Loading…
Biotransformation of Ginsenoside Rb1 to Prosapogenins, Gypenoside XVII, Ginsenoside Rd, Ginsenoside F2, and Compound K by Leuconostoc mesenteroides DC102
Ginsenoside Rb1is the main component in ginsenosides. It is a protopanaxadiol-type ginsenoside that has a dammarane-type triterpenoid as an aglycone. In this study, ginsenoside Rb1 was transformed into gypenoside XVII, ginsenoside Rd, ginsenoside F2 and compound K by glycosidase from Leuconostoc mes...
Saved in:
Published in: | Journal of ginseng research 2011-09, Vol.35 (3), p.344-351 |
---|---|
Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | |
---|---|
cites | |
container_end_page | 351 |
container_issue | 3 |
container_start_page | 344 |
container_title | Journal of ginseng research |
container_volume | 35 |
creator | Quan, Lin-Hu Piao, Jin-Ying Min, Jin-Woo Kim, Ho-Bin Kim, Sang-Rae Yang, Dong-Uk Yang, Deok Chun |
description | Ginsenoside Rb1is the main component in ginsenosides. It is a protopanaxadiol-type ginsenoside that has a dammarane-type triterpenoid as an aglycone. In this study, ginsenoside Rb1 was transformed into gypenoside XVII, ginsenoside Rd, ginsenoside F2 and compound K by glycosidase from Leuconostoc mesenteroides DC102. The optimum time for the conversion was about 72 h at a constant pH of 6.0 to 8.0 and the optimum temperature was about 30℃. Under optimal conditions, ginsenoside Rb1 was decomposed and converted into compound K by 72 h post-reaction (99%). The enzymatic reaction was analyzed by highperformance liquid chromatography, suggesting the transformation pathway: ginsenoside Rb1→ gypenoside XVII and ginsenoside Rd→ginsenoside F2→compound K. |
doi_str_mv | 10.5142/jgr.2011.35.3.344 |
format | article |
fullrecord | <record><control><sourceid>nurimedia_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3659545</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><nurid>NODE01697828</nurid><sourcerecordid>NODE01697828</sourcerecordid><originalsourceid>FETCH-LOGICAL-n211t-60df0684ae0b4a6980201147789cfe5ab3ee76309b60cafb41ae7575c908b45c3</originalsourceid><addsrcrecordid>eNpVkU2P0zAQhi0EYkvhB3BBviBxaIK_HV-Qlu5uqahYhABxi5xkUrxq7GAnSP0p_FuM9kP0NDN6n5l3NIPQS0pKSQV7e7OPJSOUllyWvORCPEILRgwvhBH6MVpQxlRRCcnP0LOUbghRmmnxFJ0xrqkm2izQn_cuTNH61Ic42MkFj0OPN84n8CG5DvCXhuIp4M8xJDuGPfisrfDmON4DP75vt6vTlu60vmIrbH2H12EYw5yTj7g54h3MbcjEFFo8QIYniCHjCV-sKWHP0ZPeHhK8uItL9O3q8uv6Q7G73mzX57vCM0qnQpGuJ6oSFkgjrDIV-XcRoXVl2h6kbTiAVpyYRpHW9o2gFrTUsjWkaoRs-RK9u507zs0AXZv3iPZQj9ENNh7rYF19qnj3s96H3zVX0sh83CV6czcghl8zpKkeXGrhcLAewpxqyqUyUnNBM_rqf68Hk_t_ZOD1LeDnLEHn7APz6friklBldMUq_hd4IJvU</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1356957341</pqid></control><display><type>article</type><title>Biotransformation of Ginsenoside Rb1 to Prosapogenins, Gypenoside XVII, Ginsenoside Rd, Ginsenoside F2, and Compound K by Leuconostoc mesenteroides DC102</title><source>PubMed Central</source><creator>Quan, Lin-Hu ; Piao, Jin-Ying ; Min, Jin-Woo ; Kim, Ho-Bin ; Kim, Sang-Rae ; Yang, Dong-Uk ; Yang, Deok Chun</creator><creatorcontrib>Quan, Lin-Hu ; Piao, Jin-Ying ; Min, Jin-Woo ; Kim, Ho-Bin ; Kim, Sang-Rae ; Yang, Dong-Uk ; Yang, Deok Chun</creatorcontrib><description>Ginsenoside Rb1is the main component in ginsenosides. It is a protopanaxadiol-type ginsenoside that has a dammarane-type triterpenoid as an aglycone. In this study, ginsenoside Rb1 was transformed into gypenoside XVII, ginsenoside Rd, ginsenoside F2 and compound K by glycosidase from Leuconostoc mesenteroides DC102. The optimum time for the conversion was about 72 h at a constant pH of 6.0 to 8.0 and the optimum temperature was about 30℃. Under optimal conditions, ginsenoside Rb1 was decomposed and converted into compound K by 72 h post-reaction (99%). The enzymatic reaction was analyzed by highperformance liquid chromatography, suggesting the transformation pathway: ginsenoside Rb1→ gypenoside XVII and ginsenoside Rd→ginsenoside F2→compound K.</description><identifier>ISSN: 1226-8453</identifier><identifier>EISSN: 2093-4947</identifier><identifier>DOI: 10.5142/jgr.2011.35.3.344</identifier><identifier>PMID: 23717079</identifier><language>eng</language><publisher>Korea (South): 고려인삼학회</publisher><ispartof>Journal of ginseng research, 2011-09, Vol.35 (3), p.344-351</ispartof><rights>Copyright ©2011, The Korean Society of Ginseng 2011</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3659545/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3659545/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23717079$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Quan, Lin-Hu</creatorcontrib><creatorcontrib>Piao, Jin-Ying</creatorcontrib><creatorcontrib>Min, Jin-Woo</creatorcontrib><creatorcontrib>Kim, Ho-Bin</creatorcontrib><creatorcontrib>Kim, Sang-Rae</creatorcontrib><creatorcontrib>Yang, Dong-Uk</creatorcontrib><creatorcontrib>Yang, Deok Chun</creatorcontrib><title>Biotransformation of Ginsenoside Rb1 to Prosapogenins, Gypenoside XVII, Ginsenoside Rd, Ginsenoside F2, and Compound K by Leuconostoc mesenteroides DC102</title><title>Journal of ginseng research</title><addtitle>J Ginseng Res</addtitle><description>Ginsenoside Rb1is the main component in ginsenosides. It is a protopanaxadiol-type ginsenoside that has a dammarane-type triterpenoid as an aglycone. In this study, ginsenoside Rb1 was transformed into gypenoside XVII, ginsenoside Rd, ginsenoside F2 and compound K by glycosidase from Leuconostoc mesenteroides DC102. The optimum time for the conversion was about 72 h at a constant pH of 6.0 to 8.0 and the optimum temperature was about 30℃. Under optimal conditions, ginsenoside Rb1 was decomposed and converted into compound K by 72 h post-reaction (99%). The enzymatic reaction was analyzed by highperformance liquid chromatography, suggesting the transformation pathway: ginsenoside Rb1→ gypenoside XVII and ginsenoside Rd→ginsenoside F2→compound K.</description><issn>1226-8453</issn><issn>2093-4947</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><recordid>eNpVkU2P0zAQhi0EYkvhB3BBviBxaIK_HV-Qlu5uqahYhABxi5xkUrxq7GAnSP0p_FuM9kP0NDN6n5l3NIPQS0pKSQV7e7OPJSOUllyWvORCPEILRgwvhBH6MVpQxlRRCcnP0LOUbghRmmnxFJ0xrqkm2izQn_cuTNH61Ic42MkFj0OPN84n8CG5DvCXhuIp4M8xJDuGPfisrfDmON4DP75vt6vTlu60vmIrbH2H12EYw5yTj7g54h3MbcjEFFo8QIYniCHjCV-sKWHP0ZPeHhK8uItL9O3q8uv6Q7G73mzX57vCM0qnQpGuJ6oSFkgjrDIV-XcRoXVl2h6kbTiAVpyYRpHW9o2gFrTUsjWkaoRs-RK9u507zs0AXZv3iPZQj9ENNh7rYF19qnj3s96H3zVX0sh83CV6czcghl8zpKkeXGrhcLAewpxqyqUyUnNBM_rqf68Hk_t_ZOD1LeDnLEHn7APz6friklBldMUq_hd4IJvU</recordid><startdate>20110901</startdate><enddate>20110901</enddate><creator>Quan, Lin-Hu</creator><creator>Piao, Jin-Ying</creator><creator>Min, Jin-Woo</creator><creator>Kim, Ho-Bin</creator><creator>Kim, Sang-Rae</creator><creator>Yang, Dong-Uk</creator><creator>Yang, Deok Chun</creator><general>고려인삼학회</general><general>The Korean Society of Ginseng</general><scope>DBRKI</scope><scope>TDB</scope><scope>NPM</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20110901</creationdate><title>Biotransformation of Ginsenoside Rb1 to Prosapogenins, Gypenoside XVII, Ginsenoside Rd, Ginsenoside F2, and Compound K by Leuconostoc mesenteroides DC102</title><author>Quan, Lin-Hu ; Piao, Jin-Ying ; Min, Jin-Woo ; Kim, Ho-Bin ; Kim, Sang-Rae ; Yang, Dong-Uk ; Yang, Deok Chun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-n211t-60df0684ae0b4a6980201147789cfe5ab3ee76309b60cafb41ae7575c908b45c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Quan, Lin-Hu</creatorcontrib><creatorcontrib>Piao, Jin-Ying</creatorcontrib><creatorcontrib>Min, Jin-Woo</creatorcontrib><creatorcontrib>Kim, Ho-Bin</creatorcontrib><creatorcontrib>Kim, Sang-Rae</creatorcontrib><creatorcontrib>Yang, Dong-Uk</creatorcontrib><creatorcontrib>Yang, Deok Chun</creatorcontrib><collection>DBpia</collection><collection>DBpia - NuriMedia Korean Studies Journals</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of ginseng research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Quan, Lin-Hu</au><au>Piao, Jin-Ying</au><au>Min, Jin-Woo</au><au>Kim, Ho-Bin</au><au>Kim, Sang-Rae</au><au>Yang, Dong-Uk</au><au>Yang, Deok Chun</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Biotransformation of Ginsenoside Rb1 to Prosapogenins, Gypenoside XVII, Ginsenoside Rd, Ginsenoside F2, and Compound K by Leuconostoc mesenteroides DC102</atitle><jtitle>Journal of ginseng research</jtitle><addtitle>J Ginseng Res</addtitle><date>2011-09-01</date><risdate>2011</risdate><volume>35</volume><issue>3</issue><spage>344</spage><epage>351</epage><pages>344-351</pages><issn>1226-8453</issn><eissn>2093-4947</eissn><abstract>Ginsenoside Rb1is the main component in ginsenosides. It is a protopanaxadiol-type ginsenoside that has a dammarane-type triterpenoid as an aglycone. In this study, ginsenoside Rb1 was transformed into gypenoside XVII, ginsenoside Rd, ginsenoside F2 and compound K by glycosidase from Leuconostoc mesenteroides DC102. The optimum time for the conversion was about 72 h at a constant pH of 6.0 to 8.0 and the optimum temperature was about 30℃. Under optimal conditions, ginsenoside Rb1 was decomposed and converted into compound K by 72 h post-reaction (99%). The enzymatic reaction was analyzed by highperformance liquid chromatography, suggesting the transformation pathway: ginsenoside Rb1→ gypenoside XVII and ginsenoside Rd→ginsenoside F2→compound K.</abstract><cop>Korea (South)</cop><pub>고려인삼학회</pub><pmid>23717079</pmid><doi>10.5142/jgr.2011.35.3.344</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1226-8453 |
ispartof | Journal of ginseng research, 2011-09, Vol.35 (3), p.344-351 |
issn | 1226-8453 2093-4947 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3659545 |
source | PubMed Central |
title | Biotransformation of Ginsenoside Rb1 to Prosapogenins, Gypenoside XVII, Ginsenoside Rd, Ginsenoside F2, and Compound K by Leuconostoc mesenteroides DC102 |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-04T13%3A48%3A33IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-nurimedia_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Biotransformation%20of%20Ginsenoside%20Rb1%20to%20Prosapogenins,%20Gypenoside%20XVII,%20Ginsenoside%20Rd,%20Ginsenoside%20F2,%20and%20Compound%20K%20by%20Leuconostoc%20mesenteroides%20DC102&rft.jtitle=Journal%20of%20ginseng%20research&rft.au=Quan,%20Lin-Hu&rft.date=2011-09-01&rft.volume=35&rft.issue=3&rft.spage=344&rft.epage=351&rft.pages=344-351&rft.issn=1226-8453&rft.eissn=2093-4947&rft_id=info:doi/10.5142/jgr.2011.35.3.344&rft_dat=%3Cnurimedia_pubme%3ENODE01697828%3C/nurimedia_pubme%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-n211t-60df0684ae0b4a6980201147789cfe5ab3ee76309b60cafb41ae7575c908b45c3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1356957341&rft_id=info:pmid/23717079&rft_nurid=NODE01697828&rfr_iscdi=true |