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441 related items for PubMed ID: 7487064

  • 1. The primary sequence of cytochrome P450tyr, the multifunctional N-hydroxylase catalyzing the conversion of L-tyrosine to p-hydroxyphenylacetaldehyde oxime in the biosynthesis of the cyanogenic glucoside dhurrin in Sorghum bicolor (L.) Moench.
    Koch BM, Sibbesen O, Halkier BA, Svendsen I, Møller BL.
    Arch Biochem Biophys; 1995 Oct 20; 323(1):177-86. PubMed ID: 7487064
    [Abstract] [Full Text] [Related]

  • 2. Characterization of cytochrome P450TYR, a multifunctional haem-thiolate N-hydroxylase involved in the biosynthesis of the cyanogenic glucoside dhurrin.
    Halkier BA, Sibbesen O, Koch B, Møller BL.
    Drug Metabol Drug Interact; 1995 Oct 20; 12(3-4):285-97. PubMed ID: 8820857
    [Abstract] [Full Text] [Related]

  • 3. Cytochrome P-450TYR is a multifunctional heme-thiolate enzyme catalyzing the conversion of L-tyrosine to p-hydroxyphenylacetaldehyde oxime in the biosynthesis of the cyanogenic glucoside dhurrin in Sorghum bicolor (L.) Moench.
    Sibbesen O, Koch B, Halkier BA, Møller BL.
    J Biol Chem; 1995 Feb 24; 270(8):3506-11. PubMed ID: 7876084
    [Abstract] [Full Text] [Related]

  • 4. Cloning of three A-type cytochromes P450, CYP71E1, CYP98, and CYP99 from Sorghum bicolor (L.) Moench by a PCR approach and identification by expression in Escherichia coli of CYP71E1 as a multifunctional cytochrome P450 in the biosynthesis of the cyanogenic glucoside dhurrin.
    Bak S, Kahn RA, Nielsen HL, Moller BL, Halkier BA.
    Plant Mol Biol; 1998 Feb 24; 36(3):393-405. PubMed ID: 9484480
    [Abstract] [Full Text] [Related]

  • 5. Purification and characterization of recombinant cytochrome P450TYR expressed at high levels in Escherichia coli.
    Halkier BA, Nielsen HL, Koch B, Møller BL.
    Arch Biochem Biophys; 1995 Oct 01; 322(2):369-77. PubMed ID: 7574710
    [Abstract] [Full Text] [Related]

  • 6. Isolation and reconstitution of cytochrome P450ox and in vitro reconstitution of the entire biosynthetic pathway of the cyanogenic glucoside dhurrin from sorghum.
    Kahn RA, Bak S, Svendsen I, Halkier BA, Møller BL.
    Plant Physiol; 1997 Dec 01; 115(4):1661-70. PubMed ID: 9414567
    [Abstract] [Full Text] [Related]

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  • 8. The presence of CYP79 homologues in glucosinolate-producing plants shows evolutionary conservation of the enzymes in the conversion of amino acid to aldoxime in the biosynthesis of cyanogenic glucosides and glucosinolates.
    Bak S, Nielsen HL, Halkier BA.
    Plant Mol Biol; 1998 Nov 01; 38(5):725-34. PubMed ID: 9862490
    [Abstract] [Full Text] [Related]

  • 9. Substrate specificity of the cytochrome P450 enzymes CYP79A1 and CYP71E1 involved in the biosynthesis of the cyanogenic glucoside dhurrin in Sorghum bicolor (L.) Moench.
    Kahn RA, Fahrendorf T, Halkier BA, Møller BL.
    Arch Biochem Biophys; 1999 Mar 01; 363(1):9-18. PubMed ID: 10049494
    [Abstract] [Full Text] [Related]

  • 10. Transgenic tobacco and Arabidopsis plants expressing the two multifunctional sorghum cytochrome P450 enzymes, CYP79A1 and CYP71E1, are cyanogenic and accumulate metabolites derived from intermediates in Dhurrin biosynthesis.
    Bak S, Olsen CE, Halkier BA, Møller BL.
    Plant Physiol; 2000 Aug 01; 123(4):1437-48. PubMed ID: 10938360
    [Abstract] [Full Text] [Related]

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  • 12. Cloning and expression of cytochrome P450 enzymes catalyzing the conversion of tyrosine to p-hydroxyphenylacetaldoxime in the biosynthesis of cyanogenic glucosides in Triglochin maritima.
    Nielsen JS, Møller BL.
    Plant Physiol; 2000 Apr 01; 122(4):1311-21. PubMed ID: 10759528
    [Abstract] [Full Text] [Related]

  • 13. The biosynthesis of cyanogenic glucosides in higher plants. The (E)- and (Z)-isomers of p-hydroxyphenylacetaldehyde oxime as intermediates in the biosynthesis of dhurrin in Sorghum bicolor (L.) Moench.
    Halkier BA, Olsen CE, Møller BL.
    J Biol Chem; 1989 Nov 25; 264(33):19487-94. PubMed ID: 2684955
    [Abstract] [Full Text] [Related]

  • 14. Cytochrome P450 CYP79A2 from Arabidopsis thaliana L. Catalyzes the conversion of L-phenylalanine to phenylacetaldoxime in the biosynthesis of benzylglucosinolate.
    Wittstock U, Halkier BA.
    J Biol Chem; 2000 May 12; 275(19):14659-66. PubMed ID: 10799553
    [Abstract] [Full Text] [Related]

  • 15. Regiospecific cytochrome P450 limonene hydroxylases from mint (Mentha) species: cDNA isolation, characterization, and functional expression of (-)-4S-limonene-3-hydroxylase and (-)-4S-limonene-6-hydroxylase.
    Lupien S, Karp F, Wildung M, Croteau R.
    Arch Biochem Biophys; 1999 Aug 01; 368(1):181-92. PubMed ID: 10415126
    [Abstract] [Full Text] [Related]

  • 16. Involvement of Cytochrome P-450 in the Biosynthesis of Dhurrin in Sorghum bicolor (L.) Moench.
    Halkier BA, Møller BL.
    Plant Physiol; 1991 May 01; 96(1):10-7. PubMed ID: 16668136
    [Abstract] [Full Text] [Related]

  • 17. The bifurcation of the cyanogenic glucoside and glucosinolate biosynthetic pathways.
    Clausen M, Kannangara RM, Olsen CE, Blomstedt CK, Gleadow RM, Jørgensen K, Bak S, Motawie MS, Møller BL.
    Plant J; 2015 Nov 01; 84(3):558-73. PubMed ID: 26361733
    [Abstract] [Full Text] [Related]

  • 18. The biosynthesis of cyanogenic glucosides in higher plants. Identification of three hydroxylation steps in the biosynthesis of dhurrin in Sorghum bicolor (L.) Moench and the involvement of 1-ACI-nitro-2-(p-hydroxyphenyl)ethane as an intermediate.
    Halkier BA, Møller BL.
    J Biol Chem; 1990 Dec 05; 265(34):21114-21. PubMed ID: 2250015
    [Abstract] [Full Text] [Related]

  • 19. The CYP79A1 catalyzed conversion of tyrosine to (E)-p-hydroxyphenylacetaldoxime unravelled using an improved method for homology modeling.
    Vazquez-Albacete D, Montefiori M, Kol S, Motawia MS, Møller BL, Olsen L, Nørholm MH.
    Phytochemistry; 2017 Mar 05; 135():8-17. PubMed ID: 28088302
    [Abstract] [Full Text] [Related]

  • 20. Ferulate-5-hydroxylase from Arabidopsis thaliana defines a new family of cytochrome P450-dependent monooxygenases.
    Meyer K, Cusumano JC, Somerville C, Chapple CC.
    Proc Natl Acad Sci U S A; 1996 Jul 09; 93(14):6869-74. PubMed ID: 8692910
    [Abstract] [Full Text] [Related]

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