Photosynthetic Electron Transport Inhibition by Buthidazole

Weed Science ◽  
1981 ◽  
Vol 29 (1) ◽  
pp. 59-64 ◽  
Author(s):  
A. C. York ◽  
C. J. Arntzen ◽  
F. W. Slife

The effects of buthidazole {3-[5-(1,1-dimethylethyl)-1,3,4-thiadiazol-2-yl]-4-hydroxy-1-methyl-2-imidazolidinone} on the photochemical reactions of isolated pea (Pisum sativumL.) chloroplast thylakoids were analyzed. Buthidazole was found to inhibit electron transport at two distinct sites in the photosynthetic electron transport chain. The major site of inhibition was on the reducing side of photosystem II at the site of diuron [3-(3,4-dichlorophenyl)-1,1-dimethylurea] and atrazine [2-chloro-4-(ethylamino)-6-(isopropylamino)-s-triazine] inhibition. Buthidazole also had a secondary site of electron transport inhibition on the oxidizing side of photosystem II. No evidence was found for buthidazole to act as an uncoupler or as an energy transfer inhibitor.

Molecules ◽  
2021 ◽  
Vol 26 (19) ◽  
pp. 5958
Author(s):  
Nia Petrova ◽  
Momchil Paunov ◽  
Petar Petrov ◽  
Violeta Velikova ◽  
Vasilij Goltsev ◽  
...  

Single-walled carbon nanotubes (SWCNT) have recently been attracting the attention of plant biologists as a prospective tool for modulation of photosynthesis in higher plants. However, the exact mode of action of SWCNT on the photosynthetic electron transport chain remains unknown. In this work, we examined the effect of foliar application of polymer-grafted SWCNT on the donor side of photosystem II, the intersystem electron transfer chain and the acceptor side of photosystem I. Analysis of the induction curves of chlorophyll fluorescence via JIP test and construction of differential curves revealed that SWCNT concentrations up to 100 mg/L did not affect the photosynthetic electron transport chain. SWCNT concentration of 300 mg/L had no effect on the photosystem II donor side but provoked inactivation of photosystem II reaction centres and slowed down the reduction of the plastoquinone pool and the photosystem I end acceptors. Changes in the modulated reflection at 820 nm, too, indicated slower re-reduction of photosystem I reaction centres in SWCNT-treated leaves. We conclude that SWCNT are likely to be able to divert electrons from the photosynthetic electron transport chain at the level of photosystem I end acceptors and plastoquinone pool in vivo. Further research is needed to unequivocally prove if the observed effects are due to specific interaction between SWCNT and the photosynthetic apparatus.


Plants ◽  
2021 ◽  
Vol 10 (2) ◽  
pp. 276
Author(s):  
Wanying Chen ◽  
Bo Jia ◽  
Junyu Chen ◽  
Yujiao Feng ◽  
Yue Li ◽  
...  

The mutual shading among individual field-grown maize plants resulting from high planting density inevitably reduces leaf photosynthesis, while regulating the photosynthetic transport chain has a strong impact on photosynthesis. However, the effect of high planting density on the photosynthetic electron transport chain in maize currently remains unclear. In this study, we simultaneously measured prompt chlorophyll a fluorescence (PF), modulated 820 nm reflection (MR) and delayed chlorophyll a fluorescence (DF) in order to investigate the effect of high planting density on the photosynthetic electron transport chain in two maize hybrids widely grown in China. PF transients demonstrated a gradual reduction in their signal amplitude with increasing planting density. In addition, high planting density induced positive J-step and G-bands of the PF transients, reduced the values of PF parameters PIABS, RC/CSO, TRO/ABS, ETO/TRO and REO/ETO, and enhanced ABS/RC and N. MR kinetics showed an increase of their lowest point with increasing high planting density, and thus the values of MR parameters VPSI and VPSII-PSI were reduced. The shapes of DF induction and decay curves were changed by high planting density. In addition, high planting density reduced the values of DF parameters I1, I2, L1 and L2, and enhanced I2/I1. These results suggested that high planting density caused harm on multiple components of maize photosynthetic electron transport chain, including an inactivation of PSII RCs, a blocked electron transfer between QA and QB, a reduction in PSI oxidation and re-reduction activities, and an impaired PSI acceptor side. Moreover, a comparison between PSII and PSI activities demonstrated the greater effect of plant density on the former.


2020 ◽  
Vol 13 (9) ◽  
pp. 2903-2914 ◽  
Author(s):  
Andrey Kanygin ◽  
Yuval Milrad ◽  
Chandrasekhar Thummala ◽  
Kiera Reifschneider ◽  
Patricia Baker ◽  
...  

Photosystem I-hydrogenase chimera intercepts electron flow directly from the photosynthetic electron transport chain and directs it to hydrogen production.


1979 ◽  
Vol 34 (5-6) ◽  
pp. 427-430 ◽  
Author(s):  
Ursula Lehmann-Kirk ◽  
Georg H. Schmid ◽  
Alfons Radunz

Abstract An antiserum to violaxanthin in hibits photosynthetic electron transport between water, iodide or tetramethylbenzidine and various electron acceptors in chloroplasts from green tobacco (Nicotian a tabacum var. John William’s Broadleaf). However, electron transport from manganese or diphenyl-carbazide to these acceptors is not impaired. The typical photosystem I reaction from DPIP / ascorbate to anthraquinone-2-sulfonate in the presence of DCMU shows no inhibition. From this it is concluded that the effect of violaxanthin on the photosynthetic electron transport chain lies on the oxygen-evolving side of photosystem II before the site from which diphenylcarbazide or manganese donate electrons.In the presence of DCMU after preillumination we find an effect of the antiserum on fluorescence.The reaction of the antibodies to violaxanthin with stroma-freed chloroplasts depends on the condition of the thylakoid membrane. Chloroplasts which are still swellable react in a bivalent manner and are agglutinated. Non swellable chloroplasts react only in a monovalent manner. This specific binding was demonstrated by means of the Coombs-test.From these reactions it follows that the antigenic determinants of violaxanthin are accessible to the antibodies, hence, they must be located in the outer surface of the thylakoid membrane.


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