# Single-cell pigment analysis of phototrophic and phyllosphere bacteria using simultaneous detection of Raman and autofluorescence spectra

## TL;DR

This paper introduces a nondestructive method to analyze pigments in single microbial cells, helping to understand their biology and find useful microbes.

## Contribution

A new method for simultaneous detection of Raman and autofluorescence spectra in single microbial cells is developed.

## Key findings

- Resonance Raman spectra reveal carotenoid structure and chain length in phototrophic bacteria.
- Autofluorescence spectra differ based on bacteriochlorophyll type, indicating distinct origins.
- Pigment diversity was observed on leaf surfaces, revealing potential for discovering new microbes.

## Abstract

Microbes produce various types of pigments that are essential for their biological activities. Microbial pigments are important for humans because they are used in the food industry and medicine. The visualization and evaluation of the pigment diversity of microbial cells living in natural environments will contribute not only to the understanding of their ecophysiology but also to the screening of useful microbes. Here, we demonstrate the simultaneous, nondestructive detection of the resonance Raman and autofluorescence spectra of pigments in model purple phototrophic bacteria at the single-cell level. The single-cell Raman spectra measured using confocal laser Raman microspectroscopy with 632.8 nm excitation covered the wavenumber range of 660–3,022 cm−1 (corresponding to 661–783 nm), in which the autofluorescence spectra from the pigments can be detected simultaneously as a baseline. The peak position of the resonance Raman spectra of the carotenoids in the cells provided information on the length of the polyene chain and structural characteristics, such as conjugated keto groups and terminal rings. By contrast, the extracted autofluorescence spectra of purple phototrophic bacteria differed in pattern depending on bacteriochlorophyll type (a or b), suggesting that their autofluorescence originates from bacteriochlorophyll-related molecules. In addition, we revealed the pigment diversity in microbial cells on the leaf surface and isolated pigmented bacteria that could contribute to the pigment diversity of the environmental sample. Our study shows that Raman and fluorescence microspectroscopy is a useful tool for finding novel pigmented microbes and uncovering yet unknown relationships between microbes and light.

To understand the activities of microbes in natural environments, it is important to know the types of biomolecules they express in situ. In this study, we report a method using resonance Raman and autofluorescence signatures to detect and distinguish the types of carotenoid and bacteriochlorophyll pigments in intact, living cells. We have shown that this method can be used to estimate the expression status and pigment types in purple phototrophic bacteria and carotenoid-producing bacteria as well as the diversity of the pigments expressed by microbes on the leaf surface. Our method requires little pretreatment and can analyze pigments without destroying cells, making it a useful tool for visualizing phototrophic activity and searching for unidentified microbes.