ハロゲン置換サリチル酸類のクロコウジカビに対する抗かび作用

書誌事項

タイトル別名
  • Antifungal Activity of Halogeno-Salicylic Acids against Growth of <i>Aspergillus niger</i>
  • ハロゲン置換サリチル酸類のクロコウジカビに対する抗かび作用 化学構造と抗かび性に関する研究 (第2報)
  • ハロゲン チカン サリチルサンルイ ノ クロコウジカビ ニ タイスル コウカビ

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抄録

The relationship between the chemical structures of thirteen kinds of halogeno-salicylic acids and their antifungal activity against Aspergillus niger was examined by using the agar plate filter paper disc method at pH 3.7. The degrees of inhibition of fungal growth were estimated in terms of both initial strength of the activity (IS), which was obtained by measuring the diameter of the inhibition zone, and its durability in a plate culture of each sample. As a control test, the IS value of salicylic acid obtained at pH 3.7 with incubation for 3 days at 25° was defined as f=100. The durability was indicated in terms of the size of the final inhibition zone or the period required for the initial inhibition zone to disappear (below 6mm), under continuous incubation.<br>In all examiniations, the presence of halogens (bromine, chlorine, and iodine) in the aromatic ring increased the antifungal activity. Among five kinds of monohalogeno-salicylic acids, the initial activity and the durability of the 3-chloro form were superior to those of other mono-chloro isomers, and the IS value of the 5-bromo form was higher than that of 4-bromo form. The IS value of the 3, 5-dichloro, dibromo, and diiodo forms were reduced in that order. The IS value of the 5-bromo-3-chloro form was as high as that of the 3-bromo-5-chloro form and was superior to that of dichloro form, although their duability was inferior to that of the 4, 5-dichloro form. In general, increasing the number of substituted halogen atoms resulted in higher antifungal activity. However, among all of the halogeno-salicylic acids tested, the 4, 5-dichloro form was more effective than the 3, 4, 5-tribromo or 4, 6-dibromo-3, 5-dichloro forms. In all tests, an inhibition zone of conidiogenesis was observed, and is shown as a p value (p=f1×(f1-f2)/100, f1; the inhibition factor of conidiogenesis, f2; the inhibition factor) in Table 3.

収録刊行物

  • 食品衛生学雑誌

    食品衛生学雑誌 34 (2), 142-147_1, 1993

    公益社団法人 日本食品衛生学会

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