NATURAL ANTI-MICROBIAL COMBINATION IN STABLE DRY POWDERED FORM

Abstract

An antimicrobial powder, which includes a low molecular weight antimicrobial organic acid and a hygroscopic ingredient, is prepared according to a process wherein the components are combined in a solution to form a liquid slurry composition prior to drying to form a powder, such that drying the liquid slurry composition involves co-drying the components. The low molecular weight antimicrobial organic acid in the antimicrobial powder can be present in a crystal phase of both anhydrous and hydrate forms. The antimicrobial powder exhibits excellent properties, such as shelf stability, without the requirement of encapsulating agents. Methods for preparing the antimicrobial powders as well as applications of the antimicrobial powders in food and beverage products are also disclosed.

Claims

1. A process of producing an antimicrobial powder, the process comprising the steps of combining a hygroscopic ingredient and a low molecular weight antimicrobial organic acid in an aqueous solution to obtain a liquid slurry composition and drying the liquid slurry composition to produce an antimicrobial powder.

2. The process of claim 1, wherein the hygroscopic ingredient and the low molecular weight antimicrobial organic acid are combined in a weight ratio of 1:100 to 100:100 w/w hygroscopic ingredient solids to organic acid solids.

3. The process of claim 1, wherein the antimicrobial powder comprises less than about 91% of a carrier.

4. The process of claim 1, wherein prior to the step of drying the liquid slurry composition, the process comprises the steps of adjusting the pH of the liquid slurry composition to between about 4.0 and 10.0, and heating the liquid slurry composition at a temperature between about 40° F. and about 180° F., wherein during the heating step the temperature is maintained until the liquid slurry composition has a dissolved percent organic acid solids in the range of about 5% to 70%.

5. The process of claim 1, wherein the low molecular weight antimicrobial organic acid is a neutralized vinegar.

6. The process of claim 5, wherein the neutralized vinegar is selected from the group consisting of sodium acetate, magnesium acetate, potassium acetate, calcium acetate, and combinations thereof.

7. The process of claim 1, wherein the hygroscopic ingredient is selected from the group consisting of celery, beet, cabbage, cucumber, eggplant, mushroom, lettuce, squash, zucchini, mixed salad greens, carrot, artichoke, green beans, lima beans, broccoli, cauliflower, collard greens, corn, mustard, okra, onion, chinese pea pods, black eyed peas, green peas, potatoes, turnips, radishes, spinach, swiss chard, apple, apricot, banana, bilberry, blackberry, blackcurrant, blueberry, coconut, currant, cherry, cherimoya, clementine, cloudberry, date, damson, durian, elderberry, fig, feijoa, gooseberry, grape, grapefruit, huckleberry, jackfruit, jambul, jujube, kiwifruit, kumquat, lemon, lime, loquat, lychee, mango, melon, cantaloupe, honeydew, watermelon, rock melon, nectarine, orange, passionfruit, peach, pear, plum, plumcot, prune, pineapple, pomegranate, pomelo, purple mangosteen, raisin, raspberry, rambutan, redcurrant, satsuma, strawberry, tangerine, tomato, ugli fruit, and combinations thereof.

8. The process of claim 7, wherein the hygroscopic ingredient is cultured.

9. The process of claim 1, wherein the low molecular weight antimicrobial organic acid is sodium acetate and the hygroscopic ingredient is cultured celery juice.

10. The process of claim 1, further comprising a step of packaging the antimicrobial powder in a container.

11. An antimicrobial powder obtainable by the process according to claim 1, wherein the low molecular weight antimicrobial organic acid is present in the antimicrobial powder in both anhydrous and hydrate forms in a ratio of about 1:5 to 5:1 parts w/w anhydrous form to hydrate form.

12. An antimicrobial powder obtainable by the process according to claim 5, wherein the neutralized vinegar is sodium acetate and is present in the antimicrobial powder in a glassy-crystal phase of both anhydrous and tri-hydrate forms in a ratio of about 1:5 to 5:1 parts w/w anhydrous form to tri-hydrate form.

13. The antimicrobial powder of claim 11, wherein the antimicrobial powder comprises less than about 91% of a carrier.

14. The antimicrobial powder of claim 13, wherein the antimicrobial powder when stored at a temperature of about 20° C. and about a 70% equilibrium relative humidity for at least 6 months has a water content of no more than about 5%.

15. An antimicrobial powder, comprising a low molecular weight antimicrobial organic acid and a hygroscopic ingredient, wherein the low molecular weight antimicrobial organic acid is present in both anhydrous and hydrate forms in a ratio of between 1:5 to 5:1 parts w/w anhydrous form to hydrate form.

16. The antimicrobial powder of claim 15, wherein the low molecular weight antimicrobial organic acid and the hygroscopic ingredient are present in a ratio of between about 1:100 and 100:100 parts w/w hygroscopic ingredient solids to organic acid solids.

17. The antimicrobial powder of claim 15, wherein the antimicrobial powder comprises less than about 91% of a carrier.

18. The antimicrobial powder of claim 17, wherein the antimicrobial powder when stored at a temperature of about 20° C. and about a 70% equilibrium relative humidity for at least 6 months has a water content of no more than about 5%.

19. The antimicrobial powder of claim 15, wherein the low molecular weight antimicrobial organic acid is a neutralized vinegar selected from the group consisting of sodium acetate, magnesium acetate, potassium acetate, calcium acetate, and combinations thereof.

20. The antimicrobial powder of claim 19, wherein the neutralized vinegar is sodium acetate and is present in the antimicrobial powder in a glassy-crystal phase of both anhydrous and tri-hydrate forms in a ratio of between 1:5 to 5:1 parts w/w anhydrous form to tri-hydrate form.

21. The antimicrobial powder of claim 15, wherein the hygroscopic ingredient is selected from the group consisting of celery, beet, cabbage, cucumber, eggplant, mushroom, lettuce, squash, zucchini, mixed salad greens, carrot, artichoke, green beans, lima beans, broccoli, cauliflower, collard greens, corn, mustard, okra, onion, chinese pea pods, black eyed peas, green peas, potatoes, turnips, radishes, spinach, swiss chard, apple, apricot, banana, bilberry, blackberry, blackcurrant, blueberry, coconut, currant, cherry, cherimoya, clementine, cloudberry, date, damson, durian, elderberry, fig, feijoa, gooseberry, grape, grapefruit, huckleberry, jackfruit, jambul, jujube, kiwifruit, kumquat, lemon, lime, loquat, lychee, mango, melon, cantaloupe, honeydew, watermelon, rock melon, nectarine, orange, passionfruit, peach, pear, plum, plumcot, prune, pineapple, pomegranate, pomelo, purple mangosteen, raisin, raspberry, rambutan, redcurrant, satsuma, strawberry, tangerine, tomato, ugli fruit, and combinations thereof.

22. The antimicrobial powder of claim 21, wherein the hygroscopic ingredient is cultured.

23. The antimicrobial powder of claim 19, wherein the neutralized vinegar is sodium acetate and the hygroscopic ingredient is cultured celery juice.

24. The antimicrobial powder of claim 15, wherein the antimicrobial powder is packaged in a container, and the packaged antimicrobial powder includes less than about 91% of a carrier.

25. A method of producing a foodstuff or beverage, comprising the steps of combining the antimicrobial powder of claim 15 with one or more edible or potable ingredients.

26. A foodstuff or beverage prepared by contacting one or more edible or potable ingredients with the antimicrobial powder of claim 15.

27. A foodstuff or beverage comprising an edible or potable ingredient and the antimicrobial powder of claim 15, wherein the antimicrobial powder is contained in an amount of between about 0.1% to about 5% by weight of the edible or potable ingredient.

Description

FIGURES

[0027] These and other advantages of the present invention are best understood with reference to the drawings, in which:

[0028] FIG. 1 is a differential scanning calorimeter (DSC) scan of a sodium acetate anhydrous glassy amorphous standard

[0029] FIG. 2 is a DSC scan of a sodium acetate tri-hydrate crystal standard

[0030] FIG. 3 is a DSC scan of a spray dried neutralized vinegar

[0031] FIG. 4 is a DSC scan of a spray dried neutralized vinegar-11% cultured celery juice concentrate

[0032] FIG. 5 is a DSC scan of a spray dried neutralized vinegar-26% cultured celery juice concentrate

[0033] FIG. 6 is a macroscopic time elapse comparison of spray dried neutralized vinegar and co-dried neutralized vinegar and cultured celery juice solids solution

[0034] FIG. 7 is a microscopic time elapse comparison of spray dried neutralized vinegar and co-dried neutralized vinegar and cultured celery juice solids solution

[0035] FIG. 8 is a photograph of a bag of dry neutralized vinegar powder (sodium acetate) that has formed a large lump due to sodium acetate crystal conversion from anhydrous to tri-hydrate

[0036] FIG. 9 is a microscopic view (40×) under semi-polar light showing the darker anhydrous sodium acetate powder turning into tri-hydrate crystal form (bright crystals), which bond particles to each other

[0037] FIG. 10 is a side-by-side comparison of vacuum-dried celery juice before and after exposure to ambient 20° C. air at 78% equilibrium relative humidity for one hour

[0038] FIG. 11 is a side-by-side comparison of vacuum dried cultured celery product (left) and 24% celery solids juice dried with buffered vinegar under 75% equilibrium relative humidity for 48 hours

[0039] FIG. 12 is a side by side comparison of vacuum dried cultured celery product (right) and 24% celery solids juice dried with buffered vinegar (left) under 75% equilibrium relative humidity for 96 hours

DETAILED DESCRIPTION OF NON-LIMITING EMBODIMENTS OF THE DISCLOSURE

[0040] There is disclosed herein antimicrobial powder compositions and methods of producing and using the same. As can be seen by comparison of the FIG. 1 DSC scan of a sodium acetate anhydrous glassy amorphous form standard and the FIG. 3 DSC scan of a spray dried neutralized vinegar (sodium acetate), spray drying a solution of neutralized vinegar results in most all sodium acetate anhydrous glassy amorphous form and no measurable tri-hydrate crystals.

[0041] As can be seen by comparison of the FIG. 2 DSC scan of a sodium acetate tri-hydrate crystal standard with FIG. 4, 5 DSC scans of a spray dried neutralized vinegar with 11% and 26% cultured celery juice concentrate, unexpectedly, co-drying a solution of a low molecular weight antimicrobial organic acid (e.g., sodium acetate) and a hygroscopic ingredient (e.g., cultured celery juice concentrate) results in a distinct composition that includes both hydrate crystal form and anhydrous glassy amorphous form. In the preferred example where sodium acetate is the low molecular weight antimicrobial organic acid, the sodium acetate is in the predominant preferred tri-hydrate crystal form, but with enough anhydrous glassy amorphous form to render the product capable of being dry processed in a spray-drum dryer, where the drying chamber temperature is well above the 58° C. melt point of the tri-hydrate crystal. The antimicrobial powder compositions may contain at least about 20% anhydrous glassy amorphous form w/w on a total organic acid (e.g., sodium acetate) crystal basis for dryability, and at least about 20% hydrate crystal form w/w on a total organic acid crystal basis for shelf stability. In one embodiment, the neutralized vinegar in the antimicrobial powder may be at least about 50% tri-hydrate crystal form w/w on a total neutralized vinegar crystal basis for shelf stability. In another embodiment, the low molecular weight antimicrobial organic acid in the antimicrobial powder may be about 80% hydrate crystal form w/w on a total organic acid crystal basis for shelf stability. In yet a further embodiment, the antimicrobial composition may contain the low molecular weight antimicrobial organic acid in a glassy-crystal phase of both anhydrous and hydrate forms in a ratio of about 1:5 to 5:1 parts w/w anhydrous form to hydrate form, preferably about 1:2 parts w/w anhydrous form to hydrate form. In one preferred example, the antimicrobial powder composition contains sodium acetate in a glassy-crystal phase of both anhydrous and tri-hydrate forms in a ratio of about 1:5 to 5:1 parts w/w anhydrous form to tri-hydrate form, preferably about 1:2 parts w/w anhydrous form to tri-hydrate form.

[0042] To demonstrate the advantages of the co-dried multiple component anti-microbial invention, a comparison was made to the same composition with independently dried components that were blended after drying, as is currently practiced in the art. FIG. 6 shows the result of leaving these two samples on a sheet of white paper at a temperature of 20° C. and 78% equilibrium relative humidity for a period of 28 hours. As can be seen in FIG. 6, the blend of independently dried components on the left absorbed water and became syrup-like, so much so that the paper underneath became wet and wrinkled. On the other hand, the co-dried product of the invention on the right remained in a usable powder form.

[0043] This behavior can be seen in closer view with the microscopic images of FIG. 7. The time elapse images on the left shows a 40× view of the particles in the blend of independently dried components at a temperature of 20° C. and 78% equilibrium relative humidity for 180 minutes from top to bottom, compared to the time elapse images on the right of the co-dried invention under the same conditions. As can be seen, the particles on the left became melted and fused, whereas the particles of the co-dried invention on the right maintained their singularity and flowability.

[0044] As yet further demonstrations of advantages of the co-dried antimicrobial powder composition, FIGS. 11 and 12 compare cultured celery products and co-dried 24% celery solids juice dried with neutralized vinegar (sodium acetate).

[0045] FIG. 11 depicts vacuum dried cultured celery product (left) versus 24% celery solids juice dried with neutralized vinegar (right) under 75% relative humidity at 22° C. for 48 hours. The results indicate that vacuum dried cultured celery product is highly hygroscopic compared to 24% celery solids juice co-dried with neutralized vinegar at 48 hours. The moisture induced phase transition of vacuum dried cultured celery product indicates the poor shelf stability under the tested conditions.

[0046] FIG. 12 depicts 24% celery solids juice co-dried with neutralized vinegar (sodium acetate) (left) versus vacuum dried cultured celery product (right) under 75% relative humidity at 22° C. for 96 hours. The results indicate that the co-dried multiple component antimicrobial powder composition of the invention was only partially liquefied, as shown by the crystalline materials remaining at the end of storage. On the other hand, vacuum dried cultured celery product became completely pourable by the end of the 96-hour testing period.

[0047] As can be seen from the above, the co-dried multiple component antimicrobial powder composition of the invention has an advantageous shelf life over a dry blended composition of the separately processed ingredients, as well as vacuum dried cultured celery product alone. This embodiment of the invention without any carrier offers a tremendous improvement to a carrier-free (vacuum dried) version of cultured celery juice.

[0048] The low molecular weight antimicrobial organic acids include but are not restricted to neutralized vinegars, such as sodium acetate, magnesium acetate, potassium acetate, and calcium acetate, as well as salts of propionic acid, citric acid, lactic acid, formic acid, glycolic acid, malic acid, and mixtures thereof.

[0049] The neutralized vinegars may be purchased from commercial sources or prepared by buffering a vinegar composition with a neutralizing agent. The vinegar composition may be in a liquid or powder form. Examples of vinegars that may be used in the present process include malt vinegar, wine vinegar, sherry vinegar, apple cider vinegar, fruit vinegars, rice vinegar, and combinations thereof.

[0050] The neutralized vinegar may be prepared through the addition of a neutralizing agent to a vinegar composition to adjust the pH of the vinegar composition to a value within the range of about 4.0 to 8.0. In a preferred embodiment, the pH of the vinegar composition is adjusted to a value of about 4.5 to 7.0. In a more preferred embodiment, the pH of the vinegar composition is adjusted to a value of about 5.0 to 6.0. Similar preferred pH ranges would likewise apply to other low molecular weight antimicrobial organic acids discussed herein.

[0051] The neutralizing agent for adjusting the pH of the low molecular weight antimicrobial organic acids is selected from the group consisting of sodium hydroxide, potassium hydroxide, magnesium hydroxide, calcium hydroxide, sodium (bi)carbonate, potassium (bi)carbonate, and mixtures thereof.

[0052] In addition to cultured celery juice, other hygroscopic ingredients may be substituted, whether or not they have anti-microbial properties. For example, such hygroscopic ingredients include other hygroscopic vegetable juices, cultured or not, such as carrot, cabbage, tomato, or the like; non vegetable hygroscopic ingredients, such as high DE corn syrup, dextrose, arabinose, ammo acids, short peptides, protein hydrolysates, honey, or the like; and hygroscopic fruit juices such as orange, blueberry, pineapple or the like.

[0053] In certain embodiments, the hydroscopic ingredients can be cultured or non-cultured sources of vegetable or fruit substrates isolated from roots, stems, leaves and/or the flower. By way of example, plant material may be selected from celery, beet, cabbage, cucumber, eggplant, mushroom, lettuce, squash, zucchini, mixed salad greens, carrot, artichoke, green beans, lima beans, broccoli, cauliflower, collard greens, corn, mustard, okra, onion, Chinese pea pods, black eyed peas, green peas, potatoes, turnips, radishes, spinach, Swiss chard and combinations thereof. The fruit substrates are selected from the group of apple, Apricot, Banana, Bilberry, Blackberry, Blackcurrant, Blueberry, Coconut, Currant, Cherry, Cherimoya, Clementine, Cloudberry, Date, Damson, Durian, Elderberry, Fig, Feijoa, Gooseberry, Grape, Grapefruit, Huckleberry, Jackfruit, Jambul, Jujube, Kiwifruit, Kumquat, Lemon, Lime Loquat, Lychee, Mango, Melon, Cantaloupe, Honeydew, Watermelon, Rock melon, Nectarine, Orange, Passionfruit, Peach, Pear, Plum, Plumcot, Prune, Pineapple, Pomegranate, Pomelo, Purple mangosteen, Raisin, Raspberry, Rambutan, Redcurrant, Satsuma, Strawberry, Tangerine, Tomato, Ugli Fruit.

[0054] The hygroscopic ingredients may be cultured using strains, including but not is limited to, Micrococcus, Kocuria Staphylococcus, Lactobacillus, Lactococcus, Streptococcus, Pediococcus, Leuconostoc, Propionibacterium, Xanthomonas, Bifidobacterium, Acetobacter, Bacillus coagulans, Enterococcus and combinations thereof.

[0055] Metabolites of the components can include organic acids or salts thereof. Such examples include glycolic, hydroxyacetic, lactic, propionic, acetic, sorbic, formic, propanoic, butyric, valeric, adipic, gluconic, glycolic, malic, fumaric, citric, tartaric, ascorbic, salicylic, benzoic, or carnosic), nitrite salts, peptides, botanicals, extracts, enzymes or a mixture thereof.

[0056] The compositions of the disclosure can include one or more additives, such as one or more of an antimicrobial compound, a surfactant, a pH adjusting agent, a cryoprotectant, anti-foaming agent, a chelating and thickening ingredient.

[0057] In certain embodiments, compositions of the disclosure can include less than about 91% of a carrier. As used herein, such carriers include those known in the art, including but not limited to maltodextrin, corn syrup, gums, proteins, etc. Preferably, the composition includes fess than about 50% of carrier. More preferably, the composition does not include a carrier.

[0058] Non-limiting processing conditions for obtaining the aforementioned product combination of low molecular weight antimicrobial organic acids (e.g., sodium acetate) and hygroscopic ingredient (e.g., celery juice) can include conditions as provided below.

[0059] Preparation of the Liquid Slurry Composition:

[0060] Prepare a solution by combining between about 1 to 100 parts of a hygroscopic ingredient (on a dry w/w basis such as celery juice solids, to 100 parts of neutralized vinegar solids or other low molecular weight antimicrobial organic acid, such as sodium acetate-acetic acid solids, at a total dissolved solids of between about 5 and 70 (w/w) percent in water. In another embodiment, the liquid slurry composition is prepared by combining between about 1 to 50 parts of a hygroscopic ingredient (on a dry w/w basis) to 100 parts of neutralized vinegar solids or other low molecular weight antimicrobial organic acid. In a preferred embodiment, the liquid slurry composition includes between about 10% to 30% (w/w) hygroscopic ingredient and about 70% to 90% (w/w) neutralized vinegar. In one preferred example, the liquid slurry composition includes about 25% (w/w) hygroscopic ingredient and about 75% (w/w) neutralized vinegar. Again, the foregoing percentages are on a dry w/w basis of the final antimicrobial powder composition.

[0061] After preparing the liquid slurry composition, the temperature of the slurry is adjusted to between about 40° F. to 180° F.; preferably about 130° F., so as to attain a high dissolved percent organic acid solids (e.g., acetate-acetic acid solids), without being so hot as to volatilize significant amount of organic acid (e.g., acetic acid). In one embodiment, the liquid slurry composition is heated until the composition has a dissolved percent acetate-acetic acid solids in the range of about 5-70%. In a preferred embodiment, the liquid slurry composition is heated until the composition has a dissolved percent acetate-acetic acid solids in the range of about 20-50%. Even more preferably, the liquid slurry composition is heated until the composition has a dissolved percent acetate-acetic acid solids in the range of about 25-35%. In one preferred example, the liquid slurry composition is heated until the composition has a dissolved percent acetate-acetic acid solids of about 30%. The pH of the resultant liquid slurry composition can be adjusted to between about 4.0 to 10.0; preferably to about 5.8.

[0062] Co-Drying the Liquid Slurry Composition:

[0063] Exemplary processes for drying the liquid slurry composition can include spray drying the liquid slurry through an APV or Niro Minor type convective dryer with inlet temperature of between about 220-550° F. and adjust product feed rate so as to maintain an exhaust temperature of between about 130-210° F. The product fed through a hydraulic pressure atomizing nozzle operating at between about 100 and 10,000 psi (preferably 2500 psi), or an air atomizing nozzle operating at a product pressure of between about 0 and 40 psi and an air pressure of between about 10 and 250 psi (preferably 0 and 35 psi respectively), or a centrifugal atomizing wheel operating at between about 10,000 and 50,000 RPM (preferably 20,000 RPM).

[0064] Another exemplary drying process includes drum drying the liquid slurry with a Bufflovac type dryer with a surface temperature of between about 225-500° F. (preferably 325° F.), and a residence time of between about 5 and 90 seconds (preferably 30 seconds).

[0065] Yet another exemplary drying process includes vacuum or freeze drying the liquid slurry in a tray or belt dryer at a pressure of between about 0.05 and 70 mm mercury (preferably 0.3-4 mm mercury) with a tray or belt temperature of initially about 0-100° F. (preferably 15° F.), and increasing temperature to a value of between about 50-200° F. (preferably 130° F.) at the end of process. Window refractance and infrared drying are yet further drying processes according to alternative embodiments.

[0066] After drying, the resulting powder or flakes can be collected by sifting through a mesh screen, such as a US#10 mesh screen, or equivalent methods to remove lumps.

[0067] The final composition is packaged in an appropriate container per intended quantity of use. For example, a container may have 2 mil or thicker polyethylene liner to deter absorption of humidity from environment.

[0068] In one preferred example, a mixture of about 25% w/w cultured celery juice solids and about 75% w/w sodium acetate neutralized vinegar in solution is dried by one of spray drying, drum drying, vacuum drying or freeze drying. This drying process provides a powder composition of sodium acetate in a glassy-crystal phase of both the thermally stable (to spray drying) anhydrous form and the non-hygroscopic (shelf stable) tri-hydrate crystal form in a ratio of about 1:2 parts w/w anhydrous to tri-hydrate and a bound form of the cultured celery juice, which has enhanced stability to hygroscopic melt degradation.

[0069] In another preferred example, an antimicrobial powder composition is provided that is free from conventionally d encapsulating materials (carriers). The antimicrobial powder composition includes a neutralized vinegar in a glassy-crystal phase of both the thermally stable (to spray drying) anhydrous form and non-hygroscopic (shelf stable) hydrate crystal form a ratio of between about 1:5 to 5:1 parts w/w anhydrous to hydrate and preferably in a ratio of between about 1:2 parts w/w anhydrous to hydrate. The antimicrobial powder composition further includes a nitrite or nitrate containing cultured or non-cultured celery juice concentrate distributed between or within the neutralized vinegar glassy-crystals in a ratio of between about 1:100 and 100:100 parts cultured or non-cultured celery juice solids (on a dry w/w basis) to neutralized vinegar solids (on a dry w/w basis), preferably 1:100 to 50:100 parts w/w cultured or non-cultured celery juice solids to neutralized vinegar solids. The antimicrobial of this embodiment provides a flowable shelf stable powder.

[0070] In certain embodiments of the disclosure, the co-dried powder composition of low molecular weight antimicrobial organic acid and a hygroscopic ingredient has a pH in the range of between about 3.5 to 12. In other embodiments, the co-dried powder composition has a pH in the range of between about 6.5 to 8.0. In yet further embodiments, the co-dried powder composition has a pH of about 7.0.

[0071] The disclosed co-processed powder compositions can be stored under different conditions, including atmospheric conditions, under vacuum, or MAP packaged.

[0072] The disclosed co-dried powder compositions are suitable for use in a range of food, beverage and personal care applications. Such applications include, but are not limited to, meat, seasoning, refrigerated salad, beverage, dressing, spread, sauce, dip, filling, marinade and dairy. In these embodiments, the co-processed powder composition can be added by various methods, such as direct addition.

[0073] By way of example, the co-processed powder composition can be directly added to a substrate at an application rate of about 0.1-5% on a w/w basis to substrate. In such applications, the co-processed powder composition inhibits or delays the outgrowth of spoilage and pathogenic microorganisms, such as E. coli, Staphylococcus, Campylobacter, Salmonella, yeast, mold, bacillus, LAB as well as Clostridium species and Listeria monocytogenes.

EXAMPLES

[0074] The following examples have been included to illustrate the presently disclosed subject matter. Certain aspects of the following examples are described in terms of techniques and procedures found or contemplated by the present inventors to work well in the practice of the presently disclosed subject matter. These examples illustrate standard practices of the inventors. In light of the present disclosure and the general level of skill in the art, those of skill will appreciate that the following examples are intended to be exemplary only and that numerous changes, modifications, and alterations can be employed without departing from the scope of the presently disclosed subject matter.

Example 1

[0075] 11% cultured celery juice powder:

TABLE-US-00001 TABLE 1 Qty Component (grams) RM % TS Solids (g) % SB Buffered Vinegar Powder 2,100.50 98 2058.49 89% Cultured Celery Juice 623.7 42.61 265.75857 11% Concentrate Water 2,722.90 TOTAL 5,447.10 2,324.25 Batch % solids 43%

[0076] In the amounts provided in Table 1, vinegar powder buffered with sodium to a pH of 5.8 was combined with cultured celery juice in water to form a liquid slurry composition having a pH of 6.78. The liquid slurry composition was subsequently heated to a temperature of 130° F. until the liquid slurry composition had a dissolved percent acetate-acetic acid solids of about 27%, as measured in the liquid.

[0077] The liquid slurry composition was fed into a spray dryer, such as an APV “Minor”, and an exhaust temperature of about 190° F. was maintained with a constant inlet air temperature of about 350° F. for about 30 minutes.

[0078] The resultant powder was collected after the dryer cooled to about 130° F.

Example 2

[0079] 25% cultured celery juice powder:

TABLE-US-00002 TABLE 2 Component Qty (LB) Rm % TS Solids (LB) % SB Buffered Vinegar Powder 4.01 98 3.928268767 76% Cultured Celery Juice 2.89 42.61 1.231731233 24% Concentrate Water 5.10 TOTAL 12.00 LB 5.16 Batch % solids 43%

[0080] In the amounts provided in Table 2, vinegar powder buffered with sodium to a pH of 5.8 was combined with cultured celery juice in water to form a liquid slurry composition having a pH of 7.00. The liquid slurry composition was subsequently heated to a temperature of 130° F. until the liquid slurry composition has a dissolved percent acetate-acetic acid solids of about 23%, as measured in the liquid.

[0081] The liquid slurry composition was fed into a spray dryer, such as an APV “Minor”, and an exhaust temperature of about 190° F. was maintained with a constant inlet air temperature of about 350° F. for about 30 minutes.

[0082] The resultant powder was collected after the dryer cooled to about 130° F.

[0083] As can be appreciated by a person of ordinary skill in the art, other similar convective or conductive forms of drying could be employed, such as drum drying or flash drying.

[0084] Recitation of ranges of values herein are merely intended to serve as a shorthand method of referring individually to each separate value falling within the range, unless otherwise indicated herein, and each separate value is incorporated into the specification as if it were individually recited herein. The use of any and all examples, or exemplary language (e.g., “such as”) provided herein, is intended merely to better illuminate the invention and does not pose a limitation on the scope of the invention unless otherwise claimed. No language in the specification should be construed as indicating any non-claimed element as essential to the practice of the invention. Preferred embodiments of this invention are described herein, including the best mode known to the inventors for carrying out the invention. Variations of those preferred embodiments may become apparent to those of ordinary skill in the art upon reading the foregoing description. The inventors expect skilled artisans to employ such variations as appropriate, and the inventors intend for the invention to be practiced otherwise than as specifically described herein. Accordingly, this invention includes all modifications and equivalents of the subject matter recited in the claims appended hereto as permitted by applicable law. Moreover, any combination of the above-described elements in all possible variations thereof is encompassed by the invention unless otherwise indicated herein or otherwise clearly contradicted by context.