JPH048037B2 - - Google Patents
Info
- Publication number
- JPH048037B2 JPH048037B2 JP57202087A JP20208782A JPH048037B2 JP H048037 B2 JPH048037 B2 JP H048037B2 JP 57202087 A JP57202087 A JP 57202087A JP 20208782 A JP20208782 A JP 20208782A JP H048037 B2 JPH048037 B2 JP H048037B2
- Authority
- JP
- Japan
- Prior art keywords
- lipase
- oils
- decomposition
- fats
- added
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 238000000354 decomposition reaction Methods 0.000 claims description 25
- 102000004882 Lipase Human genes 0.000 claims description 23
- 108090001060 Lipase Proteins 0.000 claims description 23
- 239000004367 Lipase Substances 0.000 claims description 23
- 235000019421 lipase Nutrition 0.000 claims description 23
- 239000003925 fat Substances 0.000 claims description 22
- 239000003921 oil Substances 0.000 claims description 21
- NHTMVDHEPJAVLT-UHFFFAOYSA-N Isooctane Chemical compound CC(C)CC(C)(C)C NHTMVDHEPJAVLT-UHFFFAOYSA-N 0.000 claims description 6
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 claims description 6
- JVSWJIKNEAIKJW-UHFFFAOYSA-N dimethyl-hexane Natural products CCCCCC(C)C JVSWJIKNEAIKJW-UHFFFAOYSA-N 0.000 claims description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 6
- YCOZIPAWZNQLMR-UHFFFAOYSA-N heptane - octane Natural products CCCCCCCCCCCCCCC YCOZIPAWZNQLMR-UHFFFAOYSA-N 0.000 claims description 4
- 238000000034 method Methods 0.000 claims description 4
- 235000019197 fats Nutrition 0.000 description 20
- 235000019198 oils Nutrition 0.000 description 18
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 10
- 239000003960 organic solvent Substances 0.000 description 10
- 235000014113 dietary fatty acids Nutrition 0.000 description 6
- 229930195729 fatty acid Natural products 0.000 description 6
- 239000000194 fatty acid Substances 0.000 description 6
- 150000004665 fatty acids Chemical class 0.000 description 6
- 235000011187 glycerol Nutrition 0.000 description 5
- 235000015278 beef Nutrition 0.000 description 4
- 239000003760 tallow Substances 0.000 description 4
- 238000007796 conventional method Methods 0.000 description 3
- 239000004006 olive oil Substances 0.000 description 3
- 235000008390 olive oil Nutrition 0.000 description 3
- 239000002994 raw material Substances 0.000 description 3
- 241001465754 Metazoa Species 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 239000007853 buffer solution Substances 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 241000251468 Actinopterygii Species 0.000 description 1
- 241000222120 Candida <Saccharomycetales> Species 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 235000019482 Palm oil Nutrition 0.000 description 1
- 108010019160 Pancreatin Proteins 0.000 description 1
- 235000004443 Ricinus communis Nutrition 0.000 description 1
- 241000179532 [Candida] cylindracea Species 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003240 coconut oil Substances 0.000 description 1
- 235000019864 coconut oil Nutrition 0.000 description 1
- 235000021588 free fatty acids Nutrition 0.000 description 1
- 235000019626 lipase activity Nutrition 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 230000000813 microbial effect Effects 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
- 239000002540 palm oil Substances 0.000 description 1
- 229940055695 pancreatin Drugs 0.000 description 1
- 239000008363 phosphate buffer Substances 0.000 description 1
- 235000015277 pork Nutrition 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 238000004448 titration Methods 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 235000019871 vegetable fat Nutrition 0.000 description 1
Landscapes
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Fats And Perfumes (AREA)
Description
リパーゼを用いて油脂を分解する方法について
は古くから報告があるが、工業的に用いられてい
る例は少ない。その原因としてはリパーゼの価格
が高く大量に用いられないので分解率を上げられ
ない点にある。
本発明者は、これらの点を改良すべく種々研究
を進めた結果、リパーゼを用いる油脂の分解反応
において、ヘプタン又はイソオクタンを添加して
分解を行なうと、分解速度が速くなり油脂の分解
率を上昇させ、リパーゼの添加量を減少させるこ
とができることを見出し、本発明を完成するに到
つた。
即ち、本発明は、リパーゼを用いて油脂を分解
するに際し、分解反応系にヘプタン又はイソオク
タンを添加することを特徴とするリパーゼによる
油脂の分解方法である。
本発明において用いられるリパーゼとしては、
油脂の分解力の強いものであれば動植物、微生物
の起源を問わずすべて用いることができる。その
具体例として、パンクレアチンのリパーゼ、ヒマ
種子のリパーゼ、或はキヤンデイダ(Candida)
属の微生物、例えばキヤンデイダ・シリンドラセ
(Candida cylindracea)の生産するリパーゼ、
さらに市販のリパーゼなどが挙げられる。
また油脂分解の原料となる油脂としては、例え
ば牛脂、豚脂、魚脂などの動物油脂、或はヤシ
油、パーム油、大豆油、オリーブ油などの植物油
脂が使用できる。
この油脂を分解するに際し添加する水の量は、
通常油脂1に対し0.3〜7、好ましくは0.5〜3.0の
割合とするのがよいが、原料油脂の種類、及びリ
パーゼの種類とその添加量によつても異る。
ヘプタン又はイソオクタンの添加量は、水の使
用量の5〜70%、好ましくは10〜50%である。そ
してこれらの有機溶媒は油脂の分解反応の最初か
ら加えておいてもよく、また反応途中で添加して
もよい。
分解反応の温度および時間としては、リパーゼ
による油脂の分解反応に通常使用される温度およ
び時間が用いられる。
本発明によつて油脂を分解した場合、反応終了
後に静置すると、反応生成物は二層、即ち脂肪酸
を含んだ有機溶媒層である上層とグリセリンを含
んだ水層である下層に分離する。この二層は容易
に分離するので、遠心分離機などを使う必要はな
い。上層の有機溶媒層は蒸留して有機溶媒と脂肪
酸に分け、有機溶媒は再び次の分解に使用する。
また、下層の水層は通常の方法により濃縮してグ
リセリンを回収する。更に水層中にはリパーゼ活
性が残存しているので、この水層をそのまま次回
の分解に用い、不足分のリパーゼを添加して油脂
の分解をすることにより、リパーゼの使用量を節
減することができる。
本発明によれば、リパーゼによる油脂の分解速
度が速くなり分解率を上昇させ、リパーゼの添加
量を減少させることができるので、本発明はリパ
ーゼによる油脂の分解方法として有用な方法であ
る。
次に本発明の実施例を示す。
実施例 1
リン酸緩衝液(PH7.7、1/15モル)240mlと牛脂
40gにキヤンデイダ・シリンドラセの生産するリ
パーゼを牛脂1g当り24単位(1単位は1分間に
1マイクロモルの脂肪酸を生成させるリパーゼ
量)になるように加えた2個のサンプルにそれぞ
れヘプタン60mlとイソオクタン60mlを加えて37℃
で撹拌しつつ分解を行つた。
また有機溶媒を加えない以外は、上記と同じ条
件で牛脂を分解し、緩衝液だけの場合と有機溶媒
を添加した場合とを比較した。
その結果を分解率%として次表に示す。なお分
解率は遊離脂肪酸量をアルカリ滴定して酸価
(AV)を求め、原料油脂がすべて分解した時の
酸価(AV0)との比率(AV/AV0×100)で示した。
Methods for decomposing fats and oils using lipase have been reported for a long time, but there are few examples of this being used industrially. The reason for this is that lipase is expensive and cannot be used in large quantities, making it impossible to increase the decomposition rate. As a result of conducting various studies to improve these points, the present inventor found that in the decomposition reaction of fats and oils using lipase, when heptane or isooctane is added to perform the decomposition, the decomposition rate becomes faster and the decomposition rate of fats and oils is reduced. The present inventors have discovered that it is possible to increase the amount of lipase and reduce the amount of lipase added, and have completed the present invention. That is, the present invention is a method for decomposing fats and oils using lipase, which is characterized by adding heptane or isooctane to the decomposition reaction system when decomposing fats and oils using lipase. The lipase used in the present invention includes:
Any material that has a strong ability to decompose fats and oils can be used regardless of its origin, whether animal, plant, or microbial. Specific examples include pancreatin lipase, castor seed lipase, or Candida.
Lipase produced by microorganisms of the genus, such as Candida cylindracea;
Further examples include commercially available lipases. In addition, as the fats and oils that serve as raw materials for fat decomposition, animal fats and oils such as beef tallow, pork fat, and fish fat, or vegetable fats and oils such as coconut oil, palm oil, soybean oil, and olive oil can be used. The amount of water added when decomposing this oil is
Usually, the ratio is preferably 0.3 to 7, preferably 0.5 to 3.0, per 1 of fat or oil, but it varies depending on the type of raw material oil and fat, and the type and amount of lipase added. The amount of heptane or isooctane added is 5 to 70%, preferably 10 to 50% of the amount of water used. These organic solvents may be added from the beginning of the fat and oil decomposition reaction, or may be added during the reaction. As the temperature and time for the decomposition reaction, the temperature and time normally used for the decomposition reaction of fats and oils by lipase are used. When fats and oils are decomposed according to the present invention, when left to stand after the reaction is completed, the reaction product separates into two layers: an upper layer that is an organic solvent layer containing fatty acids and a lower layer that is an aqueous layer containing glycerin. These two layers are easily separated, so there is no need to use a centrifuge. The upper organic solvent layer is distilled and separated into organic solvent and fatty acid, and the organic solvent is used again for the next decomposition.
Further, the lower aqueous layer is concentrated by a conventional method to recover glycerin. Furthermore, since lipase activity remains in the aqueous layer, the amount of lipase used can be reduced by using this aqueous layer as it is for the next decomposition and adding the insufficient amount of lipase to decompose the fats and oils. I can do it. According to the present invention, the rate of decomposition of fats and oils by lipase becomes faster, the decomposition rate increases, and the amount of lipase added can be reduced, so the present invention is a useful method for decomposing fats and oils by lipase. Next, examples of the present invention will be shown. Example 1 Add lipase produced by Candeida Cylindrace to 240 ml of phosphate buffer (PH 7.7, 1/15 mol) and 40 g of beef tallow at 24 units per 1 g of beef tallow (1 unit produces 1 micromole of fatty acids per minute). 60 ml of heptane and 60 ml of isooctane were added to each of the two samples, and the mixture was heated to 37°C.
Decomposition was carried out while stirring. In addition, beef tallow was decomposed under the same conditions as above, except that no organic solvent was added, and the cases in which only a buffer solution was used and the cases in which an organic solvent was added were compared. The results are shown in the following table as decomposition rate %. The decomposition rate was determined by alkaline titration of the amount of free fatty acids to determine the acid value (AV), and was expressed as a ratio (AV/AV 0 ×100) to the acid value (AV 0 ) when all the raw material fats and oils were decomposed.
【表】
上記の表から、いずれの有機溶媒を加えた場合
も緩衝液だけの場合と比べ分解速度は速くなり分
解率も上昇させることができることがわかる。
つぎに上記分解物を静置して二層に分解させ
た。そして上層の脂肪酸を含んだ有機溶媒層から
常法により有機溶媒を留去して脂肪酸を得、また
下層のグリセリンを含んだ水層から水を蒸発させ
てグリセリンを得た。
実施例 2
水240mlとオリーブ油50gに市販のリパーゼ
(名糖産業株式会社製)をオリーブ油1g当り50単
位になるように加え、更にイソオクタン80mlを加
えて30℃で撹拌しつつ分解を行つた。5時間後の
分解率は90%、10時間後の分解率は98%であつ
た。
10時間後に分解物を静置して二層に分解し、上
層からは常法によりオクタンを留去して脂肪酸を
採取し、下層からは水を蒸発させてグリセリンを
採取した。[Table] From the table above, it can be seen that when any organic solvent is added, the decomposition rate becomes faster and the decomposition rate can also be increased compared to when only a buffer solution is used. Next, the decomposition product was allowed to stand still and decomposed into two layers. Then, the organic solvent was distilled off from the upper organic solvent layer containing fatty acids by a conventional method to obtain fatty acids, and the water was evaporated from the lower aqueous layer containing glycerin to obtain glycerin. Example 2 Commercially available lipase (manufactured by Meito Sangyo Co., Ltd.) was added to 240 ml of water and 50 g of olive oil in an amount of 50 units per 1 g of olive oil, and 80 ml of isooctane was added and decomposition was carried out with stirring at 30°C. The decomposition rate after 5 hours was 90%, and the decomposition rate after 10 hours was 98%. After 10 hours, the decomposition product was allowed to stand still and decomposed into two layers, octane was distilled off from the upper layer by a conventional method to collect fatty acids, and water was evaporated from the lower layer to collect glycerin.
Claims (1)
を必須成分として含む分解反応系にヘプタン又は
イソオクタンを添加することを特徴とするリパー
ゼによる油脂の分解方法。1. A method for decomposing fats and oils using lipase, which comprises adding heptane or isooctane to a decomposition reaction system containing water as an essential component when decomposing fats and oils using lipase.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP57202087A JPS5991889A (en) | 1982-11-19 | 1982-11-19 | Method for decomposing fat or oil |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP57202087A JPS5991889A (en) | 1982-11-19 | 1982-11-19 | Method for decomposing fat or oil |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5991889A JPS5991889A (en) | 1984-05-26 |
JPH048037B2 true JPH048037B2 (en) | 1992-02-13 |
Family
ID=16451747
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP57202087A Granted JPS5991889A (en) | 1982-11-19 | 1982-11-19 | Method for decomposing fat or oil |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5991889A (en) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2588272B1 (en) * | 1985-10-07 | 1988-12-02 | Gattefosse Ets Sa | PROCESS FOR THE SYNTHESIS OF ORGANIC ACID ESTERS AND ALCOHOLS IN THE HETEROGENEOUS PHASE BY ENZYMATIC CATALYSIS |
JP2547330B2 (en) * | 1987-10-09 | 1996-10-23 | 株式会社平和 | Wiring device for pachinko machines |
JPH07116467B2 (en) * | 1990-06-01 | 1995-12-13 | 日本碍子株式会社 | Hydrolyzer |
JPH07116466B2 (en) * | 1990-06-01 | 1995-12-13 | 日本碍子株式会社 | Method of hydrolyzing fats and oils |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS576480A (en) * | 1980-06-13 | 1982-01-13 | Nec Corp | Buffer memory control system |
-
1982
- 1982-11-19 JP JP57202087A patent/JPS5991889A/en active Granted
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS576480A (en) * | 1980-06-13 | 1982-01-13 | Nec Corp | Buffer memory control system |
Also Published As
Publication number | Publication date |
---|---|
JPS5991889A (en) | 1984-05-26 |
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