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Protein Expression and Purification, Vol.88, No.1, 164-171, 2013
PMT1 gene plays a major role in O-mannosylation of insulin precursor in Pichia pastoris
Protein mannosyltransferases (PMTs) catalyze the O-mannosylation of serine and threonine residues of proteins in the endoplasmic reticulum. The five PMT genes coding for protein mannosyltransferases, designated as PMT1, 2, 4, 5 and 6, were identified from Pichia pastoris genome based on the homology to PMT genes in Saccharomyces cerevisiae genome, which has seven PMT genes. The homologues of S. cerevisiae PMT 3 & 7 genes are absent in P. pastoris genome. Approximately 5% of the recombinant insulin precursor expressed in P. pastoris is O-mannosylated. In this study, we attempted to prevent O-mannosylation of insulin precursor in vivo, through inactivation of the Pichia PMT genes. Since multiple PMTs are found to be expressed, it was important to understand which of these are involved in O-mannosylation of the insulin precursor. The genes encoding PMT1, 4, 5 and 6 were knocked out by insertional inactivation method. Inactivation of PMT genes 4, 5 and 6 showed similar to 16-28% reductions in the O-mannosylation of insulin precursor. The PMT1 gene disrupted Pichia clone showed similar to 60% decrease in O-mannosylated insulin precursor, establishing its role as an important enzyme for insulin precursor O-mannosylation. (c) 2013 Elsevier Inc. All rights reserved.
Keywords:Insertional inactivation;Insulin precursor;O-mannosylation;Pichia pastoris;Protein mannosyltransferase