Acid/Base-Induced Exchange of Adenine Nucleotides on Chloroplast Coupling Factor (CF1)

1977 ◽  
Vol 32 (9-10) ◽  
pp. 803-809 ◽  
Author(s):  
Bernhard Huchzermeyer ◽  
Heinrich Strotmann
Keyword(s):  
Adenine Nucleotides ◽  
Coupling Factor ◽  
Prolonged Treatment ◽  
Outer Side ◽  
Exchange Reactions ◽  
Acid Base ◽  
Ph Values ◽  
Base Transition ◽  
Acid And Base ◽  
Back Exchange

Abstract Exchange of CF1-bound adenine nucleotides was shown to take place when isolated broken chloroplasts were subjected to an acid/base treatment. This process was measured in forward (in­ corporation of 14C-labeled nucleotides) as well as back exchange reactions (release of bound labeled nucleotides). In the presence of unlabeled ADP and Pi a high precentage of labeled ATP was found to be released into the medium.Exchange is highly specific for exogenous ADP and ATP. Acid/base-induced adenylate exchange and acid/base-induced phosphorylation were measured in dependence of several external factors. The substrate constant for ADP in exchange was 1.6 μм, whereas an apparent Km of 5 μм was determined for ADP in the phosphorylation process.Acid/base-induced exchange of adenine nucleotides and acid/base-induced phosphorylation depend in a similar way on the pH values of the acid and base stages.Acid/base-induced ATP formation was sensitive to prolonged treatment in the acid stage whereas exchange was not. Mg2+ was strictly required in phosphorylation but less important in exchange. The phosphorylation ability decreased within seconds after acid/base transition; however, the ability of [14C]ADP incorporation persisted for minutes. The formation of ATP depended on an acid/base transition, whereas some adenylate exchange was also induced by an acid treatment alone.The results suggest that appropriate pH values at the inner and outer side of the thylakoid membrane rather than energy from a pH gradient is sufficient for adenylate exchange to take place on membrane-bound CF1.

Synthesis, Characterization and Thermal studies of Novel Organomercury Driven from Sulfa Drugs Part 1

2011 ◽  
Vol 7 (2) ◽  
pp. 1338-1347
Author(s):  
Tarek Ali Fahad ◽  
Shaker.A.N. AL-Jadaan
Keyword(s):  
Thermal Decomposition ◽  
Thermal Behavior ◽  
1H Nmr ◽  
Elemental Analysis ◽  
Thermal Studies ◽  
Spectroscopic Techniques ◽  
Sulfa Drugs ◽  
Acid Base ◽  
Ph Values ◽  
Multi Stage

Two new heterocyclic Organmercury compounds   were prepared from the reaction of Sulfamethaxazole and Sulfadiazine with 4-acetaminophenol as a coupler and separated as solids with characteristic colors. these compounds were characterized by F.T.IR-spectroscopy 1H-NMR , Micro-elemental Analysis and UV-Vis spectroscopic techniques . The work involves a study of acid – base properties compounds at different pH values, the ionization and protonation constants were calculated. The thermal behavior of these two compounds   were investigated on the basis of thermogravimetric (TGA) and differential thermogravimetric (DTG) analyses, Thermal decomposition of these compounds is multi-stage processes.

scholarly journals Stimulation of mitochondrial calcium ion efflux by thiol-specific reagents and by thyroxine. The relationship to adenosine diphosphate retention and to mitochondrial permeability

1979 ◽  
Vol 182 (2) ◽  
pp. 455-464 ◽  
Author(s):  
E J Harris ◽  
M Al-Shaikhaly ◽  
H Baum
Keyword(s):  
Thyroid Hormones ◽  
Calcium Ion ◽  
Adenine Nucleotides ◽  
Adenosine Diphosphate ◽  
Ruthenium Red ◽  
Reduced Form ◽  
Factors Affecting ◽  
Ph Values ◽  
Rat Heart Mitochondria ◽  
The Relationship

Respiring rat heart mitochondria were loaded with Ca2+ and then treated with Ruthenium Red. The factors affecting the subsequent Ca2+-efflux were studied. Addition of rotenone or antimycin led to a decline of efflux except at pH values above 7.2, provided the load was less than about 80 nmol per mg of protein. Oligomycin reversed the effect of the respiratory inhibitors. Independently of respiration, efflux was stimulated by the uncoupler trifluoromethyltetrachlorbenzimadazole, by mersalyl and by thyroid hormones. The stimulated efflux could be diminished by ADP, with Mg2+ as cofactor if efflux was rapid. With respiration in progress, efflux could be stimulated by N-ethylmaleimide and 5,5′-dithiobis-(2-nitrobenzoate). The effects of mersalyl and of thyroid hormones could be diminished with dithiothreitol. In the absence of stimulating agents, the Ca2+ efflux was proportional to the load up to some critical amount, this critical amount was decreased by the agents. Thyroxine and mersalyl caused not only loss of Ca2+, but also simultaneous, but not necessarily proportional, loss of internal adenine nucleotides. Both efflux rates were kept at a low value by bongkrekic acid added before the stimulating agent. It is concluded that Ca2+ efflux is a measure of a permeability controlled by the binding of ADP (an Mg2+) to the inner membrane, and that this in turn depends on the maintenance of certain thiol gropus in a reduced form by a reaction that uses NADH and ATP and the energy-linked transhydrogenase.

scholarly journals Lewis acid / Base-free Strategy for the Synthesis of 2-Arylthio and Selenyl Benzothiazole / Thiazole and Imidazole

2021 ◽  
Vol 27 (1) ◽  
pp. 17-23
Author(s):  
Guniganti Balakishan ◽  
Gullapalli Kumaraswamy ◽  
Vykunthapu Narayanarao ◽  
Pagilla Shankaraiah
Keyword(s):  
Lewis Acid ◽  
Bond Formation ◽  
Acid Base ◽  
Mechanistic Pathway ◽  
Wide Range ◽  
Acid And Base ◽  
Lewis Acid And Base ◽  
Sulfur Bond

Abstract A Cu(II)-catalyzed Csp2-Se and Csp2-Sulfur bond formation was achieved with moderate to good yields without the aid of Lewis acid and base. The reaction is compatible with a wide range of heterocycles such as benzothiazole, thiazole, and imidazole. Also, this typical protocol is found to be active in thio-selenation via S-H activation. Additionally, we proposed a plausible mechanistic pathway involving Cu(III) putative intermediate.

One-pot synthesis of furfural derivatives from pentoses using solid acid and base catalysts

2014 ◽  
Vol 4 (4) ◽  
pp. 971-978 ◽  
Author(s):  
Mahiro Shirotori ◽  
Shun Nishimura ◽  
Kohki Ebitani
Keyword(s):  
Solid Acid ◽  
Acid Base ◽  
One Pot ◽  
Amberlyst 15 ◽  
Base Catalysts ◽  
One Pot Synthesis ◽  
Combined Use ◽  
Acid And Base

One-pot synthesis of (2-furanylmethylene)malononitrile, a Knoevenagel product of furfural with malononitrile, from xylose efficiently proceeded by combined use of acid Amberlyst-15 and acid-base Cr/hydrotalcites in 44% yield.

scholarly journals ACID-BASE PROPERTIES OF -UNSATURATED KETONES OBTAINED FROM REACTION OF 5-FORMYL-8-HYDROXYQUINOLINE WITH P-SUBSTITUTED ACETOPHENONES

2019 ◽  
Vol 16 (31) ◽  
pp. 755-764
Author(s):  
Roberto FERNANDEZ-MAESTRE ◽  
Alonso J MARRUGO-GONZÁLEZ
Keyword(s):  
Electron Donor ◽  
Opposite Effect ◽  
Dissociation Constants ◽  
Phenyl Group ◽  
Hydroxyl Group ◽  
Ultraviolet Spectroscopy ◽  
Acid Base ◽  
Unsaturated Ketones ◽  
Ph Values ◽  
Phenyl Fragment

Chalcones (α,β-unsaturated ketones) containing aromatic or heterocyclic radicals are highly reactive, allowing the synthesis of novel organic compounds. In this study, the dissociation constants (pKa) of seven chalcones derived from 8-hydroxyquinoline were determined and the influence on dissociation of substituents in the phenyl group (-CH3, -OCH3, -N(CH3)2, -Cl, -Br, and -NO2) was analysed. pKa values are important because they determine the pH at which ligands are fully deprotonated -when they show their maximum chelating properties- and determine the ligands interactions at different pH values. The chalcones’ pKa’s were calculated by visible ultraviolet spectroscopy in a water-ethanol (1:1) mixture using the Henderson-Hasselbach equation. It was shown that the 8-hydroxyquinolinic fragment has a large electron donor effect on the π system of the chalcones. The introduction of substituents (R) in the phenyl fragment of the chalcones slightly affected the dissociation of the hydroxyl group and the protonation of the nitrogen in the hydroxyquinoline fragment. The acceptor substituents (Cl, Br, NO2) increased the polarity of OH- and its acidity. Nitrogen protonation decreased electron donor properties of this fragment, and deprotonation of the hydroxyl caused the opposite effect. Substituents introduction in the phenyl fragment slightly affected hydroxyl group dissociation and nitrogen protonation.

scholarly journals Effects of External Acidification on the Blood Acid-Base Status and Ion Concentrations of Lamprey

1988 ◽  
Vol 136 (1) ◽  
pp. 351-361
Author(s):  
LEONA MATTSOFF ◽  
MIKKO NIKINMAA
Keyword(s):  
High Sensitivity ◽  
Co2 Concentration ◽  
Acid Base ◽  
Ion Concentrations ◽  
Ph Response ◽  
Ph Values ◽  
Blood Ph ◽  
Acid Base Status ◽  
The Difference ◽  
K Concentration

We studied the effects of acute external acidification on the acid-base status and plasma and red cell ion concentrations of lampreys. Mortality was observed within 24 h at pH5 and especially at pH4. The main reason for the high sensitivity of lampreys to acid water appears to be the large drop in blood pH: 0.6 and 0.8 units after 24 h at pH5 and pH4, respectively. The drop of plasma pH is much larger than in teleost fishes exposed to similar pH values. The difference in the plasma pH response between lampreys and teleosts probably results from the low buffering capacity of lamprey blood, since red cells cannot participate in buffering extracellular acid loads. Acidification also caused a decrease in both Na+ and C− concentrations and an elevation in K+ concentration of plasma. The drop in plasma Na+ concentration occurred faster than the drop in plasma Cl− concentration which, in turn, coincided with the decrease in total CO2 concentration of the blood.

scholarly journals Inventarisasi Tanaman Berpotensi Sebagai Indikator Asam-Basa Alami Di Kota Kupang

bionature ◽  
2019 ◽  
Vol 19 (1) ◽  
Author(s):  
Nur R. Adawiyah Mahmud ◽  
Ihwan Ihwan ◽  
Nur Jannah
Keyword(s):  
Color Change ◽  
Curcuma Longa ◽  
Piper Betle ◽  
Acid Base ◽  
Sesbania Grandiflora ◽  
Base Solution ◽  
Synthetic Indicator ◽  
Acid Base Titration ◽  
Acid And Base ◽  
Bougainvillea Spectabilis

Abstract.  This study investigated a natural acid-base indicator which is extracted from plants in Kupang city. There are 14 plants that potential as a source of natural indicator for acid base titration, i.e, Kol Ungu (Brassica oleracea Capitata Group), Turi Merah flower (Sesbania grandiflora L. Pers), Belimbing Wuluh flower (Averhoa bilimbi L), Kaktus Merah fruit (Opuntia vulgaris Mill), Ruelia flower (Ruellia simplex), Flamboyan flower (Delonix regia), bugenvil flower (Bougainvillea spectabilis Willd.), Bayam Merah leaves (Amaranthus tricolor L.) Jamblang fruit (Syzygium cumini L.), Murbey fruit (Morus alba L.), Pinang fruit (Areca catechu L.), Sirih fruit (Piper betle L.), Kunyit (Curcuma longa Linn), and Nanas Kerang leaves (Rhoeo discolor). Plants extract shows a sharp color change in acid and base solution. Promising results as a natural indicator also shown in acid base titration which is have similar equivalent point to synthetic indicator. We can use these natural indicators as an alternative to synthetic indicator because they are found to be simple, very useful, cheap, easy to extract, accurate, and eco-friendly. Keywords: Plant, Natural indicator, Acid-Base

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