Manipulation of Purified DNA

Similar documents
Molecular Cell Biology - Problem Drill 11: Recombinant DNA

Gene Cloning & DNA Analysis

Amplified segment of DNA can be purified from bacteria in sufficient quantity and quality for :

Synthetic Biology for

Manipulating DNA. Nucleic acids are chemically different from other macromolecules such as proteins and carbohydrates.

13-2 Manipulating DNA Slide 1 of 32

Group Members: Lab Station: BIOTECHNOLOGY: Gel Electrophoresis

Plasmids. BIL 333 Lecture I. Plasmids. Useful Plasmids. Useful Plasmids. Useful Plasmids. ( Transfection ) v Small, circular, double-stranded DNA

Molecular Biology (2)

B. Incorrect! Ligation is also a necessary step for cloning.

DNA Technology. Asilomar Singer, Zinder, Brenner, Berg

Chapter 6 - Molecular Genetic Techniques

Computational Biology I LSM5191

Recitation CHAPTER 9 DNA Technologies

NB536: Bioinformatics

7.1 Techniques for Producing and Analyzing DNA. SBI4U Ms. Ho-Lau

Goal: Move the Gene for Miraculin into an Expression Vector

Lecture Four. Molecular Approaches I: Nucleic Acids

Researchers use genetic engineering to manipulate DNA.

Restriction Enzymes (endonucleases)

XXII DNA cloning and sequencing. Outline

Biotechnology DNA technology

Genetics and Genomics in Medicine Chapter 3. Questions & Answers

NCERT. 2. An enzyme catalysing the removal of nucleotides from the ends of DNA is: a. endonuclease b. exonuclease c. DNA ligase d.

Lab 9 Restriction Enzyme Analysis

_ DNA absorbs light at 260 wave length and it s a UV range so we cant see DNA, we can see DNA only by staining it.

Molecular Genetics II - Genetic Engineering Course (Supplementary notes)

CONSTRUCTION OF GENOMIC LIBRARY

PreLab Activity I: Restriction Enzymes 1. What is the sequence of the complementary DNA strand? Draw it.

Bootcamp: Molecular Biology Techniques and Interpretation

2014 Pearson Education, Inc. CH 8: Recombinant DNA Technology

Biotechnology. Chapter 20. Biology Eighth Edition Neil Campbell and Jane Reece. PowerPoint Lecture Presentations for

Recombinant DNA recombinant DNA DNA cloning gene cloning

MCB 102 University of California, Berkeley August 11 13, Problem Set 8

Regulation of enzyme synthesis

CH 8: Recombinant DNA Technology

7.02 Recombinant DNA Methods Spring 2005 Exam Study Questions Answer Key

Overview: The DNA Toolbox

BIOLOGY - CLUTCH CH.20 - BIOTECHNOLOGY.

Molecular Biology Techniques Supporting IBBE

Mission (Im)possible: Plasmid Mapping Student Materials

BIOTECHNOLOGY. Sticky & blunt ends. Restriction endonucleases. Gene cloning an overview. DNA isolation & restriction

Objectives Introduction restriction endonucleases Examples: Hind III: Eco RI: Pst I:

PRODUCT INFORMATIOIN DNA blunting and Ligation

Exploring DNA. Copying DNA in a laboratory the polymerase chain reaction

Chapter 10 (Part II) Gene Isolation and Manipulation

4. Analysing genes II Isolate mutants*

10X ligation buffer ligase 1 vector DNA insert DNA H 2 O. 10 µl Total Volume. 10X ligation buffer ligase 1 vector DNA insert DNA

10 Restriction Analysis of Genomic DNA

CHAPTER 9 DNA Technologies

The Biotechnology Toolbox

Genetic Engineering & Recombinant DNA

SELECTED TECHNIQUES AND APPLICATIONS IN MOLECULAR GENETICS

Antisense RNA Targeting the First Periplasmic Domain of YidC in Escherichia coli Appears to Induce Filamentation but Does Not Affect Cell Viability

Molecular Scissors: Lambda Digest Student Materials

Fun with DNA polymerase

CHAPTER 4A MAKING SURE YOU VE GOT A RECOMBINANT PLASMID. CHAPTER 4A STUDENT GUIDE 2013 Amgen Foundation. All rights reserved.

Answer sheet. Student number:

Biotechnology (Chapter 20) Objectives

Downloaded from

Mission (Im)possible: Determine the Identity of Unknown Plasmids. Student Materials. Introduction Lab Protocol... 5

GENETICS EXAM 3 FALL a) is a technique that allows you to separate nucleic acids (DNA or RNA) by size.

Chapter 8: Recombinant DNA. Ways this technology touches us. Overview. Genetic Engineering

BIOTECHNOLOGY : PRINCIPLES AND PROCESSES

A Lot of Cutting and Pasting Going on Here Recombinant DNA and Biotechnology

1. Why do DNA restriction fragments and plasmids separate when analyzed by gel electrophoresis?

Biology Teach Yourself Series Topic 12: Molecular Biology (Unit 4)

Restriction Endonucleases, (Cutting DNA) (Ligation) Ligase & Phosphatase

Genetics and Biotechnology 13.2 DNA Technology

Biology Chapter 9 & Honors Biology Chapter 13. Frontiers Of Biotechnology

Bi 8 Lecture 4. Ellen Rothenberg 14 January Reading: from Alberts Ch. 8

Computational Biology 2. Pawan Dhar BII

Genetics and Biotechnology. Section 1. Applied Genetics

HE Swift Cloning Kit

GenBuilder TM Cloning Kit User Manual

Chapter 10 Genetic Engineering: A Revolution in Molecular Biology

Justin Veazey. Experiment 3; Analysis of digestion products of puc19, GFPuv, and pgem-t easy

TIANgel Mini DNA Purification Kit

Multiple choice questions (numbers in brackets indicate the number of correct answers)

DNA Restriction Digestion Analysis

Genes to Proteins. Nucleic Acid Structure

Chapter 11. Restriction mapping. Objectives

Recombinant DNA Technology. The Role of Recombinant DNA Technology in Biotechnology. yeast. Biotechnology. Recombinant DNA technology.

EcoR1 is a type IIP restriction endonuclease which cleaves the palindromic

Essential Questions Real-World Reading Link Have you seen a handmade patchwork quilt? Patchwork quilts are

MOLECULAR GENETICS: TRANSFORMATION AND CLONING adapted by Dr. D. L. Vogelien

2054, Chap. 14, page 1

WSSP-04 Chapter 4 Mapping

FROM EXPERIMENTS IN BACTERIAL GENETICS AND GENE TECHNIQUE

Bio 101 Sample questions: Chapter 10

GenBuilder TM Plus Cloning Kit User Manual

GenBuilder TM Plus Cloning Kit User Manual

#FD µl (for 200 rxns) Expiry Date: Description. 1 ml of 10X FastDigest Green Buffer. Store at -20 C

Biotechnology: DNA Technology & Genomics

Student Manual. Pre-Lab Introduction to DNA Fingerprinting STUDENT MANUAL BACKGROUND

Amira A. AL-Hosary PhD of infectious diseases Department of Animal Medicine (Infectious Diseases) Faculty of Veterinary Medicine Assiut

3 Designing Primers for Site-Directed Mutagenesis

Chapter 20 DNA Technology & Genomics. If we can, should we?

Recombinant DNA Technology

DNA Restriction Digestion Analysis

Transcription:

Manipulation of Purified DNA To produce the recombinant DNA molecule, the vector, as well as the DNA to be cloned, must be cut at specific points and then joined together in a controlled manner by DNA manipulative enzymes. 1.Nucleases: are enzymes that cut, shorten, or degrade nucleic acid molecules. DNA manipulative enzymes 2.Ligases: join nucleic acid molecules together. 3.Polymerases: make copies of molecules. 4.Modifying enzymes: remove or add chemical groups. The cutting and joining manipulations that underlie gene cloning are carried out by enzymes called restriction endonucleases (for cutting) and ligases (for joining).

Enzymes for cutting DNA restriction endonucleases Each vector molecule must be cleaved at a single position, to open up the circle so that new DNA can be inserted: a molecule that is cut more than once will be broken into two or more separate fragments and will be of no use as a cloning vector. Furthermore, each vector molecule must be cut at exactly the same position on the circle. Thus a very special type of nuclease is needed to carry out this manipulation.

Function of restriction endonucleases Restriction endonucleases are synthesized by many, perhaps all, species of bacteria: over 2500 different ones have been isolated and more than 300 are available for use in the laboratory. Type II restriction endonucleases cut DNA at specific nucleotide sequences The recognition sequences for some of the most frequently used restriction endonucleases

Some examples: The ends produced by cleavage of DNA with different restriction endonucleases. A blunt end produced by AluI. A sticky end produced by EcoRI. The same sticky ends produced by BamHI, BglII and Sau3A.

Performing a restriction digest in the laboratory How to digest a sample of λ DNA? What is the number of fragments produced by cleavage with each of these restriction endonucleases?

Digest a sample of λ DNA with BglII: 1 unit of enzyme is defined as the quantity needed to cut 1 µg of DNA in 1 hour. Here we need 2 units of BglII to cut 2 µg of λ DNA.

Analyzing the result of restriction endonuclease cleavage A way of determining the number and sizes of the fragments is needed if restriction endonucleases are to be of use in gene cloning. Using gel electrophoresis Separation of molecules by gel electrophoresis: This technique uses differences in electrical charge to separate the molecules in a mixture. DNA molecules have negative charges, and so when placed in an electric field they migrate toward the positive pole. The smaller the DNA molecule, the faster it can migrate through the gel. Gel electrophoresis therefore separates DNA molecules according to their size.

Visualizing DNA molecules in an agarose gel Visualizing DNA bands in an agarose gel by EtBr staining and ultraviolet (UV) irradiation:

Estimation of the sizes of DNA molecules More common method More accurate measurement of fragment size is gained by using the mobilities of the HindIII λ fragments to construct a calibration curve; the sizes of the unknown fragments can then be determined from the distances they have migrated. The relevant formula is: D = a b(log M)

Mapping the positions of different restriction sites in a DNA molecule Only when a restriction map is available can the correct restriction endonucleases be selected for the particular cutting manipulation that is required. What restriction enzyme should be used to obtain gene B and D?

Ligation joining DNA molecules together The final step in construction of a recombinant DNA molecule is the joining together of the vector molecule and the DNA to be cloned. This process is referred to as ligation, and the enzyme that catalyzes the reaction is called DNA ligase.

The different joining reactions catalysed by DNA ligase:

Introduction of DNA into Living Cells The next step in a gene cloning experiment is to introduce these molecules into living cells, usually bacteria, which then grow and divide to produce clones. Cloning serves two main purposes Amplification Purification

Cloning can supply large amounts of recombinant DNA:

Cloning is analogous to purification. From a mixture of different molecules, clones containing copies of just one molecule can be obtained: