Analysis of gene expression in Escherichia coli in response to changes of growth-limiting nutrient in chemostat cultures.
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Construction of Escherichia coli K-12 in-frame, single-gene knockout mutants: the Keio collectionGlobal regulation of gene expression and cell differentiation in Caulobacter crescentus in response to nutrient availabilityCulture history and population heterogeneity as determinants of bacterial adaptation: the adaptomics of a single environmental transitionEvolution of E. coli on [U-13C]Glucose Reveals a Negligible Isotopic Influence on Metabolism and PhysiologyThe functional basis of adaptive evolution in chemostatsGlobal physiological analysis of carbon- and energy-limited growing Escherichia coli confirms a high degree of catabolic flexibility and preparedness for mixed substrate utilization.Identification of regulatory network topological units coordinating the genome-wide transcriptional response to glucose in Escherichia coli.Exploring and dissecting genome-wide gene expression responses of Penicillium chrysogenum to phenylacetic acid consumption and penicillinG productionEnterohemorrhagic Escherichia coli O157:H7 gene expression profiling in response to growth in the presence of host epithelia.Transcription analysis of central metabolism genes in Escherichia coli. Possible roles of sigma38 in their expression, as a response to carbon limitation.E Unibus Plurum: genomic analysis of an experimentally evolved polymorphism in Escherichia coli.Transcriptional response of Escherichia coli to ammonia and glucose fluctuationsResolution of gene regulatory conflicts caused by combinations of antibiotics.Decrease of energy spilling in Escherichia coli continuous cultures with rising specific growth rate and carbon wastingThe ColRS system is essential for the hunger response of glucose-growing Pseudomonas putida.Physiological and proteomic analysis of Escherichia coli iron-limited chemostat growth.Metaproteomics of a gutless marine worm and its symbiotic microbial community reveal unusual pathways for carbon and energy use.Genetic changes during a laboratory adaptive evolution process that allowed fast growth in glucose to an Escherichia coli strain lacking the major glucose transport system.Solubility of disulfide-bonded proteins in the cytoplasm of Escherichia coli and its "oxidizing" mutantCarbon catabolite repression correlates with the maintenance of near invariant molecular crowding in proliferating E. coli cells.Contribution of gene expression to metabolic fluxes in hypermetabolic livers induced through burn injury and cecal ligation and puncture in ratsPredicting growth conditions from internal metabolic fluxes in an in-silico model of E. coli.Accumulation of d-glucose from pentoses by metabolically engineered Escherichia coli.Interplay between CRP-cAMP and PII-Ntr systems forms novel regulatory network between carbon metabolism and nitrogen assimilation in Escherichia coli.The PEP-pyruvate-oxaloacetate node as the switch point for carbon flux distribution in bacteria.Physiological, biomass elemental composition and proteomic analyses of Escherichia coli ammonium-limited chemostat growth, and comparison with iron- and glucose-limited chemostat growth.Starvation, detoxification, and multidrug resistance in cancer therapyMeasuring Escherichia coli Gene Expression during Human Urinary Tract InfectionsGenome-scale models of metabolism and gene expression extend and refine growth phenotype prediction.Metabolic flux analysis of Escherichia coli creB and arcA mutants reveals shared control of carbon catabolism under microaerobic growth conditions.Transcriptome-wide analysis of compression-induced microRNA expression alteration in breast cancer for mining therapeutic targetsInfluence of the RelA Activity on E. coli Metabolism by Metabolite Profiling of Glucose-Limited Chemostat Cultures.Nutritional indicators and their uses in ecology.Bacterial responses to antibiotics and their combinations.Metabolic Regulation of a Bacterial Cell System with Emphasis on Escherichia coli Metabolism.DsdX is the second D-serine transporter in uropathogenic Escherichia coli clinical isolate CFT073.Metabolic suppression identifies new antibacterial inhibitors under nutrient limitation.A mathematical model of metabolism and regulation provides a systems-level view of how Escherichia coli responds to oxygen.Metabolic regulation analysis of an ethanologenic Escherichia coli strain based on RT-PCR and enzymatic activities.Volvox: A simple algal model for embryogenesis, morphogenesis and cellular differentiation.
P2860
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P2860
Analysis of gene expression in Escherichia coli in response to changes of growth-limiting nutrient in chemostat cultures.
description
2004 nî lūn-bûn
@nan
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
2004年论文
@zh
2004年论文
@zh-cn
name
Analysis of gene expression in ...... utrient in chemostat cultures.
@en
type
label
Analysis of gene expression in ...... utrient in chemostat cultures.
@en
prefLabel
Analysis of gene expression in ...... utrient in chemostat cultures.
@en
P2093
P2860
P1476
Analysis of gene expression in ...... utrient in chemostat cultures.
@en
P2093
Hirotada Mori
Kazuyuki Shimizu
Taku Oshima
P2860
P304
P356
10.1128/AEM.70.4.2354-2366.2004
P407
P577
2004-04-01T00:00:00Z