2013
DOI: 10.1016/j.carres.2012.12.003
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A heteroglycan from the mycelia of Pleurotus ostreatus: structure determination and study of antioxidant properties

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Cited by 50 publications
(10 citation statements)
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“…Interestingly, the carbohydrate composition of the exopolysaccharide resembles the carbohydrate compositions in other fungal systems (other heteroglycans), which are known about their immunostimulatory activity and antioxidant properties [13,14]. Thus, research focused on exopolysaccharide from G. lucidum and all aspects of the immune system is certainly promising and should guide future studies.…”
Section: Resultsmentioning
confidence: 97%
“…Interestingly, the carbohydrate composition of the exopolysaccharide resembles the carbohydrate compositions in other fungal systems (other heteroglycans), which are known about their immunostimulatory activity and antioxidant properties [13,14]. Thus, research focused on exopolysaccharide from G. lucidum and all aspects of the immune system is certainly promising and should guide future studies.…”
Section: Resultsmentioning
confidence: 97%
“…[30] A heteroglycan of Pleurotus ostreatus showed EC 50 value of 553 μg/ml. [31] Some transition metals, e.g., Fe 2+ , Cu + , Pb 2+ and Co 2+ , can trigger process of free radical reaction such as hydroxyl radical formation. [29] At 0.05-0.5 mg/ml, the chelating ability of Floridan was between 8.82% and 54.3%.…”
Section: Discussionmentioning
confidence: 99%
“…74, 4.93, 5.08, 5.15, 5.19, and 5.26 ppm, respectively. Therefore, the H-1/C-1 signal at 4.74/103.0 ppm indicated that the residues should be assigned to (1 → 3)-linked ␤-d-mannopyranosyl (Patra et al, 2013;Prestegard, Miner, & Tyrell, 1983). However, the anomeric chemical shifts of H-1/C-1 at 5.08/104.6, 5.15/104.8, and 5.19/96.6 ppm should be assigned to (1 → 3)-linked ␣-d-mannopyranose residues (Cui, 2005;Ližičárová, Matulová, Machová, & Capek, 2007;Takahashi, Kudoh, Okawa, & Shibata, 2012).…”
Section: Mannosyl Residuementioning
confidence: 99%
“…However, the anomeric chemical shifts of H-1/C-1 at 5.08/104.6, 5.15/104.8, and 5.19/96.6 ppm should be assigned to (1 → 3)-linked ␣-d-mannopyranose residues (Cui, 2005;Ližičárová, Matulová, Machová, & Capek, 2007;Takahashi, Kudoh, Okawa, & Shibata, 2012). The signal of anomeric chemical shift of H-1/C-1 at 4.93/102.1 ppm corresponded to (1 → 3,6)-linked ␣-d-mannopyranose residues (Liu et al, 2013;Patra et al, 2013). The H-6/H-6 signals at 3.83/3.97 and 3.87/3.99 ppm indicated that the residues could be assigned to (1 → 6)-linked ␣-d-mannopyranose residues (Yan et al, 2014).…”
Section: Mannosyl Residuementioning
confidence: 99%