UPLC‐Q‐TOF‐MS/MS analysis of the guaiane sesquiterpenoids oxytropiols A–J and detection of undescribed analogues from the locoweed endophytic fungus Alternaria oxytropis (Pleosporaceae). Issue 3 (9th November 2021)
- Record Type:
- Journal Article
- Title:
- UPLC‐Q‐TOF‐MS/MS analysis of the guaiane sesquiterpenoids oxytropiols A–J and detection of undescribed analogues from the locoweed endophytic fungus Alternaria oxytropis (Pleosporaceae). Issue 3 (9th November 2021)
- Main Title:
- UPLC‐Q‐TOF‐MS/MS analysis of the guaiane sesquiterpenoids oxytropiols A–J and detection of undescribed analogues from the locoweed endophytic fungus Alternaria oxytropis (Pleosporaceae)
- Authors:
- Tan, Xiang‐Mei
Li, Qi
Wang, Yan‐Duo
Wang, Tie‐Lin
Yang, Jian
Sun, Bing‐Da
Guo, Lan‐Ping
Ding, Gang - Abstract:
- Abstract: Introduction: In addition to the mycotoxin swainsonine, the locoweed endophytic fungus Alternaria oxytropis (Pleosporaceae) also produces a series of rarely reported, highly oxygenated bicyclic guaiane sesquiterpenoids. Few investigations on the electrospray tandem mass fragmentation pattern of this sesquiterpenoid have been reported. Objectives: We aimed to analyze and detect new guaiane sesquiterpenoid analogues from crude extracts of the locoweed endophytic fungus A. oxytropis by UPLC‐Q‐TOF‐MS/MS experiments. Materials and Methods: Oxytropiols A–J (1 –10 ) and the extract of the locoweed endophytic fungus A. oxytropis were analyzed by UPLC‐Q‐TOF‐MS/MS in positive mode. Results: Typical neutral losses, McLafferty rearrangement, 1, 2‐rearrangement, and 1, 3‐rearrangement were considered to be the main fragmentation patterns for the [M + H] + /[M + Na] + ions of 1 –10 by UPLC‐Q‐TOF‐MS/MS experiments, and possible fragmentation pathways of 1 –10 were suggested. A unique and undescribed analogue named oxytropiol K (11 ) was found in the extract based on UPLC‐Q‐TOF‐MS/MS analysis. Compound 11 was isolated and elucidated by NMR spectrometry, and its UPLC‐Q‐TOF‐MS/MS analysis was consistent with the fragmentation pathways of 1 –10 . Conclusion: The results further support that UPLC‐Q‐TOF‐MS/MS is a powerful and sensitive tool for the characterization of known compounds (dereplication) and the detection of new analogues from crude extracts and imply that the locoweedAbstract: Introduction: In addition to the mycotoxin swainsonine, the locoweed endophytic fungus Alternaria oxytropis (Pleosporaceae) also produces a series of rarely reported, highly oxygenated bicyclic guaiane sesquiterpenoids. Few investigations on the electrospray tandem mass fragmentation pattern of this sesquiterpenoid have been reported. Objectives: We aimed to analyze and detect new guaiane sesquiterpenoid analogues from crude extracts of the locoweed endophytic fungus A. oxytropis by UPLC‐Q‐TOF‐MS/MS experiments. Materials and Methods: Oxytropiols A–J (1 –10 ) and the extract of the locoweed endophytic fungus A. oxytropis were analyzed by UPLC‐Q‐TOF‐MS/MS in positive mode. Results: Typical neutral losses, McLafferty rearrangement, 1, 2‐rearrangement, and 1, 3‐rearrangement were considered to be the main fragmentation patterns for the [M + H] + /[M + Na] + ions of 1 –10 by UPLC‐Q‐TOF‐MS/MS experiments, and possible fragmentation pathways of 1 –10 were suggested. A unique and undescribed analogue named oxytropiol K (11 ) was found in the extract based on UPLC‐Q‐TOF‐MS/MS analysis. Compound 11 was isolated and elucidated by NMR spectrometry, and its UPLC‐Q‐TOF‐MS/MS analysis was consistent with the fragmentation pathways of 1 –10 . Conclusion: The results further support that UPLC‐Q‐TOF‐MS/MS is a powerful and sensitive tool for the characterization of known compounds (dereplication) and the detection of new analogues from crude extracts and imply that the locoweed endophytic fungus A. oxytropis, with few chemical investigations, is an important resource for undescribed metabolites. Abstract : Oxytropiols A‐J (1‐10 ) and the extract of the locoweed endophytic fungus A. oxytropis were analysed by UPLC‐Q‐TOF‐MS/MS in positive mode. Neutral losses, and different rearrangements were considered to be the main fragmentation patterns for the [M+H] + /[M+Na] + ions of 1‐10 . A unique and undescribed analogue named oxytropiol K (11) was found in the A. oxytropis extract based on UPLC‐Q‐TOF‐MS/MS analysis. … (more)
- Is Part Of:
- Phytochemical analysis. Volume 33:Issue 3(2022)
- Journal:
- Phytochemical analysis
- Issue:
- Volume 33:Issue 3(2022)
- Issue Display:
- Volume 33, Issue 3 (2022)
- Year:
- 2022
- Volume:
- 33
- Issue:
- 3
- Issue Sort Value:
- 2022-0033-0003-0000
- Page Start:
- 344
- Page End:
- 354
- Publication Date:
- 2021-11-09
- Subjects:
- Alternaria oxytropis (Pleosporaceae) -- bicyclic guaiane sesquiterpenoids -- endophytic fungus -- oxytropiols A–K (1–11) -- rearrangement reactions -- UPLC‐Q‐TOF‐MS/MS
Plants -- Analysis -- Periodicals
Plants -- chemistry -- Periodicals
572.2 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1002/pca.3092 ↗
- Languages:
- English
- ISSNs:
- 0958-0344
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6489.695000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 21211.xml