Spatial in situ mapping of cellulose and other biopolymers reveals the 3D tissue architecture in the green algae Ulva fenestrata.

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Autores principales: Schmidt, Alina E M, Steinhagen, Sophie, Nilsson, K Peter R, Edlund, Ulrica, Richter-Dahlfors, Agneta
Formato: Artículo científico
Lenguaje:en
Publicado: International journal of biological macromolecules 2025
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author Schmidt, Alina E M
Steinhagen, Sophie
Nilsson, K Peter R
Edlund, Ulrica
Richter-Dahlfors, Agneta
author_facet Schmidt, Alina E M
Steinhagen, Sophie
Nilsson, K Peter R
Edlund, Ulrica
Richter-Dahlfors, Agneta
Schmidt, Alina E M
Steinhagen, Sophie
Nilsson, K Peter R
Edlund, Ulrica
Richter-Dahlfors, Agneta
collection PubMed - marine biology
contents Spatial in situ mapping of cellulose and other biopolymers reveals the 3D tissue architecture in the green algae Ulva fenestrata. Schmidt, Alina E M Steinhagen, Sophie Nilsson, K Peter R Edlund, Ulrica Richter-Dahlfors, Agneta Cellulose Ulva Biopolymers Imaging, Three-Dimensional Cell Wall Microscopy, Fluorescence The macroalga Ulva fenestrata plays a key role in marine ecosystems and has increasing potential in aquaculture. However, its three-dimensional tissue architecture remains underexplored. This study applies multimodal fluorescence microscopy combined with optotracing to spatially map biopolymers and structural features in native Ulva tissue. Using Carbotrace 680, cellulose was localized in situ within the cell walls, while oligo/polyaromatic compounds were visualized across multiple scaffold layers via autofluorescence. Lambda scanning validated the fluorescence detection settings for cellulose (Exitation wavelength (Ex.) 561 nm, Emission wavelength (Em.) 570-631 nm), oligo/polyaromatics (Ex. 405 nm, Em. 408-505 nm), and chlorophyll (Ex. 639 nm, Em. 649-693 nm). Spatially resolved biopolymer anatomy maps were generated for blade and rhizoidal tissues, and 3D tissue models were constructed. The outermost blade layer exhibited a sandwich-like architecture, and a previously undescribed median layer was identified separating the two cell layers. This layer was >11 times thicker in rhizoidal tissue than in blade tissue, comprising 56 % and 7 % of the total thickness, respectively. Spectral differences in rhizoidal cells indicated cellular heterogeneity. Collectively, the observed biopolymer and architectural differences may reflect tissue-specific functional specialization of the macroalga. This imaging-based approach provides new perspectives on algal biology and supports the multisectoral valorization of Ulva.
format Artículo científico
id pubmed_40582662
institution PubMed
language en
publishDate 2025
publisher International journal of biological macromolecules
record_format pubmed
spellingShingle Spatial in situ mapping of cellulose and other biopolymers reveals the 3D tissue architecture in the green algae Ulva fenestrata.
Schmidt, Alina E M
Steinhagen, Sophie
Nilsson, K Peter R
Edlund, Ulrica
Richter-Dahlfors, Agneta
Cellulose
Ulva
Biopolymers
Imaging, Three-Dimensional
Cell Wall
Microscopy, Fluorescence
Spatial in situ mapping of cellulose and other biopolymers reveals the 3D tissue architecture in the green algae Ulva fenestrata. Schmidt, Alina E M Steinhagen, Sophie Nilsson, K Peter R Edlund, Ulrica Richter-Dahlfors, Agneta Cellulose Ulva Biopolymers Imaging, Three-Dimensional Cell Wall Microscopy, Fluorescence The macroalga Ulva fenestrata plays a key role in marine ecosystems and has increasing potential in aquaculture. However, its three-dimensional tissue architecture remains underexplored. This study applies multimodal fluorescence microscopy combined with optotracing to spatially map biopolymers and structural features in native Ulva tissue. Using Carbotrace 680, cellulose was localized in situ within the cell walls, while oligo/polyaromatic compounds were visualized across multiple scaffold layers via autofluorescence. Lambda scanning validated the fluorescence detection settings for cellulose (Exitation wavelength (Ex.) 561 nm, Emission wavelength (Em.) 570-631 nm), oligo/polyaromatics (Ex. 405 nm, Em. 408-505 nm), and chlorophyll (Ex. 639 nm, Em. 649-693 nm). Spatially resolved biopolymer anatomy maps were generated for blade and rhizoidal tissues, and 3D tissue models were constructed. The outermost blade layer exhibited a sandwich-like architecture, and a previously undescribed median layer was identified separating the two cell layers. This layer was >11 times thicker in rhizoidal tissue than in blade tissue, comprising 56 % and 7 % of the total thickness, respectively. Spectral differences in rhizoidal cells indicated cellular heterogeneity. Collectively, the observed biopolymer and architectural differences may reflect tissue-specific functional specialization of the macroalga. This imaging-based approach provides new perspectives on algal biology and supports the multisectoral valorization of Ulva.
title Spatial in situ mapping of cellulose and other biopolymers reveals the 3D tissue architecture in the green algae Ulva fenestrata.
topic Cellulose
Ulva
Biopolymers
Imaging, Three-Dimensional
Cell Wall
Microscopy, Fluorescence
url https://pubmed.ncbi.nlm.nih.gov/40582662/