(2) Descristion of Related Art Foods and feeds are particularly labile to microbial deterioration, and can serve as vehicles for transmission of pathogens, food-boirne infections and intoxications. The microorganisms involved include bacteria, yeasts, molds and viruses. Some examples of food and feed-borne pathogens are for instance Staphylococcus aureus, Salmonella spp., Clos tri di um spp., Listeria monocytogenes, Yersinia spp., Vibrio spp., Escherichia coli serotype 0157:H7, and Shigella spp. Enterotoxins produced by staphylococci, clostridia, and mycotoxins secreted by molds are also transmitted through foods and feeds.

Several different approaches are used to prevent microbial deterioration of foods and feeds, and transmission of microbial pathogens and/or their toxins through foods and feeds. Most of these strategies include using adequate processing methods and avoiding and preventing post-process contamination.

Supplementing these steps are the use of preservatives, packaging techniques, such as vacuum shrinking films, and modified atmosphere packaging. Recently there has

been an increased interest in searching for "natural inhibitors" of unwanted flora in foods and feeds. These inhibitors have included using antagonistic "safe" microorganisms such as lactic acid bacteria, microbial metabolites, such as organic acids, bacteriocins, and certain naturally derived components like spice and plant extracts.

The health promoting and antibacterial properties of a fermented Mexican drink, Pozol, have been recognized by the Mayan civilization for centuries.

Pozol is made by dissolving fermented nixtamalized corn (maize) flour dough or masa in water. Only recently, have there been careful microbiological studies on this fermented native drink. The microflora of Pozol is quite complex. Wacher et al. (World S. Microbiol.

Biochem. 9:269-274 (1993)) and Nuraida et al. (World J.

Microbiol. Biochem. 11:567:571 (1995)) reported that the predominant microflora of Pozol consisted of lactic acid bacteria (lactobacilli, lactococci, and leuconostocs), aerobic catalase-positive mesophiles, members of the Enterobacteriaceae family, yeasts (predominantly Geotrichum candidum) and molds.

Earlier studies by Mexican researchers showed that Pozol contained Agrobacterium azotophilum (Ulloa and Herrera. Rev. Latin-amer. Microbiol-. 14:15-24 (1972)), which showed a wide antibacterial activity (Herrera and Ulloa. Rev. Latin-amer. Microbiol. 17:143- 147 (1975)). The Agrobacterium azotophilum isolate was a Gram-negative, non-spore forming, coccoid-bacillus, which was capsulated, and motile (Ulloa and Herrera.

Rev. Latin-amer. Microbiol. 14:15-24 (1972)). They also noted that the bacterium inhibited the growth of several Gram-positive and Gram-negative bacteria, yeasts and molds. Later studies by others also attributed the antimicrobial properties of Pozol to isolates similar to Agrobacterium azotophilum (Sanchez-Fernandez and McKay.

Abst. IFT Annu. Meet. Food Expo (1994)). This was a

misidentification of the bacterium involved and in fact it is the strain of the present invention.

There are previous reports in the literature describing the inhibitory properties of Bacillus subtilis strains isolated from other habitats. Wilson et al., (SIM News 46:237-242 (1996)) referred to a Bacillus subtilis isolate B-3, that was effective in controlling brown rot of peaches, and was tested successfully on a semi-commercial basis in packing houses (Pusey et al., Plant Disease 72:622-626 (1988)).

This strain was patented in 1984 (Pusey, L., and Wilson, C. L., U.S. Patent No. 4,764,371). The principal agent involved in the antagonistic activity of the strain B-3 against brown rot pathogen of peaches, was found to be an antibiotic, iturin, secreted by the Bacillus (Gueldner et al., J. Agric. Food Chem. 36:366-370 (1988)). Asaka and Shoda (Appl. Environ. Microbiol.

62:4081-4085 (1996)) described the use of a strain of Bacillus subtilis, designated RB14, for controlling damping-off in tomato seedlings caused by a mold.- This strain was shown to be active against several phytopathogens in in vitro studies. This strain produced two antibiotics, iturin A and surfactin, which were found in cell-free culture supernatants. Asaka and Shoda also cited other investigations, where Bacillus subtilis strains have been used to control phytopathogens in plant growth studies. No application studies on the use of microorganisms from Pozol to control unwanted flora in foods or feeds or other systems have been reported. Other U.S. patents of interest are U.S. Patent Nos. 5,218,101 to Hansen and 5,516,682 to Hansen which relate to mutant subtilins.

DESCRIPTION OF PREFERRED EMBODIMENTS The present invention relates to a method for inhibiting undesirable microorganisms in a material containing or exposed to the microorganisms which comprises:

exposing the material to an inhibitor of the undesired microorganisms from a pure culture of a Bacillus subtilis deposited as NL-B-21974 so that the undesired microorganisms in the material are inhibited.

Preferably the material to be protected is a food or a material in contact with a food. The food can be for any animal, particularly mammals.

The present invention also relates to an isolated pure culture of Bacillus subtilis deposited as NRRL-B-21974.

The culture was deposited under the Budapest Treaty with the Agricultural Research Service Culture Collection, Peoria, Illinios, USA on 11th April, 1998 as NRRL-B- 21974. It is available as required by the Budapest Treaty, The culture of the Bacillus subtilis MRnL-B-71974 can be living or non-living. If living, it can be frozen or lyophilized or otherwise dried for preservation. The inhibition is produced by a component of the Bacillus subtilis and thus i can be non-living.

It can be sonicated or otherwise disrupted for preservation prior to use. All of these variations are known to those skilled in the art.

Preferably the culture of living cells contains between about 103 and 1012 cell forming units (cfu) per ml or gram. Most preferred is 106 to 109 cfu per ml.

The material being preserved preferably contains between about 102 and 109 cfu per ml or gram.

The amount selected depends upon the material and the undesirable microorganisms which are present. If the culture is non-living, an amount of inhibitory cellular material is used for inhibition.

The culture material can be incorporated into a bulking agent for distribution into the materials.

Most conveniently the culture material is incorporated into a dry edible particulate material, such as flour,

non-fat dry milk, salt, or pepper, which can be incorporated into the food.

The following Example 1 shows the growth and preservation of theBacillus subtilis. In the following Examples 2 to 7, application of the Bacillus subtilis Pozol isolate in food systems to inhibit unwanted flora is described. A broad application of the isolate to control undesirable microflora in various food and feed systems is evident from the Examples described hereunder.

EXAMPLE 1 The isolate from Pozol that exhibited the wide spectrum of inhibition is a Gram-positive, aerobic, spore-forming rod. The spores are sub-terminal to terminal, and the sporangia are swollen at the position of the endospore. Active, young cultures exhibit good motility. The rods are medium-sized, and usually occur as single cells. Older cells exhibit Gram-variable reaction. Extensive sporulation is observed on solid media, and very little or no sporulation occurs in broth cultures. Broth cultures fortified with minerals and starch, incubated for long periods (72 hours or greater) on a shaker show a fair amount of sporulation.

Biochemical data indicate that the organism is an atypical strain of Bacillus subtilis. One of the unique properties of the organism is its ability to grow on a nitrogen-free medium, but containing a carbon source.

The organism survives well in dough systems without any supplementation with exogenous sugar or nitrogen compounds. The biochemical characteristics of the organism as determined by the API system is given in Tables 1 and 2.

TABLE 1. Biochemical reactions of Pozol isolate as determined by API 50 CHB sugar fermentation system Sugar Fermentation Sugar Fermentation Control Esculin Glycerol ++++ Salicin Erythritol Cellobiose ++++ D-Arabinose Maltose ++++ L-Arabinose ++++ Lactose ++++ Ribose ++++ Melibiose +++ D-Xylose +++ Sucrose ++++ L-Xylose Trehalose +++ + Adonitol - Inuline - P-Methyl-C-Xyloside - Melezitose - Galactose Raffinose ++++ Glucose ++++ Starch Fructose +++ + Glycogen ++++ Mannose ++++ Xylitol + Sorbose - -Gentiobiose + Rhamnose D-Turanose ++++ Dulcitol D-Lyxose - Inositol ++++ D-Tagatose - Mannitol ++++ D-Fucose - Sorbitol ++++ L-Fucose - α-Methyl-D- - D-Arabitol - Mannoside α-Methyl-D-Glucoside +++ L-Arabitol - N-Acetyl-Glucosamine - Gluconate - Amygdalin +++ 2-Keto- - gluconate Arbutin +++ 5-Keto- - gluconate

++++ full acidification (yellow) +++ less acidification (less intense yellow) ++ minor acidification (orange/yellow) + slight acidification (red/orange) - no acidification TABLE 2 Biochemical reactions of Pozol isolate as determined by API 20E 24h 48h Ortho-Nitrophenyl N- - - Acetyl-α-D- Galactosaminide Hydrolysis Aginine Dihydrolase + + Lysine Decarboxylase - + Ornithine Decarboxylase +/- + Citrate Utilization - - Hydrogen Sulfide - - Urease + + Tryptophane Deaminase a - Indole from Tryptophane a - Voges-Proskauer a + Gelatin Liquefaction + + Glucose - - Nitrate Reduction a + a reading after addition chemicals to cupule after 48 h.

+ positive reaction after 24 hours or 48 hours at 370, according color change necessary for positive result as listed in the instructions.

- negative reaction after 24 hours and 48 hours.

+/- slight positive reaction.

The inhibitory spectrum of the bacterium against some of the spoilage flora in foods is given in Table 3.

TABLE 3 - Inhibitory spectrum of the Pozol isolate against certain common spoilage and pathogenic microflora in foods.a Microorganism Strain No./Designationb Inhibitionc I. BACTERIA Gram - positive Enterococcus faecium QRHy +++ Lactobacillus spp.d QR196 +++ Lactobacillus spp.d QR396 +++ Listeria monocytogenes QRLMO36 ++ Listeria monocytogenes ATCC43256 +++ Staphylococcus aureus ATCC10390 - Gram - negative Escherichia coli ATCC12955 +++ Pseudomonas aeruginosa ATCC10145 +++ Pseudomonas fluorescens QR22 +++ Salmonella enteritidis ATCC13076 +++ II. YEASTS Candiad glabrata ATCC2001 +++ Debaryomyces ATCC20280 +++ polymorphus Rhodotorula mucilaginosa ATCC9449 +++ var. mucilaginosa Saccharomyces spp.e QR96 +++ III. MOLDS Aspergillus flavus QN25581 + Fusarium avenaceum QN25565 + Fusarium culmorum QN25656 ++ Fusarium oxysporum ATCC48112 +++ Geotrichum candidum ATCC34614 + Penicillium spp.f QR15 +++

a Determined by deferred agar overlay assay. b ATCC - American Type Culture Collection QN - Quest, Naarden Culture Collection QR - Quest, Rochester Culture Collection<BR> c - No inhibition.

+ - Zone of inhibition <5mm.

++ - Zone of inhibition >5mm but <10 mm.

+++ - Zone of inhibition > 10 mm. d Isolates from spoiled processed meats. e Isolate from sour dough bread starter. isolate from moldy tortilla.

The organism is active against Gram-negative and Gram- positive bacteria, molds and yeasts, which are common spoilage flora in foods. Many Gram-negative bacteria such as Salmonella, Shigella, certain serological types of Escherichia, and the like are food-borne pathogens.

To insure the uniformity of inoculum used in the following Examples, a frozen concentrate of the strain was maae in the laboratory using a 1.0 liter fermentor. The strain was grown in a medium consisting of the following: NZ-Amine EKC - 0.5%; Amberex 1003 yeast extract - 0.5%; dextrose - 2.0%; mannitol - 1.0%; sodium citrate - 0.1%; magnesium sulfate - 0.1%; dipotassium hydrogen phosphate - 0.2%; and calcium chloride - 0.1%; tap water - 1.0 liter. The medium was sterilized in-place in the fermentor at 1210C for 15 minutes. The pH after sterilization was 6.2. The medium was tempered to 300C, and the initial pH was adjusted to 6.5. The fermentor was inoculated at 1.0%.

The growth of the strain in the fermentor was carried out at 300C, with agitation set at 250 RPM and the pH control set at 5.0. After 24 hours of growth, the cells were harvested by centrifugation, and the cell pellet was resuspended in the supernatant to give 20X concentration. Ten percent (v/v) of glycerol was added as cryoprotectant, and the cell concentrate was distributed in 5.0 ml volumes into sterile plastic tubes and were frozen and held at -800C. The count of the bacteria in the frozen concentrate was 1.9 X 109 cfu/ml

as determined on Tryptone Soy Agar fortified with 1.0% mannitol.

EXAMPLE 2 Moist grains and cereals are prone to spoilage through mold growth, which in many cases lead to the elaboration of mycotoxins in the molding grains, cereals, and feeds. If mold growth could be retarded or prevented in stored grains or cereals, a lot of wastage could be avoided. The efficacy of the Bacillus subtilis strain in inhibiting mold growth was tested in a moist grain system using barley grains.

Barley grains were purchased from a local store. The mold count of the grain was determined. The grain was thoroughly mixed, and a representative 11.0 g sample was added to a 99.0 ml dilution blank, mixed well, and 0.1 ml aliquots from the dilution bottle were spread-plated on 10 plates of Acidified Potato Dextrose Agar (Difco, Detroit, MI). After incubation at 280C for 4 days, the mold colonies formed on the 10 plates were counted and reported as cfu/g. The count of molds/g of the barley grains were 6 molds (cfu)/g.

One hundred grams of barley grains were weighed out into a shallow rectangular porcelain dish.

Using a graduated cylinder, 50 ml of tap water was measured and used to moisten the barley evenly. This was done by stirring the grain thoroughly with a spatula. Another dish was prepared identically. The excess moisture in the dishes was carefully drained out.

The dishes were labeled A and B. To dish A, 10 ml of sterile Tryptone Soy Broth containing 1% mannitol (TSM broth) was added and mixed well to get homogeneity. To the dish labeled B, 10 ml of 1 X 10-4 dilution of the concentrate of the Bacillus subtilis strain made with sterile TSM broth was added, and mixed to get uniform distribution. This delivered approximately 1 X 104 CFU/g of barley. The dishes were covered tightly with plastic wrap, and placed in an incubator held at 280C. The

dishes were examined every day until mold growth was noticed.

For the first three days no visible mold growth was observed. On the fourth day, the dish to which sterile TSM broth was added was totally covered with mold mycelia all over the surface. The dish to which the Bacillus subtilis strain diluted in TSM broth was added had only three isolated spots of mold on the entire surface. There was definite inhibition of indigenous mold flora in the moistened barley, when the Bacillus subtilis strain was present. The experiment was repeated with duplicate dishes for the control and experimental barley grains, using different inoculation rates of the Pozol isolate. Addition of the Bacillus subtilis strain inhibited mold development on moistened barley grains. The results are summarized in Tables 4 and 5.

TABLE 4 Effect of adding Bacillus subtilis strain on molding of barley grains. Treatmenta Days at 28°C Smell Presence of mold Dish A 0 Normal None Dish B 0 Normal None Dish A 1 Normal None Dish B 1 Normal None Dish A 2 Normal None Dish B 2 Normal None Dish A 3 Normal None Dish B 3 Normal None Dish A 4 Musty, +++++b moldy Dish B 4 Moldy +c a Control barley with sterile TSM broth added (Dish A) Experimental barley with 1 x 104 CFU/g of Bacillus <BR> <BR> <BR> <BR> <BR> subtilis strain (Dish B)<BR> <BR> @ Entire surface of the barley was covered with mold<BR> <BR> <BR> <BR> mycelia<BR> <BR> <BR> <BR> c Three isolated patches of mold mycelia

TABLE 5 Effect of adding Bacillus subtilis strain on molding of barley grains Mold developmentb,c Treatmenta Day 0 Day 1 Day 4 Day 5 Day 6 1A None None +++ 1B None None +++ ++++ 2A None None + + + 2B None None + ++ ++ 3A None None None ++ ++ 3B None None None None None 4 None None None ++ ++ a 1A - Uninoculated control 1B - Duplicate of uninoculated control 2A - With 1 x 10 Bacillus subtilis/g of barley 2B - Duplicate of 2A 3A - With 1 x 10@ Bacillus subtilis/g of barley 3B - Duplicate of 3A 4 - With 1 x 10 Bacillus subtilis/g of barley b No observations were made on days 2 and 3.

Experiment terminated on day 6 c + A few isolated spots of mold ++ About 15-20t of the surface covered with mold +++ >S0% of the surface covered with mold ++++ >75% of the surface covered with mold ++++(+) >80% of the surface covered with thick mat of mycelia None No mold development

These results indicate that the Bacillus subtilis strain in the form of a spray can be used to control mold growth in grains in general, and underground crops like peanuts. Such a treatment can be used to prevent mycotoxin formation in various cereal grains, and peanuts. Similar treatment can be used to control mold development, and accompanying.defects like "gushing", during steeping and malting of cereals used in brewing industries.

EXAMPLE 3 The nixtamalized corn flour made into dough is not only used for making Pozol, but also for making tortillas. One of the major problems in the distribution and marketing of tortillas is the appearance of mold spots and patches of mold discoloration on packaged tortillas. In this Example, the efficacy of adding the Bacillus subtilis strain to the corn dough in controlling mold growth in packaged tortillas is demonstrated. Additionally, the efficacy of adding the Bacillus subtilis strain in controlling the spoilage, and molding of stored dough is also demonstrated.

Nixtamalized, vitamin fortified corn flour sold by Quaker Oats Company (Chicago, IL) under the registered trademark QUAKER MASA HARINA DE MAIZE was purchased from a local grocery store. Masa dough was made according to the instructions on the package.

Using 3 cup measures of Masa flour and mixing in 2 1/4, cup measures of warm tap water, about 800 g of Masa dough was made. This was divided into two portions of 400 g each, and placed in two separate beakers, labeled A and B. To the dough in beaker A, 4.0 ml of sterile TSM broth was added. To beaker B, 4.0 ml of a 10-3 dilution of the cell concentrate of the Bacillus subtilis strain was added. The diluent used was sterile TSM broth. Both samples were thoroughly mixed avoiding cross-contamination. The diluted culture added to the

dough would deliver 1 X 104 organisms/g of dough. After removing about 50 g of dough from each beaker for tortilla making, the beakers were covered with aluminum foil, and placed in a 28"C incubator. Two tortillas from each sample were made using an electric tortilla- maker (Vitantonio Mfg. Co., East Lake OH 44094). Each tortilla was placed separately in a ZIPLOC bag, sealed, labeled for identity, and placed in an incubator at 280C.

Every day, the dough samples and corresponding tortillas made from the uninoculated and inoculated dough were examined for the presence of mold growth by macroscopic observation for spots or patches of mycelial growth. Total microbial counts were also made on the dough using TSM agar. The smell (olfactory response) of the dough samples and the corresponding tortillas were also recorded.

For the first two days no mold growth was seen in any of the dough samples. After the first day, the uninoculated and inoculated dough samples were found to have slightly sour smell. On the second day, the uninoculated dough had a strong sour odor, while the inoculated sample did not differ in smell from the previous day. On the third day, relatively extensive white mycelial growth was seen on the uninoculated sample, while the inoculated dough had limited, localized mold spots. The control dough retained the strong sour smell; the inoculated dough only had a slightly sour odor.

On the second day, the uninoculated dough sample had slimy patches on the surface, while the inoculated sample appeared normal. The plate counts assayed on the dough after 3 days showed that on the control sample there was a confluent growth of contaminants at 10-4 dilution on the third day. On the same day, and at the same dilution, the inoculated sample had much thinner growth of contaminants (clearly discernable individual colonies could be seen). The results are summarized in Table 6.

TABLE 6 Effect of adding Bacillus subtilis on the shelf-life and mold development on masa dough. Treatmenta Days Appearance Odor Mold Bacterial at count 28°C (CFU/g)b Control 0 Normal Normal None 3.6 x 104 Experimental 0 Normal Normal None 1.9 x 104 Control 1 Moist S1.sour None NDc Experimental 1 Moist Sl.sour None ND Control 2 Slimy Sour None 1.8 x 109 d Experimental 2 Moist Sl.sour None 1.8 x 109 d Control 3 Slimy Sour +++e TNTCf Experimental 3 Moist Sl.sour +e TNTCf Control 4 ~g Moldy ++++e TNTCf Experimental 4 ~g Sl.sour ++e TNTCf a Control - Uninoculated dough Experimental - Inoculated with 1 x 104 Bacillus subtilis/g of dough b Count made on TSM agar c Not determined counts made in parallel on Minimal agar showed 6.1 x 108 CFU/g for control and 1.5 x 106 CFU/g for the experimental sample e + Small, isolated spots of mold mycelia ++ Isolated patches of mold mycelia +++ Confluent mat of mycelia ++++ Extensive growth of mycelia f TNTC - Too numerous to count. Confluent growth of bacteria at 1 x 104 dilution. Control sample was heavily contaminated by yellow pigmented bacteria.

Yellow contaminants were absent on the experimental dough. g Appearance could not be determined because the surface was covered by mold growth.

Tortillas made from the uninoculated and inoculated dough were also examined daily for mold growth and for the development of off-odors. For the first two days,

no molds were seen in any of the tortillas. On the fourth day, the control tortillas showed mold spots (4 spots on two tortillas); by the sixth day both the control tortillas were totally covered with mold. In contrast no mold patches were seen on the tortillas made from inoculated dough until the fifth day. On the sixth day, only one spot was seen on one of the tortillas; no increase of mold growth was seen on further incubation.

Tortillas made with control dough developed off-odor after the fourth day. Tortillas made from inoculated dough was judged to be slightly off in odor on the fifth day (Table 7).

TABLE 7 Effect of adding Bacillus subtilis strain to masa dough on mold development in tortillas made from the dough. Days at I Controla Experimental 280 C Odor I Mold Odor Mold O Normal None Normal None 1 Normal None Normal None 2 | Normal None Normal None 3 Normal 1 spot/2c Normal None 4 Sl.Sourd 4 spots/2 Sl.Sour None 5 Sour 5 spots/2 S1.Sour None 6 Sour +++++e Sour 1 spot/2 7 Off +++++ Off 1 spot/2 8 | Off +++++ Off 1 spot/2 a Tortillas made from uninoculated dough. b Tortillas made from inoculated dough.

C Indicates number of mold spots on two tortillas. d Sl. Sour - slightly sour e Tortilla completely covered with mold growth.

In a repeat trial, dough that was not inoculated with the Bacillus subtilis isolate developed mold growth on the second day, which on the third day covered the surface completely. The odor of the dough was also

found to be off by the second day. The inoculated dough had no mold growth for the first two days1 and had a few isolated spots of mycelial growth on the third day.

These observations on two trials showed that by inoculating masa dough with the Bacillus subtilis strain, the shelf-life of the dough and tortillas made from the dough can be extended. Similar treatment of various dough Products, used in the production of various breads, indigenous flat breads, bakery goods, and pastas, can be used to extend shelf-life.

EXAMPLE 4 To further determine the amount of inoculated dough needed in a masa dough mix to inhibit contaminants, and development of off odors, dough mixes containing different levels of inoculated dough (inoculated with 1 X 104 cells of Bacillus subtilis strain/g of dough and incubated for 48 hours at 280C) were made. The levels of inoculated dough used were 0%, 25%, 50% and 100%. The dough samples were placed in clean glass beakers, covered with aluminum foil, and placed in an incubator at 280C. The samples were examined every day for mold growth and off-odors.

The odor of the samples containing different proportions of inoculated dough were scored to be sour after the first day. The control dough retained the normal flavor. After the second day, the control sample was very sour, which progressed to an off-odor by the third day. On the third day, the sample containing 25% inoculated dough was also considered to have an off odor. Samples containing higher levels of inoculated dough, namely, 50% and 100% were found to be devoid of off odor.

For the first three days, no mold growth was observed on any of the samples. After the third day, the control sample was totally covered with mold. There was limited, localized mold spots on the sample containing 25% inoculated dough. No mold growth was noted on samples containing 50% and 100% inoculated dough (Table 8).

TABLE 8<BR> Molding of masa dough containing different levels of cultured dougha. Days % Cultured dough in dough mix at 0 25 50 100 28°C Odor Mold Odor Mold Odor Mold Odor Mold 0 Normal none Normal None Sl. None Sour None Sourb 1 Sl. None Sl. None Sour None Sour None Sour Sour 2 Very None Sour None Sour None Off None Sour 3 Off ++++c Off ++ Off None Off None 4 Off ++++ Off ++ Off None Off + + 5 Off ++++ Off +++ Off None Off + + @ Masa dough was inoculated with 1 x 10@<BR> Bacillus subtilis/gram of dough and cultured<BR> for 48 hours at 28° C.<BR> b Sl. Sour - slightly sour.<BR> c None - no mold development<BR> + - one or two isolated spots.<BR> <P>++ - a few patches of mold.<BR> <P>++++ - >80% of the surface covered by mold.<BR> <P>+++++ - entire surface covered with mold.

From the foregoing observations, it is apparent that the use of inoculated dough would aid in controlling mold growth and offer shell-life extension in dough products.

EXAMPLE 5 In an additional trial, masa dough inoculated with the Bacillus subtilis strain and incubated for 48 hours at 280C was lyophilized, and 50% of the lyophilized dough powder was mixed with an equal amount of fresh masa flour, and made into dough. As a control, dough was made entirely from fresh masa flour. Both samples were placed in separate beakers, covered with foil, and incubated at 280C. Observations were made for mold growth and off odors every day.

No mold growth was seen for the first three days in either sample. On the third day, the control dough was completely covered over with mould. The dough made out of a mixture of fresh masa flour and 50% lyophilized cultured dough, was totally free of mold.

The dough also had a fresh odor and appearance (Table 9)

TABLE 9 Effect of adding lyophilized cultured dough powder to fresh masa flour on molding of masa dough during storage at 280Ca. Days at Control doughb Experimental doughc 28°C old 0 Normal None Normal None 1 Normal None Normal None 2 Sl. Offd 2 spots Normal None 4e | Off f Normal None a Masa dough inoculated with 1 x 104 Bacillus subtilis /gram of dough was incubated at 280C for 48 hours <BR> <BR> <BR> b and lyophilized.<BR> <P> Control dough was made from fresh masa flour.<BR> <BR> <BR> c Experimental dough was made from a mixture of equal portions of fresh masa flour and lyophilized dough powder.<BR> <BR> d 51. Off - slightly off. e No observations were made on the third day. f +++++ - Entire surface of the dough was covered by mold.

This observation showed that cultured dough that has been dried is as effective as using moist dough. The culturing can be done on a thin suspension of dough, for example 5% to 10% in water, or even lower, using the Bacillus subtilis strain, and dried by lyophilization, or spray drying, or roller drying, or fluidized bed drying or by any other means available, and mixed with fresh masa flour at various proportions in the range of 5 to 50% or higher if necessary and used for various applications. Similar preparations can be used for various breads, baked goods and the like, where dough is the starting material. The Bacillus subtilis strain can be used for inhibiting molds, extending shelf-life, and preserving dough during handling or transportation to a separate baking site.

EXAMPLE 6 To examine if application of the Bacillus subtilis strain can be used to suppress molds and extend shelf-life in dairy products, shredded cheese was chosen as the test system.

Shredded Mozzarella cheese containing no added preservatives or antimicrobials, purchased from a local supermarket, was used for this application. The shredded cheese was taken out of the package, mixed uniformly on a plastic sheet using a clean spatula. The pooled cheese was then divided into four equal quarters, and 50 g portions were weighed out from each divided pool. Using a spray bottle, two of the portions were evenly sprayed with sterile dilution buffer (used for bacterial dilutions for counting), turning the cheese particles with a spatula to get an even spray.

Approximately 15 minutes were allowed for the cheese to drain excess moisture. The two portions were then separately placed into two ZIPLOC bags, and sealed. The other two portions were similarly treated with 1 X 10-4 dilution of the cell concentrate of the Bacillus subtilis strain made in the same dilution buffer. These portions were placed in two other ZIPLOC bags, and sealed One each of the control and experimental bags were placed in a refrigerator held at 40C, and the remaining bags were placed in an incubator set at 150C.

The cheeses were examined every day for the appearance of mold spots. The higher temperature was chosen to accelerate the growth of molds, and other deterioration of the cheese. No mold development was noticed in the samples held at 4"C even after 2 weeks, and no deteriorative changes were found. No perceptible changes were seen on both samples stored at the higher temperature for the first 4 days. On the fifth day, the control sample stored at 15°C had 3 spots of mold growth; the sample sprayed with cells, however, was completely free of molds. With the progression of

storage at the higher temperature, the mold spots on the control samples got larger and began to taint the surrounding cheese particles. Mold spots on the sample treated with the culture spray appeared only after the 7th day (Table 10).

TABLE 10 Effect of spraying suspended cells of Bacillus subtilis on molding of shredded Mozzarella cheese stored at 15°Ca. Days at Control cheese Cheese sprayed with 15°C cell suspension Odor Mold Odor Mold 0 Normal None Normal None 1 Normal None Normal None 2 Normal None Normal None 3 Normal None Normal None 4 Normal None Normal None 5 Normal 3 spots Normal None 6 Normal 3 spots Normal None 7 Off 5 spots Musty? 3 spots 8 Off 6 spots Off 5 spots 9 Off 7 spots Off 5 spots 12 Moldy ++++b Off 6 spots a Control cheese was evenly sprayed with sterile dilution buffer. Experimental cheese was evenly sprayed with a diluted culture concentr5ate of Bacillus subtilis containing 1.0 x l0cfu/ml. b Cheese particles tainted with mold extensively.

Based on the foregoing results, mold development, and deterioration in cheese can be retarded using the Bacillus subtilis strain. Similar methods can be used to control microbial deterioration in other dairy products including different cheeses, evaporated and condensed milks, creams, dairy spreads and the like.

EXAMPLE 7 The application of the Bacillus subtilis strain in packaging materials to suppress microflora of foods was examined. Tortillas were used as the test system.

Masa flour was converted to dough according to the instruct ions on the package to obtain approximately 300 g of dough. The dough was made into uniformly sized tortillas. Four ZIPLOC bags were turned inside out and the inner surface was uniformly sprayed with sterile dilution buffer using a spray-bottle. After the excess moisture had drained off, the bags were turned over so that the sprayed surface was on the inside. One tortilla was placed and sealed in each of the bags.

Another set of ZIPLOC bags were sprayed with a suspension of Bacillus subtilis strain made in dilution buffer such that the suspension contained 1 x 107 CFU/ml.

The bags were turned over and four tortillas were individually placed in these bags. All the bags were labeled for identity, sealed, and placed in a 280C incubator. The tortillas were daily examined for mold development. No mold development was seen on any the samples for the first four days. After the fifth day, three out of the four control tortillas (tortillas in bags sprayed with sterile dilution buffer) showed mold growth. One of the tainted tortillas had 5 spots of mold growth. Another one 4 mold spots, and the third one had one spot. Among the experimental tortillas (placed in bags sprayed with the Bacillus subtilis strain), only one showed two small spots of mold growth on the fifth day. By the sixth day molds in the infested control packages had spread to form large patches almost covering the entire surface of the tortillas. Three tortillas in the bags treated with Bacillus subtilis strain, in contrast were free of molds; the two spots of mold on the fourth tortilla in the experimental group remained confined to the same

areas noted on the previous day. Treating the bags with a spray of the Bacillus subtilis strain definitely controlled mold development on the tortillas.

The Bacillus subtilis strain can thus be used to treat films, casings, and other packaging material to control mold growth on various food products like breads, cheeses, sausages, wieners, vegetables, fruits and the like.

In all the foregoing Examples, the Bacillus subtilis strain was found to be effective against mold development in various food systems. This strain can also be used to control molds in other food systems like dried fruits, vegetables, meats, fish and livestock feeds, silage and other forage crops.

It is intended that the foregoing description be only illustrative of the present invention and that the present invention be limited only by the hereinafter appended claims.

INDICATIONS RELATING TO A DEPOSITED MICROORGANISM (PCT Rule 13bis) A. The indications made below relate to the microorganism referred to in the description on page ~~~~~~~~~~~~~~~~~~~~~~~ , lineline 2-17 onpage B. IDENTIFICATION OF DEPOSIT Further deposits are identified on an additional sheet Name of depositary institution Agricultural Research Service Culture Collection Address of depositary institution (including postal code and country) 1815 North University Street Peoria, Illinios 61604 United States of America Date ofdeposit 11 April 1998 Accession Number NRRL B-21974 C. ADDITIONAL INDICATIONS (leave blank if not applicable) This information is continued on an additional sheet D. DESIGNATED STATES FOR WHICH INDICATIONS ARE MADE (if the indications are not for all designated States) I E. SEPARATE FURNISHING OF INDICATIONS (leave blank at not applicable) The indications listed below will be submitted to the International Bureau later (speciA"thegeneralnatue o(the indicationse.g, "Accession Number of Deposit'7 For receiving Office use only For international Bureau use only This I This sheet was received with the international application El This sheet was received by the International Bureau on: Authorized officer tR Authorized officer BUD@@EST TREATY ON THE INTERNATIONAL RECOGNI@@ON OF THE DEPOSIT OF MICROOR@ANISMS FOR THE PURPOSE OF PATENT PROSCEDURES INTERNATIONAL FORM TO RECEIPT IN THE CASE OF AN ORIGINAL DEPOSIT Dr. Ebenezer Vedamuthu issued pursuant to Rule 7.1 by the Quest International INTERNATIONAL DEPOSITARY AUTHORITY 2413 7th Street, NW identified at tho bottom of this page Rochester, MN 55901 NAME AND ADDRESS OF DEPOSITOR r. fDErsTTFICAIOW OP nl nLcRooIlohalsx fdeneficatlon roiorence gFven by the cion number Siven by the DEPOGITbar rNTRNLoNAt DEOQSITARY AUTHDECrTY: Bac131vs subtifle nQ NRRL 8-t1974 II, SCIENTIFIC DESCR«PTION AND OR PROPOSED TAXONOHZC DESIGNATION The microorganism identified under z above wae accompanied by: D a scientific description El a propoced taxonomie leignation tMark with a cross where applicable) lix. RECEIPT AND ACCEPTANCE This International Depositary Authority accepts the mlcroorganlssn identified under I. above, which waa received by it on April 11. 1998(date of the, original deposit)' XV. RECEIPT OF REQUEST FOR CONVERSION She mleroogganism identified under X. above was received by this snternational Depositary Authority on (date of- the original deposit) and a request to convert the original deposit to a deposit under the Budapest Treaty wae received by it on ,(date of receipt of request for convereion). V, rNrERNATraMUI DEPOSITAR AU?MoiLZT" Name: Agricultural Research Culture Signature(a} of peteon(e) having the power Collection (NRRt) to repreeent the international Depositary International Depositary Authority Authority or of tpthosy ed officialts): Address: 181S N. Univcrsity Street C: ,.?.. Peoria Illinois~61604 V.S.A. ~ Date: .,-. r Where Rule 6.4 (d) applies, such date is the date on which the status of international depositary authority was acquired.