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Plant defense responses Hypersensitive response

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Presentation on theme: "Plant defense responses Hypersensitive response"— Presentation transcript:

1 Plant defense responses Hypersensitive response
Prepare a 10’ talk for Friday March 3 on plant defense responses or describe interactions between plants& pathogens, pests or symbionts Plant defense responses Hypersensitive response Systemic acquired resistance Innate immunity Phytoalexin synthesis Defensins and other proteins Oxidative burst Some possible pests Nematodes Rootworms Aphids Thrips Gypsy moths hemlock woolly adelgid Some possible pathogens Agrobacterium tumefaciens Agrobacterium rhizogenes Pseudomonas syringeae Pseudomonas aeruginosa Viroids DNA viruses RNA viruses Fungi Oomycetes Some possible symbionts N-fixing bacteria N-fixing cyanobacteria Endomycorrhizae Ectomycorrhizae

2 Photosynthesis 2 sets of rxns in separate parts of chloroplast

3 Light-independent (dark) reactions
Overall Reaction: 3 CO2 + 3 RuBP + 9 ATP + 6 NADPH = 3 RuBP + 9 ADP + 9 Pi + 6 NADP+ + 1 Glyceraldehyde 3-P

4 Light-independent (dark) reactions
1) fixing CO2 2) reversing glycolysis 3) regenerating RuBP

5 fixing CO2 1) RuBP binds CO2

6 fixing CO2 1) CO2 is bound to RuBP 2) rapidly splits into two 3-Phosphoglycerate therefore called C3 photosynthesis detected by immediately killing cells fed 14CO2

7 fixing CO2 1) CO2 is bound to RuBP 2) rapidly splits into two 3-Phosphoglycerate 3) catalyzed by Rubisco (ribulose 1,5 bisphosphate carboxylase/oxygenase) the most important & abundant protein on earth Lousy Km Rotten Vmax! Makes lots of mistakes!

8 Reversing glycolysis converts 3-Phosphoglycerate to G3P consumes 1 ATP & 1 NADPH

9 Reversing glycolysis G3P has 2 possible fates 1) 1 in 6 becomes (CH2O)n

10 Reversing glycolysis G3P has 2 possible fates 1) 1 in 6 becomes (CH2O)n 2) 5 in 6 regenerate RuBP

11 Reversing glycolysis 1 in 6 G3P becomes (CH2O)n either becomes starch in chloroplast (to store in cell)

12 Reversing glycolysis 1 in 6 G3P becomes (CH2O)n either becomes starch in chloroplast (to store in cell) or is converted to DHAP & exported to cytoplasm to make sucrose

13 Reversing glycolysis 1 in 6 G3P becomes (CH2O)n either becomes starch in chloroplast (to store in cell) or is converted to DHAP & exported to cytoplasm to make sucrose Pi/triosePO4 antiporter only trades DHAP for Pi

14 Reversing glycolysis 1 in 6 G3P becomes (CH2O)n either becomes starch in chloroplast (to store in cell) or is converted to DHAP & exported to cytoplasm to make sucrose Pi/triosePO4 antiporter only trades DHAP for Pi mechanism to regulate PS

15 Regenerating RuBP G3P has 2 possible fates 5 in 6 regenerate RuBP necessary to keep cycle going

16 Regenerating RuBP Basic problem: converting a 3C to a 5C compound feed in five 3C sugars, recover three 5C sugars

17 Regenerating RuBP Basic problem: converting a 3C to a 5C compound must assemble intermediates that can be broken into 5 C sugars after adding 3C subunit

18 Regenerating RuBP making intermediates that can be broken into 5 C sugars after adding 3C subunits 3C + 3C + 3C = 5C + 4C

19 Regenerating RuBP making intermediates that can be broken into 5 C sugars after adding 3C subunits 3C + 3C + 3C = 5C + 4C 4C + 3C = 7C

20 Regenerating RuBP making intermediates that can be broken into 5 C sugars after adding 3C subunits 3C + 3C + 3C = 5C + 4C 4C + 3C = 7C 7C + 3C = 5C + 5C

21 Regenerating RuBP making intermediates that can be broken into 5 C sugars after adding 3C subunits 3C + 3C + 3C = 5C + 4C 4C + 3C = 7C 7C + 3C = 5C + 5C Uses 1 ATP/RuBP

22 Light-independent (dark) reactions
build up pools of intermediates , occasionally remove one very complicated book-keeping

23 Light-independent (dark) reactions
build up pools of intermediates , occasionally remove one very complicated book-keeping Use 12 NADPH and 18 ATP to make one 6C sugar

24 Regulating the Calvin Cycle
Rubisco is main rate-limiting step

25 Regulating the Calvin Cycle
Rubisco is main rate-limiting step indirectly regulated by light 2 ways 1) Rubisco activase: Rubisco must be carbamylated & bind Mg2+ to be active!

26 Regulating the Calvin Cycle
Rubisco is main rate-limiting step indirectly regulated by light 2 ways 1) Rubisco activase : uses ATP to activate rubisco

27 Regulating the Calvin Cycle
Rubisco is main rate-limiting step Rubisco must be carbamylated & bind Mg2+ to be active! RuBP binds & inactivates uncarbamylated rubisco Rubisco activase removes this RuBP

28 Regulating the Calvin Cycle
Rubisco is main rate-limiting step Rubisco must be carbamylated & bind Mg2+ to be active! RuBP binds & inactivates uncarbamylated rubisco Rubisco activase removes this RuBP In the dark many species phosphorylate carboxyarabinotol to form carboxyarabinitol 1-phosphate which binds the rubisco active site

29 Regulating the Calvin Cycle
Rubisco activase removes this RuBP In the dark many species phosphorylate carboxyarabinotol to form carboxyarabinitol 1-phosphate which binds the rubisco active site Rubisco activase also removes CA1P in the light CA1P phosphatase then removes the PO4

30 Regulating the Calvin Cycle
Availability of CO2 Demand is set by mesophyll, stomata control supply Ci is usually much lower than Ca A vs Ci plots tattle on the Calvin cycle

31 Regulating the Calvin Cycle
A vs Ci plots tattle on the Calvin cycle In linear phase rubisco is limiting When curves RuBP or Pi regeneration is limiting

32 Regulating the Calvin Cycle
Currently Rubisco usually limits C3 plants Will increase plant growth until hit new limiting factor

33 Regulating the Calvin Cycle
Currently Rubisco usually limits C3 plants Will increase plant growth until hit new limiting factor Free-Air CO2 Enrichment Experiments show initial gains, but taper off w/in a few years Now are limited by nutrients or water

34 Regulating the Calvin Cycle
Rubisco is main rate-limiting step indirectly regulated by light 2 ways 1) Rubisco activase 2) Light-induced changes in stroma

35 Regulating the Calvin Cycle
Rubisco is main rate-limiting step indirectly regulated by light 2 ways 1) Rubisco activase 2) Light-induced changes in stroma a) pH: rubisco is most active at pH > 8 (in dark pH is ~7.2)

36 Regulating the Calvin Cycle
Rubisco is main rate-limiting step indirectly regulated by light 2 ways 1) Rubisco activase 2) Light-induced changes in stroma a) pH: rubisco is most active at pH > 8 b) [Mg2+]: in light [Mg2+] in stroma is ~ 10x greater than in dark

37 Regulating the Calvin Cycle
Rubisco is main rate-limiting step indirectly regulated by light 2 ways 1) Rubisco activase 2) Light-induced changes in stroma a) pH: rubisco is most active at pH > 8 b) [Mg2+]: in light [Mg2+] in stroma is ~ 10x greater than in dark Mg2+ moves from thylakoid lumen to stroma to maintain charge neutrality

38 Regulating the Calvin Cycle
Rubisco is main rate-limiting step indirectly regulated by light 2 ways 1) Rubisco activase 2) Light-induced changes in stroma a) pH: rubisco is most active at pH > 8 b) [Mg2+]: in light [Mg2+] in stroma is ~ 10x greater than in dark c) CO2 is an allosteric activator of rubisco that only binds at high pH and high [Mg2+] also: stomates open in the light

39 Regulating the Calvin Cycle
Rubisco is main rate-limiting step indirectly regulated by light 2 ways 1) Rubisco activase 2) Light-induced changes in stroma Several other Calvin cycle enzymes (e.g.Fructose-1,6-bisphosphatase) are also activated by high pH & [Mg2+]

40 Regulating the Calvin Cycle
Several Calvin cycle enzymes (e.g.Fructose-1,6-bisphosphatase) are also regulated by thioredoxin contain disulfide bonds which get oxidized in the dark

41 Regulating the Calvin Cycle
Several Calvin cycle enzymes (e.g.Fructose-1,6-bisphosphatase) are also regulated by thioredoxin contain disulfide bonds which get oxidized in the dark in light, ferredoxin reduces thioredoxin, thioredoxin reduces these disulfide bonds to activate the enzyme S - S 2Fdox 2Fdred PSI + PSII light 2e- oxidized thioredoxin reduced SH enzyme (inactive) (active)

42 Regulating the Calvin Cycle
Several Calvin cycle enzymes (e.g.Fructose-1,6-bisphosphatase) are also regulated by thioredoxin contain disulfide bonds which get oxidized in the dark in light, ferredoxin reduces thioredoxin, thioredoxin reduces these disulfide bonds to activate the enzyme How light reactions talk to the Calvin cycle S - S 2Fdox 2Fdred PSI + PSII light 2e- oxidized thioredoxin reduced SH enzyme (inactive) (active)

43 RuBP + O2 <=> 3-phosphoglycerate + phosphoglycolate
PHOTORESPIRATION Rubisco can use O2 as substrate instead of CO2 RuBP + O2 <=> 3-phosphoglycerate + phosphoglycolate

44 RuBP + O2 <=> 3-phosphoglycerate + Phosphoglycolate
PHOTORESPIRATION Rubisco can use O2 as substrate instead of CO2 RuBP + O2 <=> 3-phosphoglycerate + Phosphoglycolate Releases CO2 without making ATP or NADH

45 PHOTORESPIRATION Releases CO2 without making ATP or NADH Called photorespiration : undoes photosynthesis

46 RuBP + O2 <=> 3-phosphoglycerate + Phosphoglycolate
PHOTORESPIRATION Rubisco can use O2 as substrate instead of CO2 RuBP + O2 <=> 3-phosphoglycerate + Phosphoglycolate C3 plants can lose 25%-50% of their fixed carbon

47 RuBP + O2 <=> 3-phosphoglycerate + Phosphoglycolate
PHOTORESPIRATION Rubisco can use O2 as substrate instead of CO2 RuBP + O2 <=> 3-phosphoglycerate + Phosphoglycolate C3 plants can lose 25%-50% of their fixed carbon Both rxns occur at same active site

48 PHOTORESPIRATION C3 plants can lose 25%-50% of their fixed carbon phosphoglycolate is converted to glycolate : poison!

49 Detoxifying Glycolate
1) glycolate is shuttled to peroxisomes

50 Detoxifying Glycolate
1) glycolate is shuttled to peroxisomes 2) peroxisomes convert it to glycine produce H2O2

51 Detoxifying Glycolate
1) glycolate is shuttled to peroxisomes 2) peroxisomes convert it to glycine 3) glycine is sent to mitochondria

52 Detoxifying Glycolate
1) glycolate is shuttled to peroxisomes 2) peroxisomes convert it to glycine 3) glycine is sent to mitochondria 4) mitochondria convert 2 glycine to 1 serine + 1 CO2 Why photorespiration loses CO2

53 Detoxifying Glycolate
1) glycolate is shuttled to peroxisomes 2) peroxisomes convert it to glycine 3) glycine is sent to mitochondria 4) mitochondria convert 2 glycine to 1 serine + 1 CO2 5) serine is returned to peroxisome

54 Detoxifying Glycolate
1) glycolate is shuttled to peroxisomes 2) peroxisomes convert it to glycine 3) glycine is sent to mitochondria 4) mitochondria convert 2 glycine to 1 serine + 1 CO2 5) serine is returned to peroxisome 6) peroxisome converts it to glycerate & returns it to chloroplast

55 Detoxifying Glycolate
Why peroxisomes are next to cp and mito in C3 plants Mitochondrion

56 C4 and CAM photosynthesis
Rubisco can use O2 as substrate instead of CO2 [CO2] is 1/600 [O2] _-> usually discriminate well

57 C4 and CAM photosynthesis
Rubisco can use O2 as substrate instead of CO2 [CO2] is 1/600 [O2] Photorespiration increases with temperature

58 C4 and CAM photosynthesis
Rubisco can use O2 as substrate instead of CO2 [CO2] is 1/600 [O2] Photorespiration increases with temperature Solution: increase [CO2] at rubisco

59 C4 and CAM photosynthesis
Solution: increase [CO2] at rubisco C4 & CAM = adaptations that reduce PR & water loss

60 C4 and CAM photosynthesis
Adaptations that reduce PR & water loss Both fix CO2 with a different enzyme

61 C4 and CAM photosynthesis
Adaptations that reduce PR & water loss Both fix CO2 with a different enzyme later release CO2 to be fixed by rubisco use energy to increase [CO2] at rubisco

62 C4 and CAM photosynthesis
Adaptations that reduce PR & water loss Both fix CO2 with a different enzyme later release CO2 to be fixed by rubisco use energy to increase [CO2] at rubisco C4 isolates rubisco spatially (e.g. corn)

63 C4 and CAM photosynthesis
Adaptations that reduce PR & water loss Both fix CO2 with a different enzyme later release CO2 to be fixed by rubisco use energy to increase [CO2] at rubisco C4 isolates rubisco spatially (e.g. corn) CAM isolates rubisco temporally (e.g. cacti)

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