Search engine for discovering works of Art, research articles, and books related to Art and Culture
ShareThis
Javascript must be enabled to continue!

Distributional variation of lignin and non-cellulosic polysaccharide epitopes in different pit membranes of Scots pine and Norway spruce seedlings

View through CrossRef
Microdistribution of non-cellulosic polysaccharides in pit membranes of bordered pits (intertracheid pits between adjacent tracheids), cross-field pits (half bordered pits between tracheids and ray parenchyma cells) and ray pits (simple pits in nodular end walls of ray parenchyma cells) was investigated in mature earlywood of juvenile Scots pine and Norway spruce seedlings using immunocytochemistry combined with monoclonal antibodies specific to (1→4)-β-galactan (LM5), (1→5)-α-arabinan (LM6), homogalacturonan (HG, LM19, LM20), xyloglucan (LM15), xylan (LM10, LM11) and mannan (LM21, LM22) epitopes. Using phloroglucinol-HCl and KMnO4 staining, lignin distribution in pit membranes was also examined. Apart from cross-field pit membranes in Scots pine, all pit membranes observed showed a positive reaction for lignin with differences in staining intensity. Ray pit membranes showed strongest reaction with lignin staining in both species. Intensity of lignin staining in bordered pit membranes was stronger in Norway spruce than in Scots pine. With localization of non-cellulosic polysaccharide epitopes, Scots pine showed differences in cross-field pit membranes (rhamnogalacturonan-I (RG-I), HG and xyloglucan epitopes) from bordered and ray pit membranes (RG-I and HG epitopes). In contrast, Norway spruce showed significant differences in ray pit membranes (RG-I, HG, xyloglucan, xylan and mannan epitopes) from bordered and cross-field pit membranes (HG and no/trace amount of RG-I epitopes). Distributional differences in HG epitopes depending on antibody type/ membrane regions were also observed in cross-field pit membranes between the two species. Together, the results suggest that distribution patterns of lignin and non-cellulosic polysaccharides in pit membranes differ significantly between pit types and between Scots pine and Norway spruce. Compared with the same types of pit membranes in hardwoods, the results for Scots pine and Norway spruce (softwoods) differed significantly.
Title: Distributional variation of lignin and non-cellulosic polysaccharide epitopes in different pit membranes of Scots pine and Norway spruce seedlings
Description:
Microdistribution of non-cellulosic polysaccharides in pit membranes of bordered pits (intertracheid pits between adjacent tracheids), cross-field pits (half bordered pits between tracheids and ray parenchyma cells) and ray pits (simple pits in nodular end walls of ray parenchyma cells) was investigated in mature earlywood of juvenile Scots pine and Norway spruce seedlings using immunocytochemistry combined with monoclonal antibodies specific to (1→4)-β-galactan (LM5), (1→5)-α-arabinan (LM6), homogalacturonan (HG, LM19, LM20), xyloglucan (LM15), xylan (LM10, LM11) and mannan (LM21, LM22) epitopes.
Using phloroglucinol-HCl and KMnO4 staining, lignin distribution in pit membranes was also examined.
Apart from cross-field pit membranes in Scots pine, all pit membranes observed showed a positive reaction for lignin with differences in staining intensity.
Ray pit membranes showed strongest reaction with lignin staining in both species.
Intensity of lignin staining in bordered pit membranes was stronger in Norway spruce than in Scots pine.
With localization of non-cellulosic polysaccharide epitopes, Scots pine showed differences in cross-field pit membranes (rhamnogalacturonan-I (RG-I), HG and xyloglucan epitopes) from bordered and ray pit membranes (RG-I and HG epitopes).
In contrast, Norway spruce showed significant differences in ray pit membranes (RG-I, HG, xyloglucan, xylan and mannan epitopes) from bordered and cross-field pit membranes (HG and no/trace amount of RG-I epitopes).
Distributional differences in HG epitopes depending on antibody type/ membrane regions were also observed in cross-field pit membranes between the two species.
Together, the results suggest that distribution patterns of lignin and non-cellulosic polysaccharides in pit membranes differ significantly between pit types and between Scots pine and Norway spruce.
Compared with the same types of pit membranes in hardwoods, the results for Scots pine and Norway spruce (softwoods) differed significantly.

Related Results

Cationic Lignin Polymers as Flocculant for Municipal Wastewater
Cationic Lignin Polymers as Flocculant for Municipal Wastewater
The radical polymerization of acid-washed and unwashed softwood kraft lignin with [2-(methacryloyloxy) ethyl] trimethylammonium chloride (METAC) was attempted to investigate the pr...
Productivity of seedlings of Scots pine on alluvial sands of natural and man-made origin
Productivity of seedlings of Scots pine on alluvial sands of natural and man-made origin
Purpose. To find out quantitative physical and water indicators for which there are significant changes in forest vegetation properties in alluvial sands, as well as to trace their...
Forest Edge Effects on Seedlings in Mixed Oriental Beech (Fagus orientalis Lipsky) - Scots Pine (Pinus sylvestris L.) Stands
Forest Edge Effects on Seedlings in Mixed Oriental Beech (Fagus orientalis Lipsky) - Scots Pine (Pinus sylvestris L.) Stands
Forest edges created by silvicultural treatment influence micro-climatic conditions and available light in forest stands. Studies regarding the impacts of forest edges on regenerat...
Pit-1 Gene Expression in Human Pituitary Adenomas
Pit-1 Gene Expression in Human Pituitary Adenomas
The anterior pituitary-specific transcription factor Pit-1 (also known as GHF-1) was initially identified and cloned as a transactivator of the GH and PRL genes, and later as a reg...
Morphometry of an hexagonal pit crater in Pavonis Mons, Mars
Morphometry of an hexagonal pit crater in Pavonis Mons, Mars
<p><strong>Introduction:</strong></p> <p>Pit craters are peculiar depressions found in almost every terrestria...
Tamarind seed polysaccharide isolation from tamarind kernel powder by protease enzyme and high-intensity ultrasound
Tamarind seed polysaccharide isolation from tamarind kernel powder by protease enzyme and high-intensity ultrasound
Tamarind seed polysaccharide, xyloglucan (XG), is obtained from Tamarind Kernel Powder (TKP). In food industry, XG is widely used as a thickener, stabilizer, fat replacer, or starc...

Back to Top