A strain of Bifidobacterium longum and its application in inhibiting filamentous fungi
A technology of Bifidobacterium longum and filamentous fungi, applied in the direction of bifidobacteria, applications, fungi, etc., can solve the problems of short residence time, non-sustainable physical control methods, and poor effects of biological control methods, achieving Effect of good acid stability
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Embodiment 1
[0051] Example 1: Bifidobacterium longum (Bifidobacterium longum) screening, identification, culture and observation
[0052] 1 screening
[0053] 1g taken from healthy adult Wuxi in stool samples, after diluted with saline gradient coating on a solid medium mMRS, anaerobic conditions at 37 ℃ 72h culture, colony morphology observed and recorded; Colonies were picked in mMRS streaked onto solid medium and purified cultured at 37 [deg.] C in anaerobic environment, the purified single colonies; single colony was picked mMRS streaked on solid medium, 37 [deg.] C anaerobic culture 48h, the resulting colonies were leather Gram stain (Gram stain method reference textbook "industrial Microbiology breeding" author: Zhuge Jian forward), recorded colony morphology, and according to the textbook "common bacterial systems identification Handbook" (author: East Xiuzhu) physiological and biochemical characteristics of the study strains reserved Gram positive colonies are smooth, rounded, catalas...
Embodiment 2
[0068] Example 2: Effect of Bifidobacterius CCFM1109 and its fermentation supernatant on spore rate of filamentous fungus
[0069] 1. Effect of Bifidobacterius CCFM1109 on spore rate of filamentous fungus (double flat plate - growth inhibition)
[0070] Picking Example 1 Single Silition of the Bifidobacterius CCFM1109 of Example 1 was discharged from the MMRS solid medium, and the anaerobic environment was cultured at 37 ° C for 48 h, resulting in a single colony; picking a single bacterius into the MMRS liquid In the medium, 37 ° C in an anaerobic environment was cultured for culture, and this operation was repeated 3 times to obtain a bacterial liquid culture to the third generation.
[0071] The expanded pyrectomer in the inoculated ring was inoculated into PDA medium, 28 ° C, 200 rpm culture 7d, resulting in mycelial body and spores; picking spores on the PDA slope, 28 ° C, 200 rpm culture 7d, This operation was repeated 2 times to obtain a third generation of extension pupil;...
Embodiment 3
[0086] Example 3: Effect of Bifidobacterius CCFM1109 Fermented Supermourization on Growth of Filamentous Fungal Fungi
[0087] MMRS liquid medium was mixed with PDA medium in 1: 9, 1.5: 8.5, 2: 8, 2.5: 7.5, 3: 7 (MMRS liquid medium: PDA medium), respectively. The concentration of 10, 15, 20, 20, 30% (v / v) control group mixed liquid; the fermentation supernatant obtained in Example 2 was 1: 9, 1.5: 8.5, 2: 8, 2.5, respectively: The volume ratio of 7.5, 3: 7 (fermented supernatant: PDA medium) is mixed with PDA medium to obtain an experimental group of 10, 15, 20, 25, 30% (V / V), respectively. The mixture was mixed; the mixture of the control group and the experimental group was poured; 10 μl of the expanded Popular spore suspension obtained by adding 10 μl of Example 2, at 28 ° C, during culture, and measured each tablet through each 2D measurement The fungus diameter, detecting the effect of Bifidobacterium CCFM1109 fermentation supernatant on the growth of the polyfusions, the...
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Abstract
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