Carnivorous plants inhabit nutrient-poor environments and supplement nutrient acquisition by capturing and digesting insect prey. Carnivorous adaptations have been hypothesized to be beneficial only in environments with high water and light availability. We hypothesized that plant morphology would change in response to resource availability, exhibiting traits that increase carnivory when light is abundant and exhibiting traits that increase photosynthesis when light is limited. In a field manipulation in Leon County, Texas, we examined the effects of feeding, shading, and their interaction on the morphology of the pitcher plant, Sarracenia alata. We employed a two-factor, cross-classified design, with shading (two levels, shaded and unshaded) and prey capture (two levels, fed and unfed) as factors. Eighty plants were haphazardly assigned to one of four treatments: (1) unshaded and fed (control); (2) shaded and fed; (3) unshaded and unfed; and (4) shaded and unfed. When light availability was reduced, plants produced pitchers that had smaller diameters, which is reflective of a photosynthetic morphology. Unfed plants exhibited reduced growth (produced fewer pitchers and had lower sum of pitcher heights). There was a significant interaction effect on estimated seasonal aboveground biomass: shading had no effect on the mass of unfed plants, but shading reduced the mass of fed plants. As the season progressed, competing vegetation reduced light availability to all pitchers. Plants in all treatments began to produce pitchers that were blade-like with a small, non-functional opening and a widened keel. This morphology would maximize light capture at the expense of prey capture. This experiment provides support for a theoretical model that suggests that carnivorous traits are only beneficial under conditions of high light availability. It also emphasizes the importance of periodic burns of carnivorous plant bogs to remove vegetation, thereby reducing light competition.

Micellization is a phenomenon of central importance in surfactant solutions. Here, we demonstrate that the diffusion-based spreading of the free boundary between a micellar aqueous solution and pure water yields a one-dimensional spatial profile of surfactant concentration that can be used to identify the critical micelle concentration, here denoted as C*. This can be achieved because dilution of micelles into water leads to their dissociation at a well-defined position along the concentration profile and an abrupt increase in diffusion coefficient. Rayleigh interferometry was successfully employed to determine C* values for three well-known surfactants in water at 25 ºC: Triton X-100 (TX-100), Sodium Dodecyl Sulfate (SDS), and Polyoxyethylene(4)Lauryl Ether (Brij-30). The dependence of C* on salt concentration was also characterized for TX-100 in the presence of Na2SO4, NaCl, and NaSCN. Accurate values of C* can be directly identified by visual inspection of the corresponding concentration-gradient profiles. To apply the method of least squares to experimental concentration profiles, a mathematical expression was derived from Fick’s law and the pseudo-phase separation model of micellization with the inclusion of appropriate modifications. While Rayleigh interferometry was employed in our experiments, this approach can be extended to any experimental technique that yields one-dimensional profiles of surfactant concentration. Moreover, diffusion-driven surfactant disaggregation is precise, non-invasive, requires single-sample preparation, and applies to both non-ionic and ionic surfactants. Thus, this work provides the foundation of diffusion-driven dilution methods, thereby representing a valuable addition to existing techniques for the determination of C*.

Oxidative stress is a result of an imbalance between reactive oxygen species (ROS) and the availability/activity of antioxidants. The catalase family of enzymes mitigate the risk from ROS by facilitating the disproportionation of hydrogen peroxide into molecular oxygen and water. Manganese containing catalase (MnCAT) consists of a binuclear manganese core bridged by carboxylate and single-atom ligands, likely water or hydroxide. In this work, hydrogen peroxide disproportionation using complexes of manganese with cyclen and pyclen were investigated due to the spectroscopic similarities of the latter with the native MnCAT enzyme. Potentiometric titrations were used to construct speciation curves to identify what complex compositions were present at different pH values. Based on these results, the complexes were made in situ by mixing stock solutions of ligand, buffer, and metal. The hydrogen peroxide disproportionation reaction was carried out in a sealed cell and PO2 measured using a microsensor (Unisense). When hydrogen peroxide was injected into the cell, disproportionation activity of the complexes was evident by (1) appearance of bubbles in solution, and (2) noticeable increase in PO2 as measured by the sensor. Spectroscopic investigation before, during, and after the reaction was used to follow changes in the UV-visible absorption of the complexes to collect information about the structure of the initial catalyst and any possible intermediate. Both, pyclen and cyclen were determined to form a dimeric structure under the reaction conditions used.

The aptamer domain of a naturally occurring glycine riboswitches was randomized to generate a library containing billions of different variants. The dual genetic selection of this library was performed for sarcosine, a prostate cancer marker, and successfully led to the identification of sarcosine-specific synthetic riboswitches. When a chloramphenicol-resistance gene was expressed under control of these riboswitches, E. coli cells showed chloramphenicol resistance only in the presence of sarcosine. For a colorimetric assay, the sarcosine riboswitch gene was inserted upstream of the lacZ gene. When tested with various concentrations of sarcosine, the enzymatic activity of LacZ was proportional to the amount of sarcosine, clearly indicating the sarcosine-dependent gene regulation by the sarcosine riboswitch.

Triazines appear in pharmaceuticals, agrochemicals, and as building blocks for polymers used in materials science and medicine. Predicting the structure and dynamics in water as a function of pH requires reliable simulations of the pKa values for different sites for protonation. We present the initial DFT methods and continuum solvent for pKa of amines, ring nitrogens, and 2,4,6-triamino-1,3,5-triazine (melamine) derivatives. These M06-2X/6-311++G(2d,2p) calculations in SMD continuum solvent provide consistent accuracy for tested systems, use for future studies of more complex structures.