Characterising the Multiple-Plastic Degrading Strain of Bacillus subtilis GM_03 From the Galleria mellonella Microbiome

dc.contributor.authorFacey, Fiona S.B.en
dc.contributor.authorMaharjan, Ramen
dc.contributor.authorDinh, Hueen
dc.contributor.authorBuchanan, Jason S.en
dc.contributor.authorConnal, Luke A.en
dc.contributor.authorTay, Aidan P.en
dc.contributor.authorPaulsen, Ian T.en
dc.contributor.authorCain, Amy K.en
dc.date.accessioned2026-02-26T14:40:47Z
dc.date.available2026-02-26T14:40:47Z
dc.date.issued2025en
dc.description.abstractPlastic waste is a mounting global problem with over 400 million tons of plastic produced annually and over 50% ending up in landfill after its intended use. Two types of plastics are particularly problematic and are difficult to recycle: low-density polyethylene (LDPE) and polyurethane (PU). Fortuitously, nature may offer a potential solution; Galleria mellonella larvae can digest various plastics, including LDPE, which is believed to be driven by microbes in their gut microbiome. Although some studies have examined their gut microbiota on a metagenomic level, little is known about their ability to degrade plastics. Here, we isolated six bacterial strains from G. mellonella larvae feeding on LDPE. One of them, identified as Bacillus subtilis GM_03, has the capacity to break down commercial PU (Impranil), in addition to LDPE. This bacterium encodes a suite of genes required for plastic degradation. Directed evolution was used to enhance this strain's plastic degrading rate by over six-fold. Sequencing of the evolved culture revealed four genes, srfAB, fadD, appA and citS, associated with this increased PU degradation rate. This is the first time that B. subtilis isolated from G. mellonella larvae has been shown to be capable of degrading multiple types of plastics.en
dc.description.sponsorshipFunding: This work was supported by the US Department of Defense (W911NF2320155) and the Australian Research Council Future Fellowship (FT220100152) and FSBF was supported by Macquarie University Research Excellence Scholarship (20235185). We would like to sincerely thank Darren Hill and Caspak Products PTY Ltd. for their generous donation of LDPE film. We would like to acknowledge the Macquarie University Faculty of Science and Engineering Microscopy Unit for access to its instrumentation and staff. We would like to thank Dr. Theo Colin at the Macquarie University apiary for providing yellow beeswax for G. mellonella diet. We would like to thank Samual Clay for his critical reading of this manuscript. This work was funded by the US Department of Defence project grant W911NF2320155 and Australian Research Council Future Fellowship (FT220100152) and FSBF was supported by Macquarie University Research Excellence Scholarship Programme (20235185). Open access publishing facilitated by Macquarie University, as part of the Wiley - Macquarie University agreement via the Council of Australian University Librarians. We would like to sincerely thank Darren Hill and Caspak Products PTY Ltd. for their generous donation of LDPE film. We would like to acknowledge the Macquarie University Faculty of Science and Engineering Microscopy Unit for access to its instrumentation and staff. We would like to thank Dr. Theo Colin at the Macquarie University apiary for providing yellow beeswax for G. mellonella diet. We would like to thank Samual Clay for his critical reading of this manuscript. This work was funded by the US Department of Defence project grant W911NF2320155 and Australian Research Council Future Fellowship (FT220100152) and FSBF was supported by Macquarie University Research Excellence Scholarship Programme (20235185). Open access publishing facilitated by Macquarie University, as part of the Wiley ‐ Macquarie University agreement via the Council of Australian University Librarians. This work was supported by the US Department of Defense (W911NF2320155) and the Australian Research Council Future Fellowship (FT220100152) and FSBF was supported by Macquarie University Research Excellence Scholarship (20235185). Funding:en
dc.description.statusPeer-revieweden
dc.format.extent11en
dc.identifier.issn1758-2229en
dc.identifier.otherWOS:001597916900001en
dc.identifier.otherPubMed:41115834en
dc.identifier.otherORCID:/0009-0007-6252-6568/work/206441922en
dc.identifier.otherORCID:/0000-0001-7519-977X/work/206443768en
dc.identifier.scopus105019183995en
dc.identifier.urihttps://hdl.handle.net/1885/733806631
dc.language.isoenen
dc.provenanceThis is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.en
dc.rights © 2025 The Author(s). en
dc.sourceEnvironmental Microbiology Reportsen
dc.subjectBacillus subtilisen
dc.subjectbiodegradationen
dc.subjectGalleria mellonellaen
dc.subjectpolyethyleneen
dc.subjectpolyurethaneen
dc.titleCharacterising the Multiple-Plastic Degrading Strain of Bacillus subtilis GM_03 From the Galleria mellonella Microbiomeen
dc.typeJournal articleen
dspace.entity.typePublicationen
local.contributor.affiliationFacey, Fiona S.B.; Macquarie Universityen
local.contributor.affiliationMaharjan, Ram; Macquarie Universityen
local.contributor.affiliationDinh, Hue; Macquarie Universityen
local.contributor.affiliationBuchanan, Jason S.; The Australian National Universityen
local.contributor.affiliationConnal, Luke A.; Research School of Chemistry, ANU College of Science and Medicine, The Australian National Universityen
local.contributor.affiliationTay, Aidan P.; Macquarie Universityen
local.contributor.affiliationPaulsen, Ian T.; Macquarie Universityen
local.contributor.affiliationCain, Amy K.; Macquarie Universityen
local.identifier.citationvolume17en
local.identifier.doi10.1111/1758-2229.70216en
local.identifier.pure15626969-1fb2-471f-89fc-8002564d5714en
local.identifier.urlhttps://www.scopus.com/pages/publications/105019183995en
local.type.statusPublisheden

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