1989
DOI: 10.1007/bf00184973
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Continuous cultivation of Streptomyces tendae in different media

Abstract: The strain Streptomyces tendae is well suited for continuous cultivation because of its ability to grow and produce secondary metabolites simultaneously. Continuous culture experiments on defined medium show that growth is limited by nitrogen during steady state for the given medium composition. It is supposed that this also holds for complex medium. Production of antibiotics (several nikkomycins) occurs simultaneously with exponential growth. After switching from batch to continuous operation the fraction of … Show more

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Cited by 10 publications
(3 citation statements)
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“…To study quantitatively the effect of nutrients on the regulation of antibiotic pathways and to determine the limiting nutrient a synthetic medium, established for S. tendae by Lohr et al (1989) was essential. In contrast to nikkomycins, which have a cytotoxic effect on fungi, the juglomycins are active against some bacteria, for example Bacillus subtilis, Staphylococcus aureus, and Mycobacterium tuberculosis , as well as against the producer strain itself.…”
Section: Introductionmentioning
confidence: 99%
“…To study quantitatively the effect of nutrients on the regulation of antibiotic pathways and to determine the limiting nutrient a synthetic medium, established for S. tendae by Lohr et al (1989) was essential. In contrast to nikkomycins, which have a cytotoxic effect on fungi, the juglomycins are active against some bacteria, for example Bacillus subtilis, Staphylococcus aureus, and Mycobacterium tuberculosis , as well as against the producer strain itself.…”
Section: Introductionmentioning
confidence: 99%
“…Because phosphate is known to regulate many antibiotic syntheses (Martin Offprint requests to: K.-P. Kuhn 1977), batch fermentations were carried out on a defined salts medium with phosphate as the growth-limiting substrate. These investigations have been described by Lohr et al (1989) and Lohr (1989).…”
Section: Introductionmentioning
confidence: 99%
“…The culture was cultivated for 48 h at 140 rpm and 27°C on a rotary shaker. From this culture 45 mL was transferred into 2.0-L Erlenmeyer flasks containing 900 mL of a defined medium (Lohr et al, 1989). After 48 h, 2.5 L was used to inoculate the 50-L bioreactor (MBR, Wetzikon, Switzerland).…”
Section: Culture and Growth Conditionsmentioning
confidence: 99%