266 research outputs found
Transformation of 1,1,1-trichloroethane in an anaerobic packed-bed reactor at various concentrations of 1,1,1-trichloroethane, acetate and sulfate
Biotransformation of 1,1,1-trichloroethane (CH3CCl3) was observed in an anaerobic packed-bed reactor under conditions of both sulfate reduction and methanogenesis. Acetate (1 mM) served as an electron donor. CH3CCl3 was completely converted up to the highest investigated concentration of 10 µM. 1,1-Dichloroethane and chloroethane were found to be the main transformation products. A fraction of the CH3CCl3 was completely dechlorinated via an unknown pathway. The rate of transformation and the transformation products formed depended on the concentrations of CH3CCl3, acetate and sulfate. With an increase in sulfate and CH3CCl3 concentrations and a decrease in acetate concentration, the degree of CH3CCl3 dechlorination decreased. Both packed-bed reactor studies and batch experiments with bromoethanesulfonic acid, an inhibitor of methanogenesis, demonstrated the involvement of methanogens in CH3CCl3 transformation. Batch experiments with molybdate showed that sulfate-reducing bacteria in the packed-bed reactor were also able to transform CH3CCl3. However, packed-bed reactor experiments indicated that sulfate reducers only had a minor contribution to the overall transformation in the packed-bed reactor.
The prodrug activator EtaA from Mycobacterium tuberculosis is a Baeyer-Villiger monooxygenase
EtaA is a newly identified FAD-containing monooxygenase that is responsible for activation of several thioamide prodrugs in Mycobacterium tuberculosis. It was found that purified EtaA displays a remarkably low activity with the antitubercular prodrug ethionamide. Hinted by the presence of a Baeyer-Villiger monooxygenase sequence motif in the EtaA sequence, we have been able to identify a large number of novel EtaA substrates. It was discovered that the enzyme converts a wide range of ketones to the corresponding esters or lactones via a Baeyer-Villiger reaction, indicating that EtaA represents a Baeyer-Villiger monooxygenase. With the exception of aromatic ketones (phenylacetone and benzylacetone), long-chain ketones (e.g. 2-hexanone and 2-dodecanone) also are converted. EtaA is also able to catalyze enantioselective sulfoxidation of methyl-ptolylsulfide. Conversion of all of the identified substrates is relatively slow with typical kcat values of around 0.02 s-1. The best substrate identified so far is phenylacetone (Km = 61 μM, kcat = 0.017 s-1). Redox monitoring of the flavin cofactor during turnover of phenylacetone indicates that a step in the reductive half-reaction is limiting the rate of catalysis. Intriguingly, EtaA activity could be increased by one order of magnitude by adding bovine serum albumin. This reactivity and substrate acceptance-profiling study provides valuable information concerning this newly identified prodrug activator from M. tuberculosis
Comparison of stimulation patterns for FES-cycling using measures of oxygen cost and stimulation cost
<b>Aim</b><p></p>
The energy efficiency of FES-cycling in spinal cord injured subjects is very much lower than that of normal cycling, and efficiency is dependent upon the parameters of muscle stimulation. We investigated measures which can be used to evaluate the effect on cycling performance of changes in stimulation parameters, and which might therefore be used to optimise them. We aimed to determine whether oxygen cost and stimulation cost measurements are sensitive enough to allow discrimination between the efficacy of different activation ranges for stimulation of each muscle group during constant-power cycling. <p></p>
<b>Methods</b><p></p>
We employed a custom FES-cycling ergometer system, with accurate control of cadence and stimulated exercise workrate. Two sets of muscle activation angles (“stimulation patterns”), denoted “P1” and “P2”, were applied repeatedly (eight times each) during constant-power cycling, in a repeated measures design with a single paraplegic subject. Pulmonary oxygen uptake was measured in real time and used to determine the oxygen cost of the exercise. A new measure of stimulation cost of the exercise is proposed, which represents the total rate of stimulation charge applied to the stimulated muscle groups during cycling. A number of energy-efficiency measures were also estimated. <p></p>
<b>Results</b><p></p>
Average oxygen cost and stimulation cost of P1 were found to be significantly lower than those for P2 (paired <i>t</i>-test, <i>p</i> < 0.05): oxygen costs were 0.56 ± 0.03 l min<sup>−1</sup> and 0.61 ± 0.04 l min<sup>−1</sup>(mean ± S.D.), respectively; stimulation costs were 74.91 ± 12.15 mC min<sup>−1</sup> and 100.30 ± 14.78 mC min<sup>−1</sup> (mean ± S.D.), respectively. Correspondingly, all efficiency estimates for P1 were greater than those for P2. <p></p>
<b>Conclusion</b><p></p>
Oxygen cost and stimulation cost measures both allow discrimination between the efficacy of different muscle activation patterns during constant-power FES-cycling. However, stimulation cost is more easily determined in real time, and responds more rapidly and with greatly improved signal-to-noise properties than the ventilatory oxygen uptake measurements required for estimation of oxygen cost. These measures may find utility in the adjustment of stimulation patterns for achievement of optimal cycling performance. <p></p>
The hyperon-nucleon interaction: conventional versus effective field theory approach
Hyperon-nucleon interactions are presented that are derived either in the
conventional meson-exchange picture or within leading order chiral effective
field theory. The chiral potential consists of one-pseudoscalar-meson exchanges
and non-derivative four-baryon contact terms. With regard to meson-exchange
hyperon-nucleon models we focus on the new potential of the Juelich group,
whose most salient feature is that the contributions in the scalar--isoscalar
(\sigma) and vector--isovector (\rho) exchange channels are constrained by a
microscopic model of correlated \pi\pi and KKbar exchange.Comment: 28 pages, 8 figures, submitted to Lecture Notes in Physic
Nonequilibrium wetting
When a nonequilibrium growing interface in the presence of a wall is
considered a nonequilibrium wetting transition may take place. This transition
can be studied trough Langevin equations or discrete growth models. In the
first case, the Kardar-Parisi-Zhang equation, which defines a very robust
universality class for nonequilibrium moving interfaces, with a soft-wall
potential is considered. While in the second, microscopic models, in the
corresponding universality class, with evaporation and deposition of particles
in the presence of hard-wall are studied. Equilibrium wetting is related to a
particular case of the problem, it corresponds to the Edwards-Wilkinson
equation with a potential in the continuum approach or to the fulfillment of
detailed balance in the microscopic models. In this review we present the
analytical and numerical methods used to investigate the problem and the very
rich behavior that is observed with them.Comment: Review, 36 pages, 16 figure
Experimental pulse technique for the study of microbial kinetics in continuous culture
A novel technique was developed for studying the growth kinetics of microorganisms in continuous culture. The method is based on following small perturbations of a chemostat culture by on-line measurement of the dynamic response in oxygen consumption rates. A mathematical model, incorporating microbial kinetics and mass transfer between gas and liquid phases, was applied to interpret the data. Facilitating the use of very small disturbances, the technique is non-disruptive as well as fast and accurate. The technique was used to study the growth kinetics of two cultures, Methylosinus trichosporium OB3b growing on methane, both in the presence and in the absence of copper, and Burkholderia (Pseudomonas) cepacia G4 growing on phenol. Using headspace flushes, gas blocks and liquid substrate pulse experiments, estimates for limiting substrate concentrations, maximum conversion rates Vmax and half saturation constants Ks could rapidly be obtained. For M. trichosporium OB3b it was found that it had a far higher affinity for methane when particulate methane monooxygenase (pMMO) was expressed than when the soluble form (sMMO) was expressed under copper limitation. While for B. cepacia G4 the oxygen consumption pattern during a phenol pulse in the chemostat indicated that phenol was transiently converted to an intermediate (4-hydroxy-2-oxovalerate), so that initially less oxygen was used per mole of phenol.
Universality and scaling study of the critical behavior of the two-dimensional Blume-Capel model in short-time dynamics
In this paper we study the short-time behavior of the Blume-Capel model at
the tricritical point as well as along the second order critical line. Dynamic
and static exponents are estimated by exploring scaling relations for the
magnetization and its moments at early stage of the dynamic evolution. Our
estimates for the dynamic exponents, at the tricritical point, are  and .Comment: 12 pages, 9 figure
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