β-(1→6)-D-glucan secreted during the optimised production of exopolysaccharides by Paecilomyces variotii has immunostimulatory activity.

Erica F Osaku, Rafael A Menolli, Claudia R L de M Costa, Fernando Henrique G Tessaro, Renan H de Melo, Alex E do Amaral, Péricles A D Duarte, Arquimedes Paixão de Santana Filho, Andrea Caroline Ruthes, José Luis da C Silva, Rosiane G Mello

Journal: Antonie van Leeuwenhoek 2018;111(6):981-994

PMID: 29236232

Abstract

Paecilomyces variotii is a filamentous fungus that occurs worldwide in soil and decaying vegetation. Optimization of the fermentation process for exopolysaccharide (EPS) production from the fungus P. variotii, structure determination and immuno-stimulating activity of EPS were performed. Response surface methodology (RSM) coupled with central composite design (CCD) was used to optimize the physical and chemical factors required to produce EPS in submerged fermentation. Preliminary investigations to choose the three factors for the present work were made using a factorial experimental design. Glucose, ammonium nitrate (NHNO) and pH were used as variables for which, with constant temperature of 28 °C and agitation of 90 rpm, the optimal process parameters were determined as glucose values of 0.96%, NHNO 0.26% and pH 8.0. The three parameters presented significant effects. In this condition of culture, the main composition of the isolated EPS was a linear β-(1 → 6)-linked-D-glucan, as determined by Nuclear Magnetic Resonance (NMR) and methylation analysis. This polysaccharide is a very unusual as an EPS from fungi, especially a filamentous fungus such as P. variotii. Murine peritoneal macrophages cultivated with β-glucan for 6 and 48 h showed an increase in TNF-α, IL-6 and nitric oxide release with increased polysaccharide concentrations. Therefore, we conclude that the β-(1 → 6)-linked-D-glucan produced in optimised conditions of P. variotii cultivation has an immune-stimulatory activity on murine macrophages.

Address: Centro de Ciências Biológicas e da Saúde, Universidade Estadual do Oeste do Paraná, Caixa Postal 711, CEP 85819-110, Cascavel, PR, Brazil.; Centro de Ciências Médicas e Farmacêuticas, Universidade Estadual do Oeste do Paraná, Caixa Postal 711, Cascavel, PR, CEP 85819-110, Brazil. [email protected].; Faculdade de Ciências Farmacêuticas, Universidade de São Paulo, São Paulo, SP, CEP 05508-000, Brazil.; Centro de Ciências Médicas e Farmacêuticas, Universidade Estadual do Oeste do Paraná, Caixa Postal 711, Cascavel, PR, CEP 85819-110, Brazil.; Programa de Pós-Graduação em Farmácia, Universidade Federal de Santa Catarina, Florianópolis, SC, CEP 88040-900, Brazil.; Departamento de Bioquímica e Biologia Molecular, Universidade Federal do Paraná, C.P. 19046, Curitiba, PR, 81531-990, Brazil.; Division of Glycoscience, School of Biotechnology, KTH Royal Institute of Technology, AlbaNova University Centre, 106 91, Stockholm, Sweden.; Faculdades Pequeno Príncipe e Instituto de Pesquisa Pelé Pequeno Príncipe, Avenida Iguaçu, 333 Rebouças, Curitiba, PR, Brazil.

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