Aspergillus clavatus Ac-32 strain producing lovastatin and its application
A technology of ac-32 and lovastatin, applied in the field of biotechnology microorganisms, can solve the problems of lack of excellent industrial strains of lovastatin, etc., and achieve the effects of large spore production, fast growth rate and simple cultivation.
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Embodiment 1
[0027] Example 1 Isolation, screening and identification of Aspergillus clavatus (Aspergillus clavatus) Ac-32 bacterial strain
[0028] 1 medium
[0029] ①PDA medium: 20% potato, 2% glucose, 2.0% agar powder, 1L water, pH 5.5-6.0. For the isolation, purification and identification of Aspergillus strains.
[0030] ②PD medium: 20% potato, 2% glucose, 0.5% beef extract, 1L water, pH 5.5-6.0. For the screening of Lovastatin-producing Aspergillus strains.
[0031] 2 Experimental methods
[0032] 2.1 Isolation and purification of Aspergillus strains
[0033] Pick a small amount of mycelia from the surface of natural fermentation samples (food, soil, organic matter, etc.) collected from different habitats and insert them on the surface of the PDA medium plate, and cultivate them at 28°C for 24 hours. After being connected to another PDA medium plate to continue culturing for 3 days to produce spores, the typical characteristics of Aspergillus were observed under a microscope, an...
Embodiment 2
[0046] The growth curve and Lovastatin production rule of embodiment 2 Aspergillus clavatus (Aspergillus clavatus) Ac-32 strain in 5L fermentor
[0047] 1 strain: Ac-32 Aspergillus strain.
[0048] 2 media
[0049] ① PDA medium: the formula is the same as in Example 1.
[0050] ②PD medium: the formula is the same as that in Example 1.
[0051] ③Seed medium: lactose 10%, glycerol 1%, peptone 0.5%, soybean flour 1%, KH 2 PO 4 0.1%, MgSO 4 ·7H 2 O 0.1%, NaNO 3 0.2%, water 1L, pH 5.5.
[0052] ④Fermentation medium: lactose 20%, glycerin 2%, soybean 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%, water 1L, pH 5.2.
[0053] 3 Experimental methods
[0054] 3.1 Cultivation of Ac-32 strain
[0055] Use an inoculation needle to pick a small amount of Ac-32 strain mycelium, transfer it to a PDA medium plate, and activate it for 3 days; take 1 bacteria cake (0.8 mm in diameter) from the plate and inoculate it in PD medium,...
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