With the formula C5H5N5O, guanine is a derivative ofpurine, consisting of a fusedpyrimidine-imidazole ring system with conjugated double bonds. This unsaturated arrangement means thebicyclic molecule is planar.
Guanine, along with adenine and cytosine, is present in both DNA and RNA, whereas thymine is usually seen only in DNA, and uracil only in RNA.
Guanine has multipletautomeric forms. For both the imidazole and pyrimidine rings, the proton can reside on either of the ring nitrogens. But a single tautomeric form dominates in nucleoside or nucleotide versions of guanine.[2]
Guanine binds to cytosine through threehydrogen bonds. In cytosine, the amino group acts as the hydrogen bond donor and the C-2 carbonyl and the N-3 amine as the hydrogen-bond acceptors. Guanine has the C-6 carbonyl group that acts as the hydrogen bond acceptor, while a group at N-1 and the amino group at C-2 act as the hydrogen bond donors.[citation needed]
Cytosine and guanine with the direction of hydrogen bonding indicated (arrow points positive to negative charge)
Guanine can behydrolyzed with strong acid toglycine,ammonia,carbon dioxide, andcarbon monoxide. First, guanine getsdeaminated to becomexanthine.[3] Guanine oxidizes more readily than adenine, the other purine-derivative base in DNA. Its high melting point of 350 °C reflects the intermolecular hydrogen bonding between the oxo and amino groups in the molecules in the crystal. Because of this intermolecular bonding, guanine is relatively insoluble in water, but it is soluble in dilute acids and bases.
The first isolation of guanine was reported in 1844 by the German chemistJulius Bodo Unger [de] (1819–1885), who obtained it as a mineral formed from the excreta of sea birds, which is known asguano and which was used as a source of fertilizer; guanine was named in 1846.[4] Between 1882 and 1906,Emil Fischer determined the structure and also showed thaturic acid can be converted to guanine.[5]
AFischer–Tropsch synthesis can be used to form guanine, along withadenine,uracil, andthymine. Heating an equimolar gas mixture of CO, H2, and NH3 to 700 °C for 15 to 24 minutes, followed by quick cooling and then sustained reheating to 100 to 200 °C for 16 to 44 hours with an alumina catalyst, yielded guanine and uracil:
10CO + H2 + 10NH3 → 2C5H8N5O (guanine) + 8H2O
Trace amounts of guanine form by thepolymerization ofammonium cyanide (NH 4CN). Two experiments conducted by Levy et al. showed that heating 10 mol·L−1NH 4CN at 80 °C for 24 hours gave a yield of 0.0007%, while using 0.1 mol·L−1NH 4CN frozen at −20 °C for 25 years gave a 0.0035% yield. These results indicate guanine could arise in frozen regions of the primitive earth. In 1984, Yuasa reported a 0.00017% yield of guanine after the electrical discharge ofNH 3,CH 4,C 2H 6, and 50 mL of water, followed by a subsequent acid hydrolysis. However, it is unknown whether the presence of guanine was not simply a resultant contaminant of the reaction.[6]
The word guanine derives from the Spanish loanwordguano ('bird/bat droppings'), which itself is from theQuechua wordwanu, meaning 'dung'. As theOxford English Dictionary notes, guanine is "A white amorphous substance obtained abundantly from guano, forming a constituent of the excrement of birds".[9]
In 1656 in Paris, a Mr. Jaquin extracted from the scales of the fishAlburnus alburnus so-called "pearl essence",[10] which is crystalline guanine.[11] In the cosmetics industry, crystalline guanine is used as an additive to various products (e.g., shampoos), where it provides a pearlyiridescent effect. It is also used in metallic paints and simulated pearls and plastics. It provides shimmering luster to eye shadow andnail polish. Facial treatments using the droppings, or guano, from Japanese nightingales have been used in Japan and elsewhere, because the guanine in thedroppings makes the skin look paler.[12] Guanine crystals are rhombic platelets composed of multiple transparent layers, but they have a highindex of refraction that partially reflects and transmits light from layer to layer, thus producing a pearly luster. It can be applied by spray, painting, or dipping. It may irritate the eyes. Its alternatives aremica, faux pearl (from ground shells),[13] andaluminium andbronze particles.
Guanine has a very wide variety of biological uses that include a range of functions ranging in both complexity and versatility. These include camouflage, display, and vision among other purposes.[14]
Spiders, scorpions, and some amphibians convert ammonia, as a product of protein metabolism in the cells, to guanine, as it can be excreted with minimal water loss.[14]
On 8 August 2011, a report, based onNASA studies withmeteorites found on Earth, was published suggesting building blocks of DNA and RNA (guanine,adenine and relatedorganic molecules) may have been formed extra-terrestrially in outer space.[16][17][18]
B. Unger (1846)"Bemerkungen zu obiger Notiz" (Comments on the above notice),Annalen der Chemie und Pharmacie,58 : 18-20. From page 20:" ... desshalb möchte ich den NamenGuanin vorschlagen, welcher an seine Herkunft erinnert." ( ... therefore I would like to suggest the nameguanine, which is reminiscent of its origin.)
^Levy, Matthew; Stanley L. Miller; John Oró (August 1999). "Production of Guanine from NH4CN Polymerizations".Journal of Molecular Evolution.49 (2):165–8.Bibcode:1999JMolE..49..165L.doi:10.1007/PL00006539.PMID10441668.S2CID32194418. - quotes the Yuasa paper and cites the possibility of there being a contaminant in the reaction.
^Traube, Wilhelm; Schottlander, Friedrich; Goslich, Carl; Peter, Robert; Meyer, F. A.; Schlüter, Heinrich; Steinbach, Wilhelm; Bredow, Karl (1923). "Über Ortho-diamino-pyrimidine und ihre Überführung in Purine" [o-Diaminopyrimidines and their transformation into purines].Justus Liebigs Annalen der Chemie.432: 266-96.doi:10.1002/jlac.19234320111.{{cite journal}}: CS1 maint: multiple names: authors list (link)
^Johann Rudolf von Wagner, Ferdinand Fischer, and L. Gautier,Traité de chimie industrielle (Treatise on industrial chemistry), 4th ed., (Paris, France: Masson & Co., 1903), vol. 2,pp. 64–65.
