US20100178303A1

US20100178303A1 - Stable organic-carrier-based microbial inoculants and method for producing the same

Info

Publication number: US20100178303A1
Application number: US12/663,222
Authority: US
Inventors: Saturnina Halos; Ponciano Halos
Original assignee: Individual
Current assignee: Individual
Priority date: 2007-06-21
Filing date: 2007-06-21
Publication date: 2010-07-15
Also published as: EP2126043A2; WO2008156380A2; EP2126043A4; WO2008156380A3; AU2007355202A1; US20130239633A1; WO2008156380A4; US9499447B2; AU2007355202B2

Abstract

The present invention relates to methods for producing microbial preparations for crop production and microbial preparations produced through such methods. The formulations contain microbial inoculants like Azospirillum spp. which are grown in a complex medium, lyophilized with powdered milk and further supplemented with minerals and vitamins, starch and inert substances such as talc, chalk and diatomaceous earth. The products manufactured by such methods have shelf-lives of more than 3 years. They are used to inoculate seeds, seedlings and planting materials among different agriculture and forestry species for enhancing root, root hair an shoot formation, enabling plants to efficiently use soil nutrients, supplying plants with nitrogen from the air, tolerating drought and protecting plants from root pathogenes.

Description

FIELD OF INVENTION

The present invention relates to microbial preparations for crop production.

BACKGROUND ART

The present invention relates to microbial preparations for crop production, specifically microbial inoculants incorporated in carriers that provide protection for the colonizing microorganisms and the method for producing the same.
In theory, microbial inoculants, without human intervention, have a low survival rate and efficiency in their natural soil environment because of the insufficient colony forming units per gram soil. Since the 1950's, biofertilizers that have an increased colony increased inoculum potential concentration have been developed and commercialized. There are three basic types of biofertilizers: liquid-phase, suspension- or, solid carrier-based microbial inoculants. Commercial biofertilizers effectively enhance soil fertility because they contain sufficient cells of efficient strains of specific microorganisms, that can fix atmospheric nitrogen, solubilize/mineralize phosphorous and potash or decompose organic wastes and augment plant growth with hormones and other growth promoting substances with their biological activities.
The present invention is a carrier-based biofertilizer that promotes growth of plants of any type of terrestrial biome, using special biological inoculants, such as plant growth promoting rhizobacteria. The invention induces extensive root and root hair formation, enable plants to efficiently use soil nutrients, supply plants with nitrogen from the air, increase drought tolerance and protect the plants from pathogens. Further, the inoculant can be mixed with an insecticide or fungicide without any appreciable decrease in effectivity.
The closest prior art are reported in WO 2007/014974 (“Aseptic Mycorrhization Inoculant and In vitro and Ex vitro Application Methods”), WO 1994/006732 (“Method for Obtaining a Wettable Powder Inoculant for Use with Leguminous Crops”), WO 2006/070061 (“Stable Microbial Inoculants and Methods for Production of Them”), WO 2002/015702 (“A Thermo-stable Bio-matrix”), and WO 2000/034440 (“Microorganisms for Improving Plant Productivity”).
According to WO 2007/014974 (“Aseptic Mycorrhization Inoculant and In vitro and Ex vitro Application Methods”), a low-viscosity, light, semi-solid agar-type base culture medium is used to facilitate the penetration of the root in the inoculant, as well as to potentiate and preserve the infectiousness of arbuscular mycorrhizal fungi, such as those of the present invention. WO 2007/014974 sought to obtain the advantage of being as effective in in vitro as well as ex vitro inoculation by using a semi-solid inoculant. However, it is gel-based and has a short shelf-life, which the present invention seeks to address.
WO 1994/006732 (“Method for Obtaining a Wettable Powder Inoculant for Use with Leguminous Crops”) reports a method for obtaining a wettable powder inoculant formulation for use with leguminous crops, comprising the industrialization of an inoculant for leguminous from a centrifugated biological mass of Rhizobium spp twice immersed in a cryogenic protective solution rich in sugar and protein which is subjected to a lyophilization method. Like the present invention, it is formulated with substances rich in polysaccharides and associated with a cellular protector which substitutes the previously used peat support. It also has a long shelf life of up to 25 months even when stored at room temperature. However, WO 1994/006732 can only be used for leguminous crops. Further, the formulation of the carrier uses sugar and protein while the present invention uses milk and glycerin. Also, WO 1994/006732 does not teach that the powder inoculant with a pest protectant such as an insecticide.
WO 2006/070061 (“Stable Microbial Inoculants and Methods for Production of Them”) teaches away from the present invention. It describes water containing microbial inoculants in paste form with shelf life of at least 3 months, preferably 12 months. It reports that drying, which is a method utilized in the present invention is complicated, expensive and may even be impossible.
WO 2002/015702 (“A Thermo-stable Bio-matrix”) reports a method for producing a thermo-stable biodegradable medium for storage of biological materials wherein the biological material includes: a pesticide; a viricide; a bacteriacide; a fungicide; and a combination of these. While the method is similar in that the biological material can be safely mixed with potentially degradative substances such as pesticides, viricides, bacteriacides, fungicides or a combination of these, the medium is structurally different because it is gel-based and contains a biopolymer selected from the group of xanthan gum, acacia gum, guar gum, gellan, starch or a combination thereof, unlike the present invention which is in powder form. Thus, it is no surprise that WO 2002/015702 discloses a maximum shelf life of only eighteen (18) months, which is considerably shorter than that of the present invention which allows storage of at least three (3) years.
WO 2000/034440 (“Microorganisms for Improving Plant Productivity”) is directed to microbes which includes the microorganism Azospirillum brasilense, which belongs to the same genus as some of those in the present invention. As with the present invention, two specific strains of microbial inoculant of WO 2000/034440 is effective for increasing the productivity of both nonlegume and legume plants as well as vegetable plants over a wide variety of soil types and climates. However, the WO 2000/034440 is narrowly directed only to the Azospirillum brasilense, a microorganism not covered by the present application. Further, it does not teach an inventive carrier nor the method of production that prolongs its shelf life.
The present invention, the microbes, method and product, are absolutely different and improve over other known methods and products and have considerable advantages over the nature and quality of the methods and products, particularly in the storage life of the microbial preparation.

DISCLOSURE OF THE INVENTION

The present invention relates to microbial preparations for crop production such as seed, seedling and other planting material inoculants have been the subject of many researches in the past 25 years in the Philippines. They have been shown to be useful in increasing and protecting crop yields. However, they have not been put into commercial production because of their short shelf-lives which limit their effective distribution. This is also true of microbial inoculants for processing foods. Prior art discloses a shelf life of a maximum of only eighteen (18) months. This invention is intended to solve this problem of short shelf-lives and allow for the viable commercialization of microbial inoculants. The invention is expected to produce products with a huge market since biochemical catalysts including microbial preparations have agricultural, food and forestry applications.
The invention covers dried, semi-solid and related formulations of microbial inoculants like Azospirillum spp. and Bacillus pumilus. These bacteria are used to inoculate seeds and seedlings of different agriculture and forestry species to promote among others, the extensive root and root hair formation, enable plants to efficiently use soil nutrients, supply plants with nitrogen from the air, increase drought tolerance and protect the plants from root pathogens. These formulations are prepared in the following manner:
The microbes such as Azospirillum spp. And Bacillus pumilus are grown in fermentors using special media which contain substrates including high protein feed ingredients such as fish meal/bone meal/blood meal/soya meal, table sugar and tablet salt at 30° C. The baterial cells are harvested by methods like filtration or centrifugation, added with powdered milk/glycerol to wet the cells and the Azospirillum mixture lyophilized. The products are formulated under sterile conditions with different proportions of components like the bacterial preparations, minerals, milk, vitamins and flour with or without talc/chalk/diatomaceous earth using standard mechanical devices. The dried and semi-solid products are packed or the tablets are made usually under sterile conditions.
The products as invented have extended the shelf-lives of the biochemical catalysts/microbial preparations by at least 3 years way beyond the 3 months observed with the non-lyophilized or other inoculants now available in very limited amounts in the market. The special media used to grow the bacteria improve the tolerance of the bacteria to lyophilization. Milk not only improves the tolerance of the bacteria to lyophilization; it also provides some vitamins, carbohydrates and minerals for a good start of the bacteria with inoculated plants. Bacillus pumilus need not be lyophilized because it is a spore former and can resist adverse conditions for many years. The added vitamins, minerals, flour and talc/chalk/diatomaceous earth also provide additional nutrients to selectively enrich the growth of the desired bacteria and the inoculated plants in problem soils with limiting micronutrients.

Characteristics of the Microorganisms

Azospirillum is made up of curved rod cells, 1 mm in diameter with varying sizes and shapes. It can have polar and peritrichous flagella and undergoes encystment. Its pinkish, whitish orange colonies vary in shape and surface characteristics. Carbon sources include organic acids and sugars. The nitrogen sources are amino acids, N₂, NH₄ ⁺ and NO₃. Respiration can be aerobic, microaerophilic or anaerobic. It is capable of aerotaxis, chemotaxis and can form clumps.
Bacillus pumilus consists of rod-shaped cells, which can form endospores that are very resistant to many adverse conditions. Sporulation is not repressed by exposure to air. It is gram positive, or positive only in the early stages of growth, or negative. The flagellation is peritrichous or degenerately peritrichous. It can be aerobic or facultatively anaerobic. Oxygen is the terminal electron acceptor. Colony morphology and size are very variable on some media. It exhibits a wide diversity of physiological ability; psychrophilic to thermophilic; acidophilic to alkaliphilic. Some strains are salt tolerant while others have a specific requirement for salts. Catalase is formed but may be oxidase positive or negative. It requires biotin and some strains also require amino acids. Spores formed occur ubiquitously. The mole % G+C of the DNA ranges from 39.0-46.9 for 37 strains. DNA-DNA hybridization studies indicate that the species is genetically homogenous.
The depository institution for these isolates is the UP-NSRI Culture Collection at Diliman, Quezon City. File numbers of some culture deposits are stated below while others will be submitted when already available.


	Azospirillum halopraeferens	UPCC 1370
	Azospirillum lipoferum	UPCC 1371
	Bacillus pumilus	UPCC 1372
	Azospirillum SC/PH	UPCC 1373
	Azospirillum AH/EH	UPCC 1374

Shelf Life

Extensive literature attests that such dried dormant microbial cells can remain viable for years. To further protect the product from environmental assault, nutrients that serve as buffer against changes in temperature and other environmental shock as well as provide the initial growth factors for the microbes to grow once the product gets wet and the cells start metabolizing. However, the product is vulnerable to fungal growth and/or grain beetles which considerably shorten its shelf life. Experiments were then conducted to test the inclusion in the product of fungicides and insecticides.
Two commercial fungicidal preparations and two insecticidal preparations (organic and synthetic) were added to the microbial preparation following manufacturer's recommended dosages. Liquid organic pesticides were absorbed in flour and added to the microbial preparation. These products were kept in storage for 6 months-3 years.
All products added with fungicides and insecticides did not show any infection nor infestation within the 3 years that these were kept in storage. All products tested showed the expected effect of a viable, healthy microbe: reduced inorganic fertilizer requirement in all the crops tested (rice, corn, pepper, onions, garlic, et. al), protection from bacterial leaf blight infection in rice and fungal root rot in onion, early maturity in rice, robustness and greenness of treated crops.
In an alternative embodiment, a pesticide, a viricide, a bacteriacide, a fungicide, or a combination of these may be added to the microbial inoculant to further prolong its shelf life.
Protection is being sought for preparation of biochemical catalysts/biofertilizers characterized by the 1) addition of vitamins and minerals among others, 2) harvesting by methods including centrifugation/filtration, and 3) lyophilization accompanied by skim milk with myo-inositol or glycerol or b) skim milk with honey, 4) the mixing of plant growth promoting rhizobacteria like Azospirillum halopraeferens, Azospirillum lipoferum, Azospirillum SC/PH or Azospirillum AH/EH cells with carriers like sugar, flour, talc/chalk/diatomaceous earth 5) an insecticide, a viricide, a fungicide, or a combination of these and 6) in powder, semi-solid, liquid or other forms, the products have extended shelf-lives of more than 3 years. These innovations make these products different from other formulations. They can induce changes like extensive root proliferation, drought tolerance, increased crop growth, yield and farmers' net incomes, beside being environment-friendly.

Claims

1. A method for producing and formulating microbial inoculants with a prolonged shelf-life, comprising:

isolating a microbial colony from a culture of a bacterial microorganism;

growing the colony in an organic medium;

harvesting the microbial cells from the organic medium;

mixing the harvested cells with milk and glycerol;

drying the microbial cells by lyophilization;

grinding the dried microbial cells into powder; and

mixing the microbial powder with nutrients, anti-contaminant and a dessicant.

2. The method according to claim 1 wherein the organic medium consists of a mixture of high protein and vitamin-supplemented feed formula.

3. The method according to claim 1 wherein harvesting of the microbial cells comprises filtration or centrifugation.

4. The method according to claim 1 wherein the anti-contaminant agent is an anti-fungal agent.

5. The method according to claim 1 wherein the pest protectant agent is an anti-viral agent.

6. The method according to claim 1 wherein the nutrients mixed with the microbial powder is selected from the group consisting of vitamins, minerals and flour and, wherein the dessicant is selected from the group consisting of talc, chalk and diatomaceous earth.

7. (canceled)

8. The method according to claim 1 wherein the bacterial microorganism is Azospirillum halopraeferens.

9. The method according to claim 1 wherein the bacterial microorganism is Azospirillum lipoferum.

10. The method according to claim 1 wherein the bacterial microorganism is Bacillus pumilus.

11. The method according to claim 1 wherein the bacterial microorganism is Azospirillum SC/PH.

12. The method according to claim 1 wherein the bacterial microorganism is Azospirillum AH/EH.

13. A biologically pure culture of Azospirillum SC/PH produced by the method comprising:

isolating a microbial colony from a culture of a bacterial microorganism, wherein the microorganism is Azospirillum SC/PH;

growing the colony in an organic medium;

harvesting the microbial cells from the organic medium;

mixing the harvested cells with milk and glycerol;

drying the microbial cells by lyophilization;

grinding the dried microbial cells into powder; and

mixing the microbial powder with nutrients, anti-contaminant and a dessicant.

14. A biologically pure culture of Azospirillum AH/EH produced by the method comprising:

isolating a microbial colony from a culture of a bacterial microorganism, wherein the microorganism is Azospirillum AH/EH;

growing the colony in an organic medium;

harvesting the microbial cells from the organic medium;

mixing the harvested cells with milk and glycerol;

drying the microbial cells by lyophilization;

grinding the dried microbial cells into powder; and

mixing the microbial powder with nutrients, anti-contaminant and a dessicant.

15. The biologically pure culture of claim 13 comprising a shelf life of at least 36 months or 3 years.

16. The biologically pure culture of claim 14 comprising a shelf life of at least 36 months or 3 years.

17. The biologically pure culture of Azospirillum SC/PH of claim 13, wherein the organic medium comprises a mixture of high protein and vitamin-supplemented feed formula.

18. The biologically pure culture of Azospirillum SC/PH of claim 13, wherein harvesting of the microbial cells comprises filtration or centrifugation.

19. The biologically pure culture of Azospirillum SC/PH of claim 13, wherein the anti-contaminant agent is an anti-fungal agent.

20. The biologically pure culture of Azospirillum SC/PH of claim 13, wherein the pest protectant agent is an anti-viral agent.

21. The biologically pure culture of Azospirillum SC/PH of claim 13, wherein the nutrients mixed with the microbial powder is selected from the group consisting of vitamins, minerals and flour and wherein, the dessicant is selected from group consisting of talc, chalk and diatomaceous earth.

22. The biologically pure culture of Azospirillum AH/EH of claim 14, wherein the organic medium comprises a mixture of high protein and vitamin-supplemented feed formula.

23. The biologically pure culture of Azospirillum AH/EH of claim 14, wherein harvesting of the microbial cells comprises filtration or centrifugation.

24. The biologically pure culture of Azospirillum AH/EH of claim 14, wherein the anti-contaminant agent is an anti-fungal agent.

25. The biologically pure culture of Azospirillum AH/EH of claim 14, wherein the pest protectant agent is an anti-viral agent.

26. The biologically pure culture of Azospirillum AH/EH of claim 14, wherein the nutrients mixed with the microbial powder is selected from the group consisting of vitamins, minerals and flour and wherein, the dessicant is selected from group consisting of talc, chalk and diatomaceous earth.

27. The bacterial microorganism of claim 8, wherein a representative sample of Azospirillum halopraeferens was deposited under UPCC 1370.

28. The bacterial microorganism of claim 9, wherein a representative sample of Azospirillum lipoferum was deposited under UPCC 1371.

29. The bacterial microorganism of claim 10, wherein a representative sample of Bacillus pumilus was deposited under UPCC 1372.

30. The bacterial microorganism of claim 11, wherein a representative sample of Azospirillum SC/PH was deposited under NRRL B-50317.

31. The bacterial microorganism of claim 12, wherein a representative sample of Azospirillum AH/EH was deposited under NRRL B-50318.