Regulation of hydrolase formation and phosphate release in turimycin fermentations.

During the turimycin fermentation hydrolytic enzymes are excreted responsible for orthophosphate release from phosphate-containing dissolved and undissolved complex medium constituents. Following a phosphate-limited growth period the phosphate release leads to a second growth period (diauxic growth). Depending on the rate of phosphate release the length of the lag phase of diauxic growth changes in different fermentations. The resulting second growth period is correlated with a transient delay in the formation of turimycin, of phosphatases and of nucleases. The amylolytic activities are formed already within the first hours after the beginning of fermentations. Phosphatases, nucleases and protease are excreted parallel to turimycin formation after extracellular phosphate limitation in presence of ammonia and glucose. A special role of phosphate limitation initiating enzyme synthesis is proposed.

[1]  H. Pape,et al.  Relationship between macrotetrolide production and specific activity of some hydrolases in a high and a low producing strain of Streptomyces griseus , 1981, European journal of applied microbiology and biotechnology.

[2]  J. Gibson,et al.  Phosphate utilization and alkaline phosphatase activity in Anacystis nidulans (Synechococcus) , 2004, Archives of Microbiology.

[3]  P. Müller,et al.  Parallel regulation of cAMP phosphodiesterase and phosphatase activities in turimycin fermentations. , 1983, Zeitschrift fur allgemeine Mikrobiologie.

[4]  M. Menner,et al.  Phosphate release in turimycin fermentations. , 1982, Zeitschrift fur allgemeine Mikrobiologie.

[5]  G. Hanlon,et al.  Bacitracin and protease production in relation to sporulation during exponential growth of Bacillus licheniformis on poorly utilized carbon and nitrogen sources , 1981, Journal of bacteriology.

[6]  T. Va,et al.  Hydrolase activity characteristics of actinomycetes during antibiotic biosynthesis , 1981 .

[7]  I. Shuvalova,et al.  [Regulation of alkaline exoprotease and cephalosporin C synthesis in Acremonium chrysogenum by different carbon and nitrogen sources]. , 1981, Antibiotiki.

[8]  S. Jensen,et al.  Nutritional factors controlling exocellular protease production by Pseudomonas aeruginosa , 1980, Journal of bacteriology.

[9]  Y. Aharonowitz Nitrogen metabolite regulation of antibiotic biosynthesis. , 1980, Annual review of microbiology.

[10]  J F Martin,et al.  Control of antibiotic biosynthesis. , 1980, Microbiological reviews.

[11]  L. Vining,et al.  Intracellular cyclic adenosine 3',5'-monophosphate levels and streptomycin production in cultures of Streptomyces griseus. , 1978, Canadian journal of microbiology.

[12]  D. Tempest The biochemical significance of microbial growth yields: A reassessment , 1978 .

[13]  L. Vining,et al.  Intracellular levels of guanosine 5'-diphosphate 3'-diphosphate (ppGpp) and guanosine 5'-triphosphate 3'-diphosphate (pppGpp) in cultures of Streptomyces griseus producing streptomycin. , 1978, Canadian journal of microbiology.

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

[15]  A. L. Koch,et al.  Unused protein synthetic capacity of Escherichia coli grown in phosphate-limited chemostats. , 1974, Journal of molecular biology.

[16]  Egorov Ns,et al.  [Alkaline phosphatase of a culture of Proactinomyces fructiferi var. ristomycini--producer of the antibiotic ristomycin]. , 1973 .

[17]  W. Schill,et al.  Radial diffusion in gel for micro determination of enzymes. I. Muramidase, alpha-amylase, DNase 1, RNase A, acid phosphatase, and alkaline phosphatase. , 1972, Analytical biochemistry.

[18]  M. Majumdar,et al.  Relationship between alkaline phosphatase and neomycin formation in Streptomyces fradiae. , 1971, The Biochemical journal.

[19]  A. Miller,et al.  Accumulation of Streptomycin-Phosphate in Cultures of Streptomycin Producers Grown on a High-Phosphate Medium , 1970, Journal of bacteriology.

[20]  P. S. Chen,et al.  Microdetermination of Phosphorus , 1956 .

[21]  O. H. Lowry,et al.  Protein measurement with the Folin phenol reagent. , 1951, The Journal of biological chemistry.