GNPS-guided discovery of xylacremolide C and D, evaluation of their putative biosynthetic origin and bioactivity studies of xylacremolide A and B

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GNPS-guided discovery of xylacremolide C and D, evaluation of their putative biosynthetic origin and bioactivity studies of xylacremolide A and B. / Schalk, Felix; Fricke, Janis; Um, Soohyun; Conlon, Benjamin H.; Maus, Hannah; Jäger, Nils; Heinzel, Thorsten; Schirmeister, Tanja; Poulsen, Michael; Beemelmanns, Christine.

I: RSC Advances, Bind 31, Nr. 11, 2021, s. 18748-18756.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Schalk, F, Fricke, J, Um, S, Conlon, BH, Maus, H, Jäger, N, Heinzel, T, Schirmeister, T, Poulsen, M & Beemelmanns, C 2021, 'GNPS-guided discovery of xylacremolide C and D, evaluation of their putative biosynthetic origin and bioactivity studies of xylacremolide A and B', RSC Advances, bind 31, nr. 11, s. 18748-18756. https://doi.org/10.1039/d1ra00997d

APA

Schalk, F., Fricke, J., Um, S., Conlon, B. H., Maus, H., Jäger, N., Heinzel, T., Schirmeister, T., Poulsen, M., & Beemelmanns, C. (2021). GNPS-guided discovery of xylacremolide C and D, evaluation of their putative biosynthetic origin and bioactivity studies of xylacremolide A and B. RSC Advances, 31(11), 18748-18756. https://doi.org/10.1039/d1ra00997d

Vancouver

Schalk F, Fricke J, Um S, Conlon BH, Maus H, Jäger N o.a. GNPS-guided discovery of xylacremolide C and D, evaluation of their putative biosynthetic origin and bioactivity studies of xylacremolide A and B. RSC Advances. 2021;31(11):18748-18756. https://doi.org/10.1039/d1ra00997d

Author

Schalk, Felix ; Fricke, Janis ; Um, Soohyun ; Conlon, Benjamin H. ; Maus, Hannah ; Jäger, Nils ; Heinzel, Thorsten ; Schirmeister, Tanja ; Poulsen, Michael ; Beemelmanns, Christine. / GNPS-guided discovery of xylacremolide C and D, evaluation of their putative biosynthetic origin and bioactivity studies of xylacremolide A and B. I: RSC Advances. 2021 ; Bind 31, Nr. 11. s. 18748-18756.

Bibtex

@article{4ccb5ed7f45d4207a1da931969319a74,
title = "GNPS-guided discovery of xylacremolide C and D, evaluation of their putative biosynthetic origin and bioactivity studies of xylacremolide A and B",
abstract = "Targeted HRMS2-GNPS-based metabolomic analysis ofPseudoxylariasp. X187, a fungal antagonist of the fungus-growing termite symbiosis, resulted in the identification of two lipopeptidic congeners of xylacremolides, named xylacremolide C and D, which are built fromd-phenylalanine,l-proline and an acetyl-CoA starter unit elongated by four malonyl-CoA derived ketide units. The putativexyagene cluster was identified from a draft genome generated by Illumina and PacBio sequencing and RNAseq studies. Biological activities of xylacremolide A and B were evaluated and revealed weak histone deacetylase inhibitory (HDACi) and antifungal activities, as well as moderate protease inhibition activity across a panel of nine human, viral and bacterial proteases.",
author = "Felix Schalk and Janis Fricke and Soohyun Um and Conlon, {Benjamin H.} and Hannah Maus and Nils J{\"a}ger and Thorsten Heinzel and Tanja Schirmeister and Michael Poulsen and Christine Beemelmanns",
note = "Funding Information: Funded by the Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) under Germany's Excellence Strategy - EXC 2051 with Project-ID 390713860 and CRC 1127 with Project-ID 239748522 to CB and TH. Funded by the European Research Council (ERC-CoG - 771349) and The Danish Council for Independent Research (DFF - 7014-00178) to MP. We thank the Humboldt Foundation for a postdoctoral fellowship to SU, and Mrs Heike Heinecke (Hans Kn?ll Institute) for recording NMR spectra. Funding Information: Funded by the Deutsche Forschungsgemeinscha (DFG, German Research Foundation) under Germany's Excellence Strategy – EXC 2051 with Project-ID 390713860 and CRC 1127 with Project-ID 239748522 to CB and TH. Funded by the European Research Council (ERC-CoG – 771349) and The Danish Council for Independent Research (DFF – 7014-00178) to MP. We thank the Humboldt Foundation for a postdoctoral fellowship to SU, and Mrs Heike Heinecke (Hans Kn{\"o}ll Institute) for recording NMR spectra. Publisher Copyright: {\textcopyright} The Royal Society of Chemistry 2021.",
year = "2021",
doi = "10.1039/d1ra00997d",
language = "English",
volume = "31",
pages = "18748--18756",
journal = "RSC Advances",
issn = "2046-2069",
publisher = "RSC Publishing",
number = "11",

}

RIS

TY - JOUR

T1 - GNPS-guided discovery of xylacremolide C and D, evaluation of their putative biosynthetic origin and bioactivity studies of xylacremolide A and B

AU - Schalk, Felix

AU - Fricke, Janis

AU - Um, Soohyun

AU - Conlon, Benjamin H.

AU - Maus, Hannah

AU - Jäger, Nils

AU - Heinzel, Thorsten

AU - Schirmeister, Tanja

AU - Poulsen, Michael

AU - Beemelmanns, Christine

N1 - Funding Information: Funded by the Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) under Germany's Excellence Strategy - EXC 2051 with Project-ID 390713860 and CRC 1127 with Project-ID 239748522 to CB and TH. Funded by the European Research Council (ERC-CoG - 771349) and The Danish Council for Independent Research (DFF - 7014-00178) to MP. We thank the Humboldt Foundation for a postdoctoral fellowship to SU, and Mrs Heike Heinecke (Hans Kn?ll Institute) for recording NMR spectra. Funding Information: Funded by the Deutsche Forschungsgemeinscha (DFG, German Research Foundation) under Germany's Excellence Strategy – EXC 2051 with Project-ID 390713860 and CRC 1127 with Project-ID 239748522 to CB and TH. Funded by the European Research Council (ERC-CoG – 771349) and The Danish Council for Independent Research (DFF – 7014-00178) to MP. We thank the Humboldt Foundation for a postdoctoral fellowship to SU, and Mrs Heike Heinecke (Hans Knöll Institute) for recording NMR spectra. Publisher Copyright: © The Royal Society of Chemistry 2021.

PY - 2021

Y1 - 2021

N2 - Targeted HRMS2-GNPS-based metabolomic analysis ofPseudoxylariasp. X187, a fungal antagonist of the fungus-growing termite symbiosis, resulted in the identification of two lipopeptidic congeners of xylacremolides, named xylacremolide C and D, which are built fromd-phenylalanine,l-proline and an acetyl-CoA starter unit elongated by four malonyl-CoA derived ketide units. The putativexyagene cluster was identified from a draft genome generated by Illumina and PacBio sequencing and RNAseq studies. Biological activities of xylacremolide A and B were evaluated and revealed weak histone deacetylase inhibitory (HDACi) and antifungal activities, as well as moderate protease inhibition activity across a panel of nine human, viral and bacterial proteases.

AB - Targeted HRMS2-GNPS-based metabolomic analysis ofPseudoxylariasp. X187, a fungal antagonist of the fungus-growing termite symbiosis, resulted in the identification of two lipopeptidic congeners of xylacremolides, named xylacremolide C and D, which are built fromd-phenylalanine,l-proline and an acetyl-CoA starter unit elongated by four malonyl-CoA derived ketide units. The putativexyagene cluster was identified from a draft genome generated by Illumina and PacBio sequencing and RNAseq studies. Biological activities of xylacremolide A and B were evaluated and revealed weak histone deacetylase inhibitory (HDACi) and antifungal activities, as well as moderate protease inhibition activity across a panel of nine human, viral and bacterial proteases.

U2 - 10.1039/d1ra00997d

DO - 10.1039/d1ra00997d

M3 - Journal article

C2 - 34046176

AN - SCOPUS:85106938119

VL - 31

SP - 18748

EP - 18756

JO - RSC Advances

JF - RSC Advances

SN - 2046-2069

IS - 11

ER -

ID: 271616053