Aspergillus clavatus-32 strain capable of highly yielding Lovastatin and application of Aspergillus clavatus-32 strain
A technology of ac-32 and lovastatin, which is applied in the field of biotechnology microorganisms, can solve the problems of lack of excellent industrial strains of Lovastatin, and achieve the effects of large spore production, fast growth speed and simple cultivation
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Embodiment 1
[0027] Example 1 Aspergillus clavatus ( Aspergillusclavatus ) Isolation, screening and identification of Ac-32 strain
[0028] 1 medium
[0029] ① PDA medium: potato 20%, glucose 2%, agar powder 2.0%, 1L water, pH 5.5~6.0. Used for the separation, purification and identification of Aspergillus strains.
[0030] ②PD medium: potato 20%, glucose 2%, beef extract 0.5%, water 1L, pH 5.5~6.0. Used for the screening of high-yielding Aspergillus strains of Lovastatin.
[0031] 2 Experimental methods
[0032] 2.1 Separation and purification of Aspergillus strains
[0033] Pick a small amount of hyphae from the surface of natural fermentation samples (food, soil, organic matter, etc.) collected from different habitats and connect them to the surface of the PDA medium plate, and incubate at 28°C for 24 hours. After the white fluffy hyphae grow out, take a few hyphae to transfer After being connected to another PDA medium plate and continuing to culture for 3 days to produce spores, the micro...
Embodiment 2
[0046] Example 2 Aspergillus clavatus ( Aspergillusclavatus ) The growth curve of Ac-32 strain in a 5L fermentor and the law of Lovastatin production
[0047] 1 strain: Ac-32 Aspergillus strain.
[0048] 2 medium
[0049] ① PDA culture medium: the formula is the same as in Example 1.
[0050] ②PD medium: the formula is the same as in Example 1.
[0051] ③Seed culture medium: lactose 10%, glycerol 1%, peptone 0.5%, soybean powder 1%, KH 2 PO 4 0.1%, MgSO 4 7H 2 O0.1%, NaNO 3 0.2%, 1L water, pH 5.5.
[0052] ④ Fermentation medium: lactose 20%, glycerol 2%, soy peptone 1%, yeast extract 0.5%, MgSO 4 7H 2 O0.1%, NaNO 3 0.2%, KH 2 PO 4 0.1%, ZnSO 4 0.2%, 1L water, pH 5.2.
[0053] 3 experimental methods
[0054] 3.1 Cultivation of Ac-32 strain
[0055] Pick a small amount of Ac-32 strain hyphae with an inoculating needle, transfer to a PDA medium plate, and activate and culture for 3 days; take 1 bacterial cake (0.8 mm in diameter) from the plate and inoculate it into PD medium, and culture...
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