scholarly journals Deciphering the physiological response of Escherichia coli under high ATP demand

2021 ◽  
Vol 17 (12) ◽  
Author(s):  
Simon Boecker ◽  
Giulia Slaviero ◽  
Thorben Schramm ◽  
Witold Szymanski ◽  
Ralf Steuer ◽  
...  
2020 ◽  
Vol 30 (10) ◽  
pp. 1592-1596 ◽  
Author(s):  
Alvaro R. Lara ◽  
Janet Galindo ◽  
Karim E. Jaén ◽  
Mariana Juárez ◽  
Juan-Carlos Sigala

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Shlomo E. Blum ◽  
Dan E. Heller ◽  
Shamay Jacoby ◽  
Oleg Krifuks ◽  
Uzi Merin ◽  
...  

An amendment to this paper has been published and can be accessed via a link at the top of the paper.


2016 ◽  
Vol 186-187 ◽  
pp. 27-36 ◽  
Author(s):  
Dongjie Fan ◽  
Chuanpeng Liu ◽  
Lushan Liu ◽  
Lingxiang Zhu ◽  
Fang Peng ◽  
...  

2017 ◽  
Vol 100 (10) ◽  
pp. 8385-8397 ◽  
Author(s):  
Alice de Boyer des Roches ◽  
Marion Faure ◽  
Alexandra Lussert ◽  
Vincent Herry ◽  
Pascal Rainard ◽  
...  

2011 ◽  
Vol 77 (19) ◽  
pp. 7040-7049 ◽  
Author(s):  
Stéphanie Heux ◽  
Benjamin Philippe ◽  
Jean-Charles Portais

ABSTRACTMiniaturization and high-throughput screening are currently the focus of emerging research areas such as systems biology and systems biotechnology. A fluorescence-based screening assay for the online monitoring of oxygen and pH and a numerical method to mine the resulting online process data are described. The assay employs commercial phosphorescent oxygen- and pH-sensitive probes in standard 48- or 96-well plates on a plate reader equipped with a shaker. In addition to dual parametric analysis of both pH and oxygen in a single well, the assay allows monitoring of growth, as measured by absorbance. Validation of the assay is presented and compared with commercially available plates equipped with optical sensors for oxygen and pH. By using model-free fitting to the readily available online measurements, the length and rate of each phase such as the duration of lag and transition phase or acidification, growth, and oxygen consumption rates are automatically detected. In total, nine physiological descriptors, which can be used for further statistical and comparison analysis, are extracted from the pH, oxygen partial pressure (pO2), and optical density (OD) profiles. The combination of a simple mix-and-measure procedure with an automatic data mining method allows high sample throughput and good reproducibility while providing a physiological state identification and characterization of test cells. As a proof of concept, the utility of the workflow in assessing the physiological response ofEscherichia colito environmental and genetic perturbations is demonstrated.


Author(s):  
G. Stöffler ◽  
R.W. Bald ◽  
J. Dieckhoff ◽  
H. Eckhard ◽  
R. Lührmann ◽  
...  

A central step towards an understanding of the structure and function of the Escherichia coli ribosome, a large multicomponent assembly, is the elucidation of the spatial arrangement of its 54 proteins and its three rRNA molecules. The structural organization of ribosomal components has been investigated by a number of experimental approaches. Specific antibodies directed against each of the 54 ribosomal proteins of Escherichia coli have been performed to examine antibody-subunit complexes by electron microscopy. The position of the bound antibody, specific for a particular protein, can be determined; it indicates the location of the corresponding protein on the ribosomal surface.The three-dimensional distribution of each of the 21 small subunit proteins on the ribosomal surface has been determined by immuno electron microscopy: the 21 proteins have been found exposed with altogether 43 antibody binding sites. Each one of 12 proteins showed antibody binding at remote positions on the subunit surface, indicating highly extended conformations of the proteins concerned within the 30S ribosomal subunit; the remaining proteins are, however, not necessarily globular in shape (Fig. 1).


Author(s):  
Manfred E. Bayer

Bacterial viruses adsorb specifically to receptors on the host cell surface. Although the chemical composition of some of the cell wall receptors for bacteriophages of the T-series has been described and the number of receptor sites has been estimated to be 150 to 300 per E. coli cell, the localization of the sites on the bacterial wall has been unknown.When logarithmically growing cells of E. coli are transferred into a medium containing 20% sucrose, the cells plasmolize: the protoplast shrinks and becomes separated from the somewhat rigid cell wall. When these cells are fixed in 8% Formaldehyde, post-fixed in OsO4/uranyl acetate, embedded in Vestopal W, then cut in an ultramicrotome and observed with the electron microscope, the separation of protoplast and wall becomes clearly visible, (Fig. 1, 2). At a number of locations however, the protoplasmic membrane adheres to the wall even under the considerable pull of the shrinking protoplast. Thus numerous connecting bridges are maintained between protoplast and cell wall. Estimations of the total number of such wall/membrane associations yield a number of about 300 per cell.


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