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Originally published In Press as doi:10.1074/jbc.M110809200 on January 28, 2002

J. Biol. Chem., Vol. 277, Issue 15, 13175-13183, April 12, 2002
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Global Expression Profiling of Acetate-grown Escherichia coli*

Min-Kyu Oh, Lars Rohlin, Katy C. Kao, and James C. LiaoDagger

From the Department of Chemical Engineering, UCLA, Los Angeles, California 90095

This study characterized the transcript profile of Escherichia coli in acetate cultures using DNA microarray on glass slides. Glucose-grown cultures were used as a reference. At the 95% confidence level, 354 genes were up-regulated in acetate, while 370 genes were down-regulated compared with the glucose-grown culture. Generally, more metabolic genes were up-regulated in acetate than other gene groups, while genes involved in cell replication, transcription, and translation machinery tended to be down-regulated. It appears that E. coli commits more resources to metabolism at the expense of growth when cultured in the poor carbon source. The expression profile confirms many known features in acetate metabolism such as the induction of the glyoxylate pathway, tricarboxylic acid cycle, and gluconeogenic genes. It also provided many previously unknown features, including induction of malic enzymes, ppsA, and the glycolate pathway and repression of glycolytic and glucose phosphotransferase genes in acetate. The carbon flux delivered from the malic enzymes and PpsA in acetate was further confirmed by deletion mutations. In general, the gene expression profiles qualitatively agree with the metabolic flux changes and may serve as a predictor for gene function and metabolic flux distribution.


* This work was supported by National Science Foundation Grant EEC-0087589 and National Institute of Standards and Technology Grant 70NANBOH0064.The costs of publication of this article were defrayed in part by the payment of page charges. The article must therefore be hereby marked "advertisement" in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

Dagger To whom correspondence should be addressed: Dept. of Chemical Engineering, 5531 Boelter Hall, UCLA, Los Angeles, CA 90095. Tel.: 310-825-1656; Fax: 310-206-1642; E-mail: liaoj@ucla.edu.


Copyright © 2002 by The American Society for Biochemistry and Molecular Biology, Inc.
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