scholarly journals Modeling and CFD simulation of nutrient distribution in picoliter bioreactors for bacterial growth studies on single-cell level

Lab on a Chip ◽  
2015 ◽  
Vol 15 (21) ◽  
pp. 4177-4186 ◽  
Author(s):  
Christoph Westerwalbesloh ◽  
Alexander Grünberger ◽  
Birgit Stute ◽  
Sophie Weber ◽  
Wolfgang Wiechert ◽  
...  

A microfluidic device for microbial single-cell cultivation of bacteria was modeled and simulated to identify potential substrate limitations or product accumulations.

2008 ◽  
Vol 23 (8) ◽  
pp. 1303-1306 ◽  
Author(s):  
Jin-Hee Han ◽  
Brian C. Heinze ◽  
Jeong-Yeol Yoon

2021 ◽  
Author(s):  
Dongwei Chen ◽  
Mengyue Nie ◽  
Wei Tang ◽  
Yuwei Zhang ◽  
Yuxin Qiao ◽  
...  

Streptomyces is a model filamentous prokaryote to study multicellular differentiation and a rich reservoir for antibiotics discovery. In their natural conditions, Streptomyces grows at the interface of porous soil, air, and water. The morphological development of Streptomyces is traditionally performed on agar plates and mostly studied at the population levels. However, the detailed lifecycle of Streptomyces has not been well studied due to its complexity and lack of research tools which can mimic their natural conditions in the soil. Here, we developed a simple assembled microfluidic device for cultivation and the entire lifecycle observation of Streptomyces development from single-cell level. The microfluidic device composed of a microchannel for loading samples and supplying nutrients, microwell arrays for seeding and growth of single spores, and air-filled chambers aside of the microwells that facilitate growth of aerial hyphae and spores. A unique feature of this device is that each microwell is surrounded by a 1.5 μm gap connected to an air-filled chamber which provide stabilized water-air interface. We used this device to observe the development of single Streptomyces spores and found that unlike those in bulk liquid culture, Streptomyces can differentiate at water-air interfaces in microscale liquid culture. Finally, we demonstrated that phenotypic A-Factor assay can be performed at defined time point of its lifecycle. This microfluidic device could become a robust tool for studying Streptomyces multi-cellular differentiation and interaction at single cell level.


2017 ◽  
Vol 9 (3) ◽  
pp. 238-247 ◽  
Author(s):  
Ariel S. Kniss-James ◽  
Catherine A. Rivet ◽  
Loice Chingozha ◽  
Hang Lu ◽  
Melissa L. Kemp

Integration of a microfluidic device with live cell imaging enables the application of control theory for analyzing features T cell signaling at the single cell level.


Author(s):  
Felix Weber ◽  
Tatiana Zaliznyak ◽  
Virginia P. Edgcomb ◽  
Gordon T. Taylor

The suitability of stable isotope probing (SIP) and Raman microspectroscopy to measure growth rates of heterotrophic bacteria at the single-cell level was evaluated. Label assimilation into E. coli biomass during growth on a complex 13 C-labeled carbon source was monitored in time course experiments. 13 C-incorporation into various biomolecules was measured by spectral “red shifts” of Raman-scattered emissions. The 13 C- and 12 C-isotopologues of the amino acid phenylalanine (Phe) proved to be a quantitatively accurate reporter molecules of cellular isotopic fractional abundances ( f cell ). Values of f cell determined by Raman microspectroscopy and independently by isotope-ratio mass spectrometry (IRMS) over a range of isotopic enrichments were statistically indistinguishable. Progressive labeling of Phe in E. coli cells among a range of 13 C/ 12 C organic substrate admixtures occurred predictably through time. Relative isotopologue abundances of Phe determined by Raman spectral analysis enabled accurate calculation of bacterial growth rates as confirmed independently by optical density (OD) measurements. Results demonstrate that combining stable isotope probing (SIP) and Raman microspectroscopy can be a powerful tool for studying bacterial growth at the single-cell level when grown on defined or complex organic 13 C-carbon sources even in mixed microbial assemblages. Importance: Population growth dynamics and individual cell growth rates are the ultimate expressions of a microorganism’s fitness to its environmental conditions, whether natural or engineered. Natural habitats and many industrial settings harbor complex microbial assemblages. Their heterogeneity in growth responses to existing and changing conditions is often difficult to grasp by standard methodologies. In this proof of concept study, we tested whether Raman microspectroscopy can reliably quantify assimilation of isotopically-labeled nutrients into E. coli cells and enable determination of individual growth rates among heterotrophic bacteria. Raman-derived growth rate estimates were statistically indistinguishable from those derived by standard optical density measurements of the same cultures. Raman microspectroscopy also can be combined with methods for phylogenetic identification. We report development of Raman-based techniques that enable researchers to directly link genetic identity to functional traits and rate measurements of single cells within mixed microbial assemblages, currently a major technical challenge in microbiological research.


The Analyst ◽  
2019 ◽  
Vol 144 (8) ◽  
pp. 2811-2819
Author(s):  
Chenyu Wang ◽  
Lufeng Ren ◽  
Wenwen Liu ◽  
Qingquan Wei ◽  
Manqing Tan ◽  
...  

We present an integrated microfluidic device for quantifying intracellular materials at the single-cell level.


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