Enhanced productivity through gratuitous induction in recombinant yeast fermentations. 1994

S J Napp, and N A Da Silva
Department of Chemical and Biochemical Engineering, University of California at Irvine 92717.

The advantages of gratuitous induction for GAL-regulated cloned gene (lacZ) product synthesis were evaluated for the yeast Saccharomyces cerevisiae. The growth, yield, and productivity of a gratuitous (gal1) strain were compared with those of an otherwise isogenic, nongratuitous (GAL1) strain. Batch studies clearly demonstrated the improvements possible in product synthesis when the inducer is not metabolized by the yeast cells; both beta-galactosidase specific and volumetric activities were superior for the gal1 strain. At equivalent metabolizable sugar concentrations, the productivity of the gratuitous strain exceeded that of the nongratuitous strain by 180%. The effects of initial inducer concentration and induction time were also examined. For the gratuitous strain, galactose:glucose ratios as low as 0.1 still gave maximum beta-galactosidase volumetric activity. A 5-fold higher ratio was necessary for full induction with the nongratuitous strain, and productivity was substantially lower relative to the gal1 strain. A comparison of various times for galactose addition indicated that productivity is highest when the gratuitous culture is induced for the entire batch fermentation.

UI MeSH Term Description Entries
D011994 Recombinant Proteins Proteins prepared by recombinant DNA technology. Biosynthetic Protein,Biosynthetic Proteins,DNA Recombinant Proteins,Recombinant Protein,Proteins, Biosynthetic,Proteins, Recombinant DNA,DNA Proteins, Recombinant,Protein, Biosynthetic,Protein, Recombinant,Proteins, DNA Recombinant,Proteins, Recombinant,Recombinant DNA Proteins,Recombinant Proteins, DNA
D002455 Cell Division The fission of a CELL. It includes CYTOKINESIS, when the CYTOPLASM of a cell is divided, and CELL NUCLEUS DIVISION. M Phase,Cell Division Phase,Cell Divisions,Division Phase, Cell,Division, Cell,Divisions, Cell,M Phases,Phase, Cell Division,Phase, M,Phases, M
D005285 Fermentation Anaerobic degradation of GLUCOSE or other organic nutrients to gain energy in the form of ATP. End products vary depending on organisms, substrates, and enzymatic pathways. Common fermentation products include ETHANOL and LACTIC ACID. Fermentations
D001616 beta-Galactosidase A group of enzymes that catalyzes the hydrolysis of terminal, non-reducing beta-D-galactose residues in beta-galactosides. Deficiency of beta-Galactosidase A1 may cause GANGLIOSIDOSIS, GM1. Lactases,Dairyaid,Lactaid,Lactogest,Lactrase,beta-D-Galactosidase,beta-Galactosidase A1,beta-Galactosidase A2,beta-Galactosidase A3,beta-Galactosidases,lac Z Protein,Protein, lac Z,beta D Galactosidase,beta Galactosidase,beta Galactosidase A1,beta Galactosidase A2,beta Galactosidase A3,beta Galactosidases
D012441 Saccharomyces cerevisiae A species of the genus SACCHAROMYCES, family Saccharomycetaceae, order Saccharomycetales, known as "baker's" or "brewer's" yeast. The dried form is used as a dietary supplement. Baker's Yeast,Brewer's Yeast,Candida robusta,S. cerevisiae,Saccharomyces capensis,Saccharomyces italicus,Saccharomyces oviformis,Saccharomyces uvarum var. melibiosus,Yeast, Baker's,Yeast, Brewer's,Baker Yeast,S cerevisiae,Baker's Yeasts,Yeast, Baker

Related Publications

S J Napp, and N A Da Silva
November 1984, Journal of molecular biology,
S J Napp, and N A Da Silva
January 1995, Advances in applied microbiology,
S J Napp, and N A Da Silva
May 1991, Biotechnology and bioengineering,
S J Napp, and N A Da Silva
February 1991, Biotechnology and bioengineering,
S J Napp, and N A Da Silva
January 2018, Advances in applied microbiology,
S J Napp, and N A Da Silva
January 1983, Biochemical Society symposium,
S J Napp, and N A Da Silva
April 2008, DNA research : an international journal for rapid publication of reports on genes and genomes,
S J Napp, and N A Da Silva
January 1977, Biotechnology and bioengineering,
S J Napp, and N A Da Silva
January 1999, Biotechnology progress,
Copied contents to your clipboard!