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Damage-free light-induced assembly of intestinal bacteria with a bubble-mimetic substrate
Rapid evaluation of functions in densely assembled bacteria is a crucial issue in the efficient study of symbiotic mechanisms. If the interaction between many living microbes can be controlled and accelerated via remote assembly, a cultivation process requiring a few days can be ommitted, thus leadi...
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Published in: | Communications biology 2021-03, Vol.4 (1), p.385-385, Article 385 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Rapid evaluation of functions in densely assembled bacteria is a crucial issue in the efficient study of symbiotic mechanisms. If the interaction between many living microbes can be controlled and accelerated via remote assembly, a cultivation process requiring a few days can be ommitted, thus leading to a reduction in the time needed to analyze the bacterial functions. Here, we show the rapid, damage-free, and extremely dense light-induced assembly of microbes over a submillimeter area with the “bubble-mimetic substrate (BMS)”. In particular, we successfully assembled 10
4
–10
5
cells of lactic acid bacteria (
Lactobacillus casei
), achieving a survival rate higher than 95% within a few minutes without cultivation process. This type of light-induced assembly on substrates like BMS, with the maintenance of the inherent functions of various biological samples, can pave the way for the development of innovative methods for rapid and highly efficient analysis of functions in a variety of microbes.
Hayashi et al. propose a method to realise rapid, damage-free, remote light-induced assembly of microbes over a submillimeter area with the “bubble-mimetic substrate”. They assemble 10
4
–10
5
cells of lactic acid bacteria with a survival rate higher than 95% around a laser spot. This technique is promising in developing methods for rapid and high-efficiency functional analysis of microbes. |
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ISSN: | 2399-3642 2399-3642 |
DOI: | 10.1038/s42003-021-01807-w |