메뉴 건너뛰기




Volumn 30, Issue 2, 2013, Pages 97-109

A lignan O-methyltransferase catalyzing the regioselective methylation of matairesinol in Carthamus tinctorius

Author keywords

Carthamus tinctorius; Lignan; Matairesinol; O methyltransferase; Regioselective methylation

Indexed keywords


EID: 84881033781     PISSN: 13424580     EISSN: 13476114     Source Type: Journal    
DOI: 10.5511/plantbiotechnology.12.1230a     Document Type: Article
Times cited : (20)

References (68)
  • 2
    • 32944457064 scopus 로고    scopus 로고
    • Identification of arctigenin as an antitumor agent having the ability to eliminate the tolerance of cancer cells to nutrient starvation
    • Awale S, Lu J, Kalauni SK, Kurashima Y, Tezuka Y, Kadota S, Esumi H (2006) Identification of arctigenin as an antitumor agent having the ability to eliminate the tolerance of cancer cells to nutrient starvation. Cancer Res 66: 1751-1757
    • (2006) Cancer Res , vol.66 , pp. 1751-1757
    • Awale, S.1    Lu, J.2    Kalauni, S.K.3    Kurashima, Y.4    Tezuka, Y.5    Kadota, S.6    Esumi, H.7
  • 3
    • 0037049272 scopus 로고    scopus 로고
    • Hemisynthesis of all the O-monomethylated analogues of quercetin including the major metabolites, through selective protection of phenolic functions
    • Bouktaib M, Lebrun S, Atmani A, Rolando C (2002) Hemisynthesis of all the O-monomethylated analogues of quercetin including the major metabolites, through selective protection of phenolic functions. Tetrahedron 58: 10001-10009
    • (2002) Tetrahedron , vol.58 , pp. 10001-10009
    • Bouktaib, M.1    Lebrun, S.2    Atmani, A.3    Rolando, C.4
  • 4
    • 0026409291 scopus 로고
    • CDNA cloning, sequence analysis and seasonal expression of lignin-bispecifc cafeic acid/5-hydroxyferulic acid O-methyltransferase of aspen
    • Bugos RC, Chiang VLC, Campbell WH (1991) CDNA cloning, sequence analysis and seasonal expression of lignin-bispecifc cafeic acid/5-hydroxyferulic acid O-methyltransferase of aspen. Plant Mol Biol 17: 1203-1215
    • (1991) Plant Mol Biol , vol.17 , pp. 1203-1215
    • Bugos, R.C.1    Chiang, V.L.C.2    Campbell, W.H.3
  • 6
    • 0000362615 scopus 로고    scopus 로고
    • Structural elucidation of three dibenzyl-γ-butyrolactone type lignans isolated from taiwania (Taiwania cryptomerioides Hayata) heartwood: 7-oxohinokinin, sventenin and arctigenin
    • Chang S-T, Wang S-Y, Su Y-C, Kuo Y-H (1999) Structural elucidation of three dibenzyl-γ-butyrolactone type lignans isolated from taiwania (Taiwania cryptomerioides Hayata) heartwood: 7-oxohinokinin, sventenin and arctigenin. Q Jour Chin For 32: 121-129
    • (1999) Q Jour Chin For , vol.32 , pp. 121-129
    • Chang, S.-T.1    Wang, S.-Y.2    Su, Y.-C.3    Kuo, Y.-H.4
  • 8
    • 4143102621 scopus 로고    scopus 로고
    • Arctigenin, a phenylpropanoid dibenzylbutyrolactone lignan, inhibits MAP kinases and AP-1 activation via potent MKK inhibition: The role in TNF-α inhibition
    • Cho MK, Jang Y P, Kim YC, Kim SG (2004) Arctigenin, a phenylpropanoid dibenzylbutyrolactone lignan, inhibits MAP kinases and AP-1 activation via potent MKK inhibition: the role in TNF-α inhibition. Int Immunopharmacol 4: 1419-1429
    • (2004) Int Immunopharmacol , vol.4 , pp. 1419-1429
    • Cho, M.K.1    Jang, Y.P.2    Kim, Y.C.3    Kim, S.G.4
  • 9
    • 0001438984 scopus 로고
    • Biosynthesis of lignans
    • Structure elucidation (part B). (Atta-ur-Rahman, ed) Elsevier, Amsterdam
    • Dewick PM (1989) Biosynthesis of lignans. In Studies in natural products chemistry, vol 5. Structure elucidation (part B). (Atta-ur-Rahman, ed) Elsevier, Amsterdam, pp 459-503
    • (1989) Studies In Natural Products Chemistry , vol.5 , pp. 459-503
    • Dewick, P.M.1
  • 10
    • 0029825803 scopus 로고    scopus 로고
    • (+)-Pinoresinol/(+)-lariciresinol reductase from Forsythia intermedia. Protein purifcation, cDNA cloning, heterologous expression and comparison to isofavone reductase
    • Dinkova-Kostova AT, Gang DR, Davin LB, Bedgar DL, Chu A, Lewis NG (1996) (+)-Pinoresinol/(+)-lariciresinol reductase from Forsythia intermedia. Protein purifcation, cDNA cloning, heterologous expression and comparison to isofavone reductase. J Biol Chem 271: 29473-29482
    • (1996) J Biol Chem , vol.271 , pp. 29473-29482
    • Dinkova-Kostova, A.T.1    Gang, D.R.2    Davin, L.B.3    Bedgar, D.L.4    Chu, A.5    Lewis, N.G.6
  • 11
    • 77955709841 scopus 로고    scopus 로고
    • Two O-methyltransferases involved in the biosynthesis of methoxypyrazines: Grape-derived aroma compounds important to wine favour
    • Dunlevy JD, Soole KL, Perkins MV, Dennis EG, Keyzers RA, Kalua CM, Boss PK (2010) Two O-methyltransferases involved in the biosynthesis of methoxypyrazines: grape-derived aroma compounds important to wine favour. Plant Mol Biol 74: 77-89
    • (2010) Plant Mol Biol , vol.74 , pp. 77-89
    • Dunlevy, J.D.1    Soole, K.L.2    Perkins, M.V.3    Dennis, E.G.4    Keyzers, R.A.5    Kalua, C.M.6    Boss, P.K.7
  • 12
    • 0001541240 scopus 로고
    • Phenolic and Terpenoid Heartwood Constituents of Libocedrus yateensis
    • Erdtman H, Harmatha J (1979) Phenolic and Terpenoid Heartwood Constituents of Libocedrus yateensis. Phytochemistry 18: 1495-1500
    • (1979) Phytochemistry , vol.18 , pp. 1495-1500
    • Erdtman, H.1    Harmatha, J.2
  • 13
    • 33745683964 scopus 로고    scopus 로고
    • Lignans from Saussurea conica and their NO production suppressing activity
    • Fan C-Q, Zhu X-Z, Zhan Z-J, Ji X-Q, Li H, Yue J-M (2006) Lignans from Saussurea conica and their NO production suppressing activity. Planta Med 72: 590-595
    • (2006) Planta Med , vol.72 , pp. 590-595
    • Fan, C.-Q.1    Zhu, X.-Z.2    Zhan, Z.-J.3    Ji, X.-Q.4    Li, H.5    Yue, J.-M.6
  • 14
    • 34247403338 scopus 로고    scopus 로고
    • Knockdown of berberine bridge enzyme by RNAi accumulates (S)-reticuline and activates a silent pathway in cultured California poppy cells
    • Fujii N, Inui T, Iwasa K, Morishige T, Sato F (2007) Knockdown of berberine bridge enzyme by RNAi accumulates (S)-reticuline and activates a silent pathway in cultured California poppy cells. Transgenic Res 16: 363-375
    • (2007) Transgenic Res , vol.16 , pp. 363-375
    • Fujii, N.1    Inui, T.2    Iwasa, K.3    Morishige, T.4    Sato, F.5
  • 15
    • 0026658155 scopus 로고
    • Studies on the Chinese Crude Drug "Luoshiteng" (II) On the Biologically Active Components in the Stem Part of Luoshiteng Originating from Trachelospermum jasminoides
    • Fujimoto T, Nose M, Takeda T, Ogihara Y, Nishibe S, Minami M (1992) Studies on the Chinese Crude Drug "Luoshiteng" (II) On the Biologically Active Components in the Stem Part of Luoshiteng Originating from Trachelospermum jasminoides. Shoyakugaku Zasshi 46: 224-229
    • (1992) Shoyakugaku Zasshi , vol.46 , pp. 224-229
    • Fujimoto, T.1    Nose, M.2    Takeda, T.3    Ogihara, Y.4    Nishibe, S.5    Minami, M.6
  • 17
    • 0002051540 scopus 로고    scopus 로고
    • Bioedit: A user friendly biological sequence alignment editor and analysis program for Windows 95/98/NT
    • Hall TA (1999) Bioedit: a user friendly biological sequence alignment editor and analysis program for Windows 95/98/NT. Nucl Acids Symp Ser 41: 95-98
    • (1999) Nucl Acids Symp Ser , vol.41 , pp. 95-98
    • Hall, T.A.1
  • 18
    • 4544321383 scopus 로고
    • Das Lignanglykosid Arctiin als chemotaxonomisches Merkmal in der Familie der Compositae
    • Hänsel von R, Schulz H, Leuckert C (1964) Das Lignanglykosid Arctiin als chemotaxonomisches Merkmal in der Familie der Compositae. Z Naturforsch B 19b: 727-734
    • (1964) Z Naturforsch B , vol.19 , pp. 727-734
    • von Hänsel, R.1    Schulz, H.2    Leuckert, C.3
  • 19
    • 23844550925 scopus 로고    scopus 로고
    • Biological activities of lignans and stilbenoids associated with plant-insect chemical interactions
    • Harmatha J, Dinan L (2003) Biological activities of lignans and stilbenoids associated with plant-insect chemical interactions. Phytochem Rev 2: 321-330
    • (2003) Phytochem Rev , vol.2 , pp. 321-330
    • Harmatha, J.1    Dinan, L.2
  • 20
    • 31344444146 scopus 로고    scopus 로고
    • Isolation and Identifcation of Potent Stimulatory Allelopathic Substances Exuded from Germinating Burdock (Arctium lappa) Seeds
    • Higashinakasu K, Yamada K, Shigemori H, Hasegawa K (2005) Isolation and Identifcation of Potent Stimulatory Allelopathic Substances Exuded from Germinating Burdock (Arctium lappa) Seeds. Heterocycles 65: 1431-1437
    • (2005) Heterocycles , vol.65 , pp. 1431-1437
    • Higashinakasu, K.1    Yamada, K.2    Shigemori, H.3    Hasegawa, K.4
  • 22
    • 0031882371 scopus 로고    scopus 로고
    • Plant O-methyltransferases: Molecular analysis, common signature and classifcation
    • Ibrahim RK, Bruneau A, Bantignies B (1998) Plant O-methyltransferases: molecular analysis, common signature and classifcation. Plant Mol Biol 36: 1-10
    • (1998) Plant Mol Biol , vol.36 , pp. 1-10
    • Ibrahim, R.K.1    Bruneau, A.2    Bantignies, B.3
  • 24
    • 0032126760 scopus 로고    scopus 로고
    • Conserved sequence motifs in plant S- adenosyl-l-methionine-dependent methyltransferases
    • Joshi C P, Chiang VL (1998) Conserved sequence motifs in plant S- adenosyl-l-methionine-dependent methyltransferases. Plant Mol Biol 37: 663-674
    • (1998) Plant Mol Biol , vol.37 , pp. 663-674
    • Joshi, C.P.1    Chiang, V.L.2
  • 25
    • 0001000967 scopus 로고    scopus 로고
    • Antioxidative Activity of Phenolic Compounds in Roasted safower (Carthamus tinctorius L.) Seeds
    • Kang G-H, Chang E-J, Choi S-W (1999) Antioxidative Activity of Phenolic Compounds in Roasted safower (Carthamus tinctorius L.) Seeds. J Food Sci Nutr 4: 221-225
    • (1999) J Food Sci Nutr , vol.4 , pp. 221-225
    • Kang, G.-H.1    Chang, E.-J.2    Choi, S.-W.3
  • 26
    • 39149122828 scopus 로고    scopus 로고
    • Anti-infammatory activity of arctigenin from Forsythiae Fructus
    • Kang HS, Lee JY, Kim CJ (2008) Anti-infammatory activity of arctigenin from Forsythiae Fructus. J Ethnopharmacol 116: 305-312
    • (2008) J Ethnopharmacol , vol.116 , pp. 305-312
    • Kang, H.S.1    Lee, J.Y.2    Kim, C.J.3
  • 27
    • 13744252890 scopus 로고    scopus 로고
    • MAFFT version 5: Improvement in accuracy of multiple sequence alignment
    • Katoh K, Kuma K, Toh H, Miyata T (2005) MAFFT version 5: improvement in accuracy of multiple sequence alignment. Nucleic Acids Res 33: 511-518
    • (2005) Nucleic Acids Res , vol.33 , pp. 511-518
    • Katoh, K.1    Kuma, K.2    Toh, H.3    Miyata, T.4
  • 28
    • 2142768713 scopus 로고    scopus 로고
    • 4-induced toxicity in primary cultured rat hepatocytes
    • Kim SH, Jang YP, Sung SH, Kim CJ, Kim JW, Kim YC (2003) Hepatoprotective dibenzylbutyrolactone lignans of Torreya nucifera against CCl4-induced toxicity in primary cultured rat hepatocytes. Biol Pharm Bull 26: 1202-1205
    • (2003) Biol Pharm Bull , vol.26 , pp. 1202-1205
    • Kim, S.H.1    Jang, Y.P.2    Sung, S.H.3    Kim, C.J.4    Kim, J.W.5    Kim, Y.C.6
  • 30
    • 0141571275 scopus 로고    scopus 로고
    • β-Peltatin 6-O-methyltransferase from suspension cultures of Linum nodiforum
    • Kranz K, Petersen M (2003) β-Peltatin 6-O-methyltransferase from suspension cultures of Linum nodiforum. Phytochemistry 64: 453-458
    • (2003) Phytochemistry , vol.64 , pp. 453-458
    • Kranz, K.1    Petersen, M.2
  • 31
    • 0034927211 scopus 로고    scopus 로고
    • Te last step of syringyl monolignol biosynthesis in angiosperms is regulated by a novel gene encoding sinapyl alcohol dehydrogenase
    • Li L, Cheng XF, Leshkevich J, Umezawa T, Harding SA, Chiang VL (2001) Te last step of syringyl monolignol biosynthesis in angiosperms is regulated by a novel gene encoding sinapyl alcohol dehydrogenase. Plant Cell 13: 1567-1586
    • (2001) Plant Cell , vol.13 , pp. 1567-1586
    • Li, L.1    Cheng, X.F.2    Leshkevich, J.3    Umezawa, T.4    Harding, S.A.5    Chiang, V.L.6
  • 32
    • 0030973546 scopus 로고    scopus 로고
    • A novel multifunctional O-methyltransferase implicated in a dual methylation pathway associated with lignin biosynthesis in loblolly pine
    • Li L, Popko JL, Zhang X-H, Osakabe K, Tsai CJ, Joshi C P, Chiang VL (1997) A novel multifunctional O-methyltransferase implicated in a dual methylation pathway associated with lignin biosynthesis in loblolly pine. Proc Natl Acad Sci USA 94: 5461-5466
    • (1997) Proc Natl Acad Sci USA , vol.94 , pp. 5461-5466
    • Li, L.1    Popko, J.L.2    Zhang, X.-H.3    Osakabe, K.4    Tsai, C.J.5    Joshi, C.P.6    Chiang, V.L.7
  • 33
    • 0034054073 scopus 로고    scopus 로고
    • 5-Hydroxyconiferyl aldehyde modulates enzymatic methylation for syringyl monolignol formation, a new view of monolignol biosynthesis in angiosperms
    • Li L, Popko JL, Umezawa T, Chiang VL (2000) 5-Hydroxyconiferyl aldehyde modulates enzymatic methylation for syringyl monolignol formation, a new view of monolignol biosynthesis in angiosperms. J Biol Chem 275: 6537-6545
    • (2000) J Biol Chem , vol.275 , pp. 6537-6545
    • Li, L.1    Popko, J.L.2    Umezawa, T.3    Chiang, V.L.4
  • 34
    • 0009736326 scopus 로고
    • Biological Activities of Lignans
    • MacRae WD, Towers GHN (1984) Biological Activities of Lignans. Phytochemistry 23: 1207-1220
    • (1984) Phytochemistry , vol.23 , pp. 1207-1220
    • Macrae, W.D.1    Towers, G.H.N.2
  • 35
    • 0026345966 scopus 로고
    • Isotope effect in gas-liquid chromatography of labeled compounds
    • Matucha M, Jockisch W, Verner P, Anders G (1991) Isotope effect in gas-liquid chromatography of labeled compounds. J Chromatogr A 588: 251-258
    • (1991) J Chromatogr A , vol.588 , pp. 251-258
    • Matucha, M.1    Jockisch, W.2    Verner, P.3    Anders, G.4
  • 36
    • 33644996863 scopus 로고    scopus 로고
    • Antiproliferative and apoptotic efects of butyrolactone lignans from Arctium lappa on leukemic cells
    • Matsumoto T, Hosono-Nishiyama K, Yamada H (2006) Antiproliferative and apoptotic efects of butyrolactone lignans from Arctium lappa on leukemic cells. Planta Med 72: 276-278
    • (2006) Planta Med , vol.72 , pp. 276-278
    • Matsumoto, T.1    Hosono-Nishiyama, K.2    Yamada, H.3
  • 37
    • 0032008254 scopus 로고    scopus 로고
    • Formation of (+)-eudesmin in Magnolia kobus DC. var. borealis Sarg
    • Miyauchi T, Ozawa S (1998) Formation of (+)-eudesmin in Magnolia kobus DC. var. borealis Sarg. Phytochemistry 47: 665-670
    • (1998) Phytochemistry , vol.47 , pp. 665-670
    • Miyauchi, T.1    Ozawa, S.2
  • 38
    • 0036264951 scopus 로고    scopus 로고
    • Isolation and characterization of a Pinus radiata lignin biosynthesis-related O-methyltransferase promoter
    • Moyle R, Moody J, Phillips L, Walter C, Wagner A (2002) Isolation and characterization of a Pinus radiata lignin biosynthesis-related O-methyltransferase promoter. Plant Cell Rep 20: 1052-1060
    • (2002) Plant Cell Rep , vol.20 , pp. 1052-1060
    • Moyle, R.1    Moody, J.2    Phillips, L.3    Walter, C.4    Wagner, A.5
  • 39
    • 43549093139 scopus 로고    scopus 로고
    • EST analysis of hop glandular trichomes identifes an O-methyltransferase that catalyzes the biosynthesis of xanthohumol
    • Nagel J, Culley LK, Lu Y, Liu E, Matthews PD, Stevens JF, Page JE (2008) EST analysis of hop glandular trichomes identifes an O-methyltransferase that catalyzes the biosynthesis of xanthohumol. Plant Cell 20: 186-200
    • (2008) Plant Cell , vol.20 , pp. 186-200
    • Nagel, J.1    Culley, L.K.2    Lu, Y.3    Liu, E.4    Matthews, P.D.5    Stevens, J.F.6    Page, J.E.7
  • 41
    • 47049125619 scopus 로고    scopus 로고
    • Characterization of Arabidopsis thaliana pinoresinol reductase, a new type of enzyme involved in lignan biosynthesis
    • Nakatsubo T, Mizutani M, Suzuki S, Hattori T, Umezawa T (2008) Characterization of Arabidopsis thaliana pinoresinol reductase, a new type of enzyme involved in lignan biosynthesis. J Biol Chem 283: 15550-15557
    • (2008) J Biol Chem , vol.283 , pp. 15550-15557
    • Nakatsubo, T.1    Mizutani, M.2    Suzuki, S.3    Hattori, T.4    Umezawa, T.5
  • 43
    • 0037470030 scopus 로고    scopus 로고
    • Daphnetin methylation by a novel O-methyltransferase is associated with cold acclimation and photosystem II excitation pressure in rye
    • NDong C, Anzellotti D, Ibrahim RK, Huner N P, Sarhan F (2003) Daphnetin methylation by a novel O-methyltransferase is associated with cold acclimation and photosystem II excitation pressure in rye. J Biol Chem 278: 6854-6861
    • (2003) J Biol Chem , vol.278 , pp. 6854-6861
    • Ndong, C.1    Anzellotti, D.2    Ibrahim, R.K.3    Huner, N.P.4    Sarhan, F.5
  • 46
    • 77957028431 scopus 로고    scopus 로고
    • Integrative Phytochemistry: from Ethnobotany to Molecular Ecology (Romeo, J. T., ed), Pergamon, Amsterdam
    • Noel J P, Dixon RA, Pichersky E, Zubieta C, Ferrer J-L (2003) in Recent Advances in Phytochemistry Vol. 37, Integrative Phytochemistry: from Ethnobotany to Molecular Ecology (Romeo, J. T., ed), Pergamon, Amsterdam, pp 37-58
    • (2003) Recent Advances In Phytochemistry , vol.37 , pp. 37-58
    • Noel, J.P.1    Dixon, R.A.2    Pichersky, E.3    Zubieta, C.4    Ferrer, J.-L.5
  • 47
    • 0347317979 scopus 로고    scopus 로고
    • R,S-Reticuline 7-O-methyltransferase and (R,S)-norcoclaurine 6-O-methyltransferase of Papaver somniferum- cDNA cloning and characterization of methyl transfer enzymes of alkaloid biosynthesis in opium poppy
    • Ounaroon A, Decker G, Schmidt J, Lottspeich F, Kutchan TM (2003) (R,S)-Reticuline 7-O-methyltransferase and (R,S)-norcoclaurine 6-O-methyltransferase of Papaver somniferum- cDNA cloning and characterization of methyl transfer enzymes of alkaloid biosynthesis in opium poppy. Plant J 36: 808-819
    • (2003) Plant J , vol.36 , pp. 808-819
    • Ounaroon, A.1    Decker, G.2    Schmidt, J.3    Lottspeich, F.4    Kutchan, T.M.5
  • 48
    • 0001608844 scopus 로고
    • Formation of (-)-Arctigenin in Forsythia intermedia
    • Ozawa S, Davin LB, Lewis NG (1993) Formation of (-)-Arctigenin in Forsythia intermedia. Phytochemistry 32: 643-652
    • (1993) Phytochemistry , vol.32 , pp. 643-652
    • Ozawa, S.1    Davin, L.B.2    Lewis, N.G.3
  • 49
    • 1642535462 scopus 로고
    • A Bitter Principle of Safflower; Matairesinol Monoglucoside
    • Palter R, Lundin RE (1970) A Bitter Principle of Safflower; Matairesinol Monoglucoside. Phytochemistry 9: 2407-2409
    • (1970) Phytochemistry , vol.9 , pp. 2407-2409
    • Palter, R.1    Lundin, R.E.2
  • 50
    • 0000666747 scopus 로고
    • A cathartic lignin glycoside isolated from Carthamus tinctorus
    • Palter R, Lundin RE, Haddon WF (1972) A cathartic lignin glycoside isolated from Carthamus tinctorus. Phytochemistry 11: 2871-2874
    • (1972) Phytochemistry , vol.11 , pp. 2871-2874
    • Palter, R.1    Lundin, R.E.2    Haddon, W.F.3
  • 51
    • 2142673468 scopus 로고
    • Te Complete Structure of Matairesinol Monoglucoside
    • Palter R, Haddon WF, Lundin RE (1971) Te Complete Structure of Matairesinol Monoglucoside. Phytochemistry 10: 1587-1589
    • (1971) Phytochemistry , vol.10 , pp. 1587-1589
    • Palter, R.1    Haddon, W.F.2    Lundin, R.E.3
  • 52
    • 0029555307 scopus 로고
    • Antiproliferative efect of Arctigenin and Arctiin
    • Ryu SY, Ahn JW, Kang YH, Han BH (1995) Antiproliferative efect of Arctigenin and Arctiin. Arch Pharm Res 18: 462-463
    • (1995) Arch Pharm Res , vol.18 , pp. 462-463
    • Ryu, S.Y.1    Ahn, J.W.2    Kang, Y.H.3    Han, B.H.4
  • 53
    • 33847175515 scopus 로고    scopus 로고
    • Metabolic analysis of the cinnamate/ monolignol pathway in Carthamus tinctorius seeds by a stable-isotope-dilution method
    • Sakakibara N, Nakatsubo T, Suzuki S, Shibata D, Shimada M, Umezawa T (2007) Metabolic analysis of the cinnamate/ monolignol pathway in Carthamus tinctorius seeds by a stable-isotope-dilution method. Org Biomol Chem 5: 802-815
    • (2007) Org Biomol Chem , vol.5 , pp. 802-815
    • Sakakibara, N.1    Nakatsubo, T.2    Suzuki, S.3    Shibata, D.4    Shimada, M.5    Umezawa, T.6
  • 55
    • 0001057634 scopus 로고
    • Conjugated Serotonins and Phenolic Constituents in Safower Seed (Carthamus tinctorius L.)
    • Sakamura S, Terayama Y, Kawakatsu S, Ichihara A, Saito H (1980) Conjugated Serotonins and Phenolic Constituents in Safower Seed (Carthamus tinctorius L.). Agric Biol Chem 44: 2951-2954
    • (1980) Agric Biol Chem , vol.44 , pp. 2951-2954
    • Sakamura, S.1    Terayama, Y.2    Kawakatsu, S.3    Ichihara, A.4    Saito, H.5
  • 56
    • 0037116416 scopus 로고    scopus 로고
    • Predicting the substrates of cloned plant O-methyltransferases
    • Schröder G, Wehinger E, Schröder J (2002) Predicting the substrates of cloned plant O-methyltransferases. Phytochemistry 59: 1-8
    • (2002) Phytochemistry , vol.59 , pp. 1-8
    • Schröder, G.1    Wehinger, E.2    Schröder, J.3
  • 57
    • 25844502482 scopus 로고    scopus 로고
    • Plant-based anticancer molecules: A chemical and biological profle of some important leads
    • Srivastava V, Negi AS, Kumar JK, Gupta MM, Khanuja SPS (2005) Plant-based anticancer molecules: a chemical and biological profle of some important leads. Bioorg Med Chem 13: 5892-5908
    • (2005) Bioorg Med Chem , vol.13 , pp. 5892-5908
    • Srivastava, V.1    Negi, A.S.2    Kumar, J.K.3    Gupta, M.M.4    Khanuja, S.P.S.5
  • 58
    • 78651504429 scopus 로고    scopus 로고
    • Arctigenin suppresses unfolded protein response and sensitizes glucose deprivation-mediated cytotoxicity of cancer cells
    • Sun S, Wang X, Wang C, Nawaz A, Wei W, Li J, Wang L, Yu D-H (2011) Arctigenin suppresses unfolded protein response and sensitizes glucose deprivation-mediated cytotoxicity of cancer cells. Planta Med 77: 141-145
    • (2011) Planta Med , vol.77 , pp. 141-145
    • Sun, S.1    Wang, X.2    Wang, C.3    Nawaz, A.4    Wei, W.5    Li, J.6    Wang, L.7    Yu, D.-H.8
  • 59
    • 34547842287 scopus 로고    scopus 로고
    • Biosynthesis of lignans and norlignans
    • Suzuki S, Umezawa T (2007) Biosynthesis of lignans and norlignans. J Wood Sci 53: 273-284
    • (2007) J Wood Sci , vol.53 , pp. 273-284
    • Suzuki, S.1    Umezawa, T.2
  • 60
    • 0035543965 scopus 로고    scopus 로고
    • Norlignan biosynthesis in Asparagus ofcinalis L.: The norlignan originates from two non-identical phenylpropane units
    • Suzuki S, Umezawa T, Shimada M (2001) Norlignan biosynthesis in Asparagus ofcinalis L.: the norlignan originates from two non-identical phenylpropane units. J Chem Soc, Perkin Trans 13252-13257
    • (2001) J Chem Soc, Perkin Trans , pp. 13252-13257
    • Suzuki, S.1    Umezawa, T.2    Shimada, M.3
  • 61
    • 0036616918 scopus 로고    scopus 로고
    • First in vitro norlignan formation with Asparagus officinalis enzyme preparation. Chem Commun (Camb) 1088-1089 Suzuki S, Umezawa T, Shimada M (2002b) Stereochemical diversity in lignan biosynthesis of Arctium lappa L
    • Suzuki S, Nakatsubo T, Umezawa T, Shimada M (2002a) First in vitro norlignan formation with Asparagus officinalis enzyme preparation. Chem Commun (Camb) 1088-1089 Suzuki S, Umezawa T, Shimada M (2002b) Stereochemical diversity in lignan biosynthesis of Arctium lappa L. Biosci Biotechnol Biochem 66: 1262-1269
    • (2002) Biosci Biotechnol Biochem , vol.66 , pp. 1262-1269
    • Suzuki, S.1    Nakatsubo, T.2    Umezawa, T.3    Shimada, M.4
  • 62
    • 16844385289 scopus 로고    scopus 로고
    • A heartwood norlignan, (E)-hinokiresinol, is formed from 4-coumaryl 4-coumarate by a Cryptomeria japonica enzyme preparation. Chem Commun (Camb) 2838-2839 Umezawa T (2003a) Diversity in lignan biosynthesis
    • Suzuki S, Yamamura M, Shimada M, Umezawa T (2004) A heartwood norlignan, (E)-hinokiresinol, is formed from 4-coumaryl 4-coumarate by a Cryptomeria japonica enzyme preparation. Chem Commun (Camb) 2838-2839 Umezawa T (2003a) Diversity in lignan biosynthesis. Phytochem Rev 2: 371-390
    • (2004) Phytochem Rev , vol.2 , pp. 371-390
    • Suzuki, S.1    Yamamura, M.2    Shimada, M.3    Umezawa, T.4
  • 63
    • 77949916538 scopus 로고    scopus 로고
    • Phylogenetic Distribution of Lignan Producing Plants. Wood Research 90: 27-110 Umezawa T (2010) Te cinnamate/monolignol pathway
    • Umezawa T (2003b) Phylogenetic Distribution of Lignan Producing Plants. Wood Research 90: 27-110 Umezawa T (2010) Te cinnamate/monolignol pathway. Phytochem Rev 9: 1-17
    • (2003) Phytochem Rev , vol.9 , pp. 1-17
    • Umezawa, T.1
  • 65
    • 0041876084 scopus 로고    scopus 로고
    • Two O-methyltransferases isolated from fower petals of Rosa chinensis var. spontanea involved in scent biosynthesis
    • Wu S, Watanabe N, Mita S, Ueda Y, Shibuya M, Ebizuka Y (2003) Two O-methyltransferases isolated from fower petals of Rosa chinensis var. spontanea involved in scent biosynthesis. J Biosci Bioeng 96: 119-128
    • (2003) J Biosci Bioeng , vol.96 , pp. 119-128
    • Wu, S.1    Watanabe, N.2    Mita, S.3    Ueda, Y.4    Shibuya, M.5    Ebizuka, Y.6
  • 66
    • 0035918142 scopus 로고    scopus 로고
    • Secoisolariciresinol dehydrogenase purifcation, cloning, and functional expression. Implications for human health protection
    • Xia Z-Q, Costa MA, Pélissier HC, Davin LB, Lewis NG (2001) Secoisolariciresinol dehydrogenase purifcation, cloning, and functional expression. Implications for human health protection. J Biol Chem 276: 12614-12623
    • (2001) J Biol Chem , vol.276 , pp. 12614-12623
    • Xia, Z.-Q.1    Costa, M.A.2    Pélissier, H.C.3    Davin, L.B.4    Lewis, N.G.5
  • 67
    • 18744373344 scopus 로고    scopus 로고
    • Podophyllotoxin derivatives: Current synthetic approaches for new anticancer agents
    • You Y (2005) Podophyllotoxin derivatives: current synthetic approaches for new anticancer agents. Curr Pharm Des 11: 1695-1717
    • (2005) Curr Pharm Des , vol.11 , pp. 1695-1717
    • You, Y.1
  • 68
    • 0035119588 scopus 로고    scopus 로고
    • Structures of two natural product methyltransferases reveal the basis for substrate specificity in plant O-methyltransferases
    • Zubieta C, He X-Z, Dixon RA, Noel JP (2001) Structures of two natural product methyltransferases reveal the basis for substrate specificity in plant O-methyltransferases. Nat Struct Biol 8: 271-279
    • (2001) Nat Struct Biol , vol.8 , pp. 271-279
    • Zubieta, C.1    He, X.-Z.2    Dixon, R.A.3    Noel, J.P.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.