JP2012055186A - Food utilizing polyphenol component of sorghum - Google Patents

Food utilizing polyphenol component of sorghum Download PDF

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JP2012055186A
JP2012055186A JP2010199114A JP2010199114A JP2012055186A JP 2012055186 A JP2012055186 A JP 2012055186A JP 2010199114 A JP2010199114 A JP 2010199114A JP 2010199114 A JP2010199114 A JP 2010199114A JP 2012055186 A JP2012055186 A JP 2012055186A
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sorghum
millet
polyphenol
food
components
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Nobumasa Ayusawa
信昌 鮎澤
Tsubasa Matsuoka
翼 松岡
Daisuke Uchimatsu
大輔 内松
Toshiki Kobayashi
敏樹 小林
Koji Endo
好司 遠藤
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HAKUBAKU KK
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Abstract

PROBLEM TO BE SOLVED: To provide food utilizing polyphenol components of Sorghum which is obtained as a result of product development for making use of the functionality of the polyphenol components while focusing attention on the polyphenol components richly falling in the Sorghum, and effectively utilizing the polyphenol components of miscellaneous cereals such as the Sorghum particularly, to give additional value to the miscellaneous cereals richly containing fibers, minerals, physiologically active components and the like which are limited in such easy use as to be mixed with rice and boiled.SOLUTION: The food is obtained by utilizing polyphenol components richly falling in kernels of red grain seeds and black grain seeds of Sorghum (otherwise known as corn, kaoliang, or Sorghum bicolor L. in scientific name).

Description

本発明は、雑穀「タカキビ」の成分を利用した食品の製品に属する。 The present invention belongs to a food product using components of millet “Takakibi”.

雑穀は、繊維、ミネラル、生理活性成分等が多く含まれているが、その多くは米に混ぜて炊く等の簡単な利用にとどまっている。タカキビは、日本で古くから栽培されており、家畜の飼料などに使われてきたが、その消化性の悪さから重要な飼料・食品原料とはみなされてこなかった。 Millet grains contain a lot of fiber, minerals, physiologically active ingredients, etc., but most of them are simply used for mixing with rice and cooking. Although it has been cultivated for a long time in Japan and used for livestock feed, it has not been regarded as an important feed or food ingredient due to its poor digestibility.

近年、過食による肥満等の健康問題がクローズアップされ、低カロリーの食品や飲料が数多く開発されている。雑穀は繊維質が多く含まれていることから、多種類の雑穀を米に混ぜて炊飯し、健康増進のために日常食べる米飯の繊維含量を高める方向での利用法が奨励されている。
また、現在、食品素材等に含まれる成分の消化液阻害作用などが、肥満防止の観点から注目されるようになり、消化液阻害作用のある素材やその成分を利用した多様な製品が開発されてきている。
In recent years, health problems such as obesity due to overeating have been highlighted, and many low-calorie foods and beverages have been developed. Because millet contains a lot of fiber, it is encouraged to use it in the direction of increasing the fiber content of cooked rice by mixing many kinds of millet with rice and cooking it for health promotion.
In addition, the digestive juice inhibitory action of ingredients contained in food materials, etc. is now attracting attention from the viewpoint of obesity prevention, and various products using digestive juice inhibitory ingredients and their components have been developed. It is coming.

タカキビ (Sorghum bicolor L.)には、主にその色から黄穀種、紅穀種、蛇眼穀種、黒穀種、白穀種などに分けられており、紅穀種、黒穀種は、タンニン系、アントシアニン系などのポリフェノール色素を多く含んでいることが明らかになった。 Takaraki (Sorghum bicolor L.) is mainly divided into yellow cereals, red cereals, snake-eye cereals, black cereals, white cereals, etc. It has been revealed that it contains a large amount of tannin-based and anthocyanin-based polyphenol pigments.

タカキビ (Sorghum bicolor L.)は、その消化性の悪さからこれまで重要な飼料・食品原料とはみなされてこなかったが、当社では、これまでの穀物研究の実績を活かし、消化性の悪い原因について検討し、それがタカキビ (Sorghum bicolor L.)に大量に含まれるポリフェノール成分に由来することを突きとめた。 Takaraki (Sorghum bicolor L.) has not been regarded as an important feed and food ingredient because of its poor digestibility, but we have made use of our experience in grain research to determine the cause of poor digestibility. And found out that it is derived from polyphenols contained in large amounts in Sorghum bicolor L.

特にありません。Nothing in particular.

雑穀は、繊維、ミネラル、生理活性成分などが多く含まれているが、米に混ぜて炊く等の簡単な利用にとどまっている。雑穀の成分を高度に利用し、雑穀に付加価値をつけて製品開発していく必要があり、本発明においては、タカキビ (Sorghum bicolor L.)に豊富に含まれるポリフェノール成分に着目し、その機能性を活用する製品開発を行った。 Millet contains a lot of fiber, minerals, bioactive ingredients, etc., but it is only used for simple mixing such as cooking with rice. It is necessary to develop products with high value of millet components and added value to millet grains.In the present invention, attention is paid to polyphenol components that are abundant in oyster millet (Sorghum bicolor L.). Developed products that make use of sexuality.

タカキビ (Sorghum bicolor L.)の着色種の穀実および穀子(護頴)、花梗、茎等の未利用部分に含まれるポリフェノール成分の含量を明らかにすると共に、穀実から抽出したポリフェノール成分のもつ消化酵素阻害能等の生理活性を確認し、従来問題点であった難消化性を逆に利用して、肥満防止等に利用できる食品、飲料を開発した。 Clarify the content of polyphenols contained in unused seeds such as cereals and grains of oyster millet (Sorghum bicolor L.), cereals, flower stems, stems, etc., and possess polyphenols extracted from cereals Developed foods and beverages that can be used to prevent obesity, etc. by confirming physiological activities such as digestive enzyme inhibitory ability and using the indigestibility that has been a problem in the past.

タカキビの高付加価値化を実現するための技術としては、精製した穀実としての利用、穀実の微粉砕によるポリフェノール成分の抽出効率の向上と成分の利用、焙煎による香味の付加と茶としての利用、穀子(護頴)、花梗、茎等の未利用部分に含まれるポリフェノール色素類の飲料としての利用、消化酵素阻害能等の生理活性を利用した機能性食品としての利用などである。 Technology for realizing high added value of oyster millet includes use as refined cereal, improvement of polyphenol component extraction efficiency by pulverization of cereal and use of ingredients, addition of flavor by roasting and tea Use, polyphenol pigments contained in unused parts such as cereals (garden), flower stems, stems, etc., as functional beverages utilizing physiological activities such as digestive enzyme inhibitory ability.

本発明においてタカキビのポリフェノールは、焙煎、抽出を行うことで、被験物質中のポリフェノール含量を増加させ、効率的な抽出ができる。さらに抗糖尿病作用、抗肥満作用を有することから、本発明によるタカキビのポリフェノールを利用し、機能性食品等として利用できる。 In the present invention, the polyphenol of oyster mill can be efficiently extracted by increasing the polyphenol content in the test substance by performing roasting and extraction. Furthermore, since it has an anti-diabetic action and an anti-obesity action, it can be used as a functional food or the like by using the polyphenol of oyster mill according to the present invention.

タカキビ茶のマルターゼ阻害活性の測定結果を示すグラフである。It is a graph which shows the measurement result of the maltase inhibitory activity of oyster mill tea. タカキビ茶のリパーゼ阻害活性の測定結果を示すグラフである。It is a graph which shows the measurement result of the lipase inhibitory activity of Takakibi tea.

本発明に使用するタカキビ (Sorghum bicolor L.) はタカキビ穀粒であり、タカキビであれば品種は問わないが、赤色色素を有し、ポリフェノール含量が高い品種が好ましい。また、タカキビポリフェノールが担保できれば、抽出方法は熱水抽出でも有機溶媒抽出でも良い。加工については搗精や粉砕、焙煎など通常の加工を加えても良い。原料の状態は搗精したタカキビを使用することも出来るが、精白度合いが低いほど、ポリフェノール含量が高くなるため、玄タカキビが最も好ましい。また、粉砕することでポリフェノールの抽出効率を上げても良い。穀粒の調整及び焙煎は一般的などの加工を加えても良い。例えば、炒ったり、蒸したり、レトルト加工を加えてもよい。

以下、本発明を実施例により、さらに具体的に説明するが、本発明はこれら実施例に限定されるものではない。
The persimmon millet (Sorghum bicolor L.) used in the present invention is a persimmon grain, and any cultivar is acceptable as long as it is a persimmon millet, but a cultivar having a red pigment and a high polyphenol content is preferred. In addition, as long as the millet polyphenol can be secured, the extraction method may be hot water extraction or organic solvent extraction. About processing, you may add usual processing, such as scouring, crushing, and roasting. Finely ground persimmon can be used as the raw material, but the lower the degree of whitening, the higher the polyphenol content. Moreover, you may raise the extraction efficiency of polyphenol by grind | pulverizing. The grain adjustment and roasting may be performed by any general processing. For example, roasting, steaming, or retorting may be added.

Hereinafter, the present invention will be described more specifically with reference to examples, but the present invention is not limited to these examples.

表1に示した各種雑穀の粉砕品100gに75%アセトンを1L加え、ホモジナイザーを用いて2500rpmにて15分間抽出した。これを、5Aの濾紙を用いて吸引濾過しポリフェノール抽出溶液を得た。残査は回収し、再度75%アセトンを700ml加え、同様にホモジナイザーで抽出処理した。抽出液は、5Aの濾紙を用いて吸引濾過し、先の濾液と合わせた。尚、抽出残査は棄却した。抽出液は、ロータリーエバポレーターを用いて、45℃以下にて濃縮しアセトン成分を留去した。得られた濃縮水溶液は、高速冷却遠心機にて、10,000rpm、10℃、15分間遠心処理した。上清は、5Aの濾紙にて吸引濾過を行い、抽出液を得た。得られた抽出液は、ステンレス又はアルミ製のバットに空け、-23℃の冷凍庫にて一晩凍結した後、凍結乾燥を行った。得られた抽出粉末をポリフェノール濃度が200mg%となるように蒸留水に溶解し被検物質とし、抗糖尿病作用試験に供試した。
1 L of 75% acetone was added to 100 g of pulverized grains of various grains shown in Table 1, and the mixture was extracted for 15 minutes at 2500 rpm using a homogenizer. This was suction filtered using 5A filter paper to obtain a polyphenol extraction solution. The residue was recovered, 700 ml of 75% acetone was added again, and extraction processing was performed with a homogenizer in the same manner. The extract was suction filtered using 5A filter paper and combined with the previous filtrate. The extraction residue was rejected. The extract was concentrated at 45 ° C. or less using a rotary evaporator to distill off the acetone component. The obtained concentrated aqueous solution was centrifuged at 10,000 rpm, 10 ° C. for 15 minutes in a high-speed cooling centrifuge. The supernatant was subjected to suction filtration with 5A filter paper to obtain an extract. The obtained extract was emptied into a stainless or aluminum vat, frozen in a freezer at -23 ° C. overnight, and then freeze-dried. The obtained extracted powder was dissolved in distilled water so that the polyphenol concentration was 200 mg% to obtain a test substance, which was used for an antidiabetic action test.

α−アミラーゼ阻害活性は、4%デンプン溶液(0.1Mリン酸緩衝液(pH7.0))0.9mlに各種雑穀の被検物質0.9ml添加し、37℃、5分間保温後、α−アミラーゼ溶液を0.024ml(8.62units)加え、37℃にて、30、60、120分間反応した。ブランクにはデンプン溶液の代わりにリン酸緩衝液をのみを用いたものを供し、抽出物中に元来含まれるマルトース及び酵素の作用により抽出物から遊離してくるマルトースを定量した。コントロールには供試サンプル溶液の代わりにリン酸緩衝液のみを添加したものを供し、抽出物非存在下での酵素活性を確認した。反応終了後は沸騰水中で10分間加熱して酵素を失活させた。反応停止後、遠心分離(3000rpm、10min.)し、その上清中のマルトース量をHPLCを用いてポストカラム法にて測定し、生成されるマルトース量を酵素活性の判断基準とした。尚、α−アミラーゼは、豚膵液由来のα−アミラーゼ(SIGMA社製:A-3176)を359Unit/mlになるように0.1Mリン酸ナトリウム緩衝液(pH7.0)にて希釈し調製した.
α-Amylase inhibitory activity is obtained by adding 0.9 ml of various cereal test substances to 0.9 ml of 4% starch solution (0.1 M phosphate buffer (pH 7.0)), and incubating at 37 ° C. for 5 minutes. 0.024 ml (8.62 units) was added and reacted at 37 ° C. for 30, 60, 120 minutes. A blank was prepared using only a phosphate buffer instead of a starch solution, and maltose originally contained in the extract and maltose released from the extract by the action of the enzyme were quantified. As a control, a sample to which only a phosphate buffer was added instead of the test sample solution was used to confirm the enzyme activity in the absence of the extract. After completion of the reaction, the enzyme was inactivated by heating in boiling water for 10 minutes. After stopping the reaction, the mixture was centrifuged (3000 rpm, 10 min.), The amount of maltose in the supernatant was measured by a post-column method using HPLC, and the amount of maltose produced was used as a criterion for determining enzyme activity. The α-amylase was prepared by diluting porcine pancreatic juice-derived α-amylase (manufactured by SIGMA: A-3176) with 0.1 M sodium phosphate buffer (pH 7.0) so as to be 359 Unit / ml.

マルターゼ阻害活性は、各種雑穀の被験物質0.5mlに2%マルトース溶液を0.5ml添加し、37℃ウォーターバス中にて5分間インキュベートした後、酵素液0.5mlを添加、酵素反応を開始した。反応60分後、120分後にサンプリングを行い、酵素反応を煮沸処理により停止させ、グルコース濃度測定し、糖質分解酵素阻害活性を測定した。また2%マルトース溶液は56mMマレイン酸緩衝液(pH6.0)にて作製した。酵素液は市販ラット腸管アセトン粉末(SIGMA社製)に18倍量の56mMマレイン酸緩衝液(pH6.0)を加え、氷冷しながらホモジナイザーで均質化した後、遠心分離(5,000rpm、10min、4℃)し、上清を酵素液とした。マルタ−ゼ反応には酵素液を10倍希釈して用いた。
For maltase inhibitory activity, 0.5 ml of a 2% maltose solution was added to 0.5 ml of various cereal test substances and incubated in a 37 ° C. water bath for 5 minutes, and then 0.5 ml of an enzyme solution was added to start the enzyme reaction. Sampling was performed 60 minutes after the reaction and 120 minutes later, the enzyme reaction was stopped by boiling treatment, the glucose concentration was measured, and the carbohydrase inhibitor activity was measured. A 2% maltose solution was prepared with 56 mM maleate buffer (pH 6.0). The enzyme solution was added to a commercially available rat intestinal acetone powder (manufactured by SIGMA) with 18 volumes of 56 mM maleate buffer (pH 6.0) and homogenized with a homogenizer while cooling with ice, followed by centrifugation (5,000 rpm, 10 min, And the supernatant was used as an enzyme solution. For the maltase reaction, the enzyme solution was diluted 10 times.

表2は、各被検物質のα−アミラーゼに対する50%阻害濃度と各雑穀中のポリフェノール濃度を示す。阻害能については、表より「タカキビ、ソバ、小豆」が阻害能の高いことが確認された。
表3は、各被検物質のマルターゼに対する50%阻害濃度と各雑穀中のポリフェノール濃度を示す。表より、「タカキビ、小豆、ソバ」は、阻害能が高いことが確認された。特に、タカキビについては、最もIC50が低く、阻害能が高いことがわかった。

Figure 2012055186

Figure 2012055186

Figure 2012055186
Table 2 shows the 50% inhibitory concentration of each test substance for α-amylase and the polyphenol concentration in each millet. As for the inhibitory ability, it was confirmed from the table that “Takaki, buckwheat, red beans” have a high inhibitory ability.
Table 3 shows the 50% inhibitory concentration of each test substance against maltase and the polyphenol concentration in each millet. From the table, it was confirmed that “Takaki, red beans, buckwheat” have high inhibitory ability. In particular, it was found that oyster millet had the lowest IC 50 and the highest inhibitory ability.
Figure 2012055186

Figure 2012055186

Figure 2012055186

以上のように、タカキビの75%アセトン抽出物において、α−アミラーゼ、マルターゼ阻害活性が確認された。このことは、タカキビが含むポリフェノールによりなされた結果であると考えられ、タカキビを用いた食品への利用が期待された。そこで、加工方法としてタカキビの焙煎試験と抽出試験を行った。 As described above, α-amylase and maltase inhibitory activity were confirmed in a 75% acetone extract of oyster millet. This is considered to be a result of polyphenol contained in oysters, and was expected to be used in foods using oysters. Therefore, a roasting test and an extraction test for oysters were performed as processing methods.

岩手県産の玄タカキビ100gを家庭用コーヒー豆焙煎機(iROAST, Hearthware製)にて160、180、200、250℃、5分間焙煎を行い、20gをパックに包装した。抽出は5分間煮出した後、1時間放置し、得られた茶を仮スペックのタカキビ茶とした。試料に用いたタカキビ茶は、Folin-Denis法によりポリフェノール量を測定した。その結果を表4に示した。表から焙煎することでポリフェノールの抽出量が増えている。これは焙煎によりタカキビ穀粒の組織が膨化し、より効率的に抽出できたのではないかと推測している。色調については焙煎度合いが浅いほど色調が鮮やかで焙煎していないタカキビの熱水抽出物はオレンジ色に近い色調を呈していた。焙煎が進むと色は暗くなり、250℃焙煎ではタカキビの鮮やかな赤色はほとんど感じられず、200℃以下の焙煎条件が視覚的に好ましいと考えた。また、風味については焙煎することで、タカキビの特徴的な苦味に香ばしさが付加され飲みやすくなった。色調、風味の両面から茶として好ましい焙煎条件は160℃から200℃に焙煎した条件と判断した。

Figure 2012055186

次にこのタカキビ茶の抗糖尿病作用と抗肥満作用を調べた。
100 g of brown oysters from Iwate Prefecture were roasted at 160, 180, 200, 250 ° C. for 5 minutes using a household coffee bean roasting machine (iROAST, manufactured by Hearthware), and 20 g was packaged in a pack. Extraction was boiled for 5 minutes and then left for 1 hour, and the resulting tea was used as a temporary speck tea. The amount of polyphenols in the oyster tea used for the sample was measured by the Folin-Denis method. The results are shown in Table 4. The amount of polyphenol extracted is increasing by roasting from the table. It is speculated that the roasting of the millet grains expanded the roasting and could be extracted more efficiently. Regarding the color tone, the shallower the degree of roasting, the brighter the color tone, and the hot water extract of oyster millet that was not roasted had a color tone close to orange. As roasting progressed, the color became darker, and the vivid red color of the millet was hardly felt when roasted at 250 ° C., and roasting conditions of 200 ° C. or lower were considered visually favorable. Also, by roasting the flavor, flavor was added to the characteristic bitterness of oysters, making it easier to drink. The preferred roasting conditions for tea from both the color tone and flavor were judged to be roasted from 160 ° C to 200 ° C.
Figure 2012055186

Next, the anti-diabetic action and anti-obesity action of this millet tea were examined.

ガラがついた状態の岩手県産タカキビ100gを家庭用コーヒー豆焙煎機(iROAST, Hearthware製)にて180℃または200℃、5分間焙煎を行い、20gをパックに包装した。抽出は5分間煮出した後、1時間放置をし、得られた茶飲料を仮スペックのタカキビ茶とした。試料に用いたタカキビ茶、蕃爽麗茶(ヤクルト本社)及び黒烏龍茶(サントリー)は凍結乾燥を行い粗抽出物とした。各抽出物は1500mg%となるように蒸留水に溶解し、3000 rpm、10分間遠心分離を行い沈殿物を除去した溶液を、Folin-Denis法によりポリフェノール量を測定した。このサンプルを抗糖尿病作用試験、抗肥満作用試験に供試した。
100 g of Iwate-grown oyster millet with a sack was roasted at 180 ° C. or 200 ° C. for 5 minutes with a household coffee bean roasting machine (manufactured by iROAST, Hearthware), and 20 g was packaged in a pack. Extraction was boiled for 5 minutes and then left for 1 hour. The oyster milled tea, bonsai tea (Yakult Honsha) and black oolong tea (Suntory) used as samples were freeze-dried to obtain crude extracts. Each extract was dissolved in distilled water to 1500 mg%, centrifuged at 3000 rpm for 10 minutes to remove the precipitate, and the amount of polyphenol was measured by the Folin-Denis method. This sample was subjected to an anti-diabetic action test and an anti-obesity action test.

図1はタカキビ茶と蕃爽麗茶の各抽出物濃度と阻害率の関係を示す。また表5は各試料のIC50の抽出物濃度とポリフェノ−ル濃度を示す。結果、図および表から明らかなようにタカキビ茶は市販されている蕃爽麗茶よりも阻害率は高く、好ましい結果であった。

Figure 2012055186
FIG. 1 shows the relationship between the concentration and the inhibition rate of each extract of oyster mill tea and sweet refreshing tea. Table 5 shows the IC 50 extract concentration and polyphenol concentration of each sample. As a result, as is clear from the figures and tables, octopus tea had a higher inhibition rate than the commercially available sweet refreshing tea, which was a favorable result.

Figure 2012055186

リパーゼ阻害能測定に関してはブタ膵臓由来リパーゼ(和光純薬工業)を用い、キット (リパーゼキットS、DSファーマバイオメディカル)の分析方法の一部を変更して行った。すなわち、抽出液を含む試料サンプル溶液300 μl (盲検用は蒸留水300 μl )、酵素溶液(ブタ膵リパーゼ0.1mg/ml 125 mMトリス塩酸(pH 7.5))80 μl、発色液0.1 mg/ml 5,5'- ジチオビス(2- ニトロ安息香酸)を含む緩衝液)1000 μlを入れて混和した後、エステラーゼ阻害液(3.48 mg/ml フェニルメチルスルホニルフルオリド)20 μl を添加した。これらを30 ℃で5分間予熱し、基質液(6.69 mg/ml 三酪酸ジメルカプロール+5.73 mg/mlドデシル硫酸ナトリウム)100 μl を加え混和後、遮光下にて30℃で30分間反応させた。その後、反応停止液2 mlを添加し反応を停止した。ブランクはサンプル溶液、酵素溶液、発色液、エステラーゼ阻害液を添加して30℃で5分間、および30℃で30分間加熱し、反応停止液を加えた後基質液を添加した。それぞれのサンプルの吸光度を層長1 cmのセルを用いて波長412 nmで測定した。リパーゼ活性は(測定用と盲目用の測定値の差)×0.147の計算式を用いて国際単位(IU/L)に換算した。また、被検物質を添加しないサンプル(0 mg%)に対するリパーゼ活性を算出し、リパーゼ活性が50%となるポリフェノール濃度をIC50として算出した。
The lipase inhibitory ability was measured by using porcine pancreatic lipase (Wako Pure Chemical Industries) and changing a part of the analysis method of the kit (Lipase Kit S, DS Pharma Biomedical). That is, 300 μl of sample solution containing the extract (300 μl of distilled water for blind use), 80 μl of enzyme solution (pig pancreatic lipase 0.1 mg / ml 125 mM Tris-HCl (pH 7.5)), 0.1 mg / ml of coloring solution After adding 1000 μl of 5,5′-dithiobis (2-nitrobenzoic acid buffer solution) 1000 μl and mixing, esterase inhibitor (3.48 mg / ml phenylmethylsulfonyl fluoride) 20 μl was added. Preheat them at 30 ° C for 5 minutes, add 100 μl of the substrate solution (6.69 mg / ml dimercaprol tributyrate + 5.73 mg / ml sodium dodecyl sulfate), mix, and react at 30 ° C for 30 minutes in the dark. It was. Thereafter, 2 ml of a reaction stop solution was added to stop the reaction. The blank was added with a sample solution, an enzyme solution, a color developing solution, and an esterase inhibitor, heated at 30 ° C. for 5 minutes, and 30 ° C. for 30 minutes, added with a reaction stopping solution, and then added with a substrate solution. The absorbance of each sample was measured at a wavelength of 412 nm using a cell having a layer length of 1 cm. The lipase activity was converted to international units (IU / L) using a formula of (difference between measurement values for blind and blind) × 0.147. Moreover, calculating the lipase activity for the sample (0 mg%) without addition of the test substance was calculated polyphenol concentration of lipase activity is 50% as IC 50.

結果を図2、表6に示した。IC50の値は黒烏龍茶、タカキビ茶180℃、200℃の順に低く、黒烏龍茶とタカキビ茶180℃の阻害能はほぼ同等と考えられた。黒烏龍茶のポリフェノール濃度はタカキビ茶50.0 mg%に対して100.5 mg%と約2倍の濃度含まれているため、仕上がりの飲料としての機能は黒烏龍茶に劣ってはいるものの、脂肪の吸収を抑制する効果は期待できることが分かった。

Figure 2012055186
The results are shown in FIG. The values of IC 50 were low in the order of black oolong tea, cricket tea 180 ° C, and 200 ° C, and the inhibition ability of black oolong tea and cricket tea 180 ° C was considered to be almost the same. Black oolong tea has a polyphenol concentration of 100.5 mg% compared to 50.0 mg of black millet tea, which is approximately twice as high as that of black oolong tea. It turns out that the effect to do can be expected.

Figure 2012055186

本発明においてタカキビのポリフェノールは、焙煎、抽出を行うことで、被験物質中のポリフェノールが増加したことから、効率的な抽出ができる。さらに抗糖尿病作用、抗肥満作用を有することから、本発明によるタカキビのポリフェノールを利用し、各種の食品として利用できる。 In the present invention, the polyphenol of oyster mill can be efficiently extracted because the polyphenol in the test substance is increased by roasting and extraction. Furthermore, since it has an anti-diabetic action and an anti-obesity action, it can be used as various foods by utilizing the polyphenols of oysters according to the present invention.

Claims (5)

タカキビ(モロコシ、コウリャン、学名Sorghum bicolor L.)の紅穀種、黒穀種の穀粒に豊富に含まれるポリフェノール成分を利用して製造した食品。 Food produced by using polyphenol components that are abundant in grains of red and black grains of oyster millet (sorghum, sorghum, Sorghum bicolor L.). タカキビの紅穀種、黒穀種に豊富に含まれるポリフェノール等を抽出・濃縮して得られる成分を用いて製造した機能性食品、機能性飲料。 Functional foods and functional beverages manufactured using components obtained by extracting and concentrating polyphenols, etc., abundantly contained in red and black cereals. タカキビの紅穀種、黒穀種を焙煎して得られる原料を用い、ポリフェノール等のもつ消化酵素の阻害作用を期待したタカキビ食品、タカキビ飲料。 Takakibi food and Takakibi beverages, which are expected to inhibit digestive enzymes such as polyphenols, using raw materials obtained by roasting red and black cereal seeds. タカキビの穀実を脱穀し、製粉して得られるタカキビ粉を用いて製造した低消化性の麺類、ミックス類。 Low-digestible noodles and mixes produced using pearl millet obtained by threshing and milling pearl millet. タカキビの穀子(護頴)、花梗、茎等の未利用部分を微粉砕し、豊富に含まれるポリフェノール成分を抽出・濃縮して得た美しい色素を利用した機能性飲料。 A functional beverage using beautiful pigments obtained by finely crushing unused parts such as oyster millet (garden), flower stems, stems, etc., and extracting and concentrating polyphenols contained in abundance.
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CN110771801A (en) * 2019-12-02 2020-02-11 黑龙江元态农业科技有限公司 High-activity coarse cereal nutritional powder rich in polyphenol
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