Study on secondary metabolites of endophytic fungus Diaporthe sp. AC1 induced by tryptophan analogs

Small molecule-induced fermentation of the endophytic fungus Diaporthe sp. AC1 originated from Artemisia argyi was executed to investigate its secondary metabolites. It was fermented in a culture medium containing 5-hydroxytryptophan (5-HTP), 1-methyl-L-tryptophan (1-MT), and tryptamine (TA), respec...

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Main Authors: Shikai Zhang, Qing Xu, Changbo Ji, Xiaoyu Han, Yang Zhou, Chao Liang, Linran Ma, Weijian Sun, Yanling Li, Zhengyou Yang, Fengchun Zhao, Yuan Tian
Format: Article
Language:English
Published: Frontiers Media S.A. 2023-10-01
Series:Frontiers in Microbiology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fmicb.2023.1254609/full
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author Shikai Zhang
Qing Xu
Changbo Ji
Xiaoyu Han
Yang Zhou
Chao Liang
Linran Ma
Weijian Sun
Yanling Li
Zhengyou Yang
Fengchun Zhao
Yuan Tian
author_facet Shikai Zhang
Qing Xu
Changbo Ji
Xiaoyu Han
Yang Zhou
Chao Liang
Linran Ma
Weijian Sun
Yanling Li
Zhengyou Yang
Fengchun Zhao
Yuan Tian
author_sort Shikai Zhang
collection DOAJ
description Small molecule-induced fermentation of the endophytic fungus Diaporthe sp. AC1 originated from Artemisia argyi was executed to investigate its secondary metabolites. It was fermented in a culture medium containing 5-hydroxytryptophan (5-HTP), 1-methyl-L-tryptophan (1-MT), and tryptamine (TA), respectively. The antibacterial activities of crude extracts against pathogenic bacteria and pathogenic fungi were determined by using the Oxford cup method, while the cytotoxicity of crude extracts against cancer cells was determined by using the MTT method. The results showed that the secondary metabolites of Diaporthe sp. AC1 induced by 1-MT exhibited optimal antibacterial activity and tumor cytotoxicity. The induction conditions of 1-MT were optimized, and the antibacterial activities and tumor cytotoxicity of crude extracts under different induction conditions were investigated. As indicated, the optimal moment for 1-MT addition was before inoculation and its optimal concentration was 0.25 mM. Under these conditions, Diaporthe sp. AC1 was fermented and approximately 12 g of crude extracts was obtained. The crude extracts were then separated and purified to acquire nine monomer compounds, including three new compounds (1–3) and six known compounds (4–9). The antibacterial activities of the compounds against pathogenic bacteria and pathogenic fungi were investigated by using the microdilution method, while their cytotoxicity against cancer cells was analyzed by using the MTT method. The results demonstrated that Compound 1 exhibited moderate antibacterial activities against Verticillium dahlia, Fusarium graminearum, and Botrytis cinerea, as well as a low inhibitory activity against Listeria monocytogenes. Nevertheless, Compound 1 showed significant cytotoxicity against five cancer cells, with IC50 ranging from 12.26 to 52.52 μM. Compounds 2 and 3 exhibited negligible biological activity, while other compounds showed detectable inhibitory activities against pathogenic bacteria and cancer cells.
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spelling doaj.art-cdcc2db0305042e39db3eb0fe599de312023-10-09T11:05:12ZengFrontiers Media S.A.Frontiers in Microbiology1664-302X2023-10-011410.3389/fmicb.2023.12546091254609Study on secondary metabolites of endophytic fungus Diaporthe sp. AC1 induced by tryptophan analogsShikai Zhang0Qing Xu1Changbo Ji2Xiaoyu Han3Yang Zhou4Chao Liang5Linran Ma6Weijian Sun7Yanling Li8Zhengyou Yang9Fengchun Zhao10Yuan Tian11Department of Microbiology, College of Life Science, Key Laboratory for Agriculture Microbiology, Shandong Agricultural University, Taian, ChinaDepartment of Microbiology, College of Life Science, Key Laboratory for Agriculture Microbiology, Shandong Agricultural University, Taian, ChinaCollege of Life Science, Shandong First Medical University & Shandong Academy of Medical Sciences, Taian, ChinaCollege of Life Science, Shandong First Medical University & Shandong Academy of Medical Sciences, Taian, ChinaCollege of Life Science, Shandong First Medical University & Shandong Academy of Medical Sciences, Taian, ChinaCollege of Life Science, Shandong First Medical University & Shandong Academy of Medical Sciences, Taian, ChinaCollege of Life Science, Shandong First Medical University & Shandong Academy of Medical Sciences, Taian, ChinaCollege of Life Science, Shandong First Medical University & Shandong Academy of Medical Sciences, Taian, ChinaCollege of Life Science, Shandong First Medical University & Shandong Academy of Medical Sciences, Taian, ChinaDepartment of Microbiology, College of Life Science, Key Laboratory for Agriculture Microbiology, Shandong Agricultural University, Taian, ChinaDepartment of Microbiology, College of Life Science, Key Laboratory for Agriculture Microbiology, Shandong Agricultural University, Taian, ChinaCollege of Life Science, Shandong First Medical University & Shandong Academy of Medical Sciences, Taian, ChinaSmall molecule-induced fermentation of the endophytic fungus Diaporthe sp. AC1 originated from Artemisia argyi was executed to investigate its secondary metabolites. It was fermented in a culture medium containing 5-hydroxytryptophan (5-HTP), 1-methyl-L-tryptophan (1-MT), and tryptamine (TA), respectively. The antibacterial activities of crude extracts against pathogenic bacteria and pathogenic fungi were determined by using the Oxford cup method, while the cytotoxicity of crude extracts against cancer cells was determined by using the MTT method. The results showed that the secondary metabolites of Diaporthe sp. AC1 induced by 1-MT exhibited optimal antibacterial activity and tumor cytotoxicity. The induction conditions of 1-MT were optimized, and the antibacterial activities and tumor cytotoxicity of crude extracts under different induction conditions were investigated. As indicated, the optimal moment for 1-MT addition was before inoculation and its optimal concentration was 0.25 mM. Under these conditions, Diaporthe sp. AC1 was fermented and approximately 12 g of crude extracts was obtained. The crude extracts were then separated and purified to acquire nine monomer compounds, including three new compounds (1–3) and six known compounds (4–9). The antibacterial activities of the compounds against pathogenic bacteria and pathogenic fungi were investigated by using the microdilution method, while their cytotoxicity against cancer cells was analyzed by using the MTT method. The results demonstrated that Compound 1 exhibited moderate antibacterial activities against Verticillium dahlia, Fusarium graminearum, and Botrytis cinerea, as well as a low inhibitory activity against Listeria monocytogenes. Nevertheless, Compound 1 showed significant cytotoxicity against five cancer cells, with IC50 ranging from 12.26 to 52.52 μM. Compounds 2 and 3 exhibited negligible biological activity, while other compounds showed detectable inhibitory activities against pathogenic bacteria and cancer cells.https://www.frontiersin.org/articles/10.3389/fmicb.2023.1254609/fullDiaportheendophytic fungi1-methyl-L-tryptophansecondary metabolitesbiological activity
spellingShingle Shikai Zhang
Qing Xu
Changbo Ji
Xiaoyu Han
Yang Zhou
Chao Liang
Linran Ma
Weijian Sun
Yanling Li
Zhengyou Yang
Fengchun Zhao
Yuan Tian
Study on secondary metabolites of endophytic fungus Diaporthe sp. AC1 induced by tryptophan analogs
Frontiers in Microbiology
Diaporthe
endophytic fungi
1-methyl-L-tryptophan
secondary metabolites
biological activity
title Study on secondary metabolites of endophytic fungus Diaporthe sp. AC1 induced by tryptophan analogs
title_full Study on secondary metabolites of endophytic fungus Diaporthe sp. AC1 induced by tryptophan analogs
title_fullStr Study on secondary metabolites of endophytic fungus Diaporthe sp. AC1 induced by tryptophan analogs
title_full_unstemmed Study on secondary metabolites of endophytic fungus Diaporthe sp. AC1 induced by tryptophan analogs
title_short Study on secondary metabolites of endophytic fungus Diaporthe sp. AC1 induced by tryptophan analogs
title_sort study on secondary metabolites of endophytic fungus diaporthe sp ac1 induced by tryptophan analogs
topic Diaporthe
endophytic fungi
1-methyl-L-tryptophan
secondary metabolites
biological activity
url https://www.frontiersin.org/articles/10.3389/fmicb.2023.1254609/full
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