The E-coli molecular phenotype under different growth conditions

被引:37
|
作者
Caglar, Mehmet U. [1 ,2 ,3 ]
Houser, John R. [3 ,4 ,5 ]
Barnhart, Craig S. [3 ,4 ]
Boutz, Daniel R. [3 ,4 ,5 ]
Carroll, Sean M. [6 ,7 ]
Dasgupta, Aurko [3 ,4 ,8 ]
Lenoir, Walter F. [5 ]
Smith, Bartram L. [1 ,2 ,3 ]
Sridhara, Viswanadham [2 ,3 ]
Sydykova, Dariya K. [1 ,2 ,3 ]
Vander Wood, Drew [3 ,5 ]
Marx, Christopher J. [9 ,10 ]
Marcotte, Edward M. [3 ,4 ,5 ]
Barrick, Jeffrey E. [3 ,4 ,5 ]
Wilke, Claus O. [3 ,4 ,5 ]
机构
[1] Univ Texas Austin, Dept Integrat Biol, Austin, TX 78712 USA
[2] Univ Texas Austin, Ctr Computat Biol & Bioinformat, Austin, TX 78712 USA
[3] Univ Texas Austin, Inst Cellular & Mol Biol, Austin, TX 78712 USA
[4] Univ Texas Austin, Ctr Syst & Synthet Biol, Austin, TX 78712 USA
[5] Univ Texas Austin, Dept Mol Biosci, Austin, TX 78712 USA
[6] Harvard Univ, Dept Organism & Evolutionary Biol, Cambridge, MA 02138 USA
[7] Axcella Hlth Inc, Cambridge, MA USA
[8] Washington Univ, Sch Med, Dept Internal Med, Ctr Womens Infect Dis Res,Div Infect Dis, St Louis, MO 63110 USA
[9] Univ Idaho, Dept Biol Sci, Moscow, ID 83843 USA
[10] Univ Idaho, Inst Bioinformat & Evolutionary Studies, Moscow, ID 83843 USA
来源
SCIENTIFIC REPORTS | 2017年 / 7卷
关键词
PROTEOME; SEQUENCE; SYSTEM; OPERON; GENES;
D O I
10.1038/srep45303
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Modern systems biology requires extensive, carefully curated measurements of cellular components in response to different environmental conditions. While high-throughput methods have made transcriptomics and proteomics datasets widely accessible and relatively economical to generate, systematic measurements of both mRNA and protein abundances under a wide range of different conditions are still relatively rare. Here we present a detailed, genome-wide transcriptomics and proteomics dataset of E. coli grown under 34 different conditions. Additionally, we provide measurements of doubling times and in-vivo metabolic fluxes through the central carbon metabolism. We manipulate concentrations of sodium and magnesium in the growth media, and we consider four different carbon sources glucose, gluconate, lactate, and glycerol. Moreover, samples are taken both in exponential and stationary phase, and we include two extensive time-courses, with multiple samples taken between 3 hours and 2 weeks. We find that exponential-phase samples systematically differ from stationary-phase samples, in particular at the level of mRNA. Regulatory responses to different carbon sources or salt stresses are more moderate, but we find numerous differentially expressed genes for growth on gluconate and under salt and magnesium stress. Our data set provides a rich resource for future computational modeling of E. coli gene regulation, transcription, and translation.
引用
收藏
页数:15
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