% IMPORTANT: The following is UTF-8 encoded. This means that in the presence
% of non-ASCII characters, it will not work with BibTeX 0.99 or older.
% Instead, you should use an up-to-date BibTeX implementation like “bibtex8” or
% “biber”.
@INPROCEEDINGS{Matsubara:865232,
author = {Matsubara, Shizue and Thiele, Björn and Banh, Anh and
Chlubek and Hombach, Thomas and Neuwohner, Andrea and
Janzik, Ingar and Jahnke, Siegfried and Kleist, Einhard},
title = {{T}oward understanding the regulation of carotenoid
turnover in plants},
reportid = {FZJ-2019-04763},
year = {2019},
abstract = {Progress in plant carotenoid research has brought the
scientific community genetic and molecular tools to
manipulate carotenoid composition and accumulation in model
plants and crops. However, the outcome of such manipulation
often remains unpredictable due to many “unknowns” in
feedback regulation, protein modification and interaction,
or compartmentalization. Unravelling the mechanisms that
control flux, partitioning and sequestration in carotenoid
biosynthesis and degradation pathways necessitates, among
other things, turnover analysis of pathway intermediates and
products. Isotopic labelling has been a powerful tool for
investigation of metabolic pathways in cells and plants.
Photosynthetic CO2 fixation enables convenient incorporation
of carbon isotopes in various metabolites under various
conditions. While incorporation can be observed within
seconds to minutes in and around primary metabolism, it can
take hours to days for specialized metabolism, including
that of carotenoids and apocarotenoids in photosynthetic and
non-photosynthetic organs. Despite high sensitivity of
detection, radioactive 14C is difficult to quantify at the
molecular level and experiments inevitably generate
radioactive waste. Here, we present whole-plant 13CO2
labelling systems combined with LC-MS and FTICR-MS analysis
to study carotenoid turnover. Two experiments were conducted
to test the applicability of the method. In the first
experiment, a walk-in climate chamber was used to obtain
13C-labelled peppermint plants. Subsequently, changes in
carotenoid isotopologue composition were monitored in leaves
of these plants in ambient air. In the second experiment,
Arabidopsis plants grown in ambient air were transferred to
a small 13CO2 labelling chamber to analyze 13C incorporation
in leaf pigments for up to seven days. The mass spectra of
carotenoids obtained from the two experiments showed similar
patterns of isotopologue peaks, indicating that the method
is compatible with pulse-chase labelling experiments in both
directions (13CO2/12CO2 and 12CO2/13CO2). This approach
opens up new possibilities to elucidate the regulation of
carotenoid metabolism in plants.},
month = {Nov},
date = {2019-11-25},
organization = {International Conference on Carotenoid
Research, Lemesos (Cyprus), 25 Nov 2019
- 28 Nov 2019},
subtyp = {Other},
cin = {IBG-2},
cid = {I:(DE-Juel1)IBG-2-20101118},
pnm = {582 - Plant Science (POF3-582)},
pid = {G:(DE-HGF)POF3-582},
typ = {PUB:(DE-HGF)6},
url = {https://juser.fz-juelich.de/record/865232},
}