Chemistry of fungal meroterpenoid cyclases

dc.contributor.authorBarra, Lena
dc.contributor.authorAbe, Ikuro
dc.date.accessioned2022-05-17T08:47:07Z
dc.date.available2022-05-17T08:47:07Z
dc.date.issued2021eng
dc.description.abstractungal meroterpenoid cyclases are a recently discovered emerging family of membrane-integrated, non-canonical terpene cyclases. They catalyze the conversion of hybrid isoprenic precursors towards complex scaffolds and are therefore of great importance in the structure diversification in meroterpenoid biosynthesis. The products of these pathways exhibit intriguing molecular scaffolds and highly potent bioactivities, making them privileged structures from Nature and attractive candidates for drug development or industrial applications. This review will provide a comprehensive and comparative view on fungal meroterpenoid cyclases, their intriguing chemistries and importance for the scaffold formation step towards polycyclic meroterpenoid natural products.eng
dc.description.versionpublishedeng
dc.identifier.doi10.1039/D0NP00056Feng
dc.identifier.ppn1842773836
dc.identifier.urihttps://kops.uni-konstanz.de/handle/123456789/57548
dc.language.isoengeng
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dc.subject.ddc540eng
dc.titleChemistry of fungal meroterpenoid cyclaseseng
dc.typeJOURNAL_ARTICLEeng
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@article{Barra2021Chemi-57548,
  year={2021},
  doi={10.1039/D0NP00056F},
  title={Chemistry of fungal meroterpenoid cyclases},
  number={3},
  volume={38},
  issn={0265-0568},
  journal={Natural Product Reports},
  pages={566--585},
  author={Barra, Lena and Abe, Ikuro}
}
kops.citation.iso690BARRA, Lena, Ikuro ABE, 2021. Chemistry of fungal meroterpenoid cyclases. In: Natural Product Reports. Royal Society of Chemistry (RSC). 2021, 38(3), pp. 566-585. ISSN 0265-0568. eISSN 1460-4752. Available under: doi: 10.1039/D0NP00056Fdeu
kops.citation.iso690BARRA, Lena, Ikuro ABE, 2021. Chemistry of fungal meroterpenoid cyclases. In: Natural Product Reports. Royal Society of Chemistry (RSC). 2021, 38(3), pp. 566-585. ISSN 0265-0568. eISSN 1460-4752. Available under: doi: 10.1039/D0NP00056Feng
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    <dcterms:abstract xml:lang="eng">ungal meroterpenoid cyclases are a recently discovered emerging family of membrane-integrated, non-canonical terpene cyclases. They catalyze the conversion of hybrid isoprenic precursors towards complex scaffolds and are therefore of great importance in the structure diversification in meroterpenoid biosynthesis. The products of these pathways exhibit intriguing molecular scaffolds and highly potent bioactivities, making them privileged structures from Nature and attractive candidates for drug development or industrial applications. This review will provide a comprehensive and comparative view on fungal meroterpenoid cyclases, their intriguing chemistries and importance for the scaffold formation step towards polycyclic meroterpenoid natural products.</dcterms:abstract>
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kops.sourcefieldNatural Product Reports. Royal Society of Chemistry (RSC). 2021, <b>38</b>(3), pp. 566-585. ISSN 0265-0568. eISSN 1460-4752. Available under: doi: 10.1039/D0NP00056Fdeu
kops.sourcefield.plainNatural Product Reports. Royal Society of Chemistry (RSC). 2021, 38(3), pp. 566-585. ISSN 0265-0568. eISSN 1460-4752. Available under: doi: 10.1039/D0NP00056Fdeu
kops.sourcefield.plainNatural Product Reports. Royal Society of Chemistry (RSC). 2021, 38(3), pp. 566-585. ISSN 0265-0568. eISSN 1460-4752. Available under: doi: 10.1039/D0NP00056Feng
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source.periodicalTitleNatural Product Reportseng
source.publisherRoyal Society of Chemistry (RSC)eng

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