Experimental identification of carbohydrate-binding modules (CBM) and determination of ligand specificity of each CBM are complementary and compulsory steps for their characterization. Some CBMs are very specific for their primary substrate (e.g., cellulose), whereas others are relatively promiscuous or nonspecific in their substrate preference. Here we describe a simple procedure based on in-tube adsorption of a CBM to various insoluble polysaccharides, followed by sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS PAGE) for determining the distribution of the CBM between the bound and unbound fractions. This technique enables qualitative assessment of the binding strength and ligand specificity for each CBM.
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http://dx.doi.org/10.1007/978-1-61779-956-3_10 | DOI Listing |
J Fungi (Basel)
December 2024
College of Agronomy, Guangxi University, Nanning 530004, China.
Carbohydrate-binding modules (CBMs) are essential virulence factors in phytopathogens, particularly the extensively studied members from the CBM50 gene family, which are known as lysin motif (LysM) effectors and which play crucial roles in plant-pathogen interactions. However, the function of CBM50 in has yet to be fully studied. In this study, we identified seven CBM50 genes from the genome through complete sequence analysis and functional annotation.
View Article and Find Full Text PDFArch Biochem Biophys
November 2024
Carbohydrate Enzyme Biotechnology Laboratory, Department of Biosciences and Bioengineering, Indian Institute of Technology Guwahati, Guwahati, Assam, 781039, India. Electronic address:
Int J Biol Macromol
December 2024
College of Food Science and Engineering, Ocean University of China, 1299 Sansha Road, Qingdao 266404, China; Laboratory for Marine Drugs and Bioproducts, Pilot National Laboratory for Marine Science and Technology, Qingdao 266237, China.
Quantification is essential in the research and development of polysaccharides. However, achieving simplicity and specificity in polysaccharide quantification remains a challenging task. Enzyme-linked immunosorbent assay (ELISA) based on antibodies provides a straightforward and specific quantification strategy.
View Article and Find Full Text PDFInt J Biol Macromol
December 2024
Jiangsu Co-Innovation Center for Efficient Processing and Utilization of Forest Resources and International Innovation Center for Forest Chemicals and Materials, Nanjing Forestry University, Nanjing 210037, China. Electronic address:
Bacterial cellulose (BC) has been extensively applied to fabricate advanced biomaterials, although it remains challenging due to its poor toughness and water stability. Herein a genetically engineered protein-conjugated synthetic polymer is designed to improve BC film's strength and flexibility. Initially, the hybrid polymer is constructed by grafting Family 3 carbohydrate-binding modules (CBM3) to amphoteric polyacrylamide polymer (AmPAM), one of the paper industry's most widely used dry-strength agents.
View Article and Find Full Text PDFInt J Mol Sci
November 2024
College of Agronomy, Guangxi University, Nanning 530004, China.
is a pathogenic basidiomycete fungus that causes foxtail millet kernel smut (FMKS), a devastating grain disease in most foxtail millet growing regions of the world. Carbohydrate-Binding Modules (CBMs) are one of the important families of carbohydrate-active enzymes (CAZymes) in fungi and play a crucial role in fungal growth and development, as well as in pathogen infection. However, there is little information about the CBM family in .
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