Adenine
(A, Ade) is a nucleobase associated with biochemistry. As a purine derivative, it has several essential roles in biological processes. This article explores the structure, synthesis, function, and history of adenine.
Overview
Adenine is an integral part of cellular respiration, specifically in the formation of the energy-rich molecule adenosine triphosphate (ATP). Moreover, it acts as a constituent of the cofactors nicotinamide adenine dinucleotide (NAD) and flavin adenine dinucleotide (FAD). Furthermore, it is pivotal in protein synthesis, being a primary component of both DNA and RNA. In DNA, adenine pairs with thymine, whereas in RNA, it complements uracil.<ref>Genetics Home Reference - National Institutes of Health</ref>
Structure
Several tautomers of adenine exist, which can rapidly interconvert, leading them often to be treated as equivalent. Notably, under specific isolated conditions, such as in an inert gas matrix or in the gas phase, the 9H-adenine tautomer predominantly exists.<ref>Plützer, Chr., Kleinermanns, K.,
Tautomers and electronic states of jet-cooled adenine, Phys.Chem.Chem.Phys., 2002, Vol. 4(Issue: 20), pp. 4877–4882, DOI: 10.1039/b204595h,</ref><ref>M. J. Nowak et al., Infrared spectra studies on purine, adenine, and 2-chloroadenine, Spectrochimica Acta Part A: Molecular Spectroscopy, 1994, Vol. 50, pp. 1081–1094, DOI: 10.1016/0584-8539(94)80030-8,</ref>
Biosynthesis
The metabolic pathway of Purine metabolism oversees the formation of both adenine and guanine. These nucleobases trace back to the nucleotide inosine monophosphate (IMP). This nucleotide is synthesized on a pre-existing ribose phosphate backbone. The pathway incorporates atoms from amino acids like glycine, glutamine, and aspartic acid, and it also fuses with the enzyme tetrahydrofolate.
Function
Among the purine nucleobases, adenine and guanine are crucial for constructing the nucleic acids. In DNA structures, adenine's role is to bind with thymine through two hydrogen bonds, ensuring stability. For protein synthesis in RNA, adenine pairs with uracil.
File:Base pair AT.svg File:Base pair AU.svg File:Base pair AD.svg File:Base pair APsi.svg
- Pairs: A-T (DNA) | A-U (RNA) | A-D (RNA) | A-Ψ (RNA)
When attached to ribose, adenine forms the nucleoside known as adenosine. When linked to deoxyribose, it produces deoxyadenosine. The addition of three phosphate groups to adenosine results in the formation of adenosine triphosphate (ATP). This nucleotide is vital in cellular metabolism, facilitating energy transfer between chemical reactions.
History
Historically, adenine was referred to as Vitamin B4 in older scientific literature.<ref>Vera Reader,
The assay of vitamin B4, Biochem J., 1930, Vol. 24(Issue: 6), pp. 1827–31,</ref> Although it is no longer classified as a true vitamin or part of the Vitamin B complex, it does associate with the B vitamins, niacin and riboflavin. These vitamins combine with adenine to create essential cofactors nicotinamide adenine dinucleotide (NAD) and flavin adenine dinucleotide (FAD).
Adenine was named by Albrecht Kossel in 1885, inspired by the pancreas (in Greek, "aden") from which his sample was derived.<ref>Online Etymology Dictionary by Douglas Harper</ref> Experiments in 1961 revealed that adenine could be synthesized from the polymerization of ammonia with five hydrogen cyanide molecules.<ref>Oró J, Kimball AP,
Synthesis of adenine from hydrogen cyanide, Archives of biochemistry and biophysics, 1961, Vol. 94, pp. 217–27,</ref> The implications of these findings on the origin of life on Earth are still debated.<ref>Shapiro, Robert, The prebiotic role of adenine, Origins of Life and Evolution of Biospheres, 1995, DOI: 10.1007/BF01581575,</ref>
In 2011, studies on meteorites suggested that adenine might have extraterrestrial origins, indicating that the building blocks of DNA and RNA could form in outer space.<ref>
Carbonaceous meteorites contain a wide range of extraterrestrial nucleobases(link). {{{website}}}. PNAS.
</ref>
References
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External links
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