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The basic metabolic potentials to convert those substrates are available in the respective microorganisms.
AbOPHI211A showed significant activities toward MP and ethyl-paraoxon, while the activities of wild-type AbOPH toward those substrates were not detected.
Moreover, it is believed that laccase can only oxidize those substrates which have a redox potential below that of the enzyme (Xu et al. 2000).
The results of this study show that those substrates with nano-topographical feature have a significant impact on the cells, and thus on the success of engineered tissue.
As model pollutants, PNP and DNP were used in this study, and the effects of the initial concentration of those substrates and radial thickness of the packed bed for the decomposition properties were examined.
Those substrates that were membrane bound were further scrutinized to identify the topological location of the cleavage site.
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From these data, those substrate features that are important in controlling the regiochemistry and stereochemistry of these oxidative bioconversions are identified.
More importantly, we show that many of those substrate cycles are not identified if alternative partition metrics are used instead of ShReD to determine the hierarchical modularity, demonstrating the value of our ShReD-based algorithm for discovering substrate cycles.
If this would be the case, those microorganisms could be enriched on those alternative substrates instead of on CH4.
The binding interactions resemble those of known small-molecule inhibitors as opposed to those of substrates and peptidic inhibitors.
The ordered GeSi nanorings were then grown on those patterned substrates.
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