Title: Bio 226: Cell and Molecular Biology
1 Plant Respiration Releases 50 of fixed
CO2 Provides energy for all sinks, source leaves
at night helps source during day!
2Plant Respiration Similar, but more complex than
in animals Making precursors, recycling products,
releasing energy are also important
3- Plant Respiration
- Glycolysis in cytosol
- Pyruvate oxidation in mito
- Krebs cycle in mito
- Electron transport
- chemiosmosis in mito
4- Plant Respiration
- Glycolysis in cytosol
- 1 glucose -gt 2 pyruvate
- Yields 2 NADH 2 ATP
- per glucose
- Unique features in plants
- May start with DHAP
- from cp instead of glucose
5- Unique features in plants
- May start with DHAP from cp instead of glucose
- May yield malate cf pyr
- PEP -gtOAA by PEPC, then reduced to malate
6- Plant Respiration
- May yield malate cf pyr
- PEP -gtOAA by PEPC, then reduced to malate
- Get more ATP/NADH in mito
7- Unique features in plants
- May yield malate cf pyr
- PEP -gtOAA by PEPC, then reduced to malate
- Get more ATP/NADH in mito
- Replaces substrates
8- Plant Respiration
- Glycolysis in cytosol
- 1 glucose -gt 2 pyruvate
- Yields 2 NADH 2 ATP
- per glucose
- Anaerobic plants ferment
- pyr to regenerate NAD
- Form EtOH
9- Plant Respiration
- Glycolysis in cytosol
- 1 glucose -gt 2 pyruvate
- Yields 2 NADH 2 ATP
- per glucose
- Anaerobic plants ferment
- pyr to regenerate NAD
- Form EtOH
- Less toxic than lactate
- because diffuses away
10- Plant Respiration
- Krebs cycle
- Similar, but
- more complex
- Key role is making
- intermediates
- recycling products
11- Plant Respiration
- Krebs cycle
- Similar, but
- more complex
- Key role is making
- intermediates
- recycling products
- Many ways to feed in
- other substrates to burn
12- Plant Respiration
- Krebs cycle
- Similar, but
- more complex
- Key role is making
- intermediates
- recycling products
- Many ways to feed in
- other substrates to burn
- or replace intermediates
- used for biosynthesis
13- Plant Respiration
- Many ways to feed in other substrates to burn or
replace - intermediates used
- for biosynthesis
- Needed to keep
- cycle going
14- Plant Respiration
- Many ways to feed in other substrates to burn or
replace - intermediates used
- for biosynthesis
- Needed to keep
- cycle going
15- Plant Respiration
- Many ways to feed in other substrates to burn or
replace - intermediates used
- for biosynthesis
- Needed to keep
- cycle going
- Malic enzyme is key
- lets cell burn malate
- or citrate from other
- sources
16- Plant Respiration
- Many ways to feed in other substrates to
- burn or replace intermediates used
- for biosynthesis
- Needed to keep cycle going
- Malic enzyme is key lets cell burn
- malate or citrate from other sources
- PEPCarboxylase lets cell replace Krebs
- intermediates used for synthesis
17- Plant Respiration
- Pentose phosphate shunt in cytosol or cp
- 6 glucose-6P 12NADP 7 H2O -gt 5 glucose-6P 6
CO2 12 NADPH 12 H makes NADPH
intermediates
18- Plant Respiration
- Pentose phosphate shunt in cytosol or cp
- makes NADPH intermediates
- Uses many Calvin Cycle enzymes
19- Plant Respiration
- Pentose phosphate shunt in cytosol or cp
- makes NADPH intermediates
- Uses many Calvin Cycle enzymes
- Makes nucleotide
- phenolic precursors
20- Plant Respiration
- Uses many Calvin Cycle enzymes
- Makes nucleotide phenolic precursors
- Gets Calvin cycle started at dawn
21ATP generation 2 stages 1) e- transport 2)
chemiosmotic ATP synthesis
22Three steps transport H across membrane 1) NADH
dehydrogenase pumps 4 H/ 2 e- 2) Cyt bc1 pumps
4 H/ 2 e- 3) Cyt c oxidase pumps 2 H/ 2 e- and
adds 2 H to O to form H2O
23- e- transport
- Plants have additional enzymes!
- NADH dehydrogenase in matrix that transfers e-
from NADH to UQ w/o pumping H
24- Additional e- transport enzymes!
- NADH dehydrogenase in matrix that transfers e-
from NADH to UQ w/o pumping H Insensitive to
rotenone
25- Additional e- transport enzymes!
- NADH dehydrogenase in matrix that transfers e-
from NADH to UQ w/o pumping H Insensitive to
rotenone - Helps burn off excess NADH from making precursors
26- Additional e- transport enzymes!
- NADH dehydrogenase in matrix that transfers e-
from NADH to UQ w/o pumping H Insensitive to
rotenone - Helps burn off excess NADH from making precursors
- Much lower affinity for NADH than complex I
27- Additional e- transport enzymes!
- NADH dehydrogenase in matrix that transfers e-
from NADH to UQ w/o pumping H Insensitive to
rotenone - Helps burn off excess NADH from making precursors
- Energy is released as heat
- NADH dehydrogenase in intermembrane space that
transfers e- from NADH to UQ w/o pumping H
28- Additional e- transport enzymes!
- NADH dehydrogenase in intermembrane space that
transfers e- from NADH to UQ w/o pumping H
Insensitive to rotenone - "imports" e- from cytoplasmic NADH
- Much lower affinity for NADH than complex I
- Energy is released as heat
29- Additional e- transport enzymes!
- NADPH dehydrogenase in intermembrane space that
transfers e- from NADPH to UQ w/o pumping H
Insensitive to rotenone - "imports" e- from cytoplasmic NADPH
30- Additional e- transport enzymes!
- Alternative oxidase on matrix side of IM
transfers e- from UQ to O2 w/o pumping H - Insensitive to Cyanide, Azide
- or CO
- Sensitive to SHAM
- (salicylhydroxamic acid)
31- Additional e- transport enzymes!
- Alternative oxidase on matrix side of IM
transfers e- from UQ to O2 w/o pumping H - Insensitive to Cyanide, Azide or CO
- Sensitive to SHAM (salicylhydroxamic acid,)
- Also found in fungi, trypanosomes Plasmodium
32- Additional e- transport enzymes!
- Alternative oxidase on matrix side of IM
transfers e- from UQ to O2 w/o pumping H - Also found in fungi, trypanosomes Plasmodium
- Energy lost as heat
- can raise Voodoo lilies
- 25 C
33- Additional e- transport enzymes!
- Alternative oxidase on matrix side of IM
transfers e- from UQ to O2 w/o pumping H - Plants also have an uncoupler protein lets H
in w/o doing work!
34Additional e- transport enzymes! Why so many
ways to reduce ATP synthesis efficiency?
Additional e- transport enzymes! Why so many
ways to reduce ATP synthesis efficiency?
35- Additional e- transport enzymes!
- Why so many ways to reduce ATP synthesis
efficiency? - Regenerate NAD needed for precursor synthesis
- Generate heat
- Burn off excess energy captured by
photosynthesis - Prevalence says they're doing something
important!
- Additional e- transport enzymes!
- Why so many ways to reduce ATP synthesis
efficiency? - Regenerate NAD needed for precursor synthesis
- Generate heat
- Burn off excess energy captured by
photosynthesis - Prevalence says they're doing something
important!
36Regulating Respiration Regulated by demand for
ATP, NADPH and substrates
37Glycolysis is allosterically regulated at 3
irreversible steps Hexokinase is allosterically
inhibited by its product G-6P Allosteric site
has lower affinity than active site
38Glycolysis is allosterically regulated at 3
irreversible steps Hexokinase is allosterically
inhibited by its product G-6P Pyr kinase is
allosterically inhibited by ATP citrate
39Regulating Glycolysis Main regulatory step is
Phosphofructokinase Rate-limiting step Committed
step
40Regulating Glycolysis Main regulatory step is
Phosphofructokinase Inhibited by Citrate, PEP
ATP Stimulated by ADP
41- Regulating Pyruvate DH
- Mainly by a kinase
- Inhibited when Pi added
42- Regulating Pyruvate DH
- Mainly by a kinase
- Inhibited when Pi added
- NADH, Acetyl CoA, ATP
- NH4 inhibit PDH
- activate kinase
43- Regulating Pyruvate DH
- Mainly by a kinase
- Inhibited when Pi added
- NADH, Acetyl CoA, ATP
- NH4 inhibit PDH
- activate kinase
- Activated when no Pi
- ADP, pyruvate inhibit
- kinase
44- REGULATING THE KREBS CYCLE
- Krebs cycle is allosterically regulated at 4
enzymes - citrate synthase
- Isocitrate dehydrogenase
- 3) a-ketoglutarate dehydrogenase
- 4) Malate dehydrogenase
45- REGULATING THE KREBS CYCLE
- Krebs cycle is allosterically regulated at 4
enzymes - citrate synthase
- Isocitrate dehydrogenase
- 3) a-ketoglutarate dehydrogenase
- 4) Malate dehydrogenase
- All are inhibited by NADH
- products
46- Environmental factors
- Temperature
- Rate doubles for each 10 C increase up to
40 - At higher T start to denature
47- Environmental factors
- Temperature
- Rate doubles for each 10 C increase up to
40 - At higher T start to denature
- 2) pO2
- Respiration declines if pO2 lt5
48- Environmental factors
- Temperature
- Rate doubles for each 10 C increase up to
40 - At higher T start to denature
- 2) pO2
- Respiration declines if pO2 lt5
- Problem for flooded roots
49- Environmental factors
- Temperature
- Rate doubles for each 10 C increase up to
40 - At higher T start to denature
- 2) pO2
- Respiration declines if pO2 lt5
- Problem for flooded roots
- pCO2
- Inhibits respiration at 3
50- Environmental factors
- Temperature
- Rate doubles for each 10 C increase up to
40 - At higher T start to denature
- 2) pO2
- Respiration declines if pO2 lt5
- Problem for flooded roots
- pCO2
- Inhibits respiration at 3
- No obvious effects at 700 ppm, yet biomass reduced
51Mineral Nutrition Studied by soil-free culture in
nutrient solutions
52- Mineral Nutrition
- Studied by soil-free culture in nutrient
solutions Hoaglands is best known
53- Mineral Nutrition
- Soil-free culture
- Sand culture dont really control nutrients
54- Mineral Nutrition
- Soil-free culture
- Sand culture dont really control nutrients
- Hydroponics immerse roots in nutrient solution
55- Mineral Nutrition
- Soil-free culture
- Sand culture dont really control nutrients
- Hydroponics immerse roots in nutrient solution
- Rapidly deplete nutrients O2 alter pH
56- Mineral Nutrition
- Soil-free culture
- Sand culture dont really control nutrients
- Hydroponics immerse roots in nutrient solution
- Rapidly deplete nutrients O2 alter pH
- Slanted film maintains nutrients O2
57- Mineral Nutrition
- Soil-free culture
- Sand culture
- Hydroponics immerse roots in nutrient solution
- Slanted film maintains nutrients O2
- Aeroponics sprays nutrient solution on roots
58- Mineral Nutrition
- Macronutrients
- CHOPKNS