-
1
-
-
77957192530
-
Function and evolution of plant cytochrome P450
-
Kahn R., Durst F. Function and evolution of plant cytochrome P450. Recent Adv. Phytochem. 34:2000;151-189.
-
(2000)
Recent Adv. Phytochem.
, vol.34
, pp. 151-189
-
-
Kahn, R.1
Durst, F.2
-
2
-
-
0347861780
-
Cytochromes P450
-
Edited by Somerville CR, Meyerowitz EM. American Society of Plant Biologists, Rockville MD, 2002, doi/10.1199/tab.0028
-
Werck-Reichhart D, Bak S, Paquette S: Cytochromes P450. In The Arabidopsis Book. Edited by Somerville CR, Meyerowitz EM. American Society of Plant Biologists, Rockville MD, 2002, doi/10.1199/tab.0028 URL: http://www.aspb.org/publications/Arabidopsis.
-
The Arabidopsis Book
-
-
Werck-Reichhart, D.1
Bak, S.2
Paquette, S.3
-
3
-
-
0030801551
-
Taxol biosynthesis: An update
-
Hezari M., Croteau R. Taxol biosynthesis: an update. Planta. Med. 63:1997;291-295.
-
(1997)
Planta. Med.
, vol.63
, pp. 291-295
-
-
Hezari, M.1
Croteau, R.2
-
5
-
-
0034789998
-
Taxol: Biosynthesis, molecular genetics, and biotechnological applications
-
Jennewein S., Croteau R. Taxol: biosynthesis, molecular genetics, and biotechnological applications. Appl. Microbiol. Biotechnol. 57:2001;13-19.
-
(2001)
Appl. Microbiol. Biotechnol.
, vol.57
, pp. 13-19
-
-
Jennewein, S.1
Croteau, R.2
-
6
-
-
0032560946
-
Multiple oxygenase reactions in the biosynthesis of taxoids
-
Eisenreich W., Menhard B., Lee M.S., Zenk M.H., Bacher A. Multiple oxygenase reactions in the biosynthesis of taxoids. J. Am. Chem. Soc. 120:1998;9694-9695.
-
(1998)
J. Am. Chem. Soc.
, vol.120
, pp. 9694-9695
-
-
Eisenreich, W.1
Menhard, B.2
Lee, M.S.3
Zenk, M.H.4
Bacher, A.5
-
7
-
-
27244462261
-
Taxol biosynthesis: Differential transformations of taxadien-5 α-ol and its acetate ester by cytochrome P450 hydroxylases from Taxus suspension cells
-
Wheeler A.L., Long R.M., Ketchum R.E., Rithner C.D., Williams R.M., Croteau R. Taxol biosynthesis: differential transformations of taxadien-5 α-ol and its acetate ester by cytochrome P450 hydroxylases from Taxus suspension cells. Arch. Biochem. Biophys. 390:2001;265-278.
-
(2001)
Arch. Biochem. Biophys.
, vol.390
, pp. 265-278
-
-
Wheeler, A.L.1
Long, R.M.2
Ketchum, R.E.3
Rithner, C.D.4
Williams, R.M.5
Croteau, R.6
-
8
-
-
0029775816
-
Microsome preparation from woody plant tissues
-
Hefner J., Croteau R. Microsome preparation from woody plant tissues. Methods Enzymol. 272:1996;243-249.
-
(1996)
Methods Enzymol.
, vol.272
, pp. 243-249
-
-
Hefner, J.1
Croteau, R.2
-
9
-
-
0030154837
-
Cytochrome P450-catalyzed hydroxylation of taxa-4(5),11(12)-diene to taxa-4(20),11(12)-dien-5α-ol: The first oxygenation step in taxol biosynthesis
-
Hefner J., Rubenstein S.M., Ketchum R.E., Gibson D.M., Williams R.M., Croteau R. Cytochrome P450-catalyzed hydroxylation of taxa-4(5),11(12)-diene to taxa-4(20),11(12)-dien-5α-ol: the first oxygenation step in taxol biosynthesis. Chem. Biol. 3:1996;479-489.
-
(1996)
Chem. Biol.
, vol.3
, pp. 479-489
-
-
Hefner, J.1
Rubenstein, S.M.2
Ketchum, R.E.3
Gibson, D.M.4
Williams, R.M.5
Croteau, R.6
-
10
-
-
0033524365
-
The kinetics of taxoid accumulation in cell suspension cultures of Taxus following elicitation with methyl jasmonate
-
Ketchum R.E., Gibson D.M., Croteau R.B., Shuler M.L. The kinetics of taxoid accumulation in cell suspension cultures of Taxus following elicitation with methyl jasmonate. Biotechnol. Bioeng. 62:1999;97-105.
-
(1999)
Biotechnol. Bioeng.
, vol.62
, pp. 97-105
-
-
Ketchum, R.E.1
Gibson, D.M.2
Croteau, R.B.3
Shuler, M.L.4
-
11
-
-
0035852639
-
Molecular cloning of a cytochrome P450 taxane 10 β-hydroxylase cDNA from Taxus and functional expression in yeast
-
Provides the description of the mRNA differential display RT-PCR strategy that allowed isolation of 23 P450 genes from jasmonate-elicited Taxus cells. A subgroup of 13 of these genes are taxoid biosynthetic candidate genes and the function of several of them has already been confirmed (although only published for two of them so far).
-
Schoendorf A., Rithner C.D., Williams R.M., Croteau R.B. Molecular cloning of a cytochrome P450 taxane 10 β-hydroxylase cDNA from Taxus and functional expression in yeast. Proc. Natl. Acad. Sci. U.S.A. 98:2001;1501-1506 Provides the description of the mRNA differential display RT-PCR strategy that allowed isolation of 23 P450 genes from jasmonate-elicited Taxus cells. A subgroup of 13 of these genes are taxoid biosynthetic candidate genes and the function of several of them has already been confirmed (although only published for two of them so far).
-
(2001)
Proc. Natl. Acad. Sci. U.S.A.
, vol.98
, pp. 1501-1506
-
-
Schoendorf, A.1
Rithner, C.D.2
Williams, R.M.3
Croteau, R.B.4
-
12
-
-
0035923612
-
Taxol biosynthesis: Taxane 13 α-hydroxylase is a cytochrome P450-dependent monooxygenase
-
Describes the problems that might be encountered for the expression of some plant P450s in yeast or insect cells, in particular the elusive character of some CO-difference spectra. This paper also provides evidence for oxygenation of multiple taxoid structures by a single enzyme.
-
Jennewein S., Rithner C.D., Williams R.M., Croteau R.B. Taxol biosynthesis: taxane 13 α-hydroxylase is a cytochrome P450-dependent monooxygenase. Proc. Natl. Acad. Sci. U.S.A. 98:2001;13595-13600 Describes the problems that might be encountered for the expression of some plant P450s in yeast or insect cells, in particular the elusive character of some CO-difference spectra. This paper also provides evidence for oxygenation of multiple taxoid structures by a single enzyme.
-
(2001)
Proc. Natl. Acad. Sci. U.S.A.
, vol.98
, pp. 13595-13600
-
-
Jennewein, S.1
Rithner, C.D.2
Williams, R.M.3
Croteau, R.B.4
-
13
-
-
0028855024
-
A cytochrome P-450 monooxygenase catalyzes the first step in the conversion of tabersonine to vindoline in Catharanthus roseus
-
St-Pierre B., De Luca V. A cytochrome P-450 monooxygenase catalyzes the first step in the conversion of tabersonine to vindoline in Catharanthus roseus. Plant Physiol. 109:1995;131-139.
-
(1995)
Plant Physiol.
, vol.109
, pp. 131-139
-
-
St-Pierre, B.1
De Luca, V.2
-
14
-
-
0033977809
-
Secologanin synthase which catalyzes the oxidative cleavage of loganin into secologanin is a cytochrome P450
-
Yamamoto H., Katano N., Ooi A., Inoue K. Secologanin synthase which catalyzes the oxidative cleavage of loganin into secologanin is a cytochrome P450. Phytochemistry. 53:2000;7-12.
-
(2000)
Phytochemistry
, vol.53
, pp. 7-12
-
-
Yamamoto, H.1
Katano, N.2
Ooi, A.3
Inoue, K.4
-
15
-
-
0035839086
-
7-Deoxyloganin 7-hydroxylase in Lonicera japonica cell cultures
-
Katano N., Yamamoto H., Iio R., Inoue K. 7-Deoxyloganin 7-hydroxylase in Lonicera japonica cell cultures. Phytochemistry. 58:2001;53-58.
-
(2001)
Phytochemistry
, vol.58
, pp. 53-58
-
-
Katano, N.1
Yamamoto, H.2
Iio, R.3
Inoue, K.4
-
16
-
-
0142036457
-
Light-induced cytochrome P450-dependent enzyme in indole alkaloid biosynthesis: Tabersonine16-hydroxylase
-
Schroder G., Unterbusch E., Kaltenbach M., Schmidt J., Strack D., De Luca V., Schroder J. Light-induced cytochrome P450-dependent enzyme in indole alkaloid biosynthesis: tabersonine16-hydroxylase. FEBS Lett. 458:1999;97-102.
-
(1999)
FEBS Lett.
, vol.458
, pp. 97-102
-
-
Schroder, G.1
Unterbusch, E.2
Kaltenbach, M.3
Schmidt, J.4
Strack, D.5
De Luca, V.6
Schroder, J.7
-
17
-
-
0034490132
-
Indole alkaloid biosynthesis in Catharanthus roseus: New enzyme activities and identification of cytochrome P450 CYP72A1 as secologanin synthase
-
This paper illustrates the long way from the isolation of a P450 gene to the determination of its biochemical function. The authors show how tissue-specific expression and co-localisation with other enzymes in a pathway can provide a clue to gene function. CYP72A1 is the first ring-opening plant P450 to be described.
-
Irmler S., Schroder G., St-Pierre B., Crouch N.P., Hotze M., Schmidt J., Strack D., Matern U., Schroder J. Indole alkaloid biosynthesis in Catharanthus roseus: new enzyme activities and identification of cytochrome P450 CYP72A1 as secologanin synthase. Plant J. 24:2000;797-804 This paper illustrates the long way from the isolation of a P450 gene to the determination of its biochemical function. The authors show how tissue-specific expression and co-localisation with other enzymes in a pathway can provide a clue to gene function. CYP72A1 is the first ring-opening plant P450 to be described.
-
(2000)
Plant J.
, vol.24
, pp. 797-804
-
-
Irmler, S.1
Schroder, G.2
St-Pierre, B.3
Crouch, N.P.4
Hotze, M.5
Schmidt, J.6
Strack, D.7
Matern, U.8
Schroder, J.9
-
18
-
-
0035900382
-
Geraniol 10-hydroxylase, a cytochrome P450 enzyme involved in terpenoid indole alkaloid biosynthesis
-
Collu G., Unver N., Peltenburg-Looman A.M., van der Heijden R., Verpoorte R., Memelink J. Geraniol 10-hydroxylase, a cytochrome P450 enzyme involved in terpenoid indole alkaloid biosynthesis. FEBS Lett. 508:2001;215-220.
-
(2001)
FEBS Lett.
, vol.508
, pp. 215-220
-
-
Collu, G.1
Unver, N.2
Peltenburg-Looman, A.M.3
Van der Heijden, R.4
Verpoorte, R.5
Memelink, J.6
-
19
-
-
0032871966
-
Effects of alkaloid precursor feeding and elicitation on the accumulation of secologanin in a Catharanthus roseus cell suspension culture
-
Contin A., van der Heidjen R., Verpoorte R. Effects of alkaloid precursor feeding and elicitation on the accumulation of secologanin in a Catharanthus roseus cell suspension culture. Plant Cell Tissue Organ. Cult. 56:1999;111-119.
-
(1999)
Plant Cell Tissue Organ. Cult
, vol.56
, pp. 111-119
-
-
Contin, A.1
Van der Heidjen, R.2
Verpoorte, R.3
-
20
-
-
0036536289
-
Engineering secondary metabolite production in plants
-
Verpoorte R., Memelink J. Engineering secondary metabolite production in plants. Curr. Opin. Biotechnol. 13:2002;181-187.
-
(2002)
Curr. Opin. Biotechnol.
, vol.13
, pp. 181-187
-
-
Verpoorte, R.1
Memelink, J.2
-
21
-
-
0033045549
-
The effect of phenobarbital and ketoconazole on the alkaloid biosynthesis in Catharanthus roseus cell suspension cultures
-
Contin A., Collu G., Van der Heijden R., Verpoorte R. The effect of phenobarbital and ketoconazole on the alkaloid biosynthesis in Catharanthus roseus cell suspension cultures. Plant Physiol. Biochem. 37:1999;139-144.
-
(1999)
Plant Physiol. Biochem.
, vol.37
, pp. 139-144
-
-
Contin, A.1
Collu, G.2
Van der Heijden, R.3
Verpoorte, R.4
-
22
-
-
0034177601
-
The cell and developmental biology of alkaloid biosynthesis
-
A very interesting review on the developmental control, tissue and subcellular localisation of enzymes involved in alkaloid biosynthesis. Shows that alkaloid synthesis involves several subcellular compartments and different tissues/organs, and that differential expression of enzymes in the pathway implies mobility of metabolic intermediates.
-
De Luca V., St Pierre B. The cell and developmental biology of alkaloid biosynthesis. Trends Plant Sci. 5:2000;168-173 A very interesting review on the developmental control, tissue and subcellular localisation of enzymes involved in alkaloid biosynthesis. Shows that alkaloid synthesis involves several subcellular compartments and different tissues/organs, and that differential expression of enzymes in the pathway implies mobility of metabolic intermediates.
-
(2000)
Trends Plant Sci.
, vol.5
, pp. 168-173
-
-
De Luca, V.1
St Pierre, B.2
-
23
-
-
0035213471
-
ORCAnization of jasmonate-responsive gene expression in alkaloid metabolism
-
An update on the recent advances on transcription factors and signalling cascades that regulate alkaloid metabolism. The authors describe the potential applications of manipulating gene regulators for improving alkaloid production.
-
Memelink J., Verpoorte R., Kijne J.W. ORCAnization of jasmonate-responsive gene expression in alkaloid metabolism. Trends Plant Sci. 6:2001;212-219 An update on the recent advances on transcription factors and signalling cascades that regulate alkaloid metabolism. The authors describe the potential applications of manipulating gene regulators for improving alkaloid production.
-
(2001)
Trends Plant Sci.
, vol.6
, pp. 212-219
-
-
Memelink, J.1
Verpoorte, R.2
Kijne, J.W.3
-
24
-
-
0034892702
-
Biotransformation of tryptamine and secologanin into plant terpenoid indole alkaloids by transgenic yeast
-
Geerlings A., Redondo F.J., Contin A., Memelink J., van der Heijden R., Verpoorte R. Biotransformation of tryptamine and secologanin into plant terpenoid indole alkaloids by transgenic yeast. Appl. Microbiol. Biotechnol. 56:2001;420-424.
-
(2001)
Appl. Microbiol. Biotechnol.
, vol.56
, pp. 420-424
-
-
Geerlings, A.1
Redondo, F.J.2
Contin, A.3
Memelink, J.4
Van der Heijden, R.5
Verpoorte, R.6
-
25
-
-
0032143041
-
Enzymatic oxidations in the biosynthesis of complex alkaloids
-
Chou W.M., Kutchan T.M. Enzymatic oxidations in the biosynthesis of complex alkaloids. Plant J. 15:1998;289-300.
-
(1998)
Plant J.
, vol.15
, pp. 289-300
-
-
Chou, W.M.1
Kutchan, T.M.2
-
26
-
-
0033167088
-
Molecular characterization of the enzyme catalyzing the aryl migration reaction of isoflavonoid biosynthesis in soybean
-
Steele C.L., Gijzen M., Qutob D., Dixon R.A. Molecular characterization of the enzyme catalyzing the aryl migration reaction of isoflavonoid biosynthesis in soybean. Arch. Biochem. Biophys. 367:1999;146-150.
-
(1999)
Arch. Biochem. Biophys.
, vol.367
, pp. 146-150
-
-
Steele, C.L.1
Gijzen, M.2
Qutob, D.3
Dixon, R.A.4
-
27
-
-
0033230703
-
Cloning and functional expression of a cytochrome P450 cDNA encoding 2-hydroxyisoflavanone synthase involved in biosynthesis of the isoflavonoid skeleton in licorice
-
Akashi T., Aoki T., Ayabe S. Cloning and functional expression of a cytochrome P450 cDNA encoding 2-hydroxyisoflavanone synthase involved in biosynthesis of the isoflavonoid skeleton in licorice. Plant Physiol. 121:1999;821-828.
-
(1999)
Plant Physiol.
, vol.121
, pp. 821-828
-
-
Akashi, T.1
Aoki, T.2
Ayabe, S.3
-
28
-
-
0033951110
-
Identification and expression of isoflavone synthase, the key enzyme for biosynthesis of isoflavones in legumes
-
Describes the isolation of isoflavone synthase genes from a large number of leguminous species and from sugar beet. This work shows that the expression of the soybean enzyme in Arabidopsis allows the production of genistein in this non-legume plant.
-
Jung W., Yu O., Lau S.M., O'Keefe D.P., Odell J., Fader G., McGonigle B. Identification and expression of isoflavone synthase, the key enzyme for biosynthesis of isoflavones in legumes. Nat. Biotechnol. 18:2000;208-212 Describes the isolation of isoflavone synthase genes from a large number of leguminous species and from sugar beet. This work shows that the expression of the soybean enzyme in Arabidopsis allows the production of genistein in this non-legume plant.
-
(2000)
Nat. Biotechnol.
, vol.18
, pp. 208-212
-
-
Jung, W.1
Yu, O.2
Lau, S.M.3
O'Keefe, D.P.4
Odell, J.5
Fader, G.6
McGonigle, B.7
-
29
-
-
0037030807
-
Genistein
-
A broad and interesting overview of the biological activity of isoflavonoids, and in particular genistein, with an emphasis on health benefits.
-
Dixon R.A., Ferreira D. Genistein. Phytochemistry. 60:2002;205-211 A broad and interesting overview of the biological activity of isoflavonoids, and in particular genistein, with an emphasis on health benefits.
-
(2002)
Phytochemistry
, vol.60
, pp. 205-211
-
-
Dixon, R.A.1
Ferreira, D.2
-
30
-
-
0033791950
-
Production of the isoflavones genistein and daidzein in non-legume dicot and monocot tissues
-
An analysis of genistein production in tobacco, Arabidopsis and maize cells transformed with the isoflavone synthase gene from soybean. Provides an insight into the requirements for metabolic engineering isoflavone production in non-legume dicots and monocots. The main requirement is activity of the flavonoid branch of the phenylpropanoid pathway in the analysed tissues.
-
Yu O., Jung W., Shi J., Croes R.A., Fader G.M., McGonigle B., Odell J.T. Production of the isoflavones genistein and daidzein in non-legume dicot and monocot tissues. Plant Physiol. 124:2000;781-794 An analysis of genistein production in tobacco, Arabidopsis and maize cells transformed with the isoflavone synthase gene from soybean. Provides an insight into the requirements for metabolic engineering isoflavone production in non-legume dicots and monocots. The main requirement is activity of the flavonoid branch of the phenylpropanoid pathway in the analysed tissues.
-
(2000)
Plant Physiol.
, vol.124
, pp. 781-794
-
-
Yu, O.1
Jung, W.2
Shi, J.3
Croes, R.A.4
Fader, G.M.5
McGonigle, B.6
Odell, J.T.7
-
31
-
-
0031841398
-
Identification of elicitor-induced cytochrome P450s of soybean (Glycine max L.) using differential display of mRNA
-
Schopfer C.R., Ebel J. Identification of elicitor-induced cytochrome P450s of soybean (Glycine max L.) using differential display of mRNA. Mol. Gen. Genet. 258:1998;315-322.
-
(1998)
Mol. Gen. Genet.
, vol.258
, pp. 315-322
-
-
Schopfer, C.R.1
Ebel, J.2
-
32
-
-
0035910557
-
Flavonoid 6-hydroxylase from soybean (Glycine max L.), a novel plant P-450 monooxygenase
-
Latunde-Dada A.O., Cabello-Hurtado F., Czittrich N., Didierjean L., Schopfer C., Hertkorn N., Werck-Reichhart D., Ebel J. Flavonoid 6-hydroxylase from soybean (Glycine max L.), a novel plant P-450 monooxygenase. J. Biol. Chem. 276:2001;1688-1695.
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 1688-1695
-
-
Latunde-Dada, A.O.1
Cabello-Hurtado, F.2
Czittrich, N.3
Didierjean, L.4
Schopfer, C.5
Hertkorn, N.6
Werck-Reichhart, D.7
Ebel, J.8
-
33
-
-
0034813330
-
Flavonoids with epidermal growth factor receptor tyrosine kinase inhibitory activity stimulate PEPT1-mediated cefixime uptake into human intestinal epithelial cells
-
Wenzel U., Kuntz S., Daniel H. Flavonoids with epidermal growth factor receptor tyrosine kinase inhibitory activity stimulate PEPT1-mediated cefixime uptake into human intestinal epithelial cells. J. Pharm. Exp. Ther. 299:2001;1-7.
-
(2001)
J. Pharm. Exp. Ther.
, vol.299
, pp. 1-7
-
-
Wenzel, U.1
Kuntz, S.2
Daniel, H.3
-
34
-
-
0035965253
-
CYP98A3 from Arabidopsis thaliana is a 3′-hydroxylase of phenolic esters, a missing link in the phenylpropanoid pathway
-
Characterisation of the gene coding for the P450 that synthesises chlorogenic acid. This study provides indications that the same P450 is needed for the biosynthesis of lignin monomers and that the 3-hydroxylation step in the phenylpropanoid pathway is catalysed on shikimate or quinate esters. A good example of the hints on gene function that can be obtained from analysis of genomic data.
-
Schoch G., Goepfert S., Morant M., Hehn A., Meyer D., Ullmann P., Werck-Reichhart D. CYP98A3 from Arabidopsis thaliana is a 3′-hydroxylase of phenolic esters, a missing link in the phenylpropanoid pathway. J. Biol. Chem. 276:2001;36566-36574 Characterisation of the gene coding for the P450 that synthesises chlorogenic acid. This study provides indications that the same P450 is needed for the biosynthesis of lignin monomers and that the 3-hydroxylation step in the phenylpropanoid pathway is catalysed on shikimate or quinate esters. A good example of the hints on gene function that can be obtained from analysis of genomic data.
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 36566-36574
-
-
Schoch, G.1
Goepfert, S.2
Morant, M.3
Hehn, A.4
Meyer, D.5
Ullmann, P.6
Werck-Reichhart, D.7
-
35
-
-
0037070631
-
CYP98A6 from Lithospermum erythrorhizon encodes 4-coumaroyl-4′-hydroxyphenyllactic acid 3-hydroxylase involved in rosmarinic acid biosynthesis
-
Matsuno M., Nagatsu A., Ogihara Y., Ellis B.E., Mizukami H. CYP98A6 from Lithospermum erythrorhizon encodes 4-coumaroyl-4′-hydroxyphenyllactic acid 3-hydroxylase involved in rosmarinic acid biosynthesis. FEBS Lett. 514:2002;219-224.
-
(2002)
FEBS Lett.
, vol.514
, pp. 219-224
-
-
Matsuno, M.1
Nagatsu, A.2
Ogihara, Y.3
Ellis, B.E.4
Mizukami, H.5
-
36
-
-
0036852155
-
Differential production of phenylpropanoids in sweet basil (Ocimum basilicum L.) peltate glandular trichomes and leaves is controlled by the activities of specific acyltransferases and hydroxylases
-
Shows that one of the major components of basil flavour, eugenol, is very probably formed like lignin monomers via a shikimate or quinate ester of p-coumaric acid.
-
Gang D., Beuerle T., Ullmann P., Werck-Reichhart D., Pichersky E. Differential production of phenylpropanoids in sweet basil (Ocimum basilicum L.) peltate glandular trichomes and leaves is controlled by the activities of specific acyltransferases and hydroxylases. Plant Physiol. 130:2002;1536-1544 Shows that one of the major components of basil flavour, eugenol, is very probably formed like lignin monomers via a shikimate or quinate ester of p-coumaric acid.
-
(2002)
Plant Physiol.
, vol.130
, pp. 1536-1544
-
-
Gang, D.1
Beuerle, T.2
Ullmann, P.3
Werck-Reichhart, D.4
Pichersky, E.5
-
37
-
-
0036011027
-
The Arabidopsis REF8 gene encodes the 3-hydroxylase of phenylpropanoid metabolism
-
Franke R., Humphreys J.M., Hemm M.R., Denault J.W., Ruegger M.O., Cusumano J.C., Chapple C. The Arabidopsis REF8 gene encodes the 3-hydroxylase of phenylpropanoid metabolism. Plant J. 30:2002;33-45.
-
(2002)
Plant J.
, vol.30
, pp. 33-45
-
-
Franke, R.1
Humphreys, J.M.2
Hemm, M.R.3
Denault, J.W.4
Ruegger, M.O.5
Cusumano, J.C.6
Chapple, C.7
-
38
-
-
0036011028
-
Changes in secondary metabolism and deposition of an unusual lignin in the ref8 mutant of Arabidopsis
-
••], this work demonstrates that 3-hydroxylation of caffeate and all its derivatives proceeds via shikimate or quinate esters in this plant.
-
••], this work demonstrates that 3-hydroxylation of caffeate and all its derivatives proceeds via shikimate or quinate esters in this plant.
-
(2002)
Plant J.
, vol.30
, pp. 47-59
-
-
Franke, R.1
Hemm, M.R.2
Denault, J.W.3
Ruegger, M.O.4
Humphreys, J.M.5
Chapple, C.6
-
39
-
-
0037414824
-
Purification, cloning and properties of an acyltransferase controlling shikimate and quinate ester intermediates in phenylpropanoid metabolism
-
Hoffmann L., Maury S., Martz F., Geoffroy P., Legrand M. Purification, cloning and properties of an acyltransferase controlling shikimate and quinate ester intermediates in phenylpropanoid metabolism. J. Biol. Chem. 278:2003;95-103.
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 95-103
-
-
Hoffmann, L.1
Maury, S.2
Martz, F.3
Geoffroy, P.4
Legrand, M.5
-
40
-
-
0036615409
-
Glucosinolate research in the Arabidopsis era
-
Wittstock U., Halkier B.A. Glucosinolate research in the Arabidopsis era. Trends Plant Sci. 7:2002;263-270.
-
(2002)
Trends Plant Sci.
, vol.7
, pp. 263-270
-
-
Wittstock, U.1
Halkier, B.A.2
-
41
-
-
0034695491
-
Cytochromes P-450 from cassava (Manihot esculenta Crantz) catalyzing the first steps in the biosynthesis of the cyanogenic glucosides linamarin and lotaustralin. Cloning, functional expression in Pichia pastoris, and substrate specificity of the isolated recombinant enzymes
-
One of the rare examples of advanced biotechnology research in crops specific to the Third World.
-
Andersen M.D., Busk P.K., Svendsen I., Møller B.L. Cytochromes P-450 from cassava (Manihot esculenta Crantz) catalyzing the first steps in the biosynthesis of the cyanogenic glucosides linamarin and lotaustralin. Cloning, functional expression in Pichia pastoris, and substrate specificity of the isolated recombinant enzymes. J. Biol. Chem. 275:2000;1966-1975 One of the rare examples of advanced biotechnology research in crops specific to the Third World.
-
(2000)
J. Biol. Chem.
, vol.275
, pp. 1966-1975
-
-
Andersen, M.D.1
Busk, P.K.2
Svendsen, I.3
Møller, B.L.4
-
42
-
-
0033998717
-
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 J.S., Møller B.L. Cloning and expression of cytochrome P450 enzymes catalyzing the conversion of tyrosine to p-hydroxyphenylacetaldoxime in the biosynthesis of cyanogenic glucosides in Triglochin maritima. Plant Physiol. 122:2000;1311-1321.
-
(2000)
Plant Physiol.
, vol.122
, pp. 1311-1321
-
-
Nielsen, J.S.1
Møller, B.L.2
-
43
-
-
0037149532
-
Biochemical ecology: How plants fight dirty
-
Schultz J.C. Biochemical ecology: how plants fight dirty. Nature. 416:2002;267.
-
(2002)
Nature
, vol.416
, pp. 267
-
-
Schultz, J.C.1
-
44
-
-
0035800894
-
Fatty acid hydroperoxide lyase: A plant cytochrome P450 enzyme involved in wound healing and pest resistance
-
Noordermeer M.A., Veldink G.A., Vliegenthart J.F. Fatty acid hydroperoxide lyase: a plant cytochrome P450 enzyme involved in wound healing and pest resistance. Chembiochem. 2:2001;494-504.
-
(2001)
Chembiochem.
, vol.2
, pp. 494-504
-
-
Noordermeer, M.A.1
Veldink, G.A.2
Vliegenthart, J.F.3
-
46
-
-
0036581314
-
Fatty acid-derived signals in plants
-
Weber H. Fatty acid-derived signals in plants. Trends Plant Sci. 7:2002;217-224.
-
(2002)
Trends Plant Sci.
, vol.7
, pp. 217-224
-
-
Weber, H.1
-
47
-
-
0038741782
-
Divinyl ether fatty acid synthesis in late blight-diseased potato leaves
-
Weber H., Chetelat A., Caldelari D., Farmer E.E. Divinyl ether fatty acid synthesis in late blight-diseased potato leaves. Plant Cell. 11:1999;485-494.
-
(1999)
Plant Cell
, vol.11
, pp. 485-494
-
-
Weber, H.1
Chetelat, A.2
Caldelari, D.3
Farmer, E.E.4
-
48
-
-
0035984161
-
A knock-out mutation in allene oxide synthase results in male sterility and defective wound signal transduction in Arabidopsis due to a block in jasmonic acid biosynthesis
-
Park J.H., Halitschke R., Kim H.B., Baldwin I.T., Feldmann K.A., Feyereisen R. A knock-out mutation in allene oxide synthase results in male sterility and defective wound signal transduction in Arabidopsis due to a block in jasmonic acid biosynthesis. Plant J. 31:2002;1-12.
-
(2002)
Plant J.
, vol.31
, pp. 1-12
-
-
Park, J.H.1
Halitschke, R.2
Kim, H.B.3
Baldwin, I.T.4
Feldmann, K.A.5
Feyereisen, R.6
-
49
-
-
0033921659
-
Transgenic Nicotiana tabacum and Arabidopsis thaliana plants overexpressing allene oxide synthase
-
Laudert D., Schaller F., Weiler E.W. Transgenic Nicotiana tabacum and Arabidopsis thaliana plants overexpressing allene oxide synthase. Planta. 211:2000;163-165.
-
(2000)
Planta
, vol.211
, pp. 163-165
-
-
Laudert, D.1
Schaller, F.2
Weiler, E.W.3
-
50
-
-
0032216816
-
C6-volatiles derived from the lipoxygenase pathway induce a subset of defense-related genes
-
Bate N.J., Rothstein S.J. C6-volatiles derived from the lipoxygenase pathway induce a subset of defense-related genes. Plant J. 16:1998;561-569.
-
(1998)
Plant J.
, vol.16
, pp. 561-569
-
-
Bate, N.J.1
Rothstein, S.J.2
-
51
-
-
0034940472
-
Hydroperoxide lyase depletion in transgenic potato plants leads to an increase in aphid performance
-
Demonstrates that the CYP74B hydroperoxide lyase pathway has a direct impact on sucking insect colonisation.
-
Vancanneyt G., Sanz C., Farmaki T., Paneque M., Ortego F., Castanera P., Sanchez-Serrano J.J. Hydroperoxide lyase depletion in transgenic potato plants leads to an increase in aphid performance. Proc. Natl. Acad. Sci. U.S.A. 98:2001;8139-8144 Demonstrates that the CYP74B hydroperoxide lyase pathway has a direct impact on sucking insect colonisation.
-
(2001)
Proc. Natl. Acad. Sci. U.S.A.
, vol.98
, pp. 8139-8144
-
-
Vancanneyt, G.1
Sanz, C.2
Farmaki, T.3
Paneque, M.4
Ortego, F.5
Castanera, P.6
Sanchez-Serrano, J.J.7
-
52
-
-
0035144016
-
Tomato allene oxide synthase and fatty acid hydroperoxide lyase, two cytochrome P450s involved in oxylipin metabolism, are targeted to different membranes of chloroplast envelope
-
Froehlich J.E., Itoh A., Howe G.A. Tomato allene oxide synthase and fatty acid hydroperoxide lyase, two cytochrome P450s involved in oxylipin metabolism, are targeted to different membranes of chloroplast envelope. Plant Physiol. 125:2001;306-317.
-
(2001)
Plant Physiol.
, vol.125
, pp. 306-317
-
-
Froehlich, J.E.1
Itoh, A.2
Howe, G.A.3
-
53
-
-
0034666096
-
Fatty acid 9- and 13-hydroperoxide lyases from cucumber
-
Matsui K., Ujita C., Fujimoto S., Wilkinson J., Hiatt B., Knauf V., Kajiwara T., Feussner I. Fatty acid 9- and 13-hydroperoxide lyases from cucumber. FEBS Lett. 481:2000;183-188.
-
(2000)
FEBS Lett.
, vol.481
, pp. 183-188
-
-
Matsui, K.1
Ujita, C.2
Fujimoto, S.3
Wilkinson, J.4
Hiatt, B.5
Knauf, V.6
Kajiwara, T.7
Feussner, I.8
-
54
-
-
0035864382
-
Biogenesis of volatile aldehydes from fatty acid hydroperoxides: Molecular cloning of a hydroperoxide lyase (CYP74C) with specificity for both the 9- and 13-hydroperoxides of linoleic and linolenic acids
-
Tijet N., Schneider C., Muller B.L., Brash A.R. Biogenesis of volatile aldehydes from fatty acid hydroperoxides: molecular cloning of a hydroperoxide lyase (CYP74C) with specificity for both the 9- and 13-hydroperoxides of linoleic and linolenic acids. Arch. Biochem. Biophys. 386:2001;281-289.
-
(2001)
Arch. Biochem. Biophys.
, vol.386
, pp. 281-289
-
-
Tijet, N.1
Schneider, C.2
Muller, B.L.3
Brash, A.R.4
-
55
-
-
0037195876
-
Identification of a jasmonate-regulated allene oxide synthase that metabolizes 9-hydroperoxides of linoleic and linolenic acids
-
This work shows, unexpectedly, that both allene oxide synthases and hydroperoxide lyases are found in the CYP74D subfamily that seems to have evolved for specific recognition and metabolism of 9-hydroperoxides and specific functions.
-
Itoh A., Schilmiller A.L., McCaig B.C., Howe G.A. Identification of a jasmonate-regulated allene oxide synthase that metabolizes 9-hydroperoxides of linoleic and linolenic acids. J. Biol. Chem. 277:2003;46051-46058 This work shows, unexpectedly, that both allene oxide synthases and hydroperoxide lyases are found in the CYP74D subfamily that seems to have evolved for specific recognition and metabolism of 9-hydroperoxides and specific functions.
-
(2003)
J. Biol. Chem.
, vol.277
, pp. 46051-46058
-
-
Itoh, A.1
Schilmiller, A.L.2
McCaig, B.C.3
Howe, G.A.4
-
56
-
-
0035793589
-
Molecular cloning of a divinyl ether synthase. Identification as a CYP74 cytochrome P-450
-
Itoh A., Howe G.A. Molecular cloning of a divinyl ether synthase. Identification as a CYP74 cytochrome P-450. J. Biol. Chem. 276:2001;3620-3627.
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 3620-3627
-
-
Itoh, A.1
Howe, G.A.2
-
57
-
-
0035798193
-
A pathogen-inducible divinyl ether synthase (CYP74D) from elicitor-treated potato suspension cells
-
Stumpe M., Kandzia R., Gobel C., Rosahl S., Feussner I. A pathogen-inducible divinyl ether synthase (CYP74D) from elicitor-treated potato suspension cells. FEBS Lett. 507:2001;371-376.
-
(2001)
FEBS Lett.
, vol.507
, pp. 371-376
-
-
Stumpe, M.1
Kandzia, R.2
Gobel, C.3
Rosahl, S.4
Feussner, I.5
-
58
-
-
0037026708
-
Oxylipin profiling in pathogen-infected potato leaves
-
Reports a selective activation of the 9-lipoxygenase pathway and accumulation of the derived products during potato non-host and compatible interaction.
-
Göbel C., Feussner I., Hamberg M., Rosahl S. Oxylipin profiling in pathogen-infected potato leaves. Biochim. Biophys. Acta. 584:2002;55-64 Reports a selective activation of the 9-lipoxygenase pathway and accumulation of the derived products during potato non-host and compatible interaction.
-
(2002)
Biochim. Biophys. Acta.
, vol.584
, pp. 55-64
-
-
Göbel, C.1
Feussner, I.2
Hamberg, M.3
Rosahl, S.4
-
59
-
-
0035072835
-
Suppression of a P450 hydroxylase gene in plant trichome glands enhances natural-product-based aphid resistance
-
A very interesting paper that, unexpectedly, shows increased aphid resistance can be achieved via a P450 gene suppression. A nice example of engineering trichome exudate.
-
Wang E., Wang R., DeParasis J., Loughrin J.H., Gan S., Wagner G.J. Suppression of a P450 hydroxylase gene in plant trichome glands enhances natural-product-based aphid resistance. Nat. Biotechnol. 19:2001;371-374 A very interesting paper that, unexpectedly, shows increased aphid resistance can be achieved via a P450 gene suppression. A nice example of engineering trichome exudate.
-
(2001)
Nat. Biotechnol.
, vol.19
, pp. 371-374
-
-
Wang, E.1
Wang, R.2
DeParasis, J.3
Loughrin, J.H.4
Gan, S.5
Wagner, G.J.6
-
60
-
-
0036707552
-
Isolation and characterization of the CYP71D16 trichome-specific promoter from Nicotiana tabacum L
-
Wang E., Gan S., Wagner G.J. Isolation and characterization of the CYP71D16 trichome-specific promoter from Nicotiana tabacum L. J. Exp. Bot. 53:2002;1891-1897.
-
(2002)
J. Exp. Bot.
, vol.53
, pp. 1891-1897
-
-
Wang, E.1
Gan, S.2
Wagner, G.J.3
-
61
-
-
0035883986
-
Cloning, heterologous expression, and functional characterization of 5-epi-aristolochene-1,3-dihydroxylase from tobacco (Nicotiana tabacum)
-
Describes the isolation of elicitor-induced P450 genes in tobacco by a PCR strategy and the characterisation of a P450 that catalyses two sequential hydroxylations at two different positions on 5-epi-aristolochene, apparently without release of the intermediate.
-
Ralston L., Kwon S.T., Schoenbeck M., Ralston J., Schenk D.J., Coates R.M., Chappell J. Cloning, heterologous expression, and functional characterization of 5-epi-aristolochene-1,3-dihydroxylase from tobacco (Nicotiana tabacum). Arch. Biochem. Biophys. 393:2001;222-235 Describes the isolation of elicitor-induced P450 genes in tobacco by a PCR strategy and the characterisation of a P450 that catalyses two sequential hydroxylations at two different positions on 5-epi-aristolochene, apparently without release of the intermediate.
-
(2001)
Arch. Biochem. Biophys.
, vol.393
, pp. 222-235
-
-
Ralston, L.1
Kwon, S.T.2
Schoenbeck, M.3
Ralston, J.4
Schenk, D.J.5
Coates, R.M.6
Chappell, J.7
-
62
-
-
0035991203
-
Plant defense genes associated with quantitative resistance to potato late blight in Solanum phureja × dihaploid S. tuberosum hybrids
-
Trognitz F., Manosalva P., Gysin R., Ninio-Liu D., Simon R., del Herrera M.R., Trognitz B., Ghislain M., Nelson R. Plant defense genes associated with quantitative resistance to potato late blight in Solanum phureja × dihaploid S. tuberosum hybrids. Mol. Plant Microbe Interact. 15:2002;587-597.
-
(2002)
Mol. Plant Microbe Interact.
, vol.15
, pp. 587-597
-
-
Trognitz, F.1
Manosalva, P.2
Gysin, R.3
Ninio-Liu, D.4
Simon, R.5
Del Herrera, M.R.6
Trognitz, B.7
Ghislain, M.8
Nelson, R.9
-
63
-
-
0002970532
-
Biosynthesis of cyanogenic glucosides, cyanolipids, and related compounds
-
Edited by Singh BK. Marcel Dekker Inc New York
-
Møller BL, Seigler D: Biosynthesis of cyanogenic glucosides, cyanolipids, and related compounds. In Plant Amino Acids. Biochemistry and Biotechnology. Edited by Singh BK. Marcel Dekker Inc New York, pp 563-609.
-
Plant Amino Acids. Biochemistry and Biotechnology
, pp. 563-609
-
-
Møller, B.L.1
Seigler, D.2
-
64
-
-
0035823153
-
Resistance to an herbivore through engineered cyanogenic glucoside synthesis
-
Reports the first example of insect-resistant plants obtained by transfer of an entire pathway for synthesis of a complex natural product.
-
Tattersall D.B., Bak S., Jones P.R., Olsen C.E., Nielsen J.K., Hansen M.L., Hoj P.B., Moller B.L. Resistance to an herbivore through engineered cyanogenic glucoside synthesis. Science. 293:2001;1826-1828 Reports the first example of insect-resistant plants obtained by transfer of an entire pathway for synthesis of a complex natural product.
-
(2001)
Science
, vol.293
, pp. 1826-1828
-
-
Tattersall, D.B.1
Bak, S.2
Jones, P.R.3
Olsen, C.E.4
Nielsen, J.K.5
Hansen, M.L.6
Hoj, P.B.7
Moller, B.L.8
-
66
-
-
0036169716
-
Prospects and limitations of phytoremediation for the removal of persistent pesticides in the environment
-
Chaudhry Q., Schroder P., Werck-Reichhart D., Grajek W., Marecik R. Prospects and limitations of phytoremediation for the removal of persistent pesticides in the environment. Environ. Sci. Pollut. Res. Int. 9:2002;4-17.
-
(2002)
Environ. Sci. Pollut. Res. Int.
, vol.9
, pp. 4-17
-
-
Chaudhry, Q.1
Schroder, P.2
Werck-Reichhart, D.3
Grajek, W.4
Marecik, R.5
-
67
-
-
0036166380
-
Phytoremediation of polyaromatic hydrocarbons, anilines and phenols
-
Harvey P.J., Campanella B.F., Castro P.M., Harms H., Lichtfouse E., Schaffner A.R., Smrcek S., Werck-Reichhart D. Phytoremediation of polyaromatic hydrocarbons, anilines and phenols. Environ. Sci. Pollut. Res. Int. 9:2002;29-47.
-
(2002)
Environ. Sci. Pollut. Res. Int.
, vol.9
, pp. 29-47
-
-
Harvey, P.J.1
Campanella, B.F.2
Castro, P.M.3
Harms, H.4
Lichtfouse, E.5
Schaffner, A.R.6
Smrcek, S.7
Werck-Reichhart, D.8
-
68
-
-
0035818858
-
Trichloroethylene oxidative metabolism in plants: The trichloroethanol pathway
-
Shang T.Q., Doty S.L., Wilson A.M., Howald W.N., Gordon M.P. Trichloroethylene oxidative metabolism in plants: the trichloroethanol pathway. Phytochemistry. 58:2001;1055-1065.
-
(2001)
Phytochemistry
, vol.58
, pp. 1055-1065
-
-
Shang, T.Q.1
Doty, S.L.2
Wilson, A.M.3
Howald, W.N.4
Gordon, M.P.5
-
69
-
-
0001382541
-
The chemically inducible plant cytochrome P450 CYP76B1 actively metabolizes phenylureas and other xenobiotics
-
Robineau T., Batard Y., Nedelkina S., Cabello-Hurtado F., LeRet M., Sorokine O., Didierjean L., Werck-Reichhart D. The chemically inducible plant cytochrome P450 CYP76B1 actively metabolizes phenylureas and other xenobiotics. Plant Physiol. 118:1998;1049-1056.
-
(1998)
Plant Physiol.
, vol.118
, pp. 1049-1056
-
-
Robineau, T.1
Batard, Y.2
Nedelkina, S.3
Cabello-Hurtado, F.4
LeRet, M.5
Sorokine, O.6
Didierjean, L.7
Werck-Reichhart, D.8
-
70
-
-
0033574012
-
Expression of a soybean cytochrome P450 monooxygenase cDNA in yeast and tobacco enhances the metabolism of phenylurea herbicides
-
Siminszky B., Corbin F.T., Ward E.R., Fleischmann T.J., Dewey R.E. Expression of a soybean cytochrome P450 monooxygenase cDNA in yeast and tobacco enhances the metabolism of phenylurea herbicides. Proc. Natl. Acad. Sci. U.S.A. 96:1999;1750-1755.
-
(1999)
Proc. Natl. Acad. Sci. U.S.A.
, vol.96
, pp. 1750-1755
-
-
Siminszky, B.1
Corbin, F.T.2
Ward, E.R.3
Fleischmann, T.J.4
Dewey, R.E.5
-
71
-
-
0034459652
-
Molecular cloning of novel cytochrome P450 species induced by chemical treatments in cultured tobacco cells
-
Yamada T., Kambara Y., Imaishi H., Ohkawa H. Molecular cloning of novel cytochrome P450 species induced by chemical treatments in cultured tobacco cells. Pestic. Biochem. Physiol. 68:2000;11-25.
-
(2000)
Pestic. Biochem. Physiol.
, vol.68
, pp. 11-25
-
-
Yamada, T.1
Kambara, Y.2
Imaishi, H.3
Ohkawa, H.4
-
72
-
-
0035215088
-
A general cloning strategy for divergent plant cytochrome P450 genes and its application in Lolium rigidum and Ocimum basilicum
-
Fischer T.C., Klattig J.T., Gierl A. A general cloning strategy for divergent plant cytochrome P450 genes and its application in Lolium rigidum and Ocimum basilicum. Theor. Appl. Genet. 103:2001;1014-1021.
-
(2001)
Theor. Appl. Genet.
, vol.103
, pp. 1014-1021
-
-
Fischer, T.C.1
Klattig, J.T.2
Gierl, A.3
-
73
-
-
0038745725
-
Conservation and diversity of gene families explored using the CODEHOP strategy in higher plants
-
Validation of a new and very efficient method for targeted isolation of P450 genes from various plant species.
-
Morant M., Hehn A., Werck-Reichhart D. Conservation and diversity of gene families explored using the CODEHOP strategy in higher plants. BMC Plant Biol. 2:2002;7 Validation of a new and very efficient method for targeted isolation of P450 genes from various plant species.
-
(2002)
BMC Plant Biol.
, vol.2
, pp. 7
-
-
Morant, M.1
Hehn, A.2
Werck-Reichhart, D.3
-
74
-
-
0028057047
-
Plant expression of a bacterial cytochrome P450 that catalyzes activation of a sulfonylurea pro-herbicide
-
O'Keefe D.P., Tepperman J.M., Dean C., Leto K.J., Erbes D.L., Odell J.T. Plant expression of a bacterial cytochrome P450 that catalyzes activation of a sulfonylurea pro-herbicide. Plant Physiol. 105:1994;473-482.
-
(1994)
Plant Physiol.
, vol.105
, pp. 473-482
-
-
O'Keefe, D.P.1
Tepperman, J.M.2
Dean, C.3
Leto, K.J.4
Erbes, D.L.5
Odell, J.T.6
-
75
-
-
0033197609
-
Negative selection systems for transgenic barley (Hordeum vulgare L.): Comparison of bacterial codA- and cytochrome P450 gene-mediated selection
-
Koprek T., McElroy D., Louwerse J., Williams-Carrier R., Lemaux P.G. Negative selection systems for transgenic barley (Hordeum vulgare L.): comparison of bacterial codA- and cytochrome P450 gene-mediated selection. Plant J. 19:1999;719-726.
-
(1999)
Plant J.
, vol.19
, pp. 719-726
-
-
Koprek, T.1
McElroy, D.2
Louwerse, J.3
Williams-Carrier, R.4
Lemaux, P.G.5
-
76
-
-
0035649032
-
Metabolism of herbicides and other chemicals in human cytochrome P450 species and in transgenic potato plants co-expressing human CYP1A1, CYP2B6 and CYP2C19
-
Inui H., Shiota N., Motoi Y., Ido Y., Inoue T., Kodama T., Ohkawa Y., Ohkawa H. Metabolism of herbicides and other chemicals in human cytochrome P450 species and in transgenic potato plants co-expressing human CYP1A1, CYP2B6 and CYP2C19. J. Pestic. Sci. 26:2001;28-40.
-
(2001)
J. Pestic. Sci.
, vol.26
, pp. 28-40
-
-
Inui, H.1
Shiota, N.2
Motoi, Y.3
Ido, Y.4
Inoue, T.5
Kodama, T.6
Ohkawa, Y.7
Ohkawa, H.8
-
77
-
-
0034296561
-
Expression of human cytochromes P4501A1 and P4501A2 as fused enzymes with yeast NADPH-cytochrome P450 oxidoreductase in transgenic tobacco
-
Shiota N., Kodama S., Inui H., Ohkawa H. Expression of human cytochromes P4501A1 and P4501A2 as fused enzymes with yeast NADPH-cytochrome P450 oxidoreductase in transgenic tobacco. Biosci. Biotechnol. Biochem. 64:2000;2025-2033.
-
(2000)
Biosci. Biotechnol. Biochem.
, vol.64
, pp. 2025-2033
-
-
Shiota, N.1
Kodama, S.2
Inui, H.3
Ohkawa, H.4
-
78
-
-
0034008241
-
Herbicide metabolism and cross-tolerance in transgenic potato plants co-expressing human CYP1A1, CYP2B6 and CYP2C19
-
Inui H., Kodama T., Ohkawa Y., Ohkawa H. Herbicide metabolism and cross-tolerance in transgenic potato plants co-expressing human CYP1A1, CYP2B6 and CYP2C19. Pestic. Biochem. Physiol. 66:2000;116-129.
-
(2000)
Pestic. Biochem. Physiol.
, vol.66
, pp. 116-129
-
-
Inui, H.1
Kodama, T.2
Ohkawa, Y.3
Ohkawa, H.4
-
79
-
-
0035695657
-
Herbicide metabolism and tolerance in the transgenic rice plants expressing human CYP2C9 and CYP2C19
-
Inui H., Shiota N., Ido Y., Inoue T., Hirose S., Kawahigashi H., Ohkawa Y., Ohkawa H. Herbicide metabolism and tolerance in the transgenic rice plants expressing human CYP2C9 and CYP2C19. Pestic. Biochem. Physiol. 71:2001;156-169.
-
(2001)
Pestic. Biochem. Physiol.
, vol.71
, pp. 156-169
-
-
Inui, H.1
Shiota, N.2
Ido, Y.3
Inoue, T.4
Hirose, S.5
Kawahigashi, H.6
Ohkawa, Y.7
Ohkawa, H.8
-
80
-
-
0036738079
-
Engineering herbicide metabolism in tobacco and Arabidopsis with CYP76B1, a cytochrome P450 enzyme from Jerusalem artichoke
-
The first extensive analysis of the gain in herbicide tolerance that can be achieved via heterologous expression of a plant P450 gene.
-
Didierjean L., Gondet L., Perkins R., Lau S.M., Schaller H., O'Keefe D.P., Werck-Reichhart D. Engineering herbicide metabolism in tobacco and Arabidopsis with CYP76B1, a cytochrome P450 enzyme from Jerusalem artichoke. Plant Physiol. 130:2002;179-189 The first extensive analysis of the gain in herbicide tolerance that can be achieved via heterologous expression of a plant P450 gene.
-
(2002)
Plant Physiol.
, vol.130
, pp. 179-189
-
-
Didierjean, L.1
Gondet, L.2
Perkins, R.3
Lau, S.M.4
Schaller, H.5
O'Keefe, D.P.6
Werck-Reichhart, D.7
-
81
-
-
0034612301
-
Enhanced metabolism of halogenated hydrocarbons in transgenic plants containing mammalian cytochrome P450 2E1
-
The first demonstration that the ectopic expression of a P450 gene in higher plants can drive an increased absorption and effective detoxification of a major industrial pollutant.
-
Doty S.L., Shang T.Q., Wilson A.M., Tangen J., Westergreen A.D., Newman L.A., Strand S.E., Gordon M.P. Enhanced metabolism of halogenated hydrocarbons in transgenic plants containing mammalian cytochrome P450 2E1. Proc. Natl. Acad. Sci. U.S.A. 97:2000;6287-6291 The first demonstration that the ectopic expression of a P450 gene in higher plants can drive an increased absorption and effective detoxification of a major industrial pollutant.
-
(2000)
Proc. Natl. Acad. Sci. U.S.A.
, vol.97
, pp. 6287-6291
-
-
Doty, S.L.1
Shang, T.Q.2
Wilson, A.M.3
Tangen, J.4
Westergreen, A.D.5
Newman, L.A.6
Strand, S.E.7
Gordon, M.P.8
-
82
-
-
0035692238
-
Mutations that reduce sinapoylmalate accumulation in Arabidopsis thaliana define loci with diverse roles in phenylpropanoid metabolism
-
Ruegger M., Chapple C. Mutations that reduce sinapoylmalate accumulation in Arabidopsis thaliana define loci with diverse roles in phenylpropanoid metabolism. Genetics. 159:2001;1741-1749.
-
(2001)
Genetics
, vol.159
, pp. 1741-1749
-
-
Ruegger, M.1
Chapple, C.2
-
83
-
-
0032838615
-
Brassinosteroid biosynthesis inhibitors
-
Asami T., Yoshida S. Brassinosteroid biosynthesis inhibitors. Trends Plant Sci. 9:1999;348-353.
-
(1999)
Trends Plant Sci.
, vol.9
, pp. 348-353
-
-
Asami, T.1
Yoshida, S.2
-
84
-
-
0342696170
-
Characterization of brassinazole, a triazole-type brassinosteroid biosynthesis inhibitor
-
Asami T., Min Y.K., Nagata N., Yamagishi K., Takatsuto S., Fujioka S., Murofushi N., Yamaguchi I., Yoshida S. Characterization of brassinazole, a triazole-type brassinosteroid biosynthesis inhibitor. Plant Physiol. 123:2000;93-100.
-
(2000)
Plant Physiol.
, vol.123
, pp. 93-100
-
-
Asami, T.1
Min, Y.K.2
Nagata, N.3
Yamagishi, K.4
Takatsuto, S.5
Fujioka, S.6
Murofushi, N.7
Yamaguchi, I.8
Yoshida, S.9
-
85
-
-
0035854669
-
Selective interaction of triazole derivatives with DWF4, a cytochrome P450 monooxygenase of the brassinosteroid biosynthetic pathway, correlates with brassinosteroid deficiency in planta
-
Asami T., Mizutani M., Fujioka S., Goda H., Min Y.K., Shimada Y., Nakano T., Takatsuto S., Matsuyama T., Nagata N.et al. Selective interaction of triazole derivatives with DWF4, a cytochrome P450 monooxygenase of the brassinosteroid biosynthetic pathway, correlates with brassinosteroid deficiency in planta. J. Biol. Chem. 276:2001;25687-25691.
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 25687-25691
-
-
Asami, T.1
Mizutani, M.2
Fujioka, S.3
Goda, H.4
Min, Y.K.5
Shimada, Y.6
Nakano, T.7
Takatsuto, S.8
Matsuyama, T.9
Nagata, N.10
-
86
-
-
0034741032
-
Obtusifoliol 14α-demethylase (CYP51) antisense Arabidopsis shows slow growth and long life
-
Kushiro M., Nakano T., Sato K., Yamagishi K., Asami T., Nakano A., Takatsuto S., Fujioka S., Ebizuka Y., Yoshida S. Obtusifoliol 14α-demethylase (CYP51) antisense Arabidopsis shows slow growth and long life. Biochem. Biophys. Res. Commun. 285:2001;98-104.
-
(2001)
Biochem. Biophys. Res. Commun.
, vol.285
, pp. 98-104
-
-
Kushiro, M.1
Nakano, T.2
Sato, K.3
Yamagishi, K.4
Asami, T.5
Nakano, A.6
Takatsuto, S.7
Fujioka, S.8
Ebizuka, Y.9
Yoshida, S.10
-
87
-
-
0034922518
-
Overexpression of DWARF4 in the brassinosteroid biosynthetic pathway results in increased vegetative growth and seed yield in Arabidopsis
-
Choe S., Fujioka S., Noguchi T., Takatsuto S., Yoshida S., Feldmann K.A. Overexpression of DWARF4 in the brassinosteroid biosynthetic pathway results in increased vegetative growth and seed yield in Arabidopsis. Plant J. 26:2001;573-582.
-
(2001)
Plant J.
, vol.26
, pp. 573-582
-
-
Choe, S.1
Fujioka, S.2
Noguchi, T.3
Takatsuto, S.4
Yoshida, S.5
Feldmann, K.A.6
-
88
-
-
0347928762
-
Triadimefon, a fungicidal triazole-type P450 inhibitor, induces brassinosteroid deficiency-like phenotypes in plants and binds to DWF4 protein in the brassinosteroid biosynthesis pathway
-
Asami T., Mizutani M., Shimada Y., Kitahata N., Sekimata K., Han S.Y., Fujioka S., Takatsuto S., Sakata K., Yoshida S. Triadimefon, a fungicidal triazole-type P450 inhibitor, induces brassinosteroid deficiency-like phenotypes in plants and binds to DWF4 protein in the brassinosteroid biosynthesis pathway. Biochem. J. 369:2002;71-76.
-
(2002)
Biochem. J.
, vol.369
, pp. 71-76
-
-
Asami, T.1
Mizutani, M.2
Shimada, Y.3
Kitahata, N.4
Sekimata, K.5
Han, S.Y.6
Fujioka, S.7
Takatsuto, S.8
Sakata, K.9
Yoshida, S.10
-
89
-
-
0035859901
-
Functional analysis of the LACERATA gene of Arabidopsis provides evidence for different roles of fatty acid ω-hydroxylation in development
-
Shows that knockout of CYP86A8, which codes for a fatty acid hydroxylase in Arabidopsis, leads to organ fusion, altered epidermis structure and an overall phenotype similar to that obtained by ectopic expression of a fungal cutinase gene.
-
Wellesen K., Durst F., Pinot F., Benveniste I., Nettesheim K., Wisman E., Steiner-Lange S., Saedler H., Yephremov A. Functional analysis of the LACERATA gene of Arabidopsis provides evidence for different roles of fatty acid ω-hydroxylation in development. Proc. Natl. Acad. Sci. U.S.A. 98:2001;9694-9699 Shows that knockout of CYP86A8, which codes for a fatty acid hydroxylase in Arabidopsis, leads to organ fusion, altered epidermis structure and an overall phenotype similar to that obtained by ectopic expression of a fungal cutinase gene.
-
(2001)
Proc. Natl. Acad. Sci. U.S.A.
, vol.98
, pp. 9694-9699
-
-
Wellesen, K.1
Durst, F.2
Pinot, F.3
Benveniste, I.4
Nettesheim, K.5
Wisman, E.6
Steiner-Lange, S.7
Saedler, H.8
Yephremov, A.9
-
90
-
-
0034234633
-
Increasing expression of P450 and P450-reductase proteins from monocots in heterologous systems
-
Shows that codon optimisation near the translation start is critical for efficient P450 protein expression in yeast and plants.
-
Batard Y., Hehn A., Nedelkina S., Schalk M., Pallett K., Schaller H., Werck-Reichhart D. Increasing expression of P450 and P450-reductase proteins from monocots in heterologous systems. Arch. Biochem. Biophys. 379:2000;161-169 Shows that codon optimisation near the translation start is critical for efficient P450 protein expression in yeast and plants.
-
(2000)
Arch. Biochem. Biophys.
, vol.379
, pp. 161-169
-
-
Batard, Y.1
Hehn, A.2
Nedelkina, S.3
Schalk, M.4
Pallett, K.5
Schaller, H.6
Werck-Reichhart, D.7
-
91
-
-
0036525713
-
Protein engineering of oxygenases for biocatalysis
-
A recent update on P450 gene in vitro evolution.
-
Cirino P.C., Arnold F.H. Protein engineering of oxygenases for biocatalysis. Curr. Opin. Chem. Biol. 6:2002;130-135 A recent update on P450 gene in vitro evolution.
-
(2002)
Curr. Opin. Chem. Biol.
, vol.6
, pp. 130-135
-
-
Cirino, P.C.1
Arnold, F.H.2
-
92
-
-
0035478927
-
The 'biodrug' concept: An innovative approach to therapy
-
Describes advantages of genetically engineered microorganisms for the delivery of enzymatic activities to absorption or reaction sites of the metabolites.
-
Blanquet S., Marol-Bonnin S., Beyssac E., Pompon D., Renaud M., Alric M. The 'biodrug' concept: an innovative approach to therapy. Trends Biotechnol. 19:2001;393-400 Describes advantages of genetically engineered microorganisms for the delivery of enzymatic activities to absorption or reaction sites of the metabolites.
-
(2001)
Trends Biotechnol.
, vol.19
, pp. 393-400
-
-
Blanquet, S.1
Marol-Bonnin, S.2
Beyssac, E.3
Pompon, D.4
Renaud, M.5
Alric, M.6
|