Purification and on-column refolding of EGFP overexpressed as inclusion bodies in Escherichia coli with expanded bed anion exchange chromatography
被引:27
作者:
Cabanne, C
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Univ Bordeaux 2, Ecole Super Technol Biomol Bordeauc, F-33076 Bordeaux, FranceUniv Bordeaux 2, Ecole Super Technol Biomol Bordeauc, F-33076 Bordeaux, France
Cabanne, C
[1
]
Noubhani, AM
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Univ Bordeaux 2, Ecole Super Technol Biomol Bordeauc, F-33076 Bordeaux, FranceUniv Bordeaux 2, Ecole Super Technol Biomol Bordeauc, F-33076 Bordeaux, France
Noubhani, AM
[1
]
Hocquellet, A
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Univ Bordeaux 2, Ecole Super Technol Biomol Bordeauc, F-33076 Bordeaux, FranceUniv Bordeaux 2, Ecole Super Technol Biomol Bordeauc, F-33076 Bordeaux, France
Hocquellet, A
[1
]
Dole, R
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Univ Bordeaux 2, Ecole Super Technol Biomol Bordeauc, F-33076 Bordeaux, FranceUniv Bordeaux 2, Ecole Super Technol Biomol Bordeauc, F-33076 Bordeaux, France
Dole, R
[1
]
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Dieryck, W
[1
]
Santarelli, X
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Univ Bordeaux 2, Ecole Super Technol Biomol Bordeauc, F-33076 Bordeaux, FranceUniv Bordeaux 2, Ecole Super Technol Biomol Bordeauc, F-33076 Bordeaux, France
Santarelli, X
[1
]
机构:
[1] Univ Bordeaux 2, Ecole Super Technol Biomol Bordeauc, F-33076 Bordeaux, France
来源:
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES
|
2005年
/
818卷
/
01期
关键词:
expanded bed adsorption;
EGFP;
purification;
chromatography;
refolding;
inclusion bodies;
D O I:
10.1016/j.jchromb.2004.10.023
中图分类号:
Q5 [生物化学];
学科分类号:
071010 ;
081704 ;
摘要:
The enhanced green fluorescent protein (EGFP) was over-expressed in Escherichia coli as inclusion bodies to increase its quantity and to facilitate its purification. Insoluble EGFP has been purified on Q Hyper Z matrix by expanded bed adsorption after solubilization in 8 M urea. The adsorption was made in expanded bed mode to avoid centrifugation. EBA-column refolding was done by elimination of urea and elution with NaCl. The EGFP was obtained as a highly purified soluble form with similar behavior in fluorescence and electrophoresis as native EGFP. (C) 2004 Elsevier B.V. All rights reserved.