The mechanism of cyclic phosphorylation by illuminated chloroplasts

In the reaction discovered by Hill (1937, 1939), chloroplasts isolated from the cell were shown to be capable, upon illumination, of reducing an artificial hydrogen acceptor with the concurrent evolution of oxygen. The ‘Hill reaction’ was regarded as a partial model of the light reaction in photosynthesis where limited reducing power and molecular oxygen arose from the photolysis of water. Attempts to relate this reaction to the photochemical events preceding the dark reduction of carbon dioxide in photosynthesis received their first direct support from the finding of San Pietro & Lang (1958) that nicotinamide adenine dinucleotide phosphate ( NADP )can serve as an effective acceptor of hydrogen in the photochemical reaction when the system is supplemented with a catalytic amount of a soluble protein extracted from leaves. Added significance was given to this finding by the further observation of Amon, Whatley & Allen (1959), that hydrogen transport in the reaction could be coupled to the phosphorylation of adenosine diphosphate { ADP ) to yield adenosine triphosphate { ATP ) concurrently with the reduction of NADP and the production of oxygen in the stoicheiometric proportions: l NADP LL 2 jl ATP /^0 2 . They had previously demonstrated a similar coupling of phosphorylation to hydrogen transport when the artificial reagent, ferricyanide, served as hydrogen acceptor (Arnon, Whatley & Allen 1958). In this work, Amon et al. made the further important observation that hydrogen transport in the ferricyanide reaction is strongly stimulated when phosphorylation occurs concurrently.

1964 ◽  
Vol 17 (1) ◽  
pp. 93 ◽  
Author(s):  
Jan M Anderson ◽  
NK Boardman

A study of the photochemical activity of plastids isolated from etiolated bean leaves which had been illuminated for increasing periods was undertaken. Proplastids isolated from etiolated leaves were inactive in the Hill reaction. Photochemical ferricyanide reduction was obtained with plastids isolated from etiolated leaves which had been illuminated for 6 hr. The reduction increased to a maximum value of 400 p.lloles ferricyanide/mg chlorophyll/hr after 10 hr of illumina� tion and thereafter decreased to 300,umoles ferricyanidejmg chlorophylljhr for mature bean chloroplasts. Plastids isolated from etiolated leaves illuminated for 16 hr reduced nicotinamide adenine dinucleotide phosphate (NADP) at a rate less than half that of mature chloroplasts, while B�hr plastids showed no NADP reduction.


1969 ◽  
Vol 47 (2) ◽  
pp. 299-308 ◽  
Author(s):  
Beatrice M. Sweeney

In Gonyaulax polyedra it is possible to measure overt rhythms in luminescence, photosynthesis, and cell division. A common endogenous oscillator appears to control all three processes. The question of concern here is the manner in which the information regarding period and phase is transduced from oscillator to overt rhythm. In the rhythm of photosynthetic capacity, the path of electron flow through systems I and II appears not to be the site of transduction, since there is no rhythm in cells in flashing light, in the Hill reaction, or in sensitivity to such specific inhibitors as dichlorophenyl dimethyl urea (DCMU), and carbonyl cyanide m-chlorophenylhydrazone (CCmP). The probable site of control is in the Calvin cycle, since the activity of the first enzyme in this cycle, ribulose diphosphate dicarboxylase, varies with the phase of the cells from which the enzyme is derived. The low activity of this enzyme in crude extracts from cells in the night phase in continuous light can be overcome by increasing the concentration of bicarbonate in the reaction mixture. In vivo also, increasing the concentration of bicarbonate decreases the amplitude of the rhythm markedly. The activity of mixtures of extracts prepared during the day and the night phase is intermediate between that of either enzyme preparation alone, suggesting that the differences in activity are not caused by the presence of activators or inhibitors. The activity of ribulose diphosphate carboxylase is reduced by high temperature and by the presence of parachloromercuribenzonate (pCMB) and both adenosine triphosphate (ATP) and adenosine diphosphate (ADP), but differences in sensitivity to inhibitors between "day" and "night" enzyme preparations are not observed. The concentration of ATP extractable from cells does not vary with the phase of the rhythm.Transduction in the luminescent rhythm appears to be via changes in the mechanism by which luminescence is stimulated in vivo, since it is possible to obtain large and almost equal amounts of light from cells throughout the rhythmic cycle by the addition of acid. Eliciting luminescence in this way appears to bypass the normal mechanism of stimulation. This conclusion is strengthened by the observation that the inhibitory effect of light on cell luminescence is also eliminated when acid is used.


1987 ◽  
Vol 42 (6) ◽  
pp. 684-689 ◽  
Author(s):  
John L. Huppatz ◽  
John N. Phillips

Optically active α-methylbenzylamino 2-cyanoacrylic esters were synthesized and assayed as inhibitors of the Hill reaction in isolated pea chloroplast fragments. The 5-isomers were more potent inhibitors than the S-isomers with discriminations of from ten to greater than 100-fold being observed. A β-alkyl substituent in the cyanoacrylate molecule affected both the level of activity and the difference in activity between the isomers. An α,α-dimethylbenzylamino derivative was also active at about the same level as the corresponding α-methylbenzylamino racemate. This result could be explained in terms of the orientation of the phenyl ring in the receptor site. Replacement of the α-methylbenzylamino group by other α-alkyl and α-phenyl substituents had little effect on activity. However, an α-benzyl group was beneficial.


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.


Weed Science ◽  
1974 ◽  
Vol 22 (1) ◽  
pp. 10-14 ◽  
Author(s):  
R. E. Holm ◽  
D. E. Stallard

Five 2,5-dimethyl-1-pyrrolidinecarboxanilides were effective inhibitors of the Hill reaction. However, only thecisisomers were active; thetransisomers were totally inactive. Experiments were conducted using14C-5328 (cis-2,5-dimethyl-1-pyrrolidinecarboxanilide). A correlation existed between resistance of various plants to 5328 and their ability to metabolize it to water soluble metabolites. Velvetleaf (Abutilon theophrastiMedic.) and proso millet (Panicum miliaceumL.) seedlings were very susceptible to 5328 and were unable to metabolize it. Tall morningglory [Ipomoea purpurea(L.) Roth] seedlings were highly tolerant to 5328 and converted it completely to its metabolites. Corn (Zea maysL. ‘DeKalb variety XL-45′) seedlings which were slightly susceptible to 5328 injury were able to metabolize up to 90% of the parent compound. Corn foliage uptake of14C-5328 applied to the soil surface occurred through the adventitious roots.


1961 ◽  
Vol 1 (5) ◽  
pp. 377-388 ◽  
Author(s):  
Rajni Govindjee ◽  
Eugene Rabinowitch
Keyword(s):  

Antioxidants ◽  
2018 ◽  
Vol 7 (11) ◽  
pp. 152 ◽  
Author(s):  
Daniel Wittmann ◽  
Sigri Kløve ◽  
Peng Wang ◽  
Bernhard Grimm

Thiol-based redox control is one of the important posttranslational mechanisms of the tetrapyrrole biosynthesis pathway. Many enzymes of the pathway have been shown to interact with thioredoxin (TRX) and Nicotinamide adenine dinucleotide phosphate (NADPH)-dependent thioredoxin reductase C (NTRC). We examined the redox-dependency of 5-aminolevulinic acid dehydratase (ALAD), which catalyzed the conjugation of two 5-aminolevulinic acid (ALA) molecules to porphobilinogen. ALAD interacted with TRX f, TRX m and NTRC in chloroplasts. Consequently, less ALAD protein accumulated in the trx f1, ntrc and trx f1/ntrc mutants compared to wild-type control resulting in decreased ALAD activity. In a polyacrylamide gel under non-reducing conditions, ALAD monomers turned out to be present in reduced and two oxidized forms. The reduced and oxidized forms of ALAD differed in their catalytic activity. The addition of TRX stimulated ALAD activity. From our results it was concluded that (i) deficiency of the reducing power mainly affected the in planta stability of ALAD; and (ii) the reduced form of ALAD displayed increased enzymatic activity.


1974 ◽  
Vol 15 (4) ◽  
pp. 727-731 ◽  
Author(s):  
Kazuhiko Satoh ◽  
Atusi Takamiya ◽  
Sakae Katoh

1971 ◽  
Vol 26 (5) ◽  
pp. 435-446 ◽  
Author(s):  
Alfons Radunz ◽  
Georg H. Schmid ◽  
Wilhelm Menke

Antibodies to chlorophyll are specifically adsorbed onto the membrane surface of thylakoids. The antibodies inhibit photosynthetic electron flow from water to NADP⊕. This inhibition is presumably caused by adsorption of the antibodies onto the centre chlorophyll of light reaction II. Fragments of the thylakoid membrane, obtained by ultrasonication and subsequent fractioning centrifugation, exhibit only photosystem-I activity. Conversely, the specific adsorption of antibodies to sensitizer chlorophyll has no inhibitory effect on electron transport. The ferricyanide Hill reaction of chloroplast preparations is inhibited by chlorophyll antibodies. From these observations it is concluded that the centre chlorophyll of light reaction II and at least part of the sensitizer chlorophyll is located on the surface of the thylakoids. As agglutination is sterically inhibited by the membrane protein, it is assumed that the chlorophyll is located in gaps or pores of the protein layer.Two fractions of the lamellar system exhibit photosystem I activity of different characteristic electron donor specificity. These fractions can be further distinguished in terms of their circular dichroism and protein composition.


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