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Protein-Carbohydrate Interactions

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Cover of 'Protein-Carbohydrate Interactions'

Table of Contents

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    Book Overview
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    Chapter 1 A Low-Volume, Parallel Copper-Bicinchoninic Acid (BCA) Assay for Glycoside Hydrolases
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    Chapter 2 Quantitative Kinetic Characterization of Glycoside Hydrolases Using High-Performance Anion-Exchange Chromatography (HPAEC)
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    Chapter 3 Measuring Enzyme Kinetics of Glycoside Hydrolases Using the 3,5-Dinitrosalicylic Acid Assay
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    Chapter 4 An Improved Kinetic Assay for the Characterization of Metal-Dependent Pectate Lyases
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    Chapter 5 Colorimetric Detection of Acetyl Xylan Esterase Activities
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    Chapter 6 Methods for Determining Glycosyltransferase Kinetics
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    Chapter 7 Analyzing Activities of Lytic Polysaccharide Monooxygenases by Liquid Chromatography and Mass Spectrometry
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    Chapter 8 Carbohydrate Depolymerization by Intricate Cellulosomal Systems
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    Chapter 9 Affinity Electrophoresis for Analysis of Catalytic Module-Carbohydrate Interactions
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    Chapter 10 Quantifying CBM Carbohydrate Interactions Using Microscale Thermophoresis
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    Chapter 11 Characterization of Protein-Carbohydrate Interactions by NMR Spectroscopy
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    Chapter 12 Measuring the Biomechanical Loosening Action of Bacterial Expansins on Paper and Plant Cell Walls
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    Chapter 13 Bioinspired Assemblies of Plant Cell Walls for Measuring Protein-Carbohydrate Interactions by FRAP
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    Chapter 14 CBMs as Probes to Explore Plant Cell Wall Heterogeneity Using Immunocytochemistry
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    Chapter 15 Determining the Localization of Carbohydrate Active Enzymes Within Gram-Negative Bacteria
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    Chapter 16 Analysis of Complex Carbohydrate Composition in Plant Cell Wall Using Fourier Transformed Mid-Infrared Spectroscopy (FT-IR)
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    Chapter 17 Separation and Visualization of Glycans by Fluorophore-Assisted Carbohydrate Electrophoresis
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    Chapter 18 A Rapid Procedure for the Purification of 8-Aminopyrene Trisulfonate (APTS)-Labeled Glycans for Capillary Electrophoresis (CE)-Based Enzyme Assays
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    Chapter 19 Probing the Complex Architecture of Multimodular Carbohydrate-Active Enzymes Using a Combination of Small Angle X-Ray Scattering and X-Ray Crystallography
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    Chapter 20 Metagenomics and CAZyme Discovery
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    Chapter 21 Identification of Genes Involved in the Degradation of Lignocellulose Using Comparative Transcriptomics
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    Chapter 22 Isolation and Preparation of Extracellular Proteins from Lignocellulose Degrading Fungi for Comparative Proteomic Studies Using Mass Spectrometry
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    Chapter 23 Erratum to: Colorimetric Detection of Acetyl Xylan Esterase Activities
Attention for Chapter 8: Carbohydrate Depolymerization by Intricate Cellulosomal Systems
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Chapter title
Carbohydrate Depolymerization by Intricate Cellulosomal Systems
Chapter number 8
Book title
Protein-Carbohydrate Interactions
Published in
Methods in molecular biology, April 2017
DOI 10.1007/978-1-4939-6899-2_8
Pubmed ID
Book ISBNs
978-1-4939-6898-5, 978-1-4939-6899-2
Authors

Stern, Johanna, Artzi, Lior, Moraïs, Sarah, Fontes, Carlos M. G. A., Bayer, Edward A., Johanna Stern, Lior Artzi, Sarah Moraïs, Carlos M. G. A. Fontes, Edward A. Bayer

Editors

D. Wade Abbott, Alicia Lammerts van Bueren

Abstract

Cellulosomes are multi-enzymatic nanomachines that have been fine-tuned through evolution to efficiently deconstruct plant biomass. Integration of cellulosomal components occurs via highly ordered protein-protein interactions between the various enzyme-borne dockerin modules and the multiple copies of the cohesin modules located on the scaffoldin subunit. Recently, designer cellulosome technology has been established to provide insights into the architectural role of catalytic (enzymatic) and structural (scaffoldin) cellulosomal constituents for the efficient degradation of plant cell wall polysaccharides. Owing to advances in genomics and proteomics, highly structured cellulosome complexes have recently been unraveled, and the information gained has inspired the development of designer cellulosome technology to new levels of complex organization. These higher-order designer cellulosomes have in turn fostered our capacity to enhance the catalytic potential of artificial cellulolytic complexes. In this chapter, methods to produce and employ such intricate cellulosomal complexes are reported.

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X Demographics

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Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 11 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 11 100%

Demographic breakdown

Readers by professional status Count As %
Researcher 4 36%
Student > Master 3 27%
Student > Ph. D. Student 2 18%
Student > Postgraduate 1 9%
Unknown 1 9%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 4 36%
Agricultural and Biological Sciences 3 27%
Physics and Astronomy 1 9%
Materials Science 1 9%
Unknown 2 18%
Attention Score in Context

Attention Score in Context

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 19 April 2017.
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#21,648,551
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Outputs from Methods in molecular biology
#10,428
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#275,191
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Outputs of similar age from Methods in molecular biology
#196
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