메뉴 건너뛰기




Volumn 55, Issue 21, 2007, Pages 8589-8595

Fungal-stressed germination of black soybeans leads to generation of oxooctadecadienoic acids in addition to glyceollins

Author keywords

Black soybeans; Glyceollins; Oxooctadecadienoic acids; Phytoalexins

Indexed keywords

BENZOPYRAN DERIVATIVE; GLYCEOLLIN; OCTADECADIENOIC ACID; OXYLIPIN; UNCLASSIFIED DRUG; UNSATURATED FATTY ACID;

EID: 35548975785     PISSN: 00218561     EISSN: None     Source Type: Journal    
DOI: 10.1021/jf0716735     Document Type: Article
Times cited : (36)

References (35)
  • 1
    • 33846498148 scopus 로고    scopus 로고
    • Variation of anthocyanins and isoflavones between yellow-cotyledon and green-cotyledon seeds of black soybean
    • Kim, S.-L.; Kim, H.-B.; Chi, H.-Y.; Park, N.-K.; Son, J.-R.; Yun, H.-T.; Kim, S.-J. Variation of anthocyanins and isoflavones between yellow-cotyledon and green-cotyledon seeds of black soybean. Food Sci. Biotechnol. 2005, 14, 778-782.
    • (2005) Food Sci. Biotechnol , vol.14 , pp. 778-782
    • Kim, S.-L.1    Kim, H.-B.2    Chi, H.-Y.3    Park, N.-K.4    Son, J.-R.5    Yun, H.-T.6    Kim, S.-J.7
  • 2
    • 0035217152 scopus 로고    scopus 로고
    • Isolation and characterization of an active compound from black soybean [Glycine max (L.) Merrill] and its effect on proliferation and differentiation of human leukemic U937 cells
    • Liao, H. F.; Chou, C. J.; Wu, S. H.; Khoo, K. H.; Chen, C. F.; Wang, S. Y. Isolation and characterization of an active compound from black soybean [Glycine max (L.) Merrill] and its effect on proliferation and differentiation of human leukemic U937 cells. Anti-Cancer Drugs 2001, 12 (10), 841-846.
    • (2001) Anti-Cancer Drugs , vol.12 , Issue.10 , pp. 841-846
    • Liao, H.F.1    Chou, C.J.2    Wu, S.H.3    Khoo, K.H.4    Chen, C.F.5    Wang, S.Y.6
  • 3
    • 33745491279 scopus 로고    scopus 로고
    • Bioactive compounds in legumes and their germinated products
    • Lin, P. Y.; Lai, H. M. Bioactive compounds in legumes and their germinated products. J. Agric. Food Chem. 2006, 54 (11), 3807-3814.
    • (2006) J. Agric. Food Chem , vol.54 , Issue.11 , pp. 3807-3814
    • Lin, P.Y.1    Lai, H.M.2
  • 4
    • 20744445973 scopus 로고    scopus 로고
    • Antioxidant activities of black and yellow soybeans against low-density lipoprotein oxidation
    • Takahashi, R.; Ohmori, R.; Kiyose, C.; Momiyama, Y.; Ohsuzu, F.; Kondo, K. Antioxidant activities of black and yellow soybeans against low-density lipoprotein oxidation. J. Agric. Food Chem. 2005, 53 (11), 4578-4582.
    • (2005) J. Agric. Food Chem , vol.53 , Issue.11 , pp. 4578-4582
    • Takahashi, R.1    Ohmori, R.2    Kiyose, C.3    Momiyama, Y.4    Ohsuzu, F.5    Kondo, K.6
  • 5
    • 19344365460 scopus 로고
    • Treatment on 38 cases of leucopenia with Xuesu Tang
    • Wang, D. Treatment on 38 cases of leucopenia with Xuesu Tang. Traditional Chin. Med. Res. 1992, 5, 35-36.
    • (1992) Traditional Chin. Med. Res , vol.5 , pp. 35-36
    • Wang, D.1
  • 6
    • 85051558991 scopus 로고
    • Progress in phytoalexin research during the past 50 years
    • Daniel, M, Purkayastha, R. P, Eds, Marcel Dekker, Inc, New York
    • Purkayastha, R. P. Progress in phytoalexin research during the past 50 years, In Handbook of phytoalexin metabolism and action; Daniel, M., Purkayastha, R. P., Eds.; Marcel Dekker, Inc.: New York, 1995; pp 1-39.
    • (1995) Handbook of phytoalexin metabolism and action , pp. 1-39
    • Purkayastha, R.P.1
  • 7
    • 0035859039 scopus 로고    scopus 로고
    • Natural products and disease resistance
    • Dixon, R. A. Natural products and disease resistance. Nature 2001, 411, 843-847.
    • (2001) Nature , vol.411 , pp. 843-847
    • Dixon, R.A.1
  • 9
    • 33847764645 scopus 로고    scopus 로고
    • Aging, adiposity, and calorie restriction
    • Fontana, L.; Klein, S. Aging, adiposity, and calorie restriction. JAMA, J. Am. Med. Assoc. 2007, 297, 986-994.
    • (2007) JAMA, J. Am. Med. Assoc , vol.297 , pp. 986-994
    • Fontana, L.1    Klein, S.2
  • 10
    • 33745962138 scopus 로고    scopus 로고
    • Therapeutic potential of resveratrol: The in vivo evidence
    • Sinclair, D. A. Therapeutic potential of resveratrol: the in vivo evidence. Nat. Rev. Drug Discovery 2006, 5, 493-506.
    • (2006) Nat. Rev. Drug Discovery , vol.5 , pp. 493-506
    • Sinclair, D.A.1
  • 11
    • 0141719702 scopus 로고    scopus 로고
    • Small molecule activators of sirtuins extend Saccharomyces cerevisiae lifespan
    • Howitz, K. T. Small molecule activators of sirtuins extend Saccharomyces cerevisiae lifespan. Nature 2003, 425, 191-196.
    • (2003) Nature , vol.425 , pp. 191-196
    • Howitz, K.T.1
  • 12
  • 13
    • 0010441831 scopus 로고
    • Minor pterocarpinoids of soybean
    • Lyne, R. L.; Mulheirn, L. J. Minor pterocarpinoids of soybean. Tetrahedron Lett. 1978, 19, 3127-8.
    • (1978) Tetrahedron Lett , vol.19 , pp. 3127-3128
    • Lyne, R.L.1    Mulheirn, L.J.2
  • 14
    • 0002162602 scopus 로고
    • Glyceollin: Its role in restricting fungal growth in resistant soybean hypocotyls infected with Phytophthora megasperma var sojae
    • Yoshikawa, M.; Yamauchi, K.; Masago, H. Glyceollin: its role in restricting fungal growth in resistant soybean hypocotyls infected with Phytophthora megasperma var sojae. Physiol. Plant Pathol. 1978, 12 (1), 73-82.
    • (1978) Physiol. Plant Pathol , vol.12 , Issue.1 , pp. 73-82
    • Yoshikawa, M.1    Yamauchi, K.2    Masago, H.3
  • 16
    • 0033934953 scopus 로고    scopus 로고
    • Induction of the soybean phytoalexins coumestrol and glyceollin by Aspergillus
    • Boué, S. M.; Carter, C. H.; Ehrlich, K. C.; Cleveland, T. E. Induction of the soybean phytoalexins coumestrol and glyceollin by Aspergillus. J. Agric. Food Chem. 2000, 48, 2167-2172.
    • (2000) J. Agric. Food Chem , vol.48 , pp. 2167-2172
    • Boué, S.M.1    Carter, C.H.2    Ehrlich, K.C.3    Cleveland, T.E.4
  • 17
    • 0003024075 scopus 로고    scopus 로고
    • Banks, S. W.; Dewick, P. M. Biosynthesis of glyceollins I, II, and III in soybean. Phytochemistry 1983, 22, 2729-2733.
    • Banks, S. W.; Dewick, P. M. Biosynthesis of glyceollins I, II, and III in soybean. Phytochemistry 1983, 22, 2729-2733.
  • 18
    • 27644517709 scopus 로고    scopus 로고
    • Regio- and stereoselective oxidation of linoleic acid bound to serum albumin: Identification by ESI-mass spectrometry and NMR of the oxidation products
    • Dufor, C.; Loonis, M. Regio- and stereoselective oxidation of linoleic acid bound to serum albumin: identification by ESI-mass spectrometry and NMR of the oxidation products. Chem. Phys. Lipids 2005, 138, 60-80.
    • (2005) Chem. Phys. Lipids , vol.138 , pp. 60-80
    • Dufor, C.1    Loonis, M.2
  • 19
    • 0036854723 scopus 로고    scopus 로고
    • Aldehyde dehydrogenase inhibitors from the mushroom Clitocybe clavipes
    • Kawagishi, H.; Miyazawa, T.; Kume, H.; Arimoto, Y.; Inakuma, T. Aldehyde dehydrogenase inhibitors from the mushroom Clitocybe clavipes. J. Nat. Prod. 2002, 65, 1712-1714.
    • (2002) J. Nat. Prod , vol.65 , pp. 1712-1714
    • Kawagishi, H.1    Miyazawa, T.2    Kume, H.3    Arimoto, Y.4    Inakuma, T.5
  • 20
    • 0030948290 scopus 로고    scopus 로고
    • Oxidative burst: An early plant response to pathogen infection
    • Wojtaszek, P. Oxidative burst: an early plant response to pathogen infection. Biochem. J. 1997, 322, 681-692.
    • (1997) Biochem. J , vol.322 , pp. 681-692
    • Wojtaszek, P.1
  • 21
    • 0033788518 scopus 로고    scopus 로고
    • Homologous and heterologous desensitization and synergy in pathways leading to the soybean oxidative burst
    • Chandra, S.; Cessna, S. G.; Yahraus, T.; Devine, R.; Low, P. S. Homologous and heterologous desensitization and synergy in pathways leading to the soybean oxidative burst. Planta 2000, 211, 736-742.
    • (2000) Planta , vol.211 , pp. 736-742
    • Chandra, S.1    Cessna, S.G.2    Yahraus, T.3    Devine, R.4    Low, P.S.5
  • 23
    • 0001147274 scopus 로고    scopus 로고
    • Potentiation of the oxidative burst and isoflavonoid phytoalexin accumulation by serine protease inhibitors
    • Guo, Z.; Lamb, C.; Dixon, R. A. Potentiation of the oxidative burst and isoflavonoid phytoalexin accumulation by serine protease inhibitors. Plant Physiol. 1998, 118, 1487-1494.
    • (1998) Plant Physiol , vol.118 , pp. 1487-1494
    • Guo, Z.1    Lamb, C.2    Dixon, R.A.3
  • 24
    • 0000685955 scopus 로고
    • Rapid stimulation of an oxidative burst during elicitation of cultured plant cells
    • Apostol, I.; Heinstein, P. F.; Low, P. S. Rapid stimulation of an oxidative burst during elicitation of cultured plant cells. Plant Physiol. 1989, 90, 109-116.
    • (1989) Plant Physiol , vol.90 , pp. 109-116
    • Apostol, I.1    Heinstein, P.F.2    Low, P.S.3
  • 25
    • 11944253250 scopus 로고
    • Involvement of the oxidative burst in phytoalexin accumulation and the hypersensitive reaction
    • Devlin, W. S.; Gustine, D. L. Involvement of the oxidative burst in phytoalexin accumulation and the hypersensitive reaction. Plant Physiol. 1992, 100, 1189-1195.
    • (1992) Plant Physiol , vol.100 , pp. 1189-1195
    • Devlin, W.S.1    Gustine, D.L.2
  • 26
    • 13844269347 scopus 로고    scopus 로고
    • Peroxidation of polyunsaturated fatty acid methyl esters catalyzed by N-methyl benzohydroxamic acid: A new and convenient method for selective synthesis of hydroperoxides and alcholols
    • Punta, C.; Rector, C. L.; Porter, N. A. Peroxidation of polyunsaturated fatty acid methyl esters catalyzed by N-methyl benzohydroxamic acid: A new and convenient method for selective synthesis of hydroperoxides and alcholols. Chem Res. Toxicol. 2005, 18, 349-356.
    • (2005) Chem Res. Toxicol , vol.18 , pp. 349-356
    • Punta, C.1    Rector, C.L.2    Porter, N.A.3
  • 27
    • 0015135670 scopus 로고
    • Steric analysis of hydroperoxydes formed by lipoxygenase oxygenation of linoleic acid
    • Hamberg, M. Steric analysis of hydroperoxydes formed by lipoxygenase oxygenation of linoleic acid. Anal. Biochem. 1971, 43, 515-526.
    • (1971) Anal. Biochem , vol.43 , pp. 515-526
    • Hamberg, M.1
  • 28
    • 0017596280 scopus 로고    scopus 로고
    • A simple method for the preparation of pure 9-d-hydroperoxide of linoleic acid and methyl linoleate based on the positional specificity of lipoxygenase in tomato fruit
    • Matthew, M. A.; Chan, H. W.; Galliard, T. A simple method for the preparation of pure 9-d-hydroperoxide of linoleic acid and methyl linoleate based on the positional specificity of lipoxygenase in tomato fruit. Lipids 1997, 12, 324-326.
    • (1997) Lipids , vol.12 , pp. 324-326
    • Matthew, M.A.1    Chan, H.W.2    Galliard, T.3
  • 29
    • 0034968191 scopus 로고    scopus 로고
    • Method to produce 9(S)-hydroperoxides of linoleic and linolenic acids by maize lipoxygenase
    • Gardner, H. W.; Grove, M. J. Method to produce 9(S)-hydroperoxides of linoleic and linolenic acids by maize lipoxygenase. Lipids 2001, 36, 529-533.
    • (2001) Lipids , vol.36 , pp. 529-533
    • Gardner, H.W.1    Grove, M.J.2
  • 30
    • 0025323824 scopus 로고
    • Preparation and purification of soybean lipoxygenase-derived unsaturated hydroperoxy and hydroxyl fatty acids and determination of molar absorptivities of hydroxyl fatty acids
    • Graff, G.; Anderson, A.; Jaques, L. W. Preparation and purification of soybean lipoxygenase-derived unsaturated hydroperoxy and hydroxyl fatty acids and determination of molar absorptivities of hydroxyl fatty acids. Anal. Biochem. 1990, 188, 38-47.
    • (1990) Anal. Biochem , vol.188 , pp. 38-47
    • Graff, G.1    Anderson, A.2    Jaques, L.W.3
  • 31
    • 0027333092 scopus 로고
    • Increases in 13-hydroxyoctadecadienoic acid (13-HODE) dehydrogenase activity during differentiation of cultured cells
    • Bull, A. W.; Branting, C.; Bronstein, J. C.; Blackburn, M. L.; Rafter, J. J. Increases in 13-hydroxyoctadecadienoic acid (13-HODE) dehydrogenase activity during differentiation of cultured cells. Carcinogenesis 1993, 14, 2239-2243.
    • (1993) Carcinogenesis , vol.14 , pp. 2239-2243
    • Bull, A.W.1    Branting, C.2    Bronstein, J.C.3    Blackburn, M.L.4    Rafter, J.J.5
  • 32
    • 0037052584 scopus 로고    scopus 로고
    • Conjugation of the linoleic acid oxidation product, 13-oxooctadeca-9, 11-dienoic acid, a bioactive endogenous substrate for mammalian glutathione transferase
    • (a) Arthur, W.; Bull, A. W.; Seeley, S. K.; Geno, J.; Mannervik, B. Conjugation of the linoleic acid oxidation product, 13-oxooctadeca-9, 11-dienoic acid, a bioactive endogenous substrate for mammalian glutathione transferase. Biochim. Biophys. Acta 2002, 1571, 77-82.
    • (2002) Biochim. Biophys. Acta , vol.1571 , pp. 77-82
    • Arthur, W.1    Bull, A.W.2    Seeley, S.K.3    Geno, J.4    Mannervik, B.5
  • 33
    • 0031444925 scopus 로고    scopus 로고
    • Characterization of the enzymatic and nonenzymatic reaction of 13 oxooctadecadienoic acid with glutathione
    • (b) Blackburn, M. L.; Ketterer, B.; Meyer, D. J.; Juett, A. M.; Bull, A. W. Characterization of the enzymatic and nonenzymatic reaction of 13 oxooctadecadienoic acid with glutathione. Chem. Res. Toxicol. 1997, 10, 1364-1371.
    • (1997) Chem. Res. Toxicol , vol.10 , pp. 1364-1371
    • Blackburn, M.L.1    Ketterer, B.2    Meyer, D.J.3    Juett, A.M.4    Bull, A.W.5
  • 34
    • 0011740616 scopus 로고    scopus 로고
    • 9-Oxooctadeca-10, 12-dienoic acids as acetyl-CoA carboxylase inhibitors from red pepper (Capsicum annuum L.)
    • Watanebe, J.; Kawabata, J.; Kasai, T. 9-Oxooctadeca-10, 12-dienoic acids as acetyl-CoA carboxylase inhibitors from red pepper (Capsicum annuum L.). Biosci. Biotechnol. Biochem. 1999, 63 (3), 489-493.
    • (1999) Biosci. Biotechnol. Biochem , vol.63 , Issue.3 , pp. 489-493
    • Watanebe, J.1    Kawabata, J.2    Kasai, T.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.