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In Vitro Mutagenesis

Overview of attention for book
In Vitro Mutagenesis
Springer New York

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 18: Engineering Gram-Negative Microbial Cell Factories Using Transposon Vectors.
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Chapter title
Engineering Gram-Negative Microbial Cell Factories Using Transposon Vectors.
Chapter number 18
Book title
In Vitro Mutagenesis
Published in
Methods in molecular biology, January 2017
DOI 10.1007/978-1-4939-6472-7_18
Pubmed ID
Book ISBNs
978-1-4939-6470-3, 978-1-4939-6472-7
Authors

Esteban Martínez-García, Tomás Aparicio, Víctor de Lorenzo, Pablo I. Nikel

Editors

Andrew Reeves

Abstract

The construction of microbial cell factories à la carte largely depends on specialized molecular biology and synthetic biology tools needed to reprogram bacteria for modifying their existing functions or for bestowing them with new-to-Nature tasks. In this chapter, we document the use of a series of broad-host-range mini-Tn5 vectors for the delivery of gene(s) into the chromosome of Gram-negative bacteria and for the generation of saturated, random mutagenesis libraries for studies of gene function. The application of these tailored mini-transposon vectors, which could also be used for chromosomal engineering of a wide variety of Gram-negative microorganisms, is demonstrated in the platform environmental bacterium Pseudomonas putida KT2440.

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Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 46 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
United States 1 2%
China 1 2%
Brazil 1 2%
Unknown 43 93%

Demographic breakdown

Readers by professional status Count As %
Student > Master 10 22%
Student > Bachelor 8 17%
Researcher 7 15%
Student > Ph. D. Student 5 11%
Student > Doctoral Student 3 7%
Other 5 11%
Unknown 8 17%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 23 50%
Agricultural and Biological Sciences 12 26%
Arts and Humanities 2 4%
Immunology and Microbiology 2 4%
Chemistry 1 2%
Other 0 0%
Unknown 6 13%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 2. 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.
All research outputs
#14,570,412
of 23,337,345 outputs
Outputs from Methods in molecular biology
#4,303
of 13,337 outputs
Outputs of similar age
#232,137
of 422,972 outputs
Outputs of similar age from Methods in molecular biology
#369
of 1,075 outputs
Altmetric has tracked 23,337,345 research outputs across all sources so far. This one is in the 35th percentile – i.e., 35% of other outputs scored the same or lower than it.
So far Altmetric has tracked 13,337 research outputs from this source. They receive a mean Attention Score of 3.4. This one has gotten more attention than average, scoring higher than 64% of its peers.
Older research outputs will score higher simply because they've had more time to accumulate mentions. To account for age we can compare this Altmetric Attention Score to the 422,972 tracked outputs that were published within six weeks on either side of this one in any source. This one is in the 42nd percentile – i.e., 42% of its contemporaries scored the same or lower than it.
We're also able to compare this research output to 1,075 others from the same source and published within six weeks on either side of this one. This one has gotten more attention than average, scoring higher than 61% of its contemporaries.