Structure and reaction mechanisms of a two-component indole monooxygenase from Acinetobacter baumannii

dc.contributor.authorSuksomjaisaman K.
dc.contributor.authorThananon K.
dc.contributor.authorMangkalee M.
dc.contributor.authorThotsaporn K.
dc.contributor.authorTinikul R.
dc.contributor.authorSchulte A.
dc.contributor.authorWangkanont K.
dc.contributor.authorSirikantaramas S.
dc.contributor.authorSucharitakul J.
dc.contributor.authorChaiyen P.
dc.contributor.correspondenceSuksomjaisaman K.
dc.contributor.otherMahidol University
dc.date.accessioned2026-02-07T18:30:22Z
dc.date.available2026-02-07T18:30:22Z
dc.date.issued2026-02-01
dc.description.abstractThe indole monooxygenase system from Acinetobacter baumannii is a two-component flavoprotein that catalyzes the monooxygenation of indole. The system consists of the flavoprotein reductase (IndR) and the oxygenase (IndOx). IndR generates reduced FAD (FADH<sup>−</sup>) to IndOx using NADH. The pre-equilibration of IndOx with FADH<sup>−</sup> inhibits the formation of C4a-hydroperoxyflavin. In contrast, the presence of indole facilitates the formation of C4a-hydroperoxyflavin. The structural study reveals a dynamic loop at the active site, which has never been demonstrated in this class of enzyme, resulting in two conformations of IndOx. The closed conformation prevents the formation of the C4a-hydroperoxyflavin, whereas the binding of indole directs the open conformation, allowing for the formation of C4a-hydroperoxyflavin. The kinetic mechanism of both components was elucidated using rapid kinetics. The binding of indole to form a ternary complex is a preferential random-order mechanism in which indole preferentially binds to IndOx:C4a-hydroperoxyflavin, compared with IndOx:FADH<sup>−</sup> complex. The turnover number in the presence of both components to produce 3-hydroxyindole demonstrated that either the release of oxidized FAD or the release of monooxygenated product from the IndOx active site, or partially both, entirely limits the catalytic reaction. The solvent isotope effect on the step of the structural rearrangement of the monooxygenated product to form 3-hydroxyindole in this study supports the previously proposed epoxide-dihydrodiol model. This step is significantly slower than the turnover number, indicating that the monooxygenated indole is released and then undergoes a non-enzymatic structural rearrangement outside the active site, leading to the formation of 3-hydroxyindole.
dc.identifier.citationArchives of Biochemistry and Biophysics Vol.776 (2026)
dc.identifier.doi10.1016/j.abb.2025.110681
dc.identifier.eissn10960384
dc.identifier.issn00039861
dc.identifier.pmid41325957
dc.identifier.scopus2-s2.0-105023972047
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/114864
dc.rights.holderSCOPUS
dc.subjectBiochemistry, Genetics and Molecular Biology
dc.titleStructure and reaction mechanisms of a two-component indole monooxygenase from Acinetobacter baumannii
dc.typeArticle
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=105023972047&origin=inward
oaire.citation.titleArchives of Biochemistry and Biophysics
oaire.citation.volume776
oairecerif.author.affiliationChulalongkorn University
oairecerif.author.affiliationFaculty of Science, Mahidol University
oairecerif.author.affiliationVidyasirimedhi Institute of Science and Technology

Files

Collections