2021
DOI: 10.1007/s11120-020-00812-0
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The different patterns of post-heat stress responses in wheat genotypes: the role of the transthylakoid proton gradient in efficient recovery of leaf photosynthetic capacity

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Cited by 23 publications
(16 citation statements)
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“…The sensitive plants had much lower ECS t than expected according to a low ETR PSII , but, at the same time, they showed a high proton conductivity (gH + ) resulting in a high proton flux, which was, evidently, not proportional to the observed electron transport rate. We previously observed a similar trend in wheat exposed to high temperatures (Chovancek et al 2021 ), which can be well explained by the leaks of H + through the thylakoid membrane (Bukhov et al 1999 ; Havaux et al 1996 ).…”
Section: Discussionsupporting
confidence: 66%
See 1 more Smart Citation
“…The sensitive plants had much lower ECS t than expected according to a low ETR PSII , but, at the same time, they showed a high proton conductivity (gH + ) resulting in a high proton flux, which was, evidently, not proportional to the observed electron transport rate. We previously observed a similar trend in wheat exposed to high temperatures (Chovancek et al 2021 ), which can be well explained by the leaks of H + through the thylakoid membrane (Bukhov et al 1999 ; Havaux et al 1996 ).…”
Section: Discussionsupporting
confidence: 66%
“…Data are presented as the mean value ± standard error (SE) from 10 to 20 leaves the proper regulation of linear electron transport is crucial, which requires the buildup of the transthylakoid proton gradient (Joliot and Johnson 2011). A low ECS t in salt-stress exposed plants of susceptible genotypes in our experiment shows that the accumulation of H + in thylakoid lumen was insufficient, which leads to a poor regulation of electron transport and over reduction of PSI acceptor side (Miyake et al 2005;Chovancek et al 2021). The related excessive production of reactive oxygen species may be responsible for the observed damage of photosynthetic components evident in chlorophyll fluorescence measurements as well as the decrease of chlorophyll content in leaves of susceptible wheat genotypes.…”
Section: Discussionmentioning
confidence: 78%
“…However, none of these studies capture the extent of the reversal of physiological or molecular responses during the post-stress recovery phase to ascertain the level of phenotypic plasticity in plants. There are some papers that address this question in trees (Ameye et al, 2012;Haldimann & Feller, 2004;Hamerlynck & Knapp, 1996;Rueher et al, 2016) and in crops, including grape leaves (Liu et al, 2012), rice seedlings (Mangrauthia et al, 2017) and recent work on the recovery of photosynthetic capacity in wheat and spinach (Agrawal & Jajoo, 2021;Chovancek, Zivcak, Brestic, Hussain, & Allakhverdiev, 2021) and starch levels in cotton leaves (Loka, Oosterhuis, Baxevanos, Noulas, & Hu, 2020). Additionally, post-stress photosynthetic recovery in fieldgrown maize and soybeans (Siebers et al, 2015(Siebers et al, , 2017 has been recorded, as has the rapid recovery of leaf total non-structural carbohydrate levels after 12 hr of stress (Siebers et al, 2015).…”
Section: Developmental Stage Is a Crucial Determinant Of Plant Vulnerability To Heatmentioning
confidence: 99%
“…Similarly, wheat genotypes of different origins have been evaluated to assess stress responses and mechanisms of stress tolerance [33][34][35]. Although multiple studies have focused on different traits associated with drought tolerance in wheat, including cuticular transpiration, studies providing information on variability in a diverse collection of wheat genetic responses are rather scarce.…”
Section: Introductionmentioning
confidence: 99%