34 research outputs found
Development of metabolic engineering approaches to regulate the content of total phenolics, antiradical activity and organic acids in callus cultures of the highbush blueberry (Vaccinium corymbosum L.)
Blueberry (Vaccinium corymbosum L.) is increasingly cultivated to produce high
quality berries for consumption and potential applications in medicine, nutrition and as industrial
precursors. Seasonal availability sets limitations on chemical compound isolation from cultivated
plants. Biotechnological solutions, such as tissue cultures and metabolic engineering, can provide
sufficient amounts of plant material with reasonably high metabolite levels, which may be
adjusted by different strategies. Here, we describe our approach to modifying total phenolic
content (TPC), antiradical activity (ARA) and amounts of selected organic acids in in vitro
cultures of two varieties of V. corymbosum by varying the growth media. TPC, ARA and acid
levels were determined in mature leaves of field-grown plants and in stable callus cultures derived
from leaves of varieties ‘Bluecrop’ and ‘Duke’ grown on Murashige-Skoog (MS) and Woody
plant (WP) media supplemented with varying concentrations and combinations of different plant
growth hormones. TPC varied from 83 mg g
-1 dry weight (DW) to 142 mg g
-1 DW in leaves of
‘Bluecrop’ and ‘Duke’, respectively, and correlated with their ARA with ‘Duke’ at the lead. For
callus cultures the highest ARA, as well as the highest TPC of 94 mg g
-1 DW was observed in
‘Bluecrop’ grown on WP medium with 2,4-dichlorophenoxyacetic acid (2,4-D). High level of
quinic acid was found in the mature leaves of all tested varieties, while callus cultures exhibited
relative increase in amounts of malic, succinic and citric acids instead. Oxalic acid was found
only in callus cultures
Structures and Properties of Newton Black Films Characterized Using Molecular Dynamics Simulations
Measurement of the dynamic surface excess of the non-ionic surfactant C<sub>8</sub>E<sub>4</sub>OMe by neutron reflection and ellipsometry
Determination of the dynamic surface excess of a homologous series of cationic surfactants by ellipsometry
Measurement of the dynamic surface excess of the non-ionic surfactant C<sub>8</sub>E<sub>4</sub>OMe by neutron reflection and ellipsometry
Streaming potential effect on the drainage of thin liquid films stabilized by ionic surfactants
Dynamic effects originating from the electric double layers (EDL) are studied in thin liquid films (TLF) containing ionic and nonionic surfactants. To account for such effects, the EDL are to be incorporated into the differential equations describing the TLF drainage. Numerical simulations in the literature have shown that foam films containing ionic surfactants can drain at a slower rate than that predicted by the Reynolds equation (V(Re)) which postulates rigid planar film surfaces. However, the physical reason of the trend has remained unclarified, and the numerical results have not been validated by any experimental data. In the present study, experiments on the drainage of planar foam films were conducted with the anionic surfactant sodium dodecylsulfate (SIDS) in the presence of additional electrolyte (0.02 M NaCl) and with the cationic tetrapentylammonium bromide (TPAB). The obtained results are in accord with the numerical simulations from the literature (V/V(Re) < 1). Such behavior was observed already in our preceding experiments on planar TLF with SIDS without added electrolyte. These results were compared to the data of the experiments with TLF containing nonionic surfactant, and differences in the drainage pattern between ionics and nonionics were established. A new theoretical model seas developed to account for the dynamic effects arising from EDL. According to the present model, the liquid outflow drags the bulk charges of EDL toward the film border, thus generating streaming potential (as in capillary tubes), which in turn brings the charges back toward the center to maintain the state of zero total electrical current. This creates reverse convection of the liquid near the surfaces, resulting in a velocity of film drainage smaller than V(Re). The present theory predicts kinetic dependence closer to the experiment than the Reynolds equation. The limitations of this new model are specified: it is valid for high ionic strength or low value of the surface potential