JPH0347051A - Preparation of raw solution of seasoning - Google Patents
Preparation of raw solution of seasoningInfo
- Publication number
- JPH0347051A JPH0347051A JP1329999A JP32999989A JPH0347051A JP H0347051 A JPH0347051 A JP H0347051A JP 1329999 A JP1329999 A JP 1329999A JP 32999989 A JP32999989 A JP 32999989A JP H0347051 A JPH0347051 A JP H0347051A
- Authority
- JP
- Japan
- Prior art keywords
- koji
- animal protein
- total nitrogen
- seasoning
- fermentation
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 235000011194 food seasoning agent Nutrition 0.000 title claims abstract description 34
- 238000002360 preparation method Methods 0.000 title description 10
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims abstract description 88
- 229910052757 nitrogen Inorganic materials 0.000 claims abstract description 44
- 235000021120 animal protein Nutrition 0.000 claims abstract description 26
- 150000001413 amino acids Chemical class 0.000 claims abstract description 22
- 102000004190 Enzymes Human genes 0.000 claims abstract description 20
- 108090000790 Enzymes Proteins 0.000 claims abstract description 20
- 108090000765 processed proteins & peptides Proteins 0.000 claims abstract description 19
- 108091005804 Peptidases Proteins 0.000 claims abstract description 15
- 238000000034 method Methods 0.000 claims abstract description 12
- 150000001412 amines Chemical class 0.000 claims abstract description 11
- 239000000203 mixture Substances 0.000 claims abstract description 11
- 235000013555 soy sauce Nutrition 0.000 claims abstract description 10
- 240000006439 Aspergillus oryzae Species 0.000 claims abstract description 9
- 238000006243 chemical reaction Methods 0.000 claims abstract description 9
- 235000002247 Aspergillus oryzae Nutrition 0.000 claims abstract description 8
- 241000251468 Actinopterygii Species 0.000 claims abstract description 5
- 244000063299 Bacillus subtilis Species 0.000 claims abstract description 4
- 235000014469 Bacillus subtilis Nutrition 0.000 claims abstract description 4
- 238000000855 fermentation Methods 0.000 claims description 17
- 230000004151 fermentation Effects 0.000 claims description 17
- 239000011550 stock solution Substances 0.000 claims description 14
- 102000035195 Peptidases Human genes 0.000 claims description 12
- 238000004519 manufacturing process Methods 0.000 claims description 11
- 235000019645 odor Nutrition 0.000 claims description 10
- 102000004196 processed proteins & peptides Human genes 0.000 claims description 10
- 239000000243 solution Substances 0.000 claims description 9
- 150000003839 salts Chemical class 0.000 claims description 5
- 238000006460 hydrolysis reaction Methods 0.000 claims 1
- 239000000126 substance Substances 0.000 abstract description 10
- 235000019688 fish Nutrition 0.000 abstract description 5
- 102100037486 Reverse transcriptase/ribonuclease H Human genes 0.000 abstract description 3
- 235000013372 meat Nutrition 0.000 abstract description 3
- 239000000413 hydrolysate Substances 0.000 abstract 2
- 235000015097 nutrients Nutrition 0.000 abstract 1
- 235000015170 shellfish Nutrition 0.000 abstract 1
- 239000007788 liquid Substances 0.000 description 19
- 229940088598 enzyme Drugs 0.000 description 17
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 12
- 229960004279 formaldehyde Drugs 0.000 description 12
- 235000019256 formaldehyde Nutrition 0.000 description 12
- 239000002994 raw material Substances 0.000 description 10
- 241000269821 Scombridae Species 0.000 description 9
- 235000020640 mackerel Nutrition 0.000 description 9
- 235000018102 proteins Nutrition 0.000 description 7
- 102000004169 proteins and genes Human genes 0.000 description 7
- 108090000623 proteins and genes Proteins 0.000 description 7
- 238000000354 decomposition reaction Methods 0.000 description 6
- 235000019833 protease Nutrition 0.000 description 6
- 235000015067 sauces Nutrition 0.000 description 6
- 241000228212 Aspergillus Species 0.000 description 5
- 108010082495 Dietary Plant Proteins Proteins 0.000 description 5
- 239000004278 EU approved seasoning Substances 0.000 description 4
- 239000004365 Protease Substances 0.000 description 4
- 235000010469 Glycine max Nutrition 0.000 description 3
- 241001465754 Metazoa Species 0.000 description 3
- 108010064851 Plant Proteins Proteins 0.000 description 3
- 210000000988 bone and bone Anatomy 0.000 description 3
- 235000014633 carbohydrates Nutrition 0.000 description 3
- 150000001720 carbohydrates Chemical class 0.000 description 3
- 235000013339 cereals Nutrition 0.000 description 3
- 244000144972 livestock Species 0.000 description 3
- 235000021118 plant-derived protein Nutrition 0.000 description 3
- XINQFOMFQFGGCQ-UHFFFAOYSA-L (2-dodecoxy-2-oxoethyl)-[6-[(2-dodecoxy-2-oxoethyl)-dimethylazaniumyl]hexyl]-dimethylazanium;dichloride Chemical compound [Cl-].[Cl-].CCCCCCCCCCCCOC(=O)C[N+](C)(C)CCCCCC[N+](C)(C)CC(=O)OCCCCCCCCCCCC XINQFOMFQFGGCQ-UHFFFAOYSA-L 0.000 description 2
- 241000193830 Bacillus <bacterium> Species 0.000 description 2
- 241000196324 Embryophyta Species 0.000 description 2
- 244000068988 Glycine max Species 0.000 description 2
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 2
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical group [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 2
- 241000209140 Triticum Species 0.000 description 2
- 235000021307 Triticum Nutrition 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000003797 essential amino acid Substances 0.000 description 2
- 235000020776 essential amino acid Nutrition 0.000 description 2
- 239000003925 fat Substances 0.000 description 2
- 239000012634 fragment Substances 0.000 description 2
- 230000003301 hydrolyzing effect Effects 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 235000019419 proteases Nutrition 0.000 description 2
- 235000014102 seafood Nutrition 0.000 description 2
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 2
- 235000019583 umami taste Nutrition 0.000 description 2
- 210000001835 viscera Anatomy 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 108010068370 Glutens Proteins 0.000 description 1
- 240000001931 Ludwigia octovalvis Species 0.000 description 1
- 241000269851 Sarda sarda Species 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000012190 activator Substances 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 235000008429 bread Nutrition 0.000 description 1
- 239000013043 chemical agent Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 238000006911 enzymatic reaction Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000000796 flavoring agent Substances 0.000 description 1
- 235000019634 flavors Nutrition 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000013505 freshwater Substances 0.000 description 1
- 235000021312 gluten Nutrition 0.000 description 1
- 235000013402 health food Nutrition 0.000 description 1
- 238000004128 high performance liquid chromatography Methods 0.000 description 1
- 235000021109 kimchi Nutrition 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 235000016709 nutrition Nutrition 0.000 description 1
- 235000011164 potassium chloride Nutrition 0.000 description 1
- 239000001103 potassium chloride Substances 0.000 description 1
- 229940024999 proteolytic enzymes for treatment of wounds and ulcers Drugs 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000003053 toxin Substances 0.000 description 1
- 231100000765 toxin Toxicity 0.000 description 1
- 235000021419 vinegar Nutrition 0.000 description 1
- 239000000052 vinegar Substances 0.000 description 1
Landscapes
- Seasonings (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は、醤油のような調味液を製造する際の調味料原
液の製造方法に関し、さらに詳しくは動物性蛋白を使用
した調味料原液の製造方法に関するものである。[Detailed Description of the Invention] [Industrial Application Field] The present invention relates to a method for producing a seasoning stock solution when producing a seasoning liquid such as soy sauce, and more specifically, to a method for producing a seasoning stock solution using animal protein. This relates to a manufacturing method.
醤油のような調味液は、主として、大豆や小麦に含まれ
ている植物性蛋白′を麹菌の産生ずる酵素や種々の起源
の酵素剤あるいは化学剤で加水分解して製造されるが、
このような調味液中には、蛋白質、ベブタイド、アミノ
酸などのほかに、種々の炭水化物分解物質や脂肪分解物
質などが含まれている。現在一般に製造されている上記
のような調味液は、主として植物性蛋白を原料としてお
り、魚介類や畜肉などの動物性蛋白を原料として使用し
た調味料は開発口においてはごくまれである。Seasoning liquids such as soy sauce are mainly produced by hydrolyzing vegetable proteins contained in soybeans and wheat using enzymes produced by Aspergillus ore, enzymes or chemical agents of various origins.
Such a seasoning liquid contains various carbohydrate decomposition substances, fat decomposition substances, and the like in addition to proteins, bebutide, amino acids, and the like. Currently, the above-mentioned seasoning liquids that are generally produced are mainly made from vegetable proteins, and seasonings that use animal proteins such as seafood and livestock meat as raw materials are extremely rare in development.
他方、東南アジアでは、小魚を原料とし、それ自体の内
臓などに存在する諸酵素を利用して自己消化させ、動物
性蛋白を分解した物質を含んだ調味液を使用する例があ
る。このように動物性蛋白の分解物質を多く含んだ調味
液においては、植物性蛋白を原料として製造された調味
液に比して、栄養学的に見て必須アミノ酸を多く含んで
いて栄養価が高く、且つ旨味成分を多く含んでいる。On the other hand, in Southeast Asia, there are examples of seasoning liquids made from small fish that are self-digested using various enzymes present in the fish's internal organs, and contain substances that have been broken down from animal proteins. In this way, seasoning liquids containing a large amount of decomposed substances of animal protein contain more essential amino acids and have lower nutritional value than seasoning liquids manufactured using vegetable protein as raw materials. It is expensive and contains many umami ingredients.
しかしながら、上記のような動物性蛋白を使用して製造
された従来の調味液は、脂肪成分や動物質特有のメチル
アミン及びトリメチルアミンのような揮発性アミンなど
を含みそれらが不快臭となることから日本国においては
動物性蛋白を原料として製造した調味料はほとんど普及
していないのが現状である。However, conventional seasoning liquids manufactured using animal proteins as mentioned above contain fatty components and volatile amines such as methylamine and trimethylamine, which are unique to animal substances, and these produce unpleasant odors. In Japan, seasonings made from animal protein are currently not widely available.
本発明は、上記した発明の背景に鑑み、動物性蛋白を原
料として製造された調味液であっても不快臭が発生しな
いようにした調味料原液の製造方法を提案することを目
的とするものである。In view of the background of the invention described above, it is an object of the present invention to propose a method for producing a seasoning stock solution that does not generate unpleasant odors even when the seasoning solution is produced using animal protein as a raw material. It is.
本発明の調味料原液の製造方法は、動物性蛋白又はその
源にプロテナーゼ酵素を作用させて上記動物性蛋白を主
してペプタイドまで加水分解させ、この加水分解物を、
麹中の酵素と醗酵させ、アミノ酸に分解させ、しかも生
成された揮発性アミンを吸着した麹未分解物を醗酵混合
物から除去することにより不快臭を除去することよりな
る。The method for producing a seasoning stock solution of the present invention involves treating animal protein or its source with a proteinase enzyme to hydrolyze the animal protein mainly into peptides, and converting this hydrolyzate into
This process involves fermenting with enzymes in koji, decomposing it into amino acids, and removing undecomposed koji products that have adsorbed volatile amines from the fermentation mixture to remove unpleasant odors.
このように、本発明は動物性蛋白質を酵素の作用により
ペプチドの段階まで分解する第1段階、及び生成ペブタ
イドをベブチターゼ作用を有する麹菌を発育させた植物
蛋白を含有する麹により醗酵させる第2段階よりなり、
この際動物蛋白のアミノ酸への分解に際し出現する揮発
性アミンは、麹未分解物に吸着するのでこれを除去する
際に除かれるという発明思想に基づくのである。As described above, the present invention comprises a first step in which animal protein is broken down to the peptide stage by the action of enzymes, and a second step in which the produced peptide is fermented using koji containing plant protein grown by koji mold having bebutitase action. It becomes more,
The invention is based on the idea that the volatile amines that appear during the decomposition of animal proteins into amino acids are adsorbed to the undecomposed matter of the koji, and are therefore removed when this is removed.
以下に本発明の詳細な説明する。The present invention will be explained in detail below.
本発明に用いられる動物性蛋白は、魚介類、家畜などを
初めとする動物の可食蛋白であって、特に精製する必要
はないが、使用酵素の不消化成分を除去したものが好ま
しい。しかし骨、生皮、油脂、内臓など酵素不消化物の
若干の含有は許容され、それらは製法の途中で除去する
ことができる。The animal protein used in the present invention is an edible protein from animals such as seafood and livestock, and does not need to be particularly purified, but it is preferably one from which indigestible components of the enzyme used have been removed. However, some enzyme-indigestible substances such as bones, rawhide, fats, and internal organs are allowed, and can be removed during the manufacturing process.
魚類は塩水、淡水産を問わず適当な原料であり、魚体の
比較的小さなものはそのまま丸ごとこの方法に利用する
ことができる。家畜類ではくず肉が原料となろう。Fish are suitable raw materials regardless of whether they come from saltwater or freshwater, and relatively small fish can be used whole in this method. For livestock, offal meat is likely to be the raw material.
用いられるプロテナーゼ酵素は、毒素非産生の動物性、
植物性ならびに微生物産生何れのものであってもよいが
、中性付近で作用するものが好ましく、入手容易なこと
から微生物由来の蛋白分解酵素、例えば枯草菌、麹菌な
どの産生蛋白分解酵素が適当である。これらの酵素は単
用又は連用して蛋白質を速かに加水分解して主としてペ
ブタイドを生成する。The proteinase enzyme used is of non-toxin-producing animal origin;
Both plant-derived and microbial-produced enzymes may be used, but those that act near neutrality are preferred, and proteases derived from microorganisms, such as those produced by Bacillus subtilis and Aspergillus, are suitable because they are easy to obtain. It is. These enzymes, used alone or in combination, rapidly hydrolyze proteins to produce primarily peptides.
本発明の第一段階は、動物性蛋白をプロテナーゼで加水
分解して主としてペブタイドとするものであって、方法
は、蛋白原料を加熱し原料自体内の酵素作用を不活化し
、次いでプロテナーゼと反応するもので、反応温度及び
pHは酵素の至適条件により選ばれる。例えば枯草菌産
生プロテナーゼでは、50〜60℃、pH6,0〜7.
0であり、麹菌ブロテナーゼでは40〜50℃、pH6
,0〜8,0となる。反応は酵素との接触をよくするた
めかきまぜ、要すれば原料をミンチとして蛋白質が主と
し、てペブタイドになるまで続けられる。反応過程は遊
離のアミノ酸の生成をホルモール体窒素の生成により検
定し、遊離アミノ酸が全窒素の少なくとも5%、好まし
くは10〜20%となるまで続ける。この段階で動物蛋
白は主としてベブタイドまで加水分解される。反応は、
濃厚なペブタイド液を得るため比較的に濃度の高い水媒
質中で行なわれ、2種以上のプロテナーゼを連続して作
用させる場合は、先に使用された酵素を加熱不活化して
から次の酵素をその至適条件のもとで作用させる。反応
時間は使用酵素の力価及びその使用量に依存するが数時
間で足りる。The first step of the present invention is to hydrolyze animal protein with proteinase to mainly produce peptides. The reaction temperature and pH are selected depending on the optimum conditions for the enzyme. For example, proteinase produced by Bacillus subtilis is used at 50-60°C and at a pH of 6.0-7.
0, and for Aspergillus aspergillus proteinase at 40-50℃, pH 6
,0 to 8,0. The reaction is continued by stirring to improve contact with the enzyme, and if necessary, mincing the raw materials until they become peptides, which consist mainly of protein. The reaction process is assayed for the production of free amino acids by the production of formol nitrogen and is continued until free amino acids account for at least 5% of the total nitrogen, preferably 10-20%. At this stage, animal proteins are mainly hydrolyzed to bebutide. The reaction is
In order to obtain a concentrated peptide solution, the process is carried out in a relatively highly concentrated aqueous medium, and when two or more types of proteinases are reacted in succession, the enzyme used first must be inactivated by heat before the next enzyme is applied. to operate under its optimal conditions. The reaction time depends on the titer of the enzyme used and the amount used, but several hours is sufficient.
酵素反応を終った液は加熱して不活化した後、ペブタイ
ドエキス層と不消化の油層、骨片などをそれぞれ分離し
、エキス層を回収する。After the enzymatic reaction is completed, the liquid is heated to inactivate it, and the peptide extract layer, indigestible oil layer, bone fragments, etc. are separated, and the extract layer is recovered.
このエキス層は要すれば濃縮し、次の麹によるペブタイ
ドをアミノ酸まで分解する第2段階の使用に際しては所
望により全窒素0.1〜0.25%に調整する。。This extract layer is concentrated if necessary, and adjusted to 0.1 to 0.25% total nitrogen when used in the second step of decomposing peptides into amino acids using koji. .
第二段階に用いられる麹は、植物性蛋白を含有する植物
原料にベブチターゼ作用を有する麹菌を接種して調製さ
れ、種々の醗酵調味料、食品の製造上汎用されるもので
ある。即ち、蛋白質を含有する穀類にアスペルギルス属
の麹菌を接種し発育させた麹は、ベブチターゼを含む各
種の加水分解酵素を産生ずる。The koji used in the second step is prepared by inoculating a plant material containing vegetable protein with koji mold having a bebutitase action, and is commonly used in the production of various fermented seasonings and foods. That is, the koji produced by inoculating protein-containing koji mold with Aspergillus koji mold produces various hydrolytic enzymes including bebutitase.
本発明では、穀類として、焙焼割砕した小麦と脱脂゛割
砕大豆に麹菌としてアスバルギルスソーイーを発育させ
た麹が推奨される。第一段階で得られたペブタイドは、
麹と共に醗酵することにより、植物蛋白に由来する全窒
素量の増加と共にホルモール態窒素により示される遊離
のアミノ酸が増加し、ペブタイドの分解が進行すること
が認められる。醗酵開始温度は室温で十分であり、また
醗酵期間は通常時1〜3ケ月で十分である。遊離アミノ
酸は全窒素の40〜5096近くまで産生ずれば十分調
味効果を発揮するが、ペプチターゼ力価の大きい麹を用
いることにより更にその産生を増加させることができる
。In the present invention, as grains, koji made by growing Aspergillus soyi as koji mold on roasted and cracked wheat and defatted and cracked soybeans is recommended. The peptide obtained in the first step is
It has been observed that by fermentation with koji, the total amount of nitrogen derived from plant proteins increases, as well as the amount of free amino acids represented by formol nitrogen, and the decomposition of peptides progresses. A fermentation starting temperature of room temperature is sufficient, and a fermentation period of 1 to 3 months is usually sufficient. Free amino acids exhibit a sufficient seasoning effect if they are produced in an amount close to 40 to 5096 of total nitrogen, but the production can be further increased by using koji with a high peptidase titer.
麹の使用量は、製品の所望の組成及び嗜好により異なる
が、ベブタイドの分解に必要な使用として、原料エキス
100重量部(全窒素0.1〜0.25%)当り35〜
45重量部である。また醗酵管理また調味に必要な食塩
を添加する。その使用料は、原料エキスの100重量部
当り12〜18重量部であって、商業的醤油成分に見合
う量である。尚、食塩の1部を塩化カリで代替して醗酵
させても醗酵管理さえ十分に留意すれば低塩の調味料が
でき健康食品への利用も可能である。The amount of koji used varies depending on the desired composition and preference of the product, but as necessary for the decomposition of Bebutide, the amount of koji used is 35 to 35 parts per 100 parts by weight of raw material extract (0.1 to 0.25% total nitrogen).
It is 45 parts by weight. Salt is also added as necessary for fermentation management and seasoning. The amount used is 12 to 18 parts by weight per 100 parts by weight of the raw material extract, which is an amount commensurate with commercial soy sauce ingredients. Incidentally, even if part of the salt is replaced with potassium chloride and fermentation is carried out, a low-salt seasoning can be made and it can be used in health foods as long as the fermentation is properly controlled.
さて、ベプタイドがアミノ酸へ分解するとき、ペブタイ
ドやタンパク質中に含まれている揮発性アミンが分離す
る。従来動物蛋白由来の調味液の難点であった、不快臭
を与えるこの揮発性アミンは、本発明においては麹中の
未分解物に吸着するので、麹未分解物を遠心分離機その
他でアミノ酸分解液中から除去する際に一緒に除かれる
。これは本発明の特徴の1つである。Now, when peptides are decomposed into amino acids, volatile amines contained in peptides and proteins are separated. This volatile amine, which gives off an unpleasant odor, has been a problem with conventional animal protein-derived seasoning liquids, but in the present invention, it is adsorbed to undecomposed substances in koji, so the undecomposed substances in koji are decomposed into amino acids using a centrifuge or other means. It is removed together with the liquid when it is removed from the liquid. This is one of the features of the present invention.
尚、ペブタイドエキスをペブチターゼ力価の高い酵素の
みでアミノ酸まで分解させることができるが、その場合
には穀類に由来する植物蛋白及び炭水化物などのアミノ
酸源及び香気成分源の欠除により生成調味料の品質が悪
くなると共に、揮発性アミンを醗酵液中から除去するた
め特別な手段が必要となる。In addition, it is possible to decompose pebutide extract into amino acids using only enzymes with high pebutidase titers, but in this case, the quality of the resulting seasoning may be affected due to the lack of amino acid sources and aroma component sources such as plant proteins and carbohydrates derived from grains. In addition, special means are required to remove volatile amines from the fermentation liquor.
以下に本発明を実施例をもって更に詳細に説明するが、
発明は実施例に限定されるものではない。The present invention will be explained in more detail with examples below.
The invention is not limited to the examples.
実施例1
動物性蛋白の原料としてサバを使用し、動物性蛋白をペ
ブタイドまで分解させるため第一段階は、蛋白分解酵素
としてプロテナーゼ力価の高い枯草菌産生蛋白分解酵素
及び麹菌産生蛋白分解酵素を順次使用し、第二段階はペ
ブチターゼ酵素として醤油麹を使用した。Example 1 Mackerel is used as a raw material for animal protein, and in order to degrade the animal protein to peptides, the first step is to use Bacillus subtilis-produced protease and Aspergillus aspergillus-protease, both of which have high proteinase titers, as proteolytic enzymes. They were used sequentially, and in the second step, soy sauce koji was used as the pebtidase enzyme.
生サバ4t (トン)を未処理のまま水4tとともに撹
拌機つき反応缶に入れ、温度80℃まで昇温させてその
温度で15分間加熱し、その後55℃まで温度を下げ、
pH6,2において枯草菌産生蛋白分解酵素4kgを添
加し、そのまま1.5時間反応させ、次で温度80℃ま
で昇−温させた状態で15分間維持した後、45℃にな
るまで冷却し、この温度にて麹菌産生蛋白分解酵素2k
gを添加し2時間反応させた。このとき、pHは6.5
であった。その後、この反応液を温度80℃まで昇温さ
せて再び酵素を不活性化させ、続いてこの反応液を遠心
分離機で常法によりエキス層、油層、骨片等未分解層に
分離し、エキス層を濾過後温度60℃において減圧濃縮
してサバエキス(濃縮サバヘプタイド液)を製造した。4 tons (tons) of untreated raw mackerel was placed in a reactor with a stirrer together with 4 tons of water, heated to 80°C, heated at that temperature for 15 minutes, and then lowered to 55°C.
At pH 6.2, 4 kg of Bacillus subtilis-produced protease was added, allowed to react for 1.5 hours, then raised to 80°C and maintained for 15 minutes, then cooled to 45°C. At this temperature, Aspergillus oryzae produced proteolytic enzyme 2k
g was added and reacted for 2 hours. At this time, the pH is 6.5
Met. Thereafter, the temperature of this reaction solution was raised to 80°C to inactivate the enzyme again, and then this reaction solution was separated into undecomposed layers such as an extract layer, an oil layer, and bone fragments using a centrifuge using a conventional method. The extract layer was filtered and concentrated under reduced pressure at a temperature of 60° C. to produce mackerel extract (concentrated mackerel heptide liquid).
この濃縮サバエキスの全窒素は8.5%でホルモール窒
素は1.1%であった。The total nitrogen content of this concentrated mackerel extract was 8.5%, and the formol nitrogen content was 1.1%.
上記の濃縮サバエキス(a縮すバベブタイド液)と水と
食塩と醤油麹とを下記の第1表の割合で配合して醗酵さ
せた。尚、第1表において単位は種箱2表
第1表に示すように、A仕込では濃縮サバベブタイド液
を75倍に稀めたペプタイド液に、又B仕込では同50
倍に稀めたベブタイド液にそれぞれ食塩及び醤油麹を上
記重量比の割合で配合し、室温で醗酵を開始し時間の経
過とともにその混合液中の全窒素ならびにホルモール窒
素の増加量を分析した。その結果を第2表に示す。尚、
第2表において単位は%である。The above-mentioned concentrated mackerel extract (condensed Babebbutide liquid), water, salt, and soy sauce koji were blended in the proportions shown in Table 1 below and fermented. In addition, in Table 1, the units are 75 times diluted peptide liquid in preparation A, and 50 times diluted peptide liquid in preparation B, as shown in Table 1 of Seed Box 2.
Salt and soy sauce koji were added to the diluted Bebutide solution at the above weight ratios, fermentation was started at room temperature, and the amount of increase in total nitrogen and formol nitrogen in the mixture was analyzed over time. The results are shown in Table 2. still,
In Table 2, the unit is %.
第2表に示す如く、原液においては全窒素に対するホル
モール態窒素の割合は、A仕込では18.2%、B仕込
では13.3%といずれも低かった。このことは蛋白ま
たはベブタイドの量が多く、アミノ酸量が少ないことを
示している。反応1ケ月後と2ケ月後の全窒素量とホル
モール態窒素量の増加量はA仕込とB仕込とではほぼ同
じであった。又、2ケ月後の全窒素量に対する1ケ月後
のの全窒素量の割合を計算比較すると、A仕込では86
.9%、B仕込では96,9%であり、大部分の窒素は
醗酵期間1ケ月で十分に生成することがわかった。又、
全窒素に対するホルモール態窒素量の割合は、混合液中
の遊離アミノ酸量率を示すが、はぼ42〜43%であっ
た。As shown in Table 2, the ratio of formol nitrogen to total nitrogen in the stock solution was low at 18.2% in charge A and 13.3% in charge B. This indicates that the amount of protein or bebutide is high and the amount of amino acids is low. The amount of increase in the total nitrogen amount and formol nitrogen amount after 1 month and 2 months of the reaction was almost the same in Charge A and Charge B. Also, when calculating and comparing the ratio of the total nitrogen amount after 1 month to the total nitrogen amount after 2 months, it is 86 for A preparation.
.. 9%, and 96.9% for B preparation, indicating that most of the nitrogen was sufficiently produced within one month of fermentation. or,
The ratio of formol nitrogen to total nitrogen, which indicates the amount of free amino acids in the mixture, was approximately 42 to 43%.
生成醗酵混合物を遠心分離して、不快・臭のない調味料
原液を得た。不快臭の原因となる揮発性アミンは不溶性
の使用済麹と共に除去された。The resulting fermentation mixture was centrifuged to obtain a seasoning stock solution with no unpleasant odor. Volatile amines that cause unpleasant odors were removed along with insoluble spent koji.
実施例2
上記実施例1で製造された濃縮サバエキス(濃縮サバペ
ブタイド液)を使用し、第3表に示す配合で仕込んだ。Example 2 The concentrated mackerel extract (concentrated mackerel pebutide liquid) produced in Example 1 was used, and the formulations shown in Table 3 were prepared.
この第3表に示すC仕込は、窒素含有量の多い調味料原
液を製造するためのものである。尚、第3表において単
位は眩である。The preparation C shown in Table 3 is for producing a seasoning stock solution with a high nitrogen content. In Table 3, the unit is dazzle.
上記C仕込みを室温にて3力月間発酵させ、その間、1
ケ月毎の全窒素、ホルモール態窒素、全窒素とホルモー
ル態窒素の割合、直糖、pHの変化について調べ、その
結果を第4表に示す。尚、第4表において材料の数値の
単位は%である。Ferment the above C preparation at room temperature for 3 months, during which time 1
Monthly changes in total nitrogen, formol nitrogen, ratio of total nitrogen to formol nitrogen, direct sugar, and pH were investigated, and the results are shown in Table 4. In addition, in Table 4, the unit of numerical value of the material is %.
第4表
第3表
このC仕込みでは、サバペプタイド(原液)のホルモー
ル態窒素に対する全窒素の割合は16.7%で、実施例
1の場合のA仕込やB仕込と同様に低かった。このとき
、残りの窒素形態を高速液クロマトグラフイーで分析し
たところ分子量分布はいずれも10,000以下であっ
た。又、1ケ月後、2ケ月後、3ケ月後の全窒素量とホ
ルモール態窒素量の増加量はほぼ同じであった。3ケ月
後の全窒素量に対する1ケ月後と2ケ月後の全窒素量の
割合を比較するとそれぞれ90.6%と、91,8%で
大部分の窒素は実施例1の場合と同様に1ケ月間で十分
に生成することがわかった。又、全窒素量に対するホル
モール態窒素量の割合は調味料原液中の遊離アミノ酸量
率を示すが41%から47%であった。このC仕込(ベ
ブタイド液を20倍に稀釈)の場合は全原液中における
醤油麹の割合が約43%となり、上記実施例1のA仕込
及びB仕込の場合より約10%だけ多いので、C仕込に
おける3ケ月後の全窒素量に対する1ケ月後と2ケ月後
の全窒素量の割合も10%程度高かった。醗酵混合物を
濾過して得た調味料原液は、全窒素が2.0%以上であ
り、醤油含有窒素よりも高く、しかも不快臭なく香気も
醤油様であり種々の液体調味料の原料としては好適であ
る。Table 4 Table 3 In this preparation C, the ratio of total nitrogen to formol nitrogen in the mackerel peptide (undiluted solution) was 16.7%, which was as low as in preparations A and B in Example 1. At this time, when the remaining nitrogen forms were analyzed by high performance liquid chromatography, the molecular weight distribution was found to be less than 10,000 in all cases. Furthermore, the increases in the total nitrogen amount and formol nitrogen amount after 1 month, 2 months, and 3 months were almost the same. Comparing the ratio of the total nitrogen amount after 1 month and after 2 months to the total nitrogen amount after 3 months, they were 90.6% and 91.8%, respectively. As in Example 1, most of the nitrogen was 1. It was found that sufficient amounts can be generated within a few months. Further, the ratio of the amount of formol nitrogen to the total amount of nitrogen, which indicates the amount of free amino acids in the seasoning stock solution, was 41% to 47%. In the case of this C preparation (bebutide solution diluted 20 times), the proportion of soy sauce koji in the whole stock solution is about 43%, which is about 10% higher than in the cases of A and B preparations in Example 1. The ratio of the total nitrogen amount after one month and after two months to the total nitrogen amount after three months during preparation was also about 10% higher. The seasoning stock solution obtained by filtering the fermentation mixture has a total nitrogen content of 2.0% or more, which is higher than the nitrogen contained in soy sauce, has no unpleasant odor, and has a soy sauce-like aroma, making it suitable as a raw material for various liquid seasonings. suitable.
本発明は所望の調味液の製造のため種々の改変が可能で
ある。例えばアミノ酸に富んだ組成は、ベブチターゼ力
価の高い麹菌を用いた麹を使用することにより達成され
る。また炭水化物分解物による風味は植物性蛋白を含む
穀類の組成及びその前処理によって調整されることは当
業者の周知のところである。The present invention can be modified in various ways to produce a desired seasoning liquid. For example, a composition rich in amino acids can be achieved by using koji using koji molds with high bebutitase titers. Furthermore, it is well known to those skilled in the art that the flavor of carbohydrate decomposition products can be adjusted by the composition of grains containing vegetable proteins and their pretreatment.
一般には、この調味料原液中には、動物性蛋白を起源と
する必須アミノ酸を含むアミノ酸が多量に含まれており
、それが旨味となっておいしい調味料原液となるととも
に、動物性蛋白特有の不快臭となる揮発性アミンが麹未
分解物とともに除去されることにより、動物性蛋白を使
用したものであってもそれによる不快臭を解消又は軽減
されている。In general, this seasoning stock solution contains a large amount of amino acids including essential amino acids originating from animal protein, which gives it umami and makes it a delicious seasoning stock solution. By removing volatile amines that cause unpleasant odors together with undecomposed products of koji, the unpleasant odors caused by animal proteins are eliminated or reduced.
本発明により製造した調味料原液の用途としては、焼肉
のたれ、キムチのたれ、すき焼のたれ、鍋物のたれ、ソ
ース、種々のすましたれ、パンやうどんのグルテン活性
化材、食酢、ボン酸がある。The seasoning stock solution produced according to the present invention can be used for yakiniku sauce, kimchi sauce, sukiyaki sauce, hotpot sauce, sauces, various souta sauces, gluten activators for bread and udon, vinegar, and bonito flakes. There is acid.
Claims (1)
せて上記動物性蛋白を主としてペプタイドまで加水分解
させ、この加水分解物を、麹中の酵素と醗酵させ、アミ
ノ酸に分解させ、しかも生成し揮発性アミンを吸着した
麹未分解物を醗酵混合物から除去することにより不快臭
を除くことよりなる調味料原液の製造方法。 2、動物蛋白源が魚である請求項1記載の方法。 3、プロテーゼ酵素が枯草菌又は麹菌由来のものである
請求項1記載の方法。 4、加水分解反応が、アミノ酸が反応液中の溶解全窒素
の少なくとも5%となるまで行われる請求項1記載の方
法。 5、麹が醤油麹である請求項1記載の方法。 6、醗酵が調味に必要な量の食塩の添加のもと行われる
請求項1記載の方法。 7、醗酵が、醗酵液中のアミノ酸が全窒素の40〜50
%生成するまで行なわれる請求項1記載の方法。 8、醗酵が、加水分解物中の全窒素が0.1〜0.25
%の濃度で行なわれる請求項1記載の方法。[Claims] 1. A proteinase enzyme is applied to animal protein or its source to hydrolyze the animal protein mainly to peptides, and this hydrolyzate is fermented with enzymes in koji to decompose it into amino acids. A method for producing a seasoning stock solution, which removes unpleasant odors by removing undecomposed koji products that have been produced and adsorbed volatile amines from the fermentation mixture. 2. The method according to claim 1, wherein the animal protein source is fish. 3. The method according to claim 1, wherein the prosthetic enzyme is derived from Bacillus subtilis or Aspergillus oryzae. 4. The method of claim 1, wherein the hydrolysis reaction is carried out until the amino acid accounts for at least 5% of the total nitrogen dissolved in the reaction solution. 5. The method according to claim 1, wherein the koji is soy sauce koji. 6. The method according to claim 1, wherein the fermentation is carried out with the addition of salt in an amount necessary for seasoning. 7. In fermentation, the amino acids in the fermentation solution account for 40-50% of the total nitrogen.
% of the process. 8. During fermentation, the total nitrogen in the hydrolyzate is 0.1-0.25
A method according to claim 1, wherein the method is carried out at a concentration of %.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1329999A JPH0347051A (en) | 1989-04-13 | 1989-12-20 | Preparation of raw solution of seasoning |
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP9504589 | 1989-04-13 | ||
JP1-95045 | 1989-04-13 | ||
JP1329999A JPH0347051A (en) | 1989-04-13 | 1989-12-20 | Preparation of raw solution of seasoning |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH0347051A true JPH0347051A (en) | 1991-02-28 |
Family
ID=26436342
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1329999A Pending JPH0347051A (en) | 1989-04-13 | 1989-12-20 | Preparation of raw solution of seasoning |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0347051A (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100215712B1 (en) * | 1997-04-30 | 1999-08-16 | 이상윤 | Production of seasoning |
KR20060092749A (en) * | 2005-02-19 | 2006-08-23 | 야마기가부시기가이샤 | Ingredient for seasonings by using residue of dried fish extract and its manufacturing method |
US7378120B2 (en) | 2000-04-14 | 2008-05-27 | Japan Tobacco, Inc. | Fish sauce and method for producing same |
US8173014B2 (en) | 2002-12-02 | 2012-05-08 | Marine Bioproducts As | Apparatus for hydrolysis of a protein containing raw material and application of the resulting hydrolysis products |
JP2013255465A (en) * | 2012-06-13 | 2013-12-26 | Bioestate:Kk | Trimeresurus flavoviridis fermented food and drink, and method for producing the same |
CN104686804A (en) * | 2015-03-02 | 2015-06-10 | 广东海洋大学 | Method for preparing active peptide feed additive from aquatic product leftovers |
-
1989
- 1989-12-20 JP JP1329999A patent/JPH0347051A/en active Pending
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100215712B1 (en) * | 1997-04-30 | 1999-08-16 | 이상윤 | Production of seasoning |
US7378120B2 (en) | 2000-04-14 | 2008-05-27 | Japan Tobacco, Inc. | Fish sauce and method for producing same |
US8173014B2 (en) | 2002-12-02 | 2012-05-08 | Marine Bioproducts As | Apparatus for hydrolysis of a protein containing raw material and application of the resulting hydrolysis products |
US9232812B2 (en) | 2002-12-02 | 2016-01-12 | Marine Bioproducts A.S. | Apparatus and method for hydrolysis of a protein containing raw material and application of the resulting hydrolysis products |
KR20060092749A (en) * | 2005-02-19 | 2006-08-23 | 야마기가부시기가이샤 | Ingredient for seasonings by using residue of dried fish extract and its manufacturing method |
JP2013255465A (en) * | 2012-06-13 | 2013-12-26 | Bioestate:Kk | Trimeresurus flavoviridis fermented food and drink, and method for producing the same |
CN104686804A (en) * | 2015-03-02 | 2015-06-10 | 广东海洋大学 | Method for preparing active peptide feed additive from aquatic product leftovers |
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