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1.
《Inorganica chimica acta》1986,115(2):169-172
2-(Methylamino)pyridine reacts with RuCl2(CO)3 to give a carbamoyl complex, [)Cl(CO)2], which yields with pyridine (py) and acetylacetone (Hacac), respectively, [)Cl(CO)2(py)] and [)(CO)2(acac)]. These complexes are characterized spectroscopically. The amino group of the ligand is carbonylated and the resulted carbamoyl ligand is chelating through a pyridine ring-N and a carbamoyl-C atom. 2-Aminopyridine and 2-aminopyrimidine react similarly with RuCl2(CO)3 to give the corresponding carbamoyl complexes. 相似文献
2.
Robert P. le Borgne 《Journal of experimental marine biology and ecology》1979,37(2):127-137
Respiration (O), ammonium (NH4), phosphate (PO4), total nitrogen (NT) and phosphorus (PT) excretions were measured on mixed zooplankton during 3-, 6-, 9-, 12-, 21-, and 24-h incubation periods at 20–23 C. The excretion rates of PO4, NT. and PT decrease during a 21-h period, while rates of respiration and excretion of NH{IN4} are constant. The percentage of inorganic nitrogen excreted increases regularly from 3 h (30–40% of total nitrogen) to 21 h (70–80%) and it could be either due to a bacterial activity which was measured or to a decrease with time of organic nitrogen excreted because of starvation. , , , and ratios increase during the first 9 h of incubation; the percentage of inorganic phosphorus excreted is higher at the very beginning and then remains constant from 6 to 24 h. and ratios are constant during a 24-h term, which makes them useful metabolic indexes. 相似文献
3.
In the glycolytic system derived from rat brain acetone powder, ammonium ion has been found to stimulate three different reactions: (a) the transphosphorylase reaction from phosphoenolpyruvate, (b) the phosphohexokinase reaction, and (c) the hexokinase reaction. The transphosphorylases are affected differently depending upon whether adenosine diphosphate or adenylic acid is the phosphate acceptor; in the case of the latter, the dependency upon is particularly marked. A highly active myokinase is present in these extracts and its activity influences the transphosphorylase reaction to a considerable extent. The phosphohexokinase reaction is stimulated to a greater extent by than is the hexokinase reaction. In contrast to these reactions which require the participation of the adenylic system, triose phosphate oxidase activity is uninfluenced by the presence of . 相似文献
4.
Clifford Harding Philip Stahl 《Biochemical and biophysical research communications》1983,113(2):650-658
Iron uptake by rat reticulocytes is blocked by 20 mM NH4Cl, while 125I-diferric transferrin (Tf) uptake is relatively unaffected. At pH 5.0 both apo- and diferric Tf bind with high affinity; at pH 7.4 diferric Tf binds avidly, but apoTf binds very poorly. The dissociation rate (4°C) of diferric Tf is extraordinarily slow at pH 5.0 (extrapolated ) and faster at pH 7.4 (). At pH 5.0 apoTf also dissociates slowly (), but at pH 7.4 apoTf exhibits a much faster dissociation rate (). 20 mM NH4Cl slows the release of Tf from cells at 37°C, but the rate of externalization of ligand is unaffected. Ligand dissociation at 37° involves both externalization of receptor-ligand complexes and receptor-ligand separation; the NH4Cl effect may result from an increased fraction of externalized Tf in the differric form which may dissociate more slowly. Receptor-mediated movement of Tf through acid intracellular compartments provides a mechanism to remove iron from Tf and for apoTf to remain receptor-bound for externalization to the cell surface and subsequent dissociation. 相似文献
5.
NH2OH-treated, non-water-splitting chloroplasts can oxidize H2O2 to O2 through Photosystem II at substantial rates (100–250 μequiv · h?1 · mg?1 chlorophyll with 5 mM H2O2) using 2,5-dimethyl-p-benzoquinone as an electron acceptor in the presence of the plastoquinone antagonist dibromothymoquinone. This H2O2 → Photosystem II → dimethylquinone reaction supports phosphorylation with a ratio of 0.25–0.35 and proton uptake with values of 0.67 (pH 8)–0.85 (pH 6). These are close to the value of 0.3–0.38 and the values of 0.7–0.93 found in parallel experiments for the H2O → Photosystem II → dimethylquinone reaction in untreated chloroplasts. Semi-quantitative data are also presented which show that the donor → Photosystem II → dibromothymoquinone (→O2) reaction can support phosphorylation when the donor used is a proton-releasing reductant (benzidine, catechol) but not when it is a non-proton carrier (I?, ferrocyanide). 相似文献
6.
The rate of reaction of ferro- and ferricytochrome c (C(II) and C(III)) with ferri- and ferrocyanide and of C(III) with O2? and CO2? was determined in H2O and in 2H2O in the temperature range 5–35 °C. No isotope effect was evident in any of the reductions of C(III); the apparent energy of activation was identical in H2O and 2H2O. An isotope effect with , depending on pH for instance was observed in the oxidation of C(II), in the slow phase of oxidation which involves conformational changes. An interpretation (supported by evidence from previous work) involving water molecules in the close vicinity of the reaction site on the protein is discussed. 相似文献
7.
Quercetin inhibited a dog kidney ( preparation without affecting for ATP or for cation activators, attributable to the slowly-reversible nature of its inhibition. Dimethyl sulfoxide, a selector of E2 enzyme conformations, blocked this inhibition, while the K+-phosphatase activity was at least as sensitive to quercetin as the ( activity, all consistent with quercetin favoring E1 conformations of the enzyme. Oligomycin, a rapidly-reversible inhibitor, decreased the for ATP and the for cation activators, and its inhibition was also diminished by dimethyl sulfoxide. Although oligomycin did not inhibit the K+-phosphatase activity under standard assay conditions, a reaction presumably catalyzed by E2 conformations, its effects are nevertheless accommodated by a quantitative model for that reaction depicting oligomycin as favoring E1 conformations. The model also accounts quantitatively for effects of both dimethyl sulfoxide and oligomycin on , for substrate, and for K+, as well as for stimulation of phosphatase activity by both these reagents at low K+ but high Na+ concentrations. 相似文献
8.
Mechanism of action of thrombin on fibrinogen. The reaction of thrombin with fibrinogen-like peptides containing 11, 14, and 16 residues 总被引:4,自引:0,他引:4
J W van Nispen T C Hageman H A Scheraga 《Archives of biochemistry and biophysics》1977,182(1):227-243
The following peptides were synthesized by classical methods in solution: Ac-Gly-Gly- Val-Arg-Gly-Pro-Arg-Val-Val-Glu-Arg-NHCH3 (A), Ac-Ala-Glu-Gly-Gly-Gly-Val- Arg-Gly-Pro-Arg-Val-Val-Glu-Arg-NHCH3 (B), and Ac-Phe-Leu-Ala-Glu-Gly-Gly- Gly-Val-Arg-Gly-Pro-Arg-Val-Val-Glu-Arg-NHCH3 (C). The rates of hydrolysis of the Arg-Gly bond of these three peptides by thrombin were measured, and the values of were found to be 0.05 × 10?7 (A), 0.02 × 10?7 (B), and 1.6 × 10?7 (C) [(NIH units/ liter)s]?1. The value of for peptide C is less than 1% of that for fibrinogen [although the value of kcat itself, for peptide C (but not for A or B), is comparable to that for fibrinogen]. These results indicate that phenylanine and leucine at positions P9 and P8, respectively, play a key role in the reaction of thrombin with fibrinogen. The data also show that factors outside of the 16 residues of peptide C are important in determining the rate of hydrolysis of fibrogen by thrombin. 相似文献
9.
J K Ladha P Rowell W D Stewart 《Biochemical and biophysical research communications》1978,83(2):688-696
5-hydroxylysine, an analogue of glutamate and lysine, causes production by N2-fixing A. cylindrica; it also reversibly inhibits GS activity in vitro but has no effect on alanine dehydrogenase or GOGAT. On adding 5-hydroxylysine intracellular pools of glutamine, glutamate and aspartate decrease; those of alanine and serine increase. 5-hydroxylysine alleviates the inhibitory effect of on heterocyst production and C2H2 reduction and in cultures results in heterocyst synthesis and in C2H2 reduction. The data suggest that the GS-GOGAT pathway is the sole route of importance in primary assimilation in A. cylindrica, that alone does not inhibit nitrogenase and heterocyst production, and that GS and/or a product is involved in regulating the production of both. 相似文献
10.
The kinetic α-secondary deuterium isotope effect, , for the pH-independent hydrolysis of nicotinamide riboside, yielding nicotinamide and ribose, in water at 25 ° is 1.14, establishing that this reaction proceeds with unimolecular substrate decomposition to yield a carboxonium ion, or related species, in the rate-determining step. Surprisingly, the corresponding isotope effect for the base-catalyzed decomposition of the same substrate is 1.12, a value indicating considerable sp2 character at the Cl′ position in the transition state for this reaction. A similar result, , was obtained for base-catalyzed hydrolysis of NAD+. The kinetic alpha deuterium isotope effect for the pig brain NAD glycohydrolasecatalyzed hydrolysis of nicotinamide riboside is 1.08. This value suggests that CN bond cleavage to form an intermediate carboxonium ion, or structurally related species, is at least partially rate-determining. In contrast, the corresponding value for the hydrolysis of this substrate catalyzed by Escherichia coli nicotinamide ribonucleotide glycohydrolase is very near unity, a result consistent with several interpretations including a rate-determining enzyme isomerization reaction. 相似文献
11.
Laser flash photolysis techniques have yielded rate constants for physical and reactive quenching modes of by nicotine, nicotinamide adenine dinucleotide (oxidized and reduced forms) and the reduced forms of nicotinamide mononucleotide, nicotinamide adenine dinucleotide phosphate and nicotinamide hypoxanthine dinucleotide. In the case of the last four named compounds, kinetic spectroscopy furnished evidence for one-electron transfers to . Specifically, production of O?2 was demonstrated unequivocally by reaction with 1,4-benzoquinone. Quantitative determinations revealed the extent of reactive quenching to be near 60% in each case. 相似文献
12.
C Grieco C Hansch C Silipo R N Smith A Vittoria K Yamada 《Archives of biochemistry and biophysics》1979,194(2):542-551
Fourteen derivatives of l-alanine of the type CH3CH(NHCO-3-C5H4N)COOR3 have been synthesized and their hydrolysis by chymotrypsin was studied with the object of characterizing enzymic space (?3) to which R3 binds. The binding of R3 () was shown via correlation analysis to correlate with molar refractivity (MR) of R3 rather than hydrophobicity (π). The results confirmed our earlier predictions. A correlation equation for the hydrolysis of 77 acyl-amino acid esters of the general formula R2CH(NHCOR1)COOR3 relating to molar refractivity of R1, R2, and R3 and to (Taft's polar parameter) of R3 was formulated. The general picture of ligand interactions with chymotrypsin as seen with correlation analysis is discussed. 相似文献
13.
An ATPase is demonstrated in plasma membrane fractions of goldfish gills. This enzyme is stimulated by Cl? and HCO3?, inhibited by SCN?.Biochemical characterization shows that HCO3? stimulation () is specifically inhibited in a competitive fashion by SCN? (). The residual Mg2+-dependent activity is weakly is weakly affected by SCN?.In the microsomal fraction chloride stimulation of the enzyme occurs in the presence of HCO3? (); no stimulation is observed in the absence of HCO3?. Thiocyanate exhibits a mixed type of inhibition () towards the Cl? stimulation of the enzyme.Bicarbonate-dependent ATPase from the mitochondrial fraction is stimulated by Cl?, but this enzyme has a relatively weak affinity for this substrate (). 相似文献
14.
W R Scowcroft A H Gibson J D Pagan 《Biochemical and biophysical research communications》1976,73(2):516-523
Nitrogenase activity in agar cultures of cowpea rhizobia, strain 32H1, was rapidly inhibited by but this was relieved by increased O2 tension. Inhibition was more rapid than that caused by inhibitors of protein synthesis and was not relieved by methionine sulfoximine or methionine sulfone. Under conditions were nitrogenase activity was inhibited by , glutamine synthetase and glutamate synthase were substantially unaffected. Glutamate dehydrogenase was undetected in either nitrogenase active or inhibited cultures. These results indicate that inhibition of nitrogenase activity in strain 32H1 is not effected through glutamine synthetase regulation of nitrogenase synthesis. 相似文献
15.
16.
Steve Burden 《Developmental biology》1977,61(1):79-85
The turnover of acetylcholine receptors labeled with 125I-labeled α-bungarotoxin was measured in the developing posterior latissimus dorsi muscle of the chick. The degradation rates for acetylcholine receptors at the neuromuscular junction and in extrajunctional regions of the muscle cell were determined. One week after hatching, the rates of junctional and extrajunctional receptor degradation are identical (). Three weeks weeks after hatching, however, the rate of junctional receptor degradation is considerably slower () and different than the rate of extrajunctional receptor degradation (). Thus, receptors which are localized at the neuromuscular junction early in embryonic life only become stable several weeks after hatching. 相似文献
17.
Wilson B. Knight Su-Jen Ting Suzan Chuang Debra Dunaway-Mariano Tuli Haromy Muttaiya Sundaralingam 《Archives of biochemistry and biophysics》1983,227(1):302-309
Monodentate Co(NH3)5PPi was determined not to be a substrate for yeast inorganic pyrophosphatase while P1,P2-bidentate Co(NH3)4PPi was turned over by the enzyme at a rate of 7.5 min?1. A kinetic analysis of the substrate activities of the P1,P2-bidentate complexes, Co(en)2PPi, Cr(NH3)4PPi, Cr(H2O)(NH3)3PPi, Cr(H2O)2(NH3)2PPi, and Cr(H2O)4PPi was carried out in order to access the potential role of the metal-water ligands in productive binding. While substitution of the H2O ligands with NH3 ligands had a minimal affect on the Km for Mg2+, the binding affinity of the complexes decreased with an increasing ligand ratio as did the turnover number of the corresponding central complexes. The Co(en)2PPi complex was hydrolyzed at a rate approximately 0.6% of that for the Co(NH3)4PPi complex. The substrate activities of β,γ-bidentate Co(NH3)4PPPi and α,β,γ-tridentate Co(NH3)3PPP with pyrophosphatase were also tested. While both complexes were shown to bind tightly to the Mg2+-activated enzyme neither was hydrolyzed. On the other hand, in the presence of the Zn2+-activated enzyme the tridentate complex was turned over at a rate of 0.17 min?1 while the bidentate complex remained inert to hydrolysis. 相似文献
18.
19.
(1) The polymorphic phase behaviour of aqueous dispersions of various synthetic phosphatidylethanolamines, both singly and in mixtures, has been investigated by 31P-NMR. (2) PE remains in the lamellar phase up to 90°C. PE exhibits a lamellar to hexagonal (HII) transition between 60°C and 63°C. For PE, the lamellar to hexagonal (HII) transition occurs between 7 and 12°C, whereas for PE, the hexagonal (HII) phase is the preferred structure above ?15°C. (3) Mixtures of PE and PE exhibit near-ideal miscibility behaviour. For mixtures of PE and PE there is evidence of fluid-solid immiscibility at temperatures below the gel-liquid crystalline transition temperature of the PE component. Mixtures of PE and PE exhibit complex phase behaviour involving limited fluid-solid immiscibility at low temperatures and formation of a phase allowing isotropic motional averaging at higher temperatures. (4) 31P-NMR provides a graphic method for investigating the miscibility properties of mixed PE systems. 相似文献
20.
The intrinsic viscosities, weight-average molecular weights (M?w), and radii of gyration [()≈] of Streptococcus salivarius levan in various solvents were respectively obtained from viscosity and light-scattering measurements. The data showed that the levan in water is not aggregated by hydrogen bonds, and that the values of both the refractive index and () are lower in water than in aqueous solutions of urea. Urea may break intramolecular hydrogen-bonds, e.g., between branches, allowing the molecule to expand. 相似文献