JPH0478260B2 - - Google Patents

Info

Publication number
JPH0478260B2
JPH0478260B2 JP58065113A JP6511383A JPH0478260B2 JP H0478260 B2 JPH0478260 B2 JP H0478260B2 JP 58065113 A JP58065113 A JP 58065113A JP 6511383 A JP6511383 A JP 6511383A JP H0478260 B2 JPH0478260 B2 JP H0478260B2
Authority
JP
Japan
Prior art keywords
culture
aroma
flavor
food
kluyveromyces
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.)
Expired - Lifetime
Application number
JP58065113A
Other languages
Japanese (ja)
Other versions
JPS59192063A (en
Inventor
Yoshitaka Kaji
Kenji Watanabe
Yoshinori Oota
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
KH Neochem Co Ltd
Original Assignee
Kyowa Hakko Kogyo Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Kyowa Hakko Kogyo Co Ltd filed Critical Kyowa Hakko Kogyo Co Ltd
Priority to JP58065113A priority Critical patent/JPS59192063A/en
Publication of JPS59192063A publication Critical patent/JPS59192063A/en
Publication of JPH0478260B2 publication Critical patent/JPH0478260B2/ja
Granted legal-status Critical Current

Links

Landscapes

  • Seasonings (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

本発明は食品の香味改善法に関する。 さらに詳しくは本発明はクルイベロマイセス属
に属し、β−フエネチルアルコール、エチルアセ
テート、エチルn−デカノエイト、iso−ブチル
アセテート及びβ−フエネチルアセテートの少な
くとも1種の果実又は花様香気物質を生産する能
力を有する微生物を培地に培養して得られる培養
物又は培養物の果実又は花様香気物質を含む処理
物(以下、「培養物の果実又は花様香気物質を含
む処理物」を「その処理物」と称す)を食品に添
加又は接触することを特徴とする食品の香味改善
法。 食品の香味は、その外観と共に食事をとること
による満足感を左右する最も重要な要素であり、
近年、嗜好性の多様化等の理由により種々の食品
が開発されていて、これらに優れた香味を賦与す
るということは、食品開発の上で常に重要な課題
となつている。従来種々の調味料、着香料、香味
賦与や香味改善を目的とした食品加工法等が提
案、開発されてきているが、それぞれに一長一短
がある。その中で、天然調味料類、天然着香料類
は、その香味の自然さ、使いやすさ、食品衛生上
から見た安全性等の面からその優位性が認められ
つつある。 天然調味料、天然着香料等による食品の香味改
善について種々検討した結果、クルイベロマイセ
ス属の微生物の培養物又はその処理物を食品に添
加又は接触することにより食品の香味が顕著に改
善されることが見い出された。 以下に、本発明を詳細に説明する。 本発明においては、クルイベロマイセス属に属
する微生物であればいずれも用いうるが、具体的
にはクルイベロマイセス・ブルガリカス
ATCC16045、クルイベロマイセス・フラギリス
ATCC8608、ATCC10022、クルイベロマイセ
ス・ラクチスATCC8599、IFO1090等が挙げられ
る。 クルイベロマイセス・ブルガリカス、クルイベ
ロマイセス・フラギリス、クルイベロマイセス・
ラクチスの菌学的性質は、The Yeasts,p332〜
(1971)に記載されている。 培地としては炭素源、窒素源、無機物、栄養要
求物質などを程よく含有するものであれば、合成
培地、天然培地のいずれも使用可能である。 炭素源としては、例えばグルコース、フラクト
ース、シユークロース、マルトース、ラクトー
ス、殿粉分解物、糖蜜、種々の果汁などの他に、
酢酸、クエン酸、リンゴ酸、パルチミン酸、ステ
アリン酸等の有機酸類、油脂酵素分解物等が単独
または組み合わせて使用出来る。 窒素源としては、例えば硫酸アンモニウム、塩
化アンモニウム等の無機窒素源、アミノ酸又はミ
ルクカゼイン、脱脂粉乳、チーズホエー等の乳製
品及びその副産物、蛋白加水分解物、酵母エキス
や肉エキス等のエキス類等の有機窒素源が単独ま
たは組み合わせて使用出来る。 無機塩物、栄養要求物質としては、例えばリン
酸−カリウム、リン酸−ナトリウム等のリン酸化
合物、硫酸マグネシウム、硫酸コバルト、ニコチ
ン酸アミド、ビオチン、パントテン酸カルシウ
ム、サイアミン塩酸塩等が使用出来る。 培養は振盪培養、攪拌培養、通気培養又は静置
培養で、PH4〜9好ましくはPH5〜7、温度10〜
40℃、好ましくは20〜30℃で1〜10日間行なう。 上記の如くして得られた培養物から遠心分離に
より菌体を除去して得た上清液は、アルコール
類、アセテート類を含み、果実又は花様香気を有
する。 本発明においては、このようにして得られた培
養物又はその処理物が用いられる。 その処理物としては、培養物から菌体を分離し
た上清液;菌体;培養物、菌体を分離した上清液
又は菌体から採取した香気濃縮物(例えば、溶剤
抽出した香気濃縮物、水蒸気蒸留した後、溶剤抽
出した香気濃縮物、アルコール蒸留した香気濃縮
物、活性炭やイオン交換樹脂に吸着させたのちア
ルコールで溶出した香気濃縮物など)などがあげ
られる。 さらに、上記香気濃縮物の採取する方法を詳細
に説明する。 培養物、菌体を分離した上清液又は菌体にエー
テル2部、ペンタン1部よりなる混合溶剤を添加
して、香気濃縮物を溶剤で抽出した後、該溶剤を
留去して得る方法、アルコールを添加した後、ア
ルコールと共に香気濃縮物を減圧蒸留するアルコ
ール蒸留法で得る方法、活性炭又はイオン交換樹
脂〔例えば、ダイヤイオンHP−20(三菱化成社
製)、アンバーライトXAD−4(オルガノ社製)〕
と接触させた後、吸着された香気濃縮物を例えば
40%エチルアルコールで溶出する方法で得る方法
などである。 又、培養物又はその処理物に食塩、砂糖などの
調味料や、エタノール、ソルビトール、殿粉及び
殿粉分解物、ガム質、乳化剤、保存安定剤等を添
加することが出来る。 培養物又はその処理物を食品に添加又は接触す
る場合には、培養物又はその処理物をそのまま液
体の状態で用いる以外に、濃縮してペースト状に
したり、デキストリン等の適当な賦型剤を用いる
ことによつて噴霧乾燥や凍結乾燥により粉末状に
して用いることが出来る。 培養物、その処理物としての菌体を分離した上
清液又は菌体の食品への添加量は0.1−10%、培
養物、上清液又は菌体から採取した香気濃縮物の
添加量は0.01−1%の範囲である。又、培養物も
しくはその処理物を食品に接触する場合には、特
に量の範囲の限定はないが、培養物、上清液又は
菌体としては少なくとも0.1%以上、又、香気濃
縮物としては、少なくとも0.01%含有しているも
のに食品を接触させることが望ましい。 培養物又はその処理物により風味を改善される
食品としては種々の食品があげられるが、たとえ
ば、ハム・ソーセージ等の食肉製品、パン・菓子
類、漬物、水産練製品、バター・チーズ等の乳製
品、ハンバーグ・シユウマイ等の惣菜、サラダド
レツシング、ソース類、スープ、麺用つゆ、焼肉
のたれ、果汁、酒類等があげられる。 以下に実施例を示す。 実施例 1 グルコース15%、硫酸アンモニウム3%、リン
酸−カリウム、リン酸−アンモニウム0.2%、硫
酸マグネシウム0.1%、酵母エキス1%、ペプト
ン1%、ニコチン酸アミド400PPb、サイアミン
塩酸塩400PPbを含むPH5.5の培地300mlを500ml容
三角フラスコに分注し、115℃15分間オートクレ
ーブにより殺菌した培地にクルイペロマイセス・
ブルガリカスATCC16045を接種して24℃、5日
間の静置培養を行なつた。培養終了後、培養液を
65℃、30分間加熱して火入れ処理を行ない、更に
遠心分離により菌体を除去して清澄な培養液(以
下、A液と称す。)を得た。 ついで、A液を5%含有する第1表に示す組成
のピツクル液を調製し、ロース肉重量に対し30%
注射して、5℃、1夜塩漬してロースハムを試作
した。このロースハムの香味について12名のパネ
ルにより官能検査した。その結果を第2表に示
す。
The present invention relates to a method for improving the flavor of foods. More specifically, the present invention belongs to the genus Kluyveromyces and has a fruity or floral aroma of at least one of β-phenethyl alcohol, ethyl acetate, ethyl n-decanoate, iso-butyl acetate and β-phenethyl acetate. A culture obtained by culturing a microorganism capable of producing a substance in a medium, or a processed product containing a cultured fruit- or flower-like aroma substance (hereinafter referred to as a "processed product containing a cultured fruit- or flower-like aroma substance") A method for improving the flavor of foods, characterized by adding or contacting them with (referred to as "the processed product") to foods. The flavor of food, along with its appearance, is the most important factor that affects the feeling of satisfaction from eating a meal.
In recent years, various foods have been developed due to the diversification of palatability, etc., and imparting excellent flavor to these foods has always been an important issue in food development. Various seasonings, flavoring agents, and food processing methods aimed at imparting flavor or improving flavor have been proposed and developed, but each has its advantages and disadvantages. Among these, natural seasonings and natural flavorings are becoming recognized for their superiority in terms of their natural flavor, ease of use, and safety from a food hygiene perspective. As a result of various studies on improving the flavor of foods using natural seasonings, natural flavorings, etc., it has been found that the flavor of foods can be significantly improved by adding or contacting cultures of microorganisms of the genus Kluyveromyces or processed products thereof. It was found that The present invention will be explained in detail below. In the present invention, any microorganism belonging to the genus Kluyveromyces can be used, but specifically Kluyveromyces bulgaricus
ATCC16045, Kluyveromyces fragilis
Examples include ATCC8608, ATCC10022, Kluyveromyces lactis ATCC8599, and IFO1090. Kluyveromyces bulgaricus, Kluyveromyces fragilis, Kluyveromyces
The mycological properties of L. lactis can be found in The Yeasts, p332~
(1971). As the medium, either a synthetic medium or a natural medium can be used as long as it contains appropriate amounts of carbon sources, nitrogen sources, inorganic substances, auxotrophic substances, and the like. Examples of carbon sources include glucose, fructose, sucrose, maltose, lactose, starch decomposition products, molasses, and various fruit juices.
Organic acids such as acetic acid, citric acid, malic acid, palmitic acid, and stearic acid, enzymatic decomposition products of fats and oils, etc. can be used alone or in combination. Examples of nitrogen sources include inorganic nitrogen sources such as ammonium sulfate and ammonium chloride, amino acids or milk casein, dairy products such as skim milk powder and cheese whey, and their by-products, protein hydrolysates, and extracts such as yeast extract and meat extract. Organic nitrogen sources can be used alone or in combination. Examples of inorganic salts and auxotrophic substances that can be used include phosphoric acid compounds such as potassium phosphate and sodium phosphate, magnesium sulfate, cobalt sulfate, nicotinamide, biotin, calcium pantothenate, and thiamine hydrochloride. Culture is performed by shaking culture, stirring culture, aeration culture, or static culture at pH 4-9, preferably pH 5-7, and temperature 10-10.
It is carried out at 40°C, preferably 20-30°C for 1-10 days. The supernatant obtained by removing the bacterial cells from the culture obtained as described above by centrifugation contains alcohols and acetates and has a fruity or floral aroma. In the present invention, the culture thus obtained or its treated product is used. Processed products include supernatant liquid from which bacterial cells have been separated from a culture; , aroma concentrates extracted with solvent after steam distillation, aroma concentrates distilled with alcohol, aroma concentrates adsorbed on activated carbon or ion exchange resin and then eluted with alcohol, etc.). Furthermore, a method for collecting the above aroma concentrate will be explained in detail. A method in which a mixed solvent consisting of 2 parts of ether and 1 part of pentane is added to the culture, the supernatant liquid from which the bacterial cells have been separated, or the bacterial cells, the aroma concentrate is extracted with the solvent, and then the solvent is distilled off. , A method of obtaining aroma concentrates by adding alcohol and distilling the aroma concentrate together with alcohol under reduced pressure, Activated carbon or ion exchange resin [e.g., Diaion HP-20 (manufactured by Mitsubishi Kasei Corporation), Amberlite XAD-4 (Organo company)]
After contacting the adsorbed aroma concentrate with e.g.
For example, it can be obtained by elution with 40% ethyl alcohol. Furthermore, seasonings such as salt and sugar, ethanol, sorbitol, starch and starch decomposition products, gums, emulsifiers, storage stabilizers, etc. can be added to the culture or its processed product. When adding or contacting a culture or its processed product with food, in addition to using the culture or its processed product in its liquid state, it may be concentrated into a paste, or an appropriate excipient such as dextrin may be added. Depending on the use, it can be made into a powder by spray drying or freeze drying. The amount of the culture, the supernatant liquid from which the bacterial cells are separated as a processed product, or the bacterial cells to be added to food is 0.1-10%, and the amount of the flavor concentrate collected from the culture, supernatant liquid, or bacterial cells to be added is 0.1-10%. It is in the range of 0.01-1%. In addition, when a culture or its processed product is brought into contact with food, there is no particular limitation on the amount, but it should be at least 0.1% as a culture, supernatant liquid, or bacterial cells, and as an aroma concentrate. It is desirable that food comes into contact with substances containing at least 0.01% of Foods whose flavor can be improved by cultured products or processed products include various foods, including meat products such as ham and sausage, bread and confectionery, pickles, seafood paste products, and dairy products such as butter and cheese. Examples include products, side dishes such as hamburgers and shumai, salad dressings, sauces, soups, noodle soups, yakiniku sauces, fruit juices, and alcoholic beverages. Examples are shown below. Example 1 PH5 containing 15% glucose, 3% ammonium sulfate, potassium phosphate, 0.2% ammonium phosphate, 0.1% magnesium sulfate, 1% yeast extract, 1% peptone, 400 PPb nicotinamide, 400 PPb thiamine hydrochloride. Dispense 300 ml of the medium from Step 5 into a 500 ml Erlenmeyer flask, and add Kluyperomyces to the medium that was sterilized by autoclaving at 115°C for 15 minutes.
bulgaricus ATCC16045 was inoculated and statically cultured at 24°C for 5 days. After culturing, remove the culture solution.
The mixture was heated at 65° C. for 30 minutes for pasteurization, and the bacterial cells were removed by centrifugation to obtain a clear culture solution (hereinafter referred to as solution A). Next, a pickling liquid having the composition shown in Table 1 containing 5% of liquid A was prepared, and 30% of the weight of loin meat was added.
A prototype roast ham was prepared by injecting the mixture and soaking it in salt at 5°C overnight. The flavor of this roast ham was sensory tested by a panel of 12 people. The results are shown in Table 2.

【表】【table】

【表】 実施例 2 実施例1において、クルイベロマイセス・ブル
ガリカスATCC16045の代わりにクルイベロマイ
セス・ラクチスATCC8599単独又はクルイベロマ
イセス・ブルガリカスATCC16045との組み合わ
せを用いる以外は実施例1と同様に行ない培養液
(ATCC8599単独の場合:B液と称す。
ATCC8599とATCC16045との組合わせの場合:
C液と称す)を得た。 ついで、実施例1と同様にロースハムを試作
し、そのロースハムについて12名のパネルにより
官能検査をした。その結果を第3表に示す。
[Table] Example 2 Same as Example 1 except that Kluyveromyces lactis ATCC8599 alone or in combination with Kluyveromyces bulgaricus ATCC16045 was used instead of Kluyveromyces bulgaricus ATCC16045. Perform the same procedure and culture solution (in the case of ATCC8599 alone: referred to as solution B).
For the combination of ATCC8599 and ATCC16045:
A liquid (referred to as liquid C) was obtained. Next, a roast ham was produced in the same manner as in Example 1, and the roast ham was subjected to a sensory test by a panel of 12 people. The results are shown in Table 3.

【表】 実施例 3 強力小麦粉350g、イーストフード0.5g、ぱん
酵母10g、水200mlを28℃、4時間中種発酵させ
た後、強力小麦粉150g、砂糖30g、食塩10g、
脱脂粉乳10g、シヨートニング20g、水130mlの
本捏原料に、実施例2で得られたC液を小麦粉に
対して2%に相当する10mlを加えて本捏し、220
℃、25分間焼成してパンを試作した。そのパンに
ついての官能検査の結果を第4表に示す。
[Table] Example 3 After fermenting 350g of strong wheat flour, 0.5g of yeast food, 10g of baker's yeast, and 200ml of water at 28℃ for 4 hours, 150g of strong wheat flour, 30g of sugar, 10g of salt,
To 10 g of skim milk powder, 20 g of skim milk powder, and 130 ml of water, 10 ml of Solution C obtained in Example 2, which is equivalent to 2% of the wheat flour, was added and kneaded.
A prototype of bread was made by baking at ℃ for 25 minutes. The results of the sensory test on the bread are shown in Table 4.

【表】 実施例 4 10%の食塩で5日間下漬けをした胡瓜を水洗、
細刻、塩抜きし、塩蔵比55%まで圧搾した原料5
Kgに対し第5表に示す組成の調味液5を添加
し、室温に2日間おいて胡瓜のしよう油漬を試作
した。その胡瓜の官能検査の結果を第6表に示
す。
[Table] Example 4 Cucumbers were pickled with 10% salt for 5 days and washed with water.
Ingredients that have been shredded, salted, and pressed to a salted ratio of 55% 5
Seasoning liquid 5 having the composition shown in Table 5 was added to Kg, and the mixture was left at room temperature for 2 days to prepare a sample of pickled cucumbers in ginger oil. Table 6 shows the results of the sensory test of the cucumber.

【表】【table】

【表】【table】

【表】 実施例 5 リンゴ5倍濃縮果汁(糖度50.8%)30%、リン
酸−カリウム0.2%、硫酸マグネシウム0.1%、
AM−B(協和醗酵製天然調味料)4%、脱脂粉
乳1%、パルミチン酸0.1%、L−バリン0.1%、
ニコチン酸アミド400PPb、サイアミン塩酸塩
400PPbを含むPH6.0の培地100mlを500ml容三角フ
ラスコに分注し、115℃、15分間オートクレーブ
殺菌した培地にクルイベロマイセス・フラギリス
ATCC10022を接種し30℃で2日間振盪培養を行
なつた。 該培養液を4N−H2SO4でPH2に調整し、1000
mlに対して99.5%エチルアルコールを50ml添加
し、減圧下10mmHg、30℃でアルコール蒸留を行
ない、強い果実様の芳香を有する香気濃縮物(以
下D液とする)100mlを得た。これを用いて第7
表に示す組成のサラダドレツシングを調製した。
そのサラダドレツシングの官能検査の結果を第8
表に示す。
[Table] Example 5 Apple 5 times concentrated fruit juice (sugar content 50.8%) 30%, potassium phosphate 0.2%, magnesium sulfate 0.1%,
AM-B (Kyowa Hakko natural seasoning) 4%, skim milk powder 1%, palmitic acid 0.1%, L-valine 0.1%,
Nicotinamide 400PPb, Thiamine Hydrochloride
Dispense 100ml of PH6.0 medium containing 400PPb into a 500ml Erlenmeyer flask, and add Kluyveromyces fragilis to the medium that was autoclaved at 115°C for 15 minutes.
ATCC10022 was inoculated and cultured with shaking at 30°C for 2 days. The culture solution was adjusted to pH 2 with 4N-H 2 SO 4 and heated to 1000
50 ml of 99.5% ethyl alcohol was added to each ml, and alcohol distillation was carried out under reduced pressure at 10 mmHg and 30°C to obtain 100 ml of an aroma concentrate (hereinafter referred to as liquid D) having a strong fruit-like aroma. Using this, the seventh
A salad dressing having the composition shown in the table was prepared.
The results of the sensory test for the salad dressing are shown in the 8th section.
Shown in the table.

【表】【table】

【表】【table】

【表】 実施例 6 リンゴ濃縮果汁(糖度58.2%)20%、リン酸−
アンモニウム0.2%、リン酸−カリウム0.2%、硫
酸マグネシウム0.1%、AM−B(協和醗酵製天然
調味料)3%、CH(協和発酵製天然調味料)1
%、L−バリン0.3%、L−フエニルアラニン0.3
%、DL−メチオニン0.1%、DL−リンゴ酸0.3%、
ニコチン酸アミド400PPb、ビオチン2PPb、パン
トテン酸カルシウム400PPb、サイアミン塩酸塩
400PPbを含むPH5.5の培地120mlを300ml容三角フ
ラスコに分注し、120℃、15分間オートクレーブ
により殺菌を行なつた。該培地はクルイベロマイ
セス・フラギリスATCC8608とクルイベロマイセ
ス・ラクチスIF01090を接種して28℃、2日間振
盪培養を行なつた。該培養液について実施例1と
同様にロースハムに添加して官能検査を実施した
結果、12名のパネル全員がハムの熟成香を連想さ
せる好ましい芳香を強く感じ、無添加区と比較し
て「とてもおいしい」と判定した。尚、培養液
100mlにエーテル100ml、n−ペンタン50mlを加え
香気成分の抽出を行ない更に2%炭酸ナトリウム
溶液10ml、1%塩酸10mlで有機溶剤層を順次洗浄
して有機溶剤層を分離、乾燥後、ビダリユー分溜
管(長さ30cm)の上端温度33〜34℃で溶剤を溜去
して香気の中性画分を得てガスクロマトグラフイ
ーにより分析を行なつた結果を第9表に示す。
[Table] Example 6 Apple concentrated fruit juice (sugar content 58.2%) 20%, phosphoric acid -
Ammonium 0.2%, potassium phosphate 0.2%, magnesium sulfate 0.1%, AM-B (Kyowa Hakko natural seasoning) 3%, CH (Kyowa Hakko natural seasoning) 1
%, L-valine 0.3%, L-phenylalanine 0.3
%, DL-methionine 0.1%, DL-malic acid 0.3%,
Nicotinamide 400PPb, biotin 2PPb, calcium pantothenate 400PPb, thiamine hydrochloride
120 ml of a pH 5.5 medium containing 400 PPb was dispensed into a 300 ml Erlenmeyer flask, and sterilized by autoclaving at 120° C. for 15 minutes. The medium was inoculated with Kluyveromyces fragilis ATCC8608 and Kluyveromyces lactis IF01090, and cultured with shaking at 28°C for 2 days. The culture solution was added to roast ham in the same manner as in Example 1, and a sensory test was conducted. As a result, all 12 panelists strongly felt a pleasant aroma reminiscent of the aroma of ripened ham, and compared it to the non-additive group, it was ``very Delicious.'' In addition, culture solution
Add 100 ml of ether and 50 ml of n-pentane to 100 ml to extract the aroma components, and then wash the organic solvent layer sequentially with 10 ml of 2% sodium carbonate solution and 10 ml of 1% hydrochloric acid to separate the organic solvent layer. After drying, separate the organic solvent layer. The solvent was distilled off at the upper end of the tube (length 30 cm) at a temperature of 33 to 34 DEG C. to obtain a neutral fraction with aroma, which was analyzed by gas chromatography. Table 9 shows the results.

【表】【table】

【表】【table】

Claims (1)

【特許請求の範囲】[Claims] 1 クルイベロマイセス属に属し、β−フエネチ
ルアルコール、エチルアセテート、エチルn−デ
カノエイト、iso−ブチルアセテート及びβ−フ
エネチルアセテートの少なくとも1種の果実又は
花様香気物質を生産する能力を有する微生物を培
地に培養して得られる培養物又は培養物の果実又
は花様香気物質を含む処理物を食品に添加又は接
触することを特徴とする食品の香味改善法。
1. Belongs to the genus Kluyveromyces and has the ability to produce at least one fruit or flower-like aroma substance of β-phenethyl alcohol, ethyl acetate, ethyl n-decanoate, iso-butyl acetate, and β-phenethyl acetate. 1. A method for improving the flavor of food, which comprises adding to or contacting food with a culture obtained by culturing microorganisms having the following in a medium, or a processed product of the culture containing fruit or flower-like aroma substances.
JP58065113A 1983-04-13 1983-04-13 Method for improving taste and flavor of food Granted JPS59192063A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP58065113A JPS59192063A (en) 1983-04-13 1983-04-13 Method for improving taste and flavor of food

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP58065113A JPS59192063A (en) 1983-04-13 1983-04-13 Method for improving taste and flavor of food

Publications (2)

Publication Number Publication Date
JPS59192063A JPS59192063A (en) 1984-10-31
JPH0478260B2 true JPH0478260B2 (en) 1992-12-10

Family

ID=13277510

Family Applications (1)

Application Number Title Priority Date Filing Date
JP58065113A Granted JPS59192063A (en) 1983-04-13 1983-04-13 Method for improving taste and flavor of food

Country Status (1)

Country Link
JP (1) JPS59192063A (en)

Also Published As

Publication number Publication date
JPS59192063A (en) 1984-10-31

Similar Documents

Publication Publication Date Title
JP6970226B2 (en) New fermented seasoning composition
EP0574586B1 (en) Process for producing food and drink
AU735139B2 (en) Production of aromatizing agent
US6759068B2 (en) Onion and garlic biohydrolysates and their use as natural flavorings
JPWO1993009681A1 (en) Food and beverage manufacturing methods
CN107581458A (en) Special barbecue sauce for black pepper steak and preparation method thereof
JP2004275097A (en) Method for enhancing saltiness of food and drink and seasonings used therein
CN114532518A (en) Pea protein isolate flavoring, preparation method thereof and application of pea protein isolate flavoring in improvement of flavor quality of vegetarian meat
CN105876662B (en) Fermented and cooked sausage prepared from morchella esculenta and preparation method thereof
WO2010050429A1 (en) Agent for enhancing flavor of stewed vegetables
JP5025362B2 (en) Flavor improver
JPH0478260B2 (en)
JPH06225721A (en) Fermented seasoning and its production method and pickled seasoning using the same
JP5354520B2 (en) Novel peptide composition having kokumi imparting function
JP5976313B2 (en) Production method of soy sauce-like seasonings
JP6983007B2 (en) Isoamyl alcohol-rich seasoning composition and its manufacturing method
JP2002000180A (en) Coffee flavor modifier, flavor modified coffee and method for producing the same
JP3530851B1 (en) New lactic acid bacteria and flavor-improving seasonings using the same
JP3697004B2 (en) Food flavor improving agent and flavor improving method
JPH01257440A (en) Soybean paste-containing food
JP2008048722A (en) Manufacturing method of mirin
JP2007028930A (en) Flavor improver
JP2008022804A (en) Anti-boiled agent
JPH0870813A (en) Method for improving taste of seasoning
HK1137302B (en) Flavor-improving agent