Enfumafungin synthase represents a novel lineage of fungal triterpene cyclases

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Autoren

  • Eric Kuhnert
  • Yan Li
  • Nan Lan
  • Qun Yue
  • Li Chen
  • Russell J. Cox
  • Zhiqiang An
  • Kenichi Yokoyama
  • Gerald F. Bills

Externe Organisationen

  • University of Texas Health Science Center at Houston
  • Chinese Academy of Agricultural Sciences
  • Duke University
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Details

OriginalspracheEnglisch
Seiten (von - bis)3325-3342
Seitenumfang18
FachzeitschriftEnvironmental microbiology
Jahrgang20
Ausgabenummer9
Frühes Online-Datum26 Juli 2018
PublikationsstatusVeröffentlicht - 27 Sept. 2018

Abstract

Enfumafungin is a glycosylated fernene-type triterpenoid produced by the fungus Hormonema carpetanum. Its potent antifungal activity, mediated by its interaction with β-1,3-glucan synthase and the fungal cell wall, has led to its development into the semi-synthetic clinical candidate, ibrexafungerp (=SCY-078). We report on the preliminary identification of the enfumafungin biosynthetic gene cluster (BGC) based on genome sequencing, phylogenetic reconstruction, gene disruption, and cDNA sequencing studies. Enfumafungin synthase (efuA) consists of a terpene cyclase domain (TC) fused to a glycosyltransferase (GT) domain and thus represents a novel multifunctional enzyme. Moreover, the TC domain bears a phylogenetic relationship to bacterial squalene–hopene cyclases (SHC) and includes a typical DXDD motif within the active centre suggesting that efuA evolved from SHCs. Phylogenetic reconstruction of the GT domain indicated that this portion of the fusion gene originated from fungal sterol GTs. Eleven genes flanking efuA are putatively involved in the biosynthesis, regulation, transport and self-resistance of enfumafungin and include an acetyltransferase, three P450 monooxygenases, a dehydrogenase, a desaturase and a reductase. A hypothetical scheme for enfumafungin assembly is proposed in which the E-ring is oxidatively cleaved to yield the four-ring system of enfumafungin. EfuA represents the first member of a widespread lineage of fungal SHCs.

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Enfumafungin synthase represents a novel lineage of fungal triterpene cyclases. / Kuhnert, Eric; Li, Yan; Lan, Nan et al.
in: Environmental microbiology, Jahrgang 20, Nr. 9, 27.09.2018, S. 3325-3342.

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Kuhnert, E, Li, Y, Lan, N, Yue, Q, Chen, L, Cox, RJ, An, Z, Yokoyama, K & Bills, GF 2018, 'Enfumafungin synthase represents a novel lineage of fungal triterpene cyclases', Environmental microbiology, Jg. 20, Nr. 9, S. 3325-3342. https://doi.org/10.1111/1462-2920.14333
Kuhnert, E., Li, Y., Lan, N., Yue, Q., Chen, L., Cox, R. J., An, Z., Yokoyama, K., & Bills, G. F. (2018). Enfumafungin synthase represents a novel lineage of fungal triterpene cyclases. Environmental microbiology, 20(9), 3325-3342. https://doi.org/10.1111/1462-2920.14333
Kuhnert E, Li Y, Lan N, Yue Q, Chen L, Cox RJ et al. Enfumafungin synthase represents a novel lineage of fungal triterpene cyclases. Environmental microbiology. 2018 Sep 27;20(9):3325-3342. Epub 2018 Jul 26. doi: 10.1111/1462-2920.14333
Kuhnert, Eric ; Li, Yan ; Lan, Nan et al. / Enfumafungin synthase represents a novel lineage of fungal triterpene cyclases. in: Environmental microbiology. 2018 ; Jahrgang 20, Nr. 9. S. 3325-3342.
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abstract = "Enfumafungin is a glycosylated fernene-type triterpenoid produced by the fungus Hormonema carpetanum. Its potent antifungal activity, mediated by its interaction with β-1,3-glucan synthase and the fungal cell wall, has led to its development into the semi-synthetic clinical candidate, ibrexafungerp (=SCY-078). We report on the preliminary identification of the enfumafungin biosynthetic gene cluster (BGC) based on genome sequencing, phylogenetic reconstruction, gene disruption, and cDNA sequencing studies. Enfumafungin synthase (efuA) consists of a terpene cyclase domain (TC) fused to a glycosyltransferase (GT) domain and thus represents a novel multifunctional enzyme. Moreover, the TC domain bears a phylogenetic relationship to bacterial squalene–hopene cyclases (SHC) and includes a typical DXDD motif within the active centre suggesting that efuA evolved from SHCs. Phylogenetic reconstruction of the GT domain indicated that this portion of the fusion gene originated from fungal sterol GTs. Eleven genes flanking efuA are putatively involved in the biosynthesis, regulation, transport and self-resistance of enfumafungin and include an acetyltransferase, three P450 monooxygenases, a dehydrogenase, a desaturase and a reductase. A hypothetical scheme for enfumafungin assembly is proposed in which the E-ring is oxidatively cleaved to yield the four-ring system of enfumafungin. EfuA represents the first member of a widespread lineage of fungal SHCs.",
author = "Eric Kuhnert and Yan Li and Nan Lan and Qun Yue and Li Chen and Cox, {Russell J.} and Zhiqiang An and Kenichi Yokoyama and Bills, {Gerald F.}",
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T1 - Enfumafungin synthase represents a novel lineage of fungal triterpene cyclases

AU - Kuhnert, Eric

AU - Li, Yan

AU - Lan, Nan

AU - Yue, Qun

AU - Chen, Li

AU - Cox, Russell J.

AU - An, Zhiqiang

AU - Yokoyama, Kenichi

AU - Bills, Gerald F.

N1 - Funding information: EK’s work at the University of Texas Health Science Centre at Houston was supported by a German Academic Exchange Service (DAAD) Postdoctoral Fellowship. In addition, work was supported by a Robert Welch Foundation Grant AU-20030616 (to ZA), the University of Texas Health Science Centre at Houston new faculty start-up funds, the Kay and Ben Fortson Endowment, and the National Institute of General Medical Sciences R01GM121458 (to GB). KY was supported by the Duke University Medical Center and the National Institute of General Medical Sciences R01GM115729. RJC thanks the Deutsche Forschungsge-meinschaft for LCMS equipment (INST 187/621). EK's work at the University of Texas Health Science Centre at Houston was supported by a German Academic Exchange Service (DAAD) Postdoctoral Fellowship. In addition, work was supported by a Robert Welch Foundation Grant AU-20030616 (to ZA), the University of Texas Health Science Centre at Houston new faculty start-up funds, the Kay and Ben Fortson Endowment, and the National Institute of General Medical Sciences R01GM121458 (to GB). KY was supported by the Duke University Medical Center and the National Institute of General Medical Sciences R01GM115729. RJC thanks the Deutsche Forschungsgemeinschaft for LCMS equipment (INST 187/621).

PY - 2018/9/27

Y1 - 2018/9/27

N2 - Enfumafungin is a glycosylated fernene-type triterpenoid produced by the fungus Hormonema carpetanum. Its potent antifungal activity, mediated by its interaction with β-1,3-glucan synthase and the fungal cell wall, has led to its development into the semi-synthetic clinical candidate, ibrexafungerp (=SCY-078). We report on the preliminary identification of the enfumafungin biosynthetic gene cluster (BGC) based on genome sequencing, phylogenetic reconstruction, gene disruption, and cDNA sequencing studies. Enfumafungin synthase (efuA) consists of a terpene cyclase domain (TC) fused to a glycosyltransferase (GT) domain and thus represents a novel multifunctional enzyme. Moreover, the TC domain bears a phylogenetic relationship to bacterial squalene–hopene cyclases (SHC) and includes a typical DXDD motif within the active centre suggesting that efuA evolved from SHCs. Phylogenetic reconstruction of the GT domain indicated that this portion of the fusion gene originated from fungal sterol GTs. Eleven genes flanking efuA are putatively involved in the biosynthesis, regulation, transport and self-resistance of enfumafungin and include an acetyltransferase, three P450 monooxygenases, a dehydrogenase, a desaturase and a reductase. A hypothetical scheme for enfumafungin assembly is proposed in which the E-ring is oxidatively cleaved to yield the four-ring system of enfumafungin. EfuA represents the first member of a widespread lineage of fungal SHCs.

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