RU97100774A - MANIPULATION BY PROPOSAL ACTIVITY OF PROTOPORPHIRINOGEN-OXIDASE IN EUCARIOT - Google Patents
MANIPULATION BY PROPOSAL ACTIVITY OF PROTOPORPHIRINOGEN-OXIDASE IN EUCARIOTInfo
- Publication number
- RU97100774A RU97100774A RU97100774/13A RU97100774A RU97100774A RU 97100774 A RU97100774 A RU 97100774A RU 97100774/13 A RU97100774/13 A RU 97100774/13A RU 97100774 A RU97100774 A RU 97100774A RU 97100774 A RU97100774 A RU 97100774A
- Authority
- RU
- Russia
- Prior art keywords
- plant
- dna molecule
- protox
- activity
- group
- Prior art date
Links
- 230000000694 effects Effects 0.000 title claims 23
- 241000196324 Embryophyta Species 0.000 claims 77
- 102000005135 EC 1.3.3.4 Human genes 0.000 claims 64
- 108020001991 EC 1.3.3.4 Proteins 0.000 claims 64
- 229920003013 deoxyribonucleic acid Polymers 0.000 claims 52
- 210000004027 cells Anatomy 0.000 claims 24
- 150000001413 amino acids Chemical group 0.000 claims 15
- 235000018102 proteins Nutrition 0.000 claims 15
- 102000004169 proteins and genes Human genes 0.000 claims 15
- 108090000623 proteins and genes Proteins 0.000 claims 15
- 241000206602 Eukaryota Species 0.000 claims 12
- 108091006028 chimera Proteins 0.000 claims 12
- 230000002363 herbicidal Effects 0.000 claims 12
- 239000004009 herbicide Substances 0.000 claims 12
- 235000001014 amino acid Nutrition 0.000 claims 9
- 230000002401 inhibitory effect Effects 0.000 claims 8
- 239000011541 reaction mixture Substances 0.000 claims 7
- 230000001131 transforming Effects 0.000 claims 7
- 238000004519 manufacturing process Methods 0.000 claims 5
- 239000004471 Glycine Substances 0.000 claims 4
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Natural products NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 claims 4
- XUJNEKJLAYXESH-REOHCLBHSA-N L-cysteine Chemical compound SC[C@H](N)C(O)=O XUJNEKJLAYXESH-REOHCLBHSA-N 0.000 claims 4
- ROHFNLRQFUQHCH-YFKPBYRVSA-N L-leucine Chemical compound CC(C)C[C@H](N)C(O)=O ROHFNLRQFUQHCH-YFKPBYRVSA-N 0.000 claims 4
- AYFVYJQAPQTCCC-GBXIJSLDSA-N L-threonine Chemical compound C[C@@H](O)[C@H](N)C(O)=O AYFVYJQAPQTCCC-GBXIJSLDSA-N 0.000 claims 4
- 239000004473 Threonine Substances 0.000 claims 4
- 240000008042 Zea mays Species 0.000 claims 4
- 235000002017 Zea mays subsp mays Nutrition 0.000 claims 4
- 235000004279 alanine Nutrition 0.000 claims 4
- 125000003295 alanine group Chemical group N[C@@H](C)C(=O)* 0.000 claims 4
- 235000018417 cysteine Nutrition 0.000 claims 4
- 125000003630 glycyl group Chemical group [H]N([H])C([H])([H])C(*)=O 0.000 claims 4
- 239000003112 inhibitor Substances 0.000 claims 4
- 239000000463 material Substances 0.000 claims 4
- UHSGPDMIQQYNAX-UHFFFAOYSA-N protoporphyrinogen Chemical class C1C(=C(C=2C=C)C)NC=2CC(=C(C=2CCC(O)=O)C)NC=2CC(N2)=C(CCC(O)=O)C(C)=C2CC2=C(C)C(C=C)=C1N2 UHSGPDMIQQYNAX-UHFFFAOYSA-N 0.000 claims 4
- 239000000523 sample Substances 0.000 claims 4
- 125000001493 tyrosinyl group Chemical group [H]OC1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])(N([H])[H])C(*)=O 0.000 claims 4
- 241000894006 Bacteria Species 0.000 claims 3
- 229920002676 Complementary DNA Polymers 0.000 claims 3
- 239000002299 complementary DNA Substances 0.000 claims 3
- 150000001875 compounds Chemical class 0.000 claims 3
- 235000005822 corn Nutrition 0.000 claims 3
- 235000005824 corn Nutrition 0.000 claims 3
- 150000003949 imides Chemical class 0.000 claims 3
- 230000004048 modification Effects 0.000 claims 3
- 238000006011 modification reaction Methods 0.000 claims 3
- 238000003976 plant breeding Methods 0.000 claims 3
- 238000002360 preparation method Methods 0.000 claims 3
- 241000219194 Arabidopsis Species 0.000 claims 2
- 235000007319 Avena orientalis Nutrition 0.000 claims 2
- 244000075850 Avena orientalis Species 0.000 claims 2
- 241000219310 Beta vulgaris subsp. vulgaris Species 0.000 claims 2
- 240000002791 Brassica napus Species 0.000 claims 2
- 235000006008 Brassica napus var napus Nutrition 0.000 claims 2
- 210000003763 Chloroplasts Anatomy 0.000 claims 2
- 229920001405 Coding region Polymers 0.000 claims 2
- 229920000742 Cotton Polymers 0.000 claims 2
- MTCFGRXMJLQNBG-UWTATZPHSA-N D-serine Chemical compound OC[C@@H](N)C(O)=O MTCFGRXMJLQNBG-UWTATZPHSA-N 0.000 claims 2
- 240000007842 Glycine max Species 0.000 claims 2
- 235000010469 Glycine max Nutrition 0.000 claims 2
- 240000006962 Gossypium hirsutum Species 0.000 claims 2
- 229960000310 ISOLEUCINE Drugs 0.000 claims 2
- AGPKZVBTJJNPAG-WHFBIAKZSA-N L-isoleucine Chemical compound CC[C@H](C)[C@H](N)C(O)=O AGPKZVBTJJNPAG-WHFBIAKZSA-N 0.000 claims 2
- OUYCCCASQSFEME-QMMMGPOBSA-N L-tyrosine Chemical compound OC(=O)[C@@H](N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-QMMMGPOBSA-N 0.000 claims 2
- KZSNJWFQEVHDMF-BYPYZUCNSA-N L-valine Chemical compound CC(C)[C@H](N)C(O)=O KZSNJWFQEVHDMF-BYPYZUCNSA-N 0.000 claims 2
- 241001465754 Metazoa Species 0.000 claims 2
- 210000003470 Mitochondria Anatomy 0.000 claims 2
- 240000008962 Nicotiana tabacum Species 0.000 claims 2
- 235000002637 Nicotiana tabacum Nutrition 0.000 claims 2
- 240000007594 Oryza sativa Species 0.000 claims 2
- 235000007164 Oryza sativa Nutrition 0.000 claims 2
- 235000007238 Secale cereale Nutrition 0.000 claims 2
- 240000002057 Secale cereale Species 0.000 claims 2
- 240000006394 Sorghum bicolor Species 0.000 claims 2
- 235000011684 Sorghum saccharatum Nutrition 0.000 claims 2
- 240000008529 Triticum aestivum Species 0.000 claims 2
- 125000000217 alkyl group Chemical group 0.000 claims 2
- 235000015097 nutrients Nutrition 0.000 claims 2
- 235000009566 rice Nutrition 0.000 claims 2
- 241000894007 species Species 0.000 claims 2
- 238000006467 substitution reaction Methods 0.000 claims 2
- 210000001519 tissues Anatomy 0.000 claims 2
- 239000004474 valine Substances 0.000 claims 2
- 235000021307 wheat Nutrition 0.000 claims 2
- WKMRIBJBDSRIMJ-UHFFFAOYSA-N (2,4-dichlorophenyl) pyrrolidine-1-carboxylate Chemical compound ClC1=CC(Cl)=CC=C1OC(=O)N1CCCC1 WKMRIBJBDSRIMJ-UHFFFAOYSA-N 0.000 claims 1
- 125000002373 5 membered heterocyclic group Chemical group 0.000 claims 1
- OEDUIFSDODUDRK-UHFFFAOYSA-N 5-phenyl-1H-pyrazole Chemical compound N1N=CC=C1C1=CC=CC=C1 OEDUIFSDODUDRK-UHFFFAOYSA-N 0.000 claims 1
- 125000004070 6 membered heterocyclic group Chemical group 0.000 claims 1
- 235000014469 Bacillus subtilis Nutrition 0.000 claims 1
- 125000003320 C2-C6 alkenyloxy group Chemical group 0.000 claims 1
- KSFOVUSSGSKXFI-GAQDCDSVSA-N CC1=C/2NC(\C=C3/N=C(/C=C4\N\C(=C/C5=N/C(=C\2)/C(C=C)=C5C)C(C=C)=C4C)C(C)=C3CCC(O)=O)=C1CCC(O)=O Chemical compound CC1=C/2NC(\C=C3/N=C(/C=C4\N\C(=C/C5=N/C(=C\2)/C(C=C)=C5C)C(C=C)=C4C)C(C)=C3CCC(O)=O)=C1CCC(O)=O KSFOVUSSGSKXFI-GAQDCDSVSA-N 0.000 claims 1
- 240000000218 Cannabis sativa Species 0.000 claims 1
- USIUVYZYUHIAEV-UHFFFAOYSA-N Diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 claims 1
- 102000004190 Enzymes Human genes 0.000 claims 1
- 108090000790 Enzymes Proteins 0.000 claims 1
- 241000588724 Escherichia coli Species 0.000 claims 1
- 241000238631 Hexapoda Species 0.000 claims 1
- 108020004999 Messenger RNA Proteins 0.000 claims 1
- DVMSBIVGIAGNNI-UHFFFAOYSA-M N-piperidin-1-ylcarbamate Chemical class [O-]C(=O)NN1CCCCC1 DVMSBIVGIAGNNI-UHFFFAOYSA-M 0.000 claims 1
- 241000209504 Poaceae Species 0.000 claims 1
- 240000004808 Saccharomyces cerevisiae Species 0.000 claims 1
- 241000293869 Salmonella enterica subsp. enterica serovar Typhimurium Species 0.000 claims 1
- 235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 claims 1
- 125000003277 amino group Chemical group 0.000 claims 1
- 230000000844 anti-bacterial Effects 0.000 claims 1
- 230000001580 bacterial Effects 0.000 claims 1
- 239000003899 bactericide agent Substances 0.000 claims 1
- 238000006243 chemical reaction Methods 0.000 claims 1
- 239000003937 drug carrier Substances 0.000 claims 1
- 230000002255 enzymatic Effects 0.000 claims 1
- 125000004185 ester group Chemical group 0.000 claims 1
- 125000001033 ether group Chemical group 0.000 claims 1
- 230000005284 excitation Effects 0.000 claims 1
- 230000000855 fungicidal Effects 0.000 claims 1
- 239000000417 fungicide Substances 0.000 claims 1
- 230000014509 gene expression Effects 0.000 claims 1
- 238000009396 hybridization Methods 0.000 claims 1
- 230000000749 insecticidal Effects 0.000 claims 1
- 239000002917 insecticide Substances 0.000 claims 1
- 235000009973 maize Nutrition 0.000 claims 1
- 229920002106 messenger RNA Polymers 0.000 claims 1
- 238000000034 method Methods 0.000 claims 1
- 239000000203 mixture Substances 0.000 claims 1
- 239000003750 molluscacide Substances 0.000 claims 1
- 230000002013 molluscicidal Effects 0.000 claims 1
- 230000001069 nematicidal Effects 0.000 claims 1
- 239000005645 nematicide Substances 0.000 claims 1
- 239000002773 nucleotide Substances 0.000 claims 1
- 125000003729 nucleotide group Chemical group 0.000 claims 1
- 230000002018 overexpression Effects 0.000 claims 1
- 239000008194 pharmaceutical composition Substances 0.000 claims 1
- 239000011253 protective coating Substances 0.000 claims 1
- 229950003776 protoporphyrin Drugs 0.000 claims 1
- 150000003222 pyridines Chemical class 0.000 claims 1
- 238000010998 test method Methods 0.000 claims 1
- 125000000101 thioether group Chemical group 0.000 claims 1
Claims (1)
где Q обозначает
R1 обозначает H, Cl или F;
R2 обозначает Cl;
R3 обозначает необязательно замещенный простой эфир, тиоэфир, сложный эфир, амино- или алкильную группу,
R2 и R3 вместе могут образовывать 5- или 6-членное гетероциклическое кольцо.61. The method according to claim 60, wherein the protox-inhibiting herbicide is an imide of the formula
where Q denotes
R 1 is H, Cl or F;
R 2 denotes Cl;
R 3 denotes an optionally substituted ether, thioether, ester, amino or alkyl group,
R 2 and R 3 together can form a 5 or 6 membered heterocyclic ring.
где R обозначает (C2 - C6алкенилокси)карбонил-C1 - C4алкил.62. The method of claim 61, wherein the imide is selected from the group consisting of
where R denotes (C 2 - C 6 alkenyloxy) carbonyl-C 1 - C 4 alkyl.
64. Способ тестирования химического соединения на его способность ингибировать активность фермента протокса из растения, включающий (а) объединение фермента протокса и протопорфириногена IX в первой реакционной смеси в условиях, при которых фермент протокс обладает способностью катализировать превращение протопорфириногена IX в протопорфирин IX; (б) объединение химического соединения, фермента протокса и протопорфириногена IX во второй реакционной смеси в таких же условиях, как и для первой реакционной смеси; (в) возбуждение первой и второй реакционных смесей волнами длиной от приблизительно 395 до приблизительно 410 нм; (г) сравнение флуоресценции первой и второй реакционных смесей при длинах волн от приблизительно 622 до приблизительно 635 нм; причем химическое соединение обладает способностью ингибировать активность фермента протокса, если флуоресценция второй реакционной смеси существенно меньше, чем флуоресценция первой реакционной смеси.63. The method according to p. 58, where the inhibiting protox herbicide has a formula selected from the group consisting of
64. A method of testing a chemical compound for its ability to inhibit the activity of the protox enzyme from a plant, including (a) combining the protox enzyme and protoporphyrinogen IX in the first reaction mixture under conditions where the protox enzyme has the ability to catalyze the conversion of protoporphyrinogen IX to protoporphyrin IX; (b) combining the chemical compound, the enzyme protox and protoporphyrinogen IX in the second reaction mixture under the same conditions as for the first reaction mixture; (c) the excitation of the first and second reaction mixtures by waves from about 395 to about 410 nm long; (d) comparing the fluorescence of the first and second reaction mixtures at wavelengths from about 622 to about 635 nm; moreover, the chemical compound has the ability to inhibit the activity of the protox enzyme, if the fluorescence of the second reaction mixture is substantially less than the fluorescence of the first reaction mixture.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US26119894A | 1994-06-16 | 1994-06-16 | |
US08/261.198 | 1994-06-16 |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
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RU2001130932/13A Division RU2266332C2 (en) | 1994-06-16 | 1995-06-08 | Chimera gene, recombinant vector and seed grain containing the same and gene uses |
Publications (2)
Publication Number | Publication Date |
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RU97100774A true RU97100774A (en) | 1999-03-20 |
RU2192468C2 RU2192468C2 (en) | 2002-11-10 |
Family
ID=22992309
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
RU97100774/13A RU2192468C2 (en) | 1994-06-16 | 1995-06-08 | Modulation of enzymatic activity of protoporphyrinogen oxidase in eucaryotes |
RU2001130932/13A RU2266332C2 (en) | 1994-06-16 | 1995-06-08 | Chimera gene, recombinant vector and seed grain containing the same and gene uses |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
RU2001130932/13A RU2266332C2 (en) | 1994-06-16 | 1995-06-08 | Chimera gene, recombinant vector and seed grain containing the same and gene uses |
Country Status (24)
Country | Link |
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US (5) | US5767373A (en) |
EP (1) | EP0769059B1 (en) |
JP (1) | JP3673925B2 (en) |
CN (3) | CN100432229C (en) |
AT (1) | ATE296888T1 (en) |
AU (2) | AU706763B2 (en) |
BG (1) | BG64394B1 (en) |
BR (1) | BR9508030A (en) |
CA (1) | CA2189349C (en) |
CZ (2) | CZ295884B6 (en) |
DE (1) | DE69534247T2 (en) |
DK (1) | DK0769059T3 (en) |
ES (1) | ES2239757T3 (en) |
FI (1) | FI964958A0 (en) |
HK (1) | HK1039794B (en) |
HU (1) | HUT76353A (en) |
MX (1) | MX237061B (en) |
PL (3) | PL184242B1 (en) |
PT (1) | PT769059E (en) |
RO (3) | RO121886B1 (en) |
RU (2) | RU2192468C2 (en) |
SK (1) | SK284895B6 (en) |
UA (1) | UA71536C2 (en) |
WO (1) | WO1995034659A1 (en) |
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- 1995-06-08 HU HU9603175A patent/HUT76353A/en not_active Application Discontinuation
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- 1995-06-08 JP JP50137096A patent/JP3673925B2/en not_active Expired - Fee Related
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