Production of recombinant proteins in high-density insect cell cultures.

The effect of the growth phase of Spodoptera frugiperda (Sf9) cells on the production of recombinant proteins (beta-galactosidase and glucocerebrosidase) was investigated. Cells infected with the recombinant Autographa californica nuclear polyhedrosis virus at the late exponential and stationary phases yielded low quantities of expressed protein. Highest enzyme yields were obtained using Sf9 cells from the early exponential phase (0.9 mg beta-galactosidase/10(6) cells and 1.7 microg glucocerebrosidase/10(6) cells). Infection of resuspension of cells collected from various phases of growth in fresh medium resulted in 75% restoration of maximal expression levels. This finding suggested either nutrient limitation or waste product accumulation as the cause of the decrease in productivity at the latter phases of growth. Further experiments revealed that the highest productivity levels could be obtained with cultures of Sf9 cells grown in a fermentor to a cell concentration of 4 x 10(6) mL(-1). The medium needed to be replaced prior to infection with the recombinant virus and supplemented with a mixture of glucose, L-glutamine, and yeastolate ultrafiltrate.

[1]  J. Shiloach,et al.  Carbohydrate Metabolism in Insect Cell Cultures during Cell Growth and Recombinant Protein Production , 1992, Annals of the New York Academy of Sciences.

[2]  C. Nicolau,et al.  Optimization of the production of full‐length rCD4 in baculovirus‐infected Sf9 cells , 1992, Biotechnology and bioengineering.

[3]  M. Goosen Large-scale insect cell culture. , 1992 .

[4]  M. King,et al.  High-level expression using baculovirus, purification, and characterization of a monomeric form of type II calmodulin-dependent protein kinase. , 1992, Protein expression and purification.

[5]  M. Fraser The baculovirus-infected insect cell as a eukaryotic gene expression system. , 1992, Current topics in microbiology and immunology.

[6]  J. Bailey,et al.  Factors influencing recombinant protein yields in an insect cell–bacuiovirus expression system: Multiplicity of infection and intracellular protein degradation , 1991, Biotechnology and bioengineering.

[7]  H. Miltenburger,et al.  HIGH CELL DENSITY PERFUSION CULTURE OF INSECT CELLS FOR PRODUCTION OF BACULOVIRUS AND RECOMBINANT PROTEIN , 1991 .

[8]  B. Massie,et al.  High‐level recombinant protein production in bioreactors using the baculovirus–insect cell expression system , 1990, Biotechnology and bioengineering.

[9]  D. Inlow,et al.  Insect cell culture and baculovirus propagation in protein-free medium , 1989 .

[10]  D. Inlow,et al.  Large-Scale Insect Cell-Culture for Recombinant Protein Production , 1988, Bio/Technology.

[11]  S. Tsuji,et al.  Glycosylation and processing of high levels of active human glucocerebrosidase in invertebrate cells using a baculovirus expression vector. , 1988, DNA.

[12]  M. Summers,et al.  Trends in the Development of Baculovirus Expression Vectors , 1988, Bio/Technology.

[13]  G. Gardiner,et al.  The influence of the condition of cells and medium on production of polyhedra of Autographa californica nuclear polyhedrosis virus in vitro , 1977 .

[14]  T. Grace,et al.  Establishment of Four Strains of Cells from Insect Tissues Grown in vitro , 1962, Nature.