Cellular Energy


Chloroplast-cyanobacterium comparison

Chloroplasts arose through a second endosymbiotic event in plants and various protists. These light harvesting organelles share similarity in structure and genome to photoautotrophic cynaboacteria.

Light Harvesting

Thylakoid membrane 3

The thylakoid membranes of chloroplasts and cyanobacteria provide additional surface area for energy capture of light to occur. The light-dependent reactions in chlorplasts utilize two protein complexes referred to as Photosystem I (PSI) and Photosystem II (PSII)located on the thylakoid membranes. At the center of each photosystem complexes are photopigments optimized to absorb specific wavelengths of light. When light is absorbed in a photosystem, an electron is excited and transferred to the electron transport chain. In PSII, the electron is regenerated by splitting of two water molecules into 4H+ + 4e + O2. As the electrons move through the ETC, protons are pumped into the thylakoid space. The ETC leads to the reduction of a high energy electron carrier NADP+ to NADPH. Since this pathway uses consumes water in a chemical reaction, the apparent loss of water in the thylakoid space is referred to as chemiosmosis.

PSI is also known as the cyclic pathway since the excited electron runs through a closed circuit of the ETC to regenerate the lost electron. This closed circuit also generates a proton gradient through powering of a proton pump but does not lead to the reduction of NADPH. As with the ETC-powered proton pump in mitochondria, the proton gradient is used to power ATP-synthase in producing ATP molecules.

Light Independent Reactions


The light independent reactions are also known as the dark reactions or Calvin Cycle and utilize the ATP and NADPH from the light-dependent reactions to fix gaseous CO2 into carbohydrate backbones. Photosynthesis is often simplified into 6CO2 + 6H2O + light –> C6H12O6 + 6O2 . However, the true product is 3-phosphoglycerate that can be used to generate longer carbohydrates like glucose. The starting point of carbon fixation is the carbohydrate Ribulose 1,5-bisphosphate. The enzyme Ribulose Bisphospate Carboxylase (RuBisCO)  captures a CO2 molecule onto Ribulose 1,5-bisphosphate to generate 2 molecules of 3-phosphoglycerate which can enter the process of gluconeogenesis to generate glucose. ATP from the light reactions can then facilitate the conversion of 3-phosphoglycerate to 1,3 bisphosphoglycerate which can be reduced by NADPH to glyceraldehyde-3-phosphate (G3P). G3P can then be used to regenerate  Ribulose 1,5-bisphosphate.

Calvin cycle step 1
1: Carbon fixation by RuBisCO
Calvin cycle step 2 (doubled)
2: Reduction by NADPH
Calvin cycle step 3
3: Ribulose ,5-bisphosphate regeneration

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