JP2006246840A - Method for producing functional food - Google Patents

Method for producing functional food Download PDF

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JP2006246840A
JP2006246840A JP2005070829A JP2005070829A JP2006246840A JP 2006246840 A JP2006246840 A JP 2006246840A JP 2005070829 A JP2005070829 A JP 2005070829A JP 2005070829 A JP2005070829 A JP 2005070829A JP 2006246840 A JP2006246840 A JP 2006246840A
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lactic acid
gaba
food
salt
sodium chloride
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JP4921721B2 (en
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Hiroaki Mizutani
寛明 水谷
Takafumi Miyake
崇文 三宅
Hiroko Matsumoto
裕子 松本
Yukinobu Kimura
幸信 木村
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YAMAMORI KK
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Abstract

<P>PROBLEM TO BE SOLVED: To provide a technology for imparting a high concentration γ-amino lactic acid in a method for producing γ-amino lactic acid by effecting lactobacillus having a glutamic acid-decaboxylating activity on a food containing glutamic acid or its salt, without requiring an aseptic equipment, inexpensively and safely. <P>SOLUTION: This method for imparting a high concentration γ-amino lactic acid efficiently by inhibiting the proliferation of sundry bacteria is provided by effecting the lactobacillus having a potent salt resistance and alcohol resistance and the glutamic acid-decaboxylating activity under a high sodium chloride concentration, or as necessary, under a high alcoholic concentration, to the food highly containing the glutamic acid or its salt. <P>COPYRIGHT: (C)2006,JPO&NCIPI

Description

本発明は、γ−アミノ酪酸(以下、「GABA」という)を、雑菌の増殖を抑えながら乳酸菌の働きにより製造する方法、及びこの方法により得られる食品に関する。   The present invention relates to a method for producing γ-aminobutyric acid (hereinafter referred to as “GABA”) by the action of lactic acid bacteria while suppressing the growth of various bacteria, and a food obtained by this method.

自然界に広く分布する非タンパク質構成アミノ酸であるGABAは、哺乳類の脳や脊髄に存在する抑制系の神経伝達物質であり、生体内で生理的に重要な働きをすることがわかっている。例えば、脳の血流を活発にさせ、酸素供給量を増大させて脳の代謝機能を亢進すること、ノルアドレナリンの分泌を抑制し腸管細動脈を収縮抑制することで血圧を降下させること、その他、免疫調節作用、リラックス作用、学習能力の向上や老化防止作用をもつことが報告されている。このGABAを含有する食品としては、茶、米、野菜、漬物等が挙げられるが、その含有量はきわめて少ない。   GABA, a non-proteinogenic amino acid that is widely distributed in nature, is a suppressive neurotransmitter present in the mammalian brain and spinal cord and is known to play a physiologically important role in vivo. For example, the blood flow of the brain is activated, the oxygen supply is increased to enhance the metabolic function of the brain, the secretion of noradrenaline is suppressed and the intestinal arterioles are contracted to lower the blood pressure, It has been reported to have an immunomodulating action, a relaxing action, an improvement in learning ability, and an anti-aging action. Examples of foods containing GABA include tea, rice, vegetables, and pickles, but their content is extremely small.

したがって、GABAを食品として摂取することにより、上述した生理作用が期待できることから、適当な処理を食品に施すことによりGABA含有量を増強させた食品がいくつも提唱されている。例えば、茶葉を嫌気処理しGABA含量を処理前の数十倍に高めたギャバロン茶(非特許文献1)や、コメ胚芽を嫌気処理してGABA含量を0.3%に高めたGABA富化コメ胚芽(オリザ油化(株))等が知られているが、原材料中に含まれる内在性酵素(グルタミン酸脱炭酸酵素)を活性化させるこれらの方法では富化できるGABA濃度が低いという課題があった。   Therefore, since the physiological effects described above can be expected by ingesting GABA as a food, a number of foods having an increased GABA content by applying appropriate treatment to the food have been proposed. For example, Gabalon tea (Non-patent Document 1) in which tea leaves were anaerobically treated to increase the GABA content several tens of times before the treatment, or GABA-enriched rice in which rice germ was anaerobically treated to increase the GABA content to 0.3% Germ (Oryza Oil Co., Ltd.) is known, but there is a problem that the concentration of GABA that can be enriched is low by these methods of activating the endogenous enzyme (glutamate decarboxylase) contained in the raw material. It was.

また、微生物の利用によりGABAを増加させた食品の製造方法として、グルタミン酸および/またはグルタミン酸塩に酵母を作用させる方法(特許文献1)、グルタミン酸およびその塩の多い食品素材に麹菌を作用させる方法(特許文献2)が報告されているが、こちらの方法についても増加できるGABA濃度が低いという課題があった。   In addition, as a method for producing a food with increased GABA by utilizing microorganisms, a method of causing yeast to act on glutamic acid and / or glutamate (Patent Document 1), a method of causing koji mold to act on a food material rich in glutamic acid and its salt ( Although Patent Document 2) has been reported, there is a problem that the GABA concentration that can be increased is low for this method as well.

一方、微生物のうち、特に乳酸菌に作用させる方法により高濃度のGABAを付与できることがわかり、近年種々の報告がされている。例えば、乳類にグルタミン酸遊離活性及びグルタミン酸デカルボキシラーゼ(グルタミン酸脱炭酸酵素)生産能を有する乳酸菌を作用させる方法(特許文献3)、グルタミン酸またはその塩類を含有する原料にキムチから単離された乳酸菌を作用させる方法(特許文献4)、グルタミン酸またはその塩類を蒸した大豆に含有させた培地に乳酸菌を作用させる方法(特許文献5)、乳酸菌によりGABA及び免疫賦活物質を製造する方法(特許文献6)、グルタミン酸及びその塩類の少なくとも一つを含有する食品素材に米ぬか、米胚芽および麸のうち少なくとも一つの成分を含有させ、乳酸菌を作用させる方法(特許文献7)が挙げられる。しかし、どの方法においても無塩又は低塩分を含んだ培地系又は食品素材に作用させるため、他の微生物の増殖を抑えなければならず、純粋培養に近い醗酵設備を要する、又は作用させる前に殺菌を行い、乳酸菌数を多量に接種しなければならないといった課題があった。   On the other hand, it has been found that a high concentration of GABA can be imparted by a method of acting on lactic acid bacteria among microorganisms, and various reports have been made in recent years. For example, a method in which lactic acid bacteria having glutamic acid releasing activity and glutamic acid decarboxylase (glutamic acid decarboxylase) producing ability are allowed to act on milk (Patent Document 3), lactic acid bacteria isolated from kimchi as raw materials containing glutamic acid or salts thereof A method of acting (Patent Document 4), a method of causing lactic acid bacteria to act on a medium containing glutamic acid or its salt in steamed soybeans (Patent Document 5), a method of producing GABA and an immunostimulatory substance by lactic acid bacteria (Patent Document 6) And a method of allowing lactic acid bacteria to act by adding at least one of rice bran, rice germ and rice bran to a food material containing at least one of glutamic acid and salts thereof (Patent Document 7). However, in any method, since it acts on a medium system or food material containing no salt or low salinity, the growth of other microorganisms must be suppressed, and a fermentation facility close to pure culture is required or before it is allowed to act. There was a problem that sterilization was required and a large number of lactic acid bacteria had to be inoculated.

また、魚醤油にラクトバチルス.プランタラムを添加して発酵食品を得る方法(特許文献8)では、醗酵期間が1〜2ヶ月と長期間要するといった課題があった。   Moreover, in the method (patent document 8) which adds Lactobacillus plantarum to fish soy sauce and obtains fermented food, there existed a subject that a fermentation period required as long as 1-2 months.

日本農芸化学学会誌,61,NO.11,p1449−1451,1987Journal of Japanese Society of Agricultural Chemistry, 61, NO.11, p1449-1451, 1987 特許第2891296号公報Japanese Patent No. 2891296 特許第3166077号公報Japanese Patent No. 3166077 特許第3172150号公報Japanese Patent No. 3172150 特開2003−70462号Japanese Patent Laid-Open No. 2003-70462 特開2004−187501号JP 2004-187501 A 特開2004−357535号JP 2004-357535 A 特開2001−352940号JP 2001-352940 A 特許第2704493号公報Japanese Patent No. 2704493

本発明の課題は、グルタミン酸またはその塩を含む食品にグルタミン酸脱炭酸酵素活性を有する乳酸菌を作用させてGABAを製造する方法において、無菌的な設備を要することなく、安価に、安全に、高濃度のGABAを付与させる技術を提供することである。   An object of the present invention is to produce GABA by allowing a lactic acid bacterium having glutamic acid decarboxylase activity to act on a food containing glutamic acid or a salt thereof at a low cost, safely, and at a high concentration without requiring aseptic equipment. It is to provide a technique for imparting GABA.

そこで本発明者らは上述した課題解決のために鋭意研究を重ねた結果、グルタミン酸脱炭酸酵素活性を有する耐塩性及びアルコール耐性の強い乳酸菌を高塩分ナトリウム濃度下において、さらにはアルコールを添加した高アルコール濃度下においてグルタミン酸及び/又はその塩を添加した食品に作用させることで、他の雑菌の増殖を抑えながら、安価に、安全に、高濃度のGABAを付与させることができることを見いだし、本発明を完成させるに至った。すなわち、本発明はグルタミン酸脱炭酸酵素活性を有する耐塩性及びアルコール耐性の強い乳酸菌を高塩化ナトリウム濃度下、さらに必要に応じてアルコールを添加した高アルコール濃度下においてグルタミン酸及び/又はその塩を添加した食品に作用させることを特徴とするGABAの製造方法であり、その方法により得られた高濃度GABA含有食品及びその加工食品である。   Therefore, as a result of intensive studies to solve the above-mentioned problems, the present inventors have found that lactic acid bacteria having glutamic acid decarboxylase activity and a salt-resistant and alcohol-resistant lactic acid bacterium are added under high salinity sodium concentration and further with alcohol added. It has been found that a high concentration of GABA can be imparted inexpensively and safely while acting on foods to which glutamic acid and / or its salts are added under alcohol concentration, while suppressing the growth of other bacteria. It came to complete. That is, in the present invention, glutamic acid and / or a salt thereof is added to a lactic acid bacterium having a glutamic acid decarboxylase activity and a salt-resistant and alcohol-resistant lactic acid bacterium under a high sodium chloride concentration and, if necessary, a high alcohol concentration to which alcohol is added. A method for producing GABA characterized by acting on a food, and a high-concentration GABA-containing food obtained by the method and a processed food thereof.

本発明は上述した手段により、グルタミン酸脱炭酸酵素活性を有する乳酸菌以外の菌、主に細菌、酵母、かびなどの雑菌の増殖を抑制できるため、無菌的な設備を要することなく、安価に、安全に、高濃度のGABAを付与させることができる。初発菌数を多く接種する必要がなく、前培養にかかる手間や、前培養にかかる費用も抑えられる。また、食品中に高濃度のGABAを付与できるため、これを任意の食品に少量添加するだけでその食品中のGABA含量を著しく増加させることができ、味、風味への影響もほとんどない食品を得ることができる。   The present invention can suppress the growth of bacteria other than lactic acid bacteria having glutamate decarboxylase activity, mainly bacteria, yeasts, fungi, and the like by the above-mentioned means, so that aseptic equipment is not required, and it is inexpensive and safe. Can be provided with a high concentration of GABA. It is not necessary to inoculate a large number of initial bacteria, and the labor and time for preculture can be reduced. In addition, since a high concentration of GABA can be added to the food, it is possible to remarkably increase the GABA content in the food only by adding a small amount of this to any food, and a food with little influence on the taste and flavor. Obtainable.

以下、本発明を詳細に説明する。本発明に用いられる5w/v%〜20w/v%の塩化ナトリウムを含有する食品とは、もともと塩化ナトリウムを含む食品以外に、塩化ナトリウムを含まない又は微量しか含まない食品に塩化ナトリウムを5w/v%〜20w/v%の濃度になるよう添加したものを含む。添加する塩化ナトリウムは原塩、並塩、天日塩等、主成分が塩化ナトリウムであればかまわない。塩化ナトリウムによりグルタミン酸脱炭酸酵素活性を有する乳酸菌以外の菌、例えば、細菌、かび、酵母などの雑菌の増殖を抑えるには、5w/v%〜20w/v%の塩化ナトリウム濃度が必要であり、8w/v%〜20w/v%がより好ましい。ただし、耐塩性の乳酸菌であっても、塩化ナトリウム濃度が高すぎるとグルタミン酸脱炭酸酵素活性が阻害されるため、雑菌の増殖抑制とGABA産生量の両面から判断すると、8w/v%〜14w/v%の範囲が最も好ましい。   Hereinafter, the present invention will be described in detail. The food containing 5 w / v% to 20 w / v% sodium chloride used in the present invention is a food containing no sodium chloride or containing only a trace amount of sodium chloride in addition to the food originally containing sodium chloride. Including those added to a concentration of v% to 20 w / v%. The sodium chloride to be added may be a raw salt, a common salt, a sun salt, etc., as long as the main component is sodium chloride. In order to suppress the growth of bacteria other than lactic acid bacteria having glutamate decarboxylase activity by sodium chloride, for example, bacteria, fungi, yeast, etc., a sodium chloride concentration of 5 w / v% to 20 w / v% is required, 8 w / v% to 20 w / v% is more preferable. However, even if it is a salt-tolerant lactic acid bacterium, glutamic acid decarboxylase activity is inhibited when the sodium chloride concentration is too high, and therefore, judging from both the growth suppression of miscellaneous bacteria and the amount of GABA production, 8 w / v% to 14 w / A range of v% is most preferred.

アルコールも塩化ナトリウムと同様、細菌、かび、酵母などの雑菌の増殖を抑制することができる。アルコール単独でも増殖を抑制できるが、グルタミン酸脱炭酸酵素活性も若干阻害されるため、塩化ナトリウムと併用した方が良い。すなわち、5w/v%〜20w/v%の塩化ナトリウム濃度を含む食品に、必要に応じて0.1w/v%〜6w/v%になるようにアルコールを添加すると良い。塩化ナトリウムを多く含有する食品であればあるほど、雑菌の増殖を抑制できるため、添加するアルコール添加量は少なくて済む。併用例として、5w/v%〜10w/v%の塩化ナトリウム濃度の食品に、3w/v%〜6w/v%になるようにアルコールを添加するのが好ましい。添加するアルコールは、食品に添加可能なエチルアルコールが主成分であれば問題なく、醸造アルコールでかまわない。   Alcohol, like sodium chloride, can inhibit the growth of bacteria, fungi, yeast and other bacteria. Alcohol alone can suppress growth, but glutamate decarboxylase activity is also somewhat inhibited, so it is better to use it together with sodium chloride. That is, it is good to add alcohol so that it may become 0.1 w / v%-6 w / v% to the foodstuff containing the sodium chloride concentration of 5 w / v%-20 w / v% as needed. The more the food contains sodium chloride, the more the growth of miscellaneous bacteria can be suppressed. Therefore, the amount of alcohol added is small. As a combination example, it is preferable to add alcohol to a food with a sodium chloride concentration of 5 w / v% to 10 w / v% so as to be 3 w / v% to 6 w / v%. The alcohol to be added may be brewed alcohol without any problem as long as ethyl alcohol that can be added to food is a main component.

塩化ナトリウムをもともと含む食品には、醤油、みそ、蛋白加水分解物、醤油様調味料などがある。特に醤油、みそには醸造過程で醗酵により作られたアルコールを一部含んでいることもあり、別途塩化ナトリウムやアルコールを添加する必要がないため、用いる食品としてより好ましい。醤油とは、大豆、小麦などを原料に醤油の常法に従い製造された調味料であり、醤油様調味料とは、穀類を原料に醤油の常法に従って作られた調味料や、醤油に魚貝または畜肉系のだしまたはエキス等を添加した調味料を指す。蛋白加水分解物は、植物性および/または動物性蛋白が酸により加水分解された後アルカリにより中和された調味料を指す。   Foods originally containing sodium chloride include soy sauce, miso, protein hydrolysates, and soy sauce-like seasonings. In particular, soy sauce and miso may contain some alcohol produced by fermentation during the brewing process, and it is not necessary to add sodium chloride or alcohol separately. Soy sauce is a seasoning manufactured according to the conventional method of soy sauce using soybeans, wheat, etc. as a raw material. Soy sauce-like seasoning is a seasoning made according to the normal method of soy sauce using cereals as a raw material, This refers to seasonings to which shellfish or livestock meat stock or extract is added. The protein hydrolyzate refers to a seasoning in which vegetable and / or animal proteins are hydrolyzed with acid and then neutralized with alkali.

乳酸菌の作用によりGABAを付与させる場合、乳酸菌の醗酵産物により味、風味の低下が起こることが多い。種々の処理により精製を行うことで、味、風味の低下は緩和できるが、コストがかかるという問題がある。しかし、できるだけ高濃度のGABAを含有させ、任意の食品に少量添加するだけでその食品中のGABA含量を著しく増加させることができれば、乳酸菌の醗酵産物由来の味、風味への影響がほとんどない食品を安価で得ることができる。GABAを高含有させるためには、5w/v%〜20w/v%の塩分を含む食品に、基質となるグルタミン酸またはその塩を多く含むことが重要である。食品中に含まれる天然のグルタミン酸量には限界があり、別途製造されたグルタミン酸またはその塩を添加する必要がある。ただし、20w/v%以上添加するとグルタミン酸脱炭酸酵素活性が阻害を受けるため、添加量は0.1w/v%〜15w/v%が好ましく、5w/v%〜12w/v%がより好ましい。このような範囲内であると、グルタミン酸脱炭酸酵素活性によりGABAを高濃度付与させるために必要な基質を十分含ませることができる。   When GABA is imparted by the action of lactic acid bacteria, the taste and flavor are often lowered by fermentation products of lactic acid bacteria. By performing purification by various treatments, deterioration of taste and flavor can be alleviated, but there is a problem that costs are increased. However, if the GABA content in the food can be remarkably increased by adding as much GABA as possible and adding a small amount to any food, there is almost no influence on the taste and flavor derived from the fermentation product of lactic acid bacteria. Can be obtained at low cost. In order to make GABA highly contained, it is important that a food containing a salt content of 5 w / v% to 20 w / v% contains a large amount of glutamic acid or a salt thereof as a substrate. There is a limit to the amount of natural glutamic acid contained in food, and it is necessary to add separately produced glutamic acid or a salt thereof. However, since the glutamic acid decarboxylase activity is inhibited when added at 20 w / v% or more, the amount added is preferably 0.1 w / v% to 15 w / v%, more preferably 5 w / v% to 12 w / v%. Within such a range, the substrate necessary for imparting a high concentration of GABA due to glutamate decarboxylase activity can be sufficiently contained.

本発明に用いる乳酸菌は、耐塩性及びアルコール耐性があり、グルタミン酸脱炭酸酵素活性を有する乳酸菌であれば特に限定しない。例として、ラクトバチルス(Lactobacillus、以下、L.と略記する)属、ストレプトコッカス(Streptococcus)属、ペディオコッカス(Pediococcus)属、及びビフィドバクテリウム(Bifidobacterium)属を挙げることができる。これらの中でもラクトバチルス属に属するものが好ましく、この例として、ラクトバチルス ブレビス(L. brevis)、ラクトバチルス ブルガリカス(L. bulgaricus)、ラクトバチルス プランタラム(L. plantarum)、ラクトバチルス アシドフィラス(L. acidophilus)、ラクトバチルス ラクティス(L. lactis)、ラクトバチルス カゼイ(L. casei)、ラクトバチルス ファーメンタム(L. fermentum)等を挙げることができる。耐塩性及びアルコール耐性のあるグルタミン酸脱炭酸酵素活性を有する乳酸菌の選抜については、グルタミン酸又はその塩と、塩化ナトリウム及びアルコールを含有させた一般的な乳酸菌用の培地(MRS培地)に分離した乳酸菌を接種して25℃〜35℃で数日培養後、この培養液のGABA含量を測定し、GABA量の多い乳酸菌株を選定すれば良い。   The lactic acid bacterium used in the present invention is not particularly limited as long as it is salt-resistant and alcohol-resistant and has glutamate decarboxylase activity. Examples include the genus Lactobacillus (hereinafter abbreviated as L.), the genus Streptococcus, the genus Pediococcus, and the genus Bifidobacterium. Among these, those belonging to the genus Lactobacillus are preferable, and examples thereof include Lactobacillus brevis (L. brevis), Lactobacillus bulgaricus (L. bulgaricus), Lactobacillus plantarum (L. plantarum), Lactobacillus acidophilus (L acidophilus), Lactobacillus lactis, Lactobacillus casei (L. casei), and Lactobacillus fermentum. For selection of lactic acid bacteria having glutamate decarboxylase activity having salt tolerance and alcohol resistance, lactic acid bacteria separated in a general medium for lactic acid bacteria (MRS medium) containing glutamic acid or a salt thereof, sodium chloride and alcohol are used. After inoculating and culturing at 25 ° C. to 35 ° C. for several days, the GABA content of this culture solution is measured, and a lactic acid strain having a large amount of GABA may be selected.

乳酸菌はあらかじめ前培養したものを作用させるのが好ましい。前培養は乳酸菌が増殖できる培地であれば特に限定しないが、その例として、グルコース、ペプトン、酵母エキス、グルタミン酸またはその塩類をそれぞれ1w/v%、塩化ナトリウムを5〜10w/v%含有し、pHを5.0〜6.0に調整した培地を挙げることができる。乳酸菌前培養液は遠沈濃縮等を行わなくても、そのまま接種して作用させることができる。接種させる乳酸菌の割合は、塩分を含む食品1ミリリットルあたり、10〜10cellsの範囲に設定することが好ましく、より好ましくは10〜10cellsの範囲に設定する。この範囲であると、グルタミン酸脱炭酸酵素活性を有する乳酸菌の生育もよく、乳酸菌以外の細菌やかび、酵母などの雑菌の増殖を抑えることが容易である。作用させる方法としては、通気、攪拌、静置、またはこれらの組み合わせにより作用させると良い。作用させる温度は20℃〜40℃、好ましくは25℃〜35℃の範囲が良く、作用させる時間は5日間〜25日間が良い。初発pHを酸またはアルカリによりpH4.5〜7.0、好ましくは5.0〜6.0に調整すると乳酸菌の生育が特に良い。乳酸菌を作用させている時のpH変動に対する調整についても、酸又はアルカリで行うことができる。 The lactic acid bacteria are preferably pre-cultured. The preculture is not particularly limited as long as it is a medium in which lactic acid bacteria can grow. Examples thereof include 1 w / v% glucose, peptone, yeast extract, glutamic acid or salts thereof, and 5-10 w / v% sodium chloride, Examples include a medium whose pH is adjusted to 5.0 to 6.0. The lactic acid bacteria preculture solution can be inoculated and act as it is without performing centrifugation or the like. The proportion of lactic acid bacteria to be inoculated is preferably set in the range of 10 1 to 10 7 cells, more preferably in the range of 10 3 to 10 7 cells per milliliter of food containing salt. Within this range, the growth of lactic acid bacteria having glutamate decarboxylase activity is good, and it is easy to suppress the growth of bacteria other than lactic acid bacteria, fungi, yeasts and the like. As a method of making it act, it is good to make it act by ventilation | gas_flowing, stirring, standing, or these combinations. The operating temperature is 20 ° C. to 40 ° C., preferably 25 ° C. to 35 ° C., and the operating time is 5 to 25 days. Growth of lactic acid bacteria is particularly good when the initial pH is adjusted to pH 4.5 to 7.0, preferably 5.0 to 6.0 with acid or alkali. Adjustment with respect to pH fluctuation when lactic acid bacteria are allowed to act can also be performed with an acid or an alkali.

塩化ナトリウム、塩化ナトリウム及びアルコールを含有する食品には、乳酸菌の増殖速度を高めるために、グルコース、フルクトース、シュークロース、ラクトース、ソルビトール、マルトースなどの糖源を0.1w/v%〜5w/v%になるように、より好ましくは0.5w/v%〜3w/v%になるように添加すると良い。糖源を添加することで乳酸菌の増殖速度が高まり、また、作用中の糖源不足を解消できるため、付与できるGABA含量を優位に高めることができる。   For foods containing sodium chloride, sodium chloride and alcohol, in order to increase the growth rate of lactic acid bacteria, sugar sources such as glucose, fructose, sucrose, lactose, sorbitol, maltose, etc. are added at 0.1 w / v% to 5 w / v. %, More preferably 0.5 w / v% to 3 w / v%. By adding a sugar source, the growth rate of lactic acid bacteria can be increased, and the shortage of the active sugar source can be eliminated, so that the GABA content that can be imparted can be increased significantly.

このようにして得られた食品はさまざまな生理機能を有するGABAが高含有されている。その食品はそのまま調味料として使用しても良く、既存の調味料からの置き換えで容易に麺類つゆ、スープ類等といった幅広い食品にGABAを高含有させることができる。任意の食品に少量添加するだけでその食品中のGABA含量を著しく増加させることができ、乳酸菌の醗酵産物由来の味、風味への影響がほとんどない食品を得ることができる。アルコール含有量が多く官能的に好まれない場合は、加熱、減圧等で気化させた後、種々の用途に用いれば良い。さらに脱塩、脱色、および脱臭といった加工を施し、粉末化することにより、お菓子、飲料などの材料としても用いることができる。   The food obtained in this way is high in GABA having various physiological functions. The food may be used as a seasoning as it is, and GABA can be highly contained in a wide range of foods such as noodle soup and soup by replacing existing seasonings. By adding a small amount to any food, the GABA content in the food can be remarkably increased, and a food having little influence on the taste and flavor derived from the fermentation product of lactic acid bacteria can be obtained. In the case where the alcohol content is high and it is not sensuously preferred, it may be vaporized by heating, decompression, etc. and then used for various purposes. Furthermore, it can also be used as a material for sweets, beverages, etc., by subjecting it to desalination, decolorization, and deodorization and making it into powder.

以下、実施例により本発明を具体的に説明する。本発明の技術的範囲はこれらの例により何ら限定されるものではない。
実施例1 <塩化ナトリウム高含有醤油中におけるGABA産生量>
L−グルタミン酸ナトリウムをそれぞれ4.9w/v%、7.4w/v%加えた醤油1,2(塩化ナトリウムはともに12w/v%)を準備し、醤油のpHを40%NaOH溶液で5.5に調整した。20LR容密閉容器に16LRづつ入れ、ラクトバチルス ブレビスYS1403(自社保有株)の前培養液を約0.27%(43ミリリットル)接種して、30℃で14日間醗酵させた。前培養液は培地(グルコース、ペプトン、酵母エキス、グルタミン酸ナトリウムをそれぞれ1w/v%、塩化ナトリウム10w/v%、pH6.0)に前述の乳酸菌株を一白金耳接種後、30℃で4日間培養し、7乗オーダーcfu/mlまで増殖させた。10日目、14日目の醗酵液に含まれる乳酸菌以外の菌数をトーマ氏血球計算盤にて測定した。また、14日間醗酵後、85℃/10分の殺菌を行い、8000rpmで10分間遠心分離後、得られた上澄み中に含まれるGABA含量を測定した。初発グルタミン酸量および得られた上澄み中に含まれるGABA含量の測定は、pH2.2クエン酸緩衝液で希釈してアミノ酸分析システム(HPLC、島津製作所社製)を用いて、オルトフタルアルデヒド法により定量した。乳酸菌以外の細菌、酵母、かびのトーマ氏血球計算盤での測定結果及びGABA含量測定結果を表1に示す。
Hereinafter, the present invention will be described specifically by way of examples. The technical scope of the present invention is not limited by these examples.
Example 1 <GABA production amount in soy sauce with high sodium chloride content>
Prepare soy sauce 1, 2 to which sodium L-glutamate was added 4.9 w / v% and 7.4 w / v%, respectively (sodium chloride is 12 w / v%), and adjust the pH of the soy sauce with 40% NaOH solution. Adjusted to 5. Each 16LR was put into a 20LR sealed container, inoculated with about 0.27% (43 ml) of a preculture of Lactobacillus brevis YS1403 (own company's own strain), and fermented at 30 ° C. for 14 days. The pre-culture solution is a medium (glucose, peptone, yeast extract, sodium glutamate 1 w / v%, sodium chloride 10 w / v%, pH 6.0, respectively) and the above-mentioned lactic acid strain is inoculated in one platinum loop and then at 30 ° C. for 4 days Cultured and grown to 7th power cfu / ml. On the 10th and 14th day, the number of bacteria other than the lactic acid bacteria contained in the fermentation solution was measured with a Thoma hemocytometer. Further, after fermentation for 14 days, sterilization at 85 ° C./10 minutes was performed, and after centrifugation at 8000 rpm for 10 minutes, the GABA content contained in the obtained supernatant was measured. The initial glutamic acid content and the GABA content contained in the obtained supernatant were measured by diluting with pH 2.2 citrate buffer and quantified by the orthophthalaldehyde method using an amino acid analysis system (HPLC, manufactured by Shimadzu Corporation). did. Table 1 shows the measurement results and GABA content measurement results of bacteria other than lactic acid bacteria, yeast, and mold by Tomoma's hemocytometer.

Figure 2006246840
Figure 2006246840

表1より、L−グルタミン酸ナトリウムを加えて基質を増やした塩化ナトリウム含有量の高い醤油1、2に耐塩性のグルタミン酸脱炭酸酵素活性を有する乳酸菌を作用させることにより、接種した乳酸菌以外の細菌、かび、酵母の増殖を抑えながらそれぞれ、3.2w/v%、4.2w/v%のGABAを付与させることができた。ちなみに醤油1の塩化ナトリウム濃度を4w/v%に調整した醤油に乳酸菌を作用させたところ、Bacillus属細菌の増殖が確認されたことから、塩化ナトリウム濃度は5w/v%以上必要である。   From Table 1, bacteria other than the inoculated lactic acid bacteria by allowing lactic acid bacteria having salt-resistant glutamate decarboxylase activity to act on soy sauces 1 and 2 having a high sodium chloride content by adding L-glutamic acid sodium and increasing the substrate, While suppressing the growth of mold and yeast, it was possible to impart 3.2 w / v% and 4.2 w / v% GABA, respectively. Incidentally, when lactic acid bacteria were allowed to act on soy sauce in which the sodium chloride concentration of soy sauce 1 was adjusted to 4 w / v%, the growth of Bacillus bacteria was confirmed, so the sodium chloride concentration must be 5 w / v% or more.

実施例2 <塩化ナトリウム及びアルコール高含有醤油様調味料中でのGABA産生量>
醤油を12.0w/w%、シュークロースを22.4w/w%、並塩を4.4w/w%、L−グルタミン酸ナトリウムを5.1w/w%、酵母エキスを0.4w/w%、サバエキスを3.3w/w%、95%アルコール3.9w/w%を含む醤油様調味料1と、醤油様調味料1の配合の並塩を6.9w/w%、95%アルコールを2.7w/w%にした醤油様調味料2のpHを乳酸で5.5に調整した。20ml容ねじつき試験管に15mlづつ分注し、ラクトバチルスsp. YD05(自社保有株)の前培養液を約0.27%(40マイクロリットル)接種して、30℃で19日間醗酵させた。前培養液は実施例1と同様に培養した。10日目、19日目の醗酵液に含まれる乳酸菌以外の菌数をトーマ氏血球計算盤にて測定した。19日間醗酵後、実施例1と同様の処理を行い、醤油様調味料中に含まれるGABA含量を測定した。乳酸菌以外の細菌、酵母、かびのトーマ氏血球計算盤での測定結果及びGABA含量測定結果を表2に示す。
Example 2 <GABA production amount in soy sauce-like seasonings containing high sodium chloride and alcohol>
Soy sauce 12.0 w / w%, sucrose 22.4 w / w%, average salt 4.4 w / w%, sodium L-glutamate 5.1 w / w%, yeast extract 0.4 w / w% , Soy sauce-like seasoning 1 containing 3.3 w / w% mackerel extract, 3.9 w / w% 95% alcohol, and 6.9 w / w% 95% alcohol The pH of the soy sauce-like seasoning 2 adjusted to 2.7 w / w% was adjusted to 5.5 with lactic acid. Dispense 15 ml each into a 20 ml threaded test tube, inoculate about 0.27% (40 microliters) of a preculture of Lactobacillus sp. YD05 (own company strain), and ferment it at 30 ° C. for 19 days. . The preculture was cultured in the same manner as in Example 1. The number of bacteria other than lactic acid bacteria contained in the fermentation liquid on the 10th and 19th days was measured with a Toma hemocytometer. After 19 days of fermentation, the same treatment as in Example 1 was performed, and the GABA content contained in the soy sauce-like seasoning was measured. Table 2 shows the measurement results and GABA content measurement results of bacteria other than lactic acid bacteria, yeast, and mold mold on a hemocytometer.

Figure 2006246840
Figure 2006246840

表2より、塩化ナトリウム及びアルコールを高含有する醤油様調味料1及び醤油様調味料2に、グルタミン酸脱炭酸酵素活性を有する耐塩性及びアルコール耐性の強い乳酸菌を作用させることにより、接種した乳酸菌以外の細菌、かび、酵母の増殖を抑えながら、それぞれ3.3w/v%、3.4w/v%のGABAを付与できた。   Table 2 shows that lactic acid bacteria other than the inoculated lactic acid bacteria by causing the lactic acid bacteria having strong glutamate decarboxylase activity to act on the soy sauce-like seasonings 1 and soy sauce-like seasonings 2 containing high sodium chloride and alcohol. While suppressing the growth of bacteria, fungi and yeast, 3.3 w / v% and 3.4 w / v% GABA could be imparted, respectively.

実施例3 <糖源の添加によるGABA産生量の増加>
L−グルタミン酸ナトリウム添加量が7.92w/v%、グルコース添加量がそれぞれ0%(加えない)、1w/v%、3w/v%である醤油3、4、5を準備した。それぞれの醤油のpHを、40%NaOH溶液で5.5に調整し、ラクトバチルスsp. YD05(自社保有株)を実施例1と同様に接種し、30℃で21日間培養した。GABA含量測定結果を表3に示す。
Example 3 <Increase of GABA production amount by addition of sugar source>
Soy sauces 3, 4, and 5 were prepared with a sodium L-glutamate addition amount of 7.92 w / v% and a glucose addition amount of 0% (not added), 1 w / v%, and 3 w / v%, respectively. The pH of each soy sauce was adjusted to 5.5 with 40% NaOH solution, Lactobacillus sp. YD05 (own company) was inoculated in the same manner as in Example 1, and cultured at 30 ° C. for 21 days. The GABA content measurement results are shown in Table 3.

Figure 2006246840
Figure 2006246840

表3より、グルコースを加えていない醤油3ではGABA含量が3.49w/v%であったのに対し、1w/v%添加した醤油4、3w/v%添加した醤油5ではそれぞれGABA含量が4.65w/v%、4.47w/v%と高くなった。グルコース以外に、フルクトース、シュークロース、ラクトース、ソルビトールなどの糖源を添加した場合でも同様の結果が得られた。塩化ナトリウムを高含有する食品にグルタミン酸脱炭酸酵素活性を有する耐塩性の乳酸菌を作用させ、雑菌の増殖を抑えながらGABAを安全に製造する方法において、グルコースなどの糖源(炭素源)を添加することでGABA含量を優位に高めることができる。ただし、グルコースを10w/v%加えた醤油で同様の試験を行ってみたが、GABA含量を優位に高めることはできなかった。適度に糖源を添加することで乳酸菌の増殖速度が高まり、また、作用中の糖源不足を解消できるため、GABA含量が高くなる。   From Table 3, the soy sauce 3 without added glucose had a GABA content of 3.49 w / v%, whereas the soy sauce 4 with 1 w / v% added and the soy sauce 5 with 3 w / v% added had a GABA content, respectively. It became high with 4.65 w / v% and 4.47 w / v%. Similar results were obtained when sugar sources such as fructose, sucrose, lactose and sorbitol were added in addition to glucose. A sugar source such as glucose (carbon source) is added in a method in which a salt-resistant lactic acid bacterium having glutamic acid decarboxylase activity is allowed to act on a food containing a high content of sodium chloride to safely produce GABA while suppressing the growth of various bacteria. Thus, the GABA content can be increased significantly. However, a similar test was performed using soy sauce to which 10 w / v glucose was added, but the GABA content could not be increased significantly. By appropriately adding a sugar source, the growth rate of lactic acid bacteria is increased, and the shortage of sugar source during the action can be eliminated, so that the GABA content is increased.

実施例4 <GABA富化食品の加工食品1>
実施例3に示した醤油4に乳酸菌を作用させて得られたGABA高含有醤油(GABA4.65w/v%含有)を1.25w/v%、市販の濃口醤油20w/v%、並塩6w/v%、グラニュー糖9w/v%、グリシン0.1w/v%、かつおエキス5w/v%を加えてGABA0.058w/v%含有濃縮そばつゆを得た。一食分40mlから約21mgのGABA摂取が可能なそばつゆであり、GABA高含有醤油の使用量は1.25w/v%と少量添加しただけなので乳酸菌の醗酵産物由来の味、風味への影響がほとんどないそばつゆであった。
Example 4 <Processed Food 1 of GABA-Enriched Food>
1.25 w / v% GABA high content soy sauce (GABA 4.65 w / v% contained) obtained by allowing lactic acid bacteria to act on soy sauce 4 shown in Example 3, commercially available concentrated soy sauce 20 w / v%, common salt 6 w / W%, granulated sugar 9w / v%, glycine 0.1w / v%, bonito extract 5w / v% was added to obtain concentrated soba soup containing GABA 0.058w / v%. The soba soup that can take about 21 mg of GABA from 40 ml per serving, and the amount of soy sauce containing a high amount of GABA is only 1.25 w / v%, so it has little effect on the taste and flavor derived from the fermentation products of lactic acid bacteria. There was no soba soup.

実施例5 <GABA富化食品の加工食品2>
実施例1に示した醤油2に乳酸菌を作用させて得られたGABA高含有醤油(GABA4.2w/v%含有)を2w/v%、市販の濃口醤油35w/v%、植物蛋白加水分解物11.8w/v%、L−グルタミン酸ナトリウム4w/v%、かつおエキス1w/v%、5’−イノシン酸ナトリウム0.1w/v%、5’−グアニル酸ナトリウム0.1w/v%、中華だし4w/v%、並塩12w/v%、にぼしエキス5w/v%を加えて、GABA0.084w/v%含有濃縮醤油ラーメンスープを得た。ラーメン一杯(スープ40ml)から約30mgのGABA摂取が可能なスープであり、GABA高含有醤油の使用量は2w/v%と少量添加しただけなので、実施例4のそばつゆと同様、乳酸菌の醗酵産物由来の味、風味への影響がほとんどないラーメンスープであった。
Example 5 <Processed Food 2 of GABA-enriched Food>
2% w / v GABA-rich soy sauce obtained by allowing lactic acid bacteria to act on soy sauce 2 shown in Example 1 (containing GABA 4.2 w / v%), commercially available concentrated soy sauce 35 w / v%, plant protein hydrolyzate 11.8 w / v%, sodium L-glutamate 4 w / v%, bonito extract 1 w / v%, 5′-sodium inosinate 0.1 w / v%, 5′-sodium guanylate 0.1 w / v%, Chinese However, 4 w / v%, average salt 12 w / v% and niboshi extract 5 w / v% were added to obtain concentrated soy sauce ramen soup containing 0.084 w / v GABA. It is a soup that can take about 30 mg of GABA from a cup of ramen (soup 40 ml), and the amount of GABA-rich soy sauce used is only 2 w / v%, so it is a fermented product of lactic acid bacteria, just like soba soup in Example 4. It was a ramen soup that had little influence on the origin and flavor.

Claims (6)

5w/v%〜20w/v%の塩化ナトリウムを含有する食品にグルタミン酸及び/又はその塩を添加し、グルタミン酸脱炭酸酵素活性を有する耐塩性の乳酸菌を作用させるγ−アミノ酪酸の製造方法。   A method for producing γ-aminobutyric acid, wherein glutamic acid and / or a salt thereof is added to a food containing 5 w / v% to 20 w / v% sodium chloride, and a salt-resistant lactic acid bacterium having glutamic acid decarboxylase activity is allowed to act. 5w/v%〜20w/v%の塩化ナトリウムを含有する食品に0.1w/v%〜6w/v%になるようにアルコールを加え、グルタミン酸及び/又はその塩を添加し、グルタミン酸脱炭酸酵素活性を有する耐塩性及びアルコール耐性の強い乳酸菌を作用させるγ−アミノ酪酸の製造方法。   Alcohol is added to a food containing 5 w / v% to 20 w / v% sodium chloride so as to be 0.1 w / v% to 6 w / v%, glutamic acid and / or a salt thereof is added, and glutamic acid decarboxylase is added. A method for producing γ-aminobutyric acid in which a lactic acid bacterium having a strong salt tolerance and alcohol resistance is allowed to act. 塩化ナトリウムを含有する食品が、醤油、みそ、蛋白加水分解物、醤油様調味料のいずれか一つ又は2つ以上を組み合わせた調味料である、請求項1又は請求項2に記載のγ−アミノ酪酸の製造方法   The γ- of claim 1 or 2, wherein the food containing sodium chloride is a seasoning obtained by combining any one or more of soy sauce, miso, protein hydrolyzate, and soy sauce-like seasoning. Method for producing aminobutyric acid 耐塩性及びアルコール耐性の強い乳酸菌がラクトバチルス属の乳酸菌である請求項1〜3に記載のγ−アミノ酪酸の製造方法。   The method for producing γ-aminobutyric acid according to claim 1, wherein the lactic acid bacterium having strong salt resistance and alcohol resistance is a lactic acid bacterium belonging to the genus Lactobacillus. 塩化ナトリウムを含有する食品に、糖源を添加する請求項1〜4に記載のγ−アミノ酪酸の製造方法。   The manufacturing method of (gamma) -aminobutyric acid of Claims 1-4 which adds a sugar source to the foodstuff containing sodium chloride. 請求項1〜5のいずれか一つに記載の製造方法により得られるγ−アミノ酪酸高含有食品及びその加工食品。
A γ-aminobutyric acid-rich food obtained by the production method according to claim 1 and a processed food thereof.
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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2008245545A (en) * 2007-03-29 2008-10-16 Oubiken:Kk Method for producing fermented sesame, and the fermented sesame
KR100921697B1 (en) 2007-10-09 2009-10-15 인하대학교 산학협력단 Method for using high osmotic pressure tolerant strain as natural flavor

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH07227245A (en) * 1994-02-18 1995-08-29 Kyoto Pref Gov Production of fermented food product
JP2000210075A (en) * 1999-01-21 2000-08-02 Taiyo Corp Lactic acid bacterium having high productivity of gamma- aminobutyric acid, fermented food with high content of gamma-aminobutyric acid using the same lactic acid bacterium and its production
JP2002360289A (en) * 2001-06-13 2002-12-17 Takara Holdings Inc METHOD FOR PRODUCING gamma-AMINOBUTYRIC ACID
JP2004290129A (en) * 2003-03-28 2004-10-21 Kikkoman Corp Common salt-containing food or beverage
JP2004357535A (en) * 2003-06-03 2004-12-24 Higashimaru Shoyu Co Ltd NEW LACTOBACILLUS HAVING IMMUNOPOTENTIATIVE ACTIVITY AND gamma-AMINOBUTYRIC ACID-PRODUCING ABILITY AND UTILIZATION THEREOF

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH07227245A (en) * 1994-02-18 1995-08-29 Kyoto Pref Gov Production of fermented food product
JP2000210075A (en) * 1999-01-21 2000-08-02 Taiyo Corp Lactic acid bacterium having high productivity of gamma- aminobutyric acid, fermented food with high content of gamma-aminobutyric acid using the same lactic acid bacterium and its production
JP2002360289A (en) * 2001-06-13 2002-12-17 Takara Holdings Inc METHOD FOR PRODUCING gamma-AMINOBUTYRIC ACID
JP2004290129A (en) * 2003-03-28 2004-10-21 Kikkoman Corp Common salt-containing food or beverage
JP2004357535A (en) * 2003-06-03 2004-12-24 Higashimaru Shoyu Co Ltd NEW LACTOBACILLUS HAVING IMMUNOPOTENTIATIVE ACTIVITY AND gamma-AMINOBUTYRIC ACID-PRODUCING ABILITY AND UTILIZATION THEREOF

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2008245545A (en) * 2007-03-29 2008-10-16 Oubiken:Kk Method for producing fermented sesame, and the fermented sesame
KR100921697B1 (en) 2007-10-09 2009-10-15 인하대학교 산학협력단 Method for using high osmotic pressure tolerant strain as natural flavor

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