Aspergillus oryzae strain and application thereof in Zhejiang rose vinegar fermentation
A technology of Aspergillus oryzae and rose vinegar, which is applied in the field of microorganisms, can solve the problems such as no content requirement of the state nitrogen index, and achieve the effects of fast growth, good spore colonization, and improved production efficiency
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Embodiment 1
[0022] Example 1: Isolation, identification and preservation of Aspergillus oryzae strain (Aspergillus oryzae) MG-6CCTCC NO.M2015764.
[0023] 1. Isolation and purification of Aspergillus oryzae strains.
[0024] 1. Material preparation:
[0025] Sample source: Zhejiang Wuweihe Food Co., Ltd. production workshop;
[0026] Potato sucrose medium: commercially available potatoes were peeled and cut into 1cm 2 For square cubes, weigh 200g of potato pieces, add 5-6 times of water, boil for half an hour, filter through eight layers of gauze, add 20g of sucrose, 20g of agar, dilute to 1000ml, and sterilize at 121°C for 20min;
[0027] Cha's medium: 30g sucrose, NaNO 3 3g, K 2 HPO 4 1.0g, MgSO 4 0.5g, KCl0.5g, FeSO 4 0.01g, yeast extract 5g, agar 15-20g, dilute to 1000ml, sterilize at 121°C for 20min;
[0028] Saccharomyces tsazii extract medium: 30g sucrose, NaNO 3 3g, K 2 HPO 4 1.0g, MgSO 4 0.5g, KCl0.5g, FeSO 4 0.01g, 15-20g agar, dilute to 1000ml, sterilize at 121℃ fo...
Embodiment 2
[0052] Determination of enzyme stability of Aspergillus oryzae strains:
[0053] Inoculate the fast-growing, sporulation-rich strain isolated in Example 1 on potato sucrose medium, and culture it at 30°C for 3 days. It can be seen that the surface of the strain is covered with spores, and the culture is mature. Basically, culture at 30°C for 3 days is one generation, and so on, and strains with different passage times can be obtained.
[0054] Potato sucrose medium: commercially available potatoes were peeled and cut into 1cm 2 For square cubes, weigh 200g of potato pieces, add 5-6 times of water, boil for half an hour, filter through eight layers of gauze, add 20g of sucrose, 20g of agar, dilute to 1000ml, and sterilize at 121°C for 20min.
[0055] Inoculate the obtained strains of each generation on the bran medium, shake well, and culture at a constant temperature at 30°C for about 18 hours, shake the flask once when the medium has a little white cake, shake the agglomerat...
Embodiment 3
[0058] Trial production of finished koji:
[0059] 1, press the method for making koji of embodiment 2, bacterial strain MG-6 is cultivated 72 hours at 30 ℃, makes the kind of koji of Erlenmeyer flask. Seed koji, good agglomeration, stable enzyme activity and good balance of enzyme activity of each component, and the color of the koji is bright green, rich in spores 2.5*10 10 pcs / g dry basis, good growth, with the inherent fragrance of Aspergillus oryzae. According to the national standard method, no aflatoxin was detected.
[0060] 2. Mix the koji material according to the ratio of bran:wheat flour=8:2, add 70% water, stir well, cook at a high temperature under 0.1MPa pressure for 30 minutes, and after the koji material cools, add 0.3% ( Raw material weight meter) inoculum amount is inserted into the seed koji prepared in step 1, and the ventilated koji making process is adopted at 31°C.
[0061] 3. After the koji making is completed, the enzyme activity and spore count ar...
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