178 A.R. Reddy <strong>and</strong> A.S. Raghavendra 9. CONCLUDING REMARKS Light is critical for growth <strong>and</strong> development <strong>of</strong> plants. It is apparent from the foregone account that plants have evolved multiple strategies <strong>of</strong> photoprotective <strong>and</strong> photoadaptive mechanisms that are critical for survival under conditions <strong>of</strong> excess photon absorption. Some <strong>of</strong> these mechanisms involve changes in pigment-protein complexes, synthesis <strong>and</strong> recruitment <strong>of</strong> enzymes with antioxidant function <strong>and</strong> abundant soluble antioxidants in the chloroplasts. Furthermore, the redox conditions in plant cells may modulate the photosystem components for acclimation to photooxidative stress. The induction <strong>of</strong> genes under photooxidative stress for optimized absorption <strong>of</strong> light by specific photoreceptors is poorly understood. Analysing the expression <strong>of</strong> these genes under different light quality/quantity conditions will enable us to make specific inferences about the nature <strong>and</strong> sensitivity <strong>of</strong> such photoreceptors in plants. Genetic regulation <strong>of</strong> antioxidant biosynthesis <strong>and</strong> overexpression several antioxidative enzymes should reveal plant acclamatory responses in response to photooxidative stress. There is a need to underst<strong>and</strong> how the photooxidative stress provoke several changes in cellular metabolism, reflecting the changed expression <strong>of</strong> a common or overlapping set <strong>of</strong> genes. Detailed information is also required on how the signaling molecules are integrated with ROS into the general signaling network <strong>of</strong> a cell <strong>and</strong>/or the intracellular production sites affect the signaling pathway. Metabolite, protein <strong>and</strong> transcript pr<strong>of</strong>iling technology could provide us a holistic underst<strong>and</strong>ing <strong>of</strong> how plants thrive in highly variable <strong>and</strong> adverse environments. 10. ACKNOWLEDGEMENTS Work in our laboratory on photosynthesis <strong>and</strong> preparation <strong>of</strong> this article are supported by grants (to ASR) from Department <strong>of</strong> Science <strong>and</strong> Technology (No. SP/SO/A12/98) <strong>and</strong> ARR from Council <strong>of</strong> Scientific <strong>and</strong> Industrial Research (No. 38 (1063)/03/EMR-II), both from New Delhi, India. 11. REFERENCES Adamska, I. (1997). ELIPs: Light-induced stress proteins. Physiol. Planta. 100, 794-805. Agrawal, G. K., Jwa, N-S. <strong>and</strong> Rakwal, R. (2002). A pathogen-induced novel rice Oryza sativa L.) gene encodes a putative protein homologous to type II glutathione S-transferases. Plant Sci. 163, 1153-1160. Allen, R. (1995). Dissection <strong>of</strong> oxidative stress tolerance using transgenic plants. Plant Physiol. 107, 1049-1054. Allen, R. D., Webb, R. P. <strong>and</strong> Schake, S. A. (1997). Use <strong>of</strong> Transgenic Plants to Study Antioxidant Defenses. Free Rad. Biol. Med. 23, 473-479. Alscher, R. G., Erturk, N., <strong>and</strong> Heath, L. S. (2002). Role <strong>of</strong> superoxide dismutases (SODs) in controlling oxidative stress in plants. J. Exp. Bot. 53, 1331-1341. Anderson, J. M., Chow, W. S. <strong>and</strong> Park, Y. I. (1995). The gr<strong>and</strong> design <strong>of</strong> photosynthesis: acclimation <strong>of</strong> the photosynthetic apparatus to environmental cues. Photosynth. Res. 46, 129-139. Aro, E.M., McCaffery, S. <strong>and</strong> Anderson, J. M. (1993). Photoinhibition <strong>and</strong> D1 Protein degradation
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(1997). Novel aspects <strong>of</strong> chlorophyll a/b-binding proteins. Physiol. Planta. 100, 769-779. Bergantino, E., Brunetta, A., Touloupakis, E., Segella, A., Szabo, I. <strong>and</strong> Glacometti, G. M. (2003). Role <strong>of</strong> PSII-H subunit in photo protection. Novel aspects <strong>of</strong> D1 turnover in Synechocystis 6803. J. Biol. Chem. 278, 41820-41829. Bergatino, E., S<strong>and</strong>ona, D., Cugini, D. <strong>and</strong> Bassi, R. (1998). The photo system II subunit CP29 can be phosphorylated in both C 3 <strong>and</strong> C 4 plants as suggested by sequence analysis. Plant Mol. Biol. 36, 11-22. Björkman, O. <strong>and</strong> Demmig-Adams, B. (1994). Regulation <strong>of</strong> photosynthetic light energy capture, conversion, <strong>and</strong> dissipation in leaves <strong>of</strong> higher plants. In: Ecophysiology <strong>of</strong> photosynthesis (Schulze, E-D. <strong>and</strong> M. M. Caldwell eds.) Springer-Verlag, pp. 17-47. Björkman, O. <strong>and</strong> Powles, S. B. (1981). Leaf movement in the shade species Oxalis oregano. I. Response to light level <strong>and</strong> light quality. Carnegie Year Book 80, 59-62. Boekema, E. J., Van Roon, H., Calkoen, H., Bassi, R. <strong>and</strong> Dekker, J. P. (1999). Multiple types <strong>of</strong> association <strong>of</strong> photosystem II <strong>and</strong> its light-harvesting antenna in partially solubilized photosystem II membranes. Biochemsitry 38, 2233-2239. Bowler, C., Montagu, M. V. <strong>and</strong> Inzé, D. (1992). Superoxide dismutase <strong>and</strong> stress tolerance. Annu. Rev. Plant Physiol. Plant Mol. Biol. 43, 83-116. Braidot, E., Petrussa, E., Vianello, A. <strong>and</strong> Macrì, F. (1999). Hydrogen peroxide generation by higher plant mitochondria oxidizing complex I or complex II substrates. FEBS Lett. 451, 347-350. Breusegem, F.V., Montagu, M. V. <strong>and</strong> Inzé, D. (2002). 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Recent advances in the role <strong>and</strong> biosynthesis <strong>of</strong> ascorbic acid in plants. Plant Cell Environ. 24, 383-394. Corpas, F.J., Barroso, J. B. <strong>and</strong> del Río, L. A. (2001). Peroxisomes as a source <strong>of</strong> reactive oxygen
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PHYSIOLOGY AND MOLECULAR BIOLOGY OF
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A C.I.P. Catalogue record for this
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About the Editors K.V. Madhava Rao
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LIST OF CONTRIBUTORS K. AKASHI Grad
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List of Contributors xiii NAVINDER
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PREFACE Increasing agricultural pro
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2 K.V. Madhava Rao Abiotic stresses
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4 K.V. Madhava Rao SOME O THE PROMI
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6 K.V. Madhava Rao 2. WATER STRESS
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8 K.V. Madhava Rao 5. FREEZING STRE
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10 K.V. Madhava Rao of these pathwa
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12 K.V. Madhava Rao Bray, E.A. (199
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14 K.V. Madhava Rao Rao, K.V. Madha
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16 A. Yokota, K. Takahara and K. Ak
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20 A. Yokota, K. Takahara and K. Ak
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36 A. Yokota, K. Takahara and K. Ak
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38 A. Yokota, K. Takahara and K. Ak
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41 CHAPTER 3 SALT STRESS ZORA DAJIC
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Salt Stress 43 activities (mainly i
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Salt Stress 45 In summary, mechanis
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Salt Stress 47 tolerance research i
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Salt Stress 49 need to rely on sodi
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Salt Stress 51 (Echeverria, 2000).
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Salt Stress 53 Therefore, the capac
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Salt Stress 55 Reduced plant growth
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Salt Stress 57 Table 3. Salt tolera
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Salt Stress 59 6.2. Nitrogen Fixati
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Salt Stress 61 A significant number
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Salt Stress 63 macromolecules, irre
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Salt Stress 65 8.2. Ion Homeostasis
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Salt Stress 67 1997), is speculated
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Salt Stress 69 together with the At
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Salt Stress 71 important role in si
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Salt Stress 73 Figure 5. Determinan
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Salt Stress 75 9.1.Transgenic Plant
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Salt Stress 77 tolerance from halop
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Salt Stress 79 sponse and yield (Su
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Salt Stress 81 Table 5. Possible ut
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Salt Stress 83 monitored with fluor
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Salt Stress 85 Func. Plant Biol. 29
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Salt Stress 87 Dajic, Z., Stevanovi
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Salt Stress 89 Gouia, H., Ghorbal,
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Salt Stress 91 Larcher, W. (1995).
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Salt Stress 93 Munns, R. and James,
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Salt Stress 95 Rausell, A., Kanhono
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Salt Stress 97 durum wheat crops gr
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Salt Stress 99 Yoshida, K. (2002).
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102 T.D. Sharkey and S.M. Schrader
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106 T.D. Sharkey and S.M. Schrader
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Heavy Metal Stress 229 following: (
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Heavy Metal Stress 231 a precursor
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Heavy Metal Stress 233 notype. Incr
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Table 1. Proposed specificity and l
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Heavy Metal Stress 237 4.2. Chapero
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Heavy Metal Stress 239 of prokaryot
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Heavy Metal Stress 241 5. HYPERACCU
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Table 2. Genes introduced into plan
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Heavy Metal Stress 245 7. CONCLUSIO
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Heavy Metal Stress 247 controlled b
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Heavy Metal Stress 249 Kägi, J.H.R
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Heavy Metal Stress 251 Murphy, A.,
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Heavy Metal Stress 253 through xyle
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255 CHAPTER 9 METABOLIC ENGINEERING
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Metabolic Engineering for Stress To
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Metabolic Engineering for Stress To
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302 A.K. Tyagi, S. Vij and N. Saini
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304 A.K. Tyagi, S. Vij and N. Saini
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Table 3. Continued... Source Resour
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332 A.K. Tyagi, S. Vij and N. Saini
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334 A.K. Tyagi, S. Vij and N. Saini
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336 Index Auxins, 146 Avena sativa
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338 Expressed sequence tags (ESTs),
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340 Index Magnesium, 195 Mairiena s
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342 Index Processes less sensitive
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344 Index Sunflecks, 104 Sunflower,