JP2011512142A5 - - Google Patents

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JP2011512142A5
JP2011512142A5 JP2010547028A JP2010547028A JP2011512142A5 JP 2011512142 A5 JP2011512142 A5 JP 2011512142A5 JP 2010547028 A JP2010547028 A JP 2010547028A JP 2010547028 A JP2010547028 A JP 2010547028A JP 2011512142 A5 JP2011512142 A5 JP 2011512142A5
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yeast extract
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parts
sodium
preparation
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JP5398745B2 (en
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本発明は既存技術の上記問題を解決した。本発明の目的は、酵母抽出物の調製方法を提供することで、その方法には、(a)原料酵母抽出物(ペースト状)や、ブドウ糖、塩化ナトリウム、グリシン、加水分解済植物プロテイン(HVP)及び水を反応窯の中でミックスし、(b)得られた混合物を熱反応させ、(c)熱反応が終わると、得られた生成物を調合し、(d)反応後の酵母抽出物をろ過して、酵母抽出物を含有するろ過液が得られる、のステップが含まれる。   The present invention has solved the above-mentioned problems of existing technology. The object of the present invention is to provide a method for preparing a yeast extract, which includes (a) raw material yeast extract (paste), glucose, sodium chloride, glycine, hydrolyzed plant protein (HVP). ) And water in a reaction kiln, (b) the resulting mixture is reacted thermally, (c) when the thermal reaction is finished, the resulting product is formulated, and (d) yeast extraction after the reaction Filtering the product to obtain a filtrate containing the yeast extract.

本発明の具体的な実施方式中、ステップ(a)において、原料は、250〜400重量部(ドライベース)のペースト状の原料酵母抽出物、6〜10重量部のブドウ糖、20〜40重量部の塩化ナトリウム、6〜10重量部のグリシン、80〜100重量部(ドライベース)の加水分解植物プロテイン及び適当量の反応物の濃度を25〜40%にさせる水などによって構成される。   In a specific implementation method of the present invention, in step (a), the raw material is 250 to 400 parts by weight (dry base) of a paste-like raw material yeast extract, 6 to 10 parts by weight of glucose, and 20 to 40 parts by weight. Of sodium chloride, 6 to 10 parts by weight of glycine, 80 to 100 parts by weight (dry base) of hydrolyzed plant protein, and water that brings the concentration of the appropriate amount of reactants to 25 to 40%.

本発明の具体的な実施方式中、ステップ(c)において、6〜10wt%のグルタミン酸ナトリウムと1.0〜3.0wt%の5”―イノシン酸二ナトリウム+5”―グアニル酸二ナトリウムを使って、得られた生成物を調合するが、好ましくは7〜9wt%のグルタミン酸と1.5〜2.5wt%の5”―イノシン酸二ナトリウム+5”―グアニル酸二ナトリウムを使用する。   In a specific implementation mode of the present invention, in step (c), 6 to 10 wt% sodium glutamate and 1.0 to 3.0 wt% 5 "-disodium inosinate + 5" -disodium guanylate are used. The resulting product is formulated, preferably using 7-9 wt% glutamic acid and 1.5-2.5 wt% 5 "-disodium inosinate + 5" -disodium guanylate.

本発明の具体的な実施方式中、ステップ(a)において、原料は、250〜400重量部(ドライベース)のペースト状酵母抽出物(ペースト状)、6〜10重量部のブドウ糖、20〜40重量部の塩化ナトリウム、6〜10重量部のグリシン、80〜100重量部(ドライベース)の加水分解植物プロテイン及び適当量の反応物の濃度を25〜40%にさせる水などによって構成される。   In the specific implementation method of the present invention, in step (a), the raw materials are 250 to 400 parts by weight (dry base) of paste-like yeast extract (paste), 6 to 10 parts by weight of glucose, 20 to 40. Consists of parts by weight of sodium chloride, 6 to 10 parts by weight of glycine, 80 to 100 parts by weight (dry base) of hydrolyzed plant protein, and water that brings the concentration of the appropriate amount of reactants to 25 to 40%.

本発明の具体的な実施方式中、ステップ(c)において、6〜10wt%のグルタミン酸ナトリウムと1.0〜3.0wt%の5”―イノシン酸二ナトリウム+5”―グアニル酸二ナトリウムを使って、得られた生成物を調合するが、好ましくは7〜9wt%のグルタミン酸と1.5〜2.5wt%の5”―イノシン酸二ナトリウム+5”―グアニル酸二ナトリウムを使用する。   In a specific implementation mode of the present invention, in step (c), 6 to 10 wt% sodium glutamate and 1.0 to 3.0 wt% 5 "-disodium inosinate + 5" -disodium guanylate are used. The resulting product is formulated, preferably using 7-9 wt% glutamic acid and 1.5-2.5 wt% 5 "-disodium inosinate + 5" -disodium guanylate.

酵母抽出物の生産
実施例1では、先ず、250重量部(ドライベース)の酵母抽出物(ペースト状)や、6重量部のブドウ糖、20重量部の塩化ナトリウム、6重量部のグリシン、80重量部(ドライベース)の加水分解植物プロテイン及び600重量部の水を反応窯の中に入れてミックスする。それから、得られた混合物を反応窯の中に移して、混合物を100℃、pH値4.5の下で、40分間熱反応させる。加熱・沈殿させてから、6wt%のグルタミン酸ナトリウムと1.0wt%の「5”−イノシン酸二ナトリウム+5”−グアニル酸二ナトリウム」を入れて調合する。最終製品の中に原料中の沈殿物が入らないように、酵母抽出物を200メッシュのフィルターでろ過する。ろ過が終わると、ろ過液をシングル・エフェクト流下液膜式蒸発器に移して、65wt%濃度以上にまで濃縮するが、好ましくは65〜70wt%にまで濃縮して、最終酵母抽出物製品が得られる。
Production of yeast extract In Example 1, first, 250 parts by weight (dry base) of yeast extract (paste form), 6 parts by weight of glucose, 20 parts by weight of sodium chloride, 6 parts by weight of glycine, 80 parts by weight Part (dry base) of hydrolyzed plant protein and 600 parts by weight of water are placed in a reaction kiln and mixed. The resulting mixture is then transferred into a reaction kiln and the mixture is allowed to react for 40 minutes at 100 ° C. and a pH value of 4.5. After heating and precipitating, 6 wt% sodium glutamate and 1.0 wt% “5” -disodium inosinate + 5 ”-disodium guanylate” are added to prepare. The yeast extract is filtered through a 200-mesh filter so that the final product does not contain precipitates in the raw material. When filtration is complete, the filtrate is transferred to a single effect falling film evaporator and concentrated to a concentration of 65 wt% or more, but preferably to 65-70 wt% to obtain the final yeast extract product. It is done.

Claims (9)

酵母抽出物の調製方法において、前記方法には、
(a)原料酵母抽出物、ブドウ糖、塩化ナトリウム、グリシン、加水分解済植物プロテイン及び水を反応窯の中でミックスし、
(b)ステップ(a)から得られた混合物を100〜130℃、pH値4.5〜6.3の下で、40〜90分間熱反応させ、
(c)ステップ(b)の前記熱反応が終わると、得られた生成物に6〜10wt%のグルタミン酸ナトリウムと1.0〜3.0wt%の味出しヌクレオチド二ナトリウムで調合し、及び
(d)反応後の酵母抽出物をろ過して、酵母抽出物を含有するろ過液を得る、
のステップを含む酵母抽出物の調製方法。
In the method for preparing a yeast extract, the method includes:
(A) Mix raw yeast extract, glucose, sodium chloride, glycine, hydrolyzed plant protein and water in a reaction kiln,
(B) The mixture obtained from step (a) is thermally reacted at 100 to 130 ° C. and a pH value of 4.5 to 6.3 for 40 to 90 minutes,
(C) Upon completion of the thermal reaction of step (b), the resulting product is formulated with 6-10 wt% sodium glutamate and 1.0-3.0 wt% flavored nucleotide disodium; and (d ) Filter the yeast extract after the reaction to obtain a filtrate containing the yeast extract.
A method for preparing a yeast extract comprising the steps of:
請求項1に記載の方法において、前記ステップ(d)の後は、また、酵母抽出物を含有するろ過液をシングル・エフェクト流下液膜式蒸発器に移して、65wt%以上にまで濃縮するステップ(e)が含まれることを特徴とする調製方法。   The method according to claim 1, wherein after the step (d), the filtrate containing the yeast extract is also transferred to a single effect falling film evaporator and concentrated to 65 wt% or more. (E) is contained, The preparation method characterized by the above-mentioned. 請求項1に記載の方法において、ステップ(a)の原料は、250〜400重量部のペースト状の原料酵母抽出物(ドライベース)、6〜10重量部のブドウ糖、20〜40重量部の塩化ナトリウム、6〜10重量部のグリシン、80〜100重量部の加水分解植物プロテイン(ドライベース)及び反応物の濃度を25〜40%にさせる水によって構成されることを特徴とする調製方法。   2. The method according to claim 1, wherein the raw material in step (a) is 250 to 400 parts by weight of a paste-like raw material yeast extract (dry base), 6 to 10 parts by weight of glucose, and 20 to 40 parts by weight of chloride. A preparation method comprising sodium, 6 to 10 parts by weight of glycine, 80 to 100 parts by weight of hydrolyzed plant protein (dry base), and water that brings the concentration of the reactants to 25 to 40%. 請求項1に記載の方法において、前記熱反応は、pH値5.0〜6.0の下で行うことを特徴とする調製方法。   The method according to claim 1, wherein the thermal reaction is performed under a pH value of 5.0 to 6.0. 請求項1に記載の方法において、前記熱反応の時間は、50〜80分間であることを特徴とする調製方法。   The method according to claim 1, wherein the thermal reaction time is 50 to 80 minutes. 請求項1に記載の方法において、前記ステップ(d)には、7〜9wt%のグルタミン酸と、合わせて1.5〜2.5wt%の5”―イノシン酸二ナトリウムと5”―グアニル酸二ナトリウムとで調合することを特徴とする調製方法。   The method according to claim 1, wherein the step (d) includes 7 to 9 wt% glutamic acid, and 1.5 to 2.5 wt% of 5 "-inosinate and 5" -guanylate dihydrate in total. A preparation method comprising blending with sodium. 請求項1〜6中のいずれかの1項に記載の方法によって得られる酵母抽出物。   The yeast extract obtained by the method of any one of Claims 1-6. 請求項1〜6中のいずれかの1項に記載の方法によって得られる酵母抽出物の栄養品、調味品及び保健品への応用。   Application of the yeast extract obtained by the method according to any one of claims 1 to 6 to nutritional products, seasonings and health products. 請求項8に記載の応用において、その中に記載の調味品は醤油であることを特徴とする応用。   9. The application according to claim 8, wherein the seasoned product is soy sauce.
JP2010547028A 2008-02-21 2008-09-01 Yeast extract, preparation method and application Active JP5398745B2 (en)

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CN200810006186.6 2008-02-21
CN2008100061866A CN101513246B (en) 2008-02-21 2008-02-21 Yeast extract, preparation method and application thereof
PCT/CN2008/072227 WO2009103206A1 (en) 2008-02-21 2008-09-01 A yeast extract, its processing method and application thereof

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JP2011512142A5 true JP2011512142A5 (en) 2012-12-20
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