JPH0484861A - Method for preparing fat and oil components and protein component from peanut seed - Google Patents
Method for preparing fat and oil components and protein component from peanut seedInfo
- Publication number
- JPH0484861A JPH0484861A JP19768290A JP19768290A JPH0484861A JP H0484861 A JPH0484861 A JP H0484861A JP 19768290 A JP19768290 A JP 19768290A JP 19768290 A JP19768290 A JP 19768290A JP H0484861 A JPH0484861 A JP H0484861A
- Authority
- JP
- Japan
- Prior art keywords
- fraction
- seeds
- cellulase
- peanut
- mixture
- 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
- 235000020232 peanut Nutrition 0.000 title claims abstract description 13
- 235000017060 Arachis glabrata Nutrition 0.000 title claims abstract description 11
- 235000010777 Arachis hypogaea Nutrition 0.000 title claims abstract description 11
- 235000018262 Arachis monticola Nutrition 0.000 title claims abstract description 11
- 241001553178 Arachis glabrata Species 0.000 title claims abstract 6
- 238000000034 method Methods 0.000 title description 16
- 235000004252 protein component Nutrition 0.000 title 1
- 108010059892 Cellulase Proteins 0.000 claims abstract description 14
- 102000004169 proteins and genes Human genes 0.000 claims abstract description 14
- 108090000623 proteins and genes Proteins 0.000 claims abstract description 14
- 108010059820 Polygalacturonase Proteins 0.000 claims abstract description 11
- 229940106157 cellulase Drugs 0.000 claims abstract description 11
- 108010093305 exopolygalacturonase Proteins 0.000 claims abstract description 11
- 239000000203 mixture Substances 0.000 claims abstract description 7
- 230000001954 sterilising effect Effects 0.000 claims abstract description 6
- 239000000839 emulsion Substances 0.000 claims description 7
- 238000004659 sterilization and disinfection Methods 0.000 claims description 5
- 238000004519 manufacturing process Methods 0.000 claims description 3
- 108090000790 Enzymes Proteins 0.000 abstract description 20
- 102000004190 Enzymes Human genes 0.000 abstract description 20
- 229940088598 enzyme Drugs 0.000 abstract description 20
- 239000003921 oil Substances 0.000 abstract description 18
- 238000000926 separation method Methods 0.000 abstract description 15
- 239000007787 solid Substances 0.000 abstract description 14
- 239000007788 liquid Substances 0.000 abstract description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 11
- 239000006071 cream Substances 0.000 abstract description 6
- 239000007921 spray Substances 0.000 abstract description 5
- 239000010779 crude oil Substances 0.000 abstract description 3
- 239000012223 aqueous fraction Substances 0.000 abstract 1
- 230000002255 enzymatic effect Effects 0.000 abstract 1
- 239000000725 suspension Substances 0.000 abstract 1
- 238000001238 wet grinding Methods 0.000 abstract 1
- 235000019198 oils Nutrition 0.000 description 17
- 244000105624 Arachis hypogaea Species 0.000 description 7
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 6
- 238000003756 stirring Methods 0.000 description 5
- 235000019483 Peanut oil Nutrition 0.000 description 4
- 239000003925 fat Substances 0.000 description 4
- 239000000312 peanut oil Substances 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 238000003825 pressing Methods 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 238000000638 solvent extraction Methods 0.000 description 4
- 241000542980 Mimidae Species 0.000 description 3
- UHPMCKVQTMMPCG-UHFFFAOYSA-N 5,8-dihydroxy-2-methoxy-6-methyl-7-(2-oxopropyl)naphthalene-1,4-dione Chemical compound CC1=C(CC(C)=O)C(O)=C2C(=O)C(OC)=CC(=O)C2=C1O UHPMCKVQTMMPCG-UHFFFAOYSA-N 0.000 description 2
- 235000000073 Amphicarpaea bracteata Nutrition 0.000 description 2
- 240000002470 Amphicarpaea bracteata Species 0.000 description 2
- 241000228245 Aspergillus niger Species 0.000 description 2
- 241000223218 Fusarium Species 0.000 description 2
- 238000007792 addition Methods 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 230000007547 defect Effects 0.000 description 2
- 230000007812 deficiency Effects 0.000 description 2
- 238000006911 enzymatic reaction Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 241000228212 Aspergillus Species 0.000 description 1
- 241001480052 Aspergillus japonicus Species 0.000 description 1
- 101710184309 Probable sucrose-6-phosphate hydrolase Proteins 0.000 description 1
- 102400000472 Sucrase Human genes 0.000 description 1
- 101710112652 Sucrose-6-phosphate hydrolase Proteins 0.000 description 1
- 241000223261 Trichoderma viride Species 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 235000015278 beef Nutrition 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 108010081495 driselase Proteins 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 239000000383 hazardous chemical Substances 0.000 description 1
- 230000002779 inactivation Effects 0.000 description 1
- 235000011073 invertase Nutrition 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 235000014593 oils and fats Nutrition 0.000 description 1
- 235000010987 pectin Nutrition 0.000 description 1
- 229920001277 pectin Polymers 0.000 description 1
- 239000001814 pectin Substances 0.000 description 1
- 108020001775 protein parts Proteins 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- 239000010802 sludge Substances 0.000 description 1
- 238000009987 spinning Methods 0.000 description 1
- 238000010025 steaming Methods 0.000 description 1
- 239000011550 stock solution Substances 0.000 description 1
- 235000020138 yakult Nutrition 0.000 description 1
Landscapes
- Fats And Perfumes (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は、乳濁状又は圧搾状落花生種子からの機械的分
離、又は、溶媒抽出法による公知の落花生油製造法とは
著しく異なった着想に基づく、改善された落花生油並び
にニュープロティンとしての含油量の著しく少ない高品
質の落花生蛋白質の製造法に関する。[Detailed Description of the Invention] [Field of Industrial Application] The present invention is based on a concept that is significantly different from known methods for producing peanut oil by mechanical separation from emulsified or pressed peanut seeds or by solvent extraction. The present invention relates to a method for producing improved peanut oil and high-quality peanut protein with a significantly lower oil content as new protein, based on the present invention.
落花生油の製造法として、圧搾法又は圧搾後へ牛サンを
用いて圧搾抽出する方法と、高温高圧条件下にて煮熟処
理後、特殊機械を用いて、高温度条件下にて遠心分離す
る方法とが知られている。Peanut oil can be produced by pressing or extracting by squeezing using beef sun after pressing, and by boiling under high temperature and high pressure conditions and then centrifuging under high temperature conditions using a special machine. The method is known.
これらは下記二つのタイプに分類することができる。These can be classified into the following two types.
その一つは、圧扁により種子組織を破壊して後、油分を
取り出す圧搾又は圧搾後油分を溶媒へキサンにより抽出
する溶媒抽出法、他の一つは、高温高圧により種子組織
を破壊して後、乳濁状液として、液成分と固形分とに分
離する遠心分離法である。One is the solvent extraction method, which involves destroying the seed tissue by pressing and then extracting the oil, or extracting the oil after pressing using the solvent hexane, and the other method is by destroying the seed tissue by high temperature and pressure. This is a centrifugal separation method in which the emulsion is then separated into a liquid component and a solid component.
上記圧搾、又は圧搾後溶媒抽出法では、高純度に蛋白質
を得るには、ヘキサンによる溶媒抽出法を採用するしか
なく、此の方法では、溶媒抽出後残余の溶媒(ヘキサン
)を、油脂分及び蛋白質分の両方から完全に除去しなけ
ればならない欠陥があり、又、この為の諸設備、例えば
、加熱蒸発釜や冷却機、危険物取扱い上の法規的諸設備
や、消火器等を設置しなければならない不利益があり、
又、絶えず火災の危険にさらされる為の万全の注意が要
求される欠陥がある。In the above-mentioned squeezing or post-squeezing solvent extraction method, the only way to obtain highly pure proteins is to adopt a solvent extraction method using hexane. There are defects that must be completely removed from both the protein content and various equipment for this purpose, such as heating evaporation pots, cooling machines, legal equipment for handling hazardous materials, and fire extinguishers, etc., must be installed. There are disadvantages to having to
Additionally, there are deficiencies that require extreme caution due to constant exposure to fire hazards.
又、溶媒ロスによる不利益もある。There is also a disadvantage due to solvent loss.
又、上記高温高圧法では、特別な耐圧釜を必要とする他
、法規上の問題点もあり、加えて高温度条件下に於て諸
摸作が要求される不利益があり、又、投設にも及ぶ繰り
返し分離操作を行なわなければならない欠陥があった。In addition, the high-temperature and high-pressure method described above requires a special pressure cooker, has legal problems, and has the disadvantage of requiring various experiments under high-temperature conditions. There was a defect in that the separation operation had to be repeated over the entire facility.
本発明は、上述の如き従来法の不利益ないし欠陥を克服
し、容易な操作で、油脂分よ蛋白買置との分離や、更に
は油分含有率の低い優れた蛋白質を、品質再現性良く、
且つ安価に提供するこまを目的とするものである。The present invention overcomes the disadvantages and deficiencies of the conventional methods as described above, and allows easy operation to separate fats and oils from protein, as well as produce excellent proteins with low oil content with good quality reproducibility. ,
The aim is to provide spinning tops at low cost.
本発明は、脱莢皮及び加熱殺菌処理後、粉砕した落花生
種子乳濁状液を、酵素の1種であるセルラーゼで処理す
るか、又は、セルラーゼとペクチナーゼを有効成分とす
る酵素の混合物で処理することにより、落花生より油脂
分と蛋白買置とを製造する方法である。In the present invention, after dehulling and heat sterilization, the ground peanut seed emulsion is treated with cellulase, which is a type of enzyme, or with a mixture of enzymes containing cellulase and pectinase as active ingredients. This is a method for producing fats and oils and protein from peanuts.
本発明者らは、脱莢皮及び加熱殺菌処理後、粉砕した落
花生種子乳濁状液をセルラーゼ、又は、セルラーゼとペ
クチナーゼ混合物を用いて処理すると、上記乳濁状液に
前記酵素が作用するに伴って、乳濁状が破壊されると共
に二層分離が生じ、しかも此の分離に際して、油分と蛋
白買置等の固形分とが、好都合に分離され易い状態にな
り、高品質の油脂分と高品質の蛋白買置とを効率よく、
比較的簡単な手段により製造できることを見いだし、本
発明をなすに到った。The present inventors have discovered that when a ground peanut seed emulsion is treated with cellulase or a mixture of cellulase and pectinase after dehulling and heat sterilization, the enzyme acts on the emulsion. As a result, the emulsion is destroyed and two-layer separation occurs, and during this separation, oil and solids such as protein are easily separated, resulting in high-quality oils and fats. Efficiently purchase and purchase high quality protein.
It has been discovered that it can be manufactured by relatively simple means, and the present invention has been completed.
従って、本発明は、従来の方法とは全く異なった方式に
よって、落花生種子より高品質の油脂分と高品質の蛋白
買置とを効率良く製造する改善しれた方法を提供するも
のである。Therefore, the present invention provides an improved method for efficiently producing high-quality fats and oils and high-quality protein from peanut seeds using a method completely different from conventional methods.
本発明方法に於て使用する酵素セルラーゼとしては、ト
リコデルマ・ビリデ、アスペルギルス・ニガー フザリ
ウム・モニリホルム系等の製剤があげられる。又、ペク
チナーゼとしては、アスペルギルス・ニガー アスペル
ギルス・ソジャー アスペルギルス・ジャポニカス、フ
ザリウム・モニリホルム、リゾーブス系等の製剤をあげ
る事が出来る。Examples of the enzyme cellulase used in the method of the present invention include preparations of Trichoderma viride, Aspergillus niger, Fusarium moniliform, and the like. Further, as pectinase, preparations such as Aspergillus niger, Aspergillus soger, Aspergillus japonicus, Fusarium moniliform, and Rhizobus can be mentioned.
本発明方法に於ては、脱莢皮及び加熱殺菌処理後、これ
を粉砕した乳濁状液中に、これらの酵素を添加して反応
せしめるものである。In the method of the present invention, after dehulling and heat sterilization, these enzymes are added to a pulverized emulsion and allowed to react.
上記の添加方法は、酵素の最適条件下、即ち40〜50
℃、pH4〜5付近であれば良く、その添加量も、酵素
活性度に応じて、脱莢皮落花生種子に対し通常0.1な
いし5wt%の範囲で、任意の量を添加する事が出来る
。又、これらの添加は、水溶液状として攪拌条件下に行
なうのが良い。又、水の量は通常脱莢皮種子の約2〜1
0倍量、好ましくは4〜8倍量程度である。The above addition method is performed under the optimum conditions of the enzyme, i.e. 40 to 50
℃ and pH around 4 to 5, and any amount can be added depending on the enzyme activity, usually in the range of 0.1 to 5 wt% based on the shelled peanut seeds. . Further, these additions are preferably carried out in the form of an aqueous solution under stirring conditions. Also, the amount of water is usually about 2 to 1 ounces per peeled seed.
The amount is 0 times, preferably about 4 to 8 times.
又、用いる酵素の種類、又、その組合せによって適当に
選択出来るが、比較的高温度条件を特徴とする特性を有
する酵素の場合、4〜5倍量程度用いるとよい。The enzyme can be appropriately selected depending on the type of enzyme used and the combination thereof, but in the case of an enzyme having characteristics that require relatively high temperature conditions, it is recommended to use about 4 to 5 times the amount.
又、添加する酵素は、異なる酵素源系製剤を複数混合し
て使用できる。セルラーゼとペクチナーゼの混合割合は
、その製剤の酵素源によって自由に選択する事が出来る
。又、酵素反応時間は、攪拌条件下、通常5〜24時間
程度であり、その使用する酵素の使用量の増減により、
短縮する事も出来れば、又延長する事も可能である。Furthermore, the enzyme to be added can be a mixture of a plurality of different enzyme source preparations. The mixing ratio of cellulase and pectinase can be freely selected depending on the enzyme source of the preparation. In addition, the enzyme reaction time is usually about 5 to 24 hours under stirring conditions, and depending on the amount of enzyme used,
If it can be shortened, it can also be lengthened.
セルラーゼ単独を使用した場合、反応液は、ペクチン質
が分解されない為か乳濁状を呈していることが多いが静
置することにより、油滴の分離と共に乳濁状の水層部分
と固形部分(蛋白質部分)とに分離でき、乳濁部分は遠
心分離機により処理することにより油分を容易に分離す
ることができる。When cellulase is used alone, the reaction solution is often milky, probably because the pectin is not decomposed, but by standing still, the oil droplets are separated and the milky water layer and solid portion are separated. (protein part), and the oil content can be easily separated from the emulsified part by processing it with a centrifuge.
また、セルラーゼとペクチナーゼを加えて反応させた液
は静置することによって油滴の分離と共にかなり清透な
水層部分と固形部分に分離することができる。Furthermore, by allowing the solution obtained by adding and reacting cellulase and pectinase to stand still, oil droplets can be separated and the solution can be separated into a fairly clear aqueous layer and a solid portion.
酵素処理された原液は、攪拌条件下、酵素の失活及び殺
菌処理を経て、任意の固液分離手段で、容易に分別する
事が出来る。The enzyme-treated stock solution is subjected to enzyme inactivation and sterilization treatment under stirring conditions, and can be easily separated using any solid-liquid separation means.
別に特別な手段を必要としないが、粗分離後、精密分離
の二段式分離手段によって、容易に高純度の製品を製造
する事が出来る。Although no special means is required, a high-purity product can be easily produced by using a two-stage separation means for precise separation after rough separation.
上記の固液分離機としては、スラッシャ−式遠心沈降機
や、分離板式遠心分離機等をあげる事が出来る。Examples of the above-mentioned solid-liquid separator include a thrasher type centrifugal sedimentation machine and a separating plate type centrifugal separator.
かようにして、得られる固形層は、蛋白装置として直ち
にスプレードライヤーによって粉末化、又はそのまま蛋
白質カードとして使用する事が出来る。The solid layer thus obtained can be immediately powdered using a spray dryer as a protein device, or can be used as it is as a protein curd.
又、分離した液層分は、連続的にクリームセパレータ(
分離板式)に導入し、透明な水分含有率0.5wt%以
下の落花生油分を得る事が出来る。In addition, the separated liquid layer is continuously passed through a cream separator (
It is possible to obtain transparent peanut oil with a moisture content of 0.5 wt% or less.
次に第1図に基いて本発明の詳細な説明する。Next, the present invention will be explained in detail based on FIG.
先づ落花生の種子を脱皮装置1で脱皮した後蒸煮殺菌機
2で蒸煮殺菌し、強いミキサー程度の粉砕機3に入れ、
導管4より所定量の水を導入しながら粉砕し、ついで酵
素反応機5に導入して酵素を加えて反応を行わせ、加熱
機6で酵素の失活及び殺菌を行った後遠心分離機(スラ
ッシャ−式)7で固液を分離する。遠心分離機で分離さ
れた液状物は、固形分から分離板式遠心分離機10で分
離された液体と共に分離板式クリームセパレータ8に導
入し、油脂分と水分とに分離し、油脂分は原油タンク9
に導き貯溜される。スラッシャ−(遠心分離機)で分離
された固形分は、分離板式遠心分離機10に導き、液分
を更に分離し、分離された液分はクリームセパレータ8
に導くと共に、固形分はスプレードライヤー11で乾燥
した後シフター12を経て自動袋詰機13等により袋詰
される。First, peanut seeds are dehulled in a dehulling device 1, then sterilized by steaming in a steam sterilizer 2, and put into a crusher 3, which is equivalent to a strong mixer.
The powder is ground while introducing a predetermined amount of water through the conduit 4, and then introduced into the enzyme reactor 5, where an enzyme is added and reacted. Separate the solid and liquid using Thrasher type (7). The liquid separated by the centrifuge is introduced into the separation plate cream separator 8 together with the liquid separated from the solid by the separation plate centrifuge 10, where it is separated into oil and water, and the oil and fat are transferred to the crude oil tank 9.
is led to and stored. The solid content separated by the thrasher (centrifugal separator) is guided to the separation plate centrifuge 10, where the liquid content is further separated, and the separated liquid content is transferred to the cream separator 8.
At the same time, the solid content is dried in a spray dryer 11, passed through a sifter 12, and then packed in bags by an automatic bagging machine 13 or the like.
次に、本発明の実施例を記載する。Next, examples of the present invention will be described.
実施例1
脱莢皮落花生種子10kgに同量の水を加えて加熱し、
温度90〜100℃にて、約60分間殺菌処理し、脱水
後同量の水を加えて、ミキサーにて粉砕し乳濁化する。Example 1 The same amount of water was added to 10 kg of dehulled peanut seeds and heated.
Sterilize at a temperature of 90 to 100°C for about 60 minutes, and after dehydration add the same amount of water and grind with a mixer to emulsify.
これに2倍量の水と酵素セルラーゼAp(大野製薬■)
とペクチナーゼ(マセロチーム2S、■ヤクルト本社)
各100g宛を加えて、47℃にて20時間、攪拌条件
下、酵素反応を行なう。次いでこの反応液を、90〜1
00℃に加熱して酵素の失活並びに殺菌処理を行なう。Add this to double the amount of water and the enzyme Cellulase Ap (Ohno Pharmaceutical ■)
and pectinase (Macero Team 2S, ■Yakult Honsha)
Add 100 g of each and perform the enzyme reaction at 47° C. for 20 hours under stirring conditions. Next, this reaction solution was heated to 90-1
The sample is heated to 00°C to deactivate the enzyme and sterilize it.
これを攪拌条件下でスラッシャ−に導入し、粗固液分離
を行なう。此の時点で、固形分中の油分は5%以下であ
った。This is introduced into a slasher under stirring conditions to perform crude solid-liquid separation. At this point, the oil content in the solid content was 5% or less.
油水層は、クリームセパレータを用いて油分と水分とに
分離し、透明な油分約4kg(水分含有率0.5wt%
以下、比重0.92 )を得た。一方、スラッジ層は、
約2倍量の熱湯を加えて、分離板型遠心分離機に導入し
て精密分離し、スプレードライヤーを用いて粉末化し、
含油分1%以下の乾燥固形公約3.5 kgを得た。The oil-water layer is separated into oil and water using a cream separator, and approximately 4 kg of transparent oil (moisture content 0.5 wt%) is obtained.
Hereinafter, a specific gravity of 0.92) was obtained. On the other hand, the sludge layer
Add about twice the amount of hot water, introduce it into a separator plate centrifuge for precise separation, and use a spray dryer to powder it.
Approximately 3.5 kg of dry solids with an oil content of less than 1% were obtained.
実施例2
実施例1の酵素セルラーゼApに代えて、ドリセラーゼ
(協和発酵工業−)100gを用いた他、実施例1と同
様に行なった。その結果、実施例1と同様な結果を得た
。Example 2 The same procedure as in Example 1 was carried out except that 100 g of Driselase (Kyowa Hakko Kogyo) was used instead of the enzyme cellulase Ap used in Example 1. As a result, the same results as in Example 1 were obtained.
実施例3
実施例2のペクチナーゼに代えて、スクラーゼS(三共
@J)及びペクチナーゼ(東洋醸造■ン各50g宛を用
いた他は、実施例2と同様に行なった。その結果は、実
施例1と同様であった。Example 3 The same procedure as in Example 2 was carried out, except that sucrase S (Sankyo@J) and pectinase (50 g each of Toyo Jojo Co., Ltd.) were used in place of the pectinase in Example 2.The results are as shown in Example 2. It was the same as 1.
第1図は本発明方法の一例の工程を示す図である。
1・・・脱皮装置、2・・・蒸煮殺菌機、3・・・ミキ
サ5・・・酵素反応機、6・・・加熱機、7・・・遠心
分離機、8・・・クリームセパレータ、9・・・原油タ
ンク、10・・・遠心分離機、11・・・スプレードラ
イヤー 13・・・自動袋詰機FIG. 1 is a diagram showing steps of an example of the method of the present invention. 1... Dehulling device, 2... Steam sterilizer, 3... Mixer 5... Enzyme reactor, 6... Heating machine, 7... Centrifugal separator, 8... Cream separator, 9...crude oil tank, 10...centrifugal separator, 11...spray dryer 13...automatic bagging machine
Claims (1)
濁状液を、セルラーゼ、又は、セルラーゼ及びペクチナ
ーゼ混合物を用いて処理する事を特徴とする、落花生種
子より油脂分と蛋白質分とを製造する方法。1. After dehulling and heat sterilization, the crushed peanut seed emulsion is treated with cellulase or a mixture of cellulase and pectinase to remove oil, fat and protein from peanut seeds. How to manufacture.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP19768290A JPH0484861A (en) | 1990-07-27 | 1990-07-27 | Method for preparing fat and oil components and protein component from peanut seed |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP19768290A JPH0484861A (en) | 1990-07-27 | 1990-07-27 | Method for preparing fat and oil components and protein component from peanut seed |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH0484861A true JPH0484861A (en) | 1992-03-18 |
Family
ID=16378593
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP19768290A Pending JPH0484861A (en) | 1990-07-27 | 1990-07-27 | Method for preparing fat and oil components and protein component from peanut seed |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0484861A (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2002105483A (en) * | 2000-09-28 | 2002-04-10 | Kanegafuchi Chem Ind Co Ltd | Method for treating pomegranate seed |
JP2009178135A (en) * | 2008-01-31 | 2009-08-13 | Kao Corp | Edible oil producing method |
JP2009232857A (en) * | 2009-06-22 | 2009-10-15 | Kizakura Co Ltd | Method for producing rice protein, rice protein produced by the method, and food |
CN104479854A (en) * | 2014-11-27 | 2015-04-01 | 江南大学 | Method for extracting peanut oil and peanut protein simultaneously |
US9615596B2 (en) | 2016-03-14 | 2017-04-11 | Kraft Foods Group Brands Llc | Protein products and methods for making the same |
CN107125430A (en) * | 2017-03-10 | 2017-09-05 | 河南工业大学 | It is a kind of while the method for preparing oil body and non-hydrolyzed protein matter |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5581549A (en) * | 1978-12-12 | 1980-06-19 | Safinco Nv | Obtaining of gel forming protein product |
-
1990
- 1990-07-27 JP JP19768290A patent/JPH0484861A/en active Pending
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5581549A (en) * | 1978-12-12 | 1980-06-19 | Safinco Nv | Obtaining of gel forming protein product |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2002105483A (en) * | 2000-09-28 | 2002-04-10 | Kanegafuchi Chem Ind Co Ltd | Method for treating pomegranate seed |
JP2009178135A (en) * | 2008-01-31 | 2009-08-13 | Kao Corp | Edible oil producing method |
JP2009232857A (en) * | 2009-06-22 | 2009-10-15 | Kizakura Co Ltd | Method for producing rice protein, rice protein produced by the method, and food |
CN104479854A (en) * | 2014-11-27 | 2015-04-01 | 江南大学 | Method for extracting peanut oil and peanut protein simultaneously |
US9615596B2 (en) | 2016-03-14 | 2017-04-11 | Kraft Foods Group Brands Llc | Protein products and methods for making the same |
US11533927B2 (en) | 2016-03-14 | 2022-12-27 | Kraft Foods Group Brands Llc | Protein products and methods for making the same |
CN107125430A (en) * | 2017-03-10 | 2017-09-05 | 河南工业大学 | It is a kind of while the method for preparing oil body and non-hydrolyzed protein matter |
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