메뉴 건너뛰기




Volumn 47, Issue 1, 2012, Pages 65-73

Linolenate 9R-dioxygenase and allene oxide synthase activities of lasiodiplodia theobromae

Author keywords

9R HPODE; Botryodiplodia theobromae; Cytochrome P450; Heme peroxidase; Jasmonic acid; Oxygenation mechanism

Indexed keywords

5,8 DIHYDROXY 9,12,15 OCTADECATRIENOIC ACID; 9 HYDROPEROXY 10,12,15 OCTADECATRIENOIC ACID; 9 HYDROXY 10 OXO 12,15 OCTADECADIENOIC ACID; ALLENE OXIDE SYNTHASE; DIOXYGENASE; JASMONIC ACID; LINOLENIC ACID; POLYUNSATURATED FATTY ACID; SYNTHETASE; UNCLASSIFIED DRUG;

EID: 84857060511     PISSN: 00244201     EISSN: 15589307     Source Type: Journal    
DOI: 10.1007/s11745-011-3622-5     Document Type: Article
Times cited : (19)

References (36)
  • 1
    • 70350507480 scopus 로고    scopus 로고
    • Enzymes in jasmonate biosynthesis-structure, function, regulation
    • Schaller A, Stintzi A (2009) Enzymes in jasmonate biosynthesis-structure, function, regulation. Phytochem 70:1532-1538
    • (2009) Phytochem , vol.70 , pp. 1532-1538
    • Schaller, A.1    Stintzi, A.2
  • 2
    • 75749086864 scopus 로고    scopus 로고
    • Jasmonates: Structural requirements for lipid-derived signals active in plant stress responses and development
    • Wasternack C, Kombrink E (2010) Jasmonates: structural requirements for lipid-derived signals active in plant stress responses and development. ACS Chem Biol 5:63-77
    • (2010) ACS Chem Biol , vol.5 , pp. 63-77
    • Wasternack, C.1    Kombrink, E.2
  • 4
    • 84857064442 scopus 로고
    • New metabolites of Gibberella fujikuroi
    • Cross BE, Webster GRB (1970) New metabolites of Gibberella fujikuroi. J Chem Soc C 1970:1838-1842
    • (1970) J Chem Soc C , vol.1970 , pp. 1838-1842
    • Cross, B.E.1    Grb, W.2
  • 6
    • 0032908693 scopus 로고    scopus 로고
    • Jasmonates and related compounds from Fusarium oxysporum
    • DOI 10.1016/S0031-9422(98)00596-2, PII S0031942298005962
    • Miersch O, Bohlmann H, Wasternack C (1999) Jasmonates and related compounds from Fusarium oxysporum. Phytochem 50:517-523 (Pubitemid 29058482)
    • (1999) Phytochemistry , vol.50 , Issue.4 , pp. 517-523
    • Miersch, O.1    Bohlmann, H.2    Wasternack, C.3
  • 7
    • 34848897179 scopus 로고    scopus 로고
    • Jasmonates: An update on biosynthesis, signal transduction and action in plant stress response, growth and development
    • DOI 10.1093/aob/mcm079
    • Wasternack C (2007) Jasmonates: an update on biosynthesis, signal transduction and action in plant stress response, growth and development. Ann Bot 100:681-697 (Pubitemid 47511777)
    • (2007) Annals of Botany , vol.100 , Issue.4 , pp. 681-697
    • Wasternack, C.1
  • 8
    • 0028809671 scopus 로고
    • The plant growth regulator methyl jasmonate inhibits aflatoxin production by Aspergillus flavus
    • Goodrich-Tanrikulu M, Mahoney NE, Rodriguez SB (1995) The plant growth regulator methyl jasmonate inhibits aflatoxin production by Aspergillus flavus. Microbiol 141:2831-2837
    • (1995) Microbiol , vol.141 , pp. 2831-2837
    • Goodrich-Tanrikulu, M.1    Mahoney, N.E.2    Rodriguez, S.B.3
  • 9
    • 70350517590 scopus 로고    scopus 로고
    • Methyl jasmonate: A plant stress hormone as an anti-cancer drug
    • Cohen S, Flescher E (2009) Methyl jasmonate: a plant stress hormone as an anti-cancer drug. Phytochem 70:1600-1609
    • (2009) Phytochem , vol.70 , pp. 1600-1609
    • Cohen, S.1    Flescher, E.2
  • 10
    • 78249260632 scopus 로고    scopus 로고
    • Biosynthesis of jasmonic acid in a plant pathogenic fungus, Lasiodiplodia theobromae
    • Tsukada K, Takahashi K, Nabeta K (2010) Biosynthesis of jasmonic acid in a plant pathogenic fungus, Lasiodiplodia theobromae. Phytochem 71:2019-2023
    • (2010) Phytochem , vol.71 , pp. 2019-2023
    • Tsukada, K.1    Takahashi, K.2    Nabeta, K.3
  • 11
    • 0000336575 scopus 로고
    • (+)-7-isojasmonic acid and related compounds from Botryodiplodia theobromae
    • Miersch O, Preiss A, Sembdner G, Schreiber K (1987) (+)-7-isojasmonic acid and related compounds from Botryodiplodia theobromae. Phytochem 26:1037-1039
    • (1987) Phytochem , vol.26 , pp. 1037-1039
    • Miersch, O.1    Preiss, A.2    Sembdner, G.3    Schreiber, K.4
  • 12
    • 52149110322 scopus 로고    scopus 로고
    • Structural insights into the evolutionary paths of oxylipin biosynthetic enzymes
    • Lee DS, Nioche P, Hamberg M, Raman CS (2008) Structural insights into the evolutionary paths of oxylipin biosynthetic enzymes. Nature 455:363-368
    • (2008) Nature , vol.455 , pp. 363-368
    • Lee, D.S.1    Nioche, P.2    Hamberg, M.3    Raman, C.S.4
  • 13
    • 0026664198 scopus 로고
    • A linoleic acid (8R)-dioxygenase and hydroperoxide isomerase of the fungus Gaeumannomyces graminis. Biosynthesis of (8R)-hydroxylinoleic acid and (7S, 8S)-dihydroxylinoleic acid from (8R)-hydroperoxylinoleic acid
    • Brodowsky ID, Hamberg M, Oliw EH (1992) A linoleic acid (8R)-dioxygenase and hydroperoxide isomerase of the fungus Gaeumannomyces graminis. Biosynthesis of (8R)-hydroxylinoleic acid and (7S, 8S)-dihydroxylinoleic acid from (8R)-hydroperoxylinoleic acid. J Biol Chem 267:14738-14745
    • (1992) J Biol Chem , vol.267 , pp. 14738-14745
    • Brodowsky, I.D.1    Hamberg, M.2    Oliw, E.H.3
  • 14
    • 66449133395 scopus 로고    scopus 로고
    • Identification of PpoA from Aspergillus nidulans as a fusion protein of a fatty acid heme dioxygenase/peroxidase and a cytochrome P450
    • Brodhun F, Göbel C, Hornung E, Feussner I (2009) Identification of PpoA from Aspergillus nidulans as a fusion protein of a fatty acid heme dioxygenase/peroxidase and a cytochrome P450. J Biol Chem 284:11792-11805
    • (2009) J Biol Chem , vol.284 , pp. 11792-11805
    • Brodhun, F.1    Göbel, C.2    Hornung, E.3    Feussner, I.4
  • 15
    • 74349117097 scopus 로고    scopus 로고
    • PpoC from Aspergillus nidulans is a fusion protein with one active heme
    • Brodhun F, Schneider S, Göbel C, Hornung E, Feussner I (2010) PpoC from Aspergillus nidulans is a fusion protein with one active heme. J Biochem 425:553-565
    • (2010) J Biochem , vol.425 , pp. 553-565
    • Brodhun, F.1    Schneider, S.2    Göbel, C.3    Hornung, E.4    Feussner, I.5
  • 16
    • 67649405066 scopus 로고    scopus 로고
    • Leucine/valine residues direct oxygenation of linoleic acid by (10R)- and (8R)-dioxygenases: Expression and site-directed mutagenesis of (10R)-dioxygenase with epoxyalcohol synthase activity
    • Garscha U, Oliw EH (2009) Leucine/valine residues direct oxygenation of linoleic acid by (10R)- and (8R)-dioxygenases: expression and site-directed mutagenesis of (10R)-dioxygenase with epoxyalcohol synthase activity. J Biol Chem 284:13755-13765
    • (2009) J Biol Chem , vol.284 , pp. 13755-13765
    • Garscha, U.1    Oliw, E.H.2
  • 17
    • 76849105358 scopus 로고    scopus 로고
    • Linoleate 9R-dioxygenase and allene oxide synthase activities of Aspergillus terreus
    • (Erratum 2010; 500; 210
    • Jernerén F, Hoffmann I, Oliw EH (2010) Linoleate 9R-dioxygenase and allene oxide synthase activities of Aspergillus terreus. Arch Biochem Biophys 495:67-73 (Erratum 2010; 500; 210)
    • (2010) Arch Biochem Biophys , vol.495 , pp. 67-73
    • Jernerén, F.1    Hoffmann, I.2    Oliw, E.H.3
  • 18
    • 49849089966 scopus 로고    scopus 로고
    • Response surface methodology to optimize the nutritional parameters for enhanced production of jasmonic acid by Lasiodiplodia theobromae
    • Dhandhukia PC, Thakkar VR (2008) Response surface methodology to optimize the nutritional parameters for enhanced production of jasmonic acid by Lasiodiplodia theobromae. J Appl Microbiol 105:636-643
    • (2008) J Appl Microbiol , vol.105 , pp. 636-643
    • Dhandhukia, P.C.1    Thakkar, V.R.2
  • 19
    • 0032170217 scopus 로고    scopus 로고
    • Culture conditions for jasmonic acid and biomass production by Botryodiplodia theobromae in submerged fermentation
    • DOI 10.1016/S0032-9592(98)00035-1, PII S0032959298000035
    • Eng F, Gutierrez-Rojas M, Favela-Torres E (1998) Culture conditions for jasmonic acid and biomass production by Botryodiplodia theobromae in submerged fermentation. Process Biochem 33:715-720 (Pubitemid 28525617)
    • (1998) Process Biochemistry , vol.33 , Issue.7 , pp. 715-720
    • Eng, F.1    Gutierrez-Rojas, M.2    Favela-Torres, E.3
  • 20
    • 0028260498 scopus 로고
    • Sequential oxygenation of linoleic acid in the fungus Gaeumannomyces graminis: Stereochemistry of dioxygenase and hydroperoxide isomerase reactions
    • DOI 10.1006/abbi.1994.1087
    • Hamberg M, Zhang LY, Brodowsky ID, Oliw EH (1994) Sequential oxygenation of linoleic acid in the fungus Gaeumannomyces graminis: stereochemistry of dioxygenase and hydroperoxide isomerase reactions. Arch Biochem Biophys 309:77-80 (Pubitemid 24171445)
    • (1994) Archives of Biochemistry and Biophysics , vol.309 , Issue.1 , pp. 77-80
    • Hamberg, M.1    Zhang, L.-Y.2    Brodowsky, I.D.3    Oliw, E.H.4
  • 21
    • 36849034824 scopus 로고    scopus 로고
    • Identification of dioxygenases required for Aspergillus development: Studies of products, stereochemistry, and the reaction mechanism
    • DOI 10.1074/jbc.M705366200
    • Garscha U, Jernerén F, Chung D, Keller NP, Hamberg M, Oliw EH (2007) Identification of dioxygenases required for Aspergillus development. Studies of products, stereochemistry, and the reaction mechanism. J Biol Chem 282:34707-34718 (Pubitemid 350232447)
    • (2007) Journal of Biological Chemistry , vol.282 , Issue.48 , pp. 34707-34718
    • Garscha, U.1    Jerneren, F.2    Chung, D.3    Keller, N.P.4    Hamberg, M.5    Oliw, E.H.6
  • 22
    • 0017596280 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 JA, Chan HW, Galliard T (1977) 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 12:324-326 (Pubitemid 8062331)
    • (1977) Lipids , vol.12 , Issue.3 , pp. 324-326
    • Matthew, J.A.1    Chan, H.W.S.2    Galliard, T.3
  • 23
    • 11144334584 scopus 로고    scopus 로고
    • Expression of manganese lipoxygenase in Pichia pastoris and site-directed mutagenesis of putative metal ligands
    • DOI 10.1016/j.abb.2004.10.026, PII S0003986104006174
    • Cristea M, Engström Å, Su C, Hörnsten L, Oliw EH (2005) Expression of manganese lipoxygenase in Pichia pastoris and site-directed mutagenesis of putative metal ligands. Arch Biochem Biophys 434:201-211 (Pubitemid 40040485)
    • (2005) Archives of Biochemistry and Biophysics , vol.434 , Issue.SPEC. ISS. , pp. 201-211
    • Cristea, M.1    Engstrom, A.2    Su, C.3    Hornsten, L.4    Oliw, E.H.5
  • 24
    • 78651229995 scopus 로고    scopus 로고
    • Manganese lipoxygenase oxidizes bis-allylic hydroperoxides and octadecenoic acids by different mechanisms
    • Oliw EH, Jernerén F, Hoffmann I, Sahlin M, Garscha U (2011) Manganese lipoxygenase oxidizes bis-allylic hydroperoxides and octadecenoic acids by different mechanisms. Biochim Biophys Acta 1811:138-147
    • (2011) Biochim Biophys Acta , vol.1811 , pp. 138-147
    • Oliw, E.H.1    Jernerén, F.2    Hoffmann, I.3    Sahlin, M.4    Garscha, U.5
  • 25
    • 80054112003 scopus 로고
    • Jernerén F Stereoselective oxidation of regioisomeric octadecenoic acids by fatty acid dioxygenases
    • Oliw EH, Wennman A, Hoffmanna I, Garscha U, Hamberg M, Jernerén F Stereoselective oxidation of regioisomeric octadecenoic acids by fatty acid dioxygenases. J Lipid Res 52:1995-2004
    • (1995) J Lipid Res , vol.52
    • Oliw, E.H.1    Wennman, A.2    Hoffmanna, I.3    Garscha, U.4    Hamberg, M.5
  • 26
    • 49849097086 scopus 로고    scopus 로고
    • Enantiomeric separation and analysis of unsaturated hydroperoxy fatty acids by chiral column chromatography-mass spectrometry
    • Garscha U, Nilsson T, Oliw EH (2008) Enantiomeric separation and analysis of unsaturated hydroperoxy fatty acids by chiral column chromatography-mass spectrometry. J Chromatogr B Analyt Technol Biomed Life Sci 872:90-98
    • (2008) J Chromatogr B Analyt Technol Biomed Life Sci , vol.872 , pp. 90-98
    • Garscha, U.1    Nilsson, T.2    Oliw, E.H.3
  • 27
    • 77949318484 scopus 로고    scopus 로고
    • Gene deletion of 7,8-linoleate diol synthase of the rice blast fungus: Studies on pathogenicity, stereochemistry, and oxygenation mechanisms
    • Jernerén F, Sesma A, Franceschetti M, Hamberg M, Oliw EH (2010) Gene deletion of 7,8-linoleate diol synthase of the rice blast fungus: studies on pathogenicity, stereochemistry, and oxygenation mechanisms. J Biol Chem 285:5308-5316
    • (2010) J Biol Chem , vol.285 , pp. 5308-5316
    • Jernerén, F.1    Sesma, A.2    Franceschetti, M.3    Hamberg, M.4    Oliw, E.H.5
  • 28
    • 34347214029 scopus 로고    scopus 로고
    • Steric analysis of 8-hydroxy- and 10-hydroxyoctadecadienoic acids and dihydroxyoctadecadienoic acids formed from 8R-hydroperoxyoctadecadienoic acid by hydroperoxide isomerases
    • DOI 10.1016/j.ab.2007.04.045, PII S0003269707002795
    • Garscha U, Oliw EH (2007) Steric analysis of 8-hydroxy- and 10-hydroxyoctadecadienoic acids and dihydroxyoctadecadienoic acids formed from 8R-hydroperoxylinoleic acid by hydroperoxide isomerases. Anal Biochem 367:238-246 (Pubitemid 47001927)
    • (2007) Analytical Biochemistry , vol.367 , Issue.2 , pp. 238-246
    • Garscha, U.1    Oliw, E.H.2
  • 29
    • 77951237915 scopus 로고    scopus 로고
    • Biochemical characterization of the oxygenation of unsaturated fatty acids by the dioxygenase and hydroperoxide isomerase of Pseudomonas aeruginosa 42A2
    • Martinez E, Hamberg M, Busquets M, Diaz P, Manresa A, Oliw EH (2010) Biochemical characterization of the oxygenation of unsaturated fatty acids by the dioxygenase and hydroperoxide isomerase of Pseudomonas aeruginosa 42A2. J Biol Chem 285:9339-9345
    • (2010) J Biol Chem , vol.285 , pp. 9339-9345
    • Martinez, E.1    Hamberg, M.2    Busquets, M.3    Diaz, P.4    Manresa, A.5    Oliw, E.H.6
  • 30
    • 0031706293 scopus 로고    scopus 로고
    • Analysis of novel hydroperoxides and other metabolites of oleic, linoleic, and linolenic acids by liquid chromatography-mass spectrometry with ion trap MS(n)
    • DOI 10.1007/s11745-998-0280-0
    • Oliw EH, Su C, Skogström T, Benthin G (1998) Analysis of novel hydroperoxides and other metabolites of oleic, linoleic, and linolenic acids by liquid chromatography-mass spectrometry with ion trap MSn. Lipids 33:843-852 (Pubitemid 28460150)
    • (1998) Lipids , vol.33 , Issue.9 , pp. 843-852
    • Oliw, E.H.1    Su, C.2    Skogstrom, T.3    Benthin, G.4
  • 31
    • 79151469191 scopus 로고    scopus 로고
    • Expression of 5,8-LDS of Aspergillus fumigatus and its dioxygenase domain. A comparison with 7,8-LDS, 10-dioxygenase, and cyclooxygenase
    • Hoffmann I, Jernerén F, Garscha U, Oliw EH (2011) Expression of 5,8-LDS of Aspergillus fumigatus and its dioxygenase domain. A comparison with 7,8-LDS, 10-dioxygenase, and cyclooxygenase. Arch Biochem Biophys 506:216-222
    • (2011) Arch Biochem Biophys , vol.506 , pp. 216-222
    • Hoffmann, I.1    Jernerén, F.2    Garscha, U.3    Oliw, E.H.4
  • 32
    • 34147096325 scopus 로고    scopus 로고
    • On the singular, dual, and multiple positional specificity of manganese lipoxygenase and its G316A mutant
    • DOI 10.1194/jlr.M600505-JLR200
    • Cristea M, Oliw EH (2007) On the singular, dual, and multiple positional specificity of manganese lipoxygenase and its G316A mutant. J Lipid Res 48:890-903 (Pubitemid 46557894)
    • (2007) Journal of Lipid Research , vol.48 , Issue.4 , pp. 890-903
    • Cristea, M.1    Oliw, E.H.2
  • 33
    • 71549116098 scopus 로고    scopus 로고
    • Omega-3 fatty acids are oxygenated at the n-7 carbon by the lipoxygenase domain of a fusion protein in the cyanobacterium Acaryochloris marina
    • Gao B, Boeglin WE, Brash AR (2010) Omega-3 fatty acids are oxygenated at the n-7 carbon by the lipoxygenase domain of a fusion protein in the cyanobacterium Acaryochloris marina. Biochim Biophys Acta 1801:58-63
    • (2010) Biochim Biophys Acta , vol.1801 , pp. 58-63
    • Gao, B.1    Boeglin, W.E.2    Brash, A.R.3
  • 34
    • 0032557580 scopus 로고    scopus 로고
    • Manganese lipoxygenase. Discovery of a bis-allylic hydroperoxide as product and intermediate in a lipoxygenase reaction
    • DOI 10.1074/jbc.273.21.13080
    • Hamberg M, Su C, Oliw E (1998) Manganese lipoxygenase. Discovery of a bis-allylic hydroperoxide as product and intermediate in a lipoxygenase reaction. J Biol Chem 273:13080-13088 (Pubitemid 28246874)
    • (1998) Journal of Biological Chemistry , vol.273 , Issue.21 , pp. 13080-13088
    • Hamberg, M.1    Su, C.2    Oliw, E.3
  • 35
    • 0034022757 scopus 로고    scopus 로고
    • New cyclopentenone fatty acids formed from linoleic and linolenic acids in potato
    • Hamberg M (2000) New cyclopentenone fatty acids formed from linoleic and linolenic acids in potato. Lipids 35:353-363 (Pubitemid 30252611)
    • (2000) Lipids , vol.35 , Issue.4 , pp. 353-363
    • Hamberg, M.1
  • 36
    • 54349090869 scopus 로고    scopus 로고
    • Tomato CYP74C3 is a multifunctional enzyme not only synthesizing allene oxide but also catalyzing its hydrolysis and cyclization
    • Grechkin AN, Mukhtarova LS, Latypova LR, Gogolev Y, Toporkova YY, Hamberg M (2008) Tomato CYP74C3 is a multifunctional enzyme not only synthesizing allene oxide but also catalyzing its hydrolysis and cyclization. Chembiochem 9:2498-2505
    • (2008) Chembiochem , vol.9 , pp. 2498-2505
    • Grechkin, A.N.1    Mukhtarova, L.S.2    Latypova, L.R.3    Gogolev, Y.4    Toporkova, Y.Y.5    Hamberg, M.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.