Streptomyces Iividans and application thereof
A technology of Streptomyces lividans and strains, applied in the field of bioengineering, to achieve the effect of stable performance and abundant germplasm resources
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Embodiment 1
[0048] Example 1 strain isolation and identification
[0049] (1) Morphological identification
[0050] A blue pigment-producing strain was screened and isolated from a soil sample in a park in Ningbo. After further screening and purification, the strain was inoculated on a plate for culture. After 3 days of culture on the plate, observe the characteristics of the blue pigment-producing colony, and find that the culture characteristics of the strain on Gaoshi No. 1 solid medium are: the growth of the bacteria is slower than that of the bacteria, and colonies begin to appear after 36-48 hours of culture, and can be observed after 60-72 hours to produce blue pigment. The surface of the colony is off-white, the aerial hyphae are lush and fluffy, and the mycelium in the base is blue, which can produce soluble blue pigment (see figure 1 ).
[0051] After further optical microscope and electron microscope observation, we preliminarily judged that the strain was actinomycetes, Gra...
Embodiment 2
[0060] Embodiment 2 bacterial strain fermentation produces blue pigment
[0061] Pick colonies from the test tubes where the strains were preserved for strain activation, and culture them at 37°C for 48 hours; the formula of the activation medium is: 2% soluble starch, 0.05% NaCl, 0.05% K 2 HPO 4 , 0.05%MgSO 4 , 0.001% FeSO 4 , 2% agar.
[0062] Then pick a single colony on the activated plate and transfer it to the seed culture solution for proliferation and culture, and cultivate it at 28°C for 12 hours with a rotation speed of 200r / min; the formula of the seed culture solution is: 2% soluble starch, 0.2% beef extract, 0.05 %NaCl, 0.05%K 2 HPO 4 , 0.05%MgSO 4 , the rest is water, 0.001% FeSO 4 ·7H 2 O.
[0063] Finally, the seed liquid is inoculated into the fermentation culture liquid, and the fermentation culture is carried out. In order to obtain the maximum yield of blue pigment, a series of optimizations were carried out on the components of the fermentation m...
Embodiment 3
[0101] Example 3 Obtain the basic data of blue pigment
[0102] A series of tests were carried out on the crude preparation of the blue pigment prepared in Example 2 to obtain the basic data of the blue pigment.
[0103] (1) Solubility
[0104] Take an equal amount of blue pigment crude preparation and dissolve them in 10mL of absolute ethanol, distilled water, methanol, acetone, dimethyl sulfoxide, ethyl acetate, and petroleum ether. After standing still for 2 hours, observe the solubility and color change.
[0105] (2) UV-Vis spectrum
[0106] Dissolve the crude blue pigment preparation in water, adjust the pH value of the blue pigment aqueous solution to 3, 5, 7, 9, 11, and 13 respectively, and use a UV-2550 ultraviolet-visible spectrophotometer to measure the pH value of the blue pigment in the range of 200-800nm. The blue pigment aqueous solution is scanned to obtain the ultraviolet-visible spectrum of the blue pigment.
[0107] From tests (1) and (2), it can be seen t...
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