Improved [beta]-glucan yield using an Aureobasidium pullulans M-2 mutant strain in a 200-L pilot scale fermentor targeting industrial mass production
(13)-D-glucans with -(16)-glycosidic linked branches are known to be immune activation agents and are incorporated in anti-cancer drugs and health-promoting supplements. [beta]-Glucan concentration was 9.2 g/L in a 200-L pilot scale fermentor using mutant strain Aureobasidium pullulans M-2 from an i...
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creator | Moriya, Naoyuki Moriya, Yukiko Nomura, Hideo Kusano, Kisato Asada, Yukoh Uchiyama, Hirofumi Park, Enoch Y Okabe, Mitsuyasu |
description | (13)-D-glucans with -(16)-glycosidic linked branches are known to be immune activation agents and are incorporated in anti-cancer drugs and health-promoting supplements. [beta]-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. [beta]-Glucan produced by A. pullulans M-2 was identified as a polysaccharide of D-glucose monomers linked by [beta]-(1[arrow right]3, 1[arrow right]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, [beta]-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 [beta]-glucan concentration was 9.9 g/L with a yield of 0.52 (g [beta]-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 [beta]-glucan without melanin-like pigments is highly expected, as a health-promoting supplement or functional food.[PUBLICATION ABSTRACT] |
doi_str_mv | 10.1007/s12257-013-0516-9 |
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[beta]-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. [beta]-Glucan produced by A. pullulans M-2 was identified as a polysaccharide of D-glucose monomers linked by [beta]-(1[arrow right]3, 1[arrow right]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, [beta]-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 [beta]-glucan concentration was 9.9 g/L with a yield of 0.52 (g [beta]-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 [beta]-glucan without melanin-like pigments is highly expected, as a health-promoting supplement or functional food.[PUBLICATION ABSTRACT]</description><identifier>ISSN: 1226-8372</identifier><identifier>EISSN: 1976-3816</identifier><identifier>DOI: 10.1007/s12257-013-0516-9</identifier><language>eng</language><publisher>Dordrecht: Springer Nature B.V</publisher><subject>Biotechnology ; Cellulase ; Dissolved oxygen ; Experimental design ; Fermentation ; Functional foods & nutraceuticals ; Health promotion ; Industrial production ; Laboratories ; Mutagenesis ; Physiology ; Productivity ; Studies ; Sucrose ; Yeast</subject><ispartof>Biotechnology and bioprocess engineering, 2013-11, Vol.18 (6), p.1083</ispartof><rights>The Korean Society for Biotechnology and Bioengineering and Springer-Verlag Berlin Heidelberg 2013</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids></links><search><creatorcontrib>Moriya, Naoyuki</creatorcontrib><creatorcontrib>Moriya, Yukiko</creatorcontrib><creatorcontrib>Nomura, Hideo</creatorcontrib><creatorcontrib>Kusano, Kisato</creatorcontrib><creatorcontrib>Asada, Yukoh</creatorcontrib><creatorcontrib>Uchiyama, Hirofumi</creatorcontrib><creatorcontrib>Park, Enoch Y</creatorcontrib><creatorcontrib>Okabe, Mitsuyasu</creatorcontrib><title>Improved [beta]-glucan yield using an Aureobasidium pullulans M-2 mutant strain in a 200-L pilot scale fermentor targeting industrial mass production</title><title>Biotechnology and bioprocess engineering</title><description>(13)-D-glucans with -(16)-glycosidic linked branches are known to be immune activation agents and are incorporated in anti-cancer drugs and health-promoting supplements. [beta]-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. [beta]-Glucan produced by A. pullulans M-2 was identified as a polysaccharide of D-glucose monomers linked by [beta]-(1[arrow right]3, 1[arrow right]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, [beta]-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 [beta]-glucan concentration was 9.9 g/L with a yield of 0.52 (g [beta]-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. 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[beta]-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. [beta]-Glucan produced by A. pullulans M-2 was identified as a polysaccharide of D-glucose monomers linked by [beta]-(1[arrow right]3, 1[arrow right]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, [beta]-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 [beta]-glucan concentration was 9.9 g/L with a yield of 0.52 (g [beta]-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 [beta]-glucan without melanin-like pigments is highly expected, as a health-promoting supplement or functional food.[PUBLICATION ABSTRACT]</abstract><cop>Dordrecht</cop><pub>Springer Nature B.V</pub><doi>10.1007/s12257-013-0516-9</doi></addata></record> |
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subjects | Biotechnology Cellulase Dissolved oxygen Experimental design Fermentation Functional foods & nutraceuticals Health promotion Industrial production Laboratories Mutagenesis Physiology Productivity Studies Sucrose Yeast |
title | Improved [beta]-glucan yield using an Aureobasidium pullulans M-2 mutant strain in a 200-L pilot scale fermentor targeting industrial mass production |
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