JP5111096B2 - Production method of tea extract - Google Patents
Production method of tea extract Download PDFInfo
- Publication number
- JP5111096B2 JP5111096B2 JP2007337521A JP2007337521A JP5111096B2 JP 5111096 B2 JP5111096 B2 JP 5111096B2 JP 2007337521 A JP2007337521 A JP 2007337521A JP 2007337521 A JP2007337521 A JP 2007337521A JP 5111096 B2 JP5111096 B2 JP 5111096B2
- Authority
- JP
- Japan
- Prior art keywords
- tea extract
- tea
- mass
- concentration
- extract
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Active
Links
- 239000000284 extract Substances 0.000 title claims description 120
- 238000004519 manufacturing process Methods 0.000 title claims description 11
- 241001122767 Theaceae Species 0.000 title claims 7
- ADRVNXBAWSRFAJ-UHFFFAOYSA-N catechin Natural products OC1Cc2cc(O)cc(O)c2OC1c3ccc(O)c(O)c3 ADRVNXBAWSRFAJ-UHFFFAOYSA-N 0.000 claims description 44
- 235000005487 catechin Nutrition 0.000 claims description 44
- 229920000642 polymer Polymers 0.000 claims description 35
- 150000001765 catechin Chemical class 0.000 claims description 33
- 238000000034 method Methods 0.000 claims description 26
- 239000012528 membrane Substances 0.000 claims description 23
- 108010038851 tannase Proteins 0.000 claims description 18
- PFTAWBLQPZVEMU-DZGCQCFKSA-N (+)-catechin Chemical compound C1([C@H]2OC3=CC(O)=CC(O)=C3C[C@@H]2O)=CC=C(O)C(O)=C1 PFTAWBLQPZVEMU-DZGCQCFKSA-N 0.000 claims description 11
- 229950001002 cianidanol Drugs 0.000 claims description 11
- 239000007787 solid Substances 0.000 claims description 9
- 230000000694 effects Effects 0.000 claims description 8
- 238000001471 micro-filtration Methods 0.000 claims description 7
- 108090000790 Enzymes Proteins 0.000 claims description 5
- 102000004190 Enzymes Human genes 0.000 claims description 5
- LNTHITQWFMADLM-UHFFFAOYSA-N gallic acid Chemical compound OC(=O)C1=CC(O)=C(O)C(O)=C1 LNTHITQWFMADLM-UHFFFAOYSA-N 0.000 claims description 5
- 239000011148 porous material Substances 0.000 claims description 4
- 238000002360 preparation method Methods 0.000 claims description 3
- 244000269722 Thea sinensis Species 0.000 description 144
- 235000013616 tea Nutrition 0.000 description 138
- 238000010438 heat treatment Methods 0.000 description 31
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 28
- 235000019640 taste Nutrition 0.000 description 23
- 235000013361 beverage Nutrition 0.000 description 20
- 238000000605 extraction Methods 0.000 description 15
- 230000000052 comparative effect Effects 0.000 description 13
- 238000011282 treatment Methods 0.000 description 13
- 235000019658 bitter taste Nutrition 0.000 description 12
- 239000007788 liquid Substances 0.000 description 12
- 238000000926 separation method Methods 0.000 description 12
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 10
- 238000001914 filtration Methods 0.000 description 10
- 239000000796 flavoring agent Substances 0.000 description 10
- 235000019634 flavors Nutrition 0.000 description 10
- 239000003960 organic solvent Substances 0.000 description 10
- 235000009569 green tea Nutrition 0.000 description 9
- 238000011156 evaluation Methods 0.000 description 8
- 235000003599 food sweetener Nutrition 0.000 description 7
- LVJJFMLUMNSUFN-UHFFFAOYSA-N gallocatechin gallate Natural products C1=C(O)C=C2OC(C=3C=C(O)C(O)=CC=3)C(O)CC2=C1OC(=O)C1=CC(O)=C(O)C(O)=C1 LVJJFMLUMNSUFN-UHFFFAOYSA-N 0.000 description 7
- -1 polyethylene Polymers 0.000 description 7
- 230000001954 sterilising effect Effects 0.000 description 7
- 239000003765 sweetening agent Substances 0.000 description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- 241000037488 Coccoloba pubescens Species 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
- 238000005119 centrifugation Methods 0.000 description 6
- 239000004927 clay Substances 0.000 description 6
- 239000012141 concentrate Substances 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- 238000004659 sterilization and disinfection Methods 0.000 description 6
- LSHVYAFMTMFKBA-PZJWPPBQSA-N (+)-catechin-3-O-gallate Chemical compound O([C@H]1CC2=C(O)C=C(C=C2O[C@@H]1C=1C=C(O)C(O)=CC=1)O)C(=O)C1=CC(O)=C(O)C(O)=C1 LSHVYAFMTMFKBA-PZJWPPBQSA-N 0.000 description 5
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 5
- 239000000919 ceramic Substances 0.000 description 5
- 238000001816 cooling Methods 0.000 description 5
- 235000019225 fermented tea Nutrition 0.000 description 5
- 229910052751 metal Inorganic materials 0.000 description 5
- 239000002184 metal Substances 0.000 description 5
- 239000011259 mixed solution Substances 0.000 description 5
- 229920006254 polymer film Polymers 0.000 description 5
- 239000004215 Carbon black (E152) Substances 0.000 description 4
- 229920000858 Cyclodextrin Polymers 0.000 description 4
- WMBWREPUVVBILR-UHFFFAOYSA-N GCG Natural products C=1C(O)=C(O)C(O)=CC=1C1OC2=CC(O)=CC(O)=C2CC1OC(=O)C1=CC(O)=C(O)C(O)=C1 WMBWREPUVVBILR-UHFFFAOYSA-N 0.000 description 4
- 239000007864 aqueous solution Substances 0.000 description 4
- 235000019606 astringent taste Nutrition 0.000 description 4
- RYYVLZVUVIJVGH-UHFFFAOYSA-N caffeine Chemical compound CN1C(=O)N(C)C(=O)C2=C1N=CN2C RYYVLZVUVIJVGH-UHFFFAOYSA-N 0.000 description 4
- 229940088598 enzyme Drugs 0.000 description 4
- 229930195733 hydrocarbon Natural products 0.000 description 4
- 150000002430 hydrocarbons Chemical class 0.000 description 4
- 238000005259 measurement Methods 0.000 description 4
- WMBWREPUVVBILR-WIYYLYMNSA-N (-)-Epigallocatechin-3-o-gallate Chemical compound O([C@@H]1CC2=C(O)C=C(C=C2O[C@@H]1C=1C=C(O)C(O)=C(O)C=1)O)C(=O)C1=CC(O)=C(O)C(O)=C1 WMBWREPUVVBILR-WIYYLYMNSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- 230000002378 acidificating effect Effects 0.000 description 3
- 150000001298 alcohols Chemical class 0.000 description 3
- 229960001948 caffeine Drugs 0.000 description 3
- XMOCLSLCDHWDHP-IUODEOHRSA-N epi-Gallocatechin Chemical compound C1([C@H]2OC3=CC(O)=CC(O)=C3C[C@H]2O)=CC(O)=C(O)C(O)=C1 XMOCLSLCDHWDHP-IUODEOHRSA-N 0.000 description 3
- 235000013305 food Nutrition 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 238000001223 reverse osmosis Methods 0.000 description 3
- HFHDHCJBZVLPGP-UHFFFAOYSA-N schardinger α-dextrin Chemical compound O1C(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(O)C2O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC2C(O)C(O)C1OC2CO HFHDHCJBZVLPGP-UHFFFAOYSA-N 0.000 description 3
- 238000001694 spray drying Methods 0.000 description 3
- WMBWREPUVVBILR-GHTZIAJQSA-N (+)-gallocatechin gallate Chemical compound O([C@H]1CC2=C(O)C=C(C=C2O[C@@H]1C=1C=C(O)C(O)=C(O)C=1)O)C(=O)C1=CC(O)=C(O)C(O)=C1 WMBWREPUVVBILR-GHTZIAJQSA-N 0.000 description 2
- LSHVYAFMTMFKBA-TZIWHRDSSA-N (-)-epicatechin-3-O-gallate Chemical compound O([C@@H]1CC2=C(O)C=C(C=C2O[C@@H]1C=1C=C(O)C(O)=CC=1)O)C(=O)C1=CC(O)=C(O)C(O)=C1 LSHVYAFMTMFKBA-TZIWHRDSSA-N 0.000 description 2
- 241000209507 Camellia Species 0.000 description 2
- LSHVYAFMTMFKBA-UHFFFAOYSA-N ECG Natural products C=1C=C(O)C(O)=CC=1C1OC2=CC(O)=CC(O)=C2CC1OC(=O)C1=CC(O)=C(O)C(O)=C1 LSHVYAFMTMFKBA-UHFFFAOYSA-N 0.000 description 2
- LPHGQDQBBGAPDZ-UHFFFAOYSA-N Isocaffeine Natural products CN1C(=O)N(C)C(=O)C2=C1N(C)C=N2 LPHGQDQBBGAPDZ-UHFFFAOYSA-N 0.000 description 2
- XMOCLSLCDHWDHP-UHFFFAOYSA-N L-Epigallocatechin Natural products OC1CC2=C(O)C=C(O)C=C2OC1C1=CC(O)=C(O)C(O)=C1 XMOCLSLCDHWDHP-UHFFFAOYSA-N 0.000 description 2
- 235000006468 Thea sinensis Nutrition 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 230000005540 biological transmission Effects 0.000 description 2
- 235000020279 black tea Nutrition 0.000 description 2
- VJEONQKOZGKCAK-UHFFFAOYSA-N caffeine Natural products CN1C(=O)N(C)C(=O)C2=C1C=CN2C VJEONQKOZGKCAK-UHFFFAOYSA-N 0.000 description 2
- HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 description 2
- 235000018597 common camellia Nutrition 0.000 description 2
- 239000003995 emulsifying agent Substances 0.000 description 2
- 235000012734 epicatechin Nutrition 0.000 description 2
- DZYNKLUGCOSVKS-UHFFFAOYSA-N epigallocatechin Natural products OC1Cc2cc(O)cc(O)c2OC1c3cc(O)c(O)c(O)c3 DZYNKLUGCOSVKS-UHFFFAOYSA-N 0.000 description 2
- 229940030275 epigallocatechin gallate Drugs 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 238000011049 filling Methods 0.000 description 2
- 238000004108 freeze drying Methods 0.000 description 2
- 235000011187 glycerol Nutrition 0.000 description 2
- 239000012510 hollow fiber Substances 0.000 description 2
- 239000003112 inhibitor Substances 0.000 description 2
- 230000002401 inhibitory effect Effects 0.000 description 2
- 150000002576 ketones Chemical class 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 235000020333 oolong tea Nutrition 0.000 description 2
- 150000007524 organic acids Chemical class 0.000 description 2
- 229920002492 poly(sulfone) Polymers 0.000 description 2
- 229920000139 polyethylene terephthalate Polymers 0.000 description 2
- 239000005020 polyethylene terephthalate Substances 0.000 description 2
- 229920000098 polyolefin Polymers 0.000 description 2
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 2
- 239000004810 polytetrafluoroethylene Substances 0.000 description 2
- 229920002981 polyvinylidene fluoride Polymers 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 238000000746 purification Methods 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 150000003457 sulfones Chemical class 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- XMOCLSLCDHWDHP-SWLSCSKDSA-N (+)-Epigallocatechin Natural products C1([C@H]2OC3=CC(O)=CC(O)=C3C[C@@H]2O)=CC(O)=C(O)C(O)=C1 XMOCLSLCDHWDHP-SWLSCSKDSA-N 0.000 description 1
- PFTAWBLQPZVEMU-ZFWWWQNUSA-N (+)-epicatechin Natural products C1([C@@H]2OC3=CC(O)=CC(O)=C3C[C@@H]2O)=CC=C(O)C(O)=C1 PFTAWBLQPZVEMU-ZFWWWQNUSA-N 0.000 description 1
- PFTAWBLQPZVEMU-UKRRQHHQSA-N (-)-epicatechin Chemical compound C1([C@H]2OC3=CC(O)=CC(O)=C3C[C@H]2O)=CC=C(O)C(O)=C1 PFTAWBLQPZVEMU-UKRRQHHQSA-N 0.000 description 1
- TUSDEZXZIZRFGC-UHFFFAOYSA-N 1-O-galloyl-3,6-(R)-HHDP-beta-D-glucose Natural products OC1C(O2)COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC1C(O)C2OC(=O)C1=CC(O)=C(O)C(O)=C1 TUSDEZXZIZRFGC-UHFFFAOYSA-N 0.000 description 1
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Natural products OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 1
- 241000228212 Aspergillus Species 0.000 description 1
- 240000006439 Aspergillus oryzae Species 0.000 description 1
- 235000002247 Aspergillus oryzae Nutrition 0.000 description 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- 241000894006 Bacteria Species 0.000 description 1
- 240000008441 Camellia sinensis var. assamica Species 0.000 description 1
- 239000004278 EU approved seasoning Substances 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 239000001263 FEMA 3042 Substances 0.000 description 1
- 240000005979 Hordeum vulgare Species 0.000 description 1
- 235000007340 Hordeum vulgare Nutrition 0.000 description 1
- 241000416395 Ixodes sinensis Species 0.000 description 1
- 241000228143 Penicillium Species 0.000 description 1
- LRBQNJMCXXYXIU-PPKXGCFTSA-N Penta-digallate-beta-D-glucose Natural products OC1=C(O)C(O)=CC(C(=O)OC=2C(=C(O)C=C(C=2)C(=O)OC[C@@H]2[C@H]([C@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)O2)OC(=O)C=2C=C(OC(=O)C=3C=C(O)C(O)=C(O)C=3)C(O)=C(O)C=2)O)=C1 LRBQNJMCXXYXIU-PPKXGCFTSA-N 0.000 description 1
- 229920012266 Poly(ether sulfone) PES Polymers 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 241000235527 Rhizopus Species 0.000 description 1
- FIAAVMJLAGNUKW-UHFFFAOYSA-N UNPD109131 Natural products OC1C(O)C(O)C(CO)OC1C1=C(O)C(C2C(C(O)C(O)C(CO)O2)O)=C(OC(=CC2=O)C=3C=CC(O)=CC=3)C2=C1O FIAAVMJLAGNUKW-UHFFFAOYSA-N 0.000 description 1
- FIAAVMJLAGNUKW-CRLPPWHZSA-N Vicenin 2 Natural products O=C1c2c(O)c([C@H]3[C@H](O)[C@@H](O)[C@H](O)[C@H](CO)O3)c(O)c([C@H]3[C@@H](O)[C@@H](O)[C@H](O)[C@H](CO)O3)c2OC(c2ccc(O)cc2)=C1 FIAAVMJLAGNUKW-CRLPPWHZSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000032683 aging Effects 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
- 235000001014 amino acid Nutrition 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 235000006708 antioxidants Nutrition 0.000 description 1
- 239000008122 artificial sweetener Substances 0.000 description 1
- 235000021311 artificial sweeteners Nutrition 0.000 description 1
- 229960005070 ascorbic acid Drugs 0.000 description 1
- 235000010323 ascorbic acid Nutrition 0.000 description 1
- 239000011668 ascorbic acid Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000001580 bacterial effect Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 150000001719 carbohydrate derivatives Chemical class 0.000 description 1
- 150000001720 carbohydrates Chemical class 0.000 description 1
- 235000014633 carbohydrates Nutrition 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 235000012000 cholesterol Nutrition 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 238000012258 culturing Methods 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 230000035622 drinking Effects 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- LPTRNLNOHUVQMS-UHFFFAOYSA-N epicatechin Natural products Cc1cc(O)cc2OC(C(O)Cc12)c1ccc(O)c(O)c1 LPTRNLNOHUVQMS-UHFFFAOYSA-N 0.000 description 1
- 238000000855 fermentation Methods 0.000 description 1
- 230000004151 fermentation Effects 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 235000011194 food seasoning agent Nutrition 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 235000015203 fruit juice Nutrition 0.000 description 1
- GDSRMADSINPKSL-HSEONFRVSA-N gamma-cyclodextrin Chemical compound OC[C@H]([C@H]([C@@H]([C@H]1O)O)O[C@H]2O[C@@H]([C@@H](O[C@H]3O[C@H](CO)[C@H]([C@@H]([C@H]3O)O)O[C@H]3O[C@H](CO)[C@H]([C@@H]([C@H]3O)O)O[C@H]3O[C@H](CO)[C@H]([C@@H]([C@H]3O)O)O[C@H]3O[C@H](CO)[C@H]([C@@H]([C@H]3O)O)O[C@H]3O[C@H](CO)[C@H]([C@@H]([C@H]3O)O)O3)[C@H](O)[C@H]2O)CO)O[C@@H]1O[C@H]1[C@H](O)[C@@H](O)[C@@H]3O[C@@H]1CO GDSRMADSINPKSL-HSEONFRVSA-N 0.000 description 1
- 229940080345 gamma-cyclodextrin Drugs 0.000 description 1
- 229940094952 green tea extract Drugs 0.000 description 1
- 235000020688 green tea extract Nutrition 0.000 description 1
- 229940093915 gynecological organic acid Drugs 0.000 description 1
- 230000002779 inactivation Effects 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 238000005342 ion exchange Methods 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- FIAAVMJLAGNUKW-VQVVXJKKSA-N isovitexin 8-C-beta-glucoside Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1C1=C(O)C([C@H]2[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O2)O)=C(OC(=CC2=O)C=3C=CC(O)=CC=3)C2=C1O FIAAVMJLAGNUKW-VQVVXJKKSA-N 0.000 description 1
- TYQCGQRIZGCHNB-JLAZNSOCSA-N l-ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(O)=C(O)C1=O TYQCGQRIZGCHNB-JLAZNSOCSA-N 0.000 description 1
- 150000002632 lipids Chemical class 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 239000008239 natural water Substances 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 235000019198 oils Nutrition 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 230000008520 organization Effects 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 230000001766 physiological effect Effects 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000000419 plant extract Substances 0.000 description 1
- 229920006255 plastic film Polymers 0.000 description 1
- 239000002985 plastic film Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920005597 polymer membrane Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229910001414 potassium ion Inorganic materials 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 229910001415 sodium ion Inorganic materials 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 235000011496 sports drink Nutrition 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- LRBQNJMCXXYXIU-NRMVVENXSA-N tannic acid Chemical compound OC1=C(O)C(O)=CC(C(=O)OC=2C(=C(O)C=C(C=2)C(=O)OC[C@@H]2[C@H]([C@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)O2)OC(=O)C=2C=C(OC(=O)C=3C=C(O)C(O)=C(O)C=3)C(O)=C(O)C=2)O)=C1 LRBQNJMCXXYXIU-NRMVVENXSA-N 0.000 description 1
- 235000015523 tannic acid Nutrition 0.000 description 1
- 229940033123 tannic acid Drugs 0.000 description 1
- 229920002258 tannic acid Polymers 0.000 description 1
- 239000008399 tap water Substances 0.000 description 1
- 235000020679 tap water Nutrition 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- CSNXTSWTBUEIJB-UHFFFAOYSA-N vicenin-II Natural products OC1C(O)C(O)C(CO)OC1OC1=C(O)C(OC2C(C(O)C(O)C(CO)O2)O)=C(OC(=CC2=O)C=3C=CC(O)=CC=3)C2=C1O CSNXTSWTBUEIJB-UHFFFAOYSA-N 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 239000000341 volatile oil Substances 0.000 description 1
Images
Landscapes
- Tea And Coffee (AREA)
Description
本発明は茶抽出物の製造法に関する。 The present invention relates to a method for producing a tea extract.
カテキン類の効果としては、コレステロール上昇抑制作用やαアミラーゼ活性阻害作用などが報告されている。このような生理効果を発現させるためには、より簡便に大量のカテキン類を摂取することが有効である。飲料に高濃度のカテキン類を配合する方法として、例えば、緑茶抽出物の濃縮物等を利用してカテキン類を飲料に溶解状態で添加する方法が知られているが、緑茶の抽出方法によってはエグ味という不快な異味が発生する場合がある。 The effects of catechins have been reported to be a cholesterol elevation inhibitory action, an α-amylase activity inhibitory action, and the like. In order to express such physiological effects, it is effective to ingest a large amount of catechins more simply. As a method of blending a high concentration of catechins into a beverage, for example, a method of adding catechins in a dissolved state to a beverage using a concentrate of a green tea extract or the like is known, but depending on the method of extracting green tea An unpleasant nasty taste such as egg taste may occur.
このようなエグ味を低減する技術として数多くの提案がなされており、例えば、スピラントール又はスピラントールを含有する植物抽出物若しくは植物精油由来の高甘味度甘味料を添加する方法(特許文献1参照)、ビセニン−2からなる呈味改善剤を添加する方法(特許文献2参照)、α,α’−トレハロースの糖質誘導体を添加する方法(特許文献3参照)等が報告されている。 Numerous proposals have been made as a technique for reducing such a taste, for example, a method of adding a high-sweetness sweetener derived from spirantol or a plant extract or plant essential oil containing spirantol (see Patent Document 1), A method of adding a taste improving agent comprising vicenin-2 (see Patent Document 2), a method of adding a carbohydrate derivative of α, α′-trehalose (see Patent Document 3), and the like have been reported.
しかしながら、これらの甘味料等を非重合体カテキン類を含有する茶抽出物に少量添加しただけでは不快なエグ味を十分に低減できず、しかも茶本来の風味や香りを損ないやすい。また、甘味料添加後の茶抽出物を精製処理する場合に、添加した甘味料が精製に悪影響を及ぼす場合がある。このように、甘味料等を用いてエグ味を低減させる手段には限界がある。
したがって、本発明の目的は、エグ味が抑制された茶抽出物の製造法、及び該製造法により得られた茶抽出物を提供することにある。
However, the addition of a small amount of these sweeteners or the like to a tea extract containing non-polymer catechins cannot sufficiently reduce the unpleasant taste and tends to impair the original flavor and aroma of tea. Moreover, when refine | purifying the tea extract after sweetener addition, the added sweetener may have a bad influence on refinement | purification. Thus, there is a limit to means for reducing the taste by using a sweetener or the like.
Therefore, the objective of this invention is providing the manufacturing method of the tea extract by which the taste was suppressed, and the tea extract obtained by this manufacturing method.
本発明者は、茶から得られた茶抽出液の濁りの状態や加熱処理の条件により、異なった風味が感じられるとの知見を得た。本発明者は更に詳細に検討したところ、茶から得られた茶抽出液を所定条件下にて固液分離し、得られた茶抽出液を更に所定条件下にて加熱処理することで、エグ味が抑制された茶抽出物が得られることを見出した。 The present inventor has obtained knowledge that different flavors can be felt depending on the turbid state of the tea extract obtained from tea and the conditions of the heat treatment. The present inventor has examined in further detail, and by separating the tea extract obtained from tea into solid and liquid under a predetermined condition and further heat-treating the obtained tea extract under a predetermined condition, It was found that a tea extract with a suppressed taste was obtained.
本発明は、茶から得られた第1の茶抽出液を、非重合体カテキン類濃度を1質量%としたときの濁度が200NTU以下になるように固液分離して、非重合体カテキン類濃度が0.2〜5質量%であり、かつ固形分中の非重合体カテキン類濃度が15〜80質量%である第2の茶抽出液を得、次いで第2の茶抽出液を温度95〜140℃、F値0.05〜40(Z=10)にて加熱処理する、茶抽出物の製造法を提供するものである。
本発明はまた、上記した製造法により得られた茶抽出物を提供するものである。
In the present invention, the first tea extract obtained from tea is subjected to solid-liquid separation so that the turbidity when the concentration of non-polymer catechins is 1% by mass is 200 NTU or less. To obtain a second tea extract having a concentration of 0.2 to 5% by mass and a non-polymer catechin concentration in the solid content of 15 to 80% by mass, and then subjecting the second tea extract to temperature The present invention provides a method for producing a tea extract, which is heat-treated at 95 to 140 ° C. and an F value of 0.05 to 40 (Z = 10).
The present invention also provides a tea extract obtained by the production method described above.
本発明の製造方法によれば、シュウ酸、タンパク質、繊維、脂質等の水難溶成分が選択的にかつ効率よく除去されるため、エグ味だけなく、苦味及び加熱異臭が抑制された茶抽出物を簡便に製造することができる。また、この茶抽出物は、エグ味、苦味及び加熱異臭が抑制されており、非重合体カテキン類を高濃度で含有することから、多量のカテキン類を手軽に摂取できる茶系又は非茶系飲料の製造原料として有用である。 According to the production method of the present invention, a poorly water-soluble component such as oxalic acid, protein, fiber, and lipid is selectively and efficiently removed, so that not only the taste but also the bitter taste and the heated odor are suppressed. Can be easily produced. In addition, this tea extract is suppressed in the taste, bitterness and unpleasant odor, and contains a high concentration of non-polymer catechins, so that a large amount of catechins can be easily consumed. It is useful as a raw material for producing beverages.
本発明において非重合体カテキン類とは、カテキン、ガロカテキン、カテキンガレート、ガロカテキンガレート等の非エピ体カテキン類、及びエピカテキン、エピガロカテキン、エピカテキンガレート、エピガロカテキンガレート等のエピ体カテキン類をあわせての総称であり、非重合体カテキン類の濃度は、上記8種の合計量に基づいて定義される。また、非エピ体率とは、上記8種の非重合体カテキン類の質量和に対する非エピカテキン類4種の質量和の100分率の値である。 In the present invention, non-polymer catechins include non-epimeric catechins such as catechin, gallocatechin, catechin gallate, and gallocatechin gallate, and epimeric catechins such as epicatechin, epigallocatechin, epicatechin gallate, and epigallocatechin gallate. The concentration of non-polymer catechins is defined based on the total amount of the above eight types. Further, the non-epimeric ratio is a value of 100 fraction of the mass sum of the four types of non-epicatechins relative to the mass sum of the eight types of non-polymer catechins.
本発明における非重合体カテキンガレート体とは、カテキンガレート、ガロカテキンガレート、エピカテキンガレート及びエピガロカテキンガレートの4種をあわせての総称であり、ガレート体率とは、上記8種の非重合体カテキン類の質量和に対する非重合体カテキンガレート体4種の質量和の100分率の値である。 The non-polymer catechin gallate body in the present invention is a general term that includes four types of catechin gallate, gallocatechin gallate, epicatechin gallate and epigallocatechin gallate. It is the value of 100 percent of the mass sum of the four non-polymer catechin gallate bodies relative to the mass sum of the combined catechins.
本発明で使用する第1の茶抽出液は茶から抽出したもので、非重合体カテキンを1種以上含有するものである。抽出に使用する茶としては、発酵度合いより、不発酵茶、半発酵茶、発酵茶が挙げられる。不発酵茶としては、Camellia属、例えばC.sinensis及びC.assamica、やぶきた種又はそれらの雑種等から得られる茶葉から製茶された、煎茶、番茶、玉露、てん茶、釜炒り茶等の緑茶類が挙げられる。半発酵茶又は発酵茶としては、Camellia属、例えばC.sinensis及びC.assamica、やぶきた種、若しくはそれらの雑種から得られる茶から半発酵又は発酵工程を経て製茶された、紅茶、烏龍茶、黒茶等が挙げられる。中でも、非重合体カテキン類の含有割合の高い不発酵茶が好ましい。 The first tea extract used in the present invention is extracted from tea and contains at least one non-polymer catechin. Examples of the tea used for extraction include non-fermented tea, semi-fermented tea, and fermented tea depending on the degree of fermentation. Non-fermented tea includes Camellia, such as C.I. sinensis and C.I. Examples include green teas such as sencha, bancha, gyokuro, tencha, and kettle roasted tea, which are made from tea leaves obtained from assamica, yabukita or hybrids thereof. Semi-fermented tea or fermented tea includes teas, oolong teas, black teas made from the genus Camellia, such as C. sinensis and C. assamica, tea obtained from hybrids, or semi-fermented or fermented tea. Tea etc. are mentioned. Among these, non-fermented tea having a high content of non-polymer catechins is preferable.
本発明においては、茶葉だけなく、茎茶、棒茶、芽茶を使用することができる。茎茶としては茶の茎の部分であって通常茎茶として用いられているものが挙げられ、また棒茶としては茶葉の軸や茎の部分であって通常棒茶として用いられているものが挙げられ、更に芽茶としては未だ葉にならない柔らかい芽の部分であって通常芽茶として用いられているものが挙げられる。 In the present invention, not only tea leaves but also stem tea, stick tea, and bud tea can be used. Examples of stem tea include tea stem parts that are usually used as stem tea, and stick tea parts that are the stems and stem parts of tea leaves that are usually used as stick tea. Furthermore, examples of bud tea include soft bud portions that have not yet become leaves and are usually used as bud tea.
茶からの抽出は、抽出溶媒として水を使用し、ニーダー抽出、撹拌抽出(バッチ抽出)、向流抽出(ドリップ抽出)、カラム抽出等の公知の方法により行うことができる。抽出の際、水にあらかじめアスコルビン酸又はそのナトリウム塩等の有機酸又はその塩類を添加してもよい。また、煮沸脱気や窒素ガス等の不活性ガスを通気して溶存酸素を除去しつつ、いわゆる非酸化的雰囲気下で抽出する方法を併用してもよい。 Extraction from tea can be performed by a known method such as kneader extraction, stirring extraction (batch extraction), countercurrent extraction (drip extraction), column extraction, etc., using water as an extraction solvent. At the time of extraction, an organic acid such as ascorbic acid or a sodium salt thereof or a salt thereof may be added to water in advance. Moreover, you may use together the method of extracting in so-called non-oxidative atmosphere, ventilating inert gas, such as boiling deaeration and nitrogen gas, and removing dissolved oxygen.
また、第1の茶抽出液として、茶抽出液の濃縮物を水に希釈又は溶解したものを用いてもよく、更に茶から抽出した抽出液と上記濃縮物の希釈液又は溶解液とを併用してもよい。ここで、茶抽出液の濃縮物とは、茶葉から熱水又は水溶性有機溶媒により抽出された抽出液を濃縮したものであり、例えば、特開昭59−219384号公報、特開平4−20589号公報、特開平5−260907号公報、特開平5−306279号公報等に記載されている方法により調製したものをいう。また、市販の茶抽出液の濃縮物として、市販の東京フードテクノ社製「ポリフェノン」、伊藤園社製「テアフラン」、太陽化学社製「サンフェノン」等の精製カテキン製剤を使用してもよい。 Moreover, what diluted or melt | dissolved the concentrate of the tea extract in water as a 1st tea extract may be used, and also the extract extracted from tea and the diluted solution or solution of the said concentrate are used together May be. Here, the concentrate of tea extract is a concentrate obtained by concentrating an extract extracted from tea leaves with hot water or a water-soluble organic solvent. For example, JP-A-59-219384, JP-A-4-20589. No. 5, 260-907, JP-A-5-306279, and the like. Further, as a concentrate of a commercially available tea extract, a purified catechin preparation such as “Polyphenone” manufactured by Tokyo Food Techno Co., “Theafuran” manufactured by ITO EN, or “Sunphenon” manufactured by Taiyo Kagaku may be used.
本発明の製造法においては、まず第1の茶抽出液を固液分離する。これにより、固形分と水溶性部分とに分離されるが、本発明においては、この水溶性部分である第2の茶抽出液を非重合体カテキン類濃度が1質量%の水溶液としたときに、その水溶液の濁度が200NTU以下となるように第1の茶抽出液を固液分離する。水溶液の濁度は200NTU以下であるが、150NTU以下、特に100NTU以下であるのが好ましい。濁度が200NTU以下であると、エグ味の低減ができる。なお、濁度の下限値は、茶抽出液の安定性の点から、0.01NTU以上、特に0.1NTU以上であるのが好ましい。ここで、濁度とは、固液分離により得られた第2の茶抽出液を、該茶抽出液中の非重合体カテキン類の濃度が1質量%なるようにイオン交換水で希釈し、波長範囲850nm、90°透過散乱比較方式にて濁度計を用いて測定したものをいう。 In the production method of the present invention, first, the first tea extract is subjected to solid-liquid separation. As a result, the solid content and the water-soluble part are separated. In the present invention, when the second tea extract that is the water-soluble part is an aqueous solution having a non-polymer catechin concentration of 1% by mass. The first tea extract is subjected to solid-liquid separation so that the turbidity of the aqueous solution is 200 NTU or less. The turbidity of the aqueous solution is 200 NTU or less, preferably 150 NTU or less, particularly preferably 100 NTU or less. If the turbidity is 200 NTU or less, the taste can be reduced. The lower limit of turbidity is preferably 0.01 NTU or more, particularly 0.1 NTU or more, from the viewpoint of the stability of the tea extract. Here, turbidity refers to diluting the second tea extract obtained by solid-liquid separation with ion-exchanged water so that the concentration of non-polymer catechins in the tea extract is 1% by mass, It means what was measured using a turbidimeter in a wavelength range of 850 nm and a 90 ° transmission scattering comparison method.
所定の濁度にするための固液分離手段としては、膜処理、濾過、遠心分離等を採用することができるが、中でも膜処理、特に精密濾過(MF)が水難溶成分をより確実に除去して所望の濁度に調整しやすい点で好ましい。また、膜処理を行う前に、濾過及び/又は遠心分離により固形分と水溶性部分とに分離すると、その後の膜処理において濾速が向上し生産効率に優れる点で好ましい。 Membrane treatment, filtration, centrifugation, etc. can be adopted as solid-liquid separation means for obtaining a predetermined turbidity, but membrane treatment, particularly microfiltration (MF), more reliably removes poorly water-soluble components. And it is preferable at the point which is easy to adjust to desired turbidity. Further, before the membrane treatment, it is preferable to separate the solid content and the water-soluble portion by filtration and / or centrifugation because the filtration speed is improved in the subsequent membrane treatment and the production efficiency is excellent.
固液分離の条件は、例えば、下記のとおりである。膜処理する場合の温度は、5〜70℃が好ましく、特に10〜60℃が好ましい。圧力は、例えば、30〜400kPa、更に50〜400kPa、特に50〜350kPaであるのが好ましい。膜孔径としては、所定の濁度に簡便に調整できる点で、0.1〜0.8μmが好ましく、更に0.1〜0.45μm、特に0.1〜0.25μmが好ましい。膜孔径の測定方法としては、水銀圧入法、バブルポイント試験、細菌ろ過法などを用いた一般的な測定方法が挙げられるが、バブルポイント試験で求めた値を用いるのが好ましい。 The conditions for solid-liquid separation are, for example, as follows. The temperature for the film treatment is preferably 5 to 70 ° C, particularly preferably 10 to 60 ° C. The pressure is, for example, preferably 30 to 400 kPa, more preferably 50 to 400 kPa, and particularly preferably 50 to 350 kPa. The membrane pore diameter is preferably 0.1 to 0.8 μm, more preferably 0.1 to 0.45 μm, and particularly preferably 0.1 to 0.25 μm in that it can be easily adjusted to a predetermined turbidity. Examples of the method for measuring the membrane pore diameter include general measurement methods using a mercury intrusion method, a bubble point test, a bacterial filtration method, and the like, but it is preferable to use values obtained by the bubble point test.
本発明で使用できる膜としては、例えば、炭化水素系、フッ素化炭化水素系又はスルホン系の高分子膜、セラミック膜が挙げられる。炭化水素系高分子膜としては、例えば、ポリオレフィン系高分子膜が挙げられ、具体的には、ポリエチレン、ポリプロピレン等が挙げられる。フッ素化炭化水素系高分子膜としては、例えば、フッ素化ポリオレフィン系高分子膜が挙げられ、具体的には、ポリテトラフルオロエチレン(PTFE)、ポリビニリデンジフルオライド(PVDF)等が挙げられる。スルホン系高分子膜としては、例えば、ポリスルフォン(PSU)、ポリエーテルスルフォン(PES)等が挙げられる。セラミック膜としては、例えば、日本ガイシ社製「Cefilt」、日本ポール社製「SCUMASIV」等が挙げられる。中でも、セラミック膜が、細孔分布がシャープであり、かつ濾過精度に優れる点で好ましい。また、膜の種類としては、平膜、スパイラル膜、中空糸膜、モノリス型膜等が挙げられ、中でもスパイラル膜、中空糸膜やモノリス型膜等の連続処理型のものが効率的に処理できる点で好ましい。 Examples of the membrane that can be used in the present invention include hydrocarbon-based, fluorinated hydrocarbon-based, or sulfone-based polymer membranes and ceramic membranes. Examples of the hydrocarbon polymer film include a polyolefin polymer film, and specific examples include polyethylene and polypropylene. Examples of the fluorinated hydrocarbon polymer film include a fluorinated polyolefin polymer film, and specific examples include polytetrafluoroethylene (PTFE) and polyvinylidene difluoride (PVDF). Examples of the sulfone polymer film include polysulfone (PSU), polyethersulfone (PES), and the like. Examples of the ceramic film include “Cefilt” manufactured by NGK and “SCUMASIV” manufactured by Nippon Pole. Among these, a ceramic membrane is preferable in that the pore distribution is sharp and the filtration accuracy is excellent. Examples of the membrane include flat membranes, spiral membranes, hollow fiber membranes, monolith type membranes, etc. Among them, continuous processing types such as spiral membranes, hollow fiber membranes and monolith type membranes can be processed efficiently. This is preferable.
遠心分離は、分離板型、円筒型、デカンター型などの一般的な機器を使用するのが好ましい。遠心分離条件としては、温度が5〜70℃、特に10〜40℃であるのが好ましい。回転数と時間は、例えば、分離板型の場合、4000〜10000rpm、更に5000〜10000rpm、特に6000〜10000rpmで、0.2〜30分、更に0.2〜20分、特に0.2〜15分であるのが好ましい。 Centrifugation is preferably performed using a general apparatus such as a separation plate type, a cylindrical type, or a decanter type. As the centrifugation conditions, the temperature is preferably 5 to 70 ° C, particularly 10 to 40 ° C. For example, in the case of a separation plate type, the number of rotations and time are 4000 to 10000 rpm, further 5000 to 10000 rpm, particularly 6000 to 10000 rpm, 0.2 to 30 minutes, further 0.2 to 20 minutes, and particularly 0.2 to 15. Minutes are preferred.
濾過は、通常、粗濾過を目的として他の固液分離手段と組み合わせて行われるが、例えば、ろ紙、ステンレス等の金属製フィルター等によるフィルター分離を採用することができる。金属製フィルターのメッシュサイズは、18〜300メッシュであるのが好ましい。 Filtration is usually performed in combination with other solid-liquid separation means for the purpose of rough filtration. For example, filter separation using a filter made of metal such as filter paper or stainless steel can be employed. The mesh size of the metal filter is preferably 18 to 300 mesh.
固液分離により得られた第2の茶抽出液は、非重合体カテキン類濃度が0.2〜5質量%であり、かつ固形分中の非重合体カテキン類濃度が15〜80質量%であるが、このような性状の茶抽出液とするために、必要により第2の抽出液から水分を一部除去して濃縮してもよい。非重合体カテキン類濃度は、加熱処理による着色の増大防止の観点から、0.2〜4質量%が好ましく、特に0.2〜3質量%が好ましい。また、固形分中の非重合体カテキン類濃度は、加熱処理によるエグ味低減の観点から、20〜70質量%が好ましく、特に25〜50質量%が好ましい。 The second tea extract obtained by solid-liquid separation has a non-polymer catechin concentration of 0.2 to 5% by mass and a non-polymer catechin concentration in the solid content of 15 to 80% by mass. However, in order to obtain a tea extract having such properties, if necessary, a part of the water may be removed from the second extract and concentrated. The concentration of the non-polymer catechins is preferably 0.2 to 4% by mass, particularly preferably 0.2 to 3% by mass, from the viewpoint of preventing increase in coloring due to heat treatment. In addition, the concentration of non-polymer catechins in the solid content is preferably 20 to 70% by mass, and particularly preferably 25 to 50% by mass, from the viewpoint of reducing taste by heat treatment.
次に、第2の茶抽出液を加熱処理する。加熱処理の条件は、温度95〜140℃、F値0.05〜40(Z=10)であるが、加熱温度は98〜135℃が好ましく、特に100〜130℃が好ましい。また、F値は0.07〜35が好ましく、特に0.07〜30が好ましい。加熱温度及びF値が下限未満であると、加熱処理してもエグ味が減少せず、他方加熱温度及びF値が上限を越えると加熱による異臭が生成して風味が低下する。
ここで、本明細書において、F値とは、加熱殺菌効果を表示する指標として用いられ、加熱温度121.1℃における殺菌効果に換算した値(単位は分)であり、具体的には下記式より算出される値をいう。
Next, the second tea extract is heated. The heat treatment conditions are a temperature of 95 to 140 ° C. and an F value of 0.05 to 40 (Z = 10), but the heating temperature is preferably 98 to 135 ° C., particularly preferably 100 to 130 ° C. The F value is preferably 0.07 to 35, and particularly preferably 0.07 to 30. If the heating temperature and the F value are less than the lower limit, even if the heat treatment is performed, the taste is not reduced.
Here, in this specification, the F value is used as an index for displaying the heat sterilization effect, and is a value (unit: minutes) converted to the sterilization effect at a heating temperature of 121.1 ° C. The value calculated from the equation.
式中、Zは定数10を示し、tは加熱温度(℃)を示し、secは加熱時間(秒)を示す。 In the formula, Z represents a constant 10, t represents a heating temperature (° C.), and sec represents a heating time (second).
本発明においては、第2の茶抽出液又は加熱処理して得られた茶抽出物を、苦み及び渋みを低減するためにタンナーゼ活性を有する酵素で処理してもよい。この場合、第2の茶抽出液をタンナーゼ処理する方が、加熱処理して得られた茶抽出物をタンナーゼ処理するよりも好ましい。
ここで使用されるタンナーゼは、非重合体カテキン類ガレート体を加水分解する活性を有するものであればよい。具体的には、アスペルギルス属、ペニシリウム属、リゾプス属などのタンナーゼ生産菌を培養して得られるタンナーゼが使用できる。このうち、アスペルギルス オリーゼ由来のものが特に好ましい。
タンナーゼ処理においては、第2の茶抽出液に粉末状又は溶液状のタンナーゼを、25〜500Unit/L、特に50〜150Unit/Lの濃度になるように添加することが好ましい。かかるタンナーゼの添加量は、非重合体カテキン類濃度が0.67質量%の茶抽出液1gに対して、0.1Unit以上、好ましくは0.2Unit以上である。ここで、1Unitは、30℃の水中においてタンニン酸に含まれるエステル結合を1マイクロモル加水分解する酵素量で定義される。
In the present invention, the second tea extract or the tea extract obtained by heat treatment may be treated with an enzyme having tannase activity in order to reduce bitterness and astringency. In this case, the tannase treatment of the second tea extract is preferable to the tannase treatment of the tea extract obtained by the heat treatment.
The tannase used here should just have the activity which hydrolyzes non-polymer catechin gallate body. Specifically, tannase obtained by culturing tannase-producing bacteria such as Aspergillus, Penicillium, Rhizopus and the like can be used. Of these, those derived from Aspergillus oryzae are particularly preferred.
In the tannase treatment, it is preferable to add powdered or solution tannase to the second tea extract so as to have a concentration of 25 to 500 Unit / L, particularly 50 to 150 Unit / L. The amount of tannase added is 0.1 Unit or more, preferably 0.2 Unit or more, per 1 g of tea extract having a non-polymer catechin concentration of 0.67% by mass. Here, 1Unit is defined as the amount of enzyme that hydrolyzes 1 micromole of an ester bond contained in tannic acid in water at 30 ° C.
タンナーゼ活性を有する酵素を添加後、非重合体カテキン類中のガレート体率が1〜60質量%に達するまで、第2の茶抽出液を20℃〜50℃、特に20℃〜40℃に保持することが好ましい。非重合体カテキン類中のガレート体率は、3〜55質量%、特に5〜50質量%に調整するのが好ましい。その後、できるだけ速やかに上記加熱温度まで昇温してタンナーゼを失活させて反応を停止すると同時に、上記F値にて加熱処理する。これにより、タンナーゼの処理による苦み及び渋みを低減させる工程と、加熱処理によるエグ味を低減させる工程とが同時に実施されるため、より一層エグ味が抑制された、色調の良好な茶抽出物が得られるとともに、製造工程の簡略化、作業コストの軽減化が実現される。また、当該タンナーゼの失活処理により、その後のガレート体率の低下が防止でき、目的とするガレート体率の茶抽出物を簡便に得ることができる。 After adding the enzyme having tannase activity, hold the second tea extract at 20 ° C. to 50 ° C., particularly 20 ° C. to 40 ° C. until the gallate content in the non-polymer catechins reaches 1 to 60% by mass. It is preferable to do. The gallate content in the non-polymer catechins is preferably adjusted to 3 to 55% by mass, particularly 5 to 50% by mass. Thereafter, the temperature is raised as quickly as possible to deactivate the tannase to stop the reaction, and at the same time, heat treatment is performed at the F value. Thereby, since the process of reducing the bitterness and astringency by the treatment of tannase and the process of reducing the taste by heat treatment are carried out at the same time, a tea extract having a good color tone with a further suppressed taste is obtained. As a result, the manufacturing process can be simplified and the operation cost can be reduced. In addition, the tannase inactivation treatment can prevent a subsequent decrease in the gallate body ratio, and a tea extract having the desired gallate body ratio can be easily obtained.
次に、加熱処理して得られた茶抽出物を、必要により濃縮又は乾燥して固形物、粉末、造粒物のような形態に高濃度化することができる。濃縮又は乾燥による高濃度化方法としては、例えば、減圧濃縮、逆浸透膜濃縮、噴霧乾燥、凍結乾燥が挙げられ、これらは組み合わせて行うことができる。中でも、減圧濃縮又は噴霧乾燥は、熱履歴が少ない点で好ましく、また逆浸透膜濃縮においては熱履歴が少なく、省エネルギーな点で好ましい。効率的な高濃度化方法として、例えば、まず減圧濃縮又は逆浸透膜濃縮により、固形分濃度30〜60質量%まで一次濃縮を行い、その後用途に応じて、噴霧乾燥又は凍結乾燥により、粉末化する方法が挙げられる。 Next, the tea extract obtained by the heat treatment can be concentrated or dried as necessary to increase the concentration into a form such as a solid, powder, or granulated product. Examples of the concentration increasing method by concentration or drying include vacuum concentration, reverse osmosis membrane concentration, spray drying, and freeze drying, and these can be performed in combination. Among these, vacuum concentration or spray drying is preferable from the viewpoint of low heat history, and reverse osmosis membrane concentration is preferable from the viewpoint of energy saving because of low heat history. As an efficient method of increasing the concentration, for example, first, primary concentration is performed to a solid content concentration of 30 to 60% by mass by vacuum concentration or reverse osmosis membrane concentration, and then powderization is performed by spray drying or freeze drying depending on the application. The method of doing is mentioned.
上記工程により、エグ味だけなく、苦味及び加熱臭が抑制され、しかも飲料配合時において安定性に優れた高濃度非重合体カテキン類含有茶抽出物が得られる。 According to the above process, not only the taste but also the bitterness and the heated odor are suppressed, and a highly concentrated non-polymer catechins-containing tea extract having excellent stability at the time of blending the beverage is obtained.
本発明の茶抽出物は、更に有機溶媒及び水の混合溶液中に分散し、次いで活性炭と、酸性白土又は活性白土とで接触処理することができる。これにより、非重合体カテキン類を高濃度に含有していながら、より一層経時安定性に優れた、高品質な低カフェイン含量の茶抽出物が得られる。 The tea extract of the present invention can be further dispersed in a mixed solution of an organic solvent and water, and then contact-treated with activated carbon and acidic clay or activated clay. As a result, a high-quality, low-caffeine content tea extract having excellent stability over time while containing a high concentration of non-polymer catechins can be obtained.
有機溶媒と水との含有質量比は、60/40〜97/3が好ましく、更に60/40〜95/5、特に85/15〜95/5とするのが、非重合体カテキン類の抽出効率、茶抽出物の精製、長期間の飲用性等の点で好ましい。 The content ratio of the organic solvent to water is preferably 60/40 to 97/3, more preferably 60/40 to 95/5, particularly 85/15 to 95/5, for extraction of non-polymer catechins. It is preferable in terms of efficiency, purification of tea extract, long-term drinking ability, and the like.
有機溶媒としては、エタノール、メタノール等のアルコール類、アセトン等のケトン類、酢酸エチル等のエステル類等が挙げられる。これらのうち、アルコール類、ケトン類の親水性有機溶媒が好ましく、特に食品への使用を考慮すると、アルコール類、特にエタノールが好ましい。水としては、イオン交換水、水道水、天然水等が挙げられる。この有機溶媒と水は、混合して又はそれぞれ別々にろ過された茶抽出物と混合してもよいが、混合溶液としてから茶抽出物と混合処理するのが好ましい。 Examples of the organic solvent include alcohols such as ethanol and methanol, ketones such as acetone, esters such as ethyl acetate, and the like. Among these, hydrophilic organic solvents such as alcohols and ketones are preferable, and alcohols, particularly ethanol are preferable in consideration of use in foods. Examples of water include ion exchange water, tap water, and natural water. The organic solvent and water may be mixed or mixed with the tea extract that has been filtered separately, but it is preferable that the organic solvent and water be mixed with the tea extract after forming a mixed solution.
茶抽出物の使用量(乾燥質量換算)は、有機溶媒と水の混合溶液100質量部に対して、10〜40質量部、更に10〜30質量部、特に15〜30質量部であるのが、効率よく処理できる点で好ましい。 The amount of tea extract used (in terms of dry mass) is 10 to 40 parts by mass, more preferably 10 to 30 parts by mass, and particularly 15 to 30 parts by mass with respect to 100 parts by mass of the mixed solution of the organic solvent and water. This is preferable in terms of efficient processing.
有機溶媒と水の混合溶液の添加終了後は10〜180分程度の熟成時間を設けると更に好ましい。これらの処理は、10〜60℃で行うことができ、特に10〜50℃、更に10〜40℃で行うのが好ましい。 It is more preferable to provide an aging time of about 10 to 180 minutes after the addition of the mixed solution of the organic solvent and water. These treatments can be carried out at 10 to 60 ° C., preferably 10 to 50 ° C., more preferably 10 to 40 ° C.
活性炭は、有機溶媒と水の混合溶液100質量部に対して0.5〜8質量部、特に0.5〜3質量部添加するのが、カフェイン除去効率、ろ過工程におけるケーク抵抗が小さい点で好ましい。また、活性炭と、酸性白土又は活性白土との配合割合は、質量比で活性炭1に対して1〜10が好ましく、活性炭:酸性白土又は活性白土=1:1〜1:6であるのが好ましい。 Activated carbon is added in an amount of 0.5 to 8 parts by mass, particularly 0.5 to 3 parts by mass with respect to 100 parts by mass of a mixed solution of an organic solvent and water. Is preferable. Moreover, the mixing ratio of the activated carbon and the acid clay or the activated clay is preferably 1 to 10 with respect to the activated carbon 1 by mass ratio, and is preferably activated carbon: acid clay or activated clay = 1: 1 to 1: 6. .
このようにして製造された茶抽出物中のカフェインは非重合体カテキン類/カフェインの質量比で4〜200、更に15〜200、特に30〜200とすることができる。 The caffeine in the tea extract thus produced can be 4 to 200, more preferably 15 to 200, particularly 30 to 200 in terms of the mass ratio of non-polymer catechins / caffeine.
本発明の茶抽出物は、エグ味、苦味及び加熱異臭が抑制されているにも拘らず、高い非重合カテキン類濃度を維持している。したがって、本発明の茶抽出物は容器詰飲料の原料として有用であり、特に緑茶、烏龍茶、ブレンド茶、紅茶、麦茶等の茶系飲料、スポーツ飲料、アイソトニック飲料、ニアウォーター等の非茶系飲料として有用である。 The tea extract of the present invention maintains a high concentration of non-polymerized catechins in spite of suppression of taste, bitterness, and heated odor. Therefore, the tea extract of the present invention is useful as a raw material for container-packed beverages, particularly tea beverages such as green tea, oolong tea, blended tea, black tea, barley tea, non-tea beverages such as sports beverages, isotonic beverages, and near water. Useful as.
容器詰飲料中には、非重合体カテキン類を、好ましくは0.03〜1.0質量%含有するが、より好ましくは0.04〜0.5質量%、より一層好ましくは0.06〜0.4質量%、更に好ましくは0.08〜0.3質量%、特に好ましくは0.1〜0.3質量%含有する。非重合体カテキン類の含有量がこの範囲にあると、多量の非重合カテキン類を容易に摂取しやすく、飲料調製直後の色調の点からも好ましい。 In the packaged beverage, non-polymer catechins are preferably contained in an amount of 0.03 to 1.0% by mass, more preferably 0.04 to 0.5% by mass, and still more preferably 0.06 to 0.4% by mass, more preferably 0.08 to 0.3% by mass, and particularly preferably 0.1 to 0.3% by mass. When the content of the non-polymer catechins is within this range, a large amount of the non-polymer catechins can be easily ingested, which is preferable from the viewpoint of the color tone immediately after the beverage preparation.
容器詰飲料には、ナトリウムイオン及び/又はカリウムイオンを含有させてもよい。これらのイオンを含有させた飲料は、スポーツドリンク、アイソトニック飲料等の飲料形態として有用である。 The packaged beverage may contain sodium ions and / or potassium ions. Beverages containing these ions are useful as beverage forms such as sports drinks and isotonic drinks.
容器詰飲料には、味を改善する目的で、甘味料を用いることができる。甘味料としては人工甘味料類、炭水化物類、グリセロール類(例えばグリセリン)が挙げられる。 A sweetener can be used in the packaged beverage for the purpose of improving the taste. Examples of the sweetener include artificial sweeteners, carbohydrates, and glycerol (for example, glycerin).
容器詰飲料のpHは2〜7、好ましくは2〜6.5、より好ましくは3〜4.5に調整するのがカテキン類の安定性上望ましい。 It is desirable for the stability of the catechins to adjust the pH of the packaged beverage to 2 to 7, preferably 2 to 6.5, more preferably 3 to 4.5.
容器詰飲料は、苦渋味抑制剤を配合すると飲用しやすくなり好ましい。苦渋味抑制剤としては、サイクロデキストリンが好ましい。サイクロデキストリンとしては、α−、β−、γ−サイクロデキストリン及び分岐サイクロデキストリンが使用できる。容器詰飲料には、酸化防止剤、香料、各種エステル類、有機酸類、有機酸塩類、無機酸類、無機酸塩類、無機塩類、色素類、乳化剤、保存料、調味料、酸味料、ガム、乳化剤、油、ビタミン、アミノ酸、果汁エキス類、野菜エキス類、花蜜エキス類、pH調整剤、品質安定剤等の添加剤を単独、あるいは併用して配合できる。 The container-packed beverage is preferable because it is easy to drink when a bitter and astringent taste inhibitor is blended. As the bitter and astringent taste inhibitor, cyclodextrin is preferred. As the cyclodextrin, α-, β-, γ-cyclodextrin and branched cyclodextrin can be used. For packaged beverages, antioxidants, fragrances, various esters, organic acids, organic acid salts, inorganic acids, inorganic acid salts, inorganic salts, pigments, emulsifiers, preservatives, seasonings, acidulants, gums, emulsifiers Additives such as oil, vitamins, amino acids, fruit juice extracts, vegetable extracts, nectar extracts, pH adjusters, quality stabilizers and the like can be used alone or in combination.
容器詰飲料に使用される容器は、一般の飲料と同様にポリエチレンテレフタレートを主成分とする成形容器(いわゆるPETボトル)、金属缶、金属箔やプラスチックフィルムと複合された紙容器、瓶等の通常の形態で提供することができる。ここでいう容器詰飲料とは希釈せずに飲用できるものをいう。 Containers used for packaged beverages are usually molded containers (so-called PET bottles) mainly composed of polyethylene terephthalate, metal cans, paper containers combined with metal foil or plastic film, bottles, etc. Can be provided. The term “packaged beverage” as used herein means a beverage that can be drunk without dilution.
容器詰飲料は、例えば、金属缶のように容器に充填後、加熱殺菌できる場合にあっては食品衛生法に定められた殺菌条件で製造されるが、PETボトル、紙容器のようにレトルト殺菌できないものについては、あらかじめ上記と同等の殺菌条件、例えばプレート式熱交換器等で高温短時間殺菌後、一定の温度迄冷却して容器に充填する等の方法が採用される。また無菌下で、充填された容器に別の成分を配合して充填してもよい。更に、酸性下で加熱殺菌後、無菌下でpHを中性に戻すことや、中性下で加熱殺菌後、無菌下でpHを酸性に戻す等の操作も可能である。 Container-packed beverages are manufactured under the sterilization conditions stipulated in the Food Sanitation Law if they can be sterilized by heating after filling them into containers such as metal cans. For those that cannot be used, a sterilization condition equivalent to the above, for example, a method of sterilizing at a high temperature and short time in a plate heat exchanger or the like and then cooling to a certain temperature and filling the container is adopted. Moreover, you may mix | blend another component with the filled container under aseptic conditions. Furthermore, after sterilization by heating under acidic conditions, the pH can be returned to neutrality under aseptic conditions, or after sterilization by heating under neutral conditions, the pH can be returned to acidic conditions under aseptic conditions.
(非重合体カテキン類の測定)
茶抽出液又は茶抽出物をイオン交換水で希釈した後、メンブランフィルター(0.8μm)でろ過し、次いで蒸留水で希釈した試料を、オクタデシル基導入液体クロマトグラフ用パックドカラム L−カラムTM ODS(4.6mmφ×250mm:財団法人 化学物質評価研究機構製)を装着した、島津製作所製、高速液体クロマトグラフ(型式SCL−10AVP)を用いて、カラム温度35℃でグラジエント法により測定した。移動相A液は酢酸を0.1mol/L含有の蒸留水溶液、B液は酢酸を0.1mol/L含有のアセトニトリル溶液とし、試料注入量は20μL、UV検出器波長は280nmの条件で行った。
(Measurement of non-polymer catechins)
A tea extract or tea extract is diluted with ion-exchanged water, filtered through a membrane filter (0.8 μm), and then diluted with distilled water, and a sample packed in an octadecyl group-introduced liquid chromatograph L-column TM ODS Using a high-performance liquid chromatograph (model SCL-10AVP) manufactured by Shimadzu Corporation equipped with (4.6 mmφ × 250 mm: manufactured by Chemical Substance Evaluation Research Organization), the measurement was performed by a gradient method at a column temperature of 35 ° C. The mobile phase A solution was a distilled aqueous solution containing 0.1 mol / L of acetic acid, the B solution was an acetonitrile solution containing 0.1 mol / L of acetic acid, the sample injection amount was 20 μL, and the UV detector wavelength was 280 nm. .
(濁度の測定)
固液分離して得られた第2の茶抽出液を、非重合体カテキン類濃度が1質量%になるようにイオン交換水で希釈し、それを試料として濁度計(Turbidimeter/TN-100 EUTECH INSTRUMENTS社製)を用いて、波長範囲850nm、90°透過散乱比較方式で測定を行った。
(Measurement of turbidity)
The second tea extract obtained by solid-liquid separation is diluted with ion-exchanged water so that the concentration of non-polymer catechins is 1% by mass, and this is used as a sample for a turbidimeter (Turbidimeter / TN-100 EUTECH INSTRUMENTS) was used, and measurement was performed by a 90 ° transmission / scattering comparison method with a wavelength range of 850 nm.
(風味の評価)
各茶抽出物を、非重合体カテキン濃度が175mg/100mLになるようにイオン交換水で希釈し、5名の男性モニターにて、風味(エグ味、苦味、加熱異臭)を下記の基準で評価した。結果を表1、2,3に示す。
(Evaluation of flavor)
Each tea extract was diluted with ion-exchanged water so that the non-polymer catechin concentration was 175 mg / 100 mL, and the flavor (egg taste, bitter taste, heated odor) was evaluated according to the following criteria on five male monitors. did. The results are shown in Tables 1, 2, and 3.
(1)エグ味の評価基準
A:感じにくい
B:やや感じにくい
C:やや感じる
D:感じる
(1) Evaluation standard of taste taste A: Difficult to feel B: Difficult to feel C: Feel somewhat D: Feel
(2)苦味の評価基準
A:感じにくい
B:やや感じにくい
C:やや感じる
D:感じる
(2) Evaluation criteria for bitterness A: Difficult to feel B: Slightly difficult to feel C: Slightly feel D: Feel
(3)加熱異臭の評価基準
A:感じにくい
B:やや感じにくい
C:やや感じる
D:感じる
(3) Evaluation Criteria for Heating Odor A: Difficult to Feel B: Difficult to Feel C: Slightly Feel D: Feel
実施例1
(1)緑茶葉(ケニア産、大葉種)100gを50℃の熱水3kg中にて、15分間攪拌してバッチ抽出を行ない第1の茶抽出液を得た。次いで、第1の茶抽出液を、70メッシュ、200メッシュの金網で粗ろ過し25℃まで冷却した後、第1の茶抽出液中の微粉を除去するためにバッチ式の遠心分離機(日立工機(株)製、高速冷却遠心機CR22G)にて、25℃、8000rpmで10分間遠心分離操作を行い、第2の茶抽出液2300gを得た。
(2)得られた第2の茶抽出液100gを100℃に設定した温浴中に9分間浸漬し、冷却後、得られた茶抽出物を凍結乾燥機(東京理化器械(株)製、FD-81)にて凍結乾燥を行い、粉末状の茶抽出物を得た。
Example 1
(1) 100 g of green tea leaves (from Kenya, large leaf type) were stirred in 3 kg of hot water at 50 ° C. for 15 minutes to perform batch extraction to obtain a first tea extract. Next, the first tea extract is roughly filtered through a 70-mesh and 200-mesh wire mesh, cooled to 25 ° C., and then a batch-type centrifuge (Hitachi) is used to remove the fine powder in the first tea extract. Centrifugation was performed at 25 ° C. and 8000 rpm for 10 minutes using a high-speed cooling centrifuge CR22G manufactured by Koki Co., Ltd. to obtain 2300 g of a second tea extract.
(2) 100 g of the obtained second tea extract was immersed in a warm bath set at 100 ° C. for 9 minutes, and after cooling, the obtained tea extract was freeze-dried (Tokyo Rika Kikai Co., Ltd., FD -81) and lyophilized to obtain a powdery tea extract.
実施例2
緑茶葉(ケニア産、大葉種)100gを80℃の熱水中にて抽出して第1の茶抽出液を得たこと以外は、実施例1と同様の方法により茶抽出物を得た。
Example 2
A tea extract was obtained in the same manner as in Example 1 except that 100 g of green tea leaves (produced in Kenya, large leaf type) were extracted in hot water at 80 ° C. to obtain a first tea extract.
実施例3
緑茶葉(ケニア産、大葉種)100gを90℃の熱水中にて抽出して第1の茶抽出液を得たこと以外は、実施例1と同様の方法により茶抽出物を得た。
Example 3
A tea extract was obtained in the same manner as in Example 1, except that 100 g of green tea leaves (produced in Kenya, large leaf type) were extracted in hot water at 90 ° C. to obtain the first tea extract.
実施例4
(1)実施例2と同様の方法により、緑茶葉(ケニア産、大葉種)100gを80℃の熱水3kg中にて、15分間攪拌してバッチ抽出を行ない第1の茶抽出液を得た。次いで、70メッシュ、200メッシュ金網で粗ろ過し25℃まで冷却した後、第1の茶抽出液を0.2μmのセラミックフィルター(日本ガイシ株式会社製、Cefilt)にて25℃、平均ろ過圧力0.1MPaで精密ろ過(MF処理)を行い、第2の抽出液を得た。
(2)得られた第2の抽出液100gを実施例1と同様の方法により加熱処理した後に、凍結乾燥を行い、粉末状の茶抽出物を得た。
Example 4
(1) By the same method as in Example 2, 100 g of green tea leaves (produced from Kenya, large leaf type) was stirred in 3 kg of hot water at 80 ° C. for 15 minutes to perform batch extraction to obtain a first tea extract. It was. Next, after roughly filtering with a 70 mesh and 200 mesh wire mesh and cooling to 25 ° C., the first tea extract was filtered at 25 ° C. with a 0.2 μm ceramic filter (Cefilt, manufactured by NGK Co., Ltd.) with an average filtration pressure of 0. Microfiltration (MF treatment) at 1 MPa was performed to obtain a second extract.
(2) After heat-treating 100 g of the obtained 2nd extract by the method similar to Example 1, it lyophilized | freeze-dried and the powdery tea extract was obtained.
実施例5
緑茶葉(ケニア産、大葉種)100gを75℃の熱水中にて抽出して第1の茶抽出液を得たこと以外は、実施例4と同様の方法により茶抽出物を得た。
Example 5
A tea extract was obtained in the same manner as in Example 4 except that 100 g of green tea leaves (produced in Kenya, large leaf type) were extracted in hot water at 75 ° C. to obtain the first tea extract.
実施例6
(1)実施例5と同様に、75℃の熱水中にて15分間攪拌してバッチ抽出を行ない第1の茶抽出液を得た。次いで、第1の茶抽出液を70メッシュ、200メッシュ金網で粗ろ過し25℃まで冷却した後、第1の茶抽出液を0.2μmのセラミックフィルター(日本ガイシ株式会社製、Cefilt)にて25℃、平均ろ過圧力0.1MPaで精密ろ過(MF処理)を行い、第2の茶抽出液を得た。
(2)得られた第2の抽出液を、110ml/minの流量にて連続式加熱処理装置(昇温;オイルバス、内径2.27mmφ×10m、ホールドディング部;内径10.7mmφ×2m)にて124℃、滞留時間1.5minの条件で加熱処理し、連続的に25℃まで冷却を行った。その後、得られた茶抽出物を凍結乾燥機にて凍結乾燥を行い、粉末状の茶抽出物を得た。
Example 6
(1) As in Example 5, batch extraction was performed by stirring in hot water at 75 ° C. for 15 minutes to obtain a first tea extract. Next, the first tea extract was roughly filtered with a 70 mesh and 200 mesh wire mesh and cooled to 25 ° C., and then the first tea extract was filtered with a 0.2 μm ceramic filter (Cefilt, manufactured by NGK Corporation). Microfiltration (MF treatment) was performed at 25 ° C. and an average filtration pressure of 0.1 MPa to obtain a second tea extract.
(2) The obtained second extract is continuously heated at a flow rate of 110 ml / min (temperature increase; oil bath, inner diameter 2.27 mmφ × 10 m, holding part; inner diameter 10.7 mmφ × 2 m) At 124 ° C. and a residence time of 1.5 min, and continuously cooled to 25 ° C. Thereafter, the obtained tea extract was freeze-dried with a freeze dryer to obtain a powdery tea extract.
実施例7
加熱処理条件を130℃、1.5minとしたこと以外は、実施例6と同様の方法により茶抽出物を得た。
Example 7
A tea extract was obtained by the same method as in Example 6 except that the heat treatment conditions were 130 ° C. and 1.5 min.
実施例8
加熱処理条件を133℃、1.5minとしたこと以外は、実施例6と同様の方法により茶抽出物を得た。
Example 8
A tea extract was obtained in the same manner as in Example 6 except that the heat treatment conditions were 133 ° C. and 1.5 min.
実施例9
加熱処理条件を138℃、0.5min、ホールドディング部;内径10.7mmφ×0.67mとしたこと以外は、実施例6と同様の方法により茶抽出物を得た。
Example 9
A tea extract was obtained in the same manner as in Example 6 except that the heat treatment conditions were 138 ° C., 0.5 min, holding part; inner diameter 10.7 mmφ × 0.67 m.
実施例10
実施例4(1)で得られた第2の茶抽出液を温度25℃に保持し、タンナーゼ(キッコーマン(株)製、タンナーゼKTFH、500U/g)を第2の茶抽出液に対して120ppm(60Unit/L)添加し、100分間保持した後、実施例6に記載の加熱処理条件にて加熱処理を行った。その後、得られた茶抽出物を凍結乾燥機にて凍結乾燥を行い、粉末状の茶抽出物を得た。
Example 10
The second tea extract obtained in Example 4 (1) was kept at a temperature of 25 ° C., and tannase (Kikkoman Corp., tannase KTFH, 500 U / g) was 120 ppm with respect to the second tea extract. (60 Unit / L) was added and held for 100 minutes, and then heat treatment was performed under the heat treatment conditions described in Example 6. Thereafter, the obtained tea extract was freeze-dried with a freeze dryer to obtain a powdery tea extract.
比較例1
第2の茶抽出液100gを加熱処理することなく凍結乾燥機にて凍結乾燥を行ったこと以外は、実施例2と同様の方法により茶抽出物を得た。
Comparative Example 1
A tea extract was obtained in the same manner as in Example 2 except that 100 g of the second tea extract was lyophilized with a freeze dryer without heat treatment.
比較例2
(1)緑茶葉(ケニア産、大葉種)100gを80℃の熱水3kg中にて、15分間攪拌してバッチ抽出を行ない第1の茶抽出液を得た。次いで、第1の茶抽出液を70メッシュ、200メッシュ金網で粗ろ過し25℃まで冷却して第2の茶抽出液を得た。
(2)得られた第2の茶抽出液100gを100℃に設定した温浴中に9分間浸漬し、冷却後、得られた茶抽出物を凍結乾燥機にて凍結乾燥を行い、粉末状の茶抽出物を得た。
Comparative Example 2
(1) 100 g of green tea leaves (from Kenya, large leaf type) were stirred in 3 kg of hot water at 80 ° C. for 15 minutes to perform batch extraction to obtain a first tea extract. Next, the first tea extract was coarsely filtered through a 70 mesh and 200 mesh wire net and cooled to 25 ° C. to obtain a second tea extract.
(2) 100 g of the obtained second tea extract is immersed in a warm bath set at 100 ° C. for 9 minutes, and after cooling, the obtained tea extract is freeze-dried with a freeze dryer, A tea extract was obtained.
比較例3
遠心分離条件を3000rpm、10分としたこと以外は、実施例2と同様の方法により茶抽出物を得た。
Comparative Example 3
A tea extract was obtained in the same manner as in Example 2 except that the centrifugation conditions were 3000 rpm and 10 minutes.
比較例4
加熱処理条件を90℃、30分としたこと以外は、実施例5と同様の方法により茶抽出物を得た。
Comparative Example 4
A tea extract was obtained by the same method as in Example 5 except that the heat treatment conditions were 90 ° C. and 30 minutes.
比較例5
加熱処理条件を100℃、3分としたこと以外は、実施例5と同様の方法により茶抽出物を得た。
Comparative Example 5
A tea extract was obtained in the same manner as in Example 5 except that the heat treatment conditions were 100 ° C. and 3 minutes.
比較例6
加熱処理条件を133℃、3分としたこと以外は、実施例6と同様の方法により茶抽出物を得た。
Comparative Example 6
A tea extract was obtained in the same manner as in Example 6 except that the heat treatment conditions were 133 ° C. and 3 minutes.
比較例7
実施例4(1)で得られた第2の茶抽出液を温度25℃に保持し、タンナーゼ(キッコーマン(株)製、タンナーゼKTFH、500U/g)を第2の茶抽出液に対して120ppm(60U/L)添加し、100分間保持した後、80℃に加熱して、3分間保持し酵素を失活させた。その後、得られた茶抽出液を凍結乾燥機にて凍結乾燥を行い、粉末状の茶抽出物を得た。
Comparative Example 7
The second tea extract obtained in Example 4 (1) was kept at a temperature of 25 ° C., and tannase (Kikkoman Corp., tannase KTFH, 500 U / g) was 120 ppm with respect to the second tea extract. (60 U / L) was added and held for 100 minutes, then heated to 80 ° C. and held for 3 minutes to inactivate the enzyme. Thereafter, the obtained tea extract was freeze-dried with a freeze dryer to obtain a powdery tea extract.
実施例1〜4、比較例1〜3で得られた茶抽出物の分析結果及び風味についての評価結果を表1に示す。
実施例5〜9、比較例4〜6で得られた茶抽出物の分析結果及び風味についての評価結果を表2に示す。
実施例10、比較例7で得られた茶抽出物の分析結果及び風味についての評価結果を表3に示す。
また、実施例5〜9及び比較例4〜6で得られた茶抽出物について加熱条件と風味との関係を図1に示す。
Table 1 shows the analysis results of the tea extracts obtained in Examples 1 to 4 and Comparative Examples 1 to 3 and the evaluation results on the flavor.
The analysis results of the tea extracts obtained in Examples 5 to 9 and Comparative Examples 4 to 6 and the evaluation results on the flavor are shown in Table 2.
Table 3 shows the analysis results of the tea extract obtained in Example 10 and Comparative Example 7 and the evaluation results on the flavor.
Moreover, the relationship between a heating condition and flavor is shown in FIG. 1 about the tea extract obtained in Examples 5-9 and Comparative Examples 4-6.
表1〜3の結果から、実施例1〜10で得られた茶抽出物は、いずれもエグ味、苦味及び加熱臭が抑制され、風味が良好であった。一方、比較例1〜5及び7で得られた茶抽出物はエグ味が強く、また比較例6で得られた茶抽出物は強い加熱異臭及び苦味が認められた。また、図1から、温度95〜140℃、F値0.05〜40(Z=10)にて加熱処理することの意義が実証された。 From the results shown in Tables 1 to 3, the tea extracts obtained in Examples 1 to 10 all had a good flavor, with a suppressed taste, bitterness and heated odor. On the other hand, the tea extracts obtained in Comparative Examples 1 to 5 and 7 had a strong taste, and the tea extract obtained in Comparative Example 6 showed a strong heated odor and bitterness. Further, FIG. 1 demonstrates the significance of heat treatment at a temperature of 95 to 140 ° C. and an F value of 0.05 to 40 (Z = 10).
Claims (3)
Priority Applications (7)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2007337521A JP5111096B2 (en) | 2007-12-27 | 2007-12-27 | Production method of tea extract |
KR1020107002677A KR101475758B1 (en) | 2007-08-08 | 2008-08-07 | Method for production of tea extract |
CN201310449807.9A CN103493928A (en) | 2007-08-08 | 2008-08-07 | Method for production of tea extract |
EP08826882.6A EP2177108B1 (en) | 2007-08-08 | 2008-08-07 | Method for production of tea extract |
PCT/JP2008/002140 WO2009019876A1 (en) | 2007-08-08 | 2008-08-07 | Method for production of tea extract |
US12/672,302 US20120121761A1 (en) | 2007-08-08 | 2008-08-07 | Method for production of tea extract |
CN2008801023431A CN101778571B (en) | 2007-08-08 | 2008-08-07 | Method for production of tea extract |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2007337521A JP5111096B2 (en) | 2007-12-27 | 2007-12-27 | Production method of tea extract |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2009153487A JP2009153487A (en) | 2009-07-16 |
JP5111096B2 true JP5111096B2 (en) | 2012-12-26 |
Family
ID=40958188
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2007337521A Active JP5111096B2 (en) | 2007-08-08 | 2007-12-27 | Production method of tea extract |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP5111096B2 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN104351402B (en) * | 2014-10-23 | 2017-01-25 | 中国农业科学院茶叶研究所 | Processing method for improving aftertaste sweet of tea drink |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2011065799A2 (en) * | 2009-11-30 | 2011-06-03 | (주)아모레퍼시픽 | Preparation method of tea water, and tea water obtained thereby |
WO2013094494A1 (en) * | 2011-12-21 | 2013-06-27 | 花王株式会社 | Method for producing purified tea extract |
JP5981234B2 (en) * | 2012-06-08 | 2016-08-31 | 長谷川香料株式会社 | Taste improving agent for tea-containing foods and drinks |
JP6230382B2 (en) * | 2012-12-27 | 2017-11-15 | 三井農林株式会社 | Method for producing low caffeine tea extract and low caffeine tea extract |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2518752B2 (en) * | 1991-08-21 | 1996-07-31 | 食品産業超高圧利用技術研究組合 | Tea beverage sterilization method |
JP3395116B2 (en) * | 1993-04-28 | 2003-04-07 | 株式会社 伊藤園 | Production method of tea beverage |
JPH10290667A (en) * | 1997-04-18 | 1998-11-04 | Sapporo Breweries Ltd | Production of clear green tea beverage |
JP2003199495A (en) * | 2001-12-28 | 2003-07-15 | Sapporo Breweries Ltd | Tea beverage and method of production for the same |
JP4554184B2 (en) * | 2003-10-31 | 2010-09-29 | アサヒ飲料株式会社 | Tea beverage astringency treatment method and tea beverage obtained by the method |
JP5191087B2 (en) * | 2005-06-08 | 2013-04-24 | 三井農林株式会社 | Containerized tea beverage |
JP4542047B2 (en) * | 2005-10-20 | 2010-09-08 | 花王株式会社 | Method for producing purified green tea extract |
-
2007
- 2007-12-27 JP JP2007337521A patent/JP5111096B2/en active Active
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN104351402B (en) * | 2014-10-23 | 2017-01-25 | 中国农业科学院茶叶研究所 | Processing method for improving aftertaste sweet of tea drink |
Also Published As
Publication number | Publication date |
---|---|
JP2009153487A (en) | 2009-07-16 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP3706370B2 (en) | Tannase-treated green tea extract | |
JP4694974B2 (en) | Method for producing purified green tea extract | |
JP4977523B2 (en) | Containerized tea beverage | |
JP4745784B2 (en) | Purified green tea extract | |
KR101475758B1 (en) | Method for production of tea extract | |
JP4800779B2 (en) | Method for producing purified green tea extract | |
JP5261167B2 (en) | Method for producing purified tea extract | |
JP5228229B2 (en) | Method for producing low caffeine tea extract | |
CN107580455B (en) | Green tea extract composition | |
JP2008125428A (en) | Packaged black tea beverage containing high concentration black tea polyphenol | |
JP5366771B2 (en) | Purified green tea extract | |
JP5111096B2 (en) | Production method of tea extract | |
JP3590028B2 (en) | Semi-fermented tea or fermented tea beverage with high catechin content | |
JP5820110B2 (en) | Purified tea extract | |
JP2011120499A (en) | Method for producing purified tea extract | |
JP4383337B2 (en) | High concentration catechin-containing container-packed oolong tea drink | |
JP3590032B2 (en) | Manufacturing method of green tea polyphenol | |
JPWO2019044474A1 (en) | Decolorized tea extract and method for producing the same | |
JP3638560B2 (en) | Production method of semi-fermented tea beverage and fermented tea beverage | |
JP5427499B2 (en) | Method for producing purified tea extract | |
JP5820604B2 (en) | Method for producing catechin-containing beverage | |
JP4673247B2 (en) | Process for producing a processed tea extraction product with improved flavor | |
JP4119829B2 (en) | Green tea bottled beverage | |
JP5830267B2 (en) | Container drink | |
JP2011019463A (en) | Packaged beverage |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20100916 |
|
A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20120703 |
|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20120829 |
|
TRDD | Decision of grant or rejection written | ||
A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 Effective date: 20121002 |
|
A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 |
|
A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20121009 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20151019 Year of fee payment: 3 |
|
R151 | Written notification of patent or utility model registration |
Ref document number: 5111096 Country of ref document: JP Free format text: JAPANESE INTERMEDIATE CODE: R151 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20151019 Year of fee payment: 3 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |