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Ayesha Siddiqui
Botany
University of Agriculture, Faisalabad
Potential for increased photosynthetic performance
and crop productivity in response to climate change:
role of CBFs and gibberellic acid
 Norman P. A. Hüner1, Keshav Dahal, Leonid V.
Kurepin1, Leonid Savitch, Jas Singh, Alexander G.
Ivanov, Khalil Kane and Fathey Sarhan
 It was published on April 2014 in FRONTIERS IN
CHEMISTRY
Impact of climate change on crop
productivity
Increased severity of stresses
Altered global climate
(sub-opt condition for
plant growth
Enhanced CO2
concentration
Drastic
temperature
changes
Urbanization
Industralization
Desertification
1.Photosynthetic performance
2. Biomass production
3. Crop seed yield
Green
revolution
Short, sturdy semi-dwarf
High HI & low tendency to lodge
Ultimate solution
Increased efficiency
of photosynthesis
required
Major concerned
Increasing population results in increased food
demand
To supplement increased food demand
by using any approach that is helpful
Improved agricultural
techniques
Improved genetic
techniques
Targeted genetic approaches for
improving yield
 To alter the structure & composition of the
photosynthetic photosystems and their
associated antenna complexes,
 To alter the structure of the CO2 fixing enzyme,
Rubisco, in order to reduce the rates of
photorespiration in C3 crop plants
 To increase the potential for C4 photosynthesis
in C3 plants such as rice
Proposal for improving yield:
cold acclimation
Cold acclimation is a novel approach to enhance plant
biomass production
1. by co-ordinating source-sink demand
2. And minimizing energy loss through NPQ
3. And enhanced over-expression of CBFs increases
1. Increased photosynthetic performance
2. Increased WUE
3. Potential for enhanced resistance to biotic stress
Leads to enhanced photosynthetic performance
Maximum potential biomass and grain
yield determinant
1
• Incident solar radiation
2
• Translocation of photosynthates to sink
3
• Partioning efficiency i.e. HI
4
• Light interception efficiency
5
• Energy conversion efficiency
Energy conversion efficiency
 is, the ratio of the biomass energy produced over a
given period to the radiative energy intercepted by the
canopy over the same period.
Theoretically, increasing this
efficiency will increase potential
biomass
Hypothesis: Maximum energy conversion
into biomass may improve yield
 Plant body Carbon 40% dry mass
Increase
Crucial
photoprotective mechanism
reduces yield
Photoprotective mechanism
reduces yield
absorbed energy
Photosynthetically
generated electrons
by C,N & S metabolism
Transformed into
reducing power
Excess energy is
dissipated
Photoprotective mechanism
is crucial
Protects
Photosynthetic apparatus
from irradiance
 Which is more than what
can be used by reductive
CO2, N & S assimilation
Need for Photoprotective Mechanism
Reduces efficiency of
CO2 assimilation as
energy is dissipated, as a
result less biomass
Reduction of this process
may increase
CO2 assimilation
Necessary evil for plant
survival against
environmental stresses
Proposal: Cold acclimation is
the solution
 Phenotypic plasticity, increased photosynthetic
surface
 Ultimately increased photosynthetic performance
 Minimizes dependance on NPQ for photoprotection
 Enhanced photosynthetic performance at elevated
CO2 and maintained during long term growth
 Inherent resistance to abiotic as well as biotic stress
Cold acclimation improves
photosynthetic performance
•It is estimated that under optimal growth
conditions only about 4.6% of the initial energy
that impinges the leaf surface is conserved as
fixed carbon and plant biomass.
•Suboptimal conditions may increase Carbon
assimilation in cold acclimated cultivars.
Winter CA or semi-dwarf
cultivars
Made by?
gai mutant
GAI controlled
i.e.
Gibberellins
responsive
transcription
factors
Winter CA cultivar
Rye, Barley etc
1. Enhanced Carbon metabolism
2. Enhanced sink capacity
3. Enhanced Pi cycling
4. Increased capacity for RUBP regeneration
5. Reduces photorespiration
6. Stimulates Carbon export from leaf
Conclusion:-
Co-ordinate system that
1. Enhances source-sink activities
2. More CO2 assimilation
1
• Increased cytosolic sucrose
biosynthetic enzymes i.e. SPS etc
2
• Increased gene expression
3
• Controlled RubisCO activities
Enhanced Carbon
metabolism
Enhanced sink
capacity
Crown leaf mesophyll
tissue cell vacoule
Sucrose export
Stored as fructans in
Cold acclimation & phenotypic
plasticity
 Regulated by redox state of chloroplast measured
as excitation pressure
Chloroplast redox signal
Regulates
Excitation pressure
is defined as a quantitative measure of
the proportion of closed PSII reaction
centers due to an imbalance between
energy absorbed vs. energy either utilized
through metabolism and growth or
dissipated as heat.
Picture explained
 Accumulation of growth-inactive GAs maintains levels
of DELLA proteins such growth and stem elongation
are repressed which generates a dwarf phenotype.
 This dwarf phenotype exhibits enhanced
photosynthetic performance and increased dry
biomass per unit plant volume coupled with enhanced
seed yield in CA wheat
CA dwarf phenotype results in improved
photosynthetic performance
Altered leaf
mesophyll cell
ultrastructure
Increase in
cytoplasmic volume
Decrease in
vacuolar volume
Increased specific
leaf weight
Increased leaf thickness
Increased mesophyll cell
size
Increased palisade
mesophyll layers
1. Increased leaf protein content
2. increased sucrose & other
structural carbohydrate
Larger extended
phenotype results in
Autumn (cold period)
• Increased total energy per unit plant
volume
Following spring
• Enhanced seed yield
 Extended Phenotype
 Increased leaf area
 Increased photosynthetic apparatus per unit leaf area
 Increased capacity to utilize absorbed light energy
 Keeps PSII reaction centers open
 Lowers excitation pressure
 Less photoinhibition of photosynthesis
Cold acclimation reduces relative
dependence on NPQ
Efficiency
light utilization for CO2
assimilation
Energy dissipation
as the apparent number of
photons required to close
50% of PSII reaction
centers
as the apparent number of
photons required to induce
one unit of NPQ
Shifting C3 to C4: short term increase in
CO2 assimilation
 It has been established that a short-term shift of C3
species from ambient to elevated CO2 results in an
increase in the rates of CO 2 assimilation
 This stimulation of photosynthesis in C3 plants due to
elevated CO2 occurs because Rubisco is CO2 substrate
limited at ambient CO2 and photorespiration is
suppressed since CO2 is a competitive inhibitor of the
oxygenation of RuBP by Rubisco
Shifting C3 to C4: Feed back inhibition
at long term exposure to CO2
Long-term growth and development of C3 plants at high
CO2 may lead to end product inhibition of
photosynthesis due to the accumulation of sucrose in
the cytosol.
This feedback inhibition of growth at elevated CO2
levels is
1. Due to chloroplast Pi limitations
2. And down regulation of the expression and
activities of key regulatory photosynthetic
enzymes
Long term growth at elevated CO2:
Cold acclimation maintains
photosynthetic performance
 However, CA maintains their superior photosynthetic
performance with respect to light and CO2 saturated
rates and do not exhibit feedback inhibition of
photosynthesis at elevated CO2.
How does it do that?
Cold acclimated cultivar
gives better yield
35–50% decrease
in excitation
pressure & non-
photochemical
energy dissipation
Cold acclimated cultivar
gives better yield
Genes upregulated
for
maintenance of
chloroplast
stability
(chaperonins)
Cold acclimation regulates expression
of CO2 at molecular level
 plant cell membrane is the primary site that
determines the potential of plants to freezing
tolerance
 Low temperature activates Ca2+ channels and rapidly
generates a Ca2+signal that activates a cytosolic
protein kinase whose substrate is ICE1.
 The phosphorylation of ICE1 is required for the
induction of a family CBF transcription factors which
regulate the expression of CO2.
Benefits of cold acclimation
 enhanced photosynthetic performance
 superior resistance to photoinhibition
 suppresses stomatal conductance due to to a
decrease in leaf stomatal density
 reduces transpiration rates by 30–40%
regardless of the measuring temperature
 3- fold increase in leaf water use efficiency
(WUE) primarily due to a combination of a
decrease in stomatal density combined with the
observed increase in light saturated rates of
photosynthesis
 increased systemic resistance to plant infection
Conclusion of proposal research
Cold acclimation of winter rye, winter wheat, and
Brassica napus establishes a new homeostatic state
which is characterized by an increased
 photosynthetic capacity for CO2 assimilation
 and its conversion into biomass or energy per unit
plant volume
 and seed production in wheat under suboptimal
growth conditions
So we predict that cold acclimation not only
1. Enhances photosynthetic
performance
2. It also enhances inherent resistance
to biotic stress.
CBF family of
transcription factors
 Targeting the CBF family of transcription factors in
major crop species improves crop productivity through
increased photosynthetic performance, WUE and
resistance to abiotic stress
Potential role of CBFs
 CBFs results in enhanced dwarf phenotype by
decreasing level of growth active GAs
 CBFs overexpression is related with changes in cell
membrane structure (lipid and fatty acid composition
and contents) requires for acclimation to low
temperature
 CBFs regulates the expression of COR genes encoding
maxmium freezing tolerance.
 CBFs affects plant development
 CBFs regulates genes associated with photosynthesis,
respiration and cytosolic carbon metabolism
Suboptimal conditions associated with future
climate change (cold climate)
Overexpression of C/repeat dehdration responsive
family of transcription factors
Enhanced photosynthetic performance
Overexpression of CBFs circumvents the requirement
of cold acclimation
CBFs expression signals
emanates from Chloroplast
 Chloroplast is the cellular energy sensor for detecting
changes in the environment
 Chloroplast redox imbalance or excitation pressure
sends operational signals for CBFs expression
 However, it must be integrated with regulation
associated changes in light quality sensed through
photoreceptors such as phytochrome as well as
through specific cell membrane, low temperature
sensors to establish a new CA homeostatic state.
Drawbacks of proposed research
 Delayed flowering time
 Low temperature of CBF induction causes activation
of expression of FLC (flowering locus L), negative
regulator of flowering
 Delayed bolting
 Overexpression of AtCBF3 delays onset of bolting at
20 celsius by 4 to 9 days.
 Reduced seed yield
 CBF overexpressors have reduced seed yield at warm
temperatures.
 Spring Vs. winter cultivar
 Spring varieties don’t exhibit phenotypic change
so photosynthetic performance appears to be
cultivar dependant

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Photosynthesis and Climate Change

  • 1. Ayesha Siddiqui Botany University of Agriculture, Faisalabad
  • 2. Potential for increased photosynthetic performance and crop productivity in response to climate change: role of CBFs and gibberellic acid  Norman P. A. Hüner1, Keshav Dahal, Leonid V. Kurepin1, Leonid Savitch, Jas Singh, Alexander G. Ivanov, Khalil Kane and Fathey Sarhan  It was published on April 2014 in FRONTIERS IN CHEMISTRY
  • 3. Impact of climate change on crop productivity Increased severity of stresses Altered global climate (sub-opt condition for plant growth Enhanced CO2 concentration Drastic temperature changes Urbanization Industralization Desertification 1.Photosynthetic performance 2. Biomass production 3. Crop seed yield
  • 4. Green revolution Short, sturdy semi-dwarf High HI & low tendency to lodge Ultimate solution Increased efficiency of photosynthesis required
  • 5. Major concerned Increasing population results in increased food demand To supplement increased food demand by using any approach that is helpful Improved agricultural techniques Improved genetic techniques
  • 6. Targeted genetic approaches for improving yield  To alter the structure & composition of the photosynthetic photosystems and their associated antenna complexes,  To alter the structure of the CO2 fixing enzyme, Rubisco, in order to reduce the rates of photorespiration in C3 crop plants  To increase the potential for C4 photosynthesis in C3 plants such as rice
  • 7. Proposal for improving yield: cold acclimation Cold acclimation is a novel approach to enhance plant biomass production 1. by co-ordinating source-sink demand 2. And minimizing energy loss through NPQ 3. And enhanced over-expression of CBFs increases 1. Increased photosynthetic performance 2. Increased WUE 3. Potential for enhanced resistance to biotic stress Leads to enhanced photosynthetic performance
  • 8. Maximum potential biomass and grain yield determinant 1 • Incident solar radiation 2 • Translocation of photosynthates to sink 3 • Partioning efficiency i.e. HI 4 • Light interception efficiency 5 • Energy conversion efficiency
  • 9. Energy conversion efficiency  is, the ratio of the biomass energy produced over a given period to the radiative energy intercepted by the canopy over the same period. Theoretically, increasing this efficiency will increase potential biomass
  • 10. Hypothesis: Maximum energy conversion into biomass may improve yield  Plant body Carbon 40% dry mass Increase
  • 12. Photoprotective mechanism reduces yield absorbed energy Photosynthetically generated electrons by C,N & S metabolism Transformed into reducing power Excess energy is dissipated
  • 13. Photoprotective mechanism is crucial Protects Photosynthetic apparatus from irradiance  Which is more than what can be used by reductive CO2, N & S assimilation
  • 14. Need for Photoprotective Mechanism Reduces efficiency of CO2 assimilation as energy is dissipated, as a result less biomass Reduction of this process may increase CO2 assimilation Necessary evil for plant survival against environmental stresses
  • 15. Proposal: Cold acclimation is the solution  Phenotypic plasticity, increased photosynthetic surface  Ultimately increased photosynthetic performance  Minimizes dependance on NPQ for photoprotection  Enhanced photosynthetic performance at elevated CO2 and maintained during long term growth  Inherent resistance to abiotic as well as biotic stress
  • 16. Cold acclimation improves photosynthetic performance •It is estimated that under optimal growth conditions only about 4.6% of the initial energy that impinges the leaf surface is conserved as fixed carbon and plant biomass. •Suboptimal conditions may increase Carbon assimilation in cold acclimated cultivars.
  • 17. Winter CA or semi-dwarf cultivars Made by? gai mutant GAI controlled i.e. Gibberellins responsive transcription factors
  • 18. Winter CA cultivar Rye, Barley etc 1. Enhanced Carbon metabolism 2. Enhanced sink capacity 3. Enhanced Pi cycling 4. Increased capacity for RUBP regeneration 5. Reduces photorespiration 6. Stimulates Carbon export from leaf Conclusion:- Co-ordinate system that 1. Enhances source-sink activities 2. More CO2 assimilation
  • 19. 1 • Increased cytosolic sucrose biosynthetic enzymes i.e. SPS etc 2 • Increased gene expression 3 • Controlled RubisCO activities Enhanced Carbon metabolism
  • 20. Enhanced sink capacity Crown leaf mesophyll tissue cell vacoule Sucrose export Stored as fructans in
  • 21. Cold acclimation & phenotypic plasticity  Regulated by redox state of chloroplast measured as excitation pressure Chloroplast redox signal Regulates
  • 22. Excitation pressure is defined as a quantitative measure of the proportion of closed PSII reaction centers due to an imbalance between energy absorbed vs. energy either utilized through metabolism and growth or dissipated as heat.
  • 23. Picture explained  Accumulation of growth-inactive GAs maintains levels of DELLA proteins such growth and stem elongation are repressed which generates a dwarf phenotype.  This dwarf phenotype exhibits enhanced photosynthetic performance and increased dry biomass per unit plant volume coupled with enhanced seed yield in CA wheat
  • 24. CA dwarf phenotype results in improved photosynthetic performance Altered leaf mesophyll cell ultrastructure Increase in cytoplasmic volume Decrease in vacuolar volume Increased specific leaf weight Increased leaf thickness Increased mesophyll cell size Increased palisade mesophyll layers 1. Increased leaf protein content 2. increased sucrose & other structural carbohydrate
  • 25. Larger extended phenotype results in Autumn (cold period) • Increased total energy per unit plant volume Following spring • Enhanced seed yield
  • 26.  Extended Phenotype  Increased leaf area  Increased photosynthetic apparatus per unit leaf area  Increased capacity to utilize absorbed light energy  Keeps PSII reaction centers open  Lowers excitation pressure  Less photoinhibition of photosynthesis
  • 27. Cold acclimation reduces relative dependence on NPQ Efficiency light utilization for CO2 assimilation Energy dissipation as the apparent number of photons required to close 50% of PSII reaction centers as the apparent number of photons required to induce one unit of NPQ
  • 28. Shifting C3 to C4: short term increase in CO2 assimilation  It has been established that a short-term shift of C3 species from ambient to elevated CO2 results in an increase in the rates of CO 2 assimilation  This stimulation of photosynthesis in C3 plants due to elevated CO2 occurs because Rubisco is CO2 substrate limited at ambient CO2 and photorespiration is suppressed since CO2 is a competitive inhibitor of the oxygenation of RuBP by Rubisco
  • 29. Shifting C3 to C4: Feed back inhibition at long term exposure to CO2 Long-term growth and development of C3 plants at high CO2 may lead to end product inhibition of photosynthesis due to the accumulation of sucrose in the cytosol. This feedback inhibition of growth at elevated CO2 levels is 1. Due to chloroplast Pi limitations 2. And down regulation of the expression and activities of key regulatory photosynthetic enzymes
  • 30. Long term growth at elevated CO2: Cold acclimation maintains photosynthetic performance  However, CA maintains their superior photosynthetic performance with respect to light and CO2 saturated rates and do not exhibit feedback inhibition of photosynthesis at elevated CO2. How does it do that?
  • 31. Cold acclimated cultivar gives better yield 35–50% decrease in excitation pressure & non- photochemical energy dissipation
  • 32. Cold acclimated cultivar gives better yield Genes upregulated for maintenance of chloroplast stability (chaperonins)
  • 33. Cold acclimation regulates expression of CO2 at molecular level  plant cell membrane is the primary site that determines the potential of plants to freezing tolerance  Low temperature activates Ca2+ channels and rapidly generates a Ca2+signal that activates a cytosolic protein kinase whose substrate is ICE1.  The phosphorylation of ICE1 is required for the induction of a family CBF transcription factors which regulate the expression of CO2.
  • 34. Benefits of cold acclimation  enhanced photosynthetic performance  superior resistance to photoinhibition  suppresses stomatal conductance due to to a decrease in leaf stomatal density  reduces transpiration rates by 30–40% regardless of the measuring temperature  3- fold increase in leaf water use efficiency (WUE) primarily due to a combination of a decrease in stomatal density combined with the observed increase in light saturated rates of photosynthesis  increased systemic resistance to plant infection
  • 35. Conclusion of proposal research Cold acclimation of winter rye, winter wheat, and Brassica napus establishes a new homeostatic state which is characterized by an increased  photosynthetic capacity for CO2 assimilation  and its conversion into biomass or energy per unit plant volume  and seed production in wheat under suboptimal growth conditions
  • 36. So we predict that cold acclimation not only 1. Enhances photosynthetic performance 2. It also enhances inherent resistance to biotic stress.
  • 37. CBF family of transcription factors  Targeting the CBF family of transcription factors in major crop species improves crop productivity through increased photosynthetic performance, WUE and resistance to abiotic stress
  • 38. Potential role of CBFs  CBFs results in enhanced dwarf phenotype by decreasing level of growth active GAs  CBFs overexpression is related with changes in cell membrane structure (lipid and fatty acid composition and contents) requires for acclimation to low temperature  CBFs regulates the expression of COR genes encoding maxmium freezing tolerance.  CBFs affects plant development  CBFs regulates genes associated with photosynthesis, respiration and cytosolic carbon metabolism
  • 39. Suboptimal conditions associated with future climate change (cold climate) Overexpression of C/repeat dehdration responsive family of transcription factors Enhanced photosynthetic performance Overexpression of CBFs circumvents the requirement of cold acclimation
  • 40. CBFs expression signals emanates from Chloroplast  Chloroplast is the cellular energy sensor for detecting changes in the environment  Chloroplast redox imbalance or excitation pressure sends operational signals for CBFs expression  However, it must be integrated with regulation associated changes in light quality sensed through photoreceptors such as phytochrome as well as through specific cell membrane, low temperature sensors to establish a new CA homeostatic state.
  • 41. Drawbacks of proposed research  Delayed flowering time  Low temperature of CBF induction causes activation of expression of FLC (flowering locus L), negative regulator of flowering  Delayed bolting  Overexpression of AtCBF3 delays onset of bolting at 20 celsius by 4 to 9 days.  Reduced seed yield  CBF overexpressors have reduced seed yield at warm temperatures.  Spring Vs. winter cultivar  Spring varieties don’t exhibit phenotypic change so photosynthetic performance appears to be cultivar dependant