Synergistic bioinoculant composition comprising bacterial strains of accession Nos. NRRL B-30486, NRRL B-30487, and NRRL B-30488 and a method of producing said composition thereof

Abstract

The present invention relates to a synergistic composition useful as bioinoculant, said composition comprising bacterial strains of accession Nos. NRRL B-30486, NRRL B-30487, and NRRL-B 30488, individually or in all possible combinations, and optionally carrier, with each of the strains showing plant promotery activity, phytopathogenic fungi controlling activity, abiotic stress conditions tolerating capability, phosphate solubilization capability under abiotic stress conditions; further, a method of producing said composition thereof, and in addition, a method of isolating said bacterial strains from cow ‘Sahiwal’.

Description

FIELD OF THE PRESENT INVENTION

[0001] The present invention relates to a synergistic composition useful as bioinoculant, said composition comprising bacterial strains of accession Nos. NRRL B-30486, NRRL B-30487, and NRRL-B 30488, individually or in all possible combinations, and optionally carrier, with each of the strains showing plant promotery activity, phytopathogenic fungi controlling activity, abiotic stress conditions tolerating capability, phosphate solubilization capability under abiotic stress conditions; further, a method of producing said composition thereof, and in addition, a method of isolating said bacterial strains from cow ‘Sahiwal’.

BACKGROUND AND PRIOR ART OF THE PRESENT INVENTION

[0002] The microbial world is a microcosm whose activities are of central importance to the biosphere. Microbial products contribute to environment, plant, public, and soil health. There is a striking diversity of microorganisms in their ecological and physiological specialization. They have evolved to cope with and flourish in almost every niche, no matter how inhospitable. Microorganisms also form a range of associations with other microbes and with other plants and animals. They can be pathogens, parasites, symbionts, commensales and saprophytes, and thus, their ecological influence infiltrates into all trophic levels of life and gamut of possible ecosystems. Microbes have proved to be an exceptionally rich source of new products, and there is every indication that they will continue to be so in the future. Therefore, exploration of biodiversity for novel microbes that are of ecologically significance or are of economic value is of importance. This has prompted microbiologists to continue to search for novel useful microbes from sources that remain uncharacterized.

[0003] According to Hindu mythology as well as the Indian traditional medical practices (both the classical systems like Ayurveda and Siddha and the oral practices of the rural villagers) cow's milk has rejuvenatory health protecting and health promotery properties and hence has been said as the best one among vitalisers [Caraka-Samhita, Editor-translator P. Sharma, Chaukhambha Orientalia, Varanasi, India, volume 1, p. 213 (1981); P. Pushpangadan, Ethnobiology in India: A status report, Ministry of Environment and Forests, Government of India, New Delhi (1994); P. Pushpangadan, All India Coordinated research project on ethnobiology: Final technical report 1982-1998, Ministry of Environment and Forests, Government of India, New Delhi (1998)].

[0004] Milk may be defined as the normal secretion of the mammary gland of the mammals. Milk as it is secreted by the gland of the mammals is free of microorganisms. However, microorganisms associated with the teat move up the teat canal and into the interior of the udder [J.C. Olsen and G. Mocquot. Milk and milk products. In: International commission on microbiological specifications for foods. Microbial ecology of foods. Food commodities. Vol. 2. New York: Academic Press (1980) pp. 470-486]. This causes even aseptically drawn milk to contain microorganisms, mostly bacteria. Bacteria in aseptically drawn milk are usually limited in number and include mostly micrococci, lactococci, staphylococci, streptococci, and bacillus [F. L. Bryan, Journal of Food Protection, Volume 46, pp. 637-649 (1983); R. A. Ledford. Raw milk and fluid milk products. In: Applied dairy microbiology. Eds. E. H. Marth and J. L. Steele, New York: Marcel Dekker, Inc. (1998) pp. 55-64].

[0005] It has been known for the past more than four decades that many of the bacteria that occur commonly in milk find it a relatively unfavorable medium and it would thus appear that milk has pronounced selective properties [T. Gibson and Y. A. Abd-El-Malek, Canadian Journal of Microbiology, Volume 3, pp. 203-213, (1957)]. Thus the bacterial flora that has invaded in the teat and/or udder must have the persistence ability for survival and multiplication, under these sub optimal conditions. Therefore, work on the milk described in this application pertains to bacterial flora persisting in the teat and/or udder, which have gained entrance into the aseptically drawn milk, in our attempt to search for novel microbes, from an ecological niche that remain uncharacterized.

[0006] Improving soil fertility is one of the most common tactics to increase agricultural and forest production. We have isolated plant beneficial bacteria from cow milk. Inoculation of seeds or soil with beneficial microorganisms for crop improvement has been practiced for a number of years. A variety of mechanisms have been identified as being responsible for such plant growth promoting activity. For example, certain microorganisms indirectly promote plant growth by inhibiting the growth of deleterious microorganisms; or directly enhance plant growth by producing growth hormones; and/or by assisting in the uptake of nutrients by the crops, e.g., phosphorus (P) [C. S. Nautiyal et al., FEMS Microbiology Letters, Volume 182, pp. 291-296 (2000)].

[0007] However, a major factor in the unsuccessful commercialisation of bioinoculants has been the inconsistency of field test results as their establishment and performance are severely effected by environmental factors especially under stress conditions encountered in soil e.g., salt, pH, and temperature [C. S. Nautiyal et al., FEMS Microbiology Letters, Volume 182, pp. 291-296 (2000)]. Therefore, it would be desirable to provide stress tolerant bacterial strains as bioinoculants [C. S. Nautiyal, Biocontrol of plant diseases for agricultural sustainability. In: Biocontrol potential and its exploitation in sustainable agriculture. Volume 1, Eds. R. K. Upahyay, K. G. Mukerji, and B. P. Chamola, Kluwer Academic/Plenum Publishers, New York (2000) pp. 9-23]. Plant growth promoting microorganisms include but are not limited to Rhizobium, Pseudomonas, Azospirillum, and Bacillus etc. [A. K. Saxena et. al., Bacterial biocontrol agents and their role in plant disease management. In: Biocontrol potential and its exploitation in sustainable agriculture. Volume 1, Eds. R. K. Upadhyay, K. G. Mukerji, and B. P. Chamola, Kluwer Academic/Plenum Publishers, New York (2000) pp. 25-37].

[0008] Usefulness of B. subtilis as a source of antagonist for plant pathogenic fungus Sclerotium rolfsii is well known [P. Broadbent et al., Australian Journal of Biological Sciences, Volume 24, pp. 975 (1971)]. Baker et al. [Phytopathology, Volume 73, 1148-1152 (1983)] also report on use of B. subtilis as biocontrol agent of fungal plant pathogens. Pusey et al. [Plant Disease, Volume 72, pp. 622-626 (1988)] and P. L. Pusey [U.S. Pat. No. 5,047,239] disclosed control of post harvest fruit rot using B. subtilis. S. D. Heins et al. [U.S. Pat. No. 6,103,228] have disclosed methods of protecting or treating plants from fungal and bacterial infections and corn rootworm infestations using B. subtilis.

[0009] B. lentimorbus is causative agent of milky disease in Japanese beetle and related scarab larvae [K. E. Rippere et al. International Journal of Systematic Bacteriology, Volume 48, pp. 395-402 (1998)], and therefore used for the biocontrol of larvae of certain insects [R. E. Gordon et al., The genus Bacillus, Agriculture handbook no. 427, United States Department of Agriculture, U.S. Government printing office, Washington D.C. (1973)]. B. lentimorbus has also been used to increase the production of fish [W. T. Logan et al., U.S. Pat. No. 5,746,155] and to treat poultry litter [W. T. Logan et al., U.S. Pat. No. 6,017,525].

[0010] For propagating bacteria commonly used carrier for commercial inoculants are vermiculite, charcoal, caboxymethyl cellulose, peat, perlite, polyvinyl-pyrrolidone, and talc. Press mud, a “waste” product obtained during sugar manufacture has also been used as a carrier for Azotobacter chroooccum and Rhizobium japonicum [K. S. Jauhri, Indian Journal Agriculture Research, Volume 24, pp. 189-197 (1990)]. Press mud like any other organic manure affects the physical, chemical and biological properties of the soils. It also helps to increase water stable aggregates in soils. It can be composted with distillery spent wash and utilized as a better organic manure than press mud alone [D. P. Yadav. Recycling of sugar factory press mud in agriculture. In: Recycling of crop, animal, human, and industrial wastes in agriculture. Ed. H. L. S. Tandon, Fertilizer development and consultation organization, New Delhi (1995) pp. 91-108]. Agricultural and environmental industry would therefore clearly benefit from a simple, less expensive method of microbial inoculants for plants, seeds and soil.

[0011] While work on microbiology of the milk so far has been on psychrotrophic bacteria because of their importance in milk and dairy products [M. A. Cousin. Journal of food protection. Volume 45, pp. 172-207 (1982); R. A. Ledford. Raw milk and fluid milk products. In: Applied dairy microbiology. Eds. E. H. Martha and J. L. Steele, New York: Marcel Dekker, Inc. (1998) pp. 55-64], no bacterial strain has been previously found from the milk of cow which has the ability to control phytopathogenic fungi, promote plant growth, tolerance for abiotic stresses, and solubilize phosphate under abiotic stress conditions.

[0012] India is one of the few countries in world, which has contributed richly to the International livestock gene pool and improvement of animal population in world. Cattle and buffalo contribute nearly 15% of the gross national income. The country possesses 23% of world bovine population. Cattle, common term for the domesticated herbivorous mammals that contribute to genus Bos, of the family Bovidae. Modern cattle are divided into two species: B. taurus, which originated in Europe and includes most modem breeds of dairy and beef cattle, and B. indicus, which originated in India and is characterized by a hump and the withers. The latter are now widespread in Africa and Asia, with lesser numbers imported to North America (primarily in southern U.S.), Central America, and Northern and Central America.

[0013] Dairy cattle are those breeds that have been developed primarily to produce milk. In North America the major breeds of dairy cattle are the Holstein-Friesian, Ayrashire, Brown Swiss, and Jersey. Among the major dairy breeds of B. indicus found primarily in India are the Gir, Hariana, Red Sindhi, Tharparker, and Sahiwal. By far Sahiwal is the best breed of the subcontinent. It is comparatively a heavy breed with symmetrical body and loose skin, when compared with Red Sindhi with which it is closely resembles. The animals are usually long and fleshy and with heavier built. The colour is redish dunn or pale red, sometimes fleshed with white patches. A number of herds of this breed are maintained in India. The milk yield ranges from 1400 to 2500 kg. The heritability of this trait is 0.2 to 0.3. The age at first calving ranges from 37 to 48 months and the calving interval is from 430 to 580 days. Sahiwal is one of the most popular breeds of the subcontinent. It has been exported to Srilanka, Kenya and many countries in Latin America and West Indies where a new breed called Jamaica Hope has been evolved out of Sahiwal and Jersey crossbreeds [P. N. Bhat, Handbook of Animal Husbandry, Directorate of Publication and Information on Agriculture, Krishi Anusandhan Bhawan, Pusa, New Delhi (1997)].

[0014] Accordingly, there has been no clear indication heretofore that any bacteria isolated from cow might act as a biocontrol agent, and certainly no showing of direct, bacterial-mediated stimulation of plant growth per se. Nevertheless, a bacterial strain capable of promoting plant growth, tolerance for abiotic stresses, and solubilize phosphate under abiotic stress conditions, if one were isolated, could find immediate application, e.g., in soils affected by phytopathogens, poor nutrient availability like phosphorus, and environment stresses etc., did not result in a desired improvement in crop development, additionally, no procedure for the selection of such bacterial strain has been reported. We have found by direct comparison on a variety of plant types that the unique combination of selected bacterial strains is effective in the enhancement of plant growth and health.

[0015] The present invention relates to novel strains of bacteria isolated from cow which have the ability to control phytopathogenic fungi, promote plant growth, tolerance for abiotic stresses, solubilize phosphate under abiotic stress conditions, and a method for the selection of these strains.

OBJECTS OF THE PRESENT INVENTION

[0016] The main object of the present invention is to isolate bacterial strains from cow, useful as bioinoculant.

[0017] Another main object of the present invention is to isolate bacterial strains from cow Sahiwal, having plant promotery activity.

[0018] Yet another object of the present invention is to isolate bacterial strains from cow Sahiwal, having plant-promoting activity of at least 5% of the dry weight.

[0019] Still another object of the present invention is to isolate bacterial stains from cow Sahiwal showing plant promotery activity in terms of less seeding mortality, better seedling germination, plant height, number of pods and seed dry weight.

[0020] Still another object of the present invention is to isolate bacterial strains from cow Sahiwal with phytopathogenic fungi controlling activity.

[0021] Still another object of the present invention is to isolate bacterial strains from cow Sahiwal with phosphate solubilization property.

[0022] Still another object of the present invention is to isolate bacterial strains from cow Sahiwal having abiotic stress condition tolerating activity.

[0023] Still another object of the present invention is to isolate bacterial strain from cow Sahiwal having 4-8% salt tolerance ability.

[0024] Still another object of the present invention is to isolate bacterial strains from cow Sahiwal having pH 4-10-tolerance ability.

[0025] Still another object of the present invention is to isolate bacterial strains from cow Sahiwal having temperature 50-60° C. tolerance ability.

[0026] Still another object of the present invention is to develop a synergistic formulation comprising three strains isolated from cow Sahiwal with said composition having properties, comprising controlling phytopathogenic fungi, promoting plant growth, having tolerance for abiotic stresses, solubilizing phosphate under abiotic stress conditions, producing anti-fungal metabolites.

[0027] Still another object of the present invention is to develop a formulation comprising three strains isolated from cow Sahiwal, useful as a bioinoculant, showing maximum viability under varied storage or greenhouse or field conditions.

[0028] Still another object of the present invention is to develop a formulation comprising the three isolated strains from cow Sahiwal with accession Nos. NRRL B-30486, NRRL B-30487, and NRRL-B 30488, wherein said formulation can be in liquid or dry form to seeds, plants, and soil.

SUMMARY OF THE PRESENT INVENTION

[0029] The present invention relates to a synergistic composition useful as bioinoculant, said composition comprising bacterial strains of accession Nos. NRRL B-30486, NRRL B-30487, and NRRL-B 30488, individually or in all possible combinations, and optionally carrier, with each of the strains showing plant promotery activity, phytopathogenic fungi controlling activity, abiotic stress conditions tolerating capability, phosphate solubilization capability under abiotic stress conditions; further, a method of producing said composition thereof, and in addition, a method of isolating said bacterial strains from cow ‘Sahiwal’.

DETAILED DESCRIPTION OF THE PRESENT INVENTION

[0030] Accordingly, the present invention relates to a synergistic composition useful as biomoculant, said composition comprising bacterial strains of accession Nos. NRRL B-30486, NRRL B-30487, and NRRL-B 30488, individually or in all possible combinations, and optionally carrier, with each of the strains showing plant promotery activity, phytopathogenic fungi controlling activity, abiotic stress conditions tolerating capability, phosphate solubilization capability under abiotic stress conditions; further, a method of producing said composition thereof, and in addition, a method of isolating said bacterial strains from cow ‘Sahiwal’.

[0031] In an embodiment of the present invention, a synergistic composition useful as bioinoculant, said composition comprising bacterial strains of accession Nos. NRRL B-30486, NRRL B-30487, and NRRL-B 30488, individually or in all possible combinations, and optionally carrier.

[0032] In another embodiment of the present invention, wherein the strains NRRL B-30486, and NRRL B-30488 belongs to the group Bacillus lentimorbus.

[0033] In yet another embodiment of the present invention, wherein the strain NRRL B-30487 belongs to the group Bacillus subtilis.

[0034] In still another embodiment of the present invention, wherein the strain NRRL B-30486 shows characteristics as shown below:

Characteristics    NRRL B-30486
Shape              Rods
Size
Width, μm          1.5-2.0
Length, μm         3.0-6.0
Gram reaction      +
Catalase reaction  −
Anaerobic growth   +
Voges-Proskauer    −
Reaction
pH in V-P broth    5.5
Acid from
D-glucose          +
L-arabinose        −
D-xylose           −
D-mannitol         −
Gas from glucose   +
Hydrolysis of
Casein             −
Gelatin            −
Starch             −
Use of citrate     −
Nitrate to nitrite −
Indole formation   −
Growth at pH
in nutrient broth
6.8                +
5.7                +
Growth in Nacl
2%                 +
5%                 +
7%                 +
10%                +
Growth at
30° C.             +
40° C.             +
50° C.             +
55° C.             +
65° C.             −

[0035] In still another embodiment of the present invention, wherein the strain NRRL B-30487 shows characteristics as shown below:

Characteristics    NRRL B-30487
Shape              Oval
Size
Width, μm          2.5
Gram reaction      +
Catalase reaction  +
Anaerobic growth   −
Voges-Proskauer    +
Reaction
pH in V-P broth    5.8
Acid from
D-glucose          +
L-arabinose        +
D-xylose           +
D-mannitol         +
Gas from glucose   −
Hydrolysis of
Casein             +
Gelatin            +
Starch             +
Use of citrate     +
Nitrate to nitrite +
Indole formation   −
Growth at pH
in nutrient broth
6.8                +
5.7                +
Growth in Nacl
2%                 +
5%                 +
7%                 −
10%                −
Growth at
30° C.             +
40° C.             +
50° C.             +
55° C.             +
65° C.             −

[0036] In still another embodiment of the present invention, wherein the strain NRRL B-30488 shows characteristics as shown below:

Characteristics    NRRL B-30488
Shape              Rods
Size
Width, μm          1.5-2.0
Length, μm         5.0-10.0
Gram reaction      +
Catalase reaction  −
Anaerobic growth   +
Voges-Proskauer    −
Reaction
pH in V-P broth    5.2
Acid from
D-glucose          +
L-arabinose        −
D-xylose           −
D-mannitol         −
Gas from glucose   +
Hydrolysis of
Casein             −
Gelatin            −
Starch             −
Use of citrate     −
Nitrate to nitrite −
Indole formation   −
Growth at pH
in nutrient broth
6.8                +
5.7                +
Growth in Nacl
2%                 +
5%                 +
7%                 +
10%                +
Growth at
30° C.             +
40° C.             +
50° C.             +
55° C.             +
65° C.             −

[0037] In still another embodiment of the present invention, wherein carrier is selected from a group comprising vermiculite, charcoal, a mixture of fermented sugar factory sulphitation press mud and distillery spent wash, and sugar factory carbonation press mud.

[0038] In still another embodiment of the present invention, wherein ratio of three strains is about 1:1:1.

[0039] In still another embodiment of the present invention, wherein total concentration of strains is 4-10 cfu/g of carrier and preferably 6-8 cfu/g of carrier.

[0040] In still another embodiment of the present invention, wherein concentration of each strain is 4-10 cfu/g of carrier and preferably 7-8 cfu/g of carrier.

[0041] In still another embodiment of the present invention, wherein generation time of the strains is 55-65 minutes at 30° C.

[0042] In still another embodiment of the present invention, wherein said strains colonize plant roots.

[0043] In still another embodiment of the present invention, wherein said strains survive all the seasons of the plant.

[0044] In still another embodiment of the present invention, wherein said strains survive for at least 2/3 years in the composition.

[0045] In another embodiment of the present invention, an in vitro method of isolating bacterial strains of accession nos. NRRL B-30486, NRRL B-30487, and NRRL-B 30488, from the milk of cow ‘Sahiwal’, said strains having properties, comprising controlling phytopathogenic fungi, promoting plant growth, having tolerance for abiotic stresses, solubilizing phosphate under abiotic stress conditions, producing anti-fungal metabolites collecting milk for cow ‘Sahiwal’,

[0046] In yet another embodiment of the present invention, plating milk on a culture medium.

[0047] In yet another embodiment of the present invention, incubating the culture at temp of 25-35° C., for about 1-3 days.

[0048] In still another embodiment of the present invention, selecting all morphologically distinct bacteria from culture.

[0049] In still another embodiment of the present invention, screening said strains selected in previous step which will suppress phytopathogenic fungi by showing a zone of inhibition of at least 2 mm, by incubating at 30-35° C. preferably 28° C., for 20-35 days, preferably 27 days.

[0050] In still another embodiment of the present invention, screening said strains selected in previous step for plant growth promotery bacteria showing at least 5% increase in dry weight of plant, by growing plants in the presence of selected bacteria in a concentration of bacteria ranging between about Log 6 to 10 CFU/seed or about Log 6 to 8 CFU/gram of soil.

[0051] In still another embodiment of the present invention, screening said strains selected in previous step at 4-8% salt stress tolerance for further selection.

[0052] In still another embodiment of the present invention, screening said strains selected in previous step at pH 4-10 stress tolerance for further selection.

[0053] In still another embodiment of the present invention, screening said strains selected in previous step at 50-60° C. temperature stress tolerance for further selection.

[0054] In still another embodiment of the present invention, screening said strains selected in previous step for ability to solubilize phosphate under abiotic stress conditions of high salt, pH, and temperature for further selection.

[0055] In still another embodiment of the present invention, isolating the desired three bacterial strains.

[0056] In still another embodiment of the present invention, wherein plant for growth promotery activity is selected from a group comprising Zea mays, Abelmoschus esculentus, Luffa cylindrica., Lycopersicon esculentum, Abelmoschus esculentus, and Cucumis sativus.

[0057] In still another embodiment of the present invention, wherein culture medium is Nutrient Agar, said medium comprising beef extract (2-10 gms), peptone (5-15 gms), sodium chloride (2-10 gms), agar (10-20 gms), distilled water (about 1.0 L), with pH ranging between 7.0-7.4.

[0058] In still another embodiment of the present invention, wherein pH tolerance is tested at 30° C.

[0059] In still another embodiment of the present invention, wherein soil moisture is ranging between 15-30%, preferably 20%.

[0060] In still another embodiment of the present invention, wherein salt is preferably NaCl.

[0061] In still another embodiment of the present invention, wherein the strains are grown on Nutrient Broth (NB) medium consisting of Beef extract (0.5%), peptone (1%), NaCl (0.5%), and distilled water, with pH of the medium is 7.2.

[0062] In still another embodiment of the present invention, wherein pathogenic fungus are selected from a group comprising F. moniliforme, C. falcatum, F. oxysporum f. sp. ciceri, R. solani, Pythium sp., Phoma sorghii, Sclerotium rolfsii, altemaria solani, curvularia lunata, sclerotinia sclerotiorum, and aspergillus niger.

[0063] In still another embodiment of the present invention, wherein concentration of the strains is ranging between 4-10 CFU/ml.

[0064] In still another embodiment of the present invention, wherein phosphate solubilization increases by about 428% upon a combined increase of temperature, salt, and pH.

[0065] In still another embodiment of the present invention, wherein phosphate solubilization increases by about 160% with increase in salt concentration.

[0066] In still another embodiment of the present invention, wherein phosphate solubilization increases by about 130% with increase in pH.

[0067] In still another embodiment of the present invention, wherein strains are selected for high pH stress tolerance at preferably pH 9.

[0068] In still another embodiment of the present invention, wherein strains are selected for 55° C. temperature stress tolerance.

[0069] In still another embodiment of the present invention, wherein selecting bacteria demonstrating best results in terms of less seedling mortality, and better seedling germination, plant height, number of pods and seed dry weight.

[0070] In still another embodiment of the present invention, wherein plant promotery activity goes up by 3-400%.

[0071] In still another embodiment of the present invention, wherein concentration of fungi is ranging between 4-7 spores/ml of culture medium.

[0072] In still another embodiment of the present invention, wherein abiotic stress conditions for solubilization of phosphate are selected from a group of conditions comprising high pH ranging between 7-9, high temp ranging between 30-45, and salt concentration ranging between 0.1-4%.

[0073] In another embodiment of the present invention, a method of preparing plant growth promotery formulation comprising bacterial strains of accession Nos. NRRL B-30486, NRRL B-30487, and NRRL-B 30488, individually or in all possible combinations, and carrier.

[0074] In yet another embodiment of the present invention, growing bacteria in a culture, individually to a concentration of about Log 8 to 11 cfu/ml, preferably log 9 to 10 cfu/ml, optionally followed by mixing the cultures in equal ratio in case of preparing a consortium.

[0075] In still another embodiment of the present invention, diluting the said culture with water in the ratio of 1:50 to 1:150, preferably 1:100, containing approximately Log 8-9 cfu/ml of bacteria.

[0076] In still another embodiment of the present invention, spraying about 1-3 liter of the culture/ton of freshly homogenized carrier preferably 2 liter of the culture/ton of freshly homogenized carrier and mixing.

[0077] In still another embodiment of the present invention, churning the windrows daily at least twice a day for about 2 days, to increase the temperature of the windrows up to 70-75° C.

[0078] In still another embodiment of the present invention, spraying spent wash or water into the churning windrow for about 40 days to maintain moisture level of about 55-65%.

[0079] In still another embodiment of the present invention, churning the windrows further for another 3-5 days, now to reduce the moisture and temperature of the fermented product to about 30% and 40-45° C.

[0080] In still another embodiment of the present invention, packaging plant growth promoting bioinoculant ready for its application.

[0081] In still another embodiment of the present invention, wherein carrier is selected from a group comprising fresh sulphinated press mud and carbonation press mud.

[0082] In still another embodiment of the present invention, wherein culture medium is NB medium.

[0083] In still another embodiment of the present invention, wherein homogenizing the mixture manually and by using an aero tiller.

[0084] In still another embodiment of the present invention, wherein said formulation demonstrating maximum viability, under varied storage or greenhouse or field condition.

[0085] In still another embodiment of the present invention, wherein ratio of the said strains is about 1:1:1.

[0086] In still another embodiment of the present invention, wherein using said formulation on plants, seeds, and soil.

[0087] In still another embodiment of the present invention, a method of using plant growth promotery formulation comprising bacterial strains of accession Nos. NRRL B-30486, NRRL B-30487, and NRRL-B 30488, individually or in all possible combinations, and carrier, said method comprising steps of applying the said bioinoculant in a liquid or dry form to seeds, plants, and soil.

[0088] In still another embodiment of the present invention, wherein the said bioinoculant also containing the gums or sugars to improve adhesion.

[0089] In still another embodiment of the present invention, wherein the strains are in the ratio of 1:1:1.

[0090] In still another embodiment of the present invention, wherein the said formulation demonstrates maximum viability, under varied storage or greenhouse or field condition.

[0091] In still another embodiment of the present invention, wherein the carrier is selected from a group comprising fresh sulphinated press mud and carbonation press mud.

[0092] In still another embodiment of the present invention, wherein the plants of the variety to be tested for plant growth promotion in the field in the presence of bacteria in a concentration of about Log 7-9 cfu/seed or about Log 6-8 cfu/gram of soil.

[0093] In still another embodiment of the present invention, wherein using formulation alone or in combination with other chemicals which is harmless to the growth and survival of bacteria.

[0094] In still another embodiment of the present invention, wherein the chemicals are selected from a group comprising pesticides, fertilizers, nematicides, and herbicides, with or without for example lime pelleting to limit the severity of the effect of these materials.

[0095] In still another embodiment of the present invention, the method of making a composition useful as biomoculant, said composition comprising one or more of novel bacterial strains of accession Nos. NRRL B-30486, NRRL B-30487, and NRRL-B 30488 and a carrier.

[0096] In still another embodiment of the present invention, culturing said bacterial strains in a growth medium to log phase.

[0097] In still another embodiment of the present invention, diluting the said culture with water in the ratio ranging between 1:10 to 1:100000, with preferable ratio of 1:100.

[0098] In still another embodiment of the present invention, mixing the said diluted culture with an inert powdered carrier, with the moisture level of the mixture ranging between 20-40%, preferably about 30% on a wet basis.

[0099] In still another embodiment of the present invention, incubating the said mixture for at least about two days, maintaining constant moisture level in said mixture.

[0100] In still another embodiment of the present invention, increasing the bacteria count in the said mixture to a range of about log 4-10 CFU/g of carrier.

[0101] In still another embodiment of the present invention, monitoring the survival rate of the bacteria over the period of at least one year in the said composition, wherein the bacterial strains are present preferably in a range from about Log 7 to 9 CFU/g of carrier, showing long survival rate of microbes as inoculate.

[0102] In still another embodiment of the present invention, wherein carrier is selected from a group comprising vermiculite, charcoal, a mixture of fermented sugar factory sulphitation press mud and distillery spent wash, and sugar factory carbonation press mud, rice husk, carboxymethyl cellulose, peat, perlite, talc, and polyvinyl pyrrolidone.

[0103] In still another embodiment of the present invention, wherein preferred carriers are selected from a group comprising vermiculite, charcoal, and fermented press mud.

[0104] In still another embodiment of the present invention, wherein bacterial count is most preferably about Log 8 CFU/g of carrier.

[0105] In still another embodiment of the present invention, wherein plants for growth promotion are selected from a group comprising chickpea, A. esculentus, and C. sativus, and Z. mays, and Triticum aestivum, and Glycine max, and Pisum sativum, and Impatiens balsamina.

[0106] In still another embodiment of the present invention, wherein ratio of strains is about 1:1:1, in case of a consortium.

[0107] In still another embodiment of the present invention, wherein growth medium is NB medium.

[0108] In still another embodiment of the present invention, wherein growing bacteria individually to a concentration of about Log 9 to 10 CFU/ml followed by mixing the cultures in the ratio of about 1:1:1.

[0109] In still another embodiment of the present invention, wherein diluting the culture with water preferably in the ratio of 1:10, containing approximately Log 8-9 cfu/ml.

[0110] In still another embodiment of the present invention, wherein moisture of the product is regulated with windrows.

[0111] In still another embodiment of the present invention, Applicants have discovered a novel method for screening bacteria to select those bacterial strains that have the ability to control phytopathogenic fungi, promote plant growth, tolerance for abiotic stresses, and solubilize phosphate under abiotic stress conditions. When used as bioinoculants, the novel bacteria obtained by our method have the ability to control phytopathogenic fungi and promote plant growth under field conditions.

[0112] Applicants have also discovered three novel strains' of Bacillis, when used individually or as a novel blend of consortium which provides a unique synergism, which have the ability to control phytopathogenic fungi under field conditions, promote plant growth under field conditions, tolerance for abiotic stresses, and solubilize phosphate under abiotic stress conditions.

[0113] Screening method comprises:

[0114] 1. Isolating strains of bacteria from milk and selecting the bacteria having potential for suppressing growth of phytopathogenic fungi Colletotrichum falcatum, Sclerotium rolfsii, Alternaria solani, Penicillium sp., Pythium aphamidermatum, Phytophthora palmivora, Curvularia lunata, Sclerotinia sclerotiorum, and Aspergillus niger, under in vitro conditions on nutrient agar plates (NA) by streaking one to four single bacterial colonies around the edge of a 90-mm diameter petri plate and incubating it at 28° C. for two day; transferring an agar plug inoculum of the fungi (5-mm square) to the centre of the plate individually from a source plate of fungi to be tested on NA for 2 to 7 days; and selecting the bacterial strains having the biocontrol activity which inhibited fungal growth.

[0115] 2. Screening of bacteria selected in step 1 in the greenhouse having potential for suppressing growth of pathogenic fungi under in vitro conditions, for plant growth promotery bacteria as follows: growing maize plants in the presence of bacteria selected in step 1 in the greenhouse in a concentration of about Log 8 colony forming units (cfu)/seed in non-sterile soil; growing control maize plants as above but without addition of the bacteria; and selecting as plant growth promotery bacteria those strains which cause the treated plants to exhibit greater dry weight.

[0116] 3. Screening of bacteria selected in step 2 as plant growth promoters for abiotic stress (salt, pH, and temperature) tolerance under in vitro conditions as follows: selecting as stress tolerant bacteria those strains selected in step 2 which exhibit tolerance to 6% salt (NaCl), 5-9 pH, and 55° C. temperature.

[0117] 4. Characterization of bacteria selected in step 3 tolerant for abiotic stress for ability to solubilize phosphate under abiotic stress (salt, pH, and temperature) conditions as follows: quantitative estimation of phosphate solubilization in broth using National Botanical Research Institute's phosphate growth medium (NBRIP); elucidating effect of salt (NaCl), pH, and temperature on solubilization of phosphate by growing the strains on NBRIP containing various amounts of NaCl (w/v), pH, and temperature as indicated; inoculating NBRIP medium with the bacterial strain with approximately Log 9 cfu/ml; autoclaved uninoculated medium served as controls.

[0118] 5. Screening of bacteria selected in step 3 tolerant for survival in carriers, for its commercial use as bioinoculant, as follows: culturing the bacteria in a growth media; adding log-phase cells to various carriers, particularly such as vermiculite, charcoal, and fermented press mud; thereafter applying the inoculum to seeds (e.g., by preparing a slurry containing the carrier/bacteria mixture and gums or sugars to improve adhesion) or by directly applying to soil or, by dripping carrier/bacteria suspensions into planting furrows or by mixing with other planting material; using the formulation demonstrating maximum viability (under varied storage or greenhouse or field condition) for plants, seeds, and soil.

[0119] 6. Field trial of bacteria selected in step 3 tolerant for abiotic stress for ability to control plant pathogens, particularly fungi, such as Fusarium oxysporum f. sp. ciceri i.e., reduce incidence or severity of the disease on field grown chickpea and for ability to control plant pathogens, particularly fungi, such as Fusarium moniliforme and Colletotrichum falcatum on field grown sugarcane, using various carriers such as vermiculite.

[0120] 7. Field trial of bacteria selected in step 3 tolerant for abiotic stress for ability to promote plant growth of field grown plants such as sugarcane, using various carriers such as vermiculite and fermented press mud.

[0121] The bacterial strains selected by the above process have the ability to control phytopathogenic fungi, promote plant growth, tolerance for abiotic stresses, and solubilise phosphate under abiotic stress conditions.

[0122] In accordance with this discovery, It is an object of the invention to provide a method for selecting those strains which have the ability to control phytopathogenic fungi, promote plant growth, tolerance for abiotic stresses, and solubilise phosphate under abiotic stress conditions, using the so-selected bacterial strains.

[0123] It is also an object of the invention to provide a means for screening bacteria to select those strains that have the ability to control phytopathogenic fungi and promote plant growth under field conditions.

[0124] A further object of the invention is the provision of novel strains of B. lentimorbus and B. subtilis that have the ability to control phytopathogenic fungi, promote plant growth, tolerance for abiotic stresses, and solubilize phosphate under abiotic stress conditions.

[0125] Another object of the invention is the provision of suitable carriers for bacterial strains, in particular, novel strains of B. lentimorbus and B. subtilis selected in step 3 for survival in various carriers, for commercial production as bioinoculant for plants, seeds, and soil.

[0126] Yet another object of the invention is the provision of novel strains of B. lentimorbus and B. subtilis that have the ability to control phytopathogenic fungi under field conditions.

[0127] Still another object of the invention is the provision of novel strains of B. lentimorbus and B. subtilis that have the ability to promote plant growth under field conditions.

[0128] Other objectives and advantages of the invention will become apparent from the ensuing description. It should be understood, however, that the detailed description and the specific examples, while indicating preferred embodiments of the invention, are given by way of illustration only, since various changes and modifications within the spirit and scope of the invention will become apparent to those skilled in the art from this detailed description.

[0129] In this description, the term “bacteria from milk” is used to denote bacteria, which have gained entrance into the aseptically drawn milk, by invading the teat and/or udder and have the persistence ability for survival and multiplication, under these suboptimal conditions. Therefore, the bacteria described in this application pertain to bacterial flora persisting in the teat and/or udder represent an ecological niche that remains uncharacterized.

[0130] It has been discovered that percent of bacterial strains showing biocontrol activity against phytopathogenic fungi was maximum in the milk of Sahiwal cow, followed by human, Holestien cow and buffalo. From this parameter milk of Sahiwal cow was superior to human, Holestien cow and buffalo. Extensive selections from a large number of bacterial strains collected from the milk of human, Sahiwal cow, Holestien cow and buffalo have shown that some of these strains, as described below, have the ability to stimulate plant growth.

[0131] Therefore one aspect of the present invention relates to method for screening useful bacteria from the milk of human, Sahiwal cow, Holestien cow and buffalo and application thereof for promoting plant growth.

[0132] First the bacteria are isolated by standard procedures such as described in Eklund and Lankford, Laboratory manual for general microbiology [Prentice-Hall, Inc., USA (1967), pp. 21-27]. For example, serial dilutions of the milk samples are prepared and may be spread-plated on various general media. Examples of general media, which propagate a broad number of bacteria, include NA and the like. Next the NA plates are incubated for 1 to 3 days at a temperature suitable for bacterial growth, generally about 25 to 35° C. The preferred temperature for incubation of plates is 30° C.

[0133] Next, individual strains of the bacteria are subjected to a first screening for selecting bacteria having potential for suppressing phytopathogenic fungi under in vitro conditions as described earlier [C. S. Nautiyal, Current Microbiology, Volume 35, pp. 52-58 (1997)]. Bacterial colonies on NA plates were streaked around the edge of a 90-mm diameter petri plate and the plates were incubated at 25-35° C. for 1 to 2 days. An agar plug inoculum of the fungi to be tested (5-mm square) was then transferred to the center of the plate individually from a source plate of the fungi. After incubation for 5 to 7 days inhibition zones were readily observed in the case of bacterial strains having the biocontrol activity.

[0134] Choice of time for incubation of the bacterial colonies on the plates before challenging with the pathogenic fungi to be tested and the time of incubation of the plates later on to observe the inhibition zone depends upon the rate of growth of the pathogenic fungi to be tested. For example if the fungi is fast grower e.g., Rhizoctonia then it is preferred that bacterial colonies on NA plates is streaked around the edge of a 90-mm diameter petri plate at least for 2 days in advance before an agar plug inoculum of the fungi to be tested is transferred to the center of the plate. On the contrary, if the fungi is slow grower e.g., Fusarium, then it is preferred that an agar plug inoculum of the fungi to be tested is transferred to the center of the plate and the plates are incubated for 2 to 3 days to allow sufficient time for the fungi to grow, before the bacterial colonies on NA plates is streaked around the edge of the petri plate.

[0135] Bacterial strains isolated in the previous step are screened to select those, which at a particular concentration promote plant growth under greenhouse conditions as described earlier [C. S. Nautiyal, Current Microbiology, Volume 34, pp. 12-17 (1997)]. In this test sterilized seeds of maize are grown in non-sterilized soil and inoculated with the bacterial strains, individually, at a concentration of Log 6-10 cfu/seed. The preferred concentration of inoculum is Log 8 cfu/seed. Trays (35×35 cm.) with 16 (4×4) places per tray (each space was of 7 cm. width, 10 cm. depth and 1 cm. apart from each other) have been found to be of a convenient size to grow maize and other plants for the greenhouse test. Each place was filled up to 8 cm. with non-sterilized soil. Although sterile soil or any other plant growth supporting material for example like vermiculite may also be used instead of non-sterile soil, it is preferred that non-sterile soil from the field where these bacteria are intended to be released is used in greenhouse test.

[0136] Tap water was added to each hole before planting seeds to adjust the soil to 15 to 30% moisture. Preferred soil moisture is 20%. Four bacterial-treated seeds were added per hole. The experiment in greenhouse was carried out in four different sets of 16 maize seedlings each, for non-bacterised (control) and bacterised (treated) seeds. In each set, data of 21-days-old seedlings was recorded with respect to an average dry weight of 16 plants. In order for the bacterial strain to be considered as plant growth promoter, the seedlings treated with the bacteria must have averaged at least 10% higher dry weight than comparable non-bacterised plants.

[0137] The bacterial strains thus selected were further subjected to abiotic stress tolerance by first screened for their ability to grow in nutrient broth (NB) containing 6% salt (NaCl; pH 7 and 30° C. temperature), overnight (14-16 hrs) on a New Brunswick Scientific, USA, Innova Model 4230 refrigerated incubator shaker at 180 rpm. The strains tolerant to 6% salt were grown at 9 pH (6% NaCl and 30° C. temperature), and finally the strains tolerant to 6% salt and pH 9 were grown at 55° C. temperature. Viable cells were counted by removing samples at various times in the presence or absence of stress, as indicated. Serial dilutions of each sample were spotted (25 μl) onto NA plates, and incubated at 30° C. in triplicate as described earlier [C. S. Nautiyal et al., FEMS Microbiology Letters, Volume 182, pp. 291-296 (2000)]. Viable cells were counted after 2-3 days.

[0138] The 3 bacterial strains tolerant to abiotic stresses (salt, pH, and temperature) selected as above were further screened for their ability to solubilize phosphate under abiotic stress conditions. Quantitative estimation of phosphate solubilization in broth was carried out using National Botanical Research Institute's phosphate growth medium (NBRIP) as described earlier [C. S. Nautiyal, FEMS Microbiology Letters, Volume 170, pp. 265-270 (1999)].

[0139] The effect of salt (NaCl), pH, and temperature on solubilisation of phosphate was tested by growing them on NBRIP in the presence of NaCl, pH, and temperature, as mated using the Fiske and Subbarow method [C. H. Fiske and Y. Subbarow, Journal of Biological Chemistry, Volume 66, pp. 375-400 (1925)].

[0140] The subject strains Bacillus lentimorbus NBRI0725, Bacillus subtilis NBRI1205, and Bacillus lentimorbus NBRI3009 have the taxonomic characteristics listed in Table 1, as compared to those of prior art strains of B. lentimorbus and B. subtilis.

[0141] Comparison of biochemical and physical characteristics of B. lentimorbus NBRI0725 (invention), B. lentimorbus NBRI3009 (invention), B. lentimorbus (descriptive), B. sublilis NBRI1205 (invention), and B. subtilis (descriptive).

	Bacillus lentimorbus	Bacillus subtilis
	NBRI	NBRI		NBRI
	0725	3009		1205
Characteristics	Invention	Invention	Descriptive*	Invention	Descriptive
Shape	Rods	Rods	Rods	Oval	Rods
Size
Width, μm	1.5-2.0	1.5-2.0	0.5-0.7	2.5	0.7-0.8
Length, μm	3.0-6.0	5.0-10.0	1.8-7.0	2.0-3.0
Gram reaction	+	+	+	+	+
Catalase reaction	−	−	−	+	+
Anaerobic growth	+	+	+	−	−
Voges-Proskauer
Reaction	−	−	−	+	+
pH in V-P broth	5.5	5.2	5.9-6.9	5.8	5.0-8.0
Acid from
D-glucose	+	+	+	+	+
L-arabinose	−	−	−	+	+
D-xylose	−	−	−	+	+
D-mannitol	−	−	−	+	+
Gas from glucose	+	+	+	−	−
Hydrolysis of
Casein	−	−	−	+	+
Gelatin	−	−	−	+	+
Starch	−	−	−	+	+
Use of citrate	−	−	−	+	+
Nitrate to nitrite	−	−	−	+	+
Indole formation	−	−	−	−	−
Growth at pH
in nutrient broth
6.8	+	+	−	+	+
5.7	+	+	−	+	+
Growth in Nacl
2%	+	+	−	+	+
5%	+	+	−	+	+
7%	+	+	−	−	+
10%	+	+	−	−	ND
Growth at
30° C.	+	+	+	+	+
40° C.	+	+	−	+	+
50° C.	+	+	−	+	+
55° C.	+	+	−	+	+
65° C.	−	−	−	−	−
*= As described in: R. E. Gordon et al., The genus Bacillus, Agriculture handbook no. 427, United States Department of Agriculture, U.S. Government printing office, Washington D.C. (1973;
ND = No data available.

[0142] The 3 strains B. lentimorbus NBRI0725, B. subtilis NBRI1205, and B. lentimorbus NBRI3009 isolated from Sahiwal cow selected by the method of screening as described above have the ability to control phytopathogenic fungi, promote plant growth, tolerance for abiotic stresses, and solubilize phosphate under abiotic stress conditions. B. lentimorbus NBRI0725, B. subtilis NBRI1205, and B. lentimorbus NBRI3009 have been deposited under the Budapest treaty on Jul. 5, 2001 into ARS Patent culture collection, United States Department of Agriculture, 1815 North University Street, Peoria, Ill. 61604, U.S.A. The bacterial strains B. lentimorbus NBRI0725, B. subtilis NBRI1205, and B. lentimorbus NBRI3009 have been allotted following NRRL number B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488, respectively.

[0143] In addition to the other properties noted above, the unexpected and surprising attributes of these specific B. lentimorbus and B. subtilis strains include the following characteristics. All the three strains have been isolated from the milk of Sahiwal cow. The strains have a rapid generation time in culture (55-65 minutes at 30° C.). In pure culture the strains inhibit the growth of many pathogenic fungi of plants. The strains are capable of colonizing plant roots. These bacteria reduce the plant disease in soil both under greenhouse and field conditions. The strains of the present invention are capable of promoting plant growth of plants in soil both under greenhouse and field conditions. Moreover the strains continue to survive in the soil throughout the growing season of the plant.

[0144] The subject Bacillus strains also have tolerance to abiotic stresses like 6% salt (NaCl), 5-9 pH, and 55° C. temperature.

[0145] The subject Bacillus strains have the ability to solubilize phosphate under abiotic stress conditions e.g., 0-4% salt (NaCl), 7-9 pH, and 30-45° C. temperature. Phosphate solubilization activity of the strains is induced in the presence of high salt, high pH, and high temperature.

[0146] It is within the compass of the invention to isolate any type of bacteria having the ability to control phytopathogenic fungi, promote plant growth, tolerance for abiotic stresses, and solubilize phosphate under abiotic stress conditions, however, Bacillus are the bacteria of choice because (1) they can easily be isolated, cultured and identified; (2) being a naturally occurring isolate or strain does not require genetic engineering to be effective; (3) being nutritionally versatile are able to utilize large number of organic substrates, including root exudates; (4) being suppressive to one or more pathogenic fungi; (5) having a stage in its life cycle that is resistant to harsh environmental conditions; (6) being tolerant to abiotic stresses (high salt, high pH, and high temperature); (7) being able to solubilize phosphate under abiotic stress (high salt, high pH, and high temperature) conditions; (8) colonizing the rhizosphere of the root system of the host plant(s) for the full growing season in the field; (9) enhancing the yield of the host plant(s) under field conditions; and (10) being relatively easy to develop for commercial purposes.

[0147] Another aspect of the invention is directed to a method of controlling plant diseases and promoting plant growth of plants in soil both under greenhouse and field conditions. The 3 bacterial strains designated B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488 are especially preferred in this process. An inoculant of the subject strain is used such that colonization is in the range of about Log 4-10 colony forming units/gram (cfu/g) root occurs and preferably Log 6-8 cfu/g. A mixture of the 3 strains (consortium) designated B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488 in the ratio of 1:1:1, consisting of about Log 6-10 cfu/ml each and preferably Log 7-8 cfu/ml each is especially preferred in this process. The inoculum can be applied directly to the seeds or plants, can be present in the soil before planting or can be distributed, e.g., by spreading, dusting or the like, over the crop or soil top or in soil furrow where the crop has been planted.

[0148] Seeds can be treated by coating with a composition containing the subject bacteria by dipping in a liquid containing these bacteria, by spraying with the liquid, or other method known in the art for applying bacteria to seeds.

[0149] According to yet another aspect of the invention cultures of B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488 may be grown individually in molasses diluted with water in the ratio of 1:1 to 1:10. However dilution of 1:5 is especially preferred in this process. The bacterial strains may be used individually, or as a consortium in the ratio of 1:1:1, consisting of about Log 6-11 cfu/ml each and preferably Log 8-9 cfu/ml each is especially preferred in this process. The consortium thus obtained may further be diluted with water in the ratio of 1:10 to 1:10000. However dilution of 1:100 is especially preferred in this process.

[0150] Growing the bacteria in molasses makes the process economically very viable. Bacteria grown in such manner may further be used to treat seeds by coating with a composition containing the subject bacteria by dipping in a liquid containing these bacteria, by spraying with the liquid, or other method known in the art for applying bacteria to seeds.

[0151] According to a further aspect the invention, the process of the invention may be used with any kind of bacteria or other microorganisms capable of surviving under abiotic stress conditions e.g., tolerance to salt, pH, and temperature. Of particular interest are bacteria, which have biocidal properties, e.g., biofungicidal, pesticidal, and other properties; promote plant growth, and solubilise phosphate under abiotic stress conditions, e.g., high salt, high pH, and high temperature that are capable of living in the soil in the presence of the plants.

[0152] The carriers that may be used to disperse the subject strains would include all those commonly used for inoculating crops and would include carriers such as rice husk, caboxymethyl cellulose, peat, perlite, polyvinyl-pyrrolidone, and talc. The bacteria in such compositions are at a level of about Log 4-10 cfu/g carrier. Carriers such as vermiculite or charcoal or fermented press mud are especially preferred in this process. The bacteria are grown in broth to the necessary amount, and then mixed with the carrier at the desired inoculum, followed by curing of the mixture by well-known methods.

[0153] According to this embodiment of the invention the optimum carrier may vary depending on the bacteria used. Any of the above compositions, liquids, powders, peat, soil, vermiculite, charcoal, fermented press mud and the like may have nutrients included therein or appropriate carrier medium such as water, oils or solid bases such as powders, peat, soil, vermiculite, charcoal, fermented press mud and any other carrier agents. However, as demonstrated by the examples below, vermiculite, charcoal, fermented press mud are preferred.

[0154] Further aspect of this invention relates to a process whereby the synergistic composition thus produced of the present invention may be used in any manner known in the art for example, including pretreatment of soil or seeds or pregerminated plant roots alone or in combination with other chemicals which is harmless to the growth and survival of bacteria for example plant growth promoting compounds, pesticides, fertilizers, nematicides, herbicides with or without for example lime pelleting to limit the severity of the effect of these materials. However, as demonstrated by the example below, compatible pesticides are preferred.

[0155] The examples given below in a nonlimiting way will make it possible to better understand the invention.

EXAMPLE 1

[0156] Isolation of Bacterial Strains from Milk

[0157] Fifty bacterial representatives of the predominant morphologically distinct colonies present on the plates were selected from healthy human, indigenous (Sahiwal) cow, exotic (Holestien Frisian) cow and buffalo's three individual milk samples, each. Therefore, a total of 600 bacterial strains were collected for further screening. Human milk was collected from three mothers with breast-fed infants in the range of 6 to 12 weeks old. Milk from pure breed native Sahiwal cows #12, #217, and #249 was collected from Gajaria farm, Department of Animal Husbandry, Government of Uttar Pradesh, Lucknow. Milk from exotic breed Holestien Frisian (15/16) cows #154, #412, and #667 was collected from Indian Military Farm, Central Command Headquarters, Indian Army, Lucknow. Milk samples from buffalo were collected from local commercial dairy farm. Milk was collected in sterile containers after taking due care to sanitise the teat and human handler. Samples of milk were collected in morning, midway from the milk stream coming out of teat directly into sterile container, without having any contact and stored in an ice box, during its transportation. Serial dilution of the milk samples was then plated within two hours of its collection on Nutrient agar (NA) plates (Beef extract 5.0 gm, peptone 10.0 gm, sodium chloride 5.0 gm, agar 15 gm, distilled water 1000 ml, pH 7.2).

[0158] Pure isolates of the individual strains were obtained of bacteria representative of the predominant morphologically distinct colonies present on the plates were selected at random and purified by sub culturing an individual strain on NA plates to obtain a pure culture. Each isolate was stored in an aqueous solution of 30% glycerol at −25° C.

[0159] Total bacterial counts from three individual milk samples collected from healthy human, Sahiwal cow, Holestien cow was Log 3 cfu/ml, compared with a log unit higher of Log 4 cfu/ml from buffalo (Table 2).

	TABLE 2
	Milk sample from
		Sahiwal	Holestien
Parameter	Human	cow	cow	Buffalo
Bacteria [cfu/ml]	Log 3.2	Log 3.1	Log 3.2	Log 4.2

EXAMPLE 2

[0160] Screening of Bacterial Strains Under in vitro Conditions for Ability to Suppress Pathogenic Fungi and Bacteria

[0161] The 600 bacterial strains, obtained by the procedure outlined in Example 1 were screened for their ability to inhibit growth of Colletotrichum falcatum, Sclerotium rolfsii, Alternaria solani, Penicillium sp., Pythium aphamidermatum, Phytophthora palmivora, Curvularia lunata, Sclerotinia sclerotiorum, and Aspergillus niger under in vitro conditions as follows: Four single bacterial colonies on NA plates were streaked around the edge of a 90-mm diameter petri plate and the plates were incubated at 28° C. for two days. An agar plug inoculum of the fungi to be tested (5-mm square) was then transferred to the center of the plate individually from a source plate of the fungi. After incubation for 5 to 7 days inhibition zones were readily observed in the case of bacterial strains having the biocontrol activity as the fungal growth around the streak was inhibited. While in case of bacterial strains not having biocontrol activity, fungal growth around the streak was not inhibited and the fungi grew towards the edge of the plate (Table 3). Strains, which show a zone of inhibition of at least 2 mm, were selected as positive and used for further work.

	TABLE 3
	% of biocontrol bacteria
Pathogenic		Sahiwal	Holestien
fungi	Human	cow	cow	Buffalo
Colletotrichum falcatum	0	17	0	8
Sclerotium rolfsii	0	8	0	0
Alternaria solani	8	8	8	8
Penicillium sp.	8	0	0	0
Pythium aphanidermatum	8	8	8	0
Phytophthora palmivora	8	8	8	0
Curvularia lunata	17	8	8	0
Sclerotinia sclerotiorum	0	17	8	0
Aspergillus niger	0	17	8	0

[0162] It was discovered that % of bacterial strains showing biocontrol activity against phytopathogenic fungi was maximum in Sahiwal cow, followed by human, Holestien cow and buffalo. From this parameter milk of Sahiwal cow was superior to human, Holestien cow and buffalo (Table 2). Strains, which show a zone of inhibition of at least 2 mm, were selected as positive and used for further work.

[0163] Of 600 strains tested in vitro, only 150 were determined to be having the biocontrol activity, according to above criteria.

EXAMPLE 3

[0164] Screening of Bacterial Strains for Ability to Promote Plant Growth in Greenhouse

[0165] The 150 bacterial strains that were suppressive to pathogenic fungi in vitro were screened in greenhouse by growing bacteria treated maize seeds in non-sterile soil and comparing the treated maize with control maize plants grown without bacterial treatment.

[0166] The process of screening of bacterial strains for ability to promote plant growth in greenhouse of the present invention is disclosed with particular reference to the plant maize. However it should not be conferred that the process of screening of bacterial strains for ability to promote plant growth in greenhouse is restricted to this plant, as any suitable other plant may be employed.

[0167] Non-sterile field soil from the farm of National Botanical Research Institute, Lucknow was used to evaluate the plant growth promotion potential of the 150 strains in greenhouse.

[0168] Bacterial inoculum for maize seeds was prepared by scraping 48 h grown culture from plates with 10 ml of 0.85% saline water. Maize seeds were surface sterilized by gently shaking (80 R.P.M. on a reciprocal shaker at 28° C.) with 70% ethanol (5 min.), 20% bleach Chlorox (10 min.), followed by three rinses in sterile water. After surface sterilization seeds were soaked in the bacterial suspension for 4 h at 28° C. on a reciprocal shaker at 100 R.P.M. Control seeds (non bacterised) were soaked in 0.85% saline water washed from uninoculated plates. Bacterisation levels of seeds were determined by agitating 4 seeds from each treatment and plated after serial dilution on NA plate. Mean cfu/seed were determined by averaging the cfu/gm values of three populations in three replicates per treatment after 48 h incubation of the plates at 28° C. Seed for treatments in which mixtures of three isolates were used, were inoculated by using the same total number of bacteria for the inoculum as was used for the single-isolate treatments. Thus, one-third the normal amount of each isolate in the mixture was used.

[0169] Trays (35×35 cm.) with 16 (4×4) places per tray (each space was of 7 cm. width, 10 cm. depth and 1 cm. apart from each other) were used, to grow maize. Each place was filled up to 8 cm. with non-sterilised soil. Tap water (25 ml.) was added to each hole before planting seeds to adjust the soil to 20% moisture. Four bacterial-treated seed was added per hole. The experiment in greenhouse was carried out in four different sets of 16 maize seedlings each, for non-bacterised (control) and bacterised (treated) seeds. In each set, data of 21-days-old seedlings was noted with respect to dry weight of plants. In order for the bacterial strain to be plant growth promoter, the seedlings treated with the bacteria must have averaged at least 10% higher dry weight than comparable non-bacterised plants.

[0170] Of the 150 bacterial strains tested in the greenhouse test, 50 were determined to be plant growth promoting according to above criteria.

EXAMPLE 4

[0171] Screening of Bacterial Strains for Abiotic Stress Tolerance

[0172] The bacterial strains that were suppressive to pathogenic fungi in vitro and enhanced plant growth of maize when screened in greenhouse by growing bacteria treated maize seeds in non-sterile soil, compared with the control maize plants grown without bacterial treatment were further screened for abiotic stress tolerance as follows: The stress tolerance of the strains towards salt (NaCl), pH, and temperature was tested by growing them on nutrient broth (NB; Beef extract 5.0 gm, peptone 10.0 gm, sodium chloride 5.0 gm, distilled water 1000 ml, pH 7.2) under various stress conditions, e.g., like 6% salt (NaCl), 5-9 pH, and 55° C. temperature. Viable cells were counted by removing samples at various times in the presence or absence of stress, as indicated. First of all, the 50 strains were subjected to 6% salt stress. Fifteen strains out of 50 were able to grow in the presence of 6% salt stress overnight (14-16 hrs) at 30° C. on a New Brunswick Scientific, USA, Innova Model 4230 refrigerated incubator shaker at 180 rpm. The 15 strains tolerant to 6% salt stress were also able to grow at pH 9.0 stress overnight. However, only 3 strains out of 15 were able to grow at 55° C. stress overnight. Serial dilutions of each sample were spotted (25 μl) onto NA plates, and incubated at 30° C. in triplicate as described earlier [C. S. Nautiyal et al., FEMS Microbiology Letters, Volume 182, pp. 291-296 (2000)]. Viable cells were counted after 2-3 days.

[0173] Of the 50 bacterial strains tested in the stress tolerance test, the 3 strains NRRL number B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488 were thus determined to be stress tolerant according to above criteria.

EXAMPLE 5

[0174] Ability of B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488 to Solubilise Phosphate Under Abiotic Stress Conditions

[0175] The 3 bacterial strains B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488 that were suppressive to pathogenic fungi in vitro, enhanced plant growth of maize when screened in greenhouse by growing bacteria treated maize seeds in non-sterile soil, compared with the control maize plants grown without bacterial treatment, and were tolerant to abiotic stresses (salt, pH, and temperature) were further screened for their ability to solubilise phosphate under abiotic stress conditions as follows: Quantitative estimation of phosphate solubilisation in broth was carried out using Erlenmeyer flasks (150 ml) containing 10 ml of medium inoculated in triplicate with the bacterial strain (100 μl inoculum with approximately Log 9 cfu/ml).

[0176] Value refers to the amount of P solubilised (μg/ml) by strains when individually grown for 3 days in National Botanical Research Institute's phosphate growth medium (NBRIP; glucose, 10 g; Ca3(PO4)2 tricalcium phosphate, 5 g; MgCl2.6H2O, 5 g; MgSO4.7H2O, 0.25 g; KCl, 0.2 g and (NH4)2SO4, 0.1 g [C. S. Nautiyal, FEMS Microbiology Letters, Volume 170, pp. 265-270 (1999)], at 30° C. in the presence of 0% salt (NaCl) at pH 7. The effect of salt (NaCl), pH, and temperature on solubilisation of phosphate was tested by growing them on NBRIP in the presence of NaCl (0, 1, 2, and 4%), pH (7 and 9), and temperature (30 and 45° C.), as indicated (Table 4). Autoclaved, uninoculated batch cultures served as negative controls. Flasks were incubated for 3 days at 30° C. on a New Brunswick Scientific, USA, Innova Model 4230 refrigerated incubator shaker at 180 rpm. The strains were harvested by centrifugation at 10000 rpm for 10 min, using a Sorvall RC SC centrifuge, Dupont, USA. The concentration of phosphate in culture supernatant was estimated using the Fiske and Subbarow method [C. H. Fiske and Y. Subbarow, Journal of Biological Chemistry, Volume 66, pp. 375-400 (1925)].

	TABLE 4
	Phosphate solubilisation (μg/ml)
	pH 7	pH 9
% Salt (NaCl)	Strain	30° C.	45° C.	30° C.	45° C.
0	NRRL B-30486	3.0	6.6	3.8	6.1
1		4.7	6.5	4.6	11.6
2		4.5	9.9	4.8	11.2
4		4.8	10.5	4.1	10.3
0	NRRL B-30487	2.4	1.3	0.83	1.5
1		3.4	6.0	2.8	3.2
2		6.2	6.0	5.5	5.7
4		2.5	12.5	5.6	13.2
0	NRRL B-30488	33.8	42.9	42.9	43.0
1		17.0	42.9	13.5	43.0
2		12.0	0.0	19.4	43.0
4		13.0	0.0	8.8	43.0

[0177] All the 3 bacterial strains B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488 demonstrated variable phosphate solubilisation induction ability, under in vitro conditions in the presence of high salt, high pH, and high temperature stress.

EXAMPLE 6

[0178] Ability of B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488 Under in vitro Conditions to Suppress Pathogenic Fungi in the Presence or Absence of High Salt and pH Stress

[0179] The 3 bacterial strains B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488 were screened for their biocontrol activity against several plant pathogenic fungi, under in vitro conditions in the presence or absence of high salt and pH stress (Table 5).

TABLE 5
Pathogenic	Inhibition zone (mm)
strain	B-30486	B-30487	B-30488
Fusarium oxysporum f. sp. ciceri
pH 3; 0% salt (NaCl)	10	20	10
pH 3; 2% salt	20	25	20
pH 3; 4% salt	10	NG*	20
pH 7; 0% salt	8	6	7
pH 7; 2% salt	17	20	15
pH 7; 4% salt	12	NG	16
pH 9; 0% salt	5	5	5
pH 9; 2% salt	20	10	15
pH 9; 4% salt	13	NG	14
pH 11; 0% salt	15	10	20
pH 11; 2% salt	20	20	20
pH 11; 4% salt	15	10	20
Sclerotium rolfsii
pH 3; 0% salt (NaCl)	5	NZ**	5
pH 3; 2% salt	10	5	NZ
pH 3; 4% salt	20	5	NG
pH 7; 0% salt	3	10	NZ
pH 7; 2% salt	4	3	2
pH 7; 4% salt	NG	NG	NG
pH 9; 0% salt	8	NZ	7
pH 9; 2% salt	13	7	13
pH 9; 4% salt	25	10	20
pH 11; 0% salt	5	NZ	NZ
pH 11; 2% salt	20	20	20
pH 11; 4% salt	20	5	25
Inhibition zone at pH 7; 0% salt
Rhizoctonia solani	6	NZ	3
Alternaria solani	10	6	8
Pythium aphanidermatum	10	4	10
Phytophthora palmivora	6	12	7
Sclerotinia sclerotiorum	14	10	11
Colletotrichum falcatum	11	10	NZ
Penicillium sp.	2	5	NZ
Curvularia lunata	2	3	10
Aspergillus niger	2	10	3
Phoma sorghii	NZ	5	NZ
Fusarium moniliforme	11	6	10
NG* = No growth of fungi;
NZ** = No inhibition zone

[0180] All the 3 bacterial strains B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488 demonstrated variable biocontrol activity against several phytopathogenic fungi, under in vitro conditions in the presence of high salt and/or pH stress. The strains also demonstrated variable biocontrol activity activity against several phytopathogenic fungi, under in vitro conditions in the presence or absence of high salt and pH stress. Therefore, the possibility of using consortium of all the three bacteria was explored.

EXAMPLE 7

[0181] Interaction of B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488 Individually and their Consortium, Under in vitro Conditions with Chickpea Phytopathogenic Fungi

[0182] Interaction of F. oxysporum f. sp. ciceri, Rhizoctonia solani, Pythium sp., and S. sclerotiorum with B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488 individually and in a consortium in liquid medium was elucidated in a dual culture test by growing the bacterium/consortium on nutrient broth in the presence and absence of the fungi. An agar disk (5-mm in diameter) of the F. oxysporum f. sp. ciceri, Rhizoctonia solani, Pythium sp., and S. sclerotiorum was individually inoculated in 150-ml Erlenmeyer flasks containing 50 ml nutrient broth.

[0183] A suspension of B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488 individually and its consortium, containing Log 8.0 cfu/ml was inoculated and the flasks were incubated at 30° C. for 7 days in an incubator shaker under static condition, and the control cultures were grown without bacteria. Consortium of the 3 bacterial strains B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488 was prepared by mixing the 3 cultures of approximately Log 8.0 cfu/ml, in the ratio of 1:1:1. Mycelial dry weight of the fungus grown in the presence and absence of B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488 individually and its consortium was determined by filtering out the spent media using a Whatman filter paper no. 1, and drying the fungal mass on the filter paper at 60° C. for 3 days. Test results of the interaction of B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488 individually and in a consortium, under in vitro conditions with F. oxysporum f. sp. ciceri, Rhizoctonia solani, Pythium sp., and S. sclerotiorum are presented in Table 6.

	TABLE 6
	Fungi
		Dry weight	% inhibition
	Treatment	(mg)	over control
	Fusarium oxysporum f. sp. ciceri(FO)
	1. FO	150	0
	2. FO + B-30486	78	48
	3. FO + B-30487	96	36
	4. FO + B-30488	84	44
	5. FO + B-30486 +	56	63
	B-30487 + B-30488
	Rhizoctonia solani (RS)
	1. RS	80	0
	2. RS + B-30486	30	63
	3. RS + B-30487	34	58
	4. RS + B-30488	48	40
	5. RS + B-30486 +	26	68
	B-30487 + B-30488
	Pythium sp. (PS)
	1. PS	50	0
	2. PS + B-30486	40	20
	3. PS + B-30487	48	4
	4. PS + B-30488	23	54
	5. PS + B-30486 +	21	58
	B-30487 + B-30488
	Sclerotinia sclerotiorum (SS)
	1. SS	313	0
	2. SS + B-30486	72	77
	3. SS + B-30487	96	69
	4. SS + B-30488	84	73
	5. SS + B-30486 +	64	80
	B-30487 + B-30488

[0184] As can be seen from the results which are presented in Table 6, all the three bacterial strains B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488 individually and their consortium effectively inhibited the growth of F. oxysporum f. sp. ciceri, Rhizoctonia solani, Pythium sp., and S. sclerotiorum under in vitro conditions. However, consortium of the bacterial strains was most effective in inhibiting the growth of the test fungi.

EXAMPLE 8

[0185] Survival of B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488 Individually and in a Consortium, on Vermiculite as Carrier

[0186] Determination of the survival of 3 bacterial strains B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488 individually and in a consortium, on vermiculite as carrier, over the period of twelve months, at 10° C. was accomplished according to following method. The 3 bacterial strains B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488 were grown individually in liquid growth medium NB. Cultures were grown in 2-liters flasks containing 1.5 litres of NB medium and incubated for 2 days at 30° C. on a New Brunswick Scientific, USA, Innova Model 4230 refrigerated incubator shaker at 180 rpm. After 2 days of growth 300 ml of the culture was added to 1 kg of sterile vermiculite containing autoclavable plastic bag, which yielded approximately 30% moisture of the product. Consortium of the 3 bacterial strains B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488 was prepared by mixing the 3 cultures of approximately Log 8.5 cfu/ml, in the ratio of 1:1:1. Incubating the sealed bags for 2 days at 30° C. did curing of the bioinoculant preparation. After curing, the sealed bags were stored at 10° C. and aliquots were periodically removed for viability measurements (Table 7). Viability of the product was determined by standard serial dilution method on NA plates.

	TABLE 7
	Log cfu/g of vermiculite
				B-30486 +
				B-30487 +
				B-30487
Months	B-30486	B-30487	B-30488	(Consortium)
0	8.4	8.8	8.4	8.5
1	10.2	9.7	10.3	9.8
2	9.8	9.7	9.9	9.2
4	9.4	9.3	9.6	9.2
6	8.8	8.3	8.9	8.8
9	8.4	8.3	8.5	8.8
12	7.9	7.7	8.3	8.1

[0187] As shown in the Table 7, all the three strains B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488 individually and in a consortium demonstrated good survival rates, during long-term storage in vermiculite at 10° C. After twelve months of storage, approximately Log 8 cfu/g of vermiculite was present. These data indicate that vermiculite works as an excellent carrier material for the strains to be later inoculated onto seeds, plants or soil, as no appreciable loss of cell viability was observed.

EXAMPLE 9

[0188] Biocontrol Activity of B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488 Individually and in a Consortium, in Greenhouse Against Chickpea Phytopathogenic Fungi

[0189] The 3 bacterial strains B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488 were screened individually and in a consortium, in greenhouse against chickpea phytopathogenic fungi. Cultivation of fungi for plant assay was accomplished using a 1000 ml-Eelenmeyer flask with 100 g corn and 400 g coarse sand was autoclaved and after autoclaving moisture was adjusted to 15% with sterile distilled water. The flask was incubated at 30° C. individually with one 10 mm diameter agar plug from a nutrient agar culture of F. oxysporum f. sp. ciceri, R. solani and Pythium sp. in dark for 4 weeks. After four weeks the mixture air-dried and grounded and sieved to obtain particles 0.5 mm in size. Each of the inoculum was intimately mixed with sterile soil at 0.15% inoculum per total weight of soil, to give a final mixture of 0.45% inoculum of F. oxysporum f. sp. ciceri, R. solani and Pythium sp. per total weight of soil as described earlier [C. S. Nautiyal, Current Microbiology, Volume 35, pp. 52-58 (1997)].

[0190] The experiment to examine the biocontrol activity of B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488 individually and in a consortium was carried out in four different sets of 30 chickpea seedlings each, for treated and non-treated seeds (control). Chickpea seeds were prepared for inoculum of B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488 individually and in a consortium as described in Example 3, except vermiculite was used as carrier as described in Example 8, instead of direct inoculum from petri plate. In each set, data was noted during five months of plant growth with respect to seedling germination, seedling mortality (dead seedlings, stunting of shoot height, drooping of leaves, root decolourisation), plant height, number of pods and seed dry weight. The results are tabulated in the following Table 8.

	TABLE 8
	Treatment
		Un-inoculated		% increase over
Observations	Inoculum	control	Inoculated	control
Seedling germination (%)	B-30486	82	93	13.41
Seedling mortality (%)		87	31	−64.36
Plant height (cm)		29	37	27.58
Number of pods/plant		39	48	23.07
Seed dry weight/		17	20	18.78
100 seeds (g)
Seedling germination (%)	B-30487	71	82	15.49
Seedling mortality (%)		87	38	−56.32
Plant height (cm)		29	34	17.24
Number of pods/plant		39	43	10.25
Seed dry weight/		17	19	12.73
100 seeds (g)
Seedling germination (%)	B-30488	82	100	21.95
Seedling mortality (%)		87	28	−67.8
Plant height (cm)		29	41	41.37
Number of pods/plant		39	52	33.33
Seed dry weight/		17	20	21.95
100 seeds (g)
Seedling germination (%)	B-30486 +	82	100	21.95
	B-30487 +
	B-30488
	(Consortium)
Seedling mortality (%)		87	10	−88.5
Plant height (cm)		29	43	48.27
Number of pods/plant		39	61	56.41
Seed dry weight/		17	23	39.5
100 seeds (g)

[0191] As can be seen from the results which are presented in Table 8, inoculated plants demonstrated less seedling mortality, and better seedling germination, plant height, number of pods and seed dry weight, compared with un-inoculated control. Among the inoculated plants, consortium showed best results in terms of less seedling mortality, and better seedling germination, plant height, number of pods and seed dry weight.

EXAMPLE 10

[0192] Plant Growth Promotion Activity of B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488, Individually and in a Consortium, in Greenhouse Using Chickpea

[0193] The experiment to examine the plant growth promotion activity of B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488 individually and in a consortium was carried out in four different sets of 30 chickpea seedlings each, for treated and non-treated seeds (control). Chickpea seeds were prepared for inoculum of B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488 individually and in a consortium using vermiculite as carrier as described in Example 9. In each set, data was noted during five months of plant growth with respect to seedling germination, plant height, number of pods and seed dry weight. The results are tabulated in the following Table 9.

	TABLE 9
	Treatment
	Un-inoculated		% increase over
Observations	control	Inoculated	control
Seedling germination (%)	B-30486	82	100	21.95
Plant height (cm)		29	38	31.03
Number of pods/plant		39	53	35.89
Seed dry weight/		17	21	27.88
100 seeds (g)
Seedling germination (%)	B-30487	82	92	12.19
Plant height (cm)		29	39	34.48
Number of pods/plant		39	46	17.95
Seed dry weight/		17	20	18.78
100 seeds (g)
Seedling germination (%)	B-30488	82	100	21.95
Plant height (cm)		29	44	51.72
Number of pods/plant		39	59	51.28
Seed dry weight/		17	23	40.0
100 seeds (g)
Seedling germination (%)	B-30486 +	82	100	21.95
	B-30487 +
	B-30488
	(Consortium)
Plant height (cm)		29	46	58.62
Number of pods/plant		39	64	64.10
Seed dry weight/		17	25	48.48
100 seeds (g)

[0194] As can be seen from the results which are presented in Table 9, inoculated plants demonstrated better seedling germination, plant height, number of pods and seed dry weight, compared with un-inoculated control. Among the inoculated plants, consortium showed best results in terms of better seedling germination, plant height, number of pods and seed dry weight.

EXAMPLE 11

[0195] Plant Growth Promotion Activity of the Consortium of B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488 in Greenhouse on Various Plants

[0196] Seeds were prepared and inoculated to test the plant growth promotion activity of the consortium of B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488 in greenhouse on various plants, as described above in example 8. The experiment in greenhouse was carried out in four different sets of 16 seedlings each, for non-bacterised (control) and bacterised (treated) seeds of Zea mays, Abelmoschus esculentus, Luffa cylindrica, Lycopersicon esculentum, and Cucumis sativus. In each set, data of 21-days-old seedlings was noted with respect to dry weight of plants. The results of the plant growth promotion activity of the consortium of B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488 in greenhouse on various plants are given in Table 10.

	TABLE 10
	Dry weight (mg)/plant
	Un-inoculated		% increase over
Test plants	control	Inoculated	control
1. Zea mays	67.5	80	18.51
2. Abelmoschus	20	35	75.0
esculentus
3. Luffa cylindrica	76	110	44.73
4. Lycopersicon	2	5	150.0
esculentum
5. Cucumis sativus	25	110	340.0

[0197] As the data in Table 10 demonstrate, variable plant growth promotery response on the dry weight of Zea mays, Abelmoschus esculentus, Luffa cylindrica, Lycopersicon esculentum, and Cucumis sativus by the consortium of B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488 in greenhouse. As can be seen from the results, the dry weight of the bacterised seedlings was higher in the range of 18-340% compared with non-bacterised seedlings.

EXAMPLE 12

[0198] Field Trial of Biocontrol Activity of the Consortium of B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488 Against Chickpea Phytopathogenic Fungi

[0199] Biocontrol activity of the consortium of B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488 against chickpea phytopathogenic fungi was field tested on the farms of Banaras Hindu University, Varanasi; Chandra Shekhar Azad University of Agriculture & Technology, Kanpur, and Indian Agricultural Research Institute, New Delhi on plots with consistent history of heavy infection of chickpea variety Radhey, by F. oxysporum f. sp. ciceri. The bacterial strains were propagated as described in Example 8. All the trials were seeded in October, 2000 and harvested after five months of growth in March, 2001. Field soil moisture at the time of seeding was in the range of 25-30% and the crop was entirely rain fed. Mechanical cultivation practices were not used after seeding. Each experiment was in a randomised block design. Six replicates per treatment within blocks consisted of plots of three 4-m rows (30 cm spacing). After 10 days of germination, seedlings were thinned out to 50 seedlings per row. All results were collected from the middle rows, excluding two adjacent rows as guard rows, for both non-bacterised (control) and bacterised (treated) seeds of chickpea with consortium of B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488 (Log 8 Cfu/ml). Values are the mean of six replications of 10 plants each, whereas values for the dry weights (g) are the mean of 100 seeds chosen at random from six replications of 10 plants each.

	TABLE 11
	Treatment
		Un-inoculated		% increase over
Observations	Location	control	Inoculated	control
Seedling survival (%)	Varanasi	55	73	33.69
Plant height (cm)		41	57	38.05
Number of pods/plant		65	79	20.39
Weight of 100 seeds (g)		17	20	19.87
Yield/plot (g)		410	725	76.83
Seedling survival (%)	Kanpur	40	83	105.19
Plant height (cm)		47	62	32.2
Number of pods/plant		62	94	51.61
Weight of 100 seeds (g)		16	20	24.68
Yield/plot (g)		345	870	152.17
Seedling survival (%)	New Delhi	47	87	85.11
Plant height (cm)		47	57	21.27
Number of pods/plant		44	104	136.36
Weight of 100 seeds (g)		15	19	26.49
Yield/plot (g)		450	900	100.0

[0200] As can be seen from the data in Table 11, at all the three locations compared to control, chickpea seeds treated with consortium of B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488 improved plant performance, in terms of enhanced % seedling survival, plant height, number of pods/plant, weight of 100 seeds, and yield/plot.

EXAMPLE 13

[0201] Survival of B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488 Individually and in a Consortium, on Charcoal as Carrier

[0202] Determination of the survival of 3 bacterial strains B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488 individually and in a consortium, on charcoal as carrier, over the period of six months, at 10° C. was accomplished according to following method. The 3 bacterial strains B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488 were grown individually in liquid growth medium NB. Cultures were grown in 2-liters flasks containing 1.5 liters of NB medium and incubated for 2 days at 30° C. on a New Brunswick Scientific, USA, Innova Model 4230 refrigerated incubator shaker at 180 rpm. After 2 days of growth 600 ml of the culture was added to 1 kg of sterile charcoal containing autoclavable plastic bag, which yielded approximately 30% moisture of the product. Consortium of the 3 bacterial strains B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488 was prepared by mixing the 3 cultures of approximately Log 8.5 cfu/ml, in the ratio of 1:1:1. Incubating the sealed bags for 2 days at 30° C. did curing of the bioinoculant preparation. After curing, the sealed bags were stored at 10° C. and aliquots were periodically removed for viability measurements. Viability of the product was determined by standard serial dilution method on NA plates.

[0203] Table 12 shows the survival of 3 bacterial strains B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488 individually and in a consortium, on charcoal as carrier, over the period of six months, at 10° C., following harvesting.

	TABLE 12
	Log cfu/g on charcoal
				B-30486 +
				B-30487 +
				B-30487
Months	B-30486	B-30487	B-30488	(Consortium)
0	8.4	8.8	8.4	8.5
1	9.2	9.5	9.6	9.2
2	9.1	9.1	9.5	9.6
4	8.7	8.4	8.9	8.7
6	7.1	7.6	7.5	7.8

[0204] As shown in the Table 12, all the three strains B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488 individually and in a consortium demonstrated good survival rates, during long-term storage in charcoal at 10° C. After six months of storage, approximately Log 7 cfu/g was present. These data indicate that charcoal works as an excellent carrier material, albeit not as effective when compared with vermiculite, for the strains to be later inoculated onto seeds, plants or soil. However, as a carrier material the cost of charcoal is 8 fold less, compared with vermiculite. Therefore, the lower cost of the charcoal makes its choice as a carrier very attractive for its large-scale commercial use.

EXAMPLE 14

[0205] Use of Sugar Factory Sulphitation Press Mud and Distillery Spent Wash as Carrier for Preparing at Commercial Scale Consortium of B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488

[0206] The following procedures were performed to utilize sugar factory sulphitation press mud and distillery spent wash as carrier for preparing at commercial scale, after its fermentation-using consortium of B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488.

[0207] Cultures of B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488 were grown individually in molasses diluted with water in the ratio of 1:5. Cultures were grown in 2-liters flasks containing 1.5 litres of molasses diluted with water in the ratio of 1:5 and incubated for 3 days at 30° C. on a New Brunswick Scientific, USA, Innova Model 4230 refrigerated incubator shaker at 180 rpm. After 3 days of growth consortium of the 3 bacterial strains B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488 was prepared by mixing the 3 cultures of approximately Log 9 cfu/ml, in the ratio of 1:1:1. Consortium of the 3 bacterial strains thus obtained was further diluted with water in the ratio of 1:10, containing approximately Log 8-9 cfu/ml. Growing the bacteria in molasses makes the process economically very viable.

[0208] About 300 tons of fresh sulphinated press mud, obtained while clarifying sugarcane juice with lime and sulphur dioxide, is laid out on cemented floor with width of 2.5 meter, 1.5 meter tall, and length of 150 meter windrows. The press mud was churned and homogenised, either manually or by the help of an aero tiller before adding about 600 liter consortium of B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488, prepared as described above, i.e., 2 liter of the consortium/ton of press mud and mixing again. Within 2-3 days, temperature of the windrows goes up to 70-75° C. Thereafter, the windrows are churned twice a day and spent wash is sprayed on daily basis to maintain 55-65% moisture, for up to 40 days. After about 40 sprays the spraying of spent wash is stopped and windrows regularly turned for 3-5 days to reduce the moisture of the fermented product to about 30%. Usually after 45 days, the temperature of the windrows goes down to 40-45° C. The product at this stage is totally fermented and ready for its application and packaging.

[0209] To monitor the presence of Bacillus strains during fermentation process of the windrows, spontaneous rifampicin-resistant (Rifr) strain derivative of B. lentimorbus NRRL B-30488R was isolated on NA plates, containing 100 μg rifampicin. Spontaneous B. lentimorbus NRRL B-30488R strain showing growth comparable to the wild type B. lentimorbus NRRL B-30488 based on the size of colony, on agar plates containing 100 μg rifampicin, was selected for further studies. Agar plates containing 100 μg rifampicin/ml, an amount sufficient to inhibit the growth of other bacteria in non-sterilised press mud and spent wash were used to recover B. lentimorbus NRRL B-30488R from the windrows during fermentation process. Presence of B. lentimorbus NRRL B-30488R Log 8 cfu/gm in the fermented product by 45 days is indicative of the survival, multiplication and continued presence of the B. lentimorbus NRRL B-30488R, during fermentation process.

EXAMPLE 15

[0210] Use of Sugar Factory Carbonation Press Mud as Carrier for Preparing at Commercial Scale Consortium of B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488

[0211] The procedures for fermenting sugar factory carbonation press mud as carrier for preparing at commercial scale, using consortium of B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488, were same as described as above in example 14, except water was used instead of spent wash, to maintain the moisture during fermentation.

EXAMPLE 16

[0212] Comparative Analysis of Plant Growth Promotion Activity of the Consortium of B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488 in Greenhouse Using Vermiculite, Charcoal, Fermented Sugar Factory Sulphitation Press Mud and Distillery Spent Wash, and Sugar Factory Carbonation Press Mud as Carrier, on Plants

[0213] Seeds were prepared and inoculated with the consortium of B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488 in greenhouse using vermiculite, charcoal, fermented sugar factory sulphitation press mud and distillery spent wash, and sugar factory carbonation press mud as carriers to test the plant growth promotion activity of the consortium of B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488 in greenhouse on various plants, as described above in Examples 8, 13, 14, and 15, respectively. The experiment in greenhouse was carried out in four different sets of 16 seedlings each, for non-bacterised (control) and bacterised (treated) seeds of A. esculentus, C. sativus, Z. mays, Triticum aestivum, Glycine max, Pisum sativum, and Impatiens balsamina. In each set, data of 21-days-old seedlings was noted with respect to dry weight of plants. The results of the plant growth promotion activity of the consortium of B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488 in greenhouse on various plants, while using vermiculite, charcoal, fermented sugar factory sulphitation press mud and distillery spent wash, and sugar factory carbonation press mud as carriers, are given in Table 13.

	TABLE 13
	Dry weight (mg)/plant
		Un-inoculated		% increase over
Plant	Carrier	control	Inoculated	control
1. A. esculentus	Vermiculite	28	47	67.85
2. C. sativus		30	95	216.67
3. Z. mays		61	74	21.31
4. Triticum aestivum		15	23	53.33
5. Glycine max		47	73	55.32
6. Pisum sativum		57	85	49.12
7. Impatiens balsamina		4	12	200.0
1. A. esculentus	Charcoal	31	50	61.23
2. C. sativus		34	94	176.4
3. Z. mays		65	83	27.63
4. Triticum aestivum		17	26	52.94
5. Glycine max		42	72	71.42
6. Pisum sativum		52	83	59.62
7. Impatiens balsamina		4	9	125.0
1. A. esculentus	Fermented sugar	25	38	52.0
	factory sulphitation
	press mud and
	distillery spent wash
2. C. sativus		28	56	100.0
3. Z. mays		57	70	22.81
4. Triticum aestivum		13	20	53.84
5. Glycine max		40	69	72.5
6. Pisum sativum		49	76	55.1
7. Impatiens balsamina		5	10	100.0
1. A. esculentus	Fermented sugar	36	54	50.0
	factory carbonation
	press mud
2. C. sativus		33	63	90.90
3. Z. mays		52	66	26.92
4. Triticum aestivum		12	20	66.62
5. Glycine max		42	71	69.05
6. Pisum sativum		48	74	54.17
7. Impatiens balsamina		4	10	150.0

[0214] As the data in Table 13 demonstrate, variable plant growth promotery response on the dry weight of different plants by the consortium of B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488 in greenhouse. As can be seen from the results, the dry weight of the bacterised seedlings of A. esculentus, C. sativus, Z. mays, Triticum aestivum, Glycine max, Pisum sativum, and Impatiens balsamina was higher in the range of 21-150% compared with non-bacterised seedlings, using vermiculite, charcoal, fermented sugar factory sulphitation press mud and distillery spent wash, and sugar factory carbonation press mud as carriers.

EXAMPLE 17

[0215] Field Trial of Biocontrol Activity of the Consortium of B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488 Against Sugarcane Phytopathogenic Fungi, Using Vermiculite as Carrier

[0216] Field trial plot size for all the field trials was of 9.0×3.5 meter plot size, consisting of four rows for each treatment, in triplicate.

[0217] Field trials using sugarcane variety Cos 95255 were conducted by placing sugarcane sets at the time of sowing directly on vermiculite, containing the consortium of B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488, to the saturation of 20%.

[0218] Inoculum of both the pathogens Fusarium moniliforme and Colletotrichum falcatum multiplied in liquid medium was prepared for a dual culture test by growing the fungus individually on NB. An agar disk (5-mm in diameter) of the F. moniliforme and C. falcatum were individually inoculated in 250-ml Erlenmeyer flasks containing 100 ml NB. The flasks were incubated at 30° C. for 10 days under static condition. The inoculum was diluted with sterile 0.85% saline Milli Q water (MQW) to spore concentration of Log 5 to 6 spores/ml. Sets were dipped in the inoculum thus prepared of F moniliforme or C. falcatum as indicated, for 30 minutes before planting. The inoculum was also used to drench the rows before planting sugarcane. Also the experiment was conducted in wilt sick plot where in previous year wilt incidence was as high as 95%.

[0219] First sugarcane trial was conducted using pots (9 inches diameter) in August, 2000, at Dhampur Sugar Mills Ltd., Rozagaon, Faizabad using the consortium. After three months of growth plants from pots were shifted into field. Number of infected plants, plant height, number of tillers, and girth of cane were noted in August, 2001. The test results are given in Table 14.

	TABLE 14
	Treatment
		Un-inoculated		% increase over
Observations	Fungi	control	Inoculated	control
Mortality (%)	Fusarium moniliforme	30	0	n.a.*
Plant height (cm)		161.8	181.4	12.11
Number of tillers/plant		3.1	6.4	106.4
Girth of cane (cm)		5.8	8.1	39.66
Mortality (%)	Colletotrichum falcatum	80	0	n.a.
Plant height (cm)		152	162	6.57
Number of tillers/plant		4.6	6.6	43.47
Girth of cane (cm)		5.8	7.8	34.48
*n.a. = Not applicable

[0220] The results presented in Table 14 clearly demonstrate effective biocontrol of sugarcane wilt and red rot fungi, increases in the number of tillers, plant height, and girth of cane inoculated with the consortium of B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488 using vermiculite as carrier, compared with un-inoculated control.

EXAMPLE 18

[0221] Field Trial of Plant Growth Promotion Activity of the Consortium of B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488 Using Vermiculite as Carrier, on Sugarcane at Rozagaon

[0222] Field trials using sugarcane were conducted by placing sugarcane sets at the time of sowing directly on vermiculite, containing the consortium of B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488, prepared as described in Example 8. Sugarcane trial was set up in October 2000 at Dhampur Sugar Mills Ltd., Rozagaon. After nine months of plant growth number of tillers, plant height, girth, millable cane, and cane yield of sugarcane were noted in December 2001. For the field trials sugarcane variety Cos-95255 was used at Dhampur Sugar Mills Ltd., Rozagaon. The test results of the field trials of plant growth promotion activity of the consortium of B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488 using vermiculite as carrier, on sugarcane are given in Table 15.

	TABLE 15
	Treatment
	Un-inoculated		% increase over
Observations	control	Inoculated	control
Number of tillers/plant	6.2	11.0	77.42
Plant height (cm)	200	246	23.0
Girth of cane (cm)	9.1	11.24	23.52
Millable cane	5	8	60.0
Cane yield/plot (kg)	128	229	78.9

[0223] The results presented in Table 15 clearly show increases in the number of tillers, plant height, girth, millable cane, and cane yield of cane inoculated with the consortium of B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488 using vermiculite as carrier, compared with un-inoculated control.

EXAMPLE 19

[0224] Field Trial of Plant Growth Promotion Activity of the Consortium of B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488 Using Vermiculite as Carrier, on Sugarcane at Dhampur

[0225] Field trials using sugarcane were conducted by placing sugarcane sets at the time of sowing directly on vermiculite, containing the consortium of B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488, prepared as described in Example 8. Sugarcane trials was set up in November, 2000 at Dhampur Sugar Mills Ltd., Dhampur, Bijnour. After thirteen months of plant growth, number of tillers, plant height, and girth of sugarcane were noted in December, 2001. For the field trials sugarcane variety Cos-95255 was used. The test results of the field trials of plant growth promotion activity of the consortium of B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488 using vermiculite as carrier, on sugarcane are given in Table 16.

	TABLE 16
	Treatment
	Un-inoculated		% increase over
Observations	control	Inoculated	control
Number of tillers/plant	6.0	8.4	40.0
Plant height (cm)	220	251	14.09
Girth of cane (cm)	7.2	9.4	30.56
Millable cane	4	9	125.0
Cane yield/plot (kg)	128	217	69.53

[0226] The results presented in Table 16 show increases in the number of tillers, plant height, girth of cane, millable cane, and cane yield inoculated with the consortium of B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488 using vermiculite as carrier, compared with un-inoculated control.

EXAMPLE 20

[0227] Field Trial of Plant Growth Promotion Activity of the Consortium of B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488 Using Charcoal as Carrier, on Sugarcane

[0228] Field trials using sugarcane were conducted by placing sugarcane sets at the time of sowing directly on vermiculite, containing the consortium of B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488, prepared as described in Example 13. Sugarcane trial was set up in April, 2001 at Dhampur Sugar Mills Ltd., Dhampur. After ten months of plant growth number of tillers, plant height, girth, millable cane, and cane yield of sugarcane were noted in December, 2001. For the field trials sugarcane variety Cos-89003 was used at Dhampur Sugar Mills Ltd., Dhampur. The test results of the field trials of plant growth promotion activity of the consortium of B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488 using charcoal as carrier, on sugarcane are given in Table 17.

	TABLE 17
	Treatment
	Un-inoculated		% increase over
Observations	control	Inoculated	control
Number of tillers/plant	7.2	10.8	50.0
Plant height (cm)	255	289	13.33
Girth of cane (cm)	9.2	10.8	17.33
Millable cane	5	9	80.0
Cane yield/plot (kg)	162	208	28.39

[0229] The results presented in Table 17 show increases in the number of tillers, plant height, and girth of cane, millable cane, and cane yield inoculated with the consortium of B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488 using charcoal as carrier, compared with un-inoculated control.

EXAMPLE 21

[0230] Field Trial of Plant Growth Promotion Activity of the Consortium of B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488 Using Fermented Sugar Factory Sulphitation Press Mud and Distillery Spent Wash as Carrier, on Sugarcane at Dhampur

[0231] Field trials using sugarcane were conducted by placing sugarcane sets at the time of sowing directly on fermented sugar factory sulphitation press mud and distillery spent wash as carrier, containing the consortium of B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488, prepared as described in Example 14. Sugarcane trial was set up in May, 2001 at Dhampur Sugar Mills Ltd., Dhampur. After ten months of plant growth number of tillers, plant height, girth of sugarcane, millable cane, and cane yield were noted in December, 2001. For the field trials sugarcane variety Cos-89003 was used at Dhampur Sugar Mills Ltd., Dhampur. The test results of the field trials of plant growth promotion activity of the consortium of B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488 using fermented sugar factory sulphitation press mud and distillery spent wash as carrier, on sugarcane are given in Table 18.

	TABLE 18
	Treatment
	Un-inoculated		% increase over
Observations	control	Inoculated	control
Number of tillers/plant	6.2	14	125.8
Plant height (cm)	248	285	14.91
Girth of cane (cm)	6.4	11.2	75.0
Millable cane	6	11	83.33
Cane yield/plot (kg)	164	237	44.51

[0232] The results presented in Table 18 show increases in the number of tillers, plant height, girth of cane, millable cane, and cane yield inoculated with the consortium of B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488 using fermented sugar factory sulphitation press mud and distillery spent wash as carrier, compared with un-inoculated control.

EXAMPLE 22

[0233] Field Trial of Plant Growth Promotion Activity of the Consortium of B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488 Using Fermented Sugar Factory Sulphitation Press Mud as Carrier, on Sugarcane at Dhampur

[0234] Field trials using sugarcane were conducted by placing sugarcane sets at the time of sowing directly on fermented sugar factory sulphitation press mud and distillery spent wash as carrier, containing the consortium of B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488, prepared as described in Example 14. Sugarcane trial was set up in May, 2001 at Dhampur Sugar Mills Ltd., Dhampur. After ten months of plant growth number of tillers, plant height, girth of sugarcane, millable cane, and cane yield were noted in December, 2001. For the field trials sugarcane variety Cos-89003 was used at Dhampur Sugar Mills Ltd., Dhampur. The test results of the field trials of plant growth promotion activity of the consortium of B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488 using fermented sugar factory sulphitation press mud as carrier, on sugarcane are given in Table 19.

	TABLE 19
	Treatment
	Un-inoculated		% increase over
Observations	control	Inoculated	control
Number of tillers/plant	6.2	16	158.0
Plant height (cm)	248	313	26.2
Girth of cane (cm)	6.4	12.0	87.5
Millable cane	6	11.8	96.6
Cane yield/plot (kg)	164	256	56.0

[0235] The results presented in Table 19 show increases in the number of tillers, plant height, girth of cane, millable cane, and cane yield inoculated with the consortium of B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488 using fermented sugar factory sulphitation press mud as carrier, compared with un-inoculated control.

EXAMPLE 23

[0236] Field Trial of Plant Growth Promotion Activity of the Consortium of B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488 Using Fermented Sugar Factory Carbonation Press Mud as Carrier, on Sugarcane at Rozagaon

[0237] Field trials using sugarcane were conducted by placing sugarcane sets at the time of sowing directly on fermented sugar factory carbonation press mud as carrier, containing the consortium of B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488, prepared as described in Example 15. Sugarcane trial was set up in May, 2001 at Dhampur Sugar Mills Ltd., Rozagaon. After eight months of plant growth number of tillers, plant height, girth of sugarcane, millable cane, and cane yield were noted in December, 2001. For the field trials sugarcane variety Cos-96258 was used at Dhampur Sugar Mills Ltd., Rozagaon. The test results of the field trials of plant growth promotion activity of the consortium of B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488 using fermented sugar factory carbonation press mud as carrier, on sugarcane are given in Table 20.

	TABLE 20
	Treatment
	Un-inoculated		% increase over
Observations	control	Inoculated	control
Number of tillers/plant	6	13	116.6
Plant height (cm)	230	265	15.22
Girth of cane (cm)	7.2	9.5	31.94
Millable cane	5	11	120.0
Cane yield/plot (kg)	182	280	53.85

[0238] The results presented in Table 20 show increases in the number of tillers, plant height, girth of cane, millable cane, and cane yield inoculated with the consortium of B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488 using fermented sugar factory carbonation press mud as carrier, compared with un-inoculated control.

EXAMPLE 24

[0239] Comparative Analysis of Effect of Pesticides on the Growth of B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488

[0240] The 3 bacterial strains B. lentimorbus, NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488 were screened to evaluate the effect of pesticides on its growth as follows: Evaluation of the effect of pesticides on the growth of the bacterial strains in broth was carried out using Erlenmeyer flasks (150 ml) containing 40 ml of medium inoculated in triplicate with the bacterial strain (100 μl inoculum with approximately Log 6 cfu/ml). Value refers to the number of cells (Log cfu/ml) of strains when individually grown for 1 day in NB, at 30° C. in the presence of pesticide, as per recommended dose of its application. The effect of pesticide on its growth has been presented in Table 20. Inoculated batch cultures, without any pesticides, served as control. Flasks were incubated for 1 day at 30° C. on a New Brunswick Scientific, USA, Innova Model 4230 refrigerated incubator shaker at 180 rpm.

TABLE 21
Pesticide	Log cfu/ml
(Active ingredient)	Recommended dose	B-30486	B-30487	B-30488
Control	0		7	9	7
FUNGICIDES
Mancozeb 75% WP*	3	g/L	2	2	NG**
Copper oxychloride 50% WP	6	g/L	5	2	3
Chlorothalonil 75% WP	3	g/L	NG	2	NG
Tridemorph 80% EC***	2	ml/L	5	6	NG
Triadimefon 25% WP	4	g/L	5	6	5
Carbendazim 50% WP	4	g/L	8	10	10
Carboxin 75% WP	4	g/L	5	3	NG
Metalaxyl 8% + Mancozeb	2	g/L	10	10	10
64% WP
Thiophanate-Methyl 70% WP	3	g/L	5	9	8
INSECTICIDES
Monocrotophos 36% SL****	1	ml/L	3	10	5
Dimethoate 30% EC	2	ml/L	4	7	5
Oxydemeton-methyl 25% EC	2	ml/L	7	9	7
Deltamethrin 2.8% EC	2	ml/L	10	10	10
Endosulfan 35% EC	2	ml/L	6	7	5
Dicofol 18.5% EC	2.7	ml/L	NG	5	3
Chlorpyriphos 20% EC	2.5	ml/L	3	5	3
*WP = Wettable powder;
**NG = No growth;
***EC = Emulsifying concentrate;
****SL = Soluble liquid

[0241] The results presented in Table 21 demonstrate variable response of pesticides on the growth of B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488. Among various pesticides tested carbendazim 50% W.P., metalaxyl 8%+mancozeb 64% W.P., and deltamethrin 2.8% E.C. were most compatible for application with B. lentimorbus NRRL B-30486, B. subtilis NRRL B-30487, and B. lentimorbus NRRL B-30488.

[0242] It is understood that the foregoing detailed description is given merely by way of illustration and that modification and variations may be made therein without departing from the spirit and scope of the invention.

Claims

1. A synergistic composition useful as bioinoculant, said composition comprising bacterial strains of accession Nos. NRRL B-30486, NRRL B-30487, and NRRL-B 30488, individually or in all possible combinations, and optionally carrier.

2. A composition as claimed in claim 1, wherein the strains NRRL B-30486, and NRRL B-30488 belongs to the group Bacillus lentimorbus.

3. A composition as claimed in claim 1, wherein the strain NRRL B-30487 belongs to the group Bacillus subtilis.

4. A composition as claimed in claim 1, wherein the strain NRRL B-30486 shows characteristics as shown below:

5. A composition as claimed in claim 1, wherein the strain NRRL B-30487 shows characteristics as shown below:

6. A composition as claimed in claim 1, wherein the strain NRRL B-30488 shows characteristics as shown below:

7. A composition as claimed in claim 1, wherein carrier is selected from a group comprising vermiculite, charcoal, a mixture of fermented sugar factory sulphitation press mud and distillery spent wash, and sugar factory carbonation press mud.

8. A composition as claimed in claim 1, wherein ratio of three strains is about 1:1:1.

9. A composition as claimed in claim 1, wherein total concentration of strains is 4-10 cfu/g of carrier and preferably 6-8 cfu/g of carrier.

10. A compositions claimed in claim 1, wherein concentration of each strain is 4-10 cfu/g of carrier and preferably 7-8 cfu/g of carrier.

11. A composition as claimed in claim 1, wherein generation time of the strains is 55-65 minutes at 30° C.

12. A composition as claimed in claim 1, wherein said strains colonize plant roots.

13. A composition as claimed in claim 1, wherein said strains survive all the seasons of the plant.

14. A composition as claimed in claim 1, wherein said strains survive for at least 2/3 years in the composition.

15. An in vitro method of isolating bacterial strains of accession nos. NRRL B-30486, NRRL B-30487, and NRRL-B 30488, from the milk of cow ‘Sahiwal’, said strains having properties, comprising controlling phytopathogenic fungi, promoting plant growth, having tolerance for abiotic stresses, solubilizing phosphate under abiotic stress conditions, producing anti-fungal metabolites, said method comprises steps of: (a) collecting milk for cow ‘Sahiwal’, (b) plating milk on a culture medium, (c) incubating the culture at temp of 25-35° C., for about 1-3 days, (d) selecting all morphologically distinct bacteria from culture, (e) screening said strains selected in step (d) which will suppress phytopathogenic fungi by showing a zone of inhibition of at least 2 mm, by incubating at 30-35° C. preferably 28° C., for 20-35 days, preferably 27 days, (f) screening said strains selected in step (e) for plant growth promotery bacteria showing at least 5% increase in dry weight of plant, by growing plants in the presence of selected bacteria in a concentration of bacteria ranging between about Log 6 to 10 CFU/seed or about Log 6 to 8 CFU/gram of soil, (g) screening said strains selected in step (f) at 4-8% salt stress tolerance for further selection, (h) screening said strains selected in step (g) at pH 4-10 stress tolerance for further selection, (i) screening said strains selected in step (h) at 50-60° C. temperature stress tolerance for further selection, (j) screening said strains selected in step (i) for ability to solubilize phosphate under abiotic stress conditions of high salt, pH, and temperature for further selection, and (k) isolating the desired three bacterial strains.

16. A method as claimed in claim 15, wherein plant for growth promotery activity is selected from a group comprising Zea mays, Abelmoschus esculentus, Laffa cylindrica, Lycopersicon esculentum, Abelmoschus esculentus, and Cucumis sativus.

17. A method as claimed in claim 15, wherein culture medium is Nutrient Agar, said medium comprising beef extract (2-10 gms), peptone (5-15 gms), sodium chloride (2-10 gms), agar (10-20 gms), distilled water (about 1.0 L), with pH ranging between 7.0-7.4.

18. A method as claimed in claim 15, wherein pH tolerance is tested at 30° C.

19. A method as claimed in claim 15, wherein soil moisture is ranging between 15-30%, preferably 20%.

20. A method as claimed in claim 15, wherein salt is preferably NaCl.

21. A method as claimed in claim 15, wherein the strains are grown on Nutrient Broth (NB) medium consisting of Beef extract (0.5%), peptone (1%), NaCl (0.5%), and distilled water, with pH of the medium is 7.2.

22. A method as claimed in claim 15, wherein pathogenic fungus are selected from a group comprising F. moniliforme, C. falcatum, F. oxysporum f. sp. ciceri, R. solani, Pythium sp., Phoma sorghii, Sclerotium rolfsii, alternaria solani, curvularia lunata, sclerotinia sclerotiorum, and aspergillus niger.

23. A method as claimed in claim 15, wherein concentration of the strains is ranging between 4-10 CFU/ml.

24. A method as claimed in claim 15, wherein phosphate solubilization increases by about 428% upon a combined increase of temperature, salt, and pH.

25. A method as claimed in claim 15, wherein phosphate solubilization increases by about 160% with increase in salt concentration.

26. A method as claimed in claim 15, wherein phosphate solubilization increases by about 130% with increase in pH.

27. A method as claimed in claim 15, wherein strains are selected for high pH stress tolerance at preferably pH 9.

28. A method as claimed in claim 15, wherein strains are selected for 55° C. temperature stress tolerance.

29. A method as claimed in claim 15, wherein selecting bacteria demonstrating best results in terms of less seedling mortality, and better seedling germination, plant height, number of pods and seed dry weight.

30. A method as claimed in claim 15, wherein plant promotery activity goes up by 3-400%.

31. A method as claimed in claim 15, wherein concentration of fungi is ranging between 4-7 spores/ml of culture medium.

32. A method as claimed in claim 15, wherein abiotic stress conditions for solubilization of phosphate are selected from a group of conditions comprising high pH ranging between 7-9, high temp ranging between 30-45, and salt concentration ranging between 0.1-4%.

33. A method of preparing plant growth promotery formulation comprising bacterial strains of accession Nos. NRRL B-30486, NRRL B-30487, and NRRL-B 30488, individually or in all possible combinations, and carrier, said method comprising steps of: (a) growing bacteria in a culture, individually to a concentration of about Log 8 to 11 cfu/ml, preferably log 9 to 10 cfu/ml, optionally followed by mixing the cultures in equal ratio in case of preparing a consortium, (b) diluting the said culture with water in the ratio of 1:50 to 1:150, preferably 1:100, containing approximately Log 8-9 cfu/ml of bacteria, (c) spraying about 1-3 liter of the culture/ton of freshly homogenized carrier preferably 2 liter of the culture/ton of freshly homogenized carrier and mixing, (d) churning the windrows daily at least twice a day for about 2 days, to increase the temperature of the windrows up to 70-75° C., (e) spraying spent wash or water into the churning windrow for about 40 days to maintain moisture level of about 55-65%, (f) churning the windrows further for another 3-5 days, now to reduce the moisture and temperature of the fermented product to about 30% and 40-45° C., and (g) packaging plant growth promoting bioinoculant ready for its application.

34. A method as claimed in claim 33, wherein carrier is selected from a group comprising fresh sulphinated press mud and carbonation press mud.

35. A method as claimed in claim 33, wherein culture medium is NB medium.

36. A method as claimed in claim 33, wherein homogenizing the mixture manually and by using an aero tiller.

37. A method as claimed in claim 33, wherein said formulation demonstrating maximum viability, under varied storage or greenhouse or field condition.

38. A method as claimed in claim 33, wherein ratio of the said strains is about 1:1:1.

39. A method as claimed in claim 33, wherein using said formulation on plants, seeds, and soil.

40. A method of using plant growth promotery formulation comprising bacterial strains of accession Nos. NRRL B-30486, NRRL B-30487, and NRRL-B 30488, individually or in all possible combinations, and carrier, said method comprising steps of applying the said biomoculant in a liquid or dry form to seeds, plants, and soil.

41. A method as claimed in claim 40, wherein the said bioinoculant also containing the gums or sugars to improve adhesion.

42. A method as claimed in claim 40, wherein the strains are in the ratio of 1:1:1.

43. A method as claimed in claim 40, wherein the said formulation demonstrates maximum viability, under varied storage or greenhouse or field condition.

44. A method as claimed in claim 40, wherein the carrier is selected from a group comprising fresh sulphinated press mud and carbonation press mud.

45. A method as claimed in claim 40, wherein the plants of the variety to be tested for plant growth promotion in the field in the presence of bacteria in a concentration of about Log 7-9 cfu/seed or about Log 6-8 cfu/gram of soil.

46. A method as claimed in claim 40, wherein using formulation alone or in combination with other chemicals which is harmless to the growth and survival of bacteria.

47. A method as claimed in claim 46, wherein the chemicals are selected from a group comprising pesticides, fertilizers, nematicides, and herbicides, with or without for example lime pelleting to limit the severity of the effect of these materials.

48. The method of making a composition useful as bioinoculant, said composition comprising one or more of novel bacterial strains of accession Nos. NRRL B-30486, NRRL B-30487, and NRRL-B 30488 and a carrier, said method comprising steps of: (a) culturing said bacterial strains in a growth medium to log phase, (b) diluting the said culture with water in the ratio ranging between 1:10 to 1:100000, with preferable ratio of 1:100, (c) mixing the said diluted culture with an inert powdered carrier, with the moisture level of the mixture ranging between 20-40%, preferably about 30% on a wet basis, (d) incubating the said mixture for at least about two days, maintaining constant moisture level in said mixture, (e) increasing the bacteria count in the said mixture to a range of about log 4-10 CFU/g of carrier, and (f) monitoring the survival rate of the bacteria over the period of at least one year in the said composition, wherein the bacterial strains are present preferably in a range from about Log 7 to 9 CFU/g of carrier, showing long survival rate of microbes as inoculate.

49. A method as claimed in claim 48, wherein carrier is selected from a group comprising vermiculite, charcoal, a mixture of fermented sugar factory sulphitation press mud and distillery spent wash, and sugar factory carbonation press mud, rice husk, carboxymethyl cellulose, peat, perlite, talc, and polyvinyl pyrrolidone.

50. A method as claimed in claim 48, wherein preferred carriers are selected from a group comprising vermiculite, charcoal, and fermented press mud.

51. A method as claimed in claim 48, wherein bacterial count is most preferably about Log 8 CFU/g of carrier.

52. A method as claimed in claim 48, wherein plants for growth promotion are selected from a group comprising chickpea, A. esculentus, and C. sativus, and Z. mays, and Triticum aestivum, and Glycine max, and Pisum sativum, and Impatiens balsamina.

53. A method as claimed in claim 48, wherein ratio of strains is about 1:1:1, in case of a consortium.

54. A method as claimed in claim 48, wherein growth medium is NB medium.

55. A method as claimed in claim 48, wherein growing bacteria individually to a concentration of about Log 9 to 10 CFU/ml followed by mixing the cultures in the ratio of about 1:1:1.

56. A method as claimed in claim 48, wherein diluting the culture with water preferably in the ratio of 1:10, containing approximately Log 8-9 cfu/ml.

57. A method as claimed in claim 48, wherein moisture of the product is regulated with windrows.