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Wood hemicelluloses exert distinct biomechanical contributions to cellulose fibrillar networks

Berglund, Jennie (författare)
KTH,Fiber- och polymerteknologi,Wallenberg Wood Science Center
Mikkelsen, Deidre (författare)
Flanagan, Bernadine M. (författare)
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Dhital, Sushil (författare)
Gaunitz, Stefan (författare)
KTH,Fiber- och polymerteknologi,Wallenberg Wood Science Center
Henriksson, Gunnar (författare)
KTH,Fiber- och polymerteknologi,Wallenberg Wood Science Center
Lindström, Mikael, Professor, 1967- (författare)
KTH,Fiber- och polymerteknologi,Wallenberg Wood Science Center
Yakubov, Gleb E. (författare)
Gidley, Michael J. (författare)
Vilaplana, Francisco, 1979- (författare)
KTH,Glykovetenskap,Wallenberg Wood Science Center
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 (creator_code:org_t)
2020-09-17
2020
Engelska.
Ingår i: Nature Communications. - : Springer Nature. - 2041-1723. ; 11:1
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Hemicelluloses, a family of heterogeneous polysaccharides with complex molecular structures, constitute a fundamental component of lignocellulosic biomass. However, the contribution of each hemicellulose type to the mechanical properties of secondary plant cell walls remains elusive. Here we homogeneously incorporate different combinations of extracted and purified hemicelluloses (xylans and glucomannans) from softwood and hardwood species into self-assembled networks during cellulose biosynthesis in a bacterial model, without altering the morphology and the crystallinity of the cellulose bundles. These composite hydrogels can be therefore envisioned as models of secondary plant cell walls prior to lignification. The incorporated hemicelluloses exhibit both a rigid phase having close interactions with cellulose, together with a flexible phase contributing to the multiscale architecture of the bacterial cellulose hydrogels. The wood hemicelluloses exhibit distinct biomechanical contributions, with glucomannans increasing the elastic modulus in compression, and xylans contributing to a dramatic increase of the elongation at break under tension. These diverging effects cannot be explained solely from the nature of their direct interactions with cellulose, but can be related to the distinct molecular structure of wood xylans and mannans, the multiphase architecture of the hydrogels and the aggregative effects amongst hemicellulose-coated fibrils. Our study contributes to understanding the specific roles of wood xylans and glucomannans in the biomechanical integrity of secondary cell walls in tension and compression and has significance for the development of lignocellulosic materials with controlled assembly and tailored mechanical properties.

Ämnesord

NATURVETENSKAP  -- Biologi -- Biokemi och molekylärbiologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Biochemistry and Molecular Biology (hsv//eng)

Nyckelord

biomechanics
cellulose
mechanical property
network analysis
wood
Bacteria (microorganisms)
(1-6)-alpha-glucomannan
hemicellulose
laxative
mannan
plant extract
polysaccharide
xylan
carbohydrate analysis
cell wall
chemistry
conformation
cytoskeleton
hydrogel
plant
Carbohydrate Conformation
Carbohydrate Sequence
Cathartics
Hydrogels
Mannans
Plant Extracts
Plants
Polysaccharides
Xylans

Publikations- och innehållstyp

ref (ämneskategori)
art (ämneskategori)

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