JP3353305B2 - Bread making method - Google Patents
Bread making methodInfo
- Publication number
- JP3353305B2 JP3353305B2 JP14807291A JP14807291A JP3353305B2 JP 3353305 B2 JP3353305 B2 JP 3353305B2 JP 14807291 A JP14807291 A JP 14807291A JP 14807291 A JP14807291 A JP 14807291A JP 3353305 B2 JP3353305 B2 JP 3353305B2
- Authority
- JP
- Japan
- Prior art keywords
- bread
- dough
- glutathione
- kneading
- test example
- 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.)
- Expired - Lifetime
Links
Description
【0001】[0001]
【産業上の利用分野】本発明はパン生地を製造するに当
たり、パン生地を冷凍保存した後でも、解凍し、発酵
し、焼成したパンの品質が優れた製パン方法に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for producing bread dough with excellent quality of bread that has been thawed, fermented and baked even after the bread dough is frozen and stored.
【0002】[0002]
【従来の技術】製パンの主要な工程は混捏、発酵、焼成
の3段階である。特に、焼成後のパンの品質に大きな影
響を与えるパン生地を得る混捏は、重要な工程とされて
いる。このため、現在、各種のパン生地改良剤が検討さ
れ、実際に使用されている。代表的なものとしては、各
種の乳化剤、酸化還元剤や酵素剤等がある。この中で
も、酸化還元剤については、パン生地中の小麦グルテン
の形成に大きな影響を及ぼすだけに多くの検討例があ
り、例えば、パン生地成分にグルタチオンのような還元
性物質を添加することは、食味的に良質のパンを製造す
るにあたり有効であるとする例(特公昭56−989
3,特公昭61−23970,特公昭61−2397
1,特開昭58−158121,特開昭62−662
6,特開平2−190138等)や、また、グルタチオ
ンの存在は好ましくないとする例(特開昭60−213
5等)等があるが、かかる還元性物質の添加が、混捏工
程、特にパン生地混捏時間への影響についは知られてい
ない。一方、パンの品質は生鮮食品と同様に、鮮度が極
めて重要視される。このため製パン工場では深夜、早
朝、休日作業を行い焼き立てのパンを供給しているが
「イート・イン・ベーカリー」の急増など鮮度維持は緊
急の関心事となっており、パン生地混捏時間の短縮や、
冷凍生地製パン法等の早期確立が望まれている。冷凍生
地製パン法とは、あらかじめ混捏を行ったパン生地を冷
凍し、必要な時に解凍・発酵・焼成を行い、焼き立ての
美味しいパンを消費者に提供しようとする方法である
が、パン生地中の酵母は、冷凍すると傷害を受け、解凍
後の発酵力が低下したり、また、死滅酵母からのグルタ
チオンの漏出により、グルテン形成が阻害されて、良質
のパンができないとされ手いる。このため製パン工程を
改変し、あらかじめ混捏・発酵まで済ませた後で冷凍
し、消費地において焼成する方法(特開昭61−247
331)、あるいは冷凍パン生地を発酵させないで冷凍
し解凍後酵母を添加して発酵させた後焼成する方法(特
開平1−191634)等が報告されている。また、予
め発酵を行ってから冷凍しても解凍後の発酵力が低下し
ない性質を保持する冷凍耐性酵母の開発等が行われてい
る(化学と生物 28,736,1990等)。2. Description of the Related Art The main processes of bread making are three stages of kneading, fermentation and baking. In particular, kneading to obtain bread dough that greatly affects the quality of bread after baking is an important step. For this reason, various bread dough improving agents are currently being studied and actually used. Representative examples include various emulsifiers, redox agents and enzyme agents. Among them, there are many studies on the oxidation-reduction agent because they have a great influence on the formation of wheat gluten in the dough.For example, adding a reducing substance such as glutathione to the dough component is edible. To be effective in producing high quality bread (Japanese Patent Publication No. 56-989)
3, JP-B-61-23970, JP-B-61-2397
1, JP-A-58-158121, JP-A-62-662.
6, JP-A-2-190138) and an example in which the presence of glutathione is not preferred (JP-A-60-213).
5) and the like, but there is no known effect of the addition of such a reducing substance on the kneading step, particularly the dough kneading time. On the other hand, as with fresh food, freshness is very important for the quality of bread. For this reason, bakery factories supply freshly baked bread by working on holidays in the middle of the night and early morning, but maintaining freshness is a matter of urgent concern, such as a sudden increase in “eat-in bakery”. And
Early establishment of the frozen dough baking method is desired. The frozen dough baking method is a method in which bread dough that has been kneaded in advance is frozen, thawed, fermented, and baked when necessary to provide consumers with delicious freshly baked bread. It has been reported that refrigerated rice is injured when frozen, and the fermentation power after thawing is reduced, and glutathione is leaked from dead yeast, thereby inhibiting gluten formation and making good-quality bread impossible. For this reason, the method of baking is modified, and after kneading and fermentation have been completed in advance, the method is frozen and baked in a consuming area (Japanese Patent Laid-Open No. 61-247).
331) or a method in which frozen bread dough is frozen without being fermented, thawed, added with yeast, fermented, and then baked (JP-A-1-191634). In addition, freezing-resistant yeast has been developed which retains the property that the fermentation power after thawing does not decrease even after fermentation and then freezing (Chemistry and Biology 28, 736, 1990, etc.).
【0003】[0003]
【発明が解決しようとする課題】しかしながら、パン生
地混捏時間はパンの製造の生産性に関係し、混捏時間の
短縮がもとめられているが、有効な手段がないまま現在
に至っているし、また冷凍生地製パン法については、前
記の工程改変法では、冷凍前に発酵を完了させると焼成
までの保存、運搬においてかさばったり、その取扱中に
押しつぶれて膨らみの悪いパンになることもあり、又、
冷凍パン生地の解凍後これに添加する酵母とのミキシン
グ用製パン器が必要であったり、また、冷凍耐性酵母に
ついては未だ十分な効果が得られておらず、しかも、冷
凍保存中の管理も面倒である等の欠点を有している。However, the dough kneading time is related to the productivity of bread production, and the kneading time has been required to be shortened. Regarding the dough baking method, in the above-mentioned process modification method, if fermentation is completed before freezing, storage until baking, bulky during transportation, or squeezing during handling may result in poor swelling bread, ,
After thawing the frozen bread dough, a bread maker for mixing with the yeast to be added to the dough is necessary, and sufficient effects have not yet been obtained for freeze-tolerant yeast, and management during frozen storage is troublesome. It has disadvantages such as
【0004】[0004]
【課題を解決するための手段】本発明者らは、以上のよ
うな問題点を解決するため、鋭意検討した結果、パン生
地成分にグルタチオンを添加し混捏することにより、驚
くべき事に、従来の工程をそのまま用いても、パン生地
生成時間が短縮され、また、混捏工程が終了し焼成工程
前の段階でパン生地を冷凍保存した後でも、以下、通常
の方法で解凍し、発酵し、焼成しても、意外にも冷凍傷
害を殆ど受けることなく良質のパンが得られることを見
いだし、本発明を完成したものである。Means for Solving the Problems The present inventors have conducted intensive studies to solve the above problems, and as a result, surprisingly, by adding glutathione to kneaded dough and kneading it, Even if the process is used as it is, the bread dough generation time is shortened, and also after the kneading process is completed and the bread dough is frozen and stored at the stage before the baking process, it is thawed, fermented, and baked in the usual manner. However, the present inventors have found that high-quality bread can be obtained with almost no freezing injury, and completed the present invention.
【0005】即ち、本発明は、請求項1 酵母を含むパ
ン生地を混捏により形成させ、これを冷凍保存し、その
後、解凍、発酵及び焼成するパンの製造方法において、
混捏前の酵母を含むパン生地に、グルタチオン成分を生
地原料の小麦粉重量に対し50〜70ppm添加するこ
とを特徴とするパンの製造方法。請求項2 グルタチオ
ン成分が精製グルタチオン及び/又はグルタチオンを含
有するイーストエキスであることを特徴とする請求項1
記載のパンの製造方法。である。More specifically, the present invention relates to a method for producing bread, wherein bread dough containing yeast is formed by kneading, the frozen dough is stored, then thawed, fermented and baked.
A method for producing bread, wherein a glutathione component is added to bread dough containing yeast before kneading in an amount of 50 to 70 ppm based on the weight of flour as a dough material. (2) The glutathione component is purified glutathione and / or a yeast extract containing glutathione.
The method for producing bread according to the above. It is.
【0006】本発明に用いられる基礎となるパン生地成
分組成は特に限定されるものではなく、通常知られたパ
ン生地成分組成を適用することができ、この基礎成分組
成に本発明の特徴であるグルタチオン成分を加えること
により本発明は達成される。本発明に用いられるグルタ
チオン成分としては特に限定されないが、精製グルタチ
オンでも良いし、あるいはイーストエキスに含まれるグ
ルタチオンであってもよく、又、その添加方法として
は、中種法では中種原料に、ストレート法ではパン生地
原料に添加すれば良く、何れの製パン方法でも用いるこ
とが出来る。[0006] The basic dough component composition used in the present invention is not particularly limited, and a commonly known dough component composition can be applied. The glutathione component, which is a feature of the present invention, can be applied to this basic component composition. The present invention is achieved by adding The glutathione component used in the present invention is not particularly limited, but it may be purified glutathione or glutathione contained in yeast extract. In the straight method, it may be added to the raw material of bread dough, and any bread making method can be used.
【0007】また、本発明に用いられるグルタチオン成
分の添加量としては、生地原料の小麦粉重量に対し50
〜70ppmの範囲で用いる。グルタチオン成分の添加
量が少なすぎると、上記の目的を達成することが出来
ず、また、添加量が多すぎると、グルタチオンの持つ還
元力により生地中のグルテン形成を阻害してすだちや膨
らみの劣るパンとなる。[0007] The amount of glutathione component used in the present invention is 50 wt.
Use in the range of 7070 ppm. If the added amount of the glutathione component is too small, the above object cannot be achieved, and if the added amount is too large, glutenthione inhibits gluten formation in the dough due to the reducing power of the dough and inferior in swollenness and swelling It becomes bread.
【0008】又、上記と同様範囲のグルタチオンと、酵
母を共に含むパン生地を混捏により形成させ、これを一
般には−20〜−30℃の冷凍庫に保存しても、解凍し
て発酵及び焼成すると、出来上りのパンは、グルタチオ
ン無添加のパンに比べ、比容積(容積/重量)が向上
し,内相及び味覚が良好なふっくらとしたパンを得る事
が出来る。[0008] Further, bread dough containing both glutathione and yeast in the same range as described above is formed by kneading, and this is generally stored in a freezer at -20 to -30 ° C. The finished bread has an improved specific volume (volume / weight) as compared to the bread without glutathione, and a plump bread with a good internal phase and good taste can be obtained.
【0009】[0009]
【実施例】以下に、試験例を挙げて本発明を更に詳しく
説明する。 試験例 1 グルタチオン成分としては、グルタチオン(結晶品)
(株式会社興人製)を用い使用小麦粉重量に対し50p
pm添加した表1に示す成分配合の内,ショートニング
以外の成分配合物を株式会社オシキリ製HM−50横型
ラボ用ミキサー(コンピュータ付)を用いて混捏した。
混捏工程中、デベロップ値を計測し、デベロップ値が急
上昇した後、デベロップ値が概ね1.4近辺で上昇勾配
がやや小さくなった時点(混捏後6〜7分後)で一旦撹
拌を止めて表1に示したショートニングを加えた後、再
び撹拌を再開した。再びデベロップ値が急上昇した後、
デベロップ値が上下し、上昇が完了したと思われる点を
パン生地混捏終了点と判断し,混捏を停止する。これに
よってデベロップ値は0に低下するが,このデベロップ
値が0を指した時点をパン生地混捏終了時間とした。以
上のようにして得られたパン生地を表2に示す工程条件
により発酵、焼成を行ない、パンを得た(ストレート
法)。又,対照例1として配合成分の内,グルタチオン
成分を無添加とした他は試験例1と同様の成分配合(表
1)とし、試験例1と同様の条件で混捏し、発酵し、焼
成を行ない、パンを得た。図1は試験例1及び対照例1
のパン生地混捏経過中のデベロップ値の変化をプロット
した図である。この図から、試験例1(精製グルタチオ
ン添加)は、対照例1(グルタチオン成分無添加)に比
べ約2分間、パン生地混捏時間が短縮されたことが明ら
かである。また、出来上りのパンの品質の評価結果を表
3に示す。この表から明らかなように本発明の方法で得
たパンの品質は対照例1に比べ特に問題はなかった。The present invention will be described below in more detail with reference to test examples. Test Example 1 As glutathione component, glutathione (crystal product)
(Produced by Kojin Co., Ltd.) and use 50p against the flour weight
Among the components shown in Table 1 to which pm was added, the components other than the shortening were kneaded using an HM-50 horizontal laboratory mixer (with a computer) manufactured by Oshikiri Corporation.
During the kneading process, the development value was measured, and after the development value rose sharply, the stirring was stopped once when the development value became slightly smaller at around 1.4 (6 to 7 minutes after kneading). After adding the shortening shown in 1, the stirring was restarted again. After the development value soared again,
The point where the development value rises and falls and the rise is considered complete is determined as the dough kneading end point, and kneading is stopped. As a result, the development value is reduced to 0, and the time when the development value indicates 0 is defined as the dough kneading end time. The bread dough obtained as described above was fermented and baked under the process conditions shown in Table 2 to obtain bread (straight method). In Comparative Example 1, the components were the same as in Test Example 1 (Table 1) except that the glutathione component was not added, and kneaded, fermented, and fired under the same conditions as in Test Example 1. I went and got the bread. FIG. 1 shows Test Example 1 and Control Example 1.
FIG. 4 is a diagram in which changes in the development value during the course of kneading dough are plotted. From this figure, it is apparent that the bread dough kneading time in Test Example 1 (purified glutathione added) was shortened by about 2 minutes as compared with Control Example 1 (no glutathione component added). Table 3 shows the evaluation results of the quality of the finished bread. As is clear from this table, the quality of the bread obtained by the method of the present invention was not particularly problematic as compared with Comparative Example 1.
【0010】[0010]
【表1】 [Table 1]
【0011】[0011]
【表2】 [Table 2]
【0012】[0012]
【表3】 [Table 3]
【0013】試験例 2 グルタチオンとしては、10重量%のグルタチオンを含
有する酵母エキスYH(株式会社興人製)を用い、使用
小麦粉重量に対しグルタチオン含量を50ppmに、更
に臭素酸カリウムを100ppmになるよう添加した他
は試験例1と同様の成分配合(表4)で試験例1と同様
の方法にて混捏を行なってパン生地を製造した。混捏工
程が終了したパン生地は直ちに−20℃に1週間冷凍保
存した。解凍後、試験例1と同様に表2に示す条件で発
酵、焼成を行ない,製パンした。又,対照例2として配
合成分の酵母エキスYHを無添加とした他は試験例2と
同様の成分配合(表4)を試験例2と同様の条件で、混
捏、冷凍、解凍、発酵、焼成して製パンした。この結
果、試験例1と同様にして測定したデベロップ値の変化
を図2に示す。この図よりパン生地の混捏工程時間は、
試験例1の場合と同様に短縮された。また、冷凍したパ
ン生地の解凍後の発酵力を調べる為、試験例2及び対照
例2の解凍したパン生地200gを1000mlのメス
シリンダーに入れ、27℃、湿度75%、210分間発
酵を行わせ、膨潤したパン生地の容積を測定した。この
結果、試験例2、対照例2の容積はそれぞれ650m
l,510mlであり、グルタチオン(酵母エキスY
H)添加の試験例2のパン生地は、グルタチオン無添加
の対照例2のパン生地と比較して発酵力が著しく向上し
ていることが明かである。又、試験例2及び対照例2の
出来上りのパンの品質を評価し、その結果を表5に示し
た。この結果より、グルタチオン添加の試験例2は、対
照例2に比べ比容積が向上し、内相及び味覚が優れてい
ることが確認された。Test Example 2 As glutathione, a yeast extract YH (produced by Kojin Co., Ltd.) containing 10% by weight of glutathione was used. The glutathione content was 50 ppm and the potassium bromate content was 100 ppm based on the weight of the flour used. Except for the addition, the kneading was carried out in the same manner as in Test Example 1 with the same ingredients (Table 4) as in Test Example 1 to produce bread dough. The bread dough after the kneading step was immediately frozen and stored at -20 ° C for one week. After thawing, fermentation and baking were performed under the conditions shown in Table 2 in the same manner as in Test Example 1, and bread was made. In Comparative Example 2, kneading, freezing, thawing, fermenting, and baking were performed under the same conditions as in Test Example 2 except that yeast extract YH was not added. And made bread. As a result, a change in the development value measured in the same manner as in Test Example 1 is shown in FIG. From this figure, the dough kneading process time is
It was shortened as in the case of Test Example 1. Further, in order to examine the fermentation power of the frozen bread dough after thawing, 200 g of the thawed bread dough of Test Example 2 and Control Example 2 were put into a 1000 ml measuring cylinder, fermented at 27 ° C. and 75% humidity for 210 minutes, and swollen. The volume of the finished dough was measured. As a result, the volumes of Test Example 2 and Control Example 2 were each 650 m.
1,510 ml, glutathione (yeast extract Y
H) It is clear that the dough of Test Example 2 with addition has significantly improved fermentability compared to the dough of Control Example 2 without glutathione. Further, the quality of the finished bread of Test Example 2 and Control Example 2 was evaluated, and the results are shown in Table 5. From these results, it was confirmed that the test example 2 in which glutathione was added had an improved specific volume and an excellent internal phase and taste compared to the control example 2.
【0014】[0014]
【表4】 [Table 4]
【0015】[0015]
【表5】 [Table 5]
【図1】試験例1及び対照例1のパン生地混捏中のデベ
ロップ値の変化を示した図である。FIG. 1 is a diagram showing a change in a development value during kneading of dough of Test Example 1 and Control Example 1.
【図2】試験例2及び対照例2のパン生地混捏中のデベ
ロップ値の変化を示した図である。FIG. 2 is a diagram showing a change in a development value during kneading of dough of Test Example 2 and Control Example 2.
───────────────────────────────────────────────────── フロントページの続き (72)発明者 久芳 啓資 大分県佐伯市11772番地の81 (56)参考文献 特開 昭62−6626(JP,A) 特開 昭61−247331(JP,A) ──────────────────────────────────────────────────続 き Continued from the front page (72) Inventor Keisuke Kuyoshi 81, 11772, Saeki City, Oita Prefecture (56) References JP-A-62-6626 (JP, A) JP-A-61-247331 (JP, A)
Claims (2)
せ、これを冷凍保存し、その後、解凍、発酵及び焼成す
るパンの製造方法において、混捏前の酵母を含むパン生
地に、グルタチオン成分を生地原料の小麦粉重量に対し
50〜70ppm添加することを特徴とするパンの製造
方法。Claims 1. A bread dough containing yeast is formed by kneading, frozen and stored, and then, in a method for producing bread that is thawed, fermented and baked, glutathione components are added to the dough containing yeast before kneading. A method for producing bread, comprising adding 50 to 70 ppm based on the weight of flour.
び/又はグルタチオンを含有するイーストエキスである
ことを特徴とする請求項1記載のパンの製造方法。2. The method for producing bread according to claim 1, wherein the glutathione component is purified glutathione and / or a yeast extract containing glutathione.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP14807291A JP3353305B2 (en) | 1991-05-24 | 1991-05-24 | Bread making method |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP14807291A JP3353305B2 (en) | 1991-05-24 | 1991-05-24 | Bread making method |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH04346745A JPH04346745A (en) | 1992-12-02 |
JP3353305B2 true JP3353305B2 (en) | 2002-12-03 |
Family
ID=15444593
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP14807291A Expired - Lifetime JP3353305B2 (en) | 1991-05-24 | 1991-05-24 | Bread making method |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP3353305B2 (en) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP4518456B2 (en) * | 2001-02-22 | 2010-08-04 | 株式会社興人 | Miso ripening accelerator and method for producing miso using the ripening accelerator |
WO2006000066A2 (en) * | 2004-06-29 | 2006-01-05 | Puratos Naamloze Vennootschap | Dough comprising nucleotide pyrophosphatase inhibitor |
EP1771073B1 (en) | 2004-06-29 | 2018-09-05 | Puratos Naamloze Vennootschap | Dough comprising nucleotide pyrophosphatase inhibitor |
US10631546B2 (en) | 2014-09-08 | 2020-04-28 | Mitsubishi Corporation Life Sciences Limited | Frozen bread dough improver |
-
1991
- 1991-05-24 JP JP14807291A patent/JP3353305B2/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
JPH04346745A (en) | 1992-12-02 |
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