Essentials Of Genetics (9th Global Edition)
Essentials Of Genetics (9th Global Edition)
9th Edition
ISBN: 9780134143637
Author: William S. Klug, Michael R. Cummings
Publisher: Pearson Global Edition
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Chapter 17, Problem 6PDQ
Summary Introduction

To review:

The palindromic recognition sequence in 5'-CAGTATGGATCCCAT-3' for a restriction enzyme. Also, show the double-stranded DNA (deoxyribonucleic acid) sequence of the palindrome and the enzymes that would cut at the palindromic sequence.

Introduction:

The deliberate change (modifications) in the genetic material of an organism by altering the nucleic acid is called genetic engineering, which is generally accomplished by RDT (recombinant DNA or deoxyribonucleic acid). The fragment of DNA to be cloned in the vector molecule is called DNA insert or foreign DNA that amplifies in a specific host. RDT involves many biological agent and tools for gene cloning, such as nucleases, DNA ligase, DNA insert, vector molecule, host cell, and kinasesor phosphatases.

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Students have asked these similar questions
The gene you are asked to clone is 30,000 bps in length. When you are choosing a suitable Restriction Endonuclease, what criteria about the enzyme can you deduce from the gene length?
If the GAATTC palindrome is repeated four times on the same piece of linear DNA, and the restriction enzyme that recognizes that base sequence is present and digests the DNA, how many DNA fragments will be produced?
Which restriction enzyme used in your simulated electrophoresis experiment produced DNA with ‘sticky ends’? Which produced blunt ends? Of these two restriction enzymes, which would you choose to use as donor DNA to graft (or splice) onto a recipient strand of DNA, and why?
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