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JPH0144311B2 - - Google Patents
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JPH0144311B2 - - Google Patents

Info

Publication number
JPH0144311B2
JPH0144311B2 JP1125282A JP1125282A JPH0144311B2 JP H0144311 B2 JPH0144311 B2 JP H0144311B2 JP 1125282 A JP1125282 A JP 1125282A JP 1125282 A JP1125282 A JP 1125282A JP H0144311 B2 JPH0144311 B2 JP H0144311B2
Authority
JP
Japan
Prior art keywords
rice
sake
enzyme
liquefied
liquefaction
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
Application number
JP1125282A
Other languages
Japanese (ja)
Other versions
JPS58129968A (en
Inventor
Juichi Akyama
Toshio Tanaka
Cheko Kumagai
Kenzo Morinaga
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.)
KH Neochem Co Ltd
Original Assignee
Kyowa Hakko Kogyo Co Ltd
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 Kyowa Hakko Kogyo Co Ltd filed Critical Kyowa Hakko Kogyo Co Ltd
Priority to JP57011252A priority Critical patent/JPS58129968A/en
Publication of JPS58129968A publication Critical patent/JPS58129968A/en
Publication of JPH0144311B2 publication Critical patent/JPH0144311B2/ja
Granted legal-status Critical Current

Links

Classifications

    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P60/00Technologies relating to agriculture, livestock or agroalimentary industries
    • Y02P60/80Food processing, e.g. use of renewable energies or variable speed drives in handling, conveying or stacking
    • Y02P60/87Re-use of by-products of food processing for fodder production

Landscapes

  • Fodder In General (AREA)
  • Alcoholic Beverages (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

本発明は米または白糠から液化液および固型粕
の製造法に関する。さらに詳しくは米または白糠
を好熱性液化酵素のみによつて液化し、ついで固
液分離することを特徴とする液化液および固型粕
の製造法に関する。 従来、酒造用白米に液化酵素および糖化酵素を
作用させて糖化し、これを清酒もろみに添加して
清酒を製造することは広く行なわれている。また
白糠、屑米、砕米等に液化酵素および糖化酵素を
作用させ、不溶物を除去し、ついでイオン交換樹
脂等で精製して得た糖化液を清酒もろみに添加し
て清酒を製造する方法も公知である(特開昭52−
79088等)。 本発明者らは従来法と異なり酵素の併用にか
え、好熱性液化酵素のみを使用する場合には得ら
れる液化液は清酒製造用に好適な性質を有し、一
方固型粕も食品原料用、飼料用等に好適な性質を
有することを見いだし本発明を完成した。 本発明で得られる液化液中の溶質成分は直糖、
少糖類、可溶性デキストリン等よりなり、アミノ
酸および可溶性蛋白の含量は液化酵素および糖化
酵素併用の場合に比べ少ない。蛋白質およびアミ
ノ酸は清酒の香味、色沢を低下させる。したがつ
て従来の清酒製造において良い品質のものを得る
ためには精白度の高い米を用いるか、イオン交換
樹脂処理等により蛋白質、アミノ酸を除く必要が
あつた。 ところが本法で得られる液化液は精製すること
なく直接清酒もろみに添加しても優れた品質の清
酒を製造し得る。 また清酒もろみに添加する糖化液の原料として
古米を使用した場合、清酒に古米酒臭が発生し品
質を低下させる。ところが、本発明で古米を使用
した場合に得られる液化液を用いて清酒を製造す
る場合は古米酒臭の発生を防止できる。 さらに本発明で得られる液化液中の直糖は全糖
に対して半分以下である。したがつて甘味度を抑
えてエキス分を付与できるので清酒の濃味を増加
させるために本発明の液化液は好都合である。 また本発明の液化液は食品または調味料の甘味
および濃味付与に利用し得る。 本発明で得られる固型粕には蛋白質および繊維
質が濃縮されており、高蛋白質のダイエツト食品
や飼料として好適である。 次に本発明をさらに詳しく説明する。 本発明で使用する米としては精白の程度にかか
わらず、新米、古米、屑米、砕米等いずれでもよ
い。白糠は酒造米の精白によつて生ずる糠であ
る。好熱性の液化酵素としては α−アミラーゼ活性(単位/g酵素)/プロテア
ーゼ活性(単位/g酵素) が5以上のものが好適に使用され、市販品として
α−アミラーゼM−30〔協和マイルス(株)製〕、スピ
ターゼXP−317〔長瀬産業(株)製〕、クライスターゼ
〔大和化成(株)製〕、アミラーゼAD1〔天野製薬(株)
製〕、コクゲン〔大和化成(株)製〕等がある。上記
でα−アミラーゼ活性およびプロテアーゼ活性は
国税庁所定分析法によつた。 好熱性液化酵素の使用量は米または白糠1Kgに
対し、α−アミラーゼM−30(α−アミラーゼ活
性:127万単位/g酵素)を用いるとして0.01−
3gが適当である。米または白糠1Kgに対して使
用する水は0.8−10が適当である。 液化温度は40−90℃が可能であるが、好熱性酵
素の特徴を生かすため65−80℃が好ましい。65−
80℃で液化を行なう場合には液化に先立つての米
および白糠の蒸煮は不要であるが、行なつてもよ
い。無蒸煮(生の原料を用いる場合の他、蒸気を
吹き抜けさせて米を加温させる程度の場合も含
む)の場合は糊状にならず、液化終了後過等の
固液分離が容易であるという利点がある。また65
−80℃で液化を行なう場合には雑菌の繁殖を抑え
るための薬剤によるPHの低下を必要としない。 上記のごとき条件下で通常2時間〜2日で液化
が終了する。液化終了後、過、遠心分離等によ
つて液化液と固型粕に分離する。 次に本発明の実施例を示す。 実施例 1 生米または生白糠各1Kgとそれぞれα−アミラ
ーゼM−30、0.34gを含んだ温水2とを混合
し、70℃で24時間液化した後綿布プレス過し
た。 得られた液化液および固型粕の性質について分
析した結果を第1表および第2表に示す。
The present invention relates to a method for producing liquefied liquid and solid lees from rice or white rice bran. More specifically, the present invention relates to a method for producing a liquefied liquid and solid lees, which is characterized by liquefying rice or white rice bran using only a thermophilic liquefying enzyme and then separating the solid and liquid. Conventionally, it has been widely practiced to saccharify polished rice for sake brewing by applying a liquefaction enzyme and a saccharifying enzyme, and then add this to sake mash to produce sake. There is also a method of producing sake by applying liquefying enzymes and saccharifying enzymes to white rice bran, scrap rice, broken rice, etc. to remove insoluble matter, and then purifying with ion exchange resin, etc., and adding the resulting saccharified liquid to sake mash. It is publicly known (Japanese Unexamined Patent Application Publication No. 1983-1999)
79088 etc.). The present inventors found that when using only a thermophilic liquefaction enzyme instead of using enzymes in combination with the conventional method, the liquefied liquid obtained has properties suitable for sake production, and on the other hand, the solid lees can also be used as a food raw material. The present invention was completed based on the discovery that it has properties suitable for use as feed, etc. The solute components in the liquefied liquid obtained by the present invention are straight sugar,
It consists of oligosaccharides, soluble dextrins, etc., and the content of amino acids and soluble proteins is lower than when liquefying enzymes and saccharifying enzymes are used together. Proteins and amino acids reduce the flavor and color of sake. Therefore, in order to obtain good quality sake in conventional sake production, it was necessary to use highly polished rice or to remove proteins and amino acids by treatment with an ion exchange resin. However, the liquefied liquid obtained by this method can be added directly to sake mash without purification to produce sake of excellent quality. Furthermore, if old rice is used as a raw material for the saccharification liquid added to sake mash, the sake will have an old rice wine smell and deteriorate in quality. However, when producing sake using the liquefied liquid obtained when old rice is used in the present invention, generation of old rice sake odor can be prevented. Furthermore, the amount of straight sugar in the liquefied liquid obtained by the present invention is less than half of the total sugar. Therefore, the liquefied liquid of the present invention is advantageous for increasing the richness of sake because it can impart an extract component while suppressing the degree of sweetness. Furthermore, the liquefied liquid of the present invention can be used to impart sweetness and richness to foods or seasonings. The solid meal obtained by the present invention has concentrated protein and fiber, and is suitable as a high-protein diet food or feed. Next, the present invention will be explained in more detail. The rice used in the present invention may be new rice, old rice, waste rice, broken rice, etc., regardless of the degree of polishing. Shiranuka is the bran produced by polishing sake-brewing rice. As thermophilic liquefaction enzymes, those with α-amylase activity (units/g enzyme)/protease activity (units/g enzyme) of 5 or more are preferably used, and the commercially available product is α-amylase M-30 [Kyowa Miles ( Co., Ltd.], Spitase XP-317 [Nagase Sangyo Co., Ltd.], Klystase [Daiwa Kasei Co., Ltd.], Amylase AD1 [Amano Pharmaceutical Co., Ltd.]
[manufactured by Daiwa Kasei Co., Ltd.] and Kokugen [manufactured by Daiwa Kasei Co., Ltd.]. The above α-amylase activity and protease activity were determined according to the analytical method prescribed by the National Tax Agency. The amount of thermophilic liquefying enzyme to be used is 0.01-0.01-kg of rice or white bran, assuming that α-amylase M-30 (α-amylase activity: 1.27 million units/g enzyme) is used.
3g is appropriate. The appropriate amount of water to use for 1 kg of rice or white bran is 0.8-10. The liquefaction temperature can be 40-90°C, but 65-80°C is preferable to take advantage of the thermophilic properties of the enzyme. 65−
When liquefying is carried out at 80°C, it is not necessary to steam the fresh rice and white bran prior to liquefaction, but it may be done. In the case of non-steamed rice (including cases in which raw raw materials are used, as well as cases in which steam is blown through to warm the rice), the rice does not become paste-like, and solid-liquid separation by filtration is easy after liquefaction. There is an advantage. 65 again
When liquefying at -80°C, there is no need to lower the pH using chemicals to suppress the growth of bacteria. Under the above conditions, liquefaction is usually completed in 2 hours to 2 days. After liquefaction, the liquefied liquid and solid lees are separated by filtration, centrifugation, etc. Next, examples of the present invention will be shown. Example 1 1 kg each of raw rice or raw white rice bran and warm water 2 containing 0.34 g of α-amylase M-30 were mixed, liquefied at 70°C for 24 hours, and then filtered through a cotton cloth press. Tables 1 and 2 show the results of analyzing the properties of the obtained liquefied liquid and solid lees.

【表】 *1:レーン氏逆滴定法により定量
*2:国税庁所定分析法により定量
[Table] *1: Quantified by Lane's back titration method *2: Quantified by the National Tax Agency prescribed analysis method

【表】 *4:国税庁所定分析法により定量
実施例 2 屑米1Kgを水に浸漬した後水切りし、こしきに
入れる。ついで下部より蒸気を通し米層を吹きぬ
けた直後、α−アミラーゼM−30、0.34gを含む
温水1570mlを加え、70−75℃で20時間液化し、つ
いで綿布プレス過した。結果を第3および4表
に示す。
[Table] *4: Quantification Example 2: Soak 1 kg of rice scraps in water, drain, and put in a strainer. Immediately after blowing steam through the rice layer from the bottom, 1570 ml of warm water containing 0.34 g of α-amylase M-30 was added, liquefied at 70-75°C for 20 hours, and then filtered through a cotton cloth press. The results are shown in Tables 3 and 4.

【表】 *5:国税庁所定分析法により定量
*6:レーン氏逆滴定法により定量
[Table] *5: Quantified using the National Tax Agency prescribed analysis method *6: Quantified using Lane's back titration method

【表】 実施例 3 古々米の精白米を水に浸漬した後、水切りし、
こしきに入れる。ついで下部より蒸気を通し米層
を吹きぬけた直後、α−アミラーゼM−30、0.34
gを含む温水1660mlを加え、70−75℃で20時間液
化し、ついで綿布プレス過した。結果を第5お
よび6表に示す。
[Table] Example 3 After soaking old polished rice in water, drain it,
Put it in a strainer. Then, immediately after blowing steam through the rice layer from the bottom, α-amylase M-30, 0.34
1,660 ml of hot water containing 70 g was added to the mixture, and the mixture was liquefied at 70-75°C for 20 hours, and then filtered through a cotton cloth press. The results are shown in Tables 5 and 6.

【表】【table】

【表】 実施例 4 α米1Kgおよび水2の混合物にα−アミラー
ゼM−30、0.34gを添加し70℃で24時間液化し、
ついで綿布プレス過した。結果を第7および8
表に示す。
[Table] Example 4 0.34 g of α-amylase M-30 was added to a mixture of 1 kg of α rice and 2 water, and the mixture was liquefied at 70°C for 24 hours.
Then, it was passed through a cotton cloth press. Results 7th and 8th
Shown in the table.

【表】【table】

【表】 実施例 5 低品位屑米(デンプン価75.0%)100gを水に
浸漬した後、水切りし、こしきに入れる。ついで
下部より蒸気を通し米層を吹きぬけた直後、各種
市販好熱性液化酵素および対照としての各種市販
醸造用酵素(至適温度50〜60℃)を所定量含む温
水152mlを加え、70〜75℃で20時間液化し、つい
で4000rpmで20分遠心分離した。結果を第9表に
示す。
[Table] Example 5 After soaking 100 g of low-grade scrap rice (starch value 75.0%) in water, drain it and put it in a strainer. Immediately after blowing steam through the rice layer from the bottom, 152 ml of warm water containing a predetermined amount of various commercially available thermophilic liquefaction enzymes and various commercially available brewing enzymes as a control (optimal temperature 50 to 60°C) was added, and the mixture was heated to 70 to 75°C. The mixture was liquefied for 20 hours and then centrifuged at 4000 rpm for 20 minutes. The results are shown in Table 9.

【表】 第9表から好熱性液化酵素を使用した場合は好
熱性でない醸造用酵素を使用した場合に比べ、一
般に液量が多く(収率が高い)、アミノ酸も少な
いことがわかる。 実施例 6 液化温度を50−55℃とする以外は実施例5と同
様に処理して第10表の結果を得た。
[Table] Table 9 shows that when a thermophilic liquefaction enzyme is used, the amount of liquid is generally larger (higher yield) and the amount of amino acids is lower than when a non-thermophilic brewing enzyme is used. Example 6 The same procedure as in Example 5 was carried out except that the liquefaction temperature was set at 50-55°C, and the results shown in Table 10 were obtained.

【表】 第10表から、好熱性液化酵素を使用した場合は
好熱性でない醸造用酵素を使用した場合に比べ、
アミノ酸が少なく、かつ全糖に対する直糖の割合
が小さいことがわかる。 参考例 1 (液化液を使用する清酒の製造試験) (1) 仕込配合 第11表のとおり。
[Table] From Table 10, when using a thermophilic liquefying enzyme, compared to using a non-thermophilic brewing enzyme,
It can be seen that there are few amino acids and the ratio of direct sugar to total sugar is small. Reference example 1 (Sake production test using liquefied liquid) (1) Brewing composition As shown in Table 11.

【表】 (2) 酒母 麹エキス10mlに協会701号酵母を培養し、酒
母として使用した。 (3) 仕込温度(℃) 第12表のとおり。
[Table] (2) Sake mash Kyokai No. 701 yeast was cultured in 10ml of koji extract and used as the mash. (3) Preparation temperature (°C) As shown in Table 12.

【表】 (4) 液化液の添加方法 留後13日目(上槽前日)に92ml添加した。 (5) 上槽 14日目 遠心分離 5000rpm、10分 (6) 製成酒の分析結果 第13表のとおり。【table】 (4) Addition method of liquefied liquid 92ml was added on the 13th day after distillation (the day before the upper tank). (5) Upper tank Day 14 Centrifugation 5000rpm, 10 minutes (6) Analysis results of manufactured sake As shown in Table 13.

【表】 第13表から明らかなごとく、本発明で製造した
液化液を添加した製成酒は無添加酒に比較し、糖
分が増して日本酒度が戻り、アミノ酸が低くな
り、官能的には液化液添加による異臭味は認めら
れず、濃熟味のある優良酒であつた。従つて、清
酒原料として使用できないような低品位の原料で
も、本発明の液化液を清酒もろみ中途で添加すれ
ば、原料の一部として充分に使用できることが明
らかになつた。
[Table] As is clear from Table 13, compared to sake with no additives added to the liquefied liquid produced according to the present invention, the sugar content increases, the sake content returns, the amino acid content decreases, and the sensuality is lower. No off-flavors or tastes due to the addition of the liquefied liquid were observed, and the sake was of excellent quality with a rich, ripe flavor. Therefore, it has become clear that even low-grade raw materials that cannot be used as raw materials for sake can be sufficiently used as part of the raw materials if the liquefied liquid of the present invention is added in the middle of sake mashing.

Claims (1)

【特許請求の範囲】 1 米または白糠を
α−アミラーゼ活性(単位/g酵素)/プロテアーゼ活
性(単位/g酵素)が5以上の 好熱性液化酵素のみによつて液化し、ついで固液
分離する工程からなる、液化液の製造法。 2 無蒸煮の米または白糠を使用する特許請求の
範囲第1項記載の製造法。
[Scope of Claims] 1. Liquefying rice or white rice bran using only a thermophilic liquefaction enzyme with α-amylase activity (units/g enzyme)/protease activity (units/g enzyme) of 5 or more, and then solid-liquid separation. A method for producing liquefied liquid, which consists of several steps. 2. The manufacturing method according to claim 1, which uses uncooked rice or white bran.
JP57011252A 1982-01-27 1982-01-27 Preparation of liquefied product and solid cake from rice or refined rice bran Granted JPS58129968A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP57011252A JPS58129968A (en) 1982-01-27 1982-01-27 Preparation of liquefied product and solid cake from rice or refined rice bran

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP57011252A JPS58129968A (en) 1982-01-27 1982-01-27 Preparation of liquefied product and solid cake from rice or refined rice bran

Publications (2)

Publication Number Publication Date
JPS58129968A JPS58129968A (en) 1983-08-03
JPH0144311B2 true JPH0144311B2 (en) 1989-09-27

Family

ID=11772743

Family Applications (1)

Application Number Title Priority Date Filing Date
JP57011252A Granted JPS58129968A (en) 1982-01-27 1982-01-27 Preparation of liquefied product and solid cake from rice or refined rice bran

Country Status (1)

Country Link
JP (1) JPS58129968A (en)

Also Published As

Publication number Publication date
JPS58129968A (en) 1983-08-03

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