scholarly journals The effects of high concentrations of salts on photosynthetic electron transport in spinach (Spinacia oleracea) chloroplasts

1982 ◽  
Vol 204 (3) ◽  
pp. 705-712 ◽  
Author(s):  
A C Stewart

1. Photosynthetic electron transport from water to lipophilic Photosystem II acceptors was stimulated 3-5-fold by high concentrations (greater than or equal to 1 M) of salts containing anions such as citrate, succinate and phosphate that are high in the Hofmeister series. 2. In trypsin-treated chloroplasts, K3Fe(CN)6 reduction insensitive to 3-(3,4-dichlorophenyl)-1,1-dimethylurea was strongly stimulated by high concentrations of potassium citrate, but there was much less stimulation of 2,6-dichloroindophenol reduction in Tris-treated chloroplasts supplied with 1,5-diphenylcarbazide as artificial donor. The results suggest that the main site of action of citrate was the O2-evolving complex of Photosystem II. 3. Photosystem I partial reactions were also stimulated by intermediate concentrations of citrate (up to 2-fold stimulation by 0.6-0.8 M-citrate), but were inhibited at the highest concentrations. The observed stimulation may have been caused by stabilizaton of plastocyanin that was complexed with the Photosystem I reaction centre, 4. At 1 M, potassium citrate protected O2 evolution against denaturation by heat or by the chaotropic agent NaNO3. 5. It is suggested that anions high in the Hofmeister series stimulated and stabilized electron transport by enhancing water structure around the protein complexes in the thylakoid membrane.

1984 ◽  
Vol 218 (2) ◽  
pp. 539-545 ◽  
Author(s):  
B Thomasset ◽  
J N Barbotin ◽  
D Thomas

Chloroplast membranes were isolated in different media containing Hepes [4-(2-hydroxyethyl)-1-piperazine-ethanesulphonic acid] and high concentrations of sorbitol (0.33 M), potassium citrate (0.75 M) or Na2SO4 (1.0 M). Due to the complexity of the media, the oxygen solubility is strongly modified by high concentrations of salts (oxygen solubility for 0.33 M-sorbitol, 0.21 mmol/litre; for 0.75 M-potassium citrate, 0.121 mmol/litre; and for 1.0 M-Na2SO4, 0.112 mmol/litre). The knowledge of these values is necessary to interpret the rate of O2 evolution. For thylakoids isolated in ‘sorbitol buffer’ and then tested in high concentrations of potassium citrate, a slight stimulation of O2 evolution is observed (143-173 mumol of O2/h per mg of chlorophyll a) with potassium ferricyanide as electron acceptor. When we monitor the potassium ferricyanide reduction, no stimulation of electron transport is obtained even if the observed phenomenon is identical with the Photosystem-II oxygen evolution. In the same experiments no stimulation of the photophosphorylation was recorded, but when thylakoids are directly isolated in 0.75 M-potassium citrate, O2 evolution, ferricyanide reduction and photophosphorylation are inhibited by high concentrations of salts. The behaviour of thylakoids seems to be influenced by their initial treatment.


1983 ◽  
Vol 210 (2) ◽  
pp. 583-589 ◽  
Author(s):  
A C Stewart ◽  
A W D Larkum

Thylakoid membrane preparations active in photosynthetic electron transport have been obtained from two marine red algae, Griffithsia monilis and Anotrichium tenue. High concentrations (0.5-1.0 M) of salts such as phosphate, citrate, succinate and tartrate stabilized functional binding of phycobilisomes to the membrane and also stabilized Photosystem II-catalysed electron-transport activity. High concentrations (1.0 M) of chloride and nitrate, or 30 mM-Tricine/NaOH buffer (pH 7.2) in the absence of salts, detached phycobilisomes and inhibited electron transport through Photosystem II. The O2-evolving system was identified as the electron-transport chain component that was inhibited under these conditions. Washing membranes with buffers containing 1.0-1.5 M-sorbitol and 5-50 mM concentrations of various salts removed the outer part of the phycobilisome but retained 30-70% of the allophycocyanin ‘core’ of the phycobilisome. These preparations were 30-70% active in O2 evolution compared with unwashed membranes. In the sensitivity of their O2-evolving apparatus to the composition of the medium in vitro, the red algae resembled blue-green algae and differed from other eukaryotic algae and higher plants. It is suggested that an environment of structured water may be essential for the functional integrity of Photosystem II in biliprotein-containing algae.


1982 ◽  
Vol 60 (4) ◽  
pp. 409-412 ◽  
Author(s):  
Rungsit Suwanketnikom ◽  
Kriton K. Hatzios ◽  
Donald Penner ◽  
Duncan Bell

The effect of bentazon (3-isopropyl-1H-2,1,3-benzathiadiazin-(4)3H-one 2,2-dioxide) on various photochemical reactions of isolated spinach (Spinacea oleracea L.) chloroplasts was studied at concentrations 0, 5, 15, 45, and 135 μM. Bentazon at a concentration of 135 μM strongly inhibited uncoupled electron transport from water to ferricyanide or to methylviologen with inhibition percentages greater than 90%. Photosystem II mediated electron transport from water to oxidized diaminodurene, with 2,5-dibromo-3-methyl-6-isopropyl-p-benzoquinone (DBMIB) blocking photosystem I, was also strongly inhibited by bentazon at 135 μM but less with lower concentrations of bentazon. Photosystem I mediated transfer of electrons from diaminodurene to methylviologen, with 3,4-dichlorophenyl-1,1-dimethylurea (DCMU) blocking photosystem II, was not inhibited by bentazon at any concentration examined. Transfer of electrons from catechol to methylviologen in hydroxylamine-treated chloroplasts was inhibited by bentazon, and the inhibition percentages were again concentration dependent. The data indicate that the site of bentazon inhibition of the photosynthetic electron transport is at the reducing side of photosystem II, between the primary electron acceptor Q and plastoquinone.


Proceedings ◽  
2019 ◽  
Vol 41 (1) ◽  
pp. 30
Author(s):  
Jiri Kos ◽  
Tomas Gonec ◽  
Tomas Strharsky ◽  
Michal Oravec ◽  
Josef Jampilek

In this study, a series of nine 3-hydroxynaphthalene-2-carboxanilides, disubstituted on the anilide ring by fluorine, chlorine and bromine in various positions, was prepared by microwave-assisted synthesis and characterized. The compounds were tested for their activity related to the inhibition of photosynthetic electron transport (PET) in spinach (Spinacia oleracea L.) chloroplasts. The PET-inhibiting activity of the compounds was within a wide range, but rather moderate; the highest activity within the series of the compounds was observed for N-(3,5-difluorophenyl)-3-hydroxynaphthalene-2-carboxamide (IC50 = 9.8 µM). The compounds were found to inhibit PET in photosystem II.


1970 ◽  
Vol 25 (10) ◽  
pp. 1157-1159 ◽  
Author(s):  
A. Trebst ◽  
E. Harth ◽  
W. Draber

A halogenated benzoquinone has been found to inhibit the photosynthetic electron transport system in isolated chloroplasts. 2·10-6ᴍ of dibromo-thymoquinone inhibit the Hill- reaction with NADP, methylviologen or anthraquinone to 100%, but do not effect the photoreduction of NADP at the expense of an artificial electron donor. The Hill - reaction with ferricyanide is inhibited even at the high concentration of 2·10-5ᴍ of dibromo-thymoquinone to only 60%. The remaining reduction in the presence of the inhibitor reflects the rate of ferricyanide reduction by photosystem II. It is concluded that the inhibition of electron transport by the quinone occurs between photosystem I and II and close to or at the functional site of plastoquinone.


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.


2014 ◽  
Vol 2014 ◽  
pp. 1-11 ◽  
Author(s):  
Ales Imramovsky ◽  
Jan Kozic ◽  
Matus Pesko ◽  
Jirina Stolarikova ◽  
Jarmila Vinsova ◽  
...  

A series of twelve 2-[(E)-2-substituted-ethenyl]-1,3-benzoxazoles was designed. All the synthesized compounds were tested against three mycobacterial strains. The compounds were also evaluated for their ability to inhibit photosynthetic electron transport (PET) in spinach (Spinacia oleraceaL.) chloroplasts. 2-[(E)-2-(4-Methoxyphenyl)ethenyl]-1,3-benzoxazole, 2-[(E)-2-(2,3-dihydro-1-benzofuran-5-yl)ethenyl]-1,3-benzoxazole and 2-{(E)-2-[4-(methylsulfanyl)phenyl]ethenyl}-1,3-benzoxazole showed the highest activity againstM. tuberculosis,M. kansasii,andM. avium, and they demonstrated significantly higher activity againstM. aviumandM. kansasiithan isoniazid. The PET-inhibiting activity of the most activeortho-substituted compound 2-[(E)-2-(2-methoxyphenyl)ethenyl]-1,3-benzoxazole was IC50= 76.3 μmol/L, while the PET-inhibiting activity ofpara-substituted compounds was significantly lower. The site of inhibitory action of tested compounds is situated on the donor side of photosystem II. The structure-activity relationships are discussed.


Weed Science ◽  
1980 ◽  
Vol 28 (6) ◽  
pp. 640-645 ◽  
Author(s):  
M. K. Pritchard ◽  
G. F. Warren ◽  
R. A. Dilley

The effects of oxyfluorfen [2-chloro-1-(3-ethoxy-4-nitrophenoxy)-4-(trifluoromethyl)benzene] were studied on electron transport and phosphorylation in isolated spinach (Spinacia oleraceaL.) chloroplasts and on the response of green bean (Phaseolus vulgarisL. ‘Spartan Arrow’) to applications of oxyfluorfen alone or in combination with other herbicides. Coupled non-cyclic electron transfer and phosphorylation through photosystems I and II (H2O å methyl viologen) were inhibited about 30% and 55%, respectively, by 10−4M oxyfluorfen. Photosystem II-linked phosphorylation with dimethylbenzoquinone (2,5-dimethyl-p-benzoquinone) as the electron acceptor (H2O å DMQ) was completely inhibited by 10−4M oxyfluorfen. Photosystem II electron transport with dimethylbenzoquinone as the electron acceptor was inhibited 60% by 10−4M oxyfluorfen, whereas photosystem I electron transport with 2,6-dichlorophenol indophenol as electron donor (DCIPH2å MV) was not susceptible to oxyfluorfen inhibition. Photosystem I-linked phosphorylation and the accompanying electron transport supported by durohydroquinone electron donation (DQH2å MV) were inhibited about 50% by 10−4M oxyfluorfen, whereas cyclic phosphorylation was not inhibited at that concentration. Increased conductivity of a solution that contained leaf discs taken from green beans treated with various combinations of foliar-applied herbicides was a measure of membrane damage caused by the herbicides, and revealed that oxyfluorfen has a different site of action than do photosynthesis inhibitor and bipyridilium herbicides. Oxyfluorfen plus dinoseb (2-sec-butyl-4,6-dinitrophenol) injury to green beans was additive, but the two herbicides did not have the same site of action. Oxyfluorfen did not appear to inhibit electron transport in chloroplasts at herbicidal rates, nor was it dependent on electron transport for activation.


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