AI Article Synopsis

  • Plant cell wall polysaccharides are challenging to analyze due to the need for expensive equipment and skilled operators, but a new simple method has been introduced.
  • The method involves hydrolyzing polysaccharides with specific glycosyl hydrolases and using large polyacrylamide gels to separate and visualize the fluorescently labeled oligosaccharides.
  • This protocol allows for detailed structural analysis, including linkage and branching information, and can be adapted to study various polysaccharides and novel glycosyl hydrolases.

Article Abstract

Plant cell wall polysaccharides are notoriously difficult to analyze, and most methods require expensive equipment, skilled operators, and large amounts of purified material. Here, we describe a simple method for gaining detailed polysaccharide structural information, including resolution of structural isomers. For polysaccharide analysis by gel electrophoresis (PACE), plant cell wall material is hydrolyzed with glycosyl hydrolases specific to the polysaccharide of interest (e.g., mannanases for mannan). Large format polyacrylamide gels are then used to separate the released oligosaccharides, which have been fluorescently labeled. Gels can be visualized with a modified gel imaging system (see Table of Materials). The resulting oligosaccharide fingerprint can either be compared qualitatively or, with replication, quantitatively. Linkage and branching information can be established using additional glycosyl hydrolases (e.g., mannosidases and galactosidases). Whilst this protocol describes a method for analyzing glucomannan structure, it can be applied to any polysaccharide for which characterized glycosyl hydrolases exist. Alternatively, it can be used to characterize novel glycosyl hydrolases using defined polysaccharide substrates.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5752419PMC
http://dx.doi.org/10.3791/56424DOI Listing

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