JPH10276736A - Production of fermented beverage containing acetic acid bacterium cellulose - Google Patents
Production of fermented beverage containing acetic acid bacterium celluloseInfo
- Publication number
- JPH10276736A JPH10276736A JP9127782A JP12778297A JPH10276736A JP H10276736 A JPH10276736 A JP H10276736A JP 9127782 A JP9127782 A JP 9127782A JP 12778297 A JP12778297 A JP 12778297A JP H10276736 A JPH10276736 A JP H10276736A
- Authority
- JP
- Japan
- Prior art keywords
- acetic acid
- fermented beverage
- cellulose
- acid bacterium
- culture
- 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
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 title claims abstract description 150
- 241000894006 Bacteria Species 0.000 title claims abstract description 21
- 235000019985 fermented beverage Nutrition 0.000 title claims abstract description 17
- 238000004519 manufacturing process Methods 0.000 title claims description 14
- 229920002678 cellulose Polymers 0.000 title abstract description 26
- 239000001913 cellulose Substances 0.000 title abstract description 26
- 239000000052 vinegar Substances 0.000 claims abstract description 23
- 235000021419 vinegar Nutrition 0.000 claims abstract description 23
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 claims abstract description 16
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 9
- 229910000019 calcium carbonate Inorganic materials 0.000 claims abstract description 8
- 235000015203 fruit juice Nutrition 0.000 claims abstract description 6
- 229920002749 Bacterial cellulose Polymers 0.000 claims description 6
- 239000005016 bacterial cellulose Substances 0.000 claims description 6
- 229920002301 cellulose acetate Polymers 0.000 claims 4
- 239000000796 flavoring agent Substances 0.000 abstract description 7
- 235000019634 flavors Nutrition 0.000 abstract description 7
- 235000002837 Acetobacter xylinum Nutrition 0.000 abstract description 4
- 238000012258 culturing Methods 0.000 abstract description 4
- 235000015205 orange juice Nutrition 0.000 abstract description 4
- 238000000855 fermentation Methods 0.000 abstract description 3
- 230000004151 fermentation Effects 0.000 abstract description 3
- 241001136169 Komagataeibacter xylinus Species 0.000 abstract 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 7
- 241001602876 Nata Species 0.000 description 7
- 230000000694 effects Effects 0.000 description 7
- 239000002609 medium Substances 0.000 description 6
- 240000007594 Oryza sativa Species 0.000 description 4
- 235000007164 Oryza sativa Nutrition 0.000 description 4
- 235000013361 beverage Nutrition 0.000 description 4
- HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 description 4
- 238000012136 culture method Methods 0.000 description 4
- 235000009566 rice Nutrition 0.000 description 4
- 244000235858 Acetobacter xylinum Species 0.000 description 3
- 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 3
- 239000001888 Peptone Substances 0.000 description 3
- 108010080698 Peptones Proteins 0.000 description 3
- 229940041514 candida albicans extract Drugs 0.000 description 3
- 230000008859 change Effects 0.000 description 3
- 239000012153 distilled water Substances 0.000 description 3
- 230000035622 drinking Effects 0.000 description 3
- 235000011389 fruit/vegetable juice Nutrition 0.000 description 3
- 239000008103 glucose Substances 0.000 description 3
- 235000019674 grape juice Nutrition 0.000 description 3
- 230000033001 locomotion Effects 0.000 description 3
- 235000013944 peach juice Nutrition 0.000 description 3
- 235000019319 peptone Nutrition 0.000 description 3
- 230000001954 sterilising effect Effects 0.000 description 3
- 238000004659 sterilization and disinfection Methods 0.000 description 3
- 239000012138 yeast extract Substances 0.000 description 3
- 150000001413 amino acids Chemical class 0.000 description 2
- 235000012000 cholesterol Nutrition 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 150000007524 organic acids Chemical class 0.000 description 2
- 235000005985 organic acids Nutrition 0.000 description 2
- 230000003068 static effect Effects 0.000 description 2
- 241000589220 Acetobacter Species 0.000 description 1
- 244000144730 Amygdalus persica Species 0.000 description 1
- 241000233866 Fungi Species 0.000 description 1
- 241000257303 Hymenoptera Species 0.000 description 1
- 244000046052 Phaseolus vulgaris Species 0.000 description 1
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 1
- 235000006040 Prunus persica var persica Nutrition 0.000 description 1
- 235000009754 Vitis X bourquina Nutrition 0.000 description 1
- 235000012333 Vitis X labruscana Nutrition 0.000 description 1
- 240000006365 Vitis vinifera Species 0.000 description 1
- 235000014787 Vitis vinifera Nutrition 0.000 description 1
- 241000385736 bacterium B Species 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 239000008280 blood Substances 0.000 description 1
- 210000004369 blood Anatomy 0.000 description 1
- 150000001720 carbohydrates Chemical class 0.000 description 1
- 235000020197 coconut milk Nutrition 0.000 description 1
- 235000021185 dessert Nutrition 0.000 description 1
- 235000011850 desserts Nutrition 0.000 description 1
- 230000003203 everyday effect Effects 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 239000001963 growth medium Substances 0.000 description 1
- 235000015243 ice cream Nutrition 0.000 description 1
- 230000000968 intestinal effect Effects 0.000 description 1
- XMGQYMWWDOXHJM-UHFFFAOYSA-N limonene Chemical compound CC(=C)C1CCC(C)=CC1 XMGQYMWWDOXHJM-UHFFFAOYSA-N 0.000 description 1
- 235000012054 meals Nutrition 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000007968 orange flavor Substances 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
Landscapes
- Non-Alcoholic Beverages (AREA)
Abstract
Description
(産業上の利用分野)本発明は、食酢のもろみより分離
したセルロース生産能を有する酢酸菌セルロースを含む
発酵飲料の製造方法に関するものである。 (従来の技術)酢酸菌が産生する可食性ゲル状セルロー
スは、フィリピンでは「ナタ」と呼ばれ、食後のデザー
トとして古くから食されており、食物繊維の持つ整腸作
用、低カロリー性、血中コレステロールの低下作用など
が知られている。この「ナタ」の製法としては、ココナ
ッツミルクに砂糖、酢酸などを加えて、煮沸、冷却した
ものを広口ビンに入れ、これにセルロース生産能を有す
る酢酸菌、アセトバクター・キシリヌム(Acetob
acter xylinum)を加え、布でフタをして
30℃で約2週間程度静置培養を行なう。これにより、
培養液表面に3〜4cmの寒天状の菌膜(ナタ)が生成
する。このナタを取り出して洗浄、酸抜き、殺菌後適当
な大きさに切り、糖液に含浸させた後、製品となる。こ
の方法により得られたナタは、独特の弾力のあるテクス
チャーを有し、みつ豆などに加えて、デザートとした
り、アイスクリームに加えたり、飲料に加えてセルロー
ス入り飲料などとして販売されている。 (発明が解決しようとする課題)上述したような従来の
製造方法では、3〜4cmのナタを生産するのに非常に
日数がかかり、又、生成したナタの洗浄、酸抜き、殺
菌、切断、糖液の含浸などに非常に手間がかかる。又、
比較的小さい容器で培養するために、大量に生産するの
に無理がある。又、セルロース入り飲料といってもただ
単に飲料にセルロースを加えただけであって、セルロー
スを含む発酵飲料とはいえないという問題点があった。
本発明は、その基本的要素である酢酸菌セルロースを得
るのに振盪培養を行なってゲル状になすことを目的とし
ており、更には、酢酸菌セルロースを含む発酵飲料に炭
酸カルシウムを適量添加して酢酸臭、酢酸味の少ない発
酵飲料を提供せんとするものである。 (課題を解決しようとする手段)上記目的を達成するた
めに、本発明者は鋭意研究を重ねた結果、食酢もろみよ
り分離したセルロース生産能を有する酢酸菌を、果汁と
水、少量の醸造酢を混合した培地に加え振盪培養を行な
うことにより、ゲル状の酢酸菌セルロースを生成させる
ことを特徴とする酢酸菌セルロースを含む発酵飲料を開
発するにいたり、本発明を完成した。本発明において使
用される酢酸菌は、食酢メーカーが食酢の発酵中、及び
貯蔵中のもろみより分離したセルロース生産能を有する
酢酸菌で、アセトバクター・キシリヌム(Acetob
acter xylinum)と呼ばれているものであ
る。又この菌は特定の食酢メーカー保有のものではなく
て、ごく一般的な多くの食酢メーカー保有の菌である。
むしろ、同定された保存株アセトバクター・キシリヌム
IFO 13772、アセトバクター・パストリアヌ
ス ATCC10245などの菌株と比較して、セルロ
ースの生産能が非常に強いのが特徴である。(図1)。
この理由は、菌の発育に適した環境内で長い間培養を持
続した結果、セルロースの生産能が強くなったものと思
われる。製造条件として上げられることは、材料をオレ
ンジ果汁、白桃果汁、グレープ果汁等に実施した場合、
各々の果汁の糖濃度、振盪数、培養温度、培養日数等を
考慮して適性に処理して課題解決の手段とする。(実施
例) 実施例については図、表を参照して説明する。本発明の
基本的要素である酢酸菌はアルコールを酸化して酢酸に
する能力ある細菌で、主に食酢の製造に使用されている
好気性のグラム陰性菌であり、酢酸菌の中にセルロース
を生産するものがあることは既に公知の事実である。こ
れを如何に利用して新規性の製品を製造するかが問題で
あって、本発明はこの点に鑑みて研究開発したものであ
る。本発明の実施において果汁の種類は特にこだわらな
いが、製造工程における材料の振盪培養条件として例え
ば、オレンジ果汁、白桃果汁、グレープ果汁等、糖濃度
の高い果汁を実施の対象とした。果汁を含む培地の糖濃
度は1〜4重量部が適当である。且つ振盪数は70〜1
20rpmとし、培養温度は26〜32℃で、培養日数
は2〜3日であればよい。醸造酢の種類はなるべくは米
酢であることが望ましい。培地の酢酸濃度は、0.1〜
0.5重量部が適当である。炭酸カルシウムの添加量
は、0.05〜0.3重量部、望ましくは0.1〜0.
2重量部が適量である。又、炭酸カルシウムを添加した
だけでも酢酸臭、酢酸味が少なく飲用として適している
が、更に少量の香料、及び適量の糖類を添加する方が風
味が増してより良い結果を得る。この振盪培養法の特徴
として、培養日数が2〜3日で終了となり、静置培養法
と比較して日数が少なくて済み、培養容器も振盪培養か
ら攪拌培養へと応用させることにより、大量生産が出来
るタンク培養が可能となる。このようにして得られた酢
酸菌セルロースを含む発酵飲料は、ゲル状セルロースを
含有しており、又、多種の有機酸、アミノ酸を含んでお
り、セルロースの持つ整腸作用、低カロリー性、血中コ
レステロール低下作用などと共に、有機酸、アミノ酸の
効果も期待出来る。(表1、2)(Field of Industrial Application) The present invention relates to a method for producing a fermented beverage containing acetic acid cellulose having a cellulose-producing ability separated from the mash of vinegar. (Prior art) Edible gelled cellulose produced by acetic acid bacteria is called "Nata" in the Philippines, and has been eaten as a dessert after meals since ancient times. It is known to have a lowering effect on medium cholesterol. As a method for producing this "nata", coconut milk is added with sugar, acetic acid, etc., boiled and cooled, put in a wide-mouth bottle, and an acetic acid bacterium having an ability to produce cellulose, Acetobacter xylinum (Acetob)
(actor xylinum), cover with a cloth, and perform stationary culture at 30 ° C. for about 2 weeks. This allows
An agar-like pellicle (nata) of 3 to 4 cm is formed on the surface of the culture solution. The nata is taken out, washed, deacidified, sterilized, cut into an appropriate size, and impregnated with a sugar solution to obtain a product. Nata obtained by this method has a unique elastic texture and is sold as desserts, ice creams, beverages containing cellulose, etc. in addition to beverages, in addition to bees and beans. (Problems to be Solved by the Invention) In the conventional manufacturing method as described above, it takes a very long time to produce 3 to 4 cm of nata, and the produced nata is washed, deacidified, sterilized, cut, and so on. It takes a lot of time to impregnate the sugar solution. or,
Since culture is performed in a relatively small container, mass production is impossible. In addition, there is a problem in that a beverage containing cellulose is simply obtained by adding cellulose to the beverage, and cannot be said to be a fermented beverage containing cellulose.
The present invention aims to form a gel by shaking cultivation to obtain acetic acid bacterial cellulose which is the basic element, and furthermore, adding an appropriate amount of calcium carbonate to a fermented beverage containing acetic acid bacterial cellulose. It is an object of the present invention to provide a fermented beverage having a low acetic acid smell and a low acetic acid taste. (Means for Solving the Problems) In order to achieve the above object, the present inventors have conducted intensive studies. As a result, acetic acid bacteria having a cellulose producing ability separated from vinegar mash are converted into fruit juice and water, a small amount of brewed vinegar. The present invention was completed by developing a fermented beverage containing acetic acid bacterial cellulose, which is characterized by producing a acetic acid bacterial cellulose in a gel form by adding the mixture to a culture medium containing the mixture and shaking culture. The acetic acid bacterium used in the present invention is an acetic acid bacterium having a cellulose-producing ability separated from mash during fermentation and storage of vinegar by a vinegar maker, and Acetobacter xylinum (Acetob)
acter xylinum). This bacterium is not owned by a specific vinegar maker, but is a common vinegar maker.
Rather, it is characterized by a very strong ability to produce cellulose as compared to the identified conserved strains such as Acetobacter xylinum IFO 13772 and Acetobacter pastorianus ATCC10245. (FIG. 1).
It is considered that the reason for this is that, as a result of maintaining the culture for a long time in an environment suitable for the growth of bacteria, the ability to produce cellulose was enhanced. What is raised as production conditions is that when the material is carried out on orange juice, white peach juice, grape juice, etc.,
Appropriate treatment is performed in consideration of the sugar concentration of each fruit juice, the number of shakes, the culturing temperature, the number of days of cultivation, and the like, so as to solve the problem. (Example) An example will be described with reference to the drawings and tables. The acetic acid bacterium, which is a basic element of the present invention, is a bacterium capable of oxidizing alcohol to acetic acid, and is an aerobic gram-negative bacterium mainly used in the production of vinegar. It is a known fact that there is something to produce. The problem is how to utilize this to produce a novel product, and the present invention has been researched and developed in view of this point. In the practice of the present invention, the kind of juice is not particularly limited, but as a shaking culture condition of the material in the production process, for example, juice having a high sugar concentration, such as orange juice, white peach juice, grape juice, was used. The sugar concentration of the medium containing the fruit juice is suitably from 1 to 4 parts by weight. And the number of shaking is 70-1
The cultivation temperature may be 26 to 32 ° C., and the number of culturing days may be 2 to 3 days. Preferably, the brewed vinegar is rice vinegar. The acetic acid concentration of the medium is 0.1 to
0.5 parts by weight is suitable. The addition amount of calcium carbonate is 0.05 to 0.3 parts by weight, preferably 0.1 to 0.1 part by weight.
2 parts by weight is an appropriate amount. Even if calcium carbonate alone is added, the acetic acid odor and acetic acid taste are small and suitable for drinking. However, the addition of a small amount of fragrance and an appropriate amount of saccharide enhances the flavor to obtain better results. As a feature of this shaking culture method, the number of days of culture is completed in two to three days, the number of days is smaller than that in the static culture method, and mass production is possible by applying the culture vessel from shaking culture to stirring culture. Tank cultivation that can be performed. The fermented beverage containing acetic acid bacterial cellulose thus obtained contains gelled cellulose, contains various organic acids and amino acids, and has an intestinal regulating action, low caloric content, and blood The effect of organic acids and amino acids can be expected, as well as the effect of lowering medium cholesterol. (Tables 1 and 2)
【表1】 [Table 1]
【表2】 実施例1 オレンジ果汁(濃縮果汁還元、糖度11%) 82ml 米酢(酸度4.5%、糖度5%) 65ml 水 503ml Total 650mlを70
℃で加熱殺菌後、室温まで冷却し、2Lの三角フラスコ
に採り、A食酢メーカーの食酢もろみより分離したセル
ロース生成能を有する酢酸菌A1株を、あらかじめ、グ
ルコース 2g、酵母エキス 0.5g、ペプトン
0.5g、エタノール 4ml、酢酸 0.5gに蒸留
水を加えて100mlにした培地で6日間静置培養した
培養液を2ml接種し、培養温度 28℃、振幅 40
mm、振盪数 80回/分(往復運動)、培養日数 3
日で振盪培養を行なった。振盪培養機は、タイテック
(株)製バイオシェーカー、BR−160LFを使用し
た。その時のゲル状セルロースの生成経過及び、培養液
のPH変化を表3に記す。[Table 2] Example 1 Orange juice (concentrated juice reduction, sugar content 11%) 82 ml Rice vinegar (acidity 4.5%, sugar content 5%) 65 ml water 503 ml Total 650 ml 70
After heat sterilization under ° C., cooled to room temperature, taken Erlenmeyer flask 2L, the acetic acid bacteria A 1 strain having the cellulose producing ability isolated from a vinegar mash A vinegar manufacturers advance, glucose 2g, yeast extract 0.5g, peptone
0.5 ml, 4 ml of ethanol and 0.5 g of acetic acid were added to distilled water to make 100 ml, and 2 ml of a culture solution which had been allowed to stand still for 6 days was inoculated, and the culture temperature was 28 ° C. and the amplitude was 40.
mm, number of shaking 80 times / min (reciprocating movement), culture days 3
Shaking culture was performed every day. As a shaking incubator, a bio-shaker, BR-160LF, manufactured by Taitec Co., Ltd. was used. Table 3 shows the progress of gel cellulose production and the pH change of the culture solution at that time.
【表3】 培養終了後、培養液を取り出して、炭酸カルシウム
0.2重量部、オレンジ香料0.2重量部添加し、異性
化糖を加えて糖度10%にした後、飲用に供した。酢酸
臭、酢酸味は非常に弱く、風味が良く、口当たりも良好
で、のどごしの味覚についても良好であった。 実施例2 天然白桃果汁(糖度12%) 20ml 米酢(酸度4.5%、糖度5%) 15ml 水 115ml Total 150mlを70℃
で加熱殺菌後、室温まで冷却し、500ml三角フラス
コに採り、B食酢メーカーの食酢もろみより分離したセ
ルロース生成能を有する酢酸菌B1株を、あらかじめ、
グルコース 2g、酵母エキス 0.5g、ペプトン
0.5g、エタノール 4ml、酢酸 0.5mlに蒸
留水を加えて100mlにした培地で6日間静置培養し
た培養液を0.5ml接種し、培養温度 28℃、振幅
40mm、振盪数 80回/分(往復運動)、培養日数
3日で振盪培養を行なった。その時のゲル状セルロー
スの生成経過及び、培養液のPH変化を表4に記す。[Table 3] After the culture is completed, remove the culture solution and add calcium carbonate
0.2 part by weight and 0.2 part by weight of an orange flavor were added, and isomerized sugar was added to bring the sugar content to 10%. The acetic acid smell and the acetic acid taste were very weak, the flavor was good, the mouthfeel was good, and the taste of the throat was good. Example 2 Natural white peach juice (12% sugar content) 20 ml Rice vinegar (4.5% acidity, 5% sugar content) 15 ml Water 115 ml Total 150 ml at 70 ° C.
In that subsequent to heat sterilization, cooled to room temperature, taken up in 500ml Erlenmeyer flask, the acetic acid bacterium B 1 strain having the cellulose producing ability isolated from a vinegar mash B vinegar manufacturer in advance,
Glucose 2g, yeast extract 0.5g, peptone
0.5 g, 0.5 ml of ethanol, 4 ml of acetic acid, 0.5 ml of acetic acid, 0.5 ml of a culture solution obtained by statically culturing for 6 days in a medium made up to 100 ml by adding distilled water, a culture temperature of 28 ° C., an amplitude of 40 mm, and the number of shaking 80 times / Shaking culture was performed for 3 minutes (reciprocating motion) and the number of days of culture. Table 4 shows the progress of gel cellulose production and the pH change of the culture solution at that time.
【表4】 培養終了後、培養液を取り出して、炭酸カルシウム
0.2重量部、白桃香料0.2重量部添加し、異性化糖
を加えて糖度10%にした後、飲用に供した。酢酸臭、
酢酸味は非常に弱く、風味が良く、口当たりも良好で、
のどごしの味覚についても良好であった。 実施例3 天然グレープ果汁(糖度15%) 16ml 米酢(酸度4.5%、糖度5%) 15ml 水 119ml Total 150mlを70
℃で加熱殺菌後、室温まで冷却し、500mlの三角フ
ラスコに採り、C食酢メーカーの食酢もろみより分離し
たセルロース生成能を有する酢酸菌C1株を、あらかじ
め、グルコース2g、酵母エキス 0.5g、ペプトン
0.5g、エタノール 4ml、酢酸0.5gに蒸留
水を加えて100mlにした培地で6日間静置培養した
培養液を0.5ml接種し、培養温度 28℃、振幅
40mm、振盪数 80回/分(往復運動)、培養日数
3日で振盪培養を行なった。その時のゲル状セルロー
スの生成経過及び、培養液のPH変化を表5に記す。[Table 4] After the culture is completed, remove the culture solution and add calcium carbonate
0.2 parts by weight and 0.2 parts by weight of white peach flavor were added, and isomerized sugar was added to bring the sugar content to 10%, followed by drinking. Acetic acid odor,
The acetic acid taste is very weak, good taste, good taste,
The taste of the throat was also good. Example 3 Natural grape juice (sugar content 15%) 16 ml Rice vinegar (acidity 4.5%, sugar content 5%) 15 ml water 119 ml Total 150 ml 70
After heat sterilization under ° C., cooled to room temperature, taken Erlenmeyer flask 500 ml, the acetic acid bacterium C 1 strain having the cellulose producing ability isolated from a vinegar mash C vinegar manufacturers advance, glucose 2g, yeast extract 0.5g, 0.5 ml of a culture solution which had been statically cultured for 6 days in a medium made up by adding distilled water to 0.5 g of peptone, 4 ml of ethanol and 0.5 g of acetic acid to make 0.5 ml was inoculated, and the culture temperature was 28 ° C.
Shaking culture was performed at 40 mm, shaking frequency 80 times / min (reciprocating motion), and culture days 3 days. Table 5 shows the progress of gel cellulose production and the pH change of the culture solution at that time.
【表5】 培養終了後、培養液を取り出して、炭酸カルシウム
0.2重量部、グレープ香料 0.2重量部添加し、異
性化糖を加えて糖度10%にした後、飲用に供した。酢
酸臭、酢酸味は非常に弱く、風味が良く、口当たりも良
好で、のどごしの味覚についても良好であった。 〔発明の効果〕本発明は以上説明したように構成されて
いるので、以下に記載されるような効果を奏する。 1.本発明は、振盪培養法によるもので、静置培養法に
比べて、発酵期間が短くて済み、面倒な手間も掛からな
いという利点がある。 2.菌の発育に適した環境内で長い間培養を持続した結
果、セルロースの生産能が強くなる要件効果が有る。 3.酢酸臭、酢酸味の少ない酢酸菌セルロースを含むの
で発酵飲料として効果は著大である。[Table 5] After the culture is completed, remove the culture solution and add calcium carbonate
0.2 parts by weight and 0.2 parts by weight of grape flavor were added, and isomerized sugar was added to adjust the sugar content to 10%, followed by drinking. The acetic acid smell and the acetic acid taste were very weak, the flavor was good, the mouthfeel was good, and the taste of the throat was good. [Effects of the Invention] The present invention is configured as described above, and has the following effects. 1. The present invention is based on the shaking culture method, and has the advantage that the fermentation period can be shortened and no troublesome labor is required as compared with the static culture method. 2. As a result of maintaining the culture for a long time in an environment suitable for the growth of fungi, there is a requirement effect that the ability to produce cellulose is enhanced. 3. Since it contains acetic acid bacterium cellulose with low acetic acid odor and low acetic acid taste, the effect as a fermented beverage is significant.
【図1】は振盪培養における酢酸菌株の種類とゲル状セ
ルロースの生成量の関係を表す。FIG. 1 shows the relationship between the type of acetic acid bacteria strain and the amount of gelled cellulose produced in shaking culture.
Claims (2)
を有する酢酸菌を、果汁と水、少量の醸造酢を混合した
培地に加え、振盪培養を行なうことにより、ゲル状の酢
酸菌セルロースを生成させることを特徴とする、酢酸菌
セルロースを含む発酵飲料の製造方法。1. A cellulose acetate-producing acetic acid bacterium isolated from vinegar mash is added to a medium in which fruit juice, water and a small amount of brewed vinegar are mixed, followed by shaking culture to produce a gel-like acetic acid bacterial cellulose. A method for producing a fermented beverage containing cellulose acetate.
ルシウムを0.05〜0.3重量部添加し、酢酸臭、酢
酸味の少ない発酵飲料を得ることを特徴とする請求項1
記載の酢酸菌セルロースを含む発酵飲料の製造方法。2. The fermented beverage containing cellulose acetate is added to the fermented beverage containing 0.05 to 0.3 parts by weight of calcium carbonate to obtain a fermented beverage having a low odor of acetic acid and a low acetic acid taste.
A method for producing a fermented beverage containing the cellulose acetate according to the above.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP9127782A JPH10276736A (en) | 1997-04-09 | 1997-04-09 | Production of fermented beverage containing acetic acid bacterium cellulose |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP9127782A JPH10276736A (en) | 1997-04-09 | 1997-04-09 | Production of fermented beverage containing acetic acid bacterium cellulose |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH10276736A true JPH10276736A (en) | 1998-10-20 |
Family
ID=14968556
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP9127782A Pending JPH10276736A (en) | 1997-04-09 | 1997-04-09 | Production of fermented beverage containing acetic acid bacterium cellulose |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH10276736A (en) |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2013192534A (en) * | 2012-03-22 | 2013-09-30 | Snow Brand Milk Products Co Ltd | Food and method for producing the food |
| CN103815511A (en) * | 2014-02-28 | 2014-05-28 | 何钰婷 | Preparation method of pawpaw fruit vinegar beverage |
| CN105942099A (en) * | 2016-05-30 | 2016-09-21 | 山西百世生物科技股份有限公司 | Red-date fermented beverage and production method thereof |
| CN106360216A (en) * | 2016-08-29 | 2017-02-01 | 四川华朴现代农业股份有限公司 | Production method for red-fleshed kiwifruit ferment liquid |
| JP2017534244A (en) * | 2014-08-21 | 2017-11-24 | シュー・シャンタン | Active fermentation production method, fermented liquor produced using the same, and fermented beverage |
| CN109259129A (en) * | 2018-10-18 | 2019-01-25 | 贵州省中国科学院天然产物化学重点实验室 | A kind of the stauntonvine ferment pulp can and production method of catharsis and toxin expelling |
| WO2023040706A1 (en) * | 2021-09-18 | 2023-03-23 | 爱发生物科技(大连)有限公司 | Suspended beverage and preparation method therefor |
-
1997
- 1997-04-09 JP JP9127782A patent/JPH10276736A/en active Pending
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2013192534A (en) * | 2012-03-22 | 2013-09-30 | Snow Brand Milk Products Co Ltd | Food and method for producing the food |
| CN103815511A (en) * | 2014-02-28 | 2014-05-28 | 何钰婷 | Preparation method of pawpaw fruit vinegar beverage |
| JP2017534244A (en) * | 2014-08-21 | 2017-11-24 | シュー・シャンタン | Active fermentation production method, fermented liquor produced using the same, and fermented beverage |
| CN105942099A (en) * | 2016-05-30 | 2016-09-21 | 山西百世生物科技股份有限公司 | Red-date fermented beverage and production method thereof |
| CN106360216A (en) * | 2016-08-29 | 2017-02-01 | 四川华朴现代农业股份有限公司 | Production method for red-fleshed kiwifruit ferment liquid |
| CN109259129A (en) * | 2018-10-18 | 2019-01-25 | 贵州省中国科学院天然产物化学重点实验室 | A kind of the stauntonvine ferment pulp can and production method of catharsis and toxin expelling |
| WO2023040706A1 (en) * | 2021-09-18 | 2023-03-23 | 爱发生物科技(大连)有限公司 | Suspended beverage and preparation method therefor |
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