| The Content Variation of Natural Product Induced by Different Factor(s) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Species Name: Pseudolagarobasidium acaciicola | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Factor Name: PDB medium | [1] | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Experiment Detail |
The fungus P. acaciicola was isolated from the healthy roots of a mangrove tree, B. gymnorrhiza, collected in November 2012 at The Mangrove Forest Learning and Development Center 2, Samut Sakhon province, Thailand. The fungus P. acaciicola was cultured on Potato Dextrose Agar (PDA) (HiMedia Laboratories, Mumbai, India) containing 10% of seawater (collected from Bang Saen Beach, Chonburi Province) for 1 week. The agar was then inoculated into 500 mL of Potato Dextrose Broth (PDB) (HiMedia Laboratories, Mumbai, India) containing 10% of seawater. After incubation for 21 days, broth (total volume of 500 mL) and fungal mycelia were separated by filtration using filter paper (Whatman, Grade 1). The second batch of fungal culture was a scaled-up cultivation of the fungus P. acaciicola. The fungus was cultured on PDA prepared in a mixture of seawater and distilled H2O (10% seawater). After incubation for 1 week at 30 ℃, the agar was then inoculated into 1000 mL Erlenmeyer flasks (forty flasks), each containing 250 mL of PDB prepared in 10% seawater. After incubation for 21 days, fungal culture was filtered to separate mycelia and broth (total volume of 10 L).
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| Factor | Part | Location | NP Content | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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PDB medium containing 10% of seawater (scaled-up cultivation) (30℃ + 21 days)
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Roots | Samut Sakhon province, Thailand |
NP Content: 6.9 mg
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| References | ||||||||||||||||||||||||
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| 1 | Cytotoxic sesquiterpenes from the endophytic fungus Pseudolagarobasidium acaciicola | |||||||||||||||||||||||