Some observations on protease production in continuous suspension cultures of Bacillus firmus

Invariance of culture conditions in steady state continuous cultures make these a very valuable tool to study the influence of various culture parameters on cell growth and synthesis of primary and secondary metabolites. The result of a parametric study on production of protease in continuous suspension cultures of Bacillus firmus NRS 783 are reported in this article. This strain is a superior producer of an alkaline protease with major application in the detergent industry. The parameters investigated include dilution rate and concentrations of yeast extract, ammonium, and inorganic phosphate in the bioreactor feed, glucose being the principal carbon source in all experiments. The regulatory effects of the key culture parameters on cell growth, synthesis and secretion of protease, and production of acetic acid are investigated. The relations among the specific cell growth rate, specific utilization rates of the principal carbon, nitrogen, and phosphorous sources, and specific production rates of two nonbiomass products, viz., acetic acid and protease, are examined, and the effects of the manipulated culture parameters on these relations, specific protease activity, and yields of cell mass, protease, and acetic acid on the basis of the principal carbon, nitrogen, and phosphorous sources are studied. An increase in dilution rate led to increases in specific utilization rates of the principal carbon, nitrogen, and phosphorous sources and specific production rates of acetic acid and protease and decreases in bulk activities/concentrations of the three products (acetic acid, cell mass, and protease). As a result, the productivities of the three species were maximized at an intermediate dilution rate. Increased supply of yeast extract (a rich source of amino acids, proteins, and vitamins, besides being an additional source of carbon, nitrogen, and phosphorus) promoted cell mass formation but reduced protease production per unit cell mass. Increased supply of nitrogen and phosphorous sources stimulated protease synthesis up to certain threshold levels and repressed the enzyme synthesis beyond the threshold levels. With increased supply of the nitrogen source, the phosphorous source was more efficiently utilized for cell growth and protease synthesis. Stable maintenance of continuous cultures of B. firmus over prolonged period is demonstrated in this study. © 1993 John Wiley & Sons, Inc.

[1]  S. J. Parulekar,et al.  Characterization of κ‐Carrageenan Gels Used for Immobilization of Bacillus firmus , 1991, Biotechnology progress.

[2]  S. J. Parulekar,et al.  A parametric study ot protease production in batch and fed‐batch cultures of Bacillus firmus , 1991, Biotechnology and bioengineering.

[3]  S. J. Parulekar,et al.  Effects of Culture Conditions on Plasmid Stability and Production of a Plasmid‐encoded Protein in Batch and Continuous Cultures of Escherichia coli JM103[pUC8] a , 1990, Annals of the New York Academy of Sciences.

[4]  S. J. Parulekar,et al.  Expression of β‐lactamase by recombinant Escherichia coli strains containing plasmids of different sizes—effects of pH, phosphate, and dissolved oxygen , 1989, Biotechnology and bioengineering.

[5]  D. Kirwan,et al.  Protease Production by Immobilized Bacillus licheniformis a , 1987, Annals of the New York Academy of Sciences.

[6]  F. Kargı,et al.  Plant Cell Bioreactors: Present Status and Future Trends , 1987 .

[7]  Patricia Layman Industrial Enzymes Battling To Remain Specialties: Consumption has gone up but prices of some key enzymes have fallen as they have suddenly slid into commodity status , 1986 .

[8]  Wil Lepkowski,et al.  Research Universities Face Major Structural Changes. , 1986 .

[9]  H. Hassan,et al.  Effects of cysteine on growth, protease production, and catalase activity of Pseudomonas fluorescens , 1986, Applied and environmental microbiology.

[10]  C. Emborg,et al.  Protease productivity in chemostat fermentations with retention of biomass on suspended particles , 1985 .

[11]  D. Day,et al.  Effects of cultural conditions on protease production by Aeromonas hydrophila , 1983, Applied and environmental microbiology.

[12]  M. Thirunavukkarasu,et al.  REGULATION OF AMYLASE SYNTHESIS IN BACILLUS LICHENIFORMIS NCIB 6346 , 1980 .

[13]  J. Wouters,et al.  Production of some exocellular enzymes by bacillus licheniformis 749/c in chemostat cultures , 1977 .

[14]  J. Morris,et al.  Regulation of two extracellular proteases of Neurospora crassa by induction and by carbon-nitrogen and sulfur-metabolite repression. , 1975, Archives of biochemistry and biophysics.

[15]  C. Schaffner,et al.  Factors Affecting the Production of Candicidin , 1975, Antimicrobial Agents and Chemotherapy.

[16]  F. G. Heineken,et al.  Continuous culture studies on the biosynthesis of alkaline protease, neutral protease and -amylase by Bacillus subtilis NRRL-B3411. , 1972, Journal of general microbiology.

[17]  W. H. Elliott,et al.  Characteristics of extracellular protease formation by Bacillus subtilis and its control by amino acid repression. , 1968, Biochimica et biophysica acta.

[18]  I. J. Mcdonald,et al.  Regulation of proteinase formation in a species of Micrococcus. , 1966, Canadian journal of microbiology.

[19]  D. Perlman,et al.  STUDIES ON THE UTILIZATION OF LIPIDS BY STREPTOMYCES GRISEUS , 1952, Journal of Bacteriology.

[20]  M. Vijayalakshmi,et al.  Continuous production of small peptides from milk proteins by extracellular proteases of free and immobilized Serratia marcescens cells , 1988 .

[21]  Jeff Hardin,et al.  The World of the Cell , 1986 .

[22]  Satish J. Parulekar,et al.  Modeling, optimization and control of semi-batch bioreactors , 1985 .

[23]  J. Martín Control of antibiotic synthesis by phosphate , 1977 .

[24]  T. Enari,et al.  The effect of phosphate on -amylase production and sporulation by Bacillus subtilis. , 1972, Acta chemica Scandinavica.

[25]  G. Stent Molecular Genetics: An Introductory Narrative , 1971 .

[26]  J. M. Prescott,et al.  Regulation of proteolytic enzyme production by Aeromonas proteolytica. I. Extracellular endopeptidase. , 1970, Canadian journal of microbiology.

[27]  J. M. Prescott,et al.  Regulation of proteolytic enzyme production by Aeromonas proteolytica. II. Extracellular aminopeptidase. , 1970, Canadian Journal of Microbiology (print).

[28]  B. Hofsten,et al.  An extracellular proteolytic enzyme from a strain of Arthrobacter I. Formation of the enzyme and isolation of mutant strains without proteolytic activity , 1965 .