Blue pigment producing bacteria and method for preparing crude preparation by using the same
A blue pigment and preparation technology, applied in the field of bioengineering, can solve the problem that the type and quantity cannot meet the needs of the research and development of natural blue pigment
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Embodiment 1
[0021] Embodiment 1: the cultivation of Flavobacterium sp.B29 CGMCC No.3699
[0022] The preserved Flavobacterium sp.B29 (Flavobacterium sp.B29) CGMCC No.3699 is subcultured and activated on the PDA medium, and whether there is contamination by bacteria while detecting the color change of the colony; the activated bacterial strain is inoculated in the liquid TGY medium ( No agar), the liquid culture medium filling volume is 100mL / bottle (500mL Erlenmeyer flask), 25 ℃ of constant temperature, culture 72 hours under 200rpm, observe thalline growth and color change.
[0023] Flavobacterium sp.B29 CGMCC No.3699 culture experiments showed that white, moist colonies were first formed on the surface of TGY medium, and then gradually formed wrinkled, dry blue to blue-purple colonies; in liquid TGY medium, cultured Obvious white cells appeared in 24 hours, and the cells appeared blue after 72 hours.
Embodiment 2
[0024] Example 2: Preparation and light-absorbing properties of blue pigment crude preparation
[0025] Flavobacterium sp.B29 (Flavobacterium sp.B29) CGMCC No.3699 fermentation broth obtained as in Example 1, with 8000rpm, 3min centrifugation process to obtain the thalline, add 50mL 50% ethanol solution with the thalline obtained by per 100mL fermentation culture , 100rpm vibration extraction treatment for 1 hour, and then 8000rpm, 5min centrifugation, the obtained supernatant is the ethanol extract of blue pigment; the ethanol extract is placed at a constant temperature of 60°C for vacuum concentration and straight drying, and the obtained is blue pigment Pigment crude extract. The obtained blue pigment crude extract was dissolved in 50% ethanol solution, and a scanning analysis of 200-800nm was carried out using a UV spectrophotometer. For the analysis results, see the attached figure 1 shown.
[0026] When analyzing the result table, the blue pigment produced by Flavoba...
Embodiment 3
[0027] Embodiment 3: Quantitative detection of blue pigment crude preparation
[0028] According to the method described in Example 2, the blue pigment crude preparation of Flavobacterium sp.B29 (Flavobacterium sp.B29) CGMCCNo.3699 was obtained and carried out vacuum freeze-drying to remove moisture; Accurately weigh the preparation of 1.000g dry treatment, use 50% The ethanol solution was fully dissolved, and the volume was adjusted to 100mL to prepare a blue pigment mother solution of 250mg / L; further dilution treatment was prepared to prepare a series of blue pigment solutions of 50, 100, 150, 200, and 250mg / L, and the blue pigment solution was prepared at a wavelength of 579nm Measure the absorbance value; draw the concentration-absorbance value standard curve with the blue pigment concentration as the horizontal axis and the absorbance value at 579nm wavelength as the vertical axis.
[0029] For the measurement results of the corresponding relationship between the concent...
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