TY - JOUR
T1 - Enhanced production of glycyrrhetic acid 3-O-mono-β-d-glucuronide by fed-batch fermentation using pH and dissolved oxygen as feedback parameters
AU - Lü, Bo
AU - Yang, Xiaogang
AU - Feng, Xudong
AU - Li, Chun
N1 - Publisher Copyright:
© 2015 The Chemical Industry and Engineering Society of China, and Chemical Industry Press. All rights reserved.
PY - 2016/4/1
Y1 - 2016/4/1
N2 - Glycyrrhetic acid 3-O-mono-β-d-glucuronide (GAMG), the major functional ingredient in licorice, has widespread applications in food, pharmacy and cosmetics industry. The production of GAMG through Penicillium purpurogenum Li-3 cultivation was for the first time performed through both batch and fed-batch processes in bioreactors. In batch process, under optimal conditions (pH 5.0, temperature 32 °C, agitation speed 100 r·min- 1), 3.55 g·L- 1 GAMG was obtained in a 2.5 L fermentor. To further enhance GAMG production, a fine fed-batch process was developed by using pH and DO as feedback parameters. Starting from 48 h, 100 ml 90 g·L- 1 substrate Glycyrrhizin (GL) was fed each time when pH increased to above 5.0 and DO was increased to above 80%. This strategy can significantly enhance GAMG production: the achieved GL conversion was 95.34% with GAMG yield of 95.15%, and GAMG concentration was 16.62 g·L- 1 which was 5 times higher than that of batch. Then, a two-step separation strategy was established to separate GAMG from fermentation broth by crude extraction of 15 ml column packed with D101 resin followed by fine purification with preparative C18 chromatography. The obtained GAMG purity was 95.79%. This study provides a new insight into the industrial bioprocess of high-level GAMG production.
AB - Glycyrrhetic acid 3-O-mono-β-d-glucuronide (GAMG), the major functional ingredient in licorice, has widespread applications in food, pharmacy and cosmetics industry. The production of GAMG through Penicillium purpurogenum Li-3 cultivation was for the first time performed through both batch and fed-batch processes in bioreactors. In batch process, under optimal conditions (pH 5.0, temperature 32 °C, agitation speed 100 r·min- 1), 3.55 g·L- 1 GAMG was obtained in a 2.5 L fermentor. To further enhance GAMG production, a fine fed-batch process was developed by using pH and DO as feedback parameters. Starting from 48 h, 100 ml 90 g·L- 1 substrate Glycyrrhizin (GL) was fed each time when pH increased to above 5.0 and DO was increased to above 80%. This strategy can significantly enhance GAMG production: the achieved GL conversion was 95.34% with GAMG yield of 95.15%, and GAMG concentration was 16.62 g·L- 1 which was 5 times higher than that of batch. Then, a two-step separation strategy was established to separate GAMG from fermentation broth by crude extraction of 15 ml column packed with D101 resin followed by fine purification with preparative C18 chromatography. The obtained GAMG purity was 95.79%. This study provides a new insight into the industrial bioprocess of high-level GAMG production.
KW - D101 resin separation
KW - Fed-batch fermentation
KW - Glycyrrhetic acid 3-O-mono-β-d-glucuronide
KW - Penicillium purpurogenum Li-3
UR - http://www.scopus.com/inward/record.url?scp=84978010027&partnerID=8YFLogxK
U2 - 10.1016/j.cjche.2015.12.003
DO - 10.1016/j.cjche.2015.12.003
M3 - Article
AN - SCOPUS:84978010027
SN - 1004-9541
VL - 24
SP - 506
EP - 512
JO - Chinese Journal of Chemical Engineering
JF - Chinese Journal of Chemical Engineering
IS - 4
ER -