Intrinsic Oxygen Use Kinetics of Transformed Plant Root Culture

Root meristem oxygen uptake, root tip extension rate, and specific growth rate are assessed as a function of dissolved oxygen level for three transformed root cultures. The influence of hydrodynamic boundary layer was considered for all measurements to permit correlation of oxygen‐dependent kinetics...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Biotechnology progress 2001, Vol.17 (3), p.481-489
Hauptverfasser: Asplund, Patrick T., Curtis, Wayne R.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 489
container_issue 3
container_start_page 481
container_title Biotechnology progress
container_volume 17
creator Asplund, Patrick T.
Curtis, Wayne R.
description Root meristem oxygen uptake, root tip extension rate, and specific growth rate are assessed as a function of dissolved oxygen level for three transformed root cultures. The influence of hydrodynamic boundary layer was considered for all measurements to permit correlation of oxygen‐dependent kinetics with the concentration of oxygen at the surface of the root meristem. Oxygen uptake rate is shown to be saturated at ambient conditions, and a saturation level of approximately 300 μmole O2/(cm3 tissue·hr) was observed for all three of these morphologically diverse root types. In nearly all cases, the observation of a minimum oxygen pressure, below which respiration, extension, or root growth would not occur, could be accounted for as a boundary layer mass transfer resistance. The critical oxygen pressure below which respiration declines is below saturated ambient oxygen conditions. In contrast, critical oxygen pressures for root tip extension were much higher; extension was nearly linear for the two thicker root types (Hyoscyamus muticus, henbain; Solanum tuberosum, potato) above ambient oxygen levels. The performance of the thinnest root, Brassica juncea (Indian mustard) was consistent with reduced internal limitations for oxygen transport. Extension rates did not correlate with biomass accumulation. The fastest growing henbain culture (μ = 0.44 day−1) displayed the slowest extension rate (0.16 mm/hr), and the slowest growing mustard culture (μ = 0.22 day−1) had the fastest tip extension rate (0.3 mm/hr). This apparent paradox is explained in terms of root branching patterns, where the root branching ratio is shown to be dependent upon the oxygen‐limited mersitem extension rate. The implications of these observations on the performance of root culture in bioreactors is discussed.
doi_str_mv 10.1021/bp010038v
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_70899011</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>18158353</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4208-da99bea48e49b5f720085064e21e3a168d8672d425bbbe48c4730d1de6e7d0b73</originalsourceid><addsrcrecordid>eNqF0LtO5DAUBmALgWC4FLzAKgVCoggc2_ElFYIRN4EAoUGUlpOcrAyZZLCTXebt1-yMgAZR2cX3Hx__hOxSOKTA6FExAwrA9Z8VMqKCQSqB81Uy0krIVOVcb5DNEJ4BQINk62SDUq6llvmIHF-1vXdtcGVy9zb_jW3yGDC5di32rgxJVycTb9tQd36KVXLf2LZPHrquT8ZD0w8et8labZuAO8tzizyen03Gl-nN3cXV-OQmLTMGOq1snhdoM41ZXohasbiKAJkho8gtlbrSUrEqY6IoCsx0mSkOFa1QoqqgUHyL7C_mznz3OmDozdSFEpu4EHZDMAp0nkP810-Qaio0FzzCgwUsfReCx9rMvJtaPzcUzHut5qPWaH8thw5F7OFTLnuMYG8JbChtU8fOShe-OBYlRAYL9tc1OP_-QXM6uX_4f42RdBFxoce3j4j1L0YqroR5ur0wIOh4wq-leeL_AOtem5c</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>18158353</pqid></control><display><type>article</type><title>Intrinsic Oxygen Use Kinetics of Transformed Plant Root Culture</title><source>MEDLINE</source><source>Access via Wiley Online Library</source><creator>Asplund, Patrick T. ; Curtis, Wayne R.</creator><creatorcontrib>Asplund, Patrick T. ; Curtis, Wayne R.</creatorcontrib><description>Root meristem oxygen uptake, root tip extension rate, and specific growth rate are assessed as a function of dissolved oxygen level for three transformed root cultures. The influence of hydrodynamic boundary layer was considered for all measurements to permit correlation of oxygen‐dependent kinetics with the concentration of oxygen at the surface of the root meristem. Oxygen uptake rate is shown to be saturated at ambient conditions, and a saturation level of approximately 300 μmole O2/(cm3 tissue·hr) was observed for all three of these morphologically diverse root types. In nearly all cases, the observation of a minimum oxygen pressure, below which respiration, extension, or root growth would not occur, could be accounted for as a boundary layer mass transfer resistance. The critical oxygen pressure below which respiration declines is below saturated ambient oxygen conditions. In contrast, critical oxygen pressures for root tip extension were much higher; extension was nearly linear for the two thicker root types (Hyoscyamus muticus, henbain; Solanum tuberosum, potato) above ambient oxygen levels. The performance of the thinnest root, Brassica juncea (Indian mustard) was consistent with reduced internal limitations for oxygen transport. Extension rates did not correlate with biomass accumulation. The fastest growing henbain culture (μ = 0.44 day−1) displayed the slowest extension rate (0.16 mm/hr), and the slowest growing mustard culture (μ = 0.22 day−1) had the fastest tip extension rate (0.3 mm/hr). This apparent paradox is explained in terms of root branching patterns, where the root branching ratio is shown to be dependent upon the oxygen‐limited mersitem extension rate. The implications of these observations on the performance of root culture in bioreactors is discussed.</description><identifier>ISSN: 8756-7938</identifier><identifier>EISSN: 1520-6033</identifier><identifier>DOI: 10.1021/bp010038v</identifier><identifier>PMID: 11386869</identifier><identifier>CODEN: BIPRET</identifier><language>eng</language><publisher>USA: American Chemical Society</publisher><subject>Biological and medical sciences ; Biotechnology ; Brassica - cytology ; Brassica - metabolism ; Culture Techniques - methods ; Establishment of new cell lines, improvement of cultural methods, mass culture ; Eukaryotic cell cultures ; Fundamental and applied biological sciences. Psychology ; Kinetics ; Meristem - cytology ; Meristem - metabolism ; Methods. Procedures. Technologies ; oxygen ; Oxygen - metabolism ; Plant cells and fungal cells ; Plant Roots - cytology ; Plant Roots - growth &amp; development ; Plant Roots - metabolism ; Solanum tuberosum - cytology ; Solanum tuberosum - metabolism</subject><ispartof>Biotechnology progress, 2001, Vol.17 (3), p.481-489</ispartof><rights>Copyright © 2001 American Institute of Chemical Engineers (AIChE)</rights><rights>2001 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4208-da99bea48e49b5f720085064e21e3a168d8672d425bbbe48c4730d1de6e7d0b73</citedby><cites>FETCH-LOGICAL-c4208-da99bea48e49b5f720085064e21e3a168d8672d425bbbe48c4730d1de6e7d0b73</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1021%2Fbp010038v$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1021%2Fbp010038v$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,4024,27923,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=1121380$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11386869$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Asplund, Patrick T.</creatorcontrib><creatorcontrib>Curtis, Wayne R.</creatorcontrib><title>Intrinsic Oxygen Use Kinetics of Transformed Plant Root Culture</title><title>Biotechnology progress</title><addtitle>Biotechnol Progress</addtitle><description>Root meristem oxygen uptake, root tip extension rate, and specific growth rate are assessed as a function of dissolved oxygen level for three transformed root cultures. The influence of hydrodynamic boundary layer was considered for all measurements to permit correlation of oxygen‐dependent kinetics with the concentration of oxygen at the surface of the root meristem. Oxygen uptake rate is shown to be saturated at ambient conditions, and a saturation level of approximately 300 μmole O2/(cm3 tissue·hr) was observed for all three of these morphologically diverse root types. In nearly all cases, the observation of a minimum oxygen pressure, below which respiration, extension, or root growth would not occur, could be accounted for as a boundary layer mass transfer resistance. The critical oxygen pressure below which respiration declines is below saturated ambient oxygen conditions. In contrast, critical oxygen pressures for root tip extension were much higher; extension was nearly linear for the two thicker root types (Hyoscyamus muticus, henbain; Solanum tuberosum, potato) above ambient oxygen levels. The performance of the thinnest root, Brassica juncea (Indian mustard) was consistent with reduced internal limitations for oxygen transport. Extension rates did not correlate with biomass accumulation. The fastest growing henbain culture (μ = 0.44 day−1) displayed the slowest extension rate (0.16 mm/hr), and the slowest growing mustard culture (μ = 0.22 day−1) had the fastest tip extension rate (0.3 mm/hr). This apparent paradox is explained in terms of root branching patterns, where the root branching ratio is shown to be dependent upon the oxygen‐limited mersitem extension rate. The implications of these observations on the performance of root culture in bioreactors is discussed.</description><subject>Biological and medical sciences</subject><subject>Biotechnology</subject><subject>Brassica - cytology</subject><subject>Brassica - metabolism</subject><subject>Culture Techniques - methods</subject><subject>Establishment of new cell lines, improvement of cultural methods, mass culture</subject><subject>Eukaryotic cell cultures</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Kinetics</subject><subject>Meristem - cytology</subject><subject>Meristem - metabolism</subject><subject>Methods. Procedures. Technologies</subject><subject>oxygen</subject><subject>Oxygen - metabolism</subject><subject>Plant cells and fungal cells</subject><subject>Plant Roots - cytology</subject><subject>Plant Roots - growth &amp; development</subject><subject>Plant Roots - metabolism</subject><subject>Solanum tuberosum - cytology</subject><subject>Solanum tuberosum - metabolism</subject><issn>8756-7938</issn><issn>1520-6033</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqF0LtO5DAUBmALgWC4FLzAKgVCoggc2_ElFYIRN4EAoUGUlpOcrAyZZLCTXebt1-yMgAZR2cX3Hx__hOxSOKTA6FExAwrA9Z8VMqKCQSqB81Uy0krIVOVcb5DNEJ4BQINk62SDUq6llvmIHF-1vXdtcGVy9zb_jW3yGDC5di32rgxJVycTb9tQd36KVXLf2LZPHrquT8ZD0w8et8labZuAO8tzizyen03Gl-nN3cXV-OQmLTMGOq1snhdoM41ZXohasbiKAJkho8gtlbrSUrEqY6IoCsx0mSkOFa1QoqqgUHyL7C_mznz3OmDozdSFEpu4EHZDMAp0nkP810-Qaio0FzzCgwUsfReCx9rMvJtaPzcUzHut5qPWaH8thw5F7OFTLnuMYG8JbChtU8fOShe-OBYlRAYL9tc1OP_-QXM6uX_4f42RdBFxoce3j4j1L0YqroR5ur0wIOh4wq-leeL_AOtem5c</recordid><startdate>2001</startdate><enddate>2001</enddate><creator>Asplund, Patrick T.</creator><creator>Curtis, Wayne R.</creator><general>American Chemical Society</general><general>American Institute of Chemical Engineers</general><scope>BSCLL</scope><scope>IQODW</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>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>2001</creationdate><title>Intrinsic Oxygen Use Kinetics of Transformed Plant Root Culture</title><author>Asplund, Patrick T. ; Curtis, Wayne R.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4208-da99bea48e49b5f720085064e21e3a168d8672d425bbbe48c4730d1de6e7d0b73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Biological and medical sciences</topic><topic>Biotechnology</topic><topic>Brassica - cytology</topic><topic>Brassica - metabolism</topic><topic>Culture Techniques - methods</topic><topic>Establishment of new cell lines, improvement of cultural methods, mass culture</topic><topic>Eukaryotic cell cultures</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Kinetics</topic><topic>Meristem - cytology</topic><topic>Meristem - metabolism</topic><topic>Methods. Procedures. Technologies</topic><topic>oxygen</topic><topic>Oxygen - metabolism</topic><topic>Plant cells and fungal cells</topic><topic>Plant Roots - cytology</topic><topic>Plant Roots - growth &amp; development</topic><topic>Plant Roots - metabolism</topic><topic>Solanum tuberosum - cytology</topic><topic>Solanum tuberosum - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Asplund, Patrick T.</creatorcontrib><creatorcontrib>Curtis, Wayne R.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Biotechnology progress</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Asplund, Patrick T.</au><au>Curtis, Wayne R.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Intrinsic Oxygen Use Kinetics of Transformed Plant Root Culture</atitle><jtitle>Biotechnology progress</jtitle><addtitle>Biotechnol Progress</addtitle><date>2001</date><risdate>2001</risdate><volume>17</volume><issue>3</issue><spage>481</spage><epage>489</epage><pages>481-489</pages><issn>8756-7938</issn><eissn>1520-6033</eissn><coden>BIPRET</coden><abstract>Root meristem oxygen uptake, root tip extension rate, and specific growth rate are assessed as a function of dissolved oxygen level for three transformed root cultures. The influence of hydrodynamic boundary layer was considered for all measurements to permit correlation of oxygen‐dependent kinetics with the concentration of oxygen at the surface of the root meristem. Oxygen uptake rate is shown to be saturated at ambient conditions, and a saturation level of approximately 300 μmole O2/(cm3 tissue·hr) was observed for all three of these morphologically diverse root types. In nearly all cases, the observation of a minimum oxygen pressure, below which respiration, extension, or root growth would not occur, could be accounted for as a boundary layer mass transfer resistance. The critical oxygen pressure below which respiration declines is below saturated ambient oxygen conditions. In contrast, critical oxygen pressures for root tip extension were much higher; extension was nearly linear for the two thicker root types (Hyoscyamus muticus, henbain; Solanum tuberosum, potato) above ambient oxygen levels. The performance of the thinnest root, Brassica juncea (Indian mustard) was consistent with reduced internal limitations for oxygen transport. Extension rates did not correlate with biomass accumulation. The fastest growing henbain culture (μ = 0.44 day−1) displayed the slowest extension rate (0.16 mm/hr), and the slowest growing mustard culture (μ = 0.22 day−1) had the fastest tip extension rate (0.3 mm/hr). This apparent paradox is explained in terms of root branching patterns, where the root branching ratio is shown to be dependent upon the oxygen‐limited mersitem extension rate. The implications of these observations on the performance of root culture in bioreactors is discussed.</abstract><cop>USA</cop><pub>American Chemical Society</pub><pmid>11386869</pmid><doi>10.1021/bp010038v</doi><tpages>9</tpages></addata></record>
fulltext fulltext
identifier ISSN: 8756-7938
ispartof Biotechnology progress, 2001, Vol.17 (3), p.481-489
issn 8756-7938
1520-6033
language eng
recordid cdi_proquest_miscellaneous_70899011
source MEDLINE; Access via Wiley Online Library
subjects Biological and medical sciences
Biotechnology
Brassica - cytology
Brassica - metabolism
Culture Techniques - methods
Establishment of new cell lines, improvement of cultural methods, mass culture
Eukaryotic cell cultures
Fundamental and applied biological sciences. Psychology
Kinetics
Meristem - cytology
Meristem - metabolism
Methods. Procedures. Technologies
oxygen
Oxygen - metabolism
Plant cells and fungal cells
Plant Roots - cytology
Plant Roots - growth & development
Plant Roots - metabolism
Solanum tuberosum - cytology
Solanum tuberosum - metabolism
title Intrinsic Oxygen Use Kinetics of Transformed Plant Root Culture
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-21T16%3A08%3A47IST&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=Intrinsic%20Oxygen%20Use%20Kinetics%20of%20Transformed%20Plant%20Root%20Culture&rft.jtitle=Biotechnology%20progress&rft.au=Asplund,%20Patrick%20T.&rft.date=2001&rft.volume=17&rft.issue=3&rft.spage=481&rft.epage=489&rft.pages=481-489&rft.issn=8756-7938&rft.eissn=1520-6033&rft.coden=BIPRET&rft_id=info:doi/10.1021/bp010038v&rft_dat=%3Cproquest_cross%3E18158353%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=18158353&rft_id=info:pmid/11386869&rfr_iscdi=true