Note to users. If you're seeing this message, it means that your browser cannot find this page's style/presentation instructions -- or possibly that you are using a browser that does not support current Web standards. Find out more about why this message is appearing, and what you can do to make your experience of our site the best it can be.


Originally published in Science Express on 22 March 2007
Science 27 April 2007:
Vol. 316. no. 5824, pp. 593 - 597
DOI: 10.1126/science.1132067

Reports

Multiple High-Throughput Analyses Monitor the Response of E. coli to Perturbations

Nobuyoshi Ishii,1,2* Kenji Nakahigashi,1,2* Tomoya Baba,1,2,3* Martin Robert,1,2* Tomoyoshi Soga,1,2,6* Akio Kanai,1,2* Takashi Hirasawa,1,2* Miki Naba,1 Kenta Hirai,1 Aminul Hoque,1,2 Pei Yee Ho,5 Yuji Kakazu,1 Kaori Sugawara,1 Saori Igarashi,1 Satoshi Harada,1 Takeshi Masuda,1,2 Naoyuki Sugiyama,6 Takashi Togashi,1 Miki Hasegawa,1 Yuki Takai,1 Katsuyuki Yugi,1,2 Kazuharu Arakawa,1 Nayuta Iwata,1,2 Yoshihiro Toya,1,2 Yoichi Nakayama,1,2 Takaaki Nishioka,1,2,4 Kazuyuki Shimizu,1,2,5 Hirotada Mori,1,2,3 Masaru Tomita1,2,6{dagger}

Analysis of cellular components at multiple levels of biological information can provide valuable functional insights. We performed multiple high-throughput measurements to study the response of Escherichia coli cells to genetic and environmental perturbations. Analysis of metabolic enzyme gene disruptants revealed unexpectedly small changes in messenger RNA and proteins for most disruptants. Overall, metabolite levels were also stable, reflecting the rerouting of fluxes in the metabolic network. In contrast, E. coli actively regulated enzyme levels to maintain a stable metabolic state in response to changes in growth rate. E. coli thus seems to use complementary strategies that result in a metabolic network robust against perturbations.

1 Institute for Advanced Biosciences, Keio University, Tsuruoka, Yamagata 997-0017, Japan.
2 Systems Biology Program, Graduate School of Media and Governance, Keio University, Fujisawa 252-8520, Japan.
3 Graduate School of Biological Sciences, Nara Institute of Science and Technology, Ikoma, Nara 630-0101, Japan.
4 Graduate School of Agriculture, Kyoto University, Kyoto 606-8502, Japan.
5 Department of Bioscience and Bioinformatics, Kyushu Institute of Technology, Iizuka, Fukuoka 820-8502, Japan.
6 Human Metabolome Technologies, Inc., Tsuruoka 997-0017, Japan.

* These authors contributed equally to this work.

{dagger} To whom correspondence should be addressed. E-mail: mt{at}sfc.keio.ac.jp

Read the Full Text



THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES:
Phylogenetic Analysis of ADP-Glucose Pyrophosphorylase Subunits Reveals a Role of Subunit Interfaces in the Allosteric Properties of the Enzyme.
N. Georgelis, J. R. Shaw, and L. C. Hannah (2009)
Plant Physiology 151, 67-77
   Abstract »    Full Text »    PDF »
Genetic modification of flux for flux prediction of mutants.
Q. Zhao and H. Kurata (2009)
Bioinformatics 25, 1702-1708
   Abstract »    Full Text »    PDF »
A divide-and-conquer approach to analyze underdetermined biochemical models.
O. Kotte and M. Heinemann (2009)
Bioinformatics 25, 519-525
   Abstract »    Full Text »    PDF »
Continued Protein Synthesis at Low [ATP] and [GTP] Enables Cell Adaptation during Energy Limitation.
M. C. Jewett, M. L. Miller, Y. Chen, and J. R. Swartz (2009)
J. Bacteriol. 191, 1083-1091
   Abstract »    Full Text »    PDF »
Principles of transcriptional regulation and evolution of the metabolic system in E. coli.
A. S.N. Seshasayee, G. M. Fraser, M. M. Babu, and N. M. Luscombe (2009)
Genome Res. 19, 79-91
   Abstract »    Full Text »    PDF »
System estimation from metabolic time-series data.
G. Goel, I-C. Chou, and E. O. Voit (2008)
Bioinformatics 24, 2505-2511
   Abstract »    Full Text »    PDF »
Integration of Metabolomic and Proteomic Phenotypes: Analysis of Data Covariance Dissects Starch and RFO Metabolism from Low and High Temperature Compensation Response in Arabidopsis Thaliana.
S. Wienkoop, K. Morgenthal, F. Wolschin, M. Scholz, J. Selbig, and W. Weckwerth (2008)
Mol. Cell. Proteomics 7, 1725-1736
   Abstract »    Full Text »    PDF »
The PduX Enzyme of Salmonella enterica Is an L-Threonine Kinase Used for Coenzyme B12 Synthesis.
C. Fan and T. A. Bobik (2008)
J. Biol. Chem. 283, 11322-11329
   Abstract »    Full Text »    PDF »
Cyclic AMP-Dependent Catabolite Repression Is the Dominant Control Mechanism of Metabolic Fluxes under Glucose Limitation in Escherichia coli.
A. Nanchen, A. Schicker, O. Revelles, and U. Sauer (2008)
J. Bacteriol. 190, 2323-2330
   Abstract »    Full Text »    PDF »
Comparative transcriptomics reveals key gene expression differences between the human and bovine pathogens of the Mycobacterium tuberculosis complex.
P. Golby, K. A. Hatch, J. Bacon, R. Cooney, P. Riley, J. Allnutt, J. Hinds, J. Nunez, P. D. Marsh, R. G. Hewinson, et al. (2007)
Microbiology 153, 3323-3336
   Abstract »    Full Text »    PDF »



To Advertise     Find Products


Science. ISSN 0036-8075 (print), 1095-9203 (online)