Suppr超能文献

多拷贝重组毕赤酵母菌株表达黄孢原毛平革菌的木质素过氧化物酶H2

Expression of lignin peroxidase H2 from Phanerochaete chrysosporium by multi-copy recombinant Pichia strain.

作者信息

Wang Wei, Wen Xianghua

机构信息

Department of Environmental Science and Engineering, Tsinghua University, Beijing 100084, China.

出版信息

J Environ Sci (China). 2009;21(2):218-22. doi: 10.1016/s1001-0742(08)62254-8.

Abstract

The lipH2 gene, encoding the expression of lignin peroxidase, was cloned from Phanerochaete chrysosporium BKM-F-1767 and expressed in Pichia pastoris X-33, a yeast. The cDNA of LiPH2 was generated from total RNA extracted from P. chrysosporium by PCR with primers that do not contain a P. chrysosporium lignin peroxidase secretion signal. The gene was then successfully inserted into the expression vector pPICZalpha, and resulted in the recombinant vector pPICZalpha-lipH2. The transformation was conducted in two ways. One was using the wild Pichia pastoris as the recipients, which results in the recombinant P. pastoris with single or low lipH2 gene copy. The second was using P. pastoris and single or low lipH2 gene copy as the recipients, which results in the recombinant P. pastoris with multi-copies of lipH2 genes. This study firstly expressed the gene lipH2 in P. pastoris and achieved the successful expression of the lipH2 depending upon the generation of a recombinant strain that contained multiple copies. The lignin peroxidase activity reached a maximum of 15 U/L after 12 h induction.

摘要

编码木质素过氧化物酶表达的lipH2基因,是从黄孢原毛平革菌BKM-F-1767中克隆出来的,并在毕赤酵母X-33(一种酵母)中表达。LiPH2的cDNA是通过PCR从黄孢原毛平革菌提取的总RNA中生成的,所用引物不含黄孢原毛平革菌木质素过氧化物酶分泌信号。然后该基因成功插入表达载体pPICZalpha,得到重组载体pPICZalpha-lipH2。转化通过两种方式进行。一种是以野生型毕赤酵母作为受体,这会产生具有单拷贝或低拷贝lipH2基因的重组毕赤酵母。第二种是以具有单拷贝或低拷贝lipH2基因的毕赤酵母作为受体,这会产生具有多拷贝lipH2基因的重组毕赤酵母。本研究首次在毕赤酵母中表达lipH2基因,并通过构建含有多拷贝的重组菌株实现了lipH2的成功表达。诱导12小时后,木质素过氧化物酶活性最高达到15 U/L。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验