JPS62239940A - Charge seed composition of swollen food - Google Patents
Charge seed composition of swollen foodInfo
- Publication number
- JPS62239940A JPS62239940A JP8419986A JP8419986A JPS62239940A JP S62239940 A JPS62239940 A JP S62239940A JP 8419986 A JP8419986 A JP 8419986A JP 8419986 A JP8419986 A JP 8419986A JP S62239940 A JPS62239940 A JP S62239940A
- Authority
- JP
- Japan
- Prior art keywords
- sake
- koji
- weight
- yeast
- dried
- 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.)
- Granted
Links
- 239000000203 mixture Substances 0.000 title claims description 32
- 235000013305 food Nutrition 0.000 title claims description 17
- 240000004808 Saccharomyces cerevisiae Species 0.000 claims description 28
- 235000014680 Saccharomyces cerevisiae Nutrition 0.000 claims description 28
- 235000007164 Oryza sativa Nutrition 0.000 claims description 23
- 235000009566 rice Nutrition 0.000 claims description 23
- 238000000855 fermentation Methods 0.000 claims description 16
- 230000004151 fermentation Effects 0.000 claims description 16
- 238000007796 conventional method Methods 0.000 claims description 10
- 239000000796 flavoring agent Substances 0.000 claims description 4
- 235000019634 flavors Nutrition 0.000 claims description 4
- 240000007594 Oryza sativa Species 0.000 claims 1
- 241000209094 Oryza Species 0.000 description 22
- 241000894006 Bacteria Species 0.000 description 19
- 235000008429 bread Nutrition 0.000 description 15
- 238000002360 preparation method Methods 0.000 description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- 240000006439 Aspergillus oryzae Species 0.000 description 8
- 235000002247 Aspergillus oryzae Nutrition 0.000 description 8
- 238000004108 freeze drying Methods 0.000 description 8
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 8
- 239000002002 slurry Substances 0.000 description 8
- 230000007423 decrease Effects 0.000 description 7
- 238000001035 drying Methods 0.000 description 7
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- 238000004519 manufacturing process Methods 0.000 description 5
- 238000001694 spray drying Methods 0.000 description 5
- 241000228212 Aspergillus Species 0.000 description 4
- 235000013334 alcoholic beverage Nutrition 0.000 description 4
- 229910000027 potassium carbonate Inorganic materials 0.000 description 4
- 102000004190 Enzymes Human genes 0.000 description 3
- 108090000790 Enzymes Proteins 0.000 description 3
- 244000068988 Glycine max Species 0.000 description 3
- 235000010469 Glycine max Nutrition 0.000 description 3
- 230000001580 bacterial effect Effects 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 238000012258 culturing Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 229940088598 enzyme Drugs 0.000 description 3
- 235000021107 fermented food Nutrition 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- 229910000029 sodium carbonate Inorganic materials 0.000 description 3
- 238000003860 storage Methods 0.000 description 3
- 241000122821 Aspergillus kawachii Species 0.000 description 2
- 241001112078 Aspergillus usamii Species 0.000 description 2
- 239000004375 Dextrin Substances 0.000 description 2
- 229920001353 Dextrin Polymers 0.000 description 2
- GXCLVBGFBYZDAG-UHFFFAOYSA-N N-[2-(1H-indol-3-yl)ethyl]-N-methylprop-2-en-1-amine Chemical compound CN(CCC1=CNC2=C1C=CC=C2)CC=C GXCLVBGFBYZDAG-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 229930006000 Sucrose Natural products 0.000 description 2
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 2
- 241000209140 Triticum Species 0.000 description 2
- 235000021307 Triticum Nutrition 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- 235000019425 dextrin Nutrition 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 210000004185 liver Anatomy 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 238000010979 pH adjustment Methods 0.000 description 2
- 239000003223 protective agent Substances 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 239000005720 sucrose Substances 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- CYDQOEWLBCCFJZ-UHFFFAOYSA-N 4-(4-fluorophenyl)oxane-4-carboxylic acid Chemical compound C=1C=C(F)C=CC=1C1(C(=O)O)CCOCC1 CYDQOEWLBCCFJZ-UHFFFAOYSA-N 0.000 description 1
- 239000004382 Amylase Substances 0.000 description 1
- 108010065511 Amylases Proteins 0.000 description 1
- 102000013142 Amylases Human genes 0.000 description 1
- 229920002307 Dextran Polymers 0.000 description 1
- 240000005979 Hordeum vulgare Species 0.000 description 1
- 235000007340 Hordeum vulgare Nutrition 0.000 description 1
- 241000283973 Oryctolagus cuniculus Species 0.000 description 1
- 108091005804 Peptidases Proteins 0.000 description 1
- 244000046052 Phaseolus vulgaris Species 0.000 description 1
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 1
- 239000004365 Protease Substances 0.000 description 1
- 102100037486 Reverse transcriptase/ribonuclease H Human genes 0.000 description 1
- 241000752058 Rugilus Species 0.000 description 1
- 230000001476 alcoholic effect Effects 0.000 description 1
- 235000019418 amylase Nutrition 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 235000009508 confectionery Nutrition 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- PXEDJBXQKAGXNJ-QTNFYWBSSA-L disodium L-glutamate Chemical compound [Na+].[Na+].[O-]C(=O)[C@@H](N)CCC([O-])=O PXEDJBXQKAGXNJ-QTNFYWBSSA-L 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 229940059442 hemicellulase Drugs 0.000 description 1
- 108010002430 hemicellulase Proteins 0.000 description 1
- 238000007602 hot air drying Methods 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 235000013923 monosodium glutamate Nutrition 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- 238000010899 nucleation Methods 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000004321 preservation Methods 0.000 description 1
- 238000004080 punching Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 235000020183 skimmed milk Nutrition 0.000 description 1
- 229940073490 sodium glutamate Drugs 0.000 description 1
- 239000001540 sodium lactate Substances 0.000 description 1
- 229940005581 sodium lactate Drugs 0.000 description 1
- 235000011088 sodium lactate Nutrition 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000010025 steaming Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
Landscapes
- Confectionery (AREA)
- Bakery Products And Manufacturing Methods Therefor (AREA)
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は酒種パン等の酒種膨化食品に使用される仕込み
種組成物に関する。DETAILED DESCRIPTION OF THE INVENTION [Industrial Field of Application] The present invention relates to a fermented soybean composition used for puffed sake soybean foods such as sakesouded bread.
従来、酒種を用いた膨化食品特にパン類を製造するには
まず酒siを用意する必要がある。その酒種は次のよう
にして作られている。Conventionally, in order to produce puffed foods, especially breads, using sake seeds, it is first necessary to prepare sake seeds. The sake type is made as follows.
まず、生米と火と水を一定の割合で混合し、36〜48
時間培養して麹中に存在する野性酵母を発育増殖させて
1番種を得る。この1番種の一部と米飯、麹、水を一定
の割合で混合し、20〜24時間培養して2番種を得る
。以下同様に2回種つぎをくり返して4番種を得るが、
この4番8t y&:用いて酒種パン等の膨化食品ヲ夷
遺しているのでこのat通常仕込み種と称している。First, mix raw rice, fire and water in a certain ratio,
The wild yeast present in the koji is grown and multiplied by culturing for a period of time to obtain the first species. A portion of this No. 1 seed is mixed with cooked rice, koji, and water at a constant ratio, and cultured for 20 to 24 hours to obtain No. 2 seed. Repeat the seeding process twice in the same way to obtain the 4th seed, but
This type is used to prepare puffed foods such as sake bread, so it is called a regular preparation type.
前記の仕込み種f、得るためには、前記したように最低
5日間の培養が必要で非常に手間がかかるが、得られる
仕込み槌の発酵力は必ずしも安定ではなく、より安定で
再現性のあるaを得るためには高度の技術と多大な労力
が要求される。また、このようにして得た種でるっても
その保存性が悪く、例えば仕込み槌全冷蔵庫等で保存し
ておくと発酵力が低下してしまう。In order to obtain the above-mentioned preparation f, it is necessary to culture for at least 5 days as mentioned above, which is very time-consuming, but the fermentation power of the obtained preparation is not necessarily stable, but it is more stable and reproducible. A high level of skill and a great deal of effort are required to obtain a. In addition, even if the seeds obtained in this way are stored, their storage stability is poor, and if they are stored in a refrigerator, for example, the fermentation power will decrease.
そこで、前記仕込み種を乾燥して保存することも考えら
れたが、冷蔵保存の場合以上に発酵力が低下する。例え
ばこの乾燥して保存し九種を用いる場合には、必要な発
酵力金有する酒種をイ0ようとするとまた数回の種つぎ
が必要であり、あまり価値のないものであった。Therefore, it has been considered to dry and preserve the seeds, but the fermentation power decreases more than in the case of refrigerated storage. For example, when using dried and preserved sake varieties, it would be necessary to pour the seeds several times in order to obtain a sake variety with the necessary fermentation power, and it was not very valuable.
よって1本発明は1回の培養で酒種パン等の膨化食品の
発酵に充分使用し得る仕込み橿を得ることが可能な組成
′、ftJヲ提供することを目的としている。Accordingly, an object of the present invention is to provide a composition, ftJ, which can be used in fermentation of leavened foods such as alcoholic bread in a single culture.
前記の目的を達成するために、本発明者らは鋭意研究を
重ねた結果本発明を完成した。In order to achieve the above object, the present inventors have completed the present invention as a result of extensive research.
すなわち、本発明は常法によって得られる酒種、硅、α
化米、麹の消化処理物および清酒様7レーバー生産罷と
イーストとしての発酵能の良好なサツカロマイセス・セ
レビシエよりする酒Mi膨化食品の仕込み種組成物に関
する。That is, the present invention is directed to alcoholic beverages, silica, and α obtained by conventional methods.
This invention relates to a preparation seed composition for fermented rice, fermented rice malt, sake-like seven liver production plants, and a fermented food made from Saccharomyces cerevisiae, which has good fermentation ability as yeast.
本発明における常法によって得られる酒種は、例えば第
1表に示される方法で製造される。The sake varieties obtained by conventional methods in the present invention are produced, for example, by the methods shown in Table 1.
第1表
この第1表中で用いられるmは本発明で使用される海と
同様のもので、一般に醸造用に使用されるものであれば
よく、例えばアスペルギルス・オリゼー(Asp、 o
ryzae) 、アスペルギルス・ンーヤー(Asp−
5oya) 、アスペルギルス拳ウサミ−(Asp、
usami)、アスペルギルス・カワチー(Asp、
kawachi )等の麹菌を米、小麦、大豆等の原料
に接種し、常法により製麹したものをいう。Table 1 m used in this Table 1 is the same as the sea used in the present invention, and may be any one commonly used for brewing, such as Aspergillus oryzae (Asp, o
ryzae), Aspergillus nyaa (Asp-
5oya), Aspergillus fist rabbit (Asp,
usami), Aspergillus kawachii (Asp,
Koji is produced by inoculating raw materials such as rice, wheat, soybeans, etc. with koji molds such as Aspergillus kawachi) and making koji using conventional methods.
本発明でいうα化米とは、米を蒸煮等でα化したもので
あればよく特に限定されない。The gelatinized rice as used in the present invention is not particularly limited as long as it is rice that has been gelatinized by steaming or the like.
本発明でいう麹の消化処理物とは、乾物換算で類1重量
部に対して、水を1〜4重量部加え、45〜65℃好ま
しくは50〜55℃で4〜60時間好ましくは15〜2
0時間処理して得たものをいう。この際、アミラーゼ、
プロテアーセまたはへミセルラーゼ等の酵素を添加する
とさらに好ましい。前記のようにして得た麹の消化処理
物は、常温では腐敗しやすいため例えば80〜85℃で
約10分間熱処理をして酵素を失活させるとよい。また
、保存性向上を目的としてこの麹の消化処理物を粉末化
するには、加水し低分解デキストラン等の賦形剤を加え
て噴霧乾燥すればよい。この麹の消化処理物中に存在す
る成分としては主に、麹菌がみずからの酵素により分解
された自己消化物、菌体から生産され次代農産物および
基質の分解物等がある。The digested product of koji in the present invention is prepared by adding 1 to 4 parts by weight of water to 1 part by weight of the same in terms of dry matter, and heating the mixture at 45 to 65°C, preferably 50 to 55°C, for 4 to 60 hours, preferably 15 to 15 parts by weight. ~2
This refers to the product obtained after 0 hours of treatment. At this time, amylase,
It is further preferred to add an enzyme such as protease or hemicellulase. Since the digested product of koji obtained as described above is easily putrefied at room temperature, it is recommended that the enzyme be deactivated by heat treatment at, for example, 80 to 85° C. for about 10 minutes. Further, in order to powderize the digested product of koji for the purpose of improving storage stability, it is sufficient to add water, add an excipient such as low decomposition dextran, and spray dry it. The components present in this digested product of koji include autolysed products of the koji mold decomposed by its own enzymes, next-generation agricultural products produced from the bacterial cells, and decomposed products of substrates.
本発明でいう清酒用フレーバー生産能とイーストとして
の発酵能の良好なサツカロマイセス・セレビシエとは、
麹中に存在する野性酵母の中から、清酒用7レーバーを
強くもち、しかもイースト発酵食品の生地発酵能の強い
酵母菌を選択分離し、これを純粋培養して増殖させたも
ので、特に酵母菌数を乾物換算で1010個/Iのオー
ダー迄したものが好ましい。このような酵母菌群の一例
としては、本出願人が昭和60年7月25日付で出願し
友「清酒様フレーバーをもったイースト発酵食品用酵母
菌」(特願昭60−163007号)に記載の5FY−
B凶(倣工研m″4f第8365号)が挙げられる。こ
のような酵母菌は前記したように麹中に存在する野性酵
母から選択分離する方法以外に、酒種から同様の性質を
もつ酵母菌を選択分離して純粋培養したものであっても
よい。In the present invention, Saccharomyces cerevisiae that has good flavor production ability for sake and fermentation ability as yeast is
Among the wild yeasts present in koji, we have selectively isolated yeast that has a strong 7 lever for sake and also has a strong ability to ferment dough for yeast-fermented foods, and grown it by pure culture. It is preferable that the number of bacteria is on the order of 1010 cells/I in terms of dry matter. As an example of such a group of yeast bacteria, the present applicant filed an application on July 25, 1985, entitled ``Yeast Bacteria for Yeast Fermented Foods with Sake-Like Flavor'' (Patent Application No. 163007-1988). 5FY- as described
B-Kyo (Imitation Koken M''4F No. 8365) is an example of this type of yeast.In addition to selective isolation from wild yeast present in koji as described above, such yeast can be isolated from sake varieties with similar properties. The yeast may be selectively isolated and pure cultured.
前記のような性質をもつサツカロマイセス・セレビシエ
は一種類だけ用いてもよいし、複数種類混合して用いて
もよい。One type of Satucharomyces cerevisiae having the above-mentioned properties may be used, or a mixture of multiple types may be used.
本発明の酒種膨化食品の仕込み種組成物は、前記の常法
によって得られる酒種s#α化米。The seed composition for the puffed sake seed food of the present invention is the sake seed s# gelatinized rice obtained by the above-mentioned conventional method.
麹の消化処理物および清酒様7レーパー生産能とイース
トとしての発酵能の良好なサツカロマイセス・セレビシ
エよりなるが、これらの乾物換算での配合割合が、常法
によって得られる酒種が1〜20重tチ特に6〜10重
量%、麹が1〜40重tチ特に4〜16′BL量チ、α
化米が20〜80重量%、麹の消化処理物が5〜25N
量チ特に10〜18重量%および清酒様フレーバー生産
能とイーストとしての発酵能の良好なサツカロマイセス
・セレビシエがα1〜3重i%であることが好ましい。It is made of digested koji and Saccharomyces cerevisiae, which has a good ability to produce sake-like 7 rapes and fermentation ability as yeast, but the proportion of these ingredients in terms of dry matter is 1 to 20% by weight for sake types obtained by conventional methods. Especially 6 to 10% by weight, 1 to 40% by weight of koji, especially 4 to 16' BL, α
20-80% by weight of converted rice, 5-25N of digested koji
The amount is preferably 10 to 18% by weight, and α1 to 3% by weight of Saccharomyces cerevisiae, which has good sake-like flavor production ability and yeast fermentation ability.
この組成物音用いて仕込み槌ヲ得る具体的な操作として
は以下のように行う。すなわち酒種、麹、α化米、麹の
消化処理物、清酒様7レーバー生産能とイーストとして
の発酵能の良好なサツカロマイセス・セレビシエおよび
水を前記の配合割合で混合して、温度15〜30℃好ま
しくは22〜26℃で20〜48時間培養して仕込み棟
を得る。The specific operation for obtaining a preparation mallet using this composition sound is as follows. That is, sake seeds, koji, pregelatinized rice, digested product of koji, Satucharomyces cerevisiae, which has good sake-like 7 liver production ability and fermentation ability as yeast, and water are mixed in the above-mentioned proportions and heated at a temperature of 15 to 30 ml. C. Preferably, culturing is carried out at 22 to 26.degree. C. for 20 to 48 hours to obtain a preparation block.
本発明でいう酒種は、前記のように常法によって得られ
るものであるが通常の場合2番種もしくは5番種で充分
である。The sake type referred to in the present invention can be obtained by a conventional method as described above, but type 2 or type 5 is usually sufficient.
本発明の組成物を、保存の目的のために乾燥品とするこ
とは非常に有効であり、その調製方法は以下のようにし
て行う。It is very effective to form the composition of the present invention into a dry product for the purpose of preservation, and the preparation method thereof is as follows.
まず、酒種については、乾燥により発酵力が低下するの
で4番種を使用するのが好ましい。First, regarding the type of sake, it is preferable to use type 4 because the fermentation power decreases due to drying.
この酒種は通常−が3〜4の範囲になるので。This type of sake usually has a - value in the range of 3 to 4.
これを乾燥して使用する場合にはpH4〜7特に5〜6
に調整することが好ましい。このpH調整に用いるもの
としては、炭酸カリウム、炭酸ナトリウム、乳酸ナトリ
ウムなどの中和剤を用いるとよい。呻Iを前記範囲に調
整する目的は、次の乾燥工程における酵母菌数の減少を
防ぎ、それによっておこる活性力の低下を抑える念めで
ある。また、このpH調整に先立って前記酒種を20メ
ツシュ以下程度に磨砕しておくと、後の乾燥工程が短時
間にすみより好ましい。When using this dry product, the pH should be 4 to 7, especially 5 to 6.
It is preferable to adjust to A neutralizing agent such as potassium carbonate, sodium carbonate, or sodium lactate may be used for this pH adjustment. The purpose of adjusting I to the above range is to prevent a decrease in the number of yeast bacteria in the next drying process and to suppress the decrease in activity that occurs due to this. Furthermore, it is preferable to grind the alcoholic beverage to a size of about 20 mesh or less before this pH adjustment because the subsequent drying step can be completed in a short time.
さらに、乾燥による活性の低下を防ぐ目的で蔗糖、脱脂
粉乳、グルタミン酸ソーダ等1fcはこれらの混合物を
保護剤として、前記酒種100重量部に対して1〜5重
を都添加混合することが好ましい。Furthermore, in order to prevent the activity from decreasing due to drying, it is preferable to add 1 to 5 parts of 1FC such as sucrose, skim milk powder, and sodium glutamate to 100 parts by weight of the alcoholic beverage, using a mixture of these as a protective agent. .
前記の酒種の乾燥は酵母菌数の減少ができるだけおこら
ないよう行うことが重要であり、できるだけ低温で短時
間に行う。この乾燥の具体的方法としては、凍結乾燥ま
たは噴霧乾燥の方法があり、特に凍結乾燥が好ましい。It is important to dry the above-mentioned sake seeds so that the number of yeast bacteria does not decrease as much as possible, and it is carried out at the lowest possible temperature and in the shortest possible time. Specific methods for this drying include freeze drying and spray drying, with freeze drying being particularly preferred.
凍結乾燥の場合は品温50℃以下特に40℃以下で行う
ことが好ましい。噴霧乾燥の場合は品温70’C以下特
に60℃以下で行うことが好ましい。なお、前記酒種中
に存在する酵母菌数が乾物換算で108〜109 s/
gのオーダーである場合、凍結乾燥法により乾物換算で
107〜108 イV1に、また噴νに乾燥法により乾
物換算で105〜105(K/1になることが本発明者
らによって確認されている。In the case of freeze-drying, it is preferable to perform the product at a temperature of 50°C or lower, especially 40°C or lower. In the case of spray drying, it is preferable to carry out the product at a temperature of 70'C or less, especially 60'C or less. In addition, the number of yeast bacteria present in the above sake type is 108 to 109 s/ in terms of dry matter.
The inventors have confirmed that when the amount is on the order of 10 g, the dry matter equivalent is 107 to 108 IV1 by freeze-drying, and the dry matter equivalent is 105 to 105 (K/1) by the spray drying method. There is.
麹の消化処理物の乾燥は、酒種の乾燥と四球の湯度条件
で噴霧乾燥または凍結乾燥を行えばよい。The digested product of koji may be dried by spray drying or freeze drying at the same temperature as the drying of sake seeds.
α化米および麹の乾燥は、焦げつく等の過度の変質がな
い方法であれば特に限定されず1例えば熱風乾燥を行う
。Drying of gelatinized rice and koji is not particularly limited as long as it does not cause excessive deterioration such as burning, and for example, hot air drying may be used.
本発明で使用するサツカロマイセス・セレビシエの乾燥
は菌数の減少を防ぐ意味で凍結乾燥を行うことが好まし
い。この凍結乾燥は単独で行なってもよいし、前記の従
来によって得られる酒種全凍結乾燥する際に、該サツカ
ロマイセス・セレビシエを添加混合して一緒に行なって
もよい。この場合の添加率は、これらの混合物中の醇母
菌数が乾物換算で108〜9gVIになるように設計し
て決定すればよい。なお、純粋培養したサツカロマイセ
ス・セレビシエは乾物換算で1010個/9程度の菌数
を有し、これ金凍結乾床したものは109〜10個/y
程度の菌数を有する。It is preferable to freeze-dry the Saccharomyces cerevisiae used in the present invention in order to prevent the number of bacteria from decreasing. This freeze-drying may be carried out alone, or the Saccharomyces cerevisiae may be added and mixed together with the freeze-drying of the entire alcoholic beverage obtained by the above-mentioned conventional method. In this case, the addition rate may be designed and determined so that the number of mother bacteria in the mixture becomes 108 to 9 gVI in terms of dry matter. In addition, pure cultured Satucharomyces cerevisiae has a bacterial count of about 1010 cells/y on a dry matter basis, and that on a gold freeze-dry bed has a bacterial count of 109 to 10 cells/y.
It has a certain number of bacteria.
11’14 Maのサツカロマイセス・セレビシエの凍
結乾燥の方法は、常法により行えばよいがさらに好まし
い方法として以下のような方法がある。Freeze-drying of Satucharomyces cerevisiae (11'14 Ma) may be carried out by a conventional method, but the following method is more preferable.
すなわち、純粋培養した酵母菌を遠心分離してスラリー
状のものを得、このスラリー〇pi4 k炭酸カリウム
等を用いて5〜6に調整し、スラリー100重量部に対
して、酒種の乾燥に用いた前記の保護剤を1〜5重量部
添加混合し、−20℃以下で凍結し1品温50℃以下で
乾燥する。That is, pure cultured yeast is centrifuged to obtain a slurry, this slurry is adjusted to 5 to 6 using Pi4K potassium carbonate, etc., and 100 parts by weight of the slurry is added to dry sake seeds. 1 to 5 parts by weight of the above-mentioned protective agent used are added and mixed, frozen at -20°C or lower, and dried at a temperature of 50°C or lower.
このようにして得られた本発明の酒種膨化食品の仕込み
種組成物の乾燥品を用いて仕込み種を得るには、これに
適量の水を加えて、温度15〜50℃好ましくは22〜
26℃で20〜72時間好ましくは30〜56時間培養
すればよい。In order to obtain a stock seed using the thus obtained dry product of the stock seed composition for the puffed liquor food of the present invention, an appropriate amount of water is added thereto, and the temperature is 15-50°C, preferably 22-22°C.
What is necessary is just to culture|cultivate at 26 degreeC for 20 to 72 hours, preferably 30 to 56 hours.
この仕込みaを用いて、常法により酒種膨化食品全製造
する。Using this preparation a, a whole fermented liquor food product is manufactured by a conventional method.
なお1本発明で云う酒種パン等の膨化食品とは、酒種パ
ン以外に妓頭、和菓子、クツキーなどの酒種を用いて膨
化させて食用に供する食品の總ぺて全包含するものであ
る。In the present invention, the term "puffed foods such as sake bread" refers to all types of foods that are puffed using sake seeds, such as gadou, Japanese sweets, and kutsuki, in addition to sake bread. be.
本発明で得られる酒種膨化食品の仕込み種組成物は、こ
れを用いて仕込み種を得る場合、1回の培養で簡単に酒
種パン等の膨化食品の発酵に適した仕込み種を得ること
ができる。When using the composition of the fermented seed composition for puffed sake-breed foods obtained in the present invention, it is possible to easily obtain a fermented seed suitable for the fermentation of puffed foods such as sake-dough bread with one cultivation. I can do it.
また、この組成物全乾燥すると日持ちがよく。Also, this composition has a long shelf life when completely dried.
これを密封包装すれば常温で6ケ月保存しても醇母菌数
の減少は見られず1発酵力が維持できる。If this is sealed and packaged, the number of fermentation bacteria will not decrease even if it is stored at room temperature for 6 months and the fermentation power will be maintained.
以下に実施例を挙げて、本発明をさらに具体的に説明す
る。The present invention will be explained in more detail with reference to Examples below.
実施例 1 麹菌としてアスはルギルス・オリゼーを用い。Example 1 Aspergillus uses Rugilus oryzae as the koji mold.
前記第1表と同様にして4番種を得た。この4番種を2
0メツシュ以下程度に磨砕し、次いで炭酸カリウムを用
いて≠6.0に調整した後品温60℃以下の条件でIl
!X2I乾燥して乾燥酒種を得た。Type 4 was obtained in the same manner as in Table 1 above. This number 4 type is 2
After grinding to about 0 mesh or less and adjusting to ≠6.0 using potassium carbonate, Il.
! X2I was dried to obtain a dry sake seed.
また、アスにルギルス・オリゼーを麹菌として得られた
米麹を品温60℃以下の条件で熱風乾燥して、乾燥!1
を得た。In addition, rice malt obtained from Aspergillus oryzae as koji mold is dried with hot air at a temperature of 60℃ or less! 1
I got it.
また、α化米については市販の乾燥α化米七使用した。As for the pregelatinized rice, commercially available dried pregelatinized rice 7 was used.
また、麹の消化処理物については、アスペルギルス・オ
リゼーヲ細菌として得られた米麹1重を部(乾物換算)
に対して、水を3重量部加え、55℃で20時間処理し
た後、85℃で10分間熱処理をした。次いでこのもの
に低分解デキストリンを加えて噴霧乾燥して乾燥品を得
た。In addition, for the digested product of koji, 1 part (dry weight equivalent) of rice koji obtained as Aspergillus oryzae bacteria was added.
3 parts by weight of water was added thereto, and the mixture was treated at 55°C for 20 hours, followed by heat treatment at 85°C for 10 minutes. Next, low decomposition dextrin was added to this product and spray-dried to obtain a dry product.
さらに5FY−B菌(微工研菌寄第8335号)全純粋
培養し、これ全遠心分離して酵母囚スラリ−を得た後、
炭酸カリウムを用いてこのスラリーのp)iを5.5に
調整し、このスラリー100重量部に対して蔗糖3重量
部添加混合し1品温−50℃で凍結し品温40℃以下で
乾燥して、5FY−B菌の乾燥品を得た。Furthermore, 5FY-B bacteria (Feikoken Bacteria No. 8335) was completely purified and centrifuged to obtain a yeast slurry.
Adjust p)i of this slurry to 5.5 using potassium carbonate, add 3 parts by weight of sucrose to 100 parts by weight of this slurry, mix, freeze at -50°C, and dry at temperature below 40°C. A dried product of 5FY-B bacteria was obtained.
以上のようにして得た各乾燥品を乾物換算で下記の配合
割合で配合して、本発明の酒種膨化食品の仕込み種組成
物の乾燥品を得た。Each of the dried products obtained as described above was blended in the following proportions in terms of dry matter to obtain a dried product of the stock composition for the puffed liquor product of the present invention.
(配合)
乾燥酒種 10重量%乾燥麹
12I
乾燥α化米 66 1
麹の消化処理物の乾燥品 10 l5FY−B園の
乾燥品 2I実施例 2
麹函としてアスペルギルス・ウサミ−を用い、前記第1
表と同様にして4番種を得た。この4番種を20メツシ
ユ以下に磨砕し、次いで炭酸ナトリウムを用いてpH5
,0に調整した。(Composition) Dried sake variety 10% by weight dried koji
12I Dry gelatinized rice 66 1 Dried product of digested koji 10 15 Dried product from FY-B garden 2I Example 2 Using Aspergillus usami as a koji box,
A No. 4 seed was obtained in the same manner as in the table. This No. 4 type was ground to 20 mesh or less, and then adjusted to pH 5 using sodium carbonate.
, adjusted to 0.
また、 5FY−B M (微工研菌寄第8335号)
を純粋培養し、これを遠心分離して酵母菌スラリーを得
、炭酸ナトリウムを用いてこのスラリーのpHを5.0
に調整した。前記4番種100重量部に対してこの5F
Y−B菌を20重量部添加混合して品温−20℃で凍結
し、品温50℃以下で乾燥した。Also, 5FY-B M (Feikoken Bibori No. 8335)
A yeast slurry was obtained by centrifuging the pure culture, and the pH of this slurry was adjusted to 5.0 using sodium carbonate.
Adjusted to. This 5F per 100 parts by weight of the above No. 4 type
20 parts by weight of Y-B bacteria were added and mixed, frozen at a temperature of -20°C, and dried at a temperature of 50°C or lower.
乾燥麹、乾燥α化米および麹の消化処理物の乾燥品につ
いては実施例1と同様にして得た。Dried koji, dried pregelatinized rice, and dried products of digested koji were obtained in the same manner as in Example 1.
以上のようにして得友各乾燥品を乾物換算で下記の配合
割合で配合して、本発明の酒種膨化食品の仕込み種組成
物の乾燥品を得た。As described above, each dried product of Tokutomo was blended in the following proportions in terms of dry matter to obtain a dried product of the stock composition for the puffed sake starter food of the present invention.
(配合)
酒種と5FY−B菌の混合物の乾燥品 10重量%乾燥
麹 101
乾燥α化米 65重量%麹の消化処理物
の乾燥品 15 1実施例 3
麹菌としてアスペルギルス・カワチーを用い、前記第1
表と同様にして2番種を得、酒種とした。(Composition) Dried product of a mixture of sake seeds and 5FY-B bacteria 10% by weight dried koji 101 Dried pregelatinized rice 65% by weight Dried product of digested koji 15 1 Example 3 Aspergillus kawachii was used as the koji mold, and the above-mentioned 1st
A second type was obtained in the same manner as in the table and used as a sake type.
また@菌としては、アスペルギルス・ウサミ−を麹蔚と
して得られ之麦麹を用意し、α化米としては精白米全常
法により炊飯したものを用意した。In addition, as @ bacteria, barley koji obtained from Aspergillus usami was prepared, and as pregelatinized rice, rice cooked using a conventional polished rice method was prepared.
また麹の消化処理物としては、低級デキストリンを加え
て噴霧乾燥する工程を省略し次以外は実施例1と同様に
処理したものを用意した。In addition, a digested product of koji was prepared in the same manner as in Example 1 except that the step of adding lower dextrin and spray drying was omitted, except for the following.
以上のようにして得た各原料と純粋培養した5FY−B
菌(微工研菌寄第8565号)ft乾物換算で下記配合
割合で配合して、本発明の酒種膨化食品の仕込み釉組成
物を得た。Each raw material obtained as above and pure cultured 5FY-B
Bacteria (Feikoken Bacteria No. 8565) were blended in the following proportions in terms of ft dry matter to obtain a glaze composition for the fermented sake fermented food of the present invention.
(配合)
酒種(2番種) 20重tチ麦 麹
51炊飯米
67I
迎の消化処理物 6.51
SFY−B菌 1.5I
試験例
実施例1および2で得られた本発明の酒種膨化食品の仕
込み種組成物100重量部に対してそれぞれ水t−25
0重景部お置部270重量部加えて、温度27℃で30
時間培養して仕込み種を得た。また実施例乙の仕込み種
組成物を温度27℃で30時間培養して仕込みF’Ji
k得た。(Blend) Sake type (2nd type) 20 weight t Chimugi Koji
51 cooked rice
67I Digested product 6.51 SFY-B bacterium 1.5I Test Example 100 parts by weight of the seed composition for the puffed sake food of the present invention obtained in Examples 1 and 2, respectively, of water t-25
In addition to 270 parts by weight of the placing part, 30 parts by weight at a temperature of 27°C.
After culturing for a period of time, a stock seed was obtained. In addition, the preparation seed composition of Example B was cultured at a temperature of 27°C for 30 hours to prepare the preparation F'Ji.
I got k.
これらの仕込み橿を用いて、下記に示す製パン配合およ
び製パン条件で山型食パンを装造した。Using these mixing rods, mountain-shaped bread was prepared using the bread-making formulation and bread-making conditions shown below.
(製パン配合)
小麦粉 1007に、iIt部食 塩
1重世部砂 糖
25 1全 卵
10 1シヨートニング
8I
前記の仕込種 25 I
水 40 I(
製パン条件)
ヨートニングを加え中速7分
捏上温度 30℃
発酵温#2.5時間パンチ後0.5時間(温度35℃、
湿度85チ)
分 割 分割型ii 25(11ベンチタイム
20分
成 型 ガス抜きし、丸めて2斤型に4個人れる。(Bread making combination) Wheat flour 1007, iIt part salt
1 layer sugar
25 1 whole egg
10 1 shortening
8I The above ingredients 25 I Water 40 I (
Bread making conditions) Add yotoning and knead on medium speed for 7 minutes Temperature: 30°C Fermentation temperature #2.5 hours 0.5 hours after punching (temperature: 35°C,
Humidity 85 degrees) Divide Divide Mold II 25 (11 bench time, 20 minutes Mold) Remove gas, roll into 2 loaf shapes and place into 4 pieces.
渚炉時間 60分(温度38℃、71度85%)焼
成 35分(温度190℃)以上のようにして得ら
れた食パンを以下の第2表に示す評価基準表に基づいて
評価し、その結果と食パンの体*1以下のrg3表に示
す。Baking time: 60 minutes (temperature 38℃, 71℃ 85%)
The bread obtained in the above manner for 35 minutes (temperature 190° C.) was evaluated based on the evaluation criteria table shown in Table 2 below, and the results and bread body *1 are shown in the rg3 table below.
また、比較として前記第1表と同様にして得た4番種を
仕込み種として用いたものを比較例1とし、前記第1表
と同様にして得た4番種を品温45℃以下で凍結乾燥し
たもの全仕込み種として用いたものを比較例2とし、前
記第1表と同様にして得た2番at仕込み種として用い
次ものを比較例3として、いずれも前記と同様の製パン
配合、製パン条件で製造して食パンを得た。これらの結
果も第3表に示す。In addition, as a comparison, the No. 4 type obtained in the same manner as in Table 1 above was used as the charging seed, and this was designated as Comparative Example 1. The freeze-dried product was used as a total preparation as Comparative Example 2, and the following was used as the No. 2 AT preparation obtained in the same manner as in Table 1 above as Comparative Example 3. Bread was obtained by blending and manufacturing under the bread-making conditions. These results are also shown in Table 3.
第 2 表(評価基準表)
応用例
実施例1で得られた本発明の酒種膨化食品の仕込み種組
成物100重量部に対して、水250重量部を加えて温
度27・℃で30時間培養して仕込み褌を得た。Table 2 (Evaluation Criteria Table) Application Example 250 parts by weight of water was added to 100 parts by weight of the seed composition for the puffed liquor food of the present invention obtained in Example 1, and the mixture was heated at a temperature of 27°C for 30 hours. It was cultured to obtain loincloth.
この仕込み種を用いて、試験例に示したものと同様の製
パン配合で、また分割工程以降を下記の条件に変えた以
外は同様の製パン条件で製造してあんパンを得た。Using this stock, anpan was produced using the same bread making formulation as shown in the test example and under the same bread making conditions except that the conditions after the dividing step were changed to the following.
(復)七ン条件)
分 割 分割型t 40g
ベンチタイム 20分
成 1i1 あん35gを包んで丸める焙炉時間
60分(温度38℃、湿度85%)焼 成 10分(
温度220℃)
以上のようにして得られ次あんパンは、体aが大きく、
形状、内相、触感、食感共にいずれも良好なものであう
念。(Re) Seven conditions) Divide Divide type t 40g Bench time 20 minutes ingredients 1i1 Roasted time to wrap and roll 35g of bean paste
60 minutes (temperature 38℃, humidity 85%) Baking 10 minutes (
Temperature: 220°C) The anpan obtained in the above manner has a large body a,
I am sure that the shape, internal structure, texture, and texture are all good.
Claims (1)
物および清酒様フレーバー生産能とイーストとしての発
酵能の良好なサツカロマイセス・セレビシエよりなる酒
種膨化食品の仕込み種組成物。Seed composition for fermented sake seed food, consisting of sake seed obtained by conventional methods, koji, pregelatinized rice, digested product of koji, and Saccharomyces cerevisiae, which has good ability to produce sake-like flavor and fermentation ability as yeast. .
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP8419986A JPH0661214B2 (en) | 1986-04-14 | 1986-04-14 | Preparation composition of liquor puffed food |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP8419986A JPH0661214B2 (en) | 1986-04-14 | 1986-04-14 | Preparation composition of liquor puffed food |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS62239940A true JPS62239940A (en) | 1987-10-20 |
JPH0661214B2 JPH0661214B2 (en) | 1994-08-17 |
Family
ID=13823805
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP8419986A Expired - Lifetime JPH0661214B2 (en) | 1986-04-14 | 1986-04-14 | Preparation composition of liquor puffed food |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0661214B2 (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH05316927A (en) * | 1992-05-14 | 1993-12-03 | Tokushima Seiko Kk | Fermentation promoter and improver for bread dough |
JP2001238665A (en) * | 2000-03-02 | 2001-09-04 | Natl Food Res Inst | Practical baker's yeast with high amino acid accumulation |
JP2008000109A (en) * | 2006-06-26 | 2008-01-10 | Takefumi Yoneya | Rice flour-containing confectionery, and method for producing the same |
JP2013102701A (en) * | 2011-11-10 | 2013-05-30 | Nisshin Flour Milling Inc | Production method of yeast mash |
JP2013102702A (en) * | 2011-11-10 | 2013-05-30 | Nisshin Flour Milling Inc | Production method of yeast mash |
-
1986
- 1986-04-14 JP JP8419986A patent/JPH0661214B2/en not_active Expired - Lifetime
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH05316927A (en) * | 1992-05-14 | 1993-12-03 | Tokushima Seiko Kk | Fermentation promoter and improver for bread dough |
JP2740073B2 (en) * | 1992-05-14 | 1998-04-15 | 徳島精工株式会社 | Bread dough fermentation accelerator and bread dough improving method |
JP2001238665A (en) * | 2000-03-02 | 2001-09-04 | Natl Food Res Inst | Practical baker's yeast with high amino acid accumulation |
JP4580055B2 (en) * | 2000-03-02 | 2010-11-10 | 独立行政法人農業・食品産業技術総合研究機構 | A baker's yeast with high amino acid accumulation |
JP2008000109A (en) * | 2006-06-26 | 2008-01-10 | Takefumi Yoneya | Rice flour-containing confectionery, and method for producing the same |
JP2013102701A (en) * | 2011-11-10 | 2013-05-30 | Nisshin Flour Milling Inc | Production method of yeast mash |
JP2013102702A (en) * | 2011-11-10 | 2013-05-30 | Nisshin Flour Milling Inc | Production method of yeast mash |
Also Published As
Publication number | Publication date |
---|---|
JPH0661214B2 (en) | 1994-08-17 |
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Date | Code | Title | Description |
---|---|---|---|
EXPY | Cancellation because of completion of term |