Method for preserving a microorganism
A method for preservation of a microorganism capable of microbial production of a polyunsaturated fatty acid or a compound comprising a polyunsaturated fatty acid as a constituent fatty acid, which method comprises: (a) forming spores in a spore-forming medium at pH 4-7 containing a nutrient source comprising an inorganic salt and a saccharide; (b) suspending the spores obtained in (a) in sterilized water, or sterilized water containing a surfactant and/or an inorganic salt to prepare a spore suspension, and adding a cryoprotectant at 5-15% to prepare a cryopreserving spore suspension; and (c) preserving the cryopreserving spore suspension obtained in (b) at between −100° C. and −20° C.
1. A method for preservation of a spore-forming microorganism capable of microbial production of a polyunsaturated fatty acid or a compound comprising a polyunsaturated fatty acid as a constituent fatty acid, wherein the spore-forming microorganism is Mortierella alpina , which method comprises:
(a) culturing the microorganism in a spore-forming medium at pH 4-7 containing a nutrient source comprising an inorganic salt and a saccharide, wherein the microorganism forms spores;
(b) suspending the spores obtained in (a) in sterilized water, or sterilized water containing a surfactant and/or an inorganic salt to prepare a spore suspension, and adding a cryoprotectant at 5-15% to prepare a cryopreserving spore suspension; and
(c) preserving the cryopreserving spore suspension obtained in (b) at between −100° C. and −20° C.
2. A method according to claim 1 , wherein said inorganic salt is at least one type of inorganic salt selected from the group consisting of sodium nitrate, dipotassium hydrogen phosphate, magnesium sulfate, potassium chloride and iron (II) sulfate.
3. A method according to claim 1 , characterized in that said spore-forming medium is Czapek agar medium or Czapek-Dox agar medium adjusted to a pH of 4-7 with hydrochloric acid and/or sulfuric acid.
4. A method according to claim 1 , characterized in that said cryoprotectant is glycerin.
5. A method for preservation of a microorganism according to claim 1 , wherein the microorganism is capable of producing a triglyceride comprising a polyunsaturated fatty acid as a constituent fatty acid or a phospholipid comprising a polyunsaturated fatty acid as a constituent fatty acid.
6. A method for preservation of a microorganism according to claim 1 , wherein the microorganism is capable of producing an ω6 unsaturated fatty acid, ω3 polyunsaturated fatty acid, ω9 polyunsaturated fatty acid, or a combination thereof, or a compound comprising an ω6 unsaturated fatty acid, ω3 polyunsaturated fatty acid, ω9 polyunsaturated fatty acid, or a combination thereof.
7. A method for preservation of a microorganism according to claim 6 , wherein the ω6 unsaturated fatty acid is 9,12-octadecadienoic acid (linoleic acid) 18:2ω6, 6,9,12-octadecatrienoic acid (γ-linolenic acid) 18:3ω6, 8,11,14-eicosatrienoic acid (dihomo-γ-linolenic acid) 20:3ω6, 5,8,11,14-eicosatetraenoic acid (arachidonic acid) 20:4ω6, 7,10,13,16-docosatetraenoic acid 22:4ω6 or 4,7,10,13,16-docosapentaenoic acid 22:5ω6.
8. A method for preservation of a microorganism according to claim 6 , wherein the ω3 unsaturated fatty acid is 9,12,15-octadecatrienoic acid α-linolenic acid) 18:3ω3, 6,9,12,15-octadecatetraenoic acid (stearidonic acid) 18:4ω3, 11,14,17-eicosatrienoic acid (dihomo-α-linolenic acid) 20:3ω3, 8,11,14,17-eicosatetraenoic acid 20:4ω3, 5,8,11,14,17-eicosapentaenoic acid 20:5ω3, 7,10,13,16,19-docosapentaenoic acid 22:5ω3 or 4,7,10,13,16,19-docosahexaenoic acid 22:6ω3.
9. A method for preservation of a microorganism according to claim 6 , wherein the ω9 unsaturated fatty acid is 6,9-octadecadienoic acid 18:2ω9, 8,11-eicosadienoic acid 20:2ω9 or 5,8,11-eicosatrienoic acid (Mead acid) 20:3ω9.