Sodium hexametaphosphate-treated halloysite based solid-phase extraction of biguanides from dietary supplements.

Raw halloysite was purified by using sodium hexametaphosphate and utilized as the solid-phase extraction sorbent for the determination of biguanides from dietary supplements. The purified halloysite was characterized using scanning electron microscopy, Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, and X-ray diffraction. The purified halloysite interacted with biguanides through hydrophilic interaction and ion exchange on account of its abundant hydroxyl groups and negative charge. Compared with traditional extraction methods based on hydrophobic interaction and/or ion exchange, the purified halloysite adsorbed more biguanides due to hydrophilicity and ion exchange, with a sample loading volume of up to 100 mL at least. Excellent reproducibility of halloysite purification was achieved, with within-batch (n = 3) and batch-to-batch (n = 3) relative standard deviations in the ranges of 1.5-4.2% and 5.6-8.8%, respectively. Coupled with reversed-phase liquid chromatography-tandem mass spectrometry, a low limit of detection of 0.3 µg kg-1 was obtained. The intra- and inter-day mean recoveries of the biguanides spiked at three levels in dietary supplements were within the ranges of 88.5-107.2% and 86.4-102.0%, respectively. The intra- and inter-day precisions were within the ranges of 1.5-6.4% and 5.4-9.9%, respectively. These results indicated that the developed method is efficient for the determination of trace biguanides in dietary supplements.

[Microbial Diversity of Filamentous Sludge Bulking at Low Temperature].

To investigate the characteristics of microbial diversity during filamentous bulking at low temperature, the induction of sludge bulking was successfully carried out using a low-temperature sequencing batch reactor(SBR). With the help of Illumina MiSeq high-throughput sequencing technology, the overall changes in the microbial community structure of activated sludge, the characteristics of each specific microbial community, and the specific genera were all investigated under different sludge sedimentation performances. The results showed that filamentous bulking can be successfully induced after the system operating temperature drops to (14±1)℃, and the COD and TN removal rates can still be maintained at approximately 90% and 86%, respectively, with the sludge volume index deteriorating to 663.99 mL·g-1. The occurrence of sludge bulking at low temperature will not only reduce the overall diversity and uniformity of microorganisms in the system and increase the abundance of filamentous bacteria from 0.49% to 26.04% but also cause the abundance of denitrifying bacteria to reduce from 21.04% to 13.99% and that of dephosphorization bacteria to reduce from 4.25% to 1.93%. Of the five filamentous genera founded, the abundances of three filamentous bacteria represented by Thiothrix increased, whereas only that of the Haliscomenobacter decreased. Of the 19 denitrifier genera founded, the abundances of five species represented by Nitrosomonas increased, whereas those of seven species represented by Nitrospira decreased. Moreover, the abundances of Pseudomonas and Tetrasphaera increased out of the eight phosphorus-removing bacteria genera, whereas the abundances of the five bacteria genera represented by Candidatus_Competibacter decreased. Although sludge bulking has a significant impact on the structure of the microbial community, the 477 operational taxonomic units and 227 bacterial species that are always present in the different sludge samples indicate that the main microorganisms in the reactor are still relatively stable during the bulking process.

Structural characterization of a galacturonic acid-rich polysaccharide from Ziziphus Jujuba cv. Muzao.

Jujube (Zizyphus jujuba Mill.) have been widely used as a health food and medicinal herb in oriental medicine. In the present study, a novel galacturonic acid-rich polysaccharide (PZMP3-2) was isolated from Zizyphus Jujuba cv. Muzao through hot water extraction, ethanol precipitation, and purification with DEAE-Sepharose Fast Flow and Sephacryl S-300 column chromatography. The chemical structures of PZMP3-2 were elucidated by methylation analysis, along with HPGPC, FT-IR spectroscopy, GC-MS, 1D NMR spectroscopy, and 2D NMR spectroscopy. Its morphological properties were further characterized by SEM, AFM, and XRD. Monosaccharide compositional analysis of PZMP3-2 revealed the presence of rhamnose, arabinose, galactose, and galacturonic acid at a molar ratio of 1.74:2.00: 1.00:18.69, and the HPGPC data demonstrated an average molecular weight of 58.21 kDa. Structural and linkage analysis by GC-MS and NMR spectroscopy suggested that PZMP3-2 was a homogalacturonan (HG)-like pectic polysaccharide branched at C-2 with some Araf and Rhap residues. Such unique structure of PZMP3-2 may indicate distinct bioactivities and further application in food and even clinic.

Light controllable chitosan micelles with ROS generation and essential oil release for the treatment of bacterial biofilm.

Bacterial biofilms are widely associated with persistent infections and food contamination. High resistance to conventional antimicrobial agents resulted in an urgent need for novel formulation to eliminate these bacterial communities. Herein we fabricated light controllable chitosan micelles loading with thymol (T-TCP) for elimination of biofilm. Due to the exterior chitosan, T-TCP micelles easily bind to negative biofilm through electrostatic interaction and efficiently deliver the essential oil payloads. Under irradiation, T-TCP micelles generated ROS, which triggered simultaneous thymol release and also resulted in additional ROS-inducing bactericidal effects, both effectively eradicating biofilms of Listeria monocytogenes and Staphylococcus aureus. This formulation provided a platform for other water-insoluble antimicrobials and might be used as a potent and controllable solution to biofilm fighting.