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Single cell ICP-MS to evaluate the interaction behaviour for Cd, Ce and U with Streptomyces coelicolor spores

dc.contributor.authorHellmann, S.
dc.contributor.authorGarcía Cancela, Paula 
dc.contributor.authorAlonso Fernández, Sergio 
dc.contributor.authorCorte Rodríguez, Mario 
dc.contributor.authorBettmer, Jörg 
dc.contributor.authorManteca Fernández, Ángel 
dc.contributor.authorMerten, D.
dc.contributor.authorGil Díaz, Teba
dc.contributor.authorSchäfer, T.
dc.contributor.authorMontes Bayón, María 
dc.date.accessioned2024-08-26T08:33:33Z
dc.date.available2024-08-26T08:33:33Z
dc.date.issued2024
dc.identifier.citationChemosphere, 347 (2024); doi:10.1016/j.chemosphere.2023.140633
dc.identifier.issn0045-6535
dc.identifier.urihttps://hdl.handle.net/10651/74223
dc.description.abstractStreptomyces are important soil bacteria used for bioremediation of metal-contaminated soils, however, it is still unknown how metal-selective Streptomyces are and which mechanisms are involved during their capture. In this work, we exposed S. coelicolor spores to environmentally relevant concentrations (0.1, 1, 10, 100 μM) of Ce, U and Cd in solid medium for one week to investigate the uptake behaviour of hyphae in the newly formed spores. Additionally, metal adsorption onto the spores was explored by incubating inactive, ungerminated spores for one day in aqueous metal solution. The spore-washing treatment was key to distinguishing between strongly spore- associated (e.g. incorporation; Tris-EDTA buffer) and weakly spore-associated metals (Tris buffer alone minus Tris-EDTA). Single cell (sc) ICP-MS was used to quantify metal-associated content in individual spores. Our results revealed element-specific adsorption onto inactive spores showing that out of the total metal exposure, both strongly (Ce: 58%; U: 54%; Cd: 28%) and weakly (Ce: 12%; U: 1%; Cd: 18%) adsorbed metals occur. However, scICP-MS showed that from metal-amended solid medium, only Ce and U were strongly spore- associated (averages 0.040 and 0.062 fg spore 1 for 10 μM exposures, respectively) while Cd was below the limit of detection (< 0.006 fg spore 1 ). We propose that hyphae only metabolically interact with Ce in a controlled manner but uncontrolled with U, as 66–73% Ce and only 2–4% U were inherited from adsorbed content. We conclude that Streptomyces spore-metal interaction starts with a relevant adsorption step of Ce, U and Cd as presented for aqueous conditions. If spores start to germinate, hyphae are capable of effectively encapsulating Ce and U, but not Cd. This study brings light into the still unknown field of metal interactions with Streptomyces and applied understanding for more efficient and metal-specific use of Streptomyces in bioremediation of metal-polluted soils.
dc.description.sponsorshipThe authors declare the following financial interests/personal relationships which may be considered as potential competing interests: Steffen Hellmann reports financial support was provided by German Research Foundation (DFG SPP, 2005), Opus Fluidum Futurum (project number 313773090, grant no. SCHA, 18547-1). Paula Garcia-Cancela reports financial support was provided by Government of Principado de Asturias (Severo Ochoa scholarship for predoctoral studies). Sergio Alonso-Fernandez reports financial support was provided by Consejeria de Ciencia, Innovacion y Universidad del Principado de Asturias (Severo Ochoa predoctoral grant (grant no. PA-20-PFBP19-006)).
dc.language.isoeng
dc.relation.ispartofChemosphere
dc.rights© 2023 The Authors.
dc.rightsCC Reconocimiento 4.0 Internacional
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceScopus
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85177483474&doi=10.1016%2fj.chemosphere.2023.140633&partnerID=40&md5=674a03c3a19040fefffc7664b41a5ce7
dc.titleSingle cell ICP-MS to evaluate the interaction behaviour for Cd, Ce and U with Streptomyces coelicolor spores
dc.typejournal article
dc.identifier.doi10.1016/j.chemosphere.2023.140633
dc.relation.projectIDPA-20-PFBP19-006
dc.relation.publisherversionhttp://dx.doi.org/10.1016/j.chemosphere.2023.140633
dc.rights.accessRightsopen access
dc.type.hasVersionVoR


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