4.6 Article

High-Pressure Microfluidics for Ultra-Fast Microbial Phenotyping

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FRONTIERS IN MICROBIOLOGY
卷 13, 期 -, 页码 -

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FRONTIERS MEDIA SA
DOI: 10.3389/fmicb.2022.866681

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high-pressure microfluidics; deep-sea microorganisms; real time investigations; phenotyping; fast screening

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In this study, a novel methodology based on high-pressure microfluidics was developed for rapid temperature-based phenotyping of microbial strains from deep-sea environments. The main advantage lies in the ability to achieve multiple on-chip temperature conditions at pressures representative of the deep-sea in a single experiment, overcoming the limitations of conventional large-scale batch metal reactors. Results showed that the growth of the model strain Thermococcus barophilus could be monitored over 40 temperature and pressure conditions in just 1 week without any decompression, which is significantly faster compared to conventional approaches. The robustness of this methodology was further demonstrated with an additional example using a hydrogenotrophic methanogen strain.
Here, we present a novel methodology based on high-pressure microfluidics to rapidly perform temperature-based phenotyping of microbial strains from deep-sea environments. The main advantage concerns the multiple on-chip temperature conditions that can be achieved in a single experiment at pressures representative of the deep-sea, overcoming the conventional limitations of large-scale batch metal reactors to conduct fast screening investigations. We monitored the growth of the model strain Thermococcus barophilus over 40 temperature and pressure conditions, without any decompression, in only 1 week, whereas it takes weeks or months with conventional approaches. The results are later compared with data from the literature. An additional example is also shown for a hydrogenotrophic methanogen strain (Methanothermococcus thermolithotrophicus), demonstrating the robustness of the methodology. These microfluidic tools can be used in laboratories to accelerate characterizations of new isolated species, changing the widely accepted paradigm that high-pressure microbiology experiments are time-consuming.

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