Enhancement of human granulocyte-colony stimulating factor production in recombinant E. coli using batch cultivation

被引:8
作者
Babaeipour, Valiollah [1 ]
Abbas, Mahdi Pesaran Haji [1 ]
Sahebnazar, Zahra [1 ]
Alizadeh, Reza [1 ]
机构
[1] Biotechnol Res Ctr, Dept Biochem Engn, Tehran, Iran
关键词
Amino acids; Batch culture; Media optimization; rh-GCSF; Yield; HIGH-CELL-DENSITY; HUMAN INTERFERON-GAMMA; ESCHERICHIA-COLI; CULTURE-CONDITIONS; PROTEINS; EXPRESSION; STRATEGIES; PROMOTER; HCDC;
D O I
10.1007/s00449-009-0380-3
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Development of inexpensive and simple culture media is always favorable for recombinant protein over-expression in E. coli. The effects of medium composition on the production of recombinant human granulocyte-colony stimulating factor (rh-GCSF) were investigated in batch culture of E. coli BL21 (DE3) [pET23a-hgcsf]. First, the optimum medium for production of rh-GCSF was determined; and, then it was shown that mixture of amino acid addition at induction time, which was determined on the basis of amino acids frequency in the recombinant protein, increases recombinant protein expression level significantly. Furthermore, the effect of glucose concentration on productivity of rh-GCSF was investigated; 20 g/l of glucose will result in maximum attainable biomass and rh-GCSF in this process. At optimum conditions, a cell dry weight of 10.5 g/l, an expression level of about 35% of total cellular protein, rh-GCSF concentration of 1.75 +/- A 0.1 g/l, and overall rh-GCSF yield of 165 +/- A 5 mg/g were obtained.
引用
收藏
页码:591 / 598
页数:8
相关论文
共 23 条
[1]   Over-production of human interferon-γ by HCDC of recombinant Escherichia coli [J].
Babaeipour, V. ;
Shojaosadati, S. A. ;
Robatjazi, S. M. ;
Khalilzadeh, R. ;
Maghsoudi, N. .
PROCESS BIOCHEMISTRY, 2007, 42 (01) :112-117
[2]   Cell engineering of Escherichia coli allows high cell density accumulation without fed-batch process control [J].
Baecklund, Emma ;
Markland, Katrin ;
Larsson, Gen .
BIOPROCESS AND BIOSYSTEMS ENGINEERING, 2008, 31 (01) :11-20
[3]  
Basu S, 2002, INT J MOL MED, V10, P3
[4]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[5]  
BURNETTE WN, 1981, ANAL BIOCHEM, V112, P195, DOI 10.1016/0003-2697(81)90281-5
[6]   Production of recombinant proteins by high cell density culture of Escherichia coli [J].
Choi, JH ;
Keum, KC ;
Lee, SY .
CHEMICAL ENGINEERING SCIENCE, 2006, 61 (03) :876-885
[7]   Review: Optimizing inducer and culture conditions for expression of foreign proteins under the control of the lac promoter [J].
Donovan, RS ;
Robinson, CW ;
Glick, BR .
JOURNAL OF INDUSTRIAL MICROBIOLOGY, 1996, 16 (03) :145-154
[8]   An on-line adaptive control based on DO/pH measurements and ANN pattern recognition model for fed-batch cultivation [J].
Duan, Shengbing ;
Shi, Zhongping ;
Feng, Haojie ;
Duan, Zuoying ;
Mao, Zhonggui .
BIOCHEMICAL ENGINEERING JOURNAL, 2006, 30 (01) :88-96
[9]   MAXIMIZING THE EXPRESSION OF RECOMBINANT PROTEINS IN ESCHERICHIA-COLI BY MANIPULATION OF CULTURE CONDITIONS [J].
GALINDO, E ;
BOLIVAR, F ;
QUINTERO, R .
JOURNAL OF FERMENTATION AND BIOENGINEERING, 1990, 69 (03) :159-165
[10]  
HAMES BD, 2002, INSTANT NOTES BIOCH