JP2009296918A - Food quality improver - Google Patents

Food quality improver Download PDF

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JP2009296918A
JP2009296918A JP2008153655A JP2008153655A JP2009296918A JP 2009296918 A JP2009296918 A JP 2009296918A JP 2008153655 A JP2008153655 A JP 2008153655A JP 2008153655 A JP2008153655 A JP 2008153655A JP 2009296918 A JP2009296918 A JP 2009296918A
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lactic acid
food
supernatant
culture
flavor
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Sachiko Maeda
幸子 前田
Sachiko Koga
祥子 古賀
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OMU MILK PRODUCTS CO Ltd
Kumamoto Flour Milling Co Ltd
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OMU MILK PRODUCTS CO Ltd
Kumamoto Flour Milling Co Ltd
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Abstract

<P>PROBLEM TO BE SOLVED: To provide a food quality improver for improving palate feeling or flavor of food without spoiling flavor inherent in the food, and further improving yield of the food. <P>SOLUTION: The food quality improver comprises a supernatant of a culture liquid obtained by eliminating insoluble substances from the culture liquid produced by stirring lactobacillus for 10-30 hours to be cultured, particularly a supernatant containing ≥50 μg/mL of low molecular peptide having a molecular amount of 2,500-7,000 and ≤50 mg/mL of lactic acid, or the concentrate or the dried substance of the supernatant. <P>COPYRIGHT: (C)2010,JPO&INPIT

Description

本発明は、乳酸菌に由来し、食品の保水力を向上させ、食品の食感、風味の改良、さらに加熱処理後の食品の歩留まりを向上させる食品の新規な品質改良剤に関する。   The present invention relates to a novel food quality improver derived from lactic acid bacteria, which improves the water retention of food, improves the food texture and flavor of food, and further improves the yield of food after heat treatment.

加工食品生産では、いかに食品廃材を減らして可食部を多く得るかが重要課題となるが、鮮度の劣る食材の中には、臭い、味などの風味が悪いために製品価値を下げたり、使用されずに廃棄される食品、畜肉、魚介類等がある。このような食材を有効利用するために、従来から、タレ、ドレッシング等の調味料に、旨みや風味を増強する目的でアミノ酸、核酸等の旨み調味料や畜肉、野菜エキス等を発酵させた旨み調味料を利用することが知られている。このような風味の改良剤として広く用いられているものに酵母エキスがあるが、酵母エキスは不快臭に対して高いマスキング効果を示す一方で、独特の呈味性があり、食材の持つ本来の風味を損なうため、低呈味性で、高いマスキング効果をもつ品質改良剤が求められている。   In processed food production, how to reduce food waste and obtain more edible parts is an important issue, but for foods with poor freshness, the product value may be lowered due to bad smell, taste, etc. There are foods, livestock meat, seafood, etc. that are discarded without being used. In order to effectively use such ingredients, flavors such as sauces and dressings have been conventionally fermented with flavors such as amino acids and nucleic acids, livestock meat, vegetable extracts, etc. for the purpose of enhancing the flavor and flavor. It is known to use seasonings. Yeast extract is widely used as such a flavor improver, and yeast extract has a high masking effect against unpleasant odors, but has a unique taste and is inherent in the ingredients. In order to impair the flavor, a quality improving agent having low taste and high masking effect is required.

また、加熱を行う食材などは、加熱により引き起こされる水分の流出による歩留まりの低下に加え、食材が堅くなるといった食感の悪化などの問題がある。この歩留まりの低下、食感の悪化を防止する方法として、みりんや酒などの一般的な調味料を用いる方法、有機酸塩を用いる方法(特開平5−15344)やリン酸塩を用いる方法が利用されている。しかし、一般的な調味料および有機酸塩による方法は効果が不十分であり、また、近年、リンの過剰摂取が、カルシウムの吸収を阻害し、カルシウム不足を促進するとの報告もあることから、食品加工の現場では、食品からリン酸塩を排除する動きが活発化しており、これらに代わる有効な品質改良剤が望まれている。
特開平5−15344号公報
In addition, foodstuffs to be heated have problems such as deterioration in texture such as a hardened foodstuff in addition to a decrease in yield due to outflow of moisture caused by heating. As a method for preventing this decrease in yield and deterioration in texture, there are a method using a general seasoning such as mirin and sake, a method using an organic acid salt (JP-A-5-15344), and a method using a phosphate salt. It's being used. However, the general seasoning and organic acid salt methods are not effective enough, and in recent years, it has been reported that excessive intake of phosphorus inhibits calcium absorption and promotes calcium deficiency. In the field of food processing, there is an active movement to remove phosphate from foods, and an effective quality improving agent to replace these is desired.
Japanese Patent Laid-Open No. 5-15344

本発明の目的は、食材の本来の風味を損なうことなく、食品の食感、風味を改良し、鮮度の劣る原材料であっても新鮮な原材料と同等な食味を与え、さらに食品の歩留まりを向上させることによって食品製造効率を向上させることのできる食品の品質改良剤を提供することにある。   The object of the present invention is to improve the texture and flavor of food without impairing the original flavor of the food, to give the same taste as fresh raw materials even if the raw material is inferior in freshness, and further improve the yield of food It is to provide a food quality improving agent capable of improving food production efficiency.

上記課題を解決するため、本発明者らは、風味改良効果を持つアミノ酸系調味料や核酸系調味料、および、魚介肉の歩留まり向上効果を持つ有機酸塩の効果に着目し、有機酸と低分子ペプチドやアミノ酸などを同時に生成することのできる乳酸菌発酵液の、様々な食材に対する品質改良効果について検討を行った。その結果、乳酸菌を攪拌培養にて一定時間培養することにより得られる培養液の上清が、高い風味改良効果および歩留まり向上効果を示し、上記課題を解決できることを見出した。   In order to solve the above problems, the present inventors focused on the effects of amino acid seasonings and nucleic acid seasonings having a flavor improving effect, and organic acid salts having an effect of improving the yield of seafood meat, We examined the quality improvement effect on various foodstuffs of lactic acid bacteria fermentation broth that can simultaneously produce low molecular weight peptides and amino acids. As a result, it was found that the supernatant of the culture solution obtained by culturing lactic acid bacteria for a certain period of time by stirring culture exhibits a high flavor improving effect and a yield improving effect and can solve the above-mentioned problems.

かくして、本発明は、乳酸菌を10〜30時間攪拌培養することにより得られる培養液より不溶物を除去した培養液の上清、またはその上清の濃縮物もしくは乾燥物からなることを特徴とする食品の品質改良剤を提供するものである。   Thus, the present invention is characterized by comprising a culture supernatant obtained by removing insolubles from a culture obtained by stirring and culturing lactic acid bacteria for 10 to 30 hours, or a concentrate or a dried product thereof. It provides food quality improvers.

本発明の食品の品質改良剤は乳酸発酵により生成される低分子ペプチドを多く含み、且つ適当濃度の乳酸を含むため、食品に適度な旨み、甘みを付与する他、pHを低く維持し、肉の保水性を高め、肉を軟らかくし、加熱後の歩留まりを向上させる効果を有する。また、本発明の食品の品質改良剤においては、乳酸菌スターターとして増殖の際に、過酸化水素、ジアセチル、抗菌性ペプチドなどの抗菌物質を産生する乳酸菌を用いることにより、さらに日持ち向上効果も期待できる。   The food quality improver of the present invention contains a large amount of low molecular weight peptides produced by lactic acid fermentation and contains an appropriate concentration of lactic acid. Has the effect of increasing the water retention, softening the meat, and improving the yield after heating. In addition, the food quality improving agent of the present invention can be expected to further improve the shelf life by using lactic acid bacteria that produce antibacterial substances such as hydrogen peroxide, diacetyl and antibacterial peptides during growth as lactic acid bacteria starters. .

本発明の品質改良剤は、乳酸菌を10〜30時間、攪拌培養して得られた発酵液から、不溶物および乳酸菌体を除去した上清(または、その上清の濃縮物もしくは乾燥物)からなる、食品の品質改良剤であり、上清中に、乳酸菌の増殖によって生成された分子量2,500〜7,000の低分子ペプチドが50μg/ml以上含まれており、かつ上清中の乳酸濃度が50mg/ml以下であることを特徴とする。   The quality improver of the present invention is obtained from a supernatant obtained by removing insolubles and lactic acid bacteria from a fermentation liquid obtained by stirring and culturing lactic acid bacteria for 10 to 30 hours (or a concentrated or dried product of the supernatant). Is a food quality improver, the supernatant contains 50 μg / ml or more of a low molecular weight peptide having a molecular weight of 2,500 to 7,000 produced by the growth of lactic acid bacteria, and the lactic acid concentration in the supernatant is 50 mg / ml. It is characterized by being less than ml.

本発明に使用する乳酸菌として特に好ましいのは、増殖の際に低分子のペプチドを産生するLactococcus lactis属の乳酸菌である。これらの乳酸菌は遺伝資源保存機関から入手でき、あるいは発酵食品用のスターターとして市販されているものを用いることができる。好ましい乳酸菌の例としては、Lactococcus lactis subsp. lactis
NCDO 497などを挙げることができるが、これに限定されるものではない。
Particularly preferred as the lactic acid bacterium used in the present invention is a lactic acid bacterium belonging to the genus Lactococcus lactis that produces a low molecular weight peptide upon growth. These lactic acid bacteria can be obtained from a genetic resource storage organization, or those commercially available as fermented food starters can be used. Examples of preferred lactic acid bacteria, Lactococcus lactis subsp. Lactis
NCDO 497 may be mentioned, but is not limited thereto.

培養にあたっては、糖源と窒素源を添加した液体培地を用いる。培地の糖源としては、グルコース、ガラクトース、ラクトースをあげることができる。また窒素源としては食品用酵母エキス、乳性蛋白濃縮物分解物、コーンペプチド、大豆ペプチド、業務用調味液原料などをあげることができる。発酵後にさわやかな芳香を得るためには、乳清蛋白濃縮物分解物を添加することが好ましく、食材に適度なコク味と熟成風味を付与するためには酵母エキスを添加することが望ましい。   In culturing, a liquid medium supplemented with a sugar source and a nitrogen source is used. Examples of the sugar source in the medium include glucose, galactose, and lactose. Examples of the nitrogen source include food-grade yeast extract, milk protein concentrate degradation product, corn peptide, soybean peptide, and seasoning liquid for commercial use. In order to obtain a refreshing aroma after fermentation, it is preferable to add a whey protein concentrate decomposition product, and it is desirable to add a yeast extract in order to impart an appropriate richness and aging flavor to the food.

本発明の食品の品質改良剤を得るため、乳酸菌の培養は上述の液体培地で攪拌しながら10〜30時間行う。すなわち、本発明においては、静置培養ではなく、発酵槽の中の培地を均一に保つように攪拌培養を行うものであり、その方法としてはスターラーや攪拌棒を用いて攪拌する方法の他に、無菌ガスを用いたエアレーションを用いる方法などを挙げることができるが、これらの方法に限定されるものではなく、30〜400rpm程度の攪拌速度に相当するように攪拌すればよい。培養温度は、一般に25〜37℃、好ましくは、30±2℃である。また、培養の際、炭酸カルシウムなどのpH緩衝剤を培地に添加する、あるいはアルカリ剤や中和剤などを適時添加するなどして、乳酸菌の増殖により生成される乳酸による培養液のpHの急激な低下を緩やかにすることが望ましい。   In order to obtain the food quality improving agent of the present invention, lactic acid bacteria are cultured for 10 to 30 hours with stirring in the above-mentioned liquid medium. That is, in the present invention, stirring culture is performed so as to keep the medium in the fermenter uniform, not stationary culture, and as a method thereof, in addition to a method of stirring using a stirrer or a stirring rod Examples thereof include a method using aeration using aseptic gas, but are not limited to these methods, and the stirring may be performed so as to correspond to a stirring speed of about 30 to 400 rpm. The culture temperature is generally 25 to 37 ° C, preferably 30 ± 2 ° C. In addition, during culture, a pH buffer such as calcium carbonate is added to the medium, or an alkaline agent or neutralizing agent is added at an appropriate time, so that the pH of the culture solution is rapidly increased by lactic acid produced by the growth of lactic acid bacteria. It is desirable to moderate this decrease.

本発明に従う乳酸菌の培養時間は10〜30時間であればよいが、培養時間が短すぎる場合、乳酸菌の増殖によって生成される低分子ペプチドの生成量が少なく、品質改良効果が少なくなり、また培養時間が長すぎる場合は乳酸菌の生産する過剰の乳酸によって食品に独特の発酵風味がつき、食材本来の風味を損なう。乳酸菌の培養時間としては、10〜30時間であるが、好ましくは12〜24時間の範囲がよい。このようにして、上清中には適度な量の乳酸と低分子ペプチドが含まれていることが望ましく、低分子ペプチド含量として50μg/ml以上であるが、250μg/ml以下であり、乳酸含量として50mg/ml以下であるが、20mg/ml以上の範囲にあるものが望ましい。   The culture time of the lactic acid bacteria according to the present invention may be 10 to 30 hours. However, if the culture time is too short, the amount of low molecular peptide produced by the growth of the lactic acid bacteria is small, the quality improvement effect is reduced, and the culture is performed. If the time is too long, the food has a unique fermentation flavor due to excess lactic acid produced by the lactic acid bacteria, and the original flavor of the food is impaired. The culture time for lactic acid bacteria is 10 to 30 hours, preferably 12 to 24 hours. Thus, it is desirable that the supernatant contains an appropriate amount of lactic acid and a low molecular peptide, and the low molecular peptide content is 50 μg / ml or more, but 250 μg / ml or less, and the lactic acid content 50 mg / ml or less, but those in the range of 20 mg / ml or more are desirable.

このようにして得られた培養液は遠心分離、ろ過等の公知の手法を用いて不溶物および菌体を除去して、本発明の品質改良剤を得る。品質改良剤はそのまま使用しても良いが、濃縮物(濃縮液)、あるいは凍結乾燥、噴霧乾燥等の公知の手法にて乾燥(粉体化)したものを使用しても良い。   The culture solution thus obtained is used to remove insoluble matters and bacterial cells using known techniques such as centrifugation and filtration to obtain the quality improver of the present invention. The quality improver may be used as it is, but a concentrate (concentrated solution) or a product dried (powdered) by a known method such as freeze drying or spray drying may be used.

<試験サンプルの調製>
グルコース(ブドウ糖;日本澱粉工業(株))3%、酵母エキス(酵母エキスSL-W;キリンフードテック(株))0.5%、炭酸カルシウム(アラゲン;(株)カルファイン)1%を配合した培地1リットルを121℃で15分間加熱殺菌を行った。次いであらかじめ同培地にて培養したLactococcus lactis subsp. lactis
NCDO 497株の培養液を上記培地に5%添加し、表1に示した培養条件(A〜D)にて培養を行った。得られた培養液を1万rpmで遠心分離し、不溶物及び菌体を除去した培養液上清を得た。培養温度は30℃、攪拌培養する場合はスターラーを用いて培地の攪拌速度を50rpmとした。得られた培養液上清をスプレードライにて粉体化したものを食材試験に用いた。
<Preparation of test sample>
Medium containing 3% glucose (dextrose; Nippon Starch Co., Ltd.), yeast extract (yeast extract SL-W; Kirin Foodtech Co., Ltd.) 0.5%, calcium carbonate (arogen; Calfine Co., Ltd.) 1% One liter was heat sterilized at 121 ° C. for 15 minutes. Then Lactococcus lactis subsp were cultured in advance the same medium. Lactis
The culture solution of NCDO 497 strain was added to the above medium at 5% and cultured under the culture conditions (AD) shown in Table 1. The obtained culture solution was centrifuged at 10,000 rpm to obtain a culture solution supernatant from which insolubles and cells were removed. The culture temperature was 30 ° C., and in the case of stirring culture, a stirrer was used and the stirring speed of the medium was 50 rpm. The obtained culture supernatant was pulverized by spray drying and used for the food test.

Figure 2009296918
Figure 2009296918

<食材試験1>
サーモンの切り身を表2に示す、水、あるいは発明品、対照品1〜3を5%添加した水、およびコントロールとして食品添加物の乳酸ナトリウムを添加した水に45分間浸漬し、水切りを行った後、沸騰水中にて5分間加熱調理を行った。加熱調理後の食感等について官能評価により食感、風味等について効果の検証を行った。官能評価は、出願人の社内選考により5種類の原味試験(甘味・酸味・旨み・塩味・苦味を判別する試験)にて中級レベルに達し、日常業務で食品の官能評価を行っている官能評価の専門パネラー5名(男性2名、女性3名、 年齢 25〜37歳)にて実施した。無処理を標準(3)とし、加熱処理後の風味、食感について無処理との違いについて5段階評価(悪い1←標準3→良い5)にて評価した。
<Food test 1>
The salmon fillets shown in Table 2 were dipped for 45 minutes in water, water added with 5% of the inventive product or the control products 1 to 3, and water added with sodium lactate as a food additive as a control. Then, cooking was performed for 5 minutes in boiling water. The effects on the texture, flavor, etc. were verified by sensory evaluation of the texture after cooking. The sensory evaluation has reached the intermediate level in five types of original taste tests (tests that distinguish sweetness, acidity, umami, salty taste, and bitterness) based on the applicant's in-house selection, and sensory evaluation of foods in daily operations 5 panelists (2 men, 3 women, age 25-37). Non-treatment was defined as standard (3), and the flavor and texture after heat treatment were evaluated by a five-step evaluation (bad 1 ← standard 3 → good 5).

官能試験の結果、表2に示すとおり、発明品(攪拌/20時間培養)が、他の試験区に対して優れた風味、食感の改良効果が得られた。具体的には、無処理では身が引き締まりすぎ、堅い食感であったが、発明品を添加した試験区では、適度な柔らかさと弾力があり、また風味も、無添加ではサーモンの脂っぽい味があったが、発明品を添加した試験区では脂臭さがマスキングされ、好ましい風味であった。   As a result of the sensory test, as shown in Table 2, the inventive product (stirring / culture for 20 hours) showed an excellent flavor and texture improvement effect with respect to other test sections. Specifically, the body was too tight without treatment and had a firm texture, but in the test zone with the addition of the invention product, it had moderate softness and elasticity, and the flavor was greasy with salmon without addition. Although there was a taste, the fat smell was masked in the test section to which the invention product was added, and it was a preferred flavor.

また、乳酸ナトリウム単独でも若干の品質改良効果が認められるが、その効果は同程度の乳酸を含む発明品には及ばないことから、発明品は乳酸菌によって生成される乳酸以外の何らかの物質が、食品の品質改良に大きく影響を及ぼしていると考えられた。   In addition, sodium lactate alone has some quality improvement effect, but the effect is not as good as the invention product containing the same level of lactic acid. It was thought that it had a great influence on quality improvement.

Figure 2009296918
Figure 2009296918

<発酵液の分析>
有機酸分析
発明品および対照品1〜3に含まれる乳酸濃度を高速液体クロマトグラフィーにより測定した。分析用カラムにWaters社製Organic Acid
Column、7.8×300mm、移動相に0.1% リン酸溶液を用い、流速1.0ml/min、検出UV 210nmにて分析を行った。シグマ社製のL-乳酸を用いて検量線を作成し、発明品および各対照品の乳酸濃度を測定した。
<Analysis of fermentation broth>
The lactic acid concentration contained in the organic acid analysis invention product and the control products 1 to 3 was measured by high performance liquid chromatography. Waters Organic Acid as analytical column
Column, 7.8 × 300 mm, 0.1% phosphoric acid solution was used for the mobile phase, analysis was performed at a flow rate of 1.0 ml / min, and detection UV of 210 nm. A calibration curve was prepared using L-lactic acid manufactured by Sigma, and the lactic acid concentration of the invention product and each control product was measured.

分子量分布分析
発明品および対照品1〜3に含まれる成分の分子量分布を、ゲルろ過クロマトグラフィーにより調べた。分析用カラムに東ソー株式会社製TSKgel G2000 SWXL、移動相に0.1%トリフルオロ酢酸含有45%アセトニトリルを用い、流速0.5ml/min、検出UV 210nmにて分析を行った。チトクロムc、インスリン、インスリンB鎖、ビタミンB12、トリプトファン、L-乳酸(いずれもシグマ社製)をスタンダードとして用いた分析結果(表3)より検量線を作成した。
Molecular weight distribution analysis The molecular weight distribution of the components contained in the invention product and the control products 1 to 3 was examined by gel filtration chromatography. TSKgel G2000 SWXL manufactured by Tosoh Corporation was used for the analytical column, 45% acetonitrile containing 0.1% trifluoroacetic acid was used for the mobile phase, and analysis was performed at a flow rate of 0.5 ml / min and detection UV of 210 nm. A calibration curve was prepared from the analysis results (Table 3) using cytochrome c, insulin, insulin B chain, vitamin B12, tryptophan, and L-lactic acid (all manufactured by Sigma) as standards.

Figure 2009296918
Figure 2009296918

発明品および対照品1〜3の分子量分布を分析した結果、発酵前の培地に比べ、発明品(攪拌/20時間培養)はリテンションタイム15〜17分の付近にピークが認められ、上記表3のスタンダードに基づく解析の結果、これは分子量2,500〜7,000の大きさに相当する物質であることが明らかとなった。(図1 リテンションタイム16.117分)また、発明品における、分子量2,500〜7,000Daの低分子ペプチドの濃度は115.2μg/mlであった。
発明品および各対照品の低分子ペプチド量および乳酸量は表4に示す通りであった。
食品の品質改善効果に大きく影響を及ぼすと考えられる低分子ペプチドは、攪拌培養することによりその生成量が増加することが明らかとなった。実施例2における、対照品2の食材試験結果に見られるように、5時間程度の攪拌培養でも50μg/ml程度の低分子ペプチドが生成され、無処理に比べて若干の品質改良効果が認められるが、その効果は不十分であり、十分な改良効果を得るためには、上清中の低分子ペプチド含量として50μg/ml以上、乳酸含量として50mg/ml以下であることが望ましい。
As a result of analyzing the molecular weight distribution of the invention product and the control products 1 to 3, the invention product (stirring / 20-hour culture) showed a peak at a retention time of 15 to 17 minutes as compared to the medium before fermentation. As a result of the analysis based on the standard, it was revealed that this was a substance corresponding to a molecular weight of 2,500 to 7,000. (FIG. 1 Retention time 16.117 minutes) Further, the concentration of the low molecular weight peptide having a molecular weight of 2,500 to 7,000 Da in the invention product was 115.2 μg / ml.
The amount of low molecular peptide and the amount of lactic acid of the invention product and each control product were as shown in Table 4.
It has been clarified that the amount of low molecular weight peptide, which is thought to have a great influence on the quality improvement effect of food, is increased by stirring culture. As can be seen from the food test results of the control product 2 in Example 2, a low molecular weight peptide of about 50 μg / ml is produced even with stirring culture for about 5 hours, and a slight quality improvement effect is recognized compared with the case of no treatment. However, the effect is insufficient, and in order to obtain a sufficient improvement effect, it is desirable that the low molecular peptide content in the supernatant is 50 μg / ml or more and the lactic acid content is 50 mg / ml or less.

Figure 2009296918
Figure 2009296918

<食材試験2>
一般的に食品の品質改良剤として広く用いられているリン酸塩を用いて、本発明品の品質改良効果について比較検討を行った。
鶏もも肉を表5に示す水、リン酸塩(対照品)を含む水、あるいは発明品を含む水に3時間浸漬し、水気を切り、唐揚げ粉を対肉20%の割合でまぶし、175℃の油にて4分間加熱調理を行った。加熱調理前後の重量比により歩留まり(重量残存率)を、また官能評価により食感、風味等について効果の検証を行った。歩留まりとは、製造において、「原料(素材)の投入量から期待される生産量に対して、実際に得られた製品生産数(量)比率」のことで、歩留まり率が高いほど生産効率性が良いことを意味する。官能評価は、専門パネラー5名(実施例2参照)にて実施し、コントロールを標準(3)として、加熱処理後の歩留まり(重量残存率)、風味、食感についてコントロールとの違いについて5段階評価(悪い1←標準3→良い5)にて評価した。
<Food test 2>
A comparative study was conducted on the quality improvement effect of the products of the present invention using phosphates that are generally widely used as food quality improvers.
Dip chicken thighs in the water shown in Table 5, water containing phosphate (control product) or water containing the invention for 3 hours, drain, and fry the deep-fried flour at a ratio of 20% to meat, 175 Heat cooking was performed for 4 minutes with oil at 0 ° C. The yield (weight residual ratio) was verified based on the weight ratio before and after cooking, and the texture, flavor, and the like were verified by sensory evaluation. Yield refers to the ratio of the number of products actually produced (quantity) to the production expected from the amount of raw materials (raw materials) used in production. The higher the yield rate, the higher the production efficiency. Means good. The sensory evaluation was conducted by 5 expert panelists (see Example 2), and the control was standard (3). The yield (weight residual ratio), flavor, and texture after heat treatment differed from the control in 5 stages. Evaluation was performed by evaluation (bad 1 ← standard 3 → good 5).

Figure 2009296918
Figure 2009296918

リン酸塩は主に加工食品において、食材の保水性を高め、加工食品の歩留まりを向上させる効果があるとされるが、表6に示すように、発明品を添加することにより、加熱調理後の歩留まり(重量残存率)が、コントロールに比べて高く、リン酸塩を添加した試験区と同等の歩留まり向上効果を示した。   Phosphate is said to have the effect of increasing the water retention of foods and improving the yield of processed foods, mainly in processed foods, but as shown in Table 6, by adding inventive products, The yield (weight residual ratio) was higher than that of the control, and the yield improvement effect was the same as that of the test group to which phosphate was added.

また、表7に示すように加熱処理後の肉の食感、風味に関しては、風味としては肉本来の風味を変えることがなく、食感として、柔らかさ、ジューシー感が増すなど、発明品を添加することによって食感の改良効果が認められた。また、その改良効果は、リン酸塩を添加した試験区と同等であった。   In addition, as shown in Table 7, with respect to the texture and flavor of the meat after heat treatment, the flavor of the meat does not change the original flavor of the meat, and the texture of the invention increases such as softness and juiciness. The effect of improving the texture was recognized by adding. Moreover, the improvement effect was equivalent to the test section to which phosphate was added.

Figure 2009296918
Figure 2009296918

Figure 2009296918
Figure 2009296918

本発明の食品の品質改良剤を得るための乳酸菌の培養液の培養前後のゲルろ過分析の結果を示す。The result of the gel filtration analysis before and behind culture | cultivation of the culture solution of the lactic acid bacteria for obtaining the quality improvement agent of the foodstuff of this invention is shown.

Claims (3)

乳酸菌を10〜30時間攪拌培養することにより得られる培養液より不溶物を除去した培養液の上清、またはその上清の濃縮物もしくは乾燥物からなることを特徴とする食品の品質改良剤。   A food quality improver comprising a culture supernatant obtained by removing insolubles from a culture obtained by stirring and culturing lactic acid bacteria for 10 to 30 hours, or a concentrate or a dried product of the supernatant. 前記上清中に、乳酸菌を培養することにより生成される分子量2,500〜7,000の低分子ペプチドを50μg/ml以上含み、かつ前記上清中の乳酸濃度が50mg/ml以下であることを特徴とする請求項1の食品の品質改良剤。   The supernatant contains a low molecular weight peptide having a molecular weight of 2,500 to 7,000 produced by culturing lactic acid bacteria in an amount of 50 μg / ml or more, and the lactic acid concentration in the supernatant is 50 mg / ml or less. The food quality improving agent according to claim 1. 乳酸菌がLactococcus
latis属の乳酸菌であることを特徴とする請求項1または2の食品の品質改良剤。
Lactic acid bacteria is Lactococcus
The quality improving agent for foods according to claim 1 or 2, which is a lactic acid bacterium of the genus latis .
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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2012019706A (en) * 2010-07-12 2012-02-02 Aoba Kasei Kk Quality improving agent of meat, curd inhibitor for meat, frozen food, and retort food
JP2014079197A (en) * 2012-10-16 2014-05-08 Nippon Beet Sugar Mfg Co Ltd New fermented flavor liquid and food product having fermented flavor liquid
WO2017014253A1 (en) * 2015-07-21 2017-01-26 テーブルマーク株式会社 Novel fermented seasoning composition

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2004057020A (en) * 2002-07-25 2004-02-26 Wakamoto Pharmaceut Co Ltd Method for producing lactic acid bacterium
JP2004283109A (en) * 2003-03-24 2004-10-14 Omu Milk Products Co Ltd Flavor-improving agent for food and beverage
JP2005110566A (en) * 2003-10-07 2005-04-28 Momoya Co Ltd Mew lactic acid bacterium, antimicrobial substance produced by the lactic acid bacterium and method for producing the same
JP2006129786A (en) * 2004-11-05 2006-05-25 Kyowa Hakko Kogyo Co Ltd Bread crumb and method for producing the same

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2004057020A (en) * 2002-07-25 2004-02-26 Wakamoto Pharmaceut Co Ltd Method for producing lactic acid bacterium
JP2004283109A (en) * 2003-03-24 2004-10-14 Omu Milk Products Co Ltd Flavor-improving agent for food and beverage
JP2005110566A (en) * 2003-10-07 2005-04-28 Momoya Co Ltd Mew lactic acid bacterium, antimicrobial substance produced by the lactic acid bacterium and method for producing the same
JP2006129786A (en) * 2004-11-05 2006-05-25 Kyowa Hakko Kogyo Co Ltd Bread crumb and method for producing the same

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2012019706A (en) * 2010-07-12 2012-02-02 Aoba Kasei Kk Quality improving agent of meat, curd inhibitor for meat, frozen food, and retort food
JP2014079197A (en) * 2012-10-16 2014-05-08 Nippon Beet Sugar Mfg Co Ltd New fermented flavor liquid and food product having fermented flavor liquid
WO2017014253A1 (en) * 2015-07-21 2017-01-26 テーブルマーク株式会社 Novel fermented seasoning composition
JPWO2017014253A1 (en) * 2015-07-21 2018-05-10 テーブルマーク株式会社 New fermented seasoning composition

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