生物技术进展 ›› 2019, Vol. 9 ›› Issue (2): 185-190.DOI: 10.19586/j.2095-2341.2019.0012

• 研究论文 • 上一篇    下一篇

一株特异腐质霉纤维素酶高产突变株的鉴定分析

陈媛1,2,李金阳2,张宇宏2,刘波2,张志伟1*,徐欣欣2*,张伟2   

  1. 1.山西农业大学林学院, 山西 太谷 030801;
    2.中国农业科学院生物技术研究所, 北京 100081
  • 收稿日期:2019-01-28 出版日期:2019-03-25 发布日期:2019-02-27
  • 通讯作者: 张志伟,教授,研究方向为林木有害生物控制与资源利用。E-mail:Zhiweizhang2012@163.com;徐欣欣,助理研究员,研究方向为微生物酶工程。E-mail: xuxinixn@caas.cn
  • 作者简介:陈媛,硕士研究生,研究方向为林木有害生物控制与资源利用。E-mail:chenyuan_0113@163.com。
  • 基金资助:
    国家自然科学基金项目(31600065);山西省留学人员科技活动择优资助项目;山西农业大学青年拔尖创新人才支持计划(TYIT201402)资助。

Identification and Analysis of a Cellulase Hyperproducing Mutant of Humicola insolens

CHEN Yuan, LI Jinyang, ZHANG Yuhong, LIU Bo, ZHANG Zhiwei, XU Xinxin, ZHANG Wei   

  1. 1.College of Forestry, Shanxi Agricultural University, Shanxi Taigu 030801, China;
    2.Biotechnology Research Institute, Chinese Academy of Agricultural Sciences, Beijing 100081, China
  • Received:2019-01-28 Online:2019-03-25 Published:2019-02-27

摘要: 高温真菌特异腐质霉(Humicola insolens)具有强大的纤维素酶分泌和纤维素降解能力,因此在生物质能源、饲料和纺织工业等领域中具有良好的应用前景。在特异腐质霉T-DNA随机插入突变体库中筛选得到一株纤维素酶高产菌株T53。在纤维素诱导培养条件下,突变株T53发酵上清中的滤纸酶活力、内切β-1,4葡聚糖酶活力、纤维二糖水解酶活力、β-葡萄糖苷酶活力以及木聚糖酶活力较野生型菌株分别提高了40%、60%、90%、10%、60%。蛋白电泳结果显示,T53菌株的胞外总蛋白特别是纤维素酶与半纤维素酶的分泌量较野生型菌株有显著提高。TAIL-PCR克隆鉴定了T53菌株中的T-DNA插入位点侧翼序列,结果表明T-DNA插入位点位于一个可能的C2H2型锌指蛋白类转录因子编码基因的上游启动子区域。这为揭示突变株T53中纤维素酶的高产分子机制奠定了重要基础,有助于理解特异腐质霉中纤维素酶的表达调控机制,为特异腐质霉纤维素酶高产工程菌的构建奠定了理论和技术基础。

关键词: 特异腐质霉, 纤维素酶, T-DNA随机插入, 锌指蛋白

Abstract: Humicola insolens holds a high capacity for neutral and thermostable cellulases secretion that has industrial applications promising, like biomass energy, feed and textile industry. In this study, we isolated a mutant T53 with enhanced cellulase and hemicellulase activities from a transfer DNA (T-DNA)-tagged mutant library of H. insolens that was developed before. The FPase, endoglucanase, cellobiohydrolase, β-glucosidase, and xylanase activities of T53, measured at the end of fermentation, were 40%, 60%, 90%, 10%, 60% higher than those of the wild-type strain, respectively. The result of SDS-PAGE showed that the secretion of extracellular proteins, especially cellulases and hemicellulases of T53 strain was significantly higher than that of wild type strain. The sequence flanking the T-DNA insertions in T53 was isolated and a putative zinc finger protein encoding gene potentially involved in cellulase and hemicellulase expression was identified. This study laid an important foundation for revealing the molecular mechanism of cellulases high-yielding in mutant T53, which would also enrich our understanding of the genetics background of H. insolens.

Key words: Humicola insolens, cellulases, T-DNA insertional mutagenesis, zinc finger protein