Pichia pastoris fermentation with mixed-feeds of glycerol and methanol: growth kinetics and production improvement

Fed-batch fermentation of a methanol utilization plus (Mut+) Pichia pastoris strain typically has a growth phase followed by a production phase (induction phase). In the growth phase glycerol is usually used as carbon for cell growth while in the production phase methanol serves as both inducer and carbon source for recombinant protein expression. Some researchers employed a mixed glycerol-methanol feeding strategy during the induction phase to improve production, but growth kinetics on glycerol and methanol and the interaction between them were not reported. The objective of this paper is to optimize the mixed feeding strategy based on growth kinetic studies using a Mut+ Pichia strain, which expresses the heavy-chain fragment C of botulinum neurotoxin serotype C [BoNT/C(Hc)] intracellularly, as a model system. Growth models on glycerol and methanol that describe the relationship between specific growth rate (μ) and specific glycerol/methanol consumption rate (νgly, νMeOH) were established. A mixed feeding strategy with desired μgly/μMeOH =1, 2, 3, 4 (desired μMeOH set at 0.015 h−1) was employed to study growth interactions and their effect on production. The results show that the optimal desired μgly/μMeOH is around 2 for obtaining the highest BoNT/C(Hc) protein content in cells: about 3 mg/g wet cells.

[1]  J. Cregg,et al.  Recombinant protein expression in Pichia pastoris , 2000, Molecular biotechnology.

[2]  R. Armitage,et al.  Expression of trimeric CD40 ligand in Pichia pastoris: use of a rapid method to detect high-level expressing transformants. , 1997, Gene.

[3]  J. Cregg,et al.  Development of the methylotrophic yeast, Pichia pastoris, as a host system for the production of foreign proteins , 1988 .

[4]  I. J. van der Klei,et al.  Alcohol oxidase from Hansenula polymorpha CBS 4732. , 1990, Methods in enzymology.

[5]  V. Titorenko,et al.  Genetic control of methanol utilization in yeasts , 1988, Journal of basic microbiology.

[6]  R. Siegel,et al.  Fermentation Development of Recombinant Pichia pastoris Expressing the Heterologous Gene: Bovine Lysozyme , 1990, Annals of the New York Academy of Sciences.

[7]  Wenhui Zhang,et al.  Design of Methanol Feed Control in Pichia pastoris Fermentations Based upon a Growth Model , 2002, Biotechnology progress.

[8]  W. Zhang,et al.  Modeling Pichia pastoris growth on methanol and optimizing the production of a recombinant protein, the heavy-chain fragment C of botulinum neurotoxin, serotype A. , 2000, Biotechnology and bioengineering.

[9]  D. Brown,et al.  Protective vaccination with a recombinant fragment of Clostridium botulinum neurotoxin serotype A expressed from a synthetic gene in Escherichia coli , 1995, Infection and immunity.

[10]  J. Baratti,et al.  Oxidation of Methanol by the Yeast, Pichia pastoris. Purification and Properties of the Alcohol Oxidase , 1980 .

[11]  A. Sols,et al.  Glycerol metabolism in yeasts. Pathways of utilization and production. , 1968, European journal of biochemistry.

[12]  R. Potenz,et al.  High-level expression, purification, and characterization of recombinant human tumor necrosis factor synthesized in the methylotrophic yeast Pichia pastoris. , 1989, Biochemistry.

[13]  Alberto Sols,et al.  Glycerol Metabolism in Yeasts , 1968 .

[14]  X. Liu,et al.  Biosynthetic production of type II fish antifreeze protein: fermentation by Pichia pastoris , 1997, Applied Microbiology and Biotechnology.

[15]  A. Daugulis,et al.  A rational approach to improving productivity in recombinant Pichia pastoris fermentation. , 2001, Biotechnology and bioengineering.

[16]  C. Scorer,et al.  Foreign gene expression in yeast: a review , 1992, Yeast.

[17]  Leonard A. Smith,et al.  Purification, Potency, and Efficacy of the Botulinum Neurotoxin Type A Binding Domain from Pichia pastoris as a Recombinant Vaccine Candidate , 1998, Infection and Immunity.

[18]  T. Omasa,et al.  Effect of methanol concentration on the production of human β2-glycoprotein I domain V by a recombinant Pichia pastoris: A simple system for the control of methanol concentration using a semiconductor gas sensor , 1998 .

[19]  S. Shioya,et al.  Maximum histidine production by fed-batch culture of Brevibacterium flavum , 1991 .

[20]  R. Fischer,et al.  Analysis of single-chain antibody production in Pichia pastoris using on-line methanol control in fed-batch and mixed-feed fermentations. , 2001, Biotechnology and bioengineering.

[21]  J. Cregg,et al.  Development of yeast transformation systems and construction of methanol-utilization-defective mutants of Pichia pastori by gene disruption , 1987 .

[22]  H. Chang,et al.  Effect of post-induction nutrient feeding strategies on the production of bioadhesive protein in Escherichia coli. , 1998, Biotechnology and bioengineering.

[23]  J. Cregg,et al.  Functional characterization of the two alcohol oxidase genes from the yeast Pichia pastoris , 1989, Molecular and cellular biology.

[24]  T. Gingeras,et al.  Expression of the lacZ gene from two methanol-regulated promoters in Pichia pastoris. , 1987, Nucleic acids research.

[25]  S. Shioya,et al.  Optimization and control in fed-batch bioreactors , 1992 .