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liu, f.

Publications and source records attributed to liu, f..

2 recordsLinked to original sources

Recombinant expression, purification, and antifungal activity of the novel antimicrobial peptide TaW662

Blumeria graminis f. sp. tritici (Bgt) is a significant wheat fungal pathogen, posing threats to both yield and quality. Antimicrobial peptides, with their broad-spectrum activities, hold promise in combating Bgt-induced wheat fungal diseases.In this study, we identified TaW662, an antifungal peptide gene sourced from the wheat-Thinopyrum intermedium disomic alien addition line SN6306. Through third-generation transcriptome sequencing, we obtained the full-length transcript of TaW662. Notably, TaW662 exhibited upregulated expression in response to powdery mildew infection in SN6306. Subcellular localization analysis revealed TaW662s extracellular secretion, suggesting its role in defense mechanisms. Additionally, the TaW662 protein was expressed in Escherichia coli, and the purified protein could inhibit the growth of Bgt in vitro. Utilizing the online alphafold2 server, we predicted the three-dimensional structure of TaW662, aiding in understanding its fungicidal mechanisms. Analysis of TaW662s physicochemical properties further supported its potential efficacy as a fungicide against Bgt. In conclusion, TaW662 emerges as a promising candidate for combating Bgt-induced wheat fungal diseases, warranting further exploration for agricultural disease management strategies. HighlightsTaW662, a secreted protein homologous to TaWIR1, is induced in wheat by Blumeria graminis f. sp. tritici (Bgt). The expression pattern of TaW662 in wheat under induced by Bgt was analysed using RNA-Seq technology. The three-dimensional structure of TaW662 was predicted using AlphaFold2. The growth of Bgt is inhibited by recombinant TaW662.

plant biology↗

An enzyme-based system for the extraction of small extracellular vesicles from plants

Plant-derived nanovesicles (NVs) and extracellular vesicles (EVs) are considered to be the next generation of nanocarrier platforms for biotherapeutics and drug delivery. However, EVs exist not only in the extracellular space, but also within the cell wall. Due to the limitation of isolation methods, the extraction efficiency is low, resulting in the waste of a large number of plants, especially rare and expensive medicinal plants.There are few studies comparing EVs and NVs. To overcome these challenges, we proposed and validated a novel method for the isolation of plant EVs by degrading the plant cell wall with enzymes to release the EVs in the cell wall, making it easier for EVs to break the cell wall barrier and be collected. We extracted EVs from the roots of Morinda officinalis by enzymatic degradation(MOEVs) and nanoparticles by grinding method (MONVs) as a comparison group. The results showed smaller diameter and higher yield of MOEVs.Both MOEVs and MONVs were readily absorbed by endothelial cells without cytotoxicity and promoted the expression of miR-155. The difference is that the promotion of miR-155 by MOEVs is dose-effective. More importantly, MOEVs and MONVs are naturally characterized by bone enrichment. These results support that EVs in plants can be efficiently extracted by enzymatic cell wall digestion and also confirm the potential of MOEVs as therapeutic agents and drug carriers.

pharmacology and toxicology↗