Method of transforming enzyme to prepare L-ornithine
A technology for ornithine and enzyme conversion, applied in the field of L-ornithine preparation, can solve the problems of high cost, long cycle, and difficult separation of L-ornithine, and achieve great industrial significance, safe production operation, and high production efficiency. The effect of mild conditions
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Embodiment 1
[0043] (1) Bacteria slant culture
[0044] Inoculate the slant culture medium of Enterococcus faecalis CGMCC NO.1786 into the test tube to make the slant strain;
[0045] Wherein the bacterial strain slant culture medium is made up of following components by weight:
[0046] 5 parts of glucose, 20 parts of urea, 3.5 parts of corn steep liquor, 1.0 parts of magnesium sulfate, 1.0 parts of dipotassium hydrogen phosphate, 5.0 parts of sodium chloride, 2.0 parts of calcium carbonate, 0.02 parts of iron sulfate, 0.02 parts of manganese sulfate, 15 parts of agar and 1000 parts of water;
[0047] The technological conditions for preparing slant strains are pH value 7.5, temperature 30° C., and culture time 24 hours.
[0048] (2) Inoculation fermentation
[0049] Expand the cultivation of the slant strain as the seed solution;
[0050] Put the seed liquid into the fermenter according to the inoculation amount of 10% to ferment;
[0051] Wherein the seed liquid and the fermented l...
Embodiment 2
[0063] (1) Bacteria slant culture
[0064] Inoculate the slant culture medium of Enterococcus faecalis CGMCC NO.1786 into the test tube to make the slant strain;
[0065] Wherein the bacterial strain slant culture medium is made up of following components by weight:
[0066] 8 parts of glucose, 15 parts of urea, 3.0 parts of corn steep liquor, 1.0 parts of magnesium sulfate, 1.0 parts of dipotassium hydrogen phosphate, 5.0 parts of sodium chloride, 2.0 parts of calcium carbonate, 0.02 parts of iron sulfate, 0.02 parts of manganese sulfate, 15 parts of agar and 1000 parts of water;
[0067] The technological conditions for preparing slant strains are pH value 8.0, temperature 40° C., and incubation time 36 hours.
[0068] (2) Inoculation fermentation
[0069] Expand the cultivation of the slant strain as the seed solution;
[0070] Put the seed liquid into the fermenter according to the inoculation amount of 10% to ferment;
[0071] Wherein the seed liquid and the fermente...
Embodiment 3
[0083] (1) Bacteria slant culture
[0084] Inoculate the slant culture medium of Enterococcus faecalis CGMCC NO.1786 into the test tube to make the slant strain;
[0085] Wherein the bacterial strain slant culture medium is made up of following components by weight:
[0086] 10 parts of glucose, 10 parts of urea, 2.5 parts of corn steep liquor, 1.0 parts of magnesium sulfate, 1.0 parts of dipotassium hydrogen phosphate, 5.0 parts of sodium chloride, 2.0 parts of calcium carbonate, 0.02 parts of iron sulfate, 0.02 parts of manganese sulfate, 15 parts of agar and 1000 parts of water;
[0087] The technological conditions for preparing the slant strain are pH value 7.0, temperature 30° C., and culture time 48 hours.
[0088] (2) Inoculation fermentation
[0089] Expand the cultivation of the slant strain as the seed solution;
[0090] Insert the seed liquid into the fermenter according to the inoculation amount of 15% to ferment;
[0091] Wherein the seed liquid and the ferm...
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