JPH088839B2 - Natto manufacturing method - Google Patents
Natto manufacturing methodInfo
- Publication number
- JPH088839B2 JPH088839B2 JP2198333A JP19833390A JPH088839B2 JP H088839 B2 JPH088839 B2 JP H088839B2 JP 2198333 A JP2198333 A JP 2198333A JP 19833390 A JP19833390 A JP 19833390A JP H088839 B2 JPH088839 B2 JP H088839B2
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- Japan
- Prior art keywords
- natto
- extract
- konbu
- soybeans
- soybean
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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Description
【発明の詳細な説明】 〔産業上の利用分野〕 本発明は、納豆菌増殖促進作用を有するとともに、納
豆の品質向上作用を有するこんぶエキスを用いる納豆の
製法に関するものである。TECHNICAL FIELD The present invention relates to a method for producing natto using Konbu extract, which has an action of promoting the growth of natto bacteria and an action of improving the quality of natto.
従来から、納豆は良質のタンパク質を豊富に含有する
とともに、炭水化物,脂質,ミネラル,ビタミン等をバ
ランス良く含んだ栄養価の高い食品であることが知られ
ている。また、最近の研究によって、納豆中に血栓溶解
酵素の存在が認められ、納豆に対する関心が高まってい
る。このように優れた食品である納豆は、つぎのように
して工業的に製造される。すなわち、水に浸漬した大豆
を蒸煮し、これに納豆菌の胞子懸濁液を噴霧して撹拌
し、これを発泡スチロール製の容器に計量する。つい
で、上記容器の開口を、孔が穿設されたポリスチレン製
フィルムで被覆し、約40℃で約20時間発酵させた後、10
℃以下で1〜2日間熟成して製造される。最近では、さ
らに、納豆の旨味を増すため、種々の方法が考え出され
ている。このようなものとして、例えば、こんぶだし汁
を用い、その呈味性成分(グルタミン酸等)で納豆自体
に旨味を付与する方法(特開昭55-58079号公報)が開示
されている。It has been conventionally known that natto is a highly nutritious food containing a good amount of high-quality protein and a good balance of carbohydrates, lipids, minerals, vitamins and the like. In addition, recent studies have confirmed the presence of thrombolytic enzymes in natto, which has increased interest in natto. Natto, which is such an excellent food, is industrially produced as follows. That is, soybeans soaked in water are steamed, a spore suspension of Bacillus natto is sprayed and stirred, and this is weighed in a polystyrene foam container. Then, the opening of the container is covered with a polystyrene film having holes, and after fermenting at about 40 ° C. for about 20 hours, 10
It is produced by aging at 1-2 ° C for 1-2 days. Recently, various methods have been devised to further enhance the taste of natto. As such, for example, a method (Japanese Patent Application Laid-Open No. 55-58079) is disclosed in which konbu-dashi soup is used to impart umami to the natto itself with its tasting component (such as glutamic acid).
しかしながら、上記の製法では、こんぶだし汁に納豆
菌を混入し、これを蒸煮した大豆に直接噴霧することに
より納豆を製造するため、噴霧量が多いと大豆が水分過
剰となり、菌体が大豆に付着し難く発酵が不均一にな
る。したがって、その噴霧量の上限は、蒸煮大豆に対し
て1重量%までに設定されるが、この程度の噴霧量で
は、こんぶだし汁を用いた利点は生じない。すなわち、
上記製法は、こんぶだしの旨味で納豆の味を向上させる
ことを目的としているものであり、使用するこんぶだし
汁も、こんぶだしの旨味を利用し料理用のだし汁を作る
場合と同様、こんぶを単に水で煮ただけの濃度の薄いも
の(屈折糖度計で、Brixが1付近の濃度)である。した
がって、上記の噴霧により、こんぶの旨味を多少は納豆
に付与することはできても、こんぶ自体の旨味以上の大
幅な旨味の向上や、栄養価の向上は実現することができ
ない。However, in the above-mentioned manufacturing method, natto is produced by mixing natto bacterium in the kombushi soup and spraying it directly onto steamed soybeans. It is difficult to do and the fermentation becomes uneven. Therefore, the upper limit of the spray amount is set up to 1% by weight with respect to the steamed soybeans, but with this amount of spray amount, the advantage of using Kombushi soup does not occur. That is,
The above method is intended to improve the taste of natto with the taste of kombu soup, and the kombu soup soup used is simply the same as when making soup stock for cooking using the taste of kombu soup. It has a low concentration just boiled in water (concentration of Brix near 1 on refractometer). Therefore, although the konbu taste can be imparted to the natto to some extent by the above-mentioned spraying, it is not possible to achieve a substantial improvement in the umami taste over that of the konbu itself or an improvement in the nutritional value.
本発明は、このような事情に鑑みなされたもので、納
豆菌の増殖を促進して製造期間の短縮を実現できるとと
もに、風味,栄養価等の品質に著しく優れた納豆の製造
が可能な納豆の製法の提供をその目的とする。The present invention has been made in view of such circumstances, and is capable of promoting the growth of natto bacteria to realize a shortened production period and capable of producing natto which is extremely excellent in quality such as flavor and nutritional value. The purpose is to provide a manufacturing method of.
上記の目的を達成するために、本発明は、大豆を水に
浸漬する工程と、浸漬した大豆を蒸煮する工程と、蒸煮
した大豆に納豆菌を接種する工程と、上記大豆を発酵さ
せる工程と、上記発酵させた大豆を熟成させる工程とを
備え、上記大豆の水浸漬液にこんぶをpH2.0〜6.5の酸性
水溶液中で抽出したこんぶエキスを含有させる納豆の製
法を第1の要旨(第1の発明)とし、水に浸漬した大豆
を蒸煮する工程と、蒸煮した大豆に納豆菌を接種する工
程と、上記大豆を発酵させる工程と、上記発酵させた大
豆を熟成させる工程とを備え、上記納豆菌を、こんぶを
pH2.0〜6.5の酸性水溶液中で抽出し濃縮したこんぶエキ
スとともに上記蒸煮した大豆に加えて接種する納豆の製
法を第2の要旨(第2の発明)とする。In order to achieve the above object, the present invention, a step of immersing soybeans in water, a step of steaming the soybeans soaked, a step of inoculating the steamed soybeans with Natto, and a step of fermenting the soybeans And a step of aging the fermented soybeans, and a method for producing natto in which the soybean soaking solution containing konbu extract obtained by extracting konbu in an acidic aqueous solution having a pH of 2.0 to 6.5 is included. 1)), the step of steaming soybeans soaked in water, the step of inoculating the steamed soybeans with Bacillus natto, the step of fermenting the soybeans, and the step of aging the fermented soybeans, The above natto fungus
A second aspect (second invention) is a method for producing natto, which is inoculated in addition to the steamed soybeans together with the kelp extract extracted and concentrated in an acidic aqueous solution of pH 2.0 to 6.5.
本発明者等は、納豆の製造期間の短縮化および納豆自
体の外観,栄養価の大幅な向上を目的として一連の研究
を重ねた。この研究の過程で、こんぶを上記特定酸性領
域の酸性水溶液中で抽出したこんぶエキスは、納豆菌の
増殖を著しく促進させる作用を有することを突き止め
た。すなわち、この特定の酸性領域で抽出したこんぶエ
キスを、蒸煮大豆に噴霧するのではなく、大豆の水浸漬
液に添加し含有させると、納豆菌の増殖が著しく促進さ
れるようになり、納豆菌により産出されるプロテアーゼ
の活性も飛躍的に高まるようになる。この結果、大豆タ
ンパク質が、アミノ酸等の呈味成分によく分解されるた
め、こんぶエキスの添加にともなうこんぶ風味付加の効
果だけではなく、納豆本来の旨みおよび栄養価が著しく
向上した高品質の納豆を短期間で製造することが可能と
なる。さらに、水分含量が多いこんぶのだし汁ではな
く、こんぶエキスを用いるため、その添加量も多くする
ことができるとともに、多量に噴霧することによる不均
一な発酵も生じなくなり、菌膜が厚くて艶等がよく、粘
りも強い高品質の納豆が短期間で得られるようになるこ
とを見出し、上記知見と併せて本発明に到達した。な
お、本件の第2の発明における濃縮したこんぶエキスと
は、屈折糖度計で測定したBrixが3.0〜20の範囲の濃度
のもののことである。また、特に、上記こんぶエキスと
して、こんぶを特定の酸性領域で抽出し、この抽出液を
活性炭処理あるいは限外濾過処理、またはこれら両方の
処理を行ったものを用いることが、好適である。すなわ
ち、特定の酸性領域で抽出したこんぶエキスに対し、上
記処理を施すことにより、さらに納豆菌増殖因子が多く
抽出されるとともに、こんぶエキスの濃度が一層濃縮さ
れることから、納豆菌の増殖が促進され、また納豆自体
の外観,品質も向上するようになる。そして、上記処理
により、比較的高分子の分画に存在するこんぶの不快味
成分(こんぶ特有の香り,色を帯同している)が除去さ
れ、風味の一層の向上効果が得られるようになる。The present inventors have conducted a series of studies for the purpose of shortening the manufacturing period of natto and significantly improving the appearance and nutritional value of natto itself. In the course of this research, it was found that the Konbu extract obtained by extracting Konbu in the acidic aqueous solution in the above-mentioned specific acidic region has an action of remarkably promoting the growth of Bacillus natto. That is, if the kumbu extract extracted in this specific acidic region is added to the soybean immersion liquid instead of being sprayed on steamed soybeans, the growth of Bacillus natto will be significantly promoted, The activity of the protease produced by is also dramatically increased. As a result, soybean protein is often decomposed into taste components such as amino acids, so that not only the effect of adding the konbu flavor associated with the addition of konbu extract but also the high quality natto with the original taste and nutritive value of natto are significantly improved. Can be manufactured in a short period of time. Furthermore, since Konbu extract is used instead of Konbu soup, which has a high water content, the amount added can be increased, and uneven fermentation due to spraying a large amount does not occur, resulting in a thick pellicle and gloss. It was found that natto of high quality and high tenacity can be obtained in a short period of time, and the present invention has been reached together with the above findings. The concentrated Konbu extract in the second aspect of the present invention has a concentration of Brix in the range of 3.0 to 20 as measured by a refractometer. Further, it is particularly preferable to use, as the above-mentioned Konbu extract, an extract obtained by extracting Konbu in a specific acidic region and subjecting the extract to an activated carbon treatment, an ultrafiltration treatment, or both treatments. That is, the konbu extract extracted in a specific acidic region is subjected to the above-mentioned treatment, and more natto growth factors are extracted, and the concentration of konbu extract is further concentrated. It also promotes the appearance and quality of natto itself. Then, the above-mentioned treatment removes the unpleasant taste component of kelp which is present in the relatively high molecular weight fraction (with the scent and color peculiar to kelp), and the effect of further improving the flavor can be obtained. .
つぎに、本発明を詳しく説明する。 Next, the present invention will be described in detail.
本発明に用いるこんぶとは、褐藻類のなかのこんぶ属
に属するもののことをいい、真こんぶ,利尻こんぶ,羅
臼こんぶ,三石こんぶ,長こんぶ,厚葉こんぶ,かごめ
こんぶ,ほそめこんぶ,とろろこんぶ等のいかなるこん
ぶでもよく、また、その産地,等級も限定されるもので
はない。The konbu used in the present invention refers to those belonging to the genus Konbu among brown algae, such as true konbu, Rishiri konbu, Rausu konbu, Mitsuishi konbu, long konbu, Atsuba konbu, kagome konbu, hosome konbu, and Tororo konbu etc. No matter what kind of kelp it is, its place of origin and grade are not limited.
本発明のこんぶエキスは、こんぶをpH2.0〜6.5の特定
の酸性領域で抽出したものである。この抽出は、例えば
つぎのようにして行われ、本件における第1の発明に用
いられる。すなわち、こんぶをpH2.0〜6.5の酸性水溶液
に浸漬して、抽出温度80〜95℃、抽出時間2〜30分の条
件で抽出を行うことによりこんぶエキス(以下「こんぶ
エキス1」という)が得られる。このこんぶエキス1を
そのまま用いてもよいし、これに活性炭処理または限外
濾過処理の一方または双方の処理を施したもの(以下
「こんぶエキス2」という)を用いてもよい。このよう
に酸性領域にpH調整された水溶液を用いてこんぶを抽出
することにより、こんぶ中の納豆菌増殖因子(例えばミ
ネラル成分)が抽出し易くなると同時に、中性域,アル
カリ性域での抽出ではこんぶ自体が溶け出しそれによっ
て水中に抽出されてしまうアルギン酸等の多糖類や不快
味成分の抽出がなくなり、良好な抽出液が得られる。ま
た、上記抽出液に、さらに活性炭処理,限外濾過処理を
施すことにより、比較的高分子の分画に存在するこんぶ
の不快味成分(こんぶ特有の香り,色を帯同している)
が除去される。その結果、上記酸性抽出のみを行い活性
炭処理,限外濾過処理のなされていない抽出液を用いた
ときに、場合によって生じる不都合(高分子分画成分に
よる納豆自体の色の褐色化,艶のなさ,香りの生臭さ)
をほとんど完全になくすことができるようになる。この
ような酸性抽出液は、そのまま用いてもよいし、中和し
て用いても差し支えない。The kelp extract of the present invention is kelp extracted in a specific acidic region of pH 2.0 to 6.5. This extraction is performed as follows, for example, and is used in the first invention in this case. That is, konbu extract (hereinafter referred to as "konbu extract 1") is obtained by immersing konbu in an acidic aqueous solution of pH 2.0 to 6.5 and performing extraction under conditions of an extraction temperature of 80 to 95 ° C and an extraction time of 2 to 30 minutes. can get. This Konbu extract 1 may be used as it is, or one obtained by subjecting it to one or both of an activated carbon treatment and an ultrafiltration treatment (hereinafter referred to as “Konbu extract 2”) may be used. By extracting Konbu using an aqueous solution whose pH is adjusted to an acidic range in this way, it becomes easier to extract the Bacillus subtilis natto growth factor (for example, mineral components) in Konbu, and at the same time, in the neutral and alkaline ranges. Extraction of polysaccharides such as alginic acid and unpleasant taste components which are dissolved in water and thereby extracted in water is eliminated, and a good extract can be obtained. Further, the above-mentioned extract is further subjected to an activated carbon treatment and an ultrafiltration treatment, whereby the unpleasant taste component of kelp present in a relatively high molecular weight fraction (the scent and color peculiar to kelp are accompanied)
Are removed. As a result, when the above-mentioned acidic extraction alone is used and an extract without activated carbon treatment or ultrafiltration treatment is used, inconvenience may occur in some cases (browning of the color of natto itself due to high molecular fraction components, dullness) , The smell of scent)
Will be almost completely eliminated. Such an acidic extract may be used as it is or may be used after being neutralized.
上記こんぶエキス1の抽出について、より詳しく説明
すると、抽出用水溶液のpH調整は、特に限定されるもの
ではないが、酢酸,クエン酸等の有機酸を単独でもしく
は併せて用いて調整することが行われ、その酸性度は通
常pH2.0〜6.5に設定される。より好ましいのはpH4.5〜
5.0の範囲である。すなわち、pHが2.0を下まわると、抽
出効率が悪くなるとともに納豆菌の生育に悪影響を及ぼ
すこととなり、逆に6.5を上まわると、こんぶから納豆
菌増殖因子の溶出状態が悪化するからである。また、抽
出温度は通常、80〜95℃で行われ、抽出所要時間は2〜
60分、好適には10〜30分に設定される。すなわち、抽出
温度が80℃を下まわると、抽出効率が低下し、逆に、95
℃を上まわるとこんぶの不快味成分の溶出が多くなる。
また、抽出所要時間も2分を下まわると抽出効率が低下
し、60分を上まわると不快味成分の溶出が多くなるから
である。このような抽出は、乾こんぶ(採取して砂おと
しし天日乾燥したもので、通常、水分を14〜17重量%含
んでいる)1重量部(以下「部」と略す)を、10〜30部
の酸性水溶液中に、上記の温度および時間浸漬すること
により行われる。このようにして得られた抽出液におけ
るこんぶエキスの抽出濃度は屈折糖度計で測定すること
にもとづき、通常Brixが0.5〜3.0になっている。The extraction of Konbu extract 1 will be described in more detail. The pH adjustment of the extraction aqueous solution is not particularly limited, but it may be adjusted using organic acids such as acetic acid and citric acid alone or in combination. The acidity is usually set to pH 2.0-6.5. More preferred is pH 4.5-
It is in the range of 5.0. That is, if the pH is lower than 2.0, the extraction efficiency will be poor and the growth of Bacillus natto will be adversely affected, and if the pH is higher than 6.5, the elution state of the Bacillus natto growth factor from kelp will be deteriorated. . The extraction temperature is usually 80 to 95 ° C, and the extraction time is 2 to
It is set to 60 minutes, preferably 10 to 30 minutes. That is, when the extraction temperature falls below 80 ° C, the extraction efficiency decreases, and conversely, 95%.
When it exceeds ℃, the unpleasant taste components of Konbu elute more.
Also, if the extraction required time is less than 2 minutes, the extraction efficiency will be reduced, and if it is more than 60 minutes, the unpleasant taste components will be eluted more. Such extraction is carried out using 1 to 10 parts by weight of dried konbu (collected and dried in the sun and usually containing 14 to 17% by weight of water) (hereinafter abbreviated as "part"). It is carried out by immersing in 30 parts of an acidic aqueous solution at the temperature and for the above time. The extraction concentration of Konbu extract in the thus obtained extract is usually Brix of 0.5 to 3.0 based on the measurement by a refractometer.
上記こんぶエキス2は、上記こんぶエキス1に対し
て、活性炭処理,限外濾過処理の一方もしくは双方を施
したものである。この場合、活性炭処理に用いる活性炭
としては、平均孔径が10〜30Åのものを用いることが好
ましく、より好ましいのは20〜30Åのものである。ま
た、上記活性炭処理は、上記活性炭を添加して、50〜90
℃で20〜40分接触させることが好ましい。限外濾過処理
は、通常、上記活性炭処理を終えた抽出液ないし未処理
抽出液を対象に行われ、分画分子量200000以下の膜を用
いて行われる。これにより高分子分画成分が確実に除去
され、不快味成分のないこんぶエキス2が得られる。The above-mentioned Konbu extract 2 is obtained by subjecting the above-mentioned Konbu extract 1 to one or both of activated carbon treatment and ultrafiltration treatment. In this case, it is preferable to use activated carbon having an average pore size of 10 to 30 Å, more preferably 20 to 30 Å, as the activated carbon used for the activated carbon treatment. The activated carbon treatment is carried out by adding the activated carbon to 50 to 90
It is preferable to contact at 20 ° C. for 20 to 40 minutes. The ultrafiltration treatment is usually performed on the extract or untreated extract that has been treated with the activated carbon, and is performed using a membrane having a molecular weight cutoff of 200,000 or less. As a result, the high molecular weight fraction components are surely removed, and Konbu extract 2 free from unpleasant taste components is obtained.
つぎに、上記こんぶエキス1またはこんぶエキス2を
用いた納豆の製法(本件の第1の発明)を具体的に説明
する。まず、大豆を、こんぶエキスを含有させた水浸漬
液に浸漬する。この場合、こんぶエキスの含有は、通
常、水溶液に対してこんぶエキスを添加混合することに
より行われ、その含有量は、0.1〜30%の範囲内に設定
される。より好ましいのは、2.0〜15%の範囲内であ
る。つぎに、上記浸漬した大豆を蒸煮し、この蒸煮した
大豆に納豆菌を接種する。納豆菌の接種は、通常、蒸煮
大豆1kgに対して、納豆菌の菌数が104〜109個の範囲に
なるように胞子懸濁液を接種することが行われる。より
好ましいのは106〜107個の範囲である。ついで、接種を
終えたものを35〜42℃、好適には40℃の発酵温度で15〜
25時間、好適には18時間発酵させ、その後、0〜15℃、
好適には10℃で24〜48時間冷蔵して熟成させる。これに
より目的とする納豆が得られる。Next, the method for producing natto using the above-mentioned Konbu extract 1 or Konbu extract 2 (first invention of the present case) will be specifically described. First, soybeans are dipped in a water dipping solution containing Konbu extract. In this case, the Konbu extract is usually contained by mixing the Konbu extract with an aqueous solution, and the content thereof is set within the range of 0.1 to 30%. More preferably, it is within the range of 2.0 to 15%. Next, the soaked soybeans are steamed, and the steamed soybeans are inoculated with Bacillus natto. Inoculation of Bacillus natto is usually carried out by inoculating 1 kg of steamed soybeans with a spore suspension so that the number of Bacillus natto is in the range of 10 4 to 10 9 . More preferred is the range of 10 6 to 10 7 . Then, after inoculation, the fermentation temperature of 35 to 42 ℃, preferably 40 ℃ 15 ~
Fermented for 25 hours, preferably 18 hours, then 0-15 ° C,
It is preferably refrigerated at 10 ° C. for 24 to 48 hours for aging. This makes it possible to obtain the desired natto.
なお、上記の製法では、予めこんぶエキスを添加含有
させた水浸漬液に大豆を浸漬しているが、まず大豆を水
に浸漬し、その後これにこんぶエキスを添加含有させる
ようにしてもよい。In the above manufacturing method, soybeans are soaked in a water dipping solution containing Konbu extract in advance, but soybeans may be first soaked in water and then Konbu extract may be added and contained therein.
つぎに、濃縮したこんぶエキスを用いる本件の第2の
発明を具体的に説明する。ここで、上記濃縮したこんぶ
エキスは、Brix3.0〜20のものが好ましい。Brixが20を
超えると、納豆菌に対する増殖効果は有するが、粘性の
増加と結晶化によって噴霧に適さない状態になるからで
ある。上記濃縮したこんぶエキスは、上記特定の酸性領
域で前記こんぶエキスを抽出したこんぶエキスを、例え
ば減圧濃縮,膜濃縮等の方法によって濃縮することによ
り得ることができるが、特に、上記こんぶエキス1また
は2を濃縮したものが好ましい。すなわち、本件の第2
の発明では、まず、大豆1部に対して水3〜4部を加え
て大豆を浸漬し、これを蒸煮する。つぎに、この蒸煮し
た大豆に、上記濃縮したこんぶエキスを混入した納豆菌
の胞子懸濁液を上記製法と同様に接種する。この場合、
108〜109菌数/mlの納豆菌の胞子懸濁液を、上記濃縮し
たこんぶエキスで106〜107菌数/mlになるように希釈し
たものが用いられる。そして、接種を終えたものを、上
記の温度および時間で発酵,熟成させることにより目的
とする納豆が得られる。Next, the second invention of the present case using the concentrated Konbu extract will be specifically described. Here, the concentrated Konbu extract is preferably Brix 3.0 to 20. When Brix exceeds 20, it has a growth effect on Bacillus natto, but the state becomes unsuitable for spraying due to increase in viscosity and crystallization. The concentrated kelp extract can be obtained by concentrating the kelp extract obtained by extracting the kelp extract in the specific acidic region by, for example, vacuum concentration, membrane concentration, or the like. A concentrate of 2 is preferable. That is, the second
In the invention, first, 3 to 4 parts of water is added to 1 part of soybean to immerse the soybean, and this is steamed. Next, this steamed soybean is inoculated with a spore suspension of Bacillus natto mixed with the concentrated Konbu extract as in the above-mentioned production method. in this case,
A spore suspension of 10 8 to 10 9 bacteria / ml of Bacillus natto is diluted with the concentrated Konbu extract to 10 6 to 10 7 bacteria / ml. Then, the target natto is obtained by fermenting and aging the inoculated product at the above temperature and time.
以上のように、本発明の納豆の製法は、こんぶを特定
の酸性領域で抽出したこんぶエキスを用いるものであ
る。すなわち、本発明の第1の方法は、大豆の水浸漬液
に上記こんぶエキスを添加し含有させるため、こんぶエ
キスの添加量を多くすることができ、かつ納豆菌の増殖
が著しく促進される。その結果、菌膜が厚くて艶等がよ
く、粘りも強い高品質の納豆が短時間で得られるように
なる。また、本発明の第2の方法は、納豆菌を、濃縮し
た上記こんぶエキスとともに、蒸煮した大豆に加えて接
種するため、濃縮したこんぶエキスによって納豆菌の増
殖を促進するプロテアーゼの活性が大幅に高められる。
その結果、大豆のたんぱく質がアミノ酸等の呈味性成分
によく分解されるため、得られる納豆は、こんぶエキス
自体の旨味だけでは到達することができない、高度な旨
味を有する高栄養価食品になる。また、このような濃縮
こんぶエキスを用いると、納豆の製造期間の短縮化も実
現できるようになる。特に、上記こんぶエキスとして、
こんぶを特定の酸性域で抽出し、さらに活性炭処理,限
外濾過処理すると、納豆菌増殖因子がさらに濃縮される
とともに、比較的高分子の分画に存在するこんぶの不快
味成分(こんぶ特有の香り,色を帯同している)が除去
され、納豆の製造期間の短縮や品質の向上がなされると
ともに、風味の向上効果が得られるようになる。As described above, the method for producing natto of the present invention uses a kelp extract obtained by extracting kelp in a specific acidic region. That is, according to the first method of the present invention, since the above-mentioned Konbu extract is added to the soybean soaking solution for inclusion, the amount of Konbu extract can be increased and the growth of Bacillus natto is significantly promoted. As a result, high quality natto with a thick pellicle, good gloss and strong stickiness can be obtained in a short time. In the second method of the present invention, the Bacillus natto is inoculated together with the concentrated Konbu extract into steamed soybeans, so that the concentrated Konbu extract significantly increases the activity of the protease that promotes the growth of Bacillus natto. To be enhanced.
As a result, soybean protein is often decomposed into tasting components such as amino acids, so that the obtained natto becomes a highly nutritious food with a high umami that cannot be reached only by the umami of konbu extract itself. . Further, by using such a concentrated Konbu extract, it becomes possible to shorten the production period of natto. In particular, as the above Konbu extract,
When kelp is extracted in a specific acidic region and further treated with activated carbon and ultrafiltration, the natto growth factor is further concentrated and the unpleasant taste component of kelp present in a relatively high molecular fraction (specific to konbu) Aroma and color are removed), the production period of natto can be shortened and the quality of natto can be improved, and the effect of improving flavor can be obtained.
つぎに、実施例について比較例と併せて説明する。 Next, examples will be described together with comparative examples.
〔実施例1〕 水2lを酢酸でpH4.0に調整し、この水中に真こんぶ150
gを添加し、全体の温度を95℃に昇温させ、その温度で1
0分間抽出を行った。このこんぶ抽出液の抽出濃度は屈
折糖度計でBrix2.8であった(以下このこんぶ抽出液を
「こんぶエキス1」という)。この得られたこんぶエキ
ス1を1%添加したスピジエン培地(SM培地)で納豆菌
を37℃で振盪培養し、12時間後に波長660nmで吸光測定
した。吸光度が高くなることは、納豆菌が増殖している
(菌の増殖によって濁りを生じる)ことを示している。[Example 1] 2 l of water was adjusted to pH 4.0 with acetic acid, and 150 ml of water was added to this water.
Add g and raise the total temperature to 95 ° C, at which temperature 1
Extraction was performed for 0 minutes. The extraction concentration of this Konbu extract was Brix 2.8 with a refractometer (hereinafter this Konbu extract is referred to as "Konbu extract 1"). Bacillus subtilis natto was cultured in a spidiene medium (SM medium) containing 1% of the obtained Konbu extract 1 at 37 ° C. with shaking, and 12 hours later, the absorbance was measured at a wavelength of 660 nm. Higher absorbance indicates that the Bacillus natto is growing (turbidity is caused by the growth of the bacterium).
〔実施例2〜6〕 上記こんぶエキス1を濾布を用いて荒濾過した後、そ
の濾過液に、活性炭(武田薬品工業社製,白鷺ニューゴ
ールド)を上記こんぶエキス1に対して0.3%加えた。
ついで、これを60℃に加熱し20分間撹拌しながら接触処
理を行った。この反応後、こんぶエキス1の一部を後記
の第1表に示す各分画分子量3000,6000,10000,50000,20
0000の限外濾過処理を行った。そして、これによって得
られた各液を1%添加したSM培地で、納豆菌を37℃で培
養し、12時間後に波長660nmで吸光測定した。[Examples 2 to 6] The above-mentioned Konbu extract 1 was roughly filtered using a filter cloth, and then activated carbon (Shirasagi New Gold, manufactured by Takeda Pharmaceutical Co., Ltd.) was added to the filtered solution in an amount of 0.3% relative to the above-mentioned Konbu extract 1. It was
Then, this was heated to 60 ° C. and subjected to contact treatment while stirring for 20 minutes. After this reaction, a part of Konbu extract 1 is shown in Table 1 below, and the molecular weight of each fraction is 3000,6000,10000,50000,20.
An ultrafiltration treatment of 0000 was performed. Then, Bacillus subtilis natto was cultivated at 37 ° C. in the SM medium containing 1% of each liquid thus obtained, and 12 hours later, the absorbance was measured at a wavelength of 660 nm.
〔比較例1〕 こんぶエキスを添加していないSM培地で、納豆菌を37
℃で培養し、12時間後に波長660nmで吸光測定した。[Comparative Example 1] 37% of Bacillus natto was added to SM medium containing no kelp extract.
The cells were cultured at ℃, and after 12 hours, the absorbance was measured at a wavelength of 660 nm.
〔比較例2〕 水1に、真こんぶ12gを添加し、全体の温度を80℃
に昇温させ、その温度で10分間抽出を行った。このこん
ぶだし汁の抽出濃度は屈折糖度計でBrix0.6であった。
この得られたこんぶだし汁を1%添加したSM培地で、納
豆菌を37℃で培養し、12時間後に波長660nmで吸光測定
した。[Comparative Example 2] To water 1, 12 g of true kelp was added, and the whole temperature was set to 80 ° C.
The temperature was raised to 10, and extraction was performed at that temperature for 10 minutes. The extraction concentration of this kombushi soup was Brix 0.6 with a refractometer.
Bacillus subtilis natto was cultivated at 37 ° C. in an SM medium containing 1% of the obtained Konbu-dashi soup, and after 12 hours, absorption was measured at a wavelength of 660 nm.
上記実施例1ないし6および比較例1,2における吸光
度測定の結果を、下記の第1表に示した。The results of the absorbance measurement in Examples 1 to 6 and Comparative Examples 1 and 2 are shown in Table 1 below.
上記第1表の結果から、こんぶエキスを用いた実施例
1ないし6の納豆菌の吸光度は、抽出液を添加しなかっ
た比較例1の納豆菌の吸光度の3倍以上の値となってお
り、こんぶだし汁を用いた比較例2の納豆菌の吸光度の
約2.4倍となっている。このことより、こんぶエキスが
納豆菌の増殖を促進することは明らかである。また、分
画分子量3000の実施例2と200000の実施例6とに、吸光
度の大きな差はなく、かつ分画分子量3000の実施例2は
比較例1の吸光度の3倍以上の値を示すことから、上記
の全ての分画(実施例2〜6)に含まれる分画分子量30
00以下に納豆菌の増殖を促進する成分が含有されている
ことがわかる。さらに、こんぶだし汁には納豆菌の増殖
を促進する成分がほとんど含有されていないことがわか
る。 From the results shown in Table 1 above, the absorbance of Bacillus natto of Examples 1 to 6 using Konbu extract is 3 times or more the absorbance of Bacillus natto of Comparative Example 1 in which the extract is not added. The absorbance is about 2.4 times that of the Bacillus subtilis natto of Comparative Example 2 using the kombushi soup. From this, it is clear that Konbu extract promotes the growth of Bacillus natto. Further, there is no large difference in absorbance between Example 2 having a molecular weight cutoff of 3000 and Example 6 having a molecular weight cutoff of 200,000, and Example 2 having a molecular weight cutoff of 3000 exhibits a value three times or more that of Comparative Example 1. Therefore, the molecular weight cutoff of 30 contained in all the above-mentioned fractions (Examples 2 to 6)
It can be seen that below 00 contains components that promote the growth of Bacillus natto. Furthermore, it can be seen that Konbu-dashi soup contains almost no components that promote the growth of Bacillus natto.
〔実施例7〕 水3lに上記実施例1のこんぶエキス1を60ml含有させ
た。これに大豆1kgを10℃で18時間浸漬し、蒸煮した
後、蒸煮大豆100g当たり106菌数/mlの納豆菌の胞子懸濁
液を噴霧し、常法(40℃で20時間発酵させたのち、10℃
で48時間熟成させる)に従って納豆を製造した。[Example 7] 60 ml of the Konbu extract 1 of Example 1 was added to 3 l of water. After soaking 1 kg of soybean in this for 18 hours at 10 ° C and steaming, a spore suspension of 10 6 bacteria / ml natto was sprayed per 100 g of steamed soybean and sprayed in a conventional manner (fermented at 40 ° C for 20 hours. After that, 10 ℃
The natto was manufactured according to the method of aging for 48 hours.
〔実施例8〕 上記実施例7のこんぶエキス1に代えて上記実施例2
の分画分子量3000以下のこんぶエキスを60ml含有させ
た。それ以外は上記実施例7と同様にして納豆を製造し
た。[Example 8] The above-mentioned Example 2 was used instead of the Konbu extract 1 of Example 7 above.
60 ml of Kumbu extract having a molecular weight cut off of 3000 or less was contained. Natto was produced in the same manner as in Example 7 except above.
〔実施例9〕 上記実施例7のこんぶエキス1に代えて上記実施例3
の分画分子量6000以下のこんぶエキスを60ml含有させ
た。それ以外は上記実施例7と同様にして納豆を製造し
た。[Example 9] The above-mentioned Example 3 was used instead of the Konbu extract 1 of Example 7.
60 ml of Kumbu extract having a molecular weight cut off of 6000 or less was contained. Natto was produced in the same manner as in Example 7 except above.
〔実施例10〕 上記実施例7のこんぶエキス1に代えて上記実施例4
の分画分子量10000以下のこんぶエキスを60ml含有させ
た。それ以外は上記実施例7と同様にして納豆を製造し
た。[Example 10] The above-mentioned Example 4 was used instead of the Konbu extract 1 of Example 7 above.
60 ml of Kumbu extract having a molecular weight cut-off of 10,000 or less was contained. Natto was produced in the same manner as in Example 7 except above.
〔実施例11〕 上記実施例7のこんぶエキス1に代えて上記実施例5
の分画分子量50000以下のこんぶエキスを60ml含有させ
た。それ以外は上記実施例7と同様にして納豆を製造し
た。[Example 11] The above-mentioned Example 5 was used in place of the Konbu extract 1 of Example 7 above.
60 ml of Kumbu extract having a molecular weight cut off of 50,000 or less was contained. Natto was produced in the same manner as in Example 7 except above.
〔実施例12〕 上記実施例7のこんぶエキス1に代えて上記実施例6
の分画分子量200000以下のこんぶエキスを60ml含有させ
た。それ以外は上記実施例7と同様にして納豆を製造し
た。[Example 12] The above-mentioned Example 6 was used in place of the Konbu extract 1 of Example 7 above.
60 ml of Kumbu extract having a molecular weight cut off of 200,000 or less was contained. Natto was produced in the same manner as in Example 7 except above.
〔比較例3〕 水3lに大豆1kgを10℃で18時間浸漬し、その大豆を蒸
煮した後、108菌数/mlの納豆菌の胞子懸濁液を滅菌水で
100倍に希釈し、これを上記蒸煮大豆100g当たり106個の
納豆菌胞子を噴霧し、常法に従って納豆を製造した。[Comparative Example 3] 1 kg of soybean was immersed in 3 liters of water at 10 ° C for 18 hours, and the soybean was steamed. Then, a spore suspension of 10 8 bacteria / ml of Bacillus natto was sterilized with water.
It was diluted 100-fold, and 10 6 natto fungus spores were sprayed per 100 g of the steamed soybeans, and natto was manufactured according to a conventional method.
上記実施例7ないし12および比較例3から得られた納
豆を、発酵終了後3日目に、専門パネラー20名により、
下記に示す品質基準にもとづき5段階評価で官能検査を
実施し、その平均値を後記の第2表に示した。The natto obtained from each of Examples 7 to 12 and Comparative Example 3 was treated by 20 professional panelists on the 3rd day after completion of fermentation.
A sensory test was carried out in a 5-level evaluation based on the quality standards shown below, and the average value is shown in Table 2 below.
〈外観〉 5…乳白色の菌膜で均一に被われていて光沢のあるも
の。<Appearance> 5 ... A glossy white uniform coating of milky white pellicle.
4…乳白色の菌膜がやや疎らで光沢のあるもの。4 ... Milky white pellicle is slightly sparse and glossy.
3…薄茶色の菌膜で均一に被われていて光沢のあるも
の。3 ... Light brown pellicle evenly covered and glossy.
2…薄茶色の菌膜で均一に被われていて光沢のないも
の。2. A light brown pellicle that is evenly coated and has no gloss.
1…茶色の菌膜が疎らで光沢のないもの。1 ... Brown pellicle is sparse and has no gloss.
〈香り〉 5…アンモニア臭がなく、納豆らしい芳香の豊かなも
の。<Aroma> 5 ... Aroma rich in natto with no ammonia odor.
4…アンモニア臭がなく、納豆らしい芳香のあるもの。4 ... It has no ammonia odor and has a natto-like aroma.
3…アンモニア臭がややあるが、納豆らしい芳香のある
もの。3 ... A little odor of ammonia, but with an aroma similar to natto.
2…アンモニア臭が出て、納豆らしい芳香の少ないも
の。2 ... An odor of ammonia, with little aroma like natto.
1…アンモニア臭が強く出て、納豆らしい芳香がないも
の。1 ... Ammonia smell is strong, and there is no natto-like aroma.
〈糸引き〉 5…粘質物が非常に多く、弾力の強いもの。<Thin pulling> 5 ... A substance with a large amount of mucilage and high elasticity.
4…粘質物が多く、弾力の強いもの。4-Much sticky material and strong elasticity.
3…粘質物がやや少なく、弾力のやや弱いもの。3 ... Slightly less viscous material and slightly less elastic.
2…粘質物が少なく、弾力のやや弱いもの。2 ... Slightly elastic with little sticky material.
1…粘質物が少なく、弾力の弱いもの。1 ... A little sticky substance and weak elasticity.
〈旨味〉 5…非常に強い。<Umami> 5 ... Very strong.
4…強い。4 ... strong.
3…普通。3 ... Normal.
2…弱い。2 ... weak.
1…非常に弱い。1 ... very weak.
〈硬さ〉 5…硬い。<Hardness> 5 ... Hard.
4…少し硬い。4 ... A little hard.
3…普通。3 ... Normal.
2…少し軟らかい。2 ... a little soft.
1…軟らかい。1 ... It's soft.
〈総合評価〉 5…良い。<Comprehensive evaluation> 5 ... Good.
4…やや良い。4… Somewhat good.
3…普通。3 ... Normal.
2…やや悪い。2 ... Slightly bad.
1…悪い。1 ... bad.
上記第2表の結果から、こんぶエキスを用いた実施例
7ないし12の納豆は、比較例3の納豆に比べ、全ての点
で好ましいと評価された。特に、菌膜の厚さ等の外観,
糸引きの強さおよび旨味等の点で優れていると評価され
た。 From the results shown in Table 2 above, it was evaluated that the natto of Examples 7 to 12 using Konbu extract was preferable in all respects to the natto of Comparative Example 3. In particular, the appearance of pellicle thickness,
It was evaluated to be excellent in terms of stringiness and umami.
〔実施例13〕 水3lに大豆1kgを10℃で18時間浸漬し、その大豆を蒸
煮した後、108菌数/mlの納豆菌の胞子懸濁液を、前記実
施例1で得られたこんぶエキス1を減圧濃縮してBrix8.
0に濃縮したもので100倍に希釈し、これを蒸煮大豆100g
当たり106菌数/ml噴霧し、常法に従って納豆を製造し
た。Example 13 1 kg of soybean was soaked in 3 liters of water at 10 ° C. for 18 hours, and the soybean was steamed, and then a spore suspension of 10 8 bacteria / ml of Bacillus natto was obtained in Example 1 above. Concentrate Konbu Extract 1 under reduced pressure and Brix 8.
Dilute 100 times with 0 concentrated and steam 100% soybeans
The natto was manufactured according to a conventional method by spraying 10 6 bacteria / ml.
〔比較例4〕 水3lに大豆1kgを10℃で18時間浸漬し、その大豆を蒸
煮した後、108菌数/mlの納豆菌の胞子懸濁液を上記比較
例2で得られたこんぶだし汁で100倍に希釈し、これを
蒸煮大豆100g当たり106菌数/ml噴霧し、常法に従って納
豆を製造した。[Comparative Example 4] 1 kg of soybean was immersed in 3 liters of water at 10 ° C for 18 hours, and the soybean was cooked, and then a spore suspension of 10 8 bacteria / ml of Natto was obtained from Comparative Example 2 above. It was diluted 100 times with soup stock and sprayed with 10 6 bacteria / ml per 100 g of steamed soybean to produce natto according to a conventional method.
上記実施例13および比較例3,4から得られた納豆を、
発酵終了後3日目に、専門パネラー20名により、前記に
示した品質基準にもとづき5段階評価で官能検査を実施
した。その結果を下記の第3表に示した。Natto obtained from Example 13 and Comparative Examples 3 and 4 above,
On the third day after completion of fermentation, a sensory test was conducted by 20 professional panelists on a 5-point scale based on the above-mentioned quality standards. The results are shown in Table 3 below.
上記第3表の結果から、こんぶエキス1を用いた実施
例13の納豆は、比較例3,4の納豆に比べ、全ての点で好
ましいと評価された。特に、菌膜の厚さ等の外観,糸引
きの強さおよび旨味等の点で優れていると評価された。 From the results of Table 3 above, it was evaluated that the natto of Example 13 using Konbu Extract 1 was preferable in all respects as compared with the natto of Comparative Examples 3 and 4. In particular, it was evaluated as excellent in appearance such as thickness of pellicle, strength of stringing and umami.
Claims (3)
を蒸煮する工程と、蒸煮した大豆に納豆菌を接種する工
程と、上記大豆を発酵させる工程と、上記発酵させた大
豆を熟成させる工程とを備え、上記大豆の水浸漬液にこ
んぶをpH2.0〜6.5の酸性水溶液中で抽出したこんぶエキ
スを含有させることを特徴とする納豆の製法。1. A step of soaking soybeans in water, a step of steaming the soaked soybeans, a step of inoculating the steamed soybeans with Bacillus natto, a step of fermenting the soybeans, and an aging of the fermented soybeans. The method for producing natto, which comprises the step of allowing the soybean soaking solution to contain Konbu extract obtained by extracting Konbu in an acidic aqueous solution having a pH of 2.0 to 6.5.
した大豆に納豆菌を接種する工程と、上記大豆を発酵さ
せる工程と、上記発酵させた大豆を熟成させる工程とを
備え、上記納豆菌を、こんぶをpH2.0〜6.5の酸性水溶液
中で抽出し濃縮したこんぶエキスとともに上記蒸煮した
大豆に加えて接種することを特徴とする納豆の製法。2. A step of steaming soybean soaked in water, a step of inoculating steamed soybean with Bacillus subtilis natto, a step of fermenting said soybean, and a step of aging said fermented soybean, A method for producing natto, which comprises inoculating natto bacterium with the above-mentioned steamed soybean together with konbu extract concentrated and extracted in an acidic aqueous solution of pH 2.0 to 6.5.
の酸性水溶液中で抽出し、この抽出液に活性炭処理また
は限外濾過処理の少なくとも一方の処理を施して得られ
たものである請求項(1)または(2)記載の納豆の製
法。3. The above-mentioned kelp extract has a kelp content of pH 2.0 to 6.5.
The method for producing natto according to claim 1 or 2, wherein the extract is obtained by subjecting the extract to an activated carbon treatment and / or an ultrafiltration treatment.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2198333A JPH088839B2 (en) | 1990-07-25 | 1990-07-25 | Natto manufacturing method |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2198333A JPH088839B2 (en) | 1990-07-25 | 1990-07-25 | Natto manufacturing method |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH0484871A JPH0484871A (en) | 1992-03-18 |
| JPH088839B2 true JPH088839B2 (en) | 1996-01-31 |
Family
ID=16389370
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2198333A Expired - Fee Related JPH088839B2 (en) | 1990-07-25 | 1990-07-25 | Natto manufacturing method |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH088839B2 (en) |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5241253A (en) * | 1975-09-22 | 1977-03-30 | Asahi Shiyokuhin Kk | Method of making fermented soybean |
| JPS533552A (en) * | 1976-06-30 | 1978-01-13 | Taishi Shiyokuhin Kougiyou Kk | Method of making fermented soybean with tangle therein |
| JPS5449369A (en) * | 1977-09-28 | 1979-04-18 | Kikkoman Shoyu Co Ltd | Production of seasoning or drink |
| JPS5530826A (en) * | 1978-08-24 | 1980-03-04 | Nec Kyushu Ltd | Method of manufacturing semiconductor device |
| JPS5558079A (en) * | 1978-10-21 | 1980-04-30 | Toshimitsu Yanagisawa | Preparation of fermented soybean seasoned with tangle |
| JPS5561777A (en) * | 1978-10-30 | 1980-05-09 | Toshimitsu Yanagisawa | "natto" (fermented soybean) seasoned with stock made from tangle |
-
1990
- 1990-07-25 JP JP2198333A patent/JPH088839B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0484871A (en) | 1992-03-18 |
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