A microfluidic system for the cultivation of cyanobacteria with precise light intensity and CO <sub>2</sub> control: enabling growth data acquisition at single-cell resolution

Quantification of cell growth is central to any study of photoautotrophic microorganisms. However, cellular self-shading and limited CO<sub>2</sub> control in conventional photobioreactors lead to heterogeneous conditions that obscure distinct correlations between the environment and cellular physiology. Here we present a microfluidic cultivation platform that enables precise analysis of cyanobacterial growth with spatio-temporal resolution. Since cyanobacteria are cultivated in monolayers, cellular self-shading does not occur, allowing homogeneous illumination and precise knowledge of the photon-flux density at single-cell resolution. A single chip contains multiple channels, each connected to several hundred growth chambers. In combination with an externally applied light gradient, this setup enables high-throughput multi-parameter analysis in short time. In addition, the multilayered microfluidic design allows continuous perfusion of defined gas mixtures. Transversal CO<sub>2</sub> diffusion across the intermediate polydimethylsiloxane membrane results in homogeneous CO<sub>2</sub> supply, with a unique exchange-surface to cultivation-volume ratio. Three cyanobacterial model strains were examined under various, static and dynamic environmental conditions. Phase-contrast and chlorophyll fluorescence images were recorded by automated time-lapse microscopy. Deep-learning trained cell segmentation was used to efficiently analyse large image stacks, thereby generating statistically reliable data. Cell division was highly synchronized, and growth was robust under continuous illumination but stopped rapidly upon initiating dark phases. CO<sub>2</sub>-Limitation, often a limiting factor in photobioreactors, was only observed when the device was operated under reduced CO<sub>2</sub> between 50 and 0 ppm. Here we provide comprehensive and precise data on cyanobacterial growth at single-cell resolution, accessible for further growth studies and modeling.

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Publication Details

Journal
Lab on a Chip
Published
2024-09-30
DOI
https://doi.org/10.1039/d4lc00567h
Citations
4
Primary Topic
Algal biology and biofuel production
Type
article
Field-Weighted Citation Impact
0.41

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article

A microfluidic system for the cultivation of cyanobacteria with precise light intensity and CO 2 control: enabling growth data acquisition at single-cell resolution

Dietrich Kohlheyer, Andreas P.M. Weber, Birgit Stute, Marion Eisenhut et al.
4 citations
Lab on a Chip
Algal biology and biofuel production
0.41
article

A microfluidic system for the cultivation of cyanobacteria with precise light intensity and CO 2 control: enabling growth data acquisition at single-cell resolution

Dietrich Kohlheyer, Andreas P.M. Weber, Birgit Stute, Marion Eisenhut, Eric von Lieres, Katharina Nöh, T. F. Schulze, Johannes Seiffarth, Lennart Witting, Jan Matthis Hofer
article en
4 citations

Abstract

Quantification of cell growth is central to any study of photoautotrophic microorganisms. However, cellular self-shading and limited CO<sub>2</sub> control in conventional photobioreactors lead to heterogeneous conditions that obscure distinct correlations between the environment and cellular physiology. Here we present a microfluidic cultivation platform that enables precise analysis of cyanobacterial growth with spatio-temporal resolution. Since cyanobacteria are cultivated in monolayers, cellular self-shading does not occur, allowing homogeneous illumination and precise knowledge of the photon-flux density at single-cell resolution. A single chip contains multiple channels, each connected to several hundred growth chambers. In combination with an externally applied light gradient, this setup enables high-throughput multi-parameter analysis in short time. In addition, the multilayered microfluidic design allows continuous perfusion of defined gas mixtures. Transversal CO<sub>2</sub> diffusion across the intermediate polydimethylsiloxane membrane results in homogeneous CO<sub>2</sub> supply, with a unique exchange-surface to cultivation-volume ratio. Three cyanobacterial model strains were examined under various, static and dynamic environmental conditions. Phase-contrast and chlorophyll fluorescence images were recorded by automated time-lapse microscopy. Deep-learning trained cell segmentation was used to efficiently analyse large image stacks, thereby generating statistically reliable data. Cell division was highly synchronized, and growth was robust under continuous illumination but stopped rapidly upon initiating dark phases. CO<sub>2</sub>-Limitation, often a limiting factor in photobioreactors, was only observed when the device was operated under reduced CO<sub>2</sub> between 50 and 0 ppm. Here we provide comprehensive and precise data on cyanobacterial growth at single-cell resolution, accessible for further growth studies and modeling.

Lab on a ChipVol. 25(3)
Forschungszentrum Jülich (DE), Bielefeld University (DE), Heinrich Heine University Düsseldorf (DE), RWTH Aachen University (DE)
Deutsche Forschungsgemeinschaft, Helmholtz Association
Openalex Percentile: Top 47%
Algal biology and biofuel production
0.41
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