Chemiosmosis is the movement of ions across a semipermeable membrane, down their electrochemical gradient. An example of this would be the generation of adenosine triphosphate (ATP) by the movement of hydrogen ions across a membrane during cellular respiration or photosynthesis.
Hydrogen ions, or protons, will diffuse from an area of high proton concentration to an area of lower proton concentration, and an electrochemical concentration gradient of protons across a membrane can be harnessed to make ATP. This process is related to osmosis, the diffusion of water across a membrane, which is why it is called "chemiosmosis".
ATP synthase is the enzyme that makes ATP by chemiosmosis. It allows protons to pass through the membrane and uses the free energy difference to phosphorylate adenosine diphosphate (ADP), making ATP. The generation of ATP by chemiosmosis occurs in mitochondria and chloroplasts, as well as in most bacteria and oarchaea, an electron transport chain pumps H+ ions in the thylakoid spaces through thylakoid membranes. The energy from the electron movement through electron transport chains cross through ATP synthase which allows the proton to pass through them and use this free energy difference to photophosphorylate ADP making ATP.
The chemiosmotic theory
Peter D. Mitchell proposed the chemiosmotic hypothesis in 1961. The theory suggests essentially that most adenosine triphosphate (ATP) synthesis in respiring cells comes from the electrochemical gradient across the inner membranes of mitochondria by using the energy of NADH and FADH2 formed from the breaking down of energy-rich molecules such as glucose.
Molecules such as glucose are metabolized to produce acetyl CoA as an energy-rich intermediate. The oxidation of acetyl coenzyme A (acetyl-CoA) in the mitochondrial matrix is coupled to the reduction of a carrier molecule such as nicotinamide adenine dinucleotide (NAD) and flavin adenine dinucleotide (FAD). The carriers pass electrons to the electron transport chain (ETC) in the inner mitochondrial membrane, which in turn pass them to other proteins in the ETC. The energy available in the electrons is used to pump protons from the matrix across the inner mitochondrial membrane, storing energy in the form of a transmembrane electrochemical gradient. The protons move back across the inner membrane through the enzyme ATP synthase. The flow of protons back into the matrix of the mitochondrion via ATP synthase provides enough energy for ADP to combine with inorganic phosphate to form ATP. The electrons and protons at the last pump in the ETC are taken up by oxygen to form water.
This was a radical proposal at the time, and was not well accepted. The prevailing view was that the energy of electron transfer was stored as a stable high potential intermediate, a chemically more conservative concept. The problem with the older paradigm is that no high energy intermediate was ever found, and the evidence for proton pumping by the complexes of the electron transfer chain grew too great to be ignored. Eventually the weight of evidence began to favor the chemiosmotic hypothesis, and in 1978, Peter Mitchell was awarded the Nobel Prize in Chemistry.
The proton-motive force
The movement of ions across the membrane depends on a combination of two factors:
- Diffusion force caused by a concentration gradient - all particles tend to diffuse from higher concentration to lower.
- Electrostatic force caused by electrical potential gradient - cations like protons H+ tend to diffuse down the electrical potential, anions in the opposite direction.
These two gradients taken together can be expressed as an electrochemical gradient.
Lipid bilayers of biological membranes, however, are barriers for ions. This is why energy can be stored as a combination of these two gradients across the membrane. Only special membrane proteins like ion channels can sometimes allow ions to move across the membrane (see also: Membrane transport). In chemiosmotic theory transmembrane ATP synthases are very important. They convert energy of spontaneous flow of protons through them into chemical energy of ATP bonds.
Hence researchers created the term proton-motive force (PMF), derived from the electrochemical gradient mentioned earlier. It can be described as the measure of the potential energy stored as a combination of proton and voltage (electrical potential) gradients across a membrane. The electrical gradient is a consequence of the charge separation across the membrane (when the protons H+ move without a counterion, such as chloride Cl−).
In most cases the proton-motive force is generated by an electron transport chain which acts as a proton pump, using the energy of electrons from an electron carrier (Gibbs free energy of redox reactions) to pump protons (hydrogen ions) out across the membrane, separating the charge across the membrane. In mitochondria, energy released by the electron transport chain is used to move protons from the mitochondrial matrix to the mitochondrial intermembrane space. Moving the protons out of the mitochondrion creates a lower concentration of positively charged protons inside it, resulting in a slight negative charge on the inside of the membrane. The electrical potential gradient is about -170 mV . These gradients - charge difference and the proton concentration difference both create a combined electrochemical gradient across the membrane, often expressed as the proton-motive force (PMF). In mitochondria, the PMF is almost entirely made up of the electrical component but in chloroplasts the PMF is made up mostly of the pH gradient because the charge of protons H+ is neutralized by the movement of Cl− and other anions. In either case, the PMF needs to be about 50 kJ/mol for the ATP synthase to be able to make ATP.
ΔG is the Gibbs free energy change (kJ·mol−1) during transfer of 1 mol of cations Xm+ from the phase A to B down the electrical potential, Δψ is the electrical potential difference (mV) between phases P and N (A and B), [Xm+]A and [Xm+]B are our cation concentrations on opposite sides of the membrane, F is the Faraday constant, R gas constant. The Gibbs free energy change here is expressed frequently also as electrochemical ion gradient Δμm+
In case of the electrochemical proton gradient the equation can be simplified to:
(pH in phase P - pH in phase N)
Mitchell defined the proton-motive force (PMF) as
ΔμH+ = 1 kJ·mol corresponds to Δp = 10.4 mV. At 25 °C (298K) this equation takes the form:
The energy expressed here as Gibbs free energy, electrochemical proton gradient, or proton-motive force (PMF), is a combination of two gradients across the membrane:
- concentration gradient expressed here as ΔpH
- electrical gradient Δψ
When a system reaches equilibrium, ΔG (Δμm+, Δp) = 0, but it does not mean that concentrations are equal on both sides of the membrane. The ions' electrical gradient, in addition to the concentration difference, affects spontaneous movement across the membrane.
The Gibbs free energy of ATP synthesis (ΔGp):
ADP + Pi → ATP
is also called phosphorylation potential. The H+ / ATP ratio value can be calculated by comparison of Δp and ΔGp, for example in case of the mitochondrion:
H+ / ATP = ΔGp / (Δp / 10.4 kJ·mol−1/mV) = 66 kJ·mol−1 / (200 mV / 10.4 kJ·mol−1/mV) = 66 / 19.2 = 3.4
For mitochondria, ΔGp takes here into account 1 H+ consumed to transfer a phosphate molecule (Pi) across the inner membrane into the matrix by the phosphate carrier (PiC). Otherwise it would be lower. In E. coli the H+ / ATP ratio is difficult to determine.
The energy of more than 3 H+ is required to generate the chemical energy to convert a single molecule of ATP. This value is slightly lower than the theoretical number of 4 H+ involved in oxidative phosphorylation of one ADP molecule to ATP during cellular respiration (3 H+ flowing through the ATP synthase / 1 ATP + 1 leaking from the cytoplasm through the phosphate carrier PiC). 
The complete breakdown of glucose in the presence of oxygen is called cellular respiration. The last steps of this process occur in mitochondria. The reduced molecules NADH and FADH2 are generated by the Krebs cycle, glycolysis, and pyruvate processing. These molecules pass electrons to an electron transport chain, which uses the energy released to create a proton gradient across the inner mitochondrial membrane. ATP synthase then uses the energy stored in this gradient to make ATP. This process is called oxidative phosphorylation because oxygen is the final electron acceptor and the energy released by reducing oxygen to water is used to phosphorylate ADP and generate ATP.
The light reactions of photosynthesis generate energy by chemiosmosis. The photons in sunlight are received by the antenna complex of Photosystem II, which excites a pair of electrons to a higher energy level. These electrons travel down an electron transport chain, causing H+ to be actively pumped across the thylakoid membrane into the inter-thylakoid space. These H+ are then transported down their concentration gradient through an enzyme called ATP-synthase, creating ATP by phosphorylation of ADP to ATP. The electrons from the initial light reaction reach Photosystem I, then are raised to a higher energy level by light energy and then received by an electron acceptor and reduce NADP+ to NADPH+H. The electrons from Photosystem II get replaced by the splitting of water, called "photolysis." Two water molecules must be split in order to gain four electrons, as well as an oxygen molecule, the oxygen eudicots require for survival.
Bacteria and archaea also can use chemiosmosis to generate ATP. Cyanobacteria, green sulfur bacteria, and purple bacteria create energy by a process called photophosphorylation. These bacteria use the energy of light to create a proton gradient using a photosynthetic electron transport chain. Non-photosynthetic bacteria such as E. coli also contain ATP synthase. In fact, mitochondria and chloroplasts are believed to have been formed when early eukaryotic cells ingested bacteria that could transfer energy using chemiosmosis. This is called the endosymbiotic theory.
Chemiosmotic phosphorylation is the third pathway that produces ATP from inorganic phosphate and an ADP molecule. This process is part of oxidative phosphorylation.
- Electrochemical gradient
- Cellular respiration
- Citric acid cycle
- Oxidative phosphorylation
- Peter Mitchell (1961). "Coupling of phosphorylation to electron and hydrogen transfer by a chemi-osmotic type of mechanism". Nature. 191 (4784): 144–148. Bibcode:1961Natur.191..144M. doi:10.1038/191144a0. PMID 13771349.
- Alberts, Bruce; Alexander Johnson; Julian Lewis; Martin Raff; Keith Roberts; Peter Walter (2002). "Proton Gradients Produce Most of the Cell's ATP". Molecular Biology of the Cell. Garland. ISBN 0-8153-4072-9.
- The Nobel Prize in Chemistry 1978.
- Cooper, Geoffrey M. (2000). "Figure 10.22: Electron transport and ATP synthesis during photosynthesis". The Cell: A Molecular Approach (2nd ed.). Sinauer Associates, Inc. ISBN 0-87893-119-8.
- Alberts, Bruce; Alexander Johnson; Julian Lewis; Martin Raff; Keith Roberts; Peter Walter (2002). "Figure 14-32: The importance of H+-driven transport in bacteria". Molecular Biology of the Cell. Garland. ISBN 0-8153-4072-9.
- Nicholls D. G.; Ferguson S. J. (1992). Bioenergetics 2 (2nd ed.). San Diego: Academic Press. ISBN 9780125181242.
- Stryer, Lubert (1995). Biochemistry (fourth ed.). New York - Basingstoke: W. H. Freeman and Company. ISBN 978-0716720096.
- Biochemistry textbook reference, from the NCBI bookshelf – Jeremy M. Berg; John L. Tymoczko; Lubert Stryer (eds.). "18.4. A Proton Gradient Powers the Synthesis of ATP". Biochemistry (5th ed.). W. H. Freeman.
- Technical reference relating one set of experiments aiming to test some tenets of the chemiosmotic theory – Seiji Ogawa & Tso Ming Lee (1984). "The Relation between the Internal Phosphorylation Potential and the Proton Motive Force in Mitochondria during ATP Synthesis and Hydrolysis". Journal of Biological Chemistry. 259 (16): 10004–10011. PMID 6469951.