Expression of lignin peroxidase H2 from Phanerochaete chrysosporium bymulti-copy recombinant Pichia strain
WANG Wei , WEN Xianghua
DOI:
Received February 06, 2008,Revised May 08, 2008, Accepted , Available online
Volume 21,2009,Pages 218-222
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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 pPICZ , and resulted in the recombinant vector pPICZ -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.
