AU645642B2 - Method for regulating plant growth - Google Patents
Method for regulating plant growth Download PDFInfo
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- AU645642B2 AU645642B2 AU90099/91A AU9009991A AU645642B2 AU 645642 B2 AU645642 B2 AU 645642B2 AU 90099/91 A AU90099/91 A AU 90099/91A AU 9009991 A AU9009991 A AU 9009991A AU 645642 B2 AU645642 B2 AU 645642B2
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- Prior art keywords
- lactic acid
- ppm
- plant
- growth
- polymers
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- 238000000034 method Methods 0.000 title claims description 38
- 230000008635 plant growth Effects 0.000 title description 12
- 230000001105 regulatory effect Effects 0.000 title description 5
- 239000002253 acid Substances 0.000 claims description 59
- 150000007513 acids Chemical class 0.000 claims description 36
- 230000012010 growth Effects 0.000 claims description 36
- 230000008569 process Effects 0.000 claims description 21
- 150000003839 salts Chemical class 0.000 claims description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 14
- 231100000331 toxic Toxicity 0.000 claims description 11
- 230000002588 toxic effect Effects 0.000 claims description 11
- 239000007864 aqueous solution Substances 0.000 claims description 2
- 241000196324 Embryophyta Species 0.000 description 78
- JVTAAEKCZFNVCJ-REOHCLBHSA-N L-lactic acid Chemical compound C[C@H](O)C(O)=O JVTAAEKCZFNVCJ-REOHCLBHSA-N 0.000 description 76
- 229920000642 polymer Polymers 0.000 description 75
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 66
- AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical compound OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 description 37
- 229960000448 lactic acid Drugs 0.000 description 31
- 244000207740 Lemna minor Species 0.000 description 30
- 235000006439 Lemna minor Nutrition 0.000 description 30
- 235000001855 Portulaca oleracea Nutrition 0.000 description 29
- 239000000203 mixture Substances 0.000 description 26
- 235000014655 lactic acid Nutrition 0.000 description 25
- 239000004310 lactic acid Substances 0.000 description 25
- 239000002609 medium Substances 0.000 description 21
- ATNHDLDRLWWWCB-AENOIHSZSA-M chlorophyll a Chemical compound C1([C@@H](C(=O)OC)C(=O)C2=C3C)=C2N2C3=CC(C(CC)=C3C)=[N+]4C3=CC3=C(C=C)C(C)=C5N3[Mg-2]42[N+]2=C1[C@@H](CCC(=O)OC\C=C(/C)CCC[C@H](C)CCC[C@H](C)CCCC(C)C)[C@H](C)C2=C5 ATNHDLDRLWWWCB-AENOIHSZSA-M 0.000 description 19
- 229930002875 chlorophyll Natural products 0.000 description 18
- 235000019804 chlorophyll Nutrition 0.000 description 18
- 230000000694 effects Effects 0.000 description 18
- 239000013535 sea water Substances 0.000 description 16
- 239000000539 dimer Substances 0.000 description 14
- 235000015097 nutrients Nutrition 0.000 description 14
- OZZQHCBFUVFZGT-IMJSIDKUSA-N (2s)-2-[(2s)-2-hydroxypropanoyl]oxypropanoic acid Chemical compound C[C@H](O)C(=O)O[C@@H](C)C(O)=O OZZQHCBFUVFZGT-IMJSIDKUSA-N 0.000 description 13
- 229920000747 poly(lactic acid) Polymers 0.000 description 12
- 239000004626 polylactic acid Substances 0.000 description 12
- 230000001965 increasing effect Effects 0.000 description 11
- 239000001963 growth medium Substances 0.000 description 10
- 229920001432 poly(L-lactide) Polymers 0.000 description 10
- 230000015572 biosynthetic process Effects 0.000 description 9
- 238000002474 experimental method Methods 0.000 description 9
- JVTAAEKCZFNVCJ-UWTATZPHSA-N D-lactic acid Chemical compound C[C@@H](O)C(O)=O JVTAAEKCZFNVCJ-UWTATZPHSA-N 0.000 description 8
- 241000220259 Raphanus Species 0.000 description 8
- 235000006140 Raphanus sativus var sativus Nutrition 0.000 description 8
- 229940022769 d- lactic acid Drugs 0.000 description 8
- 230000002829 reductive effect Effects 0.000 description 8
- 239000000243 solution Substances 0.000 description 8
- OZZQHCBFUVFZGT-UHFFFAOYSA-N 2-(2-hydroxypropanoyloxy)propanoic acid Chemical compound CC(O)C(=O)OC(C)C(O)=O OZZQHCBFUVFZGT-UHFFFAOYSA-N 0.000 description 7
- 229930182843 D-Lactic acid Natural products 0.000 description 7
- 229920000954 Polyglycolide Polymers 0.000 description 7
- 239000000654 additive Substances 0.000 description 7
- 239000010949 copper Substances 0.000 description 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- 240000008415 Lactuca sativa Species 0.000 description 6
- 235000003228 Lactuca sativa Nutrition 0.000 description 6
- 244000300264 Spinacia oleracea Species 0.000 description 6
- 235000009337 Spinacia oleracea Nutrition 0.000 description 6
- 238000009833 condensation Methods 0.000 description 6
- 230000005494 condensation Effects 0.000 description 6
- 230000000644 propagated effect Effects 0.000 description 6
- 238000012360 testing method Methods 0.000 description 6
- 238000010438 heat treatment Methods 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 239000004633 polyglycolic acid Substances 0.000 description 4
- 230000002786 root growth Effects 0.000 description 4
- 241000195649 Chlorella <Chlorellales> Species 0.000 description 3
- 244000061456 Solanum tuberosum Species 0.000 description 3
- 235000002595 Solanum tuberosum Nutrition 0.000 description 3
- 240000008042 Zea mays Species 0.000 description 3
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 3
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 3
- 230000000996 additive effect Effects 0.000 description 3
- 238000003556 assay Methods 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- 239000000306 component Substances 0.000 description 3
- 229920001577 copolymer Polymers 0.000 description 3
- 235000005822 corn Nutrition 0.000 description 3
- 230000003247 decreasing effect Effects 0.000 description 3
- 239000012153 distilled water Substances 0.000 description 3
- 230000002708 enhancing effect Effects 0.000 description 3
- 230000009422 growth inhibiting effect Effects 0.000 description 3
- 239000007952 growth promoter Substances 0.000 description 3
- 229940093915 gynecological organic acid Drugs 0.000 description 3
- 150000001261 hydroxy acids Chemical class 0.000 description 3
- 150000002500 ions Chemical class 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- 150000007524 organic acids Chemical class 0.000 description 3
- 235000005985 organic acids Nutrition 0.000 description 3
- 230000001737 promoting effect Effects 0.000 description 3
- JJTUDXZGHPGLLC-IMJSIDKUSA-N 4511-42-6 Chemical compound C[C@@H]1OC(=O)[C@H](C)OC1=O JJTUDXZGHPGLLC-IMJSIDKUSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- 241000195493 Cryptophyta Species 0.000 description 2
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- WAEMQWOKJMHJLA-UHFFFAOYSA-N Manganese(2+) Chemical compound [Mn+2] WAEMQWOKJMHJLA-UHFFFAOYSA-N 0.000 description 2
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 2
- 101150047344 Plaa gene Proteins 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
- 238000012258 culturing Methods 0.000 description 2
- 239000003337 fertilizer Substances 0.000 description 2
- 239000012737 fresh medium Substances 0.000 description 2
- 230000035784 germination Effects 0.000 description 2
- 239000003630 growth substance Substances 0.000 description 2
- 230000007062 hydrolysis Effects 0.000 description 2
- 238000006460 hydrolysis reaction Methods 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 229910052698 phosphorus Inorganic materials 0.000 description 2
- 239000011574 phosphorus Substances 0.000 description 2
- 239000006069 physical mixture Substances 0.000 description 2
- 239000005648 plant growth regulator Substances 0.000 description 2
- 239000003375 plant hormone Substances 0.000 description 2
- 239000011591 potassium Substances 0.000 description 2
- 229910052700 potassium Inorganic materials 0.000 description 2
- 239000011833 salt mixture Substances 0.000 description 2
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- 239000010455 vermiculite Substances 0.000 description 2
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- 229910052902 vermiculite Inorganic materials 0.000 description 2
- MNKRTDOUBUSQHX-UHFFFAOYSA-N 2,4-dihydroxy-2-methyl-3-oxopentanoic acid Chemical compound CC(O)C(=O)C(C)(O)C(O)=O MNKRTDOUBUSQHX-UHFFFAOYSA-N 0.000 description 1
- 229920001817 Agar Polymers 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-NJFSPNSNSA-N Carbon-14 Chemical compound [14C] OKTJSMMVPCPJKN-NJFSPNSNSA-N 0.000 description 1
- 240000009108 Chlorella vulgaris Species 0.000 description 1
- 235000007089 Chlorella vulgaris Nutrition 0.000 description 1
- JPVYNHNXODAKFH-UHFFFAOYSA-N Cu2+ Chemical compound [Cu+2] JPVYNHNXODAKFH-UHFFFAOYSA-N 0.000 description 1
- 241001057636 Dracaena deremensis Species 0.000 description 1
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 description 1
- 244000061176 Nicotiana tabacum Species 0.000 description 1
- 235000002637 Nicotiana tabacum Nutrition 0.000 description 1
- 229920002323 Silicone foam Polymers 0.000 description 1
- 229930006000 Sucrose Natural products 0.000 description 1
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 1
- JZRWCGZRTZMZEH-UHFFFAOYSA-N Thiamine Natural products CC1=C(CCO)SC=[N+]1CC1=CN=C(C)N=C1N JZRWCGZRTZMZEH-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- WDJHALXBUFZDSR-UHFFFAOYSA-N acetoacetic acid Chemical class CC(=O)CC(O)=O WDJHALXBUFZDSR-UHFFFAOYSA-N 0.000 description 1
- 238000005273 aeration Methods 0.000 description 1
- 239000008272 agar Substances 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 229910001431 copper ion Inorganic materials 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 230000000459 effect on growth Effects 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 229910001448 ferrous ion Inorganic materials 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 238000005194 fractionation Methods 0.000 description 1
- -1 glycolic acid Chemical class 0.000 description 1
- 239000004009 herbicide Substances 0.000 description 1
- 238000004128 high performance liquid chromatography Methods 0.000 description 1
- 238000011081 inoculation Methods 0.000 description 1
- CDAISMWEOUEBRE-GPIVLXJGSA-N inositol Chemical compound O[C@H]1[C@H](O)[C@@H](O)[C@H](O)[C@H](O)[C@@H]1O CDAISMWEOUEBRE-GPIVLXJGSA-N 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000003621 irrigation water Substances 0.000 description 1
- 150000004715 keto acids Chemical class 0.000 description 1
- 239000002207 metabolite Substances 0.000 description 1
- 230000036961 partial effect Effects 0.000 description 1
- 239000003415 peat Substances 0.000 description 1
- 239000010451 perlite Substances 0.000 description 1
- 235000019362 perlite Nutrition 0.000 description 1
- 238000004382 potting Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 230000002285 radioactive effect Effects 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 238000012216 screening Methods 0.000 description 1
- CDAISMWEOUEBRE-UHFFFAOYSA-N scyllo-inosotol Natural products OC1C(O)C(O)C(O)C(O)C1O CDAISMWEOUEBRE-UHFFFAOYSA-N 0.000 description 1
- 239000013514 silicone foam Substances 0.000 description 1
- 230000004936 stimulating effect Effects 0.000 description 1
- 230000000638 stimulation Effects 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 239000006228 supernatant Substances 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- KYMBYSLLVAOCFI-UHFFFAOYSA-N thiamine Chemical compound CC1=C(CCO)SCN1CC1=CN=C(C)N=C1N KYMBYSLLVAOCFI-UHFFFAOYSA-N 0.000 description 1
- 229960003495 thiamine Drugs 0.000 description 1
- 235000019157 thiamine Nutrition 0.000 description 1
- 239000011721 thiamine Substances 0.000 description 1
- 239000013638 trimer Substances 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01H—NEW PLANTS OR NON-TRANSGENIC PROCESSES FOR OBTAINING THEM; PLANT REPRODUCTION BY TISSUE CULTURE TECHNIQUES
- A01H4/00—Plant reproduction by tissue culture techniques ; Tissue culture techniques therefor
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/36—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a 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
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Developmental Biology & Embryology (AREA)
- Engineering & Computer Science (AREA)
- Environmental Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Dentistry (AREA)
- Cell Biology (AREA)
- Agronomy & Crop Science (AREA)
- Biotechnology (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Botany (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Cultivation Of Plants (AREA)
- Polyesters Or Polycarbonates (AREA)
Description
6 4 4 2 S F Ref: 200637
AUSTRALIA
PATENTS ACT 1990 COMPLETE SPECIFICATION FOR A STANDARD PATENT ORIGINAL 999 9 .99 99* *9 9 9 9.9.
@999 9999 oooo *o 9 9 r Name and Address of Applicant: Actual Inventor(s): Address for Service: Invention Title: CPC International Inc.
International Plaza Englewood Cliffs New Jersey 07632 UNITED STATES OF AMERICA Alan M. Kinnersley, Taylor C. Scott III, John H. Yopp and George H. Whitten Spruson Ferguson, Patent Attorneys Level 33 St Martins Tower, 31 Market Street Sydney, New South Wales, 2000, Australia Method for Regulating Plant Growth 9 *9 o a ft 9 9 9 A 9 The following statement is a full description of this invention, including the best method of performing it known to me/us:- 1 METHOD FOR REGULATING PLANT GROWTH FIELD OF THE INVENTION The present invention relates to a process for facilitating the growth of a plant irrigated with water containing a concentration of salts that would normally be toxic to the plant. In this process, plants are treated with dilute solutions of certain organic acids. The present specification also describes 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. The organic 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 15 growth regulators. For example, West German Patent 19 16 054 discloses 0 the use of alpha-hydroxy- or alpha-ketoalkanoic acids, having 7 to carbon atoms, and their derivatives, particularly amides, for use for promoting the growth of plants under drought conditions. U.S. Patent 3,148,049 discloses certain halogenated keto acids, such as halogenated acetoacetic acid, as plant growth regulators. U.S. Patent 3,351,653 discloses the use of fluorinated hydroxy acids and esters as herbicides.
9 q In 1970, Mikami, et al, Agr. Biol. Chem., 34, 977-97,', reported test results of a number of hydroxy acids as plant growth regulators. Several of these, particularly, certain aromatic hydroxy aoids, were shown to be 25 root growth promoters. Hcwever, some of the simpie 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 a broad form of this invention, there is provided a process of facilitating the growth of a plant irrigated with water containing a concentration of salts that would normally be toxic to the 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: TCW/1287v -2- R R HO--CHC 2--CHCL 2
H
n wherein n is a whole number 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.
The specification describes 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 structural formula I.
6o: The specification further describes a process For increasing the concentration of chlorophyll in a plant which comprises supplying to the 10 plant an effective amount of one or more acids having the structural formula I.
mo The specification also describes 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.
The specification describes a process for protecting a plant goodis 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.
Furthermore the specification describes a process for enhancing the 20 rate of formation of new plarts when the plants are propagated by means of 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, the specification describes 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: HO CHCO 2
CHCO
2
H
II
where n is a small whole number from 1 to 10, and at least some of the TCN/1287v 3 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.
15 The activity of the acids used in the practice of this invention o^ 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 method was followed by the present inventors to demonstrate 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 25 little growth-promoting ability.
This growth-promoting ability of the polymers of L-lactic acid is *ego 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 TCN/1287v 4 of polymers having formula I is that the plants accumulate more chlorophyll. The presence of such polymers in the growth medium, particularly at the concentrations 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 15 culture.
The polymers having formula I are also useful additives to tissue culture medium when plants are propagated by means of tissue culture.
These icids 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.
g* The polymers of L-lactic acid are also effective in increasing the 25 rate of root formation in a plant. Plants grown in the presence of these acids have a considerable increase in average root length.
0*6 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 TCW/1287v 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 tests, 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 15 given as "weight phosphorus is given as "weight P 2 0 5 and potassium is given as "weight K 2 0".
"'EXAMPLE 1 Duckweed (Lemna minor 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 25 days. The plants were harvested and weighed. All reported values represent 3 to 5 replicates.
*0 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. The 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 oi' such TCW/1287v 6 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., N.Y. City). The growth promotional property of this compound is clearly shown by the results given in the last item of Table I.
TABLE I DUCKNEED GROWTH ASSAY Weight (mg) Added Acid (ppm) Control 10 100 1000 DL-Lactic Acid 130 19 a) 134 7 a) 207 50 a 339 56 a) (Technical L-Lactic Acid 257 28 a) 256 28 198 64 a 175 3 2 a) 15 (Pure) D-Lactic Acid 71 7 b 66 4 b 75 11 b) 79 5 b (Pure) L-Lactyl-L-Lactic 46 6 b 50 15 b 71 26 b) 73 21 b) Acid 9 e a) Fresh weight b) Dry weight S..EXAMPLE 2 The general procedure given under Example 1 was followed. The acids used were mixed polymers of D-lactic acid, mixed polymers of 25 L-lactic acid, and mixed polymers of DL-lactic acid. The polymers were obtained by heating the corresponding acids for 2-1/2 hours at 100 0
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.
TCW/1287v 7 -7- TABLE II EFFECT OF POLYLACTIC 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 EXAMPLE 3 The general procedure of Example I 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 15 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 20 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 DP2 (100 ppm) 109 11 DP4 (200 ppm) 149 32 (250 ppm) 157 DP6 (300 ppm) 156 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, 400, 450, and 300 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 TCW/1287v 8 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-Llactic acid was added to the mixture. In ccntrol 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.
o** 15 TABLE IV o"s EFFECT OF L-LACTIC ACID DIMER ON DUCKNEED GROWN ON REDUCED NUTRIENTS Dry Weight (mg) Fraction of L-Lactyl-L-Lactic Nickell's Medium Control Acid (100 ppm) 0 1 1 1 1
S
1/16 12 2 25 1 S1/8 23 1 48 7 1. /4 27 3 46 6 25 Full Concentration 30 5 41 12 **ee s I EXAMPLE 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 'nder vacuum (20 mm) at 85 0 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 TCW/1287v mixture had about amounts of higher Table V show that of L-lactic acid, duckweed.
9 28% lactic acid, 34% DP2, 22% DP3, 9% DP4, and smaller polymers of the lactic acid. The results given in the mixed polymers of glycolic acid, the mixed polymers the dimer L-lactyl-L-lactic acid all enhance growth of 00o 0* *0 0 0600 *e 0 0000 0060 0~ .e 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, The mixture was centrifuged and absorption of the supernatant was read at 663 and 645 nm. From these readings, the number of m-rograms 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 15 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 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 CON1IIT 0
SS
a* S Dry Weight Chlorophyll (jig) Per mg Root Length (mm) Acid Polyglycolic Acid 1000 ppm 100 Poly-L-Lactic Acid 1000 ppm 100 38.3 47.3 34.3 76.3 46.3 27.3 8.5 2.4 11.3 5.8 2.3 13.7 3.2 TCW/1287v 10 Acid L-.actyl-L-Lactic Acid 1000 ppm 100 Control (No Acid) Dry Weight 39.3 7.6 46.3 10.0 28.0 4.3 20.0 2.5 Chlorophyll (g) Per mg Root Length (mm) 10.1 1.7 7.7 .so.
.90e *e 9 0000 6 0 0 *90 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 15 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.
*fees: 20 1 a 000:0 So a TABLE VI EFFECT OF MIXED POLYMERS OF GLYCOLIC AND LACTIC ACIDS ON DUCKWEED GROWTH Acid Dry Weight (ma) fees 0 00 00 5 Copolymer of Glycolic Acid and L-Lactic Acid 1000 ppm 100 Control (No Acid) 1:1 Mixture of Polymers of L-Lactic Acid and Glycolic Acid 1000 ppm 100 56.5 48.0 38.7 35.5 9.7 6.9 2.9 10.5 43.7 37.5 27.7 TCW/1287v 11 TABLE VI EFFECT OF MIXED POLYMERS OF GLYCOLIC AND LACTIC ACIDS ON DUCKNEED GROWTH Acid Dry Weight (mg) 3:1 Mixture of Polymers of L-Lactic Acid and Glycolic Acid 1000 ppm 56.0 100 44.0 10 30.7 6.8 Control (No Acid) 23 3.8 EXAMPLE 7 "e Fine vermiculite (125 ml) was placed in a l-liter Erlenmeyer flask capped with a silicone foam closure. Then 100 ml of a nutrient solution 15 containing 0.5 g/l MIRACLE-GRO® (a plant food having an N:P:K ratio of 15:30:15) was added. In addition to the nutrient solution, L-lactyl-Llactic acid at 100 or 1000 ppm was placed in certain flasks. Twelve radish seeds (Var. "Scarlet Globe", Yopp Quality Seeds, Carbondale, III.) 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.
o 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 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.
TCW/1287v 12 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 N. 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 66 experiments were run in the winter, the existing light was supplemented with 320 watts of fluorescence light. Plants were then harvested, dried, 15 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 ded at a concentration of from 1 to 10 ppm per treatment. Higher o concentrations of the lactic acid 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 *o Total Plant Acid Added (ppm) Mean Dry Weight (g) None (Control) 0.45 0.07 1 0.94 0.07 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, single-hydroponic units filled TCW/1287v 13 with 18.5 liters of medium. The medium used had the following composition:
KH
2
PO
4
KNO
3 Ca(NO 3 2 4H 2 0 MgSO 4 7H 2 0
H
3
BO
3 MnC1 2 .4H 2 0 ZnSO 4 7H 2 0 CuSO 4 .5H 2 0 NaMoO 4 .2H 2 0 FeSO 4 .7H 2 0 15 Na 2
EDTA
Concentration Per Liter 0.034 g 0.127 g 0.296 g 0.124 g 0.72 mg 0.45 mg 0.055 mg 0.020 mg 0.007 mg 0.68 mg 0.93 mg 00 0@ S
S
0000 0 5500 00 5 a
SO
50 0 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 25 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.
TCW/1287v 14 TABLE VIII EFFECT OF L-LACTIC ACID DIMER ON SPINACH AND LETTUCE GROWN HYDROPONICALLY Mean Weight Per Plant (q) Fresh Weight Dry Weight Spinach Control 100 ppm Acid Lettuce Control 100 ppm Acid 6.1 2 9.2 2 1.6 0.4 4.1 0.7 0.41 0.63 0.083 0.20 0060 0* 00 0 000 00 S.e 0 0000 0 @600 sesO 0 *009 **80 0S *0 S a 0 0 0 6 EXAMPLE Potato shoot cultures were initiated from shoot tips excised from "eyes" of potato tubers. Excised shoot tips, consisting of apical domes 15 accompanied by 4- to 6-leaf primordia, were placed upon nodal propagation medium. This medium consisted of Murashige and Skoog 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 0.
Ten replicate tubes were each inoculated with a single shoot. Each 20 tube (25 x 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 0 C. Thirty days after inoculation, the shoots were counted and recorded. The contents of each tube was cut into sections with each section containing a single shoot.
These shoots were then 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 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 TCW/1287v 15 showed increases in weights over those of the control of 20% and 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 .o added 400 ppm of Mn (as MnSO 4
.H
2 0) 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 15 the polymers of lactic and glycolic acids are able to protect duckweed S from the growth-inhibiting effects of the manganous ion. It is noted that the preferred concentrations of polyglycolic acid and L-lactyl-Llactic 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 Additives Mean Dry Weight Per Flask (mg) 25 Control 27.0 3.3 400 ppm Mn 6.5 1.3 400 ppm Mn" 1000 ppm PGAa) 2.2 400 ppm Mn" 100 ppm PGA 41.0 7.4 400 ppm Mn 10 ppm PGA 12.0 2.6 Control 23.8 4.8 400 ppm Mn 12.9 2.8 400 ppm Mn 1000 ppm PLAb) 95.7 9.8 400 ppm Mn' 100 ppm PLA 33.0 2.8 400 ppm Mn 10 ppm PLA 17.4 1.9 Control 35.5 400 ppm Mn 12.5 2.4 400 ppm Mn++ 1000 ppm LLC) All dead TCW/1287v 16 TABLE IX EFFECT OF VARIOUS ACIDS ON DUCKWEED GROWN IN PRESENCE OF Mn" S Mean Dry Weight Per Flask (mg) 100 ppm LL 51.2 8.6 10 ppm LL 17.2 5.3 Additive 400 ppm Mn" 400 ppm Mn eon.
S S Co Coo.
0 C C C. C oS.C CsoC 005Y we o000
CC,.
soa *0 S a) PGA Polyglycolic acid mixture having the composition given in Example b) PLA Poly-L-lactic acid mixture having the composition given in Example c) LL L-lactyl-L-lactic acid.
EXAMPLE 12 The general procedure of Example 11 was followed except that plants 15 were grown in flasks containing medium with various levels of Cu (as CuSO 4 .5H 2 0) 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 growthinhibiting 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 C. S
C.
we
S
C
Additives Control 6.25 ppm Cu 6.25 ppm Cu 1000 ppm PLAa) 12.5 ppm Cu' Mean Dry Weight Per Flask (mg) 56.0 7.3 31.7 87.2 5.7 16.5 3.1 TCW/1287v Additive 12.5 18.75 18.75 7.5% 15% 22.5% 22.5% ppm Cu ppm Cu ppm Cu Seawater b Seawater Seawater Seawater Seawater Seawater ii 1 17 TABLE X EFFECT OF L-LACTIC ACID POLYMERS ON DUCKNEED GROWN IN PRESENCE OF SALTS es Mean Dry Weight Per Flask (mg) )00 ppm PLA 63.5 3.1 All dead 000 ppm PLA All dead 46.0 000 ppm PLA 103.0 8.8 31.0 2.8 000 ppm PLA 46.0 5.3 10.7 1.7 000 DDm PLA 16.3 s: a a a a• so*** a* a 4 4 050* a 006* as a a 0 a as a 000 a 6 a as a a a ass« 9 @55.
0 a a) PLA Poly-L-lactic acid mixture having the composition given in Example b) MARINEMIX®, a salt mixture containing 29 different ions (Marine Enterprises, Baltimore, was dissolved in sufficient distilled water to give the specified percent of 20 seawater concentration.
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 25 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.
TCW/1287v 18 TABLE XI EFFECT OF L-LACTIC ACID POLYMERS ON CHLOROPHYLL CONTENT OF CHLORELLA GROWN IN PRESENCE OF SALTS Additives Control 1000 ppm PLAa) Seawaterb) 25% Seawater 1000 ppm PLA Seawater qn qco. rat r In nnm PI A Chlorophyll p.g/ml Extractant 2.8 0.3 8.1 0.2 2.7 2.3 6.6 1.1 1.7 0.4 6.1 1 *6sr 0 'e 0 000 6 a 0900 a *d a ease or oL to 0 0 15 jvr clUIUL~ TIVV rllVVI a) PLA Poly-L-lactic acid mixture having the composition given in Example b) MARINEMIX®, a salt mixture containing 29 different ions (Marine Enterprises, Baltimore, was dissolved in sufficient distilled water to give the specified percent of seawater concentration.
Thus, it is apparent that an improved process for increasing the 20 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 is described in the Examples. It 25 is also apparent that there has been provided, in accordance with the invention, a process for facilitating the growth of a plant irrigated with water containing a concentration of salts that would normally be toxic to the plant which fully satisfies the objectives, aims, and advantages set forth above. It is evident that many alternatives, modifications, and variations of the invention 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.
TCW/1287v
Claims (4)
1. A process of facilitating the growth of a plant irrigated with water containing a concentration of salts that would normally be toxic to the 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: R R HO--CHCO 2 CHCO2H n wherein n is a whole number from 1 to 10; the Rs are the same or 'oe different and denote H or CH 3 and if at least one R is CH 3 at least 10 some of the asymmetric centers are in the L-configuration.
2. The process of claim 1 wherein the acid is supplied to the 6,, 9 plant in an aqueous solution at a concentration of between about 1 and about 1000 parts per million on a weight/volume basis.
3. A process of facilitating the growth of a plant irrigated with water containing a concentration of salts that would normally be toxic to the plant, which process is substantially as herein described with reference to Example 12 or 13.
4. A plant whenever grown and irrigated with water containing a concentration of salts that would normally be toxic to the plant using the process of claim 3. a* DATED this THIRTIETH day of DECEMBER 1991 S r CPC International, Inc. S Patent Attorneys for the Applicant SPRUSON FERGUSON TCW/1287v
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US3419187A | 1987-04-06 | 1987-04-06 | |
US034191 | 1987-04-06 | ||
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AU615447B2 (en) * | 1987-04-06 | 1991-10-03 | Corn Products International, Inc. | Method for regulating plant growth |
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- 1988-04-06 DD DD88314461A patent/DD284153A5/en not_active IP Right Cessation
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