Abstract
THE dehydroxylation of 3,4-dihydroxyphenylacetic acid (homoprotocatechuic acid) to m-hydroxyphenylacetic acid in the animal body was first reported by Booth et al.1, and was confirmed by Scheline et al.2, with 3,4-dihydroxyphenylacetic acid labelled with carbon-14. A claim has been made recently3 that noradrenaline is converted to m-hydroxyphenylacetic acid in guinea pigs; such a conversion involves not only dehydroxylation in the aromatic nucleus but also in the aliphatic side-chain of noradrenaline.
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References
Booth, A. N., Murray, C. W., Jones, F. T., and DeEds, F., J. Biol. Chem., 223, 251 (1956).
Scheline, R. R., Williams, R. T., and Wit, J. G., Nature, 188, 849 (1960).
Smith, A. A., Biochim. Biophys. Acta, 69, 203 (1963).
Booth, A. N., Emerson, O. H., Jones, F. T., and DeEds, F., J. Biol. Chem., 229, 51 (1957).
Shaw, K. N. F., Gutenstein, M., and Jepson, J. B., Proc. Fifth Intern. Cong. Biochem., Moscow, 369 (1961).
Benjafield, J. G., Lancet, ii, 782 (1962).
Scott, T. W., Ward, P. F. V., and Dawson, R. M. C., Biochem. J., 87, 3P (1963).
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BOOTH, A., WILLIAMS, R. Dehydroxylation of Caffeic Acid by Rat and Rabbit Cæcal Contents and Sheep Rumen Liquor. Nature 198, 684–685 (1963). https://doi.org/10.1038/198684a0
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DOI: https://doi.org/10.1038/198684a0
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