TY - JOUR
T1 - Bioinspired mechanically stable all-polysaccharide based scaffold for photosynthetic production
AU - Virkkala, Tuuli
AU - Kosourov, Sergey
AU - Rissanen, Ville
AU - Siitonen, Vilja
AU - Arola, Suvi
AU - Allahverdiyeva, Yagut
AU - Tammelin, Tekla
N1 - Funding Information:
This project has received funding from the European Union's Horizon 2020 research and innovation programme under grant agreement No. 899576 and the Academy of Finland project #322752/#322754. S. A. was funded by the Academy of Finland grant #326262/311608. The authors acknowledge the support from the Academy of Finland funded flagship programme FinnCERES Materials Bioeconomy Ecosystem. This work made use of the Bioeconomy Facilities at Aalto University and VTT. Photosynthetic measurements and ethylene production experiments were performed in the University of Turku PhotoSYN infrastructure. We thank Teemu Suutari and Juan José Valle-Delgado for assistance with QCM-D and AFM measurements.
Publisher Copyright:
© 2023 The Royal Society of Chemistry
PY - 2023
Y1 - 2023
N2 - We demonstrate the construction of water-stable, biocompatible and self-standing hydrogels as scaffolds for the photosynthetic production of ethylene using a bioinspired all-polysaccharidic design combining TEMPO-oxidised cellulose nanofibers (TCNF) and a cereal plant hemicellulose called mixed-linkage glucan (MLG). We compared three different molecular weight MLGs from barley to increase the wet strength of TCNF hydrogels, and to reveal the mechanisms defining the favourable interactions between the scaffold components. The interactions between MLGs and TCNF were revealed via adsorption studies and interfacial rheology investigations using quartz crystal microbalance with dissipation monitoring (QCM-D). Our results show that both the MLG solution stability and adsorption behaviour did not exactly follow the well-known polymer adsorption and solubility theories especially in the presence of co-solute ions, in this case nitrates. We prepared hydrogel scaffolds for microalgal immobilisation, and high wet strength hydrogels were achieved with very low dosages of MLG (0.05 wt%) to the TCNF matrix. The all-polysaccharic biocatalytic architectures remained stable and produced ethylene for 120 h with yields comparable to the state-of-the-art scaffolds. Due to its natural origin and biodegradability, MLG offers a clear advantage in comparison to synthetic scaffold components, allowing the mechanical properties and water interactions to be tailored.
AB - We demonstrate the construction of water-stable, biocompatible and self-standing hydrogels as scaffolds for the photosynthetic production of ethylene using a bioinspired all-polysaccharidic design combining TEMPO-oxidised cellulose nanofibers (TCNF) and a cereal plant hemicellulose called mixed-linkage glucan (MLG). We compared three different molecular weight MLGs from barley to increase the wet strength of TCNF hydrogels, and to reveal the mechanisms defining the favourable interactions between the scaffold components. The interactions between MLGs and TCNF were revealed via adsorption studies and interfacial rheology investigations using quartz crystal microbalance with dissipation monitoring (QCM-D). Our results show that both the MLG solution stability and adsorption behaviour did not exactly follow the well-known polymer adsorption and solubility theories especially in the presence of co-solute ions, in this case nitrates. We prepared hydrogel scaffolds for microalgal immobilisation, and high wet strength hydrogels were achieved with very low dosages of MLG (0.05 wt%) to the TCNF matrix. The all-polysaccharic biocatalytic architectures remained stable and produced ethylene for 120 h with yields comparable to the state-of-the-art scaffolds. Due to its natural origin and biodegradability, MLG offers a clear advantage in comparison to synthetic scaffold components, allowing the mechanical properties and water interactions to be tailored.
UR - http://www.scopus.com/inward/record.url?scp=85171449448&partnerID=8YFLogxK
U2 - 10.1039/d3tb00919j
DO - 10.1039/d3tb00919j
M3 - Article
AN - SCOPUS:85171449448
SN - 2050-750X
VL - 11
SP - 8788
EP - 8803
JO - Journal of Materials Chemistry B
JF - Journal of Materials Chemistry B
IS - 36
ER -