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Volumn 8, Issue 3 SPEC. ISS., 2005, Pages 292-300

A role for intra- and intercellular translocation in natural product biosynthesis

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EID: 18044396993     PISSN: 13695266     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.pbi.2005.03.009     Document Type: Review
Times cited : (118)

References (32)
  • 1
    • 0040106748 scopus 로고
    • The biosynthesis of cyanogenic glucosides in higher plants
    • B. Lindberg-Møller, and E.E. Conn The biosynthesis of cyanogenic glucosides in higher plants J Biol Chem 255 1980 3049 3056
    • (1980) J Biol Chem , vol.255 , pp. 3049-3056
    • Lindberg-Møller, B.1    Conn, E.E.2
  • 2
    • 0019876872 scopus 로고
    • The in vitro biosynthesis of taxiphyllin and the channeling of intermediates in Triglochin maritima
    • A.J. Cutler, W. Hösel, M. Sternberg, and E.E. Conn The in vitro biosynthesis of taxiphyllin and the channeling of intermediates in Triglochin maritima J Biol Chem 256 1981 4253 4258
    • (1981) J Biol Chem , vol.256 , pp. 4253-4258
    • Cutler, A.J.1    Hösel, W.2    Sternberg, M.3    Conn, E.E.4
  • 3
    • 44949282472 scopus 로고
    • Chasing the enzymes of secondary metabolism: Plant cell cultures as a pot of gold
    • M.H. Zenk Chasing the enzymes of secondary metabolism: plant cell cultures as a pot of gold Phytochemistry 30 1991 3861 3863
    • (1991) Phytochemistry , vol.30 , pp. 3861-3863
    • Zenk, M.H.1
  • 4
    • 0000521129 scopus 로고
    • Phenylalanine ammonia lyase and cinnamic acid hydroxylases as assembled consecutive enzymes on microsomal membranes of cucumber cotyledons: Cooperation and subcellular distribution
    • U. Czichi, and H. Kindl Phenylalanine ammonia lyase and cinnamic acid hydroxylases as assembled consecutive enzymes on microsomal membranes of cucumber cotyledons: cooperation and subcellular distribution Planta 134 1977 133 143
    • (1977) Planta , vol.134 , pp. 133-143
    • Czichi, U.1    Kindl, H.2
  • 5
    • 3242655621 scopus 로고    scopus 로고
    • Metabolic channeling in plants
    • B.S.J. Winkel Metabolic channeling in plants Annu Rev Plant Biol 55 2004 85 107
    • (2004) Annu Rev Plant Biol , vol.55 , pp. 85-107
    • Winkel, B.S.J.1
  • 6
    • 0032725627 scopus 로고    scopus 로고
    • Transgene-mediated and elicitor-induced perturbation of metabolic channeling at the entry point into the phenylpropanoid pathway
    • S. Rasmussen, and R.A. Dixon Transgene-mediated and elicitor-induced perturbation of metabolic channeling at the entry point into the phenylpropanoid pathway Plant Cell 11 1999 1537 1551
    • (1999) Plant Cell , vol.11 , pp. 1537-1551
    • Rasmussen, S.1    Dixon, R.A.2
  • 7
    • 11144265587 scopus 로고    scopus 로고
    • Colocalization of l-phenylalanine ammonia-lyase and cinnamate 4-hydroxylase for metabolic channeling in phenylpropanoid biosynthesis
    • L. Achnine, E.B. Blancaflor, S. Rasmussen, and R.A. Dixon Colocalization of l-phenylalanine ammonia-lyase and cinnamate 4-hydroxylase for metabolic channeling in phenylpropanoid biosynthesis Plant Cell 16 2004 3098 3109 The work described in this article uses transient expression of GFP-fusion proteins to provide further evidence of the association of PAL1 and C4H with the ER in tobacco. PAL2 is found to have a cytosolic localization. Co-localization of PAL and C4H is confirmed by FRET, which suggests that the interaction between the two proteins is not tight.
    • (2004) Plant Cell , vol.16 , pp. 3098-3109
    • Achnine, L.1    Blancaflor, E.B.2    Rasmussen, S.3    Dixon, R.A.4
  • 8
    • 0034802539 scopus 로고    scopus 로고
    • Fluorescence resonance energy transfer microscopy of localized protein interactions in the living cell nucleus
    • R. Day, A. Periasamy, and F. Schaufele Fluorescence resonance energy transfer microscopy of localized protein interactions in the living cell nucleus Methods 25 2001 4 18
    • (2001) Methods , vol.25 , pp. 4-18
    • Day, R.1    Periasamy, A.2    Schaufele, F.3
  • 9
    • 0033607282 scopus 로고    scopus 로고
    • Interactions among enzymes of the Arabidopsis flavonoid biosynthetic pathway
    • I.E. Burbulis, and B. Winkel-Shirley Interactions among enzymes of the Arabidopsis flavonoid biosynthetic pathway Proc Natl Acad Sci USA 96 1999 12929 12934
    • (1999) Proc Natl Acad Sci USA , vol.96 , pp. 12929-12934
    • Burbulis, I.E.1    Winkel-Shirley, B.2
  • 10
    • 0034895650 scopus 로고    scopus 로고
    • Localization of flavonoid enzymes in Arabidopsis roots
    • D. Saslowsky, and B. Winkel-Shirley Localization of flavonoid enzymes in Arabidopsis roots Plant J 27 2001 37 48
    • (2001) Plant J , vol.27 , pp. 37-48
    • Saslowsky, D.1    Winkel-Shirley, B.2
  • 11
    • 35448947356 scopus 로고    scopus 로고
    • Structure and function of secretory cells
    • A. Fahn Structure and function of secretory cells Adv Bot Res 31 2000 38 75
    • (2000) Adv Bot Res , vol.31 , pp. 38-75
    • Fahn, A.1
  • 13
    • 0033791038 scopus 로고    scopus 로고
    • Development of peltate glandular trichomes of peppermint
    • G.W. Turner, J. Gershenzon, and R.B. Croteau Development of peltate glandular trichomes of peppermint Plant Physiol 124 2000 665 679
    • (2000) Plant Physiol , vol.124 , pp. 665-679
    • Turner, G.W.1    Gershenzon, J.2    Croteau, R.B.3
  • 14
    • 0026580576 scopus 로고
    • Isolation of secretory cells from plant glandular trichomes and their use in biosynthetic studies of monoterpenes and other gland products
    • J. Gershenzon, D. McCaskill, J.I.M. Rajaonarivony, C. Mihaliak, F. Karp, and R. Croteau Isolation of secretory cells from plant glandular trichomes and their use in biosynthetic studies of monoterpenes and other gland products Anal Biochem 200 1992 130 138
    • (1992) Anal Biochem , vol.200 , pp. 130-138
    • Gershenzon, J.1    McCaskill, D.2    Rajaonarivony, J.I.M.3    Mihaliak, C.4    Karp, F.5    Croteau, R.6
  • 15
    • 0000676137 scopus 로고
    • Morphology and monoterpene biosynthetic capabilities of secretory cell clusters isolated from glandular trichomes of peppermint (Mentha piperita L.)
    • D.G. McCaskill, J. Gershenzon, and R. Croteau Morphology and monoterpene biosynthetic capabilities of secretory cell clusters isolated from glandular trichomes of peppermint (Mentha piperita L.) Planta 187 1992 445 454
    • (1992) Planta , vol.187 , pp. 445-454
    • McCaskill, D.G.1    Gershenzon, J.2    Croteau, R.3
  • 16
    • 0030995585 scopus 로고    scopus 로고
    • Monoterpene essential oils are not of mevalonoid origin
    • W. Eisenreich, S. Sagner, M.H. Zenk, and A. Bacher Monoterpene essential oils are not of mevalonoid origin Tetrahedron Lett 38 1997 3889 3892
    • (1997) Tetrahedron Lett , vol.38 , pp. 3889-3892
    • Eisenreich, W.1    Sagner, S.2    Zenk, M.H.3    Bacher, A.4
  • 17
    • 0032817546 scopus 로고    scopus 로고
    • Limonene synthase, the enzyme responsible for monoterpene biosynthesis in peppermint, is localized to leucoplasts of oil gland secretory cells
    • G. Turner, J. Gershenzon, E.E. Nielsen, J.E. Froehlich, and R. Croteau Limonene synthase, the enzyme responsible for monoterpene biosynthesis in peppermint, is localized to leucoplasts of oil gland secretory cells Plant Physiol 120 1999 879 886
    • (1999) Plant Physiol , vol.120 , pp. 879-886
    • Turner, G.1    Gershenzon, J.2    Nielsen, E.E.3    Froehlich, J.E.4    Croteau, R.5
  • 18
    • 16644396565 scopus 로고    scopus 로고
    • Organization of monoterpene biosynthesis in Mentha. Immunocytochemical localization of geranyl diphosphate synthase, limonene 6-hydroxylase, isopiperitenol dehydrogenase, and pulegone reductase
    • G.W. Turner, and R. Croteau Organization of monoterpene biosynthesis in Mentha. Immunocytochemical localization of geranyl diphosphate synthase, limonene 6-hydroxylase, isopiperitenol dehydrogenase, and pulegone reductase Plant Physiol 136 2004 4215 4227 This article shows the bigger picture of monoterpene biosynthesis by using immunogold cytochemistry to localize four of the enzymes of monoterpene synthesis in mint. The results indicate that monoterpene synthesis is a dynamic process that involves multiple subcellular compartments within the secretory cells of mint glandular trichomes, which include plastids (which contain limonene synthase [LS]), ER (to which limonene 3-hydroxylase and limonene 6-hydroxylase localize), mitochondria (containing isopiperitenol dehydrogenase) and the cytosol (containing pulegone reductase). These results provide the basis for investigation of potential enzyme complexes or metabolite trafficking routes in mint species.
    • (2004) Plant Physiol , vol.136 , pp. 4215-4227
    • Turner, G.W.1    Croteau, R.2
  • 19
    • 0141794487 scopus 로고    scopus 로고
    • Monoterpene biosynthesis pathway construction in Escherichia coli
    • O.A. Carter, R.J. Peters, and R. Croteau Monoterpene biosynthesis pathway construction in Escherichia coli Phytochemistry 64 2003 425 433
    • (2003) Phytochemistry , vol.64 , pp. 425-433
    • Carter, O.A.1    Peters, R.J.2    Croteau, R.3
  • 20
    • 0002317514 scopus 로고    scopus 로고
    • Natural products (secondary metabolites)
    • B. Buchanan W. Gruissem R. Jones American Society of Plant Physiologists
    • R. Croteau, T.M. Kutchan, and N.G. Lewis Natural products (secondary metabolites) B. Buchanan W. Gruissem R. Jones Biochemistry and Molecular Biology of Plants 2000 American Society of Plant Physiologists 1250 1318
    • (2000) Biochemistry and Molecular Biology of Plants , pp. 1250-1318
    • Croteau, R.1    Kutchan, T.M.2    Lewis, N.G.3
  • 21
    • 77956684330 scopus 로고    scopus 로고
    • Molecular genetics of plant alkaloid biosynthesis
    • G.A. Cordell Academic Press
    • T.M. Kutchan Molecular genetics of plant alkaloid biosynthesis G.A. Cordell The Alkaloids - Chemistry and Biology, vol 50 1998 Academic Press 257 316
    • (1998) The Alkaloids - Chemistry and Biology, Vol 50 , pp. 257-316
    • Kutchan, T.M.1
  • 22
    • 0001094465 scopus 로고
    • The relationship between growth rate, differentiation and alkaloid accumulation in cell cultures
    • K. Lindsey, and M.M. Yeoman The relationship between growth rate, differentiation and alkaloid accumulation in cell cultures J Exp Bot 34 1983 1055 1065
    • (1983) J Exp Bot , vol.34 , pp. 1055-1065
    • Lindsey, K.1    Yeoman, M.M.2
  • 23
    • 0007138302 scopus 로고
    • Cytodifferentiation and alkaloid accumulation in cultured cells of Papaver bracteatum
    • T.M. Kutchan, S. Ayabe, R.J. Krueger, E.M. Coscia, and C.J. Coscia Cytodifferentiation and alkaloid accumulation in cultured cells of Papaver bracteatum Plant Cell Rep 2 1983 281 284
    • (1983) Plant Cell Rep , vol.2 , pp. 281-284
    • Kutchan, T.M.1    Ayabe, S.2    Krueger, R.J.3    Coscia, E.M.4    Coscia, C.J.5
  • 24
    • 0032720893 scopus 로고    scopus 로고
    • Multicellular compartmentation of Catharanthus roseus alkaloid biosynthesis predicts intercellular translocation of a pathway intermediate
    • B. St.-Pierre, F.A. Vazquez-Flota, and V. De Luca Multicellular compartmentation of Catharanthus roseus alkaloid biosynthesis predicts intercellular translocation of a pathway intermediate Plant Cell 11 1999 887 900
    • (1999) Plant Cell , vol.11 , pp. 887-900
    • St.-Pierre, B.1    Vazquez-Flota, F.A.2    De Luca, V.3
  • 25
    • 0034490132 scopus 로고    scopus 로고
    • Indole alkaloid biosynthesis in Catharanthus roseus: New enzyme activities and identification of cytochrome P450 CYP72A1 as secologanin synthase
    • S. Irmler, G. Schröder, B. St.-Pierre, N.P. Crouch, M. Hotze, J. Schmidt, D. Strack, U. Matern, and J. Schröder Indole alkaloid biosynthesis in Catharanthus roseus: new enzyme activities and identification of cytochrome P450 CYP72A1 as secologanin synthase Plant J 24 2000 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
  • 26
    • 1842430598 scopus 로고    scopus 로고
    • 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-derived primary metabolites
    • V. Burlat, A. Oudin, M. Courtois, M. Rideau, and B. St.-Pierre 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-derived primary metabolites Plant J 38 2004 131 141 This article provides in situ hybridization evidence that the early genes of secoiridoid formation (i.e. DXS, DXR, MECS and G10H) are expressed in internal phloem parenchyma. These results provide evidence that a third cell type, in addition to epidermal cells and laticifers/idioblasts, is involved in monoterpenoid indole alkaloid biosynthesis in Madagascar periwinkle. This additional evidence of the long-range transport of intermediates in the biosynthesis monoterpenoid indole alkaloids provides an experimental system for the study of the transport processes and transporters in Catharanthus alkaloid formation and accumulation.
    • (2004) Plant J , vol.38 , pp. 131-141
    • Burlat, V.1    Oudin, A.2    Courtois, M.3    Rideau, M.4    St.-Pierre, B.5
  • 27
    • 0032423802 scopus 로고    scopus 로고
    • The iridoid glucoside secologanin is derived from the novel triose phosphate/pyruvate pathway in a Catharanthus roseus cell culture
    • A. Contin, R. van der Heijden, Lefeber AWM, and R. Verpoorte The iridoid glucoside secologanin is derived from the novel triose phosphate/pyruvate pathway in a Catharanthus roseus cell culture FEBS Lett 434 1998 413 416
    • (1998) FEBS Lett , vol.434 , pp. 413-416
    • Contin, A.1    Van Der Heijden, R.2    Lefeber, A.W.M.3    Verpoorte, R.4
  • 29
    • 4644289320 scopus 로고    scopus 로고
    • The roles of latex and the vascular bundle in morphine biosynthesis in the opium poppy, Papaver somniferum
    • M. Weid, J. Ziegler, and T.M. Kutchan The roles of latex and the vascular bundle in morphine biosynthesis in the opium poppy, Papaver somniferum Proc Natl Acad Sci USA 101 2004 13957 13962 This article presents immunocytological evidence on the localization of four enzymes of tetrahydrobenzylisoquinoline- derived alkaloid biosynthesis in opium poppy. Two cell types, phloem parenchyma (in which 4′OMT and SalAT are localized) and laticifers (in which COR is localized), were identified as the sites of morphine biosynthesis. BBE localized to the parenchyma of root cortex, and is presumably involved in sanguinarine biosynthesis. 7OMT, which is involved in laudanine biosynthesis, was localized to distal phloem parenchyma. These results corroborate the results of earlier biochemical localization studies and refute a recent report that localizes alkaloid biosynthesis in opium poppy to sieve elements [32].
    • (2004) Proc Natl Acad Sci USA , vol.101 , pp. 13957-13962
    • Weid, M.1    Ziegler, J.2    Kutchan, T.M.3
  • 30
    • 0036834176 scopus 로고    scopus 로고
    • Immunocytological localization of two enzymes involved in berberine biosynthesis
    • A. Bock, G. Wanner, and M.H. Zenk Immunocytological localization of two enzymes involved in berberine biosynthesis Planta 216 2002 57 63
    • (2002) Planta , vol.216 , pp. 57-63
    • Bock, A.1    Wanner, G.2    Zenk, M.H.3
  • 31
    • 0029201588 scopus 로고
    • Phloem-specific expression of tyrosine/dopa decarboxylase genes and the biosynthesis of isoquinoline alkaloids in opium poppy
    • P.J. Facchini, and V. De Luca Phloem-specific expression of tyrosine/dopa decarboxylase genes and the biosynthesis of isoquinoline alkaloids in opium poppy Plant Cell 7 1995 1811 1821
    • (1995) Plant Cell , vol.7 , pp. 1811-1821
    • Facchini, P.J.1    De Luca, V.2
  • 32
    • 0345376982 scopus 로고    scopus 로고
    • A tale of three cell types: Alkaloid biosynthesis is localized to sieve elements in opium poppy
    • D.A. Bird, V.R. Franceschi, and P. Facchini A tale of three cell types: alkaloid biosynthesis is localized to sieve elements in opium poppy Plant Cell 15 2003 2626 2635
    • (2003) Plant Cell , vol.15 , pp. 2626-2635
    • Bird, D.A.1    Franceschi, V.R.2    Facchini, P.3


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