JPS59118078A - Preparation of seed malt - Google Patents

Preparation of seed malt

Info

Publication number
JPS59118078A
JPS59118078A JP22637082A JP22637082A JPS59118078A JP S59118078 A JPS59118078 A JP S59118078A JP 22637082 A JP22637082 A JP 22637082A JP 22637082 A JP22637082 A JP 22637082A JP S59118078 A JPS59118078 A JP S59118078A
Authority
JP
Japan
Prior art keywords
koji
culture medium
cultured
dried
rice
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.)
Pending
Application number
JP22637082A
Other languages
Japanese (ja)
Inventor
Makoto Sato
信 佐藤
Kinichi Nakamura
中村 欽一
Toshiteru Oba
大場 俊輝
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
TAX ADM AGENCY
Original Assignee
TAX ADM AGENCY
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by TAX ADM AGENCY filed Critical TAX ADM AGENCY
Priority to JP22637082A priority Critical patent/JPS59118078A/en
Publication of JPS59118078A publication Critical patent/JPS59118078A/en
Pending legal-status Critical Current

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  • Micro-Organisms Or Cultivation Processes Thereof (AREA)

Abstract

PURPOSE:To prepare a microbiologically pure seed malt, by culturing a microorganism belonging to Rhizopus genus in a culture medium, and drying the microbial cells obtained by the culture. CONSTITUTION:Microorganism belonging to Rhizopus genus is cultured in an agar culture medium or a liquid culture medium, and the microbial cells obtained by the cultivation are dried by heating or freezing to obtain the objective seed malt.

Description

【発明の詳細な説明】 本発明は、リゾープス属菌の種こうじの製造法に関する
ものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for producing seed koji of Rhizopus bacteria.

清酒醸造に用いられる米こうじは、散こうじ(ばらこう
じ)とも呼ばれ、蒸煮した白米にアスペルギルス・オリ
ーゼを繁殖させているのに対I−1中国や東南アジアの
酒類醸造に用いられる麦こうじ、酒やく、ラギーやチャ
ンなどは、もちこうじとも呼ばれ、無蒸煮の穀粉固形物
にリゾープス属菌やムコール属菌などを自然に繁殖させ
たものである。
The rice koji used in sake brewing is also called bara koji, and is made by breeding Aspergillus oryzae on steamed white rice. Anther, ragi, and chang, also called mochi-koji, are made by naturally breeding bacteria of the genus Rhizopus and Mucor in solid flour that has not been steamed.

もちこうじの造シ方は、無蒸煮の穀類を粗く砕き、水あ
るいは草根木皮の浸出液を加えれんが状、団子状、せん
べい状に成形1−1自然てカビや酵母を繁殖させる方法
である。
Mochi koji is made by coarsely crushing uncooked grains, adding water or exudate of bark from roots, and forming them into bricks, dumplings, or rice crackers (1-1), which allows mold and yeast to propagate naturally.

清酒醸造用米こうじの製きく方法と1〜ては、蒸し米に
種こうじを散布1−30〜グθ℃で約3日間培養するこ
とが通常行われている。この場合、散布する種こうじは
アスペルギルス・オリーゼヲ蒸煮1〜だ玄米に純粋培養
し、培養後の玄米を加熱乾燥したものであり、もやしと
も呼ばれ、専業の製造者によって製造販売されている。
The method for producing rice koji for sake brewing is usually carried out by spraying seed koji on steamed rice and culturing at 1-30°C for about 3 days. In this case, the seed koji to be sprayed is made by culturing Aspergillus oryzae in pure steamed brown rice and heating and drying the cultured brown rice, which is also called bean sprouts and is manufactured and sold by a specialized manufacturer.

しかしながら、リゾープス属菌については、種こうじに
相当するものは皆無である。この理由としては、リゾー
プス属菌は無蒸煮の穀類にはよく繁殖するが蒸煮した穀
類には繁殖が悪いため、無蒸煮の穀類にリゾープス属菌
を培養1−た場合、菌学的に純粋な種こうじが製造でき
ないこと、さらに胞子の着生が悪く菌体を回収すること
が困難であることなどがあげられる。
However, for Rhizopus genus bacteria, there is no equivalent to the seed koji. The reason for this is that Rhizopus bacteria breed well in unsteamed grains but not in steamed grains, so if Rhizopus bacteria are cultured in unsteamed grains, it will be mycologically pure. The problems include the inability to produce seed koji, and the difficulty in collecting bacterial cells due to poor spore attachment.

本発明者らは、リゾープス属菌の種こうじを製造すべく
研究を重ねた結果、リゾープス属菌を寒天培養基に培養
し、培養後菌体のみを回収し、加熱乾燥ない1〜は凍結
乾燥することにより、菌学的に純粋な種こうじの製造法
を完成するに至った。
As a result of repeated research to produce seed koji of Rhizopus bacteria, the present inventors have found that Rhizopus bacteria are cultured on an agar culture medium, only the bacterial cells are collected after culture, and 1 to 1 are freeze-dried without heat drying. This led to the completion of a method for producing mycologically pure seed koji.

本発明の種こうじ製造法の特徴は、リゾープス属菌を純
粋培養できること、純粋培養l−だ菌体を容易に回収可
能であること、回収菌体量が天然培地に比較17て多い
こと、さらに、乾燥することによシ、保存が可能である
ことである0 本発明で、製きくした種こうじを生白米に混合し製きく
1−だ結果、実施例で述べるように、対照の未乾燥の菌
体を用いて製きくしたこうじに比較して、はとんどそん
色のない良好な結果を得た。
The characteristics of the seed koji production method of the present invention are that Rhizopus bacteria can be cultured in a pure manner, that pure cultured L. bacteria cells can be easily recovered, and that the amount of recovered bacterial cells is 17 times higher than that of natural culture medium. According to the present invention, the dried seed koji is mixed with raw white rice to produce it. Compared to the koji produced using the microorganisms of this method, good results were obtained with almost no dull color.

次に、本発明の実施例を示す。Next, examples of the present invention will be shown.

実施例/ グルコースフタ、ペフトン/ r、9母:r−キスOj
2、リン酸第1カリウム0タグ、硫酸マグネシウム0.
.2f1寒天3?、水/θθ罰よりなる合成培地をオー
トクレーブで770℃、70分間加圧殺菌後、無菌箱中
で直径9 cmの殺菌したシャーレに流し込み、培地が
固まった後 Rh1zopusjavanicus工F
O3ググ2を斜面培養から一白金耳接種し、30℃の恒
温器中でy〜4日間培養1〜た。培養後菌体のみを培地
からはぎとシ回収1−150℃、60℃、70℃並びに
705℃の乾燥器中で約5時間加熱乾燥した。乾燥前後
の菌体重量を表/に示した。
Example/Glucose Futa, Pefton/r, 9 mother: r-kiss Oj
2. Potassium monophosphate 0 tag, Magnesium sulfate 0.
.. 2f1 agar 3? A synthetic medium consisting of water/θθ was sterilized under pressure in an autoclave at 770°C for 70 minutes, then poured into a sterilized petri dish with a diameter of 9 cm in a sterile box. After the medium solidified, Rh1zopus javanicus F.
One platinum loop of O3Gugu2 was inoculated from the slant culture, and cultured for 4 days in a 30°C incubator. After culturing, only the bacterial cells were recovered from the medium by heating and drying in a dryer at 1-150°C, 60°C, 70°C, and 705°C for about 5 hours. Table 1 shows the bacterial weight before and after drying.

次に、乾燥した菌体を種こうじとして使用l〜、こうじ
を製造することを行った。乾燥菌体をバイブレンダ−で
破砕後、生米に吸水させる水に懸濁1−だ。使用I−た
生白米の精米歩合は75%、吸水歩合は35%である。
Next, the dried bacterial cells were used as seed koji to produce koji. After crushing the dried bacterial cells with a vibratory blender, they are suspended in water to be absorbed by raw rice. The rice polishing ratio of the raw white rice used was 75%, and the water absorption ratio was 35%.

生米が均一に吸水後、3θ℃の恒温室にて、2〜3日間
培養1−た。
After the raw rice uniformly absorbed water, it was cultured for 2 to 3 days in a thermostatic chamber at 3θ°C.

なお、生米/却当シ直径9 Cmのシャーレに培養し、
乾燥した菌体をシャーレ/枚分使用した。
In addition, raw rice/discarded rice was cultured in a petri dish with a diameter of 9 cm,
A petri dish/petri dish of dried bacterial cells was used.

こうじの酸度並びに酵素力価を表2に示l〜だ。The acidity and enzyme titer of Koji are shown in Table 2.

なお、分析は国税庁所定分析法によった。The analysis was based on the analysis method prescribed by the National Tax Agency.

実施例β 実施例/と同様に、シャーレに培養した菌体を培地から
回収l−1凍結乾燥を行い、乾燥菌体を種こうじとして
使用1〜製きくした。
Example β In the same manner as in Example 1, the bacterial cells cultured in a Petri dish were recovered from the medium and freeze-dried.

表3に、、こうじの酸度並びに酵素力価を示した。Table 3 shows the acidity and enzyme titer of Koji.

表3 酵素力価(U/2こうじ)並びに酸度実施例3 実施例/の合成培地から寒天を除いた液体培地にRh1
zopus javanicus工FOj<l&jを斜
面培養から一白金耳接種し、30℃の恒温器中でり日間
振とり培養した。培養後菌体を培養液から回収し、6θ
℃の乾燥器中で約5時間加熱乾燥j−た。乾燥後の菌体
重量は0.b?//θθmg培養液であった。
Table 3 Enzyme titer (U/2 koji) and acidity Example 3 Rh1 was added to the liquid medium obtained by removing agar from the synthetic medium of Example/.
One platinum loop of Zopus javanicus was inoculated from a slant culture, and cultured with shaking in a thermostat at 30° C. for 1 day. After culturing, the bacterial cells are collected from the culture solution and 6θ
It was heated and dried in a dryer at ℃ for about 5 hours. The bacterial weight after drying is 0. b? //θθmg culture solution.

白米/θ02当り乾燥菌体0. / j ?使用12、
実施例/と同様にこうじを製造(−た。
Dry bacterial cells per white rice/θ02 0. /j? Use 12,
Koji was produced in the same manner as in Example.

表グに、こうじの酵素力価並びに酸度を示した。The enzyme titer and acidity of Koji are shown in the table.

表グ 酵素力価(U/2こうじ)並びに酸度特許出願人
  国税庁長官 福 1)幸 弘I
Table Enzyme titer (U/2 koji) and acidity Patent applicant Fuku, Commissioner of the National Tax Agency 1) Yuki HiroI

Claims (1)

【特許請求の範囲】[Claims] リゾープス属菌を寒天培養基ないしは液体培養基に培養
1〜、培養後菌体を加熱乾燥ない1〜は凍結乾燥するこ
とを特徴とする種こうじの製造法
A method for producing seed koji, which comprises culturing Rhizopus bacteria in an agar culture medium or liquid culture medium, and after culturing, the bacterial cells are heated and dried or freeze-dried.
JP22637082A 1982-12-24 1982-12-24 Preparation of seed malt Pending JPS59118078A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP22637082A JPS59118078A (en) 1982-12-24 1982-12-24 Preparation of seed malt

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP22637082A JPS59118078A (en) 1982-12-24 1982-12-24 Preparation of seed malt

Publications (1)

Publication Number Publication Date
JPS59118078A true JPS59118078A (en) 1984-07-07

Family

ID=16844071

Family Applications (1)

Application Number Title Priority Date Filing Date
JP22637082A Pending JPS59118078A (en) 1982-12-24 1982-12-24 Preparation of seed malt

Country Status (1)

Country Link
JP (1) JPS59118078A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01148176A (en) * 1987-12-04 1989-06-09 Getsukeikan Kk Method for reducing yield of malt in brewing of 'sake'

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01148176A (en) * 1987-12-04 1989-06-09 Getsukeikan Kk Method for reducing yield of malt in brewing of 'sake'
JPH0420592B2 (en) * 1987-12-04 1992-04-03 Gekkeikan Kk

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