Bifidobacterium adolescentis capable of inhibiting filamentous fungi and application of bifidobacterium adolescentis
A technology of filamentous fungi and bifidobacteria, applied in the field of bifidobacteria adolescentis, can solve the problems of short residence time, poor effect of biological control methods, and non-sustainable physical control methods, and achieve good acid stability and high The effect of applying the foreground
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Embodiment 1
[0048] Example 1: Screening, identification, cultivation and observation of Bifidobacterium adolescentic CCFM1108
[0049] 1. Screening
[0050] Take 1g of feces samples from healthy adults in Wuxi area, dilute them with normal saline, spread them on mMRS solid medium, culture them in an anaerobic environment at 37°C for 72 hours, observe and record the colony morphology; pick colonies in mMRS Streak on the solid medium, carry out purification culture at 37°C in an anaerobic environment, and obtain a purified single colony; pick a single colony and streak on the mMRS solid medium, culture anaerobically at 37°C for 48 hours, and test the obtained colony Gram staining (Gram staining method refers to the textbook "Industrial Microbial Breeding" author: Zhuge Jian), record the colony morphology, and investigate the physiological and biochemical characteristics of the strain according to the textbook "Common Bacterial System Identification Manual" (Author: Dong Xiuzhu) , to retain...
Embodiment 2
[0065] Example 2: Effect of Bifidobacterium adolescentic CCFM1108 and its fermentation supernatant on the germination rate of filamentous fungal spores
[0066] 1. The effect of Bifidobacterium adolescentic CCFM1108 on the germination rate of filamentous fungal spores (double-layer plate-growth inhibition method)
[0067] Pick the single colony of Bifidobacterium adolescentic (Bifidobacterium adolescentic) CCFM1108 screened in Example 1 and streak it on the mMRS solid medium, and culture it at 37°C for 48h under anaerobic environment to obtain a single colony; pick a single colony and inoculate it in the mMRS liquid In the culture medium, cultivate at 37° C. for 48 hours under anaerobic environment, repeat this operation 3 times, and obtain the bacterial liquid cultivated to the third generation.
[0068]Use an inoculation loop to inoculate the Penicillium extensa liquid in the ampoule tube on the PDA medium, and incubate at 28°C and 200rpm for 7 days to obtain mycelium and sp...
Embodiment 3
[0083] Embodiment 3: the influence of bifidobacterium adolescentic (Bifidobacterium adolescentic) CCFM1108 fermentation supernatant on the growth of Penicillium expanses mycelium
[0084] Mix the mMRS liquid medium with the PDA medium at a volume ratio of 1:9, 1.5:8.5, 2:8, 2.5:7.5, 3:7 (mMRS liquid medium: PDA medium) to obtain mMRS liquid medium Concentration is respectively the control group mixed solution of 10,15,20,25,30% (v / v); The fermentation supernatant that embodiment 2 obtains is respectively 1:9,1.5:8.5,2:8,2.5: The volume ratio of 7.5, 3:7 (fermentation supernatant: PDA medium) was mixed with PDA medium to obtain experimental groups with fermentation supernatant concentrations of 10, 15, 20, 25, 30% (v / v) respectively Mixed solution; Pour the mixed solution of the control group and the experimental group into the plate respectively; add 10 μL of the Penicillium expanse spore suspension obtained in Example 2 dropwise to the center of the plate, and cultivate it at...
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