-
1
-
-
0017184389
-
A rapid and sensitive method for the quantification of microgram quantities of protein utilizing the principle of protein-dye binding
-
Bradford, M.M., (1976) A rapid and sensitive method for the quantification of microgram quantities of protein utilizing the principle of protein-dye binding. Anal. Biochem. 72, 248-254.
-
(1976)
Anal. Biochem.
, vol.72
, pp. 248-254
-
-
Bradford, M.M.1
-
2
-
-
4544358361
-
Applications and advantages of virus-induced gene silencing for gene function studies in plants
-
Burch-Smith, T.M., Anderson, J.C., Martin, G.B., and, Dinesh-Kumar, S.P., (2004) Applications and advantages of virus-induced gene silencing for gene function studies in plants. Plant J. 39, 734-746.
-
(2004)
Plant J.
, vol.39
, pp. 734-746
-
-
Burch-Smith, T.M.1
Anderson, J.C.2
Martin, G.B.3
Dinesh-Kumar, S.P.4
-
3
-
-
1842430598
-
Co-expression of three MEP pathway genes and geraniol 10-hydroxylase in internal phloem parenchyma of Catharanthus roseus implicates multicellular translocation of intermediates during the biosynthesis of monoterpene indole alkaloids and isoprenoid-drived primary metabolites
-
Burlat, V., Oudin, A., Courtois, M., Rideau, M., and, St-Pierre, B., (2004) Co-expression of three MEP pathway genes and geraniol 10-hydroxylase in internal phloem parenchyma of Catharanthus roseus implicates multicellular translocation of intermediates during the biosynthesis of monoterpene indole alkaloids and isoprenoid-drived primary metabolites. Plant J. 38, 131-141.
-
(2004)
Plant J.
, vol.38
, pp. 131-141
-
-
Burlat, V.1
Oudin, A.2
Courtois, M.3
Rideau, M.4
St-Pierre, B.5
-
4
-
-
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., and, Memelink, J., (2001) Geraniol 10-hydroxylase, a cytochrome P450 enzyme involved in terpenoid indole alkaloid biosynthesis. FEBS Lett. 508, 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
-
5
-
-
84866478822
-
Discovery and functional analysis of monoterpenoid indole alkaloid pathways in plants
-
De Luca, V., Salim, V., Levac, D., Atsumi, S.M., and, Yu, F., (2012) Discovery and functional analysis of monoterpenoid indole alkaloid pathways in plants. Methods Enzymol. 515, 207-229.
-
(2012)
Methods Enzymol.
, vol.515
, pp. 207-229
-
-
De Luca, V.1
Salim, V.2
Levac, D.3
Atsumi, S.M.4
Yu, F.5
-
6
-
-
33847004779
-
Naturally occurring iridoids. A review, part 1
-
Dinda, B., Debnath, S., and, Harigaya, Y., (2007) Naturally occurring iridoids. A review, part 1. Chem. Pharm. Bull. 55, 159-222.
-
(2007)
Chem. Pharm. Bull.
, vol.55
, pp. 159-222
-
-
Dinda, B.1
Debnath, S.2
Harigaya, Y.3
-
7
-
-
79959791464
-
Naturally occurring iridoids and secoiridoids. An updated review, part 4
-
Dinda, B., Debnath, S., and, Banik, R., (2011) Naturally occurring iridoids and secoiridoids. An updated review, part 4. Chem. Pharm. Bull. 59, 803-833.
-
(2011)
Chem. Pharm. Bull.
, vol.59
, pp. 803-833
-
-
Dinda, B.1
Debnath, S.2
Banik, R.3
-
8
-
-
1542758456
-
Virus-induced gene silencing
-
Dinesh-Kumar, S.P., Anandalakshmi, R., Marathe, R., Schiff, M., and, Liu, Y., (2003) Virus-induced gene silencing. Methods Mol. Biol. 236, 287-294.
-
(2003)
Methods Mol. Biol.
, vol.236
, pp. 287-294
-
-
Dinesh-Kumar, S.P.1
Anandalakshmi, R.2
Marathe, R.3
Schiff, M.4
Liu, Y.5
-
9
-
-
34249875679
-
Catharanthus terpenoid indole alkaloids: Biosynthesis and regulation
-
El-Sayed, M., and, Verpoorte, R., (2007) Catharanthus terpenoid indole alkaloids: biosynthesis and regulation. Phytochem. Rev. 6, 277-305.
-
(2007)
Phytochem. Rev.
, vol.6
, pp. 277-305
-
-
El-Sayed, M.1
Verpoorte, R.2
-
10
-
-
84858070612
-
Synthetic biosystems for the production of high-value plant metabolites
-
Facchini, P.J., Bohlmann, J., Covello, P.S., De Luca, V., Mahadevan, R., Page, J.E., Ro, D.K., Sensen, C.W., Storms, R., and, Martin, V.J., (2012) Synthetic biosystems for the production of high-value plant metabolites. Trends Biotechnol. 30, 127-131.
-
(2012)
Trends Biotechnol.
, vol.30
, pp. 127-131
-
-
Facchini, P.J.1
Bohlmann, J.2
Covello, P.S.3
De Luca, V.4
Mahadevan, R.5
Page, J.E.6
Ro, D.K.7
Sensen, C.W.8
Storms, R.9
Martin, V.J.10
-
11
-
-
15444344334
-
Analysis of a chemical plant defense mechanism in grasses
-
et al.
-
Frey, M., Chomet, P., Glawischnig, E., et al. (1997) Analysis of a chemical plant defense mechanism in grasses. Science, 277, 696-699.
-
(1997)
Science
, vol.277
, pp. 696-699
-
-
Frey, M.1
Chomet, P.2
Glawischnig, E.3
-
12
-
-
84877983328
-
Combinatorial biosynthesis of legume natural and rare triterpenoids in engineered yeast
-
Fukushima, E.O., Seki, H., Sawai, S., Suzuki, M., Ohyama, K., Saito, K., and, Muranaka, T., (2013) Combinatorial biosynthesis of legume natural and rare triterpenoids in engineered yeast. Plant Cell Physiol. 54, 740-749.
-
(2013)
Plant Cell Physiol.
, vol.54
, pp. 740-749
-
-
Fukushima, E.O.1
Seki, H.2
Sawai, S.3
Suzuki, M.4
Ohyama, K.5
Saito, K.6
Muranaka, T.7
-
13
-
-
84870570366
-
An alternative route to cyclic terpenes by reductive cyclization in iridoid biosynthesis
-
Geu-Flores, F., Sherden, N.H., Courdavault, V., Burlat, V., Glenn, W.S., Wu, C., Nims, E., Cui, Y., and, O'Connor, S.E., (2012) An alternative route to cyclic terpenes by reductive cyclization in iridoid biosynthesis. Nature, 492, 138-142.
-
(2012)
Nature
, vol.492
, pp. 138-142
-
-
Geu-Flores, F.1
Sherden, N.H.2
Courdavault, V.3
Burlat, V.4
Glenn, W.S.5
Wu, C.6
Nims, E.7
Cui, Y.8
O'Connor, S.E.9
-
14
-
-
79955772476
-
A stereoselective hydroxylation step of alkaloid biosynthesis by a unique cytochrome P450 in Catharanthus roseus
-
Giddings, L.A., Liscombe, D.K., Hamilton, J.P., Childs, K.L., DellaPenna, D., Buell, C.R., and, O'Connor, S.E., (2011) A stereoselective hydroxylation step of alkaloid biosynthesis by a unique cytochrome P450 in Catharanthus roseus. J. Biol. Chem. 286, 16751-16757.
-
(2011)
J. Biol. Chem.
, vol.286
, pp. 16751-16757
-
-
Giddings, L.A.1
Liscombe, D.K.2
Hamilton, J.P.3
Childs, K.L.4
Dellapenna, D.5
Buell, C.R.6
O'Connor, S.E.7
-
15
-
-
0026562884
-
Improved method for high efficiency transformation in intact yeast cells
-
Gietz, D., St. Jean, A., Woods, R.A., and, Schiestl, R.H., (1992) Improved method for high efficiency transformation in intact yeast cells. Nucleic Acids Res. 20, 1425.
-
(1992)
Nucleic Acids Res.
, vol.20
, pp. 1425
-
-
Gietz, D.1
St. Jean, A.2
Woods, R.A.3
Schiestl, R.H.4
-
16
-
-
79951935714
-
The subcellular organization of strictosidine biosynthesis in Catharanthus roseus epidermis highlights several trans-tonoplast translocations of intermediate metabolites
-
Guirimand, G., Guihur, A., Ginis, O., Poutrain, P., Héricourt, F., Oudin, A., Lanoue, A., St-Pierre, B., Burlat, V., and, Courdavault, V., (2011) The subcellular organization of strictosidine biosynthesis in Catharanthus roseus epidermis highlights several trans-tonoplast translocations of intermediate metabolites. FEBS J. 278, 749-763.
-
(2011)
FEBS J.
, vol.278
, pp. 749-763
-
-
Guirimand, G.1
Guihur, A.2
Ginis, O.3
Poutrain, P.4
Héricourt, F.5
Oudin, A.6
Lanoue, A.7
St-Pierre, B.8
Burlat, V.9
Courdavault, V.10
-
17
-
-
1642263128
-
The Catharanthus alkaloids: Pharmacognosy and biotechnology
-
van der Heijden, R., Jacobs, D.I., Snoeijer, W., Hallard, D., and, Verpoorte, R., (2004) The Catharanthus alkaloids: pharmacognosy and biotechnology. Curr. Med. Chem. 11, 607-628.
-
(2004)
Curr. Med. Chem.
, vol.11
, pp. 607-628
-
-
Van Der Heijden, R.1
Jacobs, D.I.2
Snoeijer, W.3
Hallard, D.4
Verpoorte, R.5
-
19
-
-
0026027647
-
Acyclic monoterpene primary alcohol:NADP+ oxidoreductase of Rauwolfia serpentina cells: The key enzyme in biosynthesis of monoterpene alcohols
-
Ikeda, H., Esaki, N., Nakai, S., Hashimoto, K., Uesato, S., Soda, K., and, Fujita, T., (1991) Acyclic monoterpene primary alcohol:NADP+ oxidoreductase of Rauwolfia serpentina cells: the key enzyme in biosynthesis of monoterpene alcohols. J. Biochem. 109, 341-347.
-
(1991)
J. Biochem.
, vol.109
, pp. 341-347
-
-
Ikeda, H.1
Esaki, N.2
Nakai, S.3
Hashimoto, K.4
Uesato, S.5
Soda, K.6
Fujita, T.7
-
20
-
-
0034490132
-
Indole alkaloid biosynthesis in Catharanthus roseus: New enzyme activities and identification of cytochrome P450 CYP72A1 as secologanin synthase
-
Irmler, S., Schröder, G., St-Pierre, B., Crouch, N.P., Hotze, M., Schmidt, J., Strack, D., Matern, U., and, Schröder, J., (2000) Indole alkaloid biosynthesis in Catharanthus roseus: new enzyme activities and identification of cytochrome P450 CYP72A1 as secologanin synthase. Plant J. 24, 797-804.
-
(2000)
Plant J.
, vol.24
, pp. 797-804
-
-
Irmler, S.1
Schröder, G.2
St-Pierre, B.3
Crouch, N.P.4
Hotze, M.5
Schmidt, J.6
Strack, D.7
Matern, U.8
Schröder, J.9
-
21
-
-
0033167145
-
Flavonoid hydroxylase from Catharanthus roseus: CDNA, heterologous expression, enzyme properties and cell-type specific expression in plants
-
Kaltenbach, M., Schröder, G., Schmelzer, E., Lutz, V., and, Schröder, J., (1999) Flavonoid hydroxylase from Catharanthus roseus: cDNA, heterologous expression, enzyme properties and cell-type specific expression in plants. Plant J. 19, 183-193.
-
(1999)
Plant J.
, vol.19
, pp. 183-193
-
-
Kaltenbach, M.1
Schröder, G.2
Schmelzer, E.3
Lutz, V.4
Schröder, J.5
-
22
-
-
0035839086
-
7-deoxyloganin 7-hydroxylase in Lonicera japonica cell cultures
-
Katano, N., Yamamoto, H., Iio, R., and, Inoue, K., (2001) 7-deoxyloganin 7-hydroxylase in Lonicera japonica cell cultures. Phytochemistry, 58, 53-58.
-
(2001)
Phytochemistry
, vol.58
, pp. 53-58
-
-
Katano, N.1
Yamamoto, H.2
Iio, R.3
Inoue, K.4
-
23
-
-
85010187058
-
Iridoid glucosides from Lonicera japonica THUNB
-
Kawai, H., Kuroyanagi, M., and, Ueno, A., (1988) Iridoid glucosides from Lonicera japonica THUNB. Chem. Pharm. Bull. 36, 3664-3666.
-
(1988)
Chem. Pharm. Bull.
, vol.36
, pp. 3664-3666
-
-
Kawai, H.1
Kuroyanagi, M.2
Ueno, A.3
-
24
-
-
80052917677
-
A virus-induced gene silencing approach to understanding alkaloid metabolism in Catharanthus roseus
-
Liscombe, D., and, O'Connor, S.E., (2011) A virus-induced gene silencing approach to understanding alkaloid metabolism in Catharanthus roseus. Phytochemistry, 72, 1969-1977.
-
(2011)
Phytochemistry
, vol.72
, pp. 1969-1977
-
-
Liscombe, D.1
O'Connor, S.E.2
-
25
-
-
0015919630
-
S-Adenosyl-l-methionine:loganic acid methyltransferase
-
Madyastha, K.M., Guarnaccia, R., Baxter, C., and, Coscia, C.J., (1973) S-Adenosyl-l-methionine:loganic acid methyltransferase. J. Biol. Chem. 248, 2497-2501.
-
(1973)
J. Biol. Chem.
, vol.248
, pp. 2497-2501
-
-
Madyastha, K.M.1
Guarnaccia, R.2
Baxter, C.3
Coscia, C.J.4
-
26
-
-
77952516353
-
Diversification of P450 genes during land plant evolution
-
Mizutani, M., and, Ohta, D., (2010) Diversification of P450 genes during land plant evolution. Annu. Rev. Plant Biol. 61, 291-315.
-
(2010)
Annu. Rev. Plant Biol.
, vol.61
, pp. 291-315
-
-
Mizutani, M.1
Ohta, D.2
-
27
-
-
48249155450
-
The leaf epidermome of Catharanthus roseus reveals its biochemical specialization
-
Murata, J., Roepke, J., Gordon, H., and, De Luca, V., (2008) The leaf epidermome of Catharanthus roseus reveals its biochemical specialization. Plant Cell, 20, 524-542.
-
(2008)
Plant Cell
, vol.20
, pp. 524-542
-
-
Murata, J.1
Roepke, J.2
Gordon, H.3
De Luca, V.4
-
28
-
-
33746520558
-
Chemistry and biology of monoterpene indole alkaloid biosynthesis
-
O'Connor, S.E., and, Maresh, J.J., (2006) Chemistry and biology of monoterpene indole alkaloid biosynthesis. Nat. Prod. Rep. 23, 532-547.
-
(2006)
Nat. Prod. Rep.
, vol.23
, pp. 532-547
-
-
O'Connor, S.E.1
Maresh, J.J.2
-
29
-
-
34249874591
-
The iridoid pathway in Catharanthus roseus alkaloid biosynthesis
-
Oudin, A., Courtois, M., Rideau, M., and, Clastre, M., (2007) The iridoid pathway in Catharanthus roseus alkaloid biosynthesis. Phytochem. Rev. 6, 259-276.
-
(2007)
Phytochem. Rev.
, vol.6
, pp. 259-276
-
-
Oudin, A.1
Courtois, M.2
Rideau, M.3
Clastre, M.4
-
30
-
-
33747699127
-
Lonicera implexa leaves bearing naturally laid eggs of the specialist herbivore Euphydryas aurinia have dramatically greater concentrations of iridoid glycosides than other leaves
-
Peñuelas, J., Sardans, J., Stefanescu, C., Parella, T., and, Filella, I., (2006) Lonicera implexa leaves bearing naturally laid eggs of the specialist herbivore Euphydryas aurinia have dramatically greater concentrations of iridoid glycosides than other leaves. J. Chem. Ecol. 32, 1925-1933.
-
(2006)
J. Chem. Ecol.
, vol.32
, pp. 1925-1933
-
-
Peñuelas, J.1
Sardans, J.2
Stefanescu, C.3
Parella, T.4
Filella, I.5
-
31
-
-
33645822295
-
Isolation and identification of radical scavengers in olive tree (Olea europaea) wood
-
Pérez-Bonilla, M., Salido, S., van Beek, T.A., Linares-Palomino, P.J., Altarejos, J., Nogueras, M., and, Sánchez, A., (2006) Isolation and identification of radical scavengers in olive tree (Olea europaea) wood. J. Chromatogr. A 1112, 311-318.
-
(2006)
J. Chromatogr. A
, vol.1112
, pp. 311-318
-
-
Pérez-Bonilla, M.1
Salido, S.2
Van Beek, T.A.3
Linares-Palomino, P.J.4
Altarejos, J.5
Nogueras, M.6
Sánchez, A.7
-
32
-
-
0029776005
-
Yeast expression of animal and plant P450s in optimized redox environments
-
Pompon, D., Louerat, B., Bronine, A., and, Urban, P., (1996) Yeast expression of animal and plant P450s in optimized redox environments. Methods Enzymol. 272, 51-64.
-
(1996)
Methods Enzymol.
, vol.272
, pp. 51-64
-
-
Pompon, D.1
Louerat, B.2
Bronine, A.3
Urban, P.4
-
33
-
-
0036918780
-
Cloning, functional expression, and subcellular localization of multiple NADPH-cytochrome P450 reductases from hybrid poplar
-
Ro, D.K., Ehlting, J., and, Douglas, C.J., (2002) Cloning, functional expression, and subcellular localization of multiple NADPH-cytochrome P450 reductases from hybrid poplar. Plant Physiol. 130, 1837-1851.
-
(2002)
Plant Physiol.
, vol.130
, pp. 1837-1851
-
-
Ro, D.K.1
Ehlting, J.2
Douglas, C.J.3
-
34
-
-
57049089897
-
Induction of multiple pleiotropic drug resistance genes in yeast engineered to produce an increased level of anti-malarial drug precursor, artemisinic acid
-
Ro, D.K., Ouellet, M., Paradise, E.M., Burd, H., Eng, D., Paddon, C.J., Newman, J.D., and, Keasling, J.D., (2008) Induction of multiple pleiotropic drug resistance genes in yeast engineered to produce an increased level of anti-malarial drug precursor, artemisinic acid. BMC Technol. 8, 83.
-
(2008)
BMC Technol.
, vol.8
, pp. 83
-
-
Ro, D.K.1
Ouellet, M.2
Paradise, E.M.3
Burd, H.4
Eng, D.5
Paddon, C.J.6
Newman, J.D.7
Keasling, J.D.8
-
35
-
-
77956985981
-
Vinca drug components accumulate exclusively in leaf exudates of Madagascar periwinkle
-
Roepke, J., Salim, V., Wu, M., Thamm, A.M., Murata, J., Ploss, K., Boland, W., and, De Luca, V., (2010) Vinca drug components accumulate exclusively in leaf exudates of Madagascar periwinkle. Proc. Natl Acad. Sci. USA 107, 15287-15292.
-
(2010)
Proc. Natl Acad. Sci. USA
, vol.107
, pp. 15287-15292
-
-
Roepke, J.1
Salim, V.2
Wu, M.3
Thamm, A.M.4
Murata, J.5
Ploss, K.6
Boland, W.7
De Luca, V.8
-
36
-
-
84881012790
-
Towards complete elucidation of monoterpene indole alkaloid biosynthesis pathway: Catharanthus roseus as a pioneer system
-
Salim, V., and, De Luca, V., (2013) Towards complete elucidation of monoterpene indole alkaloid biosynthesis pathway: Catharanthus roseus as a pioneer system. Adv. Bot. Res. 68, 1-37.
-
(2013)
Adv. Bot. Res.
, vol.68
, pp. 1-37
-
-
Salim, V.1
De Luca, V.2
-
37
-
-
0142036457
-
Light-induced cytochrome P450-dependent enzyme in indole alkaloid biosynthesis: Tabersonine 16-hydroxylase
-
Schröder, G., Unterbusch, E., Kaltenbach, M., Schmidt, J., Strack, D., De Luca, V., and, Schröder, J., (1999) Light-induced cytochrome P450-dependent enzyme in indole alkaloid biosynthesis: tabersonine 16-hydroxylase. FEBS Lett. 458, 97-102.
-
(1999)
FEBS Lett.
, vol.458
, pp. 97-102
-
-
Schröder, G.1
Unterbusch, E.2
Kaltenbach, M.3
Schmidt, J.4
Strack, D.5
De Luca, V.6
Schröder, J.7
-
38
-
-
84855180697
-
Triterpene functional genomics in licorice for identification of CYP72A154 involved in the biosynthesis of glycyrrhizin
-
et al.
-
Seki, H., Sawai, S., Ohyama, K., et al. (2011) Triterpene functional genomics in licorice for identification of CYP72A154 involved in the biosynthesis of glycyrrhizin. Plant Cell, 23, 4112-4123.
-
(2011)
Plant Cell
, vol.23
, pp. 4112-4123
-
-
Seki, H.1
Sawai, S.2
Ohyama, K.3
-
39
-
-
84871290284
-
Characterization of the plastidial geraniol synthase from Madagascar periwinkle which initiates the monoterpenoid branch of the alkaloid pathway in internal phloem associated parenchyma
-
et al.
-
Simkin, A.J., Miettinen, K., Claudel, P., et al. (2013) Characterization of the plastidial geraniol synthase from Madagascar periwinkle which initiates the monoterpenoid branch of the alkaloid pathway in internal phloem associated parenchyma. Phytochemistry, 85, 36-43.
-
(2013)
Phytochemistry
, vol.85
, pp. 36-43
-
-
Simkin, A.J.1
Miettinen, K.2
Claudel, P.3
-
40
-
-
79957613599
-
MEGA5: Molecular evolutionary genetics analysis using maximum likelihood, evolutionary distance, and maximum parsimony methods
-
Tamura, K., Peterson, D., Peterson, N., Stecher, G., Nei, M., and, Kumar, S., (2011) MEGA5: molecular evolutionary genetics analysis using maximum likelihood, evolutionary distance, and maximum parsimony methods. Mol. Biol. Evol. 28, 2731-2739.
-
(2011)
Mol. Biol. Evol.
, vol.28
, pp. 2731-2739
-
-
Tamura, K.1
Peterson, D.2
Peterson, N.3
Stecher, G.4
Nei, M.5
Kumar, S.6
-
41
-
-
0027968068
-
CLUSTALW: Improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice
-
Thompson, J.D., Higgins, D.G., and, Gibson, T.J., (1994) CLUSTALW: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice. Nucleic Acids Res. 22, 4673-4680.
-
(1994)
Nucleic Acids Res.
, vol.22
, pp. 4673-4680
-
-
Thompson, J.D.1
Higgins, D.G.2
Gibson, T.J.3
-
42
-
-
0004171523
-
Biosynthesis of iridoid glucosides in Galium mollugo, G. Spurium var. Echinospermon and Deutzia crenata. Intermediacy of deoxyloganic acid, loganin, and iridodial glucoside
-
Uesato, S., Miyauchi, M., Itoh, H., and, Inouye, H., (1986) Biosynthesis of iridoid glucosides in Galium mollugo, G. spurium var. Echinospermon and Deutzia crenata. Intermediacy of deoxyloganic acid, loganin, and iridodial glucoside. Phytochemistry, 25, 2515-2521.
-
(1986)
Phytochemistry
, vol.25
, pp. 2515-2521
-
-
Uesato, S.1
Miyauchi, M.2
Itoh, H.3
Inouye, H.4
-
43
-
-
84879541446
-
Transcriptome analysis based on next-generation sequencing of non-model plants producing specialized metabolites of biotechnological interest
-
Xiao, M., Zhang, Y., Chen, X., et al,. (2013) Transcriptome analysis based on next-generation sequencing of non-model plants producing specialized metabolites of biotechnological interest. J. Biotechnol. 166, 122-134.
-
(2013)
J. Biotechnol.
, vol.166
, pp. 122-134
-
-
Xiao, M.1
Zhang, Y.2
Chen, X.3
-
44
-
-
0344629263
-
Transformation of loganin and 7-deoxyloganin into secologanin by Lonicera japonica cell suspension cultures
-
Yamamoto, H., Katano, N., Ooi, A., and, Inoue, K., (1999) Transformation of loganin and 7-deoxyloganin into secologanin by Lonicera japonica cell suspension cultures. Phytochemistry, 50, 417-422.
-
(1999)
Phytochemistry
, vol.50
, pp. 417-422
-
-
Yamamoto, H.1
Katano, N.2
Ooi, A.3
Inoue, K.4
-
45
-
-
0033977809
-
Secologanin synthase which catalyzes the oxidative cleavage of loganin into secologanin is a cytochrome P450
-
Yamamoto, H., Katano, N., Ooi, A., and, Inoue, K., (2000) Secologanin synthase which catalyzes the oxidative cleavage of loganin into secologanin is a cytochrome P450. Phytochemistry, 53, 7-12.
-
(2000)
Phytochemistry
, vol.53
, pp. 7-12
-
-
Yamamoto, H.1
Katano, N.2
Ooi, A.3
Inoue, K.4
|