Hydrogen-bonding regulated supramolecular chirality with controllable biostability

The regulation of natural helical nanostructures is principally supported and actuated by hydrogen bonds(H-bonds)formed from hydrogen-bonding groups(peptide bonds and base pairs)to realize biological activities and specific biofunctional transformations.However,studying the role of H-bonding patterns on the handedness of supramolecular assemblies is still challenging,since supramolecular assemblies will be disassembled or destabilized with slightly varying H-bonding groups for most supramolecules.To circumvent this issue,herein,two types of self-assembled C2-symmetric phenylalanine derivatives differed by a single H-bonding group(ester or amide)are systematically designed for deciphering the role of H-bonding pattern on the chirality of supramolecular assemblies and their related biostability.Opposite handedness nanofibrous structures with tailorable diameter and helical pitch are achieved with the transition from ester to amide groups in the gelators.Experimental and theoretical evidence suggests that helical orientation of ester-containing gelators ascribes to intermolecular H-bonds.In contrast,the helical direction for the amide-counterparts is mainly due to intra-and intermolecular H-bonds.Moreover,these H-bonding groups greatly influence their stability,as revealed by in vitro and in vivo degradation experiments and the left-handed assemblies are more stable than the right-handed ones.Thus,the study offers a feasible model to have valuable insight into understanding the role of H-bonding patterns in biological folding.

Structural Comportment of Extract of Bougainvillea xbuttiana Flower Incorporated in Silica Xerogel Matrix

Measurement of the fluorescence comportment of Bougainvillea xbuttiana flowers embedded in silica xerogels matrix prepared with two different water to tetraethyl-orthosilicate [Si(OC2H5)4] ratio molar of 11 and 5, without heat-treatment, we report the grade of biostability of compound. The structural comportment for the PSI and PSII present in Bougainvillea flower is similar to the structural comportment for these photosystems present in leaves when they are incorporated on inorganic matrix such as silica xerogels. The contribution of the natural pigment of this kind of flower such as betalains which consist of betaxanthins and betacyanins, determines their colors contributed in the range of wavelength from about 550 nm to 660 nm.

Thermo-Stability of Natural Products Based on Chlorophyll Species Embedded in Silica Xerogel

This work studied the thermostability and the biostability of chlorophyll species obtained from an extract of spinach leaves embedded in a silica xerogel matrix. The analysis was done by monitoring the photosystem II (PSII) using fluorescence spectroscopy. Samples were prepared using the sol gel method with a molar ratio of ethanol/H2O/TEOS of 4:11.6:1. Then, silica xerogel matrix was loaded with an extract of spinach leaves, obtained in dark conditions. The measurement of the fluorescence spectra was done at selected temperatures to the corresponding non-physiological regimen. Results indicate that the PSII band position remains unchanged when heat treatment temperature increases up 200°C. For temperatures above 100?C, the fluorescence intensity diminishes linearly when the temperature increases. The photosystem II embedded in silica xerogel matrix is decomposed at temperatures above 200°C.