A fluorescent probe based on cyclochalcone for detecting peroxynitrite.

A novel cyclic chalcone fluorescent probe C-PN was synthesized to detect ONOO-. After reaction with peroxynitrite, the double bond of C-PN in the cyclic chalcone structure was disconnected, which caused the change of intramolecular charge transfer (ICT) effect, emitting blue fluorescence and quenching orange red fluorescence. Visible to the naked eye, the color of the probe solution changed. The probe showed low sensitivity (detection limit = 20.2 nm), short response time (less than 60 s) at low concentration of ONOO-, good visibility, and good selectivity and stability for ONOO-.

Glycolic acid-based deep eutectic solvents boosting co-production of xylo-oligomers and fermentable sugars from corncob and the related kinetic mechanism.

BACKGROUND: Xylo-oligomers are a kind of high value-added products in biomass fractionation. Although there are several chemical methods to obtain xylo-oligomers from biomass, the reports about the deep eutectic solvents (DESs)-mediated co-production of xylo-oligomers and fermentable sugars and the related kinetic mechanism are limited. RESULTS: In this work, glycolic acid-based DESs were used to obtain xylo-oligomers from corncob. The highest xylo-oligomers yield of 65.9% was achieved at 120 °C for 20 min, of which the functional xylo-oligosaccharides (XOSs, DP 2-5) accounted for up to 31.8%. Meanwhile, the enzymatic digestion of cellulose and xylan in residues reached 81.0% and 95.5%, respectively. Moreover, the addition of metal inorganic salts significantly accelerated the hydrolysis of xylan and even the degradation of xylo-oligomers in DES, thus resulting in higher selectivity of xylan removal. AlCl3 showed the strongest synergistic effect with DES on accelerating the processes, while FeCl2 is best one for xylo-oligomers accumulation, affording the highest xylo-oligomers yield of 66.1% for only 10 min. Furthermore, the kinetic study indicates that the 'potential hydrolysis degree' model could well describe the xylan hydrolysis processes and glycolic acid/lactic acid (3:1) is a promising solvent for xylo-oligomers production, in particular, it worked well with FeCl2 for the excellent accumulation of xylo-oligomers. CONCLUSIONS: Glycolic acid-based deep eutectic solvents can be successfully applied in corncob fractionation with excellent xylo-oligomers and fermentable sugars yields on mild conditions, and the large amount of xylo-oligosaccharides accumulation could be achieved by specific process controlling. The strategies established here can be useful for developing high-valued products from biomass.

[Effects of economic fruit forest planting on the stability of red soil aggregates in the subtropical hilly area]. / 亚热带丘岗区经果林种植对红壤团聚体稳定性的影响.

The stability of aggregates is of great significance to evaluate water and soil environment in regions plan-ting economic fruit forest. We explored the effects of economic fruit forest types on the structure and stability of soil aggregates in the 0-50 cm soil layer from 5-year-old Amygdalus persica, Pyrus sorotina, Citrus reticulata, Camellia oleifera and Actinidia chinensis forests in the hilly area in northern Hunan. The content, distribution characteristics and stability indices of soil aggregates from each economic fruit forest were quantitatively analyzed by the Shavinov method. The results showed that most soil aggregates were mechanically stable, with a minimum content of 92.3%. After wet sieving, the size of water-stable aggregates in the soil from Camellia oleifera forest was mainly >2 mm, accounting for 55.9% of the total aggregates. The 0.25-2 mm aggregates were the dominant particles in the A. persica, P. sorotina, C. reticulata and A. chinensis forest soils, with contributions higher than 43.6%. The mean weight diameter (MWD) and the geometric mean diameter (GMD) of soil aggregates for the five economic fruit forest types ranged from 1.10 to 3.19 mm and 0.61 to 2.28 mm, respectively. Furthermore, the percentages of soil aggregate destruction (PAD) and fractal dimension (D) were in the range of 2.9%-37.3% and 2.30-2.68, respectively. With the increases of soil depth, the stability of soil aggregates from A. persica, C. oleifera and A. chinensis forest soils became worse; MWD and GMD decreased by 1.7%-57.7% and 4.5%-65.8%, respectively; PAD and D increased by 0.4%-17.3% and 1.6%-11.1%, respectively. The effects of economic fruit forest types on the stability of soil aggregates decreased with increasing soil depth. Based on the stability indices, aggregate stability from five economic fruit forests followed the order of C. oleifera > A. chinensis > P. sorotina > C. reticulata > A. persica. The type of economic fruit forest improved the stability of soil structure mainly by affecting the content of large-size aggregates. In terms of improving the distribution and stability of soil aggregates, it was suggested that C. oleifera should be given the top priority as the economic fruit forest in the subtropical hilly area, followed by A. chinensis. Whereas A. persica planting might reduce the degree of soil agglomeration, thus, the protective measures of soil loss should be considered during planting. Our results could provide theoretical basis and application guidance for the development, utilization, and ecological management of economic fruit forests in subtropical hilly areas.

Fragmented α-Amylase into Microporous Metal-Organic Frameworks as Bioreactors.

This work presents an efficient and facile strategy to prepare an α-amylase bioreactor. As enzymes are quite large to be immobilized inside metal-organic frameworks (MOFs), the tertiary and quaternary structures of α-amylase were first disrupted using a combination of urea, dithiothreitol (DTT), and iodoacetamide (IAA). After losing its tertiary structure, the unfolded proteins can now penetrate into the microporous MOFs, affording fragmented α-amylase@MOF bioreactors. Among the different MOFs evaluated, UiO-66 gave the most promising potential due to the size-matching effect of the α-helix of the fragmented α-amylase with the pore size of UiO-66. The prepared bioreactor exhibited high yields of small carbohydrate (maltose) even when reused up to 15 times (>80% conversion).

Spatiotemporal Control of Supramolecular Polymerization and Gelation of Metal-Organic Polyhedra.

In coordination-based supramolecular materials such as metallogels, simultaneous temporal and spatial control of their assembly remains challenging. Here, we demonstrate that the combination of light with acids as stimuli allows for the spatiotemporal control over the architectures, mechanical properties, and shape of porous soft materials based on metal-organic polyhedra (MOPs). First, we show that the formation of a colloidal gel network from a preformed kinetically trapped MOP solution can be triggered upon addition of trifluoroacetic acid (TFA) and that acid concentration determines the reaction kinetics. As determined by time-resolved dynamic light scattering, UV-vis absorption, and 1H NMR spectroscopies and rheology measurements, the consequences of the increase in acid concentration are (i) an increase in the cross-linking between MOPs; (ii) a growth in the size of the colloidal particles forming the gel network; (iii) an increase in the density of the colloidal network; and (iv) a decrease in the ductility and stiffness of the resulting gel. We then demonstrate that irradiation of a dispersed photoacid generator, pyranine, allows the spatiotemporal control of the gel formation by locally triggering the self-assembly process. Using this methodology, we show that the gel can be patterned into a desired shape. Such precise positioning of the assembled structures, combined with the stable and permanent porosity of MOPs, could allow their integration into devices for applications such as sensing, separation, catalysis, or drug release.

Fast multipoint immobilization of lipase through chiral L-proline on a MOF as a chiral bioreactor.

In this paper, we describe the facile preparation of a chiral catalyst by the combination of the amino acid, l-proline (Pro), and the enzyme, porcine pancreas lipase (PPL), immobilized on a microporous metal-organic framework (PPL-Pro@MOF). The multipoint immobilization of PPL onto the MOF is made possible with the aid of Pro, which also provided a chiral environment for enhanced enantioselectivity. The application of the microporous MOF is pivotal in maintaining the catalytic activity of PPL, wherein it prevented the leaching of Pro during the catalytic reaction, leading to the enhanced activity of PPL. The prepared biocatalyst was applied in asymmetric carbon-carbon bond formation, demonstrating the potential of this simple approach for chemical transformations.

Enzyme Immobilized on Nanoporous Carbon Derived from Metal-Organic Framework: A New Support for Biodiesel Synthesis.

In this study, nanoporous carbon (NPC) derived from metal-organic framework was used as support for the immobilization of Burkholderia cepacia lipase. The decorated aluminum oxide within the mesoporous NPC improved the enzyme loading efficiency as well as the catalytic ability for the transesterification of soybean oil, thus making it a promising green and sustainable catalytic system for industrial application.