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17 O and 14 N spectroscopy of 17 O‐labeled nucleic acid bases
Author(s) -
Burgar Matija I.,
Dhawan Devindra,
Fiat Daniel
Publication year - 1982
Publication title -
organic magnetic resonance
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.483
H-Index - 72
eISSN - 1097-458X
pISSN - 0030-4921
DOI - 10.1002/mrc.1270200315
Subject(s) - thymine , cytosine , chemistry , uracil , oxygen , aqueous solution , nucleic acid , nucleobase , hydrogen bond , nuclear magnetic resonance spectroscopy , chemical shift , hydrogen , photochemistry , molecule , stereochemistry , organic chemistry , dna , biochemistry
Oxygen‐17 and nitrogen‐14 nuclear magnetic resonance techniques have been utilized in studying liquid‐state hydrogen bonding interactions between nucleic acid bases and between the bases and solvent. The bases uracil and thymine have been labeled with 17 O at positions 2 and 4, cytosine at position 2 and thymine riboside at position 4. The 17 O chemical shift was found to be a sensitive structural probe and to provide information concerning the resonance forms that contribute to the total wave function. The chemical shift of the oxygen of thymine and uracil at position 2 was detected at a higher field than that of oxygen at position 4, presumably owing to an increased contribution of single bonded‐oxygen valence bond structures at position 2. The 17 O and 14 N chemical shifts of cytosine were found to be strongly pH dependent, and the results have been interpreted in terms of predominant cytosine resonance structures contributing to the aqueous cation and anion. The 17 O line width of cytosine in aqueous solution indicates the presence of hydrogen bonded dimers between neutral and cationic forms.