chapter 15 (part 3)

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Chapter 15 (part 3) Carbon Fixation (dark reactions)

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Chapter 15 (part 3). Carbon Fixation (dark reactions). Carbon Dioxide Fixation. A unique ability of plants, algae, etc. Melvin Calvin at Berkeley in 1945 showed that Chlorella could take up 14 CO 2 and produce 3-phosphoglycerate - PowerPoint PPT Presentation

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Page 1: Chapter 15 (part 3)

Chapter 15 (part 3)

Carbon Fixation (dark reactions)

Page 2: Chapter 15 (part 3)

Carbon Dioxide Fixation• A unique ability of plants, algae,

etc. • Melvin Calvin at Berkeley in 1945

showed that Chlorella could take up 14CO2 and produce 3-phosphoglycerate

• What was actually happening was that CO2 was combining with a 5-C sugar to form a 6-C intermediate

• This breaks down to two 3-P glycerates

Page 3: Chapter 15 (part 3)

Reductive Pentose Phosphate Cycle

6CO2+9ATP+5H20 9ADP+8Pi+6NADP++(DHAP or G3P)

Page 4: Chapter 15 (part 3)

Ribulose-1,5-Bisphosphate carboxylase/oxygenase

(rubbisco)• Probably the world's most abundant protein • In leaves greater than 50% of the soluble

protein is rubisco (stromal conc. 4 mM)• Rate Limiting step in RPP cycle• Rubisco is a slow enzyme (turnover number is

3 rxn per second)• Composed of 8 large subunits (LSU) (56,000

dal) and 8 small subunits (SSU) (14,000 dal). Active sites assocaited with LSU.

• LSU encoded by chloroplast genome. SSU encoded by nuclear genome.

Page 5: Chapter 15 (part 3)

Activation of Rubisco• Rubisco cycles between active and

inactive form.• Active form requires a bound Mg2+ ion,

light and high pH.• A none substrate CO2 molecule

participates in Mg2+ binding to active site.

• CO2 molecule binds reversibly to lysine residue forming carbamate adduct

• Activation facilitated by the enzyme rubisco activase.

• In the dark, carbamate adduct disassociates from active site. R 1,5-BP then binds tightly to active site and inhibits enzyme

Page 6: Chapter 15 (part 3)

Mg2+ plays role in binding and activating R 1,6-BP to accept

CO2

Page 7: Chapter 15 (part 3)

Rubisco Rxn Mechanisms

carboxylase

oxygenase

Page 8: Chapter 15 (part 3)

Reductive Pentose Phosphate Cycle

Page 9: Chapter 15 (part 3)

Phosphoglycerate kinase

Glyceraldehyde dehydrogenase

aldolase

F 1,6-bisphophatase

cytosol•Conversion of 3-phosphoglycerate to glucose is very similar to gluconeogenesis, but glyceraldehyde dehydrogenase uses NADPH not NADH.•Steps require consumption of ATP and NADPH.•3-phosphoglycerate could also be exported to cytsol and be used in normal gluconeogenesis.•Hexoses can then be used for energy or starch synthesis

Reduction Stage

Page 10: Chapter 15 (part 3)

Reductive Pentose Phosphate Cycle

Page 11: Chapter 15 (part 3)

Regeneration Step • Need to regenerate ribulose 1,5-

phosphate for subsequent rubisco reactions

• One of the two 3-phosphoglyserates goes towards regeneration.

• Need to generate 5 carbon sugar from 3 carbon and 6 carbon sugars.

• Most expensive part of RPP cycle.

Page 12: Chapter 15 (part 3)

Transketolases and Aldolases are used to make 5 carbon

sugars

Page 13: Chapter 15 (part 3)

Formation of 5 Carbon Sugars

Page 14: Chapter 15 (part 3)
Page 15: Chapter 15 (part 3)

F-6-P + 2 G3P + DHAP + 3 ATP 3 R-1,5-BP + 3 ADP

Page 16: Chapter 15 (part 3)

Regulation of RPP Cycle• Rubisco activity is

regulated by pH Mg2+

• Other enzymes regulated by redox state of chloroplast

• All factors are influenced by light

Page 17: Chapter 15 (part 3)

Thioredoxin• 12 kD protein• Contains Cysteine

residue that can cycle between reduced –SH and oxidized –S-S-.

• Reduced thioredoxin can activate enzymes by reducing disulfides in regulatory domains.

Page 18: Chapter 15 (part 3)

• thioreodxin ties light rxns to RPP cycle regulation

• In light Thioredoxin is reduced.

• Reduced thioredoxin activates RPP cycle enzymes.

• “dark Rxns” don’t really function well in the dark.

Page 19: Chapter 15 (part 3)
Page 20: Chapter 15 (part 3)

Oxygenase Activity of Rubisco• CO2 and O2 compete for binding at active

site.• Under normal conditions the rate of

carboxylation is 3 to 4 times the rate of oxygenation.

• Both require activation by carbamate adduct (therefore no oxygenation w/o CO2)

• Oxygenase activity produces 3-phosphoglycerate (normal C3 product) and 2-phosphoglycolate (C2 product)

Page 21: Chapter 15 (part 3)

Photorespiration (recycling of 2-

phosphoglycolate)• 4 of five carbons from

R 1,5-BP salvaged.• Loose one carbon as CO2

• Because O2 consumed and CO2 released the process is called photorespiration

• Wasteful process, loose carbon as CO2 w/o producing ATP or NADH

• Biochemist have been trying to engineer better rubisco (no luck)

Page 22: Chapter 15 (part 3)

Mechanisms to Avoid Photorespiration

• C4 Photosynthesis – Spatial separation of carbon fixation and carbon utilization

• CAM (Crassulacean Acid Metabolism) Photosynthesis – temporal separation of carbon fixation and carbon utilization

Page 23: Chapter 15 (part 3)

C4 Photosynthesis

• C4 cycle is way to pump CO2 into bundle sheath cells making concentration 20 fold higher than in mesophyll cells.

• Important in plants from hot climates.• Under elevated temperature rubisco favors oxygenase

function causing plants to undergoe photorespiration.• By fixing CO2 in Ms Cells with PEP carboxylase and

transferring it to the Bs Cells as a 4 carbon sugar can concentrate CO2 and prevent photorepsiration.

Page 24: Chapter 15 (part 3)
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CAM Photosynthesis• Found in succulent plants

(Crassulacea). • Drought tolerant plants. • Gas exchange occurs by

opening pores called stoma• What to import CO2 without

loosing water through stoma.

• CAM plants open stoma at night to fix CO2,

• They then store it until daytime when it is release it to rubisco

stoma

Page 26: Chapter 15 (part 3)