Guanine

From Wikipedia, the free encyclopedia
Jump to: navigation, search
Guanine
Guanin.svg
Guanine-3D-balls.png Guanine-3D-vdW.png
Identifiers
CAS number 73-40-5 YesY
ChemSpider 744 YesY
UNII 5Z93L87A1R YesY
DrugBank DB02377
KEGG C00242 YesY
ChEBI CHEBI:16235 YesY
ChEMBL CHEMBL219568 YesY
RTECS number MF8260000
Jmol-3D images Image 1
Properties
Molecular formula C5H5N5O
Molar mass 151.13 g/mol
Appearance White amorphous solid.
Density 2.200 g/cm3 (calculated)
Melting point 360 °C (633.15 K) decomp.
Boiling point Sublimes
Solubility in water Insoluble.
Acidity (pKa) 3.3 (amide), 9.2 (secondary), 12.3 (primary)[1]
Hazards
Main hazards Irritant.
NFPA 704
Flammability code 1: Must be pre-heated before ignition can occur. Flash point over 93 °C (200 °F). E.g., canola oil Health code 1: Exposure would cause irritation but only minor residual injury. E.g., turpentine Reactivity (yellow): no hazard code Special hazards (white): no codeNFPA 704 four-colored diamond
Flash point Non-flammable
Related compounds
Related compounds Cytosine; Adenine; Thymine; Uracil
Except where noted otherwise, data are given for materials in their standard state (at 25 °C (77 °F), 100 kPa)
 YesY (verify) (what is: YesY/N?)
Infobox references

Guanine /ˈɡwɑːnɨn/ (G, Gua) is one of the four main nucleobases found in the nucleic acids DNA and RNA, the others being adenine, cytosine, and thymine (uracil in RNA). In DNA, guanine is paired with cytosine. With the formula C5H5N5O, guanine is a derivative of purine, consisting of a fused pyrimidine-imidazole ring system with conjugated double bonds. Being unsaturated, the bicyclic molecule is planar. The guanine nucleoside is called guanosine.

Basic principles[edit]

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 two tautomeric forms, the major keto form (see figures) and rare enol form. It binds to cytosine through three hydrogen 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.

Cytonum2.png Guannum2.png

The first isolation of guanine was reported in 1844 from the excreta of sea birds,[citation needed] known as guano, which was used as a source of fertilizer. Between 1882 and 1906, Fischer determined the structure and also showed that uric acid can be converted to guanine.[2]

Guanine can be hydrolyzed with strong acid to glycine, ammonia, carbon dioxide, and carbon monoxide. Guanine is first deaminated to xanthine.[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.

Syntheses[edit]

Trace amounts of guanine form by the polymerization of ammonium cyanide (NH
4
CN
). Two experiments conducted by Levy et al. showed that heating 10 mol·L−1 NH
4
CN
at 80 °C for 24 hours gave a yield of 0.0007%, while using 0.1 mol·L−1 NH
4
CN
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 of NH
3
, CH
4
, C
2
H
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.[4]

10NH3 + 2CH4 + 4C2H6 + 2H2O → 2C5H8N5O (guanine) + 25H2

A Fischer-Tropsch synthesis can also be used to form guanine, along with adenine, uracil, and thymine. 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

Another possible abiotic route was explored by quenching a 90% N2–10%CO–H2O gas mixture high-temperature plasma.[5]

Traube's synthesis involves heating 2,4,5-triamino-1,6-dihydro-6-oxypyrimidine (as the sulfate) with formic acid for several hours. Traube purine synthesis

Other uses[edit]

The word guanine derives from the Spanish loanword guano ('bird/bat droppings'), which itself is from the Quechua word huanu or wanu, meaning 'dung.' As the Oxford English Dictionary notes, guanine is "A white amorphous substance obtained abundantly from guano, forming a constituent of the excrement of birds".[6]

In 1656 in Paris, François Jaquin extracted from scales of some fishes the so-called pearl essence, crystalline guanine forming G-quadruplexes. In the cosmetics industry, crystalline guanine is used as an additive to various products (e.g., shampoos), where it provides a pearly iridescent effect. It is also used in metallic paints and simulated pearls and plastics. It provides shimmering luster to eye shadow and nail polish. Facial treatments using the droppings, or guano, from Japanese nightingales have been used in Japan and elsewhere, reportedly because the guanine in the droppings produces a clear, "bright" skin tone[7] that users desire. Guanine crystals are rhombic platelets composed of multiple transparent layers, but they have a high index 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 are mica, faux pearl (from ground shells),[8] and aluminium and bronze particles.

Spiders and scorpions convert ammonia, as a product of protein metabolism in the cells, to guanine, as it can be excreted with minimal water loss.

Guanine is found in integumentary system of many fish such as sturgeon.[9] It is also present in the reflective deposits of the eyes of deep-sea fish and some reptiles such as crocodiles.[9]

On August 8, 2011, a report, based on NASA studies with meteorites found on Earth, was published suggesting building blocks of DNA and RNA (guanine, adenine and related organic molecules) may have been formed extraterrestrially in outer space.[10][11][12]

See also[edit]

References[edit]

  1. ^ Dawson, R.M.C., et al., Data for Biochemical Research, Oxford, Clarendon Press, 1959.
  2. ^ "Emil Fischer - Biographical". 
  3. ^ Angstadt. Purines and pyrimidines. Retrieved 2008-03-27. 
  4. ^ Levy, Matthew; Stanley L. Miller, John Oró (August 1999). "Production of Guanine from NH4CN Polymerizations". Journal of Molecular Evolution 49 (2): 165–8. doi:10.1007/PL00006539. PMID 10441668.  - quotes the Yuasa paper and cites the possibility of there being a contaminant in the reaction.
  5. ^ Miyakawa, S; Murasawa, K., Kobayashi, K., Sawaoka, AB. (December 2000). "Abiotic synthesis of guanine with high-temperature plasma". Orig Life Evol Biosph. 30 (6): 557–66. doi:10.1023/A:1026587607264. PMID 11196576. 
  6. ^ OED. "guanine" and also "guano".
  7. ^ Whitworth, Melissa (2008-10-16). "Geisha facial, the 'latest beauty secret' of Victoria Beckham, brought to the masses". Lifestyle. Telegraph. Retrieved 2008-11-20. 
  8. ^ How Pearls are Made...Faux, Fake, Imitation, Simulated or Man-made. 
  9. ^ a b Fox, D.L. (1979). Biochromy, natural coloration of living things. University of California Press. ISBN 978-0-520-03699-4
  10. ^ Callahan; Smith, K.E.; Cleaves, H.J.; Ruzica, J.; Stern, J.C.; Glavin, D.P.; House, C.H.; Dworkin, J.P. (11 August 2011). "Carbonaceous meteorites contain a wide range of extraterrestrial nucleobases". PNAS. doi:10.1073/pnas.1106493108. Retrieved 2011-08-15. 
  11. ^ Steigerwald, John (8 August 2011). "NASA Researchers: DNA Building Blocks Can Be Made in Space". NASA. Retrieved 2011-08-10. 
  12. ^ ScienceDaily Staff (9 August 2011). "DNA Building Blocks Can Be Made in Space, NASA Evidence Suggests". ScienceDaily. Retrieved 2011-08-09. 

External links[edit]