The effect of alpha terthienyl on photosynthesis

1982 ◽  
Vol 60 (12) ◽  
pp. 2565-2569 ◽  
Author(s):  
John Sinclair ◽  
Thor Arnason
Keyword(s):  
Electron Transport ◽  
Photosystem Ii ◽  
Photosystem I ◽  
Electron Acceptor ◽  
Hill Reaction ◽  
Spinach Chloroplasts ◽  
Near Ultraviolet ◽  
A Site ◽  
The Hill ◽  
Clark Electrode

Alpha terthienyl (α-T), an allelopathic polyacetylene derivative occurring in the Asteraceae, was examined for its photosensitizing effect on respiration in Chlorella and photosynthesis in Chlorella and isolated spinach chloroplasts. In experiments with the Clark electrode, O2 evolution in saturating light with Chlorella was much more sensitive to α-T plus near ultraviolet (UV) treatments than respiration. O2 transients at the onset of illumination as measured with the modulated O2 polarograph were also inhibited by α-T plus near UV. The Hill reaction in uncoupled spinach chloroplasts using ferricyanide as electron acceptor is sensitive to photosensitization with α-T, but electron transport through photosystem I operating on its own showed no decrease in activity. The results are interpreted as an indication of a site of inhibition near photosystem II and possibly in CO2 fixation as well.

On a new inhibitor of photosynthetic electron-transport in isolated chloroplasts

1970 ◽  
Vol 25 (10) ◽  
pp. 1157-1159 ◽  
Author(s):  
A. Trebst ◽  
E. Harth ◽  
W. Draber
Keyword(s):  
Electron Transport ◽  
Photosystem Ii ◽  
Photosystem I ◽  
Photosynthetic Electron Transport ◽  
Hill Reaction ◽  
High Concentration ◽  
Ferricyanide Reduction ◽  
The Hill ◽  
Photosystem I And Ii ◽  
Isolated Chloroplasts

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.

Effect of an Antiserum to a Thylakoid Membrane Polypeptide on the Primary Photoreaction of Photosystem II

1976 ◽  
Vol 31 (9-10) ◽  
pp. 594-600 ◽  
Author(s):  
Georg H. Schmid ◽  
Gernot Renger ◽  
Michael Gläser ◽  
Friederike Koenig ◽  
Alfons Radunz ◽  
...  
Keyword(s):  
Electron Transport ◽  
Photosystem Ii ◽  
Photosystem I ◽  
Electron Flow ◽  
Primary Electron ◽  
Hill Reaction ◽  
Ps Ii ◽  
Absorption Change ◽  
Oxygen Evolving ◽  
The Hill

Abstract As was described previously, an antiserum to polypeptide 11000 inhibited photosynthetic elec­tron transport on the oxygen evolving side of photosystem II. The effect of the antiserum on chloro­plasts from two tobacco mutants also clearly showed that the inhibition site is on the photosystem II-side of the electron transport chain. One of the two tobacco mutants lades the oxygen evolving capacity but exhibits some electron transport with tetramethyl benzidine, an artificial donor to PS II. In this mutant electron transport was barely inhibited. The effect of the antiserum on the primary photoevents showed that the initial amplitude of the absorption change of chlorophyll an at 690 nm and that of the primary electron acceptor X320 at 334 nm both diminished in the presence of the antiserum. Both signals were restored upon addition of diphenylcarbazide another artificial donor to photosystem II. Comparison of the degree of inhibition on the amplitudes of the fast and slow components of the 690 nm absorption change with the manometrically measured inhibition of electron transport shows that besides a full inactivation of a part of the reaction centers of photosystem II another part apparently mediates a fast cyclic electron flow around photosystem II as reported by Renger and Wolff earlier for tris-treated chloroplasts. Moreover, the antiserum affects the low temperature fluorescence in a way which is opposite to Murata’s effect of the Mg2+ -ion induced inhibition of energy spill-over from photosystem II to photosystem I. The antiserum under the condition in which the Hill reaction is inhibited lowered the 686 nm emission and enhanced the 732 nm emission which indicates an enhanced energy spill-over to photosystem I.

Interaction of Photosystem II Herbicides with Bicarbonate and Formate in Their Effects on Photosynthetic Electron Flow

1984 ◽  
Vol 39 (5) ◽  
pp. 374-377 ◽  
Author(s):  
J. J. S. van Rensen
Keyword(s):  
Electron Transport ◽  
Photosystem Ii ◽  
Electron Flow ◽  
Photosynthetic Electron Transport ◽  
Hill Reaction ◽  
Amaranthus Hybridus ◽  
Apparent Affinity ◽  
Photosynthetic Electron Flow ◽  
Different Characteristics ◽  
The Hill

The reactivation of the Hill reaction in CO2-depleted broken chloroplasts by various concentrations of bicarbonate was measured in the absence and in the presence of photosystem II herbicides. It appears that these herbicides decrease the apparent affinity of the thylakoid membrane for bicarbonate. Different characteristics of bicarbonate binding were observed in chloroplasts of triazine-resistant Amaranthus hybridus compared to the triazine-sensitive biotype. It is concluded that photosystem II herbicides, bicarbonate and formate interact with each other in their binding to the Qв-protein and their interference with photosynthetic electron transport.

Stimulation of electron transport from Photosystem II to Photosystem I in spinach chloroplasts

1980 ◽  
Vol 12 (3-4) ◽  
pp. 197-203 ◽  
Author(s):  
Rita Barr ◽  
Randa Melhem ◽  
Anne L. Lezotte ◽  
Frederick L. Crane
Keyword(s):  
Electron Transport ◽  
Photosystem Ii ◽  
Photosystem I ◽  
Spinach Chloroplasts ◽  
Stimulation Of

The site of electron transport inhibition by bentazon (3-isopropyl-1H-2,1,3-benzothiadiazin-(4)3H-one 2,2-dioxide) in isolated chloroplasts

1982 ◽  
Vol 60 (4) ◽  
pp. 409-412 ◽  
Author(s):  
Rungsit Suwanketnikom ◽  
Kriton K. Hatzios ◽  
Donald Penner ◽  
Duncan Bell
Keyword(s):  
Electron Transport ◽  
Photosystem Ii ◽  
Photosystem I ◽  
Electron Acceptor ◽  
Photosynthetic Electron Transport ◽  
Primary Electron ◽  
Photochemical Reactions ◽  
Spinacea Oleracea ◽  
Primary Electron Acceptor ◽  
Isolated Chloroplasts

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.

Site of Action of 2,5-Dimethoxy-3,6-Dichloro-p-Benzoquinone in the Photosynthetic Electron Transport Chain

1981 ◽  
Vol 36 (7-8) ◽  
pp. 656-661 ◽  
Author(s):  
G. Sarojini ◽  
H. Daniell
Keyword(s):  
Electron Transport ◽  
Photosystem Ii ◽  
Electron Transport Chain ◽  
Electron Transport Rate ◽  
Electron Flow ◽  
Electron Acceptors ◽  
Hill Reaction ◽  
Transport Chain ◽  
Site Of Action ◽  
The Hill

Abstract Electron Acceptors, Photosystem II, Quinones and Quinonediamines Dichlorodimethoxy-/?-benzoquinone (DCDMQ) was tested for its site of action in the photo­ synthetic electron transport chain. Hill reaction mediated by DCDMQ was insensitive to DBMIB (1 nm) but sensitive to DCMU, suggesting its site of action before plastoquinone but after Q -the primary electron acceptor of photosystem II. Extraction of freeze-dried chloroplasts with heptane and analyzing their capacity to photo-oxidize water using various Hill oxidants revealed that silicomolybdate (SiMO) and DCDMQ could effectively restore the activity. Diaminodurene (DAD) in the presence of ferricyanide could restore 40% of the activity. But ferricyanide alone failed to restore the ability to photo-oxidize water in heptane extracted chloroplasts. Similarly, N a2S 0 3 which is known to cause a bottleneck in the electron flow at plastoquinone affected the ferricyanide Hill reaction. Hill reactions mediated by SiMO and DCDMQ were insensitive to the addition of Na2SO3, suggesting that both these oxidants intercept electrons before plastoquinone. But 50% of the activity was lost when sulfite was added to the Hill reaction mediated by DADox. DNP-INT, melittin and picrylhydrazyl were recently introduced as photosystem II inhibitors inhibiting the electron flow between Q and the PQ pool. While DCBQ and DCDMQ Hill reactions were insensitive to DNP-INT, ferricyanide was highly sensitive. The quinonediamines TMPD and DADox showed 50% decrease in the electron transport rate, similar to heptane extracted or sulfite inhibited chloroplasts. Melittin increased the electron transport rate when ferricyanide or TMPD was the Hill oxidant, while DCBQ and DCDMQ reduction remained unaffected. However, DADox Hill reaction showed 50% inhibition in the presence of melittin. Picrylhydrazyl - which inhibits the electron flow between Q and the PQ pool - inhibited the Hill reaction of all the PS II electron acceptors except that of DCDMQ. It is possible that there is another site of intercepting electrons between Q and plastoquinone before the site where most of the quinonediamines accept electrons.

Site of Action of Oxyfluorfen

Weed Science ◽  
1980 ◽  
Vol 28 (6) ◽  
pp. 640-645 ◽  
Author(s):  
M. K. Pritchard ◽  
G. F. Warren ◽  
R. A. Dilley
Keyword(s):  
Electron Transport ◽  
Photosystem Ii ◽  
Photosystem I ◽  
Electron Acceptor ◽  
Spinacia Oleracea ◽  
Membrane Damage ◽  
Green Beans ◽  
Site Of Action ◽  
Cyclic Electron Transfer ◽  
Electron Donation

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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