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184 A. Fait, A. Yellin, H. Fromm LingenhoehlK,BromR,HeidJ,BeckP,FroestlW,KaupmannK,BettlerB,MosbacherJ (1999) Gamma-hydroxybutyrate is a weak agonist at recombinant GABA(B) receptors. Neuropharmacology 38:1667–1673 Lodwig E, Poole P (2003) Metabolism of Rhizobium bacteroids. Crit Rev Plant Sci 22:37–78 Maitre M (1997) The gamma-hydroxybutyrate signalling system in brain organization and functional implications. Prog Neurobiol 51:337–361 Mamelak M (1989) Gammahydroxybutyrate: an endogenous regulator of energy metabolism. Neurosci Biobehav Res 13:187–198 Mamelak M (1997) Neurodegeneration, sleep, and cerebral energy metabolism: a testable hypothesis. J Geriatr Psychiatr Neurol 10:29–32 Mathivet P., Bernasconi R, De Barry J, Marescaux C, Bittiger H (1997) Binding characteristics ofgamma-hydroxybutyricacidasaweakbutselectiveGABAB receptor agonist. Eur J Pharmacol 321:67–75 McIntire SL, Reimer RJ, Schuske K, Edwards RH, Jorgensen EM (1997) Identification and characterization of the vesicular GABA transporter. Nature 389:870–876 Miller RW, McRae DG, Joy K (1991) Glutamate and gamma-aminobutyrate metabolism in isolated Rhizobium meliloti bacteroids. Mol Plant Microbe Interact 4:37–45 Nakamura K, Bindokas VP, Kowlessur D, Elas M, Milstien S, Marks JD, Halpern HJ, Kang UJ (2001) Tetrahydrobiopterin scavenges superoxide in dopaminergic neurons. J Biol Chem 276:34402–34407 Nulton-Persson AC, Starke DW, Mieyal JJ, Szweda LI (2003) Reversible inactivation of αketoglutarate dehydrogenase in response to alterations in the mitochondrial glutathione status. Biochemistry 42:4235–4242 Okun MS, Boothby LA, Bartfield RB, Doering PL (2001) GHB: an important pharmacologic and clinical update. Pharm Pharm Sci 4:167–75 Owens DF, Kriegstein AR (2002) Is there more to GABA than synaptic inhibition? Nat Rev Neurosci 3:715–727 Palanivelu R, Brass L, Edlund AF, Preuss D (2003) Pollen tube growth and guidance is regulated by POP2, an Arabidopsis gene that controls GABA levels. Cell 114:47–59 Poole P, Allaway D (2000) Carbon and nitrogen metabolism in Rhizobium. AdvMicrob Physiol 43:117–163 Prell J, Boesten B, Poole P, Priefer UB (2002) The Rhizobium leguminosarum bv. viciae VF39 gamma-aminobutyrate (GABA) aminotransferase gene (gabT) is induced by GABA and highly expressed in bacteroids. Microbiology 148:615–23 Rentsch D, Hirner B, Schmelzer E, Frommer WB (1996) Salt stress-induced proline transporters and salt stress-repressed broad specificityaminoacidpermeasesidentified by suppression of a yeast amino acid permease-targeting mutant. Plant Cell 8:1437– 1446 Richmond JE, Jorgensen EM (1999) One GABA and two acetylcholine receptors function at the C. elegans neuromuscular junction. Nat Neurosci 2:791–797 Salminen SO, Streeter JG (1992) Labelling of carbon pools in Bradyrhizobium japonicum and Rhizobium leguminosarum bv. viciae bacteroids following incubation of intact nodules with 14 CO2. Plant Physiol 100: 597–604 Schaller M, Schaffhauser M, Sans N, Wermuth B (1999) Cloning and expression of succinic semialdehyde reductase from human brain: identity with aflatoxin B1 aldehyde reductase. Eur J Biochem 265:1056–1060 Shelp BJ, Walton CS, Snedden WA, Tuin LG, Oresnik IJ, Layzell DB (1995) GABA shunt in developing soybean seeds is associated with hypoxia. Physiol Plant 94:219–228 Snead OC (2000) Evidence for a G protein-coupled gamma-hydroxybutyric acid receptor. J Neurochem 75:1986–1996
12 GABA and GHB Neurotransmitters in Plants and Animals 185 Snedden WA, Fromm H (1999) Regulation of the γ-aminobutyrate-synthesizing enzyme, glutamate decarboxylase, by calcium/calmodulin: a mechanism for rapid activation in response to stress. In: Lerner HR (ed) Plant responses to environmental stresses: from phytohormones to genome reorganization. Dekker, New York, pp 549–574 Steward FC, Thompson JF–Dent CE (1949) γ-Aminobutyric acid: a constituent of the potato tuber? Science 110:439–440 Taberner PV, Rick JT, Kerkut GA (1972) The action of gamma-hydroxybutyric acid on cerebral glucose metabolism. J Neurochem 19:245–254 Torres GE, Gainetdinov RR, Caron MG (2003) Plasma membrane monoamine transporters: structure, regulation and function. Nat Rev Neurosci 4:13–25 Tretter L, Adam-Vizi V (2000) Inhibition of Krebs cycle enzymes by hydrogen peroxide: a key role of α-ketoglutarate dehydrogenase in limiting NADH production under oxidative stress. J Neurosci 20:8972–8979 Tunnicliff G (1992) Significance of gamma-hydroxybutyric acid in the brain. Gen Pharmacol 23:1027–1034 Turano FJ, Kramer GF, Wang C (1997) The effect of methionine, ethylene, and polyamine catabolic intermediates on polyamine accumulation in detached soybean leaves. Physiol Plant 101:510–518 Udvardi MK, Day DA (1997) Metabolite transport across symbiotic membranes of legume nodules. Annu Rev Plant Physiol Plant Mol Biol 48:493–523 Vance CP, Heichel GH (1991) Carbon in N2 fixation limitation or exquisite adaptation. Annu Rev Plant Physiol Plant Mol Biol 42:373–392 Visser JE, Smith DW, Moy SS, Breese GR, Friedmann T, Rothstein JD, Jinnah HA (2002) Oxidative stress and dopamine deficiency in a genetic mouse model of Lesch–Nyhan disease. Brain Res Dev Brain Res 133:127–139 Vissers S, Andre B, Muyldermans F, Grenson M. (1989) Positive and negative regulatory elements control the expression of the UGA gene coding for the inducible 4-aminobutyricacid-specific permease in Saccharomyces cerevisiae. Eur J Biochem 181:357–361 Walshaw DL, Wilkinson A, Mundy M, Smith M, Poole PS (1997) Regulation of the TCA cycle and the general amino acid permease by metabolism in Rhizobium leguminosarum. Microbiology 143:2209–2221 Weir E (2000) Raves: a review of the culture, the drugs and the prevention of harm. CMAJ 162:1843–1848 Wigge B, Kroemer S, Gardestroem P (1993) The redox levels and subcellular distribution of pyridine nucleotides in illuminated barley leaf protoplasts studied by rapid fractionation. Physiol Plant 88:10–18
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František Baluška · Stefano Manc
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Dr. František Baluška University
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VI Preface turn, reward the ants by
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VIII Preface of olfactory response.
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Contents 1 The Green Plant as an In
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Contents XIII 6 Signals and Targets
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Contents XV 11 Amino Acid Transport
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Contents XVII 15 Regulation of Plan
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Contents XIX 21.3 Conclusions and P
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Contents XXI 27.3.2 Catechin Induce
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XXIV Contributors Correa-Aragunde,
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XXVI Contributors Lamattina, L. (e-
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XXVIII Contributors Song, C. Depart
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1 The Green Plant as an Intelligent
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2 Neurobiological View of Plants an
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38 P.W. Barlow Thestimulipresentedt
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40 P.W. Barlow that a tropism is su
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42 P.W. Barlow the auxin flow into
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44 P.W. Barlow afferentnervousimpul
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46 P.W. Barlow analysis. In particu
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48 P.W. Barlow reception of his boo
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50 P.W. Barlow Iijima M, Kono Y (19
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4 How Can Plants Choose the Most Pr
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66 P.M. Neumann Finally, I examined
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68 P.M. Neumann evolutionary progre
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70 P.M. Neumann conclusion is that
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72 P.M. Neumann resources from matu
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6 Signals and Targets Triggered by
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6TargetsofSI 77 6.1.2 Self-Incompat
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6TargetsofSI 79 by Yang 2002) has p
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6TargetsofSI 81 al. 2002). Thus, SI
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6TargetsofSI 83 Fig.6.2. PrABP80 ha
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6TargetsofSI 85 many of the genes e
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6TargetsofSI 87 [Ca 2+ ]i may signa
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6TargetsofSI 89 is crosstalk betwee
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6TargetsofSI 91 Hepler PK, Vidali L
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6TargetsofSI 93 Snowman BN, Kovar D
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96 T. Nürnberger, B. Kemmerling Wh
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98 T. Nürnberger, B. Kemmerling Fo
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100 T. Nürnberger, B. Kemmerling p
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102 T. Nürnberger, B. Kemmerling i
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104 T. Nürnberger, B. Kemmerling r
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106 T. Nürnberger, B. Kemmerling F
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108 T. Nürnberger, B. Kemmerling M
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8 Nitric Oxide Involvement in Incom
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124 M.L. Lanteri et al. 9.1.1 Auxin
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126 M.L. Lanteri et al. Fig.9.1. Sc
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128 M.L. Lanteri et al. Fig.9.2. NO
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130 M.L. Lanteri et al. 9.3.1 Nitri
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132 M.L. Lanteri et al. Fig.9.3. Sc
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16 Physiological Roles of Nonselect
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16 Nonselective cation channels 237
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Fig.16.1. Possible roles of nonsele
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17 Touch-Responsive Behaviors and G
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18 Oscillations in Plants Sergey Sh
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18 Oscillations in Plants 263 Tempo
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18 Oscillations in Plants 265 Dries
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18 Oscillations in Plants 267 backg
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18 Oscillations in Plants 269 The f
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18 Oscillations in Plants 271 prehe
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18 Oscillations in Plants 273 Cardo
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18 Oscillations in Plants 275 Shaba
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278 K.Trebacz,H.Dziubinska,E.Krol W
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280 K.Trebacz,H.Dziubinska,E.Krol T
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282 K.Trebacz,H.Dziubinska,E.Krol E
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284 K.Trebacz,H.Dziubinska,E.Krol 1
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286 K.Trebacz,H.Dziubinska,E.Krol n
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288 K.Trebacz,H.Dziubinska,E.Krol D
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290 K.Trebacz,H.Dziubinska,E.Krol S
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292 R. Stahlberg, R.E. Cleland, E.
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310 E.Davies,B.Stankovic It is assu
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312 E.Davies,B.Stankovic 21.2 Evide
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314 E.Davies,B.Stankovic Fig.21.3.
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316 E.Davies,B.Stankovic Relative m
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318 E.Davies,B.Stankovic 1992; Beel
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320 E.Davies,B.Stankovic Hentze MW,
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322 J. Fromm, S. Lautner in the ran
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324 J. Fromm, S. Lautner cells (Sam
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326 J. Fromm, S. Lautner 22.5 Ion C
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328 J. Fromm, S. Lautner hastobedon
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330 J. Fromm, S. Lautner Beilby MJ,
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332 J. Fromm, S. Lautner Williams S
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334 S. Mancuso, S. Mugnai like the
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336 S. Mancuso, S. Mugnai 2,000 nM
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338 S. Mancuso, S. Mugnai the fourt
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340 S. Mancuso, S. Mugnai “slow-w
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342 S. Mancuso, S. Mugnai 23.6 Airb
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344 S. Mancuso, S. Mugnai that tree
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346 S. Mancuso, S. Mugnai Fort C, F
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348 S. Mancuso, S. Mugnai Pophof B,
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24 Electrophysiology and Phototropi
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370 E. Wagner et al. Table 25.1. Fl
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372 E. Wagner et al. Exudation [µl
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374 E. Wagner et al. metabolism at
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376 E. Wagner et al. The circadian
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378 E. Wagner et al. Fig.25.5. Time
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380 E. Wagner et al. Fig.25.7. Patt
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382 E. Wagner et al. Fig.25.9. Time
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384 E. Wagner et al. Fig.25.11. a K
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386 E. Wagner et al. 25.9 Conclusio
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388 E. Wagner et al. Lecharny A, Wa
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26 Signals and Signalling Pathways
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404 L.G. Perry et al. properties (S
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406 L.G. Perry et al. Fig.27.1. A s
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408 L.G. Perry et al. phytotoxins i
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410 L.G. Perry et al. monooxygenase
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412 L.G. Perry et al. 27.4 (±)-Cat
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414 L.G. Perry et al. (±)-catechin
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416 L.G. Perry et al. mineralizatio
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418 L.G. Perry et al. Dyer AR (2004
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420 L.G. Perry et al. Singh HP, Bat
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422 V.Ninkovic,R.Glinwood,J.Petters
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436 Subject Index defense 67, 95-10
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438 Subject Index sieve-tube-elemen
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