JPH04218362A - Food vinegar containing galactooligosaccharide and its preparation - Google Patents
Food vinegar containing galactooligosaccharide and its preparationInfo
- Publication number
- JPH04218362A JPH04218362A JP2411217A JP41121790A JPH04218362A JP H04218362 A JPH04218362 A JP H04218362A JP 2411217 A JP2411217 A JP 2411217A JP 41121790 A JP41121790 A JP 41121790A JP H04218362 A JPH04218362 A JP H04218362A
- Authority
- JP
- Japan
- Prior art keywords
- vinegar
- galactooligosaccharide
- fermentation
- acetic acid
- alcohol
- 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
- 239000000052 vinegar Substances 0.000 title claims abstract description 45
- 235000021419 vinegar Nutrition 0.000 title claims abstract description 45
- 235000021255 galacto-oligosaccharides Nutrition 0.000 title claims abstract description 25
- 150000003271 galactooligosaccharides Chemical class 0.000 title claims abstract description 25
- 238000002360 preparation method Methods 0.000 title abstract description 4
- 235000013305 food Nutrition 0.000 title abstract 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims abstract description 57
- 235000000346 sugar Nutrition 0.000 claims abstract description 28
- 238000000855 fermentation Methods 0.000 claims abstract description 26
- 230000004151 fermentation Effects 0.000 claims abstract description 26
- 150000008163 sugars Chemical class 0.000 claims abstract description 16
- 240000004808 Saccharomyces cerevisiae Species 0.000 claims abstract description 12
- 244000046052 Phaseolus vulgaris Species 0.000 claims abstract description 10
- 235000010627 Phaseolus vulgaris Nutrition 0.000 claims abstract description 9
- 239000000284 extract Substances 0.000 claims abstract description 8
- 230000001476 alcoholic effect Effects 0.000 claims abstract description 6
- 239000003125 aqueous solvent Substances 0.000 claims abstract description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 14
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 claims description 7
- 229930006000 Sucrose Natural products 0.000 claims description 7
- 239000005720 sucrose Substances 0.000 claims description 7
- MUPFEKGTMRGPLJ-RMMQSMQOSA-N Raffinose Natural products O(C[C@H]1[C@@H](O)[C@H](O)[C@@H](O)[C@@H](O[C@@]2(CO)[C@H](O)[C@@H](O)[C@@H](CO)O2)O1)[C@@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 MUPFEKGTMRGPLJ-RMMQSMQOSA-N 0.000 claims description 6
- UQZIYBXSHAGNOE-USOSMYMVSA-N Stachyose Natural products O(C[C@H]1[C@@H](O)[C@H](O)[C@H](O)[C@@H](O[C@@]2(CO)[C@H](O)[C@@H](O)[C@@H](CO)O2)O1)[C@@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@H](CO[C@@H]2[C@@H](O)[C@@H](O)[C@@H](O)[C@H](CO)O2)O1 UQZIYBXSHAGNOE-USOSMYMVSA-N 0.000 claims description 6
- MUPFEKGTMRGPLJ-UHFFFAOYSA-N UNPD196149 Natural products OC1C(O)C(CO)OC1(CO)OC1C(O)C(O)C(O)C(COC2C(C(O)C(O)C(CO)O2)O)O1 MUPFEKGTMRGPLJ-UHFFFAOYSA-N 0.000 claims description 6
- 150000001720 carbohydrates Chemical class 0.000 claims description 6
- MUPFEKGTMRGPLJ-ZQSKZDJDSA-N raffinose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO[C@@H]2[C@@H]([C@@H](O)[C@@H](O)[C@@H](CO)O2)O)O1 MUPFEKGTMRGPLJ-ZQSKZDJDSA-N 0.000 claims description 6
- UQZIYBXSHAGNOE-XNSRJBNMSA-N stachyose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO[C@@H]2[C@@H]([C@@H](O)[C@@H](O)[C@@H](CO[C@@H]3[C@@H]([C@@H](O)[C@@H](O)[C@@H](CO)O3)O)O2)O)O1 UQZIYBXSHAGNOE-XNSRJBNMSA-N 0.000 claims description 6
- 229930091371 Fructose Natural products 0.000 claims description 5
- 239000005715 Fructose Substances 0.000 claims description 5
- 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 claims description 5
- 239000008103 glucose Substances 0.000 claims description 5
- RFSUNEUAIZKAJO-ARQDHWQXSA-N Fructose Chemical compound OC[C@H]1O[C@](O)(CO)[C@@H](O)[C@@H]1O RFSUNEUAIZKAJO-ARQDHWQXSA-N 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 claims description 4
- DBTMGCOVALSLOR-AXAHEAMVSA-N galactotriose Natural products OC[C@@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](CO)O[C@@H](O[C@H]3[C@@H](O)[C@H](O)O[C@@H](CO)[C@@H]3O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O DBTMGCOVALSLOR-AXAHEAMVSA-N 0.000 claims description 3
- FZWBNHMXJMCXLU-YRBKNLIBSA-N manninotriose Chemical compound O[C@@H]1[C@@H](O)[C@@H](O)[C@@H](CO)O[C@@H]1OC[C@@H]1[C@H](O)[C@H](O)[C@@H](O)[C@@H](OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C=O)O1 FZWBNHMXJMCXLU-YRBKNLIBSA-N 0.000 claims description 3
- 239000000203 mixture Substances 0.000 claims description 3
- 125000002791 glucosyl group Chemical group C1([C@H](O)[C@@H](O)[C@H](O)[C@H](O1)CO)* 0.000 claims 2
- 125000003421 melibiose group Chemical group 0.000 claims 1
- 230000033228 biological regulation Effects 0.000 abstract description 3
- 238000000605 extraction Methods 0.000 abstract description 3
- 238000000034 method Methods 0.000 abstract 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 10
- 241000186000 Bifidobacterium Species 0.000 description 8
- 244000068988 Glycine max Species 0.000 description 8
- 235000010469 Glycine max Nutrition 0.000 description 8
- 241000894006 Bacteria Species 0.000 description 7
- 230000006870 function Effects 0.000 description 6
- 239000002994 raw material Substances 0.000 description 5
- 230000000694 effects Effects 0.000 description 4
- 229910017464 nitrogen compound Inorganic materials 0.000 description 4
- 150000002830 nitrogen compounds Chemical class 0.000 description 4
- 229920002472 Starch Polymers 0.000 description 3
- 150000001298 alcohols Chemical class 0.000 description 3
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 3
- 230000000968 intestinal effect Effects 0.000 description 3
- 210000000936 intestine Anatomy 0.000 description 3
- 239000008107 starch Substances 0.000 description 3
- 235000019698 starch Nutrition 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 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
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- 238000005273 aeration Methods 0.000 description 2
- DLRVVLDZNNYCBX-ZZFZYMBESA-N beta-melibiose Chemical compound O[C@@H]1[C@@H](O)[C@@H](O)[C@@H](CO)O[C@@H]1OC[C@@H]1[C@@H](O)[C@H](O)[C@@H](O)[C@H](O)O1 DLRVVLDZNNYCBX-ZZFZYMBESA-N 0.000 description 2
- 230000001164 bioregulatory effect Effects 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
- 238000000909 electrodialysis Methods 0.000 description 2
- 230000037149 energy metabolism Effects 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 230000036541 health Effects 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- PHTQWCKDNZKARW-UHFFFAOYSA-N isoamylol Chemical compound CC(C)CCO PHTQWCKDNZKARW-UHFFFAOYSA-N 0.000 description 2
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 2
- KQNPFQTWMSNSAP-UHFFFAOYSA-N isobutyric acid Chemical compound CC(C)C(O)=O KQNPFQTWMSNSAP-UHFFFAOYSA-N 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000012528 membrane Substances 0.000 description 2
- WLJVXDMOQOGPHL-UHFFFAOYSA-N phenylacetic acid Chemical compound OC(=O)CC1=CC=CC=C1 WLJVXDMOQOGPHL-UHFFFAOYSA-N 0.000 description 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
- 238000000746 purification Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- NWUYHJFMYQTDRP-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;1-ethenyl-2-ethylbenzene;styrene Chemical compound C=CC1=CC=CC=C1.CCC1=CC=CC=C1C=C.C=CC1=CC=CC=C1C=C NWUYHJFMYQTDRP-UHFFFAOYSA-N 0.000 description 1
- XYHKNCXZYYTLRG-UHFFFAOYSA-N 1h-imidazole-2-carbaldehyde Chemical compound O=CC1=NC=CN1 XYHKNCXZYYTLRG-UHFFFAOYSA-N 0.000 description 1
- GWYFCOCPABKNJV-UHFFFAOYSA-M 3-Methylbutanoic acid Natural products CC(C)CC([O-])=O GWYFCOCPABKNJV-UHFFFAOYSA-M 0.000 description 1
- ATRRKUHOCOJYRX-UHFFFAOYSA-N Ammonium bicarbonate Chemical compound [NH4+].OC([O-])=O ATRRKUHOCOJYRX-UHFFFAOYSA-N 0.000 description 1
- 239000004382 Amylase Substances 0.000 description 1
- 102000013142 Amylases Human genes 0.000 description 1
- 108010065511 Amylases Proteins 0.000 description 1
- COLNVLDHVKWLRT-QMMMGPOBSA-N L-phenylalanine Chemical compound OC(=O)[C@@H](N)CC1=CC=CC=C1 COLNVLDHVKWLRT-QMMMGPOBSA-N 0.000 description 1
- 244000076668 Mucuna gigantea Species 0.000 description 1
- 240000004713 Pisum sativum Species 0.000 description 1
- 235000010582 Pisum sativum Nutrition 0.000 description 1
- 235000003042 Salicornia europaea Nutrition 0.000 description 1
- 240000006677 Vicia faba Species 0.000 description 1
- 235000010749 Vicia faba Nutrition 0.000 description 1
- 235000002098 Vicia faba var. major Nutrition 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 239000001099 ammonium carbonate Substances 0.000 description 1
- 235000012501 ammonium carbonate Nutrition 0.000 description 1
- 235000019418 amylase Nutrition 0.000 description 1
- GWYFCOCPABKNJV-UHFFFAOYSA-N beta-methyl-butyric acid Natural products CC(C)CC(O)=O GWYFCOCPABKNJV-UHFFFAOYSA-N 0.000 description 1
- 238000005119 centrifugation Methods 0.000 description 1
- 238000005345 coagulation Methods 0.000 description 1
- 230000015271 coagulation Effects 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- ZPWVASYFFYYZEW-UHFFFAOYSA-L dipotassium hydrogen phosphate Chemical compound [K+].[K+].OP([O-])([O-])=O ZPWVASYFFYYZEW-UHFFFAOYSA-L 0.000 description 1
- 229910000396 dipotassium phosphate Inorganic materials 0.000 description 1
- 235000019797 dipotassium phosphate Nutrition 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 235000011194 food seasoning agent Nutrition 0.000 description 1
- BJHIKXHVCXFQLS-UYFOZJQFSA-N fructose group Chemical group OCC(=O)[C@@H](O)[C@H](O)[C@H](O)CO BJHIKXHVCXFQLS-UYFOZJQFSA-N 0.000 description 1
- 239000003456 ion exchange resin Substances 0.000 description 1
- 229920003303 ion-exchange polymer Polymers 0.000 description 1
- 229940035429 isobutyl alcohol Drugs 0.000 description 1
- 235000021332 kidney beans Nutrition 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 235000021590 normal diet Nutrition 0.000 description 1
- 235000016709 nutrition Nutrition 0.000 description 1
- 229960003424 phenylacetic acid Drugs 0.000 description 1
- 239000003279 phenylacetic acid Substances 0.000 description 1
- COLNVLDHVKWLRT-UHFFFAOYSA-N phenylalanine Natural products OC(=O)C(N)CC1=CC=CC=C1 COLNVLDHVKWLRT-UHFFFAOYSA-N 0.000 description 1
- 235000021110 pickles Nutrition 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
- 238000001556 precipitation Methods 0.000 description 1
- 230000035755 proliferation Effects 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 230000009711 regulatory function Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 150000005846 sugar alcohols Chemical class 0.000 description 1
- 238000011282 treatment Methods 0.000 description 1
- 230000004102 tricarboxylic acid cycle Effects 0.000 description 1
- 238000000108 ultra-filtration Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Distillation Of Fermentation Liquor, Processing Of Alcohols, Vinegar And Beer (AREA)
Abstract
Description
【0001】0001
【産業上の利用分野】本発明は、大豆に含まれる糖類を
抽出し、この中の発酵性糖類のみを酵母により資化させ
、酢酸発酵を行い、酸調味料としての機能に加えてガラ
クトオリゴ糖による腸内でのビフィズス菌増殖機能をも
同時に具備した生体調節機能を有するガラクトオリゴ糖
含有食酢及びその製造法に関する。[Industrial Application Field] The present invention extracts the sugars contained in soybeans, uses yeast to assimilate only the fermentable sugars, and performs acetic acid fermentation. The present invention relates to a galacto-oligosaccharide-containing vinegar having a bioregulatory function that also has a bifidobacteria growth function in the intestine, and a method for producing the same.
【0002】0002
【従来の技術】一般に食酢は、澱粉質を多く含有する穀
類を原料とし、この澱粉質を麹やアミラーゼ製剤で糖化
し、ついで酵母によるアルコール発酵を行い、更に酢酸
菌による酢酸発酵を行って製造されるものであって、そ
の食酢中にはガラクトオリゴ糖がほとんど含まれていな
い。[Prior Art] Vinegar is generally produced by using grains containing a lot of starch as raw materials, saccharifying this starch with koji or an amylase preparation, followed by alcohol fermentation with yeast, and then acetic acid fermentation with acetic acid bacteria. The vinegar contains almost no galactooligosaccharide.
【0003】0003
【発明が解決しようとする課題】前記従来の食酢は、調
味料又は漬物料等として用いられており、専ら嗜好には
適するけれども、エネルギー代謝改善機能以外の生体調
節機能以外は期待できなかった。即ち、腸内有用細菌で
あるビフィズス菌の増殖により生体調節機能が活性化す
ることが知られているが、従来の食酢にはそのような作
用が殆んどなかった。また、一般に澱粉質を多く含有す
る穀類を原料とし、これを糖化し、ついでアルコール発
酵させ、更に酢酸発酵させて食酢とした場合には、ガラ
クトオリゴ糖が殆んど含まれていなかった。[Problems to be Solved by the Invention] The above-mentioned conventional vinegar is used as a seasoning or a pickle, and although it is suitable for personal taste, it cannot be expected to have any biological regulation functions other than the function of improving energy metabolism. That is, it is known that the growth of bifidobacteria, which are useful bacteria in the intestines, activates biological regulatory functions, but conventional vinegar has almost no such effect. Furthermore, when vinegar is made from grains containing a large amount of starch, which is saccharified, then fermented with alcohol, and then fermented with acetic acid, it contains almost no galactooligosaccharide.
【0004】また、豆類にガラクトオリゴ糖が含まれて
いるけれども、豆類を粉砕してアルコール発酵を行って
も、殆んどアルコールの産生は認められないので、豆類
を直接加工して食酢を作ることはできなかった。[0004]Although beans contain galacto-oligosaccharides, almost no alcohol is produced even if beans are crushed and subjected to alcoholic fermentation, so it is difficult to make vinegar by directly processing beans. I couldn't.
【0005】[0005]
【課題を解決する為の手段】然るに本発明は、豆類から
糖を抽出し、これに含有する発酵性糖類のみをアルコー
ル発酵させ、ついで酢酸発酵して食酢を得たので、糖類
中のアルコール発酵しないガラクトオリゴ糖が含まれた
食酢となり、前記従来の問題点を解決したのである。[Means for Solving the Problems] However, in the present invention, sugar is extracted from beans, only the fermentable sugars contained therein are subjected to alcohol fermentation, and then acetic acid fermentation is performed to obtain vinegar. The resulting vinegar contains galactooligosaccharide, which solves the above-mentioned conventional problems.
【0006】即ち本発明は、酢酸酸度5%の食酢中に0
.5%〜10.0%のガラクトオリゴ糖を含有させるこ
とを特徴としたガラクトオリゴ糖含有食酢である。That is, the present invention provides 0.0
.. This is a galactooligosaccharide-containing vinegar characterized by containing 5% to 10.0% of galactooligosaccharides.
【0007】また他の発明は、発酵性糖類とガラクトオ
リゴ糖との混合物を酵母によりアルコール発酵させ、つ
いで酢酸発酵させて食酢とすることを特徴としたガラク
トオリゴ糖含有食酢である。次に、発酵性糖類をグルコ
ース、フラクトース、シュクロース、ラフィノース、ス
タキオースとしたものである。更に、ガラクトオリゴ糖
をメリビオース、マンニノトリオースとしたものである
。[0007] Another invention is a galactooligosaccharide-containing vinegar characterized in that a mixture of fermentable saccharides and galactooligosaccharides is subjected to alcohol fermentation using yeast, and then subjected to acetic acid fermentation to obtain vinegar. Next, the fermentable sugars are glucose, fructose, sucrose, raffinose, and stachyose. Furthermore, the galactooligosaccharides are melibiose and manninotriose.
【0008】また他の発明は、豆類の水性溶媒抽出物中
の発酵性糖類のみを、酵母により選択的にアルコール発
酵させ、ついで酢酸発酵させることを特徴としたガラク
トオリゴ糖含有食酢の製造法である。Another invention is a method for producing vinegar containing galactooligosaccharides, characterized in that only fermentable saccharides in an aqueous solvent extract of beans are selectively fermented with alcohol using yeast, and then fermented with acetic acid. .
【0009】前記におけるガラクトオリゴ糖の含有量を
0.5%以下にした場合には、生体調節機能が小さくな
り、10%以上にすると甘味が大きくなる為にに嗜好に
適しない。If the content of galacto-oligosaccharide is less than 0.5%, the bioregulatory function will be reduced, and if it is more than 10%, the sweetness will increase, making it unpalatable.
【0010】本発明には食酢の製造原料として豆類が使
用される。その種類はナタマメ、インゲンマメ、エンド
ウ、ソラマメ、大豆が考えられるが、酵母が資化しうる
、発酵性糖類と、非発酵性糖類との割合、及びその市場
における価格構成を考えた場合、大豆を原料とすること
が最も望ましい。In the present invention, beans are used as a raw material for producing vinegar. Possible types of such substances are sea beans, kidney beans, peas, broad beans, and soybeans, but considering the ratio of fermentable sugars and non-fermentable sugars that can be assimilated by yeast, and the price structure in the market, soybeans are considered to be the raw material. It is most desirable to do so.
【0011】まず大豆原料より水性溶媒にて遊離の糖を
抽出する。この抽出液中には糖類以外に可溶性窒素化合
物及び無機塩類が含まれる。前記可溶性窒素化合物が多
く含まれている場合には、アルコール発酵過程でイソア
ミルアルコール、プロピルアルコール、イソプチルアル
コール、プチルアルコール等の高級アルコールが産生さ
れやすく、更にこれらの高級アルコール類は酢酸発酵過
程によりイソ吉草酸、プロピオン酸、イソ酪酸、酪酸等
の脂肪酸に酸化される。またフェニルアラニンよりフェ
ニル酢酸も産生され、これらは全て不快臭成分として食
酢を官能的に嗜好性の著しく低いものとする。First, free sugars are extracted from soybean raw materials using an aqueous solvent. This extract contains soluble nitrogen compounds and inorganic salts in addition to sugars. When a large amount of the above-mentioned soluble nitrogen compounds are contained, higher alcohols such as isoamyl alcohol, propyl alcohol, isobutyl alcohol, and butyl alcohol are likely to be produced during the alcohol fermentation process, and furthermore, these higher alcohols are produced during the acetic acid fermentation process. Oxidized to fatty acids such as isovaleric acid, propionic acid, isobutyric acid, and butyric acid. Phenyl acetic acid is also produced from phenylalanine, and all of these are unpleasant odor components that make vinegar extremely unpalatable.
【0012】このような傾向から、糖抽出液中の窒素化
合物をできるだけ取り除く必要がある。そのため抽出液
は、まず加熱凝固沈澱をし、次いで電気透析、粒状活性
炭カラム、イオン交換樹脂などの処理を行う。[0012] From this tendency, it is necessary to remove nitrogen compounds from the sugar extract as much as possible. Therefore, the extract is first subjected to heat coagulation and precipitation, and then subjected to treatments such as electrodialysis, granular activated carbon column, and ion exchange resin.
【0013】窒素化合物の除去を行った抽出液は、アル
コール発酵に必要な糖濃度に調整する。アルコール発酵
は通常、糖固形分に対し、生酵母0.4%添加、27℃
〜30℃、72時間〜96時間の条件下で行われ、発酵
性糖類の大部分は酵母により資化され良質なアルコール
を得ることができる。次いで、醪中のアルコール濃度を
調整し酢酸菌を接種後、静置あるいは通気により酢酸発
酵を行う。The extract from which nitrogen compounds have been removed is adjusted to have a sugar concentration necessary for alcoholic fermentation. Alcoholic fermentation usually involves adding 0.4% live yeast to the sugar solids at 27°C.
The fermentation is carried out at ~30°C for 72 to 96 hours, and most of the fermentable saccharides are assimilated by yeast, making it possible to obtain high-quality alcohol. Next, after adjusting the alcohol concentration in the moromi and inoculating acetic acid bacteria, acetic acid fermentation is carried out by standing or aeration.
【0014】今、大豆原料中に含まれる遊離糖の、抽出
、精製、及び発酵終了時の各工程における糖組成推移を
食酢の酢酸濃度4.2%換算時の値で表すと表1の通り
となる。[0014] Table 1 shows the changes in sugar composition of free sugars contained in soybean raw materials in each step of extraction, purification, and completion of fermentation, expressed in terms of the acetic acid concentration of vinegar of 4.2%. becomes.
【0015】[0015]
【表1】[Table 1]
【0016】原料大豆中に含まれる遊離糖はシュクロー
スが主体で、次いでビフィズス菌増殖に有効なスタキオ
ース、ラフィノースがあるが、抽出、精製過程でシュク
ロースの一部が転化され、グルコース、及びフラクトー
スが生成する。また、酸性条件下では末端フラクトース
が加水分解されスタキオースはマンニノトリオースに、
ラフィノースはメリビオースに、それぞれ変化する傾向
が見られる。さらに発酵過程において、発酵性糖類の大
部分は資化され、グルコース、シュクロース、ラフィノ
ース、スタキオースは全く認められなくなる。この時、
その他の糖アルコールはほとんど変化を示さない。The free sugars contained in raw soybeans are mainly sucrose, followed by stachyose and raffinose, which are effective for the growth of bifidobacteria, but during the extraction and purification process, a part of sucrose is converted to glucose and fructose. is generated. In addition, under acidic conditions, terminal fructose is hydrolyzed and stachyose is converted to manninotriose.
Raffinose and melibiose each tend to change. Furthermore, during the fermentation process, most of the fermentable sugars are assimilated, and glucose, sucrose, raffinose, and stachyose are no longer observed. At this time,
Other sugar alcohols show almost no change.
【0017】以上の工程を経て、発酵性糖類は消失し、
非発酵性の糖類を多く含有する食酢が出来上がる。この
食酢は少量の活性炭処理によって酸刺激臭の少ない、香
気成分が改善された嗜好性の高いものとなり、かつ、ビ
フィズス菌増殖活性効果が著しい、生体調節機能を発揮
しうるものとなる。[0017] Through the above steps, fermentable sugars disappear,
Vinegar containing a large amount of non-fermentable sugars is produced. By treating this vinegar with a small amount of activated carbon, it becomes highly palatable with less acidic odor, improved aroma components, and has a remarkable effect on bifidobacterium proliferation and can exhibit biological regulation functions.
【0018】[0018]
【作用】ヒトにとって有用なビフィズス菌を腸内で増殖
させるためには、より選択的に資化される糖源を摂取す
ることが有効である。[Action] In order to proliferate Bifidobacterium useful to humans in the intestines, it is effective to ingest sugar sources that are more selectively assimilated.
【0019】今、その効果を、各種ヒト腸内細菌におけ
る資化性で比較した結果で示すと表2の通りとなる。Table 2 shows the results of a comparison of the assimilation ability of various human intestinal bacteria.
【0020】[0020]
【表2】[Table 2]
【0021】原料大豆中の遊離糖精製物はシュクロース
含量が高いため全ての菌に対し、資化性が認められる。
しかし、本発明食酢中の糖は一般的にビフィズス菌に、
より選択的に利用される。[0021] Since the purified free sugar in the raw soybean has a high sucrose content, it is assimilated by all bacteria. However, the sugar in the vinegar of the present invention generally inhibits bifidobacteria.
Used more selectively.
【0022】以下、本発明の実施例を詳細に述べる。Examples of the present invention will be described in detail below.
【0023】[0023]
【実施例1】脱脂大豆1kgに水10lを加え、60℃
加温下で水溶性物質の抽出を行い、これを95℃、15
分間加熱し冷却後、生じた熱凝固物を遠心分離にて除去
する。得られた清澄液を限外濾過膜にて分子量5000
以上の画分を除去し、次いで電気透析膜にて灰分の除去
、その後粒状活性炭カラムにて順次処理することによっ
て窒素成分や灰分をほとんど含まない糖95g(乾重)
が得られる。[Example 1] Add 10 liters of water to 1 kg of defatted soybeans at 60°C.
Water-soluble substances are extracted under heating, and this is heated at 95°C for 15 minutes.
After heating for a minute and cooling, the resulting thermal solidification is removed by centrifugation. The resulting clear liquid was filtered through an ultrafiltration membrane to a molecular weight of 5000.
The above fractions are removed, ash is removed using an electrodialysis membrane, and 95g (dry weight) of sugar, which contains almost no nitrogen or ash, is processed in sequence using a granular activated carbon column.
is obtained.
【0024】以上の工程で得られた糖760g(乾重)
を濃度23%に調整し酵母の栄養源として炭酸アンモニ
ウム3g、リン酸2カリウム1.5g、硫酸マグネシウ
ム0.15gを加える。pHを6.0に調整し生酵母4
.0gを添加後30℃、4日間発酵を行って9.5%ア
ルコール3.0lを得る。[0024] 760g of sugar (dry weight) obtained through the above steps
The concentration was adjusted to 23%, and 3 g of ammonium carbonate, 1.5 g of dipotassium phosphate, and 0.15 g of magnesium sulfate were added as nutritional sources for the yeast. Adjust the pH to 6.0 and add live yeast 4
.. After adding 0g, fermentation was carried out at 30°C for 4 days to obtain 3.0L of 9.5% alcohol.
【0025】このアルコール1lに本発明による7.5
%食酢420mlを加え、全量を1.58lとし、アル
コール濃度6%、初酸2%の醪を調製する。これに酢酸
菌を接種し、温度30℃、通気量150ml/min、
750rpm で72時間通気発酵を行い、7.5%酢
1.58lを得る。この酢に粉末活性炭0.12gを添
加し、その後清澄濾過、酸度調製を行う。以上の工程に
より4.2%酢、2.82lが得られる。[0025] 7.5% according to the present invention is added to 1 liter of this alcohol.
Add 420 ml of % table vinegar to bring the total volume to 1.58 liters to prepare moromi with an alcohol concentration of 6% and initial acid of 2%. This was inoculated with acetic acid bacteria, the temperature was 30℃, the aeration rate was 150ml/min,
Aerated fermentation was carried out at 750 rpm for 72 hours to obtain 1.58 liters of 7.5% vinegar. 0.12 g of powdered activated carbon is added to this vinegar, followed by clarifying filtration and acidity adjustment. Through the above steps, 2.82 liters of 4.2% vinegar is obtained.
【0026】[0026]
【実施例2】実施例1に準じて調製されたアルコール1
lに本発明による7.5%食酢250mlを加え全量を
1.9lとし、アルコール5%、初酸1%の醪を調整す
る。この液面に酢酸菌菌膜を浮遊させ30℃、7日間静
置発酵を行い、5.2%酢1.90lを得る。この酢に
粉末活性炭0.1gを添加し、その後清澄濾過、酸度調
整を行う。以上の工程により4.2%酢2.35lが得
られる。[Example 2] Alcohol 1 prepared according to Example 1
Add 250 ml of 7.5% vinegar according to the present invention to 1 to make a total volume of 1.9 liters, and prepare moromi with 5% alcohol and 1% primary acid. A film of acetic acid bacteria was suspended on the surface of the liquid, and static fermentation was performed at 30°C for 7 days to obtain 1.90 liters of 5.2% vinegar. 0.1 g of powdered activated carbon is added to this vinegar, followed by clarifying filtration and acidity adjustment. Through the above steps, 2.35 liters of 4.2% vinegar is obtained.
【0027】[0027]
【発明の効果】食酢は本来健康によいとされているが、
これはクレブスサイクルを速く回転させエネルギー代謝
を円滑にするためと言われている。本発明では腸内フロ
ーラを改善するのに有効な糖を多く含んだ食酢として、
1日20ccを通常の食生活を通して摂取することによ
り、さらに健康の維持、増進に役立つものとその効果を
期待される。[Effect of the invention] Vinegar is said to be originally good for health, but
This is said to speed up the Krebs cycle and smoothen energy metabolism. In the present invention, as vinegar containing a lot of sugar that is effective for improving intestinal flora,
By ingesting 20 cc per day through a normal diet, it is expected that it will be more helpful and effective in maintaining and improving health.
【0028】また、本発明の食酢(酢酸濃度4.2%)
を1日20cc一週間続けて5名の人に摂取してもらっ
た結果、腸内フローラに占めるビフィズス菌の比率が、
平均8.5%から29.2%に向上した。本発明の食酢
20ccに含まれる糖は約1.2gである。この結果か
ら見ても本発明による食酢のビフィズス菌増殖効果は著
しいものと言える。[0028] Also, the vinegar of the present invention (acetic acid concentration 4.2%)
As a result of having 5 people ingest 20cc per day for one week, the proportion of bifidobacteria in the intestinal flora was
This improved from an average of 8.5% to 29.2%. The sugar contained in 20 cc of the vinegar of the present invention is about 1.2 g. Judging from these results, it can be said that the vinegar according to the present invention has a remarkable effect on the growth of bifidobacteria.
Claims (6)
0.0%のガラクトオリゴ糖を含有させることを特徴と
したガラクトオリゴ糖含有食酢[Claim 1] 0.5% to 1% in vinegar with acetic acid acidity of 5%
Galactooligosaccharide-containing vinegar characterized by containing 0.0% galactooligosaccharide
合物を酵母によりアルコール発酵させ、ついで酢酸発酵
させて食酢とすることを特徴としたガラクトオリゴ糖含
有食酢[Claim 2] Galactooligosaccharide-containing vinegar, characterized in that a mixture of fermentable sugars and galactooligosaccharides is subjected to alcoholic fermentation using yeast, and then subjected to acetic acid fermentation to obtain vinegar.
ンニノトリオースとした請求項1又は2記載のガラクト
オリゴ糖含有食酢3. The galactooligosaccharide-containing vinegar according to claim 1 or 2, wherein the galactooligosaccharide is melibiose or manninotriose.
ス、シュクロース、ラフィノース、スタキオースとした
請求項2記載のガラクトオリゴ糖含有食酢4. The galactooligosaccharide-containing vinegar according to claim 2, wherein the fermentable saccharide is glucose, fructose, sucrose, raffinose, or stachyose.
豆類の水性溶媒抽出物中の発酵性糖類のみを、酵母
により選択的にアルコール発酵させ、ついで酢酸発酵さ
せることを特徴としたガラクトオリゴ糖含有食酢の製造
法[Claim 5]
A method for producing vinegar containing galactooligosaccharides, characterized in that only fermentable saccharides in an aqueous solvent extract of beans are selectively fermented with alcohol using yeast, and then fermented with acetic acid.
ス、シュクロース、ラフィノース、スタキオースとした
請求項5記載のガラクトオリゴ糖含有食酢の製造法6. The method for producing vinegar containing galactooligosaccharides according to claim 5, wherein the fermentable saccharide is glucose, fructose, sucrose, raffinose, or stachyose.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2411217A JPH04218362A (en) | 1990-12-17 | 1990-12-17 | Food vinegar containing galactooligosaccharide and its preparation |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2411217A JPH04218362A (en) | 1990-12-17 | 1990-12-17 | Food vinegar containing galactooligosaccharide and its preparation |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH04218362A true JPH04218362A (en) | 1992-08-07 |
Family
ID=18520255
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2411217A Pending JPH04218362A (en) | 1990-12-17 | 1990-12-17 | Food vinegar containing galactooligosaccharide and its preparation |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH04218362A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2008117609A1 (en) * | 2007-03-26 | 2008-10-02 | Mizkan Group Corporation | Process for producing vinegar and vinegar produced by this method |
US7754701B2 (en) | 2002-04-26 | 2010-07-13 | Fancl Corporation | Difructose anhydride-containing composition and use thereof |
JP2012521751A (en) * | 2009-03-27 | 2012-09-20 | デルバエレ,フランシャス | Water-soluble extract of defructosylated pea and its use as a prebiotic substance |
EP3755153A4 (en) * | 2018-02-20 | 2021-11-24 | Kerry Luxembourg S.a.r.l. | BUFFERED VINEGAR PRODUCTS WITH REDUCTION OF COLOR, SMELL AND TASTE AND THE PROCESS FOR THEIR PRODUCTION |
-
1990
- 1990-12-17 JP JP2411217A patent/JPH04218362A/en active Pending
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7754701B2 (en) | 2002-04-26 | 2010-07-13 | Fancl Corporation | Difructose anhydride-containing composition and use thereof |
US7964581B2 (en) | 2002-04-26 | 2011-06-21 | Fancl Corporation | Use of difructose anhydride-containing composition |
US8492363B2 (en) | 2002-04-26 | 2013-07-23 | Fancl Corporation | Use of difructose anhydride-containing composition |
WO2008117609A1 (en) * | 2007-03-26 | 2008-10-02 | Mizkan Group Corporation | Process for producing vinegar and vinegar produced by this method |
JP2008237040A (en) * | 2007-03-26 | 2008-10-09 | Mitsukan Group Honsha:Kk | Method for producing vinegar and vinegar produced by the method |
GB2460001A (en) * | 2007-03-26 | 2009-11-18 | Mizkan Group Corp | Process for producing vinegar and vinegar produced by this method |
JP2012521751A (en) * | 2009-03-27 | 2012-09-20 | デルバエレ,フランシャス | Water-soluble extract of defructosylated pea and its use as a prebiotic substance |
US9017741B2 (en) | 2009-03-27 | 2015-04-28 | Olygose | Water soluble defructosylated pea extract, and use thereof as a prebiotic agent |
US10258659B2 (en) | 2009-03-27 | 2019-04-16 | Olygose | Water soluble defructosylated pea extract, and use thereof as a prebiotic agent |
EP3755153A4 (en) * | 2018-02-20 | 2021-11-24 | Kerry Luxembourg S.a.r.l. | BUFFERED VINEGAR PRODUCTS WITH REDUCTION OF COLOR, SMELL AND TASTE AND THE PROCESS FOR THEIR PRODUCTION |
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