Comparative genomic, transcriptomic and secretomic profiling of Penicillium oxalicum HP7-1 and its cellulase and xylanase hyper-producing mutant EU2106, and identification of two novel regulatory genes of cellulase and xylanase gene expression

被引:59
作者
Zhao, Shuai [1 ]
Yan, Yu-Si [1 ]
He, Qi-Peng [1 ]
Yang, Lin [1 ]
Yin, Xin [1 ]
Li, Cheng-Xi [1 ]
Mao, Li-Chun [1 ]
Liao, Lu-Sheng [1 ]
Huang, Jin-Qun [1 ]
Xie, Shang-Bo [1 ]
Nong, Qing-Dong [1 ]
Zhang, Zheng [1 ]
Jing, Lei [1 ]
Xiong, Ya-Ru [1 ]
Duan, Cheng-Jie [1 ]
Liu, Jun-Liang [1 ]
Feng, Jia-Xun [1 ]
机构
[1] Guangxi Univ, State Key Lab Conservat & Utilizat Subtrop Agrobi, Guangxi Key Lab Subtrop Bioresources Conservat &, Minist Educ Microbial & Plant Genet Engn,Coll Lif, 100 Daxue Rd, Nanning 530004, Guangxi, Peoples R China
来源
BIOTECHNOLOGY FOR BIOFUELS | 2016年 / 9卷
基金
中国国家自然科学基金;
关键词
Penicillium oxalicum; Genomics; Transcriptomics; Secretomics; Transcription factor; Cellulase; Xylanase; Regulation; TRICHODERMA-REESEI; SUGARCANE BAGASSE; BETA-GLUCOSIDASE; ENZYMATIC-HYDROLYSIS; CELLULOLYTIC ENZYMES; FILAMENTOUS FUNGI; SACCHARIFICATION; FERMENTATION; DECUMBENS; REPRESSOR;
D O I
10.1186/s13068-016-0616-9
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background: The filamentous fungus Penicillium oxalicum is a potential alternative to Trichoderma reesei for industrial production of a complete cellulolytic enzyme system for a bio-refinery. Comparative omics approaches can support rational genetic engineering and/or breeding of filamentous fungi with improved cellulase production capacity. In this study, comparative genomic, transcriptomic and secretomic profiling of P. oxalicum HP7-1 and its cellulase and xylanase hyper-producing mutant EU2106 were employed to screen for novel regulators of cellulase and xylanase gene expression. Results: The 30.62 Mb P. oxalicum HP7-1 genome was sequenced, and 9834 protein-coding genes were annotated. Re-sequencing of the mutant EU2106 genome identified 274 single nucleotide variations and 12 insertion/deletions. Comparative genomic, transcriptomic and secretomic profiling of HP7-1 and EU2106 revealed four candidate regulators of cellulase and xylanase gene expression. Deletion of these candidate genes and measurement of the enzymatic activity of the resultant mutants confirmed the identity of three regulatory genes. POX02484 and POX08522, encoding a putative Zn(II)(2)Cys(6) DNA-binding domain and forkhead protein, respectively, were found to be novel, while PoxClrB is an ortholog of ClrB, a key transcriptional regulator of cellulolytic enzyme gene expression in filamentous fungi. Delta POX02484 and Delta POX08522 mutants exhibited significantly reduced beta-glucosidase activity, increased carboxymethylcellulose cellulase and xylanase activities, and altered transcription level of cellulase and xylanase genes compared with the parent strain Delta PoxKu70, with Avicel as the sole carbon source. Conclusions: Two novel genes, POX02484 and POX08522, were found and characterized to regulate the expression of cellulase and xylanase genes in P. oxalicum. These findings are important for engineering filamentous fungi to improve cellulase and xylanase production.
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页数:17
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