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Plant Physiology PDF

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FFiiifffttthhh EEdddiiitttiiion Lincoln Taiz Professor Emeritus University of California, Santa Cruz Eduardo Zeiger Professor Emeritus University of California, Los Angeles Sinauer Associates Inc., Publishers Sunderland, Massachusetts U.S.A. © Sinauer Associates, Inc. This material cannot be copied, reproduced, manufactured or disseminated in any form without express written permission from the publisher. ©2012SinauerAssociates,Inc.Thismaterialcannotbecopied,reproduced,manufactured TAIZ_FM_JD.indd III ordisseminatedinanyformwithoutexpresswrittenpermissionfromthepublisher. 5/19/10 4:08:58 PM Contents CHAPTER 1 Plant Cells 1 Plant Life: Unifying Principles 2 Independently Dividing, Semiautonomous Organelles 18 Overview of Plant Structure 2 Proplastids mature into specialized plastids in Plant cells are surrounded by rigid cell walls 2 different plant tissues 21 New cells are produced by dividing Chloroplast and mitochondrial division are tissues called meristems 2 independent of nuclear division 21 Three major tissue systems make up the plant body 4 The Plant Cytoskeleton 22 The plant cytoskeleton consists of microtubules Plant Cell Organelles 4 and microfi laments 22 Biological membranes are phospholipid Microtubules and microfi laments can assemble bilayers that contain proteins 4 and disassemble 23 The Endomembrane System 8 Cortical microtubules can move around the cell by The nucleus contains the majority of the “treadmilling” 24 genetic material 8 Cytoskeletal motor proteins mediate cytoplasmic Gene expression involves both transcription streaming and organelle traffi c 24 and translation 10 Cell Cycle Regulation 25 The endoplasmic reticulum is a network Each phase of the cell cycle has a specifi c set of of internal membranes 10 biochemical and cellular activities 26 Secretion of proteins from cells begins with the The cell cycle is regulated by cyclins and rough ER (RER) 13 cyclin-dependent kinases 26 Glycoproteins and polysaccharides destined Mitosis and cytokinesis involve both microtubules for secretion are processed in the Golgi and the endomembrane system 27 apparatus 14 The plasma membrane has specialized regions Plasmodesmata 29 involved in membrane recycling 16 Primary and secondary plasmodesmata help to Vacuoles have diverse functions in plant cells 16 maintain tissue developmental gradients 29 Independently Dividing Organelles Derived SUMMARY 31 from the Endomembrane System 17 Oil bodies are lipid-storing organelles 17 Microbodies play specialized metabolic roles in leaves and seeds 17 © Sinauer Associates, Inc. This material cannot be copied, reproduced, manufactured or disseminated in any form without express written permission from the publisher. ©2012SinauerAssociates,Inc.Thismaterialcannotbecopied,reproduced,manufactured TAIZ_FM_JD.indd XVI ordisseminatedinanyformwithoutexpresswrittenpermissionfromthepublisher. 5/19/10 4:09:15 PM CHAPTER 2 Genome Organization and Gene Expression 35 Nuclear Genome Organization 35 Epigenetic modifi cations help determine gene The nuclear genome is packaged into activity 48 chromatin 36 Posttranscriptional Regulation of Centromeres, telomeres, and nucleolar organizers Nuclear Gene Expression 50 contain repetitive sequences 36 RNA stability can be infl uenced by Transposons are mobile sequences within cis-elements 50 the genome 37 Noncoding RNAs regulate mRNA activity via Polyploids contain multiple copies of the entire the RNA interference (RNAi) pathway 50 genome 38 Posttranslational regulation determines Phenotypic and physiological responses to the life span of proteins 54 polyploidy are unpredictable 41 Tools for Studying Gene Function 55 Plant Cytoplasmic Genomes: Mitochondria Mutant analysis can help to elucidate and Chloroplasts 42 gene function 55 The endosymbiotic theory describes the origin Molecular techniques can measure the of cytoplasmic genomes 42 activity of genes 55 Organellar genomes consist mostly of linear Gene fusions can introduce reporter genes 56 chromosomes 43 Organellar genetics do not obey Genetic Modifi cation of Crop Plants 59 Mendelian laws 44 Transgenes can confer resistance to herbicides or plant pests 59 Transcriptional Regulation of Nuclear Genetically modifi ed organisms are Gene Expression 45 controversial 60 RNA polymerase II binds to the promoter region of most protein-coding genes 45 SUMMARY 61 UNIT I Transport and Translocation of Water and Solutes 65 CHAPTER 3 Water and Plant Cells 67 Water in Plant Life 67 Water Potential 73 The chemical potential of water represents the The Structure and Properties of Water 68 free-energy status of water 74 Water is a polar molecule that forms hydrogen Three major factors contribute to cell bonds 68 water potential 74 Water is an excellent solvent 69 Water potentials can be measured 75 Water has distinctive thermal properties relative to its size 69 Water Potential of Plant Cells 75 Water molecules are highly cohesive 69 Water enters the cell along a water potential gradient 75 Water has a high tensile strength 70 Water can also leave the cell in response to a water Diffusion and Osmosis 71 potential gradient 77 Diffusion is the net movement of molecules by Water potential and its components vary with random thermal agitation 71 growth conditions and location within the Diffusion is most effective over short distances 72 plant 77 Osmosis describes the net movement of water Cell Wall and Membrane Properties 78 across a selectively permeable barrier 73 © Sinauer Associates, Inc. This material cannot be copied, reproduced, manufactured or disseminated in any form without express written permission from the publisher. ©2012SinauerAssociates,Inc.Thismaterialcannotbecopied,reproduced,manufactured TAIZ_FM_JD.indd XVII ordisseminatedinanyformwithoutexpresswrittenpermissionfromthepublisher. 5/19/10 4:09:15 PM XVIII TABLE OF CONTENTS Small changes in plant cell volume cause large Plant Water Status 80 changes in turgor pressure 78 Physiological processes are affected by plant water The rate at which cells gain or lose water is status 80 infl uenced by cell membrane hydraulic Solute accumulation helps cells maintain turgor conductivity 79 and volume 80 Aquaporins facilitate the movement of water across SUMMARY 81 cell membranes 79 CHAPTER 4 Water Balance of Plants 85 Water in the Soil 85 Xylem transport of water in trees faces physical A negative hydrostatic pressure in soil water challenges 94 lowers soil water potential 86 Plants minimize the consequences of Water moves through the soil by bulk fl ow 87 xylem cavitation 96 Water Absorption by Roots 87 Water Movement from the Leaf to the Atmosphere 96 Water moves in the root via the apoplast, symplast, and transmembrane pathways 88 Leaves have a large hydraulic resistance 96 Solute accumulation in the xylem can generate The driving force for transpiration is the “root pressure” 89 difference in water vapor concentration 96 Water loss is also regulated by the pathway Water Transport through the Xylem 90 resistances 98 The xylem consists of two types of tracheary Stomatal control couples leaf transpiration to elements 90 leaf photosynthesis 98 Water moves through the xylem by The cell walls of guard cells have specialized pressure-driven bulk fl ow 92 features 99 Water movement through the xylem requires An increase in guard cell turgor pressure a smaller pressure gradient than movement opens the stomata 101 through living cells 93 The transpiration ratio measures the relationship What pressure difference is needed to lift water between water loss and carbon gain 101 100 meters to a treetop? 93 The cohesion–tension theory explains water trans- Overview: The Soil–Plant–Atmosphere port in the xylem 93 Continuum 102 SUMMARY 102 CHAPTER 5 Mineral Nutrition 107 Essential Nutrients, Defi ciencies, Some mineral nutrients can be absorbed by and Plant Disorders 108 leaves 118 Special techniques are used in nutritional Soil, Roots, and Microbes 119 studies 110 Negatively charged soil particles affect the adsorp- Nutrient solutions can sustain rapid tion of mineral nutrients 119 plant growth 110 Soil pH affects nutrient availability, soil microbes, Mineral defi ciencies disrupt plant metabolism and root growth 120 and function 113 Excess mineral ions in the soil limit plant Analysis of plant tissues reveals mineral growth 120 defi ciencies 117 Plants develop extensive root systems 121 Treating Nutritional Defi ciencies 117 Root systems differ in form but are based on Crop yields can be improved by addition of common structures 121 fertilizers 118 © Sinauer Associates, Inc. This material cannot be copied, reproduced, manufactured or disseminated in any form without express written permission from the publisher. ©2012SinauerAssociates,Inc.Thismaterialcannotbecopied,reproduced,manufactured TAIZ_FM_JD.indd XVIII ordisseminatedinanyformwithoutexpresswrittenpermissionfromthepublisher. 5/19/10 4:09:15 PM TABLE OF CONTENTS XIX Different areas of the root absorb different Nutrients move from mycorrhizal fungi to mineral ions 123 root cells 126 Nutrient availability infl uences root growth 124 SUMMARY 126 Mycorrhizal fungi facilitate nutrient uptake by roots 125 CHAPTER 6 Solute Transport 131 Passive and Active Transport 132 The genes for many transporters have been identifi ed 144 Transport of Ions across Membrane Transporters exist for diverse Barriers 133 nitrogen-containing compounds 146 Different diffusion rates for cations and anions Cation transporters are diverse 147 produce diffusion potentials 134 Anion transporters have been identifi ed 148 How does membrane potential relate to ion distribution? 134 Metal transporters transport essential micronutrients 149 The Nernst equation distinguishes between active and passive transport 136 Aquaporins have diverse functions 149 Proton transport is a major determinant of Plasma membrane H+-ATPases are highly regulated P-type ATPases 150 the membrane potential 137 The tonoplast H+-ATPase drives solute Membrane Transport Processes 137 accumulation in vacuoles 151 Channels enhance diffusion across H+-pyrophosphatases also pump protons at membranes 139 the tonoplast 153 Carriers bind and transport specifi c substances 140 Ion Transport in Roots 153 Primary active transport requires energy 140 Solutes move through both apoplast and Secondary active transport uses stored symplast 153 energy 142 Ions cross both symplast and apoplast 153 Kinetic analyses can elucidate transport Xylem parenchyma cells participate in xylem mechanisms 143 loading 154 Membrane Transport Proteins 144 SUMMARY 156 UNIT II Biochemistry and Metabolism 161 CHAPTER 7 Photosynthesis: The Light Reactions 163 Photosynthesis in Higher Plants 164 Photosynthesis takes place in complexes containing light-harvesting antennas and General Concepts 164 photochemical reaction centers 169 Light has characteristics of both a particle The chemical reaction of photosynthesis is and a wave 164 driven by light 170 When molecules absorb or emit light, Light drives the reduction of NADP and the they change their electronic state 165 formation of ATP 171 Photosynthetic pigments absorb the light that Oxygen-evolving organisms have two powers photosynthesis 166 photosystems that operate in series 171 Key Experiments in Understanding Organization of the Photosynthetic Photosynthesis 167 Apparatus 172 Action spectra relate light absorption to The chloroplast is the site of photosynthesis 172 photosynthetic activity 168 © Sinauer Associates, Inc. This material cannot be copied, reproduced, manufactured or disseminated in any form without express written permission from the publisher. ©2012SinauerAssociates,Inc.Thismaterialcannotbecopied,reproduced,manufactured TAIZ_FM_JD.indd XIX ordisseminatedinanyformwithoutexpresswrittenpermissionfromthepublisher. 5/19/10 4:09:15 PM XX TABLE OF CONTENTS Thylakoids contain integral membrane proteins 173 The photosystem I reaction center reduces NADP+ 185 Photosystems I and II are spatially separated in the thylakoid membrane 174 Cyclic electron fl ow generates ATP but no NADPH 185 Anoxygenic photosynthetic bacteria have a single reaction center 174 Some herbicides block photosynthetic electron fl ow 186 Organization of Light-Absorbing Antenna Systems 176 Proton Transport and ATP Synthesis in the Chloroplast 187 Antenna systems contain chlorophyll and are membrane associated 176 Repair and Regulation of the The antenna funnels energy to the Photosynthetic Machinery 189 reaction center 176 Carotenoids serve as photoprotective agents 190 Many antenna pigment–protein complexes Some xanthophylls also participate in energy have a common structural motif 176 dissipation 190 Mechanisms of Electron Transport 178 The photosystem II reaction center is easily Electrons from chlorophyll travel through damaged 191 the carriers organized in the “Z scheme” 178 Photosystem I is protected from active oxygen Energy is captured when an excited chlorophyll species 191 reduces an electron acceptor molecule 179 Thylakoid stacking permits energy partitioning The reaction center chlorophylls of the two between the photosystems 191 photosystems absorb at different Genetics, Assembly, and Evolution of wavelengths 180 Photosynthetic Systems 192 The photosystem II reaction center is a Chloroplast genes exhibit non-Mendelian patterns multisubunit pigment–protein complex 181 of inheritance 192 Water is oxidized to oxygen by Most chloroplast proteins are imported from photosystem II 181 the cytoplasm 192 Pheophytin and two quinones accept electrons The biosynthesis and breakdown of chlorophyll from photosystem II 183 are complex pathways 192 Electron fl ow through the cytochrome b f 6 Complex photosynthetic organisms have evolved complex also transports protons 183 from simpler forms 193 Plastoquinone and plastocyanin carry electrons between photosystems II and I 184 SUMMARY 194 CHAPTER 8 Photosynthesis: The Carbon Reactions 199 The Calvin–Benson Cycle 200 Light-dependent ion movements modulate en- The Calvin–Benson cycle has three stages: zymes of the Calvin–Benson cycle 208 carboxylation, reduction, and regeneration 200 Light controls the assembly of chloroplast enzymes The carboxylation of ribulose 1,5-bisphosphate fi xes into supramolecular complexes 208 CO for the synthesis of triose phosphates 201 2 The C Oxidative Photosynthetic Carbon 2 Ribulose 1,5-bisphosphate is regenerated for Cycle 208 the continuous assimilation of CO 201 2 The carboxylation and the oxygenation of ribulose An induction period precedes the steady state 1,5-bisphosphate are competing reactions 210 of photosynthetic CO assimilation 204 2 Photorespiration depends on the photosynthetic Regulation of the Calvin–Benson Cycle 205 electron transport system 213 The activity of rubisco increases in the light 206 Photorespiration protects the photosynthetic ap- paratus under stress conditions 214 Light regulates the Calvin–Benson cycle via the ferredoxin–thioredoxin system 207 Photorespiration may be engineered to increase the production of biomass 214 © Sinauer Associates, Inc. This material cannot be copied, reproduced, manufactured or disseminated in any form without express written permission from the publisher. ©2012SinauerAssociates,Inc.Thismaterialcannotbecopied,reproduced,manufactured TAIZ_FM_JD.indd XX ordisseminatedinanyformwithoutexpresswrittenpermissionfromthepublisher. 5/19/10 4:09:15 PM TABLE OF CONTENTS XXI Inorganic Carbon–Concentrating Formation and Mobilization of Mechanisms 216 Chloroplast Starch 225 Starch is synthesized in the chloroplast Inorganic Carbon–Concentrating Mechanisms: during the day 225 The C Carbon Cycle 216 4 Starch degradation at night requires the Malate and aspartate are carboxylation products of phosphorylation of amylopectin 228 the C cycle 217 4 The export of maltose prevails in the nocturnal Two different types of cells participate in the C 4 breakdown of transitory starch 230 cycle 218 Sucrose Biosynthesis and Signaling 231 The C cycle concentrates CO in the chloroplasts 4 2 of bundle sheath cells 220 Triose phosphates supply the cytosolic pool of three important hexose phosphates in the The C cycle also concentrates CO in single 4 2 light 231 cells 221 Fructose 2,6-bisphosphate regulates the hexose Light regulates the activity of key C enzymes 221 4 phosphate pool in the light 235 In hot, dry climates, the C cycle reduces photo- 4 The cytosolic interconversion of hexose phos- respiration and water loss 221 phates governs the allocation of assimilated Inorganic Carbon–Concentrating Mechanisms: carbon 235 Crassulacean Acid Metabolism (CAM) 221 Sucrose is continuously synthesized in the CAM is a versatile mechanism sensitive to environ- cytosol 235 mental stimuli 223 SUMMARY 237 Accumulation and Partitioning of Photosynthates—Starch and Sucrose 224 Photosynthesis: Physiological and Ecological CHAPTER 9 Considerations 243 Photosynthesis Is the Primary Function of There is an optimal temperature for Leaves 244 photosynthesis 256 Leaf anatomy maximizes light absorption 245 Photosynthetic Responses to Carbon Plants compete for sunlight 246 Dioxide 256 Leaf angle and leaf movement can control light Atmospheric CO concentration keeps rising 257 2 absorption 247 CO diffusion to the chloroplast is essential to 2 Plants acclimate and adapt to sun and shade photosynthesis 258 environments 248 Patterns of light absorption generate gradients of Photosynthetic Responses to Light by the CO2 fi xation 259 Intact Leaf 249 CO imposes limitations on photosynthesis 260 2 Light-response curves reveal photosynthetic How will photosynthesis and respiration change in properties 249 the future under elevated CO conditions? 261 2 Leaves must dissipate excess light energy 251 Identifying Different Photosynthetic Absorption of too much light can lead to Pathways 263 photoinhibition 253 How do we measure the stable carbon isotopes of Photosynthetic Responses to plants? 263 Temperature 254 Why are there carbon isotope ratio variations in plants? 264 Leaves must dissipate vast quantities of heat 254 Photosynthesis is temperature sensitive 255 SUMMARY 266 © Sinauer Associates, Inc. This material cannot be copied, reproduced, manufactured or disseminated in any form without express written permission from the publisher. ©2012SinauerAssociates,Inc.Thismaterialcannotbecopied,reproduced,manufactured TAIZ_FM_JD.indd XXI ordisseminatedinanyformwithoutexpresswrittenpermissionfromthepublisher. 5/19/10 4:09:15 PM XXII TABLE OF CONTENTS CHAPTER 10 Translocation in the Phloem 271 Pathways of Translocation 272 Phloem loading in the apoplastic pathway Sugar is translocated in phloem sieve involves a sucrose–H+ symporter 287 elements 273 Phloem loading is symplastic in some Mature sieve elements are living cells specialized species 288 for translocation 273 The polymer-trapping model explains Large pores in cell walls are the prominent feature symplastic loading in plants with intermediary of sieve elements 274 cells 288 Damaged sieve elements are sealed off 274 Phloem loading is passive in a number of tree species 289 Companion cells aid the highly specialized sieve elements 276 The type of phloem loading is correlated with a number of signifi cant characteristics 290 Patterns of Translocation: Source to Sink 276 Phloem Unloading and Sink-to-Source Materials Translocated in the Phloem 277 Transition 291 Phloem sap can be collected and analyzed 278 Phloem unloading and short-distance transport Sugars are translocated in nonreducing form 279 can occur via symplastic or apoplastic pathways 291 Other solutes are translocated in the phloem 280 Transport into sink tissues requires metabolic Rates of Movement 280 energy 292 The Pressure-Flow Model, a Passive The transition of a leaf from sink to source is Mechanism for Phloem Transport 281 gradual 292 An osmotically-generated pressure gradient drives Photosynthate Distribution: Allocation and translocation in the pressure-fl ow model 281 Partitioning 294 The predictions of mass fl ow have been Allocation includes storage, utilization, and confi rmed 282 transport 294 Sieve plate pores are open channels 283 Various sinks partition transport sugars 295 There is no bidirectional transport in single sieve Source leaves regulate allocation 295 elements 284 Sink tissues compete for available translocated The energy requirement for transport through the photosynthate 296 phloem pathway is small 284 Sink strength depends on sink size and Positive pressure gradients exist in the phloem activity 296 sieve elements 284 The source adjusts over the long term to changes Does translocation in gymnosperms involve a in the source-to-sink ratio 297 different mechanism? 285 The Transport of Signaling Molecules 297 Phloem Loading 285 Turgor pressure and chemical signals coordinate Phloem loading can occur via the apoplast or source and sink activities 297 symplast 285 Proteins and RNAs function as signal molecules Abundant data support the existence of in the phloem to regulate growth and apoplastic loading in some species 286 development 298 Sucrose uptake in the apoplastic pathway requires metabolic energy 286 SUMMARY 299 © Sinauer Associates, Inc. This material cannot be copied, reproduced, manufactured or disseminated in any form without express written permission from the publisher. ©2012SinauerAssociates,Inc.Thismaterialcannotbecopied,reproduced,manufactured TAIZ_FM_JD.indd XXII ordisseminatedinanyformwithoutexpresswrittenpermissionfromthepublisher. 5/19/10 4:09:16 PM TABLE OF CONTENTS XXIII CHAPTER 11 Respiration and Lipid Metabolism 305 Overview of Plant Respiration 305 Aerobic respiration yields about 60 molecules of ATP per molecule of sucrose 322 Glycolysis 309 Several subunits of respiratory complexes Glycolysis metabolizes carbohydrates from are encoded by the mitochondrial genome 324 several sources 309 Plants have several mechanisms that lower The energy-conserving phase of glycolysis the ATP yield 324 extracts usable energy 310 Short-term control of mitochondrial Plants have alternative glycolytic reactions 310 respiration occurs at different levels 326 In the absence of oxygen, fermentation Respiration is tightly coupled to other regenerates the NAD+ needed for pathways 327 glycolysis 311 Respiration in Intact Plants and Tissues 327 Plant glycolysis is controlled by its products 312 Plants respire roughly half of the daily The Oxidative Pentose Phosphate photosynthetic yield 328 Pathway 312 Respiration operates during photosynthesis 329 The oxidative pentose phosphate pathway Different tissues and organs respire at different produces NADPH and biosynthetic rates 329 intermediates 314 Environmental factors alter respiration rates 329 The oxidative pentose phosphate pathway is redox-regulated 314 Lipid Metabolism 330 The Citric Acid Cycle 315 Fats and oils store large amounts of energy 331 Mitochondria are semiautonomous Triacylglycerols are stored in oil bodies 331 organelles 315 Polar glycerolipids are the main structural lipids in Pyruvate enters the mitochondrion and is membranes 332 oxidized via the citric acid cycle 316 Fatty acid biosynthesis consists of cycles of two- The citric acid cycle of plants has unique carbon addition 334 features 317 Glycerolipids are synthesized in the plastids and the ER 335 Mitochondrial Electron Transport and Lipid composition infl uences membrane ATP Synthesis 317 function 336 The electron transport chain catalyzes a fl ow of Membrane lipids are precursors of important electrons from NADH to O 318 2 signaling compounds 336 The electron transport chain has supplementary Storage lipids are converted into carbohydrates branches 320 in germinating seeds 336 ATP synthesis in the mitochondrion is coupled to electron transport 320 SUMMARY 338 Transporters exchange substrates and products 322 © Sinauer Associates, Inc. This material cannot be copied, reproduced, manufactured or disseminated in any form without express written permission from the publisher. ©2012SinauerAssociates,Inc.Thismaterialcannotbecopied,reproduced,manufactured TAIZ_FM_JD.indd XXIII ordisseminatedinanyformwithoutexpresswrittenpermissionfromthepublisher. 5/19/10 4:09:16 PM XXIV TABLE OF CONTENTS CHAPTER 12 Assimilation of Mineral Nutrients 343 Nitrogen in the Environment 344 Establishing symbiosis requires an exchange of Nitrogen passes through several forms in a biogeo- signals 354 chemical cycle 344 Nod factors produced by bacteria act as signals Unassimilated ammonium or nitrate may be dan- for symbiosis 354 gerous 346 Nodule formation involves phytohormones 355 The nitrogenase enzyme complex fi xes N 357 Nitrate Assimilation 346 2 Amides and ureides are the transported Many factors regulate nitrate reductase 347 forms of nitrogen 358 Nitrite reductase converts nitrite to ammonium 347 Sulfur Assimilation 358 Both roots and shoots assimilate nitrate 348 Sulfate is the absorbed form of sulfur in plants 358 Ammonium Assimilation 348 Sulfate assimilation requires the reduction of Converting ammonium to amino acids requires sulfate to cysteine 359 two enzymes 348 Sulfate assimilation occurs mostly in leaves 360 Ammonium can be assimilated via an Methionine is synthesized from cysteine 360 alternative pathway 350 Transamination reactions transfer nitrogen 350 Phosphate Assimilation 360 Asparagine and glutamine link carbon and Cation Assimilation 361 nitrogen metabolism 350 Cations form noncovalent bonds with carbon Amino Acid Biosynthesis 351 compounds 361 Roots modify the rhizosphere to acquire iron 362 Biological Nitrogen Fixation 351 Iron forms complexes with carbon Free-living and symbiotic bacteria fi x and phosphate 363 nitrogen 351 Nitrogen fi xation requires anaerobic Oxygen Assimilation 363 conditions 352 The Energetics of Nutrient Assimilation 364 Symbiotic nitrogen fi xation occurs in specialized structures 354 SUMMARY 365 CHAPTER 13 Secondary Metabolites and Plant Defense 369 Secondary Metabolites 370 Some terpenes have roles in growth and Secondary metabolites defend plants against her- development 373 bivores and pathogens 370 Terpenes defend many plants against Secondary metabolites are divided into three ma- herbivores 373 jor groups 370 Phenolic Compounds 374 Terpenes 370 Phenylalanine is an intermediate in the Terpenes are formed by the fusion of fi ve-carbon biosynthesis of most plant phenolics 375 isoprene units 370 Ultraviolet light activates some simple There are two pathways for terpene phenolics 377 biosynthesis 370 The release of phenolics into the soil may IPP and its isomer combine to form larger limit the growth of other plants 377 terpenes 371 Lignin is a highly complex phenolic macromolecule 377 © Sinauer Associates, Inc. This material cannot be copied, reproduced, manufactured or disseminated in any form without express written permission from the publisher. ©2012SinauerAssociates,Inc.Thismaterialcannotbecopied,reproduced,manufactured TAIZ_FM_JD.indd XXIV ordisseminatedinanyformwithoutexpresswrittenpermissionfromthepublisher. 5/19/10 4:09:16 PM

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Most books are stored in the elastic cloud where traffic is expensive. For this reason, we have a limit on daily download.