Method for producing fermented carotenoid using carotenoid-producing bacteria obtained by using cobalt-containing culturing medium
The present invention provides a method for high yield and stable production of carotenoids through microbial culture. The present invention provides a method for culture of carotenoid-producing bacteria, which comprises culturing carotenoid-producing bacteria in a medium containing cobalt or a cobalt salt at a concentration of 0.005 μmol/L to 20 μmol/L.
1. A method for stable preparation of microbial cells containing carotenoids in an amount of at least 36 mg/g in dry microbial cells, comprising culturing bacteria belonging to the genus Paracoccus in a medium containing cobalt or a cobalt salt at a concentration of 0.005 μmol/L to 7 μmol/L, wherein the culturing step is carried out by aeration spinner culture.
2. The method of claim 1 , wherein the cobalt or cobalt salt has been added at a concentration of 0.005 μmol/L to 7 μmol/L in the medium.
3. The method according to claim 1 , wherein the carotenoids comprise at least one selected from the group consisting of astaxanthin, canthaxanthin, zeaxanthin, β-cryptoxanthin, lycopene, β-carotene, adonirubin, adonixanthin, echinenone, asteroidenone and 3-hydroxyechinenone.
4. The method according to claim 1 , wherein the bacteria belonging to the genus Paracoccus are those comprising DNA which corresponds to 16S ribosomal RNA and whose nucleotide sequence shares a homology of 95% or higher with the nucleotide sequence shown in SEQ ID NO: 1.
5. The method according to claim 1 , wherein the bacteria belonging to the genus Paracoccus are those of the strain E-396 (FERM BP-4283) or the strain A-581-1 (FERM BP-4671) or a mutant strain thereof.
6. A method for production of carotenoids, comprising culturing bacteria belonging to the genus Paracoccus in a medium containing cobalt or a cobalt salt at a concentration of 0.005 μmol/L to 7 μmol/L to thereby obtain microbial cells containing carotenoids in an amount of at least 36 mg/g in dry microbial cells, and collecting the carotenoids from the cultured product containing the microbial cells, wherein the culturing step is carried out by aeration spinner culture.
7. The method of claim 6 , wherein the cobalt or cobalt salt has been added at a concentration of 0.005 μmol/L to 7 μmol/L in the medium.
8. The method according to claim 6 , wherein the carotenoids comprise at least one selected from the group consisting of astaxanthin, canthaxanthin, zeaxanthin, β-cryptoxanthin, lycopene, β-carotene, adonirubin, adonixanthin, echinenone, asteroidenone and 3-hydroxyechinenone.
9. The method according to claim 6 , wherein the bacteria belonging to the genus Paracoccus are those comprising DNA which corresponds to 16S ribosomal RNA and whose nucleotide sequence shares a homology of 95% or higher with the nucleotide sequence shown in SEQ ID NO: 1.
10. The method according to claim 6 , wherein the bacteria belonging to the genus Paracoccus are those of the strain E-396 (FERM BP-4283) or the strain A-581-1 (FERM BP-4671) or a mutant strain thereof.
11. A method for stabilization of carotenoid levels in microbial cells such that carotenoids are contained in an amount of at least 36 mg/g in dry microbial cells, comprising culturing bacteria belonging to the genus Paracoccus in a medium containing cobalt or a cobalt salt at a concentration of 0.005 μmol/L to 7 μmol/L, wherein the culturing step is carried out by aeration spinner culture.
12. The method of claim 11 , wherein the cobalt or cobalt salt has been added at a concentration of 0.005 μmol/L to 7 μmol/L in the medium.
13. The method according to claim 11 , wherein the carotenoids comprise at least one selected from the group consisting of astaxanthin, canthaxanthin, zeaxanthin, β-cryptoxanthin, lycopene, β-carotene, adonirubin, adonixanthin, echinenone, asteroidenone and 3-hydroxyechinenone.
14. The method according to claim 11 , wherein the bacteria belonging to the genus Paracoccus are those comprising DNA which corresponds to 16S ribosomal RNA and whose nucleotide sequence shares a homology of 95% or higher with the nucleotide sequence shown in SEQ ID NO: 1.
15. The method according to claim 11 , wherein the bacteria belonging to the genus Paracoccus are those of the strain E-396 (FERM BP-4283) or the strain A-581-1 (FERM BP-4671) or a mutant strain thereof.
16. The method of claim 1 , wherein the bacteria belonging to the genus Paracoccus are at least one selected from the group consisting of Paracoccus carotinifaciens, Paracoccus marcusii, Paracoccus haeundaensis and Paracoccus zeaxanthinifaciens.
17. The method of claim 6 , wherein the bacteria belonging to the genus Paracoccus are at least one selected from the group consisting of Paracoccus carotinifaciens, Paracoccus marcusii, Paracoccus haeundaensis and Paracoccus zeaxanthinifaciens.
18. The method of claim 11 , wherein the bacteria belonging to the genus Paracoccus are at least one selected from the group consisting of Paracoccus carotinifaciens, Paracoccus marcusii, Paracoccus haeundaensis and Paracoccus zeaxanthinifaciens.