Bak S - Search Results

1

Biosynthesis of the cyanogenic glucosides linamarin and lotaustralin in cassava: isolation, biochemical characterization, and expression pattern of CYP71E7, the oxime-metabolizing cytochrome P450 enzyme.

Jørgensen K, Morant AV, Morant M, Jensen NB, Olsen CE, Kannangara R, Motawia MS, Møller BL, Bak S. Jørgensen K, et al. Among authors: bak s. Plant Physiol. 2011 Jan;155(1):282-92. doi: 10.1104/pp.110.164053. Epub 2010 Nov 2. Plant Physiol. 2011. PMID: 21045121 Free PMC article.

2

Isolation and reconstitution of the heme-thiolate protein obtusifoliol 14alpha-demethylase from Sorghum bicolor (L.) Moench.

Kahn RA, Bak S, Olsen CE, Svendsen I, Moller BL. Kahn RA, et al. Among authors: bak s. J Biol Chem. 1996 Dec 20;271(51):32944-50. doi: 10.1074/jbc.271.51.32944. J Biol Chem. 1996. PMID: 8955137 Free article.

3

Cloning and expression in Escherichia coli of the obtusifoliol 14 alpha-demethylase of Sorghum bicolor (L.) Moench, a cytochrome P450 orthologous to the sterol 14 alpha-demethylases (CYP51) from fungi and mammals.

Bak S, Kahn RA, Olsen CE, Halkier BA. Bak S, et al. Plant J. 1997 Feb;11(2):191-201. doi: 10.1046/j.1365-313x.1997.11020191.x. Plant J. 1997. PMID: 9076987 Free article.

4

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. Kahn RA, et al. Among authors: bak s. Plant Physiol. 1997 Dec;115(4):1661-70. doi: 10.1104/pp.115.4.1661. Plant Physiol. 1997. PMID: 9414567 Free PMC article.

5

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. Bak S, et al. Plant Mol Biol. 1998 Feb;36(3):393-405. doi: 10.1023/a:1005915507497. Plant Mol Biol. 1998. PMID: 9484480

6

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. Bak S, et al. Plant Mol Biol. 1998 Nov;38(5):725-34. doi: 10.1023/a:1006064202774. Plant Mol Biol. 1998. PMID: 9862490

7

Metabolic engineering of p-hydroxybenzylglucosinolate in Arabidopsis by expression of the cyanogenic CYP79A1 from Sorghum bicolor.

Bak S, Olsen CE, Petersen BL, Møller BL, Halkier BA. Bak S, et al. Plant J. 1999 Dec;20(6):663-71. doi: 10.1046/j.1365-313x.1999.00642.x. Plant J. 1999. PMID: 10652138 Free article.

8

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. Bak S, et al. Plant Physiol. 2000 Aug;123(4):1437-48. doi: 10.1104/pp.123.4.1437. Plant Physiol. 2000. PMID: 10938360 Free PMC article.

9

Resistance to an herbivore through engineered cyanogenic glucoside synthesis.

Tattersall DB, Bak S, Jones PR, Olsen CE, Nielsen JK, Hansen ML, Høj PB, Møller BL. Tattersall DB, et al. Among authors: bak s. Science. 2001 Sep 7;293(5536):1826-8. doi: 10.1126/science.1062249. Epub 2001 Jul 26. Science. 2001. PMID: 11474068

10

The involvement of two p450 enzymes, CYP83B1 and CYP83A1, in auxin homeostasis and glucosinolate biosynthesis.

Bak S, Feyereisen R. Bak S, et al. Plant Physiol. 2001 Sep;127(1):108-18. doi: 10.1104/pp.127.1.108. Plant Physiol. 2001. PMID: 11553739 Free PMC article.

The first committed step in the biosynthesis of indole glucosinolates is the conversion of indole-3-acetaldoxime into an indole-3-S-alkyl-thiohydroximate. The initial step in this conversion is catalyzed by CYP83B1 in Arabidopsis (S. Bak, F.E. Tax, K.A. Feldm …

The first committed step in the biosynthesis of indole glucosinolates is the conversion of indole-3-acetaldoxime into an indole-3-S-a …

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