INRAE, UR 1268 BIA, 44316 Nantes, France; INRAE, Université de Reims Champagne Ardenne, FARE, UMR A 614, 51100 Reims, France.
INRAE, UR 1268 BIA, 44316 Nantes, France; INRAE, BIBS Facility, 44316 Nantes, France.
Carbohydr Polym. 2024 Nov 1;343:122465. doi: 10.1016/j.carbpol.2024.122465. Epub 2024 Jul 5.
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.
溶细胞多糖单加氧酶(LPMOs)是一类依赖铜的酶,能够氧化断裂纤维素等结构稳定的多糖。有多项研究报道了 LPMO 与其他碳水化合物活性酶(CAZymes)协同作用以降解木质纤维素生物质,但在植物组织水平上直接研究 LPMO 的作用仍具有挑战性。在此,我们开发了一种 MALDI-MS 成像工作流程,以检测玉米组织中细胞活性 LPMO 释放的氧化寡糖。使用该工作流程,我们可以对 LPMO 的作用进行成像,并深入了解氧化和非氧化寡糖的空间变化和相对丰度。我们揭示了 LPMO 的靶向作用与植物细胞壁的组成和结构有关。