JPH0451862A - Soybean curd containing lactic bacterium metabolite - Google Patents
Soybean curd containing lactic bacterium metaboliteInfo
- Publication number
- JPH0451862A JPH0451862A JP2157438A JP15743890A JPH0451862A JP H0451862 A JPH0451862 A JP H0451862A JP 2157438 A JP2157438 A JP 2157438A JP 15743890 A JP15743890 A JP 15743890A JP H0451862 A JPH0451862 A JP H0451862A
- Authority
- JP
- Japan
- Prior art keywords
- lactic acid
- acid bacteria
- tofu
- culture
- group
- 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
- 241000894006 Bacteria Species 0.000 title claims abstract description 41
- 235000013527 bean curd Nutrition 0.000 title claims abstract description 39
- 239000002207 metabolite Substances 0.000 title abstract 3
- 230000001580 bacterial effect Effects 0.000 claims abstract description 16
- 239000000284 extract Substances 0.000 claims abstract description 7
- 235000013322 soy milk Nutrition 0.000 claims abstract description 4
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 claims description 52
- 239000004310 lactic acid Substances 0.000 claims description 26
- 235000014655 lactic acid Nutrition 0.000 claims description 26
- 230000002503 metabolic effect Effects 0.000 claims description 21
- 238000004519 manufacturing process Methods 0.000 claims description 10
- 238000010438 heat treatment Methods 0.000 claims description 6
- 238000001914 filtration Methods 0.000 claims description 5
- 239000000701 coagulant Substances 0.000 claims description 4
- 238000012258 culturing Methods 0.000 claims description 4
- 108090000623 proteins and genes Proteins 0.000 claims description 4
- 102000004169 proteins and genes Human genes 0.000 claims description 4
- 230000001112 coagulating effect Effects 0.000 claims description 3
- 241000186660 Lactobacillus Species 0.000 claims description 2
- 240000004808 Saccharomyces cerevisiae Species 0.000 claims description 2
- 239000000203 mixture Substances 0.000 abstract description 2
- 239000003795 chemical substances by application Substances 0.000 abstract 2
- 230000036425 denaturation Effects 0.000 abstract 1
- 238000004925 denaturation Methods 0.000 abstract 1
- 239000000047 product Substances 0.000 description 22
- 210000004027 cell Anatomy 0.000 description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- 239000000796 flavoring agent Substances 0.000 description 8
- 235000019634 flavors Nutrition 0.000 description 8
- 241000588724 Escherichia coli Species 0.000 description 7
- 238000000926 separation method Methods 0.000 description 7
- 230000006866 deterioration Effects 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 235000010469 Glycine max Nutrition 0.000 description 4
- 244000068988 Glycine max Species 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000000706 filtrate Substances 0.000 description 4
- 241001603151 Philus Species 0.000 description 3
- 239000000470 constituent Substances 0.000 description 3
- 239000000499 gel Substances 0.000 description 3
- 235000018102 proteins Nutrition 0.000 description 3
- 229920001817 Agar Polymers 0.000 description 2
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
- 108010073771 Soybean Proteins Proteins 0.000 description 2
- 239000008272 agar Substances 0.000 description 2
- 210000000805 cytoplasm Anatomy 0.000 description 2
- 235000013305 food Nutrition 0.000 description 2
- 238000000227 grinding Methods 0.000 description 2
- 239000002075 main ingredient Substances 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
- 239000002002 slurry Substances 0.000 description 2
- 235000019710 soybean protein Nutrition 0.000 description 2
- ZORQXIQZAOLNGE-UHFFFAOYSA-N 1,1-difluorocyclohexane Chemical compound FC1(F)CCCCC1 ZORQXIQZAOLNGE-UHFFFAOYSA-N 0.000 description 1
- 241000478814 Acidops Species 0.000 description 1
- 244000247812 Amorphophallus rivieri Species 0.000 description 1
- 235000001206 Amorphophallus rivieri Nutrition 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
- 102000003886 Glycoproteins Human genes 0.000 description 1
- 108090000288 Glycoproteins Proteins 0.000 description 1
- 229920002752 Konjac Polymers 0.000 description 1
- 241000194036 Lactococcus Species 0.000 description 1
- 239000001888 Peptone Substances 0.000 description 1
- 108010080698 Peptones Proteins 0.000 description 1
- 244000046052 Phaseolus vulgaris Species 0.000 description 1
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 1
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- 229940041514 candida albicans extract Drugs 0.000 description 1
- 230000002860 competitive effect Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 235000003891 ferrous sulphate Nutrition 0.000 description 1
- 239000011790 ferrous sulphate Substances 0.000 description 1
- 238000005194 fractionation Methods 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
- 230000002401 inhibitory effect Effects 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- BAUYGSIQEAFULO-UHFFFAOYSA-L iron(2+) sulfate (anhydrous) Chemical compound [Fe+2].[O-]S([O-])(=O)=O BAUYGSIQEAFULO-UHFFFAOYSA-L 0.000 description 1
- 229910000359 iron(II) sulfate Inorganic materials 0.000 description 1
- 235000015110 jellies Nutrition 0.000 description 1
- 239000008274 jelly Substances 0.000 description 1
- 239000000252 konjac Substances 0.000 description 1
- 235000010485 konjac Nutrition 0.000 description 1
- 229940039696 lactobacillus Drugs 0.000 description 1
- 150000002632 lipids Chemical class 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 229940099596 manganese sulfate Drugs 0.000 description 1
- 235000007079 manganese sulphate Nutrition 0.000 description 1
- 239000011702 manganese sulphate Substances 0.000 description 1
- SQQMAOCOWKFBNP-UHFFFAOYSA-L manganese(II) sulfate Chemical compound [Mn+2].[O-]S([O-])(=O)=O SQQMAOCOWKFBNP-UHFFFAOYSA-L 0.000 description 1
- 229910000402 monopotassium phosphate Inorganic materials 0.000 description 1
- 235000019796 monopotassium phosphate Nutrition 0.000 description 1
- 102000039446 nucleic acids Human genes 0.000 description 1
- 108020004707 nucleic acids Proteins 0.000 description 1
- 150000007523 nucleic acids Chemical class 0.000 description 1
- 235000008935 nutritious Nutrition 0.000 description 1
- 235000019319 peptone Nutrition 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- GNSKLFRGEWLPPA-UHFFFAOYSA-M potassium dihydrogen phosphate Chemical compound [K+].OP(O)([O-])=O GNSKLFRGEWLPPA-UHFFFAOYSA-M 0.000 description 1
- LWIHDJKSTIGBAC-UHFFFAOYSA-K potassium phosphate Substances [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 description 1
- 230000002062 proliferating effect Effects 0.000 description 1
- 235000011962 puddings Nutrition 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- 239000001593 sorbitan monooleate Substances 0.000 description 1
- 235000011069 sorbitan monooleate Nutrition 0.000 description 1
- 229940035049 sorbitan monooleate Drugs 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 230000001954 sterilising effect Effects 0.000 description 1
- 238000004659 sterilization and disinfection Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- 230000002123 temporal effect Effects 0.000 description 1
- 238000011282 treatment Methods 0.000 description 1
- YWYZEGXAUVWDED-UHFFFAOYSA-N triammonium citrate Chemical compound [NH4+].[NH4+].[NH4+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O YWYZEGXAUVWDED-UHFFFAOYSA-N 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 239000012138 yeast extract Substances 0.000 description 1
Landscapes
- Beans For Foods Or Fodder (AREA)
Abstract
Description
【発明の詳細な説明】
(産業上の利用分野)
本発明は豆腐の製造方法に係り、特に経時変質の少ない
風味にすぐれた豆腐の製造方法に関する。DETAILED DESCRIPTION OF THE INVENTION (Industrial Application Field) The present invention relates to a method for producing tofu, and particularly to a method for producing tofu with excellent flavor and less deterioration over time.
(従来の技術および発明の解決すべき課B)豆腐はその
主成分として大豆蛋白を含有する栄養分に冨む食品であ
るが、製造後比較的短時間で表面に細菌が繁殖しやすく
また密封した場合でも変質によって離水し食感や風味が
低下しやすい。(Conventional technology and problem to be solved by the invention B) Tofu is a nutritious food that contains soybean protein as its main ingredient, but it is easy for bacteria to grow on the surface within a relatively short period of time after production, and it is also sealed. Even in some cases, dehydration occurs and the texture and flavor are likely to deteriorate.
(課題を解決するための手段)
本発明者等は経時変質の少ない豆腐について種々研究す
る過程で、ある種の乳酸菌の代謝生成物の添加によって
風味にすぐれ経時変質の少ない豆腐の得られることを発
見して本発明を完成するに到った。(Means for Solving the Problems) In the process of conducting various studies on tofu that undergoes little deterioration over time, the present inventors discovered that tofu with excellent flavor and little deterioration over time could be obtained by adding metabolic products of certain lactic acid bacteria. This discovery led to the completion of the present invention.
すなわち、前記従来技術の課題は異なった菌株の乳酸菌
を同時培養し、培養中に菌体から生成される代謝生成物
および培養物を加熱処理し得られる菌体からの抽出物を
濾過して得られる生成物を蛋白質凝固剤と共に豆乳に対
して加えて約70℃の温度で凝固させることによって得
られる乳酸菌の代謝生成物を含む豆腐の製造方法によっ
て解決される。In other words, the problem with the prior art described above is that lactic acid bacteria of different strains are simultaneously cultured, and the metabolic products produced from the bacterial cells during the culture and the extract from the bacterial cells obtained by heating the culture are filtered. The problem is solved by a method for producing tofu containing metabolic products of lactic acid bacteria, which is obtained by adding the product obtained by adding a protein coagulant to soy milk and coagulating it at a temperature of about 70°C.
(作用)
本発明における豆腐は基本的には大豆を水中で摩砕した
水性スラリを加熱して得られる豆乳に対してMgC1,
等の凝固剤を加えて蛋白質を凝固させることによって製
造され、この凝固剤の添加と同時に又はその前後で乳酸
菌の代謝生成物を添加することによって得られる。(Function) The tofu in the present invention is basically produced by heating an aqueous slurry obtained by grinding soybeans in water.
It is produced by coagulating the protein by adding a coagulant such as, and is obtained by adding a metabolic product of lactic acid bacteria at the same time or before or after the addition of the coagulant.
このようにして得られる豆腐は後述するように経時変質
の尺度として通常知られている離水率(ゲル保水率の低
下)が通常の豆腐に比較して著しく減少し、また大腸菌
その他の雑菌の生育も大幅に抑止されると共に豆腐の風
味が著しく改善されかつ長期間一定に保たれる。As will be explained later, the tofu obtained in this way has a significantly reduced syneresis rate (reduction in gel water retention rate), which is commonly known as a measure of deterioration over time, compared to regular tofu, and is free from the growth of E. coli and other bacteria. In addition, the flavor of tofu is significantly improved and remains constant for a long period of time.
本発明において用いられる乳酸菌の代謝生成物は異なっ
た複数種の乳酸菌を同時培養し、培養中に生成される乳
酸菌からの代謝排出物および得られた培養物を加熱処理
して、菌体内部および細胞質自体からの抽出生成物を濾
過することによって得られる。The metabolic products of lactic acid bacteria used in the present invention are produced by culturing different types of lactic acid bacteria simultaneously and heat-treating the metabolic waste from the lactic acid bacteria produced during the culture and the resulting culture. Obtained by filtering the extraction product from the cytoplasm itself.
前記乳酸菌から得られる濾液中には菌体から排出された
代謝生成物に加えて加熱処理等を加えられた菌体細胞の
構成質自体に由来する各種アミノ酸、タン白質、核酸、
脂質、糖タン白質、多糖類等が含まれており、こ\では
それらを合せて代謝生成物という。The filtrate obtained from the lactic acid bacteria contains, in addition to metabolic products excreted from the bacterial cells, various amino acids, proteins, nucleic acids derived from the constituent substances of the bacterial cells themselves that have been subjected to heat treatment, etc.
It contains lipids, glycoproteins, polysaccharides, etc., and these are collectively referred to as metabolic products.
前記乳酸菌の代謝生成物の特色はそれが複数の異なった
種類の乳酸菌を同時に培養することによって相互の競合
的な生育の段階で選択的に得られる菌種からの代謝生成
物であること、そして特に、従来の乳酸菌飲料等に見ら
れるように生菌をそのま〜利用するのではなく、その培
養中に生じた菌体からの排出代謝生成物および加熱処理
等により菌体の細胞構成質自体から抽出される生成物を
用いることにある。The characteristics of the metabolic products of lactic acid bacteria are that they are metabolic products from bacterial species that can be selectively obtained during mutually competitive growth by culturing multiple different types of lactic acid bacteria at the same time; In particular, instead of using live bacteria as is, as seen in conventional lactic acid bacteria drinks, etc., the cell constituents of the bacteria are produced by using metabolic products excreted from the bacteria during cultivation and heat treatment, etc. The purpose is to use products extracted from
このような代謝生成物等が前記のようなすぐれた効果を
生じる理由は必ずしも明らかでないが、乳酸菌培養によ
って代謝生成物として得られる前記多I!類等の種々の
成分が総合的に作用して経時的なゲル保水率の低下(離
水率の増加)を抑制すると共に豆腐に好ましい風味を与
え、また競合培養中に生じる何等かの物質が大腸菌その
他の望ましくない細菌の繁殖を抑制しかつ大豆蛋白質の
分解による経時変化を低下させることによるものと思わ
れる。Although it is not necessarily clear why such metabolic products produce the above-mentioned excellent effects, the multi-I! A variety of components such as these act comprehensively to suppress the decline in gel water retention rate (increase in water separation rate) over time and give tofu a pleasant flavor. This is thought to be due to the suppression of the growth of other undesirable bacteria and the reduction of changes over time due to decomposition of soybean protein.
本発明において用いられる乳酸菌としては種々のものが
挙げられ、かつその培養方法も多岐にわたるが、たとえ
ばI (B、bu1garicus^、B、1cido
phi1us 1.M−1actisacidi) 、
II (B、bulgaricus B、B。There are various types of lactic acid bacteria used in the present invention, and there are also a wide variety of methods for culturing them.
philus 1. M-1actisacidi),
II (B, bulgaricus B, B.
acidophilus、M、1actisacidi
) 、 III(Kornchenbacillus
A、B、acidophilus、M、1actis
acidi)およびIV (Kornchcnbaci
llus B+ B、actdophilus W、1
actisacidi )のように各群毎に少なくとも
一つの乳酸桿菌および乳酸球菌を含み、かつ菌株が各群
相互間で異なる複数の乳酸菌を各群(1)〜(IV)に
夫々酵母を加えて群別に所定条件で一次培養し、得られ
た各群の培養物を合わせてさらに同時二次培養すること
によって好ましい結果が得られる。acidophilus, M. 1actisacidi
), III (Kornchenbacillus
A, B, acidophilus, M, 1actis
acidi) and IV (Kornchcnbaci)
llus B+ B, actdophilus W, 1
actisacidi), each group contains at least one Lactobacillus and Lactococcus, and the bacterial strains differ between each group. Favorable results can be obtained by performing primary culture under predetermined conditions and then combining the resulting cultures of each group and further performing simultaneous secondary culture.
この場合、一次培養の際の代謝生成物(乳酸その他)は
これを濾過等によって除去し菌体のみをさらに二次培養
することが好ましい。In this case, it is preferable to remove the metabolic products (lactic acid and others) during the primary culture by filtration or the like, and then further culture only the bacterial cells.
前記二次培養によって得られた乳酸菌には加熱殺菌その
他の処理を施して、培養中に菌体外に排出された代謝生
成物と菌体内部および菌体の細胞構成質自体からの抽出
物とをたとえば真空下でマイクロフィルタで濾過して分
別し、濾液として得られる透明な酸性の液体(pH3〜
4)をさらに精製して添加物として用いる。The lactic acid bacteria obtained by the secondary culture are subjected to heat sterilization or other treatments to separate the metabolic products excreted outside the cells during the culture and the extracts from inside the cells and from the cell constituents of the cells themselves. For example, by filtration and fractionation with a microfilter under vacuum, the filtrate is obtained as a transparent acidic liquid (pH 3~
4) is further purified and used as an additive.
本発明における前記代謝生成物の添加量は豆乳に対して
約1pp−ですでに有意な効果を生じるが、一方5 p
p閤以上を添加してもそれに伴う効果の向上はそれほど
見受けられない。In the present invention, the amount of the metabolic products added to soybean milk is already significant at about 1 pp-;
Even if more than P is added, the effect does not improve much.
尚本発明の効果は後述するように豆腐の経時離水率、大
腸菌の繁殖抑制作用およびパネラによる風味試験によっ
て評価した。The effects of the present invention were evaluated by the syneresis rate of tofu over time, the inhibiting effect on the propagation of Escherichia coli, and the flavor test by Panela, as described below.
本発明の方法に用いる乳酸菌の代謝生成物は豆腐の他、
主成分のゲル化によって得られ、経時的に離水をともな
って変質する他の食品、たとえばこんにゃく、寒天ゼリ
ー、プリン等にも適用することができる。In addition to tofu, the metabolic products of lactic acid bacteria used in the method of the present invention include
It can also be applied to other foods that are obtained by gelation of the main ingredient and deteriorate over time with syneresis, such as konjac, agar jelly, and pudding.
実施例 以下本発明を実施例によって説明する。Example The present invention will be explained below with reference to Examples.
I (B、bulgaricus A、B、acido
philus、M、1actisacidi> 、II
(B、bulgaricus B、B、acidop
hilus、 M、1actisacidi ) 、I
IICKornchenbacillus A、B、a
cid。I (B, bulgaricus A, B, acido
philus, M. 1actisacidi>, II
(B, bulgaricus B, B, acidop
hilus, M. 1actisacidi), I
IICKornchenbacillus A, B, a
cid.
philus、M、 1actisacidi)および
IV (Kornchcnbacillus B、 B
、acidophilusJ、1actisacidi
)の各群に分けられ、菌株が各群間で異なる乳酸菌群
(I)〜(IV)に対して夫々酵母を加え、下記組成か
らなる乳酸菌用の培地を用いて平均温度約37℃の条件
で夫々120時間時間培養した。philus, M, 1actisacidi) and IV (Kornchcnbacillus B, B
, acidophilus J, 1actisacidi
), yeast was added to lactic acid bacteria groups (I) to (IV) with different strains between each group, and a medium for lactic acid bacteria with the following composition was used at an average temperature of about 37°C. Each was cultured for 120 hours.
トリブチケースペプトン・・・・・・・・・10.00
0 g酵母エキス ・・・・・・・・・5.
000 gリン酸1カリウム ・・・・・・・・・
6.000 gクエン酸アンモニウム ・・・・・・・
・・2.000 gブドウ糖 ・・・・
・・・・・20.000 gソルビタンモノオリエイト
・・・1.000 g水和酢酸ナトリウム ・・・
・・−・・・25.000 g硫酸マグネシウム
・・・・・・・・・0.575 g硫酸マンガン
・・・・・・・・・0.120 g硫酸第1鉄
・・・・・・・・・0.034 gカンテン
・・・・・・・・・15.000 gpF
l 5.5
これら1〜V群の乳酸菌から得られる培養物から乳酸菌
のみを抽出し、これらを合せて前記と同様な培地および
培養条件で同時培養し、得られた培養物を約65℃で加
熱処理し、真空下マイクロフィルタで濾過し、前記培養
中に得られた乳酸菌からの代謝生成物と菌体内部の細胞
質等に由来する抽出物とを分別し、pn約3〜4の透明
な濾液を得た。Tributicase peptone・・・・・・10.00
0 g yeast extract ・・・・・・・・・5.
000 g monopotassium phosphate ・・・・・・・・・
6.000 g ammonium citrate...
・・2.000 g glucose ・・・・
...20.000 g sorbitan monooleate ...1.000 g hydrated sodium acetate ...
・・・-・・・25.000 g Magnesium sulfate
・・・・・・・・・0.575 g Manganese sulfate
......0.120 g ferrous sulfate
・・・・・・・・・0.034 g agar
・・・・・・・・・15.000 gpF
l 5.5 Extract only the lactic acid bacteria from the culture obtained from these lactic acid bacteria of Groups 1 to V, and co-cultivate them together in the same medium and culture conditions as above, and incubate the resulting culture at about 65°C. The metabolic products from the lactic acid bacteria obtained during the culture and the extracts derived from the cytoplasm inside the bacterial cells are separated by heat treatment and filtration with a microfilter under vacuum. A filtrate was obtained.
大豆]、Kgを水10Ilと共に摩砕して得られたスラ
リを約100″Cに2分間加熱して豆乳を得た。A slurry obtained by grinding Kg of soybean] with 10 Il of water was heated to about 100''C for 2 minutes to obtain soybean milk.
約70℃に保持した前記豆乳に対し前記濾液およびMg
C1,を加えて通常の豆腐の製造方法と同様にし処理し
て豆腐を得た。The filtrate and Mg
C1 was added and processed in the same manner as a normal tofu manufacturing method to obtain tofu.
試験例1 離水率テスト
前記豆g350g(約−丁分)を金網付のシャレー上に
放置し、豆腐から離水した水の量を濾紙に吸収させて経
時的に求め、通常の豆腐の場合と比較した。結果を第1
図に示す。Test Example 1 Water Separation Rate Test 350g of the beans (approximately -10 g) were left on a chalet with a wire mesh, and the amount of water released from the tofu was determined over time by being absorbed by a filter paper, and compared with that of regular tofu. did. Results first
As shown in the figure.
第1図から明らかなように、通常の豆腐の場合(曲線A
)も本願発明の方法による豆腐の場合(曲&’1jB)
も製造直後から離水が始まりゲルの保水状態に変化の生
じていることが示された。しかし、離水率の経時的な増
加は本願発明の豆腐の場合従来の豆腐に比較して明らか
に低下しており、1日経過後ですでに任意の差が認めら
れ、特に2日経時後の両者間の離水率の差は極めて大き
い。As is clear from Figure 1, in the case of normal tofu (curve A
) is also the case of tofu produced by the method of the claimed invention (song &'1jB)
It was also shown that syneresis started immediately after production, indicating that the water retention state of the gel had changed. However, the increase in syneresis rate over time is clearly lower in the case of the tofu of the present invention compared to conventional tofu, and a certain difference is already observed after 1 day, especially after 2 days. The difference in water separation rate between them is extremely large.
これは豆腐の食感や風味が大きく変化するといわれてい
る1〜2日の間での離水率の抑制に対して本発明の効果
が著しいことを示している。This shows that the present invention is significantly effective in suppressing the water separation rate during 1 to 2 days, when the texture and flavor of tofu are said to change significantly.
試験例2 細菌抑制テスト
前記実施例によって得られた本発明の製造方法による豆
腐および乳酸菌代謝生成物を加えないで得られた従来の
豆腐の試片を温度20℃の恒温室に保存して表面に繁殖
する生菌数および大腸菌数を測定した。結果を第2図に
示す。Test Example 2 Bacterial Inhibition Test Samples of tofu produced by the production method of the present invention obtained in the above example and of conventional tofu obtained without adding lactic acid bacteria metabolic products were stored in a thermostatic chamber at a temperature of 20°C, and the surface The number of viable bacteria and Escherichia coli proliferating in the sample were measured. The results are shown in Figure 2.
第2図から明らかなように豆腐の1日保ち」の尺度の一
つとして重要な一般生菌および大腸菌の生育率について
、従来の方法による豆腐(−船主菌数:曲線A1、大腸
菌数二曲線Bl)の場合に比較して本発明の製造方法に
よって得られた豆腐(−船主菌数:曲線A2、大腸菌数
−曲線Bよ)では、これら菌数が著しく減少していた(
縦軸は菌数の指数値を示す)。As is clear from Figure 2, the growth rate of general viable bacteria and Escherichia coli, which is important as a measure of the one-day shelf life of tofu, was compared to the growth rate of tofu produced using the conventional method (-ship owner bacterial count: curve A1, E. coli count double curve Bl). ), the number of these bacteria was significantly reduced in the tofu obtained by the production method of the present invention (- shipowner bacteria count: curve A2, coliform count - curve B) (
The vertical axis shows the index value of the number of bacteria).
(発明の効果)
以上のように本発明の方法によれば、豆腐の風味が著し
く改善されその経時変質が効果的に防止される。(Effects of the Invention) As described above, according to the method of the present invention, the flavor of tofu is significantly improved and its deterioration over time is effectively prevented.
第1図は豆腐の離水率を本発明および従来の製品の間で
比較して承すグラフ、第2図は豆腐表面の菌数の経時変
化を本発明および従来の製品の間で比較して示すグラフ
である。
図中:
A・・・従来豆腐の離水率
B・・・本発明豆腐の離水率
A1・−・従来豆腐における一般生菌数の経時変化^2
・・・本発明豆腐における一般生菌数の経時変化B1・
・従来豆腐における大腸菌数の経時変化B2・・・本発
明豆腐における大腸菌数の経時変化特許出願人 山
元 徳 藏
(は力(1名)Figure 1 is a graph comparing the water separation rate of tofu between the present invention and the conventional product, and Figure 2 is a graph comparing the change in the number of bacteria on the tofu surface over time between the present invention and the conventional product. This is a graph showing. In the figure: A... Water separation rate of conventional tofu B... Water separation rate of tofu of the present invention A1 - Change over time in the number of viable bacteria in conventional tofu ^2
...Temporal change in the number of viable bacteria in the tofu of the present invention B1.
・Change in the number of E. coli in conventional tofu over time B2...Change in the number of E. coli in tofu of the present invention over time Patent applicant Noriyuki Yamamoto (1 person)
Claims (2)
ら生成される代謝生成物および培養物を加熱処理するこ
とによって得られる菌体からの抽出物を濾過して得られ
る生成物を、蛋白質凝固剤と共に豆乳に対して加えて約
70℃の温度で凝固させ、次いで放冷することによって
得られる乳酸菌の代謝生成物を含む豆腐の製造方法。(1) A product obtained by co-cultivating different strains of lactic acid bacteria and filtering the metabolic products produced from the bacterial cells during the culture and the extract from the bacterial cells obtained by heating the culture. A method for producing tofu containing a metabolic product of lactic acid bacteria, which is obtained by adding a protein coagulant to soymilk, coagulating it at a temperature of about 70°C, and then allowing it to cool.
酸桿菌および乳酸球菌を含み菌株が各群間で異なる複数
群の乳酸菌を各群毎に酵母を加えて夫々一次培養し、培
養された各群の乳酸菌を合せてさらに同時二次培養し、
この二次培養物を処理して得られたものである前記請求
項1記載の製造方法。(2) A plurality of groups of lactic acid bacteria in which the metabolic products of the lactic acid bacteria contain at least lactobacilli and lactococci in each group and the bacterial strains differ between each group are cultured by adding yeast to each group and primary culturing each group. The lactic acid bacteria of each group were combined and further co-cultured,
The manufacturing method according to claim 1, which is obtained by treating this secondary culture.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2157438A JP2955637B2 (en) | 1990-06-18 | 1990-06-18 | Tofu containing lactic acid bacteria metabolites |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2157438A JP2955637B2 (en) | 1990-06-18 | 1990-06-18 | Tofu containing lactic acid bacteria metabolites |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH0451862A true JPH0451862A (en) | 1992-02-20 |
JP2955637B2 JP2955637B2 (en) | 1999-10-04 |
Family
ID=15649654
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2157438A Expired - Lifetime JP2955637B2 (en) | 1990-06-18 | 1990-06-18 | Tofu containing lactic acid bacteria metabolites |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2955637B2 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2009114163A (en) * | 2007-11-05 | 2009-05-28 | Nippon Energy Kenkyusho:Kk | Hypoglycemic agent and hypoglycemic functional food comprising cultivation product of complex microorganism as active ingredient |
-
1990
- 1990-06-18 JP JP2157438A patent/JP2955637B2/en not_active Expired - Lifetime
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2009114163A (en) * | 2007-11-05 | 2009-05-28 | Nippon Energy Kenkyusho:Kk | Hypoglycemic agent and hypoglycemic functional food comprising cultivation product of complex microorganism as active ingredient |
Also Published As
Publication number | Publication date |
---|---|
JP2955637B2 (en) | 1999-10-04 |
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