Korniłłowicz-Kowalska Teresa, Rybczyńska Kamila
Department of Environmental Microbiology, Laboratory of Mycology, University of Life Sciences, Leszczyńskiego 7, 20-069, Lublin, Poland,
World J Microbiol Biotechnol. 2014 Jun;30(6):1725-36. doi: 10.1007/s11274-014-1595-2. Epub 2014 Jan 11.
Cultures of the anamorphic fungus Bjerkandera adusta CCBAS 930 decolorizing, in stationary cultures, 0.01 % solutions of carminic acid and Poly R-478, were characterised by a strong increase in the activity of the horseradish peroxidase (HRP-like) and manganese-dependent peroxidase (MnP) at a low activity of lignin peroxidase. Genotypically modified mutants of B. adusta CCBAS 930: 930-5 and 930-14, with total or partial loss of decolorization capabilities relative to anthraquinonic dyes, showed inhibition of the activity of HRP-like peroxidase and MnP. Whereas, compared to the parental strain, in the mutant cultures there was an increase in the activity of lignin peroxidase and laccase. The paper presents a discussion of the role of the studied enzymatic activities in the process of decolorization of anthraquinonic dyes by the strain B. adusta CCBAS 930.
无性型真菌烟管菌CCBAS 930在静置培养条件下可使胭脂红酸和聚R - 478的0.01%溶液脱色,其特征是在木质素过氧化物酶活性较低时,辣根过氧化物酶(类HRP)和锰依赖性过氧化物酶(MnP)的活性大幅增加。烟管菌CCBAS 930的基因修饰突变体930 - 5和930 - 14,相对于蒽醌染料完全或部分丧失脱色能力,表现出类HRP过氧化物酶和MnP活性受到抑制。然而,与亲本菌株相比,突变体培养物中木质素过氧化物酶和漆酶的活性有所增加。本文讨论了所研究的酶活性在烟管菌CCBAS 930菌株对蒽醌染料脱色过程中的作用。