DE69519976T2 - Verfahren zur Verbesserung der Salztoleranz bei Pflanzen - Google Patents
Verfahren zur Verbesserung der Salztoleranz bei PflanzenInfo
- Publication number
- DE69519976T2 DE69519976T2 DE69519976T DE69519976T DE69519976T2 DE 69519976 T2 DE69519976 T2 DE 69519976T2 DE 69519976 T DE69519976 T DE 69519976T DE 69519976 T DE69519976 T DE 69519976T DE 69519976 T2 DE69519976 T2 DE 69519976T2
- Authority
- DE
- Germany
- Prior art keywords
- group
- salt
- aminolevulinic acid
- plant
- soil
- 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 - Lifetime
Links
- 230000015784 hyperosmotic salinity response Effects 0.000 title claims description 55
- 238000000034 method Methods 0.000 title claims description 50
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- 239000002689 soil Substances 0.000 claims description 49
- 239000004480 active ingredient Substances 0.000 claims description 33
- 238000011282 treatment Methods 0.000 claims description 26
- 229960002749 aminolevulinic acid Drugs 0.000 claims description 23
- 150000001875 compounds Chemical class 0.000 claims description 23
- -1 n-octyl group Chemical group 0.000 claims description 23
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- 229910002651 NO3 Inorganic materials 0.000 claims description 2
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 claims description 2
- 229910019142 PO4 Inorganic materials 0.000 claims description 2
- 244000104275 Phoenix dactylifera Species 0.000 claims description 2
- 235000010659 Phoenix dactylifera Nutrition 0.000 claims description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 claims description 2
- 244000088415 Raphanus sativus Species 0.000 claims description 2
- 235000006140 Raphanus sativus var sativus Nutrition 0.000 claims description 2
- 240000003768 Solanum lycopersicum Species 0.000 claims description 2
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- 235000002597 Solanum melongena Nutrition 0.000 claims description 2
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims description 2
- 235000015724 Trifolium pratense Nutrition 0.000 claims description 2
- FJJCIZWZNKZHII-UHFFFAOYSA-N [4,6-bis(cyanoamino)-1,3,5-triazin-2-yl]cyanamide Chemical compound N#CNC1=NC(NC#N)=NC(NC#N)=N1 FJJCIZWZNKZHII-UHFFFAOYSA-N 0.000 claims description 2
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 claims description 2
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims description 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 2
- 239000008280 blood Substances 0.000 claims description 2
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- 159000000007 calcium salts Chemical class 0.000 claims description 2
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 2
- 125000005448 ethoxyethyl group Chemical group [H]C([H])([H])C([H])([H])OC([H])([H])C([H])([H])* 0.000 claims description 2
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- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
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- HEBKCHPVOIAQTA-SCDXWVJYSA-N xylitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)CO HEBKCHPVOIAQTA-SCDXWVJYSA-N 0.000 description 1
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- FYGDTMLNYKFZSV-BYLHFPJWSA-N β-1,4-galactotrioside Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1O[C@@H]1[C@H](CO)O[C@@H](O[C@@H]2[C@@H](O[C@@H](O)[C@H](O)[C@H]2O)CO)[C@H](O)[C@H]1O FYGDTMLNYKFZSV-BYLHFPJWSA-N 0.000 description 1
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Classifications
-
- 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
- A01N37/44—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 at least one carboxylic group or a thio analogue, or a derivative thereof, and a nitrogen atom attached to the same carbon skeleton by a single or double bond, this nitrogen atom not being a member of a derivative or of a thio analogue of a carboxylic group, e.g. amino-carboxylic acids
-
- 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
- A01N37/44—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 at least one carboxylic group or a thio analogue, or a derivative thereof, and a nitrogen atom attached to the same carbon skeleton by a single or double bond, this nitrogen atom not being a member of a derivative or of a thio analogue of a carboxylic group, e.g. amino-carboxylic acids
- A01N37/46—N-acyl derivatives
-
- 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
- A01N55/00—Biocides, pest repellants or attractants, or plant growth regulators, containing organic compounds containing elements other than carbon, hydrogen, halogen, oxygen, nitrogen and sulfur
- A01N55/02—Biocides, pest repellants or attractants, or plant growth regulators, containing organic compounds containing elements other than carbon, hydrogen, halogen, oxygen, nitrogen and sulfur containing metal atoms
-
- 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
- A01N63/00—Biocides, pest repellants or attractants, or plant growth regulators containing microorganisms, viruses, microbial fungi, animals or substances produced by, or obtained from, microorganisms, viruses, microbial fungi or animals, e.g. enzymes or fermentates
- A01N63/10—Animals; Substances produced thereby or obtained therefrom
Landscapes
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Health & Medical Sciences (AREA)
- Zoology (AREA)
- Wood Science & Technology (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Dentistry (AREA)
- Agronomy & Crop Science (AREA)
- Environmental Sciences (AREA)
- Microbiology (AREA)
- Virology (AREA)
- Biotechnology (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Cultivation Of Plants (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP6292492A JP2896963B2 (ja) | 1994-11-28 | 1994-11-28 | 植物の耐塩性向上剤 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE69519976D1 DE69519976D1 (de) | 2001-03-01 |
| DE69519976T2 true DE69519976T2 (de) | 2001-06-21 |
Family
ID=17782526
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE69519976T Expired - Lifetime DE69519976T2 (de) | 1994-11-28 | 1995-11-28 | Verfahren zur Verbesserung der Salztoleranz bei Pflanzen |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US5661111A (enExample) |
| EP (1) | EP0714600B1 (enExample) |
| JP (1) | JP2896963B2 (enExample) |
| CN (1) | CN1102338C (enExample) |
| AU (1) | AU693953B2 (enExample) |
| DE (1) | DE69519976T2 (enExample) |
Families Citing this family (50)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6992107B1 (en) | 1995-03-10 | 2006-01-31 | Photocure Asa | Esters of 5-aminolevulinic acid and their use as photosensitizing compounds in photochemotherapy |
| US7530461B2 (en) | 1995-03-10 | 2009-05-12 | Photocure Asa | Esters of 5-aminolevulinic acid as photosensitizing agents in photochemotherapy |
| US6492420B2 (en) | 1995-03-10 | 2002-12-10 | Photocure As | Esters of 5-aminolevulinic acid as photosensitizing agents in photochemotherapy |
| AU734994B2 (en) * | 1997-02-26 | 2001-06-28 | Ab Tall (Holdings) Pty Ltd | Pest resistance enhancement method |
| AUPO529397A0 (en) * | 1997-02-26 | 1997-03-20 | Ab Tall (Holdings) Pty Ltd | Pest resistance enhancement method |
| CA2278871A1 (en) * | 1999-07-27 | 2001-01-27 | J. John Balsevich | Seed treatments for improving fall seeding survival of crucifers |
| JP3970492B2 (ja) * | 1999-12-14 | 2007-09-05 | コスモ石油株式会社 | ピーリング用組成物 |
| GB0018527D0 (en) * | 2000-07-27 | 2000-09-13 | Photocure Asa | Composition |
| GB0018528D0 (en) | 2000-07-27 | 2000-09-13 | Photocure Asa | Compounds |
| SE521121C2 (sv) * | 2001-03-19 | 2003-09-30 | Norogard Ab | Komposition för resorption av mikronäringsämnen i växter samt förfarande för dess framställning och användning |
| FR2824236B1 (fr) * | 2001-05-04 | 2004-12-17 | Jean Morelle | Enrichissement en substances actives des supports de culture naturels ou artificiels et des milieux de conservation des fleurs coupees |
| US20060005282A1 (en) * | 2002-04-23 | 2006-01-05 | Activx Biosciences, Inc | Production and use of salt tolerant and culture density tolerant organisms |
| US20040138176A1 (en) * | 2002-05-31 | 2004-07-15 | Cjb Industries, Inc. | Adjuvant for pesticides |
| US20030224939A1 (en) * | 2002-05-31 | 2003-12-04 | David Miles | Adjuvant for pesticides |
| GB0406917D0 (en) | 2004-03-26 | 2004-04-28 | Photocure Asa | Compounds |
| JP4719483B2 (ja) * | 2004-03-30 | 2011-07-06 | コスモ石油株式会社 | 5−アミノレブリン酸スルホン酸塩の製造方法 |
| ATE493382T1 (de) | 2004-03-30 | 2011-01-15 | Cosmo Oil Co Ltd | 5-aminolevulinsäure-phosphatsalz, verfahren zu dessen herstellung und dessen verwendung |
| JP4630087B2 (ja) * | 2004-03-30 | 2011-02-09 | コスモ石油株式会社 | 5−アミノレブリン酸硝酸塩及びその製造方法 |
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| JP4934292B2 (ja) * | 2005-07-05 | 2012-05-16 | コスモ石油株式会社 | 5−アミノレブリン酸エステルリン酸類塩、その製造方法及びその用途 |
| US20070225518A1 (en) * | 2006-03-22 | 2007-09-27 | Zvi Malik | 5-Aminolevulinic acid salts and their use |
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| EP2337775A4 (en) * | 2008-09-01 | 2015-07-01 | Swedish Pharma Ab | NEW 5-AMINOLAVULIC ACID PRODRUGS FOR PHOTODYNAMIC THERAPY AND PHOTODYNAMIC DIAGNOSIS |
| CN101375688B (zh) * | 2008-09-01 | 2011-04-20 | 山东省农业科学院作物研究所 | 一种提高小麦抗盐性的抗盐制剂及其应用方法 |
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| ES2755677T3 (es) * | 2010-09-30 | 2020-04-23 | Cosmo Trade & Service Co Ltd | Fertilizante sólido que contiene ácido 5-aminolevulínico y procedimiento para producir el mismo |
| CN102531778A (zh) * | 2011-12-30 | 2012-07-04 | 杭州安邦农业生物科技有限公司 | 含5-氨基乙酰丙酸化学修饰物的水溶性肥料 |
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| AT514362B1 (de) * | 2013-05-17 | 2015-03-15 | Köck Herbert | Verfahren zur Herstellung von Sauerstoff |
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| CN103828667A (zh) * | 2014-03-14 | 2014-06-04 | 广东海洋大学 | 利用水稻耐盐差异性除杂保纯的大棚育秧方法 |
| CN103975735B (zh) * | 2014-05-13 | 2016-02-10 | 谭国华 | 一种郁金香种球繁育复壮生产方法 |
| CN105230621B (zh) * | 2015-10-19 | 2017-05-17 | 中国农业科学院作物科学研究所 | 一种小麦高光效抗逆境增产调节剂及其制备方法和应用 |
| JP6917046B2 (ja) * | 2016-01-18 | 2021-08-11 | 国立研究開発法人理化学研究所 | 植物の耐塩性向上剤 |
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| JPWO2017135236A1 (ja) * | 2016-02-05 | 2018-11-29 | 積水化学工業株式会社 | 耐塩性苗の育成方法及び植物の水耕栽培方法 |
| CN108522503B (zh) * | 2018-04-16 | 2020-06-30 | 中国农业科学院蔬菜花卉研究所 | 一种黄瓜生长调节剂和日光温室黄瓜种植方法 |
| CN109452296A (zh) * | 2018-12-12 | 2019-03-12 | 四川国光农化股份有限公司 | 一种药肥组合物、制剂及其应用 |
| CN110150304A (zh) * | 2019-05-10 | 2019-08-23 | 海盐县凌特生物科技有限公司 | 含氯化血红素的植物生长调节剂 |
| CN112020930B (zh) * | 2020-07-31 | 2021-10-08 | 江苏沿海地区农业科学研究所 | 一种诱导水稻提高耐盐性的方法 |
| CN113615692A (zh) * | 2021-09-13 | 2021-11-09 | 京博农化科技有限公司 | 一种5-氨基乙酰丙酸和赤霉酸组合物及应用 |
| CN116035006B (zh) * | 2023-02-10 | 2024-05-28 | 山东大学 | 甲硫氨酸在提高植物耐盐能力中的应用及方法 |
| CN117770138B (zh) * | 2024-02-23 | 2024-06-04 | 潍坊市农业科学院(山东省农业科学院潍坊市分院) | 一种创制耐中重度盐碱芦笋种质的组培方法 |
| CN118140797B (zh) * | 2024-05-10 | 2024-07-05 | 中国农业科学院农业环境与可持续发展研究所 | 一种作物盐碱抗性锻炼方法及系统 |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ZA855561B (en) * | 1984-07-27 | 1986-03-26 | Univ Illinois | Photodynamic herbicides |
| DD255873A1 (de) * | 1986-12-23 | 1988-04-20 | Forschzent Bodenfruchtbarkeit | Mittel zur erhoehung der salztoleranz bei kulturpflanzen |
| DD255872A1 (de) * | 1986-12-23 | 1988-04-20 | Forschzent Bodenfruchtbarkeit | Mittel zur erhoehung der salztoleranz bei kulturpflanzen |
| NZ227505A (en) * | 1988-01-13 | 1992-02-25 | Univ Illinois | Insecticidal composition comprising delta-ala or inducers and enhancers thereof |
| JPH0639366B2 (ja) * | 1989-05-22 | 1994-05-25 | 資忠 松島 | 埴物成長促進剤 |
| JP2613136B2 (ja) * | 1991-05-14 | 1997-05-21 | 株式会社コスモ総合研究所 | 植物成長促進剤 |
| JPH06292492A (ja) * | 1993-04-07 | 1994-10-21 | Shimano Inc | スピニングリールの制動装置 |
-
1994
- 1994-11-28 JP JP6292492A patent/JP2896963B2/ja not_active Expired - Lifetime
-
1995
- 1995-11-22 US US08/561,702 patent/US5661111A/en not_active Expired - Lifetime
- 1995-11-27 AU AU39088/95A patent/AU693953B2/en not_active Ceased
- 1995-11-28 DE DE69519976T patent/DE69519976T2/de not_active Expired - Lifetime
- 1995-11-28 EP EP95118700A patent/EP0714600B1/en not_active Expired - Lifetime
- 1995-11-28 CN CN95121836A patent/CN1102338C/zh not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| CN1132592A (zh) | 1996-10-09 |
| JPH08151304A (ja) | 1996-06-11 |
| US5661111A (en) | 1997-08-26 |
| CN1102338C (zh) | 2003-03-05 |
| EP0714600B1 (en) | 2001-01-24 |
| DE69519976D1 (de) | 2001-03-01 |
| EP0714600A3 (enExample) | 1996-07-03 |
| EP0714600A2 (en) | 1996-06-05 |
| JP2896963B2 (ja) | 1999-05-31 |
| AU693953B2 (en) | 1998-07-09 |
| AU3908895A (en) | 1996-06-06 |
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