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Abstract
<p class="first" id="d14812153e71">Non-photochemical quenching (NPQ) is the most important
photoprotective system in
higher plants. NPQ can be divided into several steps according to the timescale of
relaxation of chlorophyll fluorescence after reaching a steady state (i.e., the fast
phase, qE; middle phase, qZ or qT; and slow phase, qI). The dissipation of excess
energy as heat during the xanthophyll cycle, a large component of NPQ, is detectable
during the fast to middle phase (sec to min). Although thermal dissipation is primarily
investigated using indirect methods such as chlorophyll a fluorescence measurements,
such analyses require dark adaptation or the application of a saturating pulse during
measurement, making it difficult to continuously monitor this process. Here, we designed
an unconventional technique for real-time monitoring of changes in thylakoid lumen
pH (as reflected by changes in xanthophyll pigment content) based on the photochemical
reflectance index (PRI), which we estimated by measuring light-driven leaf reflectance
at 531 nm. We analyzed two Arabidopsis thaliana mutants, npq1 (unable to convert violaxanthin
to zeaxanthin due to inhibited violaxanthin de-epoxidase [VDE] activity) and npq4
(lacking PsbS protein), to uncover the regulator of the PRI. The PRI was variable
in wild-type and npq4 plants, but not in npq1, indicating that the PRI is related
to xanthophyll cycle-dependent thermal energy quenching (qZ) rather than the linear
electron transport rate or NPQ. In situ lumen pH substitution using a pH-controlled
buffer solution caused a shift in PRI. These results suggest that the PRI reflects
only xanthophyll cycle conversion and is therefore a useful parameter for monitoring
thylakoid lumen pH (reflecting VDE activity) in vivo.
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