SK18572000A3 - Nukleotidové sekvencie kódujúce gény sdha, sdhb a sdhc - Google Patents
Nukleotidové sekvencie kódujúce gény sdha, sdhb a sdhc Download PDFInfo
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- SK18572000A3 SK18572000A3 SK1857-2000A SK18572000A SK18572000A3 SK 18572000 A3 SK18572000 A3 SK 18572000A3 SK 18572000 A SK18572000 A SK 18572000A SK 18572000 A3 SK18572000 A3 SK 18572000A3
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- 108010069205 aspartyl-phenylalanine Proteins 0.000 description 1
- 230000001580 bacterial effect Effects 0.000 description 1
- 150000007514 bases Chemical class 0.000 description 1
- OQFSQFPPLPISGP-UHFFFAOYSA-N beta-carboxyaspartic acid Natural products OC(=O)C(N)C(C(O)=O)C(O)=O OQFSQFPPLPISGP-UHFFFAOYSA-N 0.000 description 1
- 238000012742 biochemical analysis Methods 0.000 description 1
- 230000003115 biocidal effect Effects 0.000 description 1
- 230000004071 biological effect Effects 0.000 description 1
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- 230000001851 biosynthetic effect Effects 0.000 description 1
- 229960002685 biotin Drugs 0.000 description 1
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- 238000009395 breeding Methods 0.000 description 1
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- 239000012267 brine Substances 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
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- 229910052799 carbon Inorganic materials 0.000 description 1
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- 239000003240 coconut oil Substances 0.000 description 1
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- 230000002950 deficient Effects 0.000 description 1
- 230000006735 deficit Effects 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- MNNHAPBLZZVQHP-UHFFFAOYSA-N diammonium hydrogen phosphate Chemical compound [NH4+].[NH4+].OP([O-])([O-])=O MNNHAPBLZZVQHP-UHFFFAOYSA-N 0.000 description 1
- 229940111685 dibasic potassium phosphate Drugs 0.000 description 1
- 108010009297 diglycyl-histidine Proteins 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-M dihydrogenphosphate Chemical compound OP(O)([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-M 0.000 description 1
- AIUDWMLXCFRVDR-UHFFFAOYSA-N dimethyl 2-(3-ethyl-3-methylpentyl)propanedioate Chemical class CCC(C)(CC)CCC(C(=O)OC)C(=O)OC AIUDWMLXCFRVDR-UHFFFAOYSA-N 0.000 description 1
- ZPWVASYFFYYZEW-UHFFFAOYSA-L dipotassium hydrogen phosphate Chemical compound [K+].[K+].OP([O-])([O-])=O ZPWVASYFFYYZEW-UHFFFAOYSA-L 0.000 description 1
- 238000001962 electrophoresis Methods 0.000 description 1
- 238000004520 electroporation Methods 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 230000037433 frameshift Effects 0.000 description 1
- 230000005021 gait Effects 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 238000001502 gel electrophoresis Methods 0.000 description 1
- 230000004077 genetic alteration Effects 0.000 description 1
- 231100000118 genetic alteration Toxicity 0.000 description 1
- 108010079547 glutamylmethionine Proteins 0.000 description 1
- 230000034659 glycolysis Effects 0.000 description 1
- 108010067216 glycyl-glycyl-glycine Proteins 0.000 description 1
- XKUKSGPZAADMRA-UHFFFAOYSA-N glycyl-glycyl-glycine Natural products NCC(=O)NCC(=O)NCC(O)=O XKUKSGPZAADMRA-UHFFFAOYSA-N 0.000 description 1
- 238000000338 in vitro Methods 0.000 description 1
- 238000011534 incubation Methods 0.000 description 1
- 150000002484 inorganic compounds Chemical class 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 230000003834 intracellular effect Effects 0.000 description 1
- 229910000358 iron sulfate Inorganic materials 0.000 description 1
- BAUYGSIQEAFULO-UHFFFAOYSA-L iron(2+) sulfate (anhydrous) Chemical compound [Fe+2].[O-]S([O-])(=O)=O BAUYGSIQEAFULO-UHFFFAOYSA-L 0.000 description 1
- 108010000761 leucylarginine Proteins 0.000 description 1
- 235000020778 linoleic acid Nutrition 0.000 description 1
- OYHQOLUKZRVURQ-IXWMQOLASA-N linoleic acid Natural products CCCCC\C=C/C\C=C\CCCCCCCC(O)=O OYHQOLUKZRVURQ-IXWMQOLASA-N 0.000 description 1
- 108010038320 lysylphenylalanine Proteins 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 235000013372 meat Nutrition 0.000 description 1
- 239000002207 metabolite Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 108010005942 methionylglycine Proteins 0.000 description 1
- 239000013586 microbial product Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000007479 molecular analysis Methods 0.000 description 1
- ZIUHHBKFKCYYJD-UHFFFAOYSA-N n,n'-methylenebisacrylamide Chemical compound C=CC(=O)NCNC(=O)C=C ZIUHHBKFKCYYJD-UHFFFAOYSA-N 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 230000037434 nonsense mutation Effects 0.000 description 1
- 238000003199 nucleic acid amplification method 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
- 235000014593 oils and fats Nutrition 0.000 description 1
- 238000002515 oligonucleotide synthesis Methods 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 238000012261 overproduction Methods 0.000 description 1
- 239000000312 peanut oil Substances 0.000 description 1
- 235000019319 peptone Nutrition 0.000 description 1
- 229940066779 peptones Drugs 0.000 description 1
- 108010083476 phenylalanyltryptophan Proteins 0.000 description 1
- DTBNBXWJWCWCIK-UHFFFAOYSA-K phosphonatoenolpyruvate Chemical compound [O-]C(=O)C(=C)OP([O-])([O-])=O DTBNBXWJWCWCIK-UHFFFAOYSA-K 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 238000013492 plasmid preparation Methods 0.000 description 1
- 229920001522 polyglycol ester Polymers 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 230000002028 premature Effects 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 108010020755 prolyl-glycyl-glycine Proteins 0.000 description 1
- 108010090894 prolylleucine Proteins 0.000 description 1
- 230000004952 protein activity Effects 0.000 description 1
- 101150079601 recA gene Proteins 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 230000010076 replication Effects 0.000 description 1
- 230000003362 replicative effect Effects 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 238000004007 reversed phase HPLC Methods 0.000 description 1
- 238000012216 screening Methods 0.000 description 1
- 238000010187 selection method Methods 0.000 description 1
- 238000007086 side reaction Methods 0.000 description 1
- 230000011664 signaling Effects 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 150000008163 sugars Chemical class 0.000 description 1
- 239000002600 sunflower oil Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 230000009897 systematic effect Effects 0.000 description 1
- 235000019157 thiamine Nutrition 0.000 description 1
- KYMBYSLLVAOCFI-UHFFFAOYSA-N thiamine Chemical compound CC1=C(CCO)SCN1CC1=CN=C(C)N=C1N KYMBYSLLVAOCFI-UHFFFAOYSA-N 0.000 description 1
- 229960003495 thiamine Drugs 0.000 description 1
- 239000011721 thiamine Substances 0.000 description 1
- 108010061238 threonyl-glycine Proteins 0.000 description 1
- 238000004448 titration Methods 0.000 description 1
- 238000011426 transformation method Methods 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- 238000013519 translation Methods 0.000 description 1
- 230000004102 tricarboxylic acid cycle Effects 0.000 description 1
- 150000003722 vitamin derivatives 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
- 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
- C12N15/11—DNA or RNA fragments; Modified forms thereof; Non-coding nucleic acids having a biological activity
- C12N15/52—Genes encoding for enzymes or proenzymes
-
- 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.)
- C12N9/001—Oxidoreductases (1.) acting on the CH-CH group of donors (1.3)
-
- 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
- C12P13/00—Preparation of nitrogen-containing organic compounds
- C12P13/04—Alpha- or beta- amino acids
- C12P13/08—Lysine; Diaminopimelic acid; Threonine; Valine
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Genetics & Genomics (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Engineering & Computer Science (AREA)
- Biotechnology (AREA)
- Biomedical Technology (AREA)
- Microbiology (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Medicinal Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Biophysics (AREA)
- Physics & Mathematics (AREA)
- Plant Pathology (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
- Enzymes And Modification Thereof (AREA)
- Underground Or Underwater Handling Of Building Materials (AREA)
- Mobile Radio Communication Systems (AREA)
- Oscillators With Electromechanical Resonators (AREA)
- Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19959650A DE19959650A1 (de) | 1999-12-10 | 1999-12-10 | Neue für die Gene sdhA, sdhB und sdhC codierende Nukleotidsequenzen |
Publications (1)
Publication Number | Publication Date |
---|---|
SK18572000A3 true SK18572000A3 (sk) | 2001-12-03 |
Family
ID=7932187
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SK1857-2000A SK18572000A3 (sk) | 1999-12-10 | 2000-12-05 | Nukleotidové sekvencie kódujúce gény sdha, sdhb a sdhc |
Country Status (15)
Country | Link |
---|---|
US (1) | US20030100079A1 (fr) |
EP (1) | EP1106684B1 (fr) |
JP (1) | JP2001190297A (fr) |
KR (1) | KR20010062280A (fr) |
CN (1) | CN1312374A (fr) |
AT (1) | ATE326527T1 (fr) |
AU (1) | AU7212500A (fr) |
BR (1) | BR0006372A (fr) |
CA (1) | CA2326730A1 (fr) |
DE (2) | DE19959650A1 (fr) |
HU (1) | HUP0004877A2 (fr) |
ID (1) | ID28604A (fr) |
PL (1) | PL344389A1 (fr) |
SK (1) | SK18572000A3 (fr) |
ZA (1) | ZA200007221B (fr) |
Families Citing this family (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2006230202A (ja) * | 2003-06-23 | 2006-09-07 | Ajinomoto Co Inc | L−グルタミン酸の製造法 |
JP4469568B2 (ja) * | 2003-07-09 | 2010-05-26 | 三菱化学株式会社 | 有機酸の製造方法 |
CN100575496C (zh) | 2003-08-28 | 2009-12-30 | 三菱化学株式会社 | 产生琥珀酸的方法 |
WO2005026349A1 (fr) | 2003-09-17 | 2005-03-24 | Mitsubishi Chemical Corporation | Procede de production d'acide organique non amine |
EP1669459B1 (fr) * | 2003-09-30 | 2014-10-22 | Ajinomoto Co., Inc. | Procede de purification d'acide succinique a partir d'un liquide de fermentation |
BRPI0510919A (pt) | 2004-05-20 | 2008-05-20 | Ajinomoto Kk | bactéria produtora de ácido succìnico e processo para produzir ácido succìnico |
CN1989239B (zh) * | 2004-05-20 | 2013-07-10 | 味之素株式会社 | 生产琥珀酸的细菌和生产琥珀酸的方法 |
EP1947190B1 (fr) * | 2005-10-18 | 2017-11-29 | Ajinomoto Co., Inc. | Procédé de production d'acide succinique |
EP1995308B1 (fr) | 2006-02-24 | 2014-07-30 | Mitsubishi Chemical Corporation | Bactérie productrice d'acide organique et procédé de production d'acide organique |
JP2010041920A (ja) | 2006-12-19 | 2010-02-25 | Ajinomoto Co Inc | L−アミノ酸の製造法 |
CN102712941A (zh) * | 2009-12-30 | 2012-10-03 | 代谢探索者公司 | 通过过表达琥珀酸脱氢酶增加甲硫氨酸生产 |
CN105238874B (zh) * | 2015-11-18 | 2018-10-12 | 江苏省农业科学院 | 用于检测禾谷丝核菌RCSdhD基因突变的引物对、试剂盒及检测方法 |
WO2020208842A1 (fr) * | 2019-04-12 | 2020-10-15 | Green Earth Institute 株式会社 | Micro-organisme génétiquement modifié et procédé de production d'une substance cible l'utilisant |
CN111621454B (zh) * | 2020-04-20 | 2023-04-14 | 天津科技大学 | 基因工程高产菌株淀粉酶产色链霉菌及ε-聚赖氨酸的生产方法和应用 |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN100390283C (zh) * | 1997-11-21 | 2008-05-28 | 根瑟特公司 | 肺炎衣原体的基因组序列和其多肽,片段以及其用途特别是用于诊断、预防和治疗感染 |
TR200500004T2 (tr) * | 1999-06-25 | 2005-03-21 | Basf Aktiengesellschaft | Karbon metabolizma ve enerji üretimindeki proteinleri dodlayan korynebacterium glutamicum genleri |
JP2003180348A (ja) * | 1999-07-02 | 2003-07-02 | Ajinomoto Co Inc | L−アミノ酸の製造法 |
-
1999
- 1999-12-10 DE DE19959650A patent/DE19959650A1/de not_active Withdrawn
-
2000
- 2000-11-25 EP EP00125831A patent/EP1106684B1/fr not_active Expired - Lifetime
- 2000-11-25 AT AT00125831T patent/ATE326527T1/de not_active IP Right Cessation
- 2000-11-25 DE DE50012761T patent/DE50012761D1/de not_active Expired - Lifetime
- 2000-12-05 SK SK1857-2000A patent/SK18572000A3/sk unknown
- 2000-12-06 ZA ZA200007221A patent/ZA200007221B/xx unknown
- 2000-12-06 ID IDP20001049A patent/ID28604A/id unknown
- 2000-12-08 CN CN00136084A patent/CN1312374A/zh active Pending
- 2000-12-08 CA CA002326730A patent/CA2326730A1/fr not_active Abandoned
- 2000-12-08 AU AU72125/00A patent/AU7212500A/en not_active Abandoned
- 2000-12-08 KR KR1020000074723A patent/KR20010062280A/ko not_active Application Discontinuation
- 2000-12-08 HU HU0004877A patent/HUP0004877A2/hu unknown
- 2000-12-08 PL PL00344389A patent/PL344389A1/xx not_active IP Right Cessation
- 2000-12-11 BR BR0006372-0A patent/BR0006372A/pt not_active Application Discontinuation
- 2000-12-11 US US09/732,923 patent/US20030100079A1/en not_active Abandoned
- 2000-12-11 JP JP2000376438A patent/JP2001190297A/ja active Pending
Also Published As
Publication number | Publication date |
---|---|
ZA200007221B (en) | 2001-06-12 |
DE50012761D1 (de) | 2006-06-22 |
EP1106684B1 (fr) | 2006-05-17 |
HUP0004877A2 (en) | 2002-10-28 |
PL344389A1 (en) | 2001-06-18 |
HU0004877D0 (fr) | 2001-02-28 |
ID28604A (id) | 2001-06-14 |
ATE326527T1 (de) | 2006-06-15 |
JP2001190297A (ja) | 2001-07-17 |
US20030100079A1 (en) | 2003-05-29 |
CN1312374A (zh) | 2001-09-12 |
CA2326730A1 (fr) | 2001-06-10 |
KR20010062280A (ko) | 2001-07-07 |
DE19959650A1 (de) | 2001-06-13 |
EP1106684A1 (fr) | 2001-06-13 |
AU7212500A (en) | 2001-06-14 |
BR0006372A (pt) | 2001-08-21 |
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