In situ imaging of LPMO action on plant tissues

Carbohydr Polym. 2024 Nov 1:343:122465. doi: 10.1016/j.carbpol.2024.122465. Epub 2024 Jul 5.

Abstract

Lytic polysaccharide monooxygenases (LPMOs) are copper-dependent enzymes that oxidatively cleave recalcitrant polysaccharides such as cellulose. Several studies have reported LPMO action in synergy with other carbohydrate-active enzymes (CAZymes) for the degradation of lignocellulosic biomass but direct LPMO action at the plant tissue level remains challenging to investigate. Here, we have developed a MALDI-MS imaging workflow to detect oxidised oligosaccharides released by a cellulose-active LPMO at cellular level on maize tissues. Using this workflow, we imaged LPMO action and gained insight into the spatial variation and relative abundance of oxidised and non-oxidised oligosaccharides. We reveal a targeted action of the LPMO related to the composition and organisation of plant cell walls.

Keywords: Cellulose; MALDI-MS imaging; Oxidative enzyme; Plant cell wall.

MeSH terms

  • Cell Wall / chemistry
  • Cell Wall / metabolism
  • Cellulose / chemistry
  • Cellulose / metabolism
  • Lignin / chemistry
  • Lignin / metabolism
  • Mixed Function Oxygenases* / chemistry
  • Mixed Function Oxygenases* / metabolism
  • Oligosaccharides / chemistry
  • Oligosaccharides / metabolism
  • Oxidation-Reduction
  • Plant Proteins / chemistry
  • Plant Proteins / metabolism
  • Polysaccharides / chemistry
  • Polysaccharides / metabolism
  • Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization* / methods
  • Zea mays* / chemistry

Substances

  • Mixed Function Oxygenases
  • Cellulose
  • Oligosaccharides
  • Lignin
  • Polysaccharides
  • lignocellulose
  • Plant Proteins