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Microbial Toxins

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Cover of 'Microbial Toxins'

Table of Contents

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    Book Overview
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    Chapter 1 Detection of Cholera Toxin by an Immunochromatographic Test Strip
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    Chapter 2 Electrochemical Aptamer Scaffold Biosensors for Detection of Botulism and Ricin Proteins
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    Chapter 3 A Cell-Based Fluorescent Assay to Detect the Activity of AB Toxins that Inhibit Protein Synthesis
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    Chapter 4 Molecular Methods for Identification of Clostridium tetani by Targeting Neurotoxin
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    Chapter 5 Label-Free Immuno-Sensors for the Fast Detection of Listeria in Food
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    Chapter 6 Aptamer-Based Trapping: Enrichment of Bacillus cereus Spores for Real-Time PCR Detection
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    Chapter 7 Detection of Yersinia pestis in Complex Matrices by Intact Cell Immunocapture and Targeted Mass Spectrometry
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    Chapter 8 A Method to Prepare Magnetic Nanosilicate Platelets for Effective Removal of Microcystis aeruginosa and Microcystin-LR
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    Chapter 9 An Immunochromatographic Test Strip to Detect Ochratoxin A and Zearalenone Simultaneously
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    Chapter 10 Endotoxin Removal from Escherichia coli Bacterial Lysate Using a Biphasic Liquid System
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    Chapter 11 Fourier Transform Infrared Spectroscopy as a Tool in Analysis of Proteus mirabilis Endotoxins
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    Chapter 12 Laser Interferometry Method as a Novel Tool in Endotoxins Research
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    Chapter 13 Endotoxin Entrapment on Glass via C-18 Self-Assembled Monolayers and Rapid Detection Using Drug-Nanoparticle Bioconjugate Probes
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    Chapter 14 A Bioassay for the Determination of Lipopolysaccharides and Lipoproteins
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    Chapter 15 Capillary Electrophoresis Chips for Fingerprinting Endotoxin Chemotypes and Subclasses
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    Chapter 16 Micromethods for Isolation and Structural Characterization of Lipid A, and Polysaccharide Regions of Bacterial Lipopolysaccharides
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    Chapter 17 Mass Spectrometry for Profiling LOS and Lipid A Structures from Whole-Cell Lysates: Directly from a Few Bacterial Colonies or from Liquid Broth Cultures
Attention for Chapter 15: Capillary Electrophoresis Chips for Fingerprinting Endotoxin Chemotypes and Subclasses
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Chapter title
Capillary Electrophoresis Chips for Fingerprinting Endotoxin Chemotypes and Subclasses
Chapter number 15
Book title
Microbial Toxins
Published in
Methods in molecular biology, January 2017
DOI 10.1007/978-1-4939-6958-6_15
Pubmed ID
Book ISBNs
978-1-4939-6956-2, 978-1-4939-6958-6
Authors

Béla Kocsis, Lilla Makszin, Anikó Kilár, Zoltán Péterfi, Ferenc Kilár

Editors

Otto Holst

Abstract

Endotoxins (lipopolysaccharides, LPS; lipooligosaccharides, LOS) are components of the envelope of Gram-negative bacteria. These molecules, responsible for both advantageous and harmful biological activity of these microorganisms, are highly immunogenic and directly involved in numerous bacterial diseases in humans, such as Gram-negative sepsis. The characterization of endotoxins is of importance, since their physiological and pathophysiological effects depend on their chemical structure. The differences among the LPS from different bacterial serotypes and their mutants include variations mainly within the composition and length or missing of their O-polysaccharide chains. Microchip electrophoretic methodology enables the structural characterization of LPS molecules from several bacteria and the quantitative evaluation of components of endotoxin extracts. The improved microchip electrophoretic method is based on the direct labeling of endotoxins by covalent binding of a fluorescent dye. The classification of the S-type LPSs can be done according to their electrophoretic profiles, which are characteristics of the respective bacterial strains. According to the number, distribution, and the relative amounts of components in an endotoxin extract, it is possible to differentiate between the S-type endotoxins from different Gram-negative bacterial strains. The microchip electrophoresis affords high-resolution separation of pure and partially purified (e.g., obtained from whole-cell lysate) S and R endotoxins. This microchip technique provides a new, standardizable, fast, and sensitive method for the detection of endotoxins and for the quantitative evaluation of components of an endotoxin extract.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 8 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 8 100%

Demographic breakdown

Readers by professional status Count As %
Researcher 2 25%
Student > Master 2 25%
Student > Bachelor 1 13%
Lecturer > Senior Lecturer 1 13%
Professor 1 13%
Other 0 0%
Unknown 1 13%
Readers by discipline Count As %
Chemistry 3 38%
Biochemistry, Genetics and Molecular Biology 1 13%
Pharmacology, Toxicology and Pharmaceutical Science 1 13%
Nursing and Health Professions 1 13%
Engineering 1 13%
Other 0 0%
Unknown 1 13%