Improved β-glucan yield using an Aureobasidium pullulans M-2 mutant strain in a 200-L pilot scale fermentor targeting industrial mass production
Abstractβ-(1→3)-D-glucans with β-(1→6)-glycosidic linked branches are known to be immune activation agents and are incorporated in anti-cancer drugs and health-promoting supplements. β-Glucan concentration was 9.2 g/L in a 200-L pilot scale fermentor using mutant strain Aureobasidium pullulans M-2 from an imperfect fungal strain belonging to A. pullulans M-1. The culture broth of A. pullulans M-2 had a faint yellow color, whereas that of the wild-type had an intense dark green color caused by the accumulation of melanin-like pigments. β-Glucan produced by A. pullulans M-2 was identified as a polysaccharide of D-glucose monomers linked by β-(1→3, 1→6)-glycosidic bonds through GC/MS and NMR analysis. When a conventional medium was used in the culture of A. pullulans M-2 in a 3-L jar fermentor, β-glucan concentration was 1.4-fold that produced by the wild-type. However, when a medium optimized by statistical experimental design was used with dissolved oxygen at 10%, the β-glucan concentration was 9.9 g/L with a yield of 0.52 (g β-glucan/g consumed sucrose), 2.9-fold that of the wild-type. This level of productivity was reproduced when the fermentation was scaled up 200-L. The industrial production of high β-glucan without melanin-like pigments is highly expected, as a health-promoting supp
Optimizing β-glucan production from Aureobasidium pullulans is critical for scaling up this immunomodulatory polysaccharide for research and clinical applications.
Researchers identified improved fermentation conditions for Aureobasidium pullulans that significantly increased β-glucan yield. Optimization of carbon sources, nitrogen sources, and culture conditions led to substantially higher polysaccharide output while maintaining structural integrity and biological activity of the β-1,3/1,6-glucan product.
Efficient production of high-quality β-glucan from Aureobasidium pullulans is fundamental to making this immunomodulatory compound available for research and supplementation. Yield optimization studies directly support the commercialization of Aureobasidium-derived beta glucan products.
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Moriya, Naoyuki; Moriya, Yukiko; Nomura, Hideo; Kusano, Kisato; Asada, Yukoh; Uchiyama, Hirofumi; Park, Enoch Y.; Okabe, Mitsuyasu. Improved β-glucan Yield Using an Aureobasidium pullulans M-2 Mutant Strain in a 200-L Pilot Scale Fermentor Targeting Industrial Mass Production. Biotechnology and Bioprocess Engineering. 2013. DOI: 10.1007/s12257-013-0516-9.
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