Medium optimization based on the metabolic-flux spectrum of recombinant Escherichia coli for high expression of human-like collagen II

被引:31
作者
Guo, Jiaqing [1 ,2 ,3 ]
Luo, Yan'e [1 ,2 ,3 ]
Fan, Daidi [1 ,2 ,3 ]
Yang, Bo [3 ]
Gao, Pengfei [1 ,2 ,3 ]
Ma, Xiaoxuan [1 ,2 ,3 ]
Zhu, Chenhui [1 ,2 ,3 ]
机构
[1] NW Univ Xian, Shaanxi Key Lab Degradable Biomed Mat, Xian 710069, Shaanxi, Peoples R China
[2] NW Univ Xian, Shaanxi R&D Ctr Biomat & Fermentat Engn, Xian 710069, Shaanxi, Peoples R China
[3] NW Univ Xian, Sch Chem Engn, Xian 710069, Shaanxi, Peoples R China
基金
国家高技术研究发展计划(863计划); 中国国家自然科学基金; 高等学校博士学科点专项科研基金;
关键词
carbon/nitrogen molar ratio; fed-batch culture; human-like collagen II; metabolic-flux analysis (MFA); recombinant Escherichia coli; PATHWAY ANALYSIS; BATCH; GROWTH; HYDROXYAPATITE; CULTIVATION; CULTURE;
D O I
10.1042/BA20100081
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Recombinant Escherichia coli BL2I was used to produce human-like collagen II in fed-batch cultivation. By performing MFA (metabolic-flux analysis), the carbon/nitrogen molar ratios in both the batch and feeding media were optimized for high-level production of human-like collagen II. Three carbon/nitrogen molar ratios in both the batch and feeding media were used in the present study, and the MFA results showed that the optimal carbon/nitrogen molar ratios for the batch and feeding media were 2.36:1 and 5.12:1 respectively, yielding the highest dry-cell density (67.2 g/l dry cell weight) and human-like collagen production (10.8 g/l).
引用
收藏
页码:55 / 62
页数:8
相关论文
共 36 条
[11]  
HULYA AK, 2006, ENZYME MICROB TECHNO, V38, P727
[12]   Metabolic pathway analysis of recombinant Saccharomyces cerevisiae with a galactose-inducible promoter based on a signal flow modeling approach [J].
Jin, S ;
Ye, KM ;
Shimizu, K .
JOURNAL OF FERMENTATION AND BIOENGINEERING, 1995, 80 (06) :541-551
[13]   SIMPLE FED-BATCH TECHNIQUE FOR HIGH CELL-DENSITY CULTIVATION OF ESCHERICHIA-COLI [J].
KORZ, DJ ;
RINAS, U ;
HELLMUTH, K ;
SANDERS, EA ;
DECKWER, WD .
JOURNAL OF BIOTECHNOLOGY, 1995, 39 (01) :59-65
[14]   Metabolic pathway analysis for rational design of L-methionine production by Escherichia coli and Corynebacterium glutamicum [J].
Kroemer, Jens Olaf ;
Wittmann, Christoph ;
Schroeder, Hartwig ;
Heinzle, Elmar .
METABOLIC ENGINEERING, 2006, 8 (04) :353-369
[15]   COMPARISON OF GROWTH, ACETATE PRODUCTION, AND ACETATE INHIBITION OF ESCHERICHIA-COLI STRAINS IN BATCH AND FED-BATCH FERMENTATIONS [J].
LULI, GW ;
STROHL, WR .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1990, 56 (04) :1004-1011
[16]  
Luo Y, 2005, CHINESE J CHEM ENG, V13, P276
[17]   Analysis of metabolic flux in Escherichia coli expressing human-like collagen in fed-batch culture [J].
Luo, Yan E. ;
Fan, Dai D. ;
Shang, Long A. ;
Shi, Hui J. ;
Ma, Xiao X. ;
Mi, Yu ;
Zhao, Gui F. .
BIOTECHNOLOGY LETTERS, 2008, 30 (04) :637-643
[18]  
[马茂 MA Mao], 2007, [第四军医大学学报, Journal of the Fourth Military Medical University], V28, P1122
[19]   Viral vectors for the treatment of alcoholism: Use of metabolic flux analysis for cell cultivation and vector production [J].
Martinez, V. ;
Gerdtzen, Z. P. ;
Andrews, B. A. ;
Asenjo, J. A. .
METABOLIC ENGINEERING, 2010, 12 (02) :129-137
[20]   Systematic phenome analysis of Escherichia coli multiple-knockout mutants reveals hidden reactions in central carbon metabolism [J].
Nakahigashi, Kenji ;
Toya, Yoshihiro ;
Ishii, Nobuyoshi ;
Soga, Tomoyoshi ;
Hasegawa, Miki ;
Watanabe, Hisami ;
Takai, Yuki ;
Honma, Masayuki ;
Mori, Hirotada ;
Tomita, Masaru .
MOLECULAR SYSTEMS BIOLOGY, 2009, 5