Establishment of a Secretory Protein-Inducible CRISPR/Cas9 System for in Insect Cells.

Gene editing techniques are widely and effectively used for the control of pathogens, but it is difficult to directly edit the genes of Microsporidia due to its unique spore wall structure. Innovative technologies and methods are urgently needed to break through this limitation of microsporidia therapies. Here, we establish a microsporidia-inducible gene editing system through core components of microsporidia secreted proteins, which could edit target genes after infection with microsporidia.

Enhancement of peroxymonosulfate activation for 2,4-dichlorophenoxyacetic acid removal by MoSe induced Fe redox cycles.

The limited regeneration of Fe in the Fe-catalyzed advanced oxidation processes (AOPs) constrained its application for the removal of organic pollutants. Herein, MoSe was introduced to promote the degradation of 2,4-dichlorophenoxyacetic acid (2,4-D) in the Fe/PMS system. Compared with Fe/PMS processes, the 2,4-D degradation efficiency and PMS decomposition rate respectively increased by 73.