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    于存, 池玉杰. 一色齿毛菌对活性染料的脱色研究[J]. 北京林业大学学报, 2014, 36(4): 126-132. DOI: 10.13332/j.cnki.jbfu.2014.04.023
    引用本文: 于存, 池玉杰. 一色齿毛菌对活性染料的脱色研究[J]. 北京林业大学学报, 2014, 36(4): 126-132. DOI: 10.13332/j.cnki.jbfu.2014.04.023
    YU Cun, CHI Yu-jie. Decolorization to two reactive dyes of Cerena unicolor CB1[J]. Journal of Beijing Forestry University, 2014, 36(4): 126-132. DOI: 10.13332/j.cnki.jbfu.2014.04.023
    Citation: YU Cun, CHI Yu-jie. Decolorization to two reactive dyes of Cerena unicolor CB1[J]. Journal of Beijing Forestry University, 2014, 36(4): 126-132. DOI: 10.13332/j.cnki.jbfu.2014.04.023

    一色齿毛菌对活性染料的脱色研究

    Decolorization to two reactive dyes of Cerena unicolor CB1

    • 摘要: 为进一步鉴定试验菌株及明确一色齿毛菌CB1(Cerena unicolor CB1)对活性染料的脱色效果,在对该菌株ITS 序列克隆的基础上,进行了其对活性黑和活性红2 种活性染料脱色条件的研究。结果表明,C. unicolor CB1 与17 个同种其他菌株的ITS 序列相似性为93% ~99%,说明试验菌株为一色齿毛菌。染料脱色结果表明,250 mg/ L 的 活性黑对C. unicolor CB1 的脱色产生明显的抑制,而500 mg/ L 的活性红对该菌株的脱色抑制不明显。C. unicolor CB1 对活性黑和活性红的脱色最适碳源分别是果糖和葡萄糖;最适氮源分别是尿素和硝酸铵;最适Cu2+ 和Mn2+ 添 加浓度都为0.1 mmol/ L;最适pH 为5;最适接种量为直径d =8 mm 的新鲜菌丝7 片。

       

      Abstract: A study for determining the decolorizing capacity of white rot basidiomycete Cerena unicolor strain CB1 was carried out. Based on cloning of ITS sequence, factors affecting decolorization into two dyes, reactive black and reactive red, were carried out. The results of phylogenetic analysis showed that the ITS sequence of C. unicolor CB1 was 93% to 99% homologous to 17 different C. unicolor strains, indicating that strain CB1 was C. unicolor. The results of decolorization tests showed that the reactive black dye inhibited the decolorization reaction of C. unicolor CB1 evidently at the concentration of 250 mg/ L, whereas reactive red had no significant inhibition to the decolorization reaction even at the concentration of 500 mg/ L. The most optimal carbon source for C. unicolor CB1 to decolor reactive black and reactive red was fructose and glucose, respectively; The best nitrogen source was urea and ammonium nitrate, respectively. The optimal concentration of Cu2+ and Mn2+ both was 0.1 mmol/ L, the optimum pH was 5, and the optimum inoculum was seven fresh mycelium discs with d =8 mm.

       

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