Halkier BA - Search Results

1

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. Halkier BA, et al. J Biol Chem. 1989 Nov 25;264(33):19487-94. J Biol Chem. 1989. PMID: 2684955 Free article.

2

The biosynthesis of cyanogenic glucosides in seedlings of cassava (Manihot esculenta Crantz).

Koch B, Nielsen VS, Halkier BA, Olsen CE, Møller BL. Koch B, et al. Among authors: halkier ba. Arch Biochem Biophys. 1992 Jan;292(1):141-50. doi: 10.1016/0003-9861(92)90062-2. Arch Biochem Biophys. 1992. PMID: 1727632

3

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. Halkier BA, et al. J Biol Chem. 1990 Dec 5;265(34):21114-21. J Biol Chem. 1990. PMID: 2250015 Free article.

4

Cyanogenic glucosides: the biosynthetic pathway and the enzyme system involved.

Halkier BA, Scheller HV, Møller BL. Halkier BA, et al. Ciba Found Symp. 1988;140:49-66. doi: 10.1002/9780470513712.ch5. Ciba Found Symp. 1988. PMID: 3073062 Review.

5

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. Koch BM, et al. Among authors: halkier ba. Arch Biochem Biophys. 1995 Oct 20;323(1):177-86. doi: 10.1006/abbi.1995.0024. Arch Biochem Biophys. 1995. PMID: 7487064

6

Purification and characterization of recombinant cytochrome P450TYR expressed at high levels in Escherichia coli.

Halkier BA, Nielsen HL, Koch B, Møller BL. Halkier BA, et al. Arch Biochem Biophys. 1995 Oct 1;322(2):369-77. doi: 10.1006/abbi.1995.1477. Arch Biochem Biophys. 1995. PMID: 7574710

7

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. Sibbesen O, et al. Among authors: halkier ba. J Biol Chem. 1995 Feb 24;270(8):3506-11. doi: 10.1074/jbc.270.8.3506. J Biol Chem. 1995. PMID: 7876084 Free article.

8

Isolation of the heme-thiolate enzyme cytochrome P-450TYR, which catalyzes the committed step in the biosynthesis of the cyanogenic glucoside dhurrin in Sorghum bicolor (L.) Moench.

Sibbesen O, Koch B, Halkier BA, Møller BL. Sibbesen O, et al. Among authors: halkier ba. Proc Natl Acad Sci U S A. 1994 Oct 11;91(21):9740-4. doi: 10.1073/pnas.91.21.9740. Proc Natl Acad Sci U S A. 1994. PMID: 7937883 Free PMC article.

9

Involvement of cytochrome P450 in oxime production in glucosinolate biosynthesis as demonstrated by an in vitro microsomal enzyme system isolated from jasmonic acid-induced seedlings of Sinapis alba L.

Du L, Lykkesfeldt J, Olsen CE, Halkier BA. Du L, et al. Among authors: halkier ba. Proc Natl Acad Sci U S A. 1995 Dec 19;92(26):12505-9. doi: 10.1073/pnas.92.26.12505. Proc Natl Acad Sci U S A. 1995. PMID: 8618930 Free PMC article.

10

Isolation of plant and recombinant CYP79.

Halkier BA, Sibbesen O, Møller BL. Halkier BA, et al. Methods Enzymol. 1996;272:268-74. doi: 10.1016/s0076-6879(96)72032-3. Methods Enzymol. 1996. PMID: 8791786 No abstract available.

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