Plant physiology:
Gespeichert in:
| Hauptverfasser: | , |
|---|---|
| Format: | Buch |
| Sprache: | English |
| Veröffentlicht: |
Sunderland, Mass.
Sinauer
2010
|
| Ausgabe: | 5. ed. |
| Schlagworte: | |
| Online-Zugang: | Inhaltsverzeichnis |
| Beschreibung: | Getr. Zählung zahlr. Ill., graph. Darst. |
| ISBN: | 9780878935659 9780878938667 |
Internformat
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| 245 | 1 | 0 | |a Plant physiology |c Lincoln Taiz ; Eduardo Zeiger |
| 250 | |a 5. ed. | ||
| 264 | 1 | |a Sunderland, Mass. |b Sinauer |c 2010 | |
| 300 | |a Getr. Zählung |b zahlr. Ill., graph. Darst. | ||
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Datensatz im Suchindex
| _version_ | 1804142961785569280 |
|---|---|
| adam_text | Titel: Plant physiology
Autor: Taiz, Lincoln
Jahr: 2010
Contents
I CHAPTER 1
Plant Cells 1
Plant Life: Unifying Principles 2
Overview of Plant Structure 2
Plant cells are surrounded by rigid cell walls 2
New cells are produced by dividing
tissues called meristems 2
Three major tissue systems make up the
plant body 4
Plant Cell Organelles 4
Biological membranes are phospholipid
bilayers that contain proteins 4
The Endomembrane System 8
The nucleus contains the majority of the
genetic material 8
Gene expression involves both transcription
and translation 10
The endoplasmic reticulum is a network
of internal membranes 10
Secretion of proteins from cells begins with the
rough ER (RER) 13
Glycoproteins and polysaccharides destined
for secretion are processed in the Golgi
apparatus 14
The plasma membrane has specialized regions
involved in membrane recycling 16
Vacuoles have diverse functions in plant cells 16
Independently Dividing Organelles Derived
from the Endomembrane System 17
Oil bodies are lipid-storing organelles 17
Microbodies play specialized metabolic roles in
leaves and seeds 17
Independently Dividing, Semiautonomous
Organelles 18
Proplastids mature into specialized plastids in
different plant tissues 21
Chloroplast and mitochondrial division are
independent of nuclear division 21
The Plant Cytoskeleton 22
The plant cytoskeleton consists of microtubules
and microfilaments 22
Microtubules and microfilaments can assemble
and disassemble 23
Cortical microtubules can move around the cell by
treadmilling 24
Cytoskeletal motor proteins mediate cytoplasmic
streaming and organelle traffic 24
Cell Cycle Regulation 25
Each phase of the cell cycle has a specific set of
biochemical and cellular activities 26
The cell cycle is regulated by cyclins and
cyclin-dependent kinases 26
Mitosis and cytokinesis involve both microtubules
and the endomembrane system 27
Plasmodesmata 29
Primary and secondary plasmodesmata help to
maintain tissue developmental gradients 29
SUMMARY 31
I CHAPTER 2
Genome Organization and Gene Expression 35
Nuclear Genome Organization 35
The nuclear genome is packaged into
chromatin 36
Centromeres, telomeres, and nucleolar organizers
contain repetitive sequences 36
Transposons are mobile sequences within
the genome 37
Polyploids contain multiple copies of the entire
genome 38
Phenotypic and physiological responses to
polyploidy are unpredictable 41
Plant Cytoplasmic Genomes: Mitochondria
and Chloroplasts 42
The endosymbiotic theory describes the origin
of cytoplasmic genomes 42
Organellar genomes consist mostly of linear
chromosomes 43
Organellar genetics do not obey
Mendelian laws 44
Transcriptional Regulation of Nuclear
Gene Expression 45
RNA polymerase II binds to the promoter
region of most protein-coding genes 45
Epigenetic modifications help determine gene
activity 48
Posttranscriptional Regulation of
Nuclear Gene Expression 50
RNA stability can be influenced by
c/s-elements 50
Noncoding RNAs regulate mRNA activity via
the RNA interference (RNAi) pathway 50
Posttranslational regulation determines
the life span of proteins 54
Tools for Studying Gene Function 55
Mutant analysis can help to elucidate
gene function 55
Molecular techniques can measure the
activity of genes 55
Gene fusions can introduce reporter genes 56
Genetic Modification of Crop Plants
Transgenes can confer resistance to
herbicides or plant pests 59
Genetically modified organisms are
controversial 60
SUMMARY 61
59
UNIT I H Transport and Translocation of Water and Solutes 65
I CHAPTER 3
Water in Plant Life 67
Water and Plant Cells 67
The Structure and Properties of Water 68
Water is a polar molecule that forms hydrogen
bonds 68
Water is an excellent solvent 69
Water has distinctive thermal properties relative to
its size 69
Water molecules are highly cohesive 69
Water has a high tensile strength 70
Diffusion and Osmosis 71
Diffusion is the net movement of molecules by
random thermal agitation 71
Diffusion is most effective over short distances
Osmosis describes the net movement of water
across a selectively permeable barrier 73
72
Water Potential 73
The chemical potential of water represents the
free-energy status of water 74
Three major factors contribute to cell
water potential 74
Water potentials can be measured 75
Water Potential of Plant Cells 75
Water enters the cell along a water potential
gradient 75
Water can also leave the cell in response to a water
potential gradient 77
Water potential and its components vary with
growth conditions and location within the
plant 77
Cell Wall and Membrane Properties 78
XVIII TABLE OF CONTENTS
Small changes in plant cell volume cause large
changes in turgor pressure 78
The rate at which cells gain or lose water is
influenced by cell membrane hydraulic
conductivity 79
Aquaporins facilitate the movement of water across
cell membranes 79
Plant Water Status 80
Physiological processes are affected by plant water
status 80
Solute accumulation helps cells maintain turgor
and volume 80
SUMMARY 81
| CHAPTER 4
Water Balance of Plants 85
Water in the Soil 85
A negative hydrostatic pressure in soil water
lowers soil water potential 86
Water moves through the soil by bulk flow 87
Water Absorption by Roots 87
Water moves in the root via the apoplast,
symplast, and transmembrane pathways 88
Solute accumulation in the xylem can generate
root pressure 89
Water Transport through the Xylem 90
The xylem consists of two types of tracheary
elements 90
Water moves through the xylem by
pressure-driven bulk flow 92
Water movement through the xylem requires
a smaller pressure gradient than movement
through living cells 93
What pressure difference is needed to lift water
100 meters to a treetop? 93
The cohesion-tension theory explains water trans-
port in the xylem 93
Xylem transport of water in trees faces physical
challenges 94
Plants minimize the consequences of
xylem cavitation 96
Water Movement from the Leaf to the
Atmosphere 96
Leaves have a large hydraulic resistance 96
The driving force for transpiration is the
difference in water vapor concentration 96
Water loss is also regulated by the pathway
resistances 98
Stomatal control couples leaf transpiration to
leaf photosynthesis 98
The cell walls of guard cells have specialized
features 99
An increase in guard cell turgor pressure
opens the stornata 101
The transpiration ratio measures the relationship
between water loss and carbon gain 101
Overview: The Soil-Plant-Atmosphere
Continuum 102
SUMMARY 102
| CHAPTER 5
Mineral Nutrition 107
Essential Nutrients, Deficiencies,
and Plant Disorders 108
Special techniques are used in nutritional
studies 110
Nutrient solutions can sustain rapid
plant growth 110
Mineral deficiencies disrupt plant metabolism
and function 113
Analysis of plant tissues reveals mineral
deficiencies 117
Treating Nutritional Deficiencies 117
Crop yields can be improved by addition of
fertilizers 118
Some mineral nutrients can be absorbed by
leaves 118
Soil, Roots, and Microbes 119
Negatively charged soil particles affect the adsorp-
tion of mineral nutrients 119
Soil pH affects nutrient availability, soil microbes,
and root growth 120
Excess mineral ions in the soil limit plant
growth 120
Plants develop extensive root systems 121
Root systems differ in form but are based on
common structures 121
TABLE OF CONTENTS XIX
Different areas of the root absorb different
mineral ions 123
Nutrient availability influences root growth 124
Mycorrhizal fungi facilitate nutrient uptake
by roots 125
Nutrients move from mycorrhizal fungi to
root cells 126
SUMMARY 126
Solute Transport 131
I CHAPTER 6
Passive and Active Transport 132
Transport of Ions across Membrane
Barriers 133
Different diffusion rates for cations and anions
produce diffusion potentials 134
How does membrane potential relate to ion
distribution? 134
The Nernst equation distinguishes between
active and passive transport 136
Proton transport is a major determinant of
the membrane potential 137
Membrane Transport Processes 137
Channels enhance diffusion across
membranes 139
Carriers bind and transport specific substances 140
Primary active transport requires energy 140
Secondary active transport uses stored
energy 142
Kinetic analyses can elucidate transport
mechanisms 143
Membrane Transport Proteins 144
The genes for many transporters have
been identified 144
Transporters exist for diverse
nitrogen-containing compounds 146
Cation transporters are diverse 147
Anion transporters have been identified 148
Metal transporters transport essential
micronutrients 149
Aquaporins have diverse functions 149
Plasma membrane H+-ATPases are highly
regulated P-type ATPases 150
The tonoplast H+-ATPase drives solute
accumulation in vacuoles 151
H+-pyrophosphatases also pump protons at
the tonoplast 153
Ion Transport in Roots 153
Solutes move through both apoplast and
symplast 153
Ions cross both symplast and apoplast 153
Xylem parenchyma cells participate in xylem
loading 154
SUMMARY 156
UNIT II ¦ Biochemistry and Metabolism 161
I CHAPTER 7
Photosynthesis: The Light Reactions 163
Photosynthesis in Higher Plants 164
General Concepts 164
Light has characteristics of both a particle
and a wave 164
When molecules absorb or emit light,
they change their electronic state 165
Photosynthetic pigments absorb the light that
powers photosynthesis 166
Key Experiments in Understanding
Photosynthesis 167
Action spectra relate light absorption to
phctosynthetic activity 168
Photosynthesis takes place in complexes
containing light-harvesting antennas and
photochemical reaction centers 169
The chemical reaction of photosynthesis is
driven by light 170
Light drives the reduction of NADP and the
formation of ATP 171
Oxygen-evolving organisms have two
photosystems that operate in series 171
Organization of the Photosynthetic
Apparatus 172
The chloroplast is the site of photosynthesis
172
XX TABLE OF CONTENTS
Thylakoids contain integral membrane proteins 173
Photosystems I and II are spatially separated
in the thylakoid membrane 174
Anoxygenic photosynthetic bacteria have a
single reaction center 174
Organization of Light-Absorbing
Antenna Systems 176
Antenna systems contain chlorophyll and
are membrane associated 176
The antenna funnels energy to the
reaction center 176
Many antenna pigment-protein complexes
have a common structural motif 176
Mechanisms of Electron Transport 178
Electrons from chlorophyll travel through
the carriers organized in the Z scheme 178
Energy is captured when an excited chlorophyll
reduces an electron acceptor molecule 179
The reaction center chlorophylls of the two
photosystems absorb at different
wavelengths 180
The photosystem II reaction center is a
multisubunit pigment-protein complex 181
Water is oxidized to oxygen by
photosystem II 181
Pheophytin and two quiñones accept electrons
from photosystem II 183
Electron flow through the cytochrome bòf
complex also transports protons 183
Plastoquinone and plastocyanin carry electrons
between photosystems II and I 184
The photosystem I reaction center
reduces NADP+ 185
Cyclic electron flow generates ATP but no
NADPH 185
Some herbicides block photosynthetic
electron flow 186
Proton Transport and ATP Synthesis
in the Chloroplast 187
Repair and Regulation of the
Photosynthetic Machinery 189
Carotenoids serve as photoprotective agents 190
Some xanthophylls also participate in energy
dissipation 190
The photosystem II reaction center is easily
damaged 191
Photosystem I is protected from active oxygen
species 191
Thylakoid stacking permits energy partitioning
between the photosystems 191
Genetics, Assembly, and Evolution of
Photosynthetic Systems 192
Chloroplast genes exhibit non-Mendelian patterns
of inheritance 192
Most chloroplast proteins are imported from
the cytoplasm 192
The biosynthesis and breakdown of chlorophyll
are complex pathways 192
Complex photosynthetic organisms have evolved
from simpler forms 193
SUMMARY 194
CHAPTER
3 Photosynthesis: The Carbon Reactions 199
The Calvin-Benson Cycle 200
The Calvin-Benson cycle has three stages:
carboxylation, reduction, and regeneration 200
The carboxylation of ribulose 1,5-bisphosphate fixes
CO2 for the synthesis of trióse phosphates 201
Ribulose 1,5-bisphosphate is regenerated for
the continuous assimilation of CO2 201
An induction period precedes the steady state
of photosynthetic CO2 assimilation 204
Regulation of the Calvin-Benson Cycle 205
The activity of rubisco increases in the light 206
Light regulates the Calvin-Benson cycle via the
ferredoxin-thioredoxin system 207
Light-dependent ion movements modulate en-
zymes of the Calvin-Benson cycle 208
Light controls the assembly of chloroplast enzymes
into supramolecular complexes 208
The C2 Oxidative Photosynthetic Carbon
Cycle 208
The carboxylation and the oxygénation of ribulose
1,5-bisphosphate are competing reactions 210
Photorespiration depends on the photosynthetic
electron transport system 213
Photorespiration protects the photosynthetic ap-
paratus under stress conditions 214
Photorespiration may be engineered to increase
the production of biomass 214
TABLE OF CONTENTS XXI
Inorganic Carbon-Concentrating
Mechanisms 216
Inorganic Carbon-Concentrating Mechanisms:
The C4 Carbon Cycle 216
Malate and aspartate are carboxylation products of
the C4 cycle 217
Two different types of cells participate in the C4
cycle 218
The C4 cycle concentrates CO2 in the chloroplasts
of bundle sheath cells 220
The C4 cycle also concentrates CO2 in single
cells 221
Light regulates the activity of key C4 enzymes 221
In hot, dry climates, the C4 cycle reduces photo-
respiration and water loss 221
Inorganic Carbon-Concentrating Mechanisms:
Crassulacean Acid Metabolism (CAM) 221
CAM is a versatile mechanism sensitive to environ-
mental stimuli 223
Accumulation and Partitioning of
Photosynthates—Starch and Sucrose
Formation and Mobilization of
Chloroplast Starch 225
Starch is synthesized in the chloroplast
during the day 225
Starch degradation at night requires the
phosphorylation of amylopectin 228
The export of maltose prevails in the nocturnal
breakdown of transitory starch 230
Sucrose Biosynthesis and Signaling 231
Trióse phosphates supply the cytosolic pool
of three important hexose phosphates in the
light 231
Fructose 2,6-bisphosphate regulates the hexose
phosphate pool in the light 235
The cytosolic interconversion of hexose phos-
phates governs the allocation of assimilated
carbon 235
Sucrose is continuously synthesized in the
cytosol 235
SUMMARY 237
224
CHAPTER
Photosynthesis: Physiological and Ecological
Considerations 243
Photosynthesis Is the Primary Function of
Leaves 244
Leaf anatomy maximizes light absorption 245
Plants compete for sunlight 246
Leaf angle and leaf movement can control light
absorption 247
Plants acclimate and adapt to sun and shade
environments 248
Photosynthetic Responses to Light by the
Intact Leaf 249
Light-response curves reveal photosynthetic
properties 249
Leaves must dissipate excess light energy 251
Absorption of too much light can lead to
photoinhibition 253
Photosynthetic Responses to
Temperature 254
Leaves must dissipate vast quantities of heat 254
Photosynthesis is temperature sensitive 255
There is an optimal temperature for
photosynthesis 256
Photosynthetic Responses to Carbon
Dioxide 256
Atmospheric C02 concentration keeps rising 257
CO2 diffusion to the chloroplast is essential to
photosynthesis 258
Patterns of light absorption generate gradients of
CO2 fixation 259
CO2 imposes limitations on photosynthesis 260
How will photosynthesis and respiration change in
the future under elevated CO2 conditions? 261
Identifying Different Photosynthetic
Pathways 263
How do we measure the stable carbon isotopes of
plants? 263
Why are there carbon isotope ratio variations in
plants? 264
SUMMARY 266
XXII TABLE OF CONTENTS
I CHAPTER 1
•1 Translocation in the Phloem 271
Pathways of Translocation 272
Sugar is translocated in phloem sieve
elements 273
Mature sieve elements are living cells specialized
for translocation 273
Large pores in cell walls are the prominent feature
of sieve elements 274
Damaged sieve elements are sealed off 274
Companion cells aid the highly specialized sieve
elements 276
Patterns of Translocation: Source to Sink 276
Materials Translocated in the Phloem 277
Phloem sap can be collected and analyzed 278
Sugars are translocated in nonreducing form 279
Other solutes are translocated in the phloem 280
Rates of Movement 280
The Pressure-Flow Model, a Passive
Mechanism for Phloem Transport 281
An osmotically-generated pressure gradient drives
translocation in the pressure-flow model 281
The predictions of mass flow have been
confirmed 282
Sieve plate pores are open channels 283
There is no bidirectional transport in single sieve
elements 284
The energy requirement for transport through the
phloem pathway is small 284
Positive pressure gradients exist in the phloem
sieve elements 284
Does translocation in gymnosperms involve a
different mechanism? 285
Phloem Loading 285
Phloem loading can occur via the apoplast or
symplast 285
Abundant data support the existence of
apoplastic loading in some species 286
Sucrose uptake in the apoplastic pathway
requires metabolic energy 286
Phloem loading in the apoplastic pathway
involves a sucrose-H+ symporter 287
Phloem loading is symplastic in some
species 288
The polymer-trapping model explains
symplastic loading in plants with intermediary
cells 288
Phloem loading is passive in a number of
tree species 289
The type of phloem loading is correlated with a
number of significant characteristics 290
Phloem Unloading and Sink-to-Source
Transition 291
Phloem unloading and short-distance transport
can occur via symplastic or apoplastic
pathways 291
Transport into sink tissues requires metabolic
energy 292
The transition of a leaf from sink to source is
gradual 292
Photosynthate Distribution: Allocation and
Partitioning 294
Allocation includes storage, utilization, and
transport 294
Various sinks partition transport sugars 295
Source leaves regulate allocation 295
Sink tissues compete for available translocated
photosynthate 296
Sink strength depends on sink size and
activity 296
The source adjusts over the long term to changes
in the source-to-sink ratio 297
The Transport of Signaling Molecules 297
Turgor pressure and chemical signals coordinate
source and sink activities 297
Proteins and RNAs function as signal molecules
in the phloem to regulate growth and
development 298
SUMMARY 299
TABLE OF CONTENTS XXIII
CHAPTER 11
Respiration and Lipid Metabolism 305
Overview of Plant Respiration 305
Glycolysis 309
Glycolysis metabolizes carbohydrates from
several sources 309
The energy-conserving phase of glycolysis
extracts usable energy 310
Plants have alternative glycolytic reactions 310
In the absence of oxygen, fermentation
regenerates the NAD+ needed for
glycolysis 311
Plant glycolysis is controlled by its products 312
The Oxidative Pentose Phosphate
Pathway 312
The oxidative pentose phosphate pathway
produces NADPH and biosynthetic
intermediates 314
The oxidative pentose phosphate pathway is
redox-regulated 314
The Citric Acid Cycle 315
Mitochondria are semiautonomous
organelles 315
Pyruvate enters the mitochondrion and is
oxidized via the citric acid cycle 316
The citric acid cycle of plants has unique
features 317
Mitochondrial Electron Transport and
ATP Synthesis 317
The electron transport chain catalyzes a flow of
electrons from NADH to O2 318
The electron transport chain has supplementary
branches 320
ATP synthesis in the mitochondrion is coupled to
electron transport 320
Transporters exchange substrates and
products 322
Aerobic respiration yields about 60 molecules
of ATP per molecule of sucrose 322
Several subunits of respiratory complexes
are encoded by the mitochondrial genome
Plants have several mechanisms that lower
the ATP yield 324
Short-term control of mitochondrial
respiration occurs at different levels 326
Respiration is tightly coupled to other
pathways 327
324
327
329
Respiration in Intact Plants and Tissues
Plants respire roughly half of the daily
photosynthetic yield 328
Respiration operates during photosynthesis
Different tissues and organs respire at different
rates 329
Environmental factors alter respiration rates 329
Lipid Metabolism 330
Fats and oils store large amounts of energy 331
Triacylglycerols are stored in oil bodies 331
Polar glycerolipids are the main structural lipids in
membranes 332
Fatty acid biosynthesis consists of cycles of two-
carbon addition 334
Glycerolipids are synthesized in the plastids
and the ER 335
Lipid composition influences membrane
function 336
Membrane lipids are precursors of important
signaling compounds 336
Storage lipids are converted into carbohydrates
in germinating seeds 336
SUMMARY 338
XXIV TABLE OF CONTENTS
CHAPTER 12
Assimilation of Mineral Nutrients 343
Nitrogen in the Environment 344
Nitrogen passes through several forms in a biogeo-
chemical cycle 344
Unassimilated ammonium or nitrate may be dan-
gerous 346
Nitrate Assimilation 346
Many factors regulate nitrate reducíase 347
Nitrite reducíase converts nitrite to
ammonium 347
Both roots and shoots assimilate nitrate 348
Ammonium Assimilation 348
Converting ammonium to amino acids requires
two enzymes 348
Ammonium can be assimilated via an
alternative pathway 350
Transamination reactions transfer nitrogen 350
Asparagine and glutamine link carbon and
nitrogen metabolism 350
Amino Acid Biosynthesis 351
Biological Nitrogen Fixation 351
Free-living and symbiotic bacteria fix
nitrogen 351
Nitrogen fixation requires anaerobic
conditions 352
Symbiotic nitrogen fixation occurs in
specialized structures 354
Establishing symbiosis requires an exchange of
signals 354
Nod factors produced by bacteria act as signals
for symbiosis 354
Nodule formation involves phytohormones 355
The nitrogenase enzyme complex fixes N2 357
Amides and ureides are the transported
forms of nitrogen 358
Sulfur Assimilation 358
Sulfate is the absorbed form of sulfur in
plants 358
Sulfate assimilation requires the reduction of
sulfate to cysteine 359
Sulfate assimilation occurs mostly in leaves 360
Methionine is synthesized from cysteine 360
Phosphate Assimilation 360
Cation Assimilation 361
Cations form noncovalent bonds with carbon
compounds 361
Roots modify the rhizosphere to acquire iron 362
Iron forms complexes with carbon
and phosphate 363
Oxygen Assimilation 363
The Energetics of Nutrient Assimilation 364
SUMMARY 365
[CHAPTER 13
Secondary Metabolites and Plant Defense 369
Secondary Metabolites 370
Secondary metabolites defend plants against her-
bivores and pathogens 370
Secondary metabolites are divided into three ma-
jor groups 370
Terpenes 370
Terpenes are formed by the fusion of five-carbon
isoprene units 370
There are two pathways for terpene
biosynthesis 370
IPP and its isomer combine to form larger
terpenes 371
Some terpenes have roles in growth and
development 373
Terpenes defend many plants against
herbivores 373
Phenolic Compounds 374
Phenylalanine is an intermediate in the
biosynthesis of most plant phenolics 375
Ultraviolet light activates some simple
phenolics 377
The release of phenolics into the soil may
limit the growth of other plants 377
Lignin is a highly complex phenolic
macromolecule 377
TABLE OF CONTENTS XXV
There are four major groups of flavonoids 378
Anthocyanins are colored flavonoids that attract
animals 378
Flavones and flavonols may protect against dam-
age by ultraviolet light 379
Isoflavonoids have widespread pharmacological
activity 379
Tannins deter feeding by herbivores 380
Nitrogen-Containing Compounds 381
Alkaloids have dramatic physiological effects on
animals 381
Cyanogenic glycosides release the poison
hydrogen cyanide 384
Glucosinolates release volatile toxins 385
Nonprotein amino acids are toxic to
herbivores 385
Induced Plant Defenses against Insect
Herbivores 386
Plants can recognize specific components of
insect saliva 386
Jasmonic acid activates many defensive
responses 387
Some plant proteins inhibit herbivore
digestion 389
Damage by insect herbivores induces
systemic defenses 389
Herbivore-induced volatiles have complex
ecological functions 389
Insects have developed strategies to cope
with plant defenses 391
Plant Defenses against Pathogens 391
Pathogens have developed various strategies to
invade host plants 391
Some antimicrobial compounds are synthesized
before pathogen attack 392
Infection induces additional antipathogen
defenses 392
Phytoalexins often increase after pathogen
attack 393
Some plants recognize specific pathogen-derived
substances 393
Exposure to elicitors induces a signal transduction
cascade 394
A single encounter with a pathogen may increase
resistance to future attacks 394
Interactions of plants with nonpathogenic bacteria
can trigger induced systemic resistance 395
SUMMARY 396
UNIT III I Growth and Development 401
I CHAPTER 14
Signal Transduction 403
Signal Transduction in Plant and
Animal Cells 404
Plants and animals have similar transduction
components 404
Receptor kinases can initiate a signal
transduction cascade 406
Plants signal transduction components have
evolved from both prokaryotic and eukaryotic
ancestors 406
Signals are perceived at many locations
within plant cells 408
Plant signal transduction often involves
inactivation of repressor proteins 409
Protein degradation is a common feature in
plant signaling pathways 411
413
Several plant hormone receptors encode
components of the ubiquitination machinery
Inactivation of repressor proteins results in a
gene expression response 414
Plants have evolved mechanisms for switching
off or attenuating signaling responses 414
Cross-regulation allows signal transduction
pathways to be integrated 416
Signal Transduction in Space and Time 418
Plant signal transduction occurs over a wide range
of distances 418
The timescale of plant signal transduction ranges
from seconds to years 419
SUMMARY 421
XXVI TABLE OF CONTENTS
CHAPTER 15
Cell Walls: Structure, Biogenesis,
and Expansion 425
The Structure and Synthesis of
Plant Cell Walls 426
Plant cell walls have varied architecture 426
The primary cell wall is composed of
cellulose microfibrils embedded in a
polysaccharide matrix 428
Cellulose microfibrils are synthesized at
the plasma membrane 430
Matrix polymers are synthesized in the
Golgi apparatus and secreted via vesicles 433
Hemicelluloses are matrix polysaccharides
that bind to cellulose 433
Pectins are hydrophilic gel-forming components
of the matrix 434
Structural proteins become cross-linked in
the wall 437
New primary walls are assembled during
cytokinesis 437
Secondary walls form in some cells after
expansion ceases 438
Patterns of Cell Expansion 441
Microfibril orientation influences growth
directionality of cells with diffuse growth 441
Cortical microtubules influence the orientation
of newly deposited microfibrils 443
The Rate of Cell Elongation 443
Stress relaxation of the cell wall drives water
uptake and cell elongation 445
Acid-induced growth and wall stress relaxation
are mediated by expansins 446
Many structural changes accompany the
cessation of wall expansion 448
SUMMARY 448
| CHAPTER 16
Growth and Development 453
Overview of Plant Growth and
Development 454
Sporophytic development can be divided
into three major stages 455
Embryogenesis: The Origins of Polarity 456
Embryogenesis differs between dicots and
monocots, but also features common
fundamental processes 456
Apical-basal polarity is established early
in embryogenesis 457
Position-dependent signaling guides
embryogenesis 458
Auxin may function as a mobile chemical
signal during embryogenesis 460
Mutant analysis has helped identify genes
essential for embryo organization 461
The GNOM protein establishes a
polar distribution of auxin efflux proteins 463
MONOPTEROS encodes a transcription factor
that is activated by auxin 463
Radial patterning guides formation of tissue
layers 464
The differentiation of cortical and endodermal
cells involves the intercellular movement of a
transcription factor 465
Many developmental processes involve the
intercellular movement of macromolecules 467
Meristematic Tissues: Foundations for
Indeterminate Growth 468
The root and shoot apical meristems use similar
strategies to enable indeterminate growth 469
The Root Apical Meristem 469
The root tip has four developmental zones 469
The origin of different root tissues can be
traced to specific initial cells 470
Cell ablation experiments implicate directional
signaling processes in determination of cell
identity 471
Auxin contributes to the formation and
maintenance of the RAM 471
Responses to auxin depend on specific
transcription factors 472
Cytokinin activity in the RAM is required for root
development 473
TABLE OF CONTENTS XXVII
The Shoot Apical Meristem 474
The shoot apical meristem has distinct zones
and layers 474
Shoot tissues are derived from several discrete
sets of apical initials 475
The locations of PIN proteins influence SAM
formation 476
Embryonic SAM formation requires the
coordinated expression of transcription
factors 477
Negative feedback limits apical meristem size 478
Similar mechanisms maintain initials in the RAM
and in the SAM 479
Vegetative Organogénesis 480
Localized zones of auxin accumulation promote
leaf initiation 480
Spatially regulated gene expression determines
the planar form of the leaf 481
Distinct mechanisms initiate roots and shoots 483
Senescence and Programmed Cell Death 484
Leaf senescence is adaptive and strictly
regulated 484
Plants exhibit various types of senescence 485
Senescence involves the ordered degradation of
potentially phototoxic chlorophyll 487
Programmed cell death is a specialized type of
senescence 487
SUMMARY 488
CHAPTER 17
Phytochrome and Light Control of Plant
Development 493
The Photochemical and Biochemical Properties
of Phytochrome 494
Phytochrome can interconvert between Pr
and Pfr forms 496
Pfr is the physiologically active form of
phytochrome 496
Characteristics of Phytochrome-lnduced
Responses 497
Phytochrome responses vary in lag time and
escape time 497
Phytochrome responses can be distinguished by
the amount of light required 497
Very low-fluence responses are
nonphotoreversible 497
Low-fluence responses are photoreversible 498
High-irradiance responses are proportional to
the irradiance and the duration 499
Structure and Function of Phytochrome
Proteins 499
Phytochrome has several important functional
domains 500
Phytochrome ¡s a light-regulated protein
kinase 501
Pfr is partitioned between the cytosol and
the nucleus 501
Phytochromes are encoded by a multigene
family 502
Genetic Analysis of Phytochrome
Function 503
Phytochrome A mediates responses to
continuous far-red light 504
Phytochrome B mediates responses
to continuous red or white light 504
Roles for phytochromes C, D, and E
are emerging 504
Phy gene family interactions are complex 504
PHY gene functions have diversified during
evolution 505
Phytochrome Signaling Pathways 505
Phytochrome regulates membrane
potentials and ¡on fluxes 506
Phytochrome regulates gene expression 506
Phytochrome interacting factors (PIFs) act
early in phy signaling 507
Phytochrome associates with protein kinases
and phosphatases 507
Phytochrome-induced gene expression
involves protein degradation 508
Orcadian Rhythms 509
The circadian oscillator involves a
transcriptional negative feedback loop 510
Ecological Functions 512
Phytochrome enables plant adaptation to
changes in light quality 512
XXVIII TABLE OF CONTENTS
Decreasing the R:FR ratio causes elongation in
sun plants 512
Small seeds typically require a high R:FR ratio
for germination 513
Reducing shade avoidance responses can
improve crop yields 514
Phytochrome responses show ecotypic
variation 515
Phytochrome action can be modulated 515
SUMMARY 516
CHAPTER 1!
Blue-Light Responses: Morphogenesis and
Stomatal Movements 521
The Photophysiology of Blue-Light
Responses 522
Blue light stimulates asymmetric growth and
bending 523
Blue light rapidly inhibits stem elongation 523
Blue light stimulates stomatal opening 524
Blue light activates a proton pump at the
guard cell plasma membrane 527
Blue-light responses have characteristic
kinetics and lag times 528
Blue light regulates the osmotic balance of
guard cells 528
Sucrose is an osmotically active solute in guard
cells 530
532
The Regulation of Blue Light-Stimulated
Responses 531
Blue-Light Photoreceptors 532
Cryptochromes regulate plant development
Phototropins mediate blue light-dependent
phototropism and chloroplast movements 533
Zeaxanthin mediates blue-light photoreception
in guard cells 534
Green light reverses blue light-stimulated
opening 536
SUMMARY 539
CHAPTER 19
Auxin: The First Discovered Plant Growth
Hormone 545
The Emergence of the Auxin Concept 546
The Principal Auxin: lndole-3-Acetic Acid 546
IAA is synthesized in meristems and young
dividing tissues 549
Multiple pathways exist for the biosynthesis of
IAA 549
Seeds and storage organs contain covalently
bound auxin 550
IAA is degraded by multiple pathways 550
Auxin Transport 551
Polar transport requires energy and is gravity
independent 552
Chemiosmotic potential drives polar transport 553
PIN and ABCB transporters regulate cellular auxin
homeostasis 555
Auxin influx and efflux can be chemically
inhibited 556
Auxin transport is regulated by multiple
mechanisms 558
Auxin Signal Transduction Pathways 560
The principal auxin receptors are soluble
protein heterodimers 561
Auxin-induced genes are negatively regulated
by AUX/IAA proteins 561
Auxin binding to a TIR1/AFB-AUX/IAA
heterodimer stimulates AUX/IAA
destruction 562
Auxin-induced genes fall into two classes:
early and late 562
Rapid, nontranscriptional auxin responses
appear to involve a different receptor
protein 562
Actions of Auxin: Cell Elongation 562
Auxins promote growth in stems and coleoptiles,
while inhibiting growth in roots 563
The outer tissues of dicot stems are the targets
of auxin action 563
The minimum lag time for auxin-induced
elongation is ten minutes 565
TABLE OF CONTENTS XXIX
Auxin rapidly increases the extensibility of
the cell wall 565
Auxin-induced proton extrusion increases cell
extension 565
Auxin-induced proton extrusion involves activation
and protein mobilization 566
Actions of Auxin: Plant Tropisms 566
Phototropism is mediated by the lateral redistribu-
tion of auxin 566
Gravitropism involves lateral redistribution of
auxin 568
Dense plastids serve as gravity sensors 569
Gravity sensing may involve pH and calcium ions
(Ca2+) as second messengers 571
Auxin is redistributed laterally in the root cap 572
Developmental Effects of Auxin 573
Auxin regulates apical dominance 574
Auxin transport regulates floral bud development
and phyllotaxy 576
Auxin promotes the formation of lateral and
adventitious roots 576
Auxin induces vascular differentiation 576
Auxin delays the onset of leaf abscission 577
Auxin promotes fruit development 577
Synthetic auxins have a variety of commercial
uses 578
SUMMARY 578
CHAPTER 2
¡I Gibberellins: Regulators of Plant Height and
¦ Seed Germination 583
Gibberellins: Their Discovery and Chemical
Structure 584
Gibberellins were discovered by studying
a disease of rice 584
Gibberellic acid was first purified from Gibberella
culture filtrates 584
All gibberellins are based on an ent-gibberellane
skeleton 585
Effects of Gibberellins on Growth and
Development 586
Gibberellins promote seed germination 586
Gibberellins can stimulate stem and root
growth 586
Gibberellins regulate the transition from juvenile
to adult phases 587
Gibberellins influence floral initiation and sex
determination 588
Gibberellins promote pollen development
and tube growth 588
Gibberellins promote fruit set and
parthenocarpy 588
Gibberellins promote early seed
development 588
Commercial uses of gibberellins and
GA biosynthesis inhibitors 588
Biosynthesis and Deactivation of
Gibberellins 589
Gibberellins are synthesized via the terpenoid
pathway 589
Some enzymes in the GA pathway are
highly regulated 591
Gibberellin regulates its own metabolism 592
GA biosynthesis occurs at multiple plant organs
and cellular sites 592
Environmental conditions can influence
GA biosynthesis 593
GA, and GA4 have intrinsic bioactivity for
stem growth 594
Plant height can be genetically engineered 595
Dwarf mutants often show other phenotypic
defects 595
Auxins can regulate GA biosynthesis 595
Gibberellin Signaling: Significance of
Response Mutants 596
GID1 encodes a soluble GA receptor 596
DELLA-domain proteins are negative
regulators of GA response 600
Mutation of negative regulators of GA may
produce slender or dwarf phenotypes 600
Gibberellins signal the degradation of negative
regulators of GA response 601
F-box proteins target DELLA domain proteins
for degradation 601
Negative regulators with DELLA domains have
agricultural importance 602
Gibberellin Responses: Early Targets
of DELLA Proteins 602
XXX TABLE OF CONTENTS
DELLA proteins can activate or suppress gene
expression 603
DELLA proteins regulate transcription by interact-
ing with other proteins such as phytochrome-
interacting factors 603
Gibberellin Responses: The Cereal Aleurone
Layer 605
GA is synthesized in the embryo 605
Aleurone cells may have two types of GA recep-
tors 605
Gibberellins enhance the transcription of
cc-amylase mRNA 605
GAMYB is a positive regulator of a-amylase
transcription 607
DELLA-domain proteins are rapidly
degraded 607
Gibberellin Responses: Anther Development
and Male Fertility 607
GAMYB regulates male fertility 609
Events downstream of GAMYB in rice aleurone
and anthers are quite different 611
MicroRNAs regulate MYBs after transcription
in anthers but not in aleurone 611
Gibberellin Responses: Stem Growth 612
Gibberellins stimulate cell elongation and
cell division 612
GAs regulate the transcription of cell cycle
kinases 613
Reducing GA sensitivity may prevent crop
losses 613
SUMMARY 614
I CHAPTER 21
Cytokinins: Regulators of Cell Division 621
Cell Division and Plant Development 622
Differentiated plant cells can resume division 622
Diffusible factors control cell division 622
Plant tissues and organs can be cultured 622
The Discovery, Identification, and Properties
of Cytokinins 623
Kinetin was discovered as a breakdown
product of DNA 623
Zeatin was the first natural cytokinin
discovered 623
Some synthetic compounds can mimic
cytokinin action 624
Cytokinins occur in both free and bound
forms 625
Some plant pathogenic bacteria, fungi, insects,
and nematodes secrete free cytokinins 625
Biosynthesis, Metabolism, and Transport
of Cytokinins 625
Crown gall cells have acquired a gene for
cytokinin synthesis 626
IPT catalyzes the first step in cytokinin
biosynthesis 628
Cytokinins can act both as long distance and
local signals 628
Cytokinins are rapidly metabolized by
plant tissues 628
Cellular and Molecular Modes of Cytokinin
Action 629
A cytokinin receptor related to bacterial
two-component receptors has been
identified 629
Cytokinins increase expression of the type-A
response regulator genes via activation of the
type-B ARR genes 630
Histidine phosphotransfer proteins are also
involved in cytokinin signaling 632
The Biological Roles of Cytokinins 632
Cytokinins promote shoot growth by increasing
cell proliferation in the shoot apical
meristem 632
Cytokinins interact with other hormones and with
several key transcription factors 634
Cytokinins inhibit root growth by promoting the
exit of cells from the root apical meristem 635
Cytokinins regulate specific components of
the cell cycle 636
The auxin:cytokinin ratio regulates morphogenesis
in cultured tissues 637
Cytokinins modify apical dominance and promote
lateral bud growth 638
Cytokinins delay leaf senescence 638
Cytokinins promote movement of nutrients 639
TABLE OF CONTENTS XXXI
Cytokinins affect light signaling via
phytochrome 640
Cytokinins regulate vascular development 641
Manipulation of cytokinins to alter agriculturally
important traits 641
Cytokinins are involved in the formation of
nitrogen-fixing nodules in legumes 641
SUMMARY 643
| CHAPTER 22
Ethylene: The Gaseous Hormone 649
Structure, Biosynthesis, and Measurement
of Ethylene 650
Regulated biosynthesis determines the
physiological activity of ethylene 650
Ethylene biosynthesis is promoted by severa
factors 652
Ethylene biosynthesis can be elevated through a
stabilization of ACC synthase protein 652
Various inhibitors can block ethylene
biosynthesis 653
Ethylene Signal Transduction Pathways 653
Ethylene receptors are related to bacterial two-
component system histidine kinases 654
High-affinity binding of ethylene to its receptor
requires a copper cofactor 655
Unbound ethylene receptors are negative
regulators of the response pathway 655
A serine/threonine protein kinase is also involved
in ethylene signaling 657
EIN2 encodes a transmembrane protein 657
Ethylene Regulation of Gene Expression 657
Specific transcription factors are involved in
ethylene-regulated gene expression 657
Genetic epistasis reveals the order of the
ethylene signaling components 658
Developmental and Physiological
Effects of Ethylene 659
Ethylene promotes the ripening of some
fruits 659
Fruits that respond to ethylene exhibit a
climacteric 659
The receptors of never-ripe mutants of tomato
fail to bind ethylene 660
Leaf epinasty results when ACC from the root is
transported to the shoot 660
Ethylene induces lateral cell expansion 661
There are two distinct phases to growth
inhibition by ethylene 662
The hooks of dark-grown seedlings are
maintained by ethylene production 662
Ethylene breaks seed and bud dormancy in
some species 663
Ethylene promotes the elongation growth of
submerged aquatic species 663
Ethylene induces the formation of roots and
root hairs 664
Ethylene regulates flowering and sex determination
in some species 664
Ethylene enhances the rate of leaf
senescence 664
Ethylene mediates some defense responses 665
Ethylene acts on the abscission layer 665
Ethylene has important commercial uses 667
SUMMARY 668
CHAPTER 23
Abscisic Acid: A Seed Maturation and
Stress-Response Hormone 673
Occurrence, Chemical Structure, and
Measurement of ABA 674
The chemical structure of ABA determines its
physiological activity 674
ABA is assayed by biological, physical, and
chemical methods 674
Biosynthesis, Metabolism, and
Transport of ABA 674
ABA is synthesized from a carotenoid
intermediate 674
ABA concentrations in tissues are
highly variable 676
ABA is translocated in vascular tissue 677
XXXII TABLE OF CONTENTS
ABA Signal Transduction Pathways 678
Receptor candidates include diverse classes of
proteins 678
Secondary messengers function in ABA
signaling 680
Ca2+-dependent and Ca2+-independent pathways
mediate ABA signaling 680
ABA-induced lipid metabolism generates second
messengers 681
Protein kinases and phosphatases regulate
important steps in ABA signaling 682
PP2Cs interact directly with the PYR/PYL/RCAR
family of ABA receptors 683
ABA shares signaling intermediates with other
hormonal pathways 683
ABA Regulation of Gene Expression 683
Gene activation by ABA is mediated by
transcription factors 684
Developmental and Physiological Effects
of ABA 684
ABA regulates seed maturation 684
ABA inhibits precocious germination and
vivipary 685
ABA promotes seed storage reserve accumulation
and desiccation tolerance 686
Seed dormancy can be regulated by ABA and
environmental factors 686
Seed dormancy is controlled by the ratio of ABA
toGA 687
ABA inhibits GA-induced enzyme production 688
ABA promotes root growth and inhibits shoot
growth at low water potentials 688
ABA promotes leaf senescence independently
of ethylene 689
ABA accumulates in dormant buds 689
ABA closes stornata in response to water
stress 690
ABA regulates ¡on channels and the plasma
membrane ATPase in guard cells 690
SUMMARY 693
CHAPTER 2*
Br assi n osterò ids: Regulators of Cell Expansion
and Development 699
Brassinosteroid Structure, Occurrence,
and Genetic Analysis 700
BR-deficient mutants are impaired in
photomorphogenesis 701
The Brassinosteroid Signaling Pathway 703
BR-insensitive mutants identified the BR cell
surface receptor 703
Phosphorylation activates the BRI1 receptor 704
BIN2 is a repressor of BR-induced gene
expression 704
BES1/BZR1 regulate gene expression 706
Biosynthesis, Metabolism, and Transport of
Brassinosteroids 706
Brassinolide is synthesized from campesterol 707
Catabolism and negative feedback contribute to
BR homeostasis 708
Brassinosteroids act locally near their sites of
synthesis 710
Brassinosteroids: Effects on Growth and
Development 710
BRs promote both cell expansion and cell division
in shoots 711
BRs both promote and inhibit root growth 712
BRs promote xylem differentiation during vascular
development 713
BRs are required for the growth of pollen
tubes 714
BRs promote seed germination 714
Prospective Uses of Brassinosteroids in
Agriculture 714
SUMMARY 715
TABLE OF CONTENTS XXXIII
I CHAPTER 25
The Control of Flowering 719
Floral Meristems and Floral Organ
Development 720
The shoot apical meristem in Arabidopsis changes
with development 721
The four different types of floral organs are
initiated as separate whorls 721
Two major types of genes regulate floral
development 722
Meristem identity genes regulate meristem
function 722
Homeotic mutations led to the identification of
floral organ identity genes 723
Three types of homeotic genes control floral organ
identity 723
The ABC model explains the determination of
floral organ identity 724
Floral Evocation: Integrating Environmental
Cues 725
The Shoot Apex and Phase Changes 726
Plant development has three phases 726
Juvenile tissues are produced first and are located
at the base of the shoot 727
Phase changes can be influenced by nutrients,
gibberellins, and other signals 728
Competence and determination are two stages in
floral evocation 728
Circadian Rhythms: The Clock Within 730
Orcadian rhythms exhibit characteristic
features 730
Phase shifting adjusts circadian rhythms to
different day-night cycles 732
Phytochromes and cryptochromes entrain
the clock 732
Photoperiodism: Monitoring Day Length 732
Plants can be classified according to their
photoperiodic responses 732
The leaf is the site of perception of the
photoperiodic signal 734
Plants monitor day length by measuring the length
of the night 734
Night breaks can cancel the effect of the dark
period 735
The circadian clock and photoperiodic
timekeeping 736
The coincidence model is based on oscillating
light sensitivity 737
The coincidence of CONSTANS expression
and light promotes flowering in LDPs 737
SDPs use a coincidence mechanism to inhibit
flowering in long days 739
Phytochrome is the primary photoreceptor in
photoperiodism 739
A blue-light photoreceptor regulates flowering
in some LDPs 740
Vernalization: Promoting Flowering with
Cold 741
Vernalization results in competence to flower
at the shoot apical meristem 742
Vernalization can involve epigenetic changes in
gene expression 742
A range of vernalization pathways may have
evolved 743
Long-Distance Signaling Involved in
Flowering 744
The floral stimulus is transported in the
phloem 744
Grafting studies have provided evidence for a
transmissible floral stimulus 744
The Discovery of Florigen 745
The Arabidopsis protein FLOWERING LOCUST
is florigen 746
Gibberellins and ethylene can induce
flowering 747
Climate change has already caused measurable
changes in flowering time of wild plants 748
The transition to flowering involves multiple
factors and pathways 748
SUMMARY 749
XXXIV TABLE OF CONTENTS
I CHAPTER 26
Responses and Adaptations to Abiotic Stress 755
Adaptation and Phenotypic Plasticity 756
Adaptations involve genetic modification 756
Phenotypic plasticity allows plants to respond to
environmental fluctuations 756
The Abiotic Environment and its Biological
Impact on Plants 756
Climate and soil influence plant fitness 757
Imbalances in abiotic factors have primary and
secondary effects on plants 757
Water Deficit and Flooding 757
Soil water content and the relative humidity of the
atmosphere determine the water status of the
plant 758
Water deficits cause cell dehydration and
an inhibition of cell expansion 759
Flooding, soil compaction, and O2 deficiency are
related stresses 759
Imbalances in Soil Minerals 760
Soil mineral content can result in plant stress
in various ways 760
Soil salinity occurs naturally and as the result of
improper water management practices 761
The toxicity of high Na+ and CI in the cytosol is
due to their specific ¡on effects 761
Temperature Stress 762
High temperatures are most damaging to
growing, hydrated tissues 762
Temperature stress can result in damaged
membranes and enzymes 762
Temperature stress can inhibit photosynthesis 763
Low temperatures above freezing can
cause chilling injury 764
Freezing temperatures cause ice crystal formation
and dehydration 764
High Light Stress 764
Photoinhibition by high light leads to the
production of destructive forms of oxygen 764
Developmental and Physiological Mechanisms
that Protect Plants against Environmental
Extremes 765
Plants can modify their life cycles to avoid
abiotic stress 765
Phenotypic changes in leaf structure and behavior
are important stress responses 765
The ratio of root-to-shoot growth increases in
response to water deficit 769
Plants can regulate stomatal aperture in response
to dehydration stress 769
Plants adjust osmotically to drying soil by
accumulating solutes 769
Submerged organs develop aerenchyma tissue in
response to hypoxia 770
Plants have evolved two different strategies to
protect themselves from toxic ions: exclusion and
internal tolerance 772
Chelation and active transport contribute to
internal tolerance 773
Many plants have the capacity to acclimate to cold
temperatures 773
Plants survive freezing temperatures by limiting ice
formation 774
The lipid composition of membranes affects their
response to temperature 775
Plant cells have mechanisms that maintain protein
structure during temperature stress 776
Scavenging mechanisms detoxify reactive oxygen
species 776
Metabolic shifts enable plants to cope with
a variety of abiotic stresses 777
SUMMARY 778
APPENDIX ONE A1-1
APPENDIX TWO A2-1
APPENDIX THREE A3-1
GLOSSARY G-1
AUTHOR INDEX AI-1
SUBJECT INDEX SI-1
|
| any_adam_object | 1 |
| author | Taiz, Lincoln 1942- Zeiger, Eduardo 1939- |
| author_GND | (DE-588)141478993 (DE-588)141479027 |
| author_facet | Taiz, Lincoln 1942- Zeiger, Eduardo 1939- |
| author_role | aut aut |
| author_sort | Taiz, Lincoln 1942- |
| author_variant | l t lt e z ez |
| building | Verbundindex |
| bvnumber | BV036467062 |
| classification_rvk | WN 1000 |
| classification_tum | BIO 480f |
| ctrlnum | (OCoLC)845666599 (DE-599)BVBBV036467062 |
| dewey-full | 571.2 |
| dewey-hundreds | 500 - Natural sciences and mathematics |
| dewey-ones | 571 - Physiology & related subjects |
| dewey-raw | 571.2 |
| dewey-search | 571.2 |
| dewey-sort | 3571.2 |
| dewey-tens | 570 - Biology |
| discipline | Biologie |
| edition | 5. ed. |
| format | Book |
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| genre | 1\p (DE-588)4123623-3 Lehrbuch gnd-content |
| genre_facet | Lehrbuch |
| id | DE-604.BV036467062 |
| illustrated | Illustrated |
| indexdate | 2024-07-09T22:40:05Z |
| institution | BVB |
| isbn | 9780878935659 9780878938667 |
| language | English |
| oai_aleph_id | oai:aleph.bib-bvb.de:BVB01-020338823 |
| oclc_num | 845666599 |
| open_access_boolean | |
| owner | DE-20 DE-19 DE-BY-UBM DE-526 DE-188 |
| owner_facet | DE-20 DE-19 DE-BY-UBM DE-526 DE-188 |
| physical | Getr. Zählung zahlr. Ill., graph. Darst. |
| publishDate | 2010 |
| publishDateSearch | 2010 |
| publishDateSort | 2010 |
| publisher | Sinauer |
| record_format | marc |
| spelling | Taiz, Lincoln 1942- Verfasser (DE-588)141478993 aut Plant physiology Lincoln Taiz ; Eduardo Zeiger 5. ed. Sunderland, Mass. Sinauer 2010 Getr. Zählung zahlr. Ill., graph. Darst. txt rdacontent n rdamedia nc rdacarrier Entwicklungsphysiologie (DE-588)4152449-4 gnd rswk-swf Pflanzenphysiologie (DE-588)4045580-4 gnd rswk-swf Pflanzen (DE-588)4045539-7 gnd rswk-swf 1\p (DE-588)4123623-3 Lehrbuch gnd-content Pflanzenphysiologie (DE-588)4045580-4 s DE-604 Pflanzen (DE-588)4045539-7 s Entwicklungsphysiologie (DE-588)4152449-4 s 2\p DE-604 Zeiger, Eduardo 1939- Verfasser (DE-588)141479027 aut HBZ Datenaustausch application/pdf http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=020338823&sequence=000002&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA Inhaltsverzeichnis 1\p cgwrk 20201028 DE-101 https://d-nb.info/provenance/plan#cgwrk 2\p cgwrk 20201028 DE-101 https://d-nb.info/provenance/plan#cgwrk |
| spellingShingle | Taiz, Lincoln 1942- Zeiger, Eduardo 1939- Plant physiology Entwicklungsphysiologie (DE-588)4152449-4 gnd Pflanzenphysiologie (DE-588)4045580-4 gnd Pflanzen (DE-588)4045539-7 gnd |
| subject_GND | (DE-588)4152449-4 (DE-588)4045580-4 (DE-588)4045539-7 (DE-588)4123623-3 |
| title | Plant physiology |
| title_auth | Plant physiology |
| title_exact_search | Plant physiology |
| title_full | Plant physiology Lincoln Taiz ; Eduardo Zeiger |
| title_fullStr | Plant physiology Lincoln Taiz ; Eduardo Zeiger |
| title_full_unstemmed | Plant physiology Lincoln Taiz ; Eduardo Zeiger |
| title_short | Plant physiology |
| title_sort | plant physiology |
| topic | Entwicklungsphysiologie (DE-588)4152449-4 gnd Pflanzenphysiologie (DE-588)4045580-4 gnd Pflanzen (DE-588)4045539-7 gnd |
| topic_facet | Entwicklungsphysiologie Pflanzenphysiologie Pflanzen Lehrbuch |
| url | http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=020338823&sequence=000002&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA |
| work_keys_str_mv | AT taizlincoln plantphysiology AT zeigereduardo plantphysiology |