scholarly journals Metamitron, a Photosynthetic Electron Transport Chain Inhibitor, Modulates the Photoprotective Mechanism of Apple Trees

Plants ◽  
2021 ◽  
Vol 10 (12) ◽  
pp. 2803
Author(s):  
Yuval Tadmor ◽  
Amir Raz ◽  
Shira Reikin-Barak ◽  
Vivek Ambastha ◽  
Eli Shemesh ◽  
...  

Chemical thinning of apple fruitlets is an important practice as it reduces the natural fruit load and, therefore, increases the size of the final fruit for commercial markets. In apples, one chemical thinner used is Metamitron, which is sold as the commercial product Brevis® (Adama, Israel). This thinner inhibits the electron transfer between Photosystem II and Quinone-a within light reactions of photosynthesis. In this study, we investigated the responses of two apple cultivars—Golden Delicious and Top Red—and photosynthetic light reactions after administration of Brevis®. The analysis revealed that the presence of the inhibitor affects both cultivars’ energetic status. The kinetics of the photoprotective mechanism’s sub-processes are attenuated in both cultivars, but this seems more severe in the Top Red cultivar. State transitions of the antenna and Photosystem II repair cycle are decreased substantially when the Metamitron concentration is above 0.6% in the Top Red cultivar but not in the Golden Delicious cultivar. These attenuations result from a biased absorbed energy distribution between photochemistry and photoprotection pathways in the two cultivars. We suggest that Metamitron inadvertently interacts with photoprotective mechanism-related enzymes in chloroplasts of apple tree leaves. Specifically, we hypothesize that it may interact with the kinases responsible for the induction of state transitions and the Photosystem II repair cycle.

2021 ◽  
Vol 22 (8) ◽  
pp. 4021
Author(s):  
Monika Kula-Maximenko ◽  
Kamil Jan Zieliński ◽  
Ireneusz Ślesak

Gloeobacter violaceus is a cyanobacteria species with a lack of thylakoids, while photosynthetic antennas, i.e., phycobilisomes (PBSs), photosystem II (PSII), and I (PSI), are located in the cytoplasmic membrane. We verified the hypothesis that blue–red (BR) light supplemented with a far-red (FR), ultraviolet A (UVA), and green (G) light can affect the photosynthetic electron transport chain in PSII and explain the differences in the growth of the G. violaceus culture. The cyanobacteria were cultured under different light conditions. The largest increase in G. violaceus biomass was observed only under BR + FR and BR + G light. Moreover, the shape of the G. violaceus cells was modified by the spectrum with the addition of G light. Furthermore, it was found that both the spectral composition of light and age of the cyanobacterial culture affect the different content of phycobiliproteins in the photosynthetic antennas (PBS). Most likely, in cells grown under light conditions with the addition of FR and G light, the average antenna size increased due to the inactivation of some reaction centers in PSII. Moreover, the role of PSI and gloeorhodopsin as supplementary sources of metabolic energy in the G. violaceus growth is discussed.


2016 ◽  
Vol 11 (9) ◽  
pp. e1218587 ◽  
Author(s):  
Jasmine Theis ◽  
Michael Schroda

2018 ◽  
Vol 178 (2) ◽  
pp. 596-611 ◽  
Author(s):  
Yusuke Kato ◽  
Kiwamu Hyodo ◽  
Wataru Sakamoto

Plant Science ◽  
1996 ◽  
Vol 115 (2) ◽  
pp. 183-190 ◽  
Author(s):  
Douglas Campbell ◽  
Adrian K. Clarke ◽  
Petter Gustafsson ◽  
Gunnar Öquist

2014 ◽  
Vol 1837 (9) ◽  
pp. 1463-1471 ◽  
Author(s):  
Marjaana Suorsa ◽  
Marjaana Rantala ◽  
Ravi Danielsson ◽  
Sari Järvi ◽  
Virpi Paakkarinen ◽  
...  

2020 ◽  
Vol 117 (35) ◽  
pp. 21775-21784 ◽  
Author(s):  
Prakitchai Chotewutmontri ◽  
Alice Barkan

The D1 reaction center protein of photosystem II (PSII) is subject to light-induced damage. Degradation of damaged D1 and its replacement by nascent D1 are at the heart of a PSII repair cycle, without which photosynthesis is inhibited. In mature plant chloroplasts, light stimulates the recruitment of ribosomes specifically topsbAmRNA to provide nascent D1 for PSII repair and also triggers a global increase in translation elongation rate. The light-induced signals that initiate these responses are unclear. We present action spectrum and genetic data indicating that the light-induced recruitment of ribosomes topsbAmRNA is triggered by D1 photodamage, whereas the global stimulation of translation elongation is triggered by photosynthetic electron transport. Furthermore, mutants lacking HCF136, which mediates an early step in D1 assembly, exhibit constitutively highpsbAribosome occupancy in the dark and differ in this way from mutants lacking PSII for other reasons. These results, together with the recent elucidation of a thylakoid membrane complex that functions in PSII assembly, PSII repair, andpsbAtranslation, suggest an autoregulatory mechanism in which the light-induced degradation of D1 relieves repressive interactions between D1 and translational activators in the complex. We suggest that the presence of D1 in this complex coordinates D1 synthesis with the need for nascent D1 during both PSII biogenesis and PSII repair in plant chloroplasts.


Isolated heterocysts of the N 2 -fixing Anabaena cylindrica , prepared by a combination of lysozyme and Yeda press treatments, are metabolically active with over 90% of the measurable nitrogenase activity being located in the heterocyst preparations after disruption of the intact filaments. The photosynthetic activities of such isolated heterocysts are characterized by an inability to carry out the photolysis of water or to fix CO 2 . The lack of O 2 evolution appears to be due in part to the deple­tion during heterocyst differentiation of Mn, a central component of the photosystem II reaction centre in O 2 -evolving algae. There is evidence that components of the photosynthetic electron transport chain on the reducing side of the photosystem II reaction centre are present and functional in heterocysts. These include cytochrome c 554 , plastocyanin, plastoquinone, cytochrome b 559 , P700, cytochrome b 563 , and iron-sulphur proteins which appear to correspond to centre A and centre B of higher plant chloroplasts. Soluble, or loosely bound ferredoxin is also present and involved in electron transport from ferredoxin to NADP. Isolated heterocysts photoreduce methylviologen when reduced 2,6-dichlorophenolindophenol and diphenylcarbazide serve as electron donors. They show P700 photo-oxidation and photoreduction, photosyn­thetic electron transport which is inhibited by 2,5-dibromo-3-methyl-6-isopropyl- p -benzoquinone an antagonist of plastoquinone, photophos­phorylation, oxidative phosphorylation and ferredoxin-NADP oxido-reductase mediated reactions. The photosynthetic modifications of the heterocyst are such that electron transport and the generation of ATP for nitrogenase can occur without concomitant O 2 evolution and with­out nitrogenase having to compete with CO 2 fixation for ATP and reductant.


1980 ◽  
Vol 35 (1-2) ◽  
pp. 136-138 ◽  
Author(s):  
H. Daniell ◽  
G. Kulandaivelu ◽  
U. Chandra Singh

Abstract Substituted Benzoquinones, Photosystem II Acceptors Benzoquinones (BQ) substituted with alkyl or alkoxy groups 2,5-dimethoxy-3,6-dichloro-p-benzoquinone (DCDMQ), 2,3,5,6-tetramethoxy-p-benzoquinone (TMQ) have been tested for their electron affinity and site of action in the photosynthetic electron transport chain in whole cells and chloroplasts. Both the substituted compounds were found to be good electron acceptors of photosystem II. DCDMQ showed higher electron affinity than BQ as demonstrated by its two fold stimulation of O2 evolution in chloroplasts and efficiency in quenching DCMU fluorescence. TMQ on the other hand showed low electron affinity.


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