Method for synchronously producing hypocrellin and shiraia bambusicola polysaccharides
A technology of oleocanthal and liquid fermentation, applied in the directions of microorganism-based methods, biochemical equipment and methods, fermentation, etc., to achieve high medicinal value and improve economic benefits.
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Embodiment 1
[0026] Bacterial classification adopts bamboo yellow bacterium (Shiraia bambusicola Henn.), preservation number is CGMCCNo.2201, is collected from Yongjia County, Zhejiang Province, and its isolation and identification documents are as Wei Jingchao, "Fungus Identification Handbook", Shanghai Science and Technology Press, published in 1979, p238; Liu Tianhui, "Introduction to Edible Fungi", China Outlook Publishing House, published in 1987, p26; Zhang Hao et al., "Screening and Identification of Hypocretin-Producing Bacteria", Biotechnology, 2002, 12(4), p19~ 20.
[0027] 1. Shake flask culture Insert the preserved bamboo yellow fungus strains into the newly prepared slant medium, the culture temperature is 25°C, the slant medium formula is (in g / L): glucose 25, potato 200, and agar 20 . After the mycelium covered the slope, put 5 mg of bamboo yellow fungus mycelium into a 250 mL Erlenmeyer flask containing 50 mL of shaking flask culture medium (5 bottles in total), and place it...
Embodiment 2
[0035] The culture conditions and medium composition of the strains of this embodiment, their shake flask culture, and shake flask expansion culture are the same as those in Example 1.
[0036] Fermentation culture: Transfer 2000mL of strains grown in shake flasks into a 30L fermenter with 21L of fermentation medium for cultivation. Maintain the culture temperature of the fermenter at 25°C, the tank pressure at 0.05MPa, the stirring speed at 150 rpm, the ventilation rate at 1:0.5v / v / m, and the culture time at 120 hours. The culture medium of wherein said fermentation culture is made up of, contains following composition (unit: gram) in every liter of water: glucose 30, peptone 3, K 2 HPO 4 0.15, KCl 0.5, MgSO 4 0.5, FeSO 4 0.1, pH6.0.
[0037] After the fermentation, the mycelia and fermentation liquid were harvested, and the content of hypocretin and bamboo yellow polysaccharide was determined, and the determination method was the same as that in Example 1. As a result...
Embodiment 3
[0039] The culture conditions and medium composition of the strains of this embodiment, their shake flask culture, and shake flask expansion culture are the same as those in Example 1.
[0040] Fermentation culture: Transfer 2000mL of strains grown in shake flasks into a 30L fermenter with 21L of fermentation medium for cultivation. Maintain the culture temperature of the fermenter at 25°C, the tank pressure at 0.05MPa, the stirring speed at 150 rpm, the ventilation rate at 1:0.5v / v / m, and the culture time at 120 hours. The culture medium of wherein said fermentation culture is made up of, contains following composition (unit: gram) in every liter of water: Glucose 30, (NH 4 ) 2 SO 4 3,K 2 HPO 4 0.15, KCl 0.5, MgSO 4 0.5, FeSO 4 0.1, pH6.0.
[0041] After the fermentation, the mycelia and fermentation liquid were harvested, and the content of hypocretin and bamboo yellow polysaccharide was determined, and the determination method was the same as that in Example 1. A...
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