2005
DOI: 10.1016/j.phytochem.2005.06.001
|View full text |Cite
|
Sign up to set email alerts
|

Conformation and mobility of the arabinan and galactan side-chains of pectin

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1

Citation Types

2
39
0

Year Published

2008
2008
2023
2023

Publication Types

Select...
4
3
2

Relationship

0
9

Authors

Journals

citations
Cited by 76 publications
(41 citation statements)
references
References 47 publications
2
39
0
Order By: Relevance
“…CP contains a backbone of partially methyl esterified a-(1e4) linked galacturonosyl residues with occasional rhamnose insertions to which may be attached neutral galactan and/or oligosaccharide side chains. The neutral sugar side chains (especially arabinan) have mobile properties in solution, which may limit the association of the main chain with polyphenols (Ha, Vi€ etor, Jardine, Apperley, & Jarvis, 2005). As a result, the presence of less sugar branches on the polysaccharide backbone could allow a linear structure to more easily bind/stack with polyphenols (Ha et al, 2005;Watrelot, Le Bourvellec, Imberty, & Renard, 2014).…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…CP contains a backbone of partially methyl esterified a-(1e4) linked galacturonosyl residues with occasional rhamnose insertions to which may be attached neutral galactan and/or oligosaccharide side chains. The neutral sugar side chains (especially arabinan) have mobile properties in solution, which may limit the association of the main chain with polyphenols (Ha, Vi€ etor, Jardine, Apperley, & Jarvis, 2005). As a result, the presence of less sugar branches on the polysaccharide backbone could allow a linear structure to more easily bind/stack with polyphenols (Ha et al, 2005;Watrelot, Le Bourvellec, Imberty, & Renard, 2014).…”
Section: Discussionmentioning
confidence: 99%
“…The neutral sugar side chains (especially arabinan) have mobile properties in solution, which may limit the association of the main chain with polyphenols (Ha, Vi€ etor, Jardine, Apperley, & Jarvis, 2005). As a result, the presence of less sugar branches on the polysaccharide backbone could allow a linear structure to more easily bind/stack with polyphenols (Ha et al, 2005;Watrelot, Le Bourvellec, Imberty, & Renard, 2014). Therefore, OBG is proposed to more likely bind with tea polyphenols than WAX (which contains only monosaccharide branches), which in turn is more likely to bind than CP (which contains longer branches and a charged backbone both of which would limit binding), and thus showed the largest reducing effect on the binding of tea polyphenols with PPA due to the competitive mechanism.…”
Section: Discussionmentioning
confidence: 99%
“…The specific function of b-1,4-galactan in primary walls is poorly understood. b-1,4-Galactan has been implicated in cell elongation (McCartney et al, 2003) and has been demonstrated to be a water retaining viscoelastic component with a likely role in modulating the mechanical properties of cell walls (Tang et al, 1999;McCartney et al, 2000;Ha et al, 2005). However, potato tubers with reduced galactan content did not show any growth or developmental phenotype (Oxenboll Sørensen et al, 2000;Martín et al, 2005;Ulvskov et al, 2005), although the galactan deficient potato tubers were found to be slightly more brittle, indicating that galactan may play a role in transmitting stresses to cellulose microfibrils (Ulvskov et al, 2005).…”
Section: Introductionmentioning
confidence: 99%
“…The water binding properties of the galacturonic acid residues indicate that polymers containing these groups have the capacity to hydrate and swell and so possibly help maintain polymer separation in the wall. 5 The side chains of RGI include arabinan and galactan polymers which have been shown to be highly mobile 6,7,8 with the potential to interact with each other forming a temporally entangled matrix. 9 It is also believed that arabinan chains, which have been shown to contain ferulate residues attached to terminal arabinose groups, are able to oxidatively cross-link via the formation of diferulate bridges between arabinan chains that originate on separate RGI polysaccharides.…”
mentioning
confidence: 99%