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Journal ArticleDOI

Modeling of growth and energy metabolism of Pichia pastoris producing a fusion protein

TLDR
A kinetic model was developed that could predict biomass growth and oxygen consumption in processes with and without oxygen-enriched air and describes how the low maintenance demand of P. pastoris compared with E. coli enables this organism to grow to such high cell densities.
Abstract
A fusion protein composed of a cellulose binding domain from Neocallimastix patriciarum cellulase A and Candida antarctica lipase B (CBD-lipase) was produced by Pichia pastoris methanol utilization plus phenotype in high cell-density cultures. The genes expressing CBD-lipase were fused to the alpha-factor secretion signal sequence of Saccharomyces cerevisiae and placed under the control of the alcohol oxidase gene (AOX1) promoter. To control the repression and induction of AOX1 and oxygen demand at high cell density, a four-stage process was used. Batch growth on glycerol was used in the first step to provide biomass (28 g L–1) while product formation was prevented due to repression of the AOX1. The second stage was exponential fed-batch growth on glycerol, which caused a slight increase of the enzyme alcohol oxidase activity due to derepression of the AOX1. This procedure resulted in smooth transition to exponential fed-batch growth on methanol, the third stage, in which the AOX1 was strongly induced. The fourth stage was constant fed-batch growth on methanol used to control the oxygen demand at the high cell density. A kinetic model was developed that could predict biomass growth and oxygen consumption in processes with and without oxygen-enriched air. With oxygen enrichment to 34% O2 in the inlet air the methanol feed rate could be increased by 50% and this resulted in 14% higher final cell density (from 140 to 160 g L–1 cell dry weight). The increased methanol feed rate resulted in a proportionally increased specific rate of product secretion to the medium. After an initial decrease, the synthesis capacity of the cell was kept constant throughout the cultivation, which made the product concentration increase almost constantly during the process. The kinetic model also describes how the low maintenance demand of P. pastoris compared with E. coli enables this organism to grow to such high cell densities.

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Citations
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Journal ArticleDOI

Promoter library designed for fine-tuned gene expression in Pichia pastoris.

TL;DR: The new PAOX1 synthetic promoter library constitutes a basic toolbox to fine-tune gene expression in metabolic engineering and sequential induction of protein expression in synthetic biology.
Book ChapterDOI

Glutathione, altruistic metabolite in fungi.

TL;DR: Adaptation to carbon deprivation stress results in an increased tolerance to oxidative stress, which involves the induction of GSH-dependent elements of the antioxidant defence system.
Journal ArticleDOI

Bioprocess engineering aspects of heterologous protein production in Pichia pastoris: A review

TL;DR: Several bioprocess engineering aspects related to P. pastoris cultivation are discussed, including the different promoters available, both constitutive and inductive, on- and off-line process parameter monitoring methods, fed-batch and continuous cultivation control strategies, proteolytic degradation of products and methods to minimize associated yield reductions, and the different models devised to describe cell growth and protein production.
Journal ArticleDOI

Microbials for the production of monoclonal antibodies and antibody fragments

TL;DR: Glycosylated full length antibodies are currently produced in mammalian cells but can be produced in microbial organisms and microbials provide several advantages over mammalian cells.
Journal ArticleDOI

Temperature limited fed-batch technique for control of proteolysis in Pichia pastoris bioreactor cultures.

TL;DR: Three mechanisms that may contribute to the much higher accumulation of product in the TLFB process are: 2) reduced proteolysis due to lower temperature, 3) increased synthesis rate due to higher AOX activity.
References
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Journal ArticleDOI

A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding

TL;DR: This assay is very reproducible and rapid with the dye binding process virtually complete in approximately 2 min with good color stability for 1 hr with little or no interference from cations such as sodium or potassium nor from carbohydrates such as sucrose.
Journal ArticleDOI

Recent advances in the expression of foreign genes in Pichia pastoris

TL;DR: The Pichia pastoris heterologous gene expression system has been utilized to produce attractive levels of a variety of intracellular and extracellular proteins of interest and improvements in understanding and application have improved its utility even further.
Journal ArticleDOI

Strategies for optimal synthesis and secretion of heterologous proteins in the methylotrophic yeast Pichia pastoris

TL;DR: The inherent ability of P. pastoris to convert the zymogen (pro-enzyme) form of matrix metalloproteinases (MMP) into active mature forms (which tend to self-degrade, and in some instances also cause damage to cells), largely limits the use of this system for the production of MMP, but this problem can be partly alleviated by co-expression of tissue inhibitor of M MP (TIMP-1).
Journal ArticleDOI

Functional characterization of the two alcohol oxidase genes from the yeast Pichia pastoris.

TL;DR: In Pichia pastoris, alcohol oxidase is the first enzyme in the methanol utilization pathway and is encoded by two genes, AOX1 and AOX2, which appear to be regulated in the same manner.
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