Loading…
moss Physcomitrella patens releases a tetracyclic diterpene
The presence of the tetracyclic diterpene 16alpha-hydroxykaurane (16alpha-hydroxy-ent-kaurane, C20H34O, CAS 5524-17-4) was detected in sterile cell cultures of the moss Physcomitrella patens (Hedw.) B.S.G. using gas chromatography and mass spectrometry. 16alpha-hydroxykaurane was found to be a major...
Saved in:
Published in: | Plant cell reports 2004-05, Vol.22 (10), p.780-786 |
---|---|
Main Authors: | , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c379t-d90ef39cf003aa36fa1a10587a48ba7843d6fbec2dda25c0712aacfc46ccf7ba3 |
---|---|
cites | |
container_end_page | 786 |
container_issue | 10 |
container_start_page | 780 |
container_title | Plant cell reports |
container_volume | 22 |
creator | Schwartzenberg, K. von Schultze, W Kassner, H |
description | The presence of the tetracyclic diterpene 16alpha-hydroxykaurane (16alpha-hydroxy-ent-kaurane, C20H34O, CAS 5524-17-4) was detected in sterile cell cultures of the moss Physcomitrella patens (Hedw.) B.S.G. using gas chromatography and mass spectrometry. 16alpha-hydroxykaurane was found to be a major lipid compound in P. patens, with an estimated intracellular concentration of up to 0.84 mmol/l and an extracellular concentration of up to 9.3 micromol/l. The overall content of 16alpha-hydroxykaurane (in milligrams) produced per culture reached 0.37-fold that of chlorophyll a+b. In agar cultures with low air exchange, 16alpha-hydroxykaurane forms needle-like crystals on tissue and on the inner surface of the culture vessels, indicating that it is being released into the atmosphere. Solid phase microextraction confirmed the air-bound release of 16alpha-hydroxykaurane. To our knowledge this is the first report on the release of a plant-derived tetracyclic diterpene into the air. |
doi_str_mv | 10.1007/s00299-004-0754-6 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_71857509</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2193215001</sourcerecordid><originalsourceid>FETCH-LOGICAL-c379t-d90ef39cf003aa36fa1a10587a48ba7843d6fbec2dda25c0712aacfc46ccf7ba3</originalsourceid><addsrcrecordid>eNqFkE1LxDAQhoMo7rr6A7xo8eCtOmnSpMGTLH7BgoIueAvTNNHKdluT9rD_3ixdELx4GoZ53mHmIeSUwhUFkNcBIFMqBeApyJynYo9MKWdZmgF73ydTkBlNpaR8Qo5C-AKIQykOyYRyJZhQbEpumjaE5OVzE0zb1L23qxUmHfZ2HZLYWAw2JJj0tvdoNmZVm6Sqe-s7u7bH5MDhKtiTXZ2R5f3d2_wxXTw_PM1vF6lhUvVppcA6powDYIhMOKRIIS8k8qJEWXBWCVdak1UVZrkBSTNE4wwXxjhZIpuRy3Fv59vvwYZeN3Uw20vXth2ClrTIZQ7qX5BKmVMJPIIXf8CvdvDr-IQuoknIVQERoiNkfHTkrdOdrxv0G01Bb_3r0b-O_vXWvxYxc7ZbPJSNrX4TO-EROB8Bh63GD18HvXzNgDKI9wuuCvYDv2GKHg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>807505980</pqid></control><display><type>article</type><title>moss Physcomitrella patens releases a tetracyclic diterpene</title><source>Springer Nature</source><creator>Schwartzenberg, K. von ; Schultze, W ; Kassner, H</creator><creatorcontrib>Schwartzenberg, K. von ; Schultze, W ; Kassner, H</creatorcontrib><description>The presence of the tetracyclic diterpene 16alpha-hydroxykaurane (16alpha-hydroxy-ent-kaurane, C20H34O, CAS 5524-17-4) was detected in sterile cell cultures of the moss Physcomitrella patens (Hedw.) B.S.G. using gas chromatography and mass spectrometry. 16alpha-hydroxykaurane was found to be a major lipid compound in P. patens, with an estimated intracellular concentration of up to 0.84 mmol/l and an extracellular concentration of up to 9.3 micromol/l. The overall content of 16alpha-hydroxykaurane (in milligrams) produced per culture reached 0.37-fold that of chlorophyll a+b. In agar cultures with low air exchange, 16alpha-hydroxykaurane forms needle-like crystals on tissue and on the inner surface of the culture vessels, indicating that it is being released into the atmosphere. Solid phase microextraction confirmed the air-bound release of 16alpha-hydroxykaurane. To our knowledge this is the first report on the release of a plant-derived tetracyclic diterpene into the air.</description><identifier>ISSN: 0721-7714</identifier><identifier>EISSN: 1432-203X</identifier><identifier>DOI: 10.1007/s00299-004-0754-6</identifier><identifier>PMID: 14963693</identifier><language>eng</language><publisher>Germany: Springer Nature B.V</publisher><subject>Bryopsida - chemistry ; crystal structure ; Crystals ; Culture Media ; Diterpenes, Kaurane - chemistry ; Diterpenes, Kaurane - metabolism ; diterpenoids ; Gas chromatography ; Gas Chromatography-Mass Spectrometry ; hydroxykaurane ; Magnetic Resonance Spectroscopy ; Mass spectrometry ; Mosses ; mosses and liverworts ; nuclear magnetic resonance spectroscopy ; Physcomitrella patens ; spectral analysis ; tetracyclic diterpene ; Time Factors ; volatile organic compounds</subject><ispartof>Plant cell reports, 2004-05, Vol.22 (10), p.780-786</ispartof><rights>Copyright 2004 Springer-Verlag</rights><rights>Springer-Verlag 2004</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c379t-d90ef39cf003aa36fa1a10587a48ba7843d6fbec2dda25c0712aacfc46ccf7ba3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/14963693$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Schwartzenberg, K. von</creatorcontrib><creatorcontrib>Schultze, W</creatorcontrib><creatorcontrib>Kassner, H</creatorcontrib><title>moss Physcomitrella patens releases a tetracyclic diterpene</title><title>Plant cell reports</title><addtitle>Plant Cell Rep</addtitle><description>The presence of the tetracyclic diterpene 16alpha-hydroxykaurane (16alpha-hydroxy-ent-kaurane, C20H34O, CAS 5524-17-4) was detected in sterile cell cultures of the moss Physcomitrella patens (Hedw.) B.S.G. using gas chromatography and mass spectrometry. 16alpha-hydroxykaurane was found to be a major lipid compound in P. patens, with an estimated intracellular concentration of up to 0.84 mmol/l and an extracellular concentration of up to 9.3 micromol/l. The overall content of 16alpha-hydroxykaurane (in milligrams) produced per culture reached 0.37-fold that of chlorophyll a+b. In agar cultures with low air exchange, 16alpha-hydroxykaurane forms needle-like crystals on tissue and on the inner surface of the culture vessels, indicating that it is being released into the atmosphere. Solid phase microextraction confirmed the air-bound release of 16alpha-hydroxykaurane. To our knowledge this is the first report on the release of a plant-derived tetracyclic diterpene into the air.</description><subject>Bryopsida - chemistry</subject><subject>crystal structure</subject><subject>Crystals</subject><subject>Culture Media</subject><subject>Diterpenes, Kaurane - chemistry</subject><subject>Diterpenes, Kaurane - metabolism</subject><subject>diterpenoids</subject><subject>Gas chromatography</subject><subject>Gas Chromatography-Mass Spectrometry</subject><subject>hydroxykaurane</subject><subject>Magnetic Resonance Spectroscopy</subject><subject>Mass spectrometry</subject><subject>Mosses</subject><subject>mosses and liverworts</subject><subject>nuclear magnetic resonance spectroscopy</subject><subject>Physcomitrella patens</subject><subject>spectral analysis</subject><subject>tetracyclic diterpene</subject><subject>Time Factors</subject><subject>volatile organic compounds</subject><issn>0721-7714</issn><issn>1432-203X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><recordid>eNqFkE1LxDAQhoMo7rr6A7xo8eCtOmnSpMGTLH7BgoIueAvTNNHKdluT9rD_3ixdELx4GoZ53mHmIeSUwhUFkNcBIFMqBeApyJynYo9MKWdZmgF73ydTkBlNpaR8Qo5C-AKIQykOyYRyJZhQbEpumjaE5OVzE0zb1L23qxUmHfZ2HZLYWAw2JJj0tvdoNmZVm6Sqe-s7u7bH5MDhKtiTXZ2R5f3d2_wxXTw_PM1vF6lhUvVppcA6powDYIhMOKRIIS8k8qJEWXBWCVdak1UVZrkBSTNE4wwXxjhZIpuRy3Fv59vvwYZeN3Uw20vXth2ClrTIZQ7qX5BKmVMJPIIXf8CvdvDr-IQuoknIVQERoiNkfHTkrdOdrxv0G01Bb_3r0b-O_vXWvxYxc7ZbPJSNrX4TO-EROB8Bh63GD18HvXzNgDKI9wuuCvYDv2GKHg</recordid><startdate>20040501</startdate><enddate>20040501</enddate><creator>Schwartzenberg, K. von</creator><creator>Schultze, W</creator><creator>Kassner, H</creator><general>Springer Nature B.V</general><scope>FBQ</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QL</scope><scope>7T5</scope><scope>7T7</scope><scope>7TM</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>RC3</scope><scope>7QO</scope><scope>7X8</scope></search><sort><creationdate>20040501</creationdate><title>moss Physcomitrella patens releases a tetracyclic diterpene</title><author>Schwartzenberg, K. von ; Schultze, W ; Kassner, H</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c379t-d90ef39cf003aa36fa1a10587a48ba7843d6fbec2dda25c0712aacfc46ccf7ba3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Bryopsida - chemistry</topic><topic>crystal structure</topic><topic>Crystals</topic><topic>Culture Media</topic><topic>Diterpenes, Kaurane - chemistry</topic><topic>Diterpenes, Kaurane - metabolism</topic><topic>diterpenoids</topic><topic>Gas chromatography</topic><topic>Gas Chromatography-Mass Spectrometry</topic><topic>hydroxykaurane</topic><topic>Magnetic Resonance Spectroscopy</topic><topic>Mass spectrometry</topic><topic>Mosses</topic><topic>mosses and liverworts</topic><topic>nuclear magnetic resonance spectroscopy</topic><topic>Physcomitrella patens</topic><topic>spectral analysis</topic><topic>tetracyclic diterpene</topic><topic>Time Factors</topic><topic>volatile organic compounds</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Schwartzenberg, K. von</creatorcontrib><creatorcontrib>Schultze, W</creatorcontrib><creatorcontrib>Kassner, H</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Immunology Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Agricultural Science Collection</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biological Sciences</collection><collection>Agriculture Science Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>Genetics Abstracts</collection><collection>Biotechnology Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Plant cell reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Schwartzenberg, K. von</au><au>Schultze, W</au><au>Kassner, H</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>moss Physcomitrella patens releases a tetracyclic diterpene</atitle><jtitle>Plant cell reports</jtitle><addtitle>Plant Cell Rep</addtitle><date>2004-05-01</date><risdate>2004</risdate><volume>22</volume><issue>10</issue><spage>780</spage><epage>786</epage><pages>780-786</pages><issn>0721-7714</issn><eissn>1432-203X</eissn><abstract>The presence of the tetracyclic diterpene 16alpha-hydroxykaurane (16alpha-hydroxy-ent-kaurane, C20H34O, CAS 5524-17-4) was detected in sterile cell cultures of the moss Physcomitrella patens (Hedw.) B.S.G. using gas chromatography and mass spectrometry. 16alpha-hydroxykaurane was found to be a major lipid compound in P. patens, with an estimated intracellular concentration of up to 0.84 mmol/l and an extracellular concentration of up to 9.3 micromol/l. The overall content of 16alpha-hydroxykaurane (in milligrams) produced per culture reached 0.37-fold that of chlorophyll a+b. In agar cultures with low air exchange, 16alpha-hydroxykaurane forms needle-like crystals on tissue and on the inner surface of the culture vessels, indicating that it is being released into the atmosphere. Solid phase microextraction confirmed the air-bound release of 16alpha-hydroxykaurane. To our knowledge this is the first report on the release of a plant-derived tetracyclic diterpene into the air.</abstract><cop>Germany</cop><pub>Springer Nature B.V</pub><pmid>14963693</pmid><doi>10.1007/s00299-004-0754-6</doi><tpages>7</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0721-7714 |
ispartof | Plant cell reports, 2004-05, Vol.22 (10), p.780-786 |
issn | 0721-7714 1432-203X |
language | eng |
recordid | cdi_proquest_miscellaneous_71857509 |
source | Springer Nature |
subjects | Bryopsida - chemistry crystal structure Crystals Culture Media Diterpenes, Kaurane - chemistry Diterpenes, Kaurane - metabolism diterpenoids Gas chromatography Gas Chromatography-Mass Spectrometry hydroxykaurane Magnetic Resonance Spectroscopy Mass spectrometry Mosses mosses and liverworts nuclear magnetic resonance spectroscopy Physcomitrella patens spectral analysis tetracyclic diterpene Time Factors volatile organic compounds |
title | moss Physcomitrella patens releases a tetracyclic diterpene |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-20T17%3A20%3A01IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=moss%20Physcomitrella%20patens%20releases%20a%20tetracyclic%20diterpene&rft.jtitle=Plant%20cell%20reports&rft.au=Schwartzenberg,%20K.%20von&rft.date=2004-05-01&rft.volume=22&rft.issue=10&rft.spage=780&rft.epage=786&rft.pages=780-786&rft.issn=0721-7714&rft.eissn=1432-203X&rft_id=info:doi/10.1007/s00299-004-0754-6&rft_dat=%3Cproquest_cross%3E2193215001%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c379t-d90ef39cf003aa36fa1a10587a48ba7843d6fbec2dda25c0712aacfc46ccf7ba3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=807505980&rft_id=info:pmid/14963693&rfr_iscdi=true |