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Volumn 62, Issue 2, 1998, Pages 113-124

The mode of action of isoxaflutole: I. Physiological effects, metabolism, and selectivity

Author keywords

[No Author keywords available]

Indexed keywords

ABUTILON THEOPHRASTI; BRASSICA; DAUCUS CAROTA; IPOMEA; IPOMOEA; SACCHARUM HYBRID CULTIVAR; SINAPIS ARVENSIS; ZEA MAYS;

EID: 0031760410     PISSN: 00483575     EISSN: None     Source Type: Journal    
DOI: 10.1006/pest.1998.2378     Document Type: Article
Times cited : (185)

References (19)
  • 2
    • 0002634757 scopus 로고    scopus 로고
    • Isoxaflutole for weed control in maize
    • B. M. Luscombe and K. E. Pallett, Isoxaflutole for weed control in maize, Pestic. Outlook December, 29 (1996).
    • (1996) Pestic. Outlook , vol.DECEMBER , pp. 29
    • Luscombe, B.M.1    Pallett, K.E.2
  • 3
    • 0001867143 scopus 로고
    • Inhibition of carotenoid biosynthesis by herbicides
    • P. Boger and G. Sandmann, Eds., CRC Press, Boca Raton, FL
    • G. Sandmann and P. Böger, Inhibition of carotenoid biosynthesis by herbicides, in "Target Sites of Herbicide Action" (P. Boger and G. Sandmann, Eds.), p. 25, CRC Press, Boca Raton, FL, 1989.
    • (1989) Target Sites of Herbicide Action , pp. 25
    • Sandmann, G.1    Böger, P.2
  • 4
    • 0006381656 scopus 로고
    • Phytoene desaturase: A biochemical target of many bleaching herbicides
    • P. M. Bramley and K. E. Pallett, Phytoene desaturase: a biochemical target of many bleaching herbicides, Proc. Brighton Crop Protect. Conf.-Weeds 2, 713 (1993).
    • (1993) Proc. Brighton Crop Protect. Conf.-Weeds , vol.2 , pp. 713
    • Bramley, P.M.1    Pallett, K.E.2
  • 6
    • 0027452908 scopus 로고
    • SC-0051, a 2-benzoyl-cyclohexane-1,3-dione bleaching herbicide, is a potent inhibitor of the enzyme p-hydroxyphenylpyruvate dioxygenase
    • A. Schulz, O. Ort, P. Beyer, and H. Kleinig, SC-0051, a 2-benzoyl-cyclohexane-1,3-dione bleaching herbicide, is a potent inhibitor of the enzyme p-hydroxyphenylpyruvate dioxygenase, FEBS Lett. 318, 162 (1993).
    • (1993) FEBS Lett. , vol.318 , pp. 162
    • Schulz, A.1    Ort, O.2    Beyer, P.3    Kleinig, H.4
  • 7
    • 0030471724 scopus 로고    scopus 로고
    • Purification and characterisation of 4-hydroxyphenylpyruvate dioxygenase from maize
    • I. S. Barta and P. Böger, Purification and characterisation of 4-hydroxyphenylpyruvate dioxygenase from maize, Pestic. Sci. 48, 109 (1996).
    • (1996) Pestic. Sci. , vol.48 , pp. 109
    • Barta, I.S.1    Böger, P.2
  • 8
    • 0028313670 scopus 로고
    • Inhibition of barnyardgrass 4-hydroxyphenylpyruvate dioxygenase by sulcotrione
    • J. Secor, Inhibition of barnyardgrass 4-hydroxyphenylpyruvate dioxygenase by sulcotrione, Plant Physiol. 106, 1429 (1994).
    • (1994) Plant Physiol. , vol.106 , pp. 1429
    • Secor, J.1
  • 9
    • 0031789261 scopus 로고    scopus 로고
    • Mode of action of isoxaflutole. 2. Characterization of the inhibition of the carrot 4-hydroxyphenylpyruvate dioxygenase by the diketonitrile derivative of isoxaflutole
    • F. Viviani, J. P. Little, and K. E. Pallett, Mode of action of isoxaflutole. 2. Characterization of the inhibition of the carrot 4-hydroxyphenylpyruvate dioxygenase by the diketonitrile derivative of isoxaflutole, Pestic. Biochem. Physiol. 62, 125-134 (1998).
    • (1998) Pestic. Biochem. Physiol. , vol.62 , pp. 125-134
    • Viviani, F.1    Little, J.P.2    Pallett, K.E.3
  • 10
    • 0345276816 scopus 로고
    • The effect of diflufenican on pigment levels in carotenogenic systems
    • Wagennigen, The Netherlands
    • P. Barry and K. E. Pallett, The effect of diflufenican on pigment levels in carotenogenic systems, in "Proceedings, EWRS Symposium" Wagennigen, The Netherlands," p. 51, (1988).
    • (1988) Proceedings, EWRS Symposium , pp. 51
    • Barry, P.1    Pallett, K.E.2
  • 11
  • 12
    • 0027301953 scopus 로고
    • Development of high performance liquid chromatographic systems for the separation of radiolabelled carotenes and precursors formed in specific enzymatic reactions
    • P. Fraser, M. Albrecht, and G. Sandmann, Development of high performance liquid chromatographic systems for the separation of radiolabelled carotenes and precursors formed in specific enzymatic reactions, J. Chromatogr. 645, 265 (1993).
    • (1993) J. Chromatogr. , vol.645 , pp. 265
    • Fraser, P.1    Albrecht, M.2    Sandmann, G.3
  • 13
    • 0001020372 scopus 로고
    • Phycomyces blakesleeanus carB mutants: Their use in assays of phytoene desaturation
    • P. Fraser, J. de la Rivas, A Mackenzie, and P. M. Bramley, Phycomyces blakesleeanus carB mutants: Their use in assays of phytoene desaturation, Phytochemistry 30, 3971 (1991).
    • (1991) Phytochemistry , vol.30 , pp. 3971
    • Fraser, P.1    De La Rivas, J.2    Mackenzie, A.3    Bramley, P.M.4
  • 14
    • 85053535198 scopus 로고
    • Carotenoids
    • R. G Alscher and J. L Hess, Eds., CRC Press, Boca Raton, FL
    • K. E. Pallett and A. J. Young, Carotenoids, n "Antioxidants in Higher Plants" (R. G Alscher and J. L Hess, Eds.), p. 59, CRC Press, Boca Raton, FL, (1993).
    • (1993) Antioxidants in Higher Plants , pp. 59
    • Pallett, K.E.1    Young, A.J.2
  • 16
    • 0022049227 scopus 로고
    • Localisation and synthesis of prenylquinones in isolated outer and inner envelope membranes from spinach chloroplasts
    • J. Soil, G. Schultz, J. Joyard, R. Douce, and M. A. Block, Localisation and synthesis of prenylquinones in isolated outer and inner envelope membranes from spinach chloroplasts, Arch. Biochem. Biophys. 238, 290 (1985).
    • (1985) Arch. Biochem. Biophys. , vol.238 , pp. 290
    • Soil, J.1    Schultz, G.2    Joyard, J.3    Douce, R.4    Block, M.A.5
  • 17
    • 0025325851 scopus 로고
    • Quinone compounds are able to replace molecular oxygen as a terminal electron acceptor in phytoene desaturation in chromoplasts of Narcissus pseudonarcissus L. Eur.
    • M. Mayer, P. Beyer, and H. Kleinig, Quinone compounds are able to replace molecular oxygen as a terminal electron acceptor in phytoene desaturation in chromoplasts of Narcissus pseudonarcissus L. Eur., J. Biochem. 191, 359 (1990).
    • (1990) J. Biochem. , vol.191 , pp. 359
    • Mayer, M.1    Beyer, P.2    Kleinig, H.3
  • 18
    • 0000360598 scopus 로고
    • Purification and characterisation of a NADPH dependant oxidoreductase from chromoplasts of Narcissus pseudonarcissus: A redox mediator possibly involved in carotene desaturation
    • M. Mayer, V. Nievelstein, and P. Beyer, Purification and characterisation of a NADPH dependant oxidoreductase from chromoplasts of Narcissus pseudonarcissus: A redox mediator possibly involved in carotene desaturation, Plant. Physiol. Biochem. 30, 389 (1992).
    • (1992) Plant. Physiol. Biochem. , vol.30 , pp. 389
    • Mayer, M.1    Nievelstein, V.2    Beyer, P.3
  • 19
    • 0029556712 scopus 로고
    • Genetic dissection of carotenoid synthesis in Arabidopsis defines plastoquinone as an essential component of phytoene desaturation
    • S. R. Norris, T. R. Barrette, and D. Della Penna, Genetic dissection of carotenoid synthesis in Arabidopsis defines plastoquinone as an essential component of phytoene desaturation, Plant Cell 7, 2139 (1995).
    • (1995) Plant Cell , vol.7 , pp. 2139
    • Norris, S.R.1    Barrette, T.R.2    Della Penna, D.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.