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The benzoyl-CoA ligase from an anaerobic syntrophic culture was purified to homogeneity. It had a molecular mass of around 420 kDa and consisted of seven or eight subunits of 58 kDa. The temperature optimum was 37-40 degrees C, the optimum pH around 8.0 and optimal activity required 50-100 mM TRIS-HCl buffer, pH 8.0 and 3-7 mM MgCl2; MgCl2 in excess of 10 mM was inhibitory. The activation energy for benzoate was 11.3 kcal/mol. Although growth occurred only with benzoate as a carbon source, the benzoyl-coenzyme A (CoA) ligase formed benzoyl-CoA esters with benzoate, 2-, 3- and 4-fluorobenzoate, picolinate, nicotinate and isonicotinate. Acetate was activated to acetyl-CoA by an acetyl-CoA synthetase. The Km values for benzoate, 2-, 3- and 4-fluorobenzoate were 0.04, 0.28, 1.48 and 0.32 mM, the Vmax values 1.05, 1.0, 0.7 and 0.98 units (U)/mg, respectively. For reduced CoA (CoA-SH) a Km of 0.07 mM and a Vmax of 1.05 U/mg and for ATP a Km of 0.16 mM and a Vmax of 1.08 U/mg was determined. Benzoate activation was inhibited by more than 6 mM ATP, presumably by pyrophosphate generation from ATP. The inhibition constant (Ki) for pyrophosphate was 5.7 mM. No homology of the N-terminal amino acid sequence with that of a 2-aminobenzoyl-CoA ligase of a denitrifying Pseudomonas sp. was found.
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PMID:Purification and characterization of benzoyl-CoA ligase from a syntrophic, benzoate-degrading, anaerobic mixed culture. 136 92

The synthesis and characterization of colloidal mesoporous silica (CMS) functionalized with vinyl-, benzyl-, phenyl-, cyano-, mercapto-, aminopropyl- or dihydroimidazole moieties is reported. Uniform mesoporous particles ranging in size from 40 to 150 nm are generated in a co-condensation process of tetraethylorthosilicate (TEOS) and organotriethoxysilanes (RTES) in alkaline aqueous media containing triethanolamine (TEA) in combination with cetyltrimethylammonium chloride (CTACl) serving as a structure-directing agent. The materials are obtained as colloidal suspensions featuring long-term stability after template removal by ion exchange with an ethanolic solution of ammonium nitrate or HCl. The spherical particles exhibit a wormlike pore system with defined pore sizes and high surface areas. Samples are analyzed by a number of techniques including TEM, SEM, DLS, TGA, Raman, and cross-polarized (29)Si-MAS NMR spectroscopy, as well as nitrogen sorption measurements. We demonstrate that co-condensation and grafting methods result in similar changes in the nitrogen adsorption behavior, indicating a successful internal lining of the pores with functional groups through both procedures.
ACS Nano 2008 Apr
PMID:Colloidal suspensions of functionalized mesoporous silica nanoparticles. 1920 12

A mild, four-step purification procedure using NaOH reflux, HCl wash, and oxidation by 4 mol % molecular oxygen at 500 degrees C was developed to purify single-walled carbon nanotubes (SWCNTs) with narrow semiconducting (n,m) distribution produced from cobalt-incorporated MCM-41 (Co-MCM-41) in order to obtain bulk low-defect-density nanotubes. Three key features of Co-MCM-41 allow this mild purification technique: (1) ultrathin silica walls versus dense silica or other crystalline oxide supports are soluble in dilute NaOH aqueous solution, which avoids the damage to SWCNTs usually caused by using HF treatment to remove catalytic supports; (2) the small metallic particles are easily dissolved in HCl, a significantly milder chemical treatment compared to HF or HNO(3); (3) the high selectivity to SWCNTs with negligible multiwalled carbon nanotubes or graphite, which facilitates the removal of undesired carbon species by selective oxidation. The effectiveness of this purification procedure was evaluated by high-resolution transmission electron microscopy, scanning electron microscopy, Raman, UV-vis-NIR, and fluorescence spectroscopy, solution redox chemistry on fractionated (6,5) tubes, and SWCNT-based field effect transistor device performance. The results demonstrate that Co-MCM-41 catalyst not only provides tubes with narrow semiconducting (n,m) distribution but also allows a mild purification procedure and, therefore, produces SWCNTs with fewer defects.
ACS Nano 2007 Nov
PMID:Low-defect, purified, narrowly (n,m)-dispersed single-walled carbon nanotubes grown from cobalt-incorporated MCM-41. 1920 84

A general acid vapor oxidation (AVO) strategy has been developed to grow highly oriented hierarchically structured rutile TiO(2) nanoarrays with tunable morphologies from titanium thin films. This is a simple one-pot synthesis approach involving the reaction of a titanium surface with the vapor generated from a hydrochloric acid solution in a Teflon lined autoclave. To the best of our knowledge, this is the first successful attempt to grow ordered tree-like titania nanoarrays. A possible formation mechanism for the interesting architectures has been proposed based on series of time-dependent experiments. By adjusting the initial HCl concentration, films of different rutile structures including nanotrees, dendritic nanobundles, and nanorods can be selectively obtained. Subsequently, the surface morphologies and wettability can be readily tuned.
ACS Nano 2009 May 26
PMID:Hierarchically nanostructured rutile arrays: acid vapor oxidation growth and tunable morphologies. 1940 May 81

The interfacial diprotonation and assemblies of a free-base achiral porphyrin, 5,10,15,20-tetrakis(3,5-dimethoxyphenyl)-21H,23H-porphine, on various acidic subphases were investigated. It has been shown that the compound could be diprotonated in situ on an acidic subphase and can form assemblies. The interfacially organized supramolecular assemblies were transferred onto a solid substrate, and the assemblies showed supramolecular chirality. Interestingly, the supramolecular chirality of the assemblies of the diprotonated species showed a counterion-dependent behavior. For the assemblies fabricated from the aqueous HCl subphases, a strong Cotton effect (CE) could be observed, although the porphyrin itself is achiral. When an aqueous HBr solution was used as the subphase, the assemblies showed a weak CE, whereas no CE could be detected for the assemblies formulated from the HNO3 or HI subphase. Interestingly, when a mixture of HBr and NaCl, or HNO3 and NaCl, was employed as the subphase, the formed assemblies displayed chiral features similar to those fabricated on the HCl subphase, suggesting that the Cl(-) could be preferentially visualized in terms of supramolecular chirality, although the system itself is composed of achiral species. On the basis of the experimental facts and a theoretical calculation, an explanation with regard to the different sizes of the counterions and the distinct binding affinities of the counteranions to the diprotonated porphyrin species has been proposed. Our findings provide new insights into the assembly of the diprotonated porphyrins as well as the interfacially occurring symmetry breaking.
ACS Appl Mater Interfaces 2009 Sep
PMID:Acidification and assembly of porphyrin at an interface: counterion matching, selectivity, and supramolecular chirality. 2035 30

In this work, it was discovered and demonstrated that the combustion of rice husk is a catalytic process by the thermoanalytical technique. The catalyst involves the oxides of such transition metals as Mn, Fe, and Cu, which are mainly formed in the initial stage of rice husk combustion and remain in the rice husk ash as an impurity. Mn(2+) ions of various concentrations were reloaded into the HCl-washed husk for cocombustion. As a result, the complete combustion temperature of the husk was decreased exponentially depending on the Mn(2+) concentration. By the facile Mn loading technique using a 0.5 M solution, the combustion temperature can be decreased by approximately 100 degrees C, and the resulting ashes themselves can be a good catalyst in the complete combustion of many other organic compounds. The physicochemical properties and amorphous structure of the ashes from both the raw and HCl-washed husks were found to be strongly dependent on the burning temperature. A decreased complete rice husk combustion temperature can be beneficial in preparing porous amorphous silica with high surface area, high densification, and small Si-O-Si band angles.
ACS Appl Mater Interfaces 2009 Nov
PMID:Facile catalytic combustion of rice husk and burning temperature dependence of the ashes. 2035 21

The mesoporous bulks composed of TiO(2)-derived titanate nanotubes fabricated from a hydrothermal treatment of commercial TiO(2) particles in a concentrated NaOH aqueous solution were obtained by a hydrothermal hot-pressing (HHP) method and subsequent steam-curing process with HCl solutions. The mesopore size and sodium concentration for the bulky TiO(2)-derived titanate nanotubes were dependent on the treatment conditions on the steam curing process with HCl solutions. The effect of the sodium concentration (Na/Ti) on microstructures were examined on the steam curing process for the application of the bulky TiO(2)-derived titanate nanotubes to several new fields.
ACS Appl Mater Interfaces 2010 Apr
PMID:Microstructural control of mesoporous bulk composed of TiO(2)-derived titanate nanotubes. 2042 32

A versatile and robust adsorbent with both magnetic property and very high adsorption capacity is presented on the basis of functionalization of iron oxide-silica magnetic particles with carboxylic hyperbranched polyglycerol (Fe(3)O(4)/SiO(2)/HPG-COOH). The structure of the resulting product was confirmed by Fourier transform infrared (FTIR) spectra, thermo gravimetric analysis (TGA), zeta-potential, and transmission electron microscopy (TEM). According to the TGA results, the density of the carboxylic groups on the surface of Fe(3)O(4)/SiO(2)/HPG-COOH is calculated to be as high as 3.0 mmol/g, posing a powerful base for adsorbing dyes and drugs. Five kinds of dyes and one representative anticancer drug were chosen to investigate the adsorption capacity of the as-prepared magnetic adsorbent. The adsorbent shows highly efficient adsorption performance for all of the adsorbates especially for the cationic dyes and drug. For example, the saturated adsorption capacity of the Fe(3)O(4)/SiO(2)/HPG-COOH for methyl violet (MV) can reach 0.60 mmol/g, which is much higher than the previous magnetic adsorbents (usually lower than 0.30 mmol/g). 95% of MV and 90% of R6G could be adsorbed within 5 min, and both of the adsorptions reached equilibrium in about 15 min. The adsorption kinetics and isotherm of the adsorbents were investigated in detail and found that the kinetic and equilibrium adsorptions are well-modeled using pseudo-second-order kinetics and Langmuir isotherm model, respectively. In addition, the influences of pH and ionic strength on the adsorption capacity were also examined and found that pH has much greater effect on the adsorption capacity compared with the ionic strength. Regeneration experiments showed that the Fe(3)O(4)/SiO(2)/HPG-COOH can be well-regenerated in ethanol and partially regenerated in 1 M HCl aqueous solution. After regeneration, the magnetic adsorbents can still show high adsorption capacity even for 10 cycles of desorption-adsorption. No obvious decreases of magnetic intensity and aggregation of adsorbents can be observed even after 10 cycles of adsorption-desorption.
ACS Appl Mater Interfaces 2010 May
PMID:Magnetic dendritic materials for highly efficient adsorption of dyes and drugs. 2045 67

The CdS-sensitized solar cells (CdS-SSC) were fabricated by spray pyrolysis deposition (SPD) method. The performance of the cells was greatly improved through post-treatments that included thermal oxidation at 500 degrees C for 30 min in an air atmosphere and subsequent chemical etching by 40 mM aqueous HCl solution at room temperature for 30 min, as compared to as-deposited CdS-SSC. The CdS-SSC in a I(-)/I(3)(-) electrolyte system was resulted in the improvement of J(sc) (3.3 --> 5.2 mA/cm(2)), V(oc) (697 --> 758 mV), FF (41.4% --> 46.9%), and (0.95% --> 1.84%). Similarly, the efficiency of CdS-SSC in a noncorrosive polysulfide electrolyte system was also enhanced by the proposed thermal oxidation and etching process. The increase in the cell efficiency is attributed to the reduced charge recombination among sensitizer themselves through the mitigation of overaggregated CdS sensitizers deposited by SPD.
ACS Appl Mater Interfaces 2010 Jun
PMID:Performance enhancement through post-treatments of CdS-sensitized solar cells fabricated by spray pyrolysis deposition. 2051 59

The (68)Ge/(68)Ga generator has high potential for clinical positron emission tomography (PET) imaging. However, because of the unavailability of a suitable sorbent material, the commercially available (68)Ge/(68)Ga generators are not directly adaptable for the preparation of (68)Ga-labeled radiopharmaceuticals. In view of this, a new nanoceria-polyacrylonitrile (PAN) composite sorbent has been synthesized by decomposition of a cerium oxalate precursor to cerium oxide and its subsequent incorporation in PAN matrix for the development of a clinical grade (68)Ge/(68)Ga generator. The X-ray diffraction (XRD) studies and BET nitrogen adsorption technique revealed that nanocrystalline ceria had an average particle size of approximately 10 nm, surface area of 72 +/- 3 m(2)/g and an average pore size of 3.8 +/- 0.1 A. Investigation of the distribution ratio (K(d)) values for the prepared sorbent in 0.01 N HCl medium revealed the suitability of the sorbent for the quantitative retention of (68)Ge and efficient elution of clinical grade (68)Ga. A 370 MBq (10 mCi) (68)Ge/(68)Ga chromatographic generator was developed using this sorbent. (68)Ga could be regularly eluted from this generator with >80% elution yield. The eluted (68)Ga possess high radionuclidic purity (<1 x 10(-5)% of (68)Ge impurity), chemical purity (<0.1 ppm of Ce, Fe and Mn ions) and was amenable for the preparation of (68)Ga-labeled radiopharmaceuticals. The generator gave a consistent performance with respect to the elution yield and purity of (68)Ga over an extended period of 7 months.
ACS Appl Mater Interfaces 2010 Jul
PMID:Nanoceria-PAN composite-based advanced sorbent material: a major step forward in the field of clinical-grade 68Ge/68Ga generator. 2056 99


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