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  • 标题:STUDIES ON THE INTERMEDIATES IN THE BIO-SYNTHETIC PATHWAY OF RIBOFLAVIN
  • 本地全文:下载
  • 作者:Hisateru MITSUDA ; Kenji NAKAJIMA ; Yukiko YAMADA
  • 期刊名称:Journal of Nutritional Science and Vitaminology
  • 印刷版ISSN:0301-4800
  • 电子版ISSN:1881-7742
  • 出版年度:1977
  • 卷号:23
  • 期号:4
  • 页码:305-318
  • DOI:10.3177/jnsv.23.305
  • 出版社:Center for Academic Publications Japan
  • 摘要:Effects of sugars and carbonyl compounds (1%) on ribo-flavin formation were examined with non-growing cells of Eremothecium ashbyii . During non-growing cell incubation for 18hr, the addition of glucose markedly stimulated the formation of riboflavin, but the addition of pentoses (ribose, xylose, arabinose), ribitol and acetoin indicated no effect on the production. The supplementation of pyruvate, acetate, di-acetyl, glyoxal and acetoacetate, on the other hand, noticeably inhibited the formation of riboflavin. The effects of diacetyl monomer, dieter and trimer on the formation of riboflavin were further examined. Dimeric diacetyl (0.5%) among the diacetyl derivatives caused the accumulation of two green fluorescent compounds inside and outside of the cells during the 18hr incubation. The fraction (Compound G1), which was first eluted in Dowex 50W×4 column chromatography, was accumulated in large amounts indicating an inverse relation to riboflavin formation. Compound G1 was isolated from the mycelia and highly purified through many purification procedures. The structure of compound G1 was studied by paper chromatographic comparison, by determination of ultraviolet, emission, excitation and infrared spectra, by following the change of the maximum fluorescence of the reaction mixture containing the isolated compound in the presence of p -quinone and by examining the possibility of it as a substrate for riboflavin synthetase. The results obtained indi-cated that the isolated compound G1 is 6, 7-dimethyl-8-(1'-D-ribityl) lumazine. We speculated that dimeric diacetyl or its derivative becomes a significant inhibitor for the riboflavin synthetase reaction to result in the accumu-lation of 6, 7-dimethyl-8-ribityllumazine although the true inhibitor remains to be solved in future.
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