Biosynthesis of Cry5B-Loaded Sulfur Nanoparticles using Arthrobotrys oligospora Filtrate: Effects on Nematicidal Activity, Thermal Stability, and Pathogenicity against Caenorhabditis elegans

dc.contributor.authorJammor P.
dc.contributor.authorSanguanphun T.
dc.contributor.authorMeemon K.
dc.contributor.authorPromdonkoy B.
dc.contributor.authorBoonserm P.
dc.contributor.correspondenceJammor P.
dc.contributor.otherMahidol University
dc.date.accessioned2024-02-19T18:04:59Z
dc.date.available2024-02-19T18:04:59Z
dc.date.issued2023-01-01
dc.description.abstractCry5B, a crystal protein produced by Bacillus thuringiensis (Bt), is a bionematicide with potent nematicidal activity against various plant-parasitic and free-living nematodes. This protein, however, is susceptible to destruction by ultraviolet light, proteolytic enzymes, and high temperatures. This study aims to produce Cry5B protein for bionematicidal use and improve its stability and nematicidal efficacy by loading it intoArthrobotrys oligospora-mediated sulfur nanoparticles (AO-SNPs). Based on the mortality assay, the Cry5B protein exhibited dose-dependent nematicidal activity against the model organismCaenorhabditis elegans. The nematicidal activity, thermal stability, and pathogenic effects of Cry5B-loaded AO-SNPs (Cry5B-SNPs) were compared to those of free Cry5B. After 3 h of exposure to heat at 60 °C, Cry5B-SNPs had greater nematicidal activity than free Cry5B protein, indicating the effective formulation of Cry5B-SNPs that could be used as an alternative to current nematicide delivery strategies.
dc.identifier.citationACS Omega (2023)
dc.identifier.doi10.1021/acsomega.3c08653
dc.identifier.eissn24701343
dc.identifier.scopus2-s2.0-85184800009
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/97243
dc.rights.holderSCOPUS
dc.subjectChemical Engineering
dc.subjectChemistry
dc.titleBiosynthesis of Cry5B-Loaded Sulfur Nanoparticles using Arthrobotrys oligospora Filtrate: Effects on Nematicidal Activity, Thermal Stability, and Pathogenicity against Caenorhabditis elegans
dc.typeArticle
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85184800009&origin=inward
oaire.citation.titleACS Omega
oairecerif.author.affiliationMahidol University
oairecerif.author.affiliationThailand National Center for Genetic Engineering and Biotechnology
oairecerif.author.affiliationInstitute of Molecular Biosciences, Mahidol University

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