Publicación:
Biosynthetic Basis for Structural Diversity of Aminophenylpyrrole-Derived Alkaloids

dc.contributor.author Linares-Otoya L. es_PE
dc.contributor.author Liu Y. es_PE
dc.contributor.author Linares-Otoya V. es_PE
dc.contributor.author Armas-Mantilla L. es_PE
dc.contributor.author Crüsemann M. es_PE
dc.contributor.author Ganoza-Yupanqui M.L. es_PE
dc.contributor.author Campos-Florian J. es_PE
dc.contributor.author König G.M. es_PE
dc.contributor.author Schäberle T.F. es_PE
dc.date.accessioned 2024-05-30T23:13:38Z
dc.date.available 2024-05-30T23:13:38Z
dc.date.issued 2019
dc.description.abstract Bacterial aminophenylpyrrole-derived alkaloids (APPAs) represent high value lead compounds. Pyrrolnitrin, which was developed into globally important fungicides, is the only reported APPA produced by Proteobacteria. Recently, various APPAs showing diverse bioactivities were discovered from Bacteroidetes. Here, a bioinformatics and phylogenetic approach enabled the elucidation of the biosynthesis of the highly diverse APPAs in Cytophagales bacteria and their chemical diversification strategy. The biosynthetic gene clusters were identified in producer strains, and the biosynthesis was experimentally validated by heterologous expression experiments in E. coli. First, one enzyme-dependent biosynthetic step yields the tryptophan-derived precursor 3-(2′-aminophenyl)-pyrrole. Second, a spontaneous Pictet–Spengler-like coupling reaction enables the bacterial producer strains to create a library of tricyclic alkaloids, since several aldehydes can be applied as substrates. The diversity of this natural products class is further enlarged by the catalytic action of a methyltransferase, which adds one or more methyl groups to the aminophenyl intermediate.
dc.description.sponsorship Consejo Nacional de Ciencia, Tecnología e Innovación Tecnológica - Concytec
dc.identifier.doi https://doi.org/10.1021/acschembio.8b00993
dc.identifier.scopus 2-s2.0-85061575749
dc.identifier.uri https://hdl.handle.net/20.500.12390/539
dc.language.iso eng
dc.publisher American Chemical Society
dc.relation.ispartof ACS Chemical Biology
dc.rights info:eu-repo/semantics/openAccess
dc.subject pyrrole derivative
dc.subject alkaloid derivative es_PE
dc.subject antifungal agent es_PE
dc.subject Article es_PE
dc.subject bacterial gene es_PE
dc.subject bacterial genome es_PE
dc.subject bacterial strain es_PE
dc.subject bioinformatics es_PE
dc.subject chemical structure es_PE
dc.subject computer model es_PE
dc.subject controlled study es_PE
dc.subject.ocde https://purl.org/pe-repo/ocde/ford#1.02.03
dc.title Biosynthetic Basis for Structural Diversity of Aminophenylpyrrole-Derived Alkaloids
dc.type info:eu-repo/semantics/article
dspace.entity.type Publication
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