Amino acids are fundamental building blocks of terrestrial life as well as ubiquitous byproducts of abiotic reactions. In order to distinguish between amino acids formed by abiotic versus biotic processes it is possible to use chemical distributions to identify patterns unique to life. This article describes two capillary electrophoresis methods capable of resolving 17 amino acids found in high abundance in both biotic and abiotic samples (seven enantiomer pairs d/l-Ala, -Asp, -Glu, -His, -Leu, -Ser, -Val and the three achiral amino acids Gly, β-Ala, and GABA). To resolve the 13 neutral amino acids one method utilizes a background electrolyte containing γ-cyclodextrin and sodium taurocholate micelles. The acidic amino acid enantiomers were resolved with γ-cyclodextrin alone. These methods allow detection limits down to 5 nM for the neutral amino acids and 500 nM for acidic amino acids and were used to analyze samples collected from Mono Lake with minimal sample preparation.
This study compares the damping behavior of boron nitride nanotubes (BNNTs) and carbon nanotubes (CNTs) as reinforcement in PLC, a biodegradable copolymer. The damping behavior of PLC composites reinforced with 2 wt % or 5 wt % nanotube filler is evaluated by nanodynamic mechanical analysis (NanoDMA). The addition of 2 wt % CNT leads to the greatest enhancement in damping (tan δ) behavior. This is attributed to pullout in CNTs because of lower interfacial shear strength with the polymer matrix and a more effective sword-in-sheath mechanism as opposed to BNNTs which have bamboo-like nodes. BNNTs however have a superior distribution in the PLC polymer matrix enabling higher contents of BNNT to further enhance the damping behavior. This is in contrast with CNTs which agglomerate at higher concentrations, thus preventing further improvement at higher concentrations. It is observed that for different compositions, tan δ values show no significant changes over varying dynamic loads or prolonged cycles. This shows the ability of nanotube mechanisms to function at varying strain rates and to survive long cycles.
We present a comprehensive discussion of the role that microchip electrophoresis (ME) instrumentation could play in future NASA missions of exploration, as well as the current barriers that must be overcome to make this type of chemical investigation possible. We describe how ME would be able to fill fundamental gaps in our knowledge of the potential for past, present, or future life beyond Earth. Despite the great promise of ME for ultrasensitive portable chemical analysis, to date, it has never been used on a robotic mission of exploration to another world. We provide a current snapshot of the technology readiness level (TRL) of ME instrumentation, where the TRL is the NASA systems engineering metric used to evaluate the maturity of technology, and its fitness for implementation on missions. We explain how the NASA flight implementation process would apply specifically to ME instrumentation, and outline the scientific and technology development issues that must be addressed for ME analyses to be performed successfully on another world. We also outline research demonstrations that could be accomplished by independent researchers to help advance the TRL of ME instrumentation for future exploration missions. The overall approach described here for system development could be readily applied to a wide range of other instrumentation development efforts having broad societal and commercial impact.
We have investigated the interaction of D-amino acid oxidase (DAAO) with single walled carbon nanotubes (CNT) by spectroscopic ellipsometry. Dynamic adsorption experiments were performed at different experimental conditions. In addition, the activity of the enzyme adsorbed at different conditions was studied. Our results indicate that DAAO can be adsorbed to CNT at different pH values and concentrations by a combination of hydrophobic and electrostatic interactions. Considering that the highest enzymatic activity was obtained by adsorbing the protein at pH 5.7 and 0.1 mg.mL−1, our results indicate that DAAO can adopt multiple orientations on the surface; which are ultimately responsible for significant differences in catalytic activity.
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