KR100891720B1 - 식물병에 대한 저항성을 유도하는 슈도모나스 클로로라피스o6 유래 4-카바모일페닐아세트산 및 그의 용도 - Google Patents
식물병에 대한 저항성을 유도하는 슈도모나스 클로로라피스o6 유래 4-카바모일페닐아세트산 및 그의 용도 Download PDFInfo
- Publication number
- KR100891720B1 KR100891720B1 KR1020070093239A KR20070093239A KR100891720B1 KR 100891720 B1 KR100891720 B1 KR 100891720B1 KR 1020070093239 A KR1020070093239 A KR 1020070093239A KR 20070093239 A KR20070093239 A KR 20070093239A KR 100891720 B1 KR100891720 B1 KR 100891720B1
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- Prior art keywords
- pseudomonas
- resistance
- acid
- tobacco
- plant
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
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- ZGWAEKSJTSFZSS-UHFFFAOYSA-N 2-(4-carbamoylphenyl)acetic acid Chemical compound NC(=O)C1=CC=C(CC(O)=O)C=C1 ZGWAEKSJTSFZSS-UHFFFAOYSA-N 0.000 title claims abstract description 31
- 241000589516 Pseudomonas Species 0.000 title claims abstract description 31
- 201000010099 disease Diseases 0.000 title abstract description 39
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 title abstract description 39
- 230000001939 inductive effect Effects 0.000 claims abstract description 15
- 238000000034 method Methods 0.000 claims abstract description 14
- 230000001404 mediated effect Effects 0.000 claims abstract description 11
- 241000589615 Pseudomonas syringae Species 0.000 claims abstract description 9
- 230000006698 induction Effects 0.000 claims abstract description 6
- 241000208125 Nicotiana Species 0.000 claims description 35
- 235000002637 Nicotiana tabacum Nutrition 0.000 claims description 35
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical group CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 claims description 14
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims description 12
- 239000007864 aqueous solution Substances 0.000 claims description 7
- 239000001963 growth medium Substances 0.000 claims description 5
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- 241001008516 Pseudomonas chlororaphis O6 Species 0.000 claims description 2
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- 208000035240 Disease Resistance Diseases 0.000 abstract description 20
- 239000000126 substance Substances 0.000 abstract description 20
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- 241000589624 Pseudomonas amygdali pv. tabaci Species 0.000 abstract description 2
- 239000011021 lapis lazuli Substances 0.000 abstract description 2
- 125000001309 chloro group Chemical group Cl* 0.000 abstract 1
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- 230000000694 effects Effects 0.000 description 13
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- 238000004458 analytical method Methods 0.000 description 9
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- 239000002207 metabolite Substances 0.000 description 7
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- 238000005481 NMR spectroscopy Methods 0.000 description 4
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- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
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- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
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- OQEBBZSWEGYTPG-UHFFFAOYSA-N 3-aminobutanoic acid Chemical compound CC(N)CC(O)=O OQEBBZSWEGYTPG-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
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- 238000001644 13C nuclear magnetic resonance spectroscopy Methods 0.000 description 1
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- SQSYNRCXIZHKAI-UHFFFAOYSA-N 2,6-dichloroisonicotinic acid Chemical compound OC(=O)C1=CC(Cl)=NC(Cl)=C1 SQSYNRCXIZHKAI-UHFFFAOYSA-N 0.000 description 1
- MIIIXQJBDGSIKL-UHFFFAOYSA-N 2-morpholin-4-ylethanesulfonic acid;hydrate Chemical compound O.OS(=O)(=O)CCN1CCOCC1 MIIIXQJBDGSIKL-UHFFFAOYSA-N 0.000 description 1
- -1 4-carbamoylphenyl Chemical group 0.000 description 1
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- 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
- UELITFHSCLAHKR-UHFFFAOYSA-N acibenzolar-S-methyl Chemical group CSC(=O)C1=CC=CC2=C1SN=N2 UELITFHSCLAHKR-UHFFFAOYSA-N 0.000 description 1
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- 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
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- VILAVOFMIJHSJA-UHFFFAOYSA-N dicarbon monoxide Chemical compound [C]=C=O VILAVOFMIJHSJA-UHFFFAOYSA-N 0.000 description 1
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- GBMDVOWEEQVZKZ-UHFFFAOYSA-N methanol;hydrate Chemical compound O.OC GBMDVOWEEQVZKZ-UHFFFAOYSA-N 0.000 description 1
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- 235000015097 nutrients Nutrition 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
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- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
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Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C233/00—Carboxylic acid amides
- C07C233/01—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C233/02—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having nitrogen atoms of carboxamide groups bound to hydrogen atoms or to carbon atoms of unsubstituted hydrocarbon radicals
- C07C233/08—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having nitrogen atoms of carboxamide groups bound to hydrogen atoms or to carbon atoms of unsubstituted hydrocarbon radicals with carbon atoms of carboxamide groups bound to acyclic carbon atoms of a saturated carbon skeleton containing rings
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C233/00—Carboxylic acid amides
- C07C233/01—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C233/16—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by singly-bound oxygen atoms
- C07C233/17—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by singly-bound oxygen atoms with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom
- C07C233/22—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by singly-bound oxygen atoms with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom having the carbon atom of the carboxamide group bound to an acyclic carbon atom of a carbon skeleton containing six-membered aromatic rings
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Description
Claims (7)
- 삭제
- 삭제
- 제2항에 있어서, 4-카바모일페닐아세트산은 슈도모나스 클로로라피스(Pseudomonas chlororaphis) O6(KACC 91054) 균주의 배양액을 에틸아세테이트로 추출하여 수용액 층을 얻고, 이 수용액 층을 pH 2~4.5 조건에서 부탄올로 추출하여 얻은 부탄올 층에 함유되어 있는 것인 저항성 유도제.
- 삭제
- 제5항에 있어서, 4-카바모일페닐아세트산은 슈도모나스 클로로라피스 O6(KACC 91054) 균주의 배양액을 에틸아세테이트로 추출하여 수용액 층을 얻고, 이 수용액 층을 pH 2~4.5 조건에서 부탄올로 추출하여 얻은 부탄올 층에 함유되어 있는 것인 저항성 유도방법.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1020070093239A KR100891720B1 (ko) | 2007-09-13 | 2007-09-13 | 식물병에 대한 저항성을 유도하는 슈도모나스 클로로라피스o6 유래 4-카바모일페닐아세트산 및 그의 용도 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1020070093239A KR100891720B1 (ko) | 2007-09-13 | 2007-09-13 | 식물병에 대한 저항성을 유도하는 슈도모나스 클로로라피스o6 유래 4-카바모일페닐아세트산 및 그의 용도 |
Publications (1)
Publication Number | Publication Date |
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KR100891720B1 true KR100891720B1 (ko) | 2009-04-03 |
Family
ID=40757237
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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KR1020070093239A Expired - Fee Related KR100891720B1 (ko) | 2007-09-13 | 2007-09-13 | 식물병에 대한 저항성을 유도하는 슈도모나스 클로로라피스o6 유래 4-카바모일페닐아세트산 및 그의 용도 |
Country Status (1)
Country | Link |
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KR (1) | KR100891720B1 (ko) |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1082943A (en) * | 1963-03-27 | 1967-09-13 | Glaxo Lab Ltd | Derivatives of 7-aminocephalosporanic acid |
KR100358671B1 (ko) | 1994-04-18 | 2003-04-26 | 스벤스카 란트멘넨, 릭스푀르분트 에크. 푀르. | 식물질병제어용조성물및방법 |
KR100521744B1 (ko) | 2003-09-08 | 2005-10-17 | 전남대학교산학협력단 | 슈도모나스 크로로라피스 06 균주 및 이를 이용한 식물병 방제 및 가뭄 피해 감소 방법 |
-
2007
- 2007-09-13 KR KR1020070093239A patent/KR100891720B1/ko not_active Expired - Fee Related
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1082943A (en) * | 1963-03-27 | 1967-09-13 | Glaxo Lab Ltd | Derivatives of 7-aminocephalosporanic acid |
KR100358671B1 (ko) | 1994-04-18 | 2003-04-26 | 스벤스카 란트멘넨, 릭스푀르분트 에크. 푀르. | 식물질병제어용조성물및방법 |
KR100521744B1 (ko) | 2003-09-08 | 2005-10-17 | 전남대학교산학협력단 | 슈도모나스 크로로라피스 06 균주 및 이를 이용한 식물병 방제 및 가뭄 피해 감소 방법 |
Non-Patent Citations (1)
Title |
---|
PMPP, 2003 |
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