US2018320208A1PendingUtilityA1
Labyrinthulid microorganism capable of producing microbial oil, microbial oil, methods for producing said microorganism and for producing said microbial oil, and uses of said microorganism and said microbial oil
Est. expiryJul 3, 2035(~8.9 yrs left)· nominal 20-yr term from priority
C12P 7/6472C10G 3/00C12P 19/34C12P 7/6427C12N 15/79C12Y 602/01003C12Y 114/19C12R 2001/89C12N 9/1029C12N 1/125C12N 1/12C12N 9/0071C12R 2001/00C12N 1/00C12P 1/00C12N 15/09C12P 7/64Y02P30/20C12N 15/52C12P 7/6432
53
PatentIndex Score
0
Cited by
0
References
0
Claims
Abstract
A Labyrinthulid microorganism capable of producing a PUFA only through the elongase-desaturase pathway. A Labyrinthulid microorganism which has no ability of producing a PUFA through the endogenous PUFA-PKS pathway or has the ability at an extremely weak level and which has an ability of producing a PUFA through the endogenous elongase-desaturase pathway. The Labyrinthulid microorganism is a microorganism belonging to the genus Parietichytrium or Parietichytrium.
Claims
exact text as granted — not AI-modified1 - 39 . (canceled)
40 . Microbial oil that satisfies not less than one condition selected from the group consisting of (a) to (g), the microorganism being a labyrinthulid:
(a) ARA is not less than 5% of a total fatty acid composition; (b) DGLA is not less than 2.5% of the total fatty acid composition; (c) ETA is not less than 0.35% of the total fatty acid composition; (d) EPA is not less than 4% of the total fatty acid composition; (e) n-6 DPA is not greater than 0.20% of the total fatty acid composition; (f) DHA is not greater than 0.50% of the total fatty acid composition; (g) The total of DHA and n-6 DPA is not greater than 0.7% of the total fatty acid composition.
41 . The microbial oil according to claim 40 , wherein the microbial oil satisfies a condition that a value of n-6 DPA/DTA by GC area is not greater than 1.5.
42 . The microbial oil according to claim 40 , wherein the microbial oil satisfies a condition that a value of DHA/n-3 DPA by GC area is not greater than 4.
43 . The microbial oil according to claim 40 , wherein the microbial oil satisfies a condition that a value of C20 PUFA/C22 PUFA by GC area is not less than 0.5 and not greater than 50.
44 . The microbial oil according to claim 40 , wherein the microbial oil satisfies a condition that a value of n-6 PUFA/n-3 PUFA by GC area is not less than 1.8.
45 . The microbial oil according to claim 40 , wherein the labyrinthulid is obtained from a labyrinthulid selected from the group consisting of (A) and (B):
(A) A labyrinthulid in which a fatty acid composition is modified by disruption and/or gene silencing; (B) A labyrinthulid in which a fatty acid composition is modified by transforming a gene in addition to disruption and/or gene silencing.
46 . A microbial oil obtained from a labyrinthulid genetically modified such that a fatty acid composition is modified.
47 . The microbial oil according to claim 46 , wherein the disrupted and/or silenced gene is a PKS gene, a fatty acid elongase gene, and/or a fatty acid desaturase gene.
48 . The microbial oil according to claim 46 , wherein the transformed gene is a fatty acid elongase gene and/or a fatty acid desaturase gene.
49 . The microbial oil according to claim 47 , wherein the fatty acid elongase gene is a C20 elongase gene.
50 . The microbial oil according to claim 47 , wherein the fatty acid desaturase gene is a Δ4 desaturase gene and/or an ω3 desaturase gene.
51 . The microbial oil according to claim 46 , wherein a method for disrupting or transforming a gene of a labyrinthulid is electroporation, a gene gun method, orgene editing.
52 . The microbial oil according to claim 46 , wherein a method for gene silencing of a labyrinthulid is an antisense method or RNA interference.
53 . A microbial oil obtained from a labyrinthulid selected from the group consisting of (C) and (D):
(C) A labyrinthulid having very weak or no activity of producing PUFAs via the PUFA-PKS pathway; (D) A labyrinthulid in which the host PUFA-PKS gene is disrupted or silenced to a very weak level.
54 . The microbial oil according to claim 53 , wherein the labyrinthulid having very weak or no activity of producing PUFAs via the PUFA-PKS pathway is a labyrinthulid belonging to the genus Parietichytrium or genus Schizochytrium.
55 . The microbial oil according to claim 54 , wherein the labyrinthulid belonging to the genus Parietichytrium is a labyrinthulid belonging to Parietichytrium sarkarianum.
56 . The microbial oil according to claim 54 , wherein the labyrinthulid belonging to the genus Schizochytrium is a labyrinthulid belonging to Schizochytrium aggregatum.
57 . The microbial oil according to claim 55 , wherein the microorganism belonging to Parietichytrium sarkarianum is Parietichytrium sp. SEK358 (FERM BP-11405), Parietichytrium sarkarianum SEK364 (FERM BP-11298), or Parietichytrium sp. SEK517 (FERM BP-11406).
58 . The microbial oil according to claim 56 , wherein the microorganism belonging to Schizochytrium aggregatum is Schizochytrium aggregatum ATCC 28209.
59 . The microbial oil according to claim 53 , wherein the labyrinthulid in which the host PUFA-PKS gene is disrupted or silenced to a very weak level belongs to the genus Thraustochytrium.
60 . The microbial oil according to claim 59 , wherein the labyrinthulid belonging to the genus Thraustochytrium is Thraustochytrium aureum.
61 . The microbial oil according to claim 40 , wherein the microbial oil satisfies at least one condition selected from the group consisting of (E) to (H):
(E) A GC area ratio of ARA after modification is not less than 3 times greater than before modification; (F) A GC area ratio of DGLA after modification is not less than 4 times greater than before modification; (G) A GC area ratio of ETA after modification is not less than 7 times greater than before modification; (H) A GC area ratio of EPA after modification is not less than 7 times greater than before modification.
62 . A method for producing the microbial oil described in claim 61 , wherein the microbial oil has a value of n-6 DPA/DTA by GC area of not greater than 1.5.
63 . The method for producing the microbial oil described in claim 61 , wherein the microbial oil has a value of DHA/n-3 DPA by GC area of not greater than 4.
64 . The method for producing microbial oil according to claim 61 , wherein the microbial oil satisfies a condition that a value of C20 PUFA/C22 PUFA by GC area is not less than 0.5 and not greater than 50.
65 . The method for producing microbial oil according to claim 61 , wherein the microbial oil satisfies a condition that a value of n-6 PUFA/n-3 PUFA by GC area is not less than 1.8.
66 . A method for producing microbial oil obtained from a labyrinthulid genetically modified such that a fatty acid composition is modified.
67 . The method for producing microbial oil according to claim 66 , wherein microbial oil is produced in a labyrinthulid genetically modified such that a fatty acid composition is modified, the labyrinthulid being selected from the group consisting of (A) and (B):
(A) A labyrinthulid in which a fatty acid composition is modified by disruption and/or gene silencing gene silencing; (B) A labyrinthulid in which a fatty acid composition is modified by transforming a gene in addition to disruption and/or gene silencing.
68 . The method for producing microbial oil according to claim 67 , wherein the disrupted and/or silenced gene is a PKS gene, a fatty acid elongase gene, and/or a fatty acid desaturase gene.
69 . The method for producing microbial oil according to claim 67 , wherein the transformed gene is a fatty acid elongase gene and/or a fatty acid desaturase gene.
70 . The method for producing microbial oil according to claim 68 , wherein the fatty acid elongase gene is a C20 elongase gene.
71 . The method for producing microbial oil according to claim 68 , wherein the fatty acid desaturase gene is a Δ4 desaturase gene and/or an ω3 desaturase gene.
72 . The method for producing microbial oil according to claim 67 , wherein a method for disrupting or transforming a gene of a labyrinthulid is electroporation, a gene gun method, or gene editing.
73 . The method for producing microbial oil according to claim 67 , wherein a method for gene silencing of a labyrinthulid is an antisense method or RNA interference.
74 . The method for producing microbial oil according to claim 67 , wherein microbial oil is caused to be produced in a labyrinthulid selected from the group consisting of (C) and (D):
(C) A labyrinthulid having very weak or no activity of producing PUFAs via the PUFA-PKS pathway; (D) A labyrinthulid in which the host PUFA-PKS gene is disrupted or silenced to a very weak level.
75 . A method for producing microbial oil that satisfies at least one condition selected from the group consisting of (E) to (H):
(E) A GC area ratio of ARA after modification is not less than 3 times greater than before modification; (F) A GC area ratio of DGLA after modification is not less than 4 times greater than before modification; (G) A GC area ratio of ETA after modification is not less than 7 times greater than before modification; (H) A GC area ratio of EPA after modification is not less than 7 times greater than before modification.
76 . A food, animal feed, medication, or industrial product comprising the microbial oil described in claim 40 as a lipid composition.
77 . A labyrinthulid that is genetically modified such that a produced fatty acid composition is modified and that produces the microbial oil described in claim 40 .
78 . A method for creating the labyrinthulid genetically modified such that a produced fatty acid composition is modified described in claim 77 .Join the waitlist — get patent alerts
Track US2018320208A1 — get alerts on status changes and closely related new filings.
We store only your email — no account needed. See our privacy policy.