Analysis of Fast Fluorescence Kinetics of a Single Cyanobacterium Trapped in an Optical Microcavity

Author:

Rammler Tim12ORCID,Wackenhut Frank1ORCID,Rapp Johanna3,zur Oven-Krockhaus Sven12ORCID,Forchhammer Karl3ORCID,Meixner Alfred J.1,Harter Klaus2ORCID

Affiliation:

1. Institute for Physical and Theoretical Chemistry, University of Tübingen, 72076 Tübingen, Germany

2. Center for Plant Molecular Biology (ZMBP), University of Tübingen, 72076 Tübingen, Germany

3. Interfaculty Institute of Microbiology and Infection Medicine, University of Tübingen, 72076 Tübingen, Germany

Abstract

Photosynthesis is one the most important biological processes on earth, producing life-giving oxygen, and is the basis for a large variety of plant products. Measurable properties of photosynthesis provide information about its biophysical state, and in turn, the physiological conditions of a photoautotrophic organism. For instance, the chlorophyll fluorescence intensity of an intact photosystem is not constant as in the case of a single fluorescent dye in solution but shows temporal changes related to the quantum yield of the photosystem. Commercial photosystem analyzers already use the fluorescence kinetics characteristics of photosystems to infer the viability of organisms under investigation. Here, we provide a novel approach based on an optical Fabry–Pérot microcavity that enables the readout of photosynthetic properties and activity for an individual cyanobacterium. This approach offers a completely new dimension of information, which would normally be lost due to averaging in ensemble measurements obtained from a large population of bacteria.

Funder

VW foundation

Deutsche Forschungsgemeinschaft

Publisher

MDPI AG

Subject

Plant Science,Ecology,Ecology, Evolution, Behavior and Systematics

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