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Structural characteristics and biological effects of exopolysaccharide produced by cyanobacterium Nostoc sp

I. Uhliariková, M. Šutovská, J. Barboríková, M. Molitorisová, HJ. Kim, YI. Park, M. Matulová, J. Lukavský, Z. Hromadková, P. Capek

. 2020 ; 160 (-) : 364-371. [pub] 20200519

Language English Country Netherlands

Document type Journal Article

Complex structure of cyanobacterium Nostoc sp. exopolysaccharide (EPS), with apparent molecular weight 214 × 103 g/mol, can be deduced from its composition. Chemical and NMR analyses found four dominant sugar monomers, namely (1 → 4)-linked α-l-arabinopyranose, β-d-glucopyranose, β-d-xylopyranose and (1 → 3)-linked β-d-mannopyranose, two different uronic acids and a lactyl group, with (1 → 4,6)-linked β-d-glucopyranose as the only branch point suggest a complex structure of this polymer. The dominant uronic acid is α-linked, but it remained unidentified. β-d-Glucuronic acid was present in lower amount. Their position as well as that of lactyl remained undetermined too. Different doses of orally administered EPS in guinea pigs evoked a significant decrease in cough effort and a decrease in airway reactivity. The antitussive efficacy and bronchodilator effect of higher doses of EPS were found to be similar to that of the antitussive drug codeine and the antiasthmatic salbutamol. Without significant cytotoxicity on the RAW 264.7 cells, EPS stimulated the macrophage cells to produce pro-inflammatory cytokines tumor necrosis factor-α (TNF-α) and interleukin-6 (IL-6), and prostaglandins (PGs) and nitric oxide (NO) via induction of COX-2 and iNOS expression, respectively, suggesting that this biopolymer potentiates an early innate immune response and can therefore be used as a new immune modulator.

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$a Complex structure of cyanobacterium Nostoc sp. exopolysaccharide (EPS), with apparent molecular weight 214 × 103 g/mol, can be deduced from its composition. Chemical and NMR analyses found four dominant sugar monomers, namely (1 → 4)-linked α-l-arabinopyranose, β-d-glucopyranose, β-d-xylopyranose and (1 → 3)-linked β-d-mannopyranose, two different uronic acids and a lactyl group, with (1 → 4,6)-linked β-d-glucopyranose as the only branch point suggest a complex structure of this polymer. The dominant uronic acid is α-linked, but it remained unidentified. β-d-Glucuronic acid was present in lower amount. Their position as well as that of lactyl remained undetermined too. Different doses of orally administered EPS in guinea pigs evoked a significant decrease in cough effort and a decrease in airway reactivity. The antitussive efficacy and bronchodilator effect of higher doses of EPS were found to be similar to that of the antitussive drug codeine and the antiasthmatic salbutamol. Without significant cytotoxicity on the RAW 264.7 cells, EPS stimulated the macrophage cells to produce pro-inflammatory cytokines tumor necrosis factor-α (TNF-α) and interleukin-6 (IL-6), and prostaglandins (PGs) and nitric oxide (NO) via induction of COX-2 and iNOS expression, respectively, suggesting that this biopolymer potentiates an early innate immune response and can therefore be used as a new immune modulator.
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$a Šutovská, Martina $u Comenius University in Bratislava, Jessenius Faculty of Medicine in Martin, Department of Pharmacology, Mala Hora 11161/4B, 03601 Martin, Slovakia. Electronic address: martina.sutovska@uniba.sk
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$a Barboríková, Jana $u Comenius University in Bratislava, Jessenius Faculty of Medicine in Martin, Department of Pharmacology, Mala Hora 11161/4B, 03601 Martin, Slovakia
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$a Molitorisová, Miroslava $u Comenius University in Bratislava, Jessenius Faculty of Medicine in Martin, Department of Pharmacology, Mala Hora 11161/4B, 03601 Martin, Slovakia
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$a Kim, Hee Jin $u Department of Biotechnology, The Catholic University of Korea, Bucheon, Gyeonggi-do 14662, Republic of Korea
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$a Park, Yong Il $u Department of Biotechnology, The Catholic University of Korea, Bucheon, Gyeonggi-do 14662, Republic of Korea
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$a Matulová, Mária $u Institute of Chemistry, Center for Glycomics, Slovak Academy of Sciences, Dúbravská cesta 9, 84538 Bratislava, Slovakia
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$a Lukavský, Jaromír $u Institute of Botany, Centre for Algology, Academy of Sciences of the Czech Republic, Dukelská 135, 37901 Třeboň, Czech Republic
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$a Hromadková, Zdenka $u Institute of Chemistry, Center for Glycomics, Slovak Academy of Sciences, Dúbravská cesta 9, 84538 Bratislava, Slovakia
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$a Capek, Peter $u Institute of Chemistry, Center for Glycomics, Slovak Academy of Sciences, Dúbravská cesta 9, 84538 Bratislava, Slovakia. Electronic address: chemcape@savba.sk
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