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Arahidopsis thaliana

Wyss, U., Grundler, F.M.W. and Munch, A. (1992) The parasitic behaviour of 2nd-stage juveniles of Mehidogyne incognita, in roots of Arahidopsis thaliana. Nematologica 38, 98-111. [Pg.174]

Nair, R.B., Bastress, K.L., Ruegger, M.O., Denault, J.W. and Chappie, C. (2004) The Arahidopsis thaliana reduced epidermal fluorescencel gene encodes an aldehyde dehydrogenase involved in ferulic acid and sinapic acid biosynthesis. Plant Cell, 16, 544-54. [Pg.247]

Soltani, B.M., Ehlting, J., Hamberger, B. and Douglas, C.J. (2006) Multiple cis-regulatory elements regulate distinct and complex patterns of developmental and wound-induced expression oi Arahidopsis thaliana 4CL gene family members. Planta, 224,1226-38. [Pg.252]

McCann, M.C. and Caripta, N.C. (2005) Looking for cell wall mutants of Arahidopsis thaliana. Plant Eiosyst., 139, 80-3. [Pg.258]

Na extrusion from plant cells is powered by the operation of the plasma membrane H -ATPase generating an electrochemical gradient that allows plasma membrane Na /H antiporters to couple the passive movement of inside the cells, along its electrochemical potential, to the active extrusion of Na [21]. Recently, AtSOSl from Arahidopsis thaliana has been shown to encode a plasma membrane Na /H antiport with significant sequence similarity to plasma membrane Na /H antiporters from bacteria and fungi [32]. The overexpression of SOSl improved the salt tolerance of Aro-hidopsis, demonstrating that improved salt tolerance can be attained by limiting Na accumulation in plant cells [33] (Table 10.1). [Pg.973]

Chloroplasts fill most of the cytoplasm around the junction of three cells of Arahidopsis thaliana seen in this micrograph. Both grana stacks and stroma lamellae (pictured in more detail in Fig. 23-19) can be seen. Also present are several small mitochondria. Portions of the large vacuoles, characteristic of plant cells, are seen at top, right, and bottom. Micrograph courtesy of Kenneth Moore. [Pg.338]

BECHTOLD, N., ELLIS, J., PELLETIER, G., In planta Agrobacterium mediated gene-transfer by infiltration of adult Arahidopsis thaliana plants, C. R. Acad. Sci. Paris Life Sci., 1993,316,1194-1199. [Pg.17]

LORIDON, K., COURNOYER, B., GOUBELY, C., DEPEIGES, A., PICARD, G., Length polymorphism and allele structure of trinucleotide microsatellites in natural accessions of Arahidopsis thaliana, Theor. Appl. Genet., 1998, 97, 591-604. [Pg.17]

ABBOTT, R. J., GOMES, M. F., Population genetic structure and outcrossing rate of Arahidopsis thaliana (L) Heynh., Heredity, 1989,62,411-418. [Pg.17]

CHEN, F., D AURIA, J.C., THOLL, D., ROSS, J.R., GERSHENZON, J., NOEL, J.P., PICHERSKY, E., An Arahidopsis thaliana gene for methylsalicylate biosynthesis, identified by a biochemical genomics approach, has a role in defense. Plant J., 2003, 36, 577-588. [Pg.18]

MITCHELL-OLDS, T., Arahidopsis thaliana and its wild relatives A model system for ecology and evolution. Trends Ecol. Evol., 2001,16, 693-700. [Pg.18]

BOHLMANN, J., MARTIN, D., OLDHAM, N. J., GERSHENZON, J., Terpenoid secondary metabolism in Arahidopsis thaliana cDNA cloning, characterization, and functional expression of a myrcene/(E)- 3-ocunene synthase. Arch. Biochem. Biophys., 2000, 375, 262-269. [Pg.18]

FALDT, J., ARIMURA, G, 1., GERSHENZON, J., TAKABAYASHl, J., BOHLMANN, J., Functional identification of AtTPSOS as ( )-beta-ocimene synthase A new monoterpene S5mthase catal5 ing jasmonate- and wound-induced volatile formation in Arahidopsis thaliana, Planta, 2003,216,745-751. [Pg.18]

MEYER, K., CUSUMANO, J.C., SOMERVILLE, C., CHAPPLE, C.C.S., Ferulate-5-hydroxylase from Arahidopsis thaliana defines a new family of cytochrome P450-dependent monooxygenases, Proc. Natl. Acad. Sci. U. S. A., 1996, 93, 6869-6874. [Pg.60]

GOUJON, T., SIBOUT, R., EUDES, A., MACKAY, J., JOULANIN, L., Genes involved in the biosynthesis of lignin precursors in Arahidopsis thaliana. Plant Physiol. Biochem., 2003,41, 677-687. [Pg.66]

BARTLEY, G. E., SCOLNIK, P. A., BEYER, P., Two Arahidopsis thaliana carotene desaturases, phytoene desaturase and zeta-carotene desaturase, expressed in Escherichia coli, catalyze a poly-cis pathway to yield pro-lycopene., Eur. J. Biochem. 1999, 259, 396-403. [Pg.109]

Arahidopsis thaliana 86 arabinose 680 archaeal phospholipids 513 aroma compounds 414 artemisinin 67 5 Arxula adenivorans 678 astaxanthin 616 ATP-citrate lyase (ACL) 679 autonomously replicating sequences (ARS) 696... [Pg.715]

Zhu X, Suzuki K, Okada K, Tanaka K, Nakagawa T, Kawamukai M, Matsuda H (1997) Cloning and functional expression of a novel geranylgeranyl pyrophosphate synthase gene from Arahidopsis thaliana in Escherichia coli. Plant Cell Physiol 38 357-361... [Pg.3282]

Tardy F, Havaux M (1996) Photosynthesis, chlorophyll fluorescence, light-harvesting Systran and photoinhibition resistance of a zeaxanthin-accumulating mutant of Arahidopsis thaliana. J Photochtan Photobiol B 34 87—94... [Pg.3282]

Baeyer-Villiger-type oxidations can also be catalyzed by some P450s, for example CYP85 A2 from Arahidopsis thaliana, which catalyzes the conversion of castasterone (24) to brassinolide (25) [69] (Scheme 12.8). [Pg.428]

Nawrath C and Poirier Y (1996) Review on polyhydroxyalkanoate formation in the model plant Arahidopsis thaliana, Publ Natl Res Council of Canada Int Symp Bact Polyhydroxyalkanoates, pp. 119-126. [Pg.32]


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