Enhancement of phenazine-1-carboxylic acid production using batch and fed-batch culture of gacA inactivated Pseudomonas sp M18G

被引:18
作者
Li, Yaqian [1 ,2 ]
Jiang, Haixia [1 ]
Du, Xilin [1 ]
Huang, Xianqing [1 ]
Zhang, Xuehong [1 ]
Xu, Yuhong [2 ]
Xu, Yuquan [1 ]
机构
[1] Shanghai Jiao Tong Univ, Coll Life Sci & Biotechnol, Minist Educ, Key Lab Microbial Metab, Shanghai 200240, Peoples R China
[2] Shanghai Jiao Tong Univ, Sch Pharm, Shanghai 200240, Peoples R China
基金
国家高技术研究发展计划(863计划);
关键词
Pseudomonas sp M18G; Phenazine-1-carboxylic acid; Batch culture; Fed-batch culture; DO-stat feeding; BIOLOGICAL-CONTROL; RESPONSE-SURFACE; FLUORESCENS; 2-79; AERUGINOSA; OPTIMIZATION; BIOCONTROL; GROWTH; BIOSURFACTANT; FERMENTATION; ANTIBIOTICS;
D O I
10.1016/j.biortech.2009.12.120
中图分类号
S2 [农业工程];
学科分类号
0828 ;
摘要
The enhancement of phenazine-1-carboxylic acid (PCA) production was investigated in a 101 fermentor using a gacA chromosomally inactivated mutant Pseudomonas sp. M18G combined with DO-stat feeing strategy. In batch culture, the optimal growth conditions with a two-stage agitation and aeration at 1.72vvm improved PCA production to 1987 mg/l at 48 h fermentation. A mathematical kinetic model consisting of cell growth, high PCA production, and substrate consumption was developed to simulate the batch culture process. Further increases in PCA production were achieved in a DO-stat fed-batch system which maintained a constant DO of 20% by a two-pulse glucose feeding strategy. With a total 6.6 g/l glucose feeding, the maximum PCA production of 2597 mg/l was obtained at 72 h fermentation, resulting in a 44.5% increase in PCA production and 10-fold greater cell numbers compared to the batch culture. The combination strategies might pave a new way for the phenazine derivative commercial production using various pseudomonads. (c) 2009 Elsevier Ltd. All rights reserved
引用
收藏
页码:3649 / 3656
页数:8
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