论文引用

Alfredo Martínez, Francisco Bolívar, Octavio T. Ramírez et al.,
2005,
Journal of Molecular Microbiology and Biotechnology

We report a study to determine the role of pyruvate oxidase among Escherichia coli isogenic strains with active and inactive phosphoenolpyruvate:carbohydrate phosphotransferase system (PTS). Strain PB...

K. Hokamp, W. Hardt, J. Puente et al.,
2016,
PLoS genetics

We know a great deal about the genes used by the model pathogen Salmonella enterica serovar Typhimurium to cause disease, but less about global gene regulation. New tools for studying transcripts at t...

Alex Toftgaard Nielsen, G. Schoolnik, G. Otto et al.,
2006,
PLoS pathogens

Vibrio cholerae causes a severe diarrhoeal disease by secreting a toxin during colonization of the epithelium in the small intestine. Whereas the initial steps of the infectious process have been inte...

R. Herrmann, G. Browning, J. Weiner et al.,
2000,
Nucleic acids research

Very little is understood of the structure of mycoplasma promoters, and this limits interpretation of genomic sequence data in these species. In this study the transcriptional start points of 22 genes...

E. Groisman, A. Y. Mitrophanov, Eduardo A Groisman et al.,
2008,
Genes & development

Two-component systems (TCSs) and phosphorelays are key mediators of bacterial signal transduction. The signals activating these systems promote the phosphorylated state of a response regulator, which ...

Joshua S Weitz, Christopher J Marx, Ivana Gudelj et al.,
2010,
Ecology letters

Trade-offs have been put forward as essential to the generation and maintenance of diversity. However, variation in trade-offs is often determined at the molecular level, outside the scope of conventi...

Vivek K. Mutalik, A. Arkin, A. Deutschbauer et al.,
2020,
Microbiology

Though bacteriophages (phages) are known to play a crucial role in bacterial fitness and virulence, our knowledge about the genetic basis of their interaction, cross-resistance and host-range is spars...

C. Patten, H. Schellhorn, Guozhu Chen et al.,
2004,
Mutation research

Though RpoS, an alternative sigma factor, is required for survival and adaptation of Escherichia coli under stress conditions, many strains have acquired independent mutations in the rpoS gene. The re...

J. Helmann,
2011

This chapter summarizes the alternative sigma factors of the two model organisms (Escherichia coli and Bacillus subtilis), describes the types of regulatory pathways that have evolved to control σ act...

Hirotada Mori, Kiyotaka Y Hara, Tomoya Baba et al.,
2009,
FEMS microbiology letters

There is an ongoing demand to improve the ATP-regenerating system for industrial ATP-driven bioprocesses because of the low efficiency of ATP regeneration. To address this issue, we investigated the e...

Karsten Niehaus, Karl Friehs, Tino Polen et al.,
2007,
Journal of biotechnology

The use of Escherichia coli as a model organism has provided a great deal of basic information in biomolecular sciences. Examining trait differences among closely related strains of the same species a...

Torsten Waldminghaus, F. Narberhaus, Nadja Heidrich et al.,
2007,
Molecular microbiology

The translation of many heat shock and virulence genes is controlled by RNA thermometers. Usually, they are located in the 5′‐untranslated region (5′‐UTR) and block the Shine‐Dalgarno (SD) sequence by...

S. Harcum, Fu'ad T Haddadin, Sarah W Harcum et al.,
2005,
Biotechnology and bioengineering

The transcriptome profiles for wild-type (plasmid-free) and recombinant (plasmid-bearing) Escherichia coli during well-controlled synchronized high-cell-density fed-batch cultures were analyzed by DNA...

Thomas Nyström, T. Nyström, T. Silhavy et al.,
2007,
Genes & development

The sigma(S) subunit of RNA polymerase is a master regulator of Escherichia coli that retards cellular senescence and bestows cells with general stress protective functions during growth arrest. We sh...

S. Gottesman, X. Tu, T. Latifi et al.,
2006,
Proceedings of the National Academy of Sciences

The sigma factor RpoS regulates the expression of many stress response genes and is required for virulence in several bacterial species. We now report that RpoS accumulates when Salmonella enterica se...

Francisco Bolívar, César Aguilar, Noemí Flores et al.,
2008,
Journal of Molecular Microbiology and Biotechnology

The ptsHIcrr operon was deleted from Escherichia coli wild-type JM101 to generate strain PB11 (PTS–). In a mutant derived from PB11 that partially recovered its growth capacity on glucose by an adapti...

S. Rosenberg, P. Hastings, Susan M Rosenberg et al.,
2004,
Research in microbiology

The neo-Darwinists suggested that evolution is constant and gradual, and thus that genetic changes that drive evolution should be too. However, more recent understanding of phenomena called adaptive m...

T. Cebula, M. Kotewicz, E. Brown et al.,
2003,
Trends in microbiology

The mutS-rpoS intergenic region of enteric bacteria ranges in size from 88 bp in Yersinia to > 12000 bp in Salmonella. We interpret this expansion as the result of the horizontal transfer of segments ...

G. Schoolnik, M. Voskuil, M I Voskuil et al.,
2004,
Tuberculosis

The innate mechanisms used by Mycobacterium tuberculosis to persist during periods of non-proliferation are central to understanding the physiology of the bacilli during latent disease. We have used w...

Regine Hengge, Franziska Mika, R. Hengge et al.,
2005,
Genes & development

The general stress sigma factor sigma(S) (RpoS) in Escherichia coli is controlled at the levels of transcription, translation, and proteolysis. Here we demonstrate that the phosphorylated response reg...