Bacillus amyloliquefaciens for inhibiting soy sauce from forming albuginea and application of bacillus amyloliquefaciens
A technology of amylolytic spores and bacilli, which is applied in the field of microorganisms, and can solve problems such as the reduction of soy sauce quality
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Embodiment 1
[0038]Embodiment 1: Powdered Pichia pastoris produces white film in soy sauce and culture medium
[0039] Take 250mL of fermented soy sauce and 250mL of YPD medium, respectively with 1.0×10 5 CFU / mL was added with powdered Pichia pastoris CM-1, and no strain was added as a negative control. Static fermentation at 30°C for 3 days, compared with the control without adding Pichia powder. Adding powdered Pichia pastoris to the medium and soy sauce produced white film (such as figure 1 ).
Embodiment 2
[0040] Embodiment 2: Powdery Pichia pastoris produces albuginea and growth situation under different conditions
[0041] (1) Growth and film production of Pichia powder under different sodium chloride concentrations
[0042] Inoculate the strain in YPD liquid, culture it statically at 30°C for 3 days, take 1mL of the bacterial liquid for 10000r·min -1 Centrifuge for 10 min. Wash twice with 0.8% (w:v) sterile physiological saline, resuspend with 1mL sterile water, add the bacterial solution to 0%, 5 %, 10%, 15%, 20% NaCl in the YPD medium, 30 ℃ static culture, the number of viable bacteria at the beginning and end of the culture is expressed in C 0 and C 1 Indicates that the unit is CFU·mL -1 , relative growth rate=(lg C 1 -lg C 0 ) / twenty four. The results showed that the relative growth rate decreased gradually with the increase of salt concentration, but at a salt concentration of 18%, Pichia powderylum CM-1 could also maintain a relative growth rate of 45%, which pro...
Embodiment 3
[0049] Embodiment 3: Inhibit the screening of powdery Pichia pastoris to produce Bacillus amyloliquefaciens
[0050] Take 5g of soy mash in 100mL beef extract-peptone liquid medium with glass beads, shake well, and culture at 37°C for 1-3 days; centrifuge the supernatant of the cultured bacterial liquid at 4°C and 12000rpm for 5min, and take supernatant; the supernatant was serially diluted 10 -2 、10 -3 、10 -4 、10 -5 、10 -6 , absorb 0.1mL of each gradient bacterial solution and spread it on the beef extract peptone medium respectively, and incubate at 37°C for 1-3 days; pick different forms of colonies to streak on the beef extract peptone solid medium, and then culture at 30°C 1-3d until colonies grow; follow the above steps to streak and isolate 3 times to obtain a single colony of each strain. The single colony was cultured in liquid, and the inoculation amount of 1% was inserted into the medium with powdered Pichia pastoris, and the culture was static for 3 days, and ...
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