USRE35320E - Method for regulating plant growth - Google Patents

Method for regulating plant growth Download PDF

Info

Publication number
USRE35320E
USRE35320E US08/369,604 US36960495A USRE35320E US RE35320 E USRE35320 E US RE35320E US 36960495 A US36960495 A US 36960495A US RE35320 E USRE35320 E US RE35320E
Authority
US
United States
Prior art keywords
plant
acid
lactic acid
concentration
growth
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
Application number
US08/369,604
Inventor
Alan M. Kinnersley
Taylor C. Scott, III
John H. Yopp
George H. Whitten
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Unilever Bestfoods North America
Original Assignee
Unilever Bestfoods North America
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=26710675&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=USRE35320(E) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Unilever Bestfoods North America filed Critical Unilever Bestfoods North America
Priority to US08/369,604 priority Critical patent/USRE35320E/en
Application granted granted Critical
Publication of USRE35320E publication Critical patent/USRE35320E/en
Assigned to BESTFOODS reassignment BESTFOODS MERGER (SEE DOCUMENT FOR DETAILS). Assignors: CPC INTERNATIONAL INC.
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION 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
    • A01N37/00Biocides, 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
    • A01N37/12Biocides, 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, wherein Cn means a carbon skeleton not containing a ring; Thio analogues thereof
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION 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
    • A01N37/00Biocides, 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
    • A01N37/36Biocides, 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 singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01HNEW PLANTS OR NON-TRANSGENIC PROCESSES FOR OBTAINING THEM; PLANT REPRODUCTION BY TISSUE CULTURE TECHNIQUES
    • A01H3/00Processes for modifying phenotypes, e.g. symbiosis with bacteria
    • A01H3/04Processes for modifying phenotypes, e.g. symbiosis with bacteria by treatment with chemicals
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01HNEW PLANTS OR NON-TRANSGENIC PROCESSES FOR OBTAINING THEM; PLANT REPRODUCTION BY TISSUE CULTURE TECHNIQUES
    • A01H4/00Plant reproduction by tissue culture techniques ; Tissue culture techniques therefor

Definitions

  • the present invention relates to a process for increasing the rate of plant growth, increasing chlorophyll concentration, increasing rate of root formation decreasing the amount of added nutrients required for plant growth, and protecting plants against the toxic effects of salts.
  • plants are treated with dilute solutions of certain organic acids. These acids also increase the rate of new plant formation when plants are propagated by tissue culture.
  • West German Pat. No. 19 16 054 discloses the use of alpha-hydroxy- or alpha-ketoalkanoic acids, having 7 to 10 carbon atoms, and their derivatives, particularly amides, for use for promoting the growth of plants under drought conditions.
  • U.S. Pat. No. 3,148,049 discloses certain halogenated keto acids, such as halogenated acetoacetic acid, as plant growth regulators.
  • U.S. Pat. No. 3,351,653 discloses the use of fluorinated hydroxy acids and esters as herbicides. In 1970, Mikami, et al, Agr. Biol.
  • Chem., 34, 977-979 reported test results of a number of hydroxy acids as plant growth regulators. Several of these, particularly, certain aromatic hydroxy acids, were shown to be root growth promoters. However, some of the simple acids, such as glycolic acid, caused suppression of root growth rather than root growth promotion. None of the hydroxy acids revealed any activity in the straight growth-promotion test used.
  • condensation polymers of the simple acids, glycolic acid and L-lactic acid do act as growth promoters and have other advantages when applied to growing plants.
  • a process for increasing the rate of growth of a plant which comprises supplying to the plant an effective amount of one or more acids having the following structural formula: ##STR1## where n is a small whole from 1 to 10; the Rs are the same or different and denote H or CH 3 ; and if at least one R is CH 3 , at least some of the asymmetric centers are in the L-configuration.
  • a process for increasing the concentration of chlorophyll in a plant which comprises supplying to the plant an effective amount of one or more acids having the structural Formula I.
  • Another provision, in accordance with this invention is a process for protecting a plant against the toxic effects of salts which comprises supplying to the plant an effective amount of one or more acids having the structural Formula I.
  • a process for enhancing the rate of formation of new plants when the plants are propagated by means of a tissue culture which comprises culturing tissues of the plant on a growth medium which contains an effective amount of one or more acids having the structural Formula I.
  • a process for increasing the rate of root formation of a plant which comprises supplying to the plant an effective amount of one or more acids having the following structural formula: ##STR2## where n is a small whole number from 1 to 10, and at least some of the asymmetric centers are in the L-configuration.
  • the acids generally useful in the practice of this invention are the linear condensation polymers of lactic acid and glycolic acid. These may be obtained by condensing two or more molecules of the acids with the elimination of water. Mixed polymers of the two acids may also be used. When the polymers contain at least one lactic acid unit, at least some of the asymmetric centers must be in the L-configuration since polymers of D-lactic acid are not useful in this process.
  • the polymers having Formula I used in the process of this invention are readily obtained by heating the monomeric acids, preferably under reduced pressure.
  • the mixtures of polymers so obtained can be used without further purification. If desired, the mixtures can be separated into their components by various fractionation techniques.
  • the rate of duckweed growth is slower and a smaller plant yield is obtained.
  • the polymers having Formula I are added to the growth medium, the amount of nutrients needed for good growth of the duckweed is greatly reduced.
  • the use of these polymers not only enhances the growth of plants but also reduces the amount of nutrients which must be supplied to the plant.
  • An additional benefit derived from growing plants in the presence of polymers having Formula I is that the plants accumulate more chlorophyll.
  • the growth-promoting ability of these polymers having Formula I are general properties as shown by their ability to enhance the growth of such diverse plants as lettuce, radishes, spinach, and corn. They are particularly useful in promoting the growth of plants in hydroponic culture.
  • the polymers having Formula I are also useful additives to tissue culture medium when plants are propagated by means of tissue culture. These acids enhance the formation of new shoots from the culture tissue, thus, increasing the rate of formation of new plants. Preferably they are used at a concentration between about 10 and about 1000 ppm on a weight/volume basis. This is a particularly useful property of these acids since many plants are now propagated commercially by means of tissue culture.
  • the polymers of L-lactic acid are also effective in increasing the rate of root formation in a plant. Plants grown in the presence of these acids have a considerable increase in average root length.
  • the acids used in the process of the present invention are thus seen to produce a wide variety of growth-regulant effects in the plants.
  • the particular growth-regulant effect produced in a plant depends, of course, on a number of variables, including the acid or mixture of acids used, the concentrations and total amounts of the acids used, the time at which the acids are applied, and the type of plant species which is treated.
  • the amount of material added is the effective amount needed to obtain the response desired.
  • the acids are utilized in dilute aqueous solutions which contain the acids in concentrations of from about 1 to about 1000 ppm on a weight/volume basis.
  • the preferred concentrations are from about 10 ppm to about 100 ppm.
  • the preferred ranges are from about 100 ppm to about 1000 ppm.
  • the most suitable concentrations for a particular application are readily determined by well-known screening test, such as those given in the examples.
  • Solutions of the acids are conveniently applied to the plants in the water added for plant growth. This water may also contain nutrients required by the plants. Optionally, solutions of the acids may be sprayed onto or otherwise applied to the roots, stems, or leaves of the plants.
  • Duckweed (Lemna minor L.) was grown following the general procedure of Mitchell and Livingston, Methods of Studying Plant Hormones and Growth Regulating Substances, USDA-ARS Agriculture Handbook, 336, pp. 66-67 (1968). Plants were grown on Nickell's medium as described in the handbook with the iron being present as the ferrous ion chelated with EDTA. One plant at the three-frond stage was placed in each flask. Flasks were incubated in continuous light (500 lux) at 28° ⁇ 2° C. for 14 days. The plants were harvested and weighed. All reported values represent 3 to 5 replicates.
  • lactyllactic acid formed by the condensation of 2 moles of lactic acid. This was demonstrated by testing L-lactyl-L-lactic acid obtained by the partial hydrolysis of the cyclic dimer of lactic acid, L-lactide (available from Henley and Co., New York City). The growth promotional property of this component is clearly shown by the results given in the last item of Table I.
  • Example II The general procedure given under Example I was followed.
  • the acids used were mixed polymers of D-lactic acid, mixed polymers of L-lactic acid, and mixed polymers of DL-lactic acid.
  • the polymers were obtained by heating the corresponding acids for 21/2 hours at 100° C. under vacuum.
  • the material was added to the duckweed flasks at the level of 1000 ppm. No lactic acid was added in the control.
  • Table II show that the growth enhancement effect of the polymers of lactic acid is due to the polymers of L-lactic acid and is not exhibited by the polymers of D-lactic acid.
  • Example 1 The general procedure of Example 1 was followed in which various polymers of L-lactic acid were added to the duckweed growth medium. The amounts of polymers added were such as to give equivalent number of molecules in each flask. Dimer of lactic acid (DP2) was obtained by hydrolysis of L-lactide. Higher polymers of L-lactic acid containing from 4 to 6 lactic acid units (DP4-DP6) were obtained by heating the dimer of lactic acid under reduced pressure. They were separated by high-performance liquid chromatography (HPLC). The results given in Table III show that each of these polymers of L-lactic acid are growth promoters for duckweed and that the polymers containing 4 to 6 lactic acid units are somewhat more effective than the polymers containing 2 lactic acid units when they are used on an equimolar basis.
  • DP2 dimer of lactic acid
  • HPLC high-performance liquid chromatography
  • Duckweed was also grown on media containing reduced amounts of Nickell's growth components, but, in each case, 100 ppm of L-lactyl-L-lactic acid was added to the mixture.
  • duckweed was grown in reduced amounts of Nickell's growth medium components. The duckweed was grown and harvested in the usual manner, and the dry plants were then weighed.
  • Table IV show that the dimer of L-lactic acid produces excellent growth of the plants when only a fraction of the normal amount of nutrients is present. This shows that such polymers not only enhance growth of plants, but also reduce the amount of added nutrients required for growth.
  • the mixed polymers of lactic acid were prepared in a similar manner to that used to make the polymers of glycolic acid. This mixture had about 28% lactic acid, 34% DP2, 22% DP3, 9% DP4, and smaller amounts of higher polymers of the lactic acid.
  • the results given in Table V show that the mixed polymers of glycolic acid, the mixed polymers of L-lactic acid, the dimer L-lactyl-L-lactic acid all enhance growth of duckweed.
  • duckweed was harvested, dried, suspended in 80% acetone, and homogenized for 30 seconds using a POLYTRON® brand homogenizer (Brinkman Instruments, Westbury, N.Y.). The mixture was centrifuged and absorption of the supernatant was read at 663 and 645 nm. From these readings, the number of micrograms of chlorophyll per milligram of dry weight was determined using the nomogram of Kirk, Planta, 78, 200-207 (1968). The results also given in Table V show that the polymers of both lactic acid and glycolic acid increase chlorophyll content of the plants, particularly when present in the growth medium at from 100 to 1000 ppm.
  • the average length of the duckweed roots was measured for 50 plants grown in the controls and for 50 plants grown in the flasks containing 1000 ppm of each of the added acids.
  • the results also given in Table V show that the polymers of lactic acid increase the root length.
  • Example 5 The general procedure of Example 5 was followed except that the material added to the duckweed flasks was a copolymer prepared by heating an equimolar mixture of glycolic acid and L-lactic acid for 90 minutes under reduced pressure. The procedure was repeated using physical mixtures of glycolic and lactic acid polymers containing two different proportions of the poly acids. These were the same polymers used in Example 5. The results of these tests given in Table VI show that both physical mixtures of the polymers and copolymers of the acids enhance growth of duckweed.
  • Fine vermiculite (125 ml) was placed in a 1-liter Erlenmeyer flask capped with a silicone foam closure. Then 100 ml of a nutrient solution containing 0.5 g/l MIRACLE-GRO® (a plant food having an N:P:K radio of 15:30:15) was added. In addition to the nutrient solution, L-lactyl-L-lactic acid at 100 or 1000 ppm was placed in certain flasks. Twelve radish seeds (Var. "Scarlet Globe", Yopp Quality Seeds, Carbondale, Ill.) were planted in each flask. After 10 days, all plants in each flask were pooled, dried, and weighed.
  • MIRACLE-GRO® a plant food having an N:P:K radio of 15:30:15
  • the plants grown on the medium containing 1000 ppm of L-lactyl-L-lactic acid had an average dry weight (average of 4 flasks) of about 30% greater than that of the plants grown on the same medium, but containing none of the lactic acid dimer.
  • the plants grown on medium containing 100 ppm of the lactic acid dimer had an average dry weight about 5% greater than that of the controls.
  • the experiment with radish seeds was repeated except that the lactic acid dimer was replaced by varying concentrations (10, 100 and 1000 ppm) of the mixture of L-lactic acid polymers used in Example 5. Plants were grown for 16 days before they were harvested. The plants grown on a medium containing 1000 ppm of the mixture of lactic acid polymers on the average weighed about 20% more than those grown on the nutrient medium without any lactic acid polymers. The shoots of the radishes grown on the medium containing the lactic acid polymers also contained about 30% more chlorophyll per milligram of dry weight than did the corresponding shoots of radishes grown on the control medium which contained no lactic acid polymers. These results clearly show the ability of the lactic acid polymers to increase the growth and chlorophyll content of radishes.
  • Corn was planted in 15-cm diameter pots filled with an autoclaved mixture of greenhouse potting soil and field soil. Fertilizer solution having an N:P:K ratio of 4:2:2 was diluted with water so that it was applied at a rate of 28 kg of nitrogen/hectare when 100 ml was added per pot.
  • Fertilizer solution having an N:P:K ratio of 4:2:2 was diluted with water so that it was applied at a rate of 28 kg of nitrogen/hectare when 100 ml was added per pot.
  • Four seeds of George W. Park Seed Company's 5145 Trucker's Favorite White Corn were planted in each pot in the greenhouse. The pots were watered twice a week. After 1 week, the pots were thinned to two plants per pot.
  • the medium flow rate was 80 ml/min with no aeration of the reservoir tank. Fresh medium, adjusted to pH 6.0, was added each week. To certain of the hydroponic units was added the dimer of L-lactic acid at a concentration of 100 ppm.
  • Potato shoot cultures were initiated from shoot tips excised from "eyes" of potato tubers. Excised shoot tips, consisting of apical domes accompanied by 4- to 6-leaf primordia, were placed upon nodal propagation medium. This medium consisted of Murashige and Skog salts (Physiol. Plant., 15, 473-497 (1962)) plus 30 g/l sucrose, 0.4 mg/l thiamine, 100 mg/l i-inositol, and 0.17 g/l NaH 2 PO 4 .H 2 O.
  • Each tube (25 ⁇ 150 mm) contained 20 ml of medium, which was adjusted to pH 6.0 and solidified with 1% agar. Sealed tubes were kept under 16 hr/day light at about 5000 lux at a constant 25° C. Thirty days after inoculation, the shoots were counted and recorded. The contacts of each tube was cut into sections with each section containing a single shoot. These shoots were than transferred to fresh media. After an additional 30 days, the number of shoots was again counted. The experiments were repeated with two levels of the dimer of L-lactic acid added to the medium and two levels of a mixed polymer of L-lactic acid added to the medium.
  • Duckweed was grown using the general procedure of Example 1. Plants were grown in control flasks which contained only the culture medium. Other plants were grown in flasks containing medium to which was added 400 ppm of Mn ++ (as MnSO 4 H 2 O) with and without added polyglycolic acid, poly-L-lactic acid, or L-lactyl-L-lactic acid.
  • Mn ++ as MnSO 4 H 2 O
  • the results given in Table IX show that the dimer of lactic acid as well as the polymers of lactic and glycolic acids are able to protect duckweed from the growth-inhibiting effects of the manganous ion. It is noted that the preferred concentrations of polyglycolic acid and L-lactyl-L-lactic acid for this purpose are about 100 ppm, whereas, the preferred concentration of poly-L-lactic acid is about 1000 ppm for this purpose.
  • Example 11 The general procedure of Example 11 was followed except that plants were grown in flasks containing medium with various levels of Cu ++ (as CuSO 4 .5H 2 O) and seawater with and without added L-lactic acid polymers.
  • the results given in Table X show the effectiveness of L-lactic acid polymers in protecting the plants against the growth-inhibiting effects of the copper ion and of the mixture of ions present in seawater.
  • Chlorella vulgaris was grown in Chu-Gerloff medium (Gerloff, et al, pp. 27-44, in The Culturing of Algae: A Symposium, Antioch Press, Yellow Springs, Ohio (1950)) in 250-ml Erlenmeyer flasks sealed with rubber closures. The flasks were shaken at 40 rpm and exposed to about 4000 lux of light for 16 hrs per day. After 8 days of growth, 5-ml samples of each culture were dried, and the chlorophyll content of the cells was measured using the procedure given in Example 5. Tests were repeated on chlorella grown in the presence of added poly-L-lactic acid, and on chlorella grown in the presence of seawater with and without added poly-L-lactic acid.
  • Table XI The results given in Table XI are the averages of determinations made on contents of four different flasks at each concentration level. They demonstrate the ability of lactic acid polymers to increase the amount of the metabolite, chlorophyll, even when the algae are grown in the presence of substantial concentrations of the salts found in seawater.

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • Environmental Sciences (AREA)
  • Developmental Biology & Embryology (AREA)
  • Engineering & Computer Science (AREA)
  • Botany (AREA)
  • Dentistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Plant Pathology (AREA)
  • Pest Control & Pesticides (AREA)
  • Agronomy & Crop Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Biotechnology (AREA)
  • Cell Biology (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Cultivation Of Plants (AREA)
  • Hydroponics (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Fertilizers (AREA)
  • Micro-Organisms Or Cultivation Processes Thereof (AREA)
  • Polyesters Or Polycarbonates (AREA)

Abstract

A process for increasing the rate of plant growth. Plants are treated with one or more acids, which are condensation products of glycolic and/or L-lactic acid. These acids also increase the concentration of chlorophyll, increase the rate of new plant formation when plants are propagated by tissue culture, decrease the amount of added nutrients required for plant growth, and protect plants against the toxic effects of salts. Certain of the acids are useful for increasing the rate of root formation in the plant.
The questions raised in reexamination request Nos. 90/002,306, filed Mar. 26, 1991 and 90/003,035 filed Apr. 27, 1993, have been considered and the results thereof are reflected in this reissue patent which constitutes the reexamination certificate required by 35 U.S.C. 307 as provided in 37 CFR 1.570(e).

Description

This is a continuation-in-part of copending application, Ser. No. 034,191, filed Apr. 6, 1987 now abandoned.
FIELD OF THE INVENTION
The present invention relates to a process for increasing the rate of plant growth, increasing chlorophyll concentration, increasing rate of root formation decreasing the amount of added nutrients required for plant growth, and protecting plants against the toxic effects of salts. In this process, plants are treated with dilute solutions of certain organic acids. These acids also increase the rate of new plant formation when plants are propagated by tissue culture.
BACKGROUND OF THE INVENTION
Various derivatives of organic acids have been proposed as plant growth regulators. For example, West German Pat. No. 19 16 054 discloses the use of alpha-hydroxy- or alpha-ketoalkanoic acids, having 7 to 10 carbon atoms, and their derivatives, particularly amides, for use for promoting the growth of plants under drought conditions. U.S. Pat. No. 3,148,049 discloses certain halogenated keto acids, such as halogenated acetoacetic acid, as plant growth regulators. U.S. Pat. No. 3,351,653 discloses the use of fluorinated hydroxy acids and esters as herbicides. In 1970, Mikami, et al, Agr. Biol. Chem., 34, 977-979, reported test results of a number of hydroxy acids as plant growth regulators. Several of these, particularly, certain aromatic hydroxy acids, were shown to be root growth promoters. However, some of the simple acids, such as glycolic acid, caused suppression of root growth rather than root growth promotion. None of the hydroxy acids revealed any activity in the straight growth-promotion test used.
We have now discovered, to our surprise, that certain condensation polymers of the simple acids, glycolic acid and L-lactic acid, do act as growth promoters and have other advantages when applied to growing plants.
SUMMARY OF THE INVENTION
In accordance with this invention, there is provided a process for increasing the rate of growth of a plant which comprises supplying to the plant an effective amount of one or more acids having the following structural formula: ##STR1## where n is a small whole from 1 to 10; the Rs are the same or different and denote H or CH3 ; and if at least one R is CH3, at least some of the asymmetric centers are in the L-configuration.
Further provided, in accordance with this invention, is a process for increasing the concentration of chlorophyll in a plant which comprises supplying to the plant an effective amount of one or more acids having the structural Formula I.
Also provided, in accordance with this invention, is a process for decreasing the amount of added nutrients required for growth of a plant which comprises supplying to the plant an effective amount of one or more acids having the structural Formula I.
Another provision, in accordance with this invention, is a process for protecting a plant against the toxic effects of salts which comprises supplying to the plant an effective amount of one or more acids having the structural Formula I.
In addition, in accordance with this invention, there is provided a process for enhancing the rate of formation of new plants when the plants are propagated by means of a tissue culture which comprises culturing tissues of the plant on a growth medium which contains an effective amount of one or more acids having the structural Formula I.
Finally, in accordance with this invention, there is provided a process for increasing the rate of root formation of a plant which comprises supplying to the plant an effective amount of one or more acids having the following structural formula: ##STR2## where n is a small whole number from 1 to 10, and at least some of the asymmetric centers are in the L-configuration.
DETAILED DESCRIPTION OF THE INVENTION
The acids generally useful in the practice of this invention are the linear condensation polymers of lactic acid and glycolic acid. These may be obtained by condensing two or more molecules of the acids with the elimination of water. Mixed polymers of the two acids may also be used. When the polymers contain at least one lactic acid unit, at least some of the asymmetric centers must be in the L-configuration since polymers of D-lactic acid are not useful in this process.
The polymers having Formula I used in the process of this invention are readily obtained by heating the monomeric acids, preferably under reduced pressure. The mixtures of polymers so obtained can be used without further purification. If desired, the mixtures can be separated into their components by various fractionation techniques.
The activity of the acids used in the practice of this invention was discovered when they were tested in the duckweed promotion assay of Mitchell and Livingston, Methods of Studying Plant Hormones and Growth-Regulating Substances, USDA-ARS Agriculture Handbook, 336, pp. 66-67 (1968). This test showed that polymers having Formula I have growth-promoting abilities when used in the concentration of from between about 1 and about 1000 ppm (parts per million) on a weight/volume basis. Neither pure L-lactic acid nor pure D-lactic acid shows such growth-promoting properties. Likewise, the condensation polymers of D-lactic acid show little growth-promoting ability.
This growth-promoting ability of the polymers of L-lactic acid is even shown by the dimer of L-lactic acid, L-lactyl-L-lactic acid. It is also shown by the individual condensation polymers of L-lactic acid containing up to 10 lactic acid units.
Generally, when the concentration of nutrients present in the nutrient solution used for growing duckweed in the growth-promotion assay is reduced, the rate of duckweed growth is slower and a smaller plant yield is obtained. Surprisingly, if the polymers having Formula I are added to the growth medium, the amount of nutrients needed for good growth of the duckweed is greatly reduced. Thus, the use of these polymers not only enhances the growth of plants but also reduces the amount of nutrients which must be supplied to the plant.
An additional benefit derived from growing plants in the presence of polymers having Formula I is that the plants accumulate more chlorophyll. The presence of such polymers in the growth medium, particularly at the concentration of from about 100 to about 1000 ppm on a weight/volume basis, greatly enhances the amount of chlorophyll accumulated per milligram of plant weight.
When the polymers having Formula I are supplied to plants they enable the plant to grow in water containing concentrations of salts that would normally be toxic to the plants. This shows special utility for the process of this invention in applications using irrigation water of high salinity.
The growth-promoting ability of these polymers having Formula I are general properties as shown by their ability to enhance the growth of such diverse plants as lettuce, radishes, spinach, and corn. They are particularly useful in promoting the growth of plants in hydroponic culture.
The polymers having Formula I are also useful additives to tissue culture medium when plants are propagated by means of tissue culture. These acids enhance the formation of new shoots from the culture tissue, thus, increasing the rate of formation of new plants. Preferably they are used at a concentration between about 10 and about 1000 ppm on a weight/volume basis. This is a particularly useful property of these acids since many plants are now propagated commercially by means of tissue culture.
The polymers of L-lactic acid are also effective in increasing the rate of root formation in a plant. Plants grown in the presence of these acids have a considerable increase in average root length.
The acids used in the process of the present invention are thus seen to produce a wide variety of growth-regulant effects in the plants. The particular growth-regulant effect produced in a plant depends, of course, on a number of variables, including the acid or mixture of acids used, the concentrations and total amounts of the acids used, the time at which the acids are applied, and the type of plant species which is treated. The amount of material added is the effective amount needed to obtain the response desired.
In general, the acids are utilized in dilute aqueous solutions which contain the acids in concentrations of from about 1 to about 1000 ppm on a weight/volume basis. For most applications, the preferred concentrations are from about 10 ppm to about 100 ppm. However, for certain applications, the preferred ranges are from about 100 ppm to about 1000 ppm. The most suitable concentrations for a particular application are readily determined by well-known screening test, such as those given in the examples.
Solutions of the acids are conveniently applied to the plants in the water added for plant growth. This water may also contain nutrients required by the plants. Optionally, solutions of the acids may be sprayed onto or otherwise applied to the roots, stems, or leaves of the plants.
The following specific examples illustrate the present invention. They are not intended to limit the invention in any way. When concentrations are given in ppm, they are on a weight/volume basis. When ratios of nitrogen, phosphorus, and potassium are given herein, they refer to the conventional fertilizer ratios in which the nitrogen is given as "weight % N", phosphorus is given as "weight % P2 O5 ", and potassium is given as "weight % K2 O".
EXAMPLE 1
Duckweed (Lemna minor L.) was grown following the general procedure of Mitchell and Livingston, Methods of Studying Plant Hormones and Growth Regulating Substances, USDA-ARS Agriculture Handbook, 336, pp. 66-67 (1968). Plants were grown on Nickell's medium as described in the handbook with the iron being present as the ferrous ion chelated with EDTA. One plant at the three-frond stage was placed in each flask. Flasks were incubated in continuous light (500 lux) at 28°±2° C. for 14 days. The plants were harvested and weighed. All reported values represent 3 to 5 replicates.
Experiments were performed in which 85% DL-lactic acid (Sigma Chemical Co.) was added at concentrations of 10, 100, and 1000 ppm. A control was run in which no acid was added. The results given in Table I demonstrate that growth is greatly enhanced when the lactic acid is present in the concentrations of 100 and 1000 ppm. This same effect was seen using DL-lactic acid from Fisher Scientific. The fact that pure D-lactic acid (Sigma Chemical Co., St. Louis, Mo.) and pure L-lactic acid (Fitz Chemical Co., Chicago, Ill.) do not give this growth enhancement is also shown by comparable experiments which are reported in Table I. It was discovered that the growth-promoting material in technical DL-lactic acid was due to larger molecules formed by condensation of 2 or more molecules of lactic acid. Growth is promoted by the simplest of such molecules, lactyllactic acid, formed by the condensation of 2 moles of lactic acid. This was demonstrated by testing L-lactyl-L-lactic acid obtained by the partial hydrolysis of the cyclic dimer of lactic acid, L-lactide (available from Henley and Co., New York City). The growth promotional property of this component is clearly shown by the results given in the last item of Table I.
              TABLE I                                                     
______________________________________                                    
DUCKWEED GROWTH ASSAY                                                     
       Weight (mg)                                                        
       Added Acid (ppm)                                                   
       Control 10        100       1000                                   
______________________________________                                    
DL-Lactic                                                                 
         130 ± 19.sup.d                                                
                   134 ± 7.sup.d                                       
                             207 ± 50.sup.d                            
                                     339 ± 56.sup.a                    
Acid                                                                      
(Technical                                                                
(85%)                                                                     
L-Lactic Acid                                                             
         257 ± 28.sup.d                                                
                   256 ± 28.sup.d                                      
                             198 ± 64.sup.d                            
                                     175 ± 32.sup.d                    
(Pure)                                                                    
D-Lactic 71 ± 7b                                                       
                   66 ± 4.sup.b                                        
                             75 ± 11.sup.b                             
                                     79 ± 5.sup.b                      
Acid (Pure)                                                               
L-Lactyl-L-                                                               
         46 ± 6.sup.b                                                  
                    30 ± 15.sup.b                                      
                             71 ± 26.sup.b                             
                                      73 ± 21.sup.b                    
Lactic Acid                                                               
______________________________________                                    
 .sup.d Fresh weight                                                      
 .sup.b Dry weight                                                        
EXAMPLE 2
The general procedure given under Example I was followed. The acids used were mixed polymers of D-lactic acid, mixed polymers of L-lactic acid, and mixed polymers of DL-lactic acid. The polymers were obtained by heating the corresponding acids for 21/2 hours at 100° C. under vacuum. The material was added to the duckweed flasks at the level of 1000 ppm. No lactic acid was added in the control. The results given in Table II show that the growth enhancement effect of the polymers of lactic acid is due to the polymers of L-lactic acid and is not exhibited by the polymers of D-lactic acid.
When duckweed was grown in the presence of poly-L-lactic acid uniformly labelled with carbon-14, it was found that 12% of the radioactive carbon was incorporated in the plant tissue. This indicates that the acid is acting as a true growth regulator.
              TABLE II                                                    
______________________________________                                    
EFFECT OF POLYLACRIC ACID ISOMERS ON                                      
DUCKWEED                                                                  
                 Mean Dry Weight                                          
Treatment        Per Flask (mg)                                           
______________________________________                                    
Control (No acid)                                                         
                 23 ± 2                                                
Poly-D-Lactic Acid                                                        
                 28 ± 4                                                
Poly-L-Lactic Acid                                                        
                 64 ± 7                                                
Poly-DL-Lactic Acid                                                       
                  53 ± 10                                              
______________________________________                                    
EXAMPLE 3
The general procedure of Example 1 was followed in which various polymers of L-lactic acid were added to the duckweed growth medium. The amounts of polymers added were such as to give equivalent number of molecules in each flask. Dimer of lactic acid (DP2) was obtained by hydrolysis of L-lactide. Higher polymers of L-lactic acid containing from 4 to 6 lactic acid units (DP4-DP6) were obtained by heating the dimer of lactic acid under reduced pressure. They were separated by high-performance liquid chromatography (HPLC). The results given in Table III show that each of these polymers of L-lactic acid are growth promoters for duckweed and that the polymers containing 4 to 6 lactic acid units are somewhat more effective than the polymers containing 2 lactic acid units when they are used on an equimolar basis.
              TABLE III                                                   
______________________________________                                    
EFFECT OF L-LACTIC ACID POLYMERS ON                                       
DUCKWEED                                                                  
                 Dry Weight                                               
Additive         (mg)                                                     
______________________________________                                    
Control (No acid)                                                         
                  70 ± 40                                              
DP2 (100 ppm)    109 ± 11                                              
DP4 (200 ppm)    149 ± 32                                              
DP5 (250 ppm)    157 ± 15                                              
DP6 (300 ppm)    154 ± 28                                              
______________________________________                                    
A similar experiment was run in which higher polymers of lactic acid (DP8, DP9, and DP10) were added to the growth medium for the duckweed. These showed similar enhancement of growth when they were used at equivalent molarities, i.e., 400, 450, and 500 ppm, respectively. When high concentrations (4000-5000 ppm) of these higher molecular weight polymers were added to the growth medium, the plants were very small and had tiny roots. This indicates that such polymers have promise in dwarfing or in growth management where slow growth is desired, such as in turf management.
EXAMPLE 4
Duckweed was also grown on media containing reduced amounts of Nickell's growth components, but, in each case, 100 ppm of L-lactyl-L-lactic acid was added to the mixture. In control experiments, duckweed was grown in reduced amounts of Nickell's growth medium components. The duckweed was grown and harvested in the usual manner, and the dry plants were then weighed. The results of these experiments given in Table IV show that the dimer of L-lactic acid produces excellent growth of the plants when only a fraction of the normal amount of nutrients is present. This shows that such polymers not only enhance growth of plants, but also reduce the amount of added nutrients required for growth.
              TABLE IV                                                    
______________________________________                                    
EFFECT OF L-LACTIC ACID DIMER ON                                          
DUCKWEED GROWN ON REDUCED NUTRIENTS                                       
             Dry weight (mg)                                              
Fraction of             L-Lacryl-L-Lactic                                 
Nickell's Medium                                                          
               Control  Acid (100 ppm)                                    
______________________________________                                    
0               1 ± 1                                                  
                         1 ± 1                                         
1/16           12 ± 2                                                  
                        25 ± 1                                         
1/8            23 ± 1                                                  
                        44 ± 7                                         
1/4            27 ± 3                                                  
                        46 ± 6                                         
Full           30 ± 5                                                  
                         41 ± 12                                       
Concentration                                                             
______________________________________                                    
EXAMPLE 5
The general procedure of Example 1 was followed using a mixture of polymers of glycolic acid, a mixture of polymers of L-lactic acid, and the dimer L-lactyl-L-lactic acid. The material was added to the duckweed flasks at levels of 10, 100, and 1000 ppm. The mixed polymers of glycolic acid were obtained by heating glycolic acid under vacuum (20 mm) at 85° C. for 21 hours. This mixture had about 27% glycolic acid, 20% DP2, 11% DP3, 20% DP4, 12% DP5, and smaller amounts of higher polymers of glycolic acid. (DP2=the dimer, DP3=the trimer, etc., of glycolic acid). The mixed polymers of lactic acid were prepared in a similar manner to that used to make the polymers of glycolic acid. This mixture had about 28% lactic acid, 34% DP2, 22% DP3, 9% DP4, and smaller amounts of higher polymers of the lactic acid. The results given in Table V show that the mixed polymers of glycolic acid, the mixed polymers of L-lactic acid, the dimer L-lactyl-L-lactic acid all enhance growth of duckweed.
The duckweed grown in the presence of the acids appeared much darker green than that of the control. In order to measure chlorophyll content, duckweed was harvested, dried, suspended in 80% acetone, and homogenized for 30 seconds using a POLYTRON® brand homogenizer (Brinkman Instruments, Westbury, N.Y.). The mixture was centrifuged and absorption of the supernatant was read at 663 and 645 nm. From these readings, the number of micrograms of chlorophyll per milligram of dry weight was determined using the nomogram of Kirk, Planta, 78, 200-207 (1968). The results also given in Table V show that the polymers of both lactic acid and glycolic acid increase chlorophyll content of the plants, particularly when present in the growth medium at from 100 to 1000 ppm.
The average length of the duckweed roots was measured for 50 plants grown in the controls and for 50 plants grown in the flasks containing 1000 ppm of each of the added acids. The results also given in Table V show that the polymers of lactic acid increase the root length.
              TABLE V                                                     
______________________________________                                    
COMPARISON OF GLYCOLIC ACID AND LACTIC ACID                               
POLYMERS ON DUCKWEED GROWTH AND                                           
CHLOROPHYLL CONTENT                                                       
                                   Root                                   
           Dry Weight Chlorophyll (μg)                                 
                                   Length                                 
Acid       (mg)       Per mg       (mm)                                   
______________________________________                                    
Polyglycolic Acid                                                         
1000 ppm   38.3 ± 3.5                                                  
                      5.5           8.3 ± 1.0                          
100        47.3 ± 2.1                                                  
                      5.7                                                 
10         34.3 ± 2.5                                                  
                      2.4                                                 
Poly-L-Lactic                                                             
Acid                                                                      
1000 ppm    76.3 ± 11.3                                                
                      6.5          13.7 ± 3.2                          
100        46.3 ± 5.8                                                  
                      2.7                                                 
10         27.3 ± 2.3                                                  
                      2.1                                                 
L-Lactyl-L-Lactic                                                         
Acid                                                                      
1000 ppm   39.3 ± 7.6                                                  
                      6.0          10.1 ± 1.7                          
100         46.3 ± 10.0                                                
                      4.5                                                 
10         28.0 ± 4.3                                                  
                      1.6                                                 
Control    20.0 ± 2.5                                                  
                      2.0           7.7 ± 2.0                          
(No Acid)                                                                 
______________________________________                                    
EXAMPLE 6
The general procedure of Example 5 was followed except that the material added to the duckweed flasks was a copolymer prepared by heating an equimolar mixture of glycolic acid and L-lactic acid for 90 minutes under reduced pressure. The procedure was repeated using physical mixtures of glycolic and lactic acid polymers containing two different proportions of the poly acids. These were the same polymers used in Example 5. The results of these tests given in Table VI show that both physical mixtures of the polymers and copolymers of the acids enhance growth of duckweed.
              TABLE VI                                                    
______________________________________                                    
EFFECT OF MIXED POLYMERS OF GLYCOLIC                                      
AND LACTIC ACIDS ON DUCKWEED GROWTH                                       
                     Dry Weight                                           
Acid                 (mg)                                                 
______________________________________                                    
Copolymer of                                                              
Glycolic Acid and L-Lactic Acid                                           
1000 ppm             56.5 ± 9.7                                        
100                  48.0 ± 6.9                                        
10                   38.7 ± 2.9                                        
Control (No Acid)     35.5 ± 10.5                                      
1:1 Mixture of Polymers of                                                
L-Lactic Acid and Glycolic Acid                                           
1000 ppm             43.7 ± 6.9                                        
100                  37.5 ± 1.4                                        
10                   27.7 ± 1.9                                        
3:1 Mixture of Polymers of                                                
L-Lactic Acid and Glycolic Acid                                           
1000 ppm             56.0 ± 10                                         
100                  44.0 ± 9.5                                        
10                   30.7 ± 6.3                                        
Control (No Acid)      23 ± 3.8                                        
______________________________________                                    
EXAMPLE 7
Fine vermiculite (125 ml) was placed in a 1-liter Erlenmeyer flask capped with a silicone foam closure. Then 100 ml of a nutrient solution containing 0.5 g/l MIRACLE-GRO® (a plant food having an N:P:K radio of 15:30:15) was added. In addition to the nutrient solution, L-lactyl-L-lactic acid at 100 or 1000 ppm was placed in certain flasks. Twelve radish seeds (Var. "Scarlet Globe", Yopp Quality Seeds, Carbondale, Ill.) were planted in each flask. After 10 days, all plants in each flask were pooled, dried, and weighed. The plants grown on the medium containing 1000 ppm of L-lactyl-L-lactic acid had an average dry weight (average of 4 flasks) of about 30% greater than that of the plants grown on the same medium, but containing none of the lactic acid dimer. The plants grown on medium containing 100 ppm of the lactic acid dimer had an average dry weight about 5% greater than that of the controls.
The experiment with radish seeds was repeated except that the lactic acid dimer was replaced by varying concentrations (10, 100 and 1000 ppm) of the mixture of L-lactic acid polymers used in Example 5. Plants were grown for 16 days before they were harvested. The plants grown on a medium containing 1000 ppm of the mixture of lactic acid polymers on the average weighed about 20% more than those grown on the nutrient medium without any lactic acid polymers. The shoots of the radishes grown on the medium containing the lactic acid polymers also contained about 30% more chlorophyll per milligram of dry weight than did the corresponding shoots of radishes grown on the control medium which contained no lactic acid polymers. These results clearly show the ability of the lactic acid polymers to increase the growth and chlorophyll content of radishes.
EXAMPLE 8
Corn was planted in 15-cm diameter pots filled with an autoclaved mixture of greenhouse potting soil and field soil. Fertilizer solution having an N:P:K ratio of 4:2:2 was diluted with water so that it was applied at a rate of 28 kg of nitrogen/hectare when 100 ml was added per pot. Four seeds of George W. Park Seed Company's 5145 Trucker's Favorite White Corn were planted in each pot in the greenhouse. The pots were watered twice a week. After 1 week, the pots were thinned to two plants per pot. One hundred ml of a solution containing varying concentrations of L-lactic acid dimer, adjusted to pH 6.6, was added each week for 4 weeks. The plants were then allowed to grow for an additional month with watering but without the addition of more lactic acid dimer. Since the experiments were run in the winter, the existing light was supplemented with 320 watts of fluorescence light. Plants were then harvested, dried, and weighed. The results given in Table VII show that the dimer of L-lactic acid stimulates the early growth of corn plants when it is added at a concentration of from 1 to 10 ppm per dimer give less stimulation of plant growth. When radish seeds were grown under these conditions with varying amounts of the L-lactic acid dimer, no significant effect on growth was observed. However, the lactic acid dimer did promote growth of radishes under slightly different conditions (Example 7).
              TABLE VII                                                   
______________________________________                                    
EFFECT OF L-LACTIC ACID DIMER ON GROWTH OF                                
CORN                                                                      
               Total Plant                                                
Acid Added (ppm)                                                          
               Mean Dry Weight (g)                                        
______________________________________                                    
None (Control) 0.45 ± 0.07                                             
 1             0.94 ± 0.07                                             
10             1.2 ± 0.2                                               
100            0.64 ± 0.07                                             
______________________________________                                    
EXAMPLE 9
Spinach seeds were germinated in a mixture of peat moss, vermiculite, and perlite. After 9 days, seedlings were transferred to hydroponic units. Lettuce seeds were germinated on filter paper discs wet with distilled water. After 3 days, seedlings were transferred to hydroponic units. The units used were Jewel-Hubbard Scientific (Carolina Biological Supply Co., Burlington, N.C.) single-hydroponic units filled with 18.5 liters of medium. The medium used had the following composition:
______________________________________                                    
                  Concentration                                           
                  Per Liter                                               
______________________________________                                    
KH.sub.2 PO.sub.4   0.034   g                                             
KNO.sub.3           0.127   g                                             
Ca(NO.sub.3).sub.2.4H.sub.2 O                                             
                    0.296   g                                             
MgSO.sub.4.7H.sub.2 O                                                     
                    0.124   g                                             
H.sub.3 BO.sub.3    0.72    mg                                            
MnCl.sub.2.4H.sub.2 O                                                     
                    0.45    mg                                            
ZnSO.sub.4.7H.sub.2 O                                                     
                    0.055   mg                                            
CaSO.sub.4.5H.sub.2 O                                                     
                    0.020   mg                                            
NaMoO.sub.4.2H.sub.2 O                                                    
                    0.007   mg                                            
FeSO.sub.4.7H.sub.2 O                                                     
                    0.68    mg                                            
Na.sub.2 EDTA       0.93    mg                                            
______________________________________                                    
The medium flow rate was 80 ml/min with no aeration of the reservoir tank. Fresh medium, adjusted to pH 6.0, was added each week. To certain of the hydroponic units was added the dimer of L-lactic acid at a concentration of 100 ppm.
Spinach was harvested 38 days after germination, lettuce was harvested 30 days after germination. The fresh weight of individual plants was recorded, and all plants for each treatment were then pooled and dried at 70° C. for 16 hours for a single total dry weight for each treatment. The results given in Table VIII show that the dimer of L-lactic acid, when employed at a concentration of 100 ppm, is effective in stimulating the growth of both spinach and lettuce when grown hydroponically.
              TABLE VIII                                                  
______________________________________                                    
EFFECT OF L-LACTIC ACID DIMER ON SPINACH AND                              
LETTUCE GROWN HYDROPONICALLY                                              
            Mean Weight Per Plant (g)                                     
            Fresh Weight                                                  
                     Dry Weight                                           
______________________________________                                    
Spinach                                                                   
Control       6.1 ± 2 0.41                                             
100 ppm Acid  9.2 ± 2 0.63                                             
Lettuce                                                                   
Control       1.6 ± 0.4                                                
                         0.083                                            
100 ppm Acid  4.1 ± 0.7                                                
                         0.20                                             
______________________________________                                    
EXAMPLE 10
Potato shoot cultures were initiated from shoot tips excised from "eyes" of potato tubers. Excised shoot tips, consisting of apical domes accompanied by 4- to 6-leaf primordia, were placed upon nodal propagation medium. This medium consisted of Murashige and Skog salts (Physiol. Plant., 15, 473-497 (1962)) plus 30 g/l sucrose, 0.4 mg/l thiamine, 100 mg/l i-inositol, and 0.17 g/l NaH2 PO4.H2 O.
Ten replicate tubes were each inoculated with a single shoot. Each tube (25×150 mm) contained 20 ml of medium, which was adjusted to pH 6.0 and solidified with 1% agar. Sealed tubes were kept under 16 hr/day light at about 5000 lux at a constant 25° C. Thirty days after inoculation, the shoots were counted and recorded. The contacts of each tube was cut into sections with each section containing a single shoot. These shoots were than transferred to fresh media. After an additional 30 days, the number of shoots was again counted. The experiments were repeated with two levels of the dimer of L-lactic acid added to the medium and two levels of a mixed polymer of L-lactic acid added to the medium. When the dimer of L-lactic acid or the mixed polymers of L-lactic acid were added to the tissue culture medium at levels from 100 to 1000 ppm, the number of shoots produced increased by from 5% to 20% over those of the controls. Mixed polymers of L-lactic acid were somewhat more effective than the dimers of L-lactic acid in this promotion.
The general procedure outlined for potato shoot cultures was followed for shoot primordial cultures of tobacco. The plantlets grown in media containing 50 ppm and 100 ppm of mixed polymers of L-lactic acid showed increases in weights over those of the control of 20% and 50%, respectively. Higher concentrations of the polymers of lactic acid in the medium (500-1000 ppm) inhibited growth of the cultures but gave products with a higher concentration of chlorophyll.
These examples show that the polymers of L-lactic acid are useful in enhancing the rate of formation of new plants when the plants are propagated by means of tissue culture.
EXAMPLE 11
Duckweed was grown using the general procedure of Example 1. Plants were grown in control flasks which contained only the culture medium. Other plants were grown in flasks containing medium to which was added 400 ppm of Mn++ (as MnSO4 H2 O) with and without added polyglycolic acid, poly-L-lactic acid, or L-lactyl-L-lactic acid. The results given in Table IX show that the dimer of lactic acid as well as the polymers of lactic and glycolic acids are able to protect duckweed from the growth-inhibiting effects of the manganous ion. It is noted that the preferred concentrations of polyglycolic acid and L-lactyl-L-lactic acid for this purpose are about 100 ppm, whereas, the preferred concentration of poly-L-lactic acid is about 1000 ppm for this purpose.
              TABLE IX                                                    
______________________________________                                    
EFFECT OF VARIOUS ACIDS ON                                                
DUCKWEED GROWN IN PRESENCE OF Mn.sup.++                                   
                     Mean Dry Weight                                      
Additives            Per Flask (mg)                                       
______________________________________                                    
Control              27.0 ± 3.3                                        
400 ppm Mn.sup.++     6.4 ± 1.3                                        
400 ppm Mn.sup.++  + 1000 ppm PGA.sup.a                                   
                      2.2 ± 0.5                                        
400 ppm Mn.sup.++  + 100 ppm PGA                                          
                     41.0 ± 7.4                                        
400 ppm Mn.sup.++  + 10 ppm PGA                                           
                     12.0 ± 2.6                                        
Control              23.8 ± 4.8                                        
400 ppm Mn.sup.++    12.9 ± 2.8                                        
400 ppm Mn.sup.++  + 1000 ppm PLA.sup.b                                   
                     95.7 ± 9.8                                        
400 ppm Mn.sup.++  + 100 ppm PLA                                          
                     33.0 ± 2.8                                        
400 ppm Mn.sup.++  + 10 ppm PLA                                           
                     17.4 ± 1.9                                        
Control              35.5 ± 7.5                                        
400 ppm Mn.sup.++    12.5 ± 2.4                                        
400 ppm Mn.sup.++  + 1000 ppm LL.sup.c                                    
                     All dead                                             
400 ppm Mn.sup.++  + 100 ppm LL                                           
                     51.2 ± 8.6                                        
400 ppm Mn.sup.++  + 10 ppm LL                                            
                     17.2 ± 5.3                                        
______________________________________                                    
 .sup.a PGA = Polyglycolic acid mixture having the composition given as   
 Example 5                                                                
 .sup.b PLA = PolyL-lactic acid mixture having the composition given as   
 Example 5                                                                
 .sup.c LL = Llactyl-L-lactic acid.                                       
EXAMPLE 12
The general procedure of Example 11 was followed except that plants were grown in flasks containing medium with various levels of Cu++ (as CuSO4.5H2 O) and seawater with and without added L-lactic acid polymers. The results given in Table X show the effectiveness of L-lactic acid polymers in protecting the plants against the growth-inhibiting effects of the copper ion and of the mixture of ions present in seawater.
In a similar experiment, it was shown that 10 to 100 ppm of the L-lactic acid dimer protected the plants from the growth-inhibiting effect of 15% seawater. However, a growth medium containing 1000 ppm of the lactic acid dimer and 15% seawater was toxic to the plants.
              TABLE X                                                     
______________________________________                                    
EFFECT OF L-LACTIC ACID POLYMERS ON                                       
DUCKWEED GROWN IN PRESENCE OF SALTS                                       
                     Mean Dry Weight                                      
Additives            Per Flask (mg)                                       
______________________________________                                    
Control              56.0 ± 7.3                                        
6.25 ppm Cu.sup.++   31.7 ± 4.0                                        
6.25 ppm Cu.sup.++  + 1000 ppm PLA.sup.a                                  
                     87.2 ± 5.7                                        
12.5 ppm Cu.sup.++   16.5 ± 3.1                                        
12.5 ppm Cu.sup.++  + 1000 ppm PLA                                        
                     63.5 ± 3.1                                        
18.75 ppm Cu.sup.++  All dead                                             
18.75 ppm Cu.sup.++  + 1000 ppm PLA                                       
                     All dead                                             
7.5% Seawater.sup.b  46.0 ± 8.5                                        
7.5% Seawater + 1000 ppm PLA                                              
                     103.0 ± 8.8                                       
15% Seawater         31.0 ± 2.8                                        
15% Seawater + 1000 ppm PLA                                               
                     46.0 ± 5.3                                        
22.5% Seawater       10.7 ± 1.7                                        
22.5% Seawater + 1000 ppm PLA                                             
                     16.3 ± 2.5                                        
______________________________________                                    
 .sup.a PLA = PolyL-lactic acid mixture having the composition given in   
 Example 5.                                                               
 .sup.b MARINEMIX ® a salt mixture containing 29 different acids      
 (Marine Enterprises, Baltimore, MD), was dissolved in sufficient distille
 water to give the specified percent of seawater concentrations.          
EXAMPLE 13
Chlorella vulgaris was grown in Chu-Gerloff medium (Gerloff, et al, pp. 27-44, in The Culturing of Algae: A Symposium, Antioch Press, Yellow Springs, Ohio (1950)) in 250-ml Erlenmeyer flasks sealed with rubber closures. The flasks were shaken at 40 rpm and exposed to about 4000 lux of light for 16 hrs per day. After 8 days of growth, 5-ml samples of each culture were dried, and the chlorophyll content of the cells was measured using the procedure given in Example 5. Tests were repeated on chlorella grown in the presence of added poly-L-lactic acid, and on chlorella grown in the presence of seawater with and without added poly-L-lactic acid. The results given in Table XI are the averages of determinations made on contents of four different flasks at each concentration level. They demonstrate the ability of lactic acid polymers to increase the amount of the metabolite, chlorophyll, even when the algae are grown in the presence of substantial concentrations of the salts found in seawater.
              TABLE XI                                                    
______________________________________                                    
EFFECT OF L-LACTIC ACID POLYMERS ON                                       
CHLOROPHYLL CONTENT OF CHLORELLA                                          
GROWN IN PRESENCE OF SALTS                                                
                    Chlorophyll                                           
Additives           μg/ml Extractast                                   
______________________________________                                    
Control             2.8 ± 0.3                                          
1000 ppm PLA.sup.a  8.1 ± 0.2                                          
25% Seawater.sup.b  2.7 ± 2.3                                          
25% Seawater + 1000 ppm PLA                                               
                    6.6 ± 1.1                                          
30% Seawater        1.7 ± 0.4                                          
30% Seawater + 1000 ppm PLA                                               
                    6.1 ± 1.0                                          
______________________________________                                    
 .sup.a PLA = PolyL-lactic acid mixture having the composition given in   
 Example 5.                                                               
 .sup.b MARINEMIX ® a salt mixture containing 29 different acids      
 (Marine Enterprises, Baltimore, MD), was dissolved in sufficient distille
 water to give the specified percent of seawater concentrations.          
Thus, it is apparent that there has been provided, in accordance with the invention, an improved process for increasing the rate of plant growth, for increasing root growth and the chlorophyll content, for protecting a plant against the toxic effects of salts, for decreasing the amount of added nutrients required for growth of a plant, and for enhancing the rate of formation of new plants when the plants are propagated by means of tissue culture, which fully satisfies the objectives, aims, and advantages set forth above. While the invention has been described in conjunction with specific embodiments thereof, it is evident that many alternatives, modifications, and variations will be apparent to those skilled in the art in light of the foregoing description. Accordingly, it is intended to include all such alternatives, modifications, and variations as set forth within the spirit and scope of the appended claims.

Claims (7)

    What is claimed is: .[.1. A process for increasing the rate of growth of a plant which comprises supplying to the roots, stems and foliage of the plant an effective amount of one or more acids having the structural formula: ##STR3## where n is a whole number from 1 to 10; the Rs are the same or different and denote H or CH3 ; and if at least one R is CH3, at least
  1. some of the asymmetric centers are in the L-configuration..]..[.2. The process of claim 1 wherein the acid is supplied to the plant in an aqueous solution at a concentration of between about 1 and about 1000 parts per million on a weight/volume basis..]..[.3. The process of claim 1 wherein the plant is Lemna minor L..]..[.4. The process of claim 1 wherein th plant is selected from the group: lettuce, spinach, and corn..]..[.5. The process of claim 4 wherein the plant is grown in hydroponic culture..]..[.6. A process for increasing the concentration of chlorophyll in a plant which comprises supplying to the roots, stems and foliage of the plant an effective amount of one or more acids having the structural formula: ##STR4## where n is a whole number from 1 to 10; the Rs are the same or different and denote H or CH3 ; and if at least one R is CH3, at least
  2. some of the asymmetric centers are in the L-configuration..]..[.7. The process of claim 6 wherein the acid is supplied to the plant in an aqueous solution at a concentration of between about 100 and about 1000 parts per million on a weight/volume basis..]..[.8. The process of claim 6 wherein the plant is selected from the group: Lemna minor L. and Chlorella vulgaris..]..[.9. A process for increasing the rate of root formation in a plant which comprises supplying to the roots, stems and foliage of the plant an effective amount of one or more acids having the structural formula: ##STR5## where n is a whole number from 1 to 10, and at least some of the
  3. asymmetric centers are in the L-configuration..]..[.10. The process of claim 9 wherein the acid is supplied to the plant in an aqueous solution at a concentration of between about 1 and about 1000 parts per million on a weight/volume basis..]..[.11. The process of claim 9 wherein the plant is selected from the group: Lemna minor L., lettuce, and corn..]..[.12. A process for decreasing the concentration of the basic nutrient medium required for growth of a plant which comprises supplying to the roots, stems or foliage of the plant an effective amount of one or more acids having the structural formula: ##STR6## where n is a whole number from 1 to 10; the Rs are the same or different and denote H or CH3 ; and if at least one R is CH3, at least
  4. some of the asymmetric centers are in the L-configuration..]..[.13. The process of claim 12 wherein the acid is supplied to the plant in an aqueous solution at a concentration of between about 1 and about 1,000 parts per million on a weight/volume basis..]..[.14. The process of claim 12 wherein the plant is Lemna minor L..]..[.15. A process for protecting a plant against the toxic effects of salts which comprises supplying to the roots, stems and foliage of the plant an effective amount of one or more acids having the structural formula: ##STR7## where n is a whole number from 1 to 10; the Rs are the same or different and denote H or CH3 ; and if at least one R is CH3, at least
  5. some of the asymmetric centers are in the L-configuration..]..[.16. The process of claim 15 wherein the acid is supplied to the plant in an aqueous solution at a concentration of between about 1 and about 1000 parts per million on a weight/volume basis..]..[.17. The process of claim 15 wherein the plant is selected from the group: Lemna minor L. and
  6. Chlorella vulgaris..]..Iadd.18. A process for increasing the rate of growth of a plant which comprises supplying to the roots and stems and foliage an effective amount of a condensation product of glycolic acid having from two to eleven acid units per molecule. .Iaddend..Iadd.19. The process of claim 18 wherein the acid is supplied to the plant in an aqueous solution at a concentration of between about 1 and about 1000 parts per million on a weight/volume basis. .Iaddend..Iadd.20. A process for increasing the concentration of chlorophyll in a plant which comprises supplying to the roots, stems and foliage of a plant an effective amount of a condensation product of glycolic acid having from two to eleven acid units per molecule. .Iaddend..Iadd.21. The process of claim 20 wherein the acid is supplied to the plant in an aqueous solution at a concentration of between about 100 and about 1000 parts per million on a weight/volume basis. .Iaddend..Iadd.22. A process for decreasing the concentration of the basic nutrient medium required for growth of a plant which comprises supplying to the roots, stems and foliage of the plant an effective amount of a condensation product of glycolic acid having from two to eleven acid units per molecule. .Iaddend..Iadd.23. The process of claim 22 wherein the acid is supplied to the plant in an aqueous solution at a concentration of between about 1 and about 1000 parts per million on a weight/volume basis.
  7. .Iaddend..Iadd.24. A process for protecting a plant against toxic effects of salts which comprises supplying to the roots, stems and foliage of a plant an effective amount of a condensation product of glycolic acid having from two to eleven acid units per molecule. .Iaddend..Iadd.25. The process of claim 24 wherein the acid is supplied to the plant in an aqueous solution at a concentration of between about 1 and about 1000 parts per million on a weight/volume basis. .Iaddend.
US08/369,604 1987-04-06 1995-01-06 Method for regulating plant growth Expired - Lifetime USRE35320E (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US08/369,604 USRE35320E (en) 1987-04-06 1995-01-06 Method for regulating plant growth

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US3419187A 1987-04-06 1987-04-06
US07052824 US4813997B1 (en) 1987-04-06 1987-05-22 Method for regulating plant growth
US08/369,604 USRE35320E (en) 1987-04-06 1995-01-06 Method for regulating plant growth

Related Parent Applications (2)

Application Number Title Priority Date Filing Date
US3419187A Continuation-In-Part 1987-04-06 1987-04-06
US07052824 Reissue US4813997B1 (en) 1987-04-06 1987-05-22 Method for regulating plant growth

Publications (1)

Publication Number Publication Date
USRE35320E true USRE35320E (en) 1996-08-27

Family

ID=26710675

Family Applications (2)

Application Number Title Priority Date Filing Date
US07052824 Ceased US4813997B1 (en) 1987-04-06 1987-05-22 Method for regulating plant growth
US08/369,604 Expired - Lifetime USRE35320E (en) 1987-04-06 1995-01-06 Method for regulating plant growth

Family Applications Before (1)

Application Number Title Priority Date Filing Date
US07052824 Ceased US4813997B1 (en) 1987-04-06 1987-05-22 Method for regulating plant growth

Country Status (21)

Country Link
US (2) US4813997B1 (en)
EP (1) EP0355117B2 (en)
JP (1) JP2619512B2 (en)
KR (1) KR960014735B1 (en)
CN (1) CN1022972C (en)
AT (1) ATE79212T1 (en)
AU (1) AU615447B2 (en)
BR (1) BR8807449A (en)
CA (1) CA1312476C (en)
CS (1) CS273649B2 (en)
DE (1) DE3873759T3 (en)
DK (1) DK493389A (en)
ES (1) ES2006399A6 (en)
GR (1) GR1000514B (en)
IE (1) IE61358B1 (en)
IS (1) IS1474B6 (en)
MX (1) MX167764B (en)
MY (1) MY103073A (en)
NO (1) NO173581C (en)
PL (1) PL152018B1 (en)
WO (1) WO1988007815A1 (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5876995A (en) * 1996-02-06 1999-03-02 Bryan; Bruce Bioluminescent novelty items
US5900266A (en) 1997-05-29 1999-05-04 The Curators Of The University Of Missouri Heat-treated lactic and/or glycolic acid compositions and methods of use
US6326042B1 (en) 1997-05-29 2001-12-04 The Curators Of The University Of Missouri Antimicrobial use of heat-treated lactic and/or glycolic acid compositions for treatment of ground meats
US6331505B1 (en) 1998-10-29 2001-12-18 Emerald Bioagriculture Corporation Method for increasing plant productivity using glutamic acid and glycolic acid
US6432883B1 (en) 2000-04-20 2002-08-13 Emerald Bioagriculture Corporation Methods of treating plants with glycolic acid

Families Citing this family (37)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4863506A (en) * 1983-07-06 1989-09-05 Union Oil Company Of California Methods for regulating the growth of plants and growth regulant compositions
US5059241A (en) * 1983-07-06 1991-10-22 Union Oil Company Of California Plant growth regulation
AR243319A1 (en) * 1987-04-06 1993-08-31 Cpc International Inc Method for regulating plant growth
IL95873A (en) * 1990-10-02 1995-03-15 Porath Dan Aquaculture for high protein crop production of a duckweed clone suitable for human consumption and comestible products for human consumption produced thereby
US5464760A (en) * 1990-04-04 1995-11-07 University Of Chicago Fermentation and recovery process for lactic acid production
US5186738A (en) * 1990-04-05 1993-02-16 Texas A&M University System Vanadyl compositions and methods for applying the compositions to promote plant growth
JP2613136B2 (en) * 1991-05-14 1997-05-21 株式会社コスモ総合研究所 Plant growth promoter
US5573669A (en) * 1992-06-02 1996-11-12 Jensen; Kyle R. Method and system for water purification by culturing and harvesting attached algal communities
US5527456A (en) * 1992-06-02 1996-06-18 Jensen; Kyle R. Apparatus for water purification by culturing and harvesting attached algal communities
US5591341A (en) * 1992-06-02 1997-01-07 Jensen; Kyle R. Method and system for water bioremediation utilizing a conical attached algal culture system
US5814582A (en) * 1992-11-05 1998-09-29 Donlar Corporation Method for enhanced plant productivity
US5661103A (en) * 1992-11-05 1997-08-26 Donlar Corporation Seed treatment composition and method
US5350735A (en) * 1992-11-05 1994-09-27 Donlar Corporation Composition and method for enhanced fertilizer uptake by plants
US5580840A (en) * 1992-11-05 1996-12-03 Donlar Corporation Method and composition for preservation of cut flowers
US5783523A (en) * 1992-11-05 1998-07-21 Donlar Corporation Method and composition for enhanced hydroponic plant productivity with polyamino acids
US5854177A (en) * 1992-11-05 1998-12-29 Donlar Corporation Method for enhanced hydroponic plant productivity with polymeric acids
US5840656A (en) * 1994-02-23 1998-11-24 Auxein Corporation Method for increasing fertilizer efficiency
US5439873A (en) * 1994-02-23 1995-08-08 Plant Growth Development Corporation Method for stimulating plant growth using GABA
US5935909A (en) * 1997-09-16 1999-08-10 Donlar Corporation Treatment of tree seedlings to enhance survival rate
US6124241A (en) * 1998-10-29 2000-09-26 Auxien Corporation Method for increasing plant productivity using glutamic acid and glycolic acid
JP3571626B2 (en) * 1999-08-23 2004-09-29 株式会社資生堂 Plant activator
JP3805599B2 (en) * 2000-04-10 2006-08-02 花王株式会社 Plant vitality agent
JP2001316204A (en) * 2000-04-28 2001-11-13 Kao Corp Agent for vitalizing plant
JP3768380B2 (en) * 2000-04-28 2006-04-19 花王株式会社 Plant vitality agent
EP1296555A4 (en) * 2000-07-03 2004-04-28 Nft Ind Llc Controlled release agricultural products and processes for making same
TW200733880A (en) * 2005-09-09 2007-09-16 Suntory Ltd Method for low light cultivation and plant growth-promoting agent
WO2011026796A1 (en) * 2009-09-01 2011-03-10 Basf Se Synergistic fungicidal mixtures comprising lactylates and method for combating phytopathogenic fungi
WO2015176076A2 (en) 2014-05-12 2015-11-19 Gary David Mcknight Improving the efficiency of man-made and/or natural organic based animal manure fertilizers by liberating the bound nutrients (macro and micro) through the use of organic, non-aqueous liquid delivery formulations containing organic poly (organicacids) and/or their salts
KR102213059B1 (en) 2015-01-06 2021-02-05 에스케이케미칼 주식회사 Composite material panel for ship and menufacturing method thereof
US10464858B2 (en) 2015-05-13 2019-11-05 World Source Enterprises, Llc Non-aqueous organo liquid delivery systems containing dispersed poly (organic acids) that improve availability of macro and micro-nutrients to plants
JP6800834B2 (en) * 2016-12-20 2020-12-16 アース製薬株式会社 Methods for increasing plant chlorophyll, methods for inhibiting pest colonization, and compositions applicable to these methods.
US11198655B2 (en) 2018-02-11 2021-12-14 Gary David McKnight Non-aqueous Organo Liquid Delivery Systems containing dispersed Organo Polycarboxylate Functionalities that improves efficiencies and properties of nitrogen sources
US11553656B2 (en) 2019-04-30 2023-01-17 AVA Technologies Inc. Gardening apparatus
USD932346S1 (en) 2020-01-10 2021-10-05 AVA Technologies Inc. Planter
USD932345S1 (en) 2020-01-10 2021-10-05 AVA Technologies Inc. Plant pod
CN114620838A (en) * 2022-04-07 2022-06-14 辽宁大学 Method for repairing copper-polluted water body by strengthening duckweed
CN116102427B (en) * 2022-12-08 2024-02-27 江西省科学院微生物研究所(江西省流域生态研究所) Low polylactic acid, preparation method and application thereof

Citations (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SU193218A1 (en) * Н. В. Болтенков , К. Мурадов
US3148049A (en) * 1961-08-24 1964-09-08 Crown Zellerbach Corp Method for controlling plant growth
US3351653A (en) * 1962-03-08 1967-11-07 Hooker Chemical Corp Fluorine-containing hydroxy acids and esters and methods for the manufacture thereof
DE1916054A1 (en) * 1969-03-28 1970-10-15 Lentia Gmbh Chem Und Pharm Erz 2-keto- and 2-hydroxy-alkanoic acids for use - in regulation of plant growth and metabol-ism
US3679392A (en) * 1969-06-18 1972-07-25 Union Oil Co Plant growth stimulated by a combination of glycolic acid and gibberellin
JPS50157167A (en) * 1974-06-07 1975-12-18
JPS5369164A (en) * 1976-11-29 1978-06-20 Jujo Paper Co Ltd Agents for inducing adventitious roots at trunks of plants and method for using same
US4272398A (en) * 1978-08-17 1981-06-09 The United States Of America As Represented By The Secretary Of Agriculture Microencapsulation process
US4313752A (en) * 1980-08-26 1982-02-02 W. R. Grace & Co. 2,2-Dimethylvaleric acid for growth enhancement of sugarcane
SU1060163A1 (en) * 1982-01-25 1983-12-15 Новочеркасский политехнический институт Stimulating agent for growth of winter wheat
JPS5910501A (en) * 1982-07-07 1984-01-20 Hirotoshi Miyajima Agent for preserving plant and its preparation
US4471077A (en) * 1982-05-14 1984-09-11 Akzo Nv Microporous polylactide powders and a process for their preparation
US4473648A (en) * 1982-05-14 1984-09-25 International Plant Research Institute Process and nutrient medium for micropropagation of cassava
JPS6013703A (en) * 1983-07-04 1985-01-24 Mitsubishi Chem Ind Ltd Rooting promotor of rice seedling for culture for mechanical transplanting
US4536474A (en) * 1981-09-30 1985-08-20 Nippon Paint Co., Ltd. Tissue culture of lichens
JPS60169404A (en) * 1984-02-15 1985-09-02 Mikata Shokai:Kk Lawn growth promoter
US4554252A (en) * 1981-12-18 1985-11-19 Eszakmagyarorszagi Vegyimuvek Plant tissue cultivation process
US4626277A (en) * 1984-06-12 1986-12-02 Agro-Kanesho Co., Ltd. Plant growth regulator
US4634674A (en) * 1983-03-25 1987-01-06 Atlantic Richfield Company Plant regeneration from protoplasts
US4863506A (en) * 1983-07-06 1989-09-05 Union Oil Company Of California Methods for regulating the growth of plants and growth regulant compositions
US4976767A (en) * 1986-01-29 1990-12-11 Cpc International Inc. Plant food and method for its use

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6013703B2 (en) * 1977-09-09 1985-04-09 三菱電機株式会社 aroma generator
JPS5910501B2 (en) * 1978-06-29 1984-03-09 カ−ル・ドイツチエ・プリユフンド・メスゲラテバウ Method and device for generating acoustic pulses
JPS59199604A (en) * 1983-04-25 1984-11-12 Kanesho Kk Agricultural chemical composition for foliar application containing delayed-release polymer
JPS59199603A (en) * 1983-04-25 1984-11-12 Kanesho Kk Agricultural chemical composition for soil treatment containing delayed-release polymer

Patent Citations (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SU193218A1 (en) * Н. В. Болтенков , К. Мурадов
US3148049A (en) * 1961-08-24 1964-09-08 Crown Zellerbach Corp Method for controlling plant growth
US3351653A (en) * 1962-03-08 1967-11-07 Hooker Chemical Corp Fluorine-containing hydroxy acids and esters and methods for the manufacture thereof
DE1916054A1 (en) * 1969-03-28 1970-10-15 Lentia Gmbh Chem Und Pharm Erz 2-keto- and 2-hydroxy-alkanoic acids for use - in regulation of plant growth and metabol-ism
US3679392A (en) * 1969-06-18 1972-07-25 Union Oil Co Plant growth stimulated by a combination of glycolic acid and gibberellin
JPS50157167A (en) * 1974-06-07 1975-12-18
JPS5369164A (en) * 1976-11-29 1978-06-20 Jujo Paper Co Ltd Agents for inducing adventitious roots at trunks of plants and method for using same
US4272398A (en) * 1978-08-17 1981-06-09 The United States Of America As Represented By The Secretary Of Agriculture Microencapsulation process
US4313752A (en) * 1980-08-26 1982-02-02 W. R. Grace & Co. 2,2-Dimethylvaleric acid for growth enhancement of sugarcane
US4536474A (en) * 1981-09-30 1985-08-20 Nippon Paint Co., Ltd. Tissue culture of lichens
US4554252A (en) * 1981-12-18 1985-11-19 Eszakmagyarorszagi Vegyimuvek Plant tissue cultivation process
SU1060163A1 (en) * 1982-01-25 1983-12-15 Новочеркасский политехнический институт Stimulating agent for growth of winter wheat
US4471077A (en) * 1982-05-14 1984-09-11 Akzo Nv Microporous polylactide powders and a process for their preparation
US4473648A (en) * 1982-05-14 1984-09-25 International Plant Research Institute Process and nutrient medium for micropropagation of cassava
JPS5910501A (en) * 1982-07-07 1984-01-20 Hirotoshi Miyajima Agent for preserving plant and its preparation
US4634674A (en) * 1983-03-25 1987-01-06 Atlantic Richfield Company Plant regeneration from protoplasts
JPS6013703A (en) * 1983-07-04 1985-01-24 Mitsubishi Chem Ind Ltd Rooting promotor of rice seedling for culture for mechanical transplanting
US4863506A (en) * 1983-07-06 1989-09-05 Union Oil Company Of California Methods for regulating the growth of plants and growth regulant compositions
JPS60169404A (en) * 1984-02-15 1985-09-02 Mikata Shokai:Kk Lawn growth promoter
US4626277A (en) * 1984-06-12 1986-12-02 Agro-Kanesho Co., Ltd. Plant growth regulator
US4976767A (en) * 1986-01-29 1990-12-11 Cpc International Inc. Plant food and method for its use

Non-Patent Citations (37)

* Cited by examiner, † Cited by third party
Title
Bacskai, "Hot Melt Adhesive With Increased Heat Stability", CA., 92, 42874t (1980).
Bacskai, Hot Melt Adhesive With Increased Heat Stability , CA., 92, 42874t (1980). *
Die Makromolekulare Chemie, vol. 140 (No. 3429), 1970 pp. 41 54, Basel, CH; H. G. Buhrer et al.: Polythiolester II. Polythiolactic . *
Die Makromolekulare Chemie, vol. 140 (No. 3429), 1970 pp. 41-54, Basel, CH; H. G. Buhrer et al.: "Polythiolester II. Polythiolactic".
Die Makromolekulare Chemie, vol. 37, 1960, pp. 64 70, Basel, CH: A. Schoberl: Uber Polythioglykolide . *
Die Makromolekulare Chemie, vol. 37, 1960, pp. 64-70, Basel, CH: A. Schoberl: "Uber Polythioglykolide".
Ivanov, et al., "Hydroxy Acids of Black Liquors", CA., 80, 61258p (1974).
Ivanov, et al., Hydroxy Acids of Black Liquors , CA., 80, 61258p (1974). *
Justus Liebigs Annalen Der Chemie, 595, 1955, p. 101. *
Kanesho Co., "Carriers For Controlled Release Agrochemicals", CA. 102, 108271c, 1985.
Kanesho Co., "Soil Amendment", CA. 102, 162201t, 1985.
Kanesho Co., Carriers For Controlled Release Agrochemicals , CA. 102, 108271c, 1985. *
Kanesho Co., Soil Amendment , CA. 102, 162201t, 1985. *
Kirk Othmer, Encyclopedia of Chemical Technology, 3rd ed., vol. 13, pp. 80 82 (1981). *
Kirk-Othmer, Encyclopedia of Chemical Technology, 3rd ed., vol. 13, pp. 80-82 (1981).
Leopold et al. "Plant Growth and Development", NY: McGraw-Hill Book Co. 1975, pp. 9-10.
Leopold et al. Plant Growth and Development , NY: McGraw Hill Book Co. 1975, pp. 9 10. *
Mikami, Ag. Biol. Chem., 34, 977 (1970). *
PCT International Search Report dated Jul. 14, 1988. *
Richards, "Degradation of Lactose by Interaction With Casein", CA., 64, 14477b (1966).
Richards, Degradation of Lactose by Interaction With Casein , CA., 64, 14477b (1966). *
The Merck Index 10th ed. Entry 5173. "Di-Lactic Acid". 1983.
The Merck Index 10th ed. Entry 5173. Di Lactic Acid . 1983. *
Thorpe, Thorpe s Dictionary of Applied Chemistry, 4th Edition, vol. 3, pp. 161 166, 1948. *
Thorpe, Thorpe's Dictionary of Applied Chemistry, 4th Edition, vol. 3, pp. 161-166, 1948.
Ueda et al., Fermentation Engineering Journal, No. 36, pp. 368 371 (1958). *
Ueda et al., Fermentation Engineering Journal, No. 36, pp. 368-371 (1958).
Ueda et al., Fermentation Engineering Journal, No. 36, pp. 371 374 (1958). *
Ueda et al., Fermentation Engineering Journal, No. 36, pp. 371-374 (1958).
Watson et al, "Improved Turf From Corn Gluten and Corn Hulls", The Gulf Course Reporter Jun., 1958.
Watson et al, Improved Turf From Corn Gluten and Corn Hulls , The Gulf Course Reporter Jun., 1958. *
Yamauchi, et al., "Grafted Polyester Fibers", CA., 76, 128657f (1972).
Yamauchi, et al., Grafted Polyester Fibers , CA., 76, 128657f (1972). *
Zelitch, "Biochemical Control of Stomatal Opening and the Synthesis of Glycolic Acid in Leaves", Fed. Proc., 24, 868-872 (1965).
Zelitch, Biochemical Control of Stomatal Opening and the Synthesis of Glycolic Acid in Leaves , Fed. Proc., 24, 868 872 (1965). *
Zelitch, I., "The Relationship of Glycolic Acid to Respiration and Photosynthesis in Tobacco Leaves", J. Biol. Chem., 234, 3077-3081 (1959).
Zelitch, I., The Relationship of Glycolic Acid to Respiration and Photosynthesis in Tobacco Leaves , J. Biol. Chem., 234, 3077 3081 (1959). *

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5876995A (en) * 1996-02-06 1999-03-02 Bryan; Bruce Bioluminescent novelty items
US6113886A (en) 1996-02-06 2000-09-05 Bruce Bryan Bioluminescent novelty items
US6152358A (en) 1996-02-06 2000-11-28 Bruce Bryan Bioluminescent novelty items
US20060053505A1 (en) * 1996-02-06 2006-03-09 Bruce Bryan Bioluminescent novelty items
US5900266A (en) 1997-05-29 1999-05-04 The Curators Of The University Of Missouri Heat-treated lactic and/or glycolic acid compositions and methods of use
US6326042B1 (en) 1997-05-29 2001-12-04 The Curators Of The University Of Missouri Antimicrobial use of heat-treated lactic and/or glycolic acid compositions for treatment of ground meats
US6331505B1 (en) 1998-10-29 2001-12-18 Emerald Bioagriculture Corporation Method for increasing plant productivity using glutamic acid and glycolic acid
US6432883B1 (en) 2000-04-20 2002-08-13 Emerald Bioagriculture Corporation Methods of treating plants with glycolic acid

Also Published As

Publication number Publication date
MX167764B (en) 1993-04-12
ES2006399A6 (en) 1989-04-16
NO885402D0 (en) 1988-12-05
US4813997A (en) 1989-03-21
GR880100222A (en) 1989-01-31
IE61358B1 (en) 1994-11-02
IS1474B6 (en) 1991-09-24
PL271679A1 (en) 1989-02-06
EP0355117A1 (en) 1990-02-28
EP0355117B2 (en) 1997-04-23
KR960014735B1 (en) 1996-10-19
IE880994L (en) 1988-10-06
GR1000514B (en) 1992-07-30
US4813997B1 (en) 1995-07-18
CS273649B2 (en) 1991-03-12
MY103073A (en) 1993-04-30
JP2619512B2 (en) 1997-06-11
CN1022972C (en) 1993-12-08
DK493389A (en) 1989-12-04
JPH02502909A (en) 1990-09-13
NO885402L (en) 1989-02-03
PL152018B1 (en) 1990-10-31
CN88102348A (en) 1988-10-26
DK493389D0 (en) 1989-10-06
NO173581C (en) 1994-01-05
AU615447B2 (en) 1991-10-03
DE3873759T3 (en) 1997-07-17
KR890700312A (en) 1989-04-24
WO1988007815A1 (en) 1988-10-20
DE3873759D1 (en) 1992-09-17
DE3873759T2 (en) 1992-12-24
NO173581B (en) 1993-09-27
ATE79212T1 (en) 1992-08-15
IS3329A7 (en) 1988-08-31
CS231788A2 (en) 1990-06-13
EP0355117A4 (en) 1990-06-26
EP0355117B1 (en) 1992-08-12
AU1701388A (en) 1988-11-04
CA1312476C (en) 1993-01-12
BR8807449A (en) 1990-03-27

Similar Documents

Publication Publication Date Title
USRE35320E (en) Method for regulating plant growth
EP0514776B1 (en) Method for promoting plant growth
US5604177A (en) Method for stimulating plant growth using GABA and succinic acid
KR101120973B1 (en) Methods for improving growth and crop productivity of plants by adjusting plant hormone levels, ratios and/or co-factors
CA1229983A (en) Process for the production of propagating material of plants
Lam Plantlet formation from potato tuber discs in vitro
US5238841A (en) Method for regulating plant growth
US4171968A (en) Method for increasing the rate and/or yield of seed germination by treatment with surfactants
CN114403147B (en) Application of 1-methylpyrrolidine-2-carboxylic acid in promoting plant growth
AU645642B2 (en) Method for regulating plant growth
JP2002528470A (en) Method for increasing plant productivity using glutamic acid and glycolic acid
JPS63297304A (en) Method for culturing and cultivating araceous plant
US5069707A (en) Method for regulating the flowering of plants and flowering regulators of plants
PT87168B (en) PROCESS FOR REGULATING PLANT GROWTH
SU1172512A1 (en) Nutrient media for aftergrowing cut cereal crops
Petkova et al. Possibilities for regulation stem growth of tobacco seedlings by treatment with some growth retardants
JPH02231402A (en) Plant growth regulating agent

Legal Events

Date Code Title Description
AS Assignment

Owner name: BESTFOODS, NEW JERSEY

Free format text: MERGER;ASSIGNOR:CPC INTERNATIONAL INC.;REEL/FRAME:009396/0275

Effective date: 19971124

FPAY Fee payment

Year of fee payment: 12