OMICRON-QUINONES FORMED IN PLANT EXTRACTS - THEIR REACTIONS WITH AMINO ACIDS AND PEPTIDES
OMICRON-QUINONES FORMED IN PLANT EXTRACTS - THEIR REACTIONS WITH AMINO ACIDS AND PEPTIDES
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DOI:
10.1042/bj1120609
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发表时间:
1969-01-01
影响因子:
4.1
通讯作者:
PIERPOINT, WS
中科院分区:
文献类型:
--
作者:
PIERPOINT, WS
1. The reactions of amino acids and peptides with theo-quinones produced by the enzymic oxidation of chlorogenic acid and caffeic acid have been studied manometrically and spectrophotometrically. 2. Amino acids, except lysine and cysteine, react primarily through their α-amino groups to give red or brown products. These reactions, which compete with the polymerization of the quinones, are followed by secondary reactions that may absorb oxygen and give products with other colours. 3. The ∈-amino group of lysine reacts with theo-quinones in a similar way. The thiol group of cysteine reacts with the quinones, without absorbing oxygen, giving colourless products. 4. Peptides containing cysteine react with theo-quinones through their thiol group. 5. Other peptides, such as glycyl-leucine and leucylglycine, react primarily through their α-amino group and the overall reaction resembles that of theN-terminal amino acid except that it is quicker. 6. With some peptides, the secondary reactions differ from those that occur between theo-quinones and theN-terminal amino acids. The colours produced from carnosine resemble those produced from histidine rather than those from β-alanine, and the reactions of prolylalanine witho-quinones are more complex than those of proline.