초록
<P><B>Abstract</B></P><P><B>BACKGROUND</B></P><P>Biochemical reaction network of <I>Pichia pastoris</I> was improved by including <I>N</I>‐ glycosylation pathway reactions to determine the intracellular reaction rates for glycosylated protein production.</P><P><B>RESULTS</B></P><P>When co‐substrate sorbitol was replaced with mannitol, 12‐fold increase in erythropoietin flux was obtained as a result of 1.2‐ and 2.4‐fold increase in glucose‐6‐phosphate (G6P) formation from fructose‐6‐phosphate (F6P) and 3‐phospho‐D‐glycerate (3PG) formation from glyceraldehyde‐3‐phosphate (G3P), respectively. Thus, to analyse the fluxes around F6P and the fluxes of the glycosylation pathway reactions in depth, the biochemical reaction network of <I>P. pastoris</I> containing 204 reactions and 129 metabolites was developed and used. The flux analysis for glycosylated erythropoietin production with three glycan residues having 12 mannoses (EPO‐Man12) reveals that the fluxes from G3P and guanosine 5′‐diphosphate (GDP) to F6P synthesis were 1.6‐ and 3‐fold higher than that of the fluxes determined for erythropoietin production with no glycans (EPO), respectively. Furthermore, the results of theoretical data‐based overproduction capacity show that the fluxes of EPO‐Man12 and partially humanized EPO with three glycan residues having five mannoses (EPO‐Man5) were 3.6 and 3.8 µmol gDCW<SUP>‐1</SUP> h<SUP>‐1</SUP>, respectively, when the methanol and mannitol uptake rates were 2.10 mmol gDCW<SUP>‐1</SUP> h<SUP>‐1</SUP> and 1.49 mmol gDCW<SUP>‐1</SUP> h<SUP>‐1</SUP>. For glycoprotein production, fluxes around F6P were found to be important as UDP‐N‐acetyl‐α‐D‐glucosamine (UDP‐GlcNAc) and guanosine 5′‐diphosphate‐D‐Mannose (GDP‐Man) were produced from F6P. Thus the co‐substrate mannitol does not repress <I>AOX</I> promoter but is easily converted to F6P, enhancing glycoprotein production.</P><P><B>CONCLUSION</B></P><P>A metabolic reaction network for <I>P. pastoris</I> with glycosylation reactions is proposed for the determination of fluxes for glycoprotein production by <I>P. pastoris</I>. © 2013 Society of Chemical Industry</P>