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The inhibitory effect of tavaborole on the invasion of in grapes and tomatoes, as well as the potential mechanism involved, was discovered in this study. Our findings showed that tavaborole inhibited spore germination and mycelial expansion in vitro and that the control efficiency in vivo on fruit decay was dose-dependent, which was effective in reducing disease severity and maintaining the organoleptic quality of the fruit, such as reducing weight loss and retaining fruit hardness and titratable acid contents during storage. Furthermore, the precise mechanism of action was investigated further. Propidium iodide staining revealed that treated with tavaborole lost membrane integrity. For further validation, cytoplasmic malondialdehyde accumulation and leakage of cytoplasmic constituents were determined. Notably, the inhibitory effect was also dependent on inhibiting the activities of aminoacyl-tRNA synthetases involved in the aminoacyl-tRNA biosynthesis pathway in . The above findings concluded that tavaborole was effective against infection in postharvest fruit, and a related mechanism was also discussed, which may provide references for the drug repurposing of tavaborole as a postharvest fungicide.
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http://dx.doi.org/10.1021/acs.jafc.2c03441 | DOI Listing |
J Biol Chem
September 2025
Department of Integrative Structural and Computational Biology, The Scripps Research Institute, La Jolla, California, USA.
Aminoacyl-tRNA synthetases (aaRSs) catalyze the aminoacylation of tRNA with their cognate amino acids, an essential step in protein biosynthesis. While biallelic mutations in aaRSs often result in severe multi-organ dysfunction accompanied by developmental delays, monoallelic mutations typically cause milder, tissue-specific symptoms. However, a de novo monoallelic nonsense mutation (R534*) in the asparaginyl-tRNA synthetase (AsnRS)-resulting in a premature stop codon and 15-residue C-terminal truncation-has been identified in multiple families and is associated with severe neurodevelopmental symptoms.
View Article and Find Full Text PDFExp Ther Med
October 2025
Department of Surgery, Shanghai Jiading District Hospital of Traditional Chinese Medicine, Shanghai 201800, P.R. China.
The aim of the present study was to characterize the metabolomic signatures associated with colorectal polyps (CPs) in the gut. A metabolomics analysis was conducted on fecal samples collected from patients diagnosed with CPs as well as from healthy participants. A total of 60 participants were selected for analysis, including 30 patients diagnosed with CPs (CP group) and 30 healthy individuals serving as controls [healthy control (HC) group].
View Article and Find Full Text PDFNat Commun
September 2025
Department of Chemistry and Biochemistry, University of Arkansas, Fayetteville, AR, USA.
Rigorous studies have characterized the aa-tRNA selection mechanism in bacteria, which is essential for maintaining translational fidelity. Recent investigations have identified critical distinctions in humans, such as the requirement of subunit rolling and a tenfold slower proofreading step. Although these studies captured key intermediates involved in tRNA selection, they did not elucidate the transitions of aa-tRNA between intermediates.
View Article and Find Full Text PDFPlants (Basel)
August 2025
School of Life Science and Technology, Lingnan Normal University, Zhanjiang 524048, China.
As a key tropical economic tree species, the girth of the rubber tree () not only reflects its growth rate and timber yield but also determines tapping schedules and non-productive periods. This trait critically influences both the species' economic value and latex production potential. Despite recent advances in genetic analyses of girth driven by genomic technologies, the number of identified key genes remains insufficient to support molecular breeding programs.
View Article and Find Full Text PDFNature
August 2025
Department of Chemistry, University College London, London, UK.
To orchestrate ribosomal peptide synthesis, transfer RNAs (tRNAs) must be aminoacylated, with activated amino acids, at their 2',3'-diol moiety, and so the selective aminoacylation of RNA in water is a key challenge that must be resolved to explain the origin of protein biosynthesis. So far, there have been no chemical methods to effectively and selectively aminoacylate RNA-2',3'-diols with the breadth of proteinogenic amino acids in water. Here we demonstrate that (biological) aminoacyl-thiols (1) react selectively with RNA diols over amine nucleophiles, promoting aminoacylation over adventitious (non-coded) peptide bond formation.
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