Chitin and chitosan quantification in fungal cell wall via Raman spectroscopy

被引:0
作者
Barroso-Solares, Suset [1 ,2 ]
Lopez-Moya, Federico [3 ]
Fraile, Teresa [3 ]
Prieto, Angel Carmelo [1 ]
Lopez-Llorca, Luis [3 ]
Pinto, Javier [1 ,2 ]
机构
[1] Univ Valladolid, Fac Sci, Condensed Matter Phys Crystallog & Mineral Dept, Study Preservat & Recovery Archaeol Hist Environm, Valladolid 47011, Spain
[2] Univ Valladolid, BioEcoUVA Res Inst Bioecon, Valladolid, Spain
[3] Univ Alicante, Dept Marine Sci & Appl Biol, Lab Plant Pathol, Alicante 03690, Spain
关键词
Biocontrol fungi; Chitin; Chitosan; Aminopolysaccharides; Raman spectroscopy; BETA-GLUCAN; IDENTIFICATION;
D O I
10.1016/j.saa.2025.125928
中图分类号
O433 [光谱学];
学科分类号
0703 ; 070302 ;
摘要
Investigation of cell wall composition is necessary to understand the interactions between fungi and the environment as it is the external layer exposed to stimuli and detected by other organisms. Pochonia chlamydosporia and Akanthomyces lecanii, two fungal species living in the soil and infecting nematodes and insects, exhibit endophytic interactions with various plant species. Determination of cell wall composition is essential to understand the mechanisms underlying these interactions. Therefore, in this study, for the first time, we assessed the relative amounts of chitin and chitosan in the cell walls of P. chlamydosporia (PC123) and A. lecanii (69NZ, 85SCT, 126KNY, and 447SAF) via Raman spectroscopy. The isolate with the highest chitosan percentage was 69NZ, followed by 85SCT, PC123, 447SAF, and 126KNY. Moreover, combination with conventional approaches for chitin and chitosan quantification yielded quantitative results for all cell wall components. Overall, these results highlight the mechanisms by which fungi exhibit chitosan resistance and avoid detection by the host plant during root colonization.
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页数:7
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