In situ imaging of LPMO action on plant tissues

被引:0
|
作者
Leroy, Amandine [1 ,2 ]
Fanuel, Mathieu [1 ,3 ]
Alvarado, Camille [1 ]
Rogniaux, Helene [1 ,3 ]
Grisel, Sacha [4 ,5 ]
Haon, Mireille [4 ,5 ]
Berrin, Jean-Guy [4 ]
Paes, Gabriel [2 ]
Guillon, Fabienne [1 ]
机构
[1] INRAE, UR BIA 1268, F-44316 Nantes, France
[2] Univ Reims, UMR A 614, INRAE, FARE, F-51100 Reims, France
[3] INRAE, BIBS Facil, F-44316 Nantes, France
[4] Aix Marseille Univ, INRAE, Biodivers & Biotechnol Fong BBF, F-13009 Marseille, France
[5] Aix Marseille Univ, INRAE, 3PE Platform, F-13009 Marseille, France
关键词
Oxidative enzyme; Plant cell wall; Cellulose; MALDI-MS imaging; LYTIC POLYSACCHARIDE MONOOXYGENASE; ENZYMATIC-HYDROLYSIS; RECALCITRANCE;
D O I
10.1016/j.carbpol.2024.122465
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
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.
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页数:8
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