Abstract

Microalga-based biomaterial production has attracted attention as a new source of drugs, foods, and biofuels. For enhancing the production efficiency, it is essential to understand its differences between heterogeneous microalgal subpopulations. However, existing techniques are not adequate to address the need due to the lack of single-cell resolution or the inability to perform large-scale analysis and detect small molecules. Here we demonstrated large-scale single-cell analysis of Euglena gracilis (a unicellular microalgal species that produces paramylon as a potential drug for HIV and colon cancer) with our recently developed high-throughput broadband Raman flow cytometer at a throughput of >1,000 cells/s. Specifically, we characterized the intracellular content of paramylon from single-cell Raman spectra of 10,000 E. gracilis cells cultured under five different conditions and found that paramylon contents in E. gracilis cells cultured in an identical condition is given by a log-normal distribution, which is a good model for describing the number of chemicals in a reaction network. The capability of characterizing distribution functions in a label-free manner is an important basis for isolating specific cell populations for synthetic biology via directed evolution based on the intracellular content of metabolites.

Highlights

  • Natural products of microalgae have great potential for use in industry and medicine [1,2]

  • We demonstrate large-scale single-cell analysis of Euglena gracilis with our recently developed high-throughput broadband Raman flow cytometer at a throughput of >1,000 cells/s. [19]

  • We found that the intracellular paramylon content was well fitted by a log-normal distribution, which is a good model for describing the amount of chemicals in a reaction network [24]

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Summary

Introduction

Natural products of microalgae have great potential for use in industry and medicine [1,2]. Fluorescence-based flow cytometry is a powerful method for quantifying relatively larger intracellular biomolecules such as proteins and nucleic acids, its application to small metabolites is limited by the low binding specificity of fluorescent tags for smaller target molecules. To circumvent this problem, Raman microscopy has been exploited as a tool for evaluating various metabolites due to the availability of information about small molecules found in Raman spectra. Our findings pave the way towards a rapid and easy approach to assessing the biomaterial productivity of microalgae without the need for pretreatment of cells such as staining or target molecule extraction

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