Lactobacillus sake capable of reducing nitrite and application of lactobacillus sake in fermented sausages
A technology of lactobacillus sake and nitrite, applied in the directions of lactobacillus, application, fermentation, etc., can solve problems such as safety performance to be improved, increase cost, etc., achieve high polypeptide content and antioxidant performance, improve texture, and excellent color and luster. Effect
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Embodiment 1
[0035] The screening of embodiment 1 nitrite-reducing lactic acid bacteria
[0036] (1) Isolation, purification and colony morphological characteristics of nitrite-reducing lactic acid bacteria strains
[0037] Take pickle juice 0.1mL, carry out gradient dilution with 0.90% sterile saline, the dilution concentration is 10 -1 -10 -6 CFU / mL; solid sausage and salted fish were shredded and soaked in sterile normal saline for 24 hours, and the filtrate was diluted tenfold with sterile normal saline, and the dilution concentration was 10 -1 -10 -6 CFU / mL. After 48 hours of spreading and culturing the treated samples, more colonies appeared, but the colony morphology was relatively simple. After the single colony was streaked and purified repeatedly, 5 strains were isolated, and their numbers were P1, P2, Y1, Y2, and C. The colony size and Gram staining results of the 5 strains were as follows in Table 1 and figure 1 As shown, the 5 strains are all Gram-positive, rod-shaped and c...
Embodiment 2
[0049] Physiological and probiotic properties of embodiment 2 lactic acid bacteria
[0050] (1) Growth curve and determination of acid production capacity
[0051] Growth curve such as image 3 As shown in (A), the bacterial solution of strain P1 became more and more turbid after being cultured for 3 hours, OD 600nm The value began to increase rapidly and entered a stable period after 15h. The logarithmic growth phase of the strain Y1 is 6-15h, and enters the stable phase after 21h. Acid production capacity as image 3 As shown in (B), at the beginning of acid production, the pH values of the two strains were both 5.69±0.01, and as the strains grew, the acid production rate of the two strains accelerated. However, P1 has a faster acid production rate and stronger acid production capacity. This is because P1 enters the logarithmic phase earlier and then the metabolism speed is accelerated, so that the pH value of the bacterial solution drops rapidly. After 24 hours of fin...
Embodiment 3
[0061] The preparation of embodiment 3 astaxanthin nanoparticles
[0062] (1) Extraction of Haematococcus Pluvialls Astaxanthin
[0063] Weigh a certain amount of Haematococcus pluvialis powder, add it to a 0.2mol / L acetic acid-sodium acetate buffer solution with a pH value of 6.0, the concentration ratio is 20:1 (mg / mL), add 0.4mg / mL helicase, Enzymatic hydrolysis at 35°C for 4h. After the enzyme inactivation treatment, the residue was added to absolute ethanol at a ratio of 5:1 (mg / mL), placed in a 50°C water bath for extraction for 1 hour, the supernatant was collected, repeated three times, and filtered through a 0.45 μm syringe filter for later use.
[0064] (2) Preparation of astaxanthin nanoparticles
[0065] After the astaxanthin stock solution was freeze-dried, a certain amount of astaxanthin stock solution was dissolved in food-grade ethanol to prepare Haematococcus pluvialis astaxanthin-ethanol solution. Hilmar 7500 whey protein powder with a protein content of 7...
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