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Complexes 1 and 2 were synthesized in basic medium and under mild hydrothermal conditions.
For that purpose, the isolate was grown in the same medium and under the same conditions used in the bio-decolorization study.
Interesting analytical results, in terms of sensitivity and temporal reproducibility, in alkaline medium and under constant applied potentials (i.e., −1.45 and −0.6 V vs. SCE), were obtained.
In addition, zeolites have mechanical strength, good stability in aggressive medium and under thermal treatment, ability to sorb the trace amounts of analytes, high sorption capacity and selectivity, possibility of easy modification and regeneration of the sorbent, low cost and accessibility.
We therefore assessed the binding of the aptamers at 37°C, in culture medium, and under both conditions simultaneously.
For the nickel enrichment DNA microarray assays, biofilm cells were cultured for 24 h at 37°C in LB glu medium, and under these conditions the hha mutant makes 3-fold more biofilm than the wild-type.
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We manage to fix five GNGs under the minimal medium and three under the YP medium by using this procedure.
Two NGG inconsistencies under the minimal medium and one under the YP medium were resolved by relaxing the irreversibility of at least two reactions.
Overall, by using the GrowMatch procedure along with literature searches we were able to fix thirteen NGGs under the minimal medium and eleven under the YP medium (see Figure 1).
The monopile is considered as a single phase medium and behaves under a linear elastic law.
These mutants were transferred from the solid to liquid medium and kept under phototrophic growth conditions (photon flux density 120 μmol photons m−2 s−1).
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