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Applied and Environmental Microbiology, July 1999, p. 3027-3032, Vol. 65, No. 7
Department of Chemical Engineering and
BioProcess Engineering Research Center, Korea Advanced Institute of
Science and Technology, Yusong-gu, Taejon 305-701, Korea
Received 3 March 1999/Accepted 30 April 1999
Human leptin is a 16-kDa (146-amino-acid) protein that is secreted
from adipocytes and influences body weight homeostasis. In order to
obtain high-level production of leptin, the human obese
gene coding for leptin was expressed in Escherichia coli BL21(DE3) under the strong inducible T7 promoter. The recombinant leptin was produced as inclusion bodies in E. coli, and the
recombinant leptin content was as high as 54% of the total protein
content. For production of recombinant human leptin in large amounts,
pH-stat fed-batch cultures were grown. Expression of leptin was induced at three different cell optical densities at 600 nm
(OD600), 30, 90, and 140. When cells were induced at an
OD600 of 90, the amount of leptin produced was 9.7 g/liter
(37% of the total protein). After simple purification steps consisting
of inclusion body isolation, denaturation and refolding, and
anion-exchange chromatography, 144.9 mg of leptin that was more than
90% pure was obtained from a 50-ml culture, and the recovery yield was
41.1%.
0099-2240/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
High-Level Production of Human Leptin by Fed-Batch
Cultivation of Recombinant Escherichia coli and Its
Purification
*
Corresponding author. Mailing address: Department of
Chemical Engineering and BioProcess Engineering Research Center, Korea Advanced Institute of Science and Technology, 373-1 Kusong-dong, Yusong-gu, Taejon 305-701, Korea. Phone: 82-42-869-3930. Fax: 82-42-869-8800. E-mail: leesy{at}sorak.kaist.ac.kr.
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