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Sorokiniol: a new enzymes inhibitory metabolite from fungal endophyte Bipolaris sorokiniana LK12

BACKGROUND: Medicinal plants harboring endophytic fungi could carry significant potential for producing bioactive secondary metabolites. Endophytic fungi serve as alternate source of interesting compounds in their natural and modified synthetic forms to treat different diseases. In this regard, endo...

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Autores principales: Ali, Liaqat, Khan, Abdul Latif, Hussain, Javid, Al-Harrasi, Ahmed, Waqas, Muhammad, Kang, Sang-Mo, Al-Rawahi, Ahmed, Lee, In-Jung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4899901/
https://www.ncbi.nlm.nih.gov/pubmed/27277006
http://dx.doi.org/10.1186/s12866-016-0722-7
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author Ali, Liaqat
Khan, Abdul Latif
Hussain, Javid
Al-Harrasi, Ahmed
Waqas, Muhammad
Kang, Sang-Mo
Al-Rawahi, Ahmed
Lee, In-Jung
author_facet Ali, Liaqat
Khan, Abdul Latif
Hussain, Javid
Al-Harrasi, Ahmed
Waqas, Muhammad
Kang, Sang-Mo
Al-Rawahi, Ahmed
Lee, In-Jung
author_sort Ali, Liaqat
collection PubMed
description BACKGROUND: Medicinal plants harboring endophytic fungi could carry significant potential for producing bioactive secondary metabolites. Endophytic fungi serve as alternate source of interesting compounds in their natural and modified synthetic forms to treat different diseases. In this regard, endophytic microflora associated with alkaloid-rich medicinal plants Rhazya stricta is least known. RESULTS: We isolated one new bioactive compound sorokiniol (1) along with two known cyclic peptides BZR-cotoxin I (2) and BZR-cotoxin IV (3) from fungal endophyte Bipolaris sorokiniana LK12. The structures of the isolated new and known compounds were elucidated through spectroscopic data, including 1D and 2D NMR ((1)H, (13)C, HSQC, HMBC, and NOESY), mass, and UV. The known peptides (2–3) were characterized by ESI-MS, MS/MS, and by comparing the NMR data with the literature. The isolated metabolites were assayed for their role against enzyme inhibition. Compound 1 was significantly inhibitory towards acetyl cholinestrase while the other compounds (2–3) had moderate anti-lipid peroxidation and urease activities. CONCLUSION: The present results suggest that the endophytic microorganism associated with indigenously important medicinal plants can offer a rich source of biologically active chemical constituents which could help in discovering enzyme inhibitory lead drugs. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12866-016-0722-7) contains supplementary material, which is available to authorized users.
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spelling pubmed-48999012016-06-10 Sorokiniol: a new enzymes inhibitory metabolite from fungal endophyte Bipolaris sorokiniana LK12 Ali, Liaqat Khan, Abdul Latif Hussain, Javid Al-Harrasi, Ahmed Waqas, Muhammad Kang, Sang-Mo Al-Rawahi, Ahmed Lee, In-Jung BMC Microbiol Research Article BACKGROUND: Medicinal plants harboring endophytic fungi could carry significant potential for producing bioactive secondary metabolites. Endophytic fungi serve as alternate source of interesting compounds in their natural and modified synthetic forms to treat different diseases. In this regard, endophytic microflora associated with alkaloid-rich medicinal plants Rhazya stricta is least known. RESULTS: We isolated one new bioactive compound sorokiniol (1) along with two known cyclic peptides BZR-cotoxin I (2) and BZR-cotoxin IV (3) from fungal endophyte Bipolaris sorokiniana LK12. The structures of the isolated new and known compounds were elucidated through spectroscopic data, including 1D and 2D NMR ((1)H, (13)C, HSQC, HMBC, and NOESY), mass, and UV. The known peptides (2–3) were characterized by ESI-MS, MS/MS, and by comparing the NMR data with the literature. The isolated metabolites were assayed for their role against enzyme inhibition. Compound 1 was significantly inhibitory towards acetyl cholinestrase while the other compounds (2–3) had moderate anti-lipid peroxidation and urease activities. CONCLUSION: The present results suggest that the endophytic microorganism associated with indigenously important medicinal plants can offer a rich source of biologically active chemical constituents which could help in discovering enzyme inhibitory lead drugs. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12866-016-0722-7) contains supplementary material, which is available to authorized users. BioMed Central 2016-06-09 /pmc/articles/PMC4899901/ /pubmed/27277006 http://dx.doi.org/10.1186/s12866-016-0722-7 Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Ali, Liaqat
Khan, Abdul Latif
Hussain, Javid
Al-Harrasi, Ahmed
Waqas, Muhammad
Kang, Sang-Mo
Al-Rawahi, Ahmed
Lee, In-Jung
Sorokiniol: a new enzymes inhibitory metabolite from fungal endophyte Bipolaris sorokiniana LK12
title Sorokiniol: a new enzymes inhibitory metabolite from fungal endophyte Bipolaris sorokiniana LK12
title_full Sorokiniol: a new enzymes inhibitory metabolite from fungal endophyte Bipolaris sorokiniana LK12
title_fullStr Sorokiniol: a new enzymes inhibitory metabolite from fungal endophyte Bipolaris sorokiniana LK12
title_full_unstemmed Sorokiniol: a new enzymes inhibitory metabolite from fungal endophyte Bipolaris sorokiniana LK12
title_short Sorokiniol: a new enzymes inhibitory metabolite from fungal endophyte Bipolaris sorokiniana LK12
title_sort sorokiniol: a new enzymes inhibitory metabolite from fungal endophyte bipolaris sorokiniana lk12
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4899901/
https://www.ncbi.nlm.nih.gov/pubmed/27277006
http://dx.doi.org/10.1186/s12866-016-0722-7
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