Inhibition of nitrate uptake by ammonium in barley. Analysis of component fluxes
NO3- uptake by plant roots is rapidly inhibited by exposure to NH4+. The rapidity of the effect has led to the presumption that the inhibition results from the direct effects of NH4+ at the plasma membrane. The mechanism of this inhibition, however, has been in contention. In the present study we us...
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description | NO3- uptake by plant roots is rapidly inhibited by exposure to NH4+. The rapidity of the effect has led to the presumption that the inhibition results from the direct effects of NH4+ at the plasma membrane. The mechanism of this inhibition, however, has been in contention. In the present study we used the radiotracer 13N to determine the relative effects of short-term exposures to NH4+ on the 13NO3- influx, efflux, and partitioning of absorbed 13N in barley (Hordeum vulgare) roots. Plants were grown without NO3- or NO2- (uninduced for NO3- uptake), or with 0.1, 1.0, 10 mM NO3-, or 0.1 mM NO2- (to generate plant roots induced for NO3- uptake). Exposure to 1 mM NH4+ strongly reduced influx; the effect was most pronounced in plants induced for NO3- uptake when NO3- absorption was measured at low external NO3-. At higher [NO3-] and in uninduced plants the inhibitory effect was much diminished, indicating that NH4+ inhibition of influx was mediated via effects on the inducible high-affinity transport system rather than on the constitutive high-affinity transport system or the low-affinity transport system. Exposure to NH4+ also caused increased NO3- efflux; the largest effect was at low external [NO3-] in uninduced plants. In absolute terms, the reduction of influx made the dominant contribution to the observed reduction of net uptake of NO3-. Differences in response between plants induced with NO3- and those induced with NO2- indicate that NO2- may not be an appropriate analog for NO3- under all conditions. |
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Analysis of component fluxes</title><source>Jstor Complete Legacy</source><source>Oxford University Press Journals All Titles (1996-Current)</source><source>EZB-FREE-00999 freely available EZB journals</source><creator>Kronzucker, H.J ; Glass, A.D.M ; Siddiqi, M.Y</creator><creatorcontrib>Kronzucker, H.J ; Glass, A.D.M ; Siddiqi, M.Y</creatorcontrib><description>NO3- uptake by plant roots is rapidly inhibited by exposure to NH4+. The rapidity of the effect has led to the presumption that the inhibition results from the direct effects of NH4+ at the plasma membrane. The mechanism of this inhibition, however, has been in contention. In the present study we used the radiotracer 13N to determine the relative effects of short-term exposures to NH4+ on the 13NO3- influx, efflux, and partitioning of absorbed 13N in barley (Hordeum vulgare) roots. Plants were grown without NO3- or NO2- (uninduced for NO3- uptake), or with 0.1, 1.0, 10 mM NO3-, or 0.1 mM NO2- (to generate plant roots induced for NO3- uptake). Exposure to 1 mM NH4+ strongly reduced influx; the effect was most pronounced in plants induced for NO3- uptake when NO3- absorption was measured at low external NO3-. At higher [NO3-] and in uninduced plants the inhibitory effect was much diminished, indicating that NH4+ inhibition of influx was mediated via effects on the inducible high-affinity transport system rather than on the constitutive high-affinity transport system or the low-affinity transport system. Exposure to NH4+ also caused increased NO3- efflux; the largest effect was at low external [NO3-] in uninduced plants. In absolute terms, the reduction of influx made the dominant contribution to the observed reduction of net uptake of NO3-. Differences in response between plants induced with NO3- and those induced with NO2- indicate that NO2- may not be an appropriate analog for NO3- under all conditions.</description><identifier>ISSN: 0032-0889</identifier><identifier>EISSN: 1532-2548</identifier><identifier>DOI: 10.1104/pp.120.1.283</identifier><identifier>PMID: 10318705</identifier><language>eng</language><publisher>United States: American Society of Plant Physiologists</publisher><subject>Ammonium ; ammonium compounds ; application rate ; Barley ; efflux ; Elution ; Half lives ; Hordeum vulgare ; inhibition ; isotope labeling ; Kinetics ; Nitrates ; Nitrites ; nitrogen ; nitrogen metabolism ; nutrient sources ; nutrient transport ; nutrient uptake ; Plant roots ; Plants ; plasma membrane ; Quaternary ammonium compounds ; roots ; Seedlings ; stable isotopes ; Whole-Plant Processes</subject><ispartof>Plant physiology (Bethesda), 1999-05, Vol.120 (1), p.283-291</ispartof><rights>Copyright 1999 American Society of Plant Physiologists</rights><rights>Copyright American Society of Plant Physiologists May 1999</rights><rights>1999</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.jstor.org/stable/pdf/4278799$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/4278799$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,776,780,799,881,27904,27905,57997,58230</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10318705$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kronzucker, H.J</creatorcontrib><creatorcontrib>Glass, A.D.M</creatorcontrib><creatorcontrib>Siddiqi, M.Y</creatorcontrib><title>Inhibition of nitrate uptake by ammonium in barley. Analysis of component fluxes</title><title>Plant physiology (Bethesda)</title><addtitle>Plant Physiol</addtitle><description>NO3- uptake by plant roots is rapidly inhibited by exposure to NH4+. The rapidity of the effect has led to the presumption that the inhibition results from the direct effects of NH4+ at the plasma membrane. The mechanism of this inhibition, however, has been in contention. In the present study we used the radiotracer 13N to determine the relative effects of short-term exposures to NH4+ on the 13NO3- influx, efflux, and partitioning of absorbed 13N in barley (Hordeum vulgare) roots. Plants were grown without NO3- or NO2- (uninduced for NO3- uptake), or with 0.1, 1.0, 10 mM NO3-, or 0.1 mM NO2- (to generate plant roots induced for NO3- uptake). Exposure to 1 mM NH4+ strongly reduced influx; the effect was most pronounced in plants induced for NO3- uptake when NO3- absorption was measured at low external NO3-. At higher [NO3-] and in uninduced plants the inhibitory effect was much diminished, indicating that NH4+ inhibition of influx was mediated via effects on the inducible high-affinity transport system rather than on the constitutive high-affinity transport system or the low-affinity transport system. Exposure to NH4+ also caused increased NO3- efflux; the largest effect was at low external [NO3-] in uninduced plants. In absolute terms, the reduction of influx made the dominant contribution to the observed reduction of net uptake of NO3-. Differences in response between plants induced with NO3- and those induced with NO2- indicate that NO2- may not be an appropriate analog for NO3- under all conditions.</description><subject>Ammonium</subject><subject>ammonium compounds</subject><subject>application rate</subject><subject>Barley</subject><subject>efflux</subject><subject>Elution</subject><subject>Half lives</subject><subject>Hordeum vulgare</subject><subject>inhibition</subject><subject>isotope labeling</subject><subject>Kinetics</subject><subject>Nitrates</subject><subject>Nitrites</subject><subject>nitrogen</subject><subject>nitrogen metabolism</subject><subject>nutrient sources</subject><subject>nutrient transport</subject><subject>nutrient uptake</subject><subject>Plant roots</subject><subject>Plants</subject><subject>plasma membrane</subject><subject>Quaternary ammonium compounds</subject><subject>roots</subject><subject>Seedlings</subject><subject>stable isotopes</subject><subject>Whole-Plant Processes</subject><issn>0032-0889</issn><issn>1532-2548</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNpdUU1PGzEQtVBRSdPeOFat1ROXpOOvrFfqBaG2ICGBRDlbtmOD0117a-9Wzb_HUSgCLjMjvffmPc0gdExgSQjwr8OwJLTOSyrZAZoRweiCCi7foBlAnUHK9gi9K2UDAIQR_hYdEWBENiBm6Poi3gcTxpAiTh7HMGY9OjwNo_7tsNli3fcphqnHIWKjc-e2S3wadbctoewUNvVDii6O2HfTP1feo0Ovu-I-PPY5uv3x_dfZ-eLy6ufF2enlwrMGxoXVwlvrhCOstUZyxkXDtTScc7P2VgijvVgDcwSc9S1d21XDV40UxrbgCWNz9G2_d5hM79a2Jsi6U0MOvc5blXRQL5EY7tVd-qtES1dQ5SeP8pz-TK6Mqg_Fuq7T0aWpKCJFy0A0tc7Rl1fUTZpyPUFRlMgVSBCykj49j_OU4_-lK-HjnrApY8pPOKeNbNqdyec97HVS-i6Hom5vaP0X0HZnItgD5D-TqQ</recordid><startdate>19990501</startdate><enddate>19990501</enddate><creator>Kronzucker, H.J</creator><creator>Glass, A.D.M</creator><creator>Siddiqi, M.Y</creator><general>American Society of Plant Physiologists</general><general>American Society of Plant Biologists</general><scope>FBQ</scope><scope>NPM</scope><scope>3V.</scope><scope>4T-</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8AO</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</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>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>M2P</scope><scope>M7P</scope><scope>MBDVC</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>S0X</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>19990501</creationdate><title>Inhibition of nitrate uptake by ammonium in barley. Analysis of component fluxes</title><author>Kronzucker, H.J ; Glass, A.D.M ; Siddiqi, M.Y</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-f370t-ca5fcce5e139cb8434574a8b444bdfc55baf5d03e10ecf92dc6746785bc90f133</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Ammonium</topic><topic>ammonium compounds</topic><topic>application rate</topic><topic>Barley</topic><topic>efflux</topic><topic>Elution</topic><topic>Half lives</topic><topic>Hordeum vulgare</topic><topic>inhibition</topic><topic>isotope labeling</topic><topic>Kinetics</topic><topic>Nitrates</topic><topic>Nitrites</topic><topic>nitrogen</topic><topic>nitrogen metabolism</topic><topic>nutrient sources</topic><topic>nutrient transport</topic><topic>nutrient uptake</topic><topic>Plant roots</topic><topic>Plants</topic><topic>plasma membrane</topic><topic>Quaternary ammonium compounds</topic><topic>roots</topic><topic>Seedlings</topic><topic>stable isotopes</topic><topic>Whole-Plant Processes</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kronzucker, H.J</creatorcontrib><creatorcontrib>Glass, A.D.M</creatorcontrib><creatorcontrib>Siddiqi, M.Y</creatorcontrib><collection>AGRIS</collection><collection>PubMed</collection><collection>ProQuest Central (Corporate)</collection><collection>Docstoc</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>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>ProQuest Pharma Collection</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>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</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>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Agricultural Science Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>SIRS Editorial</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Plant physiology (Bethesda)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kronzucker, H.J</au><au>Glass, A.D.M</au><au>Siddiqi, M.Y</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Inhibition of nitrate uptake by ammonium in barley. Analysis of component fluxes</atitle><jtitle>Plant physiology (Bethesda)</jtitle><addtitle>Plant Physiol</addtitle><date>1999-05-01</date><risdate>1999</risdate><volume>120</volume><issue>1</issue><spage>283</spage><epage>291</epage><pages>283-291</pages><issn>0032-0889</issn><eissn>1532-2548</eissn><abstract>NO3- uptake by plant roots is rapidly inhibited by exposure to NH4+. The rapidity of the effect has led to the presumption that the inhibition results from the direct effects of NH4+ at the plasma membrane. The mechanism of this inhibition, however, has been in contention. In the present study we used the radiotracer 13N to determine the relative effects of short-term exposures to NH4+ on the 13NO3- influx, efflux, and partitioning of absorbed 13N in barley (Hordeum vulgare) roots. Plants were grown without NO3- or NO2- (uninduced for NO3- uptake), or with 0.1, 1.0, 10 mM NO3-, or 0.1 mM NO2- (to generate plant roots induced for NO3- uptake). Exposure to 1 mM NH4+ strongly reduced influx; the effect was most pronounced in plants induced for NO3- uptake when NO3- absorption was measured at low external NO3-. At higher [NO3-] and in uninduced plants the inhibitory effect was much diminished, indicating that NH4+ inhibition of influx was mediated via effects on the inducible high-affinity transport system rather than on the constitutive high-affinity transport system or the low-affinity transport system. Exposure to NH4+ also caused increased NO3- efflux; the largest effect was at low external [NO3-] in uninduced plants. In absolute terms, the reduction of influx made the dominant contribution to the observed reduction of net uptake of NO3-. Differences in response between plants induced with NO3- and those induced with NO2- indicate that NO2- may not be an appropriate analog for NO3- under all conditions.</abstract><cop>United States</cop><pub>American Society of Plant Physiologists</pub><pmid>10318705</pmid><doi>10.1104/pp.120.1.283</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Ammonium ammonium compounds application rate Barley efflux Elution Half lives Hordeum vulgare inhibition isotope labeling Kinetics Nitrates Nitrites nitrogen nitrogen metabolism nutrient sources nutrient transport nutrient uptake Plant roots Plants plasma membrane Quaternary ammonium compounds roots Seedlings stable isotopes Whole-Plant Processes |
title | Inhibition of nitrate uptake by ammonium in barley. Analysis of component fluxes |
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