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Volumn 170, Issue 9, 2013, Pages 814-821

Branched-chain amino acid biosynthesis inhibitors: Herbicide efficacy is associated with an induced carbon-nitrogen imbalance

Author keywords

Acetolactate synthase; Branched chain amino acid; Herbicide; Ketol acid reductoisomerase; Mode of action

Indexed keywords

ACETOLACTATE SYNTHASE; ACETOLACTIC ACID; ADENOSINE; ALPHA-ACETOLACTATE; BRANCHED CHAIN AMINO ACID; CARBON; DRUG DERIVATIVE; HERBICIDE; KETOL ACID REDUCTOISOMERASE; LACTIC ACID DERIVATIVE; N CYCLOPROPYL ADENOSINE 5' CARBOXAMIDE; N-CYCLOPROPYL ADENOSINE-5'-CARBOXAMIDE; NITROGEN; QUINIC ACID;

EID: 84877630110     PISSN: 01761617     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jplph.2013.01.003     Document Type: Article
Times cited : (20)

References (35)
  • 1
    • 33751214823 scopus 로고    scopus 로고
    • Changes in organic acids and sugars during early stages of development of acidic and acidless citrus fruit
    • Albertini M.V., Carcouet E., Pailly O., Gambotti C., Luro F., Berti L. Changes in organic acids and sugars during early stages of development of acidic and acidless citrus fruit. J Agric Food Chem 2006, 54:8335-8339.
    • (2006) J Agric Food Chem , vol.54 , pp. 8335-8339
    • Albertini, M.V.1    Carcouet, E.2    Pailly, O.3    Gambotti, C.4    Luro, F.5    Berti, L.6
  • 2
    • 0001297351 scopus 로고
    • Evidence for the interaction of an imidazolinone herbicide with leucine, valine, and isoleucine metabolism
    • Anderson P.C., Hibberd K.A. Evidence for the interaction of an imidazolinone herbicide with leucine, valine, and isoleucine metabolism. Weed Sci 1985, 33:479-483.
    • (1985) Weed Sci , vol.33 , pp. 479-483
    • Anderson, P.C.1    Hibberd, K.A.2
  • 3
    • 0030949330 scopus 로고    scopus 로고
    • Induction of alternative oxidase synthesis by herbicides inhibiting branched-chain amino acid synthesis
    • Aubert S., Bligny R., Day D.A., Whelan J., Douce R. Induction of alternative oxidase synthesis by herbicides inhibiting branched-chain amino acid synthesis. Plant J 1996, 11:649-657.
    • (1996) Plant J , vol.11 , pp. 649-657
    • Aubert, S.1    Bligny, R.2    Day, D.A.3    Whelan, J.4    Douce, R.5
  • 4
    • 0025366343 scopus 로고
    • Oxalyl hydroxamates as reaction-intermediate analogues for ketol-acid reductoisomerase
    • Aulabaugh A., Schloss J.V. Oxalyl hydroxamates as reaction-intermediate analogues for ketol-acid reductoisomerase. Biochem 1990, 29:2824-2830.
    • (1990) Biochem , vol.29 , pp. 2824-2830
    • Aulabaugh, A.1    Schloss, J.V.2
  • 5
    • 0004362752 scopus 로고    scopus 로고
    • The inhibition of amino acid biosynthesis
    • Wiley-Blackwell, Oxford, UK, A.H. Cobb, J.P.H. Reade (Eds.)
    • Cobb A.H., Reade J.P.H. The inhibition of amino acid biosynthesis. Herbicides and plant physiology 2010, 176-199. Wiley-Blackwell, Oxford, UK. A.H. Cobb, J.P.H. Reade (Eds.).
    • (2010) Herbicides and plant physiology , pp. 176-199
    • Cobb, A.H.1    Reade, J.P.H.2
  • 6
    • 84858055012 scopus 로고    scopus 로고
    • Why have no new herbicide modes of action appeared in recent years?
    • Duke S.O. Why have no new herbicide modes of action appeared in recent years?. Pest Manag Sci 2012, 68:505-512.
    • (2012) Pest Manag Sci , vol.68 , pp. 505-512
    • Duke, S.O.1
  • 7
    • 0028018345 scopus 로고
    • Interactions of plant acetohydroxy acid isomeroreductase with reaction intermediate analogues: correlation of the slow, competitive, inhibition kinetics of enzyme activity and herbicidal effects
    • Dumas R., Cornillon-Bertrand C., Guigue-Talet P., Genix P., Douce R., Job D. Interactions of plant acetohydroxy acid isomeroreductase with reaction intermediate analogues: correlation of the slow, competitive, inhibition kinetics of enzyme activity and herbicidal effects. Biochem J 1994, 301:813-820.
    • (1994) Biochem J , vol.301 , pp. 813-820
    • Dumas, R.1    Cornillon-Bertrand, C.2    Guigue-Talet, P.3    Genix, P.4    Douce, R.5    Job, D.6
  • 8
    • 0027135082 scopus 로고
    • Ketol-acid reductoisomerase from barley (Hordeum vulgare)
    • Durner J., Knorzer O., Böger P. Ketol-acid reductoisomerase from barley (Hordeum vulgare). Plant Physiol 1993, 103:903-910.
    • (1993) Plant Physiol , vol.103 , pp. 903-910
    • Durner, J.1    Knorzer, O.2    Böger, P.3
  • 9
    • 0000833514 scopus 로고
    • New aspects on inhibition of plant acetolactate synthase by chlorsulfuron and imazaquin
    • Durner J., Valérie Gailus V., Böger P. New aspects on inhibition of plant acetolactate synthase by chlorsulfuron and imazaquin. Plant Physiol 1991, 95:1144-1149.
    • (1991) Plant Physiol , vol.95 , pp. 1144-1149
    • Durner, J.1    Valérie Gailus, V.2    Böger, P.3
  • 10
    • 0345392629 scopus 로고    scopus 로고
    • Changes in mitochondrial electron partitioning in response to herbicides inhibiting branched-chain amino acid biosynthesis in soybean
    • Gaston S., Ribas-Carbo M., Busquets S., Berry J.A., Zabalza A., Royuela M. Changes in mitochondrial electron partitioning in response to herbicides inhibiting branched-chain amino acid biosynthesis in soybean. Plant Physiol 2003, 133:1351-1359.
    • (2003) Plant Physiol , vol.133 , pp. 1351-1359
    • Gaston, S.1    Ribas-Carbo, M.2    Busquets, S.3    Berry, J.A.4    Zabalza, A.5    Royuela, M.6
  • 11
    • 0036242666 scopus 로고    scopus 로고
    • Imazethapyr, an inhibitor of the branched-chain amino acid biosynthesis, induces aerobic fermentation in pea plants
    • Gaston S., Zabalza A., Gonzalez E.M., Arrese-Igor C., Aparicio-Tejo P.M., Royuela M. Imazethapyr, an inhibitor of the branched-chain amino acid biosynthesis, induces aerobic fermentation in pea plants. Physiol Plant 2002, 114:524-532.
    • (2002) Physiol Plant , vol.114 , pp. 524-532
    • Gaston, S.1    Zabalza, A.2    Gonzalez, E.M.3    Arrese-Igor, C.4    Aparicio-Tejo, P.M.5    Royuela, M.6
  • 13
    • 79957984988 scopus 로고    scopus 로고
    • Thirty years of herbicide discovery: surveying the past and contemplating the future
    • Gerwick B.C. Thirty years of herbicide discovery: surveying the past and contemplating the future. Agrow 2010, 600:vii-ix.
    • (2010) Agrow , vol.600 , pp. 7-9
    • Gerwick, B.C.1
  • 14
    • 0011208459 scopus 로고
    • Imidazolinones: factors determining their herbicidal efficacy
    • VCH Publishers, New York, USA, Z. Barak, D.M. Chipman, J.V. Schloss (Eds.)
    • Hawkes T.R., Thomas S.E. Imidazolinones: factors determining their herbicidal efficacy. Biosynthesis of branched chain amino acids 1990, 373-389. VCH Publishers, New York, USA. Z. Barak, D.M. Chipman, J.V. Schloss (Eds.).
    • (1990) Biosynthesis of branched chain amino acids , pp. 373-389
    • Hawkes, T.R.1    Thomas, S.E.2
  • 16
    • 13944269884 scopus 로고    scopus 로고
    • Cyclopropane-1,1-dicarboxylate is a slow-, tight-binding inhibitor of rice ketol-acid reductoisomerase
    • Lee Y.T., Ta H.T., Duggleby R.G. Cyclopropane-1,1-dicarboxylate is a slow-, tight-binding inhibitor of rice ketol-acid reductoisomerase. Plant Sci 2005, 168:1035-1040.
    • (2005) Plant Sci , vol.168 , pp. 1035-1040
    • Lee, Y.T.1    Ta, H.T.2    Duggleby, R.G.3
  • 17
    • 67349187292 scopus 로고    scopus 로고
    • 2+ and NADPH binding as revealed by two crystal structures
    • 2+ and NADPH binding as revealed by two crystal structures. J Mol Biol 2009, 89:167-182.
    • (2009) J Mol Biol , vol.89 , pp. 167-182
    • Leung, E.W.W.1    Guddat, L.W.2
  • 18
    • 34250219961 scopus 로고    scopus 로고
    • Synthesis, bioactivity, theoretical and molecular docking study of 1-cyano-N-substituted-cyclopropanecarboxamide as ketol-acid reductoisomerase inhibitor
    • Liu X.H., Chen P.Q., Wang B.L., Li Y.H., Wang S.H., Li Z.M. Synthesis, bioactivity, theoretical and molecular docking study of 1-cyano-N-substituted-cyclopropanecarboxamide as ketol-acid reductoisomerase inhibitor. Bioorg Medic Chem Let 2007, 17:3784-3788.
    • (2007) Bioorg Medic Chem Let , vol.17 , pp. 3784-3788
    • Liu, X.H.1    Chen, P.Q.2    Wang, B.L.3    Li, Y.H.4    Wang, S.H.5    Li, Z.M.6
  • 19
    • 81555214164 scopus 로고    scopus 로고
    • Synthesis, crystal structure, bioactivity and DFT calculation of new oxime ester derivatives containing cyclopropane moiety
    • Liu X.H., Pan L., Tan C.X., Weng J.Q., Wang B.L., Li Z.M. Synthesis, crystal structure, bioactivity and DFT calculation of new oxime ester derivatives containing cyclopropane moiety. Pest Biochem Physiol 2011, 101:143-147.
    • (2011) Pest Biochem Physiol , vol.101 , pp. 143-147
    • Liu, X.H.1    Pan, L.2    Tan, C.X.3    Weng, J.Q.4    Wang, B.L.5    Li, Z.M.6
  • 20
    • 76749121964 scopus 로고    scopus 로고
    • The possible role of quinate in the mode of action of glyphosate and acetolactate synthase inhibitors
    • Orcaray L., Igal M., Marino D., Zabalza A., Royuela M. The possible role of quinate in the mode of action of glyphosate and acetolactate synthase inhibitors. Pest Manag Sci 2010, 66:262-269.
    • (2010) Pest Manag Sci , vol.66 , pp. 262-269
    • Orcaray, L.1    Igal, M.2    Marino, D.3    Zabalza, A.4    Royuela, M.5
  • 21
    • 80053099654 scopus 로고    scopus 로고
    • 2011 Role of exogenously supplied ferulic and p-coumaric acids in mimicking the mode of action of acetolactate synthase inhibiting herbicides
    • Orcaray L., Igal M., Zabalza A., Royuela M. 2011 Role of exogenously supplied ferulic and p-coumaric acids in mimicking the mode of action of acetolactate synthase inhibiting herbicides. J Agric Food Chem 2011, 59:10162-10168.
    • (2011) J Agric Food Chem , vol.59 , pp. 10162-10168
    • Orcaray, L.1    Igal, M.2    Zabalza, A.3    Royuela, M.4
  • 22
    • 83355163274 scopus 로고    scopus 로고
    • Impairment of carbon metabolism induced by the herbicide glyphosate
    • Orcaray L., Zulet A., Zabalza A., Royuela M. Impairment of carbon metabolism induced by the herbicide glyphosate. J Plant Physiol 2012, 169:27-33.
    • (2012) J Plant Physiol , vol.169 , pp. 27-33
    • Orcaray, L.1    Zulet, A.2    Zabalza, A.3    Royuela, M.4
  • 23
    • 76749165972 scopus 로고
    • Spatial organization of quinic and shikimic acid biosynthesis in autotrophic cells of Pinus sylvestris needles 1982
    • Osipov V.I., Aleksandrova L.P. Spatial organization of quinic and shikimic acid biosynthesis in autotrophic cells of Pinus sylvestris needles 1982. Soviet Plant Physiol 1982, 29:286-292.
    • (1982) Soviet Plant Physiol , vol.29 , pp. 286-292
    • Osipov, V.I.1    Aleksandrova, L.P.2
  • 24
    • 77952492421 scopus 로고    scopus 로고
    • Evolution in action: plants resistant to herbicides
    • Powles S.B., Yu Q. Evolution in action: plants resistant to herbicides. Annu Rev Plant Biol 2010, 61:317-347.
    • (2010) Annu Rev Plant Biol , vol.61 , pp. 317-347
    • Powles, S.B.1    Yu, Q.2
  • 25
    • 0000766950 scopus 로고
    • Amino-acid metabolism of Lemna minor L.2. Responses to chlorsulfuron
    • Rhodes D., Hogan A.L., Deal L., Jamieson G.C., Haworth P. Amino-acid metabolism of Lemna minor L.2. Responses to chlorsulfuron. Plant Physiol 1987, 84:775-780.
    • (1987) Plant Physiol , vol.84 , pp. 775-780
    • Rhodes, D.1    Hogan, A.L.2    Deal, L.3    Jamieson, G.C.4    Haworth, P.5
  • 26
    • 0024283582 scopus 로고
    • The herbicidally active experimental compound Hoe 704 is a potent inhibitor of the enzyme acetolactate reductoisomerase
    • Schulz A., Sponemann P., Kocher H., Wegenmayer F. The herbicidally active experimental compound Hoe 704 is a potent inhibitor of the enzyme acetolactate reductoisomerase. FEBS Lett 1988, 238:375-378.
    • (1988) FEBS Lett , vol.238 , pp. 375-378
    • Schulz, A.1    Sponemann, P.2    Kocher, H.3    Wegenmayer, F.4
  • 27
    • 0022606920 scopus 로고
    • Physiological responses of corn (Zea mays) to Ac 243,997 in combination with valine, leucine, and isoleucine
    • Shaner D.L., Reider M.L. Physiological responses of corn (Zea mays) to Ac 243,997 in combination with valine, leucine, and isoleucine. Pest Biochem Physiol 1986, 25:248-257.
    • (1986) Pest Biochem Physiol , vol.25 , pp. 248-257
    • Shaner, D.L.1    Reider, M.L.2
  • 28
    • 0000959598 scopus 로고    scopus 로고
    • Biosynthesis of valine leucine e isoleucine
    • Marcel Dekker, New York, B.K. Singh (Ed.)
    • Singh B.K. Biosynthesis of valine leucine e isoleucine. Plant amino acids 1999, 227-247. Marcel Dekker, New York. B.K. Singh (Ed.).
    • (1999) Plant amino acids , pp. 227-247
    • Singh, B.K.1
  • 29
    • 0001159978 scopus 로고    scopus 로고
    • Inhibition of valine leucine and isoleucine biosynthesis
    • Marcel Dekker, New York, B.K. Singh (Ed.)
    • Wittenbach V.A., Abell L.M. Inhibition of valine leucine and isoleucine biosynthesis. Plant amino acids: biochemistry and biotechnology 1999, 385-416. Marcel Dekker, New York. B.K. Singh (Ed.).
    • (1999) Plant amino acids: biochemistry and biotechnology , pp. 385-416
    • Wittenbach, V.A.1    Abell, L.M.2
  • 30
  • 31
    • 0001694417 scopus 로고
    • Occurrence of shikimic and quinic acids in angiosperms
    • Yoshida S., Tazaki K., Minamikawa T. Occurrence of shikimic and quinic acids in angiosperms. Phytochem 1975, 14:195-197.
    • (1975) Phytochem , vol.14 , pp. 195-197
    • Yoshida, S.1    Tazaki, K.2    Minamikawa, T.3
  • 33
    • 26244452739 scopus 로고    scopus 로고
    • Fermentative metabolism is induced by inhibiting different enzymes of the branched-chain amino acid biosynthesis pathway in pea plants
    • Zabalza A., Gonzalez E.M., Arrese-Igor C., Royuela M. Fermentative metabolism is induced by inhibiting different enzymes of the branched-chain amino acid biosynthesis pathway in pea plants. J Agric Food Chem 2005, 53:7486-7493.
    • (2005) J Agric Food Chem , vol.53 , pp. 7486-7493
    • Zabalza, A.1    Gonzalez, E.M.2    Arrese-Igor, C.3    Royuela, M.4
  • 34
    • 10644223431 scopus 로고    scopus 로고
    • Carbohydrate accumulation in leaves of plants treated with the herbicide chlorsulfuron or imazethapyr is due to a decrease in sink strength
    • Zabalza A., Orcaray L., Gaston S., Royuela M. Carbohydrate accumulation in leaves of plants treated with the herbicide chlorsulfuron or imazethapyr is due to a decrease in sink strength. J Agric Food Chem 2004, 52:7601-7606.
    • (2004) J Agric Food Chem , vol.52 , pp. 7601-7606
    • Zabalza, A.1    Orcaray, L.2    Gaston, S.3    Royuela, M.4
  • 35
    • 79959376376 scopus 로고    scopus 로고
    • Unraveling the role of fermentation in the mode of action of acetolactate synthase inhibitors by metabolic profiling
    • Zabalza A., Orcaray L., Igal M., Schauer N., Fernie A.R., Geigenberger P., et al. Unraveling the role of fermentation in the mode of action of acetolactate synthase inhibitors by metabolic profiling. J Plant Physiol 2011, 168:1568-1575.
    • (2011) J Plant Physiol , vol.168 , pp. 1568-1575
    • Zabalza, A.1    Orcaray, L.2    Igal, M.3    Schauer, N.4    Fernie, A.R.5    Geigenberger, P.6


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