Application of dipeptide in increasing content of parastarch in euglena
A technology of paramylon and euglena, applied to single-celled algae, methods based on microorganisms, and the use of added compounds to stimulate growth, etc., can solve the problem of low paramylon content, achieve the effect of solving bottleneck problems and promoting research progress
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[0018] In the present invention, the preparation method of Glu-Ala comprises the following steps: the α-carboxyl group of Glu and the α-amino group of Ala are dehydrated and condensed to form an amide bond to obtain Glu-Ala.
[0019] In the present invention, the preparation method of Asp-Gly comprises the following steps: the α-carboxyl group of Asp and the α-amino group of Gly are dehydrated and condensed to form an amide bond to obtain Glu-Ala.
[0020] In the present invention, the preparation method of Arg-His comprises the following steps: the α-carboxyl group of Arg and the α-amino group of His are dehydrated and condensed to form an amide bond to obtain Glu-Ala.
[0021] In the present invention, the Glu-Ala, Asp-Gly and Arg-His were purchased from Bioengineering (Shanghai) Co., Ltd.
[0022] In the present invention, the application preferably includes the following steps:
[0023] 1) Carry out amplified culture to euglena until the OD of the algae liquid 750 When t...
Embodiment 1
[0045] 1. Source of algal species
[0046] The algal species used in the present invention: Euglena. gracilis CCAP 1224 / 5Z, purchased from CultureCollection of Algae and Protozoa.
[0047] 2. Culture medium composition
[0048] See Table 1 for common media formulations for euglena. Microelements a See Table 2 for the formula. The special medium for euglena is the usual medium for euglena plus 15g / L glucose.
[0049] 3. Algae cultivation method
[0050] Pick euglena from the euglena preservation plate and put it into a 150mL conical flask with 50mL of sterilized euglena common medium for activation. After it is cultivated to the logarithmic phase, transfer it to 1L of fresh euglena common medium solution for further expansion. Cultured, placed in a light incubator, cultured at 23±1°C, and the light intensity was 100±5μmol / m 2 the s 1 , continuous light. The whole operation process was carried out in accordance with the standard microbiological experimental method under ...
Embodiment 2
[0059] Except that Glu-Ala in Comparative Document 1 is replaced by Arg-His, the rest is the same as Example 1.
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