Biologists have tools to cut, separate, read and splice together DNA sequences.
Bacterial Transformation
4/26/2010 BIOTECHNOLOGY.
DNA Manipulation Diabetes Genetic Engineering Bacterial Plasmid
Aim: What are some applications of Genetic Engineering?
Transgenic Organisms Ms. Cuthrell.
Recombinant DNA Technology (a new approach in Biotechnology)
Metabolism and Survival
Gene transfer © 2016 Paul Billiet ODWS.
Genetic Egineering Isolation Cutting Ligation and Insertion
Presentation transcript:

 What is different between these 2 sequences? GGAATTCCTAGCAAT CCTTAAGGATCGTTA CTACGTGAGGAATTC GATGCACTCCTTAAG

 Only color & order of bases!  The actual chemical nucleotides are the SAME, even though the blue is sequence from US (eukaryotes) and the green is from bacteria (prokaryotes)!  So, DNA in plants, bacteria and us is chemically the SAME!!! That means, bacteria can “read” our DNA! (transcribe & translate our genes!)  Because of this, we can put our genes (or plant genes) in bacteria- this is what Recombinant DNA technology does!

 Plasmid : a small circular DNA molecule that is not part of the bacterial chromosome; replicates independently  Restriction Enzyme: Molecular scissors that cut DNA at a specific nucleotide sequence  Ex.: EcoRI CATCGAATTCAC GTAGCTTAAGTG

 DNA Ligase: An enzyme that joins 2 DNA fragments together (the “glue gun”).  Escherichia coli strains: Weakened strains of bacteria that are used to grow the plasmids.  Transformation: Process used to put the plasmid back into the bacteria

 Make lots of copies of the sequence  More of an issue before the human genome project  Mutate or change 1 human gene separate from the other 28,000 genes….  Make lots of a human protein cheap & easily! (ex. is human insulin)