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Tall fescue seed extraction and partial purification of ergot alkaloids

Many substances in the tall fescue/endophyte association (Schedonorus arundinaceus/Epichloë coenophiala) have biological activity. Of these compounds only the ergot alkaloids are known to have significant mammalian toxicity and the predominant ergot alkaloids are ergovaline and ergovalinine. Because...

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Autores principales: Ji, Huihua, Fannin, F., Klotz, J., Bush, Lowell
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4263182/
https://www.ncbi.nlm.nih.gov/pubmed/25566528
http://dx.doi.org/10.3389/fchem.2014.00110
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author Ji, Huihua
Fannin, F.
Klotz, J.
Bush, Lowell
author_facet Ji, Huihua
Fannin, F.
Klotz, J.
Bush, Lowell
author_sort Ji, Huihua
collection PubMed
description Many substances in the tall fescue/endophyte association (Schedonorus arundinaceus/Epichloë coenophiala) have biological activity. Of these compounds only the ergot alkaloids are known to have significant mammalian toxicity and the predominant ergot alkaloids are ergovaline and ergovalinine. Because synthetically produced ergovaline is difficult to obtain, we developed a seed extraction and partial purification protocol for ergovaline/ergovalinine that provided a biologically active product. Tall fescue seed was ground and packed into several different sized columns for liquid extraction. Smaller particle size and increased extraction time increased efficiency of extraction. Our largest column was a 114 × 52 × 61 cm (W × L × D) stainless steel tub. Approximately 150 kg of seed could be extracted in this tub. The extraction was done with 80% ethanol. When the solvent front migrated to bottom of the column, flow was stopped and seed was allowed to steep for at least 48 h. Light was excluded from the solvent from the beginning of this step to the end of the purification process. Following elution, ethanol was removed from the eluate by evaporation at room temperature and the resulting syrup was freeze-dried. About 80% recovery of alkaloids was achieved with 18-fold increase in concentration of ergovaline. Initial purification of the dried product was accomplished by extracting with hexane/water (6:1, v/v). The aqueous fraction was extracted with chloroform, the aqueous layer discarded, after which the chloroform was removed with a resulting 20-fold increase of ergovaline. About 65% of the ergovaline was recovered from the chloroform residue for an overall recovery of 50%. The resultant partially purified ergovaline had biological activities in in vivo and in vitro bovine bioassays that approximate that of synthetic ergovaline.
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spelling pubmed-42631822015-01-06 Tall fescue seed extraction and partial purification of ergot alkaloids Ji, Huihua Fannin, F. Klotz, J. Bush, Lowell Front Chem Chemistry Many substances in the tall fescue/endophyte association (Schedonorus arundinaceus/Epichloë coenophiala) have biological activity. Of these compounds only the ergot alkaloids are known to have significant mammalian toxicity and the predominant ergot alkaloids are ergovaline and ergovalinine. Because synthetically produced ergovaline is difficult to obtain, we developed a seed extraction and partial purification protocol for ergovaline/ergovalinine that provided a biologically active product. Tall fescue seed was ground and packed into several different sized columns for liquid extraction. Smaller particle size and increased extraction time increased efficiency of extraction. Our largest column was a 114 × 52 × 61 cm (W × L × D) stainless steel tub. Approximately 150 kg of seed could be extracted in this tub. The extraction was done with 80% ethanol. When the solvent front migrated to bottom of the column, flow was stopped and seed was allowed to steep for at least 48 h. Light was excluded from the solvent from the beginning of this step to the end of the purification process. Following elution, ethanol was removed from the eluate by evaporation at room temperature and the resulting syrup was freeze-dried. About 80% recovery of alkaloids was achieved with 18-fold increase in concentration of ergovaline. Initial purification of the dried product was accomplished by extracting with hexane/water (6:1, v/v). The aqueous fraction was extracted with chloroform, the aqueous layer discarded, after which the chloroform was removed with a resulting 20-fold increase of ergovaline. About 65% of the ergovaline was recovered from the chloroform residue for an overall recovery of 50%. The resultant partially purified ergovaline had biological activities in in vivo and in vitro bovine bioassays that approximate that of synthetic ergovaline. Frontiers Media S.A. 2014-12-11 /pmc/articles/PMC4263182/ /pubmed/25566528 http://dx.doi.org/10.3389/fchem.2014.00110 Text en Copyright © 2014 Ji, Fannin, Klotz and Bush. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Chemistry
Ji, Huihua
Fannin, F.
Klotz, J.
Bush, Lowell
Tall fescue seed extraction and partial purification of ergot alkaloids
title Tall fescue seed extraction and partial purification of ergot alkaloids
title_full Tall fescue seed extraction and partial purification of ergot alkaloids
title_fullStr Tall fescue seed extraction and partial purification of ergot alkaloids
title_full_unstemmed Tall fescue seed extraction and partial purification of ergot alkaloids
title_short Tall fescue seed extraction and partial purification of ergot alkaloids
title_sort tall fescue seed extraction and partial purification of ergot alkaloids
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4263182/
https://www.ncbi.nlm.nih.gov/pubmed/25566528
http://dx.doi.org/10.3389/fchem.2014.00110
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