Light Microscopy and Raman Imaging of Carotenoids in Plant Cells In Situ and in Released Carotene Crystals.

Tomasz Oleszkiewicz, Marta Z Pacia, Ewa Grzebelus, Rafal Baranski

Journal: Methods in molecular biology (Clifton, N.J.) 2021;2083():245-260

PMID: 31745927

Abstract

Light microscopy with a bright field mode offers an easy and fast examination of plant specimen for carotenoid presence in its cells. Using basic techniques such as hand sectioned or squashed preparations, carotenoid-rich chromoplasts can be identified without applying any staining procedure and their localization within the cell, their shape and number can be assessed. More detailed information can be obtained by using Raman spectroscopy which is suitable for the analysis of carotenoids due to their unique Raman spectra and allows semiquantification of their contents. Raman imaging (mapping) can be additionally used to show the distribution of carotenoids within the sample. Raman spectra can be taken from extracted carotenoids but can be also obtained directly from plant tissues or cells as Raman measurements are nondestructive for the sample. Here we describe preparations of intact tissue samples, monolayer cell samples, isolated protoplasts as well as carotene crystals released from chromoplasts that are suitable for subsequent observations using light microscopy and for analysis using Raman spectroscopy.

Address: Faculty of Biotechnology and Horticulture, Department of Plant Biology and Biotechnology, University of Agriculture in Krakow, Krakow, Poland.; Jagiellonian Centre for Experimental Therapeutics (JCET), Jagiellonian University, Krakow, Poland.; Faculty of Biotechnology and Horticulture, Department of Plant Biology and Biotechnology, University of Agriculture in Krakow, Krakow, Poland. [email protected].

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