CN1732812A - 利用多种生物酶增强和改善烟草浸膏香气的方法 - Google Patents
利用多种生物酶增强和改善烟草浸膏香气的方法 Download PDFInfo
- Publication number
- CN1732812A CN1732812A CN 200510029565 CN200510029565A CN1732812A CN 1732812 A CN1732812 A CN 1732812A CN 200510029565 CN200510029565 CN 200510029565 CN 200510029565 A CN200510029565 A CN 200510029565A CN 1732812 A CN1732812 A CN 1732812A
- Authority
- CN
- China
- Prior art keywords
- tobacco extract
- enzyme
- enzymolysis
- temperature
- tobacco
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 235000002637 Nicotiana tabacum Nutrition 0.000 title claims abstract description 81
- 241000208125 Nicotiana Species 0.000 title claims abstract description 80
- 108090000790 Enzymes Proteins 0.000 title claims abstract description 52
- 102000004190 Enzymes Human genes 0.000 title claims abstract description 52
- 238000000034 method Methods 0.000 title claims abstract description 15
- 239000000284 extract Substances 0.000 claims abstract description 83
- 229940088598 enzyme Drugs 0.000 claims abstract description 51
- 229940059442 hemicellulase Drugs 0.000 claims abstract description 13
- 108010002430 hemicellulase Proteins 0.000 claims abstract description 13
- 108010047754 beta-Glucosidase Proteins 0.000 claims abstract description 10
- 102000006995 beta-Glucosidase Human genes 0.000 claims abstract description 10
- 239000003205 fragrance Substances 0.000 claims description 29
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 26
- 238000003756 stirring Methods 0.000 claims description 24
- 239000012141 concentrate Substances 0.000 claims description 15
- 108010059892 Cellulase Proteins 0.000 claims description 12
- 229940106157 cellulase Drugs 0.000 claims description 12
- 230000001954 sterilising effect Effects 0.000 claims description 11
- 238000004659 sterilization and disinfection Methods 0.000 claims description 11
- 230000007071 enzymatic hydrolysis Effects 0.000 claims description 10
- 238000006047 enzymatic hydrolysis reaction Methods 0.000 claims description 10
- 238000001816 cooling Methods 0.000 claims description 8
- 239000002826 coolant Substances 0.000 claims description 4
- 238000010438 heat treatment Methods 0.000 claims description 4
- 239000006185 dispersion Substances 0.000 claims description 3
- 239000002994 raw material Substances 0.000 claims description 3
- 230000002708 enhancing effect Effects 0.000 claims 5
- 239000000376 reactant Substances 0.000 claims 1
- 239000001913 cellulose Substances 0.000 abstract description 7
- 229920002678 cellulose Polymers 0.000 abstract description 7
- 150000001720 carbohydrates Chemical class 0.000 abstract description 2
- AEMOLEFTQBMNLQ-DTEWXJGMSA-N beta-D-galacturonic acid Chemical compound O[C@@H]1O[C@H](C(O)=O)[C@H](O)[C@H](O)[C@H]1O AEMOLEFTQBMNLQ-DTEWXJGMSA-N 0.000 abstract 1
- 235000014633 carbohydrates Nutrition 0.000 abstract 1
- 239000000470 constituent Substances 0.000 abstract 1
- 239000000463 material Substances 0.000 description 30
- 239000000047 product Substances 0.000 description 22
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 19
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- 235000019504 cigarettes Nutrition 0.000 description 9
- 229930182478 glucoside Natural products 0.000 description 9
- 150000008131 glucosides Chemical class 0.000 description 9
- 239000000203 mixture Substances 0.000 description 7
- 239000001814 pectin Substances 0.000 description 7
- 229920001277 pectin Polymers 0.000 description 7
- 235000010987 pectin Nutrition 0.000 description 7
- 235000013599 spices Nutrition 0.000 description 7
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 6
- 230000002255 enzymatic effect Effects 0.000 description 6
- 229920002521 macromolecule Polymers 0.000 description 6
- 238000010010 raising Methods 0.000 description 5
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 4
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 4
- 229920002488 Hemicellulose Polymers 0.000 description 4
- 108010059820 Polygalacturonase Proteins 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 108010093305 exopolygalacturonase Proteins 0.000 description 4
- 239000008103 glucose Substances 0.000 description 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- PYMYPHUHKUWMLA-WDCZJNDASA-N arabinose Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)C=O PYMYPHUHKUWMLA-WDCZJNDASA-N 0.000 description 3
- PYMYPHUHKUWMLA-UHFFFAOYSA-N arabinose Natural products OCC(O)C(O)C(O)C=O PYMYPHUHKUWMLA-UHFFFAOYSA-N 0.000 description 3
- SRBFZHDQGSBBOR-UHFFFAOYSA-N beta-D-Pyranose-Lyxose Natural products OC1COC(O)C(O)C1O SRBFZHDQGSBBOR-UHFFFAOYSA-N 0.000 description 3
- WQZGKKKJIJFFOK-FPRJBGLDSA-N beta-D-galactose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@H]1O WQZGKKKJIJFFOK-FPRJBGLDSA-N 0.000 description 3
- 230000033228 biological regulation Effects 0.000 description 3
- 230000007062 hydrolysis Effects 0.000 description 3
- 238000006460 hydrolysis reaction Methods 0.000 description 3
- 239000002304 perfume Substances 0.000 description 3
- 239000002243 precursor Substances 0.000 description 3
- ULWHHBHJGPPBCO-UHFFFAOYSA-N propane-1,1-diol Chemical class CCC(O)O ULWHHBHJGPPBCO-UHFFFAOYSA-N 0.000 description 3
- 239000003643 water by type Substances 0.000 description 3
- 238000005303 weighing Methods 0.000 description 3
- QPUYECUOLPXSFR-UHFFFAOYSA-N 1-methylnaphthalene Chemical compound C1=CC=C2C(C)=CC=CC2=C1 QPUYECUOLPXSFR-UHFFFAOYSA-N 0.000 description 2
- OWEGMIWEEQEYGQ-UHFFFAOYSA-N 100676-05-9 Natural products OC1C(O)C(O)C(CO)OC1OCC1C(O)C(O)C(O)C(OC2C(OC(O)C(O)C2O)CO)O1 OWEGMIWEEQEYGQ-UHFFFAOYSA-N 0.000 description 2
- GUBGYTABKSRVRQ-PICCSMPSSA-N Maltose Natural products O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1O[C@@H]1[C@@H](CO)OC(O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-PICCSMPSSA-N 0.000 description 2
- FLIACVVOZYBSBS-UHFFFAOYSA-N Methyl palmitate Chemical compound CCCCCCCCCCCCCCCC(=O)OC FLIACVVOZYBSBS-UHFFFAOYSA-N 0.000 description 2
- 244000006449 Nicotiana forgetiana Species 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
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 2
- GUBGYTABKSRVRQ-QUYVBRFLSA-N beta-maltose Chemical compound OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O)[C@H](O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1O GUBGYTABKSRVRQ-QUYVBRFLSA-N 0.000 description 2
- 239000008367 deionised water Substances 0.000 description 2
- 229910021641 deionized water Inorganic materials 0.000 description 2
- 238000007598 dipping method Methods 0.000 description 2
- MMXKVMNBHPAILY-UHFFFAOYSA-N ethyl laurate Chemical compound CCCCCCCCCCCC(=O)OCC MMXKVMNBHPAILY-UHFFFAOYSA-N 0.000 description 2
- 235000011187 glycerol Nutrition 0.000 description 2
- NDJKXXJCMXVBJW-UHFFFAOYSA-N heptadecane Chemical compound CCCCCCCCCCCCCCCCC NDJKXXJCMXVBJW-UHFFFAOYSA-N 0.000 description 2
- DCAYPVUWAIABOU-UHFFFAOYSA-N hexadecane Chemical compound CCCCCCCCCCCCCCCC DCAYPVUWAIABOU-UHFFFAOYSA-N 0.000 description 2
- IYRMWMYZSQPJKC-UHFFFAOYSA-N kaempferol Chemical compound C1=CC(O)=CC=C1C1=C(O)C(=O)C2=C(O)C=C(O)C=C2O1 IYRMWMYZSQPJKC-UHFFFAOYSA-N 0.000 description 2
- MWDZOUNAPSSOEL-UHFFFAOYSA-N kaempferol Natural products OC1=C(C(=O)c2cc(O)cc(O)c2O1)c3ccc(O)cc3 MWDZOUNAPSSOEL-UHFFFAOYSA-N 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 229960002715 nicotine Drugs 0.000 description 2
- SNICXCGAKADSCV-UHFFFAOYSA-N nicotine Natural products CN1CCCC1C1=CC=CN=C1 SNICXCGAKADSCV-UHFFFAOYSA-N 0.000 description 2
- RZJRJXONCZWCBN-UHFFFAOYSA-N octadecane Chemical compound CCCCCCCCCCCCCCCCCC RZJRJXONCZWCBN-UHFFFAOYSA-N 0.000 description 2
- YCOZIPAWZNQLMR-UHFFFAOYSA-N pentadecane Chemical compound CCCCCCCCCCCCCCC YCOZIPAWZNQLMR-UHFFFAOYSA-N 0.000 description 2
- 150000003384 small molecules Chemical class 0.000 description 2
- 238000002470 solid-phase micro-extraction Methods 0.000 description 2
- 238000005728 strengthening Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000000341 volatile oil Substances 0.000 description 2
- XMGQYMWWDOXHJM-JTQLQIEISA-N (+)-α-limonene Chemical compound CC(=C)[C@@H]1CCC(C)=CC1 XMGQYMWWDOXHJM-JTQLQIEISA-N 0.000 description 1
- SNICXCGAKADSCV-JTQLQIEISA-N (-)-Nicotine Chemical compound CN1CCC[C@H]1C1=CC=CN=C1 SNICXCGAKADSCV-JTQLQIEISA-N 0.000 description 1
- KZJWDPNRJALLNS-VPUBHVLGSA-N (-)-beta-Sitosterol Natural products O[C@@H]1CC=2[C@@](C)([C@@H]3[C@H]([C@H]4[C@@](C)([C@H]([C@H](CC[C@@H](C(C)C)CC)C)CC4)CC3)CC=2)CC1 KZJWDPNRJALLNS-VPUBHVLGSA-N 0.000 description 1
- DMHADBQKVWXPPM-PDDCSNRZSA-N (1e,3z,6e,10z,14s)-3,7,11-trimethyl-14-propan-2-ylcyclotetradeca-1,3,6,10-tetraene Chemical compound CC(C)[C@@H]\1CC\C(C)=C/CC\C(C)=C\C\C=C(\C)/C=C/1 DMHADBQKVWXPPM-PDDCSNRZSA-N 0.000 description 1
- CSVWWLUMXNHWSU-UHFFFAOYSA-N (22E)-(24xi)-24-ethyl-5alpha-cholest-22-en-3beta-ol Natural products C1CC2CC(O)CCC2(C)C2C1C1CCC(C(C)C=CC(CC)C(C)C)C1(C)CC2 CSVWWLUMXNHWSU-UHFFFAOYSA-N 0.000 description 1
- 239000001893 (2R)-2-methylbutanal Substances 0.000 description 1
- CBQXHTWJSZXYSK-DFTQQVSXSA-N (4e)-4-[(e)-but-2-enylidene]-3,5,5-trimethylcyclohex-2-en-1-one Chemical compound C\C=C\C=C1\C(C)=CC(=O)CC1(C)C CBQXHTWJSZXYSK-DFTQQVSXSA-N 0.000 description 1
- CBQXHTWJSZXYSK-VZVVJSHISA-N (4e)-4-[(z)-but-2-enylidene]-3,5,5-trimethylcyclohex-2-en-1-one Chemical compound C\C=C/C=C1/C(C)=CC(=O)CC1(C)C CBQXHTWJSZXYSK-VZVVJSHISA-N 0.000 description 1
- CBQXHTWJSZXYSK-UNKATYBDSA-N (4z)-4-[(z)-but-2-enylidene]-3,5,5-trimethylcyclohex-2-en-1-one Chemical compound C\C=C/C=C1\C(C)=CC(=O)CC1(C)C CBQXHTWJSZXYSK-UNKATYBDSA-N 0.000 description 1
- RADIRXJQODWKGQ-HWKANZROSA-N 2-Ethoxy-5-(1-propenyl)phenol Chemical compound CCOC1=CC=C(\C=C\C)C=C1O RADIRXJQODWKGQ-HWKANZROSA-N 0.000 description 1
- ZFFTZDQKIXPDAF-UHFFFAOYSA-N 2-Furanmethanethiol Chemical compound SCC1=CC=CO1 ZFFTZDQKIXPDAF-UHFFFAOYSA-N 0.000 description 1
- MJZMNZLYXAGWBI-UHFFFAOYSA-N 2-cyclohexa-1,3-dien-1-ylacetaldehyde Chemical compound O=CCC1=CC=CCC1 MJZMNZLYXAGWBI-UHFFFAOYSA-N 0.000 description 1
- JJVKJJNCIILLRP-UHFFFAOYSA-N 2-ethyl-6-methylaniline Chemical compound CCC1=CC=CC(C)=C1N JJVKJJNCIILLRP-UHFFFAOYSA-N 0.000 description 1
- WRMNZCZEMHIOCP-UHFFFAOYSA-N 2-phenylethanol Chemical compound OCCC1=CC=CC=C1 WRMNZCZEMHIOCP-UHFFFAOYSA-N 0.000 description 1
- KLEXDBGYSOIREE-UHFFFAOYSA-N 24xi-n-propylcholesterol Natural products C1C=C2CC(O)CCC2(C)C2C1C1CCC(C(C)CCC(CCC)C(C)C)C1(C)CC2 KLEXDBGYSOIREE-UHFFFAOYSA-N 0.000 description 1
- ACZGCWSMSTYWDQ-UHFFFAOYSA-N 3h-1-benzofuran-2-one Chemical compound C1=CC=C2OC(=O)CC2=C1 ACZGCWSMSTYWDQ-UHFFFAOYSA-N 0.000 description 1
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 1
- LPZCCMIISIBREI-MTFRKTCUSA-N Citrostadienol Natural products CC=C(CC[C@@H](C)[C@H]1CC[C@H]2C3=CC[C@H]4[C@H](C)[C@@H](O)CC[C@]4(C)[C@H]3CC[C@]12C)C(C)C LPZCCMIISIBREI-MTFRKTCUSA-N 0.000 description 1
- WQZGKKKJIJFFOK-QTVWNMPRSA-N D-mannopyranose Chemical compound OC[C@H]1OC(O)[C@@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-QTVWNMPRSA-N 0.000 description 1
- ARVGMISWLZPBCH-UHFFFAOYSA-N Dehydro-beta-sitosterol Natural products C1C(O)CCC2(C)C(CCC3(C(C(C)CCC(CC)C(C)C)CCC33)C)C3=CC=C21 ARVGMISWLZPBCH-UHFFFAOYSA-N 0.000 description 1
- UBSCDKPKWHYZNX-UHFFFAOYSA-N Demethoxycapillarisin Natural products C1=CC(O)=CC=C1OC1=CC(=O)C2=C(O)C=C(O)C=C2O1 UBSCDKPKWHYZNX-UHFFFAOYSA-N 0.000 description 1
- IAJILQKETJEXLJ-UHFFFAOYSA-N Galacturonsaeure Natural products O=CC(O)C(O)C(O)C(O)C(O)=O IAJILQKETJEXLJ-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- NIDGCIPAMWNKOA-WOJBJXKFSA-N Neophytadiene Natural products [C@H](CCC[C@@H](CCCC(C)C)C)(CCCC(C=C)=C)C NIDGCIPAMWNKOA-WOJBJXKFSA-N 0.000 description 1
- 244000061176 Nicotiana tabacum Species 0.000 description 1
- 241000233805 Phoenix Species 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 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
- 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
- 241000238370 Sepia Species 0.000 description 1
- 244000061458 Solanum melongena Species 0.000 description 1
- 235000002597 Solanum melongena Nutrition 0.000 description 1
- LPQOADBMXVRBNX-UHFFFAOYSA-N ac1ldcw0 Chemical compound Cl.C1CN(C)CCN1C1=C(F)C=C2C(=O)C(C(O)=O)=CN3CCSC1=C32 LPQOADBMXVRBNX-UHFFFAOYSA-N 0.000 description 1
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 1
- 150000001241 acetals Chemical class 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- IAJILQKETJEXLJ-RSJOWCBRSA-N aldehydo-D-galacturonic acid Chemical compound O=C[C@H](O)[C@@H](O)[C@@H](O)[C@H](O)C(O)=O IAJILQKETJEXLJ-RSJOWCBRSA-N 0.000 description 1
- BYGQBDHUGHBGMD-UHFFFAOYSA-N alpha-methyl butyraldehyde Natural products CCC(C)C=O BYGQBDHUGHBGMD-UHFFFAOYSA-N 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- DULCUDSUACXJJC-UHFFFAOYSA-N benzeneacetic acid ethyl ester Natural products CCOC(=O)CC1=CC=CC=C1 DULCUDSUACXJJC-UHFFFAOYSA-N 0.000 description 1
- MJVXAPPOFPTTCA-UHFFFAOYSA-N beta-Sistosterol Natural products CCC(CCC(C)C1CCC2C3CC=C4C(C)C(O)CCC4(C)C3CCC12C)C(C)C MJVXAPPOFPTTCA-UHFFFAOYSA-N 0.000 description 1
- LGJMUZUPVCAVPU-UHFFFAOYSA-N beta-Sitostanol Natural products C1CC2CC(O)CCC2(C)C2C1C1CCC(C(C)CCC(CC)C(C)C)C1(C)CC2 LGJMUZUPVCAVPU-UHFFFAOYSA-N 0.000 description 1
- POIARNZEYGURDG-FNORWQNLSA-N beta-damascenone Chemical compound C\C=C\C(=O)C1=C(C)C=CCC1(C)C POIARNZEYGURDG-FNORWQNLSA-N 0.000 description 1
- POIARNZEYGURDG-UHFFFAOYSA-N beta-damascenone Natural products CC=CC(=O)C1=C(C)C=CCC1(C)C POIARNZEYGURDG-UHFFFAOYSA-N 0.000 description 1
- NJKOMDUNNDKEAI-UHFFFAOYSA-N beta-sitosterol Natural products CCC(CCC(C)C1CCC2(C)C3CC=C4CC(O)CCC4C3CCC12C)C(C)C NJKOMDUNNDKEAI-UHFFFAOYSA-N 0.000 description 1
- ZFMQKOWCDKKBIF-UHFFFAOYSA-N bis(3,5-difluorophenyl)phosphane Chemical compound FC1=CC(F)=CC(PC=2C=C(F)C=C(F)C=2)=C1 ZFMQKOWCDKKBIF-UHFFFAOYSA-N 0.000 description 1
- DMHADBQKVWXPPM-SBHJBAJOSA-N cembrene Natural products CC(C)C1CCC(=C/CCC(=CCC=C(C)/C=C/1)C)C DMHADBQKVWXPPM-SBHJBAJOSA-N 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 125000005594 diketone group Chemical group 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 229940067592 ethyl palmitate Drugs 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 239000000796 flavoring agent Substances 0.000 description 1
- 235000019634 flavors Nutrition 0.000 description 1
- 239000003546 flue gas Substances 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- WBJINCZRORDGAQ-UHFFFAOYSA-N formic acid ethyl ester Natural products CCOC=O WBJINCZRORDGAQ-UHFFFAOYSA-N 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 238000002290 gas chromatography-mass spectrometry Methods 0.000 description 1
- HNZUNIKWNYHEJJ-FMIVXFBMSA-N geranyl acetone Chemical compound CC(C)=CCC\C(C)=C\CCC(C)=O HNZUNIKWNYHEJJ-FMIVXFBMSA-N 0.000 description 1
- HNZUNIKWNYHEJJ-UHFFFAOYSA-N geranyl acetone Natural products CC(C)=CCCC(C)=CCCC(C)=O HNZUNIKWNYHEJJ-UHFFFAOYSA-N 0.000 description 1
- 125000002791 glucosyl group Chemical group C1([C@H](O)[C@@H](O)[C@H](O)[C@H](O1)CO)* 0.000 description 1
- 150000004676 glycans Chemical class 0.000 description 1
- 125000003147 glycosyl group Chemical group 0.000 description 1
- 230000003760 hair shine Effects 0.000 description 1
- 150000002373 hemiacetals Chemical class 0.000 description 1
- XIRNKXNNONJFQO-UHFFFAOYSA-N hexadecanoic acid ethyl ester Natural products CCCCCCCCCCCCCCCC(=O)OCC XIRNKXNNONJFQO-UHFFFAOYSA-N 0.000 description 1
- 238000004128 high performance liquid chromatography Methods 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 235000008777 kaempferol Nutrition 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 239000006210 lotion Substances 0.000 description 1
- UXOUKMQIEVGVLY-UHFFFAOYSA-N morin Natural products OC1=CC(O)=CC(C2=C(C(=O)C3=C(O)C=C(O)C=C3O2)O)=C1 UXOUKMQIEVGVLY-UHFFFAOYSA-N 0.000 description 1
- NIDGCIPAMWNKOA-UHFFFAOYSA-N neophytadiene Chemical compound CC(C)CCCC(C)CCCC(C)CCCC(=C)C=C NIDGCIPAMWNKOA-UHFFFAOYSA-N 0.000 description 1
- 229940038384 octadecane Drugs 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 229940023462 paste product Drugs 0.000 description 1
- 238000009928 pasteurization Methods 0.000 description 1
- DOIRQSBPFJWKBE-UHFFFAOYSA-N phthalic acid di-n-butyl ester Natural products CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 1
- 150000008442 polyphenolic compounds Chemical class 0.000 description 1
- 235000013824 polyphenols Nutrition 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 150000003222 pyridines Chemical class 0.000 description 1
- 235000005875 quercetin Nutrition 0.000 description 1
- 229960001285 quercetin Drugs 0.000 description 1
- KZJWDPNRJALLNS-VJSFXXLFSA-N sitosterol 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)CC[C@@H](CC)C(C)C)[C@@]1(C)CC2 KZJWDPNRJALLNS-VJSFXXLFSA-N 0.000 description 1
- 229950005143 sitosterol Drugs 0.000 description 1
- NLQLSVXGSXCXFE-UHFFFAOYSA-N sitosterol Natural products CC=C(/CCC(C)C1CC2C3=CCC4C(C)C(O)CCC4(C)C3CCC2(C)C1)C(C)C NLQLSVXGSXCXFE-UHFFFAOYSA-N 0.000 description 1
- 235000015500 sitosterol Nutrition 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- RRBYUSWBLVXTQN-VZCHMASFSA-N tricyclene Natural products C([C@@H]12)C3C[C@H]1C2(C)C3(C)C RRBYUSWBLVXTQN-VZCHMASFSA-N 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 229930007850 β-damascenone Natural products 0.000 description 1
Landscapes
- Preparation Of Compounds By Using Micro-Organisms (AREA)
Abstract
Description
主要成分 | 处理前相对百分含量(%) | 处理后相对百分含量(%) |
甲酸乙酯 | 0.50 | 0.16 |
乙酸乙酯 | 1.85 | - |
2-甲基丁醛 | 0.22 | - |
Alpha-蒎烯 | - | 0.27 |
乙醇 | 1.39 | 9.16 |
柠檬烯 | - | 0.20 |
4-甲基-2-丙基-1,3-二氧杂烷 | 1.07 | - |
乙酸 | - | 0.81 |
2-乙基-6-甲基苯胺 | - | 0.13 |
十五烷 | - | 0.43 |
十六烷 | - | 0.86 |
糠硫醇 | - | 0.27 |
1,3-环己二烯-1-乙醛 | - | 0.16 |
1,2,3,4-四氢萘 | 1.40 | - |
(Z)-2-(1’-丁烯基)-1,3,5-三甲基苯 | 1.59 | 0.47 |
十七烷 | - | 0.77 |
Pine Needle Tyrol Unk | - | 7.46 |
5-甲基-2-(1-甲基)-环己醇 | 0.67 | - |
三环烯 | 10.98 | - |
1-环己烯-1-乙醛 | 0.31 | - |
苯乙酸乙酯 | 0.18 | 0.60 |
十八烷 | - | 0.36 |
Beta-大马酮 | 1.22 | 1.30 |
香叶基丙酮 | - | 0.38 |
苯甲醇 | - | 0.34 |
十二酸乙酯 | 0.22 | - |
6,10-二甲基-5,9-二烯-2-十一酮 | 0.84 | - |
尼古丁 | 6.10 | 6.29 |
苯乙醇 | - | 0.39 |
新植二烯 | 20.10 | 33.85 |
1-(1H-2-吡咯基)-乙酮 | - | 0.29 |
6,10,14-三甲基-十五-2-酮 | 0.43 | - |
新茄尼二酮 | 0.31 | - |
1,2,3,4-四氢甲基萘 | 0.44 | - |
巨豆三烯酮2 | 0.61 | 0.42 |
西柏烯 | 0.43 | - |
巨豆三烯酮1 | 2.61 | 2.07 |
十六酸甲酯 | 0.60 | - |
十六酸乙酯 | 0.72 | 0.46 |
巨豆三烯酮3 | 0.62 | 0.39 |
巨豆三烯酮4 | 1.87 | 1.32 |
5,6,7,7a-四2(4氢)苯并呋喃酮 | 0.39 | 0.15 |
2,3’-二吡啶 | 0.27 | - |
邻苯二甲酸二丁酯 | 1.85 | 0.74 |
己二酸二辛酯 | 27.24 | 18.36 |
Claims (6)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CNB2005100295653A CN100493392C (zh) | 2005-09-12 | 2005-09-12 | 利用多种生物酶增强和改善烟草浸膏香气的方法 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CNB2005100295653A CN100493392C (zh) | 2005-09-12 | 2005-09-12 | 利用多种生物酶增强和改善烟草浸膏香气的方法 |
Publications (2)
Publication Number | Publication Date |
---|---|
CN1732812A true CN1732812A (zh) | 2006-02-15 |
CN100493392C CN100493392C (zh) | 2009-06-03 |
Family
ID=36075594
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CNB2005100295653A Active CN100493392C (zh) | 2005-09-12 | 2005-09-12 | 利用多种生物酶增强和改善烟草浸膏香气的方法 |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN100493392C (zh) |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102499450A (zh) * | 2011-09-20 | 2012-06-20 | 云南还原医学生物科技有限公司 | 一种添加于无烟烟草产品中的功能性原料及制备无烟烟草产品的方法 |
CN102987546A (zh) * | 2012-12-13 | 2013-03-27 | 华宝食用香精香料(上海)有限公司 | 一种提高烟梗萃取液品质的加工方法 |
CN106036984A (zh) * | 2016-07-03 | 2016-10-26 | 陈毅忠 | 一种固定化蜗牛酶制备烟草浸膏的方法 |
CN106811381A (zh) * | 2017-02-23 | 2017-06-09 | 湖北中烟工业有限责任公司 | 一种烟草可可酒新型烟草制品及其制备方法 |
CN107802027A (zh) * | 2017-09-29 | 2018-03-16 | 昆明坤九香精香料有限公司 | 一种利用生物酶制备烟草净油的方法 |
CN110747234A (zh) * | 2019-10-21 | 2020-02-04 | 上海百润投资控股集团股份有限公司 | 一种槐花浸膏的制备方法 |
CN112493526A (zh) * | 2020-12-07 | 2021-03-16 | 广州健顺生物医药研究院有限公司 | 一种含有薄荷脑的烟草加料香精配方 |
CN113667538A (zh) * | 2021-09-02 | 2021-11-19 | 成都宏亿实业集团有限公司 | 复合香料提取方法及应用 |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1006442B (zh) * | 1987-07-24 | 1990-01-17 | 山东大学 | 微生物复合酶处理低次烟叶的方法 |
US5343879A (en) * | 1991-06-21 | 1994-09-06 | R. J. Reynolds Tobacco Company | Tobacco treatment process |
CN1039776C (zh) * | 1994-08-18 | 1998-09-16 | 山东省食品发酵工业研究设计院 | 一种制取烟用香料的方法 |
-
2005
- 2005-09-12 CN CNB2005100295653A patent/CN100493392C/zh active Active
Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102499450A (zh) * | 2011-09-20 | 2012-06-20 | 云南还原医学生物科技有限公司 | 一种添加于无烟烟草产品中的功能性原料及制备无烟烟草产品的方法 |
CN102987546A (zh) * | 2012-12-13 | 2013-03-27 | 华宝食用香精香料(上海)有限公司 | 一种提高烟梗萃取液品质的加工方法 |
CN102987546B (zh) * | 2012-12-13 | 2014-10-22 | 华宝食用香精香料(上海)有限公司 | 一种提高烟梗萃取液品质的加工方法 |
CN106036984A (zh) * | 2016-07-03 | 2016-10-26 | 陈毅忠 | 一种固定化蜗牛酶制备烟草浸膏的方法 |
CN106811381A (zh) * | 2017-02-23 | 2017-06-09 | 湖北中烟工业有限责任公司 | 一种烟草可可酒新型烟草制品及其制备方法 |
CN106811381B (zh) * | 2017-02-23 | 2020-03-10 | 湖北中烟工业有限责任公司 | 一种烟草可可酒新型烟草制品及其制备方法 |
CN107802027A (zh) * | 2017-09-29 | 2018-03-16 | 昆明坤九香精香料有限公司 | 一种利用生物酶制备烟草净油的方法 |
CN110747234A (zh) * | 2019-10-21 | 2020-02-04 | 上海百润投资控股集团股份有限公司 | 一种槐花浸膏的制备方法 |
CN110747234B (zh) * | 2019-10-21 | 2023-05-05 | 上海百润投资控股集团股份有限公司 | 一种槐花浸膏的制备方法 |
CN112493526A (zh) * | 2020-12-07 | 2021-03-16 | 广州健顺生物医药研究院有限公司 | 一种含有薄荷脑的烟草加料香精配方 |
CN113667538A (zh) * | 2021-09-02 | 2021-11-19 | 成都宏亿实业集团有限公司 | 复合香料提取方法及应用 |
Also Published As
Publication number | Publication date |
---|---|
CN100493392C (zh) | 2009-06-03 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN100493392C (zh) | 利用多种生物酶增强和改善烟草浸膏香气的方法 | |
CN1732813A (zh) | 利用生物酶制备烟草浸膏的方法 | |
CN102499461B (zh) | 一种反应型烟用香料的制备方法 | |
CN101445766B (zh) | 可可香料的制备方法、采用该方法所得到的产品及其用途 | |
CN107164094B (zh) | 增色增香脯氨酸美拉德反应物制备方法及其应用 | |
CN101638608A (zh) | 利用微生物制备的烟用无花果香料及其制备方法和应用 | |
KR20170000890A (ko) | 돼지감자 발효주 및 그 제조 방법 | |
CN107232638A (zh) | 一种葡萄干提取物的提质纯化方法及其应用 | |
CN107723092A (zh) | 一种带有甜香的发酵当归提取物的制备方法及其应用 | |
CN109349678A (zh) | 一种复合烟叶提取物的制备方法及其应用 | |
CN105542959A (zh) | 一种电子烟液香料的制备方法 | |
CN112481036A (zh) | 一种高香气烟草精油的酶解制备方法 | |
CN108707510A (zh) | 一种红枣烟草复合美拉德反应物的制备方法及其应用 | |
CN109536393A (zh) | 一种马里兰烟叶发酵提取物的制备方法及其应用 | |
CN105686068B (zh) | 一种具有白肋烟风格的电子烟液 | |
CN109393568B (zh) | 一种用于加热不燃烧卷烟的白肋烟提取物及其制备方法 | |
CN101343596A (zh) | 一种红茶精油及其制备方法和应用 | |
CN109536283B (zh) | 一种提高品质的苏合香油的制备方法及其应用 | |
CN101361559A (zh) | 纳米猪肉香精及其制备方法 | |
CN106118882B (zh) | 一种基于废弃烟末的烟用美拉德香精的制备方法 | |
CN112316862A (zh) | 一种甜叶菊酵素微胶囊的制备方法及其在卷烟中的应用 | |
CN108236127B (zh) | 一种发酵烟用鸢尾提取物的制备方法及其应用 | |
CN106190573A (zh) | 一种葫芦巴酶促增香制备挥发油的方法及其应用 | |
CN1771845A (zh) | 一种新的烟草陈化加料液 | |
CN109402101A (zh) | 一种晒黄烟提取物的吸附发酵制备方法和应用 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
C14 | Grant of patent or utility model | ||
GR01 | Patent grant | ||
EE01 | Entry into force of recordation of patent licensing contract |
Application publication date: 20060215 Assignee: Wuxi Huahai Flavor Co.,Ltd. Assignor: Huabao Flavours & Fragrances Co.,Ltd Contract record no.: 2012310000205 Denomination of invention: Method for improving tobacco extractive incense by multiple biological enzymes Granted publication date: 20090603 License type: Exclusive License Record date: 20121116 |
|
LICC | Enforcement, change and cancellation of record of contracts on the licence for exploitation of a patent or utility model | ||
C56 | Change in the name or address of the patentee | ||
CP03 | Change of name, title or address |
Address after: 850000 Lhasa economic and Technological Development Zone, Tibet autonomous region, road, investment building, Patentee after: HUABAO FLAVOURS & FRAGRANCES CO.,LTD. Address before: Lhasa economic and Technological Development Zone, 6 investment building, Sang Sang Road Patentee before: Huabao flavor Ltd. Address after: 850000 Lhasa economic and Technological Development Zone, Tibet autonomous region, road, investment building, Patentee after: Huabao flavor Ltd. Address before: 201821 Yecheng Road, Shanghai, No. 1299, No. Patentee before: Huabao Flavours & Fragrances Co.,Ltd |
|
C41 | Transfer of patent application or patent right or utility model | ||
TR01 | Transfer of patent right |
Effective date of registration: 20170216 Address after: 214112 Wuxi Jiangsu New District B61 block No. 7 standard factory building, Patentee after: Wuxi Huahai flavor Co.,Ltd. Address before: Lhasa economic and Technological Development Zone, 6 investment building, Sang Sang Road Patentee before: HUABAO FLAVOURS & FRAGRANCES CO.,LTD. |
|
TR01 | Transfer of patent right |
Effective date of registration: 20180731 Address after: 335000 Ying Nan avenue, Longgang area, Yingtan economic and Technological Development Zone, Jiangxi Patentee after: YINGTAN HUABAO ESSENCE CO.,LTD. Address before: 214112 standard workshop No. 7, B61 plot, Wuxi New District, Wuxi, Jiangsu. Patentee before: Wuxi Huahai flavor Co.,Ltd. |
|
TR01 | Transfer of patent right |