ArticlePlanta2010
Immunolocalization of beta-1-4-galactan and its relationship with lignin distribution in developing compression wood of Cryptomeria japonica.
Article in Planta, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.
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Who cites it
13 citing papers in PubMed, 25 citations in OpenAlex.
- Temporal and spatial distribution of pectin, β(1-4)-galactan, xylan and lignin during differentiation of living fibres in young shoots of Leucaena leucocephala (Lam.) de wit.BMC plant biology · 2025Article
- Article
- Xylem Parenchyma-Role and Relevance in Wood Functioning in Trees.Plants (Basel, Switzerland) · 2021Review
- Localised laccase activity modulates distribution of lignin polymers in gymnosperm compression wood.The New phytologist · 2021Article
- Structural organization of the cell wall polymers in compression wood as revealed by FTIR microspectroscopy.Planta · 2019Article
- The cell biology of secondary cell wall biosynthesis.Annals of botany · 2018Review
- Plant Fibre: Molecular Structure and Biomechanical Properties, of a Complex Living Material, Influencing Its Deconstruction towards a Biobased Composite.Materials (Basel, Switzerland) · 2016Review
- Quantification of (1→4)-β-d-Galactans in Compression Wood Using an Immuno-Dot Assay.Plants (Basel, Switzerland) · 2015Article
- Article
- Distribution of tension wood like gelatinous fibres in the roots of Acacia nilotica (Lam.) Willd.Planta · 2014Article
- Article
- Localization of cell wall polysaccharides in normal and compression wood of radiata pine: relationships with lignification and microfibril orientation.Plant physiology · 2012Article
- Article
Corrections and comments
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Authors and funding
4 authors at 2 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Compression wood (CW) contains higher quantities of beta-1-4-galactan than does normal wood (NW). However, the physiological roles and ultrastructural distribution of beta-1-4-galactan during CW formation are still not well understood. The present work investigated deposition of beta-1-4-galactan in differentiating tracheids of Cryptomeria japonica during CW formation using an immunological probe (LM5) combined with immunomicroscopy. Our immunolabeling studies clearly showed that differences in the distribution of beta-1-4-galactan between NW (and opposite wood, OW) and CW are initiated during the formation of the S(1) layer. At this stage, CW was strongly labeled in the S(1) layer, whereas no label was observed in the S(1) layer of NW and OW. Immunogold labeling showed that beta-1-4-galactan in the S(1) layer of CW tracheids significantly decreased during the formation of the S(2) layer. Most beta-1-4-galactan labeling was present in the outer S(2) region in mature CW tracheids, and was absent in the inner S(2) layer that contained helical cavities in the cell wall. In addition, delignified CW tracheids showed significantly more labeling of beta-1-4-galactan in the secondary cell wall, suggesting that lignin is likely to mask beta-1-4-galactan epitopes. The study clearly showed that beta-1-4-galactan in CW was mainly deposited in the outer portion of the secondary cell wall, indicating that its distribution may be spatially consistent with lignin distribution in CW tracheids of Cryptomeria japonica.
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