Department of Biochemistry, Maria Curie-Skłodowska University, Akademicka 19 St., 20-033, Lublin, Poland.
Department of Genetics and Microbiology, M. Curie-Skłodowska University, Akademicka 19 St., 20-033, Lublin, Poland.
Microbiol Res. 2018 Mar;207:256-268. doi: 10.1016/j.micres.2017.12.007. Epub 2017 Dec 20.
To explore the number of enzymes engaged by Cerrena unicolor FCL139 for wood degradation, the transcriptomes of the fungus growing on birch, ash, maple sawdust and the control liquid medium were analyzed. Among 12,966 gene models predicted for the C. unicolor genome, 10,396 all-unigenes were detected, of which 9567 were found to be expressed in each of the tested growth media. The highest number (107) of unique transcripts was detected during fungus growth in the control liquid medium, while the lowest number (11) - in the fungal culture comprising maple saw dust. Analysis of C. unicolor transcriptomes identified numerous genes whose expression differed substantially between the mycelia growing in control medium and each of the sawdust media used, with the highest number (828) of upregulated transcripts observed during the fungus growth on the ash medium. Among the 294 genes that were potentially engaged in wood degradation, the expression of 59 was significantly (p < .01) changed in the tested conditions. The transcripts of 37 of those genes were at least four times more abundant in the cells grown in all sawdust media when compared to the control medium. Upregulated genes coding for cellulases and, to a lower extent, hemicellulases predominated during fungus growth on sawdust. Transcripts encoding cellulolytic enzymes were the most abundant in mycelia grown on birch and maple while lower number of such transcripts was detected in fungus growing on ash. The expression pattern of lignolytic activities-coding genes was strongly dependent on the type of sawdust applied for fungus growth medium.
为了探究密纹栓孔菌 FCL139 降解木材时涉及的酶数量,分析了该真菌在桦木、灰烬、枫木锯末和对照液体培养基上生长的转录组。在密纹栓孔菌基因组预测的 12966 个基因模型中,检测到 10396 个全基因,其中 9567 个在每种测试生长培养基中均有表达。在对照液体培养基中真菌生长时检测到的独特转录本数量最多(107 个),而在包含枫木锯末的真菌培养物中检测到的独特转录本数量最少(11 个)。密纹栓孔菌转录组分析鉴定了许多表达在对照培养基中生长的菌丝和每种使用的锯末培养基中差异显著的基因,在真菌在灰烬培养基上生长时观察到的上调转录本数量最多(828 个)。在 294 个可能参与木材降解的基因中,59 个的表达在测试条件下发生了显著变化(p < .01)。与对照培养基相比,在所有锯末培养基中生长的细胞中,这些基因的转录本至少有 4 倍增加。在锯末上生长时,编码纤维素酶的上调基因和在较低程度上编码半纤维素酶的基因占主导地位。在桦木和枫木上生长的菌丝中,编码纤维素酶的转录本最为丰富,而在灰烬上生长的真菌中检测到的此类转录本数量较少。木质素降解酶编码基因的表达模式强烈依赖于用于真菌生长培养基的锯末类型。