UA61880C2 - SYNTHESIS OF g-LINOLENIC ACID UNDER THE ACTION OF DELTA-6-DESATURASE - Google Patents
SYNTHESIS OF g-LINOLENIC ACID UNDER THE ACTION OF DELTA-6-DESATURASE Download PDFInfo
- Publication number
- UA61880C2 UA61880C2 UA97063197A UA97063197A UA61880C2 UA 61880 C2 UA61880 C2 UA 61880C2 UA 97063197 A UA97063197 A UA 97063197A UA 97063197 A UA97063197 A UA 97063197A UA 61880 C2 UA61880 C2 UA 61880C2
- Authority
- UA
- Ukraine
- Prior art keywords
- desaturase
- gamma
- plant
- linolenic acid
- acid
- Prior art date
Links
- 102100034544 Acyl-CoA 6-desaturase Human genes 0.000 title claims 2
- 108010037138 Linoleoyl-CoA Desaturase Proteins 0.000 title claims 2
- 230000015572 biosynthetic process Effects 0.000 title description 13
- 238000003786 synthesis reaction Methods 0.000 title description 13
- 230000009471 action Effects 0.000 title description 5
- 229960004488 linolenic acid Drugs 0.000 title description 5
- 108090000623 proteins and genes Proteins 0.000 claims abstract description 58
- 150000007523 nucleic acids Chemical class 0.000 claims abstract description 29
- 108020004707 nucleic acids Proteins 0.000 claims abstract description 28
- 102000039446 nucleic acids Human genes 0.000 claims abstract description 28
- 238000004519 manufacturing process Methods 0.000 claims abstract 5
- VZCCETWTMQHEPK-QNEBEIHSSA-N gamma-linolenic acid Chemical compound CCCCC\C=C/C\C=C/C\C=C/CCCCC(O)=O VZCCETWTMQHEPK-QNEBEIHSSA-N 0.000 claims description 71
- VZCCETWTMQHEPK-UHFFFAOYSA-N gamma-Linolensaeure Natural products CCCCCC=CCC=CCC=CCCCCC(O)=O VZCCETWTMQHEPK-UHFFFAOYSA-N 0.000 claims description 70
- 235000020664 gamma-linolenic acid Nutrition 0.000 claims description 70
- 229960002733 gamolenic acid Drugs 0.000 claims description 69
- 241000196324 Embryophyta Species 0.000 claims description 64
- 238000000034 method Methods 0.000 claims description 57
- 239000013598 vector Substances 0.000 claims description 48
- 210000004027 cell Anatomy 0.000 claims description 36
- 244000061176 Nicotiana tabacum Species 0.000 claims description 29
- 235000002637 Nicotiana tabacum Nutrition 0.000 claims description 29
- 230000009466 transformation Effects 0.000 claims description 19
- OYHQOLUKZRVURQ-HZJYTTRNSA-N Linoleic acid Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC(O)=O OYHQOLUKZRVURQ-HZJYTTRNSA-N 0.000 claims description 18
- 235000020778 linoleic acid Nutrition 0.000 claims description 17
- OYHQOLUKZRVURQ-IXWMQOLASA-N linoleic acid Natural products CCCCC\C=C/C\C=C\CCCCCCCC(O)=O OYHQOLUKZRVURQ-IXWMQOLASA-N 0.000 claims description 15
- 239000002773 nucleotide Substances 0.000 claims description 15
- 125000003729 nucleotide group Chemical group 0.000 claims description 15
- 235000010469 Glycine max Nutrition 0.000 claims description 11
- 244000068988 Glycine max Species 0.000 claims description 10
- 230000001965 increasing effect Effects 0.000 claims description 10
- 244000020551 Helianthus annuus Species 0.000 claims description 8
- 235000003222 Helianthus annuus Nutrition 0.000 claims description 8
- 239000013604 expression vector Substances 0.000 claims description 8
- LGHXTTIAZFVCCU-SSVNFBSYSA-N (2E,4E,6E,8E)-octadeca-2,4,6,8-tetraenoic acid Chemical compound CCCCCCCCC\C=C\C=C\C=C\C=C\C(O)=O LGHXTTIAZFVCCU-SSVNFBSYSA-N 0.000 claims description 7
- 244000105624 Arachis hypogaea Species 0.000 claims description 7
- 240000002791 Brassica napus Species 0.000 claims description 7
- 244000000626 Daucus carota Species 0.000 claims description 7
- 235000002767 Daucus carota Nutrition 0.000 claims description 7
- 240000008042 Zea mays Species 0.000 claims description 7
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 claims description 7
- 235000002017 Zea mays subsp mays Nutrition 0.000 claims description 7
- 235000005822 corn Nutrition 0.000 claims description 7
- 235000020232 peanut Nutrition 0.000 claims description 7
- 235000017060 Arachis glabrata Nutrition 0.000 claims description 6
- 235000010777 Arachis hypogaea Nutrition 0.000 claims description 6
- 235000018262 Arachis monticola Nutrition 0.000 claims description 6
- 125000003275 alpha amino acid group Chemical group 0.000 claims description 6
- 238000011069 regeneration method Methods 0.000 claims description 6
- 230000001580 bacterial effect Effects 0.000 claims description 5
- 230000008929 regeneration Effects 0.000 claims description 5
- 241000894006 Bacteria Species 0.000 claims description 4
- 241000233866 Fungi Species 0.000 claims description 4
- 241001465754 Metazoa Species 0.000 claims description 4
- 230000001939 inductive effect Effects 0.000 claims description 4
- 210000004102 animal cell Anatomy 0.000 claims description 3
- 101710202365 Napin Proteins 0.000 claims description 2
- 108010083391 glycinin Proteins 0.000 claims description 2
- 235000006008 Brassica napus var napus Nutrition 0.000 claims 3
- 240000007817 Olea europaea Species 0.000 claims 3
- 230000006698 induction Effects 0.000 claims 3
- 230000002538 fungal effect Effects 0.000 claims 2
- 238000012876 topography Methods 0.000 claims 1
- 230000009261 transgenic effect Effects 0.000 abstract description 29
- 108091026890 Coding region Proteins 0.000 abstract description 14
- 239000002253 acid Substances 0.000 abstract description 9
- 238000010276 construction Methods 0.000 abstract description 7
- 230000001105 regulatory effect Effects 0.000 abstract description 7
- 150000007513 acids Chemical class 0.000 abstract description 2
- 108020004414 DNA Proteins 0.000 description 75
- 150000001413 amino acids Chemical class 0.000 description 51
- 239000012634 fragment Substances 0.000 description 33
- 239000002299 complementary DNA Substances 0.000 description 28
- 235000021537 Beetroot Nutrition 0.000 description 27
- 235000014113 dietary fatty acids Nutrition 0.000 description 25
- 239000000194 fatty acid Substances 0.000 description 25
- 229930195729 fatty acid Natural products 0.000 description 25
- 150000004665 fatty acids Chemical class 0.000 description 23
- 239000000243 solution Substances 0.000 description 16
- 241000192700 Cyanobacteria Species 0.000 description 15
- 238000001030 gas--liquid chromatography Methods 0.000 description 15
- 239000002609 medium Substances 0.000 description 13
- 108700026244 Open Reading Frames Proteins 0.000 description 11
- 239000013612 plasmid Substances 0.000 description 11
- 238000004458 analytical method Methods 0.000 description 10
- 210000001519 tissue Anatomy 0.000 description 10
- 238000009396 hybridization Methods 0.000 description 9
- 229910052751 metal Inorganic materials 0.000 description 9
- 239000002184 metal Substances 0.000 description 9
- 238000012546 transfer Methods 0.000 description 9
- 239000004165 Methyl ester of fatty acids Substances 0.000 description 8
- YZXBAPSDXZZRGB-DOFZRALJSA-N arachidonic acid Chemical compound CCCCC\C=C/C\C=C/C\C=C/C\C=C/CCCC(O)=O YZXBAPSDXZZRGB-DOFZRALJSA-N 0.000 description 8
- 235000019387 fatty acid methyl ester Nutrition 0.000 description 8
- 239000012528 membrane Substances 0.000 description 8
- 102000004169 proteins and genes Human genes 0.000 description 8
- 210000001938 protoplast Anatomy 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 108091032973 (ribonucleotides)n+m Proteins 0.000 description 7
- 108091028043 Nucleic acid sequence Proteins 0.000 description 7
- 150000002632 lipids Chemical class 0.000 description 7
- 239000000523 sample Substances 0.000 description 7
- 108010076504 Protein Sorting Signals Proteins 0.000 description 6
- 238000004817 gas chromatography Methods 0.000 description 6
- 210000002729 polyribosome Anatomy 0.000 description 6
- 108090000765 processed proteins & peptides Proteins 0.000 description 6
- 230000002194 synthesizing effect Effects 0.000 description 6
- OYHQOLUKZRVURQ-NTGFUMLPSA-N (9Z,12Z)-9,10,12,13-tetratritiooctadeca-9,12-dienoic acid Chemical compound C(CCCCCCC\C(=C(/C\C(=C(/CCCCC)\[3H])\[3H])\[3H])\[3H])(=O)O OYHQOLUKZRVURQ-NTGFUMLPSA-N 0.000 description 5
- 108090000790 Enzymes Proteins 0.000 description 5
- 102000004190 Enzymes Human genes 0.000 description 5
- 241001625930 Luria Species 0.000 description 5
- 210000002472 endoplasmic reticulum Anatomy 0.000 description 5
- 235000004977 Brassica sinapistrum Nutrition 0.000 description 4
- 229930193140 Neomycin Natural products 0.000 description 4
- 235000021342 arachidonic acid Nutrition 0.000 description 4
- 229940114079 arachidonic acid Drugs 0.000 description 4
- 208000027697 autoimmune lymphoproliferative syndrome due to CTLA4 haploinsuffiency Diseases 0.000 description 4
- 238000010367 cloning Methods 0.000 description 4
- 230000021615 conjugation Effects 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 229960004927 neomycin Drugs 0.000 description 4
- 239000002243 precursor Substances 0.000 description 4
- 238000012163 sequencing technique Methods 0.000 description 4
- 238000010561 standard procedure Methods 0.000 description 4
- 244000089742 Citrus aurantifolia Species 0.000 description 3
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 3
- 108020004635 Complementary DNA Proteins 0.000 description 3
- 241001464430 Cyanobacterium Species 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 3
- 235000011941 Tilia x europaea Nutrition 0.000 description 3
- 230000003115 biocidal effect Effects 0.000 description 3
- 210000003763 chloroplast Anatomy 0.000 description 3
- 238000004587 chromatography analysis Methods 0.000 description 3
- 238000003776 cleavage reaction Methods 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 239000013601 cosmid vector Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 125000005313 fatty acid group Chemical group 0.000 description 3
- 238000002955 isolation Methods 0.000 description 3
- 239000004571 lime Substances 0.000 description 3
- 230000014759 maintenance of location Effects 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 102000004196 processed proteins & peptides Human genes 0.000 description 3
- 239000012925 reference material Substances 0.000 description 3
- 230000007017 scission Effects 0.000 description 3
- 238000012216 screening Methods 0.000 description 3
- 241000894007 species Species 0.000 description 3
- 238000001890 transfection Methods 0.000 description 3
- 238000005406 washing Methods 0.000 description 3
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 2
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 2
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 2
- 201000001320 Atherosclerosis Diseases 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 241000972773 Aulopiformes Species 0.000 description 2
- 235000016068 Berberis vulgaris Nutrition 0.000 description 2
- 241000335053 Beta vulgaris Species 0.000 description 2
- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- 229930195725 Mannitol Natural products 0.000 description 2
- 241001318330 Nenia Species 0.000 description 2
- 206010028980 Neoplasm Diseases 0.000 description 2
- 239000005642 Oleic acid Substances 0.000 description 2
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 2
- 229910019567 Re Re Inorganic materials 0.000 description 2
- 108020004511 Recombinant DNA Proteins 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 241000251539 Vertebrata <Metazoa> Species 0.000 description 2
- 241000700605 Viruses Species 0.000 description 2
- 239000003242 anti bacterial agent Substances 0.000 description 2
- 238000005119 centrifugation Methods 0.000 description 2
- HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 description 2
- 230000000295 complement effect Effects 0.000 description 2
- 238000005520 cutting process Methods 0.000 description 2
- 235000005911 diet Nutrition 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 230000002068 genetic effect Effects 0.000 description 2
- 125000000623 heterocyclic group Chemical group 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 230000002209 hydrophobic effect Effects 0.000 description 2
- 238000011534 incubation Methods 0.000 description 2
- 208000015181 infectious disease Diseases 0.000 description 2
- 238000011081 inoculation Methods 0.000 description 2
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 2
- 229960000318 kanamycin Drugs 0.000 description 2
- 229930027917 kanamycin Natural products 0.000 description 2
- SBUJHOSQTJFQJX-NOAMYHISSA-N kanamycin Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CN)O[C@@H]1O[C@H]1[C@H](O)[C@@H](O[C@@H]2[C@@H]([C@@H](N)[C@H](O)[C@@H](CO)O2)O)[C@H](N)C[C@@H]1N SBUJHOSQTJFQJX-NOAMYHISSA-N 0.000 description 2
- 229930182823 kanamycin A Natural products 0.000 description 2
- 238000009630 liquid culture Methods 0.000 description 2
- 239000000594 mannitol Substances 0.000 description 2
- 235000010355 mannitol Nutrition 0.000 description 2
- 238000004949 mass spectrometry Methods 0.000 description 2
- 230000001404 mediated effect Effects 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 2
- 238000004806 packaging method and process Methods 0.000 description 2
- 230000010152 pollination Effects 0.000 description 2
- 229920001184 polypeptide Polymers 0.000 description 2
- 235000020777 polyunsaturated fatty acids Nutrition 0.000 description 2
- 150000003180 prostaglandins Chemical class 0.000 description 2
- 235000019515 salmon Nutrition 0.000 description 2
- 230000035945 sensitivity Effects 0.000 description 2
- 239000013605 shuttle vector Substances 0.000 description 2
- 239000001509 sodium citrate Substances 0.000 description 2
- NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 description 2
- FQENQNTWSFEDLI-UHFFFAOYSA-J sodium diphosphate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]P([O-])(=O)OP([O-])([O-])=O FQENQNTWSFEDLI-UHFFFAOYSA-J 0.000 description 2
- 229940048086 sodium pyrophosphate Drugs 0.000 description 2
- 235000019818 tetrasodium diphosphate Nutrition 0.000 description 2
- 239000001577 tetrasodium phosphonato phosphate Substances 0.000 description 2
- 230000001131 transforming effect Effects 0.000 description 2
- 241001515965 unidentified phage Species 0.000 description 2
- OVSKIKFHRZPJSS-DOMIDYPGSA-N 2-(2,4-dichlorophenoxy)acetic acid Chemical compound OC(=O)[14CH2]OC1=CC=C(Cl)C=C1Cl OVSKIKFHRZPJSS-DOMIDYPGSA-N 0.000 description 1
- TVZRAEYQIKYCPH-UHFFFAOYSA-N 3-(trimethylsilyl)propane-1-sulfonic acid Chemical compound C[Si](C)(C)CCCS(O)(=O)=O TVZRAEYQIKYCPH-UHFFFAOYSA-N 0.000 description 1
- NUKYPUAOHBNCPY-UHFFFAOYSA-N 4-aminopyridine Chemical compound NC1=CC=NC=C1 NUKYPUAOHBNCPY-UHFFFAOYSA-N 0.000 description 1
- 101100325756 Arabidopsis thaliana BAM5 gene Proteins 0.000 description 1
- 101100063253 Aspergillus desertorum desS gene Proteins 0.000 description 1
- 241000726103 Atta Species 0.000 description 1
- 241000786798 Atya Species 0.000 description 1
- 241000701489 Cauliflower mosaic virus Species 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 description 1
- 239000003155 DNA primer Substances 0.000 description 1
- 230000006820 DNA synthesis Effects 0.000 description 1
- 108700039691 Genetic Promoter Regions Proteins 0.000 description 1
- 108700007698 Genetic Terminator Regions Proteins 0.000 description 1
- 208000035150 Hypercholesterolemia Diseases 0.000 description 1
- 206010020649 Hyperkeratosis Diseases 0.000 description 1
- 241000124008 Mammalia Species 0.000 description 1
- 108091034117 Oligonucleotide Proteins 0.000 description 1
- 108020005187 Oligonucleotide Probes Proteins 0.000 description 1
- 102100026747 Osteomodulin Human genes 0.000 description 1
- 101710114565 Osteomodulin Proteins 0.000 description 1
- 108010029182 Pectin lyase Proteins 0.000 description 1
- 240000004713 Pisum sativum Species 0.000 description 1
- 235000010582 Pisum sativum Nutrition 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 235000001537 Ribes X gardonianum Nutrition 0.000 description 1
- 235000001535 Ribes X utile Nutrition 0.000 description 1
- 235000016919 Ribes petraeum Nutrition 0.000 description 1
- 244000281247 Ribes rubrum Species 0.000 description 1
- 235000002355 Ribes spicatum Nutrition 0.000 description 1
- 235000011449 Rosa Nutrition 0.000 description 1
- 241000801617 Sacada Species 0.000 description 1
- 238000012300 Sequence Analysis Methods 0.000 description 1
- 238000002105 Southern blotting Methods 0.000 description 1
- 108091081024 Start codon Proteins 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 229930006000 Sucrose Natural products 0.000 description 1
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 1
- 108020005038 Terminator Codon Proteins 0.000 description 1
- 108700019146 Transgenes Proteins 0.000 description 1
- 239000007983 Tris buffer Substances 0.000 description 1
- 230000003213 activating effect Effects 0.000 description 1
- DTOSIQBPPRVQHS-PDBXOOCHSA-N alpha-linolenic acid Chemical compound CC\C=C/C\C=C/C\C=C/CCCCCCCC(O)=O DTOSIQBPPRVQHS-PDBXOOCHSA-N 0.000 description 1
- 235000020661 alpha-linolenic acid Nutrition 0.000 description 1
- 125000000539 amino acid group Chemical group 0.000 description 1
- 229960000723 ampicillin Drugs 0.000 description 1
- AVKUERGKIZMTKX-NJBDSQKTSA-N ampicillin Chemical compound C1([C@@H](N)C(=O)N[C@H]2[C@H]3SC([C@@H](N3C2=O)C(O)=O)(C)C)=CC=CC=C1 AVKUERGKIZMTKX-NJBDSQKTSA-N 0.000 description 1
- 230000003321 amplification Effects 0.000 description 1
- 229940088710 antibiotic agent Drugs 0.000 description 1
- 208000016063 arterial thoracic outlet syndrome Diseases 0.000 description 1
- 238000003556 assay Methods 0.000 description 1
- 108010058966 bacteriophage T7 induced DNA polymerase Proteins 0.000 description 1
- 210000004369 blood Anatomy 0.000 description 1
- 239000008280 blood Substances 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 238000010805 cDNA synthesis kit Methods 0.000 description 1
- 210000000170 cell membrane Anatomy 0.000 description 1
- 239000006285 cell suspension Substances 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229960005091 chloramphenicol Drugs 0.000 description 1
- WIIZWVCIJKGZOK-RKDXNWHRSA-N chloramphenicol Chemical compound ClC(Cl)C(=O)N[C@H](CO)[C@H](O)C1=CC=C([N+]([O-])=O)C=C1 WIIZWVCIJKGZOK-RKDXNWHRSA-N 0.000 description 1
- 238000010835 comparative analysis Methods 0.000 description 1
- 239000000306 component Substances 0.000 description 1
- 238000004590 computer program Methods 0.000 description 1
- 239000000356 contaminant Substances 0.000 description 1
- 239000013068 control sample Substances 0.000 description 1
- 238000009402 cross-breeding Methods 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 239000008367 deionised water Substances 0.000 description 1
- 229910021641 deionized water Inorganic materials 0.000 description 1
- 238000012217 deletion Methods 0.000 description 1
- 230000037430 deletion Effects 0.000 description 1
- 230000030609 dephosphorylation Effects 0.000 description 1
- 238000006209 dephosphorylation reaction Methods 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 230000037213 diet Effects 0.000 description 1
- 230000000378 dietary effect Effects 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 208000035475 disorder Diseases 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 238000004520 electroporation Methods 0.000 description 1
- 239000003623 enhancer Substances 0.000 description 1
- 230000006862 enzymatic digestion Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 230000004129 fatty acid metabolism Effects 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 235000012041 food component Nutrition 0.000 description 1
- 239000005428 food component Substances 0.000 description 1
- 238000013467 fragmentation Methods 0.000 description 1
- 238000006062 fragmentation reaction Methods 0.000 description 1
- 239000003517 fume Substances 0.000 description 1
- 229940098330 gamma linoleic acid Drugs 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 238000012224 gene deletion Methods 0.000 description 1
- 238000011331 genomic analysis Methods 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- 210000002443 helper t lymphocyte Anatomy 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 238000003780 insertion Methods 0.000 description 1
- 230000037431 insertion Effects 0.000 description 1
- 230000010354 integration Effects 0.000 description 1
- 229940049918 linoleate Drugs 0.000 description 1
- KQQKGWQCNNTQJW-UHFFFAOYSA-N linolenic acid Natural products CC=CCCC=CCC=CCCCCCCCC(O)=O KQQKGWQCNNTQJW-UHFFFAOYSA-N 0.000 description 1
- 230000037356 lipid metabolism Effects 0.000 description 1
- 239000003550 marker Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000013508 migration Methods 0.000 description 1
- 230000005012 migration Effects 0.000 description 1
- 239000007003 mineral medium Substances 0.000 description 1
- 125000000896 monocarboxylic acid group Chemical group 0.000 description 1
- 208000031225 myocardial ischemia Diseases 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 238000003199 nucleic acid amplification method Methods 0.000 description 1
- 238000007899 nucleic acid hybridization Methods 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 239000002751 oligonucleotide probe Substances 0.000 description 1
- 229940094443 oxytocics prostaglandins Drugs 0.000 description 1
- 230000000149 penetrating effect Effects 0.000 description 1
- 238000000053 physical method Methods 0.000 description 1
- 239000013600 plasmid vector Substances 0.000 description 1
- 230000008488 polyadenylation Effects 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 230000003234 polygenic effect Effects 0.000 description 1
- 238000003752 polymerase chain reaction Methods 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000004321 preservation Methods 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 230000000750 progressive effect Effects 0.000 description 1
- 238000001742 protein purification Methods 0.000 description 1
- 230000037425 regulation of transcription Effects 0.000 description 1
- 230000022532 regulation of transcription, DNA-dependent Effects 0.000 description 1
- 230000008439 repair process Effects 0.000 description 1
- 230000003362 replicative effect Effects 0.000 description 1
- 230000005070 ripening Effects 0.000 description 1
- 235000021003 saturated fats Nutrition 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- 239000006152 selective media Substances 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 101150024950 sstT gene Proteins 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 238000004448 titration Methods 0.000 description 1
- 230000005030 transcription termination Effects 0.000 description 1
- 238000011426 transformation method Methods 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- 150000003626 triacylglycerols Chemical class 0.000 description 1
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 1
- 235000021081 unsaturated fats Nutrition 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
- C12N9/0004—Oxidoreductases (1.)
- C12N9/0071—Oxidoreductases (1.) acting on paired donors with incorporation of molecular oxygen (1.14)
- C12N9/0083—Miscellaneous (1.14.99)
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
- C12N15/09—Recombinant DNA-technology
- C12N15/63—Introduction of foreign genetic material using vectors; Vectors; Use of hosts therefor; Regulation of expression
- C12N15/74—Vectors or expression systems specially adapted for prokaryotic hosts other than E. coli, e.g. Lactobacillus, Micromonospora
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
- C12N15/09—Recombinant DNA-technology
- C12N15/63—Introduction of foreign genetic material using vectors; Vectors; Use of hosts therefor; Regulation of expression
- C12N15/79—Vectors or expression systems specially adapted for eukaryotic hosts
- C12N15/82—Vectors or expression systems specially adapted for eukaryotic hosts for plant cells, e.g. plant artificial chromosomes (PACs)
- C12N15/8241—Phenotypically and genetically modified plants via recombinant DNA technology
- C12N15/8242—Phenotypically and genetically modified plants via recombinant DNA technology with non-agronomic quality (output) traits, e.g. for industrial processing; Value added, non-agronomic traits
- C12N15/8243—Phenotypically and genetically modified plants via recombinant DNA technology with non-agronomic quality (output) traits, e.g. for industrial processing; Value added, non-agronomic traits involving biosynthetic or metabolic pathways, i.e. metabolic engineering, e.g. nicotine, caffeine
- C12N15/8247—Phenotypically and genetically modified plants via recombinant DNA technology with non-agronomic quality (output) traits, e.g. for industrial processing; Value added, non-agronomic traits involving biosynthetic or metabolic pathways, i.e. metabolic engineering, e.g. nicotine, caffeine involving modified lipid metabolism, e.g. seed oil composition
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P7/00—Preparation of oxygen-containing organic compounds
- C12P7/64—Fats; Fatty oils; Ester-type waxes; Higher fatty acids, i.e. having at least seven carbon atoms in an unbroken chain bound to a carboxyl group; Oxidised oils or fats
- C12P7/6409—Fatty acids
- C12P7/6427—Polyunsaturated fatty acids [PUFA], i.e. having two or more double bonds in their backbone
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P7/00—Preparation of oxygen-containing organic compounds
- C12P7/64—Fats; Fatty oils; Ester-type waxes; Higher fatty acids, i.e. having at least seven carbon atoms in an unbroken chain bound to a carboxyl group; Oxidised oils or fats
- C12P7/6436—Fatty acid esters
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P7/00—Preparation of oxygen-containing organic compounds
- C12P7/64—Fats; Fatty oils; Ester-type waxes; Higher fatty acids, i.e. having at least seven carbon atoms in an unbroken chain bound to a carboxyl group; Oxidised oils or fats
- C12P7/6436—Fatty acid esters
- C12P7/6445—Glycerides
- C12P7/6472—Glycerides containing polyunsaturated fatty acid [PUFA] residues, i.e. having two or more double bonds in their backbone
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Y—ENZYMES
- C12Y114/00—Oxidoreductases acting on paired donors, with incorporation or reduction of molecular oxygen (1.14)
- C12Y114/19—Oxidoreductases acting on paired donors, with incorporation or reduction of molecular oxygen (1.14) with oxidation of a pair of donors resulting in the reduction of molecular oxygen to two molecules of water (1.14.19)
- C12Y114/19003—Linoleoyl-CoA desaturase (1.14.19.3)
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Genetics & Genomics (AREA)
- Engineering & Computer Science (AREA)
- Zoology (AREA)
- Wood Science & Technology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biotechnology (AREA)
- General Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Biochemistry (AREA)
- Microbiology (AREA)
- Biomedical Technology (AREA)
- Molecular Biology (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Physics & Mathematics (AREA)
- Biophysics (AREA)
- Plant Pathology (AREA)
- Cell Biology (AREA)
- Nutrition Science (AREA)
- Medicinal Chemistry (AREA)
- Breeding Of Plants And Reproduction By Means Of Culturing (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Enzymes And Modification Thereof (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US08/366,779 US5614393A (en) | 1991-10-10 | 1994-12-30 | Production of γ-linolenic acid by a Δ6-desaturase |
PCT/IB1995/001167 WO1996021022A2 (en) | 1994-12-30 | 1995-12-28 | Production of gamma linolenic acid by a δ6-desaturase |
Publications (1)
Publication Number | Publication Date |
---|---|
UA61880C2 true UA61880C2 (en) | 2003-12-15 |
Family
ID=23444458
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
UA97063197A UA61880C2 (en) | 1994-12-30 | 1995-12-28 | SYNTHESIS OF g-LINOLENIC ACID UNDER THE ACTION OF DELTA-6-DESATURASE |
Country Status (14)
Country | Link |
---|---|
US (2) | US5614393A (de) |
EP (1) | EP0801680B1 (de) |
JP (2) | JP4422211B2 (de) |
CN (1) | CN1117864C (de) |
AR (1) | AR000582A1 (de) |
AU (1) | AU707061B2 (de) |
BR (1) | BR9510411A (de) |
CA (1) | CA2207906C (de) |
DE (1) | DE69535064T2 (de) |
ES (1) | ES2262146T3 (de) |
RO (1) | RO121387B1 (de) |
RU (1) | RU2181772C2 (de) |
UA (1) | UA61880C2 (de) |
WO (1) | WO1996021022A2 (de) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
RU2484137C2 (ru) * | 2006-01-04 | 2013-06-10 | Монсанто С.А.С. | Мутанты fad-2 и высокоолеиновые растения |
Families Citing this family (105)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20070130654A1 (en) * | 1991-10-10 | 2007-06-07 | Thomas Terry L | Production of gamma linolenic acid by a delta6-desaturase |
US20090077692A1 (en) * | 1991-10-10 | 2009-03-19 | Thomas Terry L | Production of gamma linolenic acid by a delta6-desaturase |
US5614393A (en) * | 1991-10-10 | 1997-03-25 | Rhone-Poulenc Agrochimie | Production of γ-linolenic acid by a Δ6-desaturase |
US7109392B1 (en) | 1996-10-09 | 2006-09-19 | Cargill, Incorporated | Methods for increasing oleic acid content in seeds from transgenic plants containing a mutant delta 12 desaturase |
US5977436A (en) * | 1997-04-09 | 1999-11-02 | Rhone Poulenc Agrochimie | Oleosin 5' regulatory region for the modification of plant seed lipid composition |
US5959175A (en) * | 1997-04-09 | 1999-09-28 | Thomas; Terry L. | Sunflower albumin 5' regulatory region for the modification of plant seed lipid composition |
US5968809A (en) * | 1997-04-11 | 1999-10-19 | Abbot Laboratories | Methods and compositions for synthesis of long chain poly-unsaturated fatty acids |
WO1998046764A1 (en) * | 1997-04-11 | 1998-10-22 | Calgene Llc | Methods and compositions for synthesis of long chain polyunsaturated fatty acids in plants |
US6075183A (en) * | 1997-04-11 | 2000-06-13 | Abbott Laboratories | Methods and compositions for synthesis of long chain poly-unsaturated fatty acids in plants |
US6051754A (en) * | 1997-04-11 | 2000-04-18 | Abbott Laboratories | Methods and compositions for synthesis of long chain poly-unsaturated fatty acids in plants |
US5972664A (en) | 1997-04-11 | 1999-10-26 | Abbott Laboratories | Methods and compositions for synthesis of long chain poly-unsaturated fatty acids |
US7745694B1 (en) | 1997-04-11 | 2010-06-29 | Monsanto Technology Llc | Methods and compositions for synthesis of long chain polyunsaturated fatty acids in plants |
US6100450A (en) * | 1997-10-22 | 2000-08-08 | Rhone-Poulenc Agrochimie | Seed specific promoters based on arabidopsis genes |
GB9724783D0 (en) * | 1997-11-24 | 1998-01-21 | Inst Arable Crops Research | Novel polypeptides |
AU761152B2 (en) * | 1998-03-17 | 2003-05-29 | Cargill Incorporated | Genes for mutant microsomal delta-12 fatty acid desaturases and related enzymes from plants |
US6635806B1 (en) * | 1998-05-14 | 2003-10-21 | Dekalb Genetics Corporation | Methods and compositions for expression of transgenes in plants |
WO1999061602A1 (en) * | 1998-05-29 | 1999-12-02 | Ohio University | Compositions and methods for the synthesis of fatty acids, their derivatives and downstream products |
WO1999064614A2 (en) | 1998-06-12 | 1999-12-16 | Calgene Llc | Polyunsaturated fatty acids in plants |
DE19828850A1 (de) * | 1998-06-27 | 1999-12-30 | Gvs Ges Fuer Erwerb Und Verwer | Sphingolipid-Desaturase |
ATE375712T1 (de) * | 1998-08-04 | 2007-11-15 | Cargill Inc | Promotoren der fettsäure-desaturase aus pflanzen |
AU1097900A (en) * | 1998-10-05 | 2000-04-26 | Abbott Laboratories | Delta 6 and delta 12 desaturases and modified fatty acid biosynthesis and products produced therefrom |
CA2346006A1 (en) * | 1998-10-09 | 2000-04-20 | Merck & Co., Inc. | Delta 6 fatty acid desaturase |
AU2163100A (en) * | 1998-12-03 | 2000-06-19 | E.I. Du Pont De Nemours And Company | Membrane-bound desaturases |
US6864077B1 (en) | 1998-12-03 | 2005-03-08 | Edgar B. Cahoon | Membrane-bound desaturases |
US6825017B1 (en) | 1998-12-07 | 2004-11-30 | Washington State University Research Foundation | Desaturases and methods of using them for synthesis of polyunsaturated fatty acids |
US8791327B2 (en) | 1998-12-07 | 2014-07-29 | Washington State University Research Foundation | Desaturases and methods of using them for synthesis of polyunsaturated fatty acids |
CA2791961A1 (en) * | 1998-12-07 | 2000-06-15 | Washington State University Research Foundation | Desaturases and methods of using them for synthesis of polyunsaturated fatty acids |
ATE273373T1 (de) | 1999-02-26 | 2004-08-15 | Martek Biosciences Corp | Verfahren zum abtrennen von einem docosahexaensäure enthaltenden triglyerid aus einem triglyceridgemisch |
WO2000075341A1 (de) | 1999-06-07 | 2000-12-14 | Basf Plant Science Gmbh | Δ6-acetylenase und δ6-desaturase aus ceratodon purpureus |
DE10030976A1 (de) | 2000-06-30 | 2002-01-10 | Basf Ag | DELTA6-Desaturasegene exprimierende Pflanzen und PUFAS enthaltende Öle aus diesen Pflanzen und ein Verfahren zur Herstellung ungesättigter Fettsäuren |
WO2001002591A1 (de) * | 1999-07-06 | 2001-01-11 | Basf Plant Science Gmbh | Δ6-desaturasegene exprimierende pflanzen und pufas enthaltende öle aus diesen pflanzen und ein verfahren zur herstellung ungesättigter fettsäuren |
WO2001004622A1 (en) * | 1999-07-13 | 2001-01-18 | The Dow Chemical Company | Method for chemical analysis of biological material |
US7135623B1 (en) * | 1999-09-10 | 2006-11-14 | Nutrinova Nutrition Specialties & Food Engredients Gmbh | Nucleic acid which is obtained from Tetrahymena and which codes for a delta-6-desaturase, the production thereof and use |
CA2301158A1 (en) * | 2000-03-24 | 2001-09-24 | Stephen J. Allen | Screening methods for compounds useful for modulating lipid metabolism in disease |
US7087432B2 (en) * | 2000-09-28 | 2006-08-08 | Bioriginal Food & Science Corp. | Fad4, Fad5, Fad5-2 and Fad6, novel fatty acid desaturase family members and uses thereof |
DE10102337A1 (de) * | 2001-01-19 | 2002-07-25 | Basf Plant Science Gmbh | Verfahren zur Herstellung mehrfach ungesättigter Fettsäuren, neue Biosynthesegene sowie neue pflanzliche Expressionskonstrukte |
AU2003206714B2 (en) * | 2002-01-30 | 2007-09-06 | Basf Plant Science Gmbh | Elongase gene and method for producing polyunsaturated fatty acids |
US7211656B2 (en) * | 2002-01-30 | 2007-05-01 | Abbott Laboratories | Desaturase genes, enzymes encoded thereby, and uses thereof |
GB2385852A (en) * | 2002-02-27 | 2003-09-03 | Rothamsted Ex Station | Delta 6-desaturases from Primulaceae |
DE10219203A1 (de) | 2002-04-29 | 2003-11-13 | Basf Plant Science Gmbh | Verfahren zur Herstellung mehrfach ungesättigter Fettsäuren in Pflanzen |
EP2216405A1 (de) | 2002-05-03 | 2010-08-11 | Monsanto Technology LLC | Saatspezifische USP-Promotoren zur Expression von Genen in Pflanzen |
US7078234B2 (en) | 2002-12-18 | 2006-07-18 | Monsanto Technology Llc | Maize embryo-specific promoter compositions and methods for use thereof |
BR0317304A (pt) * | 2002-12-19 | 2005-11-08 | Univ Bristol | Processo para a produção de compostos, sequência de ácido nucleico isolada, sequência de aminoácidos, construção gênica, vetor, e, organismo |
CA2517253C (en) * | 2003-02-27 | 2018-07-03 | Basf Plant Science Gmbh | Method for the production of polyunsaturated fatty acids |
CN1836045B (zh) | 2003-03-28 | 2012-05-09 | 孟山都技术有限公司 | 用于早期种子发育的新型植物启动子 |
CA2868312A1 (en) | 2003-03-31 | 2004-10-14 | University Of Bristol | Novel plant acyltransferases specific for long-chained, multiply unsaturated fatty acids |
AU2004227075B8 (en) * | 2003-04-08 | 2009-07-16 | Basf Plant Science Gmbh | Delta-4 Desaturases from Euglena gracilis, expressing plants, and oils containing PUFA |
AU2003252958A1 (en) * | 2003-07-31 | 2005-02-25 | The University Of York | Fatty acid biosynthesis 3 |
US11952581B2 (en) | 2003-08-01 | 2024-04-09 | Basf Plant Science Gmbh | Process for the production of polyunsaturated fatty acids in transgenic organisms |
MX353906B (es) | 2003-08-01 | 2018-02-02 | Basf Plant Science Gmbh | Metodo para la produccion de acidos grasos poli-insaturados en organismos transgenicos. |
CA2881252C (en) * | 2003-08-21 | 2017-02-28 | Monsanto Technology Llc | Soybean oil having 5 to 50% sda and less than 10% gla |
CA2450000A1 (en) | 2003-12-18 | 2005-06-18 | Alberta Research Council Inc. | Method of creating plants with reduced level of saturated fatty acid in seed oil |
ATE528403T1 (de) * | 2004-02-27 | 2011-10-15 | Basf Plant Science Gmbh | Verfahren zur herstellung von ungesättigten omega-3-fettsäuren in transgenen organismen |
EP3543324B1 (de) | 2004-02-27 | 2022-11-30 | BASF Plant Science GmbH | Verfahren zur herstellung mehrfach ungesättigten fettsäuren in transgenen pflanzen |
US20050220901A1 (en) * | 2004-03-22 | 2005-10-06 | Huttenbauer Samuel Jr | Methods of pharmaceutical separation from plants |
WO2005102310A1 (en) * | 2004-04-16 | 2005-11-03 | Monsanto Technology Llc | Expression of fatty acid desaturases in corn |
EP2357243B1 (de) | 2004-04-22 | 2018-12-12 | Commonwealth Scientific and Industrial Research Organisation | Synthese von langkettigen polyungesättigten Fettsäuren durch rekombinante Zellen |
DK1756280T3 (en) | 2004-04-22 | 2015-02-02 | Commw Scient Ind Res Org | SYNTHESIS OF CHAIN, polyunsaturated fatty acids BY RECOMBINANT CELLS |
US7364883B2 (en) | 2004-05-07 | 2008-04-29 | Yeastern Biotech Co., Ltd. | Process for producing poly-unsaturated fatty acids by oleaginous yeasts |
WO2006064043A1 (en) * | 2004-12-17 | 2006-06-22 | Agfa Graphics Nv | System and method for supplying an ink to a reciprocating printhead in an inkjet printing apparatus |
DE102004063326A1 (de) * | 2004-12-23 | 2006-07-06 | Basf Plant Science Gmbh | Verfahren zur Herstellung mehrfach ungesättigter Fettsäuren in transgenen Organismen |
CN101128591B (zh) | 2005-02-26 | 2013-02-13 | 巴斯福植物科学有限公司 | 用于植物中种子偏好性表达的表达盒 |
DE102005013779A1 (de) * | 2005-03-22 | 2006-09-28 | Basf Plant Science Gmbh | Verfahren zur Herstellung von mehrfach ungesättigten C20- und C22-Fettsäuren mit mindestens vier Doppelbindungen in transgenen Pflanzen |
US8034994B2 (en) * | 2005-04-19 | 2011-10-11 | Basf Plant Science Gmbh | Starchy-endosperm and/or germinating embryo-specific expression in mono-cotyledonous plants |
WO2006111541A2 (en) | 2005-04-20 | 2006-10-26 | Basf Plant Science Gmbh | Expression cassettes for seed-preferential expression in plants |
EP1882037A2 (de) | 2005-05-10 | 2008-01-30 | BASF Plant Science GmbH | Expressionskassetten zur bevorzugten expression in pflanzensamen |
EP1885862B1 (de) * | 2005-05-23 | 2015-07-29 | Arcadia Biosciences Inc. | Florsafran mit erhöhter gamma-linolensäure |
DE102005038036A1 (de) * | 2005-08-09 | 2007-02-15 | Basf Plant Science Gmbh | Verfahren zur Herstellung von Arachidonsäure und/oder Eicosapentaensäure in transgenen Nutzpflanzen |
GB2431158A (en) * | 2005-10-13 | 2007-04-18 | Rothamsted Res Ltd | Process for the production of arachidonic and/or eicosapentaenoic acid |
DE102005052551A1 (de) * | 2005-11-02 | 2007-05-16 | Rothamsted Res Harpenden | Verfahren zur Herstellung von y-Linolensäure und/oder Stearidonsäure in transgenen Brassicaceae und Linaceae |
GB0603160D0 (en) | 2006-02-16 | 2006-03-29 | Rothamsted Res Ltd | Nucleic acid |
AR059376A1 (es) | 2006-02-21 | 2008-03-26 | Basf Plant Science Gmbh | Procedimiento para la produccion de acidos grasos poliinsaturados |
US8629195B2 (en) | 2006-04-08 | 2014-01-14 | Bayer Materialscience Ag | Production of polyurethane foams |
US7678560B2 (en) * | 2006-05-17 | 2010-03-16 | E.I. Du Pont De Nemours And Company | Δ 5 desaturase and its use in making polyunsaturated fatty acids |
MX2009000757A (es) | 2006-07-19 | 2009-03-09 | Monsanto Technology Llc | Acido graso desaturasas de tetraselmis suecica. |
CA2659993C (en) | 2006-08-24 | 2016-01-05 | Basf Plant Science Gmbh | Isolation and characterization of a novel pythium omega 3 desaturase with specificity to all omega 6 fatty acids longer than 18 carbon chains |
EP2059588A4 (de) | 2006-08-29 | 2010-07-28 | Commw Scient Ind Res Org | Fettsäuresynthese |
CA2847007C (en) | 2006-10-06 | 2016-11-08 | Basf Plant Science Gmbh | Process for the production of polyunsaturated fatty acids in transgenic organisms |
KR20090119910A (ko) | 2007-02-16 | 2009-11-20 | 바스프 플랜트 사이언스 게엠베하 | 외떡잎 식물에서 배-특이적 발현의 조절을 위한 핵산 서열 |
CA2695112A1 (en) * | 2007-07-31 | 2009-02-05 | Basf Plant Science Gmbh | Elongases and processes for the production of polyunsaturated fatty acids in transgenic organisms |
CA2708087A1 (en) | 2007-12-14 | 2009-06-25 | Bioriginal Food & Science Corp. | Promoters from brassica napus for seed specific gene expression |
EP2281051B1 (de) * | 2008-04-30 | 2015-03-11 | Rothamsted Research Limited | Desaturase und Verfahren zur Herstellung mehrfach ungesättigter Fettsäuren in transgenen Organismen |
CA2989798C (en) | 2008-07-01 | 2019-11-05 | Basf Plant Science Gmbh | Promoters from brassica napus for seed specific gene expression |
AU2009286755B2 (en) | 2008-08-26 | 2015-10-22 | Basf Plant Science Gmbh | Nucleic acids encoding desaturases and modified plant oil |
CN113957105B (zh) | 2008-11-18 | 2024-11-01 | 联邦科学技术研究组织 | 产生ω-3脂肪酸的酶和方法 |
EP2376638B1 (de) | 2008-12-12 | 2013-08-14 | BASF Plant Science GmbH | Desaturasen und verfahren zur herstellung mehrfach ungesättigter fettsäuren in transgenen organismen |
EP2419514A4 (de) | 2009-04-17 | 2012-10-24 | Basf Plant Science Co Gmbh | In endospermata betreibbarer pflanzenpromotor und verwendungen davon |
CA3020943A1 (en) | 2009-04-22 | 2010-10-28 | Basf Plant Science Company Gmbh | Whole seed specific promoter |
WO2010130725A1 (en) | 2009-05-13 | 2010-11-18 | Basf Plant Science Company Gmbh | Acyltransferases and uses thereof in fatty acid production |
CA2766858A1 (en) | 2009-07-10 | 2011-01-13 | Basf Plant Science Company Gmbh | Expression cassettes for endosperm-specific expression in plants |
AU2010272536B2 (en) | 2009-07-17 | 2016-09-08 | Basf Plant Science Company Gmbh | Novel fatty acid desaturases and elongases and uses thereof |
CN102782141A (zh) | 2009-12-03 | 2012-11-14 | 巴斯夫植物科学有限公司 | 用于在植物中胚-特异性表达的表达盒 |
CA2804925A1 (en) | 2010-06-25 | 2011-12-29 | Basf Plant Science Company Gmbh | Acyltransferases from thraustochytrium species and uses thereof in fatty acid production |
CN102250928A (zh) * | 2011-04-07 | 2011-11-23 | 中国农业科学院北京畜牧兽医研究所 | Δ-6脂肪酸脱氢酶突变基因及其表达载体和应用 |
ES2769448T3 (es) | 2012-04-12 | 2020-06-25 | Rothamsted Res Limited | Producción de ácidos grasos poliinsaturados omega-3 de cadena larga |
UA127917C2 (uk) | 2012-06-15 | 2024-02-14 | Коммонвелт Сайнтіфік Енд Індастріел Рісерч Організейшн | Рекомбінантна клітина brassica napus, яка містить довголанцюгові поліненасичені жирні кислоти, трансгенна рослина та насіння brassica napus, спосіб отримання екстрагованого ліпіду рослин, харчового продукту та етилового ефіру поліненасичених жирних кислот |
KR101437605B1 (ko) * | 2012-06-29 | 2014-09-15 | 대한민국 | 형질 전환된 유채를 제조하는 방법 |
GB201217524D0 (en) | 2012-10-01 | 2012-11-14 | Rothamsted Res Ltd | Recombinant organisms |
JP6554099B2 (ja) | 2013-08-07 | 2019-07-31 | イェダ リサーチ アンド ディベロップメント カンパニー リミテッドYeda Research And Development Co.Ltd. | p53変異体を再活性化することの可能なペプチド |
US9725399B2 (en) | 2013-12-18 | 2017-08-08 | Commonwealth Scientific And Industrial Research Organisation | Lipid comprising long chain polyunsaturated fatty acids |
KR102527795B1 (ko) | 2014-06-27 | 2023-05-02 | 커먼웰쓰 사이언티픽 앤 인더스트리알 리서치 오거니제이션 | 도코사펜타에노산을 포함하는 지질 |
WO2017134671A1 (en) | 2016-02-04 | 2017-08-10 | Yeda Research And Development Co. Ltd. | Peptides and use of same in the treatment of diseases, disorders or conditions associated with a mutant p53 |
FR3053052B1 (fr) | 2016-06-28 | 2021-02-12 | Fermentalg | Microalgue modifiee pour une production enrichie en tag |
CN112048460B (zh) * | 2020-08-07 | 2023-06-16 | 中国科学院水生生物研究所 | 工程化细鞘丝藻及其生产gla的应用 |
WO2023108250A1 (en) * | 2021-12-16 | 2023-06-22 | Bioriginal Food & Science Corp. | Plants with ehnhanced gamma linolenic acid production |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4736866A (en) * | 1984-06-22 | 1988-04-12 | President And Fellows Of Harvard College | Transgenic non-human mammals |
NZ221259A (en) * | 1986-07-31 | 1990-05-28 | Calgene Inc | Seed specific transcriptional regulation |
DE69033816T2 (de) * | 1989-02-24 | 2002-08-08 | Monsanto Technology Llc., St. Louis | Synthetische pflanzengene und verfahren zu ihrer herstellung |
US5260379A (en) * | 1991-09-13 | 1993-11-09 | Eastman Kodak Company | Polyester blends with improved processability |
PH31293A (en) * | 1991-10-10 | 1998-07-06 | Rhone Poulenc Agrochimie | Production of y-linolenic acid by a delta6-desaturage. |
US5614393A (en) * | 1991-10-10 | 1997-03-25 | Rhone-Poulenc Agrochimie | Production of γ-linolenic acid by a Δ6-desaturase |
US7205457B1 (en) * | 1993-02-05 | 2007-04-17 | Monsanto Technology Llc | Altered linolenic and linoleic acid content in plants |
-
1994
- 1994-12-30 US US08/366,779 patent/US5614393A/en not_active Expired - Lifetime
-
1995
- 1995-12-28 CN CN95197728A patent/CN1117864C/zh not_active Expired - Lifetime
- 1995-12-28 UA UA97063197A patent/UA61880C2/uk unknown
- 1995-12-28 ES ES95944464T patent/ES2262146T3/es not_active Expired - Lifetime
- 1995-12-28 CA CA002207906A patent/CA2207906C/en not_active Expired - Lifetime
- 1995-12-28 BR BR9510411A patent/BR9510411A/pt not_active IP Right Cessation
- 1995-12-28 RO RO97-01202A patent/RO121387B1/ro unknown
- 1995-12-28 WO PCT/IB1995/001167 patent/WO1996021022A2/en active IP Right Grant
- 1995-12-28 AU AU46735/96A patent/AU707061B2/en not_active Ceased
- 1995-12-28 DE DE69535064T patent/DE69535064T2/de not_active Expired - Lifetime
- 1995-12-28 JP JP52082796A patent/JP4422211B2/ja not_active Expired - Fee Related
- 1995-12-28 AR AR33486195A patent/AR000582A1/es active IP Right Grant
- 1995-12-28 EP EP95944464A patent/EP0801680B1/de not_active Expired - Lifetime
- 1995-12-28 RU RU97112919/13A patent/RU2181772C2/ru not_active IP Right Cessation
-
1997
- 1997-01-28 US US08/789,936 patent/US5789220A/en not_active Expired - Lifetime
-
2007
- 2007-08-01 JP JP2007201265A patent/JP2007330267A/ja not_active Withdrawn
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
RU2484137C2 (ru) * | 2006-01-04 | 2013-06-10 | Монсанто С.А.С. | Мутанты fad-2 и высокоолеиновые растения |
Also Published As
Publication number | Publication date |
---|---|
DE69535064T2 (de) | 2006-12-07 |
US5614393A (en) | 1997-03-25 |
JP2007330267A (ja) | 2007-12-27 |
WO1996021022A2 (en) | 1996-07-11 |
AU707061B2 (en) | 1999-07-01 |
US5789220A (en) | 1998-08-04 |
RU2181772C2 (ru) | 2002-04-27 |
JPH10511848A (ja) | 1998-11-17 |
CA2207906C (en) | 2009-12-01 |
RO121387B1 (ro) | 2007-04-30 |
EP0801680B1 (de) | 2006-06-14 |
AR000582A1 (es) | 1997-07-10 |
AU4673596A (en) | 1996-07-24 |
BR9510411A (pt) | 1998-05-19 |
JP4422211B2 (ja) | 2010-02-24 |
ES2262146T3 (es) | 2006-11-16 |
CN1177379A (zh) | 1998-03-25 |
EP0801680A2 (de) | 1997-10-22 |
CN1117864C (zh) | 2003-08-13 |
WO1996021022A3 (en) | 1996-09-12 |
CA2207906A1 (en) | 1996-07-11 |
DE69535064D1 (de) | 2006-07-27 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
UA61880C2 (en) | SYNTHESIS OF g-LINOLENIC ACID UNDER THE ACTION OF DELTA-6-DESATURASE | |
Shibata et al. | Plant lipoxygenases | |
RU2152996C2 (ru) | Фрагмент днк (варианты), вектор, способ получения растения, способ индуцирования продукции гамма-линоленовой кислоты (варианты), способ индуцирования продукции октадекатетраеновой кислоты и дельта-6-десатураза цианобактерий | |
CN107312785A (zh) | OsKTN80b基因在降低水稻株高方面的应用 | |
JP2003512821A (ja) | 外来性遺伝子の転写調節方法 | |
JPS6322191A (ja) | 遺伝子の発現方法 | |
JP6945865B2 (ja) | Casタンパク質発現カセット | |
KR20080071190A (ko) | 델타-9 일롱가제, 및 다중불포화 지방산 생성에 있어서의이들의 용도 | |
JPH06510422A (ja) | 植物におけるポリヒドロキシアルカノコートの生産 | |
US11345937B2 (en) | Construction of Mucor circinelloides cell factory for producing stearidonic acid and fermentation technology thereof | |
CN101321872B (zh) | 高γ-亚麻酸红花 | |
CN105368851B (zh) | 一种来源于寄生疫霉的ω-3脱饱和酶、含所述脱饱和酶的载体、重组微生物及其应用 | |
CN105505930B (zh) | 花生Δ12脂肪酸脱氢酶AhFAD2-1B-m基因的启动子及其制备方法和应用 | |
CN113308481A (zh) | 一种大豆dgat2基因外显子编辑位点及其应用 | |
TW201142021A (en) | A gene of unsaturated fatty acid synthetic enzyme isolated from marchantia polymorpha and its use | |
Thimmaraju et al. | Morphometric and biochemical characterization of red beet (Beta vulgaris L.) hairy roots obtained after single and double transformations | |
CN116240231A (zh) | 一种纳米酶级联反应系统及其制备方法和应用 | |
US8148602B2 (en) | Diacylglycerol acyltransferases from flax | |
CN108659108B (zh) | 一种与黄金梨果顶硬化相关的nac转录因子 | |
CN105906696A (zh) | 一个新的棉纤维发育相关基因GhEIN3的鉴定及应用 | |
US20040103450A1 (en) | Soybean mutant strain and soybean oil therefrom | |
CN118516400B (zh) | gma-miR169c基因在调控植物脂肪酸合成中的应用 | |
CN105112419B (zh) | 花生Δ12脂肪酸脱氢酶AhFAD2-1B基因的启动子及其制备方法和应用 | |
JP5641232B2 (ja) | オゴノリ由来のシクロオキシゲナーゼの遺伝子及び該遺伝子を利用するプロスタグランジン類生産方法 | |
CN104450748B (zh) | 糙草△6‑脂肪酸脱饱和酶ApD6D基因家族及其重组表达载体和应用 |