JPH0376529A - Dough and producing of bread using the same dough - Google Patents
Dough and producing of bread using the same doughInfo
- Publication number
- JPH0376529A JPH0376529A JP21191989A JP21191989A JPH0376529A JP H0376529 A JPH0376529 A JP H0376529A JP 21191989 A JP21191989 A JP 21191989A JP 21191989 A JP21191989 A JP 21191989A JP H0376529 A JPH0376529 A JP H0376529A
- Authority
- JP
- Japan
- Prior art keywords
- bread
- dough
- phytase
- minutes
- wheat flour
- 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
Links
- 235000008429 bread Nutrition 0.000 title claims abstract description 46
- 108010011619 6-Phytase Proteins 0.000 claims abstract description 20
- 229940085127 phytase Drugs 0.000 claims abstract description 20
- 238000004519 manufacturing process Methods 0.000 claims description 9
- 238000002360 preparation method Methods 0.000 claims description 3
- 238000007493 shaping process Methods 0.000 claims description 2
- 235000013312 flour Nutrition 0.000 abstract description 24
- 238000000034 method Methods 0.000 abstract description 23
- 230000000694 effects Effects 0.000 abstract description 18
- 241000209140 Triticum Species 0.000 abstract description 15
- 235000021307 Triticum Nutrition 0.000 abstract description 15
- 230000000704 physical effect Effects 0.000 abstract description 15
- 235000012180 bread and bread product Nutrition 0.000 abstract description 3
- 230000032683 aging Effects 0.000 description 14
- 238000011156 evaluation Methods 0.000 description 11
- 102000004190 Enzymes Human genes 0.000 description 10
- 108090000790 Enzymes Proteins 0.000 description 10
- 229940088598 enzyme Drugs 0.000 description 10
- 108091005804 Peptidases Proteins 0.000 description 9
- 239000004365 Protease Substances 0.000 description 9
- 102100037486 Reverse transcriptase/ribonuclease H Human genes 0.000 description 8
- 239000002994 raw material Substances 0.000 description 8
- 238000012360 testing method Methods 0.000 description 8
- 239000004744 fabric Substances 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- 239000004382 Amylase Substances 0.000 description 5
- 102000013142 Amylases Human genes 0.000 description 5
- 108010065511 Amylases Proteins 0.000 description 5
- 108010068370 Glutens Proteins 0.000 description 5
- 239000000654 additive Substances 0.000 description 5
- 235000019418 amylase Nutrition 0.000 description 5
- 235000013305 food Nutrition 0.000 description 5
- 235000021312 gluten Nutrition 0.000 description 5
- 239000002075 main ingredient Substances 0.000 description 5
- 235000018102 proteins Nutrition 0.000 description 5
- 102000004169 proteins and genes Human genes 0.000 description 5
- 108090000623 proteins and genes Proteins 0.000 description 5
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 4
- 239000004129 EU approved improving agent Substances 0.000 description 4
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 4
- 238000010521 absorption reaction Methods 0.000 description 4
- 239000008351 acetate buffer Substances 0.000 description 4
- 239000003995 emulsifying agent Substances 0.000 description 4
- 238000000855 fermentation Methods 0.000 description 4
- 230000004151 fermentation Effects 0.000 description 4
- 239000002265 redox agent Substances 0.000 description 4
- 235000011844 whole wheat flour Nutrition 0.000 description 4
- IMQLKJBTEOYOSI-GPIVLXJGSA-N Inositol-hexakisphosphate Chemical compound OP(O)(=O)O[C@H]1[C@H](OP(O)(O)=O)[C@@H](OP(O)(O)=O)[C@H](OP(O)(O)=O)[C@H](OP(O)(O)=O)[C@@H]1OP(O)(O)=O IMQLKJBTEOYOSI-GPIVLXJGSA-N 0.000 description 3
- IMQLKJBTEOYOSI-UHFFFAOYSA-N Phytic acid Natural products OP(O)(=O)OC1C(OP(O)(O)=O)C(OP(O)(O)=O)C(OP(O)(O)=O)C(OP(O)(O)=O)C1OP(O)(O)=O IMQLKJBTEOYOSI-UHFFFAOYSA-N 0.000 description 3
- 240000004808 Saccharomyces cerevisiae Species 0.000 description 3
- 235000014680 Saccharomyces cerevisiae Nutrition 0.000 description 3
- HUTIVPWAVQGKQA-UHFFFAOYSA-N calcium;octadecyl 2-hydroxypropanoate Chemical compound [Ca].CCCCCCCCCCCCCCCCCCOC(=O)C(C)O HUTIVPWAVQGKQA-UHFFFAOYSA-N 0.000 description 3
- 238000006911 enzymatic reaction Methods 0.000 description 3
- 238000004898 kneading Methods 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 235000002949 phytic acid Nutrition 0.000 description 3
- 239000000467 phytic acid Substances 0.000 description 3
- 229940068041 phytic acid Drugs 0.000 description 3
- 239000000758 substrate Substances 0.000 description 3
- XWNSFEAWWGGSKJ-UHFFFAOYSA-N 4-acetyl-4-methylheptanedinitrile Chemical compound N#CCCC(C)(C(=O)C)CCC#N XWNSFEAWWGGSKJ-UHFFFAOYSA-N 0.000 description 2
- 244000068988 Glycine max Species 0.000 description 2
- 235000010469 Glycine max Nutrition 0.000 description 2
- 239000004153 Potassium bromate Substances 0.000 description 2
- 229920002472 Starch Polymers 0.000 description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 2
- 239000011668 ascorbic acid Substances 0.000 description 2
- 229960005070 ascorbic acid Drugs 0.000 description 2
- 235000010323 ascorbic acid Nutrition 0.000 description 2
- OGBUMNBNEWYMNJ-UHFFFAOYSA-N batilol Chemical class CCCCCCCCCCCCCCCCCCOCC(O)CO OGBUMNBNEWYMNJ-UHFFFAOYSA-N 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000004440 column chromatography Methods 0.000 description 2
- 238000000502 dialysis Methods 0.000 description 2
- 238000010828 elution Methods 0.000 description 2
- 229940094037 potassium bromate Drugs 0.000 description 2
- 235000019396 potassium bromate Nutrition 0.000 description 2
- 238000004904 shortening Methods 0.000 description 2
- 235000019698 starch Nutrition 0.000 description 2
- 239000008107 starch Substances 0.000 description 2
- OWEGMIWEEQEYGQ-UHFFFAOYSA-N 100676-05-9 Natural products OC1C(O)C(O)C(CO)OC1OCC1C(O)C(O)C(O)C(OC2C(OC(O)C(O)C2O)CO)O1 OWEGMIWEEQEYGQ-UHFFFAOYSA-N 0.000 description 1
- 241000228212 Aspergillus Species 0.000 description 1
- 240000002791 Brassica napus Species 0.000 description 1
- 235000004977 Brassica sinapistrum Nutrition 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- OUYCCCASQSFEME-QMMMGPOBSA-N L-tyrosine Chemical compound OC(=O)[C@@H](N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-QMMMGPOBSA-N 0.000 description 1
- 102000004882 Lipase Human genes 0.000 description 1
- 108090001060 Lipase Proteins 0.000 description 1
- 239000004367 Lipase Substances 0.000 description 1
- GUBGYTABKSRVRQ-PICCSMPSSA-N Maltose Natural products O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1O[C@@H]1[C@@H](CO)OC(O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-PICCSMPSSA-N 0.000 description 1
- 102000035195 Peptidases Human genes 0.000 description 1
- 108091006629 SLC13A2 Proteins 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 238000002835 absorbance Methods 0.000 description 1
- VJHCJDRQFCCTHL-UHFFFAOYSA-N acetic acid 2,3,4,5,6-pentahydroxyhexanal Chemical compound CC(O)=O.OCC(O)C(O)C(O)C(O)C=O VJHCJDRQFCCTHL-UHFFFAOYSA-N 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- 239000000872 buffer Substances 0.000 description 1
- 239000005018 casein Substances 0.000 description 1
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 1
- 235000021240 caseins Nutrition 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 235000012343 cottonseed oil Nutrition 0.000 description 1
- 238000003028 enzyme activity measurement method Methods 0.000 description 1
- 230000003100 immobilizing effect Effects 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 235000019421 lipase Nutrition 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 108090000765 processed proteins & peptides Proteins 0.000 description 1
- 235000019419 proteases Nutrition 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 230000001953 sensory effect Effects 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000002195 soluble material Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 235000013322 soy milk Nutrition 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- YNJBWRMUSHSURL-UHFFFAOYSA-N trichloroacetic acid Chemical compound OC(=O)C(Cl)(Cl)Cl YNJBWRMUSHSURL-UHFFFAOYSA-N 0.000 description 1
- OUYCCCASQSFEME-UHFFFAOYSA-N tyrosine Natural products OC(=O)C(N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-UHFFFAOYSA-N 0.000 description 1
- 238000010792 warming Methods 0.000 description 1
- 235000020985 whole grains Nutrition 0.000 description 1
Landscapes
- Bakery Products And Manufacturing Methods Therefor (AREA)
Abstract
Description
【発明の詳細な説明】
産業上の利用分野
本発明はフィターゼを含有する生地およびそれを用いる
パンの製造法に関する。DETAILED DESCRIPTION OF THE INVENTION Field of the Invention The present invention relates to a dough containing phytase and a method for producing bread using the same.
従来の技術
従来よりパン生地の物性の改善とパンの品質向上のため
、いろいろな製パン改良剤が使用されている。例えば、
各種の乳化剤(モノグリセリド、ステアリル乳酸カルシ
ウムなど)、酸化還元剤(臭素酸カリウム、アスコルビ
ン酸など)、酵素剤(アミラーゼ、プロテアーゼ、リパ
ーゼなど)が使用されている。また優れた製パン改良剤
である活性グルテン(特開昭60−30644号公報、
6〇−78549号公報〉及び、ラオスフォリパーゼA
を含有する生地を常法により処理したパンの製造法(特
開昭59−88040号公報)などが知られている。BACKGROUND OF THE INVENTION Conventionally, various bread improving agents have been used to improve the physical properties of bread dough and improve the quality of bread. for example,
Various emulsifiers (monoglycerides, calcium stearyl lactate, etc.), redox agents (potassium bromate, ascorbic acid, etc.), and enzyme agents (amylase, protease, lipase, etc.) are used. Active gluten, which is an excellent bread improving agent (Japanese Patent Application Laid-Open No. 60-30644,
Publication No. 60-78549> and Laosfolipase A
A method for producing bread (Japanese Unexamined Patent Application Publication No. 88040/1983) is known in which bread containing dough is processed by a conventional method.
フィターゼを食品(原料)に用いる例として、固定化し
て豆乳中のフィチン酸の除去に用いる例[食工誌、 3
2.174(1985) ) 、大豆および綿実のフィ
チン酸の除去に用いる例〔ジャーナル・オブ・アグリカ
ルチュラル・アンド・フード・ケミストリー(J、 ^
gric、Food Cheln、)、 36.25
9 and 1181(1988) ]などが知られて
いる。An example of using phytase in foods (raw materials) is an example of immobilizing it and using it to remove phytic acid from soy milk [Food Engineering Journal, 3
2.174 (1985)), an example of its use in the removal of phytic acid from soybeans and cottonseed [Journal of Agricultural and Food Chemistry (J, ^
gric, Food Chelln, ), 36.25
9 and 1181 (1988)] are known.
しかしフィターゼを添加してパンを製造したという報告
はこれまでにない。However, there have been no reports to date of the production of bread with the addition of phytase.
発明が解決しようとする課題
本発明の目的は優れた物性を有する生地および晶質のよ
いパン製品の提供にある。Problems to be Solved by the Invention An object of the present invention is to provide dough having excellent physical properties and bread products with good crystallinity.
課題を解決するための手段
本発明はフィターゼを含有する生地およびフィターゼを
含有する生地を調製し、ついで該調製物を分割、成型後
焼成することを特徴とするパンの製造法に関する。Means for Solving the Problems The present invention relates to a method for producing bread, which comprises preparing a phytase-containing dough and a phytase-containing dough, and then dividing the preparation, shaping it, and then baking it.
フィツーゼとしては植物、微生物由来のもので、アミラ
ーゼおよびプロテアーゼの含有量が後記参考鋼上に示し
たプロテアーゼおよびアミラーゼ活性表示法で0.25
単位以下であればいずれも用いられるが、具体的には参
考例1で得られた精製酵素が用いられる。後記参考例2
に製パンにおよぼすプロテアーゼの影響について示す。Phytuse is derived from plants and microorganisms, and the content of amylase and protease is 0.25 according to the protease and amylase activity display method shown on the reference steel below.
Although any enzyme can be used as long as it is less than one unit, specifically, the purified enzyme obtained in Reference Example 1 is used. Reference example 2 below
The effects of proteases on bread making are shown below.
フィツーゼの添加量は原料小麦粉の品質、製パン法、原
料配合などによって決定されるが、−船釣には後記参考
例1に示したフィターゼ活性表示法で、小麦粉1kgあ
たり50〜5000単位が適当である。The amount of phytuse added is determined by the quality of the raw flour, bread-making method, raw material composition, etc. - For boat fishing, 50 to 5000 units per kg of flour is appropriate according to the phytase activity display method shown in Reference Example 1 below. It is.
フィツーゼは通常、生地温握時に添加される。Fituse is usually added during dough warming.
別の方法として、小麦粉に混合させる方法や、各種副原
料を混合した製パン用小麦粉配合品に含有させる方法が
ある。Other methods include a method of mixing it with wheat flour, and a method of including it in a flour blend for bread making mixed with various auxiliary materials.
フィツーゼは他の改良剤と併用することもできる。改良
剤としては酸化還元剤例えば、臭素酸カリウム、アスコ
ルビン酸など、乳化剤例えば、モノグリセリド、ステア
リル乳酸カルシウムなど、また活性グルテンなどがあげ
られる。それらの添加量は通常小麦粉に対して酸化還元
剤の場合0.0005〜0.01%(w/w)、乳化剤
の場合0.05〜0.5%(iv/w)、活性グルテン
の場合0.5〜5.0%(w/W)である。Phytuse can also be used in combination with other improving agents. Examples of improving agents include redox agents such as potassium bromate and ascorbic acid, emulsifiers such as monoglycerides and calcium stearyl lactate, and activated gluten. The amount of these additives is usually 0.0005 to 0.01% (w/w) for redox agents, 0.05 to 0.5% (iv/w) for emulsifiers, and 0.05 to 0.5% (iv/w) for active gluten based on wheat flour. It is 0.5-5.0% (w/W).
本発明にかかわるフィツーゼは製パン法の中種法、スト
レート法いずれの方法にも適用される。The phytuse according to the present invention can be applied to both the medium bread method and the straight bread manufacturing method.
製パン法として中種法を用いる場合は小麦粉、パン酵母
を主成分とする中種原料、または小麦粉、砂糖、シa−
)ニングを主成分とする本捏原料の少なくとも一方にフ
ィツーゼ、さらに必要に応じて、酸化還元剤、乳化剤ま
たは活性グルテンを添加すればよいが、フィツーゼは中
種原料に添加しておいた方がより好ましい。When using the dough method as a bread making method, wheat flour, dough raw materials whose main ingredients are baker's yeast, or wheat flour, sugar, and
) Phytuse may be added to at least one of the main ingredients of this kneaded raw material, and if necessary, a redox agent, an emulsifier, or an active gluten may be added, but it is better to add phytuse to the intermediate raw material. More preferred.
中種法を用いてパンを製造する場合は、例えば次の如く
して行なう。小麦粉、パン酵母を主成分とする中種原料
に水を加えて混捏し、通常25〜35℃で2〜5時間発
酵(中種発酵)する。該発酵物を小麦粉、砂糖、ショー
トニングを主成分とする本捏原料と混せ水を加えて混捏
し、生地をつくる。When manufacturing bread using the dough method, it is carried out, for example, as follows. Water is added to a dough raw material whose main ingredients are wheat flour and baker's yeast, and the mixture is kneaded and fermented (dough fermentation), usually at 25 to 35°C for 2 to 5 hours. The fermented product is mixed with the main ingredients for kneading, which are flour, sugar, and shortening, and water is added and kneaded to form dough.
該生地を通常25〜35℃で10〜40分間(フロア−
タイム)放置する。ついで、目的とするパンに応じて分
割し、通常15〜35℃で10〜30分間(ベンチタイ
ム)放置する。ついで、生地を成型し、型に入れ、通常
35〜45℃で一定の高さに生地が膨張するまで最終発
酵を行った後、180〜240℃で10〜30分間焼成
を行ない、パンを製造する。The dough is usually heated at 25 to 35°C for 10 to 40 minutes (on the floor).
time) leave it alone. Then, the bread is divided into pieces according to the intended bread, and is usually left at 15 to 35°C for 10 to 30 minutes (bench time). Next, the dough is shaped, placed in a mold, and subjected to final fermentation until the dough expands to a certain height, usually at 35 to 45 degrees Celsius, and then baked at 180 to 240 degrees Celsius for 10 to 30 minutes to produce bread. do.
また、ストレート法を用いてパンを製造する場合は例え
ば次の如くして行なう。小麦粉、砂糖、ショートニング
、イーストフードなどを主成分とする原料に水を加え、
混捏した後、該混捏物を通常25〜35℃で60〜18
0分間発酵する。ついで、目的とするパンに応じて生地
を分割し、通常10〜30分間〈ベンチタイム)、15
〜35℃で放置する。放置後、生地を成型し、型に入れ
、通常35〜45℃で一定の高さに生地が膨張するまで
最終発酵を行なう。ついで、180〜240℃で10〜
30分間焼成してパンを製造する。Moreover, when bread is manufactured using the straight method, it is carried out as follows, for example. Add water to raw materials whose main ingredients are flour, sugar, shortening, yeast food, etc.
After kneading, the kneaded product is usually heated to 60 to 18 ℃ at 25 to 35℃.
Ferment for 0 minutes. Next, divide the dough into pieces depending on the desired bread and bake for 10 to 30 minutes (bench time), 15 minutes.
Leave at ~35°C. After standing, the dough is shaped, placed in a mold, and subjected to final fermentation, usually at 35 to 45°C, until the dough expands to a certain height. Then, at 180-240℃ for 10~
Bake for 30 minutes to make bread.
さらに本発明の場合、小麦粉の代わりに小麦の皮部を含
む粉(以下全粒粉と称す)を用いても前記と同様に中種
法、ストレート法が適用できる。Furthermore, in the case of the present invention, even if flour containing the skin of wheat (hereinafter referred to as whole wheat flour) is used instead of wheat flour, the dough method and the straight method can be applied in the same manner as described above.
超上の如くして得られるパンは容積が太き(、内部は良
く膜伸びした構造および適度な軟らかさを有し、また、
保存中の老化も少ないという優れた特徴を有している。The bread obtained in the above manner has a large volume (with a well-stretched internal structure and moderate softness, and
It has an excellent feature of little aging during storage.
以下に実施例および参考例を示す。Examples and reference examples are shown below.
実施例1゜
本実施例では、参考例1で調製したフイターゼの強力小
麦粉〈蛍白含量X 2.1%〉に対する製パン改良効果
を示す。Example 1 This example shows the effect of phytase prepared in Reference Example 1 on improving bread making on strong wheat flour (fluorescence content X 2.1%).
次の工程によりパンを製造した。Bread was manufactured by the following steps.
第1表に各試験区の添加剤と添加量を示し、第2表に3
日後の生地物性および製品品質(比容積、相対老化度〉
の評価を示す。Table 1 shows the additives and amounts added in each test area, and Table 2 shows the additives and amounts added.
Fabric physical properties and product quality after days (specific volume, relative aging degree)
Indicates the evaluation of
第 1 表
フロア−タイム(28℃、40分間)
分割
ベンチタイム(室温、15分間)
或 を
ブルーフ(40℃、40分間)
圭
焼 或(220℃、25分間〉
土
パン
第
表
(注)16 生地物性の評価基準(熟練技術者による
官能評価〉 :5 非常に良好。Table 1 Floor time (28℃, 40 minutes) Split bench time (room temperature, 15 minutes) Or Bruf (40℃, 40 minutes) Keiyaki (220℃, 25 minutes) Soil bread Table (Note) 16 Evaluation criteria for fabric physical properties (sensory evaluation by skilled technicians): 5 Very good.
4 良好、3 普通、2 やや劣る。4 Good, 3 Fair, 2 Slightly poor.
1 劣る
2、比容積 : なたね置換法
3、相対老化度 : クリープメーター〈山型社製)を
用いて測定し、無添加
区の懐を100とした相対値で表した。1 Inferior 2. Specific volume: Rapeseed replacement method 3. Relative aging degree: Measured using a creep meter (manufactured by Yamagata Co., Ltd.), and expressed as a relative value with the volume of the additive-free area set as 100.
無添加区に比べて試験区■および■は、いずれも生地物
性が改良され、比容積が増大し、■、■とフィターゼの
添加量が増すにつれてパンの老化は抑制された。Compared to the additive-free plots, in both test plots ① and ②, the physical properties of the dough were improved, the specific volume increased, and as the amount of phytase added increased, staleness of the bread was suppressed.
実施例2゜
本実施例では、低蛋白小麦粉(蛋白含浸8.9%)に対
するフィターゼの製パン改良効果を示す。実施例1にお
いて使用した強力小麦粉の代わりに低蛋白小麦粉を用い
る以外は実施例1と同様に行った。ただし、製パン吸水
は57とした。Example 2 This example shows the bread making improvement effect of phytase on low protein wheat flour (8.9% protein impregnation). The same procedure as in Example 1 was carried out except that low protein wheat flour was used instead of the strong wheat flour used in Example 1. However, the bread making water absorption was set at 57.
第3表に2B後の生地物性および製品品質(比容積、相
対老化度)の評価を示す。Table 3 shows evaluations of fabric properties and product quality (specific volume, relative aging degree) after 2B.
第
表
(注)評価方法:第2表の場合と同じ
低蛋白小麦粉はフィターゼ無添加の場合、生地物性、比
容積および相対老化度のいずれも強力小麦粉よりも劣る
が、フィターゼ添加により生地物性(特に非粘着性、弾
力性)、比容積および老化度いずれも大いに改養された
。Table (Note) Evaluation method: The same low-protein flour as in Table 2 is inferior to strong flour in terms of physical properties, specific volume, and relative aging when no phytase is added, but with the addition of phytase, the physical properties of the dough In particular, the non-adhesion, elasticity), specific volume and degree of aging were greatly improved.
実施例3゜
本実施例では全粒粉に対するフィクーゼの製パン改良効
果を示す。実施例1において使用した強力小麦粉の代わ
りに全粒粉を用いる以外は実施例1と同様に行った。た
だし、製パン吸水は70とした。Example 3 This example shows the bread-making improvement effect of ficuse on whole wheat flour. The same procedure as in Example 1 was conducted except that whole wheat flour was used instead of the strong wheat flour used in Example 1. However, the bread making water absorption was set at 70.
第4表に2B後の生地物性および製品品質(比容積、相
対老化度)の評価を示す。Table 4 shows evaluations of fabric properties and product quality (specific volume, relative aging degree) after 2B.
第 4 表
中種発酵く28℃、4時間)
(注〉評価方法:第2表の場合と同じ
全粒粉の場合、フィターゼ無添加区の生地物性、比容積
および相対老化度は、低蛍由小麦粉よりもさらに劣るが
、フィターゼ添加により生地物性(特に非粘着性、弾力
性)、比容積および相対老化度がいずれも大いに改善さ
れた。Table 4: Soybean fermentation at 28°C for 4 hours) (Note: Evaluation method: In the case of whole wheat flour, which is the same as in Table 2, the dough physical properties, specific volume, and relative aging degree of the phytase-free group are the same as those for low-fluorescence flour. Although even worse than that, the addition of phytase significantly improved the physical properties of the dough (particularly non-stickiness and elasticity), specific volume, and relative aging rate.
実施例4゜
本実施例では、全粒粉を60%使用した中種法にてパン
を製造した際のフィターゼの製パン改良効果を示す。Example 4 This example shows the effect of phytase on improving bread production when bread is produced using the dough method using 60% whole grain flour.
次の工程によりパンを製造する。Bread is manufactured through the following steps.
↓
フロア−タイム(室温、15分間)
↓
分割
↓
ベンチタイム(室温、15分間〉
↓
成型
ブルーフく40℃、40分間〉
焼 Fyj、(220℃、25分間)
↓
パン
第5表に2日後の生地物性および製品品質(比容積およ
び相対老化度)の評価を示す。↓ Floor time (room temperature, 15 minutes) ↓ Division ↓ Bench time (room temperature, 15 minutes) ↓ Forming dough at 40℃, 40 minutes > Baking (220℃, 25 minutes) ↓ Bread Table 5 shows the results after 2 days Evaluation of fabric physical properties and product quality (specific volume and relative aging degree) is shown.
第 5 表
第7表に2日後の生地物性および製品品質容積、相対老
化度〉の評価を示す。Table 5 Table 7 shows the evaluation of the physical properties of the dough, product quality, volume, and relative aging degree after 2 days.
第 6 表
(注)評価方法:第2表の場合と同じ
実施例1の場合と同様に試験区■および■においては、
試験区Iに比べて、生地物性、比容積および相対老化度
が改善された。Table 6 (Note) Evaluation method: Same as in Table 2 As in Example 1, in test plots ■ and ■,
Compared to Test Group I, the physical properties of the fabric, the specific volume, and the relative degree of aging were improved.
実施例5゜
本実施例ではフィターゼと他の改良剤との併用例として
、パン製造に広く使用されているステアリル乳酸カルシ
ウム(C3L)および活性グルテン〔プロピアン(協和
発酵工業株式会社製〉〕との併用効果を示す。第6表に
示した添加剤を用いる以外は実施例4と同様に行った。Example 5 In this example, as an example of the combination of phytase and other improving agents, calcium stearyl lactate (C3L), which is widely used in bread manufacturing, and active gluten [propian (manufactured by Kyowa Hakko Kogyo Co., Ltd.]) were used. The effect of combined use is shown.The same procedure as in Example 4 was carried out except that the additives shown in Table 6 were used.
(注)
第
表
評価方法:第2表の場合と同じ
CSLを単独に使用した場合(試験区■)比容積が無添
加よりも低くなるがフィツーゼの添加により(試験区■
〉無添加のレベルまで向上した。(Note) Evaluation method in Table 2: When the same CSL as in Table 2 is used alone (test area ■), the specific volume is lower than without addition, but with the addition of fituse (test area ■
〉Improved to the level of no additives.
また生地物性および相対老化度に関してはフィツーゼの
単独使用により(試験区■)かなり改善されたが、さら
にC3Lまたはプロピアンを併用することにより(試験
区■または■)、相乗的に改善された。In addition, the physical properties of the fabric and the relative degree of aging were significantly improved by using fituse alone (test group ■), but were further improved synergistically by using C3L or propian in combination (test group ■ or ■).
参考例1゜
(精製フィツーゼの調製法)
アスペルギルス起源のフィツーゼ(シグマ社製、粗酵素
)を用いて以下の方法でm製した。Reference Example 1 (Preparation method of purified phytuse) Phytose derived from Aspergillus (manufactured by Sigma, crude enzyme) was used to produce m in the following method.
粗酵素粉末
透析/1hM酢酸緩衝液(pH5,0)[][]!A巳
−ツーセファロースムクロマトグラフィー20 m−5
0mM酢酸緩衝液溶出画分CM−セルロース カラムク
ロマトグラフィー20yn〜200mM酢酸緩衝液溶出
画分よ
りEAB−セルロース カラムクロマトグラフィーO〜
0. IM NaC1/10mM酢酸緩衝液溶ib画分
透析/10mM)リス−塩酸緩衝Fi、(pH7,0)
精製フィツーゼ
酵素活性測定法
フィツーゼ活性は、〔プレバラティブ・バイオケミスト
リー(Prep、 Biochem、)、 17.
63(1987)〕の方法に準じて行った。本活性測
定法は基質に0.8mM (最終濃度)フィチン酸を用
い、pH5,5,30℃で5分間の酵素反応によって生
成するリン酸を測定するものであり、活性の定義は1分
間に1μモルのリン酸を生成する酵素量を1単位とした
。Crude enzyme powder dialysis/1 hM acetate buffer (pH 5,0) [] []! Ami-2 sepharoseme chromatography 20 m-5
0mM acetate buffer elution fraction CM-cellulose column chromatography 20yn~200mM acetate buffer elution fraction EAB-cellulose column chromatography O~
0. IM NaC1/10mM acetate buffer solution ib fraction dialysis/10mM) Lis-HCl buffer Fi, (pH 7,0)
Purified Phytuse Enzyme Activity Measurement Method Phytuse activity was determined by [Preparative Biochemistry (Prep, Biochem), 17.
63 (1987)]. This activity measurement method uses 0.8mM (final concentration) phytic acid as a substrate and measures the phosphoric acid produced by an enzymatic reaction at pH 5, 5, and 30°C for 5 minutes. The amount of enzyme that produced 1 μmol of phosphoric acid was defined as 1 unit.
プロテアーゼ活性は、基質に0.5%(最終濃度)カゼ
インを用い、pH5,5,30℃で10分間の酵素反応
を行い、生成するアミノ酸ペプチドを吸光度280nm
で測定するものであり、活性の定義は1分間に1μモル
のチロシンに相当するトリクロロ酢酸可溶物を生成する
酵素量を1単位とした。Protease activity was determined by using 0.5% (final concentration) casein as a substrate, performing an enzymatic reaction at pH 5, 5, and 30°C for 10 minutes, and measuring the resulting amino acid peptide with an absorbance of 280 nm.
The activity is defined as the amount of enzyme that produces trichloroacetic acid soluble material corresponding to 1 μmol of tyrosine per minute.
アミラーゼ活性は、基質に0.5%(最終濃度〉可溶性
デンプンを用い、pH5,5,30℃で10分間の酵素
反応によって生成する還元糖を測定するものであり、活
性の定義は1分間に1μモルのマルトースに相当する還
元糖を生成する酵素量を1単位とした。Amylase activity is a measurement of reducing sugar produced by an enzymatic reaction for 10 minutes at pH 5, 5, 30°C using 0.5% (final concentration) soluble starch as a substrate, and the definition of activity is 0.5% (final concentration) soluble starch. The amount of enzyme that produces reducing sugar equivalent to 1 μmol of maltose was defined as 1 unit.
第8表に上記の精製に用いた粗酵素と得られた精製酵素
のフィツーゼ、プロテアーゼおよびアミラーゼの比活性
(蛋白1■あたりの単位〉を示す。Table 8 shows the specific activities of phytuse, protease and amylase (units per square protein) of the crude enzyme used in the above purification and the purified enzyme obtained.
なおタンパク質はFolin−Lowry法にて測定し
た。Note that protein was measured by the Folin-Lowry method.
第 8 表
参考例2゜
(製パンにおよぼすプロテアーゼの影響〉第9表に参考
例1で得られたプロテアーゼ画分の製パンにおよぼす影
響を示す。製パンは全粒粉の代わりに中種原料の70%
強力小麦粉(製パン吸水42〉、本捏原料の30%強力
小麦粉(製パン吸水23)を用いる以外は実施例4ε同
様に行った。Table 8 Reference Example 2゜ (Influence of protease on bread making) Table 9 shows the influence of the protease fraction obtained in Reference Example 1 on bread making. 70%
The same procedure as in Example 4ε was carried out except that strong wheat flour (bread making water absorption 42) and 30% strong wheat flour (bread making water absorption 23) used as the raw material for kneading were used.
第 9 表
プロテアーゼ0.5単位の添加で明らかな悪影響がみら
れる。Table 9. Addition of 0.5 units of protease has a clear negative effect.
発明の効果
本発明の方法によりフィターゼを用いることによりパン
生地の物性(特に非粘着性、弾力性〉およびパン製品の
品質〈比容積、相対老化度〉を非常に改善することがで
きる。Effects of the Invention By using phytase according to the method of the present invention, the physical properties of bread dough (especially non-stickiness and elasticity) and the quality of bread products (specific volume, relative aging degree) can be greatly improved.
Claims (2)
製物を分割、成型後焼成することを特徴とするパンの製
造法。(2) A method for producing bread, which comprises preparing a dough containing phytase, dividing the preparation into portions, shaping them, and then baking them.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP21191989A JPH0376529A (en) | 1989-08-17 | 1989-08-17 | Dough and producing of bread using the same dough |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP21191989A JPH0376529A (en) | 1989-08-17 | 1989-08-17 | Dough and producing of bread using the same dough |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH0376529A true JPH0376529A (en) | 1991-04-02 |
Family
ID=16613839
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP21191989A Pending JPH0376529A (en) | 1989-08-17 | 1989-08-17 | Dough and producing of bread using the same dough |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0376529A (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2721804A1 (en) * | 1994-07-01 | 1996-01-05 | Keddar Alain | Sterilisation by heat treatment of powdered food product |
WO2010135588A2 (en) | 2009-05-21 | 2010-11-25 | Verenium Corporation | Phytases, nucleic acids encoding them and methods for making and using them |
EP2397486A1 (en) | 2006-09-21 | 2011-12-21 | Verenium Corporation | Phytases, nucleic acids encoding them and methods for making and using them |
WO2014067933A1 (en) | 2012-10-31 | 2014-05-08 | C-Lecta Gmbh | Bioactive carrier preparation for enhanced safety in care products and food |
RU2643712C1 (en) * | 2016-11-16 | 2018-02-05 | Федеральное государственное автономное научное учреждение "Научно-исследовательский институт хлебопекарной промышленности" (ФГАНУ НИИХП) | Method for manufacturing bakery products |
-
1989
- 1989-08-17 JP JP21191989A patent/JPH0376529A/en active Pending
Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2721804A1 (en) * | 1994-07-01 | 1996-01-05 | Keddar Alain | Sterilisation by heat treatment of powdered food product |
EP2397486A1 (en) | 2006-09-21 | 2011-12-21 | Verenium Corporation | Phytases, nucleic acids encoding them and methods for making and using them |
EP2617819A2 (en) | 2006-09-21 | 2013-07-24 | Verenium Corporation | Phytases, nucleic acids encoding them and methods for making and using them |
EP2617821A2 (en) | 2006-09-21 | 2013-07-24 | Verenium Corporation | Phytases, nucleic acids encoding them and methods for making and using them |
EP2617729A2 (en) | 2006-09-21 | 2013-07-24 | Verenium Corporation | Phytases, nucleic acids encoding them and methods for making and using them |
EP2617820A2 (en) | 2006-09-21 | 2013-07-24 | Verenium Corporation | Phytases, nucleic acids encoding them and methods for making and using them |
EP2617823A2 (en) | 2006-09-21 | 2013-07-24 | Verenium Corporation | Phytases, nucleic acids encoding them and methods for making and using them |
EP2617728A2 (en) | 2006-09-21 | 2013-07-24 | Verenium Corporation | Phytases, nucleic acids encoding them and methods for making and using them |
WO2010135588A2 (en) | 2009-05-21 | 2010-11-25 | Verenium Corporation | Phytases, nucleic acids encoding them and methods for making and using them |
WO2014067933A1 (en) | 2012-10-31 | 2014-05-08 | C-Lecta Gmbh | Bioactive carrier preparation for enhanced safety in care products and food |
RU2643712C1 (en) * | 2016-11-16 | 2018-02-05 | Федеральное государственное автономное научное учреждение "Научно-исследовательский институт хлебопекарной промышленности" (ФГАНУ НИИХП) | Method for manufacturing bakery products |
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