Campbell Biology in Focus (2nd Edition)
Campbell Biology in Focus (2nd Edition)
2nd Edition
ISBN: 9780321962751
Author: Lisa A. Urry, Michael L. Cain, Steven A. Wasserman, Peter V. Minorsky, Jane B. Reece
Publisher: PEARSON
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Chapter 13.4, Problem 1CC
Summary Introduction

To identify:

The sequence and the types of the bonds that are being cleaved in the sequence of the DNA by the restriction enzyme PvuI namely:

5'-CGATCG-3'3'-GCTAGC-5'

Concept introduction:

The enzyme PvuI cuts in between the T-C nucleotide in the sequence given. The sequence after the digestion of the restriction enzyme sequence will be:

5'-CGAT--CG-3'3'-GC--TAGC-5'

The types of the bonds that will be cleaved in between the nucleotides are the phosphate bonds between the pentose sugar and the nucleotide connecting the next nucleotide in the sequence.

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MAKE CONNECTIONS The restriction site for an enzymecalled PvuI is the following sequence:5’-CGATCG-3’3’-GCTAGC-5’
3 The restriction endonuclease Pstl cuts DNA symmetrically on both strands at the СТGCAG sequence: GACGTC On the resulting DNA fragments are left 3' overhanging ends of 4 nucleotides. PstI cleaves the phosphodiester backbone with a-type specificity. In short-hand notation, showing the identity of phosphates on the ends, draw the two fragments that result from PstI digestion of the following double-stranded oligonucleotide: 5'-рAATTGCTAСTGCAGAACCGG-3' 3'-ТТAАCGATGACGTCTTGGСС--5'
Sensors detect the flash of light. DNA polymerase Unused deoxyribonucleotides are cleaved by apyrase. ATP is consumed by luciferase and light is emitted. AMP and PP, are converted into ATP by sulfurylase. Template strand Growing strand 3' TAGGCCTACACTTACGCGAATGT 5' 5' ATCCGGAT 3' dGTP dNTPs dNDPs dNMPs + P₁ PP₁ ATP [1]
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