4.7 Article

Enzymatic-fingerprinting workflow of polysaccharides in Hericium erinaceus fruiting bodies: From HILIC-ESI--MS screening to targeted MIM profiling

Journal

INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES
Volume 173, Issue -, Pages 491-503

Publisher

ELSEVIER
DOI: 10.1016/j.ijbiomac.2021.01.093

Keywords

Structural-fingerprinting of polysaccharides; Hericium erinaceus; Enzymatic digestion; HILIC-ESI--MS; HILIC-MIM-MS

Funding

  1. Applied Technology Research and Development Plan of Heilongjiang Province [GA19C104]
  2. University Research and Development Projects of Heilongjiang Province [TSTAUR2018026]

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An uncommon enzymatic-fingerprinting workflow was proposed for the characterization and discrimination of mushroom polysaccharides using HILIC-ESI-MS. The study revealed the structural features of polysaccharides in Hericium erinaceus fruiting bodies and visually classified different polysaccharides through similarity analysis and other methods. This enzymatic-fingerprinting workflow provides an effective example for quality evaluation of fungi polysaccharides using a structural-fingerprinting strategy.
In this study, an uncommon enzymatic-fingerprinting workflow, was proposed for characterization and discrimination of mushroom polysaccharides (MPs) by hydrophilic interaction liquid chromatography-negative electrospray mass spectrometry (HILIC-ESI--MS). Firstly, the HILIC-ESI--MS was used to screen and identify the enzymatic digestion products of MPs using HILIC-Orbitrap based on full scan and MS/MS modes. Secondly, a targeted structural-fingerprinting of polysaccharides (SFP) was built in a multiple-ion monitoring (MIM) mode using the same HILIC separation with a triple quadrupole MS. Thirdly, a case study of polysaccharides in Hericium erinaceus fruiting bodies (HEP) was performed to obtain the expected SFP based on dextranase digestion that allows for visual discrimination of polysaccharides from other five edible mushrooms attributed to Agrocybe cylindracea, Arimillaria mellea, Flammulina velutipes, Pleurotus eryngii, and Lentinula edodes. Furthermore, a major structural backbone of HEP was unveiled by occurrence of -> (6)(Hex)(1) -> along withmultiple possible substitutions including of terminal GalA, Fuc, acetyl, -> (4)Hex(1) ->, and -> (3)Hex(1) ->. Finally, the similarity analysis, hierarchical cluster analysis (HCA), and partial least squares discriminant analysis (PLS-DA) were performed to visualize various MPs. As a result, the enzymatic-fingerprinting workflow presents an effective example for quality evaluation of fungi polysaccharides using a SFP strategy. (C) 2021 Elsevier B.V. All rights reserved.

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