JPH06276996A - Seasoning and its production - Google Patents
Seasoning and its productionInfo
- Publication number
- JPH06276996A JPH06276996A JP5094914A JP9491493A JPH06276996A JP H06276996 A JPH06276996 A JP H06276996A JP 5094914 A JP5094914 A JP 5094914A JP 9491493 A JP9491493 A JP 9491493A JP H06276996 A JPH06276996 A JP H06276996A
- Authority
- JP
- Japan
- Prior art keywords
- ethanol
- yeast
- seasoning
- protein
- raw material
- 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.)
- Granted
Links
- 235000011194 food seasoning agent Nutrition 0.000 title claims abstract description 55
- 238000004519 manufacturing process Methods 0.000 title claims description 16
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 120
- 240000004808 Saccharomyces cerevisiae Species 0.000 claims abstract description 46
- 102000004169 proteins and genes Human genes 0.000 claims abstract description 32
- 108090000623 proteins and genes Proteins 0.000 claims abstract description 32
- 239000013543 active substance Substances 0.000 claims abstract description 21
- 239000002994 raw material Substances 0.000 claims description 31
- 238000000855 fermentation Methods 0.000 claims description 11
- 230000004151 fermentation Effects 0.000 claims description 11
- 239000000796 flavoring agent Substances 0.000 abstract description 14
- 235000019634 flavors Nutrition 0.000 abstract description 14
- 235000019640 taste Nutrition 0.000 abstract description 14
- 150000001720 carbohydrates Chemical class 0.000 abstract 1
- 235000014680 Saccharomyces cerevisiae Nutrition 0.000 description 40
- 235000018102 proteins Nutrition 0.000 description 28
- 102000004157 Hydrolases Human genes 0.000 description 24
- 108090000604 Hydrolases Proteins 0.000 description 24
- 239000007788 liquid Substances 0.000 description 20
- 238000000034 method Methods 0.000 description 18
- 239000000047 product Substances 0.000 description 18
- 239000000126 substance Substances 0.000 description 17
- 239000007864 aqueous solution Substances 0.000 description 16
- 244000068988 Glycine max Species 0.000 description 15
- 235000010469 Glycine max Nutrition 0.000 description 15
- 230000007062 hydrolysis Effects 0.000 description 14
- 238000006460 hydrolysis reaction Methods 0.000 description 14
- 235000000346 sugar Nutrition 0.000 description 13
- 210000005253 yeast cell Anatomy 0.000 description 10
- 230000007065 protein hydrolysis Effects 0.000 description 9
- 235000019646 color tone Nutrition 0.000 description 8
- 150000003839 salts Chemical class 0.000 description 7
- 239000000243 solution Substances 0.000 description 7
- 238000003860 storage Methods 0.000 description 7
- 150000001413 amino acids Chemical class 0.000 description 6
- 238000005910 aminocarbonylation reaction Methods 0.000 description 6
- 150000008163 sugars Chemical class 0.000 description 6
- 238000000354 decomposition reaction Methods 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 239000007787 solid Substances 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 239000004278 EU approved seasoning Substances 0.000 description 4
- 240000007594 Oryza sativa Species 0.000 description 4
- 235000007164 Oryza sativa Nutrition 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 238000011156 evaluation Methods 0.000 description 4
- 239000000499 gel Substances 0.000 description 4
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 235000009566 rice Nutrition 0.000 description 4
- 235000013555 soy sauce Nutrition 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 240000006439 Aspergillus oryzae Species 0.000 description 3
- 235000002247 Aspergillus oryzae Nutrition 0.000 description 3
- 241000894006 Bacteria Species 0.000 description 3
- 241001465754 Metazoa Species 0.000 description 3
- GXCLVBGFBYZDAG-UHFFFAOYSA-N N-[2-(1H-indol-3-yl)ethyl]-N-methylprop-2-en-1-amine Chemical compound CN(CCC1=CNC2=C1C=CC=C2)CC=C GXCLVBGFBYZDAG-UHFFFAOYSA-N 0.000 description 3
- 238000004458 analytical method Methods 0.000 description 3
- 230000003385 bacteriostatic effect Effects 0.000 description 3
- 230000025938 carbohydrate utilization Effects 0.000 description 3
- 230000015556 catabolic process Effects 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 238000006731 degradation reaction Methods 0.000 description 3
- 235000013305 food Nutrition 0.000 description 3
- 235000013372 meat Nutrition 0.000 description 3
- 239000012528 membrane Substances 0.000 description 3
- 150000002972 pentoses Chemical class 0.000 description 3
- 235000021067 refined food Nutrition 0.000 description 3
- 230000001953 sensory effect Effects 0.000 description 3
- 238000011282 treatment Methods 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 108010010803 Gelatin Proteins 0.000 description 2
- 108091005804 Peptidases Proteins 0.000 description 2
- 235000021307 Triticum Nutrition 0.000 description 2
- 241000209140 Triticum Species 0.000 description 2
- 240000008042 Zea mays Species 0.000 description 2
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 2
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 2
- 235000013405 beer Nutrition 0.000 description 2
- 239000006227 byproduct Substances 0.000 description 2
- 210000004027 cell Anatomy 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 235000005822 corn Nutrition 0.000 description 2
- 239000008273 gelatin Substances 0.000 description 2
- 229920000159 gelatin Polymers 0.000 description 2
- 235000019322 gelatine Nutrition 0.000 description 2
- 235000011852 gelatine desserts Nutrition 0.000 description 2
- 230000002401 inhibitory effect Effects 0.000 description 2
- 239000004310 lactic acid Substances 0.000 description 2
- 235000014655 lactic acid Nutrition 0.000 description 2
- 235000013336 milk Nutrition 0.000 description 2
- 239000008267 milk Substances 0.000 description 2
- 210000004080 milk Anatomy 0.000 description 2
- 229920001282 polysaccharide Polymers 0.000 description 2
- 239000005017 polysaccharide Substances 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 238000011160 research Methods 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 235000014347 soups Nutrition 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- QCVGEOXPDFCNHA-UHFFFAOYSA-N 5,5-dimethyl-2,4-dioxo-1,3-oxazolidine-3-carboxamide Chemical compound CC1(C)OC(=O)N(C(N)=O)C1=O QCVGEOXPDFCNHA-UHFFFAOYSA-N 0.000 description 1
- FHVDTGUDJYJELY-UHFFFAOYSA-N 6-{[2-carboxy-4,5-dihydroxy-6-(phosphanyloxy)oxan-3-yl]oxy}-4,5-dihydroxy-3-phosphanyloxane-2-carboxylic acid Chemical compound O1C(C(O)=O)C(P)C(O)C(O)C1OC1C(C(O)=O)OC(OP)C(O)C1O FHVDTGUDJYJELY-UHFFFAOYSA-N 0.000 description 1
- 241000251468 Actinopterygii Species 0.000 description 1
- 101710152845 Arabinogalactan endo-beta-1,4-galactanase Proteins 0.000 description 1
- 241000228212 Aspergillus Species 0.000 description 1
- 241000193830 Bacillus <bacterium> Species 0.000 description 1
- 102000002322 Egg Proteins Human genes 0.000 description 1
- 108010000912 Egg Proteins Proteins 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 101710147028 Endo-beta-1,4-galactanase Proteins 0.000 description 1
- 241000287828 Gallus gallus Species 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
- 229920002488 Hemicellulose Polymers 0.000 description 1
- 235000007340 Hordeum vulgare Nutrition 0.000 description 1
- 240000005979 Hordeum vulgare Species 0.000 description 1
- 238000007696 Kjeldahl method Methods 0.000 description 1
- 241000824268 Kuma Species 0.000 description 1
- 241000442132 Lactarius lactarius Species 0.000 description 1
- 102000035195 Peptidases Human genes 0.000 description 1
- 239000004365 Protease Substances 0.000 description 1
- 108010009736 Protein Hydrolysates Proteins 0.000 description 1
- 102100037486 Reverse transcriptase/ribonuclease H Human genes 0.000 description 1
- 241000269851 Sarda sarda Species 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
- 244000061456 Solanum tuberosum Species 0.000 description 1
- 235000002595 Solanum tuberosum Nutrition 0.000 description 1
- 108010046377 Whey Proteins Proteins 0.000 description 1
- 102000007544 Whey Proteins Human genes 0.000 description 1
- 238000002835 absorbance Methods 0.000 description 1
- 229940072056 alginate Drugs 0.000 description 1
- 235000010443 alginic acid Nutrition 0.000 description 1
- 229920000615 alginic acid Polymers 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 235000015278 beef Nutrition 0.000 description 1
- 235000010410 calcium alginate Nutrition 0.000 description 1
- 229960002681 calcium alginate Drugs 0.000 description 1
- 239000000648 calcium alginate Substances 0.000 description 1
- OKHHGHGGPDJQHR-YMOPUZKJSA-L calcium;(2s,3s,4s,5s,6r)-6-[(2r,3s,4r,5s,6r)-2-carboxy-6-[(2r,3s,4r,5s,6r)-2-carboxylato-4,5,6-trihydroxyoxan-3-yl]oxy-4,5-dihydroxyoxan-3-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylate Chemical compound [Ca+2].O[C@@H]1[C@H](O)[C@H](O)O[C@@H](C([O-])=O)[C@H]1O[C@H]1[C@@H](O)[C@@H](O)[C@H](O[C@H]2[C@H]([C@@H](O)[C@H](O)[C@H](O2)C([O-])=O)O)[C@H](C(O)=O)O1 OKHHGHGGPDJQHR-YMOPUZKJSA-L 0.000 description 1
- 239000005018 casein Substances 0.000 description 1
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 1
- 235000021240 caseins Nutrition 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 235000013330 chicken meat Nutrition 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 230000029087 digestion Effects 0.000 description 1
- 235000006694 eating habits Nutrition 0.000 description 1
- 235000014103 egg white Nutrition 0.000 description 1
- 210000000969 egg white Anatomy 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 238000001879 gelation Methods 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 150000004676 glycans Chemical class 0.000 description 1
- 239000001963 growth medium Substances 0.000 description 1
- 230000003301 hydrolyzing effect Effects 0.000 description 1
- 239000012263 liquid product Substances 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 235000012054 meals Nutrition 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000002609 medium Substances 0.000 description 1
- 238000009629 microbiological culture Methods 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 235000015277 pork Nutrition 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 108090000765 processed proteins & peptides Proteins 0.000 description 1
- 239000003531 protein hydrolysate Substances 0.000 description 1
- 235000015067 sauces Nutrition 0.000 description 1
- 235000020183 skimmed milk Nutrition 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 230000001502 supplementing effect Effects 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 235000021119 whey protein Nutrition 0.000 description 1
- 235000008939 whole milk Nutrition 0.000 description 1
Landscapes
- Seasonings (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は調味料、特に無塩調味料
とその製造法に関し、ス−プ、各種のつゆ類またはたれ
類などの加工用調味液に使用して好適な、風味に優れ品
質安定性の高い調味料とその製造法を提供することにあ
る。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a seasoning, particularly a salt-free seasoning and a method for producing the same, to give a flavor suitable for use in a seasoning liquid for processing soups, various soups or sauces. It is to provide a seasoning having excellent quality stability and a method for producing the seasoning.
【0002】我が国を代表する伝統的醸造調味料である
醤油は、古くから家庭内であるいは各種食品の加工調味
料として多量に消費されてきた。しかしながら、醤油に
は多量の食塩が含まれており、近年、健康上の配慮から
その使用を控える傾向にある。また、現代の食生活の多
様化に伴い、とくに加工食品用の調味料として、従来の
調味料とは異なる機能、例えばレトルト包装加熱時にも
安定した呈味、風味および色調を維持可能な機能を有す
る調味料が求められている。[0002] Soy sauce, which is a traditional brewing seasoning that represents Japan, has been consumed in large amounts at home or as a processing seasoning for various foods since ancient times. However, soy sauce contains a large amount of salt, and in recent years, there is a tendency to refrain from using it for health reasons. In addition, with the diversification of modern dietary habits, especially as a seasoning for processed foods, a function different from conventional seasonings, for example, a function that can maintain a stable taste, flavor and color tone even when retort packaging is heated. A seasoning to have is sought.
【0003】このため、可能な限り食塩を含まずアミノ
酸を主要な呈味成分とする各種の調味料を製造する方法
が開発されている。例えば特開昭57−186455に
記載する方法がある。それらの多くは、タンパク質原料
をタンパク質加水分解酵素活性物質を使用して加水分解
し呈味性のアミノ酸を多量に含有する液状物製品を製造
する方法である。For this reason, methods have been developed for producing various seasonings which contain as little salt as possible and amino acids as main taste components. For example, there is a method described in JP-A-57-186455. Many of them are methods of producing a liquid product containing a large amount of a tasting amino acid by hydrolyzing a protein raw material using a protein hydrolase active substance.
【0004】[0004]
【発明が解決しようとする課題】しかしながら、上記の
如き方法においては、加水分解時に生成するアミノ酸お
よびタンパク質原料に由来する糖分にアミノカルボニル
化反応、「メイラ−ド(Maillard)反応」が生じ、風味
および色調を劣化せしめる褐変化物質を副生する。また
アミノカルボニル化反応生成物は製品の保存時にも引続
き生成され、風味および色調の劣化を来し品質安定性に
問題となるばかりでなく、この種の製品を使用する各種
の加工食品に対し好ましくない臭いを移転または発生せ
しめる。However, in the method as described above, the amino acid produced during the hydrolysis and the sugar derived from the protein raw material undergo an aminocarbonylation reaction, a "Maillard reaction", and the flavor is increased. And a browning substance that deteriorates the color tone is produced as a by-product. In addition, the aminocarbonylation reaction product is continuously produced even during storage of the product, which not only causes deterioration in flavor and color tone and poses a problem in quality stability, but is also preferable for various processed foods using this type of product. No odor is transferred or generated.
【0005】また、可能な限り食塩を含まない条件下で
は、タンパク質原料をタンパク質加水分解酵素活性物質
を使用して加水分解を行う際には、雑菌の混入、増殖を
回避することは実際上不可能である。In addition, it is practically impossible to avoid contamination and growth of various bacteria when the protein raw material is hydrolyzed using a protein hydrolase active substance under the condition that salt is not included as much as possible. It is possible.
【0006】なお、アミノカルボニル化反応生成物は、
タンパク質原料中に存在するペントザン、ヘミセルロ−
スなどが、代表的なタンパク質加水分解酵素活性物質で
ある麹菌の生成するガラクタナ−ゼ、キシリナ−ゼなど
の多糖加水分解酵素により加水分解をうけて生成するペ
ント−スを主成分とする糖分とアミノ酸が反応して生成
することから、ペント−スを主成分とする糖分量を低減
化する目的でペント−ス資化性乳酸菌を利用すること、
食塩水を使用してペント−スを除去するなどの報告およ
び対策が提案されている[醤油研究所雑誌,7(1),
19(1981);同誌,11,(5)189(198
5);同誌,12(4),132(1986)]。しか
し、未だ満足すべき効果を上げていない。The aminocarbonylation reaction product is
Pentosans and hemicelluloses present in protein raw materials
And sugars mainly composed of pentose produced by hydrolysis with a polysaccharide hydrolase such as galactanase or xylinase produced by Aspergillus oryzae, which is a typical protein hydrolase active substance. Since amino acids are produced by reaction, use of pentose-assimilating lactic acid bacteria for the purpose of reducing the amount of sugar having pentose as a main component,
Reports and countermeasures such as removing pentoses using saline have been proposed [Soy Sauce Research Institute Magazine, 7 (1),
19 (1981); ibid, 11, (5) 189 (198).
5); Ibid., 12 (4), 132 (1986)]. However, it has not yet produced satisfactory results.
【0007】また、食塩の使用を可能な限り低減化する
目的で、最初にグルコ−スを添加、次いで低温下で酵母
菌を増殖せしめ、そこで生成するエタノ−ルの共存下に
おいてタンパク質原料およびタンパク質加水分解酵素活
性物質を接触せしめる試み[Agric. Biol. Chem., 55
(5) 1325 (1991) ]もあるが、雑菌の増殖を抑止しつ
つ、かつ、加水分解を有効に進行させ得るに必要なエタ
ノ−ル濃度を全工程期間にわったて適度に維持すること
は困難である。For the purpose of reducing the use of salt as much as possible, glucose is added first, and then yeast is grown at a low temperature, and the protein raw material and the protein are produced in the presence of ethanol produced there. Attempt to contact hydrolase active substance [Agric. Biol. Chem., 55
(5) 1325 (1991)], but to maintain an appropriate ethanol concentration over the entire process period while suppressing the growth of bacteria and allowing hydrolysis to proceed effectively. It is difficult.
【0008】さらに、タンパク質の加水分解はペプチド
の段階で止まり、呈味性に関係あるアミノ酸の生成効率
は必ずしも高くない。また、エタノ−ル臭、原料臭、高
温分解臭が製品の調味料に残る可能性がある。[0008] Furthermore, protein hydrolysis stops at the peptide stage, and the production efficiency of amino acids related to taste is not necessarily high. Further, there is a possibility that an odor of ethanol, a raw material odor, and a high temperature decomposition odor remain in the seasoning of the product.
【0009】その他、酢酸、乳酸などの有機酸を添加し
てタンパク質加水分解を行う方法(特公昭53−187
97)、初期諸味のpHを4〜6に調整すると共に、エ
タノ−ル生産能を有する酵母菌を添加して発酵および消
化分解を行う方法(特開平4−311366)も提案さ
れているが、低pH下ではタンパク質加水分解酵素の活
性低下による分解率の低下が生じ、そのため、呈味およ
び風味とも満足できる製品は得がたい。In addition, a method of adding an organic acid such as acetic acid or lactic acid to hydrolyze protein (Japanese Patent Publication No. 53-187).
97), while adjusting the pH of the initial moromi to 4 to 6 and adding a yeast having an ethanol-producing ability to carry out fermentation and digestion decomposition (Japanese Patent Application Laid-Open No. 4-311366), At low pH, the degradation rate of proteolytic enzyme is reduced and the degradation rate is reduced. Therefore, it is difficult to obtain a product that has satisfactory taste and flavor.
【0010】さらに、タンパク質加水分解物中の褐変化
物質、褐変中間体物質を除去する目的で種々の膜処理が
おこなわれているが、これらの物質を完全に除去するこ
とは困難であり、更に残糖を膜処理で除去することも困
難であるので、膜処理を行った製品についても保存時の
品質安定性に不安が残る。Further, various membrane treatments have been carried out for the purpose of removing browning substances and browning intermediate substances in protein hydrolysates, but it is difficult to completely remove these substances. Since it is also difficult to remove residual sugar by membrane treatment, there is concern about the quality stability of the product subjected to membrane treatment during storage.
【0011】上記の通り、従来技術による無塩または低
塩の調味料の製造に関しては、製造の全工程中で静菌状
態を保持するために適切なエタノ−ル量を共存および維
持せしめることならびに製品調味料の呈味、風味および
色調を劣化せしめ、その保存時の品質安定性に不安を残
す褐変化物質、褐変中間体物質の生成防止および除去す
ることについては数多の問題があった。As described above, regarding the production of salt-free or low-salt seasonings according to the prior art, coexistence and maintenance of an appropriate amount of ethanol for maintaining a bacteriostatic state in all steps of production, and There are many problems in preventing and removing the browning substance and the browning intermediate substance which deteriorate the taste, flavor and color tone of the product seasoning and leave the quality stability during storage uneasy.
【0012】本発明は、上記問題を解消し、食塩を含有
しないと共に、呈味、風味および品質安定性の優れたの
調味料およびその製造法を提供することを目的とする。An object of the present invention is to solve the above problems, and to provide a seasoning which does not contain salt and which is excellent in taste, flavor and quality stability, and a method for producing the same.
【0013】上記目的を達成するため、請求項1に記載
の発明に係る調味料では、エタノール存在下、タンパク
質原料に、タンパク質加水分解酵素活性物質および糖分
資化性能を有する酵母菌を作用せしめてなるものとし
た。In order to achieve the above object, in the seasoning according to the invention of claim 1, in the presence of ethanol, a protein hydrolase active substance and a yeast having a sugar-utilizing ability are allowed to act on a protein raw material. I was supposed to.
【0014】また、請求項2に記載の発明に係る調味料
の製造法では、エタノール存在下、タンパク質原料に、
タンパク質加水分解酵素活性物質および糖分資化性能を
有する酵母菌を作用させるものとする。In the method for producing a seasoning according to the second aspect of the invention, the protein raw material is added to the protein raw material in the presence of ethanol.
A protein hydrolase active substance and a yeast having a sugar-utilizing ability are allowed to act.
【0015】また、請求項3に記載の調味料の製造法で
は、請求項2に記載の調味料の製造法において、前記酵
母菌を、エタノ−ル発酵能を有するものとした。Further, in the method for producing a seasoning according to claim 3, in the method for producing a seasoning according to claim 2, the yeast has an ethanol fermenting ability.
【0016】また、請求項4に記載の調味料の製造法で
は、請求項2又は請求項3に記載の調味料の製造法にお
いて、前記酵母菌として、固定化酵母菌を用いるものと
した。In the method for producing a seasoning according to claim 4, an immobilized yeast is used as the yeast in the method for producing a seasoning according to claim 2 or 3.
【0017】[0017]
【作用】本発明は、無塩あるいは低塩条件下でタンパク
質原料にタンパク質加水分解酵素活性物質のタンパク質
加水分解酵素を作用せしめて調味料を製造する方法に関
して種々検討した結果、特定範囲にエタノール濃度を維
持しつつ、タンパク質加水分解酵素活性物質に加えさら
に糖分資化性能を有する酵母菌を作用させることによっ
て、好ましい呈味、風味および色調を有し、保存時の品
質安定性を阻害する褐変化物質、褐変中間体物質の含量
も少ない調味料液が得られることを見出し本発明に至っ
たものである。[Function] The present invention has variously examined the method of producing a seasoning by allowing a protein hydrolase of a protein hydrolase active substance to act on a protein raw material under salt-free or low salt conditions, and as a result, various results have been obtained. A browning that has a favorable taste, flavor and color tone, and inhibits the quality stability during storage by allowing yeast having an ability to utilize sugars to act in addition to a protein hydrolase active substance while maintaining The inventors of the present invention have found that a seasoning liquid having a low content of substances and browning intermediate substances can be obtained, and the present invention has been completed.
【0018】これは、製品調味料の呈味、風味および色
調を劣化せしめ、その保存時の品質安定性を阻害する褐
変化物質、褐変中間体物質を生成するアミノカルボニル
化反応を有効に阻止することによって実現できるもので
あり、そのアミノカルボニル化反応の原因となるタンパ
ク質原料の加水分解時に生成する糖分を酵母菌によって
資化し、調味料中に存在する糖分を低濃度に保持するこ
とによる。なお、アミノカルボニル化反応の阻止に有効
な製品調味料中に存在する糖分濃度として1.0(重量
/容量)%以下が望ましい。This effectively inhibits the aminocarbonylation reaction which deteriorates the taste, flavor and color tone of the product seasoning and inhibits the browning substance and the browning intermediate substance which impair the quality stability during storage. This is achieved by utilizing the sugars produced during the hydrolysis of the protein raw material, which causes the aminocarbonylation reaction, by the yeast and keeping the sugars present in the seasoning at a low concentration. The sugar concentration present in the product seasoning effective for inhibiting the aminocarbonylation reaction is preferably 1.0 (weight / volume)% or less.
【0019】また、タンパク質原料にタンパク質加水分
解酵素活性物質を作用せしめる際には、当初より高濃度
のエタノ−ルを添加することなく、当初添加エタノ−ル
量および工程進行中にその場で生成するエタノ−ル量、
更に工程進行中に逸出するエタノ−ル量の合計量を考慮
して、全工程にわたってエタノ−ル濃度を静菌状態を保
持し、かつ、タンパク質加水分解酵素の活性を阻害しな
い範囲内に維持することが望ましいが、本発明において
は、用いる酵母菌をエタノール発酵能を有するものとす
ることにより、この酵母菌にタンパク質原料の加水分解
時に生成する糖分を資化させてエタノ−ルを生成させ、
該エタノールを利用することが可能となる。When the protein hydrolase active substance is allowed to act on the protein raw material, the amount of ethanol added initially and the amount of ethanol added initially are not added at the time of the process progress. The amount of ethanol to
Furthermore, considering the total amount of ethanol that escapes during the process, the concentration of ethanol is maintained in a bacteriostatic state throughout the entire process, and is maintained within a range that does not inhibit the activity of protein hydrolase. In the present invention, the yeast used has ethanol fermentability, so that the yeast can utilize the sugars produced during the hydrolysis of the protein raw material to produce ethanol. ,
It becomes possible to utilize the ethanol.
【0020】なお、静菌状態を保持し、かつ、タンパク
質加水分解酵素の活性を阻害しない条件として。少なく
とも作用後の生成液に含有されるエタノ−ル濃度が2〜
20(容量/容量)%の範囲内となることが望ましい。
これは、通常、無塩または低塩条件下において、酵母菌
による作用後にエタノール濃度が2%以下となるような
状態では作用中に雑菌が増殖する恐れがあり、20%以
上となるような場合にはタンパク質加水分解酵素による
作用が阻害されてしまう可能性があり、いずれにしても
作用後に得られる調味液の呈味が良くないためである。As conditions for maintaining the bacteriostatic state and not inhibiting the activity of the protein hydrolase. At least the concentration of ethanol contained in the product liquid after the action is 2 to
It is desirable to be in the range of 20 (volume / volume)%.
This is usually the case when the concentration of ethanol is 2% or less after the action of the yeast under salt-free or low-salt conditions, and when the concentration of ethanol is 20% or more. This is because the action of the protein hydrolase may be inhibited, and in any case, the taste of the seasoning liquid obtained after the action is not good.
【0021】また、本発明に用いるタンパク質原料とし
ては、主に大豆、小麦、大麦、米、トウモロコシ、米分
離タンパク質、ジャガイモ分離タンパク質、ビ−ル醸造
副製品(ビ−ル粕など)等の植物性原料や、ゼラチン、
卵白、脱脂粉乳、全乳粉末、乳カゼイン、乳ホエイタン
パク質、魚肉、カツオ肉抽出物、鶏肉、牛肉、豚肉、獣
肉抽出エキスまたはこれらの加工品などの動物性原料が
挙げられる。もちろんこれら原料の混合原料でもよく、
例えば大豆とトウモロコシ、大豆と小麦、大豆とゼラチ
ン、大豆分離タンパク質と白身の魚肉フィレ−など種々
の組合わせが考えられる。As the protein raw material used in the present invention, plants such as soybean, wheat, barley, rice, corn, rice isolated protein, potato isolated protein and beer brewing by-products (beer meal etc.) are mainly used. Raw materials, gelatin,
Animal raw materials such as egg white, skim milk powder, whole milk powder, milk casein, milk whey protein, fish meat, bonito meat extract, chicken, beef, pork, animal meat extract and processed products thereof can be mentioned. Of course, a mixed raw material of these raw materials may be used,
For example, various combinations such as soybean and corn, soybean and wheat, soybean and gelatin, soybean isolated protein and white fish fillet can be considered.
【0022】また本発明においては、タンパク質加水分
解酵素活性物質として、タンパク質加水分解活性を有す
る物質またはタンパク質加水分解活性に加えて多糖加水
分解活性を有する物質であれば広く使用可能であるが、
例えば分離したタンパク質加水分解酵素(プロテアー
ゼ)標品、微生物の培養物またはその加工品等がある。
またアスペルギルス(Aspergillus )属菌、バチルス
(Bacillus)属菌の液体培地培養物または固体培地培養
物、特に米麹、麦麹、豆麹、フスマ麹、醤油麹および植
物性原料に動物性原料を被覆し麹菌を培養した混合麹、
さらに、これら各種の麹を混合したものなどがある。In the present invention, as the protein hydrolase active substance, a substance having a protein hydrolysis activity or a substance having a polysaccharide hydrolysis activity in addition to the protein hydrolysis activity can be widely used.
Examples include isolated protein hydrolase (protease) preparations, microbial cultures or processed products thereof.
In addition, liquid or solid medium cultures of Aspergillus spp., Bacillus spp., Particularly rice koji, malt koji, soybean koji, fusuma koji, soy sauce koji, and vegetable raw materials coated with animal raw materials Mixed koji, which is a cultivated koji mold,
Further, there is a mixture of these various types of koji.
【0023】さらに、本発明で使用する酵母菌は、高い
糖分資化性能を有することが好ましい。さらに、エタノ
−ル発酵能の高い酵母菌であることが望ましいが、非耐
塩性の酵母菌、具体的には清酒酵母、ビ−ル酵母、ワイ
ン酵母、ウイスキ−原酒発酵用酵母およびパン酵母が適
当である。Further, the yeast used in the present invention preferably has a high sugar utilization ability. Further, it is desirable that the yeast has a high ethanol fermenting ability, but non-salt-tolerant yeasts, specifically, sake yeast, beer yeast, wine yeast, whiskey-fermenting yeast and baker's yeast are preferable. Appropriate.
【0024】また、使用する酵母はこれら各種の酵母の
高密度培養物の他に、酵母菌体を、例えばアルギン酸塩
・ゲル内に包埋した固定化酵母菌体、セラミックス担体
またはセライトに吸着、固定化した酵母菌体も使用でき
る。このような固定化酵母菌体は、長時間、連続使用が
できる可能性があり、調味料製造工程のバイオリアクタ
ーによる自動化、これに伴う全工程の高効率低コスト化
を実現可能とする。In addition to the high-density cultures of these various yeasts, the yeast to be used is adsorbed on an immobilized yeast cell, for example, a yeast cell embedded in an alginate gel, a ceramic carrier or celite, Immobilized yeast cells can also be used. Such an immobilized yeast cell may be used continuously for a long time, and it is possible to realize automation of a seasoning production process by a bioreactor, and to realize high efficiency and cost reduction of all the processes associated therewith.
【0025】タンパク質原料にタンパク質加水分解酵素
活性物質および糖分資化性の高い酵母菌を作用させる際
には、初め25〜35℃で、次いで50〜60℃で作用
させることが望ましい。When a protein hydrolase active substance and a yeast having a high sugar-utilizing ability are allowed to act on the protein raw material, it is desirable to first act at 25 to 35 ° C. and then at 50 to 60 ° C.
【0026】タンパク質原料にタンパク質加水分解酵素
活性物質および糖分資化性の高い酵母菌を作用させて得
られる調味料液を製品とするには、固液分離により生成
液中の固体成分を分離除去することが好ましい。これ
は、固体成分には製品調味料の呈味、風味および色調を
劣化せしめ、その保存時の品質安定性を阻害する褐変化
物質、褐変中間体物質が濃縮吸着されているためであ
る。In order to make a seasoning liquid obtained by reacting a protein hydrolase active substance and a yeast having a high sugar utilization with a protein raw material, solid components in the product liquid are separated and removed by solid-liquid separation. Preferably. This is because the solid component is concentrated and adsorbed with a browning substance and a browning intermediate substance which deteriorate the taste, flavor and color tone of the product seasoning and impair the quality stability during storage.
【0027】また、エタノールを含有する水溶液中でタ
ンパク質原料にタンパク質加水分解酵素活性物質および
糖分資化性の高い酵母菌を作用させる際に、使用するエ
タノ−ル水溶液として、それ以前にタンパク質原料に対
するタンパク質加水分解酵素活性物質および糖分資化性
を有する酵母菌の作用を行った後の、固体成分を分離除
去した液を減圧下に濃縮した時に回収される揮発成分を
含有する水溶液、あるいは該水溶液に適当量のエタノ−
ルまたは滅菌水を添加し、エタノ−ル濃度を調整した溶
液を利用することができる。このように濃縮時に回収さ
れる揮発成分を含有する水溶液を使用すると、製品調味
料の品質、特に風味を向上せしめる。Further, as an ethanol aqueous solution used when a protein hydrolase active substance and a yeast having a high sugar-utilizing ability are allowed to act on a protein raw material in an aqueous solution containing ethanol, the protein raw material can be used before that. An aqueous solution containing a volatile component that is recovered when the liquid from which the solid component has been separated and removed is concentrated under reduced pressure after the action of a protein hydrolase active substance and a yeast having sugar-utilizing ability, or the aqueous solution. A suitable amount of ethanol
Solution in which ethanol or sterilized water is added to adjust the ethanol concentration can be used. When the aqueous solution containing the volatile component recovered during the concentration is used, the quality of the product seasoning, particularly the flavor, can be improved.
【0028】[0028]
【実施例】以下に本発明を実施例をもって説明する。本
実施例は、エタノール含有水溶液中においてタンパク質
原料としての脱脂大豆に対するタンパク質加水分解酵素
活性物質および酵母菌の作用を各々異なる条件1〜6の
操作に従って行うことによって各々調味液を製造するも
のである。EXAMPLES The present invention will be described below with reference to examples. In this example, the seasoning liquids are produced by performing the actions of the protein hydrolase active substance and the yeast on the defatted soybeans as the protein raw material in the ethanol-containing aqueous solution according to the operations of different conditions 1 to 6, respectively. .
【0029】ここでは各条件での操作に共通して、ま
ず、市販の醤油麹「うすむらさき」(商品名:樋口松之
助商店製)より分離した麹菌をフスマ培地に接種し、3
0℃に3日間保つことによって新たにフスマ麹を製麹し
ておき、このフスマ麹300gと脱脂大豆1Kgとをエ
タノ−ル水溶液4L中に浸漬後、市販の清酒粕(メルシ
ャン株式会社製)より分離した非耐塩性酵母菌を10万
個/mlになるように添加し、エタノール発酵ならびに
加水分解を行い、生成物液を固液分離して調味液を得
た。Here, in common with the operation under each condition, first, the fusuma culture medium is inoculated with the koji mold isolated from the commercially available soy sauce koji "Usmurasaki" (trade name: manufactured by Higuchi Matsunosuke Shoten), and 3
Kuma bran malt is newly koji-made by keeping it at 0 ° C. for 3 days, and 300 g of the bran malt koji and 1 Kg of defatted soybean are soaked in 4 L of ethanol aqueous solution, and then commercially available sake sake lees (manufactured by Mercian Co., Ltd.) The separated non-salt-tolerant yeast was added at 100,000 cells / ml, ethanol fermentation and hydrolysis were performed, and the product liquid was subjected to solid-liquid separation to obtain a seasoning liquid.
【0030】条件1(a〜d)の操作では、脱脂大豆1
Kg,フスマ麹300g,酵母菌10万個/mlを添加
混合した5(容量/容量)%エタノール水溶液をまず3
0℃5日間保持してエタノール発酵を行い、その後50
℃5日間保持して加水分解を行った。In the operation of conditions 1 (a to d), defatted soybean 1
Kg, 300 g of bran koji, and 100,000 yeast cells / ml were added and mixed to prepare 5 (volume / volume)% ethanol aqueous solution.
Fermentation of ethanol is carried out at 0 ° C for 5 days, then 50
Hydrolysis was carried out by holding at 5 ° C for 5 days.
【0031】条件2の操作では、脱脂大豆1Kg,フス
マ麹300g,酵母菌10万個/mlを添加混合した5
(容量/容量)%エタノール水溶液をまず50℃5日間
保持して加水分解を行い、その後30℃5日間保持して
エタノール発酵を行った。In the operation of condition 2, 1 kg of defatted soybean, 300 g of bran koji, and 100,000 yeast cells / ml were added and mixed.
(Volume / volume)% ethanol aqueous solution was first kept at 50 ° C. for 5 days for hydrolysis, and then kept at 30 ° C. for 5 days for ethanol fermentation.
【0032】条件3の操作では、エタノ−ル発酵を、ア
ルギン酸カルシウム・ゲルに包埋した非耐塩性酵母菌を
充填したカラムに通液する方法によった。ゲル内の酵母
菌濃度は1億個/ml(ゾル状態で非耐塩性酵母菌を1
0万個/ml濃度となし、ゲル化後、該ゲルを30度C
に24時間保持し前記の菌体濃度に調整)。通液条件は
SV=1(カラム内容積量を1時間を要して流下)、R
V=5(通液量はカラム内容積量の5倍)。The operation of condition 3 was carried out by passing the ethanol fermentation through a column packed with non-salt-tolerant yeasts embedded in calcium alginate gel. The concentration of yeast in the gel is 100 million / ml (
After the gelation, the gel was set to 30 ° C.
And keep it for 24 hours to adjust to the above cell concentration). The flow conditions are SV = 1 (flowing down the volume of the column within 1 hour), R
V = 5 (the flow rate is 5 times the volume in the column).
【0033】まず、脱脂大豆1Kg,フスマ麹300
g,酵母菌10万個/mlを添加混合した5(容量/容
量)%エタノール水溶液を50℃5日間保持して加水分
解を行う。その後、上記の固定化酵母菌が充填され下部
に流出量の制御可能なコックを備えたカラムへ、加水分
解後の糖を含む分解懸濁液をカラム内容量流入せしめ
る。一時間保持後、カラム下部のコックを開いて少しづ
つ液を流出させ、その流出速度と同一の速度で残余のカ
ラム4倍量の分解懸濁液をカラムへ供給する。最後にカ
ラム内容液が全部流出したところで水を流入せしめカラ
ム内の残渣を押し出す。First, 1 kg of defatted soybean, 300 of koji bran
g, and 100,000 yeast cells / ml were added and mixed, and a 5 (volume / volume)% ethanol aqueous solution was held at 50 ° C. for 5 days for hydrolysis. After that, the decomposition suspension containing the sugar after hydrolysis is caused to flow into the column volume filled with the above-mentioned immobilized yeast and equipped with a cock having a controllable flow rate at the bottom. After holding for one hour, the cock at the bottom of the column is opened to let the liquid flow out little by little, and the remaining 4-fold amount of the decomposition suspension is supplied to the column at the same rate as the flow rate. Finally, when all the contents in the column have flowed out, water is allowed to flow in and the residue in the column is pushed out.
【0034】条件4の操作では、条件1の操作に従って
得られた調味液3Kgを減圧下に濃縮した際に分取した
揮発成分に、滅菌水およびエタノールを添加し、エタノ
ール濃度を5(容量/容量)%に調整した水溶液を用い
た。この濃縮揮発成分を含む5(容量/容量)%エタノ
ール水溶液4Lに脱脂大豆1Kg,フスマ麹300g,
酵母菌10万個/mlを添加混合し、まず30℃5日間
保持してエタノール発酵を行い、その後50℃5日間保
持して加水分解を行った。In the operation of condition 4, sterilized water and ethanol were added to the volatile components separated when 3 kg of the seasoning solution obtained according to the operation of condition 1 was concentrated under reduced pressure, and the ethanol concentration was adjusted to 5 (volume / volume). An aqueous solution adjusted to (volume)% was used. To 4 L of a 5 (volume / volume)% ethanol solution containing this concentrated volatile component, 1 kg of defatted soybeans, 300 g of bran koji,
100,000 yeast cells / ml were added and mixed, and the mixture was first kept at 30 ° C. for 5 days for ethanol fermentation, and then kept at 50 ° C. for 5 days for hydrolysis.
【0035】条件5の操作では、条件1の操作に従って
得られた調味液3Kgを減圧下に濃縮した際に分取した
揮発成分に、滅菌水およびエタノールを添加し、エタノ
ール濃度を12(容量/容量)%に調整した水溶液を用
いた。この濃縮揮発成分を含む12(容量/容量)%エ
タノール水溶液4Lに脱脂大豆1Kg,フスマ麹300
g,酵母菌10万個/mlを添加混合し、まず30℃5
日間保持してエタノール発酵を行い、その後50℃5日
間保持して加水分解を行った。In the operation of condition 5, sterilized water and ethanol were added to the volatile components separated when 3 kg of the seasoning solution obtained according to the operation of condition 1 was concentrated under reduced pressure, and the ethanol concentration was adjusted to 12 (volume / volume). An aqueous solution adjusted to (volume)% was used. 1 kg of defatted soybean, 300 ml of koji bran was added to 4 L of a 12 (volume / volume)% ethanol aqueous solution containing this concentrated volatile component.
g, 100,000 yeast cells / ml were added and mixed, and the mixture was mixed at 30 ° C for 5
It was kept for a day to carry out ethanol fermentation, and then kept at 50 ° C. for 5 days for hydrolysis.
【0036】条件6の操作では、条件1の操作に従って
得られた調味液3Kgを減圧下に濃縮した際に分取した
揮発成分に、滅菌水およびエタノールを添加し、エタノ
ール濃度を10(容量/容量)%に調整した水溶液を用
いた。この濃縮揮発成分を含む10(容量/容量)%エ
タノール水溶液4Lに脱脂大豆1Kg,フスマ麹300
g,酵母菌10万個/mlを添加混合し、まず30℃5
日間保持してエタノール発酵を行い、その後50℃5日
間保持して加水分解を行った。In the operation of condition 6, sterilized water and ethanol were added to the volatile components collected when 3 kg of the seasoning solution obtained according to the operation of condition 1 was concentrated under reduced pressure, and the ethanol concentration was adjusted to 10 (volume / volume). An aqueous solution adjusted to (volume)% was used. 1 kg of defatted soybean, 300 ml of koji bran was added to 4 L of 10 (volume / volume)% ethanol aqueous solution containing this concentrated volatile component.
g, 100,000 yeast cells / ml were added and mixed, and the mixture was mixed at 30 ° C for 5
It was kept for a day to carry out ethanol fermentation, and then kept at 50 ° C. for 5 days for hydrolysis.
【0037】以上の操作によって取得した各調味液につ
いて、ケ−ルダ−ル(Kjeldahl)法による総窒
素の分析、アミノ酸中のアミノ基をオルト・フェニルア
ルデヒドと反応せしめ生成する蛍光を測定するOPA法
[Poter, D. H., J. Agric. Food Chem., 32,334-339 (1
984)] )による分解率の測定、公定分析法であるフェ−
リング レ−マン ショウル(Fehring Lehmann Schor
l)法による還元糖濃度(g/dL)の測定、製品調味
料を100度Cに3時間保持した場合の吸光度法により
測定した色度の上昇率ならびに15名からなる官能評価
パネルによる官能評価試験を行った。結果を表1に示
す。With respect to each seasoning liquid obtained by the above operation, analysis of total nitrogen by Kjeldahl method, OPA method for measuring fluorescence generated by reacting amino group in amino acid with ortho-phenylaldehyde
[Poter, DH, J. Agric. Food Chem., 32,334-339 (1
984)]) Degradation rate measurement by the official analysis method
Fehring Lehmann Schor
l) Method for measuring reducing sugar concentration (g / dL), increase rate of chromaticity measured by absorbance method when product seasoning was kept at 100 ° C for 3 hours, and sensory evaluation by sensory evaluation panel consisting of 15 persons The test was conducted. The results are shown in Table 1.
【0038】[0038]
【表1】 [Table 1]
【0039】表1の結果からわかるように、エタノール
発酵は、タンパク質加水分解前に行っても後に行って
も、例えば条件1と条件2の結果を比較すると得られる
調味料液の評価に殆ど差ない。また、特に条件5の結果
から明らかなように、タンパク質原料に対するタンパク
質加水分解酵素活性物質および糖分資化性を有する酵母
菌の作用を行った後の、固体成分を分離除去した液を減
圧下に濃縮した時に回収される揮発成分を含有するエタ
ノール水溶液を使用してさらに調味料を製造すること
は、製品調味料の品質、特に風味を向上せしめる点から
有効である。As can be seen from the results shown in Table 1, whether the ethanol fermentation is carried out before or after the protein hydrolysis, for example, there is almost no difference in the evaluation of the seasoning liquid obtained by comparing the results of Condition 1 and Condition 2. Absent. In addition, as is clear from the result of the condition 5, in particular, after the action of the protein hydrolase active substance and the yeast having sugar-utilizing ability on the protein raw material, the liquid from which the solid components have been separated and removed is put under reduced pressure. It is effective to further produce a seasoning by using an aqueous ethanol solution containing a volatile component recovered when concentrated, from the viewpoint of improving the quality of the product seasoning, particularly the flavor.
【0040】但し、条件5、6の結果から、当初より比
較的高いエタノール濃度でタンパク質加水分解を行う場
合には、分解作用が阻害されるためか調味液の呈味は余
り良くないという傾向が見られる。なお、その他の条件
においては作用後の生成液のエタノール濃度は、初期設
定濃度(表中1EtOH(%) で表示)より1〜2%程度低い
あるいは高い値であってほぼ変わりなく維持されてい
た。However, from the results of Conditions 5 and 6, when the protein is hydrolyzed at a relatively high ethanol concentration from the beginning, there is a tendency that the taste of the seasoning liquid is not so good probably because the decomposition action is inhibited. Can be seen. Under other conditions, the ethanol concentration of the product solution after the action was maintained at almost 1 to 2% lower or higher than the initial set concentration (indicated by 1EtOH (%) in the table), which was almost unchanged. .
【0041】なお、上記実施例においては、エタノール
発酵を30℃5日間、タンパク質加水分解を50℃5日
間で行ったが、本発明はこれに限定するものではなく、
用いるタンパク質原料、タンパク質加水分解酵素活性物
質および酵母菌の種類に応じて適宜設定すれば良い。In the above examples, ethanol fermentation was carried out at 30 ° C. for 5 days and protein hydrolysis was carried out at 50 ° C. for 5 days, but the present invention is not limited to this.
It may be appropriately set depending on the protein raw material used, the protein hydrolase active substance, and the type of yeast.
【0042】また、固定化酵母菌を用いる場合、実施例
に示した固定化法以外にも種々の方法が考えられるが、
これも用いる酵母菌、タンパク質原料に応じて、あるい
はバイオリアクターに組み込む場合には物理的・化学的
耐久性等、反応系に応じて適当な方法を選択することが
好ましい。When immobilized yeast is used, various methods other than the immobilization method shown in the examples are conceivable.
It is preferable to select an appropriate method depending on the yeast, protein raw material to be used, or when it is incorporated into a bioreactor, depending on the reaction system such as physical and chemical durability.
【0043】さらに、タンパク質原料に対してタンパク
質加水分解酵素活性物質を作用させ、次いで糖分資化性
能を有する酵母菌を作用させるという順を追った工程に
限らず、両者を同時に作用させる工程としても良い。Further, it is not limited to a step in which a protein hydrolase active substance is allowed to act on a protein raw material, and then a yeast having a sugar-utilizing ability is acted on. good.
【0044】ここで、比較例として酵母の作用を関与さ
せないでタンパク質加水分解を行った。上記実施例と同
様に新たに製麹したフスマ麹300gと脱脂大豆1Kg
とを5(容量/容量)%エタノール水溶液4L中に添加
混合し、まず30℃5日間保持し、その後50℃に5日
間保持して(比較例1〜3)、あるいは2、5、7日目
にエタノール濃度を測定し、当初の濃度を維持するよう
エタノールの補充を行いながら(比較例4)タンパク質
加水分解を行った。取得した調味液について実施例と同
一の方法によって分析および官能評価試験を行った。結
果を表1に下部に示す。Here, as a comparative example, protein hydrolysis was carried out without involving the action of yeast. Similar to the above-mentioned example, 300 g of freshly malted rice koji and 1 kg of defatted soybean
And 4% of 5 (vol / vol)% ethanol aqueous solution were added and mixed, and first kept at 30 ° C. for 5 days, and then kept at 50 ° C. for 5 days (Comparative Examples 1 to 3), or 2, 5, 7 days. The ethanol concentration was measured in the eye, and protein hydrolysis was performed while supplementing ethanol so as to maintain the initial concentration (Comparative Example 4). The obtained seasoning liquid was subjected to analysis and sensory evaluation test by the same method as in the example. The results are shown in Table 1 below.
【0045】表1からわかるように、比較例では酵母に
よる作用がなく、即ちタンパク質加水分解工程を経て生
成された糖の酵母による資化が十分行われておらず、い
ずれの比較例の場合も3g/dL前後と実施例に比べ多
くの還元糖が分析された。このように、エタノール存在
下でタンパク質加水分解を行っても、糖分資化という酵
母の関与がなければ呈味が良くかつ品質安定性の良い調
味料は得られないことが明らかとなった。As can be seen from Table 1, in Comparative Examples, there was no action by yeast, that is, the sugar produced through the protein hydrolysis step was not sufficiently assimilated by yeast. Around 3 g / dL, a large amount of reducing sugars were analyzed as compared with the examples. Thus, it has been clarified that even if protein hydrolysis is performed in the presence of ethanol, a seasoning having a good taste and good quality stability cannot be obtained without the involvement of yeast of sugar utilization.
【0046】[0046]
【発明の効果】以上説明したとおり、本発明によれば、
実質上食塩を含まず調味液として好ましい呈味、風味お
よび色調を有すると共に、褐変化物質、褐変中間体物質
の含量も少なく保存時の品質安定性にも優れた調味料が
得られる。このような調味料は、健康上の点および品質
の点から、安心して種々の調味材料、加工食品に利用で
きる。As described above, according to the present invention,
A seasoning containing substantially no salt and having a preferable taste, flavor and color tone as a seasoning liquid, and having a small amount of browning substances and browning intermediate substances and excellent quality stability during storage can be obtained. Such seasonings can be safely used for various seasoning materials and processed foods in terms of health and quality.
───────────────────────────────────────────────────── フロントページの続き (72)発明者 高野 靖 神奈川県川崎市川崎区鈴木町1−1 味の 素株式会社食品総合研究所内 ─────────────────────────────────────────────────── ─── Continuation of front page (72) Inventor Yasushi Takano 1-1, Suzuki-cho, Kawasaki-ku, Kawasaki-shi, Kanagawa Ajinomoto Co., Inc. Food Research Institute
Claims (4)
ンパク質加水分解酵素活性物質および糖分資化性能を有
する酵母菌を作用せしめてなることを特徴とする調味
料。1. A seasoning characterized in that a protein hydrolase active substance and a yeast having a sugar-utilizing ability are allowed to act on a protein raw material in the presence of ethanol.
タンパク質加水分解酵素活性物質および糖分資化性能を
有する酵母菌を作用させることを特徴とする請求項1に
記載の調味料の製造法。2. A protein raw material in the presence of ethanol,
The method for producing a seasoning according to claim 1, wherein a protein hydrolase active substance and a yeast having a sugar-utilizing ability are allowed to act.
ることを特徴とする請求項2に記載の調味料の製造法。3. The method for producing a seasoning according to claim 2, wherein the yeast has an ethanol fermentation ability.
ることを特徴とする請求項2又は請求項3に記載の調味
料の製造法。4. The method for producing a seasoning according to claim 2, wherein an immobilized yeast is used as the yeast.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP09491493A JP3227893B2 (en) | 1993-03-31 | 1993-03-31 | Seasoning and its manufacturing method |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP09491493A JP3227893B2 (en) | 1993-03-31 | 1993-03-31 | Seasoning and its manufacturing method |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH06276996A true JPH06276996A (en) | 1994-10-04 |
| JP3227893B2 JP3227893B2 (en) | 2001-11-12 |
Family
ID=14123274
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP09491493A Expired - Fee Related JP3227893B2 (en) | 1993-03-31 | 1993-03-31 | Seasoning and its manufacturing method |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP3227893B2 (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2009165377A (en) * | 2008-01-15 | 2009-07-30 | Kyushu Univ | Unsalted alcohol fermented seasoning liquid and method for producing the same |
| JP2014512831A (en) * | 2011-05-03 | 2014-05-29 | ネステク ソシエテ アノニム | Hydrolyzate of protein substrate and production method thereof |
| JP2018108116A (en) * | 2016-12-27 | 2018-07-12 | アピ株式会社 | Method for producing royal jelly material, royal jelly material, royal jelly-containing food and drink, and royal jelly-containing cosmetic |
-
1993
- 1993-03-31 JP JP09491493A patent/JP3227893B2/en not_active Expired - Fee Related
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2009165377A (en) * | 2008-01-15 | 2009-07-30 | Kyushu Univ | Unsalted alcohol fermented seasoning liquid and method for producing the same |
| JP2014512831A (en) * | 2011-05-03 | 2014-05-29 | ネステク ソシエテ アノニム | Hydrolyzate of protein substrate and production method thereof |
| JP2018108116A (en) * | 2016-12-27 | 2018-07-12 | アピ株式会社 | Method for producing royal jelly material, royal jelly material, royal jelly-containing food and drink, and royal jelly-containing cosmetic |
Also Published As
| Publication number | Publication date |
|---|---|
| JP3227893B2 (en) | 2001-11-12 |
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