JPH0433408B2 - - Google Patents
Info
- Publication number
- JPH0433408B2 JPH0433408B2 JP61245400A JP24540086A JPH0433408B2 JP H0433408 B2 JPH0433408 B2 JP H0433408B2 JP 61245400 A JP61245400 A JP 61245400A JP 24540086 A JP24540086 A JP 24540086A JP H0433408 B2 JPH0433408 B2 JP H0433408B2
- Authority
- JP
- Japan
- Prior art keywords
- oligosaccharide
- acid
- alginic acid
- alginate
- oligosaccharides
- 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
- 229920001542 oligosaccharide Polymers 0.000 claims description 67
- 235000010443 alginic acid Nutrition 0.000 claims description 59
- 229920000615 alginic acid Polymers 0.000 claims description 59
- 229960001126 alginic acid Drugs 0.000 claims description 31
- 239000000783 alginic acid Substances 0.000 claims description 31
- 150000002482 oligosaccharides Chemical class 0.000 claims description 29
- 150000004781 alginic acids Chemical class 0.000 claims description 22
- 238000000034 method Methods 0.000 claims description 13
- AEMOLEFTQBMNLQ-BZINKQHNSA-N D-Guluronic Acid Chemical compound OC1O[C@H](C(O)=O)[C@H](O)[C@@H](O)[C@H]1O AEMOLEFTQBMNLQ-BZINKQHNSA-N 0.000 claims description 11
- AEMOLEFTQBMNLQ-VANFPWTGSA-N D-mannopyranuronic acid Chemical compound OC1O[C@H](C(O)=O)[C@@H](O)[C@H](O)[C@@H]1O AEMOLEFTQBMNLQ-VANFPWTGSA-N 0.000 claims description 11
- IAJILQKETJEXLJ-UHFFFAOYSA-N Galacturonsaeure Natural products O=CC(O)C(O)C(O)C(O)C(O)=O IAJILQKETJEXLJ-UHFFFAOYSA-N 0.000 claims description 11
- AEMOLEFTQBMNLQ-UHFFFAOYSA-N beta-D-galactopyranuronic acid Natural products OC1OC(C(O)=O)C(O)C(O)C1O AEMOLEFTQBMNLQ-UHFFFAOYSA-N 0.000 claims description 11
- 239000002689 soil Substances 0.000 claims description 11
- 239000000203 mixture Substances 0.000 claims description 10
- 239000003337 fertilizer Substances 0.000 claims description 9
- 238000010438 heat treatment Methods 0.000 claims description 9
- 238000006116 polymerization reaction Methods 0.000 claims description 8
- 239000000243 solution Substances 0.000 claims description 7
- 239000007864 aqueous solution Substances 0.000 claims description 5
- -1 alginic acid oligosaccharide Chemical class 0.000 description 37
- 229940072056 alginate Drugs 0.000 description 28
- 230000000694 effects Effects 0.000 description 13
- IXPNQXFRVYWDDI-UHFFFAOYSA-N 1-methyl-2,4-dioxo-1,3-diazinane-5-carboximidamide Chemical compound CN1CC(C(N)=N)C(=O)NC1=O IXPNQXFRVYWDDI-UHFFFAOYSA-N 0.000 description 10
- 229940005550 sodium alginate Drugs 0.000 description 10
- 239000000661 sodium alginate Substances 0.000 description 10
- 235000010413 sodium alginate Nutrition 0.000 description 10
- 108090000790 Enzymes Proteins 0.000 description 9
- 102000004190 Enzymes Human genes 0.000 description 9
- 229940088598 enzyme Drugs 0.000 description 9
- 230000012010 growth Effects 0.000 description 8
- 108010004131 poly(beta-D-mannuronate) lyase Proteins 0.000 description 8
- 241000196324 Embryophyta Species 0.000 description 7
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 6
- 239000002253 acid Substances 0.000 description 6
- 239000007788 liquid Substances 0.000 description 6
- 241000512259 Ascophyllum nodosum Species 0.000 description 5
- 230000001737 promoting effect Effects 0.000 description 5
- 239000002994 raw material Substances 0.000 description 5
- 235000000346 sugar Nutrition 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- 238000000354 decomposition reaction Methods 0.000 description 4
- 229920001282 polysaccharide Polymers 0.000 description 4
- 239000005017 polysaccharide Substances 0.000 description 4
- 150000004804 polysaccharides Chemical class 0.000 description 4
- 241001474374 Blennius Species 0.000 description 3
- 244000146493 Cryptotaenia japonica Species 0.000 description 3
- 235000004035 Cryptotaenia japonica Nutrition 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 238000012271 agricultural production Methods 0.000 description 3
- 230000003301 hydrolyzing effect Effects 0.000 description 3
- 239000003375 plant hormone Substances 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 229920003002 synthetic resin Polymers 0.000 description 3
- 239000000057 synthetic resin Substances 0.000 description 3
- 239000008399 tap water Substances 0.000 description 3
- 235000020679 tap water Nutrition 0.000 description 3
- 210000002268 wool Anatomy 0.000 description 3
- 229930192334 Auxin Natural products 0.000 description 2
- 240000004713 Pisum sativum Species 0.000 description 2
- 235000010582 Pisum sativum Nutrition 0.000 description 2
- 244000088415 Raphanus sativus Species 0.000 description 2
- 235000006140 Raphanus sativus var sativus Nutrition 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 240000008042 Zea mays Species 0.000 description 2
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 2
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 239000002363 auxin Substances 0.000 description 2
- 210000002421 cell wall Anatomy 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000000470 constituent Substances 0.000 description 2
- 235000005822 corn Nutrition 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 244000005700 microbiome Species 0.000 description 2
- 230000008635 plant growth Effects 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 150000008163 sugars Chemical class 0.000 description 2
- HMUNWXXNJPVALC-UHFFFAOYSA-N 1-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperazin-1-yl]-2-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethanone Chemical group C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)N1CCN(CC1)C(CN1CC2=C(CC1)NN=N2)=O HMUNWXXNJPVALC-UHFFFAOYSA-N 0.000 description 1
- 108010059892 Cellulase Proteins 0.000 description 1
- 241000195493 Cryptophyta Species 0.000 description 1
- 240000008067 Cucumis sativus Species 0.000 description 1
- 235000010799 Cucumis sativus var sativus Nutrition 0.000 description 1
- 229930191978 Gibberellin Natural products 0.000 description 1
- 244000068988 Glycine max Species 0.000 description 1
- 235000010469 Glycine max Nutrition 0.000 description 1
- IHPVFYLOGNNZLA-UHFFFAOYSA-N Phytoalexin Natural products COC1=CC=CC=C1C1OC(C=C2C(OCO2)=C2OC)=C2C(=O)C1 IHPVFYLOGNNZLA-UHFFFAOYSA-N 0.000 description 1
- 235000008331 Pinus X rigitaeda Nutrition 0.000 description 1
- 235000011613 Pinus brutia Nutrition 0.000 description 1
- 241000018646 Pinus brutia Species 0.000 description 1
- 241000589516 Pseudomonas Species 0.000 description 1
- 244000155437 Raphanus sativus var. niger Species 0.000 description 1
- 238000002835 absorbance Methods 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 244000052616 bacterial pathogen Species 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229940106157 cellulase Drugs 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000004665 defense response Effects 0.000 description 1
- 230000004069 differentiation Effects 0.000 description 1
- 230000002255 enzymatic effect Effects 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 230000002496 gastric effect Effects 0.000 description 1
- 230000035784 germination Effects 0.000 description 1
- 239000003448 gibberellin Substances 0.000 description 1
- IXORZMNAPKEEDV-OBDJNFEBSA-N gibberellin A3 Chemical class C([C@@]1(O)C(=C)C[C@@]2(C1)[C@H]1C(O)=O)C[C@H]2[C@]2(C=C[C@@H]3O)[C@H]1[C@]3(C)C(=O)O2 IXORZMNAPKEEDV-OBDJNFEBSA-N 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- SEOVTRFCIGRIMH-UHFFFAOYSA-N indole-3-acetic acid Chemical compound C1=CC=C2C(CC(=O)O)=CNC2=C1 SEOVTRFCIGRIMH-UHFFFAOYSA-N 0.000 description 1
- 230000006698 induction Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- 239000000280 phytoalexin Substances 0.000 description 1
- 150000001857 phytoalexin derivatives Chemical class 0.000 description 1
- 230000004983 pleiotropic effect Effects 0.000 description 1
- 235000011121 sodium hydroxide Nutrition 0.000 description 1
- 239000011343 solid material Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 244000045561 useful plants Species 0.000 description 1
Classifications
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A40/00—Adaptation technologies in agriculture, forestry, livestock or agroalimentary production
- Y02A40/10—Adaptation technologies in agriculture, forestry, livestock or agroalimentary production in agriculture
Landscapes
- Cultivation Of Plants (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Description
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[Industrial Application Field] The present invention promotes plant growth by applying alginic acid oligosaccharide to plants or soil,
The present invention provides a method that enables efficient production of agricultural products. [Conventional techniques and their problems] It is an important issue in agricultural production to increase yield by promoting the growth of agricultural crops, increasing the yield per unit area, and increasing the number of plantings. Plant hormones such as gibberellins and auxins have been reported as plant growth-promoting substances, but the effects of these plant hormones are multifaceted and have many effects on plants at the same time. Even if one effect is beneficial, another effect may be harmful, and its practical use is limited. On the other hand, in recent years, it has been reported that oligosaccharides obtained through the decomposition of polysaccharides that constitute the cell walls of plants play an important role as regulators of the plant's own biological defense responses and induction of differentiation. I've come to feel that way. For example, when applied to soybean, oligogalacturonic acid prepared from plant cell walls promotes the synthesis of certain antibacterial substances (phytoalexins) and enhances resistance to pathogenic bacteria; It has been reported that oligosaccharides (xylo-oligosaccharides) produced by peas have the effect of suppressing the growth-promoting effect of auxin on pea sprouting. The actions of such oligosaccharides are different from those of plant hormones, and their actions are said to be specific rather than pleiotropic. [Means for Solving the Problems] The purpose of the present invention is to discover sugars that promote the growth of agricultural crops from among various oligosaccharides, apply these oligosaccharides to agricultural production, and improve the efficiency of agricultural production. The goal is to make the world more popular. In order to achieve the above object, the present inventors extensively searched for oligosaccharides that have the effect of promoting the growth of agricultural crops, and obtained oligosaccharides obtained by decomposing alginic acid (hereinafter referred to as alginic acid oligosaccharides).
The present invention has been completed based on the new discovery that this has the effect of promoting the growth of roots and above-ground parts of agricultural crops.
That is, the present invention provides (a) an oligosaccharide having a degree of polymerization of 2 to 20 and composed only of guluronic acid, and (b) a degree of polymerization of 2 to 20.
Oligosaccharides composed only of mannuronic acid and
(C) An oligosaccharide obtained by decomposing alginic acid, which has a degree of polymerization of 2 to 20 and is a mixture of oligosaccharides composed of guluronic acid and mannuronic acid, or the oligosaccharide.
This is a method of cultivating agricultural products characterized by using crops obtained by heat treatment for 15 minutes to 180 minutes under conditions of pH 1 to 3 and 100 to 130°C. The constituent sugars of alginic acid are mannuronic acid and guluronic acid, and the oligosaccharides obtained by decomposing these polysaccharides have a completely different chemical structure from the previously reported oligogalacturonic acids and xylooligosaccharides. It is also a new fact that oligosaccharides have the effect of promoting the growth of roots and above-ground parts of agricultural crops. In the present invention, alginate oligosaccharide is defined as follows. An oligosaccharide composition obtained by decomposing alginic acid, sodium alginate, and polysaccharides originating from microorganisms and algae such as kelp containing alginic acid with an enzyme such as alginate lyase, or by hydrolyzing with an acid such as hydrochloric acid. The main constituent sugar components of sugar are guluronic acid and mannuronic acid. It is a mixture of oligosaccharides having a degree of polymerization of 2 to 20 and composed of only guluronic acid, only mannuronic acid, or a combination of guluronic acid and mannuronic acid. Furthermore, this mixture has a pH of 1
~3. A heat-treated product obtained by heating for 15 minutes to 180 minutes under conditions of 100 to 130°C can also be used in the same manner. means. Such a composition is prepared, for example, as follows. All alginic acid-containing raw materials can be used as raw materials, including commercially available alginic acid, sodium alginate, alginic acid-containing seaweeds such as kelp, kajime, lesonia, and dulberia, and alginic acid-like polysaccharides produced by microorganisms such as Pseudomonas. can. As a means of decomposing alginic acid, a method of hydrolyzing it with an acid such as hydrochloric acid or sulfuric acid, and a method of decomposing it with an enzyme such as alginate lyase can be applied. When hydrolyzing with acid, for example, add 100 parts of water to 5 parts of sodium alginate to dissolve the alginic acid, then add 3 parts of concentrated hydrochloric acid and heat at 90 to 100°C for 2 to 4 hours.
After a period of hydrolysis, the alginate oligosaccharide can be prepared by filtering, neutralizing the solution with caustic soda, and concentrating. In addition, when decomposing with alginate lyase, add 100 parts of water to 5 parts of sodium alginate to dissolve alginic acid, then
Prepare alginate oligosaccharides by adjusting the pH to the optimum pH for enzyme action, adding 100 to 4000 units of enzyme per gram of sodium alginate, and reacting for 24 to 48 hours at the optimum temperature for enzyme action. I can do it. When an abalone gastrointestinal enzyme (trade name: Avalon Acetone Powder, manufactured by Merck) is used as alginate lyase, the optimum action pH is 7 to 8 and the optimum action temperature is 20 to 35°C. Enzyme activity of alginate lyase is PH7.0, 30â
When an enzyme is applied to a 0.2% sodium alginate solution, the enzyme power that increases the absorbance at 230 nm by 0.01 in 30 minutes is expressed as one unit. In addition, when obtaining oligosaccharides directly from seaweed,
For example, add 1,300 parts of water to 40 parts of dried kelp to bring the pH to 11, grind it with a homogenizer, treat it at 60°C for 3 hours, then bring the pH to 5.5, and add cellulase (product name: Meicelase, Meiji Seika Co., Ltd.) was added at a solid content of 0.5%, and after reacting at 40â for 20 hours, the pH was adjusted to 7.0.
1000% alginate lyase per 1g of solid content.
Alginate oligosaccharides can be produced directly from kelp by adding units and reacting at 30°C for 48 hours. The alginic acid oligosaccharide obtained in this way has mannuronic acid and guluronic acid as its main sugar components, and contains only guluronic acid with a degree of polymerization of 2 to 20, only mannuronic acid, or guluronic acid and mannuronic acid. It is a mixture containing oligosaccharides composed of a combination of acids. The content of alginate oligosaccharide in the decomposition product obtained as described above takes various values depending on the decomposition raw material, but for example, when prepared by an enzymatic decomposition method using sodium alginate as the raw material, solid Monochu 40
Reach ~100%. In addition, when seaweed such as kelp is used as a raw material, it accounts for 10 to 25% of the solid material. The alginic acid oligosaccharide thus obtained can be applied to seeds, etc., added to soil as a 0.25 to 0.00025% aqueous solution, sprayed on leaves, and even added to liquid fertilizer for hydroponic cultivation. When applied to agricultural crops by adding and mixing with the composition, it promotes the growth of the roots and above-ground parts of the crops, resulting in improved yields. ~3, preferably PH2.0
~3.0. It has become clear that heat treatment can be further promoted by performing heat treatment for 15 to 180 minutes at a temperature of 100 to 120°C. It should be noted that undecomposed alginic acid or sodium alginate had no growth-promoting effect on agricultural crops, as shown in Example 1 below, for example. [Example] Next, the present invention will be explained in detail with reference to Examples. Example 1 Alginate lyase (Avalon Acetone Powder) was added to alginic acid at a rate of 4000 u/g alginic acid, and reacted at pH 7.0 and 40°C for 48 hours to prepare oligosaccharides. â2
Heat treatment was performed for a period of time. After heat treatment, the reaction solution
The pH was neutralized to 7.0, and the plant growth promoting effect of alginate oligosaccharides before and after heating was investigated using daikon radish. That is, 36 Kaiware radish seeds were sown in a glass container set with a synthetic resin wool mat, 70 ml of tap water was added, and the mixture was heated at 23°C.
The seeds were cultivated for 6 days (4 days in the dark and the following 2 days under irradiation conditions of 5000 lux). Alginate oligosaccharide was added at a rate of 2.5 to 0.000025% based on tap water. The results are shown in Table 1. Alginate oligosaccharide promotes the growth of both shoot and root length compared to the control plot without alginate oligosaccharide under any concentration condition, but the effect is enhanced in the PH3.0, 120â, 2-hour heating section. There was a tendency to
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æ·»å ã«ãããããã®å¢åãèªããããã[Table] The values in Table 1 are the stem and leaf lengths (cm) grown under conditions without additives such as alginate oligosaccharides.
Or, it is expressed as an index when the average value of root length (cm) is set as 100. (n=36) Example 2 Two seeds of Mitsuba (white-stem Mitsuba) were sown in a 4 cm square synthetic resin wool pine and immersed in a liquid fertilizer containing Otsuka House Fertilizer No. 1 0.15% and Otsuka House Fertilizer No. 2 0.1%. After that, they were cultivated for 10 days at 23â and 5,000 lux to germinate and raise seedlings, and then planted in a hydroponic cultivation device at 8,000 lux. It was cultivated for 2.5 months under the condition of 23-24â. The experimental areas are as follows. Control group: Seedlings were raised with liquid fertilizer without addition of oligosaccharide alginate, and then cultivated with liquid fertilizer without additives. Alginate oligosaccharide added area: Alginate oligosaccharide
After raising seedlings with liquid fertilizer containing 0.025%, they were subsequently cultivated with liquid fertilizer containing 0.025% oligosaccharide alginate. In addition, alginate oligosaccharides are prepared by adding alginate lyase to a 5% sodium alginate solution (PH7.0).
Added at a rate of 4000u/g alginic acid, 40â,
After reacting for 48 hours, the pH of the reaction solution was adjusted to 3.0 and 120
The mixture was heat-treated at â for 2 hours, cooled, and then neutralized to pH 7.0. The test results are shown in Table 2. An increase in the yield of Mitsuba was observed with the addition of alginate oligosaccharide.
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The plants were grown for 6 days at 23°C in the dark for 4 days and then under irradiation at 5000 lux for the next 2 days. As a control, seeds without seed coating were sown in the same manner and cultivated under the same cultivation conditions. The results are shown in Table 3.
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ïŒã«ç€ºãã[Table] A 20% increase in yield was observed by adding alginate oligosaccharide to soil. Example 5 36 corn seeds were sown per 33 m 2 and cultivated for 3.5 months under natural conditions. The experimental areas are as follows. Control group: Oligosaccharide alginate untreated group Addition group: After germination, when the length of the leaves reached 8 to 12 cm, 6 g of oligosaccharide alginate was applied as a 0.05% aqueous solution around the roots. moreover,
After 1.5 months, 6 g of alginate oligosaccharide was additionally applied in the same manner. Note that the alginate oligosaccharide prepared according to the method described in Example 2 was used. The results are shown in Table 5.
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æ¹æ³ã§èª¿è£œãããçµæã衚ïŒã«ç€ºãã[Table] A 26% increase in corn yield was observed by applying alginate oligosaccharide. Example 6 100 cucumber seeds (variety name, Lady) were sown in a tray for raising seedlings, cultivated for one week at 20 to 23°C, and then planted in three-inch pots, and the seedlings were raised for another two weeks.
The seedlings thus obtained were planted in soil at intervals of 80 cm and cultivated under natural conditions for 3 months. The experimental areas are as follows. Control group: Alginate oligosaccharide untreated and added group: Three-inch pots After planting, on the third day, alginate oligosaccharide was dissolved in 50 ml of water at a rate of 25 mg per pot and applied. Further, 50 mg of the solution was dissolved in 500 ml of water and applied additionally 3 weeks after planting. Note that alginic acid oligosaccharide was prepared in the same manner as in Example 2. The results are shown in Table 6.
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By using alginic acid oligosaccharides according to the present invention, it is possible to promote the growth of useful plants and increase their yield.
Claims (1)
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æ³ã[Scope of Claims] 1 (a) An oligosaccharide with a degree of polymerization of 2 to 20 and composed only of guluronic acid, (b) an oligosaccharide with a degree of polymerization of 2 to 20 and composed only of mannuronic acid, and (C) Degree of polymerization is 2~
The oligosaccharide obtained by decomposing alginic acid, which is a mixture of oligosaccharides composed of guluronic acid and mannuronic acid, or the oligosaccharide at pH 1 to 3, 100
A method for cultivating agricultural products characterized by using products obtained by heat treatment for 15 minutes to 180 minutes under conditions of ~130°C. 2. The method according to claim 1, wherein an oligosaccharide obtained by decomposing alginic acid or a heat-treated product thereof is applied to seeds of agricultural crops. 3. The method according to claim 1, wherein the oligosaccharide obtained by decomposing alginic acid or a heat-treated product thereof is sprayed on the leaves of agricultural crops. 4. The method according to claim 1, in which an oligosaccharide obtained by decomposing alginic acid or a heat-treated product thereof is added to and mixed with fertilizer. 5. The method according to claim 1, wherein the oligosaccharide obtained by decomposing alginic acid or a heat-treated product thereof is mixed with soil in advance, and the soil is used. 6. The method according to claim 1, wherein an oligosaccharide obtained by decomposing alginic acid or a heat-treated product thereof is made into an aqueous solution, and the soil is sprinkled with this solution.
Priority Applications (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP61245400A JPS63101302A (en) | 1986-10-17 | 1986-10-17 | Culture of plant |
| CA000549522A CA1332880C (en) | 1986-10-17 | 1987-10-16 | Plant cultivation method |
| FR8714303A FR2605185B1 (en) | 1986-10-17 | 1987-10-16 | PLANT CULTIVATION PROCESS |
| CN87107747A CN1020842C (en) | 1986-10-17 | 1987-10-17 | Plant cultivation method |
| DE3735365A DE3735365C2 (en) | 1986-10-17 | 1987-10-19 | Method for accelerating plant growth |
| US07/571,003 US5588254A (en) | 1986-10-17 | 1990-08-22 | Plant cultivation method |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP61245400A JPS63101302A (en) | 1986-10-17 | 1986-10-17 | Culture of plant |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS63101302A JPS63101302A (en) | 1988-05-06 |
| JPH0433408B2 true JPH0433408B2 (en) | 1992-06-03 |
Family
ID=17133089
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP61245400A Granted JPS63101302A (en) | 1986-10-17 | 1986-10-17 | Culture of plant |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS63101302A (en) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2795289B1 (en) * | 1999-06-25 | 2005-09-30 | Centre Nat Rech Scient | USE OF 1,4-BETA-D-GLYCURONAN POLYMERS AND GLYCURONIC OLIGOSACCHARIDES DERIVED AS PHYTOSANITARY AND / OR FERTILIZER |
| CA2430277A1 (en) * | 1999-11-30 | 2001-07-06 | Chuanxing Yu | The alginate having low molecular weight, methods of manufacturing it and its use |
| FR3080742B1 (en) * | 2018-05-07 | 2021-09-24 | Soc Detude Et Dexploitation Dalgues Et Produits Maritimes Setexam | USE OF AN EXTRACT OR A FRACTION OF EXTRACT OF RED AGAROPHYTE ALGAE AS A PLANT DEFENSE STIMULATOR AND APPLICATION OF THE SAID EXTRACT OR OF THE SAID FRACTION OF EXTRACT |
-
1986
- 1986-10-17 JP JP61245400A patent/JPS63101302A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS63101302A (en) | 1988-05-06 |
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