Bemmann W, Voigt A, Tröger R
Zentralbl Bakteriol Naturwiss. 1981;136(8):661-81.
The activities of catalase, peroxydase, and of the chitinolytic enzymes of the thermophilic hydrocarbon-utilizing fungal strains of Aspergillus fumigatus and Mucor lusitanicus, grown in n-alkane (KW) or glucose (Glc) medium at different temperatures with additions of KCN, NaNO3, 3-amino-1,2,4-triazole (ATA), and CaCl2 and with a shift culture from Glc to KW medium were determined. The enzymatic activities, able to cleave H2O2, were cytochemically shown in the hyphae with 3,3-diamino-benzidine-tetrahydrochloride (DAB) reagent. The colouring of the mycelium was most intense during the linear growth phase in the KW medium. The DAB oxydation could completely by suppressed by pre-incubation of the mycelium with the enzyme inhibitors KCN or ATA and incubation in the standard medium without H2O2. The catalase and peroxydase activities were higher in the KW medium than in the Glc medium, where highest activities occurred at the start of the linear and the stationary growth phase. The pre-incubation of the enzyme solution with the inhibitors KCN, NaNO2 or ATA gave maximum inhibition with ATA, likewise gave the addition of ATA to the medium the highest inhibition of the enzymatic activities, connected with an extension of the initial growth phase. Addition of CaCl2 increased the catalase and peroxydase activities, where catalase at 40 degrees C and peroxydase at 50 degrees C showed maximum growth. A shift of the growing mycelium from Glc to KW medium confirmed the correlation of KW utilization and high catalase activity. The highest chitinolytic activities were ascertained at the beginning of the linear growth phase at a temperature of 40 degrees C. The results were discussed.
测定了烟曲霉和葡萄牙毛霉嗜热烃利用真菌菌株在添加了KCN、NaNO₃、3-氨基-1,2,4-三唑(ATA)和CaCl₂的正构烷烃(KW)或葡萄糖(Glc)培养基中,于不同温度下培养,以及从Glc培养基转移至KW培养基的交替培养过程中过氧化氢酶、过氧化物酶和几丁质分解酶的活性。能够裂解H₂O₂的酶活性通过3,3-二氨基联苯胺四盐酸盐(DAB)试剂在菌丝中进行细胞化学显示。在KW培养基中线性生长阶段,菌丝体的染色最为强烈。通过用酶抑制剂KCN或ATA对菌丝体进行预孵育,并在不含H₂O₂的标准培养基中孵育,DAB氧化可被完全抑制。KW培养基中的过氧化氢酶和过氧化物酶活性高于Glc培养基,在Glc培养基中,最高活性出现在线性生长阶段开始和稳定生长阶段。用抑制剂KCN、NaNO₂或ATA对酶溶液进行预孵育,ATA产生的抑制作用最大,同样,向培养基中添加ATA对酶活性的抑制作用最高,这与初始生长阶段的延长有关。添加CaCl₂可提高过氧化氢酶和过氧化物酶的活性,其中40℃时过氧化氢酶和50℃时过氧化物酶显示出最大活性。生长中的菌丝体从Glc培养基转移至KW培养基证实了KW利用与高过氧化氢酶活性之间的相关性。在40℃温度下线性生长阶段开始时确定了最高的几丁质分解活性。对结果进行了讨论。