JP2006166726A - Squeezed liquid, squeezed lees extract liquid and alcohol extract liquid each comprising cherry fruit, and beverage, coloring matter, antioxidant substance and antioxidant processed food each using the cherry fruit - Google Patents

Squeezed liquid, squeezed lees extract liquid and alcohol extract liquid each comprising cherry fruit, and beverage, coloring matter, antioxidant substance and antioxidant processed food each using the cherry fruit Download PDF

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JP2006166726A
JP2006166726A JP2004360088A JP2004360088A JP2006166726A JP 2006166726 A JP2006166726 A JP 2006166726A JP 2004360088 A JP2004360088 A JP 2004360088A JP 2004360088 A JP2004360088 A JP 2004360088A JP 2006166726 A JP2006166726 A JP 2006166726A
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antioxidant
fruit
cherry
squeezed
liquid
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Tomoaki Saito
知明 齋藤
Hiroshi Kitamura
裕志 北村
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ROKKA SHUZO KK
Aomori Prefecture
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ROKKA SHUZO KK
Aomori Prefecture
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<P>PROBLEM TO BE SOLVED: To provide excellently antioxidant raw material effectively utilizing Prunus fruits, being in disuse up to now, such as Prunus Sargentii other than Ume. <P>SOLUTION: The squeezed liquid, the squeezed lees extract liquid and the extract liquid is obtained from Prunus sargentii Rehder or other cherry fruit. The beverage, coloring matter, antioxidant substance or an antioxidant processed product is obtained through addition of at least one of the squeezed liquid, the squeezed lees extract and the extract liquid. According to an antioxidant test using β-carotene linoleic acid, 2 wt.% fruit extract liquid-added distilled spirit or water suppresses β-carotene color fading by 76% and exhibits excellent antioxidant properties in comparison with water or distilled spirit added no Prunus sargentii Rehder fruit. <P>COPYRIGHT: (C)2006,JPO&NCIPI

Description

本発明はサクラ果実の圧搾液・圧搾粕抽出液・アルコール抽出液、およびそれを用いた飲料・着色料・抗酸化性物質・抗酸化性加工品に係り、特に、従来利用されていないオオヤマザクラ(Prunus sargentii Rehder)等のサクラ果実を有効利用して、抗酸化性に優れた飲料・抗酸化性物質等を得ることのできる、サクラ果実の圧搾液・圧搾粕抽出液・アルコール抽出液、およびそれを用いた飲料・着色料・抗酸化性物質・抗酸化性加工品に関する。   The present invention relates to a squeezed extract of cherry fruit, a squeezed koji extract, an alcoholic extract, and a beverage, a coloring agent, an antioxidant substance, and an antioxidant processed product using the same. (Prunus sargentii Rehder) and other cherry fruits can be used effectively to obtain beverages, antioxidants, etc. with excellent antioxidant properties. It relates to beverages, colorants, antioxidant substances, and antioxidant processed products using the same.

サクラの果実の利用技術は、サクランボを除いては、従来多くは存在せず、バラ科サクラ属ウメの果実を用いて、過剰体脂肪蓄積抑制剤、それを含有する肥満予防食品、肥満改善食品、肥満予防用の医薬組成物、肥満治療用の医薬組成物を得るとする提案がなされている程度である(特許文献1 IPDLの特実公報テキスト検索にて、要約+請求の範囲={(サクラorザクラ)and果実}による検索結果計24件の内の一つ。検索年月日=2004年8月27日)。   Except for cherries, there are not many techniques for using cherry fruits. Excessive body fat accumulation inhibitors, obesity-preventing foods, and obesity-improving foods using the fruits of Rosaceae To the extent that proposals have been made to obtain a pharmaceutical composition for obesity prevention and a pharmaceutical composition for the treatment of obesity (Patent Document 1 IPDL special fact gazette text search, summary + claims = {( One of 24 search results by Sakura or Sakura) and Fruit} (Search Date = August 27, 2004).

特開平8−198767号公報「過剰体脂肪蓄積剤及びそれを含有する組成物」。要約、特許請求の範囲。Japanese Patent Application Laid-Open No. 8-198767 "Excess body fat accumulating agent and composition containing the same". Summary, claims.

さて、サクラの中でもオオヤマザクラは他のサクラに比べて結実が良好であり、色素が豊富であるため、多方面への利用が可能と考えられる。   Of the cherry blossoms, Oyamazakura has better fruiting than other cherry blossoms and is rich in pigments, so it can be used in many ways.

本発明は、かかる従来技術の状況を踏まえ、従来利用されていないオオヤマザクラのようなウメ以外のサクラ属の果実を有効利用して、抗酸化性に優れた飲料・抗酸化性物質等を得ることのできる、サクラ果実の圧搾液・圧搾粕抽出液・アルコール抽出液、およびそれを用いた飲料・着色料・抗酸化性物質・抗酸化性加工品を提供することである。   In light of the state of the prior art, the present invention makes effective use of fruits of the genus Sakura other than ume, such as cherry salmon, which has not been used in the past, to obtain beverages, antioxidants, and the like excellent in antioxidant properties It is possible to provide a squeezed cherry fruit squeezed solution, a squeezed koji extract, an alcohol extract, and a beverage, a colorant, an antioxidant substance, and an antioxidant processed product using the same.

本願発明者は上記課題について検討した結果、本発明に至った。すなわち、上記課題を解決するための手段として本願で特許請求される発明は、以下のとおりである。   As a result of studying the above problems, the present inventor has reached the present invention. That is, the invention claimed in the present application as means for solving the above problems is as follows.

(1) オオヤマザクラ(Prunus sargentii Rehder)果実またはその他のサクラ果実の圧搾液。
(2) アルコールを用いて抽出した、オオヤマザクラ(Prunus sargentii Rehder)果実またはその他のサクラ果実の圧搾粕抽出液。
(3) アルコールを用いて抽出したオオヤマザクラ(Prunus sargentii Rehder)果実またはその他のサクラ果実の抽出液。
(1) Pressed liquid of Prunus sargentii Rehder fruit or other cherry fruit.
(2) Pressed koji extract of Prunus sargentii Rehder fruit or other cherry fruit extracted using alcohol.
(3) Extracts of Prunus sargentii Rehder fruits or other cherry fruits extracted with alcohol.

(4) オオヤマザクラ(Prunus sargentii Rehder)またはその他のサクラの、下記(I)または(II)の少なくともいずれか一を添加した飲料。
(I)果汁もしくは果実
(II)(I)を用いた抽出物
(5) 前記飲料は焼酎その他のアルコール飲料であることを特徴とする、(4)に記載の飲料。
(4) A beverage to which at least one of the following (I) or (II) of a cherry tree (Prunus sargentii Rehder) or another cherry tree is added.
(I) Fruit juice or fruit
(II) Extract using (I) (5) The beverage according to (4), wherein the beverage is shochu or other alcoholic beverage.

(6) オオヤマザクラ(Prunus sargentii Rehder)またはその他のサクラの、下記(I)または(II)の少なくともいずれか一を用いた着色料。
(I)果汁もしくは果実
(II)(I)を用いた抽出物
(7) オオヤマザクラ(Prunus sargentii Rehder)またはその他のサクラの、下記(I)または(II)の少なくともいずれか一を用いて得られる抗酸化性物質または抗酸化性加工品。
(I)果汁もしくは果実
(II)(I)を用いた抽出物
(6) A coloring agent using at least one of the following (I) or (II) of Prunus sargentii Rehder or other cherry.
(I) Fruit juice or fruit
(II) Extract using (I) (7) Antioxidant obtained by using at least one of the following (I) or (II) of Prunus sargentii Rehder or other cherry Antioxidant processed product.
(I) Fruit juice or fruit
(II) Extract using (I)

本発明のサクラ果実の圧搾液・圧搾粕抽出液・アルコール抽出液、およびそれを用いた飲料・着色料・抗酸化性物質・抗酸化性加工品は上述のように構成されるため、これによれば、従来利用されていないオオヤマザクラのようなサクラ属果実を有効利用して、抗酸化性に優れた飲料・抗酸化性物質等を得ることができる。   The cherry fruit pressing liquid, pressed rice bran extract, alcoholic extract of the present invention, and beverages, colorants, antioxidant substances, and antioxidant processed products using the same are configured as described above. According to this, it is possible to obtain a beverage, an antioxidant substance, and the like excellent in antioxidant property by effectively using a cherry genus fruit such as a cherry tree that has not been conventionally used.

本発明に適用されるサクラ属としては、オオヤマザクラ(Prunus sargentii Rehder)を好適に用いることができるが、それに限定されず、たとえばオオシマザクラなど他のサクラ属の果実も、以下主に説明に用いるオオヤマザクラと同様の効果を期待できる。   As the cherry genus applied to the present invention, a cherry tree (Prunus sargentii Rehder) can be preferably used. The same effect as Yamazakura can be expected.

以下、本発明を、オオヤマザクラについて行った実施例によりさらに詳細に説明する。
<1 試料の採取とサンプル処理>
試料の採取は平成14年(2002年)6月30日に岩木山環状道路百沢付近にて行った。採取した果実は柔らかい熟したもので暗い赤から黒色を呈し、径10mm程度の球状を呈していた。
Hereinafter, the present invention will be described in more detail with reference to examples carried out on the cherry tree.
<1 Sample collection and sample processing>
The sample was collected on June 30, 2002, near Iwakiyama Ring Road Hyakusawa. The collected fruit was soft, ripe, dark red to black, and spherical with a diameter of about 10 mm.

採取した果実は数時間以内に水洗いを行い、50%醸造用アルコールを果実100gに対して200ml入れ、暗所にて密閉し、浸漬保存した(果実エタノール浸出液)。残りの果実398gは手動圧搾機で圧搾し、果汁154mlを得、小分けし凍結保存した。また、圧搾後の粕は適当量のエタノールに浸漬し(粕エタノール浸出液)、6ヶ月以上暗所に保存した。   The collected fruit was washed with water within several hours, 200 ml of 50% brewing alcohol was added to 100 g of the fruit, sealed in a dark place, and stored by immersion (fruit ethanol leachate). The remaining fruit (398 g) was squeezed with a manual squeezer to obtain 154 ml of fruit juice, which was aliquoted and stored frozen. The squeezed squeezed soaked in an appropriate amount of ethanol (salted ethanol exudate) was stored in a dark place for 6 months or longer.

<2 試料の成分分析>
アルコール浸漬6ヵ月後から各種成分分析を行った。総ポリフェノールはFollin−Denis法、ミネラルは湿式灰化後ICPを用いて、遊離アミノ酸はアミノ酸自動分析装置を用いて分析した。また、各試料の乾物相当量はアルミ皿内の濾紙に含浸させ、減圧乾燥後の重量の差で求めた。
<2 Sample component analysis>
Various components were analyzed from 6 months after alcohol immersion. The total polyphenol was analyzed using the Follin-Denis method, the mineral was analyzed using ICP after wet ashing, and the free amino acid was analyzed using an amino acid automatic analyzer. Moreover, the dry matter equivalent amount of each sample was impregnated in the filter paper in an aluminum dish, and it calculated | required by the difference in the weight after drying under reduced pressure.

<3 抗酸化性について>
以下説明する各抗酸化性試験では、凍結保存しておいたオオヤマザクラ圧搾液と果実エタノール浸出液、粕エタノール浸出液と果実エタノール浸出液を焼酎等に添加したものを試料として行った。
<3 Antioxidant properties>
In each of the antioxidant tests described below, samples were prepared by adding frozen wild cherry extract and fruit ethanol leaching solution, salmon ethanol leaching solution and fruit ethanol leaching solution to shochu and the like.

<3.1 XYZ原理に基づくフォトン検出による抗酸化活性の検討>
<3.1.1 試薬および測定法>
試薬および測定法は、青森県産業技術開発センターにより検討(フォトン評価機器を利用したスーパーヘルシー食品の創造、青森県地域産官学共同研究事業(平成9〜10年度)成果普及講習会テキスト)された方法によった。すなわち、暗室にてchemiluminescence detector model CLD-110、chemiluminescence counter model CLD-10(東北電子産業社製)を用い、ステンレス製試料皿に試料を適当量入れ、25ul のMeOHと蒸留水を加え混合し、全量を1.0mlになるように採取した。標準として50ulの1mM Gallic acid(GA、50%MeOHに溶解)と950ulの蒸留水を混合し1.0mlとした。これらをCLD-110の試料室にセットし、XとしてH2O2を、ZとしてCH3CHOを含む溶液2.0mlをゆっくり注入し、2分間に生成するフォトン(CL)をクロマトインテグレーターに記録し、そのピーク面積値をCLとした。一方、XをHO・とした場合にはFeを試料皿内で0.5mMになるように添加し同様にCLを測定した。
<3.1 Examination of antioxidant activity by photon detection based on XYZ principle>
<3.1.1 Reagents and measurement methods>
Reagents and measurement methods were examined by Aomori Prefectural Industrial Technology Development Center (Creation of super healthy food using photon evaluation equipment, Aomori Prefectural Industry-Government-Academia Collaborative Research Project (Heisei 9-10) Results Dissemination Seminar Text) According to the method. That is, using a chemiluminescence detector model CLD-110, chemiluminescence counter model CLD-10 (Tohoku Electronics Industrial Co., Ltd.) in a dark room, put an appropriate amount of sample in a stainless steel sample dish, add 25ul of MeOH and distilled water, and mix. The total amount was collected to 1.0 ml. As a standard, 50 ul of 1 mM Gallic acid (GA, dissolved in 50% MeOH) and 950 ul of distilled water were mixed to make 1.0 ml. Set these in the sample chamber of CLD-110, slowly inject 2.0 ml of a solution containing H2O2 as X and CH3CHO as Z, and record the photons (CL) generated in 2 minutes in the chromatographic integrator, and the peak area value Was CL. On the other hand, when X was HO., Fe was added to 0.5 mM in the sample pan, and CL was measured in the same manner.

<3.1.2 抗酸化活性の評価法>
H2O2に対する抗酸化性は、下式のとおり、GA1mMのCLピーク面積の平均値を1000 unitsとして、各試料の平均CL面積値を求め、抗酸化度とした。またHO・に対する抗酸化性は0.5nM FeCl2のみのCLピーク面積をバックグランドとして差し引いて同様に求めた。
抗酸化度(units)= [試料のCLピーク面積の平均]*1000/[GA1mMのピーク面積]*希釈倍率
<3.1.2 Evaluation method for antioxidant activity>
As shown in the following formula, the antioxidant property against H 2 O 2 was determined by taking the average value of the CL peak area of GA 1 mM as 1000 units, and determining the average CL area value of each sample as the antioxidant degree. Further, the antioxidant property against HO · was similarly determined by subtracting the CL peak area of only 0.5 nM FeCl 2 as the background.
Degree of antioxidant (units) = [average of CL peak area of sample] * 1000 / [peak area of GA 1 mM] * dilution ratio

<3.2 β−カロチン・リノール酸系による抗酸化性の評価>
<3.2.1 試薬および測定法>
マイクロプレートリーダーを用いて安原ら(東京農業大学農学集報,43(4),260-267(1999))の方法によった。すなわちβ−カロチン150ul(1mg/ml クロロホルム)、リノール酸100ul(0.1g/ml クロロホルム)、ツイ−ン40 300ul(0.2g/ml クロロホルム)の混合溶液を窒素気流下で乾固させ30mlの純水に溶解し0.2Mリン酸緩衝液(pH7.0)2.7mlを加え静かに攪拌しβ−カロチン・リノール酸溶液を調整した。ただちに適宜に希釈した試料10ulを96穴マイクロタイタープレートの各ウェルに注入し、β−カロチン・リノール酸溶液を200ul添加した。振とう攪拌後、50℃、暗所でインキュベーションし、15分毎にOD492nmにおける吸光度を測定した。標準物質はブチルヒドロキシアニソール(BHA)1mg/100ml エタノール溶液を用いた。
<3.2 Evaluation of Antioxidation by β-Carotene / Linoleic Acid System>
<3.2.1 Reagents and measurement methods>
Using a microplate reader, Yasuhara et al. (Tokyo University of Agriculture, 43 (4), 260-267 (1999)). That is, a mixed solution of β-carotene 150 ul (1 mg / ml chloroform), linoleic acid 100 ul (0.1 g / ml chloroform), Tween 40 300 ul (0.2 g / ml chloroform) was dried to dryness in a nitrogen stream, and 30 ml of pure water Then, 2.7 ml of 0.2 M phosphate buffer (pH 7.0) was added and gently stirred to prepare a β-carotene / linoleic acid solution. Immediately, 10 ul of appropriately diluted sample was injected into each well of a 96-well microtiter plate, and 200 ul of β-carotene / linoleic acid solution was added. After stirring with shaking, incubation was performed at 50 ° C. in the dark, and the absorbance at OD 492 nm was measured every 15 minutes. As the standard substance, a 1 mg / 100 ml ethanol solution of butylhydroxyanisole (BHA) was used.

<3.2.2 抗酸化活性の評価法>
抗酸化活性は津志田ら(日本食品工業会誌 41(9),611-618(1994))の方法をもとに行った。すなわち試料溶液の15分と45分の吸光度の差をBHA1mg/100mlの15分と45分の吸光度の差で求めた。
試料溶液(O.D.15min−O.D.45min)/BHA1mg/100ml(O.D.15min−O.D.45min)
<3.2.2 Evaluation method of antioxidant activity>
Antioxidant activity was performed based on the method of Tsushida et al. (Japan Food Industry Association Journal 41 (9), 611-618 (1994)). That is, the difference in absorbance between 15 minutes and 45 minutes of the sample solution was determined by the difference in absorbance between 15 minutes and 45 minutes of BHA 1 mg / 100 ml.
Sample solution (OD15min-OD45min) / BHA 1mg / 100ml (OD15min-OD45min)

<3.3 DPPHを用いたラジカル補足能の検討>
<3.3.1 試薬および測定法>
マイクロプレートリーダーを用いて行った。DPPH 混液は使用直前に調整した500uMDPPH(1,1-Diphenyl-2-picrylhydrazyl)溶液と0.1M tris 緩衝液(pH7.4)を8:7に混ぜて調整した。次に適宜に希釈した試料50ulを96穴マイクロタイタープレートの各ウェルに注入し、すばやくDPPH混液を150ul加え、蓋をし、暗所に置き10分毎にOD550nmにおける吸光度を測定した。比較する標準溶液としてビタミンC,没食子酸(GA)、カテキンを20、10、5ppmに調整し同様に処理した。
<3.3 Examination of radical scavenging ability using DPPH>
<3.3.1 Reagents and measurement methods>
This was performed using a microplate reader. The DPPH mixture was prepared by mixing 8: 7 with a 500 uM DPPH (1,1-Diphenyl-2-picrylhydrazyl) solution and 0.1 M tris buffer (pH 7.4) prepared immediately before use. Next, 50ul of an appropriately diluted sample was poured into each well of a 96-well microtiter plate, 150ul of DPPH mixed solution was quickly added, the lid was put on, placed in a dark place, and the absorbance at OD550nm was measured every 10 minutes. As a standard solution for comparison, vitamin C, gallic acid (GA), and catechin were adjusted to 20, 10, and 5 ppm and treated in the same manner.

<3.3.2 評価法>
各標準溶液のデータを用いて、30分後の濃度と吸光度の検量線を作成し、試料の30分後の吸光度より相当値を求めた。
<3.3.2 Evaluation method>
Using the data of each standard solution, a calibration curve of the concentration and absorbance after 30 minutes was prepared, and an equivalent value was obtained from the absorbance after 30 minutes of the sample.

<4.結果と考察>
<4.1 オオヤマザクラより調整した溶液の成分値>
表1に、オオヤマザクラの各試料の水分とミネラル値を示した。果実一般と同様にカリウムが多く、同属のサクランボと似た組成を示した。
<4. Results and Discussion>
<4.1 Component values of the solution prepared from the cherry tree>
Table 1 shows the moisture and mineral values of each sample of Oyamazakura. As with fruits in general, it was high in potassium and showed a composition similar to the cherries of the same genus.

Figure 2006166726
Figure 2006166726

図1に、オオヤマザクラ果汁のアミノ酸分析計による遊離アミノ酸のクロマトグラムを、また、
図2に、その定量値をそれぞれ示した。多種のアミノ酸が検出されたが、主要なアミノ酸はプロリンであり、約50%を占め、次にアスパラギン、γ-アミノ酪酸、β-アラニンが多く、これら4種アミノ酸が85%を占めていた。このアミノ酸パターンはバラ科の果実の傾向とは異なり、鈴木ら(食品総合研究所報告第31号 42-70)の報告と比較すると、柑橘系に近いパターンを示した。
Fig. 1 shows the chromatogram of free amino acids by the amino acid analyzer of Oyama cherry juice.
FIG. 2 shows the quantitative values. A variety of amino acids were detected, but the main amino acid was proline, accounting for about 50%, followed by asparagine, γ-aminobutyric acid, and β-alanine, and these four amino acids accounted for 85%. This amino acid pattern was different from the tendency of fruits of the Rosaceae family, and showed a pattern close to citrus when compared with the report of Suzuki et al.

表2に、各試料の総ポリフェノール量を示した。これらの値は野菜、果物の平均的な値の50mg/100gと比較し、10倍相当の量に相当した。   Table 2 shows the total polyphenol content of each sample. These values corresponded to 10 times the amount compared to the average value of 50 mg / 100 g for vegetables and fruits.

図3に、実抽出液を50倍に希釈し、吸収スペクトルを測定した結果を示した。これらより可視部540〜550 nmと紫外部280nmに吸収ピークがあることから、アントニアニンの吸収スペクトルが大きく影響していると考えられた。しかし、塩酸酸性で鮮赤色を示すが、苛性ソーダで中和していくと中性付近で淡紫色を経て、青から紫ではなく、黄緑に変色すること、紫外部の吸光度も高いことから、有機物一般およびその他のポリフェノール類も含まれていると考えられた。   FIG. 3 shows the result of measuring the absorption spectrum after diluting the actual extract 50 times. From these, since there are absorption peaks in the visible region of 540 to 550 nm and the ultraviolet region of 280 nm, it was considered that the absorption spectrum of anthocyanin greatly influenced. However, it shows a bright red color with acidic hydrochloric acid, but when neutralized with caustic soda, it goes through a pale purple color near neutrality, discolors from blue to purple instead of purple, and also has a high UV absorbance. Organic matter and other polyphenols were also considered to be included.

Figure 2006166726
Figure 2006166726

<4.2 XYZ原理に基づくフォトン検出によるオオヤマザクラ果実の抗酸化活性>
表3に、XYZ原理に基づくフォトン検出によるオオヤマザクラ各果実資料の抗酸化活性を示した。天然の抗酸化物質として知られている没食子酸(GA)と比較した数値を掲げているが、オオヤマザクラの果実を含む試料はどれも高い抗酸化性がみられた。比較的高い抗酸化性が認められているジョミ(ガマズミ)と比較しても、圧搾液でH2O2に対する抗酸化性がほぼ30倍、HO・に対する抗酸化性がほぼ9倍と高い数値を示した。実抽出液は2倍量のエタノール溶液で静地抽出した液であり、抗酸化物質が十分に抽出されたと考えれば、ほぼ3倍相当の希釈に相当しており、実際の抗酸化活性もH2O2に対して約3分の1となっており、抗酸化物質がかなり抽出されていると考えられた。
<4.2 Antioxidant activity of cherry berries by photon detection based on XYZ principle>
Table 3 shows the antioxidant activity of each fruit material of the cherry tree by photon detection based on the XYZ principle. Although the values are compared with gallic acid (GA), which is known as a natural antioxidant, all the samples containing the fruit of lynx were highly antioxidant. Compared with Jomi (viburnum), which has a relatively high antioxidant activity, the compressed solution showed a high value of approximately 30-fold for antioxidant against H2O2 and nearly 9-fold for antioxidant against HO. . The actual extract is a solution that is statically extracted with twice the amount of ethanol solution. If you think that the antioxidants are sufficiently extracted, it corresponds to a dilution equivalent to almost three times, and the actual antioxidant activity is also H2O2. It was thought that the antioxidant substance was considerably extracted.

さらに、焼酎においては活性が認められなかったが焼酎に2%実抽出液を添加したものは活性があらわれ2%の添加で実抽出液の活性のほぼ3%を示した。また、圧搾粕を抽出した液については抽出倍率が不明であるが、少なくても2倍以上はあったものと考えられ、搾汁残渣には相当量の抗酸化物質が残存していることがわかった。特にHO・に対する活性値は圧搾液より高かった。   Furthermore, although no activity was observed in shochu, 2% actual extract added to shochu showed activity, and 2% addition showed almost 3% of the activity of the actual extract. In addition, although the extraction ratio is unknown for the liquid from which the squeezed koji was extracted, it is considered that there was at least twice or more, and a considerable amount of antioxidants remained in the juice residue. all right. In particular, the activity value against HO · was higher than that of the pressed solution.

Figure 2006166726
Figure 2006166726

なお、各試料の詳細は次のとおりである。
果実圧搾液:オオヤマザクラの実398gを手動式圧搾機で搾汁し、154mlを得た。
圧搾粕抽出液:上記搾汁粕に特級エタノール液約200mlを加え約5ヶ月浸漬した上澄液。
実抽出液:実150gに50%エタノール液300mlを加え約5ヶ月浸漬した上澄液。
焼酎:六花酒造(株)製、津軽海峡
2%実抽出液添加焼酎:上記津軽海峡に容量で2%になるように実抽出液を加えたもの。
数値は平均値±SD
抗酸化活性はGA(没食子酸)1mMのCLピーク面積を1000unitsとした。
(1) ジョミ原液:フォトン評価機器を利用したスーパーヘルシー食品の創造よりp.174
The details of each sample are as follows.
Fruit pressing solution: 398 g of Oyama cherry was squeezed with a manual press to obtain 154 ml.
Pressed koji extract: A supernatant obtained by adding about 200 ml of a special grade ethanol solution to the above koji koji and dipping for about 5 months.
Real extract: A supernatant obtained by adding 300 ml of 50% ethanol solution to 150 g of real fruit and immersing for about 5 months.
Shochu: manufactured by Rokka Sake Brewery Co., Ltd., Tsugaru Strait 2% real extract added Shochu: Tsugaru Strait added with real extract so that its volume is 2%.
Numerical values are mean ± SD
As for the antioxidant activity, the CL peak area of GA (gallic acid) 1 mM was 1000 units.
(1) Jomi Stock: From the creation of super healthy food using photon evaluation equipment p.174

表4には、各試料の1mlの抗酸化性がGA濃度にしてどのくらい相当するか換算した結果を示した。H2O2に対するオオヤマザクラ各試料の1mlあたりのGA相当量は果実圧搾液、圧搾液抽出液、実抽出液、2%実抽出液添加焼酎はそれぞれ13.52、9.30、4.70、0.17mMであり、HO・に対しては28.18、36.27、6.47、0.22mMに相当した。この値はこれまで調べられていた各種食材、天然物と比較しても非常に高い活性を示しており、生体においても各種機能を発揮する可能性が示唆された。   Table 4 shows the results of conversion of how much 1 ml of the antioxidant property of each sample corresponds to the GA concentration. The GA equivalent amount per ml of the cherry tree for H2O2 is 13.52, 9.30, 4.70, 0.17 mM for fruit pressurization liquid, press liquid extract, real extract, and 2% real extract, respectively. On the other hand, it corresponded to 28.18, 36.27, 6.47 and 0.22 mM. This value shows very high activity compared to various foods and natural products that have been examined so far, suggesting the possibility of exerting various functions in living bodies.

Figure 2006166726
Figure 2006166726

<4.3 β−カロチン・リノール酸系による抗酸化性の評価>
図4に、β−カロチン・リノール酸系による抗酸化性について示した。リノール酸の酸化によるβ―カロチンの退色は試料が加えられていない状態の焼酎、水と比較してそれらに2%実抽出液を加えた結果、76%抑制することがわかった。この結果は抗酸化物質であるBHA1mg/100mlより強かった。また、水と焼酎を比べた場合、焼酎の方が酸化しにくいといえた。またβ−カロチン・リノール酸系においては果実圧搾液、実抽出液、粕抽出液間の差は少なく、ほぼ10倍に希釈した液がBHA1mg/100mlの2倍の活性を持つと考えられた。
<4.3 Antioxidant evaluation by β-carotene / linoleic acid system>
FIG. 4 shows the antioxidant properties of the β-carotene / linoleic acid system. It was found that the fading of β-carotene due to the oxidation of linoleic acid was suppressed by 76% as a result of adding 2% actual extract to shochu and water in which no sample was added. This result was stronger than the antioxidant BHA 1mg / 100ml. In addition, when water and shochu were compared, shochu was less likely to oxidize. In the β-carotene / linoleic acid system, there was little difference between the fruit pressurized solution, the actual extract, and the koji extract, and it was considered that the solution diluted approximately 10 times had twice the activity of 1 mg / 100 ml of BHA.

<4.4 DPPHを用いたラジカル補足能の検討>
図5に、DPPHを用いたラジカル補足能について示す。オオヤマザクラの果実からの試料をラジカル補足能のある標準物質のビタミンC(V.C)、没食子酸(GA)、カテキンの5、10、20ppmと比較した結果、高いラジカル補足能が見られ、実抽出液を水、焼酎で200〜400倍に希釈した溶液を実験に用いた。
<4.4 Examination of radical scavenging ability using DPPH>
FIG. 5 shows the radical scavenging ability using DPPH. As a result of comparing the sample from the fruit of the cherry tree with the reference substances vitamin C (VC), gallic acid (GA), catechin 5, 10, 20 ppm of radical supplementing ability, high radical scavenging ability was seen, A solution obtained by diluting the actual extract with water and shochu 200 to 400 times was used in the experiment.

表5に、ラジカル補足能から各標準物質相当量を求めた結果を示した。水に実抽出液を2%添加した溶液はビタミンC、GA、カテキンそれぞれ38.4、13.2、33.6ppmに相当し、焼酎に2%添加した場合は58.0、17.6、42.0ppmに相当した。β−カロチン・リノール酸系による抗酸化性の場合と同様に水より焼酎に添加した場合に高い値を示した。なお、水による希釈割合から計算した実抽出液の相当量はビタミンC、GA、カテキンそれぞれ1916、656、1684ppmとなり、これらを実抽出液の乾物あたりに換算するとそれぞれ38332、13128、33640ppmに相当した。   Table 5 shows the result of determining the equivalent amount of each standard substance from the radical scavenging ability. A solution obtained by adding 2% of the actual extract to water corresponds to 38.4, 13.2, and 33.6 ppm of vitamin C, GA, and catechin, respectively, and corresponds to 58.0, 17.6, and 42.0 ppm when added to 2% of shochu. Similar to the case of the antioxidant property of the β-carotene / linoleic acid system, a higher value was obtained when added to shochu than water. The equivalent amount of the actual extract calculated from the dilution ratio with water was 1916, 656, and 1684 ppm for vitamin C, GA, and catechin, respectively, and these were equivalent to 38332, 13128, and 33640 ppm, respectively, when converted into dry matter of the actual extract. .

Figure 2006166726
Figure 2006166726

<5.オオヤマザクラ果実の利用>
オオヤマザクラの果実の抗酸化性について検討した結果、XYZ原理に基づくフォトン検出によるH2O2およびHO・に対する抗酸化性、β−カロチン・リノール酸系による脂肪酸酸化に対する抗酸化性、DPPHを用いたラジカルの補足能による抗酸化性いずれにおいても高い抗酸化性を示した。このことはオオヤマザクラの果実に強力な抗酸化物質が含まれていることを意味し、生体内においても酸化に起因するいろいろな疾病の防御作用、改善作用を持つ可能性が高いと考えられた。
<5. Use of cherry berries>
As a result of examining the antioxidant properties of the fruit of the cherry tree, the antioxidant activity against H2O2 and HO ・ by photon detection based on the XYZ principle, the antioxidant property against fatty acid oxidation by β-carotene and linoleic acid, the radicals using DPPH It showed high antioxidant property in all of the antioxidant properties due to the supplementary ability. This means that the fruit of the cherry tree contains a powerful antioxidant, and it is thought that there is a high possibility that it will have a protective and ameliorating action against various diseases caused by oxidation in vivo. .

果実をエタノールで抽出した抽出液においても同様に高い抗酸化性が認められたことは、アルコール浸漬によって容易に抗酸化性物質の抽出、保存が可能なことを示している。加えて、主にアントシアニンと考えられたオオヤマザクラの色素は非常に含量が多く、鮮やかな赤色を呈し、アルコール浸漬において容易に抽出可能である。   Similarly, the high antioxidant property observed in the extract obtained by extracting fruit with ethanol indicates that the antioxidant substance can be easily extracted and stored by immersion in alcohol. In addition, the pigment of Oyama cherry, which is mainly considered to be anthocyanin, has a very high content, exhibits a bright red color, and can be easily extracted in alcohol immersion.

オオヤマザクラの果実に2倍量のエタノール溶液を加え抽出した液を、2%焼酎や水に加えた溶液はきれいな赤紫色を呈すると同時に抗酸化性が付加された。2%添加時の乾物は0.01%であり、きわめて少量の抽出物で高い付加価値を生むことが可能である。たとえば食品、飲料に添加することで新たな機能性食品の製造が可能であり、抗酸化物質を分離、精製することで医薬品への適用も考えられる。また、着色料としての利用も十分可能である。   A solution obtained by adding 2 times the amount of ethanol solution to the fruit of Oyamazakura and adding it to 2% shochu or water showed a beautiful reddish purple color and at the same time added antioxidant properties. When 2% is added, the dry matter is 0.01%, and it is possible to produce high added value with a very small amount of extract. For example, a new functional food can be produced by adding it to foods and beverages, and it can be applied to pharmaceuticals by separating and purifying antioxidants. Moreover, the use as a coloring agent is also possible enough.

本発明のサクラ果実の圧搾液・圧搾粕抽出液・アルコール抽出液、およびそれを用いた飲料・着色料・抗酸化性物質・抗酸化性加工品は上述のように構成されるため、これによれば、従来利用されていないオオヤマザクラのようなサクラ属果実を有効利用して、抗酸化性に優れた飲料・抗酸化性物質等を得ることができる。したがって将来的にも、産業上利用価値が高い発明である。   The cherry fruit pressing liquid, pressed rice bran extract, alcoholic extract of the present invention, and beverages, colorants, antioxidant substances, and antioxidant processed products using the same are configured as described above. According to this, it is possible to obtain a beverage, an antioxidant substance, and the like excellent in antioxidant property by effectively using a cherry genus fruit such as a cherry tree that has not been conventionally used. Therefore, it is an invention with high industrial utility value in the future.

オオヤマザクラ果汁のアミノ酸分析計による遊離アミノ酸のクロマトグラムを示すグラフである。It is a graph which shows the chromatogram of the free amino acid by the amino acid analyzer of Aoyama cherry juice. オオヤマザクラ果汁のアミノ酸分析計による遊離アミノ酸のの定量値を示すグラフである。It is a graph which shows the quantitative value of the free amino acid by the amino acid analyzer of Aoyama cherry juice. オオヤマザクラ実抽出液を50倍に希釈し、吸収スペクトルを測定した結果を示すグラフである。It is a graph which shows the result of having diluted the cherry tree cherry extract 50 times and measuring the absorption spectrum. オオヤマザクラ果実のβ−カロチン・リノール酸系による抗酸化性について示すグラフである。It is a graph which shows about the antioxidant property by the beta-carotene * linoleic acid type | system | group of a cherry tree fruit. オオヤマザクラ果実のDPPHを用いたラジカル補足能について示すグラフである。It is a graph which shows about the radical scavenging ability using DPPH of the cherry tree fruit.

Claims (7)

オオヤマザクラ(Prunus sargentii Rehder)果実またはその他のサクラ果実の圧搾液。 Pressed liquid of Prunus sargentii Rehder fruit or other cherry fruit. アルコールを用いて抽出した、オオヤマザクラ(Prunus sargentii Rehder)果実またはその他のサクラ果実の圧搾粕抽出液。 Squeeze extract of Prunus sargentii Rehder fruit or other cherry fruit extracted with alcohol. アルコールを用いて抽出したオオヤマザクラ(Prunus sargentii Rehder)果実またはその他のサクラ果実の抽出液。 Extracts of Prunus sargentii Rehder fruits or other cherry fruits extracted with alcohol. オオヤマザクラ(Prunus sargentii Rehder)またはその他のサクラの、下記(I)または(II)の少なくともいずれか一を添加した飲料。
(I)果汁もしくは果実
(II)(I)を用いた抽出物
A beverage to which at least one of the following (I) or (II) of a cherry tree (Prunus sargentii Rehder) or other cherry tree is added.
(I) Fruit juice or fruit
(II) Extract using (I)
前記飲料は焼酎その他のアルコール飲料であることを特徴とする、請求項4に記載の飲料。 The beverage according to claim 4, wherein the beverage is shochu or other alcoholic beverage. オオヤマザクラ(Prunus sargentii Rehder)またはその他のサクラの、下記(I)または(II)の少なくともいずれか一を用いた着色料。
(I)果汁もしくは果実
(II)(I)を用いた抽出物
A coloring agent using at least one of the following (I) or (II) of Prunus sargentii Rehder or other cherry.
(I) Fruit juice or fruit
(II) Extract using (I)
オオヤマザクラ(Prunus sargentii Rehder)またはその他のサクラの、下記(I)または(II)の少なくともいずれか一を用いて得られる抗酸化性物質または抗酸化性加工品。
(I)果汁もしくは果実
(II)(I)を用いた抽出物
An antioxidant substance or an antioxidant processed product obtained by using at least one of the following (I) or (II) of Prunus sargentii Rehder or other cherry:
(I) Fruit juice or fruit
(II) Extract using (I)
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Publication number Priority date Publication date Assignee Title
JP2015051934A (en) * 2013-09-05 2015-03-19 地方独立行政法人青森県産業技術センター Dermal oxidative stress inhibitor
JP2015067546A (en) * 2013-09-26 2015-04-13 地方独立行政法人青森県産業技術センター Matrix metalloprotease-1 production inhibitor
KR101522371B1 (en) * 2013-06-05 2015-05-26 재단법인 전주생물소재연구소 Food and pharmaceutical composition comprising hot water extract of Chaenomeles sinensis fruit with improved liver function and antioxidant activity
CN110194999A (en) * 2019-05-29 2019-09-03 小金县夹金山天然野樱桃酒业有限公司 A kind of brewing method of wild cherry fruit wine

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR101522371B1 (en) * 2013-06-05 2015-05-26 재단법인 전주생물소재연구소 Food and pharmaceutical composition comprising hot water extract of Chaenomeles sinensis fruit with improved liver function and antioxidant activity
JP2015051934A (en) * 2013-09-05 2015-03-19 地方独立行政法人青森県産業技術センター Dermal oxidative stress inhibitor
JP2015067546A (en) * 2013-09-26 2015-04-13 地方独立行政法人青森県産業技術センター Matrix metalloprotease-1 production inhibitor
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