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In Vitro Mutagenesis

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Cover of 'In Vitro Mutagenesis'

Table of Contents

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    Book Overview
  2. Altmetric Badge
    Chapter 1 Design and Validation of CRISPR/Cas9 Systems for Targeted Gene Modification in Induced Pluripotent Stem Cells.
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    Chapter 2 Mutagenesis and Genome Engineering of Epstein-Barr Virus in Cultured Human Cells by CRISPR/Cas9.
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    Chapter 3 Use of CRISPR/Cas Genome Editing Technology for Targeted Mutagenesis in Rice.
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    Chapter 4 All-in-One CRISPR-Cas9/FokI-dCas9 Vector-Mediated Multiplex Genome Engineering in Cultured Cells.
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    Chapter 5 CRISPR/Cas9-Mediated Mutagenesis of Human Pluripotent Stem Cells in Defined Xeno-Free E8 Medium.
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    Chapter 6 Development of CRISPR/Cas9 for Efficient Genome Editing in Toxoplasma gondii.
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    Chapter 7 Generation of Stable Knockout Mammalian Cells by TALEN-Mediated Locus-Specific Gene Editing.
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    Chapter 8 Efficient Generation of Gene-Modified Mice by Haploid Embryonic Stem Cell-Mediated Semi-cloned Technology.
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    Chapter 9 Insertion of Group II Intron-Based Ribozyme Switches into Homing Endonuclease Genes.
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    Chapter 10 Generating a Genome Editing Nuclease for Targeted Mutagenesis in Human Cells.
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    Chapter 11 Use of Group II Intron Technology for Targeted Mutagenesis in Chlamydia trachomatis.
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    Chapter 12 In Silico Approaches to Identify Mutagenesis Targets to Probe and Alter Protein-Cofactor and Protein-Protein Functional Relationships.
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    Chapter 13 In Silico Prediction of Deleteriousness for Nonsynonymous and Splice-Altering Single Nucleotide Variants in the Human Genome.
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    Chapter 14 In Silico Methods for Analyzing Mutagenesis Targets.
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    Chapter 15 Methods for Detecting Critical Residues in Proteins.
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    Chapter 16 A Method for Bioinformatic Analysis of Transposon Insertion Sequencing (INSeq) Results for Identification of Microbial Fitness Determinants.
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    Chapter 17 Application of In Vitro Transposon Mutagenesis to Erythromycin Strain Improvement in Saccharopolyspora erythraea.
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    Chapter 18 Engineering Gram-Negative Microbial Cell Factories Using Transposon Vectors.
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    Chapter 19 PERMutation Using Transposase Engineering (PERMUTE): A Simple Approach for Constructing Circularly Permuted Protein Libraries.
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    Chapter 20 Transposon Insertion Mutagenesis for Archaeal Gene Discovery.
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    Chapter 21 Genome-Wide Transposon Mutagenesis in Mycobacterium tuberculosis and Mycobacterium smegmatis.
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    Chapter 22 Multiple Site-Directed and Saturation Mutagenesis by the Patch Cloning Method.
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    Chapter 23 Seamless Ligation Cloning Extract (SLiCE) Method Using Cell Lysates from Laboratory Escherichia coli Strains and its Application to SLiP Site-Directed Mutagenesis.
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    Chapter 24 Facile Site-Directed Mutagenesis of Large Constructs Using Gibson Isothermal DNA Assembly.
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    Chapter 25 Revised Mechanism and Improved Efficiency of the QuikChange Site-Directed Mutagenesis Method.
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    Chapter 26 An In Vitro Single-Primer Site-Directed Mutagenesis Method for Use in Biotechnology.
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    Chapter 27 Use of Megaprimer and Overlapping Extension PCR (OE-PCR) to Mutagenize and Enhance Cyclodextrin Glucosyltransferase (CGTase) Function.
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    Chapter 28 Step-By-Step In Vitro Mutagenesis: Lessons From Fucose-Binding Lectin PA-IIL.
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    Chapter 29 Analytical Methods for Assessing the Effects of Site-Directed Mutagenesis on Protein-Cofactor and Protein-Protein Functional Relationships.
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    Chapter 30 Biochemical and Biophysical Methods to Examine the Effects of Site-Directed Mutagenesis on Enzymatic Activities and Interprotein Interactions.
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    Chapter 31 Use of Random and Site-Directed Mutagenesis to Probe Protein Structure-Function Relationships: Applied Techniques in the Study of Helicobacter pylori.
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    Chapter 32 Novel Random Mutagenesis Method for Directed Evolution.
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    Chapter 33 Random Mutagenesis by Error-Prone Polymerase Chain Reaction Using a Heavy Water Solvent.
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    Chapter 34 Development and Use of a Novel Random Mutagenesis Method: In Situ Error-Prone PCR (is-epPCR).
Attention for Chapter 17: Application of In Vitro Transposon Mutagenesis to Erythromycin Strain Improvement in Saccharopolyspora erythraea.
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Chapter title
Application of In Vitro Transposon Mutagenesis to Erythromycin Strain Improvement in Saccharopolyspora erythraea.
Chapter number 17
Book title
In Vitro Mutagenesis
Published in
Methods in molecular biology, January 2017
DOI 10.1007/978-1-4939-6472-7_17
Pubmed ID
Book ISBNs
978-1-4939-6470-3, 978-1-4939-6472-7
Authors

J. Mark Weber, Andrew Reeves, William H. Cernota, Roy K. Wesley

Editors

Andrew Reeves

Abstract

Transposon mutagenesis is an invaluable technique in molecular biology for the creation of random mutations that can be easily identified and mapped. However, in the field of microbial strain improvement, transposon mutagenesis has scarcely been used; instead, chemical and physical mutagenic methods have been traditionally favored. Transposons have the advantage of creating single mutations in the genome, making phenotype to genotype assignments less challenging than with traditional mutagens which commonly create multiple mutations in the genome. The site of a transposon mutation can also be readily mapped using DNA sequencing primer sites engineered into the transposon termini. In this chapter an in vitro method for transposon mutagenesis of Saccharopolyspora erythraea is presented. Since in vivo transposon tools are not available for most actinomycetes including S. erythraea, an in vitro method was developed. The in vitro method involves a significant investment in time and effort to create the mutants, but once the mutants are made and screened, a large number of highly relevant mutations of direct interest to erythromycin production can be found.

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Mendeley readers

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Geographical breakdown

Country Count As %
Unknown 4 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 1 25%
Student > Bachelor 1 25%
Researcher 1 25%
Student > Doctoral Student 1 25%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 2 50%
Environmental Science 1 25%
Chemistry 1 25%
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This research output has an Altmetric Attention Score of 1. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 06 January 2018.
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