ATP (adenosine triphosphate) is a nucleotide (Chapter 11) bearing three phosphates in a row; the two outer bonds are phosphoanhydride bonds whose hydrolysis, , has and, at the concentrations of a cell, . ATP is the cell’s energy currency: catabolism makes it (Chapter 15), and biosynthesis, transport and movement spend it. An uphill reaction is made to go by coupling it to ATP hydrolysis through a shared intermediate, so that the sum of the two is negative.
Examples
Example 8.17 (Why ATP hydrolysis releases so much)
Three reasons: the four negative charges of ATP’s phosphates repel one another and are relieved by cleavage; the products and are better stabilised by resonance and by hydration than the anhydride; and the cell keeps ATP a thousand times above its equilibrium with ADP and phosphate. The last is the largest term: with ATP at , ADP , , .
Example 8.18 (Coupling)
Glucose glucose-6-phosphate has : at equilibrium almost no glucose would be phosphorylated. Hexokinase instead transfers the phosphate straight from ATP: glucose ATP glucose-6-phosphate ADP, , equilibrium constant , reaction essentially complete. The phosphate never appears free: the two reactions are one.
Example 8.14 (The cell’s inventory)
Of a bacterium’s dry mass, proteins are , RNA , DNA , lipids , polysaccharides , small molecules and ions the rest. By number of molecules the picture inverts: a thousand kinds of small metabolite and ion, at concentrations from nanomolar to a tenth of a mole per litre, make up most of the molecules that are not water. Potassium is at , glutamate , ATP , a transcription factor at a few molecules per cell.