Compositions containing and methods of use of an infectivity-cured Hr plasmid-bearing microorganism

TECHNICAL FIELD
This invention relates to the field of plant husbandry, and in particular relates to compositions containing and methods of use of an Hr plasmid-bearing microorganism free from pathogenicity to carrots.
BACKGROUND ART
It is known to improve seed germination, with this type of prior art being illustrarted by U.S. Pat. No. 2,553,577 to Hale et al., and U.S. Pat. No. 2,690,388 to Hale. Treatment of a seed with a microorganism, particularly with a microorganism of the genus Phizobium, is also known. This type of prior art is exemplified by U.S. Pat. Nos. 2,313,057 to Fischer, 3,168,796 to Scott et al, 3,499,748 to Fraser, 4,136,486 to Franklin, Jr. et al, 4,149,869 to Lloyd, and 4,161,397 to Bellet et al. In addition, U.S. Pat. No. 674,765 to Hartleb who discloses a seed treated with a microorganism, states that nodule formation begins very shortly after the seed has become imbedded in the soil, and mentions rapid germination at lines 37 and 38 thereof. Furthermore, U.S. Pat. No. 4,077,793 to Krupicka discloses that treating seeds of certain crops such as maize, corn, potatoes ad tomatoes with a biochemical material containing nitrogen-fixing soil microorganisms results in earlier germination, and reports unusually good yield. Also, Chemical and Engineering News, Dec. 8, 1980, p. 29 discusses the treatment of soybean seeds with nirogen-fixing bacteria.
Additionally, it is known to stimulate the sprouting of cucumber and sugar beet plants by spreading a cell suspension of Agrobacterium rhizogenes on the surface of cucumber and sugar beet seeds. Illustrative of this type of prior art is M. Stanek, Foila Microbiologica 21(3):213 (1976). In this work, the microorganism was isolated from the surface of the hyphae of the fungus Pythium debaryanum. It is also disclosed in this work that treatment of the surface of sugar beet seeds with a suspension of the A. rhizogenes cells prevented black root disease, when the seeds were simultaneously artificially contaminated with the fungus Phoma betae.
Finally, the preparation of an infectivity-cured Hr plasmid-bearing microorganism is known. Illustrative of this prior art is Moore, Warren and Strobel, Plasmid, 2:617-626 (1979). This microorganism was prepared by treating A. rhizogenes A.sub.4, which contains the Hr plasmid in nature, with ethidium bromide. This microorganism was free from pathogenicity to carrots. In this work, it is suggested in the paragraph bridging the two columns on p. 625 that induction of rooting may be a potential use of A. rhizogenes A.sub.4. Induction of rooting is a potential use of pathogenic A. rhizogenes A.sub.4 and is to be distinguished from either induction of germination (sprouting) or growth promoting activities such as the enhancement of root elongation, shoot elongation, and root development.
However, this and the other prior art of which we are aware, are deficient as failing to provide an agriculturally useful composition comprised of a seed treated with a selected infectivity-cured Hr plasmid-bearing microorganism. Furthermore, this art fails to provide methods of enhancing root elongation, shoot elongation or root development of a germinating seed that include treating a seed with a selected infectivity-cured Hr plasmid-bearing microorganism. Moreover, this prior art fails to provide a method of inducing germination of Kentucky bluegrass seed that involves treating the seed with a selected infectivity-cured Hr plasmid-bearing microorganism, and fails to provide a method of promoting plant growth at a lower soil temperature than is common at the time of planting a seed of the plant. Additionally, this prior art fails to provide an inoculant for increasing nodulation, root mass, and shoot mass in a leguminous plant, the inoculant containing a Rhizobium microorganism and a selected infectivity-cured Hr plasmid-bearing microorganism; and fails to provide an agriculturally useful composition containing a suitable seed treated with this inoculant.
DISCLOSURE OF THE INVENTION
It is accordingly one object of the present invention to provide an agriculturally useful composition comprised of a seed treated with a selected infectivity-cured Hr plasmid-bearing microorganism.
A further object is to provide methods of enhancing root elongation, shoot elongation or root development of a germinating seed that includes treating a seed with a selected infectivity-cured Hr plasmid-bearing microorganism.
An even further object is to provide a method of inducing germination of Kentucky bluegrass seed that involves treating the seed with a selected infectivity-cured Hr plasmid-bearing microorganism.
A still further object is to provide a method of promoting plant growth at a lower soil temperature than is common at the time of planting a seed of the plant.
An additional object is to provide an inoculant for increasing nodulation, root mass and shoot mass in a leguminous plant, the inoculant containing a Rhizobium microorganism and a selected infectivity-cured Hr plasmid-bearing microorganism.
An even additional object is to provide an agriculturally useful composition containing a suitable seed treated with this inoculant.
Other objects and advantages of the present invention will become apparent as the description thereof proceeds.
In satisfaction of the foregoing objects and objectives, there is provided in one aspect of this invention, an agriculturally useful composition. In one embodiment, the composition includes a seed selected from the group consisting of pea, soybean, Kentucky bluegrass and rice treated with a selected infectivity-cured Hr plasmid-bearing microorganism. The microorganism is characterized by freedom from pathogenicity to carrots and significantly greater germination induction of Kentucky bluegrass seed, when compared to A. rhizogenes A.sub.4 ATCC 31798.
In another embodiment, the composition includes a seed selected from the group consisting of pea, soybean, corn, pinto bean and rice treated with a selected infectivity-cured Hr plasmid-bearing microorganism. The microoorganism is characterized by freedom from pathogenicity to carrots and an induction of significantly enhanced shoot length in a germinating corn seed, when compared to A. rhizogenes A.sub.4 ATCC 31799.
In a second aspect of the invention, agriculturally useful methods are provided. In one embodiment, there is provided a method of enhancing root elongation of a germinating seed. In this method, a seed selected from the group consisting of pea, Newana spring wheat, shabet barley, corn, sorghum and soybean is treated with a root elongation enhancing amount of a selected infectivity-cured Hr plasmid-bearing microorganism free from pathogenicity to carrots. The microorganism is either (1) a first microorganism type characterized by an induction of significantly enhanced shoot length in a germinating corn seed, when compared to A. rhizogenes A.sub.4 ATCC 31799, or (2) a second microorganism type characterized by significantly greater germination induction of Kentucky bluegrass seed, when compared to A. rhizogenes A.sub.4 ATCC 31798. However, when the seed is sorghum, the microorganism is the first microorganism type.
In another embodiment of this aspect of the invention, there is provided a method of enhancing root development of a germinating seed. This method includes the step of treating a seed selected from the group consisting of soybean, rice, pinto bean, Newana spring wheat, corn, pea and sorghum with a root development enhancing amount of a selected infectivity-cured Hr plasmid-bearing microorganism free from pathogenicity to carrots and that is either the first microorganism type or the second microorganism type. However, when the seed is sorghum, the microorganism is the first microorganism type.
In another embodiment of this aspect of the invention, there is provided a method of enhancing shoot elongation of a germinating seed. This method includes treating a seed selected from the group consisting of cotton, pinto bean, rice, pea, Newana spring wheat, shabet barley, corn, winter rye and broccoli, with a shoot elongation enhancing amount of a selected infectivity-cured Hr plasmid-bearing microorganism free from pathogenicity to carrots and that is either the first microorganism type or the second microorganism type. However, when the seed is corn or winter rye, the microorganism is the first microorganism type.
In a third aspect of the invention, there is provided a method of inducing germination of Kentucky bluegrass seed. This method includes treating the seed with a germination inducing amount of a selected infectivity-cured Hr plasmid-bearing microorganism this is free from pathogenicity to carrots and that is the second microorganism type.
In a fourth aspect of the invention, there is provided a method of promoting plant growth at a lower soil temperature than is common at the time of planting a seed of the plant. The method includes the step of treating soybean or corn seed with a selected infectivity-cured Hr plasmid-bearing microorganism that is free from pathogenicity to carrots and that is the second microorganism type.
In a furtherw aspect of the present invention, there is provided an inoculant for increasing nodulation, root mass and shoot mass in a leguminous plant. The inoculant contains (a) a microorganism of the genus Rhizobium that is capble of inducing nodulation in the selected leguminous plant, and (b) a selected infectivity-cured Hr plasmid-bearing microorganism free from pathogenicity to carrots and that is either the first microorganism type or second microorganism type. The relative proportions of the Rhizobium microorganism and the plasmid-bearing microorganism are such that nodulation of a leguminous plant is increased as a consequence of treating a seed of the plant with a nodulation increasing amount of the inoculant.
Also provided is a agriculturally useful composition containing the inoculant and a seed of a leguminous plant in which the Rhizobium microorganism of the inoculant is capable of inducing nodulation. The inoculant is present in a nodulation increasing amount.
BEST MODE FOR CARRYING OUT THE INVENTION
As discussed, the present invention relates to compositions containing and methods of using a selected infectivity-cured Hr plasmid-bearing microorganism. By definition, for purposes of this document, an infectivity-cured Hr plasmid-bearing microorganism is free from pathogenicity to carrots and thus lacks the ability to induce root proliferation. In a preferred embodiment, the microorganism is an A. rhizogenes A.sub.4 microorganism. For ease of understanding, much of the below discussion is specific to the A. rhizogenes A.sub.4 microorganism, in which the Hr plasmid occurs in nature.
Broadly speaking, the infectivity-cured Hr plasmid-bearing microoganism is either a first microorganism type or is a second microorganism type. By a "first microorganism type" is meant a microorganism characterized by, for example, an induction of significantly enhanced shoot length in a germinating corn seed, when compared to A. rhizogenes A.sub.4 ATCC 31799. This type is exemplified by A. rhizogenes A.sub.4 ATCC 31798, and in this regard, reference is hereby made to the below Examples, which quantify other characteristics of this microorganism type. By a "second microorganism type" is meant a microorganism characterized by, for example, significantly greater germination induction of Kentucky bluegrass seed, when compared to A. rhizogenes A.sub.4 ATCC 31798. This type is exemplified by A. rhizogenes A.sub.4 ATCC 31799, and in this regard, reference is hereby made to the below Examples, which quantify other characteristics of this microorganism type.
For the purposes of this invention, for the first microorganism type, experimentation identical to that used in obtaining the data in Table 5, is used to show the characteristic of significantly enhanced shoot length in comparison with the A. rhizogenes A.sub.4 ATCC 31799 species. For the purposes of this invention, for the second microorganism type, experimentation identical to that used in obtaining the data in Table 10, is used to show the characteristic of significantly greater induction of Kentucky bluegrass seed in comparison with the A. rhizogenes A.sub.4 ATCC 31798 species.
Preferred species useful in the invention are A. rhizogenes A.sub.4 ATCC 31798 and A. rhizogenes A.sub.4 ATCC 31799. A culture of each of these preferred species has been placed on deposit with the American Type Culture Collection, and the accession numbers set forth above have been assigned thereto. In each case, the deposit is restricted until such time as a patent has been issued disclosing the above deposits, except that access is available under 37 C.F.R.1.14. After issuance of the patent, all restrictions on availability of the deposited cultures to the public will be irrevocably removed. The deposits will be maintained for a period of 30 years from the deposit date, and accordingly, the cultures will be permanently available to the public after issuance of the patent.
A. rhizogenes A.sub.4 ATCC 31798 and A. rhizogenes A.sub.4 ATCC 31799 were obtained by treating an A. rhizogenes A.sub.4 wild strain with ethidium bromide according to the procedures of Lin and Kado, Can. J. Microbiol., 23:1554-1561 (1977). The A. rhizogenes A.sub.4 microorganism is a soil-inhabiting microorganism that was originally isolated by Dr. Peter Ark (University of California, Berkeley) from naturally infected roses exhibiting hairy root symptoms. The wild strain is known and available, and is described at p. 618 of the Moore, Warren and Strobel publication discussed earlier. The wild strain induces rooting of carrots, known as the "hairy root" syndrome, and is pathogenic to carrots. On carrot root disks inoculated with as few as 100 cells thereof, root proliferation is noted within two weeks. This microorganism causes root proliferation on members of many plant families including Leguminosiae and Compositae, and hence has a wide host range. As a result of this pathogenicity, it is better not to use the wild strain for agricultural purposes.
The preferred species were made by incorporating an about 100 micromolar amount of ethidum bromide into the nutrient-containing agar culture medium described below, and placing cells of the wild strain on the agar surface. After about six days, colonies were tested for the ability ot induce root formation on carrot disks according to the carrot disk assay procedure on p. 618 of the Moore, Warren and Strobel publication. Those microorganisms that were found incapable of inducing root formation were further evaluated for growth promoting activities such as the enhancement of root elongation, shoot elongation, or root development (number of laterals, length of longest lateral, and/or adventitious root length), and for the capability to increase seed germination (sprouting). Testing of this type is discussed in detail in the below Examples. By this procedure, A. rhizogenes A.sub.4 ATCC 31798 and A. rhizogenes A.sub.4 ATCC 31799 were prepared and isolated. The preferred species are particularly characterized by freedom from pathogenicity to carrots, as shown by an inability to induce root proliferation in carrots.
By Tables 1 and 2 below, it is shown that the Hr plasmid controls the growth promoting activites mentioned above. This plasmid is correlated in the Moore, Warren and Strobel publication with the root proliferation infectivity of the A. rhizogenes A.sub.4 wild strain. Thus, the Hr plasmid controls both growth promoting activities and infectivity. It is believed that, in addition, the Hr plasmid controls germination induction; promotes plant growth at a lower soil temperature than is common at the time of planting a seed of the plant; and functions to synergistically increase nodulation, root mass and shoot mass in a leguminous plant, when combined with a suitable Rhizobium microorganism.
The Hr plasmid is not found, in nature, in either A. tumefaciens or A. radiobacter. As demonstrated in Table 1, a seed treated with the A. rhizogenes A.sub.4 wild strain or with either of the preferred species shows significant growth effects when compared to an untreated seed (control), whereas a seed treated with either A. tumefaciens or A. radiobacter does not show, on the whole, a significant growth effect. As demonstrated in Table 2, a seed treated with an A. radiobacter transconjugant that contains the Hr plasmid also shows significant growth effects, on the whole. Hence, these data show that the Hr plasmid is correlated with the growth promoting activities.
As a result of the ethidium bromide treatment described above, the infectivity gene was cured from the Hr plasmid in the case of the infectivity-cured Hr plasmid-bearing microorganism useful in the present invention. The A. radiobacter transconjugant was prepared by in vivo mating using known techniques, as a result of which the Hr plasmid was placed into this microorganism. Accordingly, it can be seen that the Hr plasmid could be placed into a microorganism other than A. rhizogenes A.sub.4, and that the resulting microorganism could be treated with ethidium bromide to cure the infectivity gene from the Hr plasmid, and to produce a microorganism having an infectivity-cured Hr plasmid that is either the first microorganism type or the second microorganism type described above. As explained earlier, these microorganism types are illustrated by A. rhizogenes A.sub.4 ATCC 31798 and A. rhizogenes A.sub.4 ATCC 31799, respectively, and as can be appreciated from the below discussion and Examples, these species are believed to differ from each other in the composition of the infectivity-cured Hr plasmid. Hence, the present invention covers any microorganism that contains an infectivity-cured Hr plasmid that is functionally equivalent to either the infectivity-cured Hr plasmid in A. rhizogenes A.sub.4 ATCC 31798 or the infectivity-cured Hr plasmid in A. rhizogenes A.sub.4 ATCC 31799.
As a result of the ethidium bromide treatment, it has been unexpectedly discovered that the grwoth-promoting activities of the infectivity-cured Hr plasmid found in a microorganism in accordance with the invention are significantly enhanced, compared to the growth-promoting activites of a naturally occurring Hr plasmid, as found in the A. rhizogenes A.sub.4 wild strain. As illustrated in the below Examples, the particular growth effect found to be enhanced varies according to the seed type, e.g., corn, pea or soybean, and varies according to whether the microorganism is the first or second microorganism type. In certain seeds such as Newana spring wheat, a significant enhancement is not observed. However, as illustrated in the below Examples, in certain of these seeds, as well as in certain seeds in which significant enhancement is observed, it has been surprisingly discovered that the first and/or second microorganism types have a significant growth effect, compared to the same seed untreated with an A. rhizogenes A.sub.4 microorganism (control of the Examples). In certain seeds such as winter wheat, a significant growth effect of this type is not observed.
A. rhizogenes A.sub.4 microorganims can be easily cultured on a medium containing the following nutrients per liter: 0.5 g KH.sub.2 PO.sub.4, 10 g mannitol, 2 g L-glutamate, 0.2 g NaCl, 0.2 g MgSO.sub.4, and 0.3 g yeast extract. An agar plate containing these nutrients is prepared by adjusting the pH of a solution containing these nutrients to 7.0, mixing 15 g/l of agar with the pH-adjusted solution, heating the resulting mixture, and pouring the hot liquid into a petri dish. The cells of A. rhizogenes A.sub.4 grown either on plates or in liquid media are harvested as a paste from plates or by centrifugation from liquid media, frozen and then subjected to drying by lyophilization. The lyophilized cells posses biological activity at the same level as those that are freshly harvested.
In one embodiment of the agriculturally useful composition of the present invention, the microorganism-treated seed is pea seed, soybean seed, Kentucky bluegrass seed (Poa pratensis) or rice seed, and the infectivity-cured Hr plasmid-bearing microorganism is the second microogranism type. In the case of pea, soybean or rice, significantly enhanced growth promoting effects are surprisingly observed when compared to the same seed treated with the A. rhizogenes A.sub.4 wild strain. These effects are advantageous agriculturally as well as for land reclamation when the seed is a legume. The preferred species is A. rhizogenes A.sub.4 ATCC 31799. Depending upon the seed selected, the growth promoting effect is enhanced shoot length and/or increased lateral root development. In the case of Kentucky bluegrass, significantly enhanced germination is observed when compared to the same seed treated with the A. rhizogenes A.sub.4 wild strain.
In another embodiment of the agriculturally useful composition of the present invention, the microorganism treated seed is pea, soybean, corn, pinto bean or rice, and the infectivity-cured Hr plasmid-bearing microorganism is the first microorganism type. In each instance, significantly enhanced growth promoting effects are surprisingly observed when compared to the same seed treated with the A. rhizogenes A.sub.4 wild strain. These effects are advantageous agriculturally as well as for land reclamation when the seed is a legume. The preferred species is A. rhizogenes A.sub.4 ATCC 31798. Depending upon the seed selected, the germinating seeds of this composition are characterized by enhanced root development (number of laterals, length of longest lateral and/or adventitious root length) and/or increased shoot length. As can be understood from the below Tables and as indicated by the above description, significantly enhanced effects are obtained when pea, soybean or rice is treated with either microorganism type, and especially with either preferred species.
In the agriculturally useful composition described above and in the methods described below, a selected seed is treated with an agriculturally efficacious amount of the infectivity-cured Hr plasmid-bearing microorganism according to the invention. Preferably, treatment of the seed is accomplished by coating the seed with cells of the microorganism.
In the case of A. rhizogenes A.sub.4, the microorganism is grown for about three days at about room temperature on the culture medium described above, and the seed is coated by being placed directly into contact with the microorganism, which occurs in a slimy growth and thus readily adheres to the seed coat. Alternatively, lyophilized cells may be used to coat the seed by reconstituting the cells in water to about the same consistency as a fresh cell growth (paste), and then contacting the seed with the paste. The lyophilized cells possess biological activity at the same level as those that are freshly harvested. Either of these procedures is used in the Examples below.
Commercially, the coating procedures described above are not satisfactory since the microorganism-coated seed should be dry, although rice could be treated with a paste of reconstituted lyophilized cells. A commercially useful coating technique advantageously involves mixing an adherence-promoting additive such as kaolin or bentonite to freeze-dried cells of the microorganism, and then contacting the seed with the mixture. When kaolin is used as the additive, it is particularly suitable to combine about 3 parts of kaolin with about 1 part of cells (weight/weight). Alternatively, the seed could be first contacted with the adherence-promoting additive and then with the freeze-dried cells.
When the seed is coated by contacting the seed with the bacterial cells, or with the mixture of cells and adherence-promoting additive, the number of cells per seed depends upon factors such as the seed size and the relative amounts of the cells and of the additive. When a seed is simply contacted with a paste of A. rhizogenes A.sub.4 cells, about 10.sup.9 -10.sup.10 cells will be coated onto a relatively larger seed such as a soybean seed, and about 10.sup.6 -10.sup.7 cells will be coated onto a relatively smaller seed such as a grass seed. Optionally, there is added during the coating procedure a fungicide such as Captan.RTM.. Experimentation has shown that either microorganism type may be compatible with a fungicide such as Captan.RTM.. Other compatible additives could be included during the coating procedure.
In a second aspect of the present invention, agriculturally useful methods are provided. These methods include the step of treating a seed with an agriculturally efficacious amount of an infectivity-cured Hr plasmid-bearing microorganism that is either the first or second microorganism type. In this aspect of the invention, it is preferred that treatment of the seed be accomplished by coating the seed with cells of the microorganism. In this regard, the above description relating to coating a seed with the microorganism according to the invention is equally applicable to the agriculturally useful methods of the present invention.
In one embodiment of the agriculturally useful methods of the present invention, there is provided a method of enhancing root elongation of a germinating seed in which the agriculturally efficacious amount of the microorganism in accordance with the invention is more particularly a root elongation enhancing amount. The seed is pea, Newana spring wheat, shabet barley, corn, sorghum or soybean. However, when the seed is sorghum, the microorganism is the first microorganism type. In each instance, significantly enhanced root elongation is surprisingly observed in comparison with the same seed that is untreated with an A. rhizogenes A.sub.4 microorganism (control of the Examples). An advantage of enhanced root elongation is that it promotes more rapid establishment of a plant in the soil.
In another embodiment, there is provided a method of enhancing root development of a germinating seed in which the agriculturally efficacious amount of the microorganism in accordance with the invention is more particularly a root development enhancing amount. Enhanced root development is characterized by an increase in the number of lateral roots, an increase in the length of the longest lateral root, and/or an increase in adventitious root length. The seed is soybean, rice, pinto bean, pea, Newana spring wheat or sorghum. However, when the seed is sorghum, the microorganism is the first microorganism type. In each instance, significantly enhanced root development is surprisingly observed in comparison with the same seed that is untreated with an A. rhizogenes A.sub.4 microorganism (control of the Examples). When the seed is soybean or pea, the microorganism is preferably the second microorganism type, and when the seed is pinto bean or corn, the microorganism is preferably the first microorganism type. Enhanced root development is agriculturally advantageous because it facilitates a more rapid establishment of the plant in the soil and promotes passage of the plant through the early seedling stage at an accelerated rate and this reduces disease impact.
In still another embodiment, there is provided a method of enhancing sheet elongation of a germinating seed in which the agriculturally efficacious amount of the microorganism in accordance with the invention is more specifically a shoot elongation enhancing amount. The seed is cotton, pinto bean, rice, pea, Newana spring wheat, shabet barley, corn, winter rye or broccoli. However, when the seed is corn or winter rye, the microorganism is the first microorganism type. In each instance, significantly enhanced shoot elongation is surprisingly observed in comparison with the same seed that is untreated with an A. rhizogenes A.sub.4 microorganism (control of the Examples). When the seed is rice, the microorganism is preferably the first microorganism type, and when the seed is shabet barley, the microorganism is preferably the second microorganism type. An advantage of enhanced shoot elongation is that, for example, in the case of beans, the time for harvest may be reduced because of more rapid development of shoots and tops, and as a result early flowering. Enhanced shoot elongation is also advantageous in the case of rice since it results in the shoot extending above the water level more rapidly and thus reduces decay.
In a third aspect of the present invention, there is provided a method of inducing germination of Kentucky bluegrass seed. Use of this method will help establish lawns, sods and so forth. This method includes treating the seed with an agriculturally efficacious amount, more precisely a germination inducing amount, of the second microorganism type described above. Significantly enhanced germination is surprisingly observed when compared to the seed treated with the A. rhizogenes A.sub.4 wild strain. The preferred species is A. rhizogenes A.sub.4 ATCC 31799. It is preferred that treatment of the seed be accomplished by coating the seed with the microorganism. In this regard, the above disclosure relating to coating a seed with the microorganism in accordance with the invention is equally applicable to this aspect of the present invention.
In a fourth aspect of the present invention, there is provided a method of promoting plant growth at a lower soil temperature than is common at the time of planting a seed of the plant. This method has the advantage of permitting earlier planting, for example, at a soil temperature of about 58.degree. F., rather than about 70.degree. F. This method includes treating a corn or soybean seed with an agriculturally efficacious, more particularly a plant growth promoting, amount of the second microorganism type. Significantly enhanced root and shoot elongation are surprisingly observed for this microorganism type when compared to the same seed that is untreated with an A. rhizogenes A.sub.4 microorganism. Enhancement is observed for the wild strain also. The preferred species is A. rhizogenes A.sub.4 ATCC 31799, and it is preferred that the treatment be accomplished by coating the seed with the microorganism. In this regard, the above disclosure relating to coating a seed with the microorganism in accordance with the invention is equally applicable to this aspect of the invention.
Advantageously, the treated seed is incubated for at least about 1 to 2 days, at about room temperature, prior to being planted. Treatment of the seed with the microorganism is suitably also at about room temperature.
In a further aspect of the present invention, there is provided an inoculant for increasing nodulation, root mass and shoot mass in a leguminous plant. Increased nodulation has the advantage of increasing nitrogn fixation. The inoculant includes (a) a microorganism of the genus Rhizobium that is capable of inducing nodulation in the selected leguminous plant, and (b) an infectivity-cured Hr plasmid-bearing microorganism that is either the first or second microorganism type. Significantly increased nodulation, root mass and shoot mass are surprisingly observed with the wild strain when compared to treatment with R. japonicum only, and thus are believed to exist for the first and second microorganism types. The relative proportions of the Rhizobium microorganism and the first or second microorganism type in the inoculant are such that nodulation of a leguminous plant is increased as a result of treating a seed of the plant with a nodulation increasing amount of the inoculant. Suitably, at least about 1% of the total amount of the Rhizobium microorganism and of the first or second microorganism type in the inoculant, is the Rhizobium microorganism. Advantageously, the two microorganisms are present in substantially equal amounts in the inoculant. When the leguminous plant is a soybean plant, the Rhizobium microorganism is Rhizobium japonicum.
Also provided by the present invention is an agriculturally useful composition that includes this inoculant and a seed of a leguminous plant in which the Rhizobium microorganism of the inoculant is capable of inducing nodulation. The seed is treated with an agriculturally efficacious, more particularly a nodulation increasing, amount of the inoculant. Preferably, treatment of the seed is accomplished by coating the seed with cells of the inoculant. Any of the coating procedures described earlier may be used, with the commercially useful techniques being preferred. These procedures are, however, modified in that the Rhizobium microorganism is in each instance mixed with the infectivity-cured Hr plasmid-bearing microorganism prior to contacting a seed with cells of the Hr plasmid-bearing microorganism. One additional alternative coating procedure involves contacting a seed with finely chopped or ground peat containing cells of the mixture of the Rhizobium microorganism and the Hr plasmid-bearing microorganism. This procedure could be used in place of any of the earlier-described procedures. The number of cells coated onto each seed depends upon factors such as those discussed above.
Specific examples of the present invention will now be set forth. It is to be understood that these examples are merely illustrative, and are in no way to be interpreted as limiting the scope of the invention.

EXAMPLE 1
Ten to fifteen pea seeds are pretreated for five minutes in 5% sodium hypochlorite and then coated with cells of the A. rhizogenes A.sub.4 wild strain in accordance with the coating procedure described above for the A. rhizogenes A.sub.4 microorganism. Either fresh cells or reconstituted lyophilized cells are used. The coated cells are immediately placed on Steel Blue Anchor Seed Germination Blotter thoroughly moistened with water until free water no longer drips from its surface, and contained within an air-tight 15 cm.times.15 cm.times.3 cm plastic box. The box is incubated at 25.degree. C. for 7 days, and the response of the germinating seeds is then evaluated.
This procedure is followed using cells of A. rhizogenes A.sub.4 ATCC 31798, using cells of A. rhizogenes A.sub.4 ATCC 31799, using cells of A. tumefaciens, and using cells of A. radiobacter, in place of cells of the wild strain. In addition, a control experiment is run in which this procedure is followed except that the seed is not treated with any microorganism.
Each experiment is carried out three times, and there is derived a value that represents an average of three replicates of 10-15 seeds, for each experiment. These values are set forth in Table 1.
EXAMPLE 2
Following the procedure of Example 1, using cells of an A. radiobacter transconjugant that contains the Hr plasmid, rather than using cells of the wild strain, and again carrying out a control experiment, the values set forth in Table 2 are obtained. Each of these values, and each of the values in Tables 3-9 and 11-14, represents an average of three replicates of 10-15 seeds.
EXAMPLE 3
Following the procedure of Example 1, except that the experimentation is limited to cells of the A. rhizogenes A.sub.4 wild strain, cells of A. rhizogenes A.sub.4 ATCC 31798, cells of A. rhizogenes A.sub.4 ATCC 31799 and carrying out a control experiment, and except that soybean seed is substituted for pea seed, the results set forth in Table 3 and relating to the number of laterals and the length of the longest lateral are obtained.
Following the procedure of the previous paragraph, except that the period of incubation is 3 days, rather than 7 days, the results set forth in Table 3 and relating to root length are obtained.
TABLE 1______________________________________ Response of Germinating Pea (Pisum sativum) - After 7 days* Root Shoot Number Length ofTreatment Length Length of Longest La-Used (mm) (mm) Laterals teral (mm)______________________________________Control 50.8.sup.y 3.6.sup.z 0.3.sup.x 0.2.sup.zWild Strain 70.4.sup.x 7.8.sup.yz 3.0.sup.y 3.0.sup.xyATCC 31798 67.4.sup.x 12.4.sup.xy 5.3.sup.z 4.2.sup.xyATCC 31799 71.6.sup.x 13.5.sup.x 5.6.sup.z 5.2.sup.xA. tumefaciens 43.5.sup.y 4.6.sup.z 0.3.sup.x 0.3.sup.zA. radiobacter 48.9.sup.y 7.4.sup.yz 0.07.sup.x 0.02.sup.z______________________________________ *Differences were significant at the 1% level. Numbers followed by the same letter(s) are in common statistically significant groups.
TABLE 2______________________________________ Response of Germinating Pea ( Pisum sativum) - After 7 days* Root Shoot Number Length ofTreatment Length Length.sup.1 of Longest La-Used (mm) (mm) Laterals teral.sup.2 (mm)______________________________________Transconjugant 76.3.sup.x 32.1 7.4.sup.x 13.7.sup.yControl 68.5.sup.x 11.8 5.6.sup.x 4.4.sup.x______________________________________ *Numbers followed by the same letter are in common statistically significant groups. .sup.1 Difference is significant at the 10% level. .sup.2 Differences are significant at the 5% level.
EXAMPLE 4
Following the procedure of the first paragraph of Example 3, except that shabet barley seed is substituted for soybean seed and the period of incubation is 5 days, rather than 7 days, the results set forth in Table 4 are obtained.
EXAMPLE 5
Following the procedure of Example 4, except that corn seed is substituted for barley seed and the period of incubation is 6 days, rather than 5 days, the results set forth in Table 5 are obtained.
EXAMPLE 6
Following the procedure of Example 4, except that rice seed is substituted for barley seed and the period of incubation is 8 days rather than 5 days, the results shown in Table 6 are obtained.
EXAMPLE 7
Following the procedure of Example 4, except that Newana spring wheat seed is substituted for barley seed, and the period of incubation is 3 days, rather than 5 days, the results set forth in Table 7 are obtained.
EXAMPLE 8
Following the procedure of Example 4, except that winter rye seed is substituted for barley seed and the period of incubation is 4 days, rather than 5 days, the results set forth in Table 8 are obtained.
EXAMPLE 9
Following the procedure of Example 4, except that sorghum seed is substituted for barley seed, and the period of incubation is 6 days, rather than 5 days, the results set forth in Table 9 are obtained.
TABLE 3______________________________________ Response of Germinating Soybean (Glycine max)* Root Number Length of Lon-Treatment Length.sup.1 of gest Lateral.sup.2Used (mm) Laterals.sup.2 (mm)______________________________________Control 16.9.sup.x 11.8.sup.x 9.5.sup.xWild Strain 37.7.sup.y 12.1.sup.x 26.4.sup.yATCC 31798 40.3.sup.y 17.7.sup.y 27.0.sup.yATCC 31799 44.4.sup.y 26.2.sup.y 36.1.sup.z______________________________________ *Numbers followed by the same letter are in common statistically significant groups. .sup.1 Results after 3 days. Differences were significant at the 5% level .sup.2 Results after 7 days. Differences were significant at the 1% level
TABLE 4______________________________________ Response of Germinating Shabet Barley (Hordeum vulgare) After 5 Days* Root Shoot NumberTreatment Length.sup.1 Length.sup.2 ofUsed (mm) (mm) Roots______________________________________Control 67.5.sup.x 21.8.sup.x 5.6.sup.xWild Strain 96.4.sup.y 32.3.sup.y 5.7.sup.xATCC 31798 90.1.sup.y 29.7.sup.xy 5.5.sup.xATCC 31799 97.0.sup.y 35.0.sup.y 6.0.sup.x______________________________________ *Numbers followed by the same letter(s) are in common statistically significant groups. .sup.1 differences were significant at the 1% level. .sup.2 Differences were significant at the 5% level.
TABLE 5______________________________________Response of Germinating Corn(Zea mays) - After 6 Days* Length Adventi- of tious Root Shoot Number Longest RootTreatment Length.sup.1 Length.sup.2 of Lateral.sup.2 Length.sup.2Used (mm) (mm) Laterals.sup.1 (mm) (mm)______________________________________Control 102.2.sup.x 18.9.sup.x 9.6.sup.x 3.6.sup.x 9.6.sup.yWild Strain 129.1.sup.y 28.4.sup.x 21.7.sup.y 8.6.sup.y 21.3.sup.xATCC 147.7.sup.y 38.4.sup.y 29.1.sup.z 12.0.sup.y 24.7.sup.x31798ATCC 142.7.sup.y 28.5.sup.x 23.9.sup.yz 11.1.sup.y 15.5.sup.xy31799______________________________________ *Numbers followed by the same letter(s) are in common statistically significant groups. .sup.1 Differences were significant at the 1% level. .sup.2 Differences were significant at the 5% level.
TABLE 6______________________________________ Response of Germinating Rice (Oryza sativa) - After 8 Days* Length of Root Shoot Number LongestTreatment Length Length.sup.1 of Lateral.sup.2Used (mm) (mm) Laterals (mm)______________________________________Control 52.7.sup.x 12.5.sup.x 47.9.sup.x 14.0.sup.xWild Strain 58.0.sup.x 18.3.sup.xy 62.9.sup.x 22.8.sup.yATCC 31798 58.8.sup.x 25.3.sup.z 65.4.sup.x 21.6.sup.yATCC 31799 62.4.sup.x 20.0.sup.yz 70.8.sup.x 20.4.sup.y______________________________________ *Numbers followed by the same letter(s) are in common statistically significant groups. .sup.1 Differences were significant at the 5% level. .sup.2 Differences were significant at the 1% level.
TABLE 7______________________________________ Response of Germinating Newana Spring Wheat (Triticum aestivum) - After 3 Days* Root Shoot NumberTreatment Length.sup.1 Length.sup.2 ofUse (mm) (mm) Roots.sup.2______________________________________Control 18.3.sup.x 2.1.sup.x 2.2.sup.xWild Strain 28.4.sup.y 4.6.sup.y 2.9.sup.yATCC 31798 30.2.sup.y 4.9.sup.y 2.9.sup.yATCC 31799 28.4.sup.y 4.3.sup.y 2.8.sup.y______________________________________ *Numbers followed by the same letter are in common statistically significant groups. .sup.1 Differences were significant at the 1% level. .sup.2 Differences were significant at the 5% level.
TABLE 8______________________________________ Response of Germinating Winter Rye (Secalis cereale) - After 4 Days* Root Shoot NumberTreatment Length Length.sup.1 ofUsed (mm) (mm) Roots______________________________________Control 53.7.sup.x 15.2 3.9.sup.xWild Strain 58.8.sup.x 18.6 4.3.sup.xATCC 31798 57.8.sup.x 21.2 4.5.sup.xATCC 31799 58.4.sup.x 17.8 3.9.sup.x______________________________________ *Numbers followed by the same letter are in common statistically significant groups. .sup.1 ATCC 31798 was statistically superior at the 10% level, when compared to the control.
EXAMPLE 10
The procedure of Example 4 is followed, except that Kentucky bluegrass seed is substituted for barley seed, except that the bluegrass seed is not pretreated with sodium hypochlorite, except that the period of incubation is 4 days, rather than 5 days, and except that 100 seeds per box, rather than 10-15 seeds per box are used. Each seed treated with an A. rhizogenes A.sub.4 microorganism is coated with 10.sup.6 -10.sup.7 bacterial cells. The results set forth in Table 10 are obtained. Each of these values represents an average of three replicates of 100 seeds. As shown, ATCC 31799 produces significantly greater germination induction than ATCC 31798, and the wild strain produces substantially equivalent germination induction to that produced by ATCC 31798.
As indicated, Kentucky bluegrass seed rot is significantly reduced for seeds treated with the infectivity-cured Hr plasmid-bearing microorganism in accordance with the invention, as well as with the A. rhizogenes A.sub.4 wild strain. Generally, seed rot is prevented by use of fungicides.
EXAMPLE 11
Following the procedure of Example 4, except that cotton seed is substituted for barley seed and the period of incubation is 4 days, rather than 5 days, the results set forth in Table 11 are obtained.
EXAMPLE 12
Following the procedure of Example 11, except that the period of incubation is 7 days, rather than 4 days, the results set forth in Table 12 are obtained.
TABLE 9______________________________________ Response of Germinating Sorghum (Sorgum vulgare var. saccharatum) - After 6 Days* Length of Root Shoot Number LongestTreatment Length.sup.1 Length.sup.2 of Lateral.sup.3Used (mm) (mm) Laterals.sup.3 (mm)______________________________________Control 74.5.sup.x 30.0 6.9 7.8Wild Strain 93.5.sup.y 43.5 3.0 4.0ATCC 31798 91.5.sup.y 40.4 7.3 8.7ATCC 31799 75.7.sup.x 41.7 6.6 6.3______________________________________ *Numbers followed by the same letter are in common statistically significant groups. .sup.1 Differences were significant at the 1% level. .sup.2 Wild strain was statistically superior at 10% level when compared to the control. .sup.3 ATCC 31798 was statistically superior at 10% level, when compared to the control.
TABLE10______________________________________ Percent of Kentucky Bluegrass (PoaTreatment Used* pratensis) Germinating After 4 Days______________________________________Control 8Wild Strain 16ATCC 31798 15ATCC 31799 24______________________________________ *Seed rot was significantly reduced on all seeds treated with the wild strain and the two mutants of A. rhizogenes A.sub.4.
TABLE 11______________________________________ Response of Germinating Cotton (Gossypium hirsutum) - After 4 Days*Treatment Root LengthUsed (mm)______________________________________Control 31.8.sup.xWild Strain 50.3.sup.yATCC 31798 45.8.sup.yATCC 31799 50.1.sup.y______________________________________ *Differences were significant at the 1% level. Numbers followed by the same letter are in common statistically significant groups.
TABLE 12______________________________________ Response of Germinating Cotton ( Gossypium hirsutum) - After 7 Days*Treatment Root Length Shoot LengthUsed (mm) (mm)______________________________________Control 58.0.sup.x 9.6.sup.xWild Strain 56.4.sup.x 11.2.sup.yATCC 31798 65.0.sup.x 11.3.sup.yATCC 31799 56.1.sup.x 11.8.sup.y______________________________________ *Differences were significant at the 5% level. Numbers followed by the same letter are in common statistically significant groups.
EXAMPLE 13
Following the procedure of Example 4, except that pinto bean seed is substituted for barley seed, and the period of incubation is 7 days, rather than 5 days, the results set forth in Table 13 are obtained.
EXAMPLE 14
Following the procedure of Example 4, except that broccoli seed is substituted for barley seed and the period of incubation is 8 days, rather than 5 days, the results set forth in Table 14 are obtained.
EXAMPLE 15
Soybean seed is treated with cells of the A. rhizogenes A.sub.4 wild strain in accordance with the procedure of Example 1. Each seed is deposited onto the surface of a 3'.times.4".times.2" column of perlite. The seeds are watered every Monday, Wednesday and Friday with 500 ml of half-strength Hoaglands solution (Hoagland and Arnon, University of California, Agricultural Experiment Station Circular No. 347, 1938) minus all sources of nitrogen. After the seeds sprout, a suspension of R. japonicum is placed on the perlite surface next to each sprouting seed. The total number of R. japonicum cells per seed is about 10.sup.8. The plants are kept at 23.degree.-25.degree. C., and natural lighting is utilized under greenhouse conditions. After 5 weeks, the plants are removed, and the results set forth in Table 15 are obtained. Each value represents an average for 10 plints.
In order to provide a control, this procedure is followed except that the soybean seeds are not treated with the A. rhizogenes A.sub.4 wild strain. Each value set forth in Table 15 for the control also represents an average for 10 plants.
TABLE 13______________________________________ Response of Germinating Pinto Bean (Phaseolus vulgaris) - After 7 Days* Length of Root Shoot Number LongestTreatment Length Length of LateralUsed (mm) (mm) Laterals (mm)______________________________________Control 87.9.sup.x 15.0.sup.x 12.3.sup.x 54.9.sup.xWild Strain 91.0.sup.x 30.2.sup.y 17.2.sup.xy 66.3.sup.xATCC 31798 114.1.sup.x 29.4.sup.y 20.7.sup.y 69.4.sup.xATCC 31799 88.2.sup.x 28.1.sup.y 15.7.sup.xy 76.6.sup.x______________________________________ *Differences were significant at the 5% level. Numbers followed by the same letter(s) are in common statistically significant groups.
TABLE 14______________________________________ Response of Germinating Broccoli ( Brassica oleracea) - After 8 Days*Treatment Root Length Shoot LengthUsed (mm) (mm)______________________________________Control 66.3.sup.x 61.4.sup.xWild Strain 75.0.sup.x 77.9.sup.yATCC 31798 76.6.sup.x 72.8.sup.yATCC 31799 79.1.sup.x 73.5.sup.y______________________________________ *Differences were significant at the 5% level. Numbers followed by the same letter are in common statistically significant groups.
TABLE 15__________________________________________________________________________ Response of Germinating Soybean Seed Length of Number Shoot Longest Root Shoot NoduleTreatment of Length.sup.3 Root Mass.sup.2 Mass.sup.1 Mass.sup.2Used Nodules.sup.1 (mm) (mm) (g) (g) (g)__________________________________________________________________________Control (treatment with 12.8 158.5 245.8 0.06 0.17 0.087R. japonicum only)Wild Strain plus 21.3 177.0 248.1 0.08 0.27 0.139R. japonicum__________________________________________________________________________ .sup.1 Differences are significant at the 1% level using the analysis of variance statistical test. .sup.2 Differences are significant at the 5% level using the analysis of variance statistical test. .sup.3 Differences are significant at the 1% level using the student's T test, but are not significant using the analysis of variance statistical test.
In the case of the data set forth above for Newana spring wheat and barley, the significant differences shown in the Tables disappeared when the observations were made after a 7 day incubation period. However, the presence of the significant differences shown in the Tables for these seed types are nevertheless expected to be of importance. When the procedure of Example 4 was followed except that winter wheat seed was substituted for barley seed and the incubation period was seven days, no significant differences were observed.
Applicability
The invention provides enhanced growth promoting effects in sprouting seeds that are advantageous agriculturally, and that are advantageous for land reclamation when the seed is a legume. Furthermore, the invention helps establish lawns and sods by germination induction and increases nitrogen-fixation, root mass, shoot mass and nodule mass in legumes.

Number	Name	Date
674765	Hartleb et al.	May 1901
2313057	Fischer	Jan 1943
2553577	Hale et al.	Jan 1951
2690388	Hale	Jan 1954
3168796	Scott et al.	Feb 1965
3361555	Herschler	Jan 1968
3499748	Fraser	Jan 1970
4061488	Mann	Dec 1977
4077793	Krupicka	Jan 1978
4136486	Franklin, Jr. et al.	Jan 1979
4149869	Lloyd	Apr 1979
4161397	Bellet et al.	Jul 1979

Compositions containing and methods of use of an infectivity-cured Hr plasmid-bearing microorganism

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US Referenced Citations (12)

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Entry
Rawls, "Nitrogen Fixation etc.," (1980) C & E News, pp. 20-30 (1980).
Moore et al., "Involvement of a Plasmid, etc.," (1978) Plasmid 2, pp. 6176 (1979).
Stanek, "Effect of A. Rhizogenes, etc.," (1976) Folia Microbiol., 21, p. 213 (1976).
Chem. & Eng. News, Dec. 8, 1980, p. 29.
Plasmid, Moore et al., 2:617-626 (1979).
Stanek, Folia Microbiologica, 21(3):213 (1976).