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dc.contributor.authorHendricks, Lauren
dc.contributor.authorReinhardt, Clorice R
dc.contributor.authorGreen, Tierani
dc.contributor.authorKunczynski, Lily
dc.contributor.authorRoberts, August Jaunzarins
dc.contributor.authorMiller, Naomi
dc.contributor.authorRafalin, Noga
dc.contributor.authorKulik, Heather J
dc.contributor.authorGroves, John T
dc.contributor.authorAustin, Rachel N
dc.date.accessioned2026-04-23T19:47:27Z
dc.date.available2026-04-23T19:47:27Z
dc.date.issued2025-03-07
dc.identifier.urihttps://hdl.handle.net/1721.1/165665
dc.description.abstractPurified alkane monooxygenase (AlkB) from Fontimonas thermophila (FtAlkB) catalyzes the defluorination of 1- fluorooctane, producing octanal, which is partially reduced under the reaction conditions to generate 1-octanol. This reaction occurs preferentially at the monofluorinated methyl group, with only a minor amount of oxidation at the nonfluorinated end of the molecule. The dehalogenation chemistry is specific to 1-fluorooctane, as neither 1-chlorooctane or 1-bromooctane are dehalogenated to an appreciable extent. Furthermore, P. putida cells containing the structurally related AlkB (PpAlkB) along with the full set of genes required for alkane metabolism, utilize 1-fluorooctane as their sole source of carbon with growth rates comparable to those for cells grown with octane.en_US
dc.language.isoen
dc.publisherAmerican Chemical Societyen_US
dc.relation.isversionof10.1021/jacs.5c00386en_US
dc.rightsArticle is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.en_US
dc.sourceauthoren_US
dc.titleFontimonas thermophila Alkane Monooxygenase (FtAlkB) Is an Alkyl Fluoride Dehalogenaseen_US
dc.typeArticleen_US
dc.identifier.citationHendricks, Lauren, Reinhardt, Clorice R, Green, Tierani, Kunczynski, Lily, Roberts, August Jaunzarins et al. 2025. "Fontimonas thermophila Alkane Monooxygenase (FtAlkB) Is an Alkyl Fluoride Dehalogenase." Journal of the American Chemical Society, 147 (11).
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemical Engineeringen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemistryen_US
dc.relation.journalJournal of the American Chemical Societyen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2026-04-23T19:39:39Z
dspace.orderedauthorsHendricks, L; Reinhardt, CR; Green, T; Kunczynski, L; Roberts, AJ; Miller, N; Rafalin, N; Kulik, HJ; Groves, JT; Austin, RNen_US
dspace.date.submission2026-04-23T19:39:42Z
mit.journal.volume147en_US
mit.journal.issue11en_US
mit.licensePUBLISHER_POLICY
mit.metadata.statusAuthority Work and Publication Information Neededen_US


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