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BIG, a regulator of polar auxin transport, is necessary to regulate the growth and development of Arabidopsis. Although mutations in the BIG gene cause severe root developmental defects, the exact mechanism remains unclear. Here, we report that disruption of the BIG gene resulted in decreased quiescent center (QC) activity and columella cell numbers, which was accompanied by the downregulation of WUSCHEL-RELATED HOMEOBOX5 (WOX5) gene expression. BIG affected auxin distribution by regulating the expression of PIN-FORMED proteins (PINs), but the root morphological defects of big mutants could not be rescued solely by increasing auxin transport. Although the loss of BIG gene function resulted in decreased expression of the PLT1 and PLT2 genes, genetic interaction assays indicate that this is not the main reason for the root morphological defects of big mutants. Furthermore, genetic interaction assays suggest that BIG affects the stem cell niche (SCN) activity through the SCRSCARECROW (SCR)/SHORT ROOT (SHR) pathway and BIG disruption reduces the expression of SCR and SHR genes. In conclusion, our findings reveal that the BIG gene maintains root meristem activity and SCN integrity mainly through the SCR/SHR pathway.

Temperature/pH-responsive carboxymethyl cellulose/poly (N-isopropyl acrylamide) interpenetrating polymer network (IPN) aerogels (CMC/Ca2+/PNIPAM aerogels) were developed as a novel drug delivery system. The aerogel has a highly open network structure with a porosity of more than 90%, which provides convenient conditions for drug release. The morphology and structure of the CMC/Ca2+/PNIPAM aerogels were characterized via scanning electron microscopy (SEM), Micro-CT, X-ray photoelectron spectroscopy (XPS), pore size analysis, and cytotoxicity analysis. The analysis results demonstrate that the aerogel is non-toxic and has more active sites, temperatures, and pH response performances. The anticancer drug 5-fluorouracil (5-FU) was successfully loaded into aerogels through physical entrapment and hydrogen bonding. The drug loading and sustained-release model of aerogels are used to fit the drug loading and sustained-release curve, revealing the drug loading and sustained-release mechanism, and providing a theoretical basis for the efficient drug loading and sustained release.

In this study, an ultrasound Fenton-like sponge iron system was used to enhance the degradation efficiency for chloramphenicol (CAP). Three single-factor experiments of reaction pH, hydrogen peroxide (H2O2) concentration, and sponge iron (Fe) concentration were used to explore the impact on CAP degradation efficiency. The response surface method revealed the interactions between various factors. The degradation efficiency for CAP was as high as 99.97% at pH = 3, 3.19 mmol/L H2O2, and a sponge iron concentration of 2.26 g/L. The degradation rate for CAP was significantly reduced upon the addition of some inorganic salts, mainly due to the quenching of OH radicals. Gram-negative (G(−)) Escherichia coli and Gram-positive (G(+)) Staphylococcus aureus were used to evaluate the changes in the antibacterial activity of CAP. Finally, gas chromatography/mass spectrometry (GC-MS) was used to identify the degradation products and the degradation path for the products was proposed based on the detected products.

Softwood kraft lignin is a renewable type of woody material that can be converted to value-added products, for example, as a paper strength additive in the paper industry. In this study, the monomers of methacryloxyethyltrimethyl ammonium chloride (DMC), acrylic acid (AA), and acrylamide (AM) were grafted on softwood kraft lignin (SKL) to prepare three different SKL copolymers. Fourier-transform infrared, proton nuclear magnetic resonance, charge density, elemental, and molecular weight analyses confirmed that the monomers were successfully grafted onto SKL. The grafting rates of SKL-DMC, SKL-AA, and SKL-AM copolymers were 80.35%, 82.70%, and 79.48%, respectively. The application of SKL copolymers as a paper additive for enhancing paper physical properties was studied. The results indicated that at a 2 wt % dosage of SKL copolymers, the increase in the physical properties of paper is maximum.

In this study, phosphorylated birchwood xylan was produced under alkali conditions using trisodium trimetaphosphate. Three single-factor experiments were used to explore the influences of time, temperature, and the molar ratio of trisodium trimetaphosphate to xylan on the degree of substitution (DS) and charge density of xylan. The response surface methodology was used to explore the interaction of these three factors. Phosphorylated xylan with a maximum DS of 0.79 and a charge density of −3.40 mmol/g was produced under the optimal conditions of 80 °C, 4 h, and a molar ratio of xylan/sodium trimetaphosphate (STMP) of 1/3. Fourier transform infrared (FTIR), ascorbic acid method analyses, and inductively coupled plasma–atomic emission spectrometer (ICP-AES) analyses confirmed that the phosphate groups were successfully attached to xylan. Thermogravimetric analysis confirmed that phosphorylated xylan was less stable than birchwood xylan. Furthermore, the phosphorylated xylan was applied as a flocculant for removing ethyl violet dye from a simulated dye solution. The results indicated that more than 95% of the dye was removed from the solution. The theoretical and experimental values of charge neutralization for the dye removal were close to one another, confirming that charge neutralization was the main mechanism for the interaction of dye and phosphorylated xylan. The impacts of salts on the flocculation efficiency of phosphorylated xylan were also analyzed.