Biotransformation of (-)-Epigallocatechin-3-O-gallate into (-)-2R,3S-Dihydromyricetin by the Endophytic Fungus Diaporthe sp. E Isolate Obtained from a Tea Plant

Endophytic fungi have been reported possess an interesting ability to mimic their host plant metabolites. Several fungi also show their specific capability to biotransform the chemical constituents of the host plant. The endophytic fungus Diaporthe sp. E isolate obtained from young stem of a tea pla...

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Main Author: ANDRIA AGUSTA
Format: Article
Language:English
Published: Bogor Agricultural University 2007-12-01
Series:Hayati Journal of Biosciences
Subjects:
3R
Online Access:http://journal.ipb.ac.id/index.php/hayati/article/viewFile/257/123
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spelling doaj-6f8aeedc74584eacbe3c87d8e2209c472020-11-24T22:03:18ZengBogor Agricultural UniversityHayati Journal of Biosciences1978-30192086-40942007-12-01144150154Biotransformation of (-)-Epigallocatechin-3-O-gallate into (-)-2R,3S-Dihydromyricetin by the Endophytic Fungus Diaporthe sp. E Isolate Obtained from a Tea PlantANDRIA AGUSTAEndophytic fungi have been reported possess an interesting ability to mimic their host plant metabolites. Several fungi also show their specific capability to biotransform the chemical constituents of the host plant. The endophytic fungus Diaporthe sp. E isolate obtained from young stem of a tea plant (Camellia sinensis) show their unique capability to biotransform (-)-epigallocatechin-3-O-gallate [(-)-EGCG] into a major product in glucose-peptone-yeast extract medium that incubated under dark condition at 27 oC for 48 h. The major biotransformation product were isolated and purified through column chromatography techniques using Sephadex LH-20 and silica gel. The chemical structure of the major product were elucidated as (-)-2R,3S-dihydromyricetin based on their IR, FAB-MS, 1D- and 2D-NMR spectra.http://journal.ipb.ac.id/index.php/hayati/article/viewFile/257/123(-)-2R3S-dihydromyricetin(-)-EGCG(-)-2R3R4R-leucodelphynidinbiotransformationDiaporthe sp. E isolateendophytic fungusCamellia sinensis
collection DOAJ
language English
format Article
sources DOAJ
author ANDRIA AGUSTA
spellingShingle ANDRIA AGUSTA
Biotransformation of (-)-Epigallocatechin-3-O-gallate into (-)-2R,3S-Dihydromyricetin by the Endophytic Fungus Diaporthe sp. E Isolate Obtained from a Tea Plant
Hayati Journal of Biosciences
(-)-2R
3S-dihydromyricetin
(-)-EGCG
(-)-2R
3R
4R-leucodelphynidin
biotransformation
Diaporthe sp. E isolate
endophytic fungus
Camellia sinensis
author_facet ANDRIA AGUSTA
author_sort ANDRIA AGUSTA
title Biotransformation of (-)-Epigallocatechin-3-O-gallate into (-)-2R,3S-Dihydromyricetin by the Endophytic Fungus Diaporthe sp. E Isolate Obtained from a Tea Plant
title_short Biotransformation of (-)-Epigallocatechin-3-O-gallate into (-)-2R,3S-Dihydromyricetin by the Endophytic Fungus Diaporthe sp. E Isolate Obtained from a Tea Plant
title_full Biotransformation of (-)-Epigallocatechin-3-O-gallate into (-)-2R,3S-Dihydromyricetin by the Endophytic Fungus Diaporthe sp. E Isolate Obtained from a Tea Plant
title_fullStr Biotransformation of (-)-Epigallocatechin-3-O-gallate into (-)-2R,3S-Dihydromyricetin by the Endophytic Fungus Diaporthe sp. E Isolate Obtained from a Tea Plant
title_full_unstemmed Biotransformation of (-)-Epigallocatechin-3-O-gallate into (-)-2R,3S-Dihydromyricetin by the Endophytic Fungus Diaporthe sp. E Isolate Obtained from a Tea Plant
title_sort biotransformation of (-)-epigallocatechin-3-o-gallate into (-)-2r,3s-dihydromyricetin by the endophytic fungus diaporthe sp. e isolate obtained from a tea plant
publisher Bogor Agricultural University
series Hayati Journal of Biosciences
issn 1978-3019
2086-4094
publishDate 2007-12-01
description Endophytic fungi have been reported possess an interesting ability to mimic their host plant metabolites. Several fungi also show their specific capability to biotransform the chemical constituents of the host plant. The endophytic fungus Diaporthe sp. E isolate obtained from young stem of a tea plant (Camellia sinensis) show their unique capability to biotransform (-)-epigallocatechin-3-O-gallate [(-)-EGCG] into a major product in glucose-peptone-yeast extract medium that incubated under dark condition at 27 oC for 48 h. The major biotransformation product were isolated and purified through column chromatography techniques using Sephadex LH-20 and silica gel. The chemical structure of the major product were elucidated as (-)-2R,3S-dihydromyricetin based on their IR, FAB-MS, 1D- and 2D-NMR spectra.
topic (-)-2R
3S-dihydromyricetin
(-)-EGCG
(-)-2R
3R
4R-leucodelphynidin
biotransformation
Diaporthe sp. E isolate
endophytic fungus
Camellia sinensis
url http://journal.ipb.ac.id/index.php/hayati/article/viewFile/257/123
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