The invention discloses an isolated, biologically pure culture of a microorganism,
1. A method for controlling fungal organism, comprising applying a formulation including a microbial inoculant 2. The method of 3. The method of 4. The method of 5. The method of 6. The method of 7. The method of 8. The method of 9. The method of 10. The method of 11. The method of 12. The method of 13. A method of 14. The method of 15. The method of
[0001] The present invention relates to a biofungicide. In particular, the present invention relates to a microorganism, [0002] Diseases caused by fungal species are considered among the most widespread and damaging of plants worldwide. Presently, control of plant fungal diseases is largely dependent upon the application of certain chemicals. Although some of these chemicals are known to have negative environmental and human health problems, nevertheless such chemical agents continue to be in wide use due to their strong activity against important fungal diseases, and availability of environmentally safer and effective alternatives. [0003] Generally, biological control of diseases commonly infecting plants in the root zone (rhizosphere) and the leaf zone (phylloplane) are preferred over more traditional synthetic chemical control methodologies. Such biocontrol agents usually cause little or no injury to the plant host or the environment, and some may even favor normal plant development. However, most such biocontrol organisms are typically very limited either in the scope of their effectiveness against fungal diseases, or in their ability to survive under practical field conditions and during treatment applications. [0004] Attempts have been made to control plant fungal diseases by using certain microorganisms. For example, U.S. Pat. No. 5,589,381 (Neyra and Sadasivan, 1996) describes a [0005] It is, therefore, an object of the present invention to provide an environmentally favorable and effective biological agent for the control of a broad range of plant fungal diseases and other fungal organisms. [0006] It is a further object of the present invention to provide a formulation and a biological method for controlling plant fungal diseases utilizing a unique strain of [0007] It is an additional object of the present invention to provide a composition containing said SB3086 strain in a form suitable for application to plants. Such a composition may contain such common components known to one of ordinary skill in the art, as non-toxic surfactants, non-toxic amounts of plant nutrients, preservatives and the like, and may be in the form of active vegetative spores, liquid, flowable powder, granules, spray dried material or with another carrier material. [0008] Another object of the present invention is to provide a method for controlling plant fungal diseases utilizing the biofungicide of the present invention. The biofungicide may be applied to the shoot, the root, the seeds, vegetative propagules or as a soil or plant treatment in any suitable form, such as a liquid, a spray, a powder, root dip, a granule, a dust and the like containing active vegetative cells [0009] Various other objects and advantages of the present invention will become evident from the following brief description of drawings and from the detailed description of the invention. [0010] In the drawings, [0011] The above and various other objects and advantages of the present invention are achieved by a biologically pure culture of [0012] An important aspect of the present invention is to control plant pathogenic fungal species using biological organisms which function by natural antagonism or growth inhibition of the disease-causing fungi, thereby limiting the damage and spread of the harmful diseases. The invention in particular relates to the discovery of a novel bacterial soil isolate, [0013] It was discovered that [0014] It should be understood that unless defined otherwise, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs. Although any methods and materials similar or equivalent to those described herein can be used in the practice or testing of the present invention, the methods and materials described herein are preferred. Unless mentioned otherwise, the techniques employed or contemplated herein are standard methodologies well known to one of ordinary skill in the art. The materials, methods and examples are only exemplary and not limiting. [0015] The term “biocontrol” or “biofungicide” as used herein means controlling or eliminating the fungal activity by biological means, such as by using a bacterium, as opposed to the use of a synthetic chemical agent. [0016] The term “biosupplement” as used herein is defined as those naturally-occurring materials recognized to be of direct or indirect benefit to plant growth, hardiness, yield, or quality, other than commonly recognized inorganic nutrients and micronutrients. Examples of such biosupplements include: i) sea plant extracts, such as that obtained from the Norwegian kelp plant [0017] The term “Propagule” as used herein refers to a component or a section of a plant containing all the essential elements to enable regrowth into a full plant and/or propagation of desired plant components. Example of such propagules include: i) seeds; ii) eyes or “seedpieces”, such as from potatoes; iii) stem cuttings which may be placed under suitable growth conditions to form new roots; iv) root or rhizome section.; and the like. [0018] The natural soil microorganism, [0019] Taxonomic characteristics of [0020] [0021] Various embodiments of the invention are now described. [0022] Soil samples and root wash material were gathered from healthy plant and turf roots and adjacent areas. Individual isolates were obtained by dilution plate analysis on a variety of solid growth media in such a way as to select for bacterial strains capable of spore-formation. Specifically, roots of vegetable and turfgrass plants were washed in a sterile phosphate buffer, then heated at 80° C. for 10 minutes. The heat-shocked washing was subsequently diluted in fresh buffer at 10-fold increments, and spread onto Standard Methods agar plates and incubated overnight at 32° C. Individual colonies were separately cultured and screened for the ability to inhibit the indicator fungus Geotrichum, as well as certain other plant-pathogenic fungi. Those able to inhibit this indicator fungus, were selected for further comparative testing against additional plant pathogenic fungal species. To assess anti-fungal activity on indicator plates, a small circular plug (4 mm) of the target fungus (taken from a culture growing on semi-solid medium) was placed in the center of a sterile 15 cm petri plate containing commercially available Potato Dextrose Agar. At the same time, 5 μl volumes of individual overnight cultures of the candidate bacterial isolates to be tested (grown in LB broth) were separately placed approximately 3 cm from the fungal plug. Evidence of inhibition were recorded after 3-4 days incubation at 23° C. [0023] While [0024] As described in Example 1, small circular plugs were taken from actively growing cultures of the plant fungal disease pathogens: [0025] The ability of a single soil microbe such as [0026] While some strains exhibit certain anti-fungal characteristics in common with SB3086, most exhibit limited activities, and none were found to have as extensive or strong an activity as SB3086. [0027] The anti-fungal ability of [0028] Having demonstrated the broad range antifungal efficacy of SB3086 by laboratory tests, studies were undertaken to demonstrate the function and hardiness of such a biocontrol microbe under actual field conditions. This field performance ability was demonstrated for [0029] For this study, an economically important turf plant, Penncross Bentgrass, widely used in golf course and sport fields, was selected as a representative test subject. A fungal pathogen, [0030] The results are presented in [0031] To further demonstrate the breadth of field capability of [0032] The data show significant disease control by [0033] Of course, the biofungicide may be applied to the plants in any suitable form, such as a spray, a powder, a granule, a liquid and the like. A formulation containing the biofungicide of the present invention may also include such common components as a surfactant, non-toxic amounts of plant nutrients (e.g. fertilizers and micronutrients) and the like as may be suggested to one of ordinary skill in the art. [0034] A composition in accordance with the present invention is a concentrated liquid formulation which includes non-toxic amounts of plant nutrients and micronutrients, such as organic nitrogen, chelated zinc, chelated iron, as well as natural organic growth enhancing agents, such as sea plant extract. Inclusion of these ingredients, in addition to the active ingredient [0035] The concentrate is usually diluted in about 2 to 300 volumes of water and applied by foliar spray. On turfgrass, the application rate is usually 18 ounces of the preferred formulation in 2 gallons of water sprayed on 1000 sq. ft. of turf surface using suitable liquid spray equipment. Such equipment might include application though a standard irrigation system. The amount of the preferred formulation which is applied may vary from about 2 to about 36 oz/1000 sq. ft. depending on disease pressure and overall plant health. Alternatively, a dry formulation of the invention may be prepared by spray-drying the [0036] Example embodiments have now been described in accordance with the objects and advantages of the present invention. It will be appreciated that these examples are merely illustrative and not limiting of the invention. Many variations and modifications will be apparent to those skilled in the art and all such variations and modifications are included within the purview and scope of the claims.
[0037] [0038] [0039] [0040] [0041]FIELD OF THE INVENTION
BACKGROUND OF THE INVENTION
SUMMARY OF THE INVENTION
BRIEF DESCRIPTION OF DRAWINGS
DETAILED DESCRIPTION OF INVENTION
EXAMPLE 1
Isolation of
EXAMPLE 2
Performance Comparison of
EXAMPLE 3
Performance comparison of
EXAMPLE 4
Ability of
EXAMPLE 5
Field Performance of
EXAMPLE 6
Field Control of Rhizoctonia Blight Disease (Brown Patch) by
EXAMPLE 7
Composition of a Formulation
Comparative Taxonomic Characteristics of (Type (Type Characteristic SB3086 Characteristics)1,2 Characteristics)1,2 Gram Reaction + + + Cell width (μm) 0.8 0.8 0.8 Ellipsoidal spores + + + Motility + + + Anaerobic growth + + − (<1.5 ppm O2) ONPG + + +/− Growth at 55° C. + + − Gelatin Hydrolysis + + + V-P Reaction + + + Nitrate Reduction + + + Growth in 7% NaCl + + + Starch Hydrolysis + + + Citrate Utilization − +/− + Catalase Positive + + + Casein + + + Decomposition Acid from Glucose + + + Acid from Mannitol + + + Acid from + + + Arabinose Egg-yolk lecithinase − − − Comparative Anti-Disease Activity of SB3086 with other strains. Dollar Gray Leaf Rhizoctonia Helminthosporium Pink Snow Strain Spot1 Spot2 blight3 Colletotrichum Blight5 Mold4 SB3086 56 5 5 5 5 4 ATCC 25972 2 1 3 1 3 1 ATCC 53757 1 0 1 0 0 1 ATCC 14580 1 0 1 1 0 1 ATCC 11946 1 NA7 1 1 0 NA PR1-36a 1 NA 4 5 5 NA 1 2 3 4 5 6Graduated scale with 5 = strong inhibition to 0 = no inhibition 7Not assessed Fungal inhibition by soil bacterial strains Culture Type Trait A Trait B Trait A Trait B Trait A Trait B SB3086 + + + + + + SB3002 − − − − − − SB3003 − − − − − − SB3006 + + − + − +/− Soy 130 − − − +/− − − UW8 Bacillus sp. + + + + +/− − 3PMN − − − − + − HC − − − − + − SB3013 + − +/− +/− + − S1−B Pseudomonas sp. − + NA NA − − BJ−2 − + + + − + G11 Bacillus sp. + − NA NA − − VT−5 − − NA NA + − S1 Erwinia sp. − − − − − − DS1 Paenebacillus sp. − − − − − − Trait A + = Culture causes mycelia to discolor at interface. − = Culture has no apparent discoloration effect on fungus. Trait B + = Culture causes clear inhibition zone. − = Culture has no apparent inhibition zone. Comparative ability of darkening of bathroom tile and grout). Bacterial Strain SB3086 5 0 1 0 4 Field Control of Rhizoctonia blight (Brown Patch) by SB3086 Percent Disease Control (Rhizoctonia blight) Daconil ® Heritage ® Untreated Location Plant Type SB3086 (chlorothalonil) (azoxystrobin) Control Ohio State University Bentgrass 78 89 81 0 Clemson University Fescue 43 81 90 0 Virginia Polytech. Inst. Fescue 58 100 100 0 Components of a Formulation. Range (per L) Ingredient Amount (w/v) (w/v) CAS No. Purpose 0.14% 0.001-12% N/A Active Ingredient SB3086 (1.1 × 109 (1.0 × 106-1.0 × 1011 CFU/ml)1 CFU/ml) Seaweed Extract 3.0% 0-10% EPA Manuf. Organic Powder No. 67016-2 biosupplement Urea 25.2% 0-48% 57-13-6 Nutrient supplement Iron EDTA Chelate, Fe 1.95% 0-8% 15708-41-5 Micronutrient 13% Powder supplement Potassium chloride KCl 0.24% 0-10% 7447-40-7 Nutrient supplement Disodium dihydro 0.00024% 0-0.002% 10102-40-6 Micronutrient molybdate supplement Na2MoO4· 2H2O Cobalt chloride 1.0 × 10−5% 0-1 × 10−3% 7791-13-1 Micronutrient hexahydrate supplement CoCl2· 6H2O Nickel chloride 1.0 × 10−5% 0-1 × 10−3% 7791-20-0 Micronutrient hexahydrate supplement NiCl2· 6H2O Kathon CG/ICP: 5.52 ppm 1-500 ppm 26172-55-4 Preservative for 5-chloro-2-methyl-4- shelf concentrate isosthiazolin-3-one 1Colony Forming Units per ml