KR20230096680A - Bread Containing Buckwheat and Kelp Ingredient, and Method for Manufacturing the Same - Google Patents
Bread Containing Buckwheat and Kelp Ingredient, and Method for Manufacturing the Same Download PDFInfo
- Publication number
- KR20230096680A KR20230096680A KR1020210186406A KR20210186406A KR20230096680A KR 20230096680 A KR20230096680 A KR 20230096680A KR 1020210186406 A KR1020210186406 A KR 1020210186406A KR 20210186406 A KR20210186406 A KR 20210186406A KR 20230096680 A KR20230096680 A KR 20230096680A
- Authority
- KR
- South Korea
- Prior art keywords
- weight
- water
- buckwheat
- parts
- bread
- Prior art date
Links
- 235000009419 Fagopyrum esculentum Nutrition 0.000 title claims abstract description 87
- 235000008429 bread Nutrition 0.000 title claims abstract description 79
- 241000512259 Ascophyllum nodosum Species 0.000 title claims abstract description 43
- 238000000034 method Methods 0.000 title claims abstract description 20
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 18
- 239000004615 ingredient Substances 0.000 title description 7
- 240000008620 Fagopyrum esculentum Species 0.000 title 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 88
- 241000219051 Fagopyrum Species 0.000 claims abstract description 87
- 239000000284 extract Substances 0.000 claims abstract description 25
- 239000000843 powder Substances 0.000 claims description 48
- 235000013339 cereals Nutrition 0.000 claims description 41
- 108090000790 Enzymes Proteins 0.000 claims description 39
- 102000004190 Enzymes Human genes 0.000 claims description 39
- 235000013312 flour Nutrition 0.000 claims description 33
- 238000000855 fermentation Methods 0.000 claims description 26
- 230000004151 fermentation Effects 0.000 claims description 26
- 240000004808 Saccharomyces cerevisiae Species 0.000 claims description 22
- UFVKGYZPFZQRLF-UHFFFAOYSA-N hydroxypropyl methyl cellulose Chemical compound OC1C(O)C(OC)OC(CO)C1OC1C(O)C(O)C(OC2C(C(O)C(OC3C(C(O)C(O)C(CO)O3)O)C(CO)O2)O)C(CO)O1 UFVKGYZPFZQRLF-UHFFFAOYSA-N 0.000 claims description 22
- 239000001866 hydroxypropyl methyl cellulose Substances 0.000 claims description 21
- 235000010979 hydroxypropyl methyl cellulose Nutrition 0.000 claims description 21
- 229920003088 hydroxypropyl methyl cellulose Polymers 0.000 claims description 21
- 241000209140 Triticum Species 0.000 claims description 17
- 235000021307 Triticum Nutrition 0.000 claims description 17
- 239000002609 medium Substances 0.000 claims description 12
- 238000002156 mixing Methods 0.000 claims description 12
- 150000003839 salts Chemical class 0.000 claims description 11
- 235000020183 skimmed milk Nutrition 0.000 claims description 11
- 238000001035 drying Methods 0.000 claims description 10
- 238000004898 kneading Methods 0.000 claims description 10
- 235000000346 sugar Nutrition 0.000 claims description 9
- 241000228212 Aspergillus Species 0.000 claims description 8
- 235000013601 eggs Nutrition 0.000 claims description 8
- 239000001963 growth medium Substances 0.000 claims description 8
- -1 hydroxypropoxy group Chemical group 0.000 claims description 8
- 239000011812 mixed powder Substances 0.000 claims description 8
- 229920002472 Starch Polymers 0.000 claims description 7
- 235000014121 butter Nutrition 0.000 claims description 7
- 235000015097 nutrients Nutrition 0.000 claims description 7
- 238000010298 pulverizing process Methods 0.000 claims description 7
- 235000019698 starch Nutrition 0.000 claims description 7
- 239000008107 starch Substances 0.000 claims description 7
- 238000012258 culturing Methods 0.000 claims description 6
- 238000010438 heat treatment Methods 0.000 claims description 6
- 239000003651 drinking water Substances 0.000 claims description 5
- 235000020188 drinking water Nutrition 0.000 claims description 5
- 238000001914 filtration Methods 0.000 claims description 5
- 240000007594 Oryza sativa Species 0.000 claims description 4
- 235000007164 Oryza sativa Nutrition 0.000 claims description 4
- 235000009566 rice Nutrition 0.000 claims description 4
- 238000006467 substitution reaction Methods 0.000 claims description 4
- 238000005406 washing Methods 0.000 claims description 4
- 244000068988 Glycine max Species 0.000 claims description 3
- 235000010469 Glycine max Nutrition 0.000 claims description 3
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 3
- 235000015099 wheat brans Nutrition 0.000 claims description 3
- 238000007872 degassing Methods 0.000 claims description 2
- 230000001954 sterilising effect Effects 0.000 claims description 2
- 238000000227 grinding Methods 0.000 claims 1
- 238000011534 incubation Methods 0.000 claims 1
- 239000000725 suspension Substances 0.000 claims 1
- 230000003078 antioxidant effect Effects 0.000 abstract description 15
- 210000000813 small intestine Anatomy 0.000 abstract description 14
- 230000000694 effects Effects 0.000 abstract description 9
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract description 8
- 201000010099 disease Diseases 0.000 abstract description 7
- 230000036541 health Effects 0.000 abstract description 6
- 230000009286 beneficial effect Effects 0.000 abstract description 4
- 210000002249 digestive system Anatomy 0.000 abstract description 3
- 229940088598 enzyme Drugs 0.000 description 36
- 235000014680 Saccharomyces cerevisiae Nutrition 0.000 description 18
- 230000000052 comparative effect Effects 0.000 description 15
- 235000013305 food Nutrition 0.000 description 9
- 239000003963 antioxidant agent Substances 0.000 description 8
- 235000006708 antioxidants Nutrition 0.000 description 8
- 239000000243 solution Substances 0.000 description 8
- 238000012360 testing method Methods 0.000 description 8
- 239000000203 mixture Substances 0.000 description 7
- 239000000047 product Substances 0.000 description 7
- 102000004169 proteins and genes Human genes 0.000 description 7
- 108090000623 proteins and genes Proteins 0.000 description 7
- 108010068370 Glutens Proteins 0.000 description 6
- 235000013325 dietary fiber Nutrition 0.000 description 6
- 241000894007 species Species 0.000 description 6
- 210000002784 stomach Anatomy 0.000 description 6
- 229920001817 Agar Polymers 0.000 description 5
- 239000008272 agar Substances 0.000 description 5
- 239000011248 coating agent Substances 0.000 description 5
- 238000000576 coating method Methods 0.000 description 5
- 238000004090 dissolution Methods 0.000 description 5
- 238000000605 extraction Methods 0.000 description 5
- 239000000499 gel Substances 0.000 description 5
- 229910052500 inorganic mineral Inorganic materials 0.000 description 5
- 239000011707 mineral Substances 0.000 description 5
- 240000006439 Aspergillus oryzae Species 0.000 description 4
- 235000002247 Aspergillus oryzae Nutrition 0.000 description 4
- JMGZEFIQIZZSBH-UHFFFAOYSA-N Bioquercetin Natural products CC1OC(OCC(O)C2OC(OC3=C(Oc4cc(O)cc(O)c4C3=O)c5ccc(O)c(O)c5)C(O)C2O)C(O)C(O)C1O JMGZEFIQIZZSBH-UHFFFAOYSA-N 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- IVTMALDHFAHOGL-UHFFFAOYSA-N eriodictyol 7-O-rutinoside Natural products OC1C(O)C(O)C(C)OC1OCC1C(O)C(O)C(O)C(OC=2C=C3C(C(C(O)=C(O3)C=3C=C(O)C(O)=CC=3)=O)=C(O)C=2)O1 IVTMALDHFAHOGL-UHFFFAOYSA-N 0.000 description 4
- 229930003935 flavonoid Natural products 0.000 description 4
- 150000002215 flavonoids Chemical class 0.000 description 4
- 235000017173 flavonoids Nutrition 0.000 description 4
- 235000021312 gluten Nutrition 0.000 description 4
- FDRQPMVGJOQVTL-UHFFFAOYSA-N quercetin rutinoside Natural products OC1C(O)C(O)C(CO)OC1OCC1C(O)C(O)C(O)C(OC=2C(C3=C(O)C=C(O)C=C3OC=2C=2C=C(O)C(O)=CC=2)=O)O1 FDRQPMVGJOQVTL-UHFFFAOYSA-N 0.000 description 4
- 235000005493 rutin Nutrition 0.000 description 4
- ALABRVAAKCSLSC-UHFFFAOYSA-N rutin Natural products CC1OC(OCC2OC(O)C(O)C(O)C2O)C(O)C(O)C1OC3=C(Oc4cc(O)cc(O)c4C3=O)c5ccc(O)c(O)c5 ALABRVAAKCSLSC-UHFFFAOYSA-N 0.000 description 4
- IKGXIBQEEMLURG-BKUODXTLSA-N rutin Chemical compound O[C@H]1[C@H](O)[C@@H](O)[C@H](C)O[C@@H]1OC[C@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](OC=2C(C3=C(O)C=C(O)C=C3OC=2C=2C=C(O)C(O)=CC=2)=O)O1 IKGXIBQEEMLURG-BKUODXTLSA-N 0.000 description 4
- 229960004555 rutoside Drugs 0.000 description 4
- 229940088594 vitamin Drugs 0.000 description 4
- 229930003231 vitamin Natural products 0.000 description 4
- 235000013343 vitamin Nutrition 0.000 description 4
- 239000011782 vitamin Substances 0.000 description 4
- 239000002253 acid Substances 0.000 description 3
- 235000005911 diet Nutrition 0.000 description 3
- 239000000796 flavoring agent Substances 0.000 description 3
- 235000019634 flavors Nutrition 0.000 description 3
- 230000002538 fungal effect Effects 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 230000003647 oxidation Effects 0.000 description 3
- 238000007254 oxidation reaction Methods 0.000 description 3
- 230000036542 oxidative stress Effects 0.000 description 3
- 235000018102 proteins Nutrition 0.000 description 3
- 150000003254 radicals Chemical class 0.000 description 3
- 239000008223 sterile water Substances 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- 150000003722 vitamin derivatives Chemical class 0.000 description 3
- GVJHHUAWPYXKBD-UHFFFAOYSA-N (±)-α-Tocopherol Chemical compound OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-UHFFFAOYSA-N 0.000 description 2
- XUDNWQSXPROHLK-OACYRQNASA-N 2-phenyl-3-[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1OC1=C(C=2C=CC=CC=2)OC2=CC=CC=C2C1=O XUDNWQSXPROHLK-OACYRQNASA-N 0.000 description 2
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 2
- 244000298479 Cichorium intybus Species 0.000 description 2
- 235000007542 Cichorium intybus Nutrition 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 102000035195 Peptidases Human genes 0.000 description 2
- 108091005804 Peptidases Proteins 0.000 description 2
- REFJWTPEDVJJIY-UHFFFAOYSA-N Quercetin Chemical compound C=1C(O)=CC(O)=C(C(C=2O)=O)C=1OC=2C1=CC=C(O)C(O)=C1 REFJWTPEDVJJIY-UHFFFAOYSA-N 0.000 description 2
- 235000021355 Stearic acid Nutrition 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 230000032683 aging Effects 0.000 description 2
- 235000021329 brown rice Nutrition 0.000 description 2
- 229940041514 candida albicans extract Drugs 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 206010012601 diabetes mellitus Diseases 0.000 description 2
- 230000000378 dietary effect Effects 0.000 description 2
- 230000029087 digestion Effects 0.000 description 2
- HHEAADYXPMHMCT-UHFFFAOYSA-N dpph Chemical compound [O-][N+](=O)C1=CC([N+](=O)[O-])=CC([N+]([O-])=O)=C1[N]N(C=1C=CC=CC=1)C1=CC=CC=C1 HHEAADYXPMHMCT-UHFFFAOYSA-N 0.000 description 2
- 239000000706 filtrate Substances 0.000 description 2
- OVBPIULPVIDEAO-LBPRGKRZSA-N folic acid Chemical compound C=1N=C2NC(N)=NC(=O)C2=NC=1CNC1=CC=C(C(=O)N[C@@H](CCC(O)=O)C(O)=O)C=C1 OVBPIULPVIDEAO-LBPRGKRZSA-N 0.000 description 2
- 230000006870 function Effects 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 230000004060 metabolic process Effects 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 235000016709 nutrition Nutrition 0.000 description 2
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 2
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 239000008213 purified water Substances 0.000 description 2
- LXNHXLLTXMVWPM-UHFFFAOYSA-N pyridoxine Chemical compound CC1=NC=C(CO)C(CO)=C1O LXNHXLLTXMVWPM-UHFFFAOYSA-N 0.000 description 2
- 230000001953 sensory effect Effects 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000008117 stearic acid Substances 0.000 description 2
- 239000012138 yeast extract Substances 0.000 description 2
- OYHQOLUKZRVURQ-NTGFUMLPSA-N (9Z,12Z)-9,10,12,13-tetratritiooctadeca-9,12-dienoic acid Chemical compound C(CCCCCCC\C(=C(/C\C(=C(/CCCCC)\[3H])\[3H])\[3H])\[3H])(=O)O OYHQOLUKZRVURQ-NTGFUMLPSA-N 0.000 description 1
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- FPIPGXGPPPQFEQ-UHFFFAOYSA-N 13-cis retinol Natural products OCC=C(C)C=CC=C(C)C=CC1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-UHFFFAOYSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- 108010088751 Albumins Proteins 0.000 description 1
- 102000009027 Albumins Human genes 0.000 description 1
- 241000894006 Bacteria Species 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 244000206911 Candida holmii Species 0.000 description 1
- 235000002965 Candida holmii Nutrition 0.000 description 1
- AUNGANRZJHBGPY-UHFFFAOYSA-N D-Lyxoflavin Natural products OCC(O)C(O)C(O)CN1C=2C=C(C)C(C)=CC=2N=C2C1=NC(=O)NC2=O AUNGANRZJHBGPY-UHFFFAOYSA-N 0.000 description 1
- ZZZCUOFIHGPKAK-UHFFFAOYSA-N D-erythro-ascorbic acid Natural products OCC1OC(=O)C(O)=C1O ZZZCUOFIHGPKAK-UHFFFAOYSA-N 0.000 description 1
- 229920000855 Fucoidan Polymers 0.000 description 1
- 108010044091 Globulins Proteins 0.000 description 1
- 102000006395 Globulins Human genes 0.000 description 1
- 206010019233 Headaches Diseases 0.000 description 1
- OVSQVDMCBVZWGM-IDRAQACASA-N Hirsutrin Natural products O([C@H]1[C@H](O)[C@H](O)[C@H](O)[C@@H](CO)O1)C1=C(c2cc(O)c(O)cc2)Oc2c(c(O)cc(O)c2)C1=O OVSQVDMCBVZWGM-IDRAQACASA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- FVQOMEDMFUMIMO-UHFFFAOYSA-N Hyperosid Natural products OC1C(O)C(O)C(CO)OC1OC1C(=O)C2=C(O)C=C(O)C=C2OC1C1=CC=C(O)C(O)=C1 FVQOMEDMFUMIMO-UHFFFAOYSA-N 0.000 description 1
- 206010020772 Hypertension Diseases 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 229920001543 Laminarin Polymers 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- OVBPIULPVIDEAO-UHFFFAOYSA-N N-Pteroyl-L-glutaminsaeure Natural products C=1N=C2NC(N)=NC(=O)C2=NC=1CNC1=CC=C(C(=O)NC(CCC(O)=O)C(O)=O)C=C1 OVBPIULPVIDEAO-UHFFFAOYSA-N 0.000 description 1
- GXCLVBGFBYZDAG-UHFFFAOYSA-N N-[2-(1H-indol-3-yl)ethyl]-N-methylprop-2-en-1-amine Chemical compound CN(CCC1=CNC2=C1C=CC=C2)CC=C GXCLVBGFBYZDAG-UHFFFAOYSA-N 0.000 description 1
- PVNIIMVLHYAWGP-UHFFFAOYSA-N Niacin Chemical compound OC(=O)C1=CC=CN=C1 PVNIIMVLHYAWGP-UHFFFAOYSA-N 0.000 description 1
- 208000001140 Night Blindness Diseases 0.000 description 1
- 208000008589 Obesity Diseases 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- 235000021314 Palmitic acid Nutrition 0.000 description 1
- 239000001888 Peptone Substances 0.000 description 1
- 108010080698 Peptones Proteins 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 206010037394 Pulmonary haemorrhage Diseases 0.000 description 1
- ZVOLCUVKHLEPEV-UHFFFAOYSA-N Quercetagetin Natural products C1=C(O)C(O)=CC=C1C1=C(O)C(=O)C2=C(O)C(O)=C(O)C=C2O1 ZVOLCUVKHLEPEV-UHFFFAOYSA-N 0.000 description 1
- LUJAXSNNYBCFEE-UHFFFAOYSA-N Quercetin 3,7-dimethyl ether Natural products C=1C(OC)=CC(O)=C(C(C=2OC)=O)C=1OC=2C1=CC=C(O)C(O)=C1 LUJAXSNNYBCFEE-UHFFFAOYSA-N 0.000 description 1
- PUTDIROJWHRSJW-UHFFFAOYSA-N Quercitrin Natural products CC1OC(Oc2cc(cc(O)c2O)C3=CC(=O)c4c(O)cc(O)cc4O3)C(O)C(O)C1O PUTDIROJWHRSJW-UHFFFAOYSA-N 0.000 description 1
- 230000002292 Radical scavenging effect Effects 0.000 description 1
- HWTZYBCRDDUBJY-UHFFFAOYSA-N Rhynchosin Natural products C1=C(O)C(O)=CC=C1C1=C(O)C(=O)C2=CC(O)=C(O)C=C2O1 HWTZYBCRDDUBJY-UHFFFAOYSA-N 0.000 description 1
- AUNGANRZJHBGPY-SCRDCRAPSA-N Riboflavin Chemical compound OC[C@@H](O)[C@@H](O)[C@@H](O)CN1C=2C=C(C)C(C)=CC=2N=C2C1=NC(=O)NC2=O AUNGANRZJHBGPY-SCRDCRAPSA-N 0.000 description 1
- 241000235070 Saccharomyces Species 0.000 description 1
- 241000582914 Saccharomyces uvarum Species 0.000 description 1
- 241000970946 Streptomyces inusitatus Species 0.000 description 1
- AUYYCJSJGJYCDS-LBPRGKRZSA-N Thyrolar Chemical class IC1=CC(C[C@H](N)C(O)=O)=CC(I)=C1OC1=CC=C(O)C(I)=C1 AUYYCJSJGJYCDS-LBPRGKRZSA-N 0.000 description 1
- FPIPGXGPPPQFEQ-BOOMUCAASA-N Vitamin A Natural products OC/C=C(/C)\C=C\C=C(\C)/C=C/C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-BOOMUCAASA-N 0.000 description 1
- 229930003451 Vitamin B1 Natural products 0.000 description 1
- 229930003471 Vitamin B2 Natural products 0.000 description 1
- 229930003268 Vitamin C Natural products 0.000 description 1
- 229930003427 Vitamin E Natural products 0.000 description 1
- 241000607479 Yersinia pestis Species 0.000 description 1
- 238000002835 absorbance Methods 0.000 description 1
- OXGUCUVFOIWWQJ-XIMSSLRFSA-N acanthophorin B Natural products O[C@H]1[C@H](O)[C@H](O)[C@H](C)O[C@H]1OC1=C(C=2C=C(O)C(O)=CC=2)OC2=CC(O)=CC(O)=C2C1=O OXGUCUVFOIWWQJ-XIMSSLRFSA-N 0.000 description 1
- 238000005903 acid hydrolysis reaction Methods 0.000 description 1
- 229920001284 acidic polysaccharide Polymers 0.000 description 1
- 150000004805 acidic polysaccharides Chemical class 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 239000000783 alginic acid Substances 0.000 description 1
- 235000010443 alginic acid Nutrition 0.000 description 1
- 229920000615 alginic acid Polymers 0.000 description 1
- 229960001126 alginic acid Drugs 0.000 description 1
- 150000004781 alginic acids Chemical class 0.000 description 1
- FPIPGXGPPPQFEQ-OVSJKPMPSA-N all-trans-retinol Chemical compound OC\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-OVSJKPMPSA-N 0.000 description 1
- 102000004139 alpha-Amylases Human genes 0.000 description 1
- 108090000637 alpha-Amylases Proteins 0.000 description 1
- 229940024171 alpha-amylase Drugs 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 230000003110 anti-inflammatory effect Effects 0.000 description 1
- 230000006851 antioxidant defense Effects 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 230000001164 bioregulatory effect Effects 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- FAPWYRCQGJNNSJ-UBKPKTQASA-L calcium D-pantothenic acid Chemical compound [Ca+2].OCC(C)(C)[C@@H](O)C(=O)NCCC([O-])=O.OCC(C)(C)[C@@H](O)C(=O)NCCC([O-])=O FAPWYRCQGJNNSJ-UBKPKTQASA-L 0.000 description 1
- 229960002079 calcium pantothenate Drugs 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 238000005119 centrifugation Methods 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 230000001055 chewing effect Effects 0.000 description 1
- WIIZWVCIJKGZOK-RKDXNWHRSA-N chloramphenicol Chemical compound ClC(Cl)C(=O)N[C@H](CO)[C@H](O)C1=CC=C([N+]([O-])=O)C=C1 WIIZWVCIJKGZOK-RKDXNWHRSA-N 0.000 description 1
- 229960005091 chloramphenicol Drugs 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000012669 compression test Methods 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 235000009508 confectionery Nutrition 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 238000010411 cooking Methods 0.000 description 1
- 230000002542 deteriorative effect Effects 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- BIXZHMJUSMUDOQ-UHFFFAOYSA-N dichloran Chemical compound NC1=C(Cl)C=C([N+]([O-])=O)C=C1Cl BIXZHMJUSMUDOQ-UHFFFAOYSA-N 0.000 description 1
- 230000037213 diet Effects 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 230000001079 digestive effect Effects 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- MGJZITXUQXWAKY-UHFFFAOYSA-N diphenyl-(2,4,6-trinitrophenyl)iminoazanium Chemical compound [O-][N+](=O)C1=CC([N+](=O)[O-])=CC([N+]([O-])=O)=C1N=[N+](C=1C=CC=CC=1)C1=CC=CC=C1 MGJZITXUQXWAKY-UHFFFAOYSA-N 0.000 description 1
- 230000006806 disease prevention Effects 0.000 description 1
- 208000035475 disorder Diseases 0.000 description 1
- 210000001198 duodenum Anatomy 0.000 description 1
- 230000003628 erosive effect Effects 0.000 description 1
- 235000020776 essential amino acid Nutrition 0.000 description 1
- 239000003797 essential amino acid Substances 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000003337 fertilizer Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 229960000304 folic acid Drugs 0.000 description 1
- 235000019152 folic acid Nutrition 0.000 description 1
- 239000011724 folic acid Substances 0.000 description 1
- 238000004108 freeze drying Methods 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- WIGCFUFOHFEKBI-UHFFFAOYSA-N gamma-tocopherol Natural products CC(C)CCCC(C)CCCC(C)CCCC1CCC2C(C)C(O)C(C)C(C)C2O1 WIGCFUFOHFEKBI-UHFFFAOYSA-N 0.000 description 1
- 210000004211 gastric acid Anatomy 0.000 description 1
- 210000004051 gastric juice Anatomy 0.000 description 1
- 210000001035 gastrointestinal tract Anatomy 0.000 description 1
- 238000001879 gelation Methods 0.000 description 1
- 229930182470 glycoside Natural products 0.000 description 1
- 150000002338 glycosides Chemical class 0.000 description 1
- 230000009931 harmful effect Effects 0.000 description 1
- 231100000869 headache Toxicity 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 238000011081 inoculation Methods 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 229960003284 iron Drugs 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- OVSQVDMCBVZWGM-QCKGUQPXSA-N isoquercetin Natural products OC[C@@H]1O[C@@H](OC2=C(Oc3cc(O)cc(O)c3C2=O)c4ccc(O)c(O)c4)[C@H](O)[C@@H](O)[C@@H]1O OVSQVDMCBVZWGM-QCKGUQPXSA-N 0.000 description 1
- MWDZOUNAPSSOEL-UHFFFAOYSA-N kaempferol Natural products OC1=C(C(=O)c2cc(O)cc(O)c2O1)c3ccc(O)cc3 MWDZOUNAPSSOEL-UHFFFAOYSA-N 0.000 description 1
- DBTMGCOVALSLOR-VPNXCSTESA-N laminarin Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)OC1O[C@@H]1[C@@H](O)C(O[C@H]2[C@@H]([C@@H](CO)OC(O)[C@@H]2O)O)O[C@H](CO)[C@H]1O DBTMGCOVALSLOR-VPNXCSTESA-N 0.000 description 1
- 230000031700 light absorption Effects 0.000 description 1
- 150000002632 lipids Chemical class 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000002075 main ingredient Substances 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 230000007721 medicinal effect Effects 0.000 description 1
- 230000000813 microbial effect Effects 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- 239000005445 natural material Substances 0.000 description 1
- 229930014626 natural product Natural products 0.000 description 1
- 229960003512 nicotinic acid Drugs 0.000 description 1
- 235000001968 nicotinic acid Nutrition 0.000 description 1
- 239000011664 nicotinic acid Substances 0.000 description 1
- 231100000344 non-irritating Toxicity 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 235000012149 noodles Nutrition 0.000 description 1
- 230000035764 nutrition Effects 0.000 description 1
- 235000020824 obesity Nutrition 0.000 description 1
- 230000009965 odorless effect Effects 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 235000021313 oleic acid Nutrition 0.000 description 1
- 230000004792 oxidative damage Effects 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 235000019319 peptone Nutrition 0.000 description 1
- 239000000575 pesticide Substances 0.000 description 1
- 230000000144 pharmacologic effect Effects 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 150000008442 polyphenolic compounds Chemical class 0.000 description 1
- 235000013824 polyphenols Nutrition 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 108060006613 prolamin Proteins 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 230000002797 proteolythic effect Effects 0.000 description 1
- RADKZDMFGJYCBB-UHFFFAOYSA-N pyridoxal hydrochloride Natural products CC1=NC=C(CO)C(C=O)=C1O RADKZDMFGJYCBB-UHFFFAOYSA-N 0.000 description 1
- 235000005875 quercetin Nutrition 0.000 description 1
- 229960001285 quercetin Drugs 0.000 description 1
- OVSQVDMCBVZWGM-QSOFNFLRSA-N quercetin 3-O-beta-D-glucopyranoside Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1OC1=C(C=2C=C(O)C(O)=CC=2)OC2=CC(O)=CC(O)=C2C1=O OVSQVDMCBVZWGM-QSOFNFLRSA-N 0.000 description 1
- OEKUVLQNKPXSOY-UHFFFAOYSA-N quercetin 3-O-beta-D-glucopyranosyl(1->3)-alpha-L-rhamnopyranosyl(1->6)-beta-d-galactopyranoside Natural products OC1C(O)C(C(O)C)OC1OC1=C(C=2C=C(O)C(O)=CC=2)OC2=CC(O)=CC(O)=C2C1=O OEKUVLQNKPXSOY-UHFFFAOYSA-N 0.000 description 1
- QPHXPNUXTNHJOF-UHFFFAOYSA-N quercetin-7-O-beta-L-rhamnopyranoside Natural products OC1C(O)C(O)C(C)OC1OC1=CC(O)=C2C(=O)C(O)=C(C=3C=C(O)C(O)=CC=3)OC2=C1 QPHXPNUXTNHJOF-UHFFFAOYSA-N 0.000 description 1
- OXGUCUVFOIWWQJ-HQBVPOQASA-N quercitrin Chemical compound O[C@@H]1[C@H](O)[C@@H](O)[C@H](C)O[C@H]1OC1=C(C=2C=C(O)C(O)=CC=2)OC2=CC(O)=CC(O)=C2C1=O OXGUCUVFOIWWQJ-HQBVPOQASA-N 0.000 description 1
- 230000000284 resting effect Effects 0.000 description 1
- 229960002477 riboflavin Drugs 0.000 description 1
- 229930187593 rose bengal Natural products 0.000 description 1
- AZJPTIGZZTZIDR-UHFFFAOYSA-L rose bengal Chemical compound [K+].[K+].[O-]C(=O)C1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1C1=C2C=C(I)C(=O)C(I)=C2OC2=C(I)C([O-])=C(I)C=C21 AZJPTIGZZTZIDR-UHFFFAOYSA-L 0.000 description 1
- 229940081623 rose bengal Drugs 0.000 description 1
- STRXNPAVPKGJQR-UHFFFAOYSA-N rose bengal A Natural products O1C(=O)C(C(=CC=C2Cl)Cl)=C2C21C1=CC(I)=C(O)C(I)=C1OC1=C(I)C(O)=C(I)C=C21 STRXNPAVPKGJQR-UHFFFAOYSA-N 0.000 description 1
- 230000035807 sensation Effects 0.000 description 1
- 235000019615 sensations Nutrition 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 238000004659 sterilization and disinfection Methods 0.000 description 1
- 239000010902 straw Substances 0.000 description 1
- 238000005728 strengthening Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L sulfate group Chemical group S(=O)(=O)([O-])[O-] QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 239000006228 supernatant Substances 0.000 description 1
- 230000009967 tasteless effect Effects 0.000 description 1
- 229960003495 thiamine Drugs 0.000 description 1
- DPJRMOMPQZCRJU-UHFFFAOYSA-M thiamine hydrochloride Chemical compound Cl.[Cl-].CC1=C(CCO)SC=[N+]1CC1=CN=C(C)N=C1N DPJRMOMPQZCRJU-UHFFFAOYSA-M 0.000 description 1
- 239000005495 thyroid hormone Substances 0.000 description 1
- 229940036555 thyroid hormone Drugs 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- 230000002792 vascular Effects 0.000 description 1
- 235000019155 vitamin A Nutrition 0.000 description 1
- 239000011719 vitamin A Substances 0.000 description 1
- 235000010374 vitamin B1 Nutrition 0.000 description 1
- 239000011691 vitamin B1 Substances 0.000 description 1
- 235000019164 vitamin B2 Nutrition 0.000 description 1
- 239000011716 vitamin B2 Substances 0.000 description 1
- 235000019158 vitamin B6 Nutrition 0.000 description 1
- 239000011726 vitamin B6 Substances 0.000 description 1
- 235000019154 vitamin C Nutrition 0.000 description 1
- 239000011718 vitamin C Substances 0.000 description 1
- 235000019165 vitamin E Nutrition 0.000 description 1
- 229940046009 vitamin E Drugs 0.000 description 1
- 239000011709 vitamin E Substances 0.000 description 1
- 229940045997 vitamin a Drugs 0.000 description 1
- 229940011671 vitamin b6 Drugs 0.000 description 1
- 238000003809 water extraction Methods 0.000 description 1
- 230000037221 weight management Effects 0.000 description 1
- 229910001656 zinc mineral Inorganic materials 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A21—BAKING; EDIBLE DOUGHS
- A21D—TREATMENT, e.g. PRESERVATION, OF FLOUR OR DOUGH, e.g. BY ADDITION OF MATERIALS; BAKING; BAKERY PRODUCTS; PRESERVATION THEREOF
- A21D2/00—Treatment of flour or dough by adding materials thereto before or during baking
- A21D2/08—Treatment of flour or dough by adding materials thereto before or during baking by adding organic substances
- A21D2/36—Vegetable material
-
- A—HUMAN NECESSITIES
- A21—BAKING; EDIBLE DOUGHS
- A21D—TREATMENT, e.g. PRESERVATION, OF FLOUR OR DOUGH, e.g. BY ADDITION OF MATERIALS; BAKING; BAKERY PRODUCTS; PRESERVATION THEREOF
- A21D8/00—Methods for preparing or baking dough
- A21D8/06—Baking processes
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
- A23V2002/00—Food compositions, function of food ingredients or processes for food or foodstuffs
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
- A23V2250/00—Food ingredients
- A23V2250/20—Natural extracts
- A23V2250/202—Algae extracts
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
- A23V2250/00—Food ingredients
- A23V2250/20—Natural extracts
- A23V2250/21—Plant extracts
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
- A23V2300/00—Processes
- A23V2300/14—Extraction
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
- A23V2300/00—Processes
- A23V2300/50—Concentrating, enriching or enhancing in functional factors
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Food Science & Technology (AREA)
- Bakery Products And Manufacturing Methods Therefor (AREA)
Abstract
Description
본 발명은 메밀 전초와 다시마의 열수추출물을 빵의 반죽에 포함시켜 메밀과 다시마의 효능을 부여한 빵의 제조방법 및 이 방법으로 제조되는 빵에 관한 것이다.The present invention relates to a method for manufacturing bread to which the efficacy of buckwheat and kelp is imparted by including hot-water extracts of buckwheat starch and kelp in bread dough, and to bread manufactured by the method.
현대인의 식생활이 점차 서구화 및 다양화되고 있으며, 편리한 식생활을 추구하는 경향과 바쁜 현대인들의 일상으로 인해 밥을 대신하여 빵의 소비가 꾸준히 증가하고 있다.Modern people's dietary life is gradually westernized and diversified, and consumption of bread instead of rice is steadily increasing due to the tendency to pursue a convenient diet and the busy daily life of modern people.
일반적으로 빵은 곡식가루에 소금, 설탕, 베이킹파우더 등을 물과 함께 반죽하여 발효시킨 다음 굽거나 찐 음식으로서, 내부에 팥 등의 소(filling)를 넣어 제조하기도 하며, 반죽의 형태, 발효, 굽기의 차이에 따라 다양한 종류의 빵을 제조할 수 있다.In general, bread is a food that is fermented by kneading grain flour with salt, sugar, baking powder, etc. together with water, and then baked or steamed. Depending on the difference in baking, various types of bread can be manufactured.
빵은 크게 효모(yeast)로 서서히 발효시키는 발효빵(이스트 브레드)과 베이킹파우더를 써서 급히 부풀리는 무발효빵(퀵브레드)으로 분류할 수 있으며, 영양적인 측면에서 탄수화물인 밀가루가 주재료이므로 칼로리원 식품으로 가치가 있고, 반죽에 포함되는 부재료, 소, 익히는 방법 등에 따라 다양한 식감 및 풍미를 가지는 빵을 제조할 수 있다.Bread can be largely classified into fermented bread (yeast bread), which is slowly fermented with yeast, and non-fermented bread (quick bread), which is rapidly raised using baking powder. It is valuable as a food and can produce bread with various textures and flavors depending on the sub-materials included in the dough, ingredients, and cooking methods.
이러한 빵의 주재료인 밀가루는 글루텐이 풍부하여 반죽에 유리하기 때문에 각종 면(麵)류 또는 과자를 제조하는데 널리 사용되어 왔으나, 밀가루의 탄수화물은 체내흡수가 빠르고 상대적으로 포만감을 덜 느끼게 하여 비만, 당뇨 등을 비롯한 성인병을 유발하는 원인으로 지목되고 있으며, 밀가루에 함유된 글루텐은 소화장애와 두통을 유발하기도 한다.Wheat flour, the main ingredient of bread, is rich in gluten and is advantageous for dough, so it has been widely used in the manufacture of various types of noodles or confectionery. It is pointed out as a cause of adult diseases, including back, and gluten contained in wheat flour can cause digestive disorders and headaches.
소비자의 식생활 수준이 다양화, 고급화되면서 맛뿐만 아니라 영양 및 기호성 면에서 소비자의 요구 수준이 높아지고 있으며, 이에 따라 빵에 여러 가지 유용성분이 함유된 부재료를 첨가하거나 주재료인 밀가루를 대신하여 영양학적으로 우수한 재료를 사용하여 빵의 기능성을 높이고자 하는 노력이 진행되고 있다.As the level of consumer's dietary life diversifies and becomes more sophisticated, the level of demand from consumers in terms of nutrition and preference as well as taste is increasing. Efforts are being made to improve the functionality of bread by using ingredients.
예를 들어, 빵 제조시 밀가루에 메밀 성분을 첨가하여 밀가루 빵의 단점을 보완하고자 하는 방안이 제시되어 있으며, 메밀은 플라보노이드(flavonoid)의 일종인 루틴(rutin)이 많이 함유되어 있어서 고혈압의 예방과 치료에 효과가 있고, 혈관계 질환의 치료, 폐출혈 예방, 항염증성의 약리효과, 모세혈관 강화 등 천연 화합물로서 의학적인 효과를 가지고 있다.For example, a plan to compensate for the disadvantages of wheat bread by adding buckwheat components to wheat flour when making bread has been proposed. It is effective in treatment, has medical effects as a natural compound such as treatment of vascular system disease, prevention of pulmonary hemorrhage, anti-inflammatory pharmacological effect, and strengthening of capillaries.
이러한 메밀의 효능을 빵에 부여한 예로서, 한국등록특허공보 제0750952호에는 발아메밀을 동결건조하여 분쇄한 후 밀가루와 혼합하고 반죽하여 굽는 발아메밀분말 함유 빵의 제조방법이 제안되었다.As an example of imparting the efficacy of buckwheat to bread, Korean Patent Registration No. 0750952 proposes a method for producing bread containing germinated buckwheat powder by freeze-drying and pulverizing germinated buckwheat, mixing it with wheat flour, and baking it.
상기 발명은 메밀을 발아시켜 인체에 유익한 루틴 함랑을 증가시키면서 제빵성을 악화시키는 주요 요인인 α-아밀라이제(α-amylase)를 억제함으로써, 빵의 기능성을 향상시키고 빵의 볼륨감과 조직감을 높여서 제빵적성이 우수한 건강 기능성 빵을 제조할 수 있다.The invention germinates buckwheat to increase the amount of rutin, which is beneficial to the human body, while suppressing α-amylase, which is a major factor in deteriorating baking properties, thereby improving the functionality of bread and increasing the volume and texture of bread. Healthy functional bread with excellent baking aptitude can be manufactured.
그러나 메밀은 보존성이 다른 식품보다 낮아서 온도, 습도가 높은 조건하에서 변질되기 쉽고, 밀가루와 같이 반죽 과정에서 글루텐을 형성할 수 없어서 점성과 탄성이 낮으므로 빵의 기호도를 떨어뜨리는 단점이 있다.However, buckwheat has lower preservability than other foods, so it is easy to deteriorate under conditions of high temperature and humidity, and like wheat flour, it cannot form gluten during the dough process, so it has low viscosity and elasticity, so it has the disadvantage of reducing the preference of bread.
이에, 한국등록특허공보 제1708972호에는 메밀로 발효력과 저장성이 좋은 발효종을 제조한 후 이를 이용하여 빵을 제조하는 방법이 제안되었으며, 메밀가루, 밀가루, 효모 및 물을 혼합하고 발효시켜 메밀 발효종을 제조한 후, 메밀가루, 밀가루, 상기 제조된 메밀 발효종, 소금 및 물을 혼합하고 반죽하여 메밀 발효종 반죽을 제조한 다음, 상기 메밀 발효종 반죽을 이용하여 빵을 제조한다.Accordingly, Korean Registered Patent Publication No. 1708972 proposes a method of manufacturing bread using buckwheat after manufacturing a fermented species with good fermentation and storability. Buckwheat is fermented by mixing and fermenting buckwheat flour, wheat flour, yeast and water. After preparing the species, buckwheat flour, wheat flour, the prepared buckwheat fermentation species, salt and water are mixed and kneaded to prepare a buckwheat fermentation species dough, and then bread is prepared using the buckwheat fermentation species dough.
상기 발명은 효모로서 사카로미세스 세레비지에(Saccharomyces cerevisiae), 샌프란시스코 발효종(San Francisco sourdough)에서 분리된 사카로마이세스 엑시구스(Saccharomyces exiguus), 스트렙토미세스 이누시타투스(Streptomyces inusitatus), 사카로마이세스 우바륨(Saccharomyces uvarum) 등을 사용하고, 수분함량이 많아서 효모의 활동이 활발하며, 짧게는 2 시간에서 최대 24 시간까지 발효와 휴지를 반복하면서 본 반죽에 일부를 떼어서 사용한다.The invention is a yeast, Saccharomyces cerevisiae , Saccharomyces exiguus isolated from San Francisco sourdough, Streptomyces inusitatus , saccharomyces Myces Uvarum ( Saccharomyces uvarum ), etc. are used, and the activity of yeast is active due to the high moisture content, and a portion of the dough is used while repeating fermentation and resting from 2 hours to a maximum of 24 hours.
반죽을 나누어 추후 반죽에 사용하여 풍미가 증가하고, 소금이 효모 이외의 미생물 생육을 억제시켜 발효력과 저장성이 좋은 발효종을 제조할 수 있으며, 이러한 발효종을 이용하여 빵을 제조함으로써 빵의 기호도와 저장성이 향상된다.Divide the dough and use it for later dough to increase the flavor, and salt inhibits the growth of microorganisms other than yeast to produce fermented species with good fermentation power and storability. storability is improved.
그런데 메밀의 유효성분인 루틴은 플라보놀 배당체의 일종으로서, 플라보놀 배당체는 강산과 접하면 산이 촉매로 작용하여 비배당체로 전환되는 산가수분해가 일어나는데, 상기 메밀 발효종 빵을 섭취하면 메밀의 루틴 성분이 위액의 강산과 접촉하여 가수분해되므로 메밀을 빵에 혼합하여도 메밀의 효능을 인체가 충분히 흡수하지 못하는 단점이 있다.By the way, rutin, which is an active ingredient of buckwheat, is a kind of flavonol glycoside, and when flavonol glycoside comes in contact with strong acid, acid acts as a catalyst to convert acid hydrolysis into a non-glycoside. Since the ingredients are hydrolyzed in contact with the strong acid of gastric juice, even if buckwheat is mixed with bread, the body does not fully absorb the efficacy of buckwheat.
본 발명은 상기의 문제를 해결하기 위한 것으로서, 메밀과 다시마 성분을 빵의 반죽에 포함시켜 이들이 가지는 유용한 효능이 인체에서 충분히 흡수될 수 있도록 하는 빵의 제조방법 및 이 방법으로 제조되는 빵을 제공하는 것이다.The present invention is to solve the above problems, to provide a bread manufacturing method and bread manufactured by this method, which include buckwheat and kelp ingredients in bread dough so that their useful effects can be sufficiently absorbed by the human body will be.
상기 과제를 해결하기 위하여, 본 발명은 메밀 전초와 다시마를 세척하여 건조한 후 분쇄하여 혼합분말을 준비하는 단계; 상기 혼합분말에 중량기준 25~35 배수의 물을 가하고 90~100 ℃에서 3~5 시간 가열한 다음 여과하여 잔사가 제거된 1차 열수추출물을 얻는 단계; 상기 잔사에 중량기준 25~35 배수의 물을 가하고 90~100 ℃에서 3~5 시간 가열한 다음 여과하여 잔사가 제거된 2차 열수추출물을 얻는 단계; 상기 1차 열수추출물과 2차 열수추출물을 혼합하고 부피가 처음의 5~15 %가 되도록 농축한 다음 건조하여 농축분말을 제조하는 단계; 물에 밀가루, 메밀가루, 계란, 설탕, 탈지분유, 소금, 효모 및 상기 농축분말을 혼합하여 반죽한 후 버터를 첨가하여 다시 반죽하는 단계; 상기 반죽물을 온도 25~30 ℃, 습도 80~90 %에서 80~100 분간 1차 발효시키는 단계; 상기 1차 발효물을 분할하여 실온에서 10~30 분간 2차 발효시키는 단계; 상기 2차 발효물의 가스를 빼고 둥글리기한 다음 온도 35~40 ℃, 습도 85~95 %에서 40~60 분간 3차 발효시키는 단계; 및 상기 3차 발효물을 굽는 단계;를 포함하는 빵의 제조방법을 제공한다.In order to solve the above problems, the present invention comprises the steps of preparing a mixed powder by washing, drying and pulverizing buckwheat outpost and kelp; Adding 25 to 35 times the water by weight to the mixed powder, heating at 90 to 100 ° C. for 3 to 5 hours, and then filtering to obtain a first hot-water extract from which residues are removed; adding 25 to 35 multiples of water by weight to the residue, heating at 90 to 100 ° C. for 3 to 5 hours, and then filtering to obtain a secondary hot-water extract from which the residue is removed; preparing a concentrated powder by mixing the first hot water extract and the second hot water extract, concentrating the volume to be 5 to 15% of the first volume, and then drying; Mixing flour, buckwheat flour, eggs, sugar, skim milk powder, salt, yeast, and the concentrated powder with water, kneading, adding butter and kneading again; Primary fermentation of the dough at a temperature of 25 to 30 ° C. and a humidity of 80 to 90% for 80 to 100 minutes; Dividing the primary fermentation product and subjecting it to secondary fermentation at room temperature for 10 to 30 minutes; Degassing and rounding the secondary fermentation, followed by third fermentation at a temperature of 35 to 40 ° C and a humidity of 85 to 95% for 40 to 60 minutes; And baking the tertiary fermented product; provides a method for producing bread including.
이때, 상기 반죽물은 물 100 중량부에 밀가루 120~160 중량부, 메밀가루 40~60 중량부, 계란 15~25 중량부, 설탕 10~20 중량부, 탈지분유 5~15 중량부, 소금 1~7 중량부, 효모 1~7 중량부, 농축분말 1~7 중량부 및 버터 15~25 중량부를 포함하는 것이 바람직하다.At this time, the dough is 100 parts by weight of water, 120 to 160 parts by weight of wheat flour, 40 to 60 parts by weight of buckwheat flour, 15 to 25 parts by weight of eggs, 10 to 20 parts by weight of sugar, 5 to 15 parts by weight of skim milk powder, 1 salt It is preferable to include ~ 7 parts by weight, yeast 1-7 parts by weight, concentrated powder 1-7 parts by weight and butter 15-25 parts by weight.
또한, 상기 반죽하는 단계의 물에 곡류 효소를 추가하며, 상기 곡류 효소는, 메밀과 서목태를 물에 침지하여 수분함량이 34~38 중량%가 되도록 한 후 물을 빼주는 단계; 상기 물을 뺀 메밀 70~90 중량%, 물을 뺀 서목태 5~15 중량% 및 다시마 분말 5~15 중량%를 혼합하여 증자한 후 냉각시키는 단계; 상기 냉각된 메밀. 서목태 및 다시마 분말에 누룩곰팡이를 0.5~3.0 중량%의 비율로 접종하고 20~30 ℃에서 45~55 시간 발효시키는 단계; 및 상기 발효물을 건조하여 분쇄하는 단계;를 통하여 제조되는 것이 바람직하다.In addition, adding a grain enzyme to the water of the kneading step, the grain enzyme, immersing buckwheat and seomoktae in water so that the water content is 34 to 38% by weight, and then draining the water; 70 to 90% by weight of buckwheat minus the water, 5 to 15% by weight of drained seomoktae, and 5 to 15% by weight of kelp powder mixed, steamed, and then cooled; The cooled buckwheat. Inoculating Aspergillus mold in seomoktae and kelp powder at a rate of 0.5 to 3.0% by weight and fermenting at 20 to 30 ° C. for 45 to 55 hours; It is preferably prepared through; and drying and pulverizing the fermented product.
또한, 상기 곡류 효소를 히드록시프로필 메틸셀룰로오스로 코팅하는 것이 바람직하고, 상기 히드록시프로필 메틸셀룰로오스는 메톡시기와 히드록시프로폭시기가 치환도 19~30:4~12의 비율로 구성되는 것이 더욱 바람직하다.In addition, it is preferable to coat the cereal enzyme with hydroxypropyl methylcellulose, and the hydroxypropyl methylcellulose is more preferably composed of a methoxy group and a hydroxypropoxy group in a ratio of substitution of 19 to 30: 4 to 12 do.
또한, 본 발명은 상기의 방법으로 제조되는 빵을 제공한다.In addition, the present invention provides bread prepared by the above method.
본 발명의 방법으로 제조되는 빵은 항산화 활성이 높은 메밀과 다시마를 빵의 반죽에 포함시켜 인체의 건강 유지 및 질환 예방에 유용한 효과를 제공하고, 빵의 섭취 후 소화기관을 거치는 동안 유용성분이 파괴되지 않고 소장까지 도달하므로 메밀과 다시마의 효능이 체내에서 온전히 발휘될 수 있다.Bread prepared by the method of the present invention includes buckwheat and kelp with high antioxidant activity in bread dough to provide useful effects for maintaining human health and preventing diseases, and useful components are not destroyed while passing through the digestive system after eating bread. Since it reaches the small intestine without stopping, the efficacy of buckwheat and kelp can be fully demonstrated in the body.
체내에는 산화 촉진물질과 산화 억제물질이 균형을 이루고 있는데, 산화 균형이 깨져 산화촉진 쪽으로 기울면 세포에 해로운 영향을 끼치게 되는 것으로 알려져 있고 이러한 유해작용을 산화적 스트레스라고 한다.Oxidation promoters and antioxidants are in balance in the body, and it is known that when the oxidative balance is broken and leans towards oxidation promotion, it has a detrimental effect on cells, and this harmful effect is called oxidative stress.
이론적으로 체내에서 산화적 스트레스와 이에 대항하는 항산화성 방어 체계가 불균형해질 때 항산화 물질을 추가하면 산화성 피해를 제한할 수 있으며, 항산화 물질 중 플라보노이드는 지질의 산화, 활성산소 및 산화적 스트레스를 막는 역할을 함으로서 노화를 예방하거나 지연하는 효과가 있다고 알려져 있다.Theoretically, when oxidative stress and the antioxidant defense system against it are imbalanced in the body, adding antioxidants can limit oxidative damage, and among antioxidants, flavonoids play a role in preventing lipid oxidation, free radicals, and oxidative stress. It is known to have the effect of preventing or delaying aging by doing.
천연물질 중에서 메밀과 다시마에 플라보노이드 성분이 다량 함유되어 있어서 이들의 항산화력이 매우 높으므로, 본 발명에서는 메밀과 다시마를 열수추출한 후 밀가루와 메밀가루의 혼합분말에 첨가하여 건강에 좋은 기능성 빵을 제조한다.Among natural substances, buckwheat and kelp contain a large amount of flavonoid components, so their antioxidant power is very high. do.
메밀은 생육기간이 60~80 일 정도로 짧고 서늘한 기후에서 잘 자라며, 병충해에 강한 특성이 있어서 많은 양의 화학비료와 농약을 사용할 필요가 없는 무공해 작물이다.Buckwheat grows well in a cool climate with a short growing period of about 60 to 80 days, and is a pollution-free crop that does not require the use of large amounts of chemical fertilizers and pesticides because it is resistant to pests and diseases.
메밀의 플라보노이드 성분으로는 루틴을 비롯하여 퀘르세틴(quercetin), 이소퀘르세틴(isoquercetin), 마이레세틴(myrecetin), 퀘르시트린(quercitrin) 등이 알려져 있고 이들 화합물의 항산화 작용, 혈압 저하 작용, 혈관 수축 작용, 항균 작용 등 생체조절기능이 밝혀져 있으며, 특히 메밀 단백질 중에는 글로불린(globulin)과 알부민(albumin) 등이 60 % 이상 함유되어 있는 반면에 프롤아민(prolamin)과 글루텔린(glutelin) 함량은 14 % 내외로 비교적 적은편이어서 글루텔린 함량이 많은 밀가루 단백질 조성과 대조를 이루고 있다.Flavonoid components of buckwheat include rutin, quercetin, isoquercetin, myrecetin, and quercitrin. Its bioregulatory functions such as antibacterial activity have been revealed. In particular, buckwheat protein contains more than 60% of globulin and albumin, while the contents of prolamin and glutelin are around 14%. It is relatively small, which contrasts with the flour protein composition, which has a high glutelin content.
또한, 메밀의 필수아미노산 함량은 밀 또는 귀리보다 많아서 영양적 가치가 높고, 메밀의 지방산은 올레익산(oleic acid)과 리놀레익산(linoleic acid)이 주성분이며, 팔미틱산(palmitic acid), 스테아릭산(stearic acid)이 다른 곡류에 비하여 높다.In addition, the essential amino acid content of buckwheat is higher than that of wheat or oat, and its nutritional value is high. The main components of buckwheat's fatty acids are oleic acid and linoleic acid, and palmitic acid and stearic acid. (stearic acid) is higher than other grains.
메밀은 과거에 구황작물로 이용되어 왔으나 최근에는 비만증, 고혈압, 당뇨 등에 유효할 뿐만 아니라 글루텐 프리 식품으로도 인정되고 있고 건강을 위한 별미식품으로 인식되어 소비량이 꾸준히 증가하는 추세이다.Buckwheat has been used as a food crop in the past, but recently it is not only effective for obesity, hypertension, diabetes, etc., but also recognized as a gluten-free food, and is recognized as a delicacy for health, and its consumption is steadily increasing.
특히, 메밀은 알곡에 비하여 전초(全草)에 식이섬유(dietary fiber), 루틴, 플라보노이드, 폴리페놀(polyphenol) 함량이 매우 높아서 메밀 전초를 사용하는 것이 바람직하고, 사용상 편의를 위하여 메밀 전초 중 경엽(莖葉) 부위를 사용하는 것이 좀 더 바람직하다.In particular, buckwheat has a very high content of dietary fiber, rutin, flavonoids, and polyphenols in the outpost compared to grains, so it is preferable to use buckwheat outpost. (莖葉) It is more preferable to use the part.
다시마는 칼륨, 나트륨, 칼슘, 마그네슘 등 인체의 생리대사에 관여하는 무기질을 다량 함유하고 갑상선 호르몬의 주성분인 요오드를 4000 ppm 이상 함유하고 있어서 인체에 부족한 무기질을 채워줄 뿐만 아니라, 우론산(uronic acid)의 복합체인 알긴산(alginic acid), 황산기를 함유한 산성 다당으로서 후코이단(fucoidan), 라미나란(laminaran)과 같은 식이섬유의 보고로 알려져 있다.Kelp contains a large amount of minerals involved in the physiological metabolism of the human body, such as potassium, sodium, calcium, and magnesium, and contains more than 4000 ppm of iodine, the main component of thyroid hormone. It is known as a report of dietary fiber such as fucoidan and laminaran as an acidic polysaccharide containing alginic acid and sulfate group.
먼저, 메밀과 다시마의 열수추출물을 제조한다.First, hot-water extracts of buckwheat and kelp are prepared.
메밀(전초 또는 경엽)과 다시마를 중량기준 2:8 내지 8:2의 비율로 혼합하여 물로 세척한 후 건조하며, 건조물을 600 ㎛ 이하의 크기가 되도록 분쇄하여 메밀과 다시마가 혼합된 분말을 준비한다.Buckwheat (outpost or foliage) and kelp are mixed in a ratio of 2:8 to 8:2 by weight, washed with water and dried, and the dried material is pulverized to a size of 600 ㎛ or less to prepare a mixed powder of buckwheat and kelp do.
상기 혼합분말에 중량기준 25~35 배수의 물을 가하고 90~100 ℃에서 3~5 시간 가열한 다음 여과하여 잔사(殘渣)가 제거된 1차 열수추출물을 얻으며, 동일한 방법으로 상기 잔사에 중량기준 25~35 배수의 물을 가하고 90~100 ℃에서 3~5 시간 가열한 다음 여과하여 잔사가 제거된 2차 열수추출물을 얻는다.25 to 35 multiples of water by weight was added to the mixed powder, heated at 90 to 100 ° C. for 3 to 5 hours, and then filtered to obtain a primary hot-water extract from which residues were removed. After adding 25 to 35 multiples of water, heating at 90 to 100 ° C for 3 to 5 hours, filtering to obtain a secondary hot water extract from which residues are removed.
상기 1차 열수추출물과 2차 열수추출물을 혼합하고 부피가 처음의 5~15 %가 되도록 농축한 다음 건조하여 메밀과 다시마의 열수추출 농축분말을 제조한다.The first hot-water extract and the second hot-water extract are mixed, concentrated to a volume of 5 to 15% of the first volume, and then dried to prepare a concentrated hot-water extract powder of buckwheat and kelp.
다음은 상기 메밀과 다시마의 열수추출 농축분말을 밀가루와 메밀가루가 혼합된 반죽에 첨가하여 빵을 제조한다.Next, bread is prepared by adding the hot water-extracted concentrated powder of buckwheat and kelp to a dough mixed with wheat flour and buckwheat flour.
물에 밀가루, 메밀가루, 계란, 설탕, 탈지분유, 소금, 효모 및 상기 열수추출 농축분말을 혼합하여 반죽한 후 버터를 첨가하여 다시 반죽하며, 상기 반죽물을 온도 25~30 ℃, 습도 80~90 %에서 80~100 분간 1차 발효시킨다.Wheat flour, buckwheat flour, eggs, sugar, skim milk powder, salt, yeast, and the above-mentioned hot water-extracted concentrated powder are mixed with water and kneaded, and then butter is added and kneaded again. First ferment at 90% for 80 to 100 minutes.
상기 재료의 혼합비는 물 100 중량부 기준 밀가루 120~160 중량부, 메밀가루 40~60 중량부, 계란 15~25 중량부, 설탕 10~20 중량부, 탈지분유 5~15 중량부, 소금 1~7 중량부, 효모 1~7 중량부, 상기 열수추출 농축분말 1~7 중량부 및 버터 15~25 중량부인 것이 바탐직하고, 물 100 중량부 기준 제빵개량제 1~5 중량부, 비타민 미네랄 믹스 0.5~3.0 중량부 및 식이섬유 0.5~3.0 중량부를 추가할 수도 있다.The mixing ratio of the above ingredients is based on 100 parts by weight of water: 120 to 160 parts by weight of wheat flour, 40 to 60 parts by weight of buckwheat flour, 15 to 25 parts by weight of eggs, 10 to 20 parts by weight of sugar, 5 to 15 parts by weight of skim milk powder, 1 to 10 parts by weight of salt 7 parts by weight, 1 to 7 parts by weight of yeast, 1 to 7 parts by weight of the concentrated powder extracted from the hot water, and 15 to 25 parts by weight of butter, preferably 1 to 5 parts by weight of a baking improver based on 100 parts by weight of water, 0.5 parts by weight of vitamin and mineral mix ~3.0 parts by weight and 0.5 to 3.0 parts by weight of dietary fiber may be added.
상기 비타민 미네랄 믹스는 비타민 A, 비타민 C, 비타민 E, 비타민 B1, 비타민 B2, 비타민 B6, 칼슘 판토테네이트(calcium pantothenate), 니아신(niacin), 엽산(folic acid) 등의 비타민과, 철, 아연 등의 미네랄을 포함할 수 있다.The vitamin-mineral mix includes vitamins such as vitamin A, vitamin C, vitamin E, vitamin B1, vitamin B2, vitamin B6, calcium pantothenate, niacin, folic acid, iron, zinc Minerals such as
상기 1차 발효물을 적당한 크기로 분할하여 실온에서 다시 10~30 분간 2차 발효시키며, 상기 2차 발효물의 가스를 빼고 둥글리기한 다음 온도 35~40 ℃, 습도 85~95 %에서 40~60 분간 3차 발효시킨다.Divide the primary fermented product into appropriate sizes, perform secondary fermentation at room temperature for 10 to 30 minutes, degas and round the secondary fermented product, and then 40 to 60 °C at a temperature of 35 to 40 ° C and a humidity of 85 to 95%. Fermented for 3 minutes.
상기 3차 발효물을 160~200 ℃에서 20~40 분간 구워서 빵을 제조한다.Bread is prepared by baking the third fermented product at 160 to 200 ° C. for 20 to 40 minutes.
상기와 같이 제조된 빵은 밀가루에 메밀이 함유되어 메밀의 향과 맛이 부가되고 경도, 탄력성, 응집성, 검성, 씹힘성이 증가하여 씹는 식감이 향상되며, 특히 메밀의 유용성분이 빵에 함유되어 영양학적으로 우수한 기능성 빵을 제조할 수 있다.The bread prepared as described above contains buckwheat in wheat flour, which adds the aroma and taste of buckwheat, and improves chewing texture by increasing hardness, elasticity, cohesiveness, gumminess, and chewiness. As a result, excellent functional bread can be prepared.
빵의 기능성을 좀 더 높이기 위하여 빵 제조시 메밀과 다시마 성분을 포함하는 곡류 효소를 첨가할 수도 있으며, 상기 곡류 효소는 메밀, 서목태 및 다시마 분말에 누룩곰팡이 종균을 접종하여 발효시킨 후 건조 및 분쇄하여 제조될 수 있으며, 상기 반죽시 물 100 중량부 기준 곡류 효소 1~5 중량부를 첨가할 수 있다.In order to further increase the functionality of bread, grain enzymes containing buckwheat and kelp components may be added during bread production, and the grain enzymes are inoculated with Aspergillus mold spawn in buckwheat, seomoktae and kelp powder, fermented, dried and pulverized 1 to 5 parts by weight of grain enzyme based on 100 parts by weight of water may be added during the kneading.
서목태는 식이섬유가 풍부하게 함유되어 있어서 포만감을 주므로 체중관리에 도움을 주고 당뇨 예방, 피부 관리, 야맹증에 효과가 있으며, 해독력이 뛰어나 체내의 독성을 풀어주는 역할을 한다.Seomoktae is rich in dietary fiber, so it gives a feeling of fullness, so it helps in weight management, and is effective in preventing diabetes, skin care, and night blindness.
먼저, 메밀과 서목태를 물로 세척하고 물에 침지하여 수분함량이 34~38 중량%가 되도록 하며, 메밀은 20~30 ℃의 물에 40~80 분간, 서목태는 20~30 ℃의 물에 100~140 분간 침지하면 상기 수분함량을 맞출 수 있고, 침지 후 40~80 분간 채반 등에 건져두어 물을 빼준다.First, buckwheat and seomoktae are washed with water and immersed in water so that the moisture content is 34 to 38% by weight. If immersed for 140 minutes, the above moisture content can be adjusted, and after immersion, drain the water by putting it on a tray for 40 to 80 minutes.
상기 메밀로서 메밀 알곡과 메밀 전초(또는 경엽)를 5~8:1~2의 중량비로 혼합하여 사용하는 것이 후공정인 발효를 원할하게 하고 효소의 항산화력 및 활성을 증대하는 점에서 가장 바람직하다.As the buckwheat, buckwheat grains and buckwheat sheath (or foliage) are mixed and used in a weight ratio of 5 to 8: 1 to 2, which is the most preferable in terms of smooth fermentation and increasing the antioxidant power and activity of enzymes. .
다시마를 물에 50~70 분간 침지한 후 40~60 ℃에서 10~15 시간 건조하고 850 ㎛ 이하의 크기가 되도록 분쇄하여 다시마 분말을 준비한다.After immersing kelp in water for 50 to 70 minutes, drying at 40 to 60 ° C. for 10 to 15 hours, and pulverizing to a size of 850 μm or less to prepare kelp powder.
메밀 70~90 중량%, 서목태 5~15 중량%, 다시마 분말 5~15 중량%의 비율로 혼합하고 95~100 ℃에서 40~80 분간 증자한 후 100~140 분간 냉각시키며, 여기에 누룩곰팡이를 0.5~3.0 중량%의 비율로 접종하고 20~30 ℃에서 45~55 시간 발효시키며, 발효 중 가끔 섞어주어 발효가 균일하게 진행되도록 한다.70-90% by weight of buckwheat, 5-15% by weight of Seomoktae, and 5-15% by weight of kelp powder are mixed, steamed at 95-100 ° C for 40-80 minutes, and then cooled for 100-140 minutes. Inoculate at a rate of 0.5 to 3.0% by weight, ferment at 20 to 30 ° C for 45 to 55 hours, and occasionally mix during fermentation to ensure uniform fermentation.
상기 발효된 곡류를 35~45 ℃에서 10~15 시간 건조하고 분쇄하여 곡류 효소를 제조한다.The fermented grains are dried at 35 to 45 ° C. for 10 to 15 hours, and then pulverized to prepare grain enzymes.
상기 곡류 효소는 생체 내의 화학반응을 매개하는 촉매로서, 음식물의 소화흡수를 돕고 신진대사를 촉진하며 신체의 기능이 원활해지도록 도와서 건강 유지 및 질환 예방에 도움을 주는 유용한 효과를 발휘한다.The cereal enzyme is a catalyst for mediating chemical reactions in the living body, helping digestion and absorption of food, promoting metabolism, and helping the body function smoothly, thereby exhibiting useful effects that help maintain health and prevent disease.
상기 발효에 사용되는 누룩곰팡이는 시중에서 구입하거나 미생물 분양기관에서 분양받아 사용할 수 있으나, 전통 누룩에서 누룩곰팡이를 분리하고 배양하여 종균을 직접 제조하여 사용할 수 있으며, 누룩곰팡이 종균의 제조방법을 예시하면 다음과 같다.Aspergillus mold used in the fermentation can be purchased on the market or sold at a microbial sales institution, but it can be used by separating and culturing the aspergillus mold from traditional yeast, and the spawner can be directly produced and used. As follows.
먼저, 누룩을 분쇄하여 멸균수와 혼합하고 100~150 rpm으로 8~12 분간 현탁한 후 멸균수를 추가하여 희석하며. 상기 희석액을 MEA(malt extract agar) 평판배지에 도말하여 23~27 ℃에서 4~6 일간 1차 배양하고 배양된 곰팡이 콜로니(colony)를 순수분리한다.First, the yeast is pulverized, mixed with sterile water, suspended at 100 to 150 rpm for 8 to 12 minutes, and then diluted by adding sterile water. The diluted solution is spread on a malt extract agar (MEA) plate medium, and is first cultured at 23 to 27 ° C for 4 to 6 days, and the cultured fungal colonies are pure.
상기 분리한 곰팡이 균주를 세균으로부터의 오염을 방지하기 위하여 DRBC(dichloran rose bengal chloramphenicol agar) 배지에 도말하여 23~27 ℃에서 4~6 일간 2차 배양하고, 상기 2차 배양액 균주를 YM(yeast malt) broth 배지에 접종하고 33~37 ℃의 진탕항온수조(shaking water bath)에서 100~150 rpm으로 교반하면서 10~15 시간 3차 배양한다.In order to prevent contamination from bacteria, the isolated fungal strain was smeared on a DRBC (dichloran rose bengal chloramphenicol agar) medium and cultured for 4 to 6 days at 23 to 27 ° C., and the secondary culture strain was YM (yeast malt ) Inoculate broth medium and incubate 3rd time for 10-15 hours while stirring at 100-150 rpm in a shaking water bath at 33-37 ° C.
상기 배양액에서 전분 및 단백질 분해활성이 높은 균주를 선발하기 위하여, 상기 3차 배양액을 0.5~2.0 %(w/v) 농도의 가용성 전분 또는 1~5 %(w/v) 농도의 탈지유가 함유된 YM 한천배지에 점적(點滴)하고 33~37 ℃에서 12~20 시간 4차 배양한 후 배지 위에 형성된 투명환의 크기가 큰 균주를 선별한다.In order to select strains with high starch and proteolytic activity in the culture medium, the tertiary culture medium contained soluble starch at a concentration of 0.5 to 2.0% (w / v) or skim milk at a concentration of 1 to 5% (w / v). After dripping on YM agar medium and culturing for 12 to 20 hours at 33 ~ 37 ℃ for the fourth time, strains with large transparent rings formed on the medium are selected.
다음은 상기 선별된 균주를 이용하여 종균을 제조한다.Next, spawners are prepared using the selected strains.
음용수 100 중량부에 밀기울 0.5~3.0 중량부, 대두분말 0.5~3.0 중량부, 미강 0.5~3.0 중량부, 효모(yeast) 0.1~1.0 중량부를 혼합하여 양액(nutrient solution)을 준비하고, 상기 양액을 고온 및 고압, 예를 들어 115~125 ℃, 10~20 psi에서 10~20 분간 살균한다.A nutrient solution was prepared by mixing 0.5 to 3.0 parts by weight of wheat bran, 0.5 to 3.0 parts by weight of soybean powder, 0.5 to 3.0 parts by weight of rice bran, and 0.1 to 1.0 parts by weight of yeast with 100 parts by weight of drinking water. Sterilize at high temperature and high pressure, for example, 115-125 ℃, 10-20 psi for 10-20 minutes.
상기 살균한 양액에 상기 선별된 균주를 접종하고 진탕항온수조를 이용하여 28~32 ℃, 100~150 rpm에서 20~30 시간 5차 배양하며, 동일한 방식으로 상기 살균한 양액에 상기 5차 배양액을 접종하고 진탕항온수조를 이용하여 28~32 ℃, 100~150 rpm에서 20~30 시간 6차 배양한다.The selected strain is inoculated into the sterilized nutrient solution and cultured 5 times for 20 to 30 hours at 28 to 32 ℃ and 100 to 150 rpm using a shaking constant temperature water bath. Inoculate and incubate 6 times for 20 to 30 hours at 28 to 32 ℃ and 100 to 150 rpm using a shaking water bath.
현미를 물로 세척하고 물에 20~30 시간 침지한 후 건져두어 물을 빼주며, 이를 90~100 ℃에서 20~30 시간 증자하고 냉각한 후 여기에 상기 6차 배양액을 접종하여 충분히 섞어주고 온도 23~27 ℃, 습도 85~95 %를 유지하면서 40~55 시간 7차 배양하여 발효 종균을 제조하고, 상기 발효 종균을 25~35 ℃에서 10~15 시간 건조하여 누룩곰팡이 종균을 제조한다.Wash brown rice with water, soak in water for 20-30 hours, drain the water, increase it at 90-100 ° C for 20-30 hours, cool it, inoculate it with the 6th culture medium, mix well, and set the temperature to 23 While maintaining ~27 ℃ and humidity of 85 ~ 95%, fermented seeds are prepared by culturing 7 times for 40 to 55 hours, and the fermentation seeds are dried at 25 ~ 35 ℃ for 10 to 15 hours to prepare Aspergillus mold seeds.
그런데 상기의 누룩곰팡이 종균으로 제조된 곡류 효소는 단백질의 일종으로서 이를 섭취하면 인체의 위에서 분비되는 위산과 소화기관에서 분비되는 단백질분해효소에 의해 분해되어 그 효능을 충분히 발휘하기 어려운 단점이 있으므로, 곡류 효소가 위에서 파괴되지 않고 소장까지 효소의 단백질 구조를 유지한 상태에서 도달되도록 하는 것이 필요하다.However, the grain enzyme produced from the yeast fungus above is a kind of protein, and when ingested, it is decomposed by gastric acid secreted from the stomach of the human body and proteolytic enzyme secreted from the digestive tract, so it is difficult to fully exert its efficacy. It is necessary to ensure that the enzyme reaches the small intestine without being destroyed in the stomach while maintaining the protein structure of the enzyme.
이를 위하여 상기 제조된 곡류 효소를 히드록시프로필 메틸셀룰로오스(hydroxypropyl methyl cellulose, HPMC)로 코팅하는 것이 바람직하며, HPMC는 비이온성을 나타내어 물에 대한 용해도가 높고 낮은 온도에서도 잘 용해되어 점성이 있는 콜로이드 용액을 형성하며, 일반적으로 무미, 무취의 백색 분말로서 자극성, 독성이 없고 인체에 무해하다.To this end, it is preferable to coat the prepared cereal enzyme with hydroxypropyl methyl cellulose (HPMC), and HPMC is nonionic, so it has high water solubility and dissolves well even at low temperatures, resulting in a viscous colloidal solution It is generally tasteless and odorless white powder, non-irritating, non-toxic and harmless to the human body.
HPMC는 셀룰로오스의 히드록시기(-OH) 또는 히드록시메틸기(-CH2OH)의 수소가 메틸기와 히드록시프로필기로 치환되어 있고 메틸기와 히드록시프로필기의 치환비율에 의해 HPMC의 타입이 결정되며, 치환기의 구조적 특성에 의해 물에 대한 용해도가 우수하고 점성 및 겔 득성 등 다양한 성질을 발현한다.In HPMC, the hydrogen of the hydroxy group (-OH) or hydroxymethyl group (-CH 2 OH) of cellulose is substituted with a methyl group and a hydroxypropyl group, and the type of HPMC is determined by the substitution ratio of the methyl group and the hydroxypropyl group, and the substituent Due to its structural characteristics, it has excellent water solubility and exhibits various properties such as viscosity and gelation.
HPMC는 구조 내의 소수성 작용기들 사이의 상호작용에 의해 그물망 구조를 형성하고 높은 온도에서는 겔(gel)로 존재하고 낮은 온도에서는 졸(sol)로 존재하는 상전이 현상을 가지고 있으며,치환도에 따라 겔이 형성되는 온도와 겔의 강도에서 차이가 나고 용액상태에서도 고점도로 존재하거나 열에 의한 겔 특정이 발현된다.HPMC forms a network structure by interaction between hydrophobic functional groups in the structure, and has a phase transition phenomenon that exists as a gel at high temperature and as a sol at low temperature. There is a difference in the temperature at which it is formed and the strength of the gel, and it exists in high viscosity even in the solution state, or the gel characteristic is expressed by heat.
이러한 특성을 이용하여, HPMC를 물에 용해시킨 후 건조하여 물을 제거하면 투명하고 강도가 우수한 코팅막을 형성하므로,HPMC를 물에 용해시킨 후 곡류 효소를 혼합하여 가열하면 HPMC가 겔화되면서 곡류 효소 표면에 결착되고 가열에 의해 물이 점차 증발하면서 곡류 효소 표면에 HPMC의 코팅막이 형성된다.Using these characteristics, when HPMC is dissolved in water and then dried to remove water, a transparent and high-strength coating is formed. When HPMC is dissolved in water and then mixed with grain enzyme and heated, HPMC gels and the surface of grain enzyme and while the water gradually evaporates by heating, a coating film of HPMC is formed on the surface of the grain enzyme.
상기 HPMC 코팅막은 느린 표면 침식 특성이 있어서 물에 용해되는 시간이 비교적 길므로 곡류 효소를 포함하는 빵의 섭취시 곡류 효소가 위에서 파괴되지 않고 효소의 단백질 구조를 유지한 상태로 소장까지 도달할 수 있다.The HPMC coating film has a slow surface erosion property, so it takes a relatively long time to dissolve in water, so when eating bread containing cereal enzymes, the cereal enzymes are not destroyed in the stomach and can reach the small intestine while maintaining the protein structure of the enzymes. .
음식물은 종류에 따라 차이가 있으나 통상 위에서 4~6 시간 정도 체류한 후 소장에 도달하고 소장에서 5~8 시간 정도 체류하며, HPMC 코팅막은 코팅두께에 따라 차이가 있으나 물에서 4 시간 후 약 20 % 용해, 6 시간 후 약 40 % 용해, 9 시간 후 약 60 % 용해, 14 시간 후 약 80 % 용해되고, HPMC는 수용액 중에서 pH에 관계없이 일정한 용해 속도를 가진다.Food varies depending on the type, but usually reaches the small intestine after staying in the stomach for about 4 to 6 hours and stays in the small intestine for about 5 to 8 hours. dissolution, about 40% dissolution after 6 hours, about 60% dissolution after 9 hours, about 80% dissolution after 14 hours, and HPMC has a constant dissolution rate regardless of pH in aqueous solution.
따라서 HPMC로 코팅된 곡류 효소는 위에서 20~40 % 용해된 후 소장으로 이송되고 소장에서 60~80 % 용해되므로, 많은 양의 곡류 효소는 효소의 단백질 구조를 유지한 채 소장으로 이송된다.Therefore, grain enzyme coated with HPMC is 20-40% dissolved in the stomach and transported to the small intestine, and 60-80% dissolved in the small intestine, so a large amount of grain enzyme is transported to the small intestine while maintaining the protein structure of the enzyme.
곡류 효소가 소장에 체류하는 동안 HPMC 코팅막이 서서히 용해되어 제거되고, HPMC 코팅막이 제거된 곡류 효소는 십이지장에서 분비된 이자액에 의해 각 성분으로 분해되며, 효소 성분은 소장에 이송된 음식물을 체내에 흡수할 수 있도록 분해하여 소화를 도우면서 효소 자체 또한 소장에서 흡수되어 건강에 유익한 작용을 한다.While the grain enzyme stays in the small intestine, the HPMC coating film is gradually dissolved and removed, and the grain enzyme with the HPMC coating film removed is broken down into each component by the pancreatic fluid secreted from the duodenum, and the enzyme component absorbs the food transported to the small intestine into the body. Enzymes themselves are also absorbed in the small intestine, which is beneficial to health.
HPMC가 위에서 용해되는 양을 최소화하여 곡류 효소가 단백질 구조를 유지한 채 소장에 도달되도록 하기 위하여 HPMC의 점도를 높여서 겔 강도를 증가시키는 것이 바람직하며, HPMC의 점도는 메톡시기(-OCH3)와 히드록시프로폭시기(-OCH2CH(CH3)OH)의 비율과 관계가 있고, 메톡시기와 히드록시프로폭시기가 치환도(degree of substitution) 19~30:4~12의 비율로 구성되는 것이 상대적으로 점도가 높다.In order to minimize the amount of HPMC dissolved in the stomach so that the cereal enzyme reaches the small intestine while maintaining the protein structure, it is desirable to increase the gel strength by increasing the viscosity of HPMC. It is related to the ratio of the hydroxypropoxyl group (-OCH 2 CH(CH 3 )OH), and the methoxy group and the hydroxypropoxyl group are composed in a ratio of 19-30:4-12 degree of substitution. It has relatively high viscosity.
상기와 같이 빵 제조시 히드록시프로필 메틸셀룰로오스로 코팅된 곡류 효소를 함유시키면 빵의 섭취 후 소화기관을 거치는 동안 곡류 효소의 유용성분이 파괴되지 않고 소장까지 도달하므로 곡류 효소가 제공하는 소화흡수 촉진, 건강 유지, 질환 예방 등의 효과를 온전히 발휘될 수 있다.As described above, when bread is prepared by including grain enzymes coated with hydroxypropyl methylcellulose, useful ingredients of grain enzymes are not destroyed and reach the small intestine while passing through the digestive system after eating bread, so that grain enzymes promote digestion and absorption, and promote health. The effects of maintenance, disease prevention, etc. can be fully exerted.
이하, 본 발명을 하기의 실시예, 비교예 및 시험예에 의거하여 좀 더 상세하게 설명한다.Hereinafter, the present invention will be described in more detail based on the following Examples, Comparative Examples and Test Examples.
단, 하기의 실시예는 본 발명을 예시하기 위한 것일 뿐, 본 발명이 하기 실시예에 의해 한정되는 것이 아니고, 본 발명의 기술적 사상을 벗어나지 않는 범위 내에서 치환 및 균등한 타 실시예로 변경할 수 있음은 본 발명이 속하는 기술분야에서 통상의 지식을 가진 자에게 있어서 명백할 것이다.However, the following examples are only for exemplifying the present invention, and the present invention is not limited by the following examples, and can be substituted and replaced by other equivalent examples without departing from the technical spirit of the present invention. It will be clear to those skilled in the art to which the present invention belongs.
<실시예 1> <Example 1>
메밀 경엽과 다시마를 동일 중량비로 혼합하여 흐르는 물에 3 회 세척한 후 65 ℃에서 5 시간 동안 건조하였으며, 이들을 분쇄기로 분쇄한 후 30 mesh(600 ㎛) 표준체로 걸러서 표준체를 통과한 혼합분말을 준비하였다.Buckwheat leaves and kelp were mixed in equal weight ratios, washed three times in running water, dried at 65 ° C for 5 hours, pulverized with a grinder, and then filtered through a 30 mesh (600 ㎛) standard sieve to prepare a mixed powder that passed through the standard sieve. did
상기 혼합분말을 여과백에 넣고 정제수를 중량 기준 30 배수 가한 후 95 ℃에서 4 시간 동안 1차 추출하였으며, 같은 방식으로 상기 1차 추출 잔사에 정제수를 중량 기준 30 배수 가한 후 95 ℃에서 4 시간 동안 2차 추출하였다.The mixed powder was placed in a filter bag, purified water was added 30 times by weight, and first extraction was performed at 95 ° C. for 4 hours. In the same way, purified water was added 30 times by weight to the residue of the first extraction, and then 95 ° C. for 4 hours. The second extraction was performed.
상기 1차 추출 여액과 2차 추출 여액을 합하고 합친 부피의 1/10이 될 때까지 가열농축한 다음 농축액을 동결건조기로 동결건조하여 메밀 전초와 다시마의 열수추출 농축분말을 제조하였다.The first extraction filtrate and the second extraction filtrate were combined, heated and concentrated until 1/10 of the combined volume, and then the concentrate was freeze-dried with a freeze dryer to prepare a hot-water extract concentrated powder of buckwheat sprouts and kelp.
밀가루(강력분)와 메밀가루를 체를 치고 건조 효모 20 g을 음용수에 완전히 녹인 다음, 음용수 500 g에 상기 밀가루 700 g, 상기 메밀가루 250 g, 계란 100 g, 설탕 80 g, 탈지분유 50 g, 소금 20 g, 상기 건조 효모액, 상기 열수추출 농축분말 20 g, 제빵개량제 10 g, 비타민 미네랄 믹스 5 g 및 치커리 식이섬유 5 g을 반죽기에 넣어서 2 분간 반죽한 후 버터 100 g을 추가하여 다시 17 분간 반죽하였으며, 반죽물을 손으로 늘여서 신장성, 점성, 글루텐의 상태를 확인하여 파이널 스테이지(final stage) 단계를 확인하였다.Sift wheat flour (strong flour) and buckwheat flour, completely dissolve 20 g of dry yeast in drinking water, then 700 g of the flour, 250 g of the buckwheat flour, 100 g of egg, 80 g of sugar, 50 g of skim milk powder, 20 g of salt, the dry yeast liquid, 20 g of the hot water extract concentrated powder, 10 g of baking improver, 5 g of vitamin mineral mix, and 5 g of chicory dietary fiber were put into a kneader, kneaded for 2 minutes, and then 100 g of butter was added and kneaded again. It was kneaded for minutes, and the final stage was confirmed by stretching the dough by hand to check the state of extensibility, viscosity, and gluten.
상기 반죽물을 볼(bowl)에 담고 랩을 씌워서 발효기에 넣고 온도 27 ℃, 습도 85 %에서 90 분간 1차 발효시켰으며, 손가락에 밀가루를 묻혀 1차 발효된 반죽물을 찔러서 모양이 잘 유지되는 상태를 확인하고, 1차 발효된 반죽물을 들어서 옆면이 실처럼 잘 늘어져있는 것을 확인하였다.The dough was placed in a bowl, covered with a wrap, placed in a fermenter, and primary fermented for 90 minutes at a temperature of 27 ° C and a humidity of 85%. After checking the state, it was confirmed that the side of the dough was well stretched like a thread by lifting the first fermented dough.
상기 1차 발효 반죽물을 210 g씩 나누어 나무판자 위에 놓고 랩으로 덮어서 실온에서 20 분간 2차 발효시킨 다음, 2차 발효 반죽물을 두께가 일정하도록 밀대(push stick)로 밀어 펴면서 가스를 빼주고 3 겹 접기를 한 후 둥글게 말고 이음매를 잘 봉해주었다.Divide the primary fermented dough by 210 g, place it on a wooden board, cover with a wrap, and ferment the secondary fermentation at room temperature for 20 minutes. After folding, I rolled it round and sealed the seam well.
빵틀에 쇼트닝(shortening)을 바르고 상기 성형된 반죽을 3 덩어리씩 넣어준 후 온도 38 ℃, 습도 90 %에서 50 분간 3차 발효시켰으며, 빵이 빵틀에서 1 ㎝ 정도 부풀었을 때 3차 발효를 끝내고 윗불과 아랫불 온도 180 ℃의 오븐에서 30 분간 구워서 식빵을 제조하였다.After applying shortening to the bread mold and putting the molded dough in 3 loaves, the third fermentation was performed at a temperature of 38 ° C and a humidity of 90% for 50 minutes. After finishing, bread was prepared by baking for 30 minutes in an oven with an upper and lower heat temperature of 180 ° C.
<실시예 2><Example 2>
메밀 알곡, 메밀 경엽 및 서목태를 물로 세척한 후 25 ℃의 물에 메밀은 1 시간, 서목태는 2 시간 동안 침지하여 수분함량이 36 중량%가 되도록 한 다음 채반에 담아서 1 시간 동안 물을 빼주었다.After washing the buckwheat grains, buckwheat leaves and seomoktae with water, the buckwheat was immersed in water at 25 ° C. for 1 hour and the seomoktae for 2 hours to make the moisture content 36% by weight, and then placed in a sieve and drained for 1 hour.
다시마를 물에 1 시간 침지하고 3 회 세척한 후 열풍건조기(JW-500ED, 진우전자, 한국)를 이용하여 50 ℃에서 12 시간 건조하고 850 ㎛(표준체 No. 20) 이하의 크기가 되도록 분쇄하여 다시마 분말을 준비하였다.After immersing kelp in water for 1 hour, washing it three times, drying it at 50 ℃ for 12 hours using a hot air dryer (JW-500ED, Jinwoo Electronics, Korea), and pulverizing it to a size of 850 ㎛ or less (standard sieve No. 20) Kelp powder was prepared.
상기 물을 뺀 메밀 알곡 60 중량%, 메밀 경엽 20 중량%, 물을 뺀 서목태 10 중량% 및 상기 다시마 분말 10 중량%를 혼합하여 95 ℃에서 1 시간 증자하고 2 시간 동안 냉각시킨 다음 여기에 한국생명공학연구원 생물자원센터(Korean Collection for Type Culture, KCTC)에서 분양받은 아스퍼질러스 오리제 균주를 1 중량%의 비율로 접종하고 25 ℃에서 48 시간 발효시켰으며, 발효 도중에 10 시간마다 뒤섞어 주었다.60% by weight of buckwheat grains minus the water, 20% by weight of buckwheat leaves, 10% by weight of drained seomoktae, and 10% by weight of the kelp powder were mixed, steamed at 95 ° C. for 1 hour, cooled for 2 hours, and then the Korea Life Insurance The Aspergillus oryzee strain obtained from the Korean Collection for Type Culture (KCTC) of the Institute of Engineering was inoculated at a rate of 1% by weight, fermented at 25 ° C. for 48 hours, and stirred every 10 hours during fermentation.
상기 발효물을 건조실에서 40 ℃의 온도로 12 시간 건조한 후 조분쇄기(SJC, 승진정밀, 한국)로 분쇄하여 곡류 효소를 제조하였다.The fermented product was dried in a drying room at a temperature of 40 ° C. for 12 hours, and then pulverized with a coarse grinder (SJC, Seungjin Precision, Korea) to prepare a grain enzyme.
실시예 1의 반죽시 상기 제조된 곡류 효소 15 g을 첨가한 것을 제외하고는, 상기 실시예 1과 동일한 방법으로 식빵을 제조하였다.Bread was prepared in the same manner as in Example 1, except that 15 g of the grain enzyme prepared above was added during the kneading of Example 1.
<실시예 3><Example 3>
전통시장에서 3 종의 누룩을 구입하여 분쇄한 후 혼합하여 누룩분말을 준비하였으며, 상기 누룩분말 10 g을 90 ㎖ 멸균수에 넣어 120 rpm에서 10 분간 현탁한 후 멸균수를 추가하여 단계적으로 10-2~10-4 배로 희석하였다.Nuruk powder was prepared by purchasing three types of Nuruk from a traditional market, crushing them, and mixing them. After suspending 10 g of the Nuruk powder in 90 ml of sterile water at 120 rpm for 10 minutes, sterilized water was added to prepare 10 - It was diluted 2 to 10 -4 times.
상기 희석액 100 ㎕를 MEA 평판배지에 도말하고 25 ℃에서 5 일 동안 1차 배양한 후 나타난 곰팡이 콜로니를 순수분리하였으며, 분리된 곰팡이 균주를 DRBC 배지에 도말하고 25 ℃에서 5 일 동안 2차 배양한 후 냉장보존하였다.100 μl of the dilution was spread on an MEA plate medium, and after primary culture at 25 ° C. for 5 days, the resulting fungal colony was purely isolated. After that, it was refrigerated.
백금이를 이용하여 상기 2차 배양액을 YM broth 배지 30 ㎖에 접종한 후 35 ℃의 진탕항온수조에서 120 rpm으로 교반하면서 12 시간 동안 3차 배양하고, 상기 3차 배양액 100 ㎕를 1 %(w/v)의 가용성 전분(Difco, 미국) 또는 2 %(w/v)의 탈지유(Difco, 미국)가 함유된 각각의 YM 한천배지(효모추출물 3.0 g, 맥아추출물 3.0 g, 펩톤 5.0 g, 덱스트로스 10.0 g, 한천 20.0 g)에 점적하고 35 ℃에서 16 시간 4차 배양하였다.After inoculating the secondary culture medium into 30 ml of YM broth medium using a platinum ear, tertiary culture was performed for 12 hours while stirring at 120 rpm in a shaking constant temperature water bath at 35 ° C., and 100 μl of the tertiary culture was 1% (w Each YM agar medium (yeast extract 3.0 g, malt extract 3.0 g, peptone 5.0 g, deck 10.0 g of Straw, 20.0 g of agar) and incubated for 16 hours at 35 °C for the fourth time.
4차 배양 후 가용성 전분 배지와 탈지유 배지 각각에 형성된 투명환의 크기를 측정하여 투명환이 큰 균주를 선별하여, 전분 및 단백질 분해효소를 다량 생산하는 균주를 분리하였다.After the 4th culture, the size of the transparent ring formed in each of the soluble starch medium and the skim milk medium was measured to select a strain having a large transparent ring, and a strain producing a large amount of starch and proteolytic enzyme was isolated.
다음은 음용수 중 밀기울 1 중량%, 대두분말 1 중량%, 미강 1 중량% 및 효모추출물 0.5 중량%를 함유하는 양액 50 ㎖를 고압멸균기(AC-14, JEIO TECH, 한국)에서 121 ℃, 15 psi에서 15 분간 살균한 다음, 여기에 상기 분리된 균주를 지름 6 ㎜ 크기로 잘라서 접종하고 진탕항온수조를 이용하여 30 ℃, 120 rpm에서 1 일간 5차 배양하였다.Next, 50 ml of a nutrient solution containing 1% by weight of wheat bran, 1% by weight of soybean powder, 1% by weight of rice bran and 0.5% by weight of yeast extract in drinking water was sterilized in a high-pressure sterilizer (AC-14, JEIO TECH, Korea) at 121 ° C. and 15 psi. After sterilization for 15 minutes, the isolated strain was cut into a size of 6 mm in diameter and inoculated therein, and cultured 5 times for 1 day at 30 ° C. and 120 rpm using a shaking constant temperature water bath.
동일한 방식으로, 상기 살균한 양액 500 ㎖에 상기 5차 배양액을 접종하고 진탕항온수조를 이용하여 30 ℃, 120 rpm에서 1 일간 6차 배양하였다.In the same way, the 5th culture medium was inoculated into 500 ml of the sterilized nutrient solution, and the 6th culture was carried out for 1 day at 30 ° C. and 120 rpm using a shaking constant temperature water bath.
현미를 깨끗한 물로 2 회 세척하고 20 ℃의 물에 24 시간 침지한 후 채반에 담아서 1 시간 동안 물을 빼주었으며, 이를 95 ℃에서 1 시간 증자하고 2 시간 동안 냉각시킨 다음 여기에 상기 6차 배양액을 접종하여 골고루 섞어준 후 발효실에 넣고 온도 25 ℃, 습도 90 %를 유지하면서 48 시간 동안 7차 배양하고 배양 중 2 시간마다 뒤섞어 주었다.Brown rice was washed twice with clean water, immersed in water at 20 ° C for 24 hours, put in a sieve and drained for 1 hour, steamed at 95 ° C for 1 hour, cooled for 2 hours, and then added to the 6th culture medium. After inoculation and mixing evenly, it was placed in a fermentation room and cultured 7 times for 48 hours while maintaining a temperature of 25 ° C and a humidity of 90%, and was stirred every 2 hours during culture.
상기 7차 배양액을 30 ℃에서 12 시간 건조하여 고체 종균을 제조하였다.Solid spawn was prepared by drying the 7 th culture solution at 30 °C for 12 hours.
실시예 2의 아스퍼질러스 오리제 균주 대신에 상기 제조된 고체 종균을 사용한 것을 제외하고는, 상기 실시예 2와 동일한 방법으로 식빵을 제조하였다.Bread was prepared in the same manner as in Example 2, except that the prepared solid spawn was used instead of the Aspergillus oryzae strain of Example 2.
<비교예 1><Comparative Example 1>
상기 실시예 1에서, 메밀 경엽 대신에 메밀 알곡을 사용하여 열수추출 농축분말을 제조한 것을 제외하고는, 상기 실시예 1과 동일한 방법으로 식빵을 제조하였다.In Example 1, bread was prepared in the same manner as in Example 1, except that hot-water extracted concentrated powder was prepared using buckwheat grains instead of buckwheat leaves.
<비교예 2><Comparative Example 2>
상기 실시예 1에서, 반죽시 열수추출 농축분말을 사용하지 않고 음용수, 밀가루, 메밀가루, 계란, 설탕, 탈지분유, 소금, 건조 효모액, 제빵개량제, 비타민 미네랄 믹스 및 치커리 식이섬유를 반죽기에 넣어서 반죽한 것을 것을 제외하고는, 상기 실시예 1과 동일한 방법으로 식빵을 제조하였다.In Example 1, drinking water, wheat flour, buckwheat flour, eggs, sugar, skim milk powder, salt, dry yeast liquid, baking improver, vitamin mineral mix and chicory dietary fiber were added to the kneader without using hot water extracted concentrated powder during kneading. Bread was prepared in the same manner as in Example 1, except that it was kneaded.
<시험예 1> 항산화능 측정<Test Example 1> Antioxidant activity measurement
상기 실시예 1~3 및 비교예 1에서 제조된 식빵의 항산화능을 측정하였으며, 항산화능은 각 군별 시료를 에탄올로 추출한 후 추출물의 전자공여능을 Blois의 방법을 변형하여 측정하였다.The antioxidant capacity of the bread prepared in Examples 1 to 3 and Comparative Example 1 was measured, and the antioxidant capacity was measured by modifying the method of Blois for the electron donating ability of the extract after extracting samples for each group with ethanol.
1,1-Diphenyl-2-picrylhydrazyl(DPPH)은 화학적으로 안정화된 수용성 자유라디칼(free radical)로서 517 ㎚에서 특징적인 광흡수를 나타내는 보라색 화합물이며, 항산화 활성이 있는 물질과 접하면 자유라디칼이 소멸되면서 노란색으로 변하게 되는데 이 방법은 육안으로도 쉽게 관찰할 수 있는 대표적인 항산화 실험이다.1,1-Diphenyl-2-picrylhydrazyl (DPPH) is a chemically stabilized water-soluble free radical, which is a purple compound that exhibits characteristic light absorption at 517 nm. As it ages, it turns yellow. This method is a representative antioxidant experiment that can be easily observed with the naked eye.
구체적으로, 각 군별 시료 25 ㎎에 80 % 에탄올 0.5 ㎖를 가한 후 실온으로 설정한 진탕항온수조(shaking water bath)에 24 시간 동안 150 rpm으로 1 회 교반하여 추출물을 얻은 다음, 각 추출물을 10 분 동안 10000 rpm으로 원심분리하고 상등액을 여과한 후 각각 0.3 mM DPPH 1 ㎖와 혼합하여 1 분 동안 반응시키고 분광광도계(spectrophotometer, Model V-560, Jasco Co., 일본)를 사용하여 517 ㎚에서 흡광도를 측정하고 그 결과를 하기 표 1에 나타내었다.Specifically, after adding 0.5 ml of 80% ethanol to 25 mg of sample for each group, the extract was obtained by stirring once at 150 rpm for 24 hours in a shaking water bath set at room temperature, and then each extract was washed for 10 minutes. After centrifugation at 10000 rpm during the process, the supernatant was filtered, mixed with 1 ml of 0.3 mM DPPH, reacted for 1 minute, and the absorbance was measured at 517 nm using a spectrophotometer (Model V-560, Jasco Co., Japan). It was measured and the results are shown in Table 1 below.
상기 표 1을 보면, 메밀 경엽과 다시마의 열수추출 농축분말을 포함하는 실시예의 빵이 메밀 알곡과 다시마의 열수추출 농축분말을 포함하는 비교예 1 및 메밀 경엽과 다시마의 열수추출 농축분말을 포함하지 않은 비교예 2에 비하여 항산화능이 좀 더 우수한 것으로 측정되었다.Referring to Table 1, the bread of Example containing the hot-water extract concentrated powder of buckwheat leaf and kelp does not contain the hot-water extract concentrated powder of buckwheat leaf and kelp and Comparative Example 1 containing the hot-water extract concentrated powder of buckwheat grain and kelp. Compared to Comparative Example 2, the antioxidant activity was measured to be more excellent.
또한, 실시예에서는 실시예 3 〉실시예 2 〉실시예 1의 순서로 항산화능이 우수하여, 빵의 반죽에 메밀, 서목태 및 다시마를 아스퍼질러스 오리제 균주로 발효시킨 곡류 효소를 추가하면 빵의 항산화 활성이 높아지고, 아스퍼질러스 오리제 균주 대신에 전통 누룩에서 분리한 누룩곰팡이 균주로 발효시킨 곡류 효소를 추가하면 빵의 항산화 활성이 더욱 높아짐을 알 수 있다.In addition, in the examples, the antioxidant activity is excellent in the order of Example 3 > Example 2 > Example 1, and adding cereal enzymes fermented with buckwheat, seomoktae and kelp with Aspergillus oryzae strains to the bread dough results in bread It can be seen that the antioxidant activity is increased, and the antioxidant activity of the bread is further increased when the grain enzyme fermented with the Aspergillus oryzae strain isolated from the traditional Nuruk is added instead of the Aspergillus oryzae strain.
상기와 같이, 빵 제조시 메밀 경엽과 다시마의 열수추출 농축분말을 포함시키면 빵의 항산화 활성이 높아지고, 높은 항산화능은 인체에 노화와 질병을 유발하는 자유라디칼을 제거하여 인체에 유익한 효과를 제공할 것으로 판단된다.As described above, when the buckwheat leaves and kelp's hot water extract concentrated powder are included in bread manufacturing, the antioxidant activity of bread increases, and the high antioxidant activity removes free radicals that cause aging and disease in the human body, providing beneficial effects to the human body. It is judged to be
<시험예 2> 식감 분석<Test Example 2> Texture analysis
상기 실시예 및 비교예에서 제조된 빵의 경도(hardness), 탄력성(springness), 응집성(cohesiveness), 검성(gumminess) 및 씹힘성(chewiness)을 분석하였다.Hardness, springness, cohesiveness, gumminess and chewiness of the bread prepared in the above examples and comparative examples were analyzed.
경도는 빵의 단단한 정도를 나타내고, 탄력성은 변형된 물질이 힘 제거시 원상태로 되돌아가려는 성질로서 입안에서는 고무와 같은 탄력이 느껴지는 감각이라고 할 수 있으며, 응집성은 식품 내 성분과 성분이 밀접하게 결합되어 씹었을 때 쉽게 풀어지지 않고 뭉쳐있어서 쫀득쫀득한 느낌을 주는 성질이라 할 수 있고, 검성은 식품을 삼킬 수 있는 상태까지 씹는 데 필요한 에너지를 나타내며, 씹힘성은 식품을 입에서 씹어야 하는 정도 또는 씹는 데 필요한 노력의 정도라고 할 수 있다.Hardness indicates the hardness of bread, elasticity is the property of a deformed material to return to its original state when force is removed, and it can be said to be a sensation of rubber-like elasticity in the mouth. It can be said to be a property that gives a chewy feeling because it is not easily released when chewed, and gumness indicates the energy required to chew food to the point where it can be swallowed. It can be said to be the degree of effort.
각 군별 빵을 물성측정기(COMPAC-100, SUN SCIENCE, 일본)를 이용하여 조직감을 분석하였으며, 분석조건은 test type:TPA, measuring type:2-bite compression test, distance format:33 % strain(10 ㎚), load cell:10 ㎏, plunger diameter:35 ㎜, test speed:120 ㎜/min, sample size(width×length×height):3×3×3 ㎝이었고 분석결과를 하기 표 2에 나타내었다.Bread for each group was analyzed for texture using a physical property measuring instrument (COMPAC-100, SUN SCIENCE, Japan), and the analysis conditions were test type: TPA, measuring type: 2-bite compression test, distance format: 33 % strain (10 nm ), load cell: 10 kg, plunger diameter: 35 mm, test speed: 120 mm/min, sample size (width × length × height): 3 × 3 × 3 cm, and the analysis results are shown in Table 2 below.
상기 표 2를 보면, 각 군별로 경도, 탄력성, 응집성, 검성 및 씹힘성에서 약간의 차이가 있으나 유의적인 결과를 나타내지는 않았으며, 실시예와 비교에 간에도 뚜렷한 차이가 나타나지 않았다.Referring to Table 2, there were slight differences in hardness, elasticity, cohesiveness, gumminess and chewiness for each group, but no significant results were shown, and no clear difference was found between the examples and comparisons.
따라서 빵 제조시 반죽에 메밀 전초와 다시마의 열수추출 농축분말을 첨가하거나 메밀, 서목태 및 다시마를 발효시킨 곡류 효소를 추가하는 것이 빵의 식감에 주는 영향은 미미한 것으로 판단된다.Therefore, it is judged that adding buckwheat starch powder and kelp hot water-extracted concentrated powder or adding fermented grain enzymes from buckwheat, seomoktae, and kelp to the dough during bread manufacturing has a negligible effect on the texture of bread.
<시험예 3> 관능검사<Test Example 3> Sensory test
상기 제조된 식빵을 훈련된 10 명의 요원을 대상으로 외부 색, 향, 맛, 조직감, 전반적인 기호도의 항목을 7점 척도법으로 평가하여 그 평균값을 하기 표 3에 나타내었다.The items of external color, aroma, taste, texture, and overall acceptability of the prepared bread were evaluated on a 7-point scale for 10 trained agents, and the average values are shown in Table 3 below.
색은 실시예 2가 가장 높게 평가되었고, 향과 맛은 실시예 3이 가장 높게 평가되었으며, 조직감은 비교예 1 및 2가 가장 높게 평가되었다.Example 2 was rated the highest for color, Example 3 was rated the highest for flavor and taste, and Comparative Examples 1 and 2 were rated the highest for texture.
즉, 메밀 전초와 다시마의 열수추출 농축분말이 빵의 색, 향 및 맛을 향상시키고, 메밀, 서목태 및 다시마를 발효시킨 곡류 효소를 추가하면 빵의 색, 향 및 맛이 더욱 좋아지는 것을 알 수 있다.In other words, it can be seen that the concentrated powder of hot water extraction of buckwheat sprouts and kelp improves the color, aroma and taste of bread, and the addition of fermented grain enzymes of buckwheat, seomoktae and kelp improves the color, aroma and taste of bread. .
또한, 반죽에 농축분말을 첨가하거나 메밀 알곡 대신에 메밀 경엽을 사용하면 빵의 조직감을 약간 감소하나 유의적인 차이를 나타내지 않았다.In addition, adding concentrated powder to the dough or using buckwheat leaves instead of buckwheat kernels slightly reduced the texture of bread, but did not show a significant difference.
전체적인 기호도에서 실시예가 비교예보다 높게 평가되어 본 발명에 따른 메밀과 다시마 성분을 함유하는 빵의 상품성을 확인할 수 있었다.In the overall preference, the example was evaluated higher than the comparative example, confirming the marketability of the bread containing buckwheat and kelp components according to the present invention.
Claims (7)
상기 혼합분말에 중량기준 25~35 배수의 물을 가하고 90~100 ℃에서 3~5 시간 가열한 다음 여과하여 잔사가 제거된 1차 열수추출물을 얻는 단계;
상기 잔사에 중량기준 25~35 배수의 물을 가하고 90~100 ℃에서 3~5 시간 가열한 다음 여과하여 잔사가 제거된 2차 열수추출물을 얻는 단계;
상기 1차 열수추출물과 2차 열수추출물을 혼합하고 부피가 처음의 5~15 %가 되도록 농축한 다음 건조하여 농축분말을 제조하는 단계;
물에 밀가루, 메밀가루, 계란, 설탕, 탈지분유, 소금, 효모 및 상기 농축분말을 혼합하여 반죽한 후 버터를 첨가하여 다시 반죽하는 단계;
상기 반죽물을 온도 25~30 ℃, 습도 80~90 %에서 80~100 분간 1차 발효시키는 단계;
상기 1차 발효물을 분할하여 실온에서 10~30 분간 2차 발효시키는 단계;
상기 2차 발효물의 가스를 빼고 둥글리기한 다음 온도 35~40 ℃, 습도 85~95 %에서 40~60 분간 3차 발효시키는 단계; 및
상기 3차 발효물을 굽는 단계;를 포함하는 빵의 제조방법.Preparing a mixed powder by washing, drying, and pulverizing buckwheat outpost and kelp;
Adding 25 to 35 times the water by weight to the mixed powder, heating at 90 to 100 ° C. for 3 to 5 hours, and then filtering to obtain a first hot-water extract from which residues are removed;
adding 25 to 35 multiples of water by weight to the residue, heating at 90 to 100 ° C. for 3 to 5 hours, and then filtering to obtain a secondary hot-water extract from which the residue is removed;
preparing a concentrated powder by mixing the first hot water extract and the second hot water extract, concentrating the volume to be 5 to 15% of the first volume, and then drying;
Mixing flour, buckwheat flour, eggs, sugar, skim milk powder, salt, yeast, and the concentrated powder with water, kneading, adding butter and kneading again;
Primary fermentation of the dough at a temperature of 25 to 30 ° C. and a humidity of 80 to 90% for 80 to 100 minutes;
Dividing the primary fermentation product and subjecting it to secondary fermentation at room temperature for 10 to 30 minutes;
Degassing and rounding the secondary fermentation, followed by third fermentation at a temperature of 35 to 40 ° C and a humidity of 85 to 95% for 40 to 60 minutes; and
Bread manufacturing method comprising the step of baking the tertiary fermented product.
상기 반죽물은 물 100 중량부에 밀가루 120~160 중량부, 메밀가루 40~60 중량부, 계란 15~25 중량부, 설탕 10~20 중량부, 탈지분유 5~15 중량부, 소금 1~7 중량부, 효모 1~7 중량부, 농축분말 1~7 중량부 및 버터 15~25 중량부를 포함하는 것을 특징으로 하는 빵의 제조방법.The method of claim 1,
The dough is 100 parts by weight of water, 120 to 160 parts by weight of wheat flour, 40 to 60 parts by weight of buckwheat flour, 15 to 25 parts by weight of eggs, 10 to 20 parts by weight of sugar, 5 to 15 parts by weight of skim milk powder, and 1 to 7 parts by weight of salt. A method for producing bread, comprising 1 to 7 parts by weight of yeast, 1 to 7 parts by weight of concentrated powder, and 15 to 25 parts by weight of butter.
상기 반죽하는 단계의 물에 곡류 효소를 추가하며,
상기 곡류 효소는, 메밀과 서목태를 물에 침지하여 수분함량이 34~38 중량%가 되도록 한 후 물을 빼주는 단계;
상기 물을 뺀 메밀 70~90 중량%, 물을 뺀 서목태 5~15 중량% 및 다시마 분말 5~15 중량%를 혼합하여 증자한 후 냉각시키는 단계;
상기 냉각된 메밀. 서목태 및 다시마 분말에 누룩곰팡이를 0.5~3.0 중량%의 비율로 접종하고 20~30 ℃에서 45~55 시간 발효시키는 단계; 및
상기 발효물을 건조하여 분쇄하는 단계;를 통하여 제조되는 것을 특징으로 하는 빵의 제조방법.The method of claim 1,
Add grain enzyme to the water in the kneading step,
The cereal enzyme, immersing buckwheat and seomoktae in water so that the water content is 34 to 38% by weight, and then draining the water;
70 to 90% by weight of buckwheat minus the water, 5 to 15% by weight of seomoktae and 5 to 15% by weight of kelp powder are mixed, steamed, and then cooled;
The cooled buckwheat. Inoculating Aspergillus mold in seomoktae and kelp powder at a rate of 0.5 to 3.0% by weight and fermenting at 20 to 30 ° C. for 45 to 55 hours; and
Method for producing bread, characterized in that produced through; drying and grinding the fermented product.
상기 누룩곰팡이는, 누룩을 분쇄하여 멸균수와 혼합하고 현탁시키는 단계;
상기 현탁액을 23~27 ℃에서 4~6 일간 1차 배양하는 단계;
상기 1차 배양액에서 콜로니를 분리하여 23~27 ℃에서 4~6 일간 2차 배양하는 단계;
상기 2차 배양액을 33~37 ℃에서 진탕하면서 10~15 시간 3차 배양하는 단계;
상기 3차 배양액을 0.5~2.0 %(w/v) 농도의 가용성 전분 또는 1~5 %(w/v) 농도의 탈지유가 함유된 배지에 점적하고 33~37 ℃에서 12~20 시간 4차 배양하는 단계;
상기 4차 배양액의 배지 위에 형성된 투명환의 크기가 큰 균주를 선별하는 단계;
음용수 100 중량부에 밀기울 0.5~3.0 중량부, 대두분말 0.5~3.0 중량부, 미강 0.5~3.0 중량부 및 효모 0.1~1.0 중량부를 혼합하여 양액을 준비하는 단계;
상기 양액을 살균한 후 상기 선별된 균주를 접종하고 28~32 ℃에서 진탕하면서 20~30 시간 5차 배양하는 단계;
상기 살균한 양액에 상기 5차 배양액을 접종하고 28~32 ℃에서 진탕하면서 20~30 시간 6차 배양하는 단계;
현미를 증자하여 냉각하고 여기에 상기 6차 배양액을 접종하여 온도 23~27 ℃, 습도 85~95 %에서 40~55 시간 7차 배양한 후 건조하는 단계;를 통하여 제조되는 것을 특징으로 하는 빵의 제조방법.The method of claim 3,
The Aspergillus mold, pulverizing the Nuruk, mixing and suspending the Nuruk with sterilized water;
Primary incubation of the suspension at 23 to 27 ° C. for 4 to 6 days;
Isolating colonies from the primary culture medium and culturing the secondary culture at 23-27 ° C for 4-6 days;
third culturing for 10 to 15 hours while shaking the secondary culture at 33 to 37 ° C;
The tertiary culture medium was added to a medium containing soluble starch at a concentration of 0.5 to 2.0% (w/v) or skim milk at a concentration of 1 to 5% (w/v), followed by 4th culture at 33 to 37 ° C for 12 to 20 hours. doing;
Selecting a strain having a large transparent ring formed on the medium of the quaternary culture;
Preparing a nutrient solution by mixing 0.5 to 3.0 parts by weight of wheat bran, 0.5 to 3.0 parts by weight of soybean powder, 0.5 to 3.0 parts by weight of rice bran, and 0.1 to 1.0 parts by weight of yeast with 100 parts by weight of drinking water;
After sterilizing the nutrient solution, inoculating the selected strain and incubating the 5th culture for 20 to 30 hours while shaking at 28 to 32 ° C;
Inoculating the 5th culture solution into the sterilized nutrient solution and culturing the 6th culture for 20-30 hours while shaking at 28-32 ° C;
Bread, characterized in that produced by manufacturing method.
상기 곡류 효소를 히드록시프로필 메틸셀룰로오스로 코팅하는 것을 특징으로 하는 빵의 제조방법.The method of claim 3,
A method for producing bread, characterized in that the grain enzyme is coated with hydroxypropyl methylcellulose.
상기 히드록시프로필 메틸셀룰로오스는 메톡시기와 히드록시프로폭시기가 치환도 19~30:4~12의 비율로 구성되는 것을 특징으로 하는 빵의 제조방법.The method of claim 5,
The hydroxypropyl methylcellulose is a method for producing bread, characterized in that the ratio of the methoxy group and the hydroxypropoxy group is 19 to 30: 4 to 12 substitution.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1020210186406A KR102653907B1 (en) | 2021-12-23 | 2021-12-23 | Method for Manufacturing Bread Containing Buckwheat and Kelp Ingredient |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1020210186406A KR102653907B1 (en) | 2021-12-23 | 2021-12-23 | Method for Manufacturing Bread Containing Buckwheat and Kelp Ingredient |
Publications (2)
Publication Number | Publication Date |
---|---|
KR20230096680A true KR20230096680A (en) | 2023-06-30 |
KR102653907B1 KR102653907B1 (en) | 2024-04-01 |
Family
ID=86960085
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1020210186406A KR102653907B1 (en) | 2021-12-23 | 2021-12-23 | Method for Manufacturing Bread Containing Buckwheat and Kelp Ingredient |
Country Status (1)
Country | Link |
---|---|
KR (1) | KR102653907B1 (en) |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100567389B1 (en) * | 2002-11-08 | 2006-04-04 | (주)바이오뉴트리젠 | Carbohydrate foods comprising powders or extracts of plants comprising polyphenol or bioflavonoid for suppressing the fatness |
KR20060095672A (en) * | 2005-02-28 | 2006-09-01 | 주식회사 다우존팜 | Method for producing flour using |
KR20100087513A (en) * | 2009-01-28 | 2010-08-05 | 충남대학교산학협력단 | Preparation method for bread containing spirulina |
-
2021
- 2021-12-23 KR KR1020210186406A patent/KR102653907B1/en active IP Right Grant
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100567389B1 (en) * | 2002-11-08 | 2006-04-04 | (주)바이오뉴트리젠 | Carbohydrate foods comprising powders or extracts of plants comprising polyphenol or bioflavonoid for suppressing the fatness |
KR20060095672A (en) * | 2005-02-28 | 2006-09-01 | 주식회사 다우존팜 | Method for producing flour using |
KR20100087513A (en) * | 2009-01-28 | 2010-08-05 | 충남대학교산학협력단 | Preparation method for bread containing spirulina |
Also Published As
Publication number | Publication date |
---|---|
KR102653907B1 (en) | 2024-04-01 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Haard | Fermented cereals: a global perspective | |
KR101249442B1 (en) | Method of preparing bread using bacilus subtilis and bread comprising fermented material by bacilus subtilis | |
Szabłowska et al. | Acorn flour properties depending on the production method and laboratory baking test results: A review | |
KR101823088B1 (en) | Method for manufacturing breads using lactic acid bacteria | |
KR20210039769A (en) | Manufacturing method of Nurungi using liquerfied Opuntia humifusa | |
KR20140034981A (en) | Method for increasing resveratrol content of peanut sprouts and foods in resveratrol of peanut sprouts | |
CN112369563A (en) | Barley seedling powder green ball and preparation method thereof | |
KR20170065452A (en) | Lotus tea beverage and manufacturing method thereof | |
KR102081990B1 (en) | Yorgurt comprising rice germ and preparation method thereof | |
KR101875189B1 (en) | Food additive composition comprising tengcha and functional food using thefeof | |
KR102073393B1 (en) | Methdo for preparing soybean sauce and paste using fermented chaga mushroom powder and bamboo salt | |
KR102653907B1 (en) | Method for Manufacturing Bread Containing Buckwheat and Kelp Ingredient | |
KR101781109B1 (en) | Method for producing colored Jocheong using colored malt and colored Jocheong produced by same method | |
KR20090081598A (en) | Method for Preparing Fermented Soybean Powder | |
KR102676272B1 (en) | Method for Manufacturing Grain Enzyme Containing Buckwheat | |
KR101866468B1 (en) | Enzyme food and diet enzyme food comprising concentrated product by fermentation of grains, and their preparation method | |
KR20190077799A (en) | Manufacturing method of grain tea having germinated GABA rice using aspergillus | |
KR102527825B1 (en) | Manufacturing method of condensed milk cream for baguette and condensed milk cream manufactured by the same | |
KR102518361B1 (en) | Manufacturing method of rice baguette and rice baguette manufactured by the same | |
KR102338680B1 (en) | Method for manufacturing functional mugwort and brown rice cake | |
KR20140050889A (en) | Manufacturing method of sunsik with fermented grain and water soluble propolis | |
KR102497862B1 (en) | Method for manufacturing natural fermented species and the natural fermented species prepared therefrom | |
KR102624478B1 (en) | Method for producing sorghum red bean rice bread comprising sorghum and red bean | |
KR20140102099A (en) | Germinated Wheat Deonjang and Its Manufacturing Method | |
KR102345350B1 (en) | Bamboo salt comprising dendropanax morbiferus and manufacturing method thereof |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
E902 | Notification of reason for refusal | ||
E701 | Decision to grant or registration of patent right | ||
GRNT | Written decision to grant |