scholarly journals Cyanoacrylate inhibitors of the Hill reaction. I. Nature of the inhibitor/receptor site interaction.

1984 ◽  
Vol 48 (1) ◽  
pp. 51-54 ◽  
Author(s):  
John N. PHILLIPS ◽  
John L. HUPPATZ
Keyword(s):  
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.


Author(s):  
Maria Waqas ◽  
Muhammad Khurram ◽  
S.M. Razaul Hasan

In the field of computational biology, electronic modeling of bio-cellular processes is in vogue for about a couple of decades. Fast, efficient and scalable electronic mimetics of recurrently found bio-chemical reactions are expected to provide better electronic circuit simulators that can also be used as bio-sensors or implantable biodevices at cellular levels. This paper presents some possible electronic circuit equivalents to model dynamics of one such bio-chemical reaction commonly involved in many bio-cellular processes, specifically pathways in living cells, known as the Hill process. The distinguishing feature of this process is cooperativity which has been modeled in silicon substrate using a pair of transistors, one transistor driving current in the other the same way ligand binding to one receptor site controls the binding affinity of the other receptor sites. Two possible circuits have been proposed and compared to electronically model cooperativity of a Hill reaction. The main idea is to exploit the natural analogies found between structures and processes of a bio-cell and electronic transistor mechanics, to efficiently model fundamental bio-chemical reactions found recurring in bio-processes. These circuits can then be combined and rearranged quickly to form larger, more complex bio-networks, thus mitigating the intricacies involved in modeling of such systems.


1987 ◽  
Vol 42 (6) ◽  
pp. 674-678 ◽  
Author(s):  
John L. Huppatz ◽  
John N. Phillips

The influence of steric factors on the activity of 2-cyanoacrylic esters as inhibitors of the Hill reaction was examined. The spatial arrangement of the different groups in the inhibitor molecule was found to be an important factor in determining potency. The positioning of the phenyl ring in aralkylamino derivatives and the steric properties of the β-substituent are particularly significant in the interaction of molecules with the) hydrophobic domain of the receptor site. The difference in activity observed with optically active α-methylbenzylamino derivatives confirmed the importance of the orientation of the phenyl ring and indicated an interaction with a specific hydrophobic region.


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):  

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.


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

1984 ◽  
Vol 39 (5) ◽  
pp. 386-388 ◽  
Author(s):  
Jan F. H. Snel ◽  
Dirk Naber ◽  
Jack J. S. van Rensen

The effects of formate on the Hill reaction in isolated broken pea chloroplasts were in­vestigated. Addition of formate to chloroplasts has two distinct effects: I. basal electron flow can be stimulated 3-fold; 2. uncoupled electron flow is inhibited. The stimulating effect is due to uncoupling by formate and appears instantaneous. Maximal inhibition by form ate is only observed after prolonged illumination. The inhibitory action of form ate on electron flow can be relieved by bicarbonate *.


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