Counteraction of Paraquat Toxicity at the Chloroplast Level

1987 ◽  
Vol 42 (6) ◽  
pp. 824-828 ◽  
Author(s):  
Brad L. Upham ◽  
Kriton K. Hatzios

Six pyridyl derivatives [benzylviologen, 2-anilinopyridine, 1,2-bis(4-pyridyl)ethane, 1,2-bis(4-pyridyl)ethylene, 2-benzoylpyridine, and 2-benzylaminopyridine] and five heme-iron derivatives [hemoglobin, hemin, hematin, ferritin, and ferrocene] were screened for their potential to counteract paraquat (1,1′-dimethyl-4.4′-bipyridinium ion) toxicity on pea (Pisum sativum L.) isolated chloroplasts. The H2O → methylviologen(MV)/O2 and H2O → ferredoxin(Fd)/NADP+ were two Hill reactions assayed with these compounds. Antagonists of paraquat toxicity should inhibit the first Hill reaction but not the latter. AU pyridyl derivatives examined did not inhibit the reaction H2O → MV/O2. Ferritin and ferrocene were also ineffective as inhibitors of this reaction. Hemoglobin inhibited the reaction H2O → MV/O2 without inhibiting the reaction H2O → Fd/NADP+, providing protection to pea chloroplasts against paraquat. Hemin and hematin inhibited both Hill reactions examined. They also inhibited H2O → diaminodurene(DAD)ox and durohydro- quinone → MV/O2 Hill reactions but not the dichlorophenol indophenolred → MV/O2 and DADred → MV/O2 Hill reactions. These results suggest that hemin and hematin are inhibiting the photo- synthetic electron transport in the plastoquinone-pool region.

1987 ◽  
Vol 42 (7-8) ◽  
pp. 824-828 ◽  
Author(s):  
Brad L. Upham ◽  
Kriton K. Hatzios

Six pyridyl derivatives [benzylviologen, 2-anilinopyridine, 1,2-bis(4-pyridyl)ethane, 1,2-bis(4- pyridyl)ethylene, 2-benzoylpyridine, and 2-benzylaminopyridine] and five heme-iron derivatives [hemoglobin, hemin, hematin, ferritin, and ferrocene] were screened for their potential to coun- teract paraquat (1,1′-dimethyl-4.4′-bipyridinium ion) toxicity on pea (Pisum sativum L.) isolated chloroplasts. The H2O -> methylviologen(MV)/O2 and H2O → ferredoxin(Fd)/NADP+ were two Hill reactions assayed with these compounds. Antagonists of paraquat toxicity should inhibit the first Hill reaction but not the latter. All pyridyl derivatives examined did not inhibit the reaction H2O → MV/O2. Ferritin and ferrocene were also ineffective as inhibitors of this reaction. Hemoglobin inhibited the reaction H2O → MV/O2 without inhibiting the reaction H2O → Fd/NADP+, providing protection to pea chloroplasts against paraquat. Hemin and hematin inhibited both Hill reactions examined. They also inhibited H2O → diaminodurene(DAD)ox and durohydro-quinone → MV/O2 Hill reactions but not the dichlorophenol indophenolred → MV/O2 and DADred → MV/O2 Hill reactions. These results suggest that hemin and hematin are inhibiting the photosynthetic electron transport in the plastoquinone-pool region.


Planta ◽  
2019 ◽  
Vol 251 (1) ◽  
Author(s):  
Daria Todorenko ◽  
Nyurgun Timofeev ◽  
Ilya Kovalenko ◽  
Galina Kukarskikh ◽  
Dmitry Matorin ◽  
...  

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.


1977 ◽  
Vol 60 (1) ◽  
pp. 165-169 ◽  
Author(s):  
James R. Brandle ◽  
William F. Campbell ◽  
William B. Sisson ◽  
Martyn M. Caldwell

1966 ◽  
Vol 21 (11) ◽  
pp. 1057-1059 ◽  
Author(s):  
R. Berzborn ◽  
W. Menke ◽  
A. Trebst ◽  
E. Pistorius

The influence of two separated globuline fractions from rabbit antisera against isolated chloroplasts from Antirrhinum majus upon photosynthetic reactions of isolated chloroplasts from spinach has been investigated. The chloroplast antibodies had no effect on electron transport in a Hill reaction with ferricyanide, but one fraction inhibited noncyclic and cyclic ATP formation. This inhibition was reversed by preincubation of the antibody with coupling factor. Both globuline fractions inhibited photosynthetic NADP reduction; the inhibition of only one fraction was reversed by preincubation with ferredoxin-NADP-reductase. We conclude from these results that three components of photosynthetic activities are located on the surface of the thylakoids: the ATP forming system, the NADP-reductase, and an unknown factor participating in photosynthetic NADP reduction but not in ferricyanide reduction or cyclic electron transport


1963 ◽  
Vol 18 (2) ◽  
pp. 105-109 ◽  
Author(s):  
Achim Trebst ◽  
Herbert Eck

Salicylaldoxime at a concentration of 10-2-m. is an inhibitor of the Hill - reaction and therefore also of aerobic photophosphorylation in isolated chloroplasts. This might indicate a functional role for copper in the electron transport system of photosynthesis.At a concentration of 10-3-m. and lower, salicylaldoxime is not an inhibitor, but a cofactor of aerobic photophosphorylation. This is due to its hydroxylation to the p-hydroquinone, which is the actual cofactor. This p-hydroxylation, which is probably catalyzed by a peroxidase, takes place only with salicylaldehyde and its oxime, but not with other phenols, whether they have a carbonyl function attached to the phenyl ring or not. A number of o- and p-hydroquinones with a carbonyl function at the phenyl ring and two naphthohydroquinones, of which the corresponding quinone cannot be prepared by chemical means, are reversibly oxidized and reduced in photosynthetic phosphorylation in chloroplasts. A possible explanation is that these hydroquinones are oxidized only to the semiquinone level and rapidly reduced again.


1986 ◽  
Vol 41 (7-8) ◽  
pp. 751-757 ◽  
Author(s):  
Tadao Asami ◽  
Nobutaka Takahashi ◽  
Shigeo Yoshida

Abstract A series of 2-(1-alkylamino)vinylidene-1,3-cyclohexanedione was synthesized and assayed as inhibitors of the Hill reaction in isolated chloroplasts. The pI50 value of this series was dramatically changed by modification of the peripheral of its hydrophilic moiety and the maximum pI50 value of this series was almost equal to that of DCMU . The results suggest that this series may be a good probe for searching the environment of inhibitors binding site because of its chemical and biological characteristics and its ease of synthesis.


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