JPH03277247A - Preparation of edible raw material using ginseng - Google Patents
Preparation of edible raw material using ginsengInfo
- Publication number
- JPH03277247A JPH03277247A JP2077420A JP7742090A JPH03277247A JP H03277247 A JPH03277247 A JP H03277247A JP 2077420 A JP2077420 A JP 2077420A JP 7742090 A JP7742090 A JP 7742090A JP H03277247 A JPH03277247 A JP H03277247A
- Authority
- JP
- Japan
- Prior art keywords
- ginseng
- engine
- fermentation
- fermented
- medicinal
- 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
- 239000002994 raw material Substances 0.000 title abstract description 4
- 235000003140 Panax quinquefolius Nutrition 0.000 title abstract 7
- 235000008434 ginseng Nutrition 0.000 title abstract 7
- 235000005035 Panax pseudoginseng ssp. pseudoginseng Nutrition 0.000 title abstract 6
- 241000208340 Araliaceae Species 0.000 title description 2
- 241000894006 Bacteria Species 0.000 claims abstract description 28
- 239000000463 material Substances 0.000 claims abstract description 20
- 239000000758 substrate Substances 0.000 claims abstract description 3
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 claims description 48
- 239000004310 lactic acid Substances 0.000 claims description 24
- 235000014655 lactic acid Nutrition 0.000 claims description 24
- 239000000284 extract Substances 0.000 claims description 7
- 238000004519 manufacturing process Methods 0.000 claims description 3
- 238000000855 fermentation Methods 0.000 abstract description 35
- 230000004151 fermentation Effects 0.000 abstract description 35
- 239000000796 flavoring agent Substances 0.000 abstract description 14
- 235000019634 flavors Nutrition 0.000 abstract description 14
- 235000013305 food Nutrition 0.000 abstract description 11
- 239000004480 active ingredient Substances 0.000 abstract description 9
- 241001632410 Eleutherococcus senticosus Species 0.000 abstract description 7
- 235000013618 yogurt Nutrition 0.000 abstract description 4
- 239000012670 alkaline solution Substances 0.000 abstract description 2
- 239000000872 buffer Substances 0.000 abstract description 2
- 235000013351 cheese Nutrition 0.000 abstract description 2
- 239000003795 chemical substances by application Substances 0.000 abstract description 2
- 235000021110 pickles Nutrition 0.000 abstract description 2
- 240000004371 Panax ginseng Species 0.000 abstract 6
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 abstract 2
- 235000002789 Panax ginseng Nutrition 0.000 abstract 1
- 241000168720 Panax japonicus Species 0.000 abstract 1
- 235000003174 Panax japonicus Nutrition 0.000 abstract 1
- 241000180649 Panax notoginseng Species 0.000 abstract 1
- 235000003143 Panax notoginseng Nutrition 0.000 abstract 1
- 240000005373 Panax quinquefolius Species 0.000 abstract 1
- 229910000019 calcium carbonate Inorganic materials 0.000 abstract 1
- 239000007788 liquid Substances 0.000 description 17
- 230000000052 comparative effect Effects 0.000 description 13
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 12
- 239000000047 product Substances 0.000 description 11
- 235000013361 beverage Nutrition 0.000 description 10
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 9
- 229930182490 saponin Natural products 0.000 description 8
- 150000007949 saponins Chemical class 0.000 description 8
- 235000017709 saponins Nutrition 0.000 description 8
- 235000000346 sugar Nutrition 0.000 description 8
- 230000000694 effects Effects 0.000 description 7
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- 206010020649 Hyperkeratosis Diseases 0.000 description 5
- 230000007423 decrease Effects 0.000 description 5
- 239000006228 supernatant Substances 0.000 description 5
- 235000019658 bitter taste Nutrition 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 239000001397 quillaja saponaria molina bark Substances 0.000 description 4
- 230000001953 sensory effect Effects 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 3
- 235000009508 confectionery Nutrition 0.000 description 3
- 239000000835 fiber Substances 0.000 description 3
- 235000011389 fruit/vegetable juice Nutrition 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- 235000015097 nutrients Nutrition 0.000 description 3
- 241000196324 Embryophyta Species 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- 229930006000 Sucrose Natural products 0.000 description 2
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 244000299461 Theobroma cacao Species 0.000 description 2
- 235000013365 dairy product Nutrition 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- 235000019441 ethanol Nutrition 0.000 description 2
- 238000000605 extraction Methods 0.000 description 2
- 238000000227 grinding Methods 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 239000000741 silica gel Substances 0.000 description 2
- 229910002027 silica gel Inorganic materials 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 230000001954 sterilising effect Effects 0.000 description 2
- 238000004659 sterilization and disinfection Methods 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 239000005720 sucrose Substances 0.000 description 2
- 235000019640 taste Nutrition 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 1
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 1
- 229930182843 D-Lactic acid Natural products 0.000 description 1
- JVTAAEKCZFNVCJ-UWTATZPHSA-N D-lactic acid Chemical compound C[C@@H](O)C(O)=O JVTAAEKCZFNVCJ-UWTATZPHSA-N 0.000 description 1
- 244000000626 Daucus carota Species 0.000 description 1
- 235000002767 Daucus carota Nutrition 0.000 description 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
- 241001558017 Gynura Species 0.000 description 1
- 241000186660 Lactobacillus Species 0.000 description 1
- 244000294411 Mirabilis expansa Species 0.000 description 1
- 235000015429 Mirabilis expansa Nutrition 0.000 description 1
- 241000208343 Panax Species 0.000 description 1
- 235000002791 Panax Nutrition 0.000 description 1
- 235000009470 Theobroma cacao Nutrition 0.000 description 1
- 230000002159 abnormal effect Effects 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 235000001014 amino acid Nutrition 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 235000015173 baked goods and baking mixes Nutrition 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 229940041514 candida albicans extract Drugs 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
- 235000019219 chocolate Nutrition 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 235000016213 coffee Nutrition 0.000 description 1
- 235000013353 coffee beverage Nutrition 0.000 description 1
- 235000011850 desserts Nutrition 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 235000013399 edible fruits Nutrition 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000002255 enzymatic effect Effects 0.000 description 1
- 235000021107 fermented food Nutrition 0.000 description 1
- 235000012041 food component Nutrition 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 230000008821 health effect Effects 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 235000015110 jellies Nutrition 0.000 description 1
- 229940039696 lactobacillus Drugs 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000013536 miso Nutrition 0.000 description 1
- 239000011259 mixed solution Substances 0.000 description 1
- 210000000496 pancreas Anatomy 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 229930004725 sesquiterpene Natural products 0.000 description 1
- 150000004354 sesquiterpene derivatives Chemical class 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 235000014347 soups Nutrition 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 150000008163 sugars Chemical class 0.000 description 1
- 235000013616 tea Nutrition 0.000 description 1
- 238000004809 thin layer chromatography Methods 0.000 description 1
- 230000001256 tonic effect Effects 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 239000012138 yeast extract Substances 0.000 description 1
Abstract
Description
【発明の詳細な説明】
産業上の利用分野
この発明は、薬用エンジンを乳酸菌で発酵して風味を改
善する際、その有効成分を損なうことな(処理しようと
するものであり、薬用エンジンを食用素材として用いる
とき利用される。DETAILED DESCRIPTION OF THE INVENTION Field of Industrial Application This invention aims to improve the flavor of medicated engine by fermenting it with lactic acid bacteria, without damaging its active ingredients. Used when used as a material.
従来の技術
オタネエンジン、アメリカエンジン、エゾウコギなどの
薬用エンジンは、保健強壮、健胃などの効果が知られて
おり、薬用として昔から広く利用されている。また、そ
の主な有効成分が各種のジン七ノサイドを含むサポニン
類であることも知られている。Conventional technology Medicinal engines such as Otane engine, American engine, and Eleuthero are known for their health tonic and stomach-boosting effects, and have been widely used for medicinal purposes since ancient times. It is also known that its main active ingredients are saponins including various gin heptansides.
薬用エンジンは、中国や韓国などでは薬膳などの材料と
して興理食品に用いられているか、特有の苦味が強く、
しかも泥臭さなどの臭いもあるため、食品に用いる場合
、使用量か著しく制限され、少し多く用いると風味か劣
るものとなる。従って、通常の食用素材としては、はと
んど利用されていない。Medicinal engine is used as an ingredient in medicinal dishes in China and Korea, or it has a unique bitter taste.
Moreover, since it has a muddy odor, the amount of use is severely limited when used in foods, and if a little too much is used, the flavor will be poor. Therefore, it is rarely used as a normal edible material.
薬用エンジンを用いた発酵食品としてヨーグルト(特開
昭63−216432号)が知られている。これは、薬
用エンジンを水と共に破砕した後固形分を除いた薬用エ
ンジンジュースを、直接又は糖若しくは乳製品を加えて
から乳酸菌を接種し、発酵させたものであり、これを直
接摂取するものである。なお、薬用エンジンを発酵させ
、他の食品の素材として利用することは、従来行われて
いなかった。Yogurt (Japanese Unexamined Patent Publication No. 63-216432) is known as a fermented food using a medicinal engine. This is made by crushing medicated engine juice with water and removing the solid content, and then fermenting it directly or by adding sugar or dairy products, inoculating lactic acid bacteria, and fermenting it. be. Note that fermenting medicinal engines and using them as ingredients for other foods has not been done in the past.
発明が解決しようとする課題
例えば比較試験例にも見られるように、この発明の発明
者らか得た知見によると、薬用エンジン成分に乳酸菌を
加えて発酵させると発酵の進行に従いpHが低下し、通
常pH3,7或はそれ以下となり、糖などの発酵栄養成
分を加えると3.5以下となることもある。このように
低いpHでは、有効+1であるジンセッサイドの減少が
みられ、pH3,0以下となるとジンセッサイドが全く
存在しないものとなることか知られた。Problems to be Solved by the Invention According to the knowledge obtained by the inventors of the present invention, as can be seen in the comparative test examples, when lactic acid bacteria are added to the medicinal engine component and fermented, the pH decreases as the fermentation progresses. The pH is usually 3.7 or lower, and may be lower than 3.5 if fermented nutritional components such as sugar are added. At such a low pH, a decrease in ginsside, which is effective +1, is observed, and when the pH falls below 3.0, no ginsside is present at all.
この発明は、薬用エンジンの有効成分を損なうことなく
乳酸菌で発酵させ、風味を改良しようとするものである
。This invention aims to improve the flavor of medicinal engines by fermenting them with lactic acid bacteria without damaging their active ingredients.
これにより薬用エンジンの有効成分を高いレベルで含み
、しかも風味の優れた食用素材を供することを目的とし
ており、薬用エンジンの有効成分を含み、風味の良好な
食品を供することも目的としている。The purpose of this is to provide an edible material that contains a high level of the active ingredient of medicinal engine and has an excellent flavor.It also aims to provide a food that contains the active ingredient of medicinal engine and has a good flavor.
課題を解決するための手段
この発明の発明者は、薬用エンジンの有効成分であるジ
ンセッサイドがpH4,0までは比較的安定であるが、
pH3,8以下となると減少することを見いだし、この
発明を完成させた。Means for Solving the Problems The inventor of the present invention discovered that ginsicide, which is an active ingredient in medicinal engines, is relatively stable up to pH 4.0;
It was discovered that this decreases when the pH is lower than 3.8, and this invention was completed.
この発明は、薬用エンジンの破砕物、磨砕物又は抽出物
或はこれらを含む基質に乳酸菌を接種し、pH4,0以
上、好ましくはpH4,5以上に保ちながら発酵させて
食用素材とするものである。In this invention, lactic acid bacteria are inoculated into crushed, ground, or extracts of medicinal engines, or substrates containing these, and fermented while maintaining the pH at 4.0 or higher, preferably at 4.5 or higher, to produce an edible material. be.
薬用エンジンとしてオタネエンジン、アメリカエンジン
、エゾウコギ、チクセツエンジン、三七エンジンなどウ
コギ科植物、特にPanaX属、Eleutheroc
occus@、Gynura属に属する植物、或はこれ
らの植物の組織培養物などが用いられる。As a medicinal engine, Araliaceae plants such as Otane engine, American engine, Eleuthero, Chikusetsu engine, Sanshichi engine, especially PanaX genus, Eleutheroc
plants belonging to the genus Gynura, or tissue cultures of these plants are used.
また、使用する部位もエゾウコギで茎、オタネエンジン
やアメリカエンジンなどのその他の薬用エンジンで根が
通常用いられるが、これに限定するものでな(、サポニ
ン類を含むそれ以外の部位も用いることかできる。また
、これらの薬用エンジンは、生のまま、又は乾燥したも
のなど任意の状態のものが利用できる。In addition, the parts used are usually the stems of Eleuthero, and the roots of other medicinal engines such as Otane engine and American engine, but the parts used are not limited to these (although other parts containing saponins may also be used). Furthermore, these medicinal engines can be used in any desired state, such as fresh or dried.
発酵処理する前に薬用エンジンは、先ず破砕、磨砕又は
抽出処理する。Before being fermented, the medicinal engine is first crushed, ground or extracted.
破砕又は磨砕するには、薬用エンジンを直接処理しても
よいが、水を加えてから行うのがよい。For crushing or grinding, the medicinal engine may be processed directly, but it is better to do so after adding water.
すなわち、薬用エンジンをフードカッターなどで細断し
、その重量の50〜400%の水を加え、ミキサーその
他公知の破砕機で破砕する、細かくした薬用エンジンを
円盤型磨砕機などの磨砕装置で磨砕する、などの方法で
処理する。In other words, the medicated engine is shredded with a food cutter, water is added to the mixture in an amount of 50 to 400% of its weight, and the mixture is crushed using a mixer or other known crusher. Process by grinding or other methods.
抽圧は、細断、破砕又は磨砕した薬用エンジンに使用目
的に応じ適量の水を加えて行う。また、アルコール水溶
液などの溶媒で抽出した後、減圧濃縮などで溶媒を除き
、乳酸菌の繁殖が可能な状態としてもよい。Extraction is carried out by adding an appropriate amount of water to the shredded, crushed or ground medicinal engine depending on the purpose of use. Alternatively, after extraction with a solvent such as an aqueous alcohol solution, the solvent may be removed by vacuum concentration or the like to create a state in which lactic acid bacteria can propagate.
次に薬用ニンジ/の破砕物、磨砕物又は抽出物などの薬
用エンジン処理物に乳酸菌を接種して、発酵させる。こ
の際、使用する乳酸菌として、ヨーグルト、チーズ、漬
物などの食品に用いられる乳酸菌など所望に応じ任意の
乳酸菌が利用可能である。Next, lactic acid bacteria are inoculated into a medicinal engine-treated product such as a crushed product, a ground product, or an extract of medicinal carrots, and fermentation is performed. At this time, any lactic acid bacteria can be used as desired, such as lactic acid bacteria used in foods such as yogurt, cheese, and pickles.
なお、薬用エンジン処理物に野菜や果実の破砕物や汁液
、乳製品、茶類、コーヒー、ココア、糖類などの食品原
料を加えてから発酵させてももよい。Note that food materials such as crushed vegetables and fruits, juices, dairy products, teas, coffee, cocoa, sugars, etc. may be added to the medicated engine-treated product before fermentation.
また、薬用エンジンの処理物は、雑菌を除き、発酵を円
滑に行わせるため、乳酸菌を接種する前に加熱殺菌など
の殺菌処理を行うようにするのが望ましい。Furthermore, in order to remove bacteria from the medicinal engine and ensure smooth fermentation, it is desirable to perform sterilization treatment such as heat sterilization before inoculating lactic acid bacteria.
発酵は、薬用エンジンの処理物に、あらかじめ炭酸力ル
ンウムなとの難溶性アルカリ剤を加える、緩衝剤を加え
る、或は発酵の進行に従いアルカリ溶液をときどき滴下
するなど公知の方法で発酵により生じる酸を中和し、p
Hが4.0以下とならないようにする。しかし、pHが
40に近い値で発酵を続けると、発酵のわずかな亢進で
思いがけないpHの低下をきたし、有効成分の減少を起
すおそれがあるので、なるへくならp H4、5前後で
発酵するのが望ましい。また、発酵によりpHが低下し
、4.3前後となったら発酵を停止し、40以下となら
ないようにしてもよい。Fermentation is carried out by adding a poorly soluble alkaline agent such as carbonic acid to the medicinal engine in advance, adding a buffer, or occasionally dropping an alkaline solution as the fermentation progresses to remove the acid produced by fermentation. neutralizes p
Make sure that H does not fall below 4.0. However, if fermentation is continued at a pH close to 40, a slight increase in fermentation may cause an unexpected drop in pH, leading to a decrease in active ingredients. It is desirable to do so. Further, when the pH decreases due to fermentation and reaches around 4.3, fermentation may be stopped to prevent the pH from dropping below 40.
なお、必要により発酵前の薬用エンジンの処理物に糖、
アミノ酸、ビタミン、ミネラルなどの発酵栄養源を添加
してから発酵を行ってもよい。In addition, if necessary, sugar,
Fermentation may be performed after adding fermentation nutrients such as amino acids, vitamins, and minerals.
発酵は、使用した乳酸菌が増殖し得る温度範囲で行えば
よく、それにより薬用エンジンの風味の改善に効果がみ
られる。具体的には、25〜40℃の温度範囲で各々の
乳酸菌の至適増殖温度の前後、或はそれより5°C位低
い温度で行うのが好ましい。Fermentation can be carried out at a temperature range that allows the lactic acid bacteria used to grow, and this is effective in improving the flavor of medicinal engines. Specifically, it is preferable to carry out the reaction at a temperature in the range of 25 to 40°C, around the optimum growth temperature of each lactic acid bacterium, or about 5°C lower than that.
また、発酵は、静置した状態又は緩やかに撹拌した状態
で行うのが好ましく、強く攪拌しながら発酵すると、乳
酸の生成が抑えられ、ときには異常発酵による異臭が生
じるので、好ましくない。In addition, it is preferable to carry out the fermentation while standing still or with gentle stirring. Fermenting while stirring strongly is not preferable because it suppresses the production of lactic acid and sometimes produces an off-odor due to abnormal fermentation.
糖その他の発酵栄養源を加えずに発酵させる場合は、原
料由来の糖が消費しつくされた時点で発酵を終了しても
、風味改善に十分な効果が得られる。When fermentation is performed without adding sugar or other fermentation nutrient sources, a sufficient effect on flavor improvement can be obtained even if the fermentation is terminated when the sugar derived from the raw material is completely consumed.
しかし、糖などの発酵栄養源を加えて発酵させる場合は
、例えば10部個/9程度の菌を接種して10”個/9
程度に増殖したとき、又は培養液に対して 0.4%程
度の乳酸が生成したとき発酵を停止するようにする。し
かし、それ以前にても風味の改善が認められ、これによ
り発酵が進んでも風味に悪い影響が見られないので、所
望により任意の段階で発酵を停止することが可能である
。However, when fermenting by adding a fermentation nutrient source such as sugar, for example, inoculating about 10 parts/9 of bacteria and 10"/9
Fermentation should be stopped when the cells have grown to a certain level or when about 0.4% lactic acid is produced in the culture solution. However, the flavor is improved even before that point, and as a result, even if the fermentation progresses, there is no negative effect on the flavor, so it is possible to stop the fermentation at any stage if desired.
このようにして乳酸菌により発酵した薬用エンジン処理
物は、苦味がなくなり、しかも泥臭さなどの不快臭も感
じなくなり、優れた風味の食用素材となる。The medicated engine-treated product fermented by lactic acid bacteria in this manner has no bitterness and no unpleasant odor such as muddy odor, making it an edible material with excellent flavor.
発明の効果
この発明により処理した薬用エンジン発酵物ハ、例えば
実施例1〜15にも示すように、発酵していない薬用エ
ンジンに比べ風味がよ(、好まれるものとなった。従っ
て、例えば、ジュース、ドリンク類、ネクターなどの飲
料、シャーベット、アイスキャンデーなどの冷菓類、キ
ャンデー、ゼリー、焼き菓子などの菓子類、スープ、甘
酒、味噌、誠理食品などの食品を製造するときの素材と
して利用できる。Effects of the Invention As shown in Examples 1 to 15, the fermented medicinal engine treated according to the present invention had a better flavor (and became more desirable) than the unfermented medicinal engine. Therefore, for example, Used as an ingredient in the production of beverages such as juices, drinks, and nectars, frozen desserts such as sherbet and popsicles, confectionery such as candies, jellies, and baked goods, and foods such as soups, amazake, miso, and Seiri foods. can.
しかも、発酵処理物をそのまま利用することにより、薬
用エンジンの繊維質などが含まれたものとなり、繊維質
を除いて利用する場合に比べ薬用エンジンの効果と繊維
の効果を有する一層健康保持に適した素材となる。また
、発酵した上澄液又は発酵物全体を乾燥して粉末として
用いてもよく、水分を嫌うチョコレートや粉末飲料など
にも利用できる新しい食用素材とすることも可能である
。Moreover, by using the fermented product as it is, it contains the fiber of the medicinal engine, and is more suitable for maintaining health by having the effect of the medicinal engine and the effect of the fiber than when using it without the fiber. It becomes a material. In addition, the fermented supernatant liquid or the whole fermented product may be dried and used as a powder, and it is also possible to create a new edible material that can be used in chocolate, powdered drinks, etc. that dislike moisture.
しかも、比較試験にもみられるように、単に乳酸菌を加
えて発酵した場合、薬用エンジンの有効成分であるサポ
ニン類が減少し、ときにはほとんど存在しないこともあ
り得るが、この発明による場合、サポニン類の減少が少
なく、保険、健康上の効果が保持されたものとなる。Furthermore, as seen in comparative tests, if lactic acid bacteria were simply added and fermented, saponins, which are the active ingredients of medicinal engines, would be reduced, and in some cases almost non-existent. The reduction is small, and the insurance and health effects are maintained.
実施例1〜10
3年もののオタネエンジンの生の根をフードカッターで
細断し、3倍量の水を加え、家庭用のミキサーで破砕し
た。これを100℃で20分間加熱して殺菌処理した。Examples 1 to 10 The raw roots of 3-year-old Otane engine were shredded with a food cutter, 3 times the amount of water was added, and crushed with a household mixer. This was sterilized by heating at 100° C. for 20 minutes.
この殺菌したオタネエンジンの処理物のpHは 5.6
であった。次いで、これに表1に示す乳酸菌を接種し、
30℃にて48時間静置発酵させ、食用素材を得た。The pH of the processed material from this sterilized Otanega engine is 5.6.
Met. Next, lactic acid bacteria shown in Table 1 were inoculated into this,
Static fermentation was performed at 30° C. for 48 hours to obtain an edible material.
なお、発酵中は定期的にpHを測定し、必要に応じIN
炭酸水素す) IJウム溶液を滴下し、発酵物のpHを
4,5以上に保った。During fermentation, the pH should be measured periodically, and the pH should be adjusted as necessary.
Hydrogen carbonate solution) was added dropwise to maintain the pH of the fermented product at 4.5 or higher.
このようにして得たオタネエンジンの発酵物からなる食
用素材を用い、その10部(重量部、以下同じ)にしょ
糖10部、クエン酸 0.2部及び水80部を加え、オ
タネエンジンの飲料を調製した。Using the edible material made of the fermented product of Otane Engine obtained in this way, 10 parts of sucrose, 0.2 parts of citric acid, and 80 parts of water were added to 10 parts (by weight, the same hereinafter) of the edible material, and a drink of Otane Engine was prepared. was prepared.
各々の乳酸菌で発酵したオタネエンジンを食用素材とし
た各実施例の飲料と、殺菌処理しただけの発酵前のすタ
ネエンジンの処理物を用い同様に調整して得た比較例の
飲料との嗜好の比較を行う官能試験を25名のパネラ−
により行った結果、表1のようになった。Preferences between the beverages of each example using the edible material of Sotanenjin fermented with each lactic acid bacterium and the beverages of comparative examples prepared in the same way using the processed product of Sotanenjin that has just been sterilized and is not fermented. A sensory test was conducted by 25 panelists to compare the
The results were as shown in Table 1.
(以下余白)
表1
生オタネエンジンの乳酸菌発酵効果
なお、官能検査結果のaは各実施例の乳酸発酵したオタ
ネエンジンを用いた飲料を好むとした人の数、bは各実
施例の飲料と比較例の飲料との間に好みの差がないとし
た人の数、Cは乳酸菌処理していないオタネエンジンを
用いた比較例の飲料を好むとした人の数をそれぞれ示す
。(Leaving space below) Table 1 Lactic acid bacteria fermentation effect of raw Otanae Engine Note that in the sensory test results, a is the number of people who preferred the beverage made using the lactic acid-fermented Otanezin of each example, and b is the number of people who preferred the beverage using the lactic acid-fermented Otanese engine of each example. C indicates the number of people who said there was no difference in their preference between the drink of the comparative example and the drink of the comparative example, and C indicates the number of people who said they preferred the drink of the comparative example using the Otanae engine that was not treated with lactic acid bacteria.
各発酵液に窒素ガスを吹き込み、テナノクス濃縮管に送
気して揮発成分を捕集し、ガスクロマトグラムを求めた
結果、いずれも未発酵液を同様に処理して得られたガス
クロマトグラムに比べ薬用エンジン特有の臭気の成分で
あるセスキテルペン類等の量が減少していた。 また、
各発酵液の上澄み液より分離した粗サポニン量を5EP
−PAKC−18カラムを使用して測定した結果、いず
れも2,000〜2,400μg/峠であり、薬用エン
ジンの未発酵液の 2,570μ9/峠と比べ発酵によ
るサポニン類の減少がいずれもわずかであった。Nitrogen gas was blown into each fermented liquid, and the volatile components were collected by blowing into the Tenanox concentrator tube, and gas chromatograms were obtained. The amount of sesquiterpenes, which are components of engine odor, was reduced. Also,
The amount of crude saponin separated from the supernatant liquid of each fermentation liquid is 5EP.
-As a result of measurement using a PAKC-18 column, the amount of saponins due to fermentation was 2,000 to 2,400 μg/touge, compared to 2,570 μg/touge for unfermented medicinal engine liquid. It was very little.
更にまた、各々の発酵液及び未発酵液の上澄み液より粗
サポニンを分離し、分離した粗サポニンをシリカゲルの
薄層クロマトグラフィー(展開液n−ブタノール 酢酸
エチル:水=4:1:5)により分離し、クロマトスキ
ャナー(島津C5−920)で各スポットの大きさを測
定した。その結果、未発酵液のスポットを 10として
各発酵液の相当するスポットを相対値で求めると、いず
れも0.8〜13の範囲にあり、はぼ等しかった。Furthermore, crude saponin was separated from the supernatant liquid of each fermented liquid and unfermented liquid, and the separated crude saponin was subjected to silica gel thin layer chromatography (developing liquid: n-butanol, ethyl acetate: water = 4:1:5). The spots were separated and the size of each spot was measured using a chromato scanner (Shimadzu C5-920). As a result, when the spots of the unfermented liquor were determined as 10 and the corresponding spots of each fermented liquor were calculated as relative values, they were all in the range of 0.8 to 13 and were not equal.
実施例11〜15
組織培養したオタネエンジンのカルスに等量の水を加え
、家庭用のミキサーで破砕した。Examples 11 to 15 An equal amount of water was added to the tissue-cultured callus of Otanenji, and the mixture was crushed using a household mixer.
次いで、これを100℃、20分間加熱殺菌してから表
2に記載の乳酸菌を接種し、37°Cにて48時間発酵
させた。Next, this was heat sterilized at 100°C for 20 minutes, then inoculated with lactic acid bacteria listed in Table 2, and fermented at 37°C for 48 hours.
なお、発酵中は定期的にpHを測定し、必要に応じIN
炭酸水素ナトリウム溶液を滴下し、pH4,5以上に保
った。During fermentation, the pH should be measured periodically, and the pH should be adjusted as necessary.
A sodium bicarbonate solution was added dropwise to maintain the pH above 4.5.
このようにして得た発酵液は、いずれも未発酵の殺菌液
に比べ苦味が少なく、しかも泥臭さがなく、ヨーグルト
に似た甘い香りあるいはされやかな酸臭を帯びた好まし
い風味となった。The fermented liquid thus obtained had less bitterness than the unfermented sterilized liquid, had no muddy odor, and had a pleasant flavor with a sweet odor similar to yogurt or a mild sour odor.
このオタネエンジンの発酵物の上澄み液を素材とし、そ
の10部にしょ糖10部、クエン酸02部、水80部を
加え飲料を調製した。A beverage was prepared using the supernatant liquid of the fermented product of Otanenji as a raw material, and adding 10 parts of sucrose, 0.2 parts of citric acid, and 80 parts of water to 10 parts of the supernatant liquid.
この実施例のオタネエンジン飲料と、未発酵のオタネエ
ンジンカルスを各実施例の発酵液と同様にして調製した
比較例の飲料との嗜好を比較する官能検査の結果は、表
2のようになった。Table 2 shows the results of a sensory test comparing the tastes of this Example's Otane Engine beverage and a Comparative Example beverage prepared from unfermented Otane Engine callus in the same manner as the fermentation liquid of each Example. Ta.
表2
オタネエンジンカルスの乳酸菌発酵
なお、官能検査結果は、表1と同様に、aは実施例の乳
酸発酵したオタネエンジンを用いた飲料を好むとした人
の数、bは実施例の飲料と比較例の飲料との間に好みの
差かないとした人の数、Cは乳酸菌処理していないオタ
ネエンジンを用いた比較例の飲料を好むとした人の数を
それぞれ示す。Table 2 Lactic acid bacteria fermentation of Pancreas enzymatic calli The sensory test results are similar to Table 1, where a is the number of people who preferred the beverage made using the lactic acid-fermented Panasonic callus, and b is the number of people who preferred the beverage using the lactic acid-fermented Panasonic callus. C indicates the number of people who said there was no difference in taste between the drinks of the comparative example and the drink of the comparative example, and C shows the number of people who said they liked the drink of the comparative example using the Otanae engine that was not treated with lactic acid bacteria.
実施例16
エゾウコギの乾燥物10部を破砕し、90部の50%エ
チルアルコール水溶液に加え、35℃で20日間浸漬後
抽出液を分離し、エバポレーターを用いて減圧濃縮し、
10部の濃縮抽出液を得た。Example 16 10 parts of dried Eleuthero was crushed, added to 90 parts of 50% ethyl alcohol aqueous solution, immersed at 35°C for 20 days, separated the extract, concentrated under reduced pressure using an evaporator,
10 parts of concentrated extract were obtained.
ここに得た濃縮抽出液10部に対し、5%ふどう糖溶液
10部及びイーストエキス 0.2部を加え、100℃
にて15分加熱殺菌した。To 10 parts of the concentrated extract obtained here, 10 parts of 5% glucose solution and 0.2 parts of yeast extract were added, and the mixture was heated at 100°C.
It was sterilized by heating for 15 minutes.
次いで、殺菌処理した濃縮抽出液にペデイオコッカス・
ベントサシアスを接種し、35℃にて24時間静置発酵
させた。24時間後に発酵液のpHが 4.3となった
ので、加熱処理して発酵を停止させた。Next, Pedeiococcus was added to the sterilized concentrated extract.
Bentosasias was inoculated and fermented for 24 hours at 35°C. After 24 hours, the pH of the fermented liquid became 4.3, so the fermentation was stopped by heat treatment.
この発酵液を素材として用い、その10部とじよ糖10
部、クエン酸0.3部及び水80部を混ぜ、エゾウコギ
の飲料とした。このエゾウコギの飲料は、苦味がなく、
まろやかな好ましい風味のものとなった。Using this fermented liquid as a material, add 10 parts of it and 10 parts of sugar.
1 part, 0.3 parts of citric acid, and 80 parts of water were mixed to prepare a drink for Eleuthero. This Eleuthero drink has no bitter taste.
It had a mellow and pleasant flavor.
比較試験結果
組織培養したオタネエンジンのカルスに等量の水を加え
、家庭用のミキサーで破砕した。次いで、これを100
で20分間加熱殺菌してからラクトバチルス・ブランフ
ルムを接種し、37℃にて静置発酵させた。Comparative Test Results An equal amount of water was added to the tissue-cultured callus of Otanenji, and the mixture was crushed using a household mixer. Next, set this to 100
The mixture was sterilized by heating for 20 minutes, then inoculated with Lactobacillus branfrum, and left to ferment at 37°C.
発Rに従いpHが低下し、72時間後にはpH3,7と
なった。 この発酵途中の発酵液をpHの低下に従い順
次サンプリングし、ジンセッサイドの量を測定した。The pH decreased as R developed and reached pH 3.7 after 72 hours. The fermented liquor during this fermentation was sampled sequentially as the pH decreased, and the amount of ginsicide was measured.
ジンセッサイド量の測定は、各サンプルより分離した粗
サポニンをシリカゲル薄層プレートにスポットし、n−
ブタノール・酢酸エチル 水−4:1:5の混合溶液を
展開液として展開した後硫酸を噴霧して105℃、5分
間加熱して発色させ、クロマトスキャナーを用いて各ス
ポットの量を求め、未発酵液を同様に処理した比較試料
のスボ。To measure the amount of ginsicide, crude saponin separated from each sample was spotted on a thin silica gel plate, and n-
After developing a mixed solution of butanol/ethyl acetate/water-4:1:5 as a developing solution, sulfuric acid was sprayed and heated at 105°C for 5 minutes to develop color. The amount of each spot was determined using a chromatography scanner. A comparative sample of subo, in which the fermented liquid was treated in the same way.
トの量を1,0としたときの相対値として求めた。It was determined as a relative value when the amount of water is set to 1.0.
測定の結果は、表3の通りである。The measurement results are shown in Table 3.
なお、対照は、比較例の試料に乳酸を加え、混合してp
H3,0としたものである。As a control, lactic acid was added to the sample of the comparative example, mixed, and p
It is set as H3.0.
なお、表3のA及びCは、Rf値が0.67及び035
のスポIトを、またBは0.57と052のスボノ)の
和をそれぞれ示す。また、Aは、ジンセッサイドRg+
に相当するスポットである。Note that A and C in Table 3 have Rf values of 0.67 and 035.
, and B indicates the sum of 0.57 and 052 (Subono), respectively. Also, A is ginsesside Rg+
It is a spot corresponding to .
Claims (1)
乳酸菌を接種し、pH4.0以上、好ましくはpH4.
5以上に保ちながら発酵させることを特徴とする薬用エ
ンジンを用いた食用素材の製造法。Lactic acid bacteria are inoculated into a substrate containing a crushed product, a ground product, or an extract of a medicinal engine, and the pH is adjusted to pH 4.0 or higher, preferably pH 4.0.
A method for producing edible materials using a medicated engine, which is characterized by fermenting while maintaining the temperature at 5 or higher.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2077420A JPH03277247A (en) | 1990-03-27 | 1990-03-27 | Preparation of edible raw material using ginseng |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2077420A JPH03277247A (en) | 1990-03-27 | 1990-03-27 | Preparation of edible raw material using ginseng |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH03277247A true JPH03277247A (en) | 1991-12-09 |
Family
ID=13633469
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2077420A Pending JPH03277247A (en) | 1990-03-27 | 1990-03-27 | Preparation of edible raw material using ginseng |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH03277247A (en) |
Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0655202A1 (en) * | 1993-11-24 | 1995-05-31 | SITIA-YOMO S.p.A. | Yogurt having healty components |
WO2000021384A1 (en) * | 1998-10-12 | 2000-04-20 | Kitii Corporation Ltd. | Fermented organic acid that changes cell and protein functions |
KR20030094827A (en) * | 2002-06-08 | 2003-12-18 | 노환진 | Ginseng Fermentation Drink |
WO2004050892A1 (en) | 2002-12-05 | 2004-06-17 | Hongrim Trading Co., Ltd. | Ginseng fermented by lactic acid bacterium, yoghurt containing the same, and lactic acid bacteria used in the preparation thereof |
KR100479803B1 (en) * | 2002-04-08 | 2005-03-30 | 홍림통산(주) | Composition containing an extract of specially treated ginseng for preventing brain cells and treating brain stroke |
KR100517899B1 (en) * | 2002-01-30 | 2005-09-30 | 주식회사 일화 | Bioconversion ginseng composite using microorganism and fabrication method thereof |
KR100773059B1 (en) * | 2003-12-02 | 2007-11-02 | 히데오 하세가와 | Novel microorganism having deglycosylating ability, the probiotics containing the same and the process for preparing them |
KR100789261B1 (en) * | 2004-12-28 | 2007-12-31 | 김재백 | A fermented ginseng containing deglycosylated ginsenosides and the preparation method thereof |
KR100789678B1 (en) * | 2005-10-07 | 2008-01-02 | (주)예당바이오 | Preparation Method Of Fermented Ginseng Or Fermented Red Ginseng Using Probiotics From Kimchi |
JP2010132625A (en) * | 2008-12-08 | 2010-06-17 | Nagase & Co Ltd | Anti-diabetic agent |
WO2023084839A1 (en) * | 2021-11-12 | 2023-05-19 | 株式会社皇漢薬品研究所 | Method for producing sarcopenia-inhibiting food product, sarcopenia-inhibiting food product, and muscle-enhancing food product |
-
1990
- 1990-03-27 JP JP2077420A patent/JPH03277247A/en active Pending
Cited By (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0655202A1 (en) * | 1993-11-24 | 1995-05-31 | SITIA-YOMO S.p.A. | Yogurt having healty components |
WO2000021384A1 (en) * | 1998-10-12 | 2000-04-20 | Kitii Corporation Ltd. | Fermented organic acid that changes cell and protein functions |
US6316035B1 (en) | 1998-10-12 | 2001-11-13 | Kitii Corporation Ltd. | Fermented organic acid that changes cell and protein functions and method of making |
KR100517899B1 (en) * | 2002-01-30 | 2005-09-30 | 주식회사 일화 | Bioconversion ginseng composite using microorganism and fabrication method thereof |
US7645465B2 (en) * | 2002-04-08 | 2010-01-12 | Kuan Industrial Co., Ltd. | Method of preparing a pharmaceutical composition comprising fermented ginseng |
KR100479803B1 (en) * | 2002-04-08 | 2005-03-30 | 홍림통산(주) | Composition containing an extract of specially treated ginseng for preventing brain cells and treating brain stroke |
KR20030094827A (en) * | 2002-06-08 | 2003-12-18 | 노환진 | Ginseng Fermentation Drink |
KR100497895B1 (en) * | 2002-12-05 | 2005-06-29 | 홍림통산(주) | Ginseng fermented by lactic acid bacterium, yoghurt containing the same, and lactic acid bacteria used in the preparation thereof |
WO2004050892A1 (en) | 2002-12-05 | 2004-06-17 | Hongrim Trading Co., Ltd. | Ginseng fermented by lactic acid bacterium, yoghurt containing the same, and lactic acid bacteria used in the preparation thereof |
KR100773059B1 (en) * | 2003-12-02 | 2007-11-02 | 히데오 하세가와 | Novel microorganism having deglycosylating ability, the probiotics containing the same and the process for preparing them |
KR100789261B1 (en) * | 2004-12-28 | 2007-12-31 | 김재백 | A fermented ginseng containing deglycosylated ginsenosides and the preparation method thereof |
KR100789678B1 (en) * | 2005-10-07 | 2008-01-02 | (주)예당바이오 | Preparation Method Of Fermented Ginseng Or Fermented Red Ginseng Using Probiotics From Kimchi |
JP2010132625A (en) * | 2008-12-08 | 2010-06-17 | Nagase & Co Ltd | Anti-diabetic agent |
WO2023084839A1 (en) * | 2021-11-12 | 2023-05-19 | 株式会社皇漢薬品研究所 | Method for producing sarcopenia-inhibiting food product, sarcopenia-inhibiting food product, and muscle-enhancing food product |
JPWO2023084839A1 (en) * | 2021-11-12 | 2023-05-19 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
KR100664687B1 (en) | Preparation method of non-fermentative carbonated beverages comprising barley concentrate and hop extract, and non-fermentative carbonated beverages prepared by the same method | |
CN101245307B (en) | Melon and fruit vinegar and manufacture method thereof | |
US4702923A (en) | Lyophilized kefir yoghurt health food | |
US20110070332A1 (en) | Method for processing cocoa beans | |
JP4616413B1 (en) | Fermented food manufacturing method and fermented food | |
KR102149951B1 (en) | Fermented material of jujube with high gaba by mixed fermentation and manufacturing method thereof | |
Kaur et al. | Traditional bio-preservation in beverages: Fermented beverages | |
KR20150064360A (en) | Fruit Jam Comprising Fermented Stevia Extracts and Method for Preparing the Same | |
KR20080103258A (en) | White lotus wine and preparation method thereof | |
US4305963A (en) | Powdered malt wort beverage product | |
KR101983039B1 (en) | Method for Manufacturing Nuruk Sauce | |
JPH03277247A (en) | Preparation of edible raw material using ginseng | |
JP7150556B2 (en) | Method for producing fermented coffee extract | |
KR20190024420A (en) | Manufacturing method of soybean-yogurt improved taste and increased number of viable lactic acid bacteria | |
JPH03277246A (en) | Preparation of new edible raw material using ginseng | |
KR102124781B1 (en) | Manufacturing method macaron using barley shoot and macaron using barley shoot manufactured by the same | |
KR101788925B1 (en) | Methods for Preparing Citron Sparkling Wine | |
CN108371325B (en) | Puffed instant sweet rice wine fried rice and preparation method thereof | |
JP2913413B2 (en) | Whey-containing alcoholic beverages | |
KR20190130334A (en) | Manufacturing method of pineapple beverages | |
JPS5913185B2 (en) | Method for producing alcoholic beverages using mushrooms as raw materials | |
JPH034766A (en) | Production of dried fruit extract and flavor modifier | |
KR102127485B1 (en) | Manufacturing method for slice for decoration of rice cake and slice for decoration of rice cake manufactured by the same | |
KR101930764B1 (en) | Method of preparing traditional liquor comprising walnut extract | |
JPH06233666A (en) | Water or hot water infusion beverage and its production |