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FEMS Yeast Res ; 18(2)2018 03 01.
Article in English | MEDLINE | ID: mdl-29514209

ABSTRACT

Glutathione is the most abundant cellular thiol and the low molecular weight peptide present in cells. The methylotrophic yeast Ogataea (Hansenula) polymorpha is considered as a promising cell factory for the synthesis of glutathione. In this study, a competitive O. polymorpha glutathione producer was constructed by overexpression of the GSH2 gene, encoding γ-glutamylcysteine synthetase, the first enzyme involved in glutathione biosynthesis, and the MET4 gene coding for central regulator of sulfur metabolism. Overexpression of MET4 gene in the background of overexpressed GSH2 gene resulted in 5-fold increased glutathione production during shake flask cultivation as compared to the wild-type strain, reaching 2167 mg L-1. During bioreactor cultivation, glutathione accumulation by obtained recombinant strain was 5-fold increased relative to that by the parental strain with overexpressed only GSH2 gene, on the first 25 h of batch cultivation in mineral medium. Obtained results suggest involvement of Met4 transcriptional activator in regulation of GSH synthesis in the methylotrophic yeast O. polymorpha.


Subject(s)
Basic-Leucine Zipper Transcription Factors/genetics , Fungal Proteins/genetics , Gene Expression Regulation, Fungal , Glutathione/biosynthesis , Pichia/genetics , Pichia/metabolism , Basic-Leucine Zipper Transcription Factors/metabolism , Biomass , Fungal Proteins/metabolism , Transcription Factors/metabolism
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