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91.
The capacity for anaerobic decolorization of a sulfonated azo dye, Congo Red, by a strain of a sulfate-reducing bacterium
was evaluated. After optimizing the growth rate of the bacteria on a simple carbon source and terminal electron acceptor pair,
lactate and sulfate, respectively, the effect of the dye concentration on their growth rate was analyzed. The decolorization
rate was affected by the dye concentration in the growth medium. The azo-bond cleavage mechanism of reductive decolorization
with the formation of benzidine was consistent with the results, as this metabolite was identified by high-performance liquid
chromatography. Several fractions of the culture medium, including lysed cell extracts, were examined for the capacity to
reduce the azo dye. This reduction capacity was found in the culture medium in which the cells had previously grown. The results
showed that the mechanism of reductive decolorization of this sulfonated azo dye was extracellular and nonenzymatic, consistent
with the production of sulfide anion by the microorganisms while growing on lactate and sulfate. The sulfide anions were the
cause of the reduction leading to the disappearance of color in the medium. To increase the rate of decolorization, the presence
of ferrous ion was also necessary together with the lactate and sulfate substrates. 相似文献
92.
Narayani Ramakrishnan Marian E. Clay Liang-YAN Xue Helen H. Evans Antonio Rodriguez-Antunez Nancy L. Oleinick 《Photochemistry and photobiology》1988,48(3):297-303
Abstract— Chloroaluminum phthalocyanine (CAPC) is an efficient photosensitizer for the inactivation of Chinese hamster V79 cells. In order to investigate possible molecular mechanisms in the photo-dynamic action of CAPC and visible light, the induction and repair rate of two classes of DNA lesions have been determined, i.e. DNA single-strand breaks and DNA-protein cross-links. In cells pretreated with 1 μ.M CAPC, a fluence of 12 kJ/m2 of red light (>600 nm) kills approximately 50% of the cells and induces 3 to 3.5 Gy-equivalents of single-strand breaks. The repair of these breaks was slower than the repair of single-strand breaks induced by -irradiation. The photodynamic action of CAPC also induces a large number of DNA-protein cross-links which, in contrast to -radiation-induced DNA-protein cross-links, do not appear to be repaired during 4 h of post-treatment incubation in fresh medium. These studies suggest that DNA may be an important target for the cytotoxicity of CAPC + red light. 相似文献
93.
Fábio C. Sampaio Paolo Torre Flávia M. Lopes Passos Célia Alencar de Moraes Patrizia Perego Attilio Converti 《Applied biochemistry and biotechnology》2007,136(2):165-181
To obtain in-depth information on the overall metabolic behavior of the new good xylitol producer Debaryomyces hansenii UFV-170, batch bioconversions were carried out using semisynthetic media with compositions simulating those of typical acidic
hemicellulose hydrolysates of sugarcane bagasse. For this purpose, we used media containing glucose (4.3–6.5 g/L), xylose
(60.1–92.1 g/L), or arabinose (5.9–9.2 g/L), or binary or ternary mixtures of them in either the presence or absence of typical
inhibitors of acidic hydrolysates, such as furfural (1.0–5.0 g/L), hydroxymethylfurfural (0.01–0.30 g/L), acetic acid (0.5–3.0
g/L), and vanillin (0.5–3.0 g/L). D. hansenii exhibited a good tolerance to high sugar concentrations as well as to the presence of inhibiting compounds in the fermentation
media. It was able to produce xylitol only from xylose, arabitol from arabinose, and no glucitol from glucose. Arabinose metabolization
was incomplete, while ethanol was mainly produced from glucose and, to a lesser less extent, from xylose and arabinose. The
results suggest potential application of this strain in xyloseto-xylitol bioconversion from complex xylose media from lignocellulosic
materials. 相似文献
94.
Blay G Bargues V Cardona L Collado AM Garcia B Munoz MC Pedro JR 《The Journal of organic chemistry》2000,65(7):2138-2144
Hydroxyester 2, easily obtained from santonin (1), has been transformed into 10 alpha-hydroxyguai-3-en-8,12-olide 6, a good intermediate for the synthesis of natural 8,12-guaianolides. Compound 6 was obtained from 2 by photochemical rearrangement of its acetyl derivative 7, stereoselective hydrogenation on Pd/C, reduction, regioselective elimination, hydrolysis, and lactonization. The synthesis of the natural guaianolides 3-5 was carried out in two sequences in which the regioselective elimination of a hydroxyl group at C10 with triflic anhydride or SOCl2 to afford, respectively, the endo or exo double bond on C10 and the regioselective opening of the C3-C4 alpha-epoxide were the key steps. 相似文献
95.
W. Klaus M. E. Garcia K. H. Bennemann 《Zeitschrift für Physik D Atoms, Molecules and Clusters》1995,35(1):43-49
The short-time behavior of small Hg n clusters immediately after single or double ionization is studied. We calculate self-consistently the ground state electronic energyE of ionized Hg n clusters. Upon ionization changes of the potential energy surface (PES) occur, which govern the atomic motion in the cluster. These changes depend on cluster size and charge and are determined by the interplay between the localization of the holes within an ionic core and the polarization energy of the neutral rest of the cluster. In the case of single ionization of the cluster the PES results mainly from hole delocalization. In contrast, in the case of double ionization the PES is governed almost only by strong environment polarization. We use our theory to explain the physical origin of the oscillations in the ionization cross-section of singly and doubly excited Hg n clusters observed in recent pump-probe experiments. 相似文献
96.
J. V. Sinisterra F. Garcia Blanco M. Iglesias J. M. Marinas 《Reaction Kinetics and Catalysis Letters》1984,25(3-4):277-282
A general and repetitive method to determine the base strength and number of basic sites of catalysts with low surface area is reported. The nature of the titrating agent is discussed. The nature of the active sites of a Ba(OH)2 catalyst with low surface area is discussed.
. . Ba(OH)2, .相似文献
97.
Variations of densities and viscosities with temperature and composition are reported for binary liquid mixtures containing propionic acid+aniline (I),+o-toluidine (II),+o-anisidine (III), and+o-chloroaniline (IV). Entropies S
m and enthalpies H
m of activation as functions of the composition of the mixtures, as well as free energies of activation G
m at 10, 20, 30, 40, and 50°C and different compositions were calculated by means of Eyring's equation. The formation of activated complexes between the components of these binary mixtures is postulated and claimed to result from acid-base and hydrogen bonding exchange interactions. 相似文献
98.
Neutral oxorhenium(V) complexes with thiosemicarbazones derived from 2‐pyridine formamide, HL1, are formed when [ReOCl3(PPh3)2] reacts with equimolar amounts of the ligands. Reduction of the metal and the formation of rhenium(III) complexes of the composition [Re(L1)2]+ occurs when an excess of thiosemicarbazones is used and the reaction is performed in boiling toluene for a prolonged period of time. The thiosemicarbazones deprotonate and act as tridentate ligands as has been confirmed by an X‐ray structure of [ReOCl2(L1b)], where HL1b is 2‐pyridineformamide‐N(4)‐ethylthiosemicarbazone and the ligand occupies the equatorial coordination sphere of the complex together with one of the chloro ligands. 相似文献
99.
100.