Phosphate
Biologic activity of cyclic and caged phosphates: a review.
Wikipedia:
A phosphate (PO3−4) is an inorganic chemical and a salt of phosphoric acid. In organic chemistry, a phosphate, or organophosphate, is an ester of phosphoric acid. Of the various phosphoric acids and phosphates, organic phosphates are important in biochemistry and biogeochemistry (ecology), and inorganic phosphates are mined to obtain phosphorus for use in agriculture and industry.[2] At elevated temperatures in the solid state, phosphates can condense to form pyrophosphates.
In biology, adding phosphates to—and removing them from—proteins in cells are both pivotal in the regulation of metabolic processes. Referred to as phosphorylation and dephosphorylation, respectively, they are important ways that energy is stored and released in living systems.
Chemical properties
This is the structural formula of the phosphoric acid functional group as found in weakly acidic aqueous solution. In more basic aqueous solutions, the group donates the two hydrogen atoms and ionizes as a phosphate group with a negative charge of 2.
The phosphate ion is a polyatomic ion with the empirical formula PO3−
4 and a molar mass of 94.97 g/mol. It consists of one central phosphorus atom surrounded by four oxygen atoms in a tetrahedral arrangement. The phosphate ion carries a −3 formal charge and is the conjugate base of the hydrogen phosphate ion, HPO2−4, which is the conjugate base of H2PO−4, the dihydrogen phosphate ion, which in turn is the conjugate base of H3PO-4, phosphoric acid. A phosphate salt forms when a positively charged ion attaches to the negatively charged oxygen atoms of the ion, forming an ionic compound. Many phosphates are not soluble in water at standard temperature and pressure. The sodium, potassium, rubidium, caesium, and ammonium phosphates are all water-soluble. Most other phosphates are only slightly soluble or are insoluble in water. As a rule, the hydrogen and dihydrogen phosphates are slightly more soluble than the corresponding phosphates. The pyrophosphates are mostly water-soluble.
Aqueous phosphate exists in four forms. In strongly basic conditions, the phosphate ion (PO3−4) predominates, whereas in weakly basic conditions, the hydrogen phosphate ion (HPO2−4) is prevalent. In weakly acidic conditions, the dihydrogen phosphate ion (H2PO−4) is most common. In strongly acidic conditions, trihydrogen phosphate (H
3PO4) is the main form.
H
3PO
4Phosphoric acid
H
2PO−
4Dihydrogen phosphate
HPO2−
4Hydrogen phosphate
PO3−
4Phosphate
However, phosphates are most commonly found in the form of adenosine phosphates (AMP, ADP, and ATP) and in DNA and RNA, and can be released by the hydrolysis of ATP or ADP. Similar reactions exist for the other nucleoside diphosphates and triphosphates. Phosphoanhydride bonds in ADP and ATP, or other nucleoside diphosphates and triphosphates, contain high amounts of energy which give them their vital role in all living organisms. They are generally referred to as high-energy phosphate, as are the phosphagens in muscle tissue. Compounds such as substituted phosphines have uses in organic chemistry, but do not seem to have any natural counterparts.
The addition and removal of phosphate from proteins in all cells is a pivotal strategy in the regulation of metabolic processes. Phosphorylation and dephosphorylation are important ways that energy is stored and released in living systems. Cells use ATP in this manner.
Reference ranges for blood tests, showing 'inorganic phosphorus' in purple at right, being almost identical to the molar concentration of phosphate
Phosphate is useful in animal cells as a buffering agent. Phosphate salts that are commonly used for preparing buffer solutions at cell pHs include Na2HPO4, NaH2PO4, and the corresponding potassium salts.
An important occurrence of phosphates in biological systems is as the structural material of bone and teeth. These structures are made of crystalline calcium phosphate in the form of hydroxyapatite. The hard dense enamel of mammalian teeth consists of fluoroapatite, a hydroxy calcium phosphate where some of the hydroxyl groups have been replaced by fluoride ions.
Plants take up phosphorus through several pathways: the arbuscular mycorrhizal pathway and the direct uptake pathway.
Ecology

Sea surface phosphate from the World Ocean Atlas

Relationship of phosphate to nitrate uptake for photosynthesis in various regions of the ocean. Note that nitrate is more often limiting than phosphate. See the Redfield ratio.
In ecological terms, because of its important role in biological systems, phosphate is a highly sought after resource. Once used, it is often a limiting nutrient in environments, and its availability may govern the rate of growth of organisms. This is generally true of freshwater environments, whereas nitrogen is more often the limiting nutrient in marine (seawater) environments. Addition of high levels of phosphate to environments and to micro-environments in which it is typically rare can have significant ecological consequences. For example, blooms in the populations of some organisms at the expense of others, and the collapse of populations deprived of resources such as oxygen (see eutrophication) can occur. In the context of pollution, phosphates are one component of total dissolved solids, a major indicator of water quality, but not all phosphorus is in a molecular form which algae can break down and consume.[13]
Calcium hydroxyapatite and calcite precipitates can be found around bacteria in alluvial topsoil.[14] As clay minerals promote biomineralization, the presence of bacteria and clay minerals resulted in calcium hydroxyapatite and calcite precipitates.[14]
Phosphate deposits can contain significant amounts of naturally occurring heavy metals. Mining operations processing phosphate rock can leave tailings piles containing elevated levels of cadmium, lead, nickel, copper, chromium, and uranium. Unless carefully managed, these waste products can leach heavy metals into groundwater or nearby estuaries. Uptake of these substances by plants and marine life can lead to concentration of toxic heavy metals in food products.[15]






