Ribulose 1,5-bisphosphate

RuBP was originally discovered by Andrew Benson in 1951 while working in the lab of Melvin Calvin at UC Berkeley. Calvin, who had been away from the lab at the time of discovery and was not listed as a co-author, controversially removed the full molecule name from the title of the initial paper, identifying it solely as "ribulose". At the time, the molecule was known as ribulose diphosphate (RDP or RuDP) but the prefix di- was changed to bis- to emphasize the nonadjacency of the two phosphate groups. ==Role in photosynthesis and the Calvin-Benson Cycle==

The enzyme ribulose-1,5-bisphosphate carboxylase-oxygenase (rubisco) catalyzes the reaction between RuBP and carbon dioxide. The product is the highly unstable six-carbon intermediate known as 3-keto-2-carboxyarabinitol 1,5-bisphosphate, or 2'-carboxy-3-keto-D-arabinitol 1,5-bisphosphate (CKABP). This six-carbon β-ketoacid intermediate hydrates into another six-carbon intermediate in the form of a gem-diol. This intermediate then cleaves into two molecules of 3-phosphoglycerate (3-PGA) which is used in a number of metabolic pathways and is converted into glucose. In the Calvin-Benson cycle, RuBP is a product of the phosphorylation of ribulose-5-phosphate (produced by glyceraldehyde 3-phosphate) by ATP. Interactions with rubisco RuBP acts as an enzyme inhibitor for the enzyme rubisco, which regulates the net activity of carbon fixation. When RuBP is bound to an active site of rubisco, the ability to activate via carbamylation with and is blocked. The functionality of rubisco activase involves removing RuBP and other inhibitory bonded molecules to re-enable carbamylation on the active site. ==Role in photorespiration==

Rubisco also catalyzes RuBP with oxygen () in an interaction called photorespiration, a process that is more prevalent at high temperatures. During photorespiration RuBP combines with to become 3-PGA and phosphoglycolic acid. Like the Calvin-Benson Cycle, the photorespiratory pathway has been noted for its enzymatic inefficiency Due to enhanced RuBP carboxylation and decreased rubisco oxygenation stemming from the increased concentration of in the bundle sheath, rates of photorespiration are decreased in plants. ==Measurement==

RuBP can be measured isotopically via the conversion of {{chem2|^{14}CO2}} and RuBP into glyceraldehyde 3-phosphate. G3P can then be measured using an enzymatic optical assay. Given the abundance of RuBP in biological samples, an added difficulty is distinguishing particular reservoirs of the substrate, such as the RuBP internal to a chloroplast vs external. One approach to resolving this is by subtractive inference, or measuring the total RuBP of a system, removing a reservoir (e.g. by centrifugation), re-measuring the total RuBP, and using the difference to infer the concentration in the given repository. ==See also==