Characterization and immunomodulatory effects of glucans from Pleurotus albidus, a promising species of mushroom for farming and biomass production

International Journal of Biological Macromolecules

Volumn 95, Issue , 2017, Pages 215-223

  Castro Alves, Victor Costa ^a   Gomes, Daniel ^b   Menolli, Nelson ^c,d   Sforça, Maurício Luís ^e   Nascimento, João Roberto Oliveira do ^a,f  

^a UNIVERSITY OF SÃO PAULO   (Brazil)

^b AGÊNCIA PAULISTA DE TECNOLOGIA DOS AGRONEGÓCIOS   (Brazil)

^c INSTITUTO FEDERAL DE EDUCAÇÃO   (Brazil)

^d Instituto de Pesquisas Ambientais do Estado de São Paulo   (Brazil)

^e BRAZILIAN CENTER FOR RESEARCH IN ENERGY AND MATERIALS CNPEM   (Brazil)

^f Food Research Center (FoRC)   (Brazil)

Author keywords

Immunomodulation; Pleurotus albidus; Polysaccharides

Indexed keywords

GLUCAN; HOT WATER; INTERLEUKIN 6; NITRIC OXIDE; POLYSACCHARIDE; TUMOR NECROSIS FACTOR; IMMUNOLOGIC FACTOR;

AGRICULTURAL PROCEDURES; ANIMAL CELL; ARTICLE; BIOMASS PRODUCTION; CELL VIABILITY; CHEMICAL COMPOSITION; CHEMICAL STRUCTURE; CONTROLLED STUDY; CYTOKINE PRODUCTION; CYTOKINE RELEASE; FUNGUS CULTURE; IMMUNOMODULATION; MACROPHAGE; MOLECULAR WEIGHT; NONHUMAN; NUCLEAR MAGNETIC RESONANCE; PHAGOCYTOSIS; PLEUROTUS; PLEUROTUS ALBIDUS; AGRICULTURE; ANIMAL; BIOMASS; CHEMISTRY; DRUG EFFECTS; GROWTH, DEVELOPMENT AND AGING; IMMUNOLOGY; METABOLISM; MOUSE; RAW 264.7 CELL LINE; SECRETION (PROCESS);

AGRICULTURE; ANIMALS; BIOMASS; GLUCANS; IMMUNOLOGIC FACTORS; MACROPHAGES; MICE; NITRIC OXIDE; PLEUROTUS; RAW 264.7 CELLS; TUMOR NECROSIS FACTOR-ALPHA;

EID: 84996920940     PISSN: 01418130     EISSN: 18790003     Source Type: Journal    
DOI: 10.1016/j.ijbiomac.2016.11.059     Document Type: Article

References (43)

1. [1] Giavasis, I., Bioactive fungal polysaccharides as potential functional ingredients in food and nutraceuticals. Curr. Opin. Biotechnol. 26 (2014), 162–173, 10.1016/j.copbio.2014.01.010.
2. [2] Ferreira, S.S., Passos, C.P., Madureira, P., Vilanova, M., Coimbra, M.A., Structure-function relationships of immunostimulatory polysaccharides: a review. Carbohydr. Polym. 132 (2015), 378–396, 10.1016/j.carbpol.2015.05.079.
3. [3] Corrêa, R.C.G., Brugnari, T., Bracht, A., Peralta, R.M., Ferreira, I.C.F.R., Biotechnological, nutritional and therapeutic uses of Pleurotus spp. (Oyster mushroom) related with its chemical composition: a review on the past decade findings. Trends Food Sci. Technol. 50 (2016), 103–117, 10.1016/j.tifs.2016.01.012.
4. [4] Lechner, B.E., Albertó, E., Search for new naturally occurring strains of Pleurotus to improve yields: Pleurotus albidus as a novel proposed species for mushroom production. Rev. Iberoam. Micol. 28 (2011), 148–154, 10.1016/j.riam.2010.12.001.
5. [5] Gambato, G., Todescato, K., Pavão, E.M., Scortegagna, A., Fontana, R.C., Salvador, M., Camassola, M., Evaluation of productivity and antioxidant profile of solid-state cultivated macrofungi Pleurotus albidus and Pycnoporus sanguineus. Bioresour. Technol. 207 (2016), 46–51, 10.1016/j.biortech.2016.01.121.
6. [6] Sartori, S.B., Ferreira, L.F.R., Messias, T.G., Souza, G., Pompeu, G.B., Monteiro, R.T.R., Pleurotus biomass production on vinasse and its potential use for aquaculture feed. Mycology 6 (2015), 28–34, 10.1080/21501203.2014.988769.
7. [7] Lechner, B.E., Wright, J.E., Albertó, E., The genus Pleurotus in Argentina. Mycologia 96 (2004), 845–858, 10.2307/3762117.
8. [8] Justo, A., Vizzini, A., Minnis, A.M., Menolli, N., Capelari, M., Rodríguez, O., Malysheva, E., Contu, M., Ghignone, S., Hibbett, D.S., Phylogeny of the Pluteaceae (Agaricales, Basidiomycota): taxonomy and character evolution. Fungal Biol. 115 (2011), 1–20, 10.1016/j.funbio.2010.09.012.
9. [9] White, T., Burns, T., Lee, S., Taylor, J., Amplification and direct sequencing of fungal ribosomal RNA genes for phylogenetics. Innis, M., Gelfand, D., Sninsky, J., White, T., (eds.) PCR Protoc. A Guid. to Methods Appl., 1990, Academic Press, San Diego, 315–322.
10. [10] Gardes, M., Bruns, T., ITS primers with enhanced specificity for basidiomycetes: application to the identification of mycorrhizae and rusts. Mol. Ecol. 2 (1993), 113–118.
11. [11] Menolli, N., Breternitz, B.S., Capelari, M., The genus Pleurotus in Brazil: a molecular and taxonomic overview. Mycoscience 55 (2014), 378–389, 10.1016/j.myc.2013.12.001.
12. [12] Stamatakis, A., Hoover, P., Rougemont, J., A rapid bootstrap algorithm for the RAxML web servers. Syst. Biol. 57 (2008), 758–771, 10.1080/10635150802429642.
13. [13] Yang, B.K., Jeong, S.C., Song, C.H., Hypolipidemic effect of exo- and endo-biopolymers produced from submerged mycelial culture of Ganoderma lucidum in rats. J. Microbiol. Biotechnol. 12 (2002), 872–877.
14. [14] Palacios, I., García-Lafuente, A., Guillamón, E., Villares, A., Novel isolation of water-soluble polysaccharides from the fruiting bodies of Pleurotus ostreatus mushrooms. Carbohydr. Res. 358 (2012), 72–77, 10.1016/j.carres.2012.06.016.
15. [15] Castro-Alves, V.C., Nascimento, J.R.O., Speeding up the extraction of mushroom polysaccharides. Food Anal. Methods, 2016, 10.1007/s12161-016-0406-9.
16. [16] Shiga, T.M., Fabi, J.P., do Nascimento, J.R.O., Petkowicz, C.L.D.O., Vriesmann, L.C., Lajolo, F.M., Cordenunsi, B.R., Changes in cell wall composition associated to the softening of ripening papaya: evidence of extensive solubilization of large molecular mass galactouronides. J. Agric. Food Chem. 57 (2009), 7064–7071, 10.1021/jf900073b.
17. [17] Castro-Alves, V.C., Sansone, M., Sansone, A.B., Nascimento, J.R.O., Polysaccharides from raw and cooked chayote modulate macrophage function. Food Res. Int. 81 (2016), 171–179, 10.1016/j.foodres.2016.01.017.
18. [18] Maxwell, E., Hotchkiss, A.T., Morris, V.J., Belshaw, N.J., Rhamnogalacturonan I containing homogalacturonan inhibits colon cancer cell proliferation by decreasing ICAM1 expression. Carbohydr. Polym. 132 (2015), 546–553, 10.13140/RG.2.1.3768.1769.
19. [19] Delaglio, F., Grzesiek, S., Vuister, G.W., Zhu, G., Pfeifer, J., Bax, A., NMRPipe: a multidimensional spectral processing system based on UNIX pipes. J. Biomol. NMR 6 (1995), 277–293, 10.1007/BF00197809.
20. [20] Fuentes, A.L., Millis, L., Vapenik, J., Sigola, L., Lipopolysaccharide-mediated enhancement of zymosan phagocytosis by RAW 264.7 macrophages is independent of opsonins, laminarin, mannan, and complement receptor 3. J. Surg. Res. 189 (2014), 304–312, 10.1016/j.jss.2014.03.024.
21. [21] Sun, L., Feng, K., Jiang, R., Chen, J., Zhao, Y., Ma, R., Tong, H., Water-soluble polysaccharide from Bupleurum chinense DC: isolation, structural features and antioxidant activity. Carbohydr. Polym. 79 (2010), 180–183, 10.1016/j.carbpol.2009.07.044.
22. [22] Synytsya, A., Novak, M., Structural analysis of glucans. Ann. Transl. Med., 2, 2014, 17, 10.3978/j.issn. 2305-5839.2014.02.07 1–1.
23. [23] Iorio, E., Torosantucci, A., Bromuro, C., Chiani, P., Ferretti, A., Giannini, M., Cassone, A., Podo, F., Candida albicans cell wall comprises a branched β-d-(1, 6)-glucan with β-d-(1, 3)-side chains. Carbohydr. Res. 343 (2008), 1050–1061, 10.1016/j.carres.2008.02.020.
24. [24] Suabjakyong, P., Nishimura, K., Toida, T., Van Griensven, L.J.L.D., Function Structural characterization and immunomodulatory effects of polysaccharides from Phellinus linteus and Phellinus igniarius on the IL-6/IL-10 cytokine balance of the mouse macrophage cell lines (RAW264.7). Food Funct. 6 (2015), 2834–2844, 10.1039/c5fo00491h.
25. [25] Tada, R., Harada, T., Nagi-Miura, N., Adachi, Y., Nakajima, M., Yadomae, T., Ohno, N., NMR characterization of the structure of a β-(1, 3)-D-glucan isolate from cultured fruit bodies of Sparassis crispa. Carbohydr. Res. 342 (2007), 2611–2618, 10.1016/j.carres.2007.08.016.
26. [26] Amari, M., Arango, L.F.G., Gabriel, V., Robert, H., Morel, S., Moulis, C., Gabriel, B., Remaud-Siméon, M., Fontagné-Faucher, C., Characterization of a novel dextransucrase from Weissella confusa isolated from sourdough. Appl. Microbiol. Biotechnol. 97 (2013), 5413–5422, 10.1007/s00253-012-4447-8.
27. [27] Bounaix, M.S., Gabriel, V., Morel, S., Robert, H., Rabier, P., Remaud-Siméon, M., Gabriel, B., Fontagné-Faucher, C., Biodiversity of exopolysaccharides produced from sucrose by sourdough lactic acid bacteria. J. Agric. Food Chem. 57 (2009), 10889–10897, 10.1021/jf902068t.
28. [28] Cheetham, N.W.H., Fiala-beer, E., Walker, G.J., Dextran structural details from high-field proton NMR spectroscopy. Carbohydr. Polym. 14 (1991), 149–158.
29. [29] van Leeuwen, S.S., Kralj, S., Gerwig, G.J., Dijkhuizen, L., Kamerling, J.P., Structural analysis of bioengineering α-D-Glucan produced by a triple mutant of the glucansucrase GTF180 enzyme from Lactobacillus reuteri strain 180: Generation of (α1, 4) linkages in a native (1, 3)(1, 6)-α-D-Glucan. Biomacromolecules 9 (2008), 2251–2258, 10.1021/bm800410w.
30. [30] Cheng, H.N., Neiss, T.G., Solution NMR spectroscopy of food polysaccharides. Polym. Rev. 52 (2012), 81–114, 10.1080/15583724.2012.668154.
31. [31] Dertli, E., Colquhoun, I.J., Gunning, A.P., Bongaerts, R.J., Le Gall, G., Bonev, B.B., Mayer, M.J., Narbad, A., Structure and biosynthesis of two exopolysaccharides produced by lactobacillus johnsonii FI9785. J. Biol. Chem. 288 (2013), 31938–31951, 10.1074/jbc.M113.507418.
32. [32] Maina, N.H., Tenkanen, M., Maaheimo, H., Juvonen, R., Virkki, L., NMR spectroscopic analysis of exopolysaccharides produced by Leuconostoc citreum and Weissella confusa. Carbohydr. Res. 343 (2008), 1446–1455, 10.1016/j.carres.2008.04.012.
33. [33] Seymour, F.R., Bishop, S.H., Correlation of the structure of dextrans to their H-NMR spectra. Carbohydr. Res. 74 (1979), 77–92.
34. [34] Souza Kirsch, L., de Macedo, A.J.P., Teixeira, M.F.S., Production of mycelial biomass by the Amazonian edible mushroom Pleurotus albidus. Braz. J. Microbiol. 47 (2016), 658–664, 10.1016/j.bjm.2016.04.007.
35. [35] Zhang, M., Cui, S.W., Cheung, P.C.K., Wang, Q., Antitumor polysaccharides from mushrooms: a review on their isolation process, structural characteristics and antitumor activity. Trends Food Sci. Technol. 18 (2007), 4–19, 10.1016/j.tifs.2006.07.013.
36. [36] Slaven, Z., Adelle, F., Alessandra, R., Corrado, F., Massimo, R., Medicinal mushrooms., 1st ed. Ray, R., Ward, O., (eds.) Microb. Technol. Hortic., vol. 3, 2008, CRC, Press, Boca Ratón, FL, USA p. 390.
37. [37] Pramanik, M., Chakraborty, I., Mondal, S., Islam, S.S., Structural analysis of a water-soluble glucan (Fr.I) of an edible mushroom, Pleurotus sajor-caju. Carbohydr. Res. 342 (2007), 2670–2675, 10.1016/j.carres.2007.08.012.
38. [38] Ruthes, A.C., Smiderle, F.R., Iacomini, M., D-Glucans from edible mushrooms: a review on the extraction, purification and chemical characterization approaches. Carbohydr. Polym. 117 (2015), 753–761, 10.1016/j.carbpol.2014.10.051.
39. [39] Duque, G.A., Descoteaux, A., Macrophage cytokines: involvement in immunity and infectious diseases. Front. Immunol. 5 (2014), 1–12, 10.3389/fimmu.2014.00491.
40. [40] Lee, J.Y., Kim, Y.J., Kim, H.J., Kim, Y.S., Park, W., Immunostimulatory effect of laminarin on RAW 264.7 mouse macrophages. Molecules 17 (2012), 5404–5411, 10.3390/molecules17055404.
41. [41] Bittencourt, V.C.B., Figueiredo, R.T., Da Silva, R.B., Mourão-Sá, D.S., Fernandez, P.L., Sassaki, G.L., Mulloy, B., Bozza, M.T., Barreto-Bergter, E., An α-glucan of Pseudallescheria boydii is involved in fungal phagocytosis and toll-like receptor activation. J. Biol. Chem. 281 (2006), 22614–22623, 10.1074/jbc.M511417200.
42. [42] Palencia, D., Werning, M.L., Sierra-filardi, E., Duen, M.T., Irastorza, A., oCorbı, A.L., Lo, P., Probiotic properties of the 2-substituted (1, 3)-β-D-glucan-producing bacterium pediococcus parvulus. Appl. Environ. Microbiol. 75 (2009), 4887–4891, 10.1128/AEM.00394-09.
43. [43] Tang, C., Kamiya, T., Liu, Y., Kadoki, M., Kakuta, S., Oshima, K., Hattor, M., Takeshita, K., Kanai, T., Saijo, S., Ohno, N., Iwakura, Y., Inhibition of dectin-1 signaling ameliorates colitis by inducing Lactobacillus-mediated regulatory T cell expansion in the intestine. Cell Host Microbe 18 (2015), 183–197.