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Sulfated steroids of Halichondriidae family sponges – Natural inhibitors of polysaccharide-degrading enzymes of bacterium Formosa algae, inhabiting brown alga Fucus evanescens
Inhibiting effects of sulfated steroids from marine sponges of Halichondriidae family: halistanol sulfate, topsentiasterol sulfate D and chlorotopsentiasterol sulfate D were investigated on three different types of enzymes degrading polysaccharides of brown algae: endo-1,3-β-d-glucanase GFA, fucoida...
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Published in: | Carbohydrate research 2019-10, Vol.484, p.107776-107776, Article 107776 |
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Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
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Online Access: | Get full text |
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Summary: | Inhibiting effects of sulfated steroids from marine sponges of Halichondriidae family: halistanol sulfate, topsentiasterol sulfate D and chlorotopsentiasterol sulfate D were investigated on three different types of enzymes degrading polysaccharides of brown algae: endo-1,3-β-d-glucanase GFA, fucoidan hydrolase FFA2 and bifunctional alginate lyase ALFA3 from marine bacterium Formosa algae KMM 3553T, inhabiting thalli of brown alga Fucus evanescens. This is the first research, devoted to influence of a marine natural compound on three functionally related enzymes that make up the complex of enzymes, necessary to degrade unique carbohydrate components of brown algae. Alginic acid, 1,3-β-D-glucan (laminaran) and fucoidan jointly constitute practically all carbohydrate biomass of brown algae, so enzymes, able to degrade such polysaccharides, are crucial for digesting brown algae biomass as well as for organisms surviving and proliferating on brown algae thalli. Halistanol sulfate irreversibly inhibited native endo-1,3-β-D-glucanases of marine mollusks, but reversibly competitively inhibited recombinant endo-1,3-β-d-glucanase GFA. This fact indicates that there are significant structural differences between the enzymes of practically the same specificity. For alginate lyase and fucoidan hydrolase halistanol sulfate was irreversible inhibitor. Topsentiasterol sulfate D was less active inhibitor whereas chlorotopsentiasterol sulfate D was the strongest inhibitor of enzymes under the study. Chlorotopsentiasterol sulfate D caused 98% irreversible inhibition of GFA. Chlorotopsentiasterol sulfate D also caused reversible and 100% inhibition of ALFA3, which is unusual for reversible inhibitors. Inhibition of FFA2 was complete and irreversible in all cases.
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•Three sulfated steroids inhibited activity of three different recombinant enzymes.•Endo-1,3-β-d-glucanase, fucoidanase and alginate lyase from bacterium Formosa algae.•Halistanol sulfate completely inhibited endo-1,3-β-D-glucanases of mollusks.•Halistanol sulfate reversibly inhibited bacterial endo-1,3-β-d-glucanase.•Fucoidanase was completely and irreversibly inhibited by all sulfated steroids. |
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ISSN: | 0008-6215 1873-426X |
DOI: | 10.1016/j.carres.2019.107776 |