Department of Biotechnology, National Institute of Technology Durgapur, Mahatma Gandhi Avenue, Durgapur, 713209, India.
Environ Sci Pollut Res Int. 2014 Jan;21(2):1444-54. doi: 10.1007/s11356-013-2040-z. Epub 2013 Aug 6.
A highly tolerant phenol-degrading yeast strain PHB5 was isolated from wastewater effluent of a coke oven plant and identified as Candida tropicalis based on phylogenetic analysis. Biodegradation experiments with C. tropicalis PHB5 showed that the strain was able to utilize 99.4% of 2,400 mg l(-1) phenol as sole source of carbon and energy within 48 h. Strain PHB5 was also observed to grow on 18 various aromatic hydrocarbons. Haldane model was used to fit the exponential growth data and the following kinetic parameters were obtained: μ max = 0.3407 h(-1), K S = 15.81 mg l(-1), K i = 169.0 mg l(-1) (R (2) = 0.9886). The true specific growth rate, calculated from μ max, was 0.2113. A volumetric phenol degradation rate (V max) was calculated by fitting the phenol consumption data with Gompertz model and specific degradation rate (q) was calculated from V max. The q values were fitted with Haldane model, yielding following parameters: q max = 0.2766 g g(-1) h(-1), K S ' = 2.819 mg l(-1), K i ' = 2,093 (R (2) = 0.8176). The yield factor (Y X/S ) varied between 0.185 to 0.96 g g(-1) for different initial phenol concentrations. Phenol degradation by the strain proceeded through a pathway involving production of intermediates such as catechol and cis,cis-muconic acid which were identified by enzymatic assays and HPLC analysis.
一株高效苯酚降解酵母 PHB5 从焦化厂废水处理厂中分离得到,基于系统发育分析,将其鉴定为热带假丝酵母。用 C. tropicalis PHB5 进行生物降解实验表明,该菌株能够在 48 小时内利用 2400mg/L 的苯酚作为唯一的碳源和能源,降解率达到 99.4%。该菌株还能利用 18 种不同的芳烃生长。用 Haldane 模型拟合指数生长数据,得到以下动力学参数:μ max = 0.3407 h-1,KS = 15.81mg/L,Ki = 169.0mg/L(R2 = 0.9886)。根据 μ max 计算的真实比生长速率为 0.2113。通过拟合苯酚消耗数据与 Gompertz 模型计算体积苯酚降解速率(V max),并从 V max 计算比降解速率(q)。q 值与 Haldane 模型拟合,得到以下参数:q max = 0.2766gg-1h-1,KS '= 2.819mg/L,Ki '= 2093(R2 = 0.8176)。不同初始苯酚浓度下的产率因子(YX/S)在 0.185 到 0.96 gg-1 之间变化。该菌株降解苯酚的途径涉及中间产物的生成,如儿茶酚和反,顺-粘康酸,这些产物通过酶促测定和 HPLC 分析得到鉴定。