WO2008111719A1

WO2008111719A1 - Bacillus amyloliquefaciens k317 for suppressing the growth of antibiotics-resistant pathogenic microorganism or enteropathogenic microorganism

Info

Publication number: WO2008111719A1
Application number: PCT/KR2007/005985
Authority: WO
Inventors: Yound-Hyo Chang; Min Young Jung; Moon-Soo Rhee
Original assignee: Korea Research Institute Of Bioscience And Biotechnology
Priority date: 2007-03-13
Filing date: 2007-11-26
Publication date: 2008-09-18
Also published as: US20100021576A1; WO2008111719A8; KR100878799B1; US9080219B2; KR20080083840A

Abstract

The present invention relates to a Bacillus amyloliquefaciens K317 strain suppressing the growth of antibiotics-resistant pathogenic microorganisms or enteropathogenic microorganisms, more precisely a Bacillus amyloliquefaciens K317 strain, a culture supernatant thereof and an antibacterial metabolite separated from the same. The Bacillus amyloliquefaciens K317 strain, the culture supernatant thereof and the antibacterial metabolite separated from the same of the invention can be effectively used for the composition, health food, and probiotics for inhibiting the growth of antibiotics-resistant pathogenic microorganisms and enteropathogenic microorganisms, since they have excellent antibacterial activity and inhibition effect on the growth of methicillin resistant pathogenic microorganism and such enteropathogenic microorganism as Edwardsiella tarda, E.coli and Staphylococcus epidermidis.

Description

[DESCRIPTION]

[invention Title]

BACILLUS AMYLOLIQUEFACIENS K317 FOR SUPPRESSING THE GROWTH OF ANTIBIOTICS-RESISTANT PATHOGENIC MICROORGANISM OR ENTEROPATHOGENIC MICROORGANISM

[Technical Field]

The present invention relates to a Bacillus amyloliquefaciens K317 strain suppressing the growth of antibiotics-resistant pathogenic microorganisms or enteropathogenic microorganisms, more precisely a Bacillus amyloliquefaciens K317 strain, a culture supernatant thereof and an antibacterial metabolite separated from the same.

[Background Art]

Among many pathogenic microorganisms, the one casing trouble most over the world is Staphylococcus aureus, which is a Gram-positive coccus detected in approximately 30% of the total earth population and is known as a pathogen causing nosocomial infection (Isabel CV, Robert S. K., Francisco A. K., J. Am. Acad. Dermatol. 50:845-849, 2004). This bacterium causes infection primarily on skin and soft tissue, leading to pyoderma, and further induces systemic infection threatening a life such as osteomyelitis, endocarditis, sepsis and bacteremia (Henry Shinefield, M. D. et al . , The New England J. of Med. 346:491-496, 2002). Antibacterial agents for Staphylococcus aureus such as penicillin and methicillin have been used as a therapeutic agent for the infection over decades owing to their excellent antibacterial effect. However, since the strain exhibiting methicillin resistance (methicillin-resistant Staphylococcus aureus: MRSA) was first reported in England in 1961, the number of such antibiotics-resistant strains has been increasing (Standing Medical Advisory Committee, Department of Health, 1998).

The appearance of antibiotics resistant strains resulted from reckless overuse of antibiotics is also a serious problem in Korea. For example, the population of methicillin resistant strains reaches around 50% and according to the recent investigation by Korean Society for Nosocomial Infection Control, the rate of MRSA strains separated from most university hospitals and general hospitals reaches 70-80%. Therefore, it is required to develop a sanitary, safe and effective therapeutic agent for MRSA.

Korean Patent Application No. 2004-55648 describes that Streptomyces laidlogenes DS684 isolated from soil has the inhibitory effect on methicillin and vancomycin resistant strains, and Korean Patent No. 654370 describes that Lactobacillus ruminus SPM0211 has the inhibitory effect on vancomycin resistant strains .

Probiotics indicate the microorganism balancing intestinal microflora, the microorganism having antibacterial and enzyme activities and the product produced by the same (Fuller, R. J Appl Bacterlol . 66(5) :365-378, 1989). Probiotics are also defined as live bacteria in the form of single strain or combined strains which can be supplied to human or animals in the form of dried cells or fermented products to improve intestinal microflora. Therefore, the probiotics use human intestines as a habitat and need to survive until they reach intestines as nonpathogenic and non-toxic. Further, the probiotics have to maintain the survival rate and activity in the product carrying the probiotics until they are consumed and have to be sensitive to antibiotics used for the prevention of infection and at the same time must not contain antibiotics resistant plasmid. Besides, the probiotics have to have resistance against acid, enzyme and bile in intestines (Mishra, C. et al. , Asia Pacific J Clin Nutr. 5:20-24, 1996).

Probiotics are exemplified by Bacillus sp. having excellent digestive enzyme (amylase, protease, lipase, cellulose and phosphatase) producing capacity, Lactobacillus sp. capable of decomposing low molecular carbohydrates by producing organic acid, Saccharomyces sp. facilitating absorption in intestine after converting into lactic acid and vitamin B synthesis and vitamin E absorption as well, and Photosynthetic bacteria suppressing foul smell by metabolizing malodorous substances (ammonia, hydrogen sulfide, amines, etc.) remaining in feces of cattle.

In particular, Bacillus sp. and Lactobacillus sp. are generally called lactic acid bacteria (LAB) and separated from food. These species include strains that produce antibacterial substances working against saprogenic bacteria to prevent food from being rotten, which makes them very valuable probiotics (Tagg, G. U. et al., Bacteriol. Rev. 40:772-756, 1976). These lactic acid bacteria produce antibacterial peptide, so called bacteriocin, having antibacterial mechanism which has nothing to do with antibiotics resistance mechanism. Bacteriocin is not like the conventional antibiotics and is difficult to be defined precisely, since bacteriocin is not typical in molecular weight, biochemical characteristics, antibacterial spectrum to host or mechanisms. Klaenhammer defined bacteriocin as protein or protein complex that has antibacterial activity direct to those species close to bacteriocin producing bacteria (Klaenhammer, TR. Biochimie 70:337- 379, 1998). The substances having antibacterial activity are suggested as "bacteriocin-like substances" even though they are not the typical ones identified according to the standard (Tagg, G. U. et al. , Bacteriol. Rev. 40:772-756, 1976). There is no boundary fixed among antibiotics, bacteriocins and microcins, but bacteriocins are classified into bacteriostatics or bacteriocidals according to their activity spectrum and belong to peptide antibiotics group. Antibiotics are produced by non-ribosomal synthesis based on several steps of enzymatic mechanism. In the meantime, bacteriocins are generated by ribosomal synthesis and rarely have resistance but seem to have potential for resistance (Hurst A. Adv Appl Microbiol 27:85-123, 1981; Harvis, B., Farr, J. Biochim Biophys Acta 227:232-340, 1971; Harris, LJ. et al., J Food Prot 52:384-387, 1989). Lots of antibiotics can be chemically synthesized but no chemical synthesis of bacteriocins has been reported, yet. With the advancement of genetic engineering techniques, bacteriocin-like substances can be reconstructed and recombinated, precisely lipids or carbohydrates take a part of bacteriocin complex. Bacteriocin can be adhered on cells or released out of the cells, can be generated before and after growth cycle, has resistance against such enzymes as protease, and is stable against pH and temperature. Antibacterial mechanism of bacteriocin has not been disclosed, yet, and only thing that has been reported is that bacteriocin is stuck in cell membrane channel to induce cell lysis. Cell lysis is directly associated with cell death and depends on sensitive bacteria having non-specific receptor site and specific receptor site (Bhunia, AK. et al._r J Appl Bacterlol 57:492-498, 1991). Bacteriocin with these characteristics is rising as alternative antibiotics and is acknowledged as a safe antibacterial agent used as a food preservative.

Bacillus is a very interesting and industrially important species applicable in various industries, particularly regarding antibacterial activity, because it can produce numbers of peptide antibiotics and is safe for food and industrial use (Paik, H. D. et al . , J. Ind. Microbiol. Biotechnol. 19:294-298, 1997). It has been known that many Bacillus species such as Bacillus cereus, Bacillus subtllls and Bacillus thuringlensis produce bacteriocins and bacteriocin-like substances (Paik, H. D. et al. , J. Ind. Microbiol. Biotechnol. 19:294-298, 1997; Zheng, G. et al. , J. Bacterid. 181:7346-7355, 1999; Bizani, D., Brandelli, A. J. Appl. Microbiol. 93:512-519, 2002).

The present inventors separated the novel Bacillus amyloliquefaciens K317 strain (KCTC 11042BP) from Kimchi, the Korean traditional safe fermented food, and further completed this invention by confirming that the culture solution of the strain and the antibacterial metabolite separated therefrom had strong inhibitory effect on various pathogenic enterobacteria including 30 kinds of MRSA strains.

[Disclosure] [Technical Problem]

It is an object of the present invention to provide a novel strain inhibiting the growth of antibiotics-resistant pathogenic microorganisms or enteropathogenic microorganisms, a supernatant of the culture solution thereof, and an antibacterial metabolite isolated from the same. [Technical Solution]

To achieve the above object, the present invention provides a Bacillus amylollquefaclens K317 strain suppressing the growth of antibiotics-resistant pathogenic microorganisms or enteropathogenic microorganisms .

The present invention also provides a supernatant of the culture solution of Bacillus amylollquefaclens K317. The present invention further provides an antibacterial metabolite isolated from the supernatant of the culture solution of Bacillus amylollquefaclens K317.

The present invention also provides probiotics comprising the above strain, the culture supernatant or the antibacterial metabolite as an active ingredient.

The present invention also provides a composition for inhibiting the growth of antibiotics-resistant pathogenic microorganisms or enteropathogenic microorganisms which comprises the above strain, the culture supernatant or the antibacterial metabolite as an active ingredient.

The present invention also provides health food for inhibiting the growth of antibiotics-resistant pathogenic microorganisms or enteropathogenic microorganisms comprising Bacillus amyloliquefaclens K317, the culture supernatant thereof or the antibacterial metabolite as an active ingredient.

The present invention also provides a feed additive for inhibiting the growth of antibiotics- resistant pathogenic microorganisms or enteropathogenic microorganisms comprising Bacillus amyloliquefaciens K317, the culture supernatant thereof or the antibacterial metabolite as an active ingredient.

[Advantageous Effect]

The novel Bacillus amyloliquefaciens K317 strain, the supernatant of the culture thereof and the antibacterial metabolite recovered from the same of the present invention can inhibit the growth of antibiotics-resistant pathogenic microorganisms including MRSA strain and enteropathogenic microorganisms effectively, so that they can be used for the composition or health food and as probiotics for inhibiting the growth of such pathogenic microorganisms .

[Description of Drawings]

The application of the preferred embodiments of the present invention is best understood with reference to the accompanying drawings, wherein:

Fig. 1 illustrates the result of growth inhibiting test with antibiotics-resistant pathogenic microorganisms to isolate Bacillus amyloliquefaclens K317.

Fig. 2 is a phylogenetic tree based on 16S rRNA sequence showing the relation of the K317 strain of the present invention and the conventional strains. Fig. 3 illustrates the antibacterial activity of Bacillus amyloliquefaclens K317 against MRSA (methicillin-resistant Staphylococcus aureus) 30.

Fig. 4 illustrates the growth inhibition observed after co-culture of Bacillus amyloliquefaclens K317 and MRSA.

Fig. 5 is a graph illustrating the growth inhibition of enteropathogenic microorganism according to the diluted concentrations of the supernatant of Bacillus amylollquefaciens K317 culture solution. Fig. 6 is a graph illustrating the growth inhibition of MRSA 1, MRSA, 2, MRSA 3, MRSA 4, and MRSA 5 according to the diluted concentrations of the supernatant of Bacillus amyloliquefaclens K317 culture solution. Fig. 7 is a graph illustrating the growth inhibition of MRSA 6, MRSA, 7, MRSA 8, MRSA 9, and MRSA 10 according to the diluted concentrations of the supernatant of Bacillus amylollquefaclens K317 culture solution. Fig. 8 is a graph illustrating the growth inhibition of MRSA 11, MRSA, 12, MRSA 13, MRSA 14, and MRSA 15 according to the diluted concentrations of the supernatant of Bacillus amyloliquefaciens K317 culture solution. Fig. 9 is a graph illustrating the growth inhibition of MRSA 16, MRSA, 17, MRSA 18, MRSA 19, and MRSA 20 according to the diluted concentrations of the supernatant of Bacillus amyloliquefaciens K317 culture solution. Fig. 10 is a graph illustrating the growth inhibition of MRSA 21, MRSA, 22, MRSA 23, MRSA 24, and MRSA 25 according to the diluted concentrations of the supernatant of Bacillus amyloliquefaciens K317 culture solution. Fig. 11 is a graph illustrating the growth inhibition of MRSA 26, MRSA, 27, MRSA 28, MRSA 29, and MRSA 30 according to the diluted concentrations of the supernatant of Bacillus amyloliquefaciens K317 culture solution. Fig. 12 is a graph illustrating the growth inhibition of MRSA 1 and MRSA 6 over the culture time and diluted concentrations of the supernatant of Bacillus amyloliquefaclens K317 culture solution.

Fig. 13 illustrates the antibacterial capacity of the antibacterial metabolite in the supernatant of Bacillus amyloliquefaciens K317 culture solution.

[Best Mode]

Hereinafter, the present invention is described in detail.

The present invention provides a Bacillus amyloliquefaciens K317 strain suppressing the growth of antibiotics-resistant pathogenic microorganisms or enteropathogenic microorganisms.

To select a microorganism exhibiting antibacterial activity against MRSA (methicillin- resistant Stapylococcus aureus), the antibiotics- resistant pathogenic microorganism, the present inventors diluted Kimchi juice in the plate on which MRSA strains were smeared, followed by culture. Colonies having clear zones were selected (see Fig. 1). The selected colonies were separated and purified and the strain identified at last was named Bacillus sp. K317, which was deposited at Korean Collection for Type Cultures, Korea Research Institute of Bioscience and Biotechnology located at Yuseong-Gu, Daejeon, Korea, on December 4, 2006 (Accession No: KCTC 11042BP).

To investigate the inhibiting activity of the strain of the invention on the growth of pathogenic microorganisms, the present inventors cultured Salmonella typhimurium, Edwardsiella tarda, E. coll, Staphylococcus epldermidls distributed from Korean Collection for Type Cultures (KCTC), Korea Research Institute of Bioscience and Biotechnology (KRIBB) and 30 strains of MRSA, the antibiotics-resistant bacteria, distributed from Culture Collection of Antimicrobial Resistant Microbes, Seoul Women's University, Seoul, Korea, in proper media, which were then smeared on MH media with fixed numbers of live cells. The Bacillus amylollquefaciens K317 strain was streaked on the media and cultured. Then, the formation of clear zone was observed. As a result, clear zone was observed around streaking of Bacillus amyloliquefaciens K317, indicating that the growth of enteropathogenic microorganisms was suppressed (see Fig. 3). Bacillus amyloliquefaciens K317 was co-cultured with MRSA. As a result, in the early stage of co-culture, both MRSA and Bacillus amyloliquefaciens K317 formed colonies, but after 24 hours of the co-cuLture, MRSA did not form a colony anymore (see Fig. 4). The above results indicate that the Bacillus amyloliquefaciens K317 of the present invention inhibits the growth of the antibiotics-resistant pathogenic microorganism MRSA and enteropathogenic microorganisms effectively.

The present invention also provides a supernatant of the culture solution of Bacillus amyloliquefaciens K317. The present inventors diluted the supernatant of Bacillus amyloliquefaciens K317 culture solution, followed by investigating the inhibitory effect on pathogenic microorganisms. The target strains for the experiment were Salmonella typhimurium, Edwardsiella tarda, E.coli, Staphylococcus epidermidis and 30 strains of MRSA, the antibiotics-resistant bacteria.

As a result, the growth of Edwardsiella tarda, E.coli, and Staphylococcus epidermidis were significantly suppressed in the undiluted supernatant or 1/2 diluted supernatant of Bacillus amyloliquefaciens K317 culture solution (see Fig. 5). In addition, the growth of most MRSA was suppressed in 1/4 diluted supernatant of Bacillus amyloliquefaciens K317 culture solution. MRSA was hardly growing in the undiluted supernatant or 1/2 diluted supernatant, suggesting that the supernatant had very strong inhibitory effect (see Figs 6 - 12). From the results, it was confirmed that the supernatant of Bacillus amyloliquefaclens K317 culture solution of the present invention suppressed the growth of antibiotics- resistant pathogenic microorganism MRSA and enteropathogenic microorganisms effectively.

The present invention further provides an antibacterial metabolite isolated from the supernatant of the culture solution of Bacillus amyloliquefaciens K317.

The present inventors separated metabolites having the molecular weight of more than 10 kDa and less than 10 kDa from the supernatant of the culture solution, followed by examination of antibacterial activities on antibiotics-resistant pathogenic microorganisms. As a result, clear zone was observed in the paper disk treated with the metabolite having the molecular weight of more than 10 kDa (see Fig. 13). Therefore, it was confirmed that the metabolite having the molecular weight of more than 10 kDa separated from the culture supernatant inhibited effectively the growth of antibiotics-resistant pathogenic microorganism MRSA and enteropathogenic microorganisms. The present invention also provides probiotics comprising the above strain, the culture supernatant or the antibacterial metabolite as an active ingredient. As explained hereinbefore, the Bacillus amylollquefaciens K317 strain, the culture supernatant thereof or the antibacterial metabolite isolated from the supernatant of the present invention had antibacterial activity against enteropathogenic microorganisms Edwardsiella tarda, E.coli and Staphylococcus epldermidis . Moreover, the strain of the present invention was isolated from the traditional safe fermented food Kimchi juice, so that it can be effectively used as non-toxic safe probiotics. The probiotics of the present invention can be applied to animals including cattle, Eood or animal feeds, in addition to medicines for animal and human.

The present invention also provides a composition for inhibiting the growth of antibiotics-resistant pathogenic microorganisms or enteropathogenic microorganisms which comprises the above strain, the culture supernatant or the antibacterial metabolite as an active ingredient. The antibiotics-resistant pathogenic microorganism herein is preferably methicillin- resistant Staphylococcus aureus (MRSA) , and the enteropathogenic microorganisms are preferably Edwardsiella tarda, E.coli and Staphylococcus epidermldls . The composition of the present invention can include, in addition to the Bacillus amylollquefaciens K317 strain, the supernatant thereof or the antibacterial metabolite, one or more effective ingredients having the same or similar function. The composition of the present invention can be administered orally or parenterally and be used in general forms of pharmaceutical formulation. The composition of the present invention can be prepared for oral or parenteral administration by mixing with generally used diluents or excipients such as fillers, extenders, binders, wetting agents, disintegrating agents and surfactant. Solid formulations for oral administration are tablets, pills, powders, granules and capsules. These solid formulations are prepared by mixing the Bacillus amylollquefaciens K317 strain, the culture supernatant thereof or the antibacterial metabolite isolated from the same with one or more suitable excipients such as starch, calcium carbonate, sucrose or lactose, gelatin, etc. Liquid formulations for oral administration are suspensions, solutions, emulsions and syrups, and the above-mentioned formulations can contain various excipients such as wetting agents, sweeteners, aromatics and preservatives in addition to generally used simple diluents such as water and liquid paraffin. Formulations for parenteral administration are sterilized aqueous solutions, water- insoluble excipients, suspensions, emulsions, lyophilized preparations, suppositories and injections. Water insoluble excipients and suspensions can contain, in addition to the active compound or compounds, propylene glycol, polyethylene glycol, vegetable oil like olive oil, injectable ester like ethylolate, etc. Suppositories can contain, in addition to the active compound or compounds, witepsol, macrogol, tween 61, cacao butter, laurin butter, glycerol, gelatin, etc.

The effective dosage of the composition can be determined according to weight, age, gender, health condition, diet, administration frequency, administration method, excretion and severity of a disease. The dosage of the Bacillus amyloliquefaclens K317 strain, the culture supernatant thereof or the antibacterial metabolite isolated from the same is

0.001-100 mg/kg per day and preferably 5-50 nig/kg per day, and administration frequency is once a day or preferably a few times a day. The Bacillus amyloliquefaciens K317 strain, the culture supernatant thereof or the antibacterial metabolite isolated from the same of the present invention was evaluated to be a safe substance since its estimated LD₅₀ value was much greater than 1,000 ing/ kg in mice, which was confirmed by acute toxicity assay with rats tested via oral administration.

The composition of the present invention can be treated independently or co-treated with surgery, hormone therapy, chemo-therapy and biological regulators, for the prevention and treatment of disease caused by pathogenic microorganisms such as MRSA and enteropathogenic microorganisms such as Edwardsiella tarda, E.coli and Staphylococcus epldermidis.

The present invention also provides health food for inhibiting the growth of antibiotics-resistant pathogenic microorganisms or enteropathogenic microorganisms comprising Bacillus amyloliquefaciens K317, the culture supernatant thereof or the antibacterial metabolite as an active ingredient.

The antibiotics-resistant pathogenic microorganism herein is preferably methicillin- resistant Staphylococcus aureus (MRSA) , and the enteropathogenic microorganisms are preferably Edwardsiella tarda, E.coli and Staphylococcus epldermidis.

Health food containing the Bacillus amyloliquefaciens K317 strain, the culture supernatant thereof or the antibacterial metabolite isolated from the same of the present invention can be folk remedies for inhibiting the growth of pathogenic microorganisms which are exemplified by tea, jelly, soup, extract, beverages, etc, containing the Bacillus amyloliquefaciens K317 strain, the culture supernatant thereof or the antibacterial metabolite isolated from the same as an active ingredient. Health food for inhibiting the growth of antibiotics-resistant pathogenic microorganisms or enteropathogenic microorganisms of the present invention processed in various forms is safe without causing side effects in human, is excellent in inhibiting the growth of pathogenic microorganisms, and facilitates the administration and long-term storage.

The Bacillus amyloliquefaciens K317 strain, the culture supernatant thereof or the antibacterial metabolite isolated from the same of the present invention can be used for health food to suppress the growth of pathogenic microorganisms. In that case, the Bacillus amyloliquefaciens K317 strain, the culture supernatant thereof or the antibacterial metabolite isolated from the same can be added as it is or as mixed with other food components according to the conventional method. The mixing ratio of active ingredients can be regulated according to the purpose of use (prevention, health enhancement or treatment). In general, to produce health food or beverages, the Bacillus amyloliquefaciens K317 strain, the culture supernatant thereof or the antibacterial metabolite isolated from the same is added preferably by up to 15 weight part and more preferably by up to weight part for 100 weight part of the raw material. However, if long term administration is required for health and hygiene or regulating health condition, the content can be lower than the above but higher content can be accepted as well since the Bacillus amyloliquefaciens K317 strain, the culture supernatant thereof or the antibacterial metabolite isolated from the same has been proved to be very safe.

The food herein is not limited. For example, the Bacillus amyloliquefaciens K317 strain, the culture supernatant thereof or the antibacterial metabolite isolated from the same can be added to meats, sausages, breads, chocolates, candies, snacks, cookies, pizza, ramyuns, flour products, gums, dairy products including ice cream, soups, beverages, tea, drinks, alcohol drinks and vitamin complex, etc, and in wide sense, almost every food applicable in the production of health food can be included.

The composition for health beverages of the present invention can additionally include various flavors or natural carbohydrates, etc, like other beverages. The natural carbohydrates above can be one of monosaccharides such as glucose and fructose, disaccharides such as maltose and sucrose, polysaccharides such as dextrin and cyclodextrin, and sugar alcohols such as xilytole, sorbitol and erythritol. Besides, natural sweetening agents such as thaumatin and stevia extract, and synthetic sweetening agents such as saccharin and aspartame can be included as a sweetening agent. The content of the natural carbohydrate is preferably 0.01-0.04 g and more preferably 0.02-0.03 g in 100 g of the Bacillus amyloliquefac±ens K317 strain, the culture supernatant thereof or the antibacterial metabolite isolated from the same.

In addition to the ingredients mentioned above, health food containing the Bacillus amyloliquefaciens K317 strain, the culture supernatant thereof or the antibacterial metabolite iso Lated from the same of the present invention can include in variety of nutrients, vitamins, minerals, flavors, coloring agents, pectic acid and its salts, alginic acid and its salts, organic acid, protective colloidal viscosifiers , pH regulators, stabilizers, antiseptics, glycerin, alcohols, carbonators which used to be added to soda, etc. Health food containing the Bacillus amyloliquefaclens K317 strain, the culture supernatant thereof or the antibacterial metabolite isolated from the same can also include natural fruit juice, fruit beverages and/or fruit flesh addable to vegetable beverages. All the mentioned ingredients can be added singly or together. The mixing ratio of those ingredients does not matter in fact, but in general, each can be added by 001-0.1 weight part per 100 weight part of the Bacillus amyloliquefaciens K317 strain, the culture supernatant thereof or the antibacterial metabolite isolated from the same of the present invention.

The antibiotics-resistant pathogenic microorganism herein is preferably methicillin- resistant Staphylococcus aureus (MRSA) , and the enteropathogenic microorganisms are preferably Edwardsiella tarda, E.coli and Staphylococcus epidermldis .

The feed additive of the present invention can be added to animal feeds . The feed additive of the invention contains Bacillus amyloliquefaciens K317 strain, the culture supernatant thereof or the antibacterial metabolite isolated from the same by 1-20 weight part, and more preferably 10-20 weight part for

100 weight part of the conventional animal feed. The feed additive of the present invention is expected to have antibacterial effect and growth inhibiting effect on MRSA and such enteropathogenic microorganisms as

Edwardsiella tarda, E.coli and Staphylococcus epidermidis (see Figs. 4 - 12).

[Mode for Invention]

Practical and presently preferred embodiments of the present invention are illustrative as shown in the following Examples . However, it will be appreciated that those skilled in the art, on consideration of this disclosure, may make modifications and improvements within the spirit and scope of the present invention.

Example 1 : Separation of the microorganism having antibacterial activity

To separate the microorganism having antibacterial activity against MRSA (methicillin- resistant Staphylococuus aureus) , the antibiotics- resistant pathogenic microorganism, Kimchi juice properly diluted was smeared on the tryptic soy agar (TSA, Difco) medium pre-smeared with MRSA, followed by culture at 37 ^°C for 48 hours. Upon completion of the culture, tens of colonies exhibiting clear zone were selected (Fig. 1). The Kimchi was prepared as follows; cleaned Chinese cabbage, cut it into two equal pieces crosswise, soaked them in approximately 7% (w/w) salt water, salted down at room temperature (approximately

25 ^°C) for 14 hours, washed the salted cabbages with tap water three times, and dehydrated them for 2 hours; and radish (cut into 4 x 4 cm), green onion and other ingredients were added to the prepared cabbages . The other ingredients were those: salted fish prepared by mixing pickled oysters, salted anchovies, salted shrimps and other salted fishes, and garlic, ginger, hot red pepper powder, glutinous rice flour, and sugar. They were all mixed and stored at 5^°C, resulting in the fermented Kimchi. The selected colonies were transferred onto fresh TSA medium and cultured 3 times, leading to pure isolation. The isolated microorganism strain was stored in 20% glycerol at -80^°C.

Example 2; Identification of the separated K317 strain The K317 strain finally selected in Example 1 was identified by morphological classification method and the newest molecular systematic method. The K317 strain was grown best when it was cultured on TSA (Tryptic Soy Agar, Difco) medium at 30-37 ^°C . Its morphological characteristics were investigated by Gram staining, and as a result, the strain was confirmed to be a Gram positive bacillus. The strain was finally identified as Bacillus amyloliquefaciens by 16S rRNA nucleotide sequencing. The nucleotide sequencing and analysis were as follows. To extract DNA, the cultured cells were resuspended in 100 μi of STES buffer (0.4 M NaCl, 0.2 M Tris-HCl (pH 7.6), 0.01 M EDTA, 1% SDS). Glass beads were added to the sample, followed by lysis for 5 minutes with TOMY (micro tube mixer MT-360) to elute cytoplasm. The eluent was suspended in 200 jA of TE buffer (pH 8.0) and 200 ≠ of phenol/chloroform, followed by centrifugation . 5 fd of RNase A was treated to the supernatant, followed by reaction for one hour at 37^°C. 200 βi of chloroform was added thereto, followed by centrifugation at 12,000 rpm for 5 minutes. The supernatant was washed with ethanol twice and then dried (vacuum dry: SpeedVac ) . The recovered DNA was dissolved in sterilized distilled water and stored. For PCR to amplify 16S rDNA, universal primer comprising PCR premix (Bioneer, Korea), forward primer (5¹ - GAG TTT GAT CCT GGC TCA G - 3¹: SEQ. ID. NO: 1) and reverse primer (5¹ - GGT TAC CTT GTT ACG ACT T - 3': SEQ. ID. NO: 2) was used. The final volume of the reaction mixture for PCR was 20 βi and PCR was performed as follows; denaturation at 94 ^°C for 1 minute, annealing at 50 ^°C for 1 minute, DNA polymerization at 72 ^°C for 1 minute and 50 seconds (30 cycles).

Nucleotide sequencing (SEQ. ID. NO: 3) and systematic analysis of the amplified DNA was performed according to the method of Chang, et al (Chang et al., Int. J. Syst. Evol. Microbiol. 52: 377-381, 2002) (Fig. 2 and Table 1). The identified K317 strain was deposited at Korean Collection for Type Cultures (KCTC), Korea Research Institute of Bioscience and Biotechnology (KRIBB) located at 52, Eoeun-Dong, Yuseong-Gu, Daejeon, Korea, on December 4, 2006 (Accession No: KCTC 11042BP)

[Table l]

Example 3: Inhibiting capacity of Bacillus amylol±quefaciens K317 on the growth of pathogenic microorganisms

To investigate the inhibiting activity of the K317 strain identified in Example 2 on the growth of pathogenic microorganisms, following experiment was performed. The K317 strain was cultured on TSA medium at 37 °C for 24 hours. Enteropathogenic microorganisms herein were Salmonella typhimurium, Edwardsiella tarda, E. coll and Staphylococcus epidermidis distributed from Korean Collection for Type Cultures (KCTC), Korea Research Institute of Bioscience and Biotechnology (KRIBB). And 30 strains of MRSA distributed from Culture Collection of Antimicrobial Resistant Microbes, Seoul Women's University, Seoul, Korea, were used as antibiotics-resistant bacteria. For the pathogenic bacteria growth inhibition test, the strains were cultured on Mueller Hinton media (MH, Difco, USA) at 37 ^°C for 48 hours. Then, the formation of clear zone was observed. The present inventors smeared live pathogenic microorganisms each cultured on TSA (Tryptic Soy Agar, Difco) medium on MH medium at the density of 10^6~7 CFU/m-C. The K317 strain was streaked on the medium and cultured. As a result, clear zones were observed around pathogenic microorganisms and MRSA strains after the culture, suggesting that the growth of those pathogenic microorganisms and MRSA strains were suppressed (Fig. 3). The inhibiting activity of the K317 strain on the growth of 2 MRSA strains (#1 and #6) presented as yellow colonies was investigated by mixed culture. The concentrations of K317 and MRSA were equally adjusted to 10^6~7 CFU/m-β. and mixed together at the ratio of 1:1 (v/v) , followed by mixed culture in MH liquid medium at 37 ^°C for 24 hours. The culture was diluted in PBS (Phosphate-Buffered Saline, Bioneer, Korea), smeared on TSA medium and measured the number of live cells.

As a result, no colonies of MRSA, which was 10^6"7 CFU/mβ. before the mixed culture, were found after 24 hours of the mixed culture with K317 (Fig. 4). The above result indicated that the K317 strain had excellent inhibiting activity on the growth of the MRSA strain .

Example 4 : Growth inhibition test using the culture solution of Bacillus amyloliquefaciens K317

K317 strain was cultured in MH liquid medium at 37 ^°C for 24 hours and the cells were eliminated from the culture solution by using 0.2 μm membrane filter (Satorius, Germany). The supernatant only was used for the following experiment. The supernatant was diluted to 1/512 by using sterilized MH broth. Each of the strains, Salmonella typhimurium, Edwardsiella tarda, E.coli, Staphylococcus epidermidis and 30 kinds of MRSA was distributed in 96-well plate, to which diluted K317 supernatant was added at. different concentrations, followed by culture 37 ^°C for 24 hours. OD₅₉₅ (optical density) was measured by using ELISA reader (Benchmark microplate reader, BIO-RAD, USA) . As a result, the growth of Edwardsiella tarda, E.coli, and Staphylococcus epidermidis was suppressed in the undiluted and 1/2 diluted supernatant of Bacillus amyloliquefaclens K317 culture solution (Fig. 5). The supernatant of Bacillus amyloliquefaciens K317 culture solution inhibited the growth of 30 kinds of MRSA even at 1/4 diluted solution and in the undiluted and 1/2 diluted supernatant, 30 kinds of MRSA were hardly grown (Figs. 6 - 11). To make accurate growth inhibition curve, the present inventors diluted the K317 supernatant further to 1/32 fold and growth inhibition curves on MRSA #1 and MRSA #6 were made every 3 hours by the same manner as described above. The sterilized MH liquid medium where the strain was not cultured was used as a negative control and the medium where MRSA was cultured without addition of the K317 supernatant was used as a positive control.

As a result, the growth of MRSAs was suppressed in all the diluted supernatants and particularly MRSAs were not grown at all at the concentrations over 1/4 fold dilution, particularly 1:1 and 1:1/2 dilutions, exhibiting the strong inhibitory effect (Fig. 12).

Example 5 : Antibacterial metabolites produced by Bacillus amyloliquefaciens K317

K317 strain was cultured in 100 vd of TSB medium, and then the cells were eliminated by using 0.2 μm filter to prepare the supernatant. The supernatant was concentrated by centrifugation at 3,000xg using Centricon YM-IO (Milipore, USA). As a result, the metabolites of less than 10 kDa in molecular weight and more than 10 kDa in molecular weight were respectively obtained. Antibacterial activity of the metabolite in the culture solution sorted according to the molecular weight was measured by paper disc (diameter: 6mm, Toyo Roshi Kaisha, Japan) method. 30 strains of MRSA were cultured on TSA (Tryptic Soy Agar, Difco) and the number of live cells was adjusted to 10^6~7 CFU/m#, which were smeared on MH medium. Paper disc was placed on the medium, to which the materials separated by the centrifugation by molecular weight were dropped and absorbed thereon by 20 /d. After culturing thereof, clear zones were observed around the paper disc absorbing the materials of more than 10 kDa in molecular weight. Therefore, it was confirmed that an antibacterial material suppressing the growth of MRSA strains is included in the supernatant of K317 culture solution and the molecular weight of the material is at least 10 kDa (Fig. 13). Example 6; Acute toxicity test

The following experiments were performed to see if the Bacillus amyloliquefaciens K317 strain, the culture supernatant thereof or the antibacterial metabolite isolated from the same of the present invention had acute toxicity in rats.

6-week old specific pathogen free (SPF) SD line rats were used in the tests for acute toxicity. The Bacillus amyloliquefaciens K.317 strain, the culture supernatant thereof or the antibacterial metabolite isolated from the same of the present invention was suspended in 0.5% methyl cellulose solution and orally administered once to 2 rats per group at the dosage of

Death, clinical symptoms, and weight change in rats were observed, hematological tests and biochemical tests of blood were performed, and any abnormal signs in the gastrointestinal organs of chest and abdomen were checked with eyes during autopsy.

The results showed that the Bacillus amyloliquefaciens K317 strain, the culture supernatant thereof or the antibacterial metabolite isolated from the same of the present invention did not cause any specific clinical symptoms, weight change, or death in rats. No change was observed in hematological tests, biochemical tests of blood, and autopsy.

The Bacillus amyloliquefaciens K317 strain, the culture supernatant thereof or the antibacterial metabolite isolated from the same of the present invention used in this experiment was evaluated to be a safe substance since it did not cause any toxic change in rats up to the level of 1,000 mg/kg and its estimated LD₅₀ value was much greater than 1,000 mg/kg in rats.

Manufacturing Example 1 : Preparation of food

Foods containing the Bacillus amyloliquefaciens K317 strain, the culture supernatant thereof or the antibacterial metabolite isolated from the same of the present invention were prepared as follows.

<1-1> Preparation of spices

Health enhancing spices were prepared by mixing 0.2-10 weight% of the Bacillus amyloliquefaciens K317 strain.

<l-2> Preparation of tomato ketchup and sauce

Health enhancing tomato ketchup and sauce were prepared by mixing 0.2-10 weight% of the supernatant of Bacillus amyloliquefaciens K317 culture solution with tomato ketchup and sauce according to the conventional method.

<l-3> Preparation of flour food

0.1-5.0 weight% of the antibacterial metabolite of the present invention was added to the flour.

Health enhancing foods such as bread, cake, cookies, crackers and noodles were prepared with the flour mixture according to the conventional method.

<l-4> Preparation of soups and gravies

0.1-1.0 weight part of the supernatant of

Bacillus amyloliquefaciens K317 culture solution was added to soups and gravies. Health enhancing meat products, soups and gravies were prepared with this mixture by the conventional method.

<l-5> Preparation of ground beef Health enhancing ground beef was prepared by mixing 10 weight% of the supernatant of Bacillus amyloliquefaciens K317 culture solution with ground beef according to the conventional method.

<l-6> Preparation of dairy products 0.1-1.0 weight% of the antibacterial metabolite of the present invention was added to milk. Health enhancing dairy products such as yoghurt, butter and ice cream were prepared with the milk mixture according to the conventional method.

<l-7> Preparation of Sun-Sik

Brown rice, barley, glutinous rice and Yulmu (Job's tears) were gelatinized according to the conventional method, dried and pulverized to obtain 60- mesh powders.

Black soybean, black sesame and wild sesame were steamed and dried according to the conventional method and pulverized to obtain 60-mesh powders. The antibacterial metabolite of the present invention was concentrated under reduced pressure, spray-dried and pulverized to obtain 60-mesh dry powders .

Sun-Sik was prepared by mixing the^' dry powders of the grains, seeds and the antibacterial metabolite of the present invention according to the below ratio.

Grains (brown rice: 30 weight part, Yulmu: 15 weight part, barley: 20 weight part),

Seeds (wild sesame: 7 weight part, black soybean: 8 weight part, black sesame: 7 weight part), Dry powders of the antibacterial metabolite of the present invention (1 weight part),

Ganoderma lucidum (0.5 weight part),

Rehmannia glutinosa (0.5 weight part)

Manufacturing Example 2 : Preparation of beverages <2-l> Preparation of carbonated beverages

Sugar (5-10%), citric acid (0.05-0.3%), caramel

(0.005-0.02%), vitamin C (0.1-1%) and the antibacterial metabolite of the present invention were all mixed, to which purified water (79-94%) was added to make syrup. The syrup was sterilized at 85-98 ^°C for 20-180 seconds and then mixed with cold water at the ratio of 1:4. Carbonated beverages containing the antibacterial metabolite of the present invention were prepared by adding carbon dioxide (0.5-0.82%) to the mixture .

<2-2> Preparation of health beverages The supernatant of Bacillus amyloliquefac±ens K317 culture solution was mixed with liquid fructose (0.5%), oligosaccharide (2%), sugar (2%), salt (0.5%), and water (75%). After mixing completely, the mixture was sterilized instantly and filled small containers such as glass bottles, pet bottles, etc, to prepare health beverages.

<2-3> Preparation of vegetable juice

Health enhancing vegetable juice was prepared by adding 0.5 g of the supernatant of Bacillus amyloliquefaciens K317 culture solution to 1,000 ι\\l of tomato or carrot juice according to the conventional method.

<2-4> Preparation of fruit juice

Health enhancing fruit juice was prepared by adding 0.1 g of the supernatant of Bacillus amyloliquefaciens K317 culture solution to 1,000 Hid of apple or grape juice according to the conventional method.

Manufacturing Example 3 ; Preparation of feeds

<3-l> Purified feeds for growing pigs up to 50 kg a) Crude protein at least 16 weight%, Lysine at least 0.8 weight%,

Crude lipid up to 8 weight%,

Crude fiber up to 6 weight%,

Starch at least 33 weight%,

Calcium at least 0.7 weight%, Phosphate at least 0.5 weight%, Sodium at least 0.15 weight%, b) Copper at least 20 mg, Zinc at least 50 mg, Vitamin A at least 4,000 IU, Vitamin D at least 500 IU, c) Supernatant of Bacillus amyloliquefaciens K-317 culture solution 0.02 - 20 ppm.

<3-2> Milk replacement feeds for growing calves at least 80 kg a) Crude protein at least 17 weight%, Lysine at least 1.25 weight%, Crude lipid 15 - 30 weight%, Crude fiber up to 2 weight%, Crude ash up to 10 weight%,

Calcium at least 0.9 weight%,

Phosphate at least 0.7 weight%,

Sodium at least 0.2 weight%,

Magnesium at least 0.13 weight%, Powdered milk at least 25 weight%, b) Copper up to 15 mg, Vitamin A at least 8,000 IU, Vitamin D at least 1,000 IU, Vitamin E at least 20 mg, c) Supernatant of Bacillus amyloliquefaciens K-317 culture solution 0.02 ~ 20 ppm.

Those skilled in the art will appreciate that the conceptions and specific embodiments disclosed in the foregoing description may be readily utilized as a basis for modifying or designing other embodiments for carrying out the same purposes of the present invention. Those skilled in the art will also appreciate that such equivalent embodiments do not depart from the spirit and scope of the invention as set forth in the appended claims.

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Claims

[CLAIMS]

[Claim l]

A Bacillus amyloiquefaciens K317 strain inhibiting the growth of antibiotics-resistant pathogenic microorganism or enteropathogenic microorganisms .

[Claim 2]

The Bacillus amyloliquefaciens K317 strain according to claim 1, wherein the antibiotics-resistant pathogenic microorganism is methicillin resistant Staphylococcus aureus.

[Claim 3] The Bacillus amyloliquefaciens K317 strain according to claim 1, wheiein the enteropathogenic microorganisms are Edwards iella tarda, E.coli, and Staphylococcus epidermidis.

[Claim 4]

The Bacillus amyloliquefaciens K317 strain according to claim 1, wherein the strain is KCTC 11042BP.

[Claim 5] The Bacillus amyloliquefaciens K317 strain according to claim 1, wherein the strain contains 16S rRNA sequence represented by SEQ. ID. NO: 3.

[Claim 6]

A culture supernatant of the Bacillus amyloliquefaciens K317 strain of claim 1.

[Claim 7] An antibacterial metabolite recovered from the supernatant of claim 6.

[Claim 8]

The antibacterial metabolite according to claim 7, wherein the recovering method is centrifugation, concentration using microfilter and recovery using adsorbent.

[Claim 9] The antibacterial metabolite according to claim I₁ wherein the molecular weight of the metabolite is at least 10 kDa.

[Claim lθ] A Probiotics comprising the strain of claim 1, the supernatant of claim 6, or the antibacteria L metabolite of claim 7 as an active ingredient.

[Claim ll] A composition for inhibiting the growth of antibiotics-resistant pathogenic microorganisms or enteropathogenic microorganisms comprising the strain of claim 1, the culture supernatant of claim 6, or the antibacterial metabolite of claim 7 as an active ingredient.

[Claim 12]

The composition for inhibiting the growth of antibiotics-resistant pathogenic microorganisms or enteropathogenic microorganisms according to claim 11, wherein the antibiotics-resistant pathogenic microorganism is methicillin resistant Staphylococcus aureus.

[Claim 13]

The composition for inhibiting the growth of antibiotics-resistant pathogenic microorganisms or enteropathogenic microorganisms according to claim 11, wherein the enteropathogenic microorganisms are Edwardsiella tarda, E.coli and Staphylococcus

AA epidermidis .

[Claim 14]

A health food for inhibiting the growth of antibiotics-resistant pathogenic microorganisms or enteropathogenic microorganisms comprising the strain of claim 1, the culture supernatant of claim 6, or the antibacterial metabolite of claim 7 as an active ingredient.

[Claim 15]

The health food for inhibiting the growth of antibiotics-resistant pathogenic microorganisms or enteropathogenic microorganisms according to claim 14, wherein the antibiotics-resistant pathogenic microorganism is methicillin resistant Staphylococcus aureus.

[Claim 16] The health food for inhibiting the growth of antibiotics-resistant pathogenic microorganisms or enteropathogenic microorganisms according to claim 14, wherein the enteropathogenic microorganisms are Edwardsiella tarda, E.coli and Staphylococcus epidermidls .

[Claim 17]

A feed additive for inhibiting the growth of antibiotics-resistant pathogenic microorganisms or enteropathogenic microorganisms comprising the strain of claim 1, the culture supernatant of claim 6, or the antibacterial metabolite of claim 7 as an active ingredient.

[Claim 18]

The feed additive for inhibiting the growth of antibiotics-resistant pathogenic microorganisms or enteropathogenic microorganisms according to claim 17, wherein the antibiotics-resistant pathogenic microorganism is methicillin resistant Staphylococcus aureus.

[Claim 19]

The feed additive for inhibiting the growth of antibiotics-resistant pathogenic microorganisms or enteropathogenic microorganisms according to claim 17, wherein the enteropathogenic microorganisms are Edwardsiella tarda, E. coll and Staphylococcus epidermidis.