JPS643464B2 - - Google Patents
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- Publication number
- JPS643464B2 JPS643464B2 JP56086634A JP8663481A JPS643464B2 JP S643464 B2 JPS643464 B2 JP S643464B2 JP 56086634 A JP56086634 A JP 56086634A JP 8663481 A JP8663481 A JP 8663481A JP S643464 B2 JPS643464 B2 JP S643464B2
- Authority
- JP
- Japan
- Prior art keywords
- water
- minutes
- fraction
- oil
- soybeans
- 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.)
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- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 22
- 235000010469 Glycine max Nutrition 0.000 claims description 21
- 244000068988 Glycine max Species 0.000 claims description 20
- 239000002245 particle Substances 0.000 claims description 16
- 235000013305 food Nutrition 0.000 claims description 12
- 238000010438 heat treatment Methods 0.000 claims description 11
- 239000007787 solid Substances 0.000 claims description 11
- 239000000463 material Substances 0.000 claims description 10
- 238000005119 centrifugation Methods 0.000 claims description 8
- 239000000725 suspension Substances 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 2
- 239000013049 sediment Substances 0.000 claims 1
- 239000003921 oil Substances 0.000 description 15
- 239000012528 membrane Substances 0.000 description 9
- 238000000034 method Methods 0.000 description 7
- 102000004169 proteins and genes Human genes 0.000 description 7
- 108090000623 proteins and genes Proteins 0.000 description 7
- 235000013322 soy milk Nutrition 0.000 description 7
- 239000000203 mixture Substances 0.000 description 5
- 239000000839 emulsion Substances 0.000 description 4
- 238000001914 filtration Methods 0.000 description 4
- 239000002244 precipitate Substances 0.000 description 4
- 238000000108 ultra-filtration Methods 0.000 description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 238000010298 pulverizing process Methods 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 238000004062 sedimentation Methods 0.000 description 3
- 238000000926 separation method Methods 0.000 description 3
- 238000002791 soaking Methods 0.000 description 3
- 239000012134 supernatant fraction Substances 0.000 description 3
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 239000006071 cream Substances 0.000 description 2
- 239000000796 flavoring agent Substances 0.000 description 2
- 235000019634 flavors Nutrition 0.000 description 2
- 238000000227 grinding Methods 0.000 description 2
- 235000013336 milk Nutrition 0.000 description 2
- 239000008267 milk Substances 0.000 description 2
- 210000004080 milk Anatomy 0.000 description 2
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 239000006228 supernatant Substances 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 229930182558 Sterol Natural products 0.000 description 1
- 239000005862 Whey Substances 0.000 description 1
- 102000007544 Whey Proteins Human genes 0.000 description 1
- 108010046377 Whey Proteins Proteins 0.000 description 1
- SMEGJBVQLJJKKX-HOTMZDKISA-N [(2R,3S,4S,5R,6R)-5-acetyloxy-3,4,6-trihydroxyoxan-2-yl]methyl acetate Chemical compound CC(=O)OC[C@@H]1[C@H]([C@@H]([C@H]([C@@H](O1)O)OC(=O)C)O)O SMEGJBVQLJJKKX-HOTMZDKISA-N 0.000 description 1
- 229940081735 acetylcellulose Drugs 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 238000003916 acid precipitation Methods 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 235000013361 beverage Nutrition 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 159000000007 calcium salts Chemical class 0.000 description 1
- 229920002301 cellulose acetate Polymers 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000010411 cooking Methods 0.000 description 1
- 239000010779 crude oil Substances 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 238000011026 diafiltration Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000002657 fibrous material Substances 0.000 description 1
- 235000011194 food seasoning agent Nutrition 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 159000000003 magnesium salts Chemical class 0.000 description 1
- 239000008268 mayonnaise Substances 0.000 description 1
- 235000010746 mayonnaise Nutrition 0.000 description 1
- 239000012466 permeate Substances 0.000 description 1
- 150000003904 phospholipids Chemical class 0.000 description 1
- 229920002492 poly(sulfone) Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 230000001376 precipitating effect Effects 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000010791 quenching Methods 0.000 description 1
- 230000000171 quenching effect Effects 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 150000003432 sterols Chemical class 0.000 description 1
- 235000003702 sterols Nutrition 0.000 description 1
- 229930003799 tocopherol Natural products 0.000 description 1
- 239000011732 tocopherol Substances 0.000 description 1
- 235000019149 tocopherols Nutrition 0.000 description 1
- 239000000052 vinegar Substances 0.000 description 1
- 235000021419 vinegar Nutrition 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- QUEDXNHFTDJVIY-UHFFFAOYSA-N γ-tocopherol Chemical class OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1 QUEDXNHFTDJVIY-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Beans For Foods Or Fodder (AREA)
- Fats And Perfumes (AREA)
Description
本発明は、丸大豆より固型分中の油分含量が50
%ないし70%の食品素材を製造する方法に関す
る。
従来、豆乳は水に浸漬した丸大豆を水中で磨砕
したのち不溶区分のオカラを除去して得られる。
又はオカラを除去せず、マントン・ゴーリンなど
の強制分散させて豆乳とする場合もある。このよ
うにして製造した豆乳は、固型分中の油分含量
は、多くてもせいぜい30%にすぎない。
本発明は、浸漬大豆を短時間加熱することによ
り蛋白質を加熱変性して水不溶性としたのち、粉
砕することにより蛋白質を不溶区分として除去
し、さらに酸沈、塩沈又は限外濾過等の手段によ
りホエー区分、又は低分子区分を除去することに
よつて、脂肪粒子よりなる区分を採取し、固型分
中の油分含量が50%ないし70%にもなる、食品素
材を製造する方法である。
本発明方法は、まず、水洗した丸大豆を1ない
し10倍の水に浸漬する。この水の温度、PH、イオ
ン強度などは特に限定する必要はないが、浸漬時
間は5時間ないし24時間程度とし、完全に膨潤し
た浸漬大豆とする。
この水浸漬した丸大豆を、80℃ないし200℃の
温度範囲で30秒ないし30分間加熱する。加熱処理
が不充分であると、蛋白区分は粉砕処理中に破壊
され、溶解してしまうため収率低下の原因とな
り、加熱処理が過ぎると、いたずらに蛋白が熱変
性を受け、食品加工に利用する際、味、風味が悪
くなるため、80℃ないし200℃で30秒ないし30分
間、好ましくは100℃ないし150℃で1分間ないし
10分間程度の加熱処理が適当である。加熱手段は
特に限定されるものではなく、水蒸気による加
熱、排騰水による加熱、マイクロ波による加熱な
どいずれの加熱方法を用いることができる。
加熱処理を施した丸大豆は、冷却した後、1な
いし10倍量の水の存在下で粒径350μ以下のもの
が50%ないし90%になるように微粉砕される。
350μ以下の粒子が50%未満であると、大豆子葉
細胞が充分破壊されないために、脂肪粒子が繊維
質とともに沈降区分に混入し、収率低下の原因と
なる。350μ以下のものが90%より多くなると、
不溶化した蛋白を再溶解するために油分含量低下
の原因となり、適当でない。
粉砕の方法は特定する必要はなく、デイスパー
ズ・ミル、ホモジナイザー、磨砕機等の装置を用
いることができる。例えば、家庭用のミキサー
で、粗砕したのち擂潰器で磨砕して、42メツシユ
(350μ)以下の区分が50%以上になるようにすれ
ば良い。
粉砕後の懸濁液より50G1分以上の遠心分離に
よつて沈降しない区分を採取する。50G1分以上
の遠心分離によつて沈降する区分とは、一般にオ
カラと呼ばれている繊維質と、加熱凝固して不溶
性となつた蛋白粒子からなる。このような区分は
自然沈降を2時間以上行なうなどの方法によつて
も得られる。50G1分以上の遠心分離によつて沈
降しない区分は、脂肪粒子が分散した乳化物と、
クリーム層及び可溶性成分からなり、これより粒
径ほぼ0.1ないし1.0μの脂肪粒子区分のみを採取
する。採取する方法は、分画分子量5万以上の特
定の親水性限外濾過膜を用いて前記の沈降しない
区分より低分子区分を除去すればよい。親水性限
外濾過膜としては、アセチルセルロース膜、芳香
族系ポリスルフオン膜、ポリオレフイン膜などの
濾過膜を使用することができる。濾過膜にかかる
圧力としては1.1Kg/cm2ないし10Kg/cm2好ましく
は1.2Kg/cm2ないし5.0Kg/cm2の範囲が適してお
り、この範囲内で透過物の量、濾過膜の目の大き
さなどによつて好ましい値が選ばれる。
このようにして脂肪粒子よりなる区分を採取す
ることもできるが、前記の沈降しない区分に酸を
添加しPHを4ないし5に調整して沈殿させるか、
あるいは、カルシウム塩、マグネシウム塩等を
0.01ないし10モル/の濃度となるように添加す
ることによつて沈澱させた後、100G1分以上の遠
心分離、濾過などの分離操作を行ない、沈澱した
区分を脂肪粒子よりなる区分として採取すること
も可能である。
上記方法によつて固型分中の油分含量が50%な
いし70%の食品素材を製造することができる。こ
の食品素材は固型分含量が10%ないし30%の白色
の乳化物であつた。更に含有されている脂肪粒子
は、ほとんど破壊されておらず丸大豆組織内にあ
つた状態とほぼ同じ状態で本発明の食品素材中に
存在しているため、粒径がほぼ0.1μないし0.5μと
非常に小さく、分散性が良く、油脂と水の分離、
即ちエマルジヨン破壊がおこりにくい食品素材で
あつた。
本発明によつて得られる食品素材は、希釈して
豆乳様飲料として利用できることはもちろん、調
味付けしてマヨネーズ、ドレツシングなどの植物
原料を主成分とする油性乳化食品としたり、風味
付けしてコーヒーホワイトナー、生クリーム代替
品などとして応用することも可能である。
更に、この食品素材を乾燥して高油分粉末油脂
として新しい食品形態として広く利用することも
できる。また、この粉末油脂よりn−ヘキサンで
油を抽出することもでき、得られる油は通常の方
法によつて得られる大豆粗原油と比べてリン脂
質、ステロール、トコフエロール含量の少ない油
である。
以下、実施例により本発明を説明する。
実施例 1
丸大豆1.0Kgを5倍量の水に浸し5℃冷蔵庫に
一晩放置して充分膨潤させたのち、3分間煮沸し
た。流水で急冷したのち、家庭用ミキサーにて1
分、さらに擂潰器で10分粉砕し、全量が7Kgにな
るように水を加えた。この時の粒子径は、
150mesh on(100μ以上)が約40%であつた。
粉砕液は1000RPMで5分間遠心分離してオカ
ラ、蛋白などからなる沈降区分を分離除去して上
澄区分を集めた。沈降区分は3Kgの水で洗浄し、
洗浄水は、同様に遠心分離して沈澱を除いたの
ち、上澄区分に加えた。上澄区分約7Kgは、6N
−硫酸を加えてPH4.4に調整して一時間放置後、
3000RPMで20分間遠心分離して上澄区分を除去
し、濃縮豆乳0.9Kgを得た(固形分含量23%、油
分含量/固型分55%)。
実施例 2
水浸漬して充分膨潤した丸大豆約2.0Kgを、3
分間煮沸したのち、500gずつ4区分に分けて粉
砕し、粉砕条件の異なる試料4点を得て、粉砕条
件が収率及び組成に及ぼす影響を調べた。分離条
件は実施例1に同じである。結果を表1に示す。
The present invention has a solid content of 50% less oil than whole soybeans.
% to 70% of food materials. Conventionally, soybean milk is obtained by soaking whole soybeans in water, grinding them in water, and then removing the insoluble okara.
Alternatively, soymilk may be made by forcibly dispersing soybean milk such as Menton Gaulin without removing okara. The soymilk produced in this way has an oil content of no more than 30% in the solid matter. The present invention involves heating soaked soybeans for a short time to thermally denature the protein to make it water-insoluble, and then removing the protein as an insoluble fraction by pulverizing the soybean, and further using means such as acid precipitation, salt precipitation, or ultrafiltration. This is a method for producing food materials with an oil content of 50% to 70% in the solid matter by removing the whey fraction or low molecular fraction by extracting the fraction consisting of fat particles. . In the method of the present invention, first, washed whole soybeans are soaked in 1 to 10 times as much water. The temperature, pH, ionic strength, etc. of this water are not particularly limited, but the soaking time is about 5 to 24 hours, and the soaked soybeans are completely swollen. The whole soybeans soaked in water are heated in a temperature range of 80°C to 200°C for 30 seconds to 30 minutes. If the heat treatment is insufficient, the protein fraction will be destroyed and dissolved during the grinding process, causing a decrease in yield. If the heat treatment is too long, the protein will be unnecessarily thermally denatured and cannot be used for food processing. When cooking, the taste and flavor will deteriorate, so the temperature is 80℃ to 200℃ for 30 seconds to 30 minutes, preferably 100℃ to 150℃ for 1 minute or 30 minutes.
Heat treatment for about 10 minutes is appropriate. The heating means is not particularly limited, and any heating method such as heating with steam, heating with rising water, heating with microwaves, etc. can be used. The heat-treated whole soybeans are cooled and then pulverized in the presence of 1 to 10 times the amount of water so that 50% to 90% of the soybeans have a particle size of 350 μm or less.
If the proportion of particles of 350μ or less is less than 50%, the soybean cotyledon cells will not be sufficiently destroyed, and fat particles will be mixed into the sedimentation section along with the fibers, causing a decrease in yield. If the proportion of 350 μ or less exceeds 90%,
It is not suitable because it causes a decrease in oil content because the insolubilized protein is redissolved. The method of pulverization does not need to be specified, and devices such as a dispersion mill, homogenizer, and attritor can be used. For example, you can coarsely crush it with a household mixer and then grind it with a grinder so that 50% or more of it is 42 mesh (350μ) or less. Collect the fraction that does not settle by centrifugation at 50G for 1 minute or more from the suspension after pulverization. The segment that settles when centrifuged at 50G for 1 minute or more consists of fibrous material generally called okara and protein particles that have become insoluble after being coagulated by heating. Such a division can also be obtained by a method such as performing natural sedimentation for 2 hours or more. The categories that do not settle by centrifugation at 50G for 1 minute or more are emulsions in which fat particles are dispersed;
It consists of a cream layer and soluble components, from which only the fat particle section with a particle size of approximately 0.1 to 1.0 μm is collected. As for the collection method, a specific hydrophilic ultrafiltration membrane with a molecular cutoff of 50,000 or more may be used to remove the lower molecular fraction than the non-sedimenting fraction. As the hydrophilic ultrafiltration membrane, a filtration membrane such as an acetyl cellulose membrane, an aromatic polysulfon membrane, or a polyolefin membrane can be used. The pressure applied to the filtration membrane is preferably in the range of 1.1Kg/cm 2 to 10Kg/cm 2 , preferably 1.2Kg/cm 2 to 5.0Kg/cm 2 , and within this range, the amount of permeate and the diameter of the filtration membrane can be adjusted. A preferable value is selected depending on the size of . It is also possible to collect a section consisting of fat particles in this way, but you can add acid to the section that does not settle and adjust the pH to 4 to 5 to precipitate it.
Alternatively, use calcium salts, magnesium salts, etc.
After precipitating by adding to a concentration of 0.01 to 10 mol/, performing separation operations such as centrifugation at 100G for 1 minute or more and filtration, and collecting the precipitated section as a section consisting of fat particles. is also possible. By the above method, a food material having an oil content of 50% to 70% in solid matter can be produced. This food material was a white emulsion with a solids content of 10% to 30%. Furthermore, the contained fat particles are almost undestructed and exist in the food material of the present invention in almost the same state as in the whole soybean tissue, so the particle size is approximately 0.1μ to 0.5μ. Very small size, good dispersibility, separation of oil and water,
In other words, it was a food material in which emulsion destruction was unlikely to occur. The food material obtained by the present invention can be diluted and used as a soy milk-like drink, seasoned to make oil-based emulsified foods based on plant materials such as mayonnaise and dressing, or flavored to make coffee. It can also be used as a whitener, fresh cream substitute, etc. Furthermore, this food material can be dried and made into a high-oil powdered fat that can be widely used as a new food form. Additionally, oil can be extracted from this powdered fat with n-hexane, and the resulting oil has a lower content of phospholipids, sterols, and tocopherols than crude soybean crude oil obtained by conventional methods. The present invention will be explained below with reference to Examples. Example 1 1.0 kg of whole soybeans was soaked in 5 times the amount of water, left in a refrigerator at 5°C overnight to sufficiently swell, and then boiled for 3 minutes. After quenching with running water, mix with a household mixer.
The mixture was crushed for another 10 minutes using a grinder, and water was added so that the total amount was 7 kg. The particle size at this time is
Approximately 40% were 150mesh on (100μ or more). The pulverized solution was centrifuged at 1000 RPM for 5 minutes to separate and remove the precipitated fraction consisting of okara, protein, etc., and the supernatant fraction was collected. The sedimentation section was washed with 3 kg of water.
The washing water was similarly centrifuged to remove the precipitate, and then added to the supernatant section. Approximately 7Kg of skim is 6N
-After adding sulfuric acid and adjusting the pH to 4.4 and leaving it for one hour,
The supernatant fraction was removed by centrifugation at 3000 RPM for 20 minutes to obtain 0.9 kg of concentrated soymilk (solid content 23%, oil content/solid content 55%). Example 2 Approximately 2.0 kg of whole soybeans soaked in water and sufficiently swollen were
After boiling for a minute, the mixture was divided into four 500g portions and crushed to obtain four samples with different crushing conditions, and the influence of the crushing conditions on yield and composition was investigated. The separation conditions are the same as in Example 1. The results are shown in Table 1.
【表】
実施例 3
充分水浸漬した丸大豆1.0Kgを120℃加圧蒸気下
で5分間加熱後冷却し、家庭用ミキサーで5分間
粉砕後水を加えて全量を5.0Kgとした。2000Gに
て10分間、遠心分離して、沈澱区分を除去したの
ち、上部、エマルジヨン区分3.0Kgに、カルシウ
ム濃度が0.5%になるようにCaCl290gを添加して
撹拌しながら1時間放置した。これを3000Gで20
分間遠心分離して上澄区分を除去し、脂肪粒子を
含んだ沈澱区分を分離した。沈澱区分をそのまま
凍結乾燥して粉末化した。得られた粉末油脂の性
状は下記のようであつた。収量102g、油分含
量/固型分58%。
実施例 4
丸大豆100gを水1に約7時間浸漬したのち、
3分間煮沸して冷却した。家庭用ミキサーで5分
間粉砕して、遠心分離機(久保田製、Model
KR−180A ローター RA−6)を用い、
3000RPM、5分の遠心分離にて沈澱区分を除去
した。上澄液500gを限外濾過膜(バイオエンヂ
ニアリング製、ダイアフイルター A−50T)を
用いて限外濾過を行ない、固型分濃度13.1%の濃
縮豆乳140gを得た(油分含量/固型分52.2%)。
この濃縮豆乳140gに、砂糖1.5g、食塩0.3g
を加えて調味付けしたのち、水で希釈して全量を
300mlにすると、青臭みがなくコク味豊かな豆乳
飲料が得られた。
参考例
実施例1により得られた濃縮豆乳100gをとり、
水に分散しながら水酸化ナトリウムで、PHを5.6
に調整し全量を150mlにした、酢30g、塩3g、
砂糖5g及びコシヨウ少々を加えて調味付けし、
よくかきまぜ、油脂と水が分離しないマヨネーズ
タイプのドレツシングを作ることができた。[Table] Example 3 1.0 kg of whole soybeans soaked in water were heated for 5 minutes at 120° C. under pressurized steam, cooled, and ground in a household mixer for 5 minutes, and then water was added to bring the total amount to 5.0 kg. After centrifugation at 2000G for 10 minutes to remove the precipitate section, 90 g of CaCl 2 was added to the upper portion of the emulsion section (3.0 kg) so that the calcium concentration was 0.5%, and the mixture was left for 1 hour with stirring. 20 of this at 3000G
The supernatant fraction was removed by centrifugation for a minute, and the precipitate fraction containing fat particles was separated. The precipitated fraction was directly freeze-dried and powdered. The properties of the obtained powdered oil and fat were as follows. Yield 102g, oil content/solids 58%. Example 4 After soaking 100g of whole soybeans in water 1 for about 7 hours,
Boiled for 3 minutes and cooled. Grind for 5 minutes with a household mixer, then use a centrifugal separator (Kubota, Model
Using KR-180A rotor RA-6),
The precipitate fraction was removed by centrifugation at 3000 RPM for 5 minutes. 500 g of the supernatant liquid was ultrafiltered using an ultrafiltration membrane (Diafilter A-50T, manufactured by Bio Engineering) to obtain 140 g of concentrated soymilk with a solid content concentration of 13.1% (oil content/solid content 52.2). %). 140g of this concentrated soy milk, 1.5g of sugar, 0.3g of salt
Add seasoning, then dilute with water to make the entire amount.
When the amount was 300 ml, a soy milk beverage with no grassy smell and rich flavor was obtained. Reference Example Take 100g of concentrated soymilk obtained in Example 1,
Sodium hydroxide while dispersing in water, pH to 5.6
Adjust the total amount to 150ml, 30g vinegar, 3g salt,
Season by adding 5g of sugar and a little koshiyo,
By stirring well, I was able to make a mayonnaise-type dressing in which the oil and water do not separate.
Claims (1)
温度範囲で、30秒ないし30分間加熱した後、水の
存在下で粒径350μ以下のものが50%ないし90%
になるように粉砕して懸濁液とし、該懸濁液より
50G1分以上の遠心分離にて沈降しない区分を得、
該区分より脂肪粒子よりなる区分を採取すること
を特徴とする固型分中の油分含量が50%ないし70
%の食品素材の製造方法。1. After heating whole soybeans soaked in water at a temperature range of 80℃ to 200℃ for 30 seconds to 30 minutes, in the presence of water, 50% to 90% of the soybeans have a particle size of 350μ or less.
Grind to make a suspension, and from the suspension
A classification that does not sediment is obtained by centrifugation at 50G for 1 minute or more.
A segment consisting of fat particles is collected from the segment, and the oil content in the solid content is between 50% and 70%.
% food material manufacturing method.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP56086634A JPS57202263A (en) | 1981-06-05 | 1981-06-05 | Preparation of food raw material |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP56086634A JPS57202263A (en) | 1981-06-05 | 1981-06-05 | Preparation of food raw material |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS57202263A JPS57202263A (en) | 1982-12-11 |
| JPS643464B2 true JPS643464B2 (en) | 1989-01-20 |
Family
ID=13892450
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP56086634A Granted JPS57202263A (en) | 1981-06-05 | 1981-06-05 | Preparation of food raw material |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS57202263A (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2007300884A (en) * | 2006-05-15 | 2007-11-22 | Michihiro Kamiya | Bean curd refuse |
-
1981
- 1981-06-05 JP JP56086634A patent/JPS57202263A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS57202263A (en) | 1982-12-11 |
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