Patent Application
20140227419
The present invention relates to an anti-fungal agent for processed cereal foods.
In order to extend the length of preservation time of food, it is necessary to suppress growth of microorganisms, particularly mold to prevent putrefaction. Generally, it is thought that putrefaction of food depends on the preservation condition (surrounding environment) after food production, and a technique of prevention against putrefaction using an anti-fungal agent, preservation pH, preservation temperature, water activity control and the like in combination is in practical use.
The production of bread, which is most typical of processed cereal foods, uses various enzymes for increasing the volume, preventing staling, improving the structure and color of the crumb of bread, and improving the color of crust. The representative examples of the enzymes include amylases, hemicellulases such as xylanase; oxidases; and lipases (Patent Document 1). Also, the use of enzymes in place of emulsifying agents used for staling prevention and dough preparation is being studied. Taking the global breadmaking market into consideration, from the point of view of reducing costs of raw materials or increasing the efficiency of production processes in the production of bread, the use of enzymes has attracted attention.
On the other hand, cakes, confectioneries, noodles and cooked rice are preserved mainly in a refrigerated state or a frozen state. Moreover, industrially, there are cases where an anti-fungal agent such as calcium propionate and alcohol is also used. However, it has been reported that the use of an anti-fungal agent can impair the flavor of foods and affect the physical properties of foods. As a result, preventing mold from growing on foods is an important problem related to the extension of preservation time of processed cereal foods, and therefore, a safe and inexpensive anti-fungal agent is desired.
Patent Document 1: Japanese Laid-Open Patent Publication No. 2007-325515
It is an object of the present invention to provide a safe and inexpensive anti-fungal agent for processed cereal foods.
As a result of intensive research to solve the foregoing problems, the inventors of the present invention found that it is possible to provide a safe and inexpensive anti-fungal agent for processed cereal foods by using chitinase, and completed the present invention.
The present invention provides an anti-fungal agent for processed cereal foods, comprising chitinase.
In one embodiment, the anti-fungal agent further contains calcium propionate.
In one embodiment, calcium propionate is contained in a ratio of 0.1 to 500 parts by mass to 1 part by mass of the chitinase.
The present invention also provides an anti-fungal agent-containing processed cereal food, which contains the anti-fungal agent.
In one embodiment, the food is bread, a cake or a confectionery.
The present invention further provides a method for producing an anti-fungal agent-containing processed cereal food, which comprises a step of incorporating the anti-fungal agent into the processed cereal food.
In one embodiment, the step is mixing the anti-fungal agent into cereal materials.
In one embodiment, the anti-fungal agent is mixed so that chitinase is contained in an amount of 1 to 10,000 μg/g of the cereal materials.
In one embodiment, the step is applying the anti-fungal agent on the surface of the processed cereal food.
In one embodiment, the anti-fungal agent is applies so that chitinase is contained in an amount of 2 to 200 μg/cm2 of the surface of the processed cereal food.
With the present invention, it is possible to provide a safe and inexpensive anti-fungal agent for processed cereal foods. Due to the inclusion of an enzyme, chitinase, the anti-fungal agent for processed cereal foods of the present invention is safe and inexpensive.
The anti-fungal agent for processed cereal foods of the present invention contains chitinase.
In the present invention, the processed cereal food means food obtained by processing cereals. For example, the processed cereal food means food obtained by using cereals as they are, or processed cereals (e.g., pulverized cereals and ground cereals) as raw materials, mixing any other materials to the raw materials as appropriate to produce a mixture (e.g., dough), processing the mixture by a method such as baking, steaming, frying and boiling, and shaping the mixture or adding other ingredients to the mixture if necessary. Examples of cereals include wheat, corn, rice, buckwheat, barley, rye, and oats. Examples of processed cereal foods include bread, cakes, confectioneries, noodles, and cooked rice. Bread, cakes, and confectioneries are preferable, and bread is more preferable. Examples of bread include white bread, sweet pastries, rolls, French bread, steamed buns, stuffed bread, bread rolls, fruit bread, corn bread, butter-enriched rolls, buns, sweet dough, croissants, Danish pastries, hardtacks, and pretzels. Examples of cakes include sponge cakes, Swiss rolls, angel cakes, pound cakes, fruitcakes, and hotcakes. Examples of confectioneries include doughnuts, madeleines, baumkuchens, crepes, waffles, castellas, cookies, biscuits, crackers, muffins, choux pastries, éclairs, millefeuilles, tarts, wafers, pies, pizzas, snack food, soufflés, Senbei (rice crackers), Okaki (fried rice cakes), Arare (cubic rice crackers), Manjuu (buns with a bean-jam filling), Dora-yaki (two small pancakes with bean jam in between), Imagawa-yaki (Japanese muffin filled with bean jam), Tai-yaki (fish-shaped pancake filled with bean jam), rice cakes, Chinese steamed buns, mooncakes, small round cookies, and fried dough cookies. Examples of noodles include udon (Japanese wheat noodles), soba (Japanese buckwheat noodles), somen (Japanese thin wheat noodles), pasta, Chinese noodles, rice vermicelli, and pho (Vietnamese noodles). Examples of cooked rice include rice, steamed rice, Chimaki (rice dumplings wrapped in bamboo leaves), rice balls, sushi, and Chinese-style fried rice.
Chitinase in the present invention is a general name referring to enzymes that degrade chitin. Chitin is β-1,4-poly-N-acetyl glucosamine, a polysaccharide in which a plurality of monosaccharides, N-acetyl glucosamines (GlcNAc) are linked via β-1,4 bonds, and is a main structural polysaccharide of arthropods, mollusks, ectoprocts, and fungi. Chitin is cleaved into GlcNAcs and oligosaccharides thereof by chitinase (EC3.2.1.14) derived from plants (e.g., papayas), mid-gut glands of mollusks, microorganisms (e.g., actinomycetes) and the like. Chitinase is a general name referring to enzymes that cleave chitin into oligosaccharides or GlcNAcs. It is known that chitinases include exo-chitinases and endo-chitinases in terms of cleavage patterns, and chitinases include family 18, family 19 and other families in terms of the homology of gene sequences, but there is no particular limitation on chitinase to be contained in the anti-fungal agent for processed cereal foods of the present invention. Chitinases of family 18 or other families are preferable.
There is no particular limitation on methods for preparing chitinase. Examples thereof include a method for preparing chitinase from plants or microorganisms containing chitinase. A method for preparing chitinase from microorganisms is preferable because the microorganisms can be mass-cultured and chitinase can be prepared inexpensively. There is no particular limitation on microorganisms. Examples thereof include actinomycetes, bacteria, mold, and yeasts. Actinomycetes are preferable. Examples of actinomycetes include Streptomyces griseus (hereinafter, “Streptomyces” is described as “S.”), S. avermitilis, S. violaceoruber and S. cinnamoneus. These strains are available from bioresource collections such as RIKEN, the National Institute of Technology and Evaluation, and the American Type Culture Collection. A method for preparing chitinase from microorganisms include the steps of, for example, culturing microorganisms producing chitinase; separating microorganism cells and a solution containing chitinase from the culture; and separating and purifying chitinase from the solution containing chitinase. For culturing microorganisms producing chitinase, the microorganisms are cultured in a culture medium containing a nutrient source which the microorganisms can utilize. The culture medium may be in a liquid form or in a solid form as long as the production of chitinase is promoted. A liquid culture medium is preferable for mass culture. Examples of the nutrient source include a carbon source, a nitrogen source and inorganic salts. Examples of the carbon source include glucose, glycerin, dextrin, starch, molasses, oil from animals and plants, and chitin. Examples of the nitrogen source include soybean flour, corn steep liquor, cottonseed cakes, meat extract, peptone, yeast extract, ammonium sulfate, sodium nitrate, and urea. Examples of the inorganic salts include sodium, potassium, calcium, magnesium, manganese, iron, cobalt, zinc, and phosphoric acid. A culturing method may be stationary culture, shaking culture, or aerated and stirred culture, and aerated and stirred culture is preferable for mass culture. A culture temperature is generally 15 to 37° C., and preferably 20 to 30° C. pH of the culture medium is preferably pH 5 to 9. A culture time is generally 2 to 7 days, and the culture is stopped when the amount of the chitinase accumulated in the culture medium reaches its maximum. For separating microorganism cells and a solution containing chitinase from the culture, known methods such as centrifugation and filtration can be used. For separating and purifying chitinase from the solution containing chitinase, known methods such as ultrafiltration using a filtration membrane with molecular weight cut off of 5,000 or 10,000, fractionation using ammonium sulfate or ethanol, and purification by chromatography can be used in combination as appropriate based on a desired purity of chitinase. As chitinase, the solution containing chitinase may be used in a liquid state as it is, or a powdered enzyme obtained by drying the solution in a vacuum or lyophilizing the solution may be used. In the present invention, it is preferable to use chitinase with high purity obtained by culturing actinomycetes in a culture medium containing a carbon source such as glucose and glycerol, which actinomycetes can relatively easily utilize, a naturally-derived nitrogen source such as meat extract and yeast extract, and inorganic salt such as calcium salt; concentrating, by ultrafiltration, the culture supernatant obtained by separating actinomycete cells from the culture; and purifying chitinase from the concentrated solution by ammonium sulfate precipitation, alcohol precipitation, column chromatography and the like.
The anti-fungal agent for processed cereal foods of the present invention may further contain calcium propionate. Calcium propionate is preferably contained in a ratio of 0.1 to 500 parts by mass and more preferably 1 to 200 parts by mass to 1 part by mass of chitinase.
There is no particular limitation on mold against which the anti-fungal agent for processed cereal foods of the present invention exhibit an anti-fungal effect. Examples of the mold includes a bread mold (Aspergillus), aspergillus (Aspergillus), penicillium (Penicillium), cladosporium (Cladosporium), rhizopus (Rhizopus), and mucor (Mucor).
The anti-fungal agent for processed cereal foods of the present invention may further contain a preservative agent, a shelf-life improving agent and alcohol. Examples of preservative agents include benzoic acid, benzoic acid salt, sorbic acid, sorbic acid salt, paraben, polylysine, milt protein degradation product, tsunaburishin, nisin, and natamycin. Examples of shelf-life improving agents include organic acid, organic acid salt (e.g., sodium acetate), and glycine. Examples of alcohol include ethanol. The rest of the anti-fungal agent for processed cereal foods of the present invention is generally water.
An anti-fungal agent-containing processed cereal food of the present invention contains the above-described anti-fungal agent. Accordingly, chitinase is contained. There is no particular limitation on the amount of chitinase contained in the anti-fungal agent-containing processed cereal food of the present invention as long as the anti-fungal effect of chitinase is exhibited. Chitinase is preferably contained in an amount of 0.5 to 100,000 μg/g of processed cereal food, more preferably 0.65 to 6,600 μg/g, and even more preferably 1.3 to 1,300 μg/g. Particularly, when chitinase is contained on the surface, chitinase is preferably contained in an amount of 5 to 500 μg/g of a processed cereal food, and more preferably 12.5 to 250 μg/g.
A method for producing the anti-fungal agent-containing a processed cereal food of the present invention includes the step of incorporating the above-described anti-fungal agent into a processed cereal food. There is no particular limitation on the step as long as chitinase is incorporated in the processed cereal food to exhibit the anti-fungal effect of chitinase. Chitinase may be added in the final stage or in the intermediate stage of the production of the processed cereal food, or to cereal materials, or in combination of at least two of these adding methods. Examples thereof include mixing the above-described anti-fungal agent into cereal materials, and applying the above-described anti-fungal agent on the surface of the processed cereal food. For mixing the above-described anti-fungal agent to cereal materials, for example, an aqueous solution, alcoholic solution, or the like containing the above-described anti-fungal agent is kneaded into raw materials, dough, or the like of the processed cereal food, or the raw materials, dough, or the like is immersed in the aqueous solution, alcoholic solution, or the like. For applying the above-described anti-fungal agent on the surface of the processed cereal food, for example, an aqueous solution, alcoholic solution, or the like containing the above-described anti-fungal agent is sprayed or coated on the surface of the processed cereal food. Spray or coating may be before or after baking the processed cereal food, and preferably after baking the processed cereal food.
When mixing into the cereal materials, the above-described anti-fungal agent is preferably contained in the processed cereal food in an amount of 1 to 10,000 μg/g of the cereal materials, and more preferably 2 to 2,000 μg/g. When applying on the surface of the processed cereal food, the above-described anti-fungal agent is preferably attached thereto in an amount of 2 to 200 μg/cm2 of the surface of the cereal materials, and more preferably 5 to 100 μg/cm2.
Hereinafter, the present invention will be described more specifically by way of examples, but the present invention is not limited to the examples below.
All chitinases used in the examples below are derived from actinomycetes. Calcium propionate used in the examples below is a preservative agent widely used in foods, and is known to exhibit the anti-fungal effect. In the examples below, “%” means “% by mass”.
Three hundred and thirty grams of bread dough (dough) of the raw materials blended in the ratio shown in Table 1 (Example 1) was mixed at a low speed for 5 minutes, and then, was mixed at a high speed for 7 minutes. The dough was retained at 35° C. for 100 minutes to be leavened, and then, was baked at 140° C. for 20 minutes to obtain a loaf of bread (hereinafter, referred to as a “loaf”).
The obtained loaf was left to room temperature, and the entire surface of the loaf (approximately 280 g) was sprayed with a spraying agent (approximately 10 μL/cm2) shown in Table 2 (“0.1% chitinase” means a concentration when 1 mg of chitinase is added with respect to 1 ml of the spraying agent). The loaves were retained in the atmosphere to dry the surface, and then, the loaves were independently put into separate plastic bags and were preserved at a room temperature. The presence or the absence of the growth of mold was checked visually. It should be noted that Denazyme CBT manufactured by Nagase ChemteX Corporation was used as chitinase XNP-161 (exo-chitinase) and Denazyme CBB manufactured by Nagase ChemteX Corporation was used as chitinase XGP-402 (chitinase, family 18). Moreover, the culture of S. violaceoruber was fractionated with ammonium sulfate and lyophilized for use as chitinase XGP-403 (chitinase, family 19), and the culture of S. griseus was fractionated with ammonium sulfate and lyophilized for use as chitinase XGP-405 (chitinase, family 19). Table 3 shows the results. Table 3 shows the length of preservation time of the loaves until the growth of mold was observed. In Table 3, “-” means that the loaf was sprayed with nothing.
As shown in Table 3, the length of preservation time of bread was extended for 3 to 6 days by adding chitinase. The length of preservation time of bread in a case of adding chitinase was extended for 2 to 5 days compared to the control which was more than in a case of adding calcium propionate. It was proved that chitinase has a stronger anti-fungal effect than calcium propionate.
The anti-fungal effects of the spraying agents 1 to 3 were evaluated in the same manner as in Example 1, except that the raw materials were blended in the ratio shown in Table 1 (Example 2) instead of the ratio shown in Table 1 (Example 1). Accordingly, in the loaf (approximately 280 g) of the present example, calcium propionate was kneaded into the dough. Table 4 shows the results. Table 4 shows the length of preservation time of the loaves until the growth of mold was observed. In Table 4, “-” means that the loaf was sprayed with nothing.
As shown in Table 4, the length of preservation time of bread was extended for 24 to 45 days by adding chitinase. The length of preservation time of bread in a case of spraying chitinase was extended for 21 to 42 days compared to the control which was more than in a case of spraying calcium propionate. In Example 2, it is thought that kneading calcium propionate into the bread dough allowed the length of preservation time of bread to be extended (for 11 days without spraying). Whereas the length of preservation time of bread was extended for 3 days more by spraying with calcium propionate (control), the length of preservation time of bread was extended for 24 to 45 days more by spraying with chitinase, which proved a remarkable anti-fungal effect.
Four hundred grams of bread dough (dough) of the raw materials blended in the ratio shown in Table 5 (“1 ppm chitinase” means a concentration when 1 μg of chitinase is added with respect to 1 g of flour) was mixed at a low speed for 2 minutes, and then, was mixed at a high speed for 6 minutes. After bench time at 26 ° C. for 10 minutes, the dough was divided and shaped. The shaped dough was retained at 30° C. for 60 minutes to be leavened, and then, baked at 220° C. for 50 minutes to obtain six loaves.
Each obtained loaf (approximately 340 g) was sliced into 8 slices with a thickness of 1.5 cm and a size of 110 to 120 cm2, so that 48 slices were obtained in total. The slices were independently put into separate plastic bags and were preserved at a room temperature. The presence or the absence of the growth of mold was checked visually and the number of the slices on which mold grew was counted over time.
As shown in
The number of the slices on which mold grew was counted in the same manner in Example 3, except that 5 ppm chitinase was used instead of 15 ppm chitinase and 0.1% calcium propionate was used instead of 0.05% calcium propionate used with chitinase.
As shown in
The number of slices on which mold grew was counted in the same manner in Example 4, except that 0.2% chitinase XGP-403 or XGP-405 was used instead of 5 or 20 ppm chitinase XGP-402 and 0.1% calcium propionate was used instead of 0.2% calcium propionate used as Comparative Example.
As shown in
With the present invention, it is possible to provide a safe and inexpensive anti-fungal agent for processed cereal foods. Due to the inclusion of an enzyme chitinase, the anti-fungal agent for processed cereal foods of the present invention is safe and inexpensive.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2011-220549 | Oct 2011 | JP | national |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/JP2012/075517 | 10/2/2012 | WO | 00 | 3/31/2014 |
