This study aimed to optimize extracellular glutathione production by a Saccharomyces cerevisiae engineered strain and to concentrate the extracellular glutathione by membrane separation processes, including ultrafiltration (UF) and nanofiltration (NF). Synthetic defined (SD) medium containing 20 g L-1 glucose was fermented for 48 h; the fermentation liquid was passed through an UF membrane to remove macromolecules. Glutathione in this permeate was concentrated for 48 h to 545.1 +/- 33.6 mg L-1 using the NF membrane; this was a significantly higher concentration than that obtained with yeast extract peptone dextrose (YPD) medium following 96 h NF concentration (217.9 +/- 57.4 mg L-1). This higher glutathione concentration results from lower cellular growth in SD medium (final OD600 = 6.9 +/- 0.1) than in YPD medium (final OD600 = 11.0 +/- 0.6) and thus higher production of extracellular glutathione (16.0 +/- 1.3 compared to 9.2 +/- 2.1 mg L-1 in YPD medium, respectively). Similar fermentation and membrane processing of sweet sorghum juice containing 20 g L-1 total sugars provided 240.3 +/- 60.6 mg L-1 glutathione. Increased extracellular production of glutathione by this engineered strain in SD medium and subsequent UF permeation and NF concentration in shortend time may help realize industrial recovery of extracellular glutathione. (C) 2015, The Society for Biotechnology, Japan. All rights reserved.
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Kyowa Hakko Kirin Co Ltd, Frontier Lab, Machida, Tokyo 1948533, JapanKyowa Hakko Kirin Co Ltd, Frontier Lab, Machida, Tokyo 1948533, Japan
Hara, Kiyotaka Y.
Shimodate, Natsuka
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Kyowa Hakko Kirin Co Ltd, Frontier Lab, Machida, Tokyo 1948533, JapanKyowa Hakko Kirin Co Ltd, Frontier Lab, Machida, Tokyo 1948533, Japan
Shimodate, Natsuka
Hirokawa, Yasutaka
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Kyowa Hakko Kirin Co Ltd, Frontier Lab, Machida, Tokyo 1948533, JapanKyowa Hakko Kirin Co Ltd, Frontier Lab, Machida, Tokyo 1948533, Japan
Hirokawa, Yasutaka
Ito, Mikito
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Kyowa Hakko Kirin Co Ltd, Frontier Lab, Machida, Tokyo 1948533, JapanKyowa Hakko Kirin Co Ltd, Frontier Lab, Machida, Tokyo 1948533, Japan
Ito, Mikito
Baba, Tomoya
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Keio Univ, Inst Adv Biosci, Yamagata, Japan
Nara Inst Sci & Technol, Nara, JapanKyowa Hakko Kirin Co Ltd, Frontier Lab, Machida, Tokyo 1948533, Japan
Baba, Tomoya
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Mori, Hirotada
Mori, Hideo
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Kyowa Hakko Kirin Co Ltd, Frontier Lab, Machida, Tokyo 1948533, JapanKyowa Hakko Kirin Co Ltd, Frontier Lab, Machida, Tokyo 1948533, Japan
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Kyowa Hakko Kirin Co Ltd, Frontier Lab, Machida, Tokyo 1948533, JapanKyowa Hakko Kirin Co Ltd, Frontier Lab, Machida, Tokyo 1948533, Japan
Hara, Kiyotaka Y.
Shimodate, Natsuka
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机构:
Kyowa Hakko Kirin Co Ltd, Frontier Lab, Machida, Tokyo 1948533, JapanKyowa Hakko Kirin Co Ltd, Frontier Lab, Machida, Tokyo 1948533, Japan
Shimodate, Natsuka
Hirokawa, Yasutaka
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Kyowa Hakko Kirin Co Ltd, Frontier Lab, Machida, Tokyo 1948533, JapanKyowa Hakko Kirin Co Ltd, Frontier Lab, Machida, Tokyo 1948533, Japan
Hirokawa, Yasutaka
Ito, Mikito
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Kyowa Hakko Kirin Co Ltd, Frontier Lab, Machida, Tokyo 1948533, JapanKyowa Hakko Kirin Co Ltd, Frontier Lab, Machida, Tokyo 1948533, Japan
Ito, Mikito
Baba, Tomoya
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Keio Univ, Inst Adv Biosci, Yamagata, Japan
Nara Inst Sci & Technol, Nara, JapanKyowa Hakko Kirin Co Ltd, Frontier Lab, Machida, Tokyo 1948533, Japan
Baba, Tomoya
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Mori, Hirotada
Mori, Hideo
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Kyowa Hakko Kirin Co Ltd, Frontier Lab, Machida, Tokyo 1948533, JapanKyowa Hakko Kirin Co Ltd, Frontier Lab, Machida, Tokyo 1948533, Japan