Two New Nonenolides from Diaporthe sp. SXZ-19, an Endophytic Fungus of Camptotheca Acuminata.


Journal

Chemistry & biodiversity
ISSN: 1612-1880
Titre abrégé: Chem Biodivers
Pays: Switzerland
ID NLM: 101197449

Informations de publication

Date de publication:
May 2021
Historique:
received: 23 12 2020
accepted: 04 03 2021
pubmed: 6 3 2021
medline: 11 8 2021
entrez: 5 3 2021
Statut: ppublish

Résumé

Two new nonenolides named diaportheolides A (1) and B (2) were isolated from the endophytic fungus Diaporthe sp. SXZ-19 of Camptotheca acuminata. The chemical structures of 1 and 2 were elucidated by spectroscopic analyses, including 1D- and 2D-NMR experiments and HR-ESI-MS data analysis. Their in vitro antibacterial activities are established to be insignificant.

Identifiants

pubmed: 33665917
doi: 10.1002/cbdv.202001055
doi:

Substances chimiques

Anti-Bacterial Agents 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e2001055

Subventions

Organisme : Natural Science Foundation of Hubei Province
ID : 2019CFB595
Organisme : Hubei University
ID : 19RC06

Informations de copyright

© 2021 Wiley-VHCA AG, Zurich, Switzerland.

Références

G. Strobel, B. Daisy, ‘Bioprospecting for microbial endophytes and their natural products’, Microbiol. Mol. Biol. Rev. 2003, 67, 491-502.
R. X. Tan, W. X. Zou, ‘Endophytes: A rich source of functional metabolites’, Nat. Prod. Rep. 2001, 18, 448-459.
H. W. Zhang, Y. C. Song, R. X. Tan, ‘Biology and chemistry of endophytes’, Nat. Prod. Rep. 2006, 23, 753-771.
X. Lin, C. Lu, Y. Huang, Z. Zheng, W. Su, Y. Shen, ‘Endophytic fungi from a pharmaceutical plant, Camptotheca acuminata: Isolation, identification and bioactivity’, World J. Microbiol. Biotechnol. 2007, 23, 1037-1040.
Y. Liu, Z. Hu, X. Lin, C. Lu, Y. Shen, ‘A new polyketide from Diaporthe sp. SXZ-19, an endophytic fungal strain of Camptotheca acuminata’, Nat. Prod. Res. 2013, 27, 2100-2104.
A. S. Ratnayake, W. Y. Yoshida, S. L. Mooberry, T. Hemscheidt, ‘The structure of microcarpalide, a microfilament disrupting agent from an endophytic fungus’, Org. Lett. 2001, 3, 3479-3481.
A. Evidente, A. Cimmino, A. Berestetskiy, G. Mitina, A. Andolfi, A. Motta, ‘Stagonolides B - F, nonenolides produced by Stagonospora cirsii, a potential mycoherbicide of Cirsium arvense’, J. Nat. Prod. 2008, 71, 31-34.
A. Evidente, A. Cimmino, A. Berestetskiy, A. Andolfi, A. Motta, ‘Stagonolides G - I and modiolide A, nonenolides produced by Stagonospora cirsii, a potential mycoherbicide for Cirsium arvense’, J. Nat. Prod. 2008, 71, 1897-1901.
A. Dalinova, V. Dubovik, L. Chisty, D. Kochura, A. Ivanov, S. Smirnov, M. Petrova, A. Zolotarev, A. Evidente, A. Berestetskiy, ‘Stagonolides J and K and stagochromene A, two new natural substituted nonenolides and a new disubstituted chromene-4,5-dione isolated from Stagonospora cirsii S-47 proposed for the biocontrol of Sonchus arvensis’, J. Agric. Food Chem. 2019, 67, 13040-13050.
Y. Li, M. Wang, Y. Huang, Y. Shen, ‘Secondary metabolites from Phomopsis sp. A123’, Mycology 2010, 1, 254-261.
E. G. Baraban, J. B. Morin, G. M. Phillips, A. J. Phillips, S. A. Strobel, J. Handelsman, ‘Xyolide, a bioactive nonenolide from an amazonian endophytic fungus, Xylaria feejeensis’, Tetrahedron Lett. 2013, 54, 4058-4060.
J. Wang, C. C. Xu, H. Tang, L. Su, Y. Chou, K. Soong, J. Li, C. L. Zhuang, Y. P. Luo, W. Zhang, ‘Osteoclastogenesis inhibitory polyketides from the sponge-associated fungus Xylaria feejeensis’, Chem. Biodiversity 2018, 15, e1800358.
R. Xu, C. Lu, X. Wu, C. Lin, Z. Zheng, ‘A new ten-membered lactone from Tubercularia sp. TF5, an endophytic fungus of Taxus mairei’, Chem. Nat. Compd. 2009, 45, 797-799.
P. R. Sudina, D. R. Motati, A. Seema, ‘Stereocontrolled total synthesis of nonenolide’, J. Nat. Prod. 2018, 81, 1399-1404.

Auteurs

Yuanzhen Liu (Y)

School of Chemistry and Life Sciences, Hubei University of Education, No. 129 Gaoxin 2nd Road, Wuhan, 430205, P. R. China.
Hubei Key Laboratory of Purification and Application of Plant Anticancer Active Ingredients, Hubei University of Education, No. 129 Gaoxin 2nd Road, Wuhan, 430205, P. R. China.
Research Center for Development and Utilization of Medicinal Plants in Eastern Hubei Province, Hubei University of Education, No. 129 Gaoxin 2nd Road, Wuhan, 430205, P. R. China.

Li Cheng (L)

School of Chemistry and Life Sciences, Hubei University of Education, No. 129 Gaoxin 2nd Road, Wuhan, 430205, P. R. China.
Research Center for Development and Utilization of Medicinal Plants in Eastern Hubei Province, Hubei University of Education, No. 129 Gaoxin 2nd Road, Wuhan, 430205, P. R. China.

Yuemao Shen (Y)

School of Life Sciences, Xiamen University, No. 4221-120 South Xiang'an Road, Xiamen, 361102, P. R. China.

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