Abstract: Provided is a method for constructing a gE gene-deleted pseudorabies virus (PRV) strain using an adenine base editor (ABE) and use thereof. The method includes: designing an sgRNA sequence using the ABE with a start codon of the gE gene in a PRV as a target site, ligating an enzyme-digested fragment to a double-stranded DNA fragment with sticky ends to obtain a ligation product; and transforming the ligation product into a competent cell to allow plate screening and culture, selecting a resulting positive bacterial strain to allow expanded culture, and extracting a plasmid from a resulting positive bacterial solution; and transferring the plasmid into a target cell to allow the transfection for 24 h, collecting a resulting virus liquid, and centrifuging the virus liquid to collect a resulting supernatant.

Abstract: A method for using a natural attapulgite is disclosed. The method includes using the natural attapulgite as a natural nano mineral enzyme. The results of the examples show that the natural attapulgite has peroxidase-like activity, catalase-like activity or superoxide dismutase-like activity, and good biocompatibility. Compared with protease, the natural attapulgite has the advantages such as large reserves, easy to obtain, low cost, high temperature resistance and wide range of pH value. Compared with a developed artificial nano enzymes, the natural attapulgite further has the advantages such as multi-function, natural non-toxic (from nature, no heavy metals), good biocompatibility, easy to obtain, no complex processing, and huge surface area which provides a place for cell growth and proliferation.