New strain of Chryseobacterium sp. And application thereof
A technology of Chryseobacterium and strains, applied in the field of wine-making microorganisms, to achieve the effect of improving the quality of wine body and broad application space
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Embodiment 1
[0036] Example 1 Isolation, screening and identification of a new strain of the genus Aureus sp. WLY-B-L9
[0037] (1) Separation and screening
[0038] The samples taken from the brewing environment of Yibin Wuliangye Co., Ltd. were screened for bacteria using PCA medium. Use a planktonic sampler (Zhejiang Sujing Purification Equipment Co., Ltd., FKC-I type) to sample for one minute (100L air), and the sampling is repeated 3 times. Incubate at 37°C for 3 days, select the colonies on the plate for streaking and culture, and repeat three times until the purified strains are isolated and stored on the slant. The strain was named WLY-B-L9.
[0039] (2) Classification and identification
[0040] 1. Morphological characteristics of strains
[0041] The isolated WLY-B-L9 strain was a gram-negative bacterium, rod-shaped, and the colony on PCA medium was yellow, the surface was moist and smooth, and the edges were irregular.
[0042] 2. Physiological and biochemical properties
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Embodiment 2
[0053] Example 2 Determination of fatty acid of new strain of the genus Aureus spp. WLY-B-L9
[0054] The strain WLY-B-L9 was inoculated in liquid NA medium for activation and cultured to logarithmic growth phase OD 600 =1.8, inoculate 250mL liquid NA medium according to the inoculum volume ratio of 5%, after culturing at 37°C for 3 days, divide the culture medium into 50mL centrifuge tubes, centrifuge at 5000r / min for 10min, discard the supernatant, collect The bacterial cells were sent to the China Industrial Microorganism Culture Collection Center (CICC) for fatty acid composition determination. Detection was performed by thin layer chromatography.
[0055] The results show that the main fatty acid composition is: anteiso-C 15:0 Content is 36.84%, C 15:0 -methyl or anteiso-C 15:0 The isoω9c content is 23.2%, C 15:0 The iso 3OH content was 17.73%.
Embodiment 3
[0056] Example 3 Determination of polar lipids of new strains of the genus Aureus spp. WLY-B-L9
[0057] The strain WLY-B-L9 was inoculated in liquid NA medium for activation and cultured to logarithmic growth phase OD 600 =1.8, inoculate 250mL liquid NA medium according to the inoculum volume ratio of 5%, after culturing at 37°C for 3 days, divide the culture medium into 50mL centrifuge tubes, centrifuge at 5000r / min for 10min, discard the supernatant, collect The bacteria were sent to the China Industrial Microorganism Collection Center (CICC) for the determination of polar lipid components. Detection by gas chromatography.
[0058] The results showed that the main polar lipid components were: phosphatidylethanolamine, aminolipid (UAL 1-3), unidentified aminoglycolipid (UAGL), glycolipid (UL 1-6), glycolipid (GL).
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