Effect of vanadate, molybdate, and azide on membrane-associated ATPase and soluble phosphatase activities of corn roots [Zea mays, maize, Avena sativa, oats]
The effects of vanadate, molybdate, and azide on ATP phosphohydrolase (ATPase) and acid phosphatase activities of plasma membrane, mitochondrial, and soluble supernatant fractions from corn (Zea mays L. WF9 × MO17) roots were investigated. Azide (0.1-10 millimolar) was a selective inhibitor of pH 9....
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Veröffentlicht in: | Plant physiology (Bethesda) 1982-11, Vol.70 (5), p.1335-1340 |
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description | The effects of vanadate, molybdate, and azide on ATP phosphohydrolase (ATPase) and acid phosphatase activities of plasma membrane, mitochondrial, and soluble supernatant fractions from corn (Zea mays L. WF9 × MO17) roots were investigated. Azide (0.1-10 millimolar) was a selective inhibitor of pH 9.0-ATPase activity of the mitochondrial fraction, while molybdate (0.01-1.0 millimolar) was a relatively selective inhibitor of acid phosphatase activity in the supernatant fraction. The pH 6.4-ATPase activity of the plasma membrane fraction was inhibited by vanadate (10-500 micromolar), but vanadate, at similar concentrations, also inhibited acid phosphatase activity. This result was confirmed for oat (Avena sativa L.) root and coleoptile tissues. While vanadate does not appear to be a selective inhibitor, it can be used in combination with molybdate and azide to distinguish the plasma membrane ATPase from mitochondrial ATPase or supernatant acid phosphatase. Vanadate appeared to be a noncompetitive inhibitor of the plasma membrane ATPase, and its effectiveness was increased by K+. K+-stimulated ATPase activity was inhibited by 50% at about 21 micromolar vanadate. The rate of K+ transport in excised corn root segments was inhibited by 66% by 500 micromolar vanadate. |
doi_str_mv | 10.1104/pp.70.5.1335 |
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Facultad de Agronomia</creatorcontrib><description>The effects of vanadate, molybdate, and azide on ATP phosphohydrolase (ATPase) and acid phosphatase activities of plasma membrane, mitochondrial, and soluble supernatant fractions from corn (Zea mays L. WF9 × MO17) roots were investigated. Azide (0.1-10 millimolar) was a selective inhibitor of pH 9.0-ATPase activity of the mitochondrial fraction, while molybdate (0.01-1.0 millimolar) was a relatively selective inhibitor of acid phosphatase activity in the supernatant fraction. The pH 6.4-ATPase activity of the plasma membrane fraction was inhibited by vanadate (10-500 micromolar), but vanadate, at similar concentrations, also inhibited acid phosphatase activity. This result was confirmed for oat (Avena sativa L.) root and coleoptile tissues. While vanadate does not appear to be a selective inhibitor, it can be used in combination with molybdate and azide to distinguish the plasma membrane ATPase from mitochondrial ATPase or supernatant acid phosphatase. Vanadate appeared to be a noncompetitive inhibitor of the plasma membrane ATPase, and its effectiveness was increased by K+. K+-stimulated ATPase activity was inhibited by 50% at about 21 micromolar vanadate. The rate of K+ transport in excised corn root segments was inhibited by 66% by 500 micromolar vanadate.</description><identifier>ISSN: 0032-0889</identifier><identifier>EISSN: 1532-2548</identifier><identifier>DOI: 10.1104/pp.70.5.1335</identifier><identifier>PMID: 16662676</identifier><language>eng</language><publisher>United States: American Society of Plant Physiologists</publisher><subject>acid phosphatase ; Adenosine triphosphatases ; adenosinetriphosphatase ; azide ; Azides ; Cell membranes ; Corn ; mitochondria ; Molybdates ; molybdic(VI) acid ; Oats ; Phosphatases ; Plant roots ; Plants ; plasma membranes ; roots ; vanadate ; Vanadates ; Zea mays</subject><ispartof>Plant physiology (Bethesda), 1982-11, Vol.70 (5), p.1335-1340</ispartof><rights>Copyright 1982 The American Society of Plant Physiologists</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c435t-aef0a2868bfc01347cf7eaf24ecf1a3257cb69d7dbe8b63b1665d42d5bfb07893</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/4267690$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/4267690$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>314,780,784,803,27924,27925,58017,58250</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16662676$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gallagher, S R</creatorcontrib><creatorcontrib>Leonard, R T</creatorcontrib><creatorcontrib>Universidad de San Carlos de Guatemala, Ciudad de Guatemala. Facultad de Agronomia</creatorcontrib><title>Effect of vanadate, molybdate, and azide on membrane-associated ATPase and soluble phosphatase activities of corn roots [Zea mays, maize, Avena sativa, oats]</title><title>Plant physiology (Bethesda)</title><addtitle>Plant Physiol</addtitle><description>The effects of vanadate, molybdate, and azide on ATP phosphohydrolase (ATPase) and acid phosphatase activities of plasma membrane, mitochondrial, and soluble supernatant fractions from corn (Zea mays L. WF9 × MO17) roots were investigated. Azide (0.1-10 millimolar) was a selective inhibitor of pH 9.0-ATPase activity of the mitochondrial fraction, while molybdate (0.01-1.0 millimolar) was a relatively selective inhibitor of acid phosphatase activity in the supernatant fraction. The pH 6.4-ATPase activity of the plasma membrane fraction was inhibited by vanadate (10-500 micromolar), but vanadate, at similar concentrations, also inhibited acid phosphatase activity. This result was confirmed for oat (Avena sativa L.) root and coleoptile tissues. While vanadate does not appear to be a selective inhibitor, it can be used in combination with molybdate and azide to distinguish the plasma membrane ATPase from mitochondrial ATPase or supernatant acid phosphatase. Vanadate appeared to be a noncompetitive inhibitor of the plasma membrane ATPase, and its effectiveness was increased by K+. K+-stimulated ATPase activity was inhibited by 50% at about 21 micromolar vanadate. The rate of K+ transport in excised corn root segments was inhibited by 66% by 500 micromolar vanadate.</description><subject>acid phosphatase</subject><subject>Adenosine triphosphatases</subject><subject>adenosinetriphosphatase</subject><subject>azide</subject><subject>Azides</subject><subject>Cell membranes</subject><subject>Corn</subject><subject>mitochondria</subject><subject>Molybdates</subject><subject>molybdic(VI) acid</subject><subject>Oats</subject><subject>Phosphatases</subject><subject>Plant roots</subject><subject>Plants</subject><subject>plasma membranes</subject><subject>roots</subject><subject>vanadate</subject><subject>Vanadates</subject><subject>Zea mays</subject><issn>0032-0889</issn><issn>1532-2548</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1982</creationdate><recordtype>article</recordtype><recordid>eNp9kU9vEzEQxS0EoqFw44iQT3BJgr22195jVJU_UiWQaC8gZI29Nt1qd721nUjpd-G74k0ieuM0o5nfzNPTQ-g1JWtKCf8wTWtJ1mJNGRNP0IIKVq0qwdVTtCCk9ESp5gy9SOmOEEIZ5c_RGa3ruqplvUB_Lr13NuPg8Q5GaCG7JR5CvzfHFsYWw0PXOhxGPLjBRBjdClIKtitAizfX3yC5A5dCvzW9w9NtSNMt5MPc5m7X5c6lWcKGOOIYQk745w8HeIB9KnLQPRSpzc6NgBOUA1jiADn9eomeeeiTe3Wq5-jm4-X1xefV1ddPXy42VyvLmcgrcJ5ApWplvC0WubReOvAVd9ZTYJWQ1tRNK1vjlKmZKfZFy6tWGG-IVA07R--Pf6cY7rcuZT10ybq-L2bDNmnJGG8IPZDv_ktSJilT9Qwuj6CNIaXovJ5iN0Dca0r0HJyeJi2JFnoOruBvT3-3ZnDtI3xKqgBvjsBdyiH-2_N52ZDHew9Bw-_YJX3znTaKkYYpLgX7C12SqEo</recordid><startdate>198211</startdate><enddate>198211</enddate><creator>Gallagher, S R</creator><creator>Leonard, R T</creator><general>American Society of Plant Physiologists</general><scope>FBQ</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>8FD</scope><scope>FR3</scope><scope>M7Z</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>198211</creationdate><title>Effect of vanadate, molybdate, and azide on membrane-associated ATPase and soluble phosphatase activities of corn roots [Zea mays, maize, Avena sativa, oats]</title><author>Gallagher, S R ; Leonard, R T</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c435t-aef0a2868bfc01347cf7eaf24ecf1a3257cb69d7dbe8b63b1665d42d5bfb07893</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1982</creationdate><topic>acid phosphatase</topic><topic>Adenosine triphosphatases</topic><topic>adenosinetriphosphatase</topic><topic>azide</topic><topic>Azides</topic><topic>Cell membranes</topic><topic>Corn</topic><topic>mitochondria</topic><topic>Molybdates</topic><topic>molybdic(VI) acid</topic><topic>Oats</topic><topic>Phosphatases</topic><topic>Plant roots</topic><topic>Plants</topic><topic>plasma membranes</topic><topic>roots</topic><topic>vanadate</topic><topic>Vanadates</topic><topic>Zea mays</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gallagher, S R</creatorcontrib><creatorcontrib>Leonard, R T</creatorcontrib><creatorcontrib>Universidad de San Carlos de Guatemala, Ciudad de Guatemala. Facultad de Agronomia</creatorcontrib><collection>AGRIS</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biochemistry Abstracts 1</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Plant physiology (Bethesda)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gallagher, S R</au><au>Leonard, R T</au><aucorp>Universidad de San Carlos de Guatemala, Ciudad de Guatemala. Facultad de Agronomia</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effect of vanadate, molybdate, and azide on membrane-associated ATPase and soluble phosphatase activities of corn roots [Zea mays, maize, Avena sativa, oats]</atitle><jtitle>Plant physiology (Bethesda)</jtitle><addtitle>Plant Physiol</addtitle><date>1982-11</date><risdate>1982</risdate><volume>70</volume><issue>5</issue><spage>1335</spage><epage>1340</epage><pages>1335-1340</pages><issn>0032-0889</issn><eissn>1532-2548</eissn><abstract>The effects of vanadate, molybdate, and azide on ATP phosphohydrolase (ATPase) and acid phosphatase activities of plasma membrane, mitochondrial, and soluble supernatant fractions from corn (Zea mays L. WF9 × MO17) roots were investigated. Azide (0.1-10 millimolar) was a selective inhibitor of pH 9.0-ATPase activity of the mitochondrial fraction, while molybdate (0.01-1.0 millimolar) was a relatively selective inhibitor of acid phosphatase activity in the supernatant fraction. The pH 6.4-ATPase activity of the plasma membrane fraction was inhibited by vanadate (10-500 micromolar), but vanadate, at similar concentrations, also inhibited acid phosphatase activity. This result was confirmed for oat (Avena sativa L.) root and coleoptile tissues. While vanadate does not appear to be a selective inhibitor, it can be used in combination with molybdate and azide to distinguish the plasma membrane ATPase from mitochondrial ATPase or supernatant acid phosphatase. Vanadate appeared to be a noncompetitive inhibitor of the plasma membrane ATPase, and its effectiveness was increased by K+. K+-stimulated ATPase activity was inhibited by 50% at about 21 micromolar vanadate. The rate of K+ transport in excised corn root segments was inhibited by 66% by 500 micromolar vanadate.</abstract><cop>United States</cop><pub>American Society of Plant Physiologists</pub><pmid>16662676</pmid><doi>10.1104/pp.70.5.1335</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | acid phosphatase Adenosine triphosphatases adenosinetriphosphatase azide Azides Cell membranes Corn mitochondria Molybdates molybdic(VI) acid Oats Phosphatases Plant roots Plants plasma membranes roots vanadate Vanadates Zea mays |
title | Effect of vanadate, molybdate, and azide on membrane-associated ATPase and soluble phosphatase activities of corn roots [Zea mays, maize, Avena sativa, oats] |
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