JP2006025669A - Method for producing beverage - Google Patents

Method for producing beverage Download PDF

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JP2006025669A
JP2006025669A JP2004207687A JP2004207687A JP2006025669A JP 2006025669 A JP2006025669 A JP 2006025669A JP 2004207687 A JP2004207687 A JP 2004207687A JP 2004207687 A JP2004207687 A JP 2004207687A JP 2006025669 A JP2006025669 A JP 2006025669A
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lactic acid
gaba
beverage
fermentation
producing
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Tomomi Aijima
知美 相島
Shunji Kadomatsu
俊志 門松
Mitsuro Uchida
充郎 内田
Yuichiro Nishi
祐一郎 西
Noriyoshi Tsuchiya
紀美 土谷
Katanori Nishimura
賢了 西村
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KUMAMOTOKEN KAJITSU NOGYO KYOD
KUMAMOTOKEN KAJITSU NOGYO KYODO KUMIAI RENGOKAI
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KUMAMOTOKEN KAJITSU NOGYO KYODO KUMIAI RENGOKAI
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Abstract

<P>PROBLEM TO BE SOLVED: To provide a method for producing beverage containing lactic fermentation fruit juice or lactic fermentation vegetable squeezed liquid, having high GABA content and excellent in flavor for performing lactic fermentation without any problem even in fruit juice or vegetable squeezed liquid with the use of lactic acid bacteria capable of producing GABA. <P>SOLUTION: This method for producing the beverage comprises adding lactic acid bacteria having γ-aminobutyric acid (GABA) producing ability to the raw material of the beverage. <P>COPYRIGHT: (C)2006,JPO&NCIPI

Description

本発明はγ−アミノ酪酸(以下、文脈によりGABAと略す)を高濃度に含有する飲料及びその製造方法に関する。   The present invention relates to a beverage containing γ-aminobutyric acid (hereinafter abbreviated as GABA depending on the context) in a high concentration and a method for producing the same.

ほ乳類においてGABAは主に脳や脊髄に存在する抑制系の神経伝達物質であり、その生理効果については脳の血量を活発にさせて脳の代謝機能を亢進するとともに、脊椎の血管運動中枢に作用して血圧を降下させ、抗利尿ホルモンであるバソプレッソンの分泌を抑制して、血管を拡張して血圧を下げること等が報告され、脳代謝賦活を目的に医薬品としても利用されている。また、GABAは自然界に広く分布しているアミノ酸であり、微生物や動植物が有するグルタミン酸デカルボキシラーゼ(GAD)酵素の作用によりL-グルタミン酸が脱炭酸されて生産される。GABAは非タンパク構成アミノ酸であるが、上述のように生体に重要な働きを有し、特に高血圧の予防に有効な機能性食品素材として近年注目を集めており、様々なGABA含有食品の開発が行われている。例えば、米胚芽を嫌気処理してGABA含有量を高めた胚芽米、茶葉を嫌気処理してGABA量を高めた緑茶などが市販されている。   In mammals, GABA is an inhibitory neurotransmitter that exists mainly in the brain and spinal cord. Its physiological effects increase the brain's blood volume and enhance the metabolic function of the brain, and the vasomotor center of the spine. It has been reported to lower blood pressure by acting to lower blood pressure, suppress secretion of vasopressone, an antidiuretic hormone, dilate blood vessels, and is also used as a medicine for the purpose of stimulating brain metabolism. GABA is an amino acid that is widely distributed in nature, and is produced by decarboxylation of L-glutamate by the action of glutamate decarboxylase (GAD) enzyme possessed by microorganisms and animals and plants. GABA is a non-protein constituent amino acid, but as mentioned above, it has an important function in the living body, and has recently attracted attention as a functional food material effective for the prevention of hypertension, and various GABA-containing foods have been developed. Has been done. For example, germinated rice in which rice germ is anaerobically treated to increase the GABA content, and green tea in which tea leaves are anaerobically treated to increase the GABA content are commercially available.

一方、微生物を利用してGABAを富化した食品の製造法として、牛乳にグルタミン酸(塩)を添加し乳酸菌を培養してGABAを含有する発酵食品を得る方法(特許文献1)、またグルタミン酸(ナトリウム)に酵母又はクロレラの細胞破砕液を作用させてGABAを富化した食品素材を製造する方法(特許文献2)、発酵乳製品中の乳酸菌の脱炭酸酵素作用によりGABAを生成する方法(特許文献3)、乳製品をプロテアーゼ処理後、乳酸菌を摂取してGABA含有発酵乳を製造する方法(特許文献4)がある。   On the other hand, as a method for producing a food enriched with GABA using microorganisms, a method of obtaining a fermented food containing GABA by adding glutamic acid (salt) to milk and culturing lactic acid bacteria (Patent Document 1), or glutamic acid ( A method of producing a food material enriched with GABA by allowing yeast or chlorella cell lysate to act on sodium) (Patent Document 2), a method of generating GABA by the decarboxylase action of lactic acid bacteria in fermented milk products (Patent Document 2) Reference 3), there is a method for producing GABA-containing fermented milk by ingesting lactic acid bacteria after protease treatment of dairy products (Patent Document 4).

特開平7-227245号公報Japanese Unexamined Patent Publication No. 7-227245 特開平9-238850号公報Japanese Patent Laid-Open No. 9-238850 特開平10-295394号公報JP-A-10-295394 特開2001-120179号公報JP 2001-120179 A 特開平1-179646号公報Japanese Unexamined Patent Publication No. 1-179646 特開平05-084066号公報JP 05-084066 A 特開平06-062814号公報Japanese Patent Laid-Open No. 06-062814

これまで多くのGABA富化食品に関する製法特許は出されているが、果物や野菜の搾汁液そのものにGABAを富化した例は見当たらない。また、これまでの事例では生成されるGABA量が少量で効率的ではなく実用化において充分とはいえない。本発明では、食品・飲料としての安全性の観点から、従来から食品製造に用いられている微生物を利用して当該飲料の原料中のグルタミン酸からGABAを生産させることが適当と考えられた。しかし、微生物として乳酸菌を利用した場合、果汁中ではポリフェノール類が乳酸発酵を抑制するため、果汁のみにより乳酸発酵を行うことはGABAの高産生を目的とする方法としては困難とされていた。これまでに、特許文献5ではpH調整済の果実処理物と乳製品の混合物中で乳酸発酵を行っており、特許文献6では果汁の静菌作用を受けにくい新規乳酸菌の開発、特許文献7では乳酸菌を多糖類ゲルで包括固定化して果汁の発酵を行っているがいずれも満足な方法とはいえない。そこで、本発明は乳酸菌の作用により当該飲料の原料中のグルタミン酸から短時間に高変換率でGABAを生産させ、GABAを高含有する飲料を提供することを目的として、その目的にかなった乳酸菌の探索を行った。   So far, many patents have been issued regarding GABA-enriched foods, but no GABA-enriched examples have been found in fruit and vegetable juices. In addition, in the past cases, the amount of GABA produced is small and not efficient, so it cannot be said that it is sufficient for practical use. In the present invention, from the viewpoint of safety as a food / beverage, it was considered appropriate to produce GABA from glutamic acid in the raw material of the beverage using microorganisms conventionally used in food production. However, when lactic acid bacteria are used as microorganisms, polyphenols suppress lactic acid fermentation in fruit juice, and it has been considered difficult to perform lactic acid fermentation only with fruit juice as a method for high GABA production. So far, in Patent Document 5, lactic acid fermentation has been carried out in a mixture of a pH-adjusted fruit processed product and a dairy product. In Patent Document 6, the development of a novel lactic acid bacterium that is less susceptible to the bacteriostatic action of fruit juice. Although lactic acid bacteria are entrapped and immobilized with a polysaccharide gel to ferment fruit juice, none of them is a satisfactory method. Therefore, the present invention aims to produce GABA with a high conversion rate in a short time from glutamic acid in the raw material of the beverage by the action of lactic acid bacteria, and to provide a beverage containing a high content of GABA. Searched.

本発明では果汁中で乳酸発酵しGABAを高濃度に生産する乳酸菌の探索を行うとともに、GABAを多量に生成し、なおかつ乳酸発酵後の果汁の風味や特性を損なわない製造条件(初発pH、発酵温度、発酵時間、果汁還元率、初発酸度、乳酸菌添加量)を検討した。GABAの基質となるグルタミン酸含量が果汁中に少ない場合はグルタミン酸の添加を行うこととしたが、発酵後の果汁中に残存するグルタミン酸が原料の味を変化させないようGABA変換率の高い乳酸菌の選抜を行い、添加量の設定を行った。   The present invention searches for lactic acid bacteria that produce lactic acid by high-concentration lactic acid fermentation in fruit juice, produces a large amount of GABA, and does not impair the flavor and characteristics of the juice after lactic acid fermentation (initial pH, fermentation Temperature, fermentation time, fruit juice reduction rate, initial acidity, and amount of lactic acid bacteria added). If the glutamic acid content of GABA substrate is low in the fruit juice, we decided to add glutamic acid, but we selected lactic acid bacteria with a high GABA conversion rate so that glutamic acid remaining in the fruit juice after fermentation does not change the taste of the raw material. The addition amount was set.

その結果、果汁中においても問題なく乳酸発酵してGABAを生産する乳酸菌を見いだし、さらには初発pHの設定や発酵温度、発酵時間、果汁還元率及び初発酸度の設定、添加グルタミン酸ナトリウム量の設定を行うことにより効率よくGABA含量の高い果汁及び野菜搾汁液を得ることが可能となり、この発明を完成するに至った。   As a result, we found lactic acid bacteria that produce GABA by lactic acid fermentation without problems even in the fruit juice, and further set the initial pH, fermentation temperature, fermentation time, juice reduction rate and initial acidity, and the amount of added sodium glutamate. As a result, fruit juice and vegetable juice with high GABA content can be obtained efficiently, and the present invention has been completed.

即ち、本発明は、飲料の原料にγ−アミノ酪酸生性能を有する乳酸菌を添加することを特徴とする飲料の製造方法である。   That is, this invention is a manufacturing method of the drink characterized by adding the lactic acid bacteria which have (gamma) -aminobutyric acid raw performance to the raw material of a drink.

上記γ−アミノ酪酸生成能を有する乳酸菌としてはラクトバチルスブレビス(Lactobacillus brevis)に属する乳酸菌が挙げられ、飲料の原料としては果汁又は野菜搾汁液が挙られる。   Examples of the lactic acid bacteria having the ability to produce γ-aminobutyric acid include lactic acid bacteria belonging to Lactobacillus brevis, and examples of beverage materials include fruit juice or vegetable juice.

さらに、本発明は、上記飲料の原料にさらにグルタミン酸及び/又はその塩を5w/v%以下添加する上記飲料の製造方法も含むものである。
さらに、本発明は、上記記載の製造方法により得られる飲料である。
Furthermore, the present invention includes a method for producing the beverage, wherein glutamic acid and / or a salt thereof is further added to the raw material of the beverage at 5 w / v% or less.
Furthermore, the present invention is a beverage obtained by the production method described above.

GABAを生産し得る乳酸菌を用いることにより果汁中や野菜搾汁液中においても問題なく乳酸発酵し、GABA含量の高い、なおかつ風味に優れた乳酸発酵果汁及び乳酸発酵野菜搾汁液を含む飲料を製造することができた。そして、この飲料はGABAを安全にかつ高濃度で摂取できるもので、更には嗜好性が高いものであるため日常的に手軽に摂取ことができ、積極的な健康保持効果が期待できる。   By using lactic acid bacteria capable of producing GABA, lactic acid fermentation can be performed without problems even in fruit juices and vegetable juices, and beverages containing lactic acid fermentation fruit juices and lactic acid fermentation vegetable juices with high GABA content and excellent flavor are produced. I was able to. And since this drink can ingest GABA safely and in high concentration, and also has high palatability, it can be easily ingested on a daily basis, and an active health maintenance effect can be expected.

以下、本発明のGABA富化果汁の製造方法について詳細に説明する。
この発明に用いる乳酸菌は、果汁や野菜汁においてGABAを生産する種類であればいずれでもよいが、ポリフェノールが豊富な果汁中において増殖及び乳酸発酵が認められ、GABAを生産する菌種について探索した。結果を表1に示す。
Hereinafter, the method for producing the GABA-enriched fruit juice of the present invention will be described in detail.
The lactic acid bacteria used in the present invention may be any kind that produces GABA in fruit juice or vegetable juice, but growth and lactic acid fermentation were observed in the fruit juice rich in polyphenols, and the bacterial species producing GABA were searched. The results are shown in Table 1.

Figure 2006025669
Figure 2006025669

表1において、乳酸菌11株の中では、Lactobacillus paracasei subsp. paracasei NBRC-12004、Lactobacillus brevis NBRC-12005、Lactobacillus plantarum NBRC-12006、Pediococcus paevulus NBRC-12233が果汁中での増殖が認められたが、GABAを高生産した株はLactobacillus brevis NBRC-12005のみであった。表1は乳酸菌の増殖を確認しやすくするためクリア(透明)タイプの温州みかん果汁(9 Bx)を用い、pH調整はせず0.5%のグルタミン酸ソーダを添加して前培養した各種乳酸菌を2%量植菌後30℃2日間発酵させたものである。菌体の増殖は、集菌菌体の水への再懸濁液の濁度を650nmにおいて測定した。この結果から、果汁や野菜汁においてGABAを生産するには、特にLactobacillus brevis (ラクトバチルスブレビス)に属するものが望ましく、この例としてNBRC-3345 (旧IFO-3345)、NBRC-3960 (旧IFO-3960)、NBRC-12005 (旧IFO-12005)等を挙げることができる。   In Table 1, among the 11 lactic acid bacteria strains, Lactobacillus paracasei subsp. Lactobacillus brevis NBRC-12005 was the only strain that produced high yields. Table 1 shows the clear (transparent) type mandarin orange juice (9 Bx) to make it easier to confirm the growth of lactic acid bacteria, and 2% of each type of lactic acid bacteria pre-cultured with 0.5% sodium glutamate without pH adjustment Fermented at 30 ° C for 2 days after mass inoculation. Cell growth was determined by measuring the turbidity of the resuspension of the collected cells in water at 650 nm. From these results, in order to produce GABA in fruit juice and vegetable juice, those belonging to Lactobacillus brevis (Lactobacillus brevis) are particularly desirable. 3960), NBRC-12005 (formerly IFO-12005) and the like.

乳酸菌はあらかじめ前培養したものを用いるのが望ましい。前培養は乳酸菌が増殖できる培地であればいずれの培地でもよく特に限定されない。前培養は静置培養でも振とう培養でもよいが、30℃で1日間を必要とする。前培養された乳酸菌懸濁液はそのまま利用することもできるが、果汁以外の培地、例えばYPD培地等の場合は、培地由来の風味が製品に移行するのを抑えるため集菌、洗浄して果汁原料に接種することが望ましい。前培養した乳酸菌の原料への添加量は、原料が温州みかん果汁の場合、0.5%以上が望ましく、2.0%量接種しても生成するGABA量には大きな変化は見られなかった(図1参照)。しかし、0.1%接種ではGABA生産量が低下した。なお、図1は、原料素材は温州みかん果汁(9゜Bx)を使用し、30℃で2日間静置培養したものである。果汁及び野菜搾汁液はその種類には制限はなく、任意の果物や野菜を原料として使用できる。様々な果物の果汁や野菜の搾汁液に乳酸菌NBRC-12005を接種し乳酸発酵後のGABA含量を図2に示す。図2は、各種飲料としては、各原料素材をpH4.2に調整しそれにグルタミン酸ソーダ0.5%を添加したものを原料として使用し、30℃で2日間静置培養したものである。原料の風味を生かすためにはpH調整をしない方が望ましいが、上述ラクトバチルスブレビスが有するグルタミン酸デカルボキシラーゼはpH中性域では活性が阻害されるため、GABA生産効率を増強させるためには乳酸菌接種時のpHを酸性域、例えばpH3.5〜pH6.0に調整することが好ましい。しかし、酸度の高い柑橘系果汁の場合は必ずしもpH調整を必要としない(実施例2)。pH調整する場合に用いる物質は、食品添加物として認められたものならばいずれでもよく特定の種類に限定されない。例えばクエン酸及びクエン酸塩または重曹が挙げられる。また発酵温度及び発酵時間は上述乳酸菌の場合は20〜40℃、1日間〜3日間で乳酸発酵及びGABA生成が認められるが、好ましくは25〜30℃、2日間である(図3参照)。なお、図3において、原料素材は温州みかん果汁(9゜Bx)を使用した。   It is desirable to use a pre-cultured lactic acid bacterium. The preculture is not particularly limited as long as it is a medium in which lactic acid bacteria can grow. The preculture may be stationary culture or shaking culture, but it requires 1 day at 30 ° C. The pre-cultured lactic acid bacteria suspension can be used as it is, but in the case of a medium other than fruit juice, such as YPD medium, the fruit juice is collected and washed to prevent the flavor derived from the medium from transferring to the product. It is desirable to inoculate the raw material. The amount of pre-cultured lactic acid bacteria added to the raw material is desirably 0.5% or more when the raw material is Unshu mandarin orange juice, and no significant change was observed in the amount of GABA produced even after inoculation of 2.0% (see FIG. 1). ). However, GABA production decreased with 0.1% inoculation. In FIG. 1, the raw material is Unshu mandarin orange juice (9 ° Bx) and statically cultured at 30 ° C. for 2 days. The types of fruit juice and vegetable juice are not limited, and any fruit or vegetable can be used as a raw material. Fig. 2 shows the GABA content after inoculating lactic acid bacteria NBRC-12005 into various fruit juices and vegetable juices and lactic acid fermentation. FIG. 2 shows various beverages obtained by adjusting each raw material to pH 4.2 and adding sodium glutamate 0.5% as a raw material, followed by stationary culture at 30 ° C. for 2 days. It is desirable not to adjust the pH in order to make use of the flavor of the raw material, but since the glutamate decarboxylase possessed by Lactobacillus brevis is inhibited in the neutral pH range, inoculation with lactic acid bacteria to enhance GABA production efficiency It is preferable to adjust the pH at the time to an acidic range, for example, pH 3.5 to pH 6.0. However, in the case of citrus fruit juice having a high acidity, pH adjustment is not necessarily required (Example 2). The substance used for pH adjustment is not limited to a specific type as long as it is recognized as a food additive. Examples include citric acid and citrate or sodium bicarbonate. In the case of the above-mentioned lactic acid bacteria, the fermentation temperature and fermentation time are 20 to 40 ° C. for 1 to 3 days. Lactic acid fermentation and GABA production are observed, but preferably 25 to 30 ° C. for 2 days (see FIG. 3). In FIG. 3, the raw material was Wenzhou orange juice (9 ° Bx).

また、果汁原料及び野菜搾汁液原料において遊離グルタミン酸含量の低いものはこの乳酸発酵による効果が得にくくなるため、GABAの基質となるグルタミン酸及び/又はその塩を添加して乳酸菌を作用させてもよい。添加量は特に制限されないが、乳酸菌によりGABAに変換されずに残存するグルタミン酸が原料由来の風味に影響を与えないように、乳酸菌が100%変換できる添加量が望ましい。また、通常、果汁や野菜汁はクリア(透明)タイプと混濁タイプに分けられるが、混濁タイプを用いた場合は果汁に対してグルタミン酸0.2%添加量が適しており、クリアタイプを用いた場合は0.5%添加量が適していた(図4参照)。混濁タイプがよりポリフェノール量が多いために発酵阻害を受けると考えられ、GABA生産効率の点ではクリアタイプのほうが適している。なお、図4は、原料素材は温州みかん果汁(9°Bx)を使用し、30℃で2日間静置培養したものである。さらに、果汁は通常濃縮液を還元して飲料とする工程が考えられるが、乳酸発酵の原料として濃縮液でも希釈された還元液でも限定されないが、高糖度の場合はGABA生成効率が低下するため、混濁タイプみかん果汁の場合Bx 10程度が好ましい(図5参照)。一方、クリアタイプにおいては糖度がBx 18であっても良好なGABA生産効率を示した。なお、図5は、原料素材としては温州みかん果汁を使用し、30℃で2日間静置培養したものである。   Moreover, since the effect by this lactic acid fermentation becomes difficult to obtain in fruit juice raw materials and vegetable juice liquid raw materials having a low free glutamic acid content, glutamic acid and / or a salt thereof as a substrate for GABA may be added to cause lactic acid bacteria to act. . The addition amount is not particularly limited, but an addition amount capable of converting 100% of lactic acid bacteria is desirable so that glutamic acid remaining without being converted to GABA by lactic acid bacteria does not affect the flavor derived from the raw material. In addition, fruit juice and vegetable juice are usually divided into clear (transparent) type and turbid type, but when using the turbid type, 0.2% glutamic acid addition amount is suitable for the fruit juice, and when using the clear type A 0.5% addition amount was suitable (see FIG. 4). The turbid type is considered to be subject to fermentation inhibition due to higher polyphenol content, and the clear type is more suitable in terms of GABA production efficiency. In FIG. 4, the raw material is Unshu mandarin orange juice (9 ° Bx), which is cultured at 30 ° C. for 2 days. Furthermore, fruit juice usually has a process of reducing the concentrated liquid to make a beverage, but it is not limited to either concentrated liquid or diluted reduced liquid as a raw material for lactic acid fermentation, but GABA production efficiency decreases when the sugar content is high In the case of turbid orange juice, about Bx 10 is preferable (see FIG. 5). On the other hand, the clear type showed good GABA production efficiency even when the sugar content was Bx 18. In addition, FIG. 5 uses static mandarin orange juice as a raw material, and is statically cultured at 30 ° C. for 2 days.

本培養は静置、撹拌のいずれでもよいが、静置培養や緩やかな撹拌培養が原料香気の飛散を防ぐ点で有利である。このような発酵工程に置いて、乳酸菌は温州ミカン原料では発酵2日目に生菌数が15倍以上に増殖し、その乳酸菌の作用によりGABAを4倍以上に富化していた(図6参照)。なお、図6は、原料素材は温州みかん果汁(9°Bx)を使用し、菌体量1%量を植菌して所定の日数培養したものである。また、上述乳酸菌はヘテロ型と考えられるが、発酵によりエタノールの生成は見られなかった。   The main culture may be either stationary or agitation, but stationary culture or gentle agitation culture is advantageous in that it prevents scattering of raw material aroma. In such a fermentation process, lactic acid bacteria grew more than 15 times the number of viable bacteria on the second day of fermentation with Unshu mandarin orange raw material, and GABA was enriched more than 4 times by the action of the lactic acid bacteria (see FIG. 6). ). In FIG. 6, the raw material is Wenzhou mandarin orange juice (9 ° Bx), inoculated with a 1% amount of cells and cultured for a predetermined number of days. Moreover, although the said lactic acid bacteria are considered to be heterotype, the production | generation of ethanol was not seen by fermentation.

こうして得られる乳酸発酵液を最終飲料製品として仕上げる手法は特に限定されず、通常の方法が用いられる。例えば、香料及び甘味料の添加あるいは低酸原料の使用や高糖度原料あるいは混濁タイプとのブレンドによって味や香りを調整することができる。また殺菌工程を経ることによって生菌含有タイプとしない方法を選択することもできる。   The method for finishing the lactic acid fermentation liquor thus obtained as a final beverage product is not particularly limited, and ordinary methods are used. For example, the taste and aroma can be adjusted by the addition of a fragrance and a sweetener, the use of a low acid raw material, a blend with a high sugar raw material or a turbid type. Moreover, the method which does not become a living microbe containing type can also be selected by passing through a sterilization process.

以下、実施例を挙げて本発明をさらに詳細に説明するが、本発明の技術的範囲はこれらの実施例に限定されるものではない。   EXAMPLES Hereinafter, although an Example is given and this invention is demonstrated further in detail, the technical scope of this invention is not limited to these Examples.

実施例1
乳酸菌ラクトバチルスNBRC-12005 (IFO-12005)を121℃15分間殺菌したYPD培地(glucose 4%, polypeptone 1%, Yeast extract 0.5%, KH2PO4 0.5%, MgSO4・7H2O 0.2%、 和光純薬工業製、pH 4.2に調整)10mlに植菌し、30℃、1日間静置培養した。この培養液を遠心分離(3000rpm, 5分間)により集菌して無菌水で再懸濁して、以下の実施例で使用する乳酸菌とした。
Example 1
YPD medium (glucose 4%, polypeptone 1%, Yeast extract 0.5%, KH 2 PO 4 0.5%, MgSO 4 7H 2 O 0.2%, sterilized with lactic acid bacteria Lactobacillus NBRC-12005 (IFO-12005) at 121 ° C for 15 minutes, Wako Pure Chemical Industries, Ltd. (adjusted to pH 4.2) was inoculated into 10 ml, and statically cultured at 30 ° C. for 1 day. The culture was collected by centrifugation (3000 rpm, 5 minutes) and resuspended in sterile water to obtain lactic acid bacteria used in the following examples.

実施例2
温州みかん濃縮果汁を9゜Bx に調整後、次の3試験区の発酵原料を各100ml調製した。殺菌処理は行っていない。次のA〜Cの原料を調製した。A: pH無調整でグルタミン酸ナトリウム添加なし、B: pH無調整でグルタミン酸ナトリウムを0.2g添加、C: 重曹でpHを4.2に調製しグルタミン酸ナトリウムを0.5g添加したものである。各試験区原料に乳酸菌再懸濁液1mlを植菌した。30℃で2日間静置培養した。発酵後80℃達温で殺菌し、乳酸発酵GABA富化果汁が得られた。発酵前後のpH、滴定酸度、グルタミン酸濃度、GABA濃度を表2に示した。滴定酸度は試料1mlを滴定するのに要した0.1M NaOHの量(ml)で示した。
Example 2
After adjusting Wenzhou mandarin orange juice to 9 ° Bx, 100 ml of fermentation raw materials for the following three test sections were prepared. There is no sterilization treatment. The following raw materials A to C were prepared. A: pH is not adjusted and sodium glutamate is not added, B: pH is not adjusted, 0.2 g of sodium glutamate is added, C: pH is adjusted to 4.2 with sodium bicarbonate, and 0.5 g of sodium glutamate is added. 1 ml of lactic acid bacteria resuspension was inoculated into the raw material of each test section. Static culture was performed at 30 ° C. for 2 days. After fermentation, it was sterilized at a temperature of 80 ° C., and lactic acid fermentation GABA-enriched fruit juice was obtained. Table 2 shows pH values before and after fermentation, titratable acidity, glutamic acid concentration, and GABA concentration. Titration acidity was indicated by the amount (ml) of 0.1M NaOH required to titrate 1 ml of sample.

比較例1
比較試験として、実施例1と同様の方法により調整した乳酸菌ラクトバチルスNBRC-12004 (IFO-12004)を用いて実施例2のCの条件に従って温州みかん濃縮果汁を発酵させた。この場合のGABA濃度を表2に示した。
Comparative Example 1
As a comparative test, Unshu orange juice concentrate was fermented according to the conditions of Example 2C using lactic acid bacteria Lactobacillus NBRC-12004 (IFO-12004) prepared by the same method as in Example 1. The GABA concentration in this case is shown in Table 2.

実施例3
ほうれん草濃縮搾汁液を3゜Bx に調整後、次の4試験区の発酵原料を各100ml調製した。殺菌処理は行っていない。A: pH無調整でグルタミン酸ナトリウム添加なし、B: クエン酸でpHを4.2に調製しグルタミン酸ナトリウム添加なし、C: pH無調整でグルタミン酸ナトリウムを0.5g添加、D: クエン酸でpHを4.2に調製しグルタミン酸ナトリウムを0.5g添加したものである。各試験区原料に乳酸菌再懸濁液1mlを植菌した。30℃で2日間静置培養した。発酵後80℃達温で殺菌し、乳酸発酵GABA富化野菜汁が得られた。発酵前後のpH、滴定酸度、グルタミン酸濃度、GABA濃度を表2に示した。
Example 3
After adjusting the spinach concentrated juice to 3 ° Bx, 100 ml of fermentation raw materials for the following 4 test sections were prepared. There is no sterilization treatment. A: No pH adjustment, no sodium glutamate added, B: Citric acid adjusted to pH 4.2 with no sodium glutamate added, C: No pH adjusted, 0.5 g sodium glutamate added, D: Citric acid adjusted to pH 4.2 0.5 g of sodium glutamate is added. 1 ml of lactic acid bacteria resuspension was inoculated into the raw material of each test section. Static culture was performed at 30 ° C. for 2 days. After fermentation, it was sterilized at a temperature of 80 ° C. to obtain lactic acid fermented GABA-enriched vegetable juice. Table 2 shows pH values before and after fermentation, titratable acidity, glutamic acid concentration, and GABA concentration.

Figure 2006025669
Figure 2006025669

乳酸菌の添加量のGABA産生量への影響を示す図。The figure which shows the influence on the GABA production amount of the addition amount of lactic acid bacteria. 各種飲料における、発酵によるGABA量の増加量を示す図。The figure which shows the increase amount of the GABA amount by fermentation in various drinks. 発酵温度のGABAの産生量への影響を調べた図。The figure which investigated the influence on the production amount of GABA of fermentation temperature. グルタミン酸ソーダの添加量と果汁中のGABA量の変化を示す図。The figure which shows the change of the addition amount of glutamic acid sodium, and the amount of GABA in fruit juice. 果汁原料の発酵初発BxとGABAの産生量との関係を示す図。The figure which shows the relationship between the fermentation initial Bx of a fruit juice raw material, and the production amount of GABA. 乳酸菌生菌数と果汁中のGABA量を示す図。The figure which shows the lactic acid bacteria viable count and the amount of GABA in fruit juice.

Claims (5)

飲料の原料にγ−アミノ酪酸生成能を有する乳酸菌を添加することを特徴とする飲料の製造方法。   A method for producing a beverage, comprising adding a lactic acid bacterium having a γ-aminobutyric acid-producing ability to a beverage raw material. 飲料の原料が果汁又は野菜搾汁液であることを特徴する請求項1に記載の果汁飲料の製造方法。   2. The method for producing a fruit juice drink according to claim 1, wherein the beverage material is fruit juice or vegetable juice. 飲料の原料にグルタミン酸及び/又はその塩を5w/v%以下添加することを特徴とする請求項1又は2に記載の飲料の製造方法。   The method for producing a beverage according to claim 1 or 2, wherein glutamic acid and / or a salt thereof is added to the beverage material in an amount of 5 w / v% or less. γ−アミノ酪酸生成能を有する乳酸菌がラクトバチルスブレビス(Lactobacillus brevis)に属する乳酸菌である請求項1乃至3のいずれかに記載の飲料の製造方法。   The method for producing a beverage according to any one of claims 1 to 3, wherein the lactic acid bacterium having γ-aminobutyric acid-producing ability is a lactic acid bacterium belonging to Lactobacillus brevis. 請求項1乃至4のいずれかの項に記載の製造方法により得られる飲料。   A beverage obtained by the production method according to any one of claims 1 to 4.
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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2015533484A (en) * 2012-09-11 2015-11-26 ティラビスコ アーベー Prebiotic thylakoid composition
CN114947027A (en) * 2022-04-27 2022-08-30 镇江恒顺生物工程有限公司 Preparation method of fermented fruit and vegetable juice rich in gamma-aminobutyric acid, acetic acid and lactic acid

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2015533484A (en) * 2012-09-11 2015-11-26 ティラビスコ アーベー Prebiotic thylakoid composition
CN114947027A (en) * 2022-04-27 2022-08-30 镇江恒顺生物工程有限公司 Preparation method of fermented fruit and vegetable juice rich in gamma-aminobutyric acid, acetic acid and lactic acid
CN114947027B (en) * 2022-04-27 2024-05-24 镇江恒顺生物工程有限公司 Preparation method of fermented fruit and vegetable juice rich in gamma-aminobutyric acid, acetic acid and lactic acid

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