Cargando…

Long-term strain improvements accumulate mutations in regulatory elements responsible for hyper-production of cellulolytic enzymes

Long-term strain improvements through repeated mutagenesis and screening have generated a hyper-producer of cellulases and hemicellulases from Penicillium decumbens 114 which was isolated 30 years ago. Here, the genome of the hyper-producer P. decumbens JU-A10-T was sequenced and compared with that...

Descripción completa

Detalles Bibliográficos
Autores principales: Liu, Guodong, Zhang, Lei, Qin, Yuqi, Zou, Gen, Li, Zhonghai, Yan, Xing, Wei, Xiaomin, Chen, Mei, Chen, Ling, Zheng, Kai, Zhang, Jun, Ma, Liang, Li, Jie, Liu, Rui, Xu, Hai, Bao, Xiaoming, Fang, Xu, Wang, Lushan, Zhong, Yaohua, Liu, Weifeng, Zheng, Huajun, Wang, Shengyue, Wang, Chengshu, Xun, Luying, Zhao, Guo-Ping, Wang, Tianhong, Zhou, Zhihua, Qu, Yinbo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3610096/
https://www.ncbi.nlm.nih.gov/pubmed/23535838
http://dx.doi.org/10.1038/srep01569
Descripción
Sumario:Long-term strain improvements through repeated mutagenesis and screening have generated a hyper-producer of cellulases and hemicellulases from Penicillium decumbens 114 which was isolated 30 years ago. Here, the genome of the hyper-producer P. decumbens JU-A10-T was sequenced and compared with that of the wild-type strain 114-2. Further, the transcriptomes and secretomes were compared between the strains. Selective hyper-production of cellulases and hemicellulases but not all the secreted proteins was observed in the mutant, making it a more specific producer of lignocellulolytic enzymes. Functional analysis identified that changes in several transcriptional regulatory elements played crucial roles in the cellulase hyper-producing characteristics of the mutant. Additionally, the mutant showed enhanced supply of amino acids and decreased synthesis of secondary metabolites compared with the wild-type. The results clearly point out that we can target gene regulators and promoters with minimal alterations of the genetic content but maximal effects in genetic engineering.