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Visualizing and isolating iron-reducing microorganisms at single cell level

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Abstract Iron-reducing microorganisms (FeRM) play key roles in many natural and engineering processes. Visualizing and isolating FeRM from multispecies samples are essential to understand the in-situ location and geochemical role of FeRM. Here, we visualized FeRM by a “turn-on” Fe 2+ -specific fluorescent chemodosimeter (FSFC) with high sensitivity, selectivity and stability. This FSFC could selectively identify and locate active FeRM from either pure culture, co-culture of different bacteria or sediment-containing samples. Fluorescent intensity of the FSFC could be used as an indicator of Fe 2+ concentration in bacterial cultures. By integrating FSFC with a single cell sorter, we obtained three FSFC-labeled cells from an enriched consortia and all of them were subsequently evidenced to be capable of iron-reduction and two unlabeled cells were evidenced to have no iron-reducing capability, further confirming the feasibility of the FSFC. Importance Visualization and isolation of FeRM from samples containing multispecies are commonly needed by researchers from different disciplines, such as environmental microbiology, environmental sciences and geochemistry. However, no available method has been reported. In this study, we provid a solution to visualize FeRM and evaluate their activity even at single cell level. Integrating with single cell sorter, FeRM can also be isolated from samples containing multispecies. This method can be used as a powerful tool to uncover the in-situ or ex-situ role of FeRM and their interactions with ambient microbes or chemicals.
Title: Visualizing and isolating iron-reducing microorganisms at single cell level
Description:
Abstract Iron-reducing microorganisms (FeRM) play key roles in many natural and engineering processes.
Visualizing and isolating FeRM from multispecies samples are essential to understand the in-situ location and geochemical role of FeRM.
Here, we visualized FeRM by a “turn-on” Fe 2+ -specific fluorescent chemodosimeter (FSFC) with high sensitivity, selectivity and stability.
This FSFC could selectively identify and locate active FeRM from either pure culture, co-culture of different bacteria or sediment-containing samples.
Fluorescent intensity of the FSFC could be used as an indicator of Fe 2+ concentration in bacterial cultures.
By integrating FSFC with a single cell sorter, we obtained three FSFC-labeled cells from an enriched consortia and all of them were subsequently evidenced to be capable of iron-reduction and two unlabeled cells were evidenced to have no iron-reducing capability, further confirming the feasibility of the FSFC.
Importance Visualization and isolation of FeRM from samples containing multispecies are commonly needed by researchers from different disciplines, such as environmental microbiology, environmental sciences and geochemistry.
However, no available method has been reported.
In this study, we provid a solution to visualize FeRM and evaluate their activity even at single cell level.
Integrating with single cell sorter, FeRM can also be isolated from samples containing multispecies.
This method can be used as a powerful tool to uncover the in-situ or ex-situ role of FeRM and their interactions with ambient microbes or chemicals.

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