| The Content Variation of Natural Product Induced by Different Factor(s) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Species Name: Streptomyces sp. TP-A0456 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Factor Name: Fermentation medium | [1] | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Experiment Detail |
The producing microorganism, strain TP-A0456, was isolated from the wild plant of Cryptomeria japonica collected in Kosugi-machi, Toyama, Japan. Streptomyces sp. TP-A0456 cultured on a slant agar medium was inoculated into five 500-ml K-l flasks each containing 100 ml of the seed medium consisting of soluble starch 1%, glucose 0.5%, NZ-case (Humco Scheffield Chemical Co.) 0.3%, yeast extract (Difco Laboratories) 0.2%, tryptone (Difco Laboratories) 0.5%, K2HPO4 0.1%, MgSO4-7H2O 0.05% and CaCO3 0.3% (pH 7.0). The inoculated flasks were cultivated on a rotary shaker (200 rpm) at 30℃ for 4days. Three-ml of the seed culture was transferred into a hundred 500-ml K-l flasks each containing 100 ml of the production mediumconsisting of glucose 0.5%, glycerol 2%, soluble starch 2%, Pharmamedia (Traders Protein) 1.5%, yeast extract (Difco Laboratories) 0.3% and Diaion HP-20 (Mitsubishi Chemical Co.) 1%. The pH of the medium was adjusted to 7.0 before sterilization. The inoculated flasks were cultured on a rotary shaker (200 rpm) at 30 ℃ for 6 days.
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| Factor | Part | Location | NP Content | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Fermentation medium containing 1% dextrin, 3% glycerol, 2% soybean flour, 1% corn steep liquor, 0.05% KH2PO4, 0.05% NaCl and 0.5% CaCO3 (30℃ + 6 days +PH7 + 200 rpm)
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Stems | Kosugi-machi, Toyama, Japan. |
NP Content: 6.3 mg
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| References | ||||||||||||||||||||||||
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| 1 | Cedarmycins A and B, new antimicrobial antibiotics from Streptomyces sp. TP-A0456 | |||||||||||||||||||||||