Marasmiellus androsaceus strain and application thereof
A technology of Anluo Xiaopi and strains, applied in the field of microorganisms, can solve the problems of low yield, complicated separation process, and small added value, and achieve high Anluo Xiaopi polysaccharide yield and simple operation
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Embodiment 1
[0029] Embodiment 1 Utilizes the mutagenesis of the starting strain to obtain the mutant strain H123
[0030] The starting strain of Anluo parsley was obtained by tissue separation method, inoculated on the wort fixed slant medium, cultured at 26°C for 48 hours, and then stored in the refrigerator at 4°C for later use. Take 8mL of spore suspension in a 6cm plate, stir it magnetically, and irradiate it with a UV lamp at 30cm for 20s, then perform the first round of irradiation. The first mutant strain was subjected to the second round of ultraviolet radiation mutagenesis for 30 seconds, and the high-yielding strain H125, which grew well and produced high levels of polysaccharides from the umbrella parsley, was obtained through primary and secondary screening.
[0031] The components in the slant medium are calculated by weight percentage: 3% glucose, 1% yeast extract, 1% beef extract, 0.1% sodium chloride, 0.05% potassium dihydrogen phosphate, 1.0% agar powder, and the pH value...
Embodiment 2
[0034] Change the composition of the slant medium, and cultivate the high-yield strain and the starting strain respectively. Each component in the slant culture medium is designed by weight percentage: glucose 2%, yeast extract 2%, beef extract 1%, sodium chloride 0.0%, potassium dihydrogen phosphate 0.05%, agar powder 1.0%, pH value 5.0 to 6.0. The sugar production of the high-yielding strain was increased by 18% compared with the starting strain.
Embodiment 3
[0036] figure 1 Provided is a process flow for producing the polysaccharide of Anluo puffyman in one embodiment.
[0037] Step 1. Cultivate high-yield strain H125
[0038] Step ① Pick from the mother seed test tube, and culture the fresh high-yielding strain H125 in a primary shake flask. In the primary shake flask culture process, 50mL seed culture medium was packed in a 500mL Erlenmeyer shake flask, 23°C, 150rpm shaking culture for 48h, and the primary shake flask strain was obtained.
[0039] In step ②, carry out secondary shake flask culture on the strains of the primary shake flask. Put 200mL of seed culture medium in a 1000mL Erlenmeyer shake flask, insert 50mL of the strain of the first shake flask, and culture at 24°C and 150rpm for 36h with shaking to obtain the strain of the second shake flask.
[0040] Step ③ Carry out primary seed culture on the secondary shake flask strain. The secondary shake flask strains were inserted into the 100L fully automatic fermenter...
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