Tailoring confocal microscopy for real-time analysis of photosynthesis at single-cell resolution

Cell Rep Methods. 2023 Sep 25;3(9):100568. doi: 10.1016/j.crmeth.2023.100568. Epub 2023 Aug 28.

Abstract

Photoautotrophs' environmental responses have been extensively studied at the organism and ecosystem level. However, less is known about their photosynthesis at the single-cell level. This information is needed to understand photosynthetic acclimation processes, as light changes as it penetrates cells, layers of cells, or organs. Furthermore, cells within the same tissue may behave differently, being at different developmental/physiological stages. Here, we describe an approach for single-cell and subcellular photophysiology based on the customization of confocal microscopy to assess chlorophyll fluorescence quenching by the saturation pulse method. We exploit this setup to (1) reassess the specialization of photosynthetic activities in developing tissues of non-vascular plants; (2) identify a specific subpopulation of phytoplankton cells in marine photosymbiosis, which consolidate energetic connections with their hosts; and (3) examine the link between light penetration and photoprotection responses inside the different tissues that constitute a plant leaf anatomy.

Keywords: 3D reconstruction; CP: Imaging; CP: Plants; confocal microscopy; fluorescence integration; light penetration; non-vascular and vascular plants; photoprotection; phytoplankton.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Ecosystem*
  • Heart Rate
  • Microscopy, Confocal
  • Photosynthesis*
  • Phytoplankton