Thiazolylidene-Ketonitriles are Efficient Inhibitors of Electron Transport in Reaction Centers from Photosynthetic Bacteria

1991 ◽  
Vol 46 (11-12) ◽  
pp. 1059-1062 ◽  
Author(s):  
Walter Oettmeier ◽  
Silvana Preuße ◽  
Michael Haefs

Thiazolylidene-ketonitriles are efficient inhibitors of photosynthetic electron flow in reaction centers from either Rhodobacter sphaeroides or Rhodobacter capsulatus. Some compounds of this class exhibit a higher inhibitory potency in the bacterial system as compared to photosystem II. Up to now, photosystem II inhibitors were generally less active in photosynthetic bacteria. An azido-thiazolylidene-ketonitrile upon illumination almost exclusively tags the L-subunit in the bacterial reaction center.

1984 ◽  
Vol 39 (5) ◽  
pp. 374-377 ◽  
Author(s):  
J. J. S. van Rensen

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.


2001 ◽  
Vol 183 (6) ◽  
pp. 2013-2024 ◽  
Author(s):  
Fevzi Daldal ◽  
Sevnur Mandaci ◽  
Christine Winterstein ◽  
Hannu Myllykallio ◽  
Kristen Duyck ◽  
...  

ABSTRACT We have recently established that the facultative phototrophic bacterium Rhodobacter sphaeroides, like the closely relatedRhodobacter capsulatus species, contains both the previously characterized mobile electron carrier cytochromec 2 (cyt c 2) and the more recently discovered membrane-anchored cytc y. However, R. sphaeroides cytc y, unlike that of R. capsulatus, is unable to function as an efficient electron carrier between the photochemical reaction center and the cyt bc 1complex during photosynthetic growth. Nonetheless, R. sphaeroides cyt c y can act at least in R. capsulatus as an electron carrier between the cytbc 1 complex and thecbb 3-type cyt c oxidase (cbb 3-Cox) to support respiratory growth. Since R. sphaeroides harbors both acbb 3-Cox and anaa 3-type cyt c oxidase (aa 3-Cox), we examined whetherR. sphaeroides cyt c y can act as an electron carrier to either or both of these respiratory terminal oxidases. R. sphaeroides mutants which lacked either cyt c 2 or cyt c y and either the aa 3-Cox or thecbb 3-Cox were obtained. These double mutants contained linear respiratory electron transport pathways between the cyt bc 1 complex and the cytc oxidases. They were characterized with respect to growth phenotypes, contents of a-, b-, andc-type cytochromes, cyt c oxidase activities, and kinetics of electron transfer mediated by cytc 2 or cyt c y. The findings demonstrated that both cyt c 2 and cytc y are able to carry electrons efficiently from the cyt bc 1 complex to either thecbb 3-Cox or theaa 3-Cox. Thus, no dedicated electron carrier for either of the cyt c oxidases is present in R. sphaeroides. However, under semiaerobic growth conditions, a larger portion of the electron flow out of the cytbc 1 complex appears to be mediated via the cytc 2-to-cbb 3-Coxand cytcy -to-cbb 3-Coxsubbranches. The presence of multiple electron carriers and cytc oxidases with different properties that can operate concurrently reveals that the respiratory electron transport pathways of R. sphaeroides are more complex than those ofR. capsulatus.


1987 ◽  
Vol 42 (6) ◽  
pp. 690-692 ◽  
Author(s):  
Walter Oettmeier ◽  
Silvana Preuße

Besides s-triazine and triazinone herbicides the chromone stigmatellin and tetrahalogen-substituted 1.4-benzoquinones are inhibitors of photosynthetic electron flow from reduced cytochrome c to ubiquinone-6 in isolated bacterial reaction centers. With isolated bacterial chromatophores binding experiments with radiolabeled herbicides can be performed in a similar way as with thylakoids from higher plants. Tetrahalogen-substituted 1.4-benzoquinones in a Michael type reaction can add onto nucleophilic groups in proteins. In bacterial reaction centers, a [14C]tetra- bromo-1.4-benzoquinone (bromanil) exclusively binds to the H-subunit.


HortScience ◽  
1999 ◽  
Vol 34 (3) ◽  
pp. 548B-548
Author(s):  
Lailiang Cheng ◽  
Leslie H. Fuchigami ◽  
Patrick J. Breen

Photosystem II (PSII) efficiency and CO2 assimilation in response to photon flux density (PFD) and intercellular CO2 concentration (Ci) were monitored simultaneously in leaves of apple, pear, apricot, and cherry with a combined system for measuring chlorophyll fluorescence and gas exchange. When photorespiration was minimized by low O2 (2%) and saturated CO2 (1300 ppm), a linear relationship was found between PSII efficiency and the quantum yield for CO2 assimilation with altering PFD, indicating CO2 assimilation in this case is closely linked to PSII activity. As PFD increased from 80 to 1900 μmol·m–2·s–1 under ambient CO2 (350 ppm) and O2 (21%) conditions, PSII efficiency decreased by increased nonphotochemical quenching and decreased concentration of open PSII reaction centers. The rate of linear electron transport showed a similar response to PFD as CO2 assimilation. As Ci increased from 50 to 1000 ppm under saturating PFD (1000 μmol·m–2·s–1) and ambient O2, PSII efficiency was increased initially by decreased nonphotochemical quenching and increased concentration of open PSII reaction centers and then leveled off with further a rise in Ci. CO2 assimilation reached a plateau at a higher Ci than PSII efficiency because increasing Ci diverted electron flow from O2 reduction to CO2 assimilation by depressing photorespiration. It is concluded that PSII efficiency is regulated by both nonphotochemical quenching and concentration of open PSII reaction centers in response to light and CO2 to meet the requirement for photosynthetic electron transport.


1998 ◽  
Vol 53 (9-10) ◽  
pp. 849-856
Author(s):  
Sujata R. Mishra ◽  
Surendra Chandra Sabat

Stimulatory effect of divalent cations like calcium (Ca2+) and magnesium (Mg2+) was investigated on electron transport activity of divalent cation deficient low-salt suspended (LS) thylakoid preparation from a submerged aquatic angiosperm, Hydrilla verticillata. Both the cations stimulated electron transport activity of LS-suspended thylakoids having an intact water oxidation complex. But in hydroxylamine (NH2OH) - or alkaline Tris - washed thylakoid preparations (with the water oxidation enzyme impaired), only Ca2+ dependent stimulation of electron transport activity was found. The apparent Km of Ca2+ dependent stimulation of electron flow from H2O (endogenous) or from artificial electron donor (exogenous) to dichlorophenol indophenol (acceptor) was found to be identical. Calcium supported stimulation of electron transport activity in NH2OH - or Tris - washed thylakoids was electron donor selective, i.e., Ca2+ ion was only effective in electron flow with diphenylcarbazide but not with NH2OH as electron donor to photosystem II. A magnesium effect was observed in thylakoids having an intact water oxidation complex and the ion became unacceptable in NH2OH - or Tris - washed thylakoids. Indirect experimental evidences have been presented to suggest that Mg2+ interacts with the water oxidation complex, while the Ca2+ interaction is localized betw een Yz and reaction center of photosystem II.


1994 ◽  
Vol 72 (2) ◽  
pp. 177-181 ◽  
Author(s):  
Ernesto Bernal-Morales ◽  
Alfonso Romo De Vivar ◽  
Bertha Sanchez ◽  
Martha Aguilar ◽  
Blas Lotina-Hennsen

The inhibition of ATP synthesis, proton uptake, and electron transport (basal, phosphorylating, and uncoupled) from water to methylviologen by ivalin (a naturally occurring sesquiterpene lactone in Zaluzania triloba and Iva microcephala) indicates that it acts as electron transport inhibitor. Since photosystem I and electron transport from DPC to QA were not affected, while the electron flow of uncoupled photosystem II from H2O to DAD and from water to silicomolybdate was inhibited, we concluded that the site of inhibition of ivalin is located at the oxygen evolution level. Key words: oxygen evolution, ivalin, photosynthesis, sesquiterpene lactone.


1996 ◽  
Vol 51 (3-4) ◽  
pp. 179-184 ◽  
Author(s):  
Surendra Chandra Sabat

Abstract The inhibitory effects of copper ion (Cu2+) on the photosynthetic electron transport func­tion was investigated both in NaCl washed (depleted in 17 and 23 kDa polypeptides) and native (unwashed) photosystem II membrane preparations from spinach (Beta vulgaris) chlo-roplasts. Copper in the range of 2.0 to 15 μᴍ strongly inhibited the electron flow from water to 2,6-dichlorobenzoquinone in NaCl washed particles in a concentration dependent manner. Com plete inhibition was noticed at 15 μᴍ Cu2+. Oppositely in native membranes, 15 μᴍ C u2+ inhibited only 10-12% of control activity. It was found that calcium ion (Ca2+) significantly reduced the Cu2+ inhibition of electron transport activity. The Ca2+ supported prevention of Cu2+ toxicity was specific to Ca2+. Further analysis indicated that both Cu2+ and Ca2+ act competitively. Since Ca2+ is known to have stimulating/stabilizing effect at the donor side of photosystem II, it is therefore suggested that Cu2+ in NaCl washed particles exerts its inhibi­tory effect(s) at the oxidizing side of photosystem stimulates/stabilizes the oxygen evolution.


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