CN106689961A - Preparation method of barley health-care solid beverage - Google Patents
Preparation method of barley health-care solid beverage Download PDFInfo
- Publication number
- CN106689961A CN106689961A CN201710045801.3A CN201710045801A CN106689961A CN 106689961 A CN106689961 A CN 106689961A CN 201710045801 A CN201710045801 A CN 201710045801A CN 106689961 A CN106689961 A CN 106689961A
- Authority
- CN
- China
- Prior art keywords
- barley
- preparation
- solid beverage
- health
- care solid
- 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.)
- Withdrawn
Links
- 235000007340 Hordeum vulgare Nutrition 0.000 title claims abstract description 98
- 235000013361 beverage Nutrition 0.000 title claims abstract description 27
- 239000007787 solid Substances 0.000 title claims abstract description 24
- 238000002360 preparation method Methods 0.000 title claims abstract description 15
- 240000005979 Hordeum vulgare Species 0.000 title 1
- 241000209219 Hordeum Species 0.000 claims abstract description 98
- 102000004190 Enzymes Human genes 0.000 claims abstract description 23
- 108090000790 Enzymes Proteins 0.000 claims abstract description 23
- 239000007788 liquid Substances 0.000 claims abstract description 17
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 claims abstract description 15
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 14
- 239000000843 powder Substances 0.000 claims abstract description 8
- 239000006228 supernatant Substances 0.000 claims abstract description 8
- 238000000227 grinding Methods 0.000 claims abstract description 7
- 229940088598 enzyme Drugs 0.000 claims description 21
- 238000009835 boiling Methods 0.000 claims description 17
- 239000002002 slurry Substances 0.000 claims description 14
- 101150039403 ams gene Proteins 0.000 claims description 12
- 241000209140 Triticum Species 0.000 claims description 8
- 235000021307 Triticum Nutrition 0.000 claims description 8
- 238000000605 extraction Methods 0.000 claims description 8
- 102000013392 Carboxylesterase Human genes 0.000 claims description 7
- 108010051152 Carboxylesterase Proteins 0.000 claims description 7
- 108010059892 Cellulase Proteins 0.000 claims description 6
- 229940106157 cellulase Drugs 0.000 claims description 6
- UOCLXMDMGBRAIB-UHFFFAOYSA-N 1,1,1-trichloroethane Chemical class CC(Cl)(Cl)Cl UOCLXMDMGBRAIB-UHFFFAOYSA-N 0.000 claims description 3
- 238000005119 centrifugation Methods 0.000 claims description 3
- 235000013312 flour Nutrition 0.000 claims description 2
- 230000008901 benefit Effects 0.000 abstract description 5
- 239000003205 fragrance Substances 0.000 abstract description 4
- 150000001875 compounds Chemical class 0.000 abstract description 3
- 238000001816 cooling Methods 0.000 abstract 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- 229960001701 chloroform Drugs 0.000 abstract 1
- 238000004140 cleaning Methods 0.000 abstract 1
- 238000001035 drying Methods 0.000 abstract 1
- 238000010438 heat treatment Methods 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 239000004615 ingredient Substances 0.000 abstract 1
- 238000010792 warming Methods 0.000 abstract 1
- 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 16
- KUBCEEMXQZUPDQ-UHFFFAOYSA-N hordenine Chemical compound CN(C)CCC1=CC=C(O)C=C1 KUBCEEMXQZUPDQ-UHFFFAOYSA-N 0.000 description 10
- 235000012000 cholesterol Nutrition 0.000 description 8
- 230000000694 effects Effects 0.000 description 7
- 229940064063 alpha tocotrienol Drugs 0.000 description 6
- RZFHLOLGZPDCHJ-DLQZEEBKSA-N alpha-Tocotrienol Natural products Oc1c(C)c(C)c2O[C@@](CC/C=C(/CC/C=C(\CC/C=C(\C)/C)/C)\C)(C)CCc2c1C RZFHLOLGZPDCHJ-DLQZEEBKSA-N 0.000 description 6
- RZFHLOLGZPDCHJ-XZXLULOTSA-N α-Tocotrienol Chemical compound OC1=C(C)C(C)=C2O[C@@](CC/C=C(C)/CC/C=C(C)/CCC=C(C)C)(C)CCC2=C1C RZFHLOLGZPDCHJ-XZXLULOTSA-N 0.000 description 6
- 235000019145 α-tocotrienol Nutrition 0.000 description 6
- 239000011730 α-tocotrienol Substances 0.000 description 6
- FYGDTMLNYKFZSV-URKRLVJHSA-N (2s,3r,4s,5s,6r)-2-[(2r,4r,5r,6s)-4,5-dihydroxy-2-(hydroxymethyl)-6-[(2r,4r,5r,6s)-4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxyoxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1OC1[C@@H](CO)O[C@@H](OC2[C@H](O[C@H](O)[C@H](O)[C@H]2O)CO)[C@H](O)[C@H]1O FYGDTMLNYKFZSV-URKRLVJHSA-N 0.000 description 5
- 229920002498 Beta-glucan Polymers 0.000 description 5
- 102000004308 Carboxylic Ester Hydrolases Human genes 0.000 description 5
- 108090000863 Carboxylic Ester Hydrolases Proteins 0.000 description 5
- 108010084185 Cellulases Proteins 0.000 description 5
- 102000005575 Cellulases Human genes 0.000 description 5
- 244000269722 Thea sinensis Species 0.000 description 5
- 238000004760 accelerator mass spectrometry Methods 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 5
- 229940071490 hordenine Drugs 0.000 description 5
- 230000007062 hydrolysis Effects 0.000 description 5
- 238000006460 hydrolysis reaction Methods 0.000 description 5
- GJJVAFUKOBZPCB-ZGRPYONQSA-N (r)-3,4-dihydro-2-methyl-2-(4,8,12-trimethyl-3,7,11-tridecatrienyl)-2h-1-benzopyran-6-ol Chemical class OC1=CC=C2OC(CC/C=C(C)/CC/C=C(C)/CCC=C(C)C)(C)CCC2=C1 GJJVAFUKOBZPCB-ZGRPYONQSA-N 0.000 description 4
- 235000013305 food Nutrition 0.000 description 4
- 230000006870 function Effects 0.000 description 4
- 239000011731 tocotrienol Substances 0.000 description 4
- 229930003802 tocotrienol Natural products 0.000 description 4
- 235000019148 tocotrienols Nutrition 0.000 description 4
- 229940068778 tocotrienols Drugs 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- -1 flavonoids Compound Chemical class 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 230000009467 reduction Effects 0.000 description 3
- 102000004286 Hydroxymethylglutaryl CoA Reductases Human genes 0.000 description 2
- 108090000895 Hydroxymethylglutaryl CoA Reductases Proteins 0.000 description 2
- REFJWTPEDVJJIY-UHFFFAOYSA-N Quercetin Chemical compound C=1C(O)=CC(O)=C(C(C=2O)=O)C=1OC=2C1=CC=C(O)C(O)=C1 REFJWTPEDVJJIY-UHFFFAOYSA-N 0.000 description 2
- 229920002472 Starch Polymers 0.000 description 2
- 230000003064 anti-oxidating effect Effects 0.000 description 2
- 239000008280 blood Substances 0.000 description 2
- 210000004369 blood Anatomy 0.000 description 2
- 229930003935 flavonoid Natural products 0.000 description 2
- 235000017173 flavonoids Nutrition 0.000 description 2
- 230000036541 health Effects 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
- 150000002632 lipids Chemical class 0.000 description 2
- 235000012054 meals Nutrition 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 238000011160 research Methods 0.000 description 2
- 238000001694 spray drying Methods 0.000 description 2
- 210000002784 stomach Anatomy 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 239000003643 water by type Substances 0.000 description 2
- 239000002076 α-tocopherol Substances 0.000 description 2
- GVJHHUAWPYXKBD-IEOSBIPESA-N α-tocopherol Chemical compound OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-IEOSBIPESA-N 0.000 description 2
- 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 description 1
- 235000019890 Amylum Nutrition 0.000 description 1
- 102000018832 Cytochromes Human genes 0.000 description 1
- 108010052832 Cytochromes Proteins 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
- 206010013954 Dysphoria Diseases 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- IKMDFBPHZNJCSN-UHFFFAOYSA-N Myricetin Chemical compound C=1C(O)=CC(O)=C(C(C=2O)=O)C=1OC=2C1=CC(O)=C(O)C(O)=C1 IKMDFBPHZNJCSN-UHFFFAOYSA-N 0.000 description 1
- 208000004880 Polyuria Diseases 0.000 description 1
- ZVOLCUVKHLEPEV-UHFFFAOYSA-N Quercetagetin Natural products C1=C(O)C(O)=CC=C1C1=C(O)C(=O)C2=C(O)C(O)=C(O)C=C2O1 ZVOLCUVKHLEPEV-UHFFFAOYSA-N 0.000 description 1
- 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
- GAMYVSCDDLXAQW-AOIWZFSPSA-N Thermopsosid Natural products O(C)c1c(O)ccc(C=2Oc3c(c(O)cc(O[C@H]4[C@H](O)[C@@H](O)[C@H](O)[C@H](CO)O4)c3)C(=O)C=2)c1 GAMYVSCDDLXAQW-AOIWZFSPSA-N 0.000 description 1
- 230000035508 accumulation Effects 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 229940087168 alpha tocopherol Drugs 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 230000000259 anti-tumor effect Effects 0.000 description 1
- 230000000840 anti-viral effect Effects 0.000 description 1
- 238000003556 assay Methods 0.000 description 1
- 230000003796 beauty Effects 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- ADRVNXBAWSRFAJ-UHFFFAOYSA-N catechin Natural products OC1Cc2cc(O)cc(O)c2OC1c3ccc(O)c(O)c3 ADRVNXBAWSRFAJ-UHFFFAOYSA-N 0.000 description 1
- 235000005487 catechin Nutrition 0.000 description 1
- 210000004027 cell Anatomy 0.000 description 1
- 210000000170 cell membrane Anatomy 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 229950001002 cianidanol Drugs 0.000 description 1
- 235000009508 confectionery Nutrition 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 230000009849 deactivation Effects 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 238000004807 desolvation Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 230000035619 diuresis Effects 0.000 description 1
- 230000035622 drinking Effects 0.000 description 1
- 238000010828 elution Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000007071 enzymatic hydrolysis Effects 0.000 description 1
- 238000006047 enzymatic hydrolysis reaction Methods 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000000284 extract Substances 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 229930003944 flavone Natural products 0.000 description 1
- 235000011949 flavones Nutrition 0.000 description 1
- 150000002215 flavonoids Chemical class 0.000 description 1
- 239000000796 flavoring agent Substances 0.000 description 1
- 235000019634 flavors Nutrition 0.000 description 1
- 235000011389 fruit/vegetable juice Nutrition 0.000 description 1
- 150000004676 glycans Chemical class 0.000 description 1
- 241000411851 herbal medicine Species 0.000 description 1
- 230000002218 hypoglycaemic effect Effects 0.000 description 1
- 230000036039 immunity Effects 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 230000002779 inactivation Effects 0.000 description 1
- 210000000936 intestine Anatomy 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 235000008777 kaempferol Nutrition 0.000 description 1
- 230000003859 lipid peroxidation Effects 0.000 description 1
- 238000004895 liquid chromatography mass spectrometry Methods 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 210000001853 liver microsome Anatomy 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 239000002932 luster Substances 0.000 description 1
- 238000004949 mass spectrometry Methods 0.000 description 1
- 239000002398 materia medica Substances 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 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
- PCOBUQBNVYZTBU-UHFFFAOYSA-N myricetin Natural products OC1=C(O)C(O)=CC(C=2OC3=CC(O)=C(O)C(O)=C3C(=O)C=2)=C1 PCOBUQBNVYZTBU-UHFFFAOYSA-N 0.000 description 1
- 235000007743 myricetin Nutrition 0.000 description 1
- 229940116852 myricetin Drugs 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 230000004792 oxidative damage Effects 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 239000002304 perfume Substances 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 230000035790 physiological processes and functions Effects 0.000 description 1
- 235000013824 polyphenols Nutrition 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 238000010298 pulverizing process Methods 0.000 description 1
- 230000000171 quenching effect Effects 0.000 description 1
- 235000005875 quercetin Nutrition 0.000 description 1
- 229960001285 quercetin Drugs 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000035807 sensation Effects 0.000 description 1
- 235000019615 sensations Nutrition 0.000 description 1
- 230000001953 sensory effect Effects 0.000 description 1
- 235000013599 spices Nutrition 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 238000002560 therapeutic procedure Methods 0.000 description 1
- 229960000984 tocofersolan Drugs 0.000 description 1
- 238000000870 ultraviolet spectroscopy Methods 0.000 description 1
- 238000001291 vacuum drying Methods 0.000 description 1
- VHBFFQKBGNRLFZ-UHFFFAOYSA-N vitamin p Natural products O1C2=CC=CC=C2C(=O)C=C1C1=CC=CC=C1 VHBFFQKBGNRLFZ-UHFFFAOYSA-N 0.000 description 1
- 235000004835 α-tocopherol Nutrition 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L2/00—Non-alcoholic beverages; Dry compositions or concentrates therefor; Their preparation
- A23L2/385—Concentrates of non-alcoholic beverages
- A23L2/39—Dry compositions
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
- A23V2002/00—Food compositions, function of food ingredients or processes for food or foodstuffs
Landscapes
- Health & Medical Sciences (AREA)
- Nutrition Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Food Science & Technology (AREA)
- Polymers & Plastics (AREA)
- Non-Alcoholic Beverages (AREA)
Abstract
The invention relates to a preparation method of a barley health-care solid beverage. The preparation method comprises the following steps of (1) cleaning high-quality barley, airing, baking for 30 to 50min at the temperature of 120 to 150 DEG C, removing water, crushing to obtain barley powder, adding into boiled water, gelatinizing for 20 to 40min, and cooling to room temperature, so as to obtain a barley pulp; (2) performing enzymolysis on the barley pulp by compound enzyme for 6 to 10h at the temperature of 40 to 60 DEG C and the pH (potential of hydrogen) value of 5 to 6; (3) heating an enzymolysis liquid obtained in step (2) to boil, warming for 5 to 10min, deactivating enzyme, cooling to room temperature, and centrifuging, so as to obtain a barley supernatant; (4) extracting the barley supernatant obtained in step (3) by trichloromethane, obtaining an upper supernatant, drying for 8 to 10h at the temperature of 60 to 80 DEG C under the vacuum atmosphere, and grinding into the powder. The prepared barley health-care solid beverage has the advantages that the content of effective functional ingredients is higher, the mouth feel and color of the beverage are good, the fragrance is heavy, and the favor of consumers is obtained.
Description
Technical field
The invention belongs to beverage/food technical field, and in particular to a kind of preparation method of barley health-care solid beverage.
Background technology
Barley is that grass family Hordeum is annual, gives birth to or perennial herb crop in more year, and alias tries to gain wheat, meal wheat, barebacked wheat.
Used as one of world's staple food crop, its food therapy function is already recognized barley by people.《Compendium of Materia Medica》Say:Barley is sweet
It is salty cool, there are a clearing away heat and promoting diuresis, and the effect of stomach intestines wide.《Mediate class is adjusted to compile》Think:Barley is mild-natured cool, helps stomach Qi.For wheat is won in face, and
Without scorching.Moderns like wheat, and dare not or would not speak up barley, surprisingly health.《It is good to help book on Chinese herbal medicine》Upper record:The hair of long term usage is not white, very benefit
People, therefore barley cures mainly dysphoria with smothery sensation of relieving summer heat, and has QI invigorating, in tune, qi-restoratives beauty treatment, the work(of disperse accumulations feed.
Contain various functional components in barley, mainly there is several amino acids, beta glucan, alpha-tocotrienol, flavonoids
Compound, polyphenol compound, ergot class compound etc..Having 75% in barley endosperm cell membrane is made up of beta glucan, β-Portugal
The research report of glycan physiological function is concentrated mainly on reduction cholesterol and hypoglycemic two aspect.Beta glucan is to animal and human body
Immunity function have a facilitation, can growth promotion, build up health, improve resistance against diseases.
Alpha-tocotrienol can be eliminated or quenching activity oxygen radical, prevent the chain reaction of lipid peroxidation, so that
With oxidation resistant function.There is research to show, during rat liver microsome membrane lipid peroxidatio, alpha-tocotrienol
Antioxidation activity protects cytochrome P much stronger than alpha-tocopherol450Ability it is also stronger than alpha-tocopherol, tocotrienols can be with
Rat heart is protected from oxidative damage.The antioxidation of tocotrienols has important at the atherosis aspect of prevention of arterial
Meaning.Alpha-tocotrienol can reduce cholesterol, and this is the earliest report of tocotrienols reduction cholesterol, causes people
Concern.Further study showed that, alpha-tocotrienol can effectively suppress the activity of HMG-COA reductases.HMG-COA
Reductase is the rate-limiting enzyme of internal cholesterol biosynthesis, it is suppressed that its activity also may refrain from the synthesis of cholesterol.Cell experiment
Prove that tocotrienols has the function of suppressing cholesterol biosynthesis with zoopery.
Flavone compound based on catechin, myricetin, Quercetin, Kaempferol, with antibacterial, it is antiviral, antitumor,
Suppress cholesterol increases with Lipid, suppresses effect that blood sugar rises.
Baked barley tea is typically barley frying into sallow, before eating, it is only necessary to can leach strong perfume (or spice) with brewed in hot water
Tea.Barley is prepared into the trend that a kind of easily tea-drinking is current barley food development through deep processing.Chinese patent
CN104171170A provides a kind of preparation method of instant baked barley tea, with high-quality barley as raw material, by rotating cone destilling tower
Method extracts the modes such as the baked barley tea slurry enzymolysis processing after fragrance elite, extraction, elite backfill and spray drying and prepares instant barley
Tea.The invention has been sufficiently reserved the active ingredient in barley, and inherits the local flavor of barley giving off a strong fragrance juice alcohol.But spray drying
Temperature it is higher so that the alpha-tocotrienol in baked barley tea is largely oxidized, made big simultaneously because the presence of hordenine
Wheat tea mouthfeel is more puckery, and consumer's drinking experience is not good.
The content of the invention
The invention provides a kind of preparation method of barley health-care solid beverage, barley in made barley health-care solid beverage
Functional component content it is higher, and functional component activity it is higher, beverage mouthfeel is more preferably.
The technical proposal for solving the technical problem of the invention is:
A kind of preparation method of barley health-care solid beverage, comprises the following steps:
(1) high-quality barley cleaned, dry, bakeed in 120-150 DEG C and remove within 30-50 minutes moisture, then be grinding to obtain big
Flour, after being gelatinized 20-40 minutes in addition boiling water, is cooled to room temperature, obtains barley slurry.Bakeed by low temperature and replace high temperature to fry
System, preferably, functional component is because of high temperature deactivation on the other hand being prevented effectively from barley for the color and luster of one side barley tea-drinking.By barley
Powder is first destroyed amylum body therein through boiling water gelatinization, and crystal structure disappears, and becomes amorphism starch, now barley particles
Expansion.
(2) step (1) gained barley slurry is used into complex enzyme in 40-60 DEG C, under PH5-6, is digested 6-10 hours, through boiling water
The expansion barley particles hydrolysis result of gelatinization is more preferable.
(3) step (2) gained enzymolysis liquid is heated to boiling, is incubated the 5-10 minutes enzyme that goes out, be cooled to room temperature, centrifugation is big
Wheat clear liquid;
(4) step (3) the gained barley stillness of night is used into chloroform extraction, takes supernatant liquor, in 60-80 DEG C of vacuum drying
After 8-10 hours, then pulverize.Contain a small amount of hordenine in barley, make it have acerbity, influence the mouth of barley tea-drinking
Sense, barley clear liquid is extracted using trichloroethanes, and further the hordenine in removal barley clear liquid, improves the mouth of barley tea-drinking
Sense.
Preferably, pearling cone meal described in step (1) is 1 with the mass ratio of boiling water:20-30.
Preferably, complex enzyme is made up of cellulase, carboxy-lesterase and AMS described in step (2), the fibre
The mass ratio of the plain enzyme of dimension, carboxy-lesterase and AMS is 1:2-5:1.5-3.Using complex enzyme coordinated enzymatic hydrolysis, compared to single
Enzyme is digested, and has the advantages that hydrolysis temperature is low, the time is short, efficiency high.AMS and cellulase are constantly by its hydrolysis
Carboxy-lesterase provide non-reducing end, effectively increase its concentration of substrate, at the same carboxy-lesterase again constantly consumption AMS and
The product of cellulase degradation, promotes the two hydrolysis, so as to improve enzymolysis efficiency, improves product purity.
Preferably, the slurry of barley described in step (2) is 1 with the mass ratio of complex enzyme:0.1-0.3.
Preferably, the rotating speed being centrifuged described in step (3) is 1200-1500r/min, centrifugation time is 8-15 minutes.
Preferably, the barley stillness of night described in step (4) is 1 with the mass ratio of trichloroethanes:8-10.
Beneficial effects of the present invention are:
1st, the present invention is bakeed using low temperature and substitutes high temperature frying, effectively reduces the functional component in barley tea-drinking because of high temperature
Inactivation, the reduction cholesterol and effect of lowering blood sugar of made barley health-care solid beverage are more preferably.
2nd, the complex enzyme zymohydrolysis constituted using cellulase, carboxy-lesterase and AMS, with hydrolysis temperature is low, the time
Short, efficiency high advantage.
3rd, solid beverage is finally reduced using hordenine in chloroform extraction method removing barley health-care solid beverage
Sour and astringent sense, makes its mouthfeel more preferably.
Specific embodiment
In order to make the purpose , technical scheme and advantage of the present invention be clearer, with reference to embodiments to the present invention
It is further elaborated.
Embodiment 1
(1) 10g high-quality barleys cleaned, dry, bakeed in 120 DEG C 50 minutes and remove moisture, then be grinding to obtain 8g barleys
Powder, after being gelatinized 40 minutes in addition 200g boiling water, is cooled to room temperature, obtains barley slurry;
(2) step (1) gained barley slurry is used into 8g cellulases, 16g carboxy-lesterases and 16g AMSs in 50 DEG C,
Under PH5.5, digest 8 hours;
(3) step (2) gained 240g enzymolysis liquids are heated to boiling, are incubated 8 minutes enzymes that go out, be cooled to room temperature, be centrifuged
Obtain 202g barley clear liquids;
(4) step (3) the gained barley stillness of night is used into 2000g chloroform extractions, takes supernatant liquor, it is dry in 60 DEG C of vacuum
After dry 10 hours, then pulverize.
Embodiment 2
(1) 10g high-quality barleys cleaned, dry, bakeed in 130 DEG C 40 minutes and remove moisture, then be grinding to obtain 8g barleys
Powder, after being gelatinized 30 minutes in addition 160g boiling water, is cooled to room temperature, obtains barley slurry;
(2) step (1) gained barley slurry is used into 3g cellulases, 9g carboxy-lesterases and 4.5g AMSs in 40 DEG C,
Under PH6, digest 10 hours;
(3) step (2) gained 180g enzymolysis liquids are heated to boiling, are incubated 5 minutes enzymes that go out, be cooled to room temperature, be centrifuged
Obtain 135g barley clear liquids;
(4) step (3) the gained barley stillness of night is used into 1350g chloroform extractions, takes supernatant liquor, it is dry in 80 DEG C of vacuum
After dry 8 hours, then pulverize.
Embodiment 3
(1) 10g high-quality barleys cleaned, dry, bakeed in 150 DEG C 30 minutes and remove moisture, then be grinding to obtain 8g barleys
Powder, after being gelatinized 20 minutes in addition 240g boiling water, is cooled to room temperature, obtains barley slurry;
(2) step (1) gained barley slurry is used into 8.5g cellulases, 41.5g carboxy-lesterases and 25g AMSs in 60
DEG C, under PH5, digest 9 hours;
(3) step (2) gained 320g enzymolysis liquids are heated to boiling, are incubated 10 minutes enzymes that go out, be cooled to room temperature, be centrifuged
Obtain 260g barley clear liquids;
(4) step (3) the gained barley stillness of night is used into 2340g chloroform extractions, takes supernatant liquor, it is dry in 70 DEG C of vacuum
After dry 9 hours, then pulverize.
Comparative example 1
Operated with embodiment 1 it is identical, unlike complex enzyme is replaced using 40g cellulases, prepare barley health-care solid
Beverage.
Comparative example 2
Operated with embodiment 1 it is identical, unlike complex enzyme is replaced using 40g carboxy-lesterases, prepare barley health-care solid
Beverage.
Comparative example 3
Operated with embodiment 1 it is identical, unlike complex enzyme is replaced using 40g AMSs, prepare barley health-care solid
Beverage.
Comparative example 4
(1) 10g high-quality barleys cleaned, dry, bakeed in 120 DEG C 50 minutes and remove moisture, then be grinding to obtain 8g barleys
Powder, after being gelatinized 40 minutes in addition 200g boiling water, is cooled to room temperature, obtains barley slurry;
(2) step (1) gained barley slurry is used into 8g cellulases, 16g carboxy-lesterases and 16g AMSs in 50 DEG C,
Under PH5.5, digest 8 hours;
(3) step (2) gained 240g enzymolysis liquids are heated to boiling, are incubated 8 minutes enzymes that go out, be cooled to room temperature, be centrifuged
202g barley clear liquids are obtained, after being vacuum dried 10 hours in 60 DEG C, then barley solid beverage of pulverizing to obtain.
The functional component assay of embodiment 4:
UV-VIS spectrophotometry detects beta glucan content.The barley health-care solid beverage for obtaining will be purified to be dissolved in
In methyl alcohol, it is measured with LC-MS instrument.
Liquid phase chromatogram condition:Chromatograph:WATERS 2690;Detector:WATERS 996;Analytical column:Lichrospher
C-18 2.1x250mm;Mobile phase:Methanol-water-gradient elution (1% acetic acid);Column temperature:30℃;Flow velocity:0.3mL/min;Sample introduction
Amount:10μL.
Mass Spectrometry Conditions:Ionic means:ESI-, ESI+:Capillary voltage:3.88KV:Taper hole voltage:30V;Ion source temperature:
120℃;Desolvation temperature:300℃;Mass range:200-800m/z:Photoelectric multiplier voltage:650V.
Test result is shown in Table 1:
Table 1:
It can be seen from Table 1 that, using beta glucan content and flavonoids in the barley solid beverage that complex enzyme zymohydrolysis are obtained
The two content is higher in the product that compounds content is digested than single enzyme.
The sensory test of embodiment 5
Embodiment 1-3 and the gained barley solid beverage of comparative example 4 are brewed using boiling water, after ten minutes, selection 10 is commented
Valency person carries out mouthfeel evaluation to four kinds of barley tea-drinkings respectively, and standards of grading are shown in Table 2.
Table 2:
It can be seen from Table 2 that:Hordenine is removed by chloroform extraction, the color of barley tea-drinking can be effectively improved
Pool, mouthfeel, proterties and fragrance.
Presently preferred embodiments of the present invention is the foregoing is only, is not intended to limit the invention, it is all in essence of the invention
Any modification, equivalent and improvement made within god and principle etc., should be included within the scope of the present invention.
Claims (6)
1. a kind of preparation method of barley health-care solid beverage, it is characterised in that the preparation method comprises the following steps:
(1) high-quality barley cleaned, dry, bakeed in 120-150 DEG C 30-50 minutes and remove moisture, then be grinding to obtain barley
Powder, after being gelatinized 20-40 minutes in addition boiling water, is cooled to room temperature, obtains barley slurry;
(2) step (1) gained barley slurry is used into complex enzyme in 40-60 DEG C, under PH5-6, is digested 6-10 hours;
(3) step (2) gained enzymolysis liquid is heated to boiling, is incubated the 5-10 minutes enzyme that goes out, be cooled to room temperature, barley is centrifuged
Clear liquid;
(4) step (3) gained barley clear liquid is used into chloroform extraction, takes supernatant liquor, 8- is vacuum dried in 60-80 DEG C
After 10 hours, then pulverize.
2. the preparation method of barley health-care solid beverage as claimed in claim 1, it is characterised in that big described in step (1)
Flour is 1 with the mass ratio of boiling water:20-30.
3. the preparation method of barley health-care solid beverage as claimed in claim 1, it is characterised in that multiple described in step (2)
Synthase is made up of cellulase, carboxy-lesterase and AMS, the mass ratio of the cellulase, carboxy-lesterase and AMS
It is 1:2-5:1.5-3.
4. the preparation method of the barley health-care solid beverage as described in claim 1 or 3, it is characterised in that described in step (2)
It is 1 that barley is starched with the mass ratio of complex enzyme:0.1-0.3.
5. the preparation method of barley health-care solid beverage as claimed in claim 1, it is characterised in that described in step (3) from
The rotating speed of the heart is 1200-1500r/min, and centrifugation time is 8-15 minutes.
6. the preparation method of barley health-care solid beverage as claimed in claim 1, it is characterised in that big described in step (4)
Wheat clear liquid is 1 with the mass ratio of trichloroethanes:8-10.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201710045801.3A CN106689961A (en) | 2017-01-22 | 2017-01-22 | Preparation method of barley health-care solid beverage |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201710045801.3A CN106689961A (en) | 2017-01-22 | 2017-01-22 | Preparation method of barley health-care solid beverage |
Publications (1)
Publication Number | Publication Date |
---|---|
CN106689961A true CN106689961A (en) | 2017-05-24 |
Family
ID=58909472
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201710045801.3A Withdrawn CN106689961A (en) | 2017-01-22 | 2017-01-22 | Preparation method of barley health-care solid beverage |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN106689961A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN107712172A (en) * | 2017-09-27 | 2018-02-23 | 浙江茶乾坤食品股份有限公司 | A kind of preparation method for the mixing instant tea powder that ferments |
CN109700027A (en) * | 2019-02-20 | 2019-05-03 | 威海百合生物技术股份有限公司 | A kind of solid beverage and preparation method thereof with anti-oxidant fat-reducing effect |
-
2017
- 2017-01-22 CN CN201710045801.3A patent/CN106689961A/en not_active Withdrawn
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN107712172A (en) * | 2017-09-27 | 2018-02-23 | 浙江茶乾坤食品股份有限公司 | A kind of preparation method for the mixing instant tea powder that ferments |
CN109700027A (en) * | 2019-02-20 | 2019-05-03 | 威海百合生物技术股份有限公司 | A kind of solid beverage and preparation method thereof with anti-oxidant fat-reducing effect |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN106418106B (en) | Instant ginger solid beverage and preparation method thereof | |
CN103540493B (en) | A kind of compound method of ganoderma lucidum tea wine | |
CN102228180B (en) | Betelnut buccal tablet and preparation method thereof | |
KR100975278B1 (en) | Extraction method of opuntia humifusa using enzyme hydrolysis | |
CN1943382B (en) | Tea capsule and its preparing method | |
KR102231913B1 (en) | Vegetable Brown Sauce having high biological active materials and preparation method thereof | |
CN100586442C (en) | Method of producing glossy ganoderma polypeptide product | |
KR102048833B1 (en) | Method for preparing extract of Ginger comprising High Pressure/Enzymatic reaction step and Active ingradients increased Ginger extract prepared by the same | |
CN106689961A (en) | Preparation method of barley health-care solid beverage | |
KR102430000B1 (en) | Extract of root plant with increased active ingredients and methods for their preparation | |
KR20110111142A (en) | Processing method of ginseng for enhancing contents of active components in the ginseng | |
Kumar et al. | Black soybean (Glycine max (L.) Merr.): paving the way toward new nutraceutical | |
CN105670846A (en) | Pomegranate beer | |
Tangkhawanit et al. | Changes in bioactive components, biological activities and starch digestibility of soymilk residues as affected by far-infrared radiation combined with hot-air and hot-air drying | |
CN115211481B (en) | Sophora flower bud tea and preparation method thereof | |
CN107019136A (en) | A kind of solid beverage with effect of lowering blood sugar and preparation method thereof | |
CN104256024A (en) | Blood-fat-reducing coffee | |
CN103503965A (en) | Anti-cancer and anti-aging cookie and making method thereof | |
KR101403526B1 (en) | method for making cooked rice with lotus leaf or Phyllostachys nigra and cooked rice thereby | |
CN114515005B (en) | Coix seed extract containing chrysanthemum components and preparation method and application thereof | |
CN108077485A (en) | A kind of blue or green money willow herbal tea and preparation method thereof | |
CN106136085A (en) | A kind of natural Semen sojae atricolor extractum and preparation method thereof | |
KR20180082362A (en) | Method for steamed Codonopsis lanceolate and composition for treating non-alcoholic fatty liver comprising thereof | |
CN108013194A (en) | A kind of production method of pearl Lee fruit tea | |
KR102159806B1 (en) | Method for preparing extract of ginger comprising ethanol treatment and active ingredients increased Ginger extract prepared by the same |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PB01 | Publication | ||
PB01 | Publication | ||
SE01 | Entry into force of request for substantive examination | ||
WW01 | Invention patent application withdrawn after publication | ||
WW01 | Invention patent application withdrawn after publication |
Application publication date: 20170524 |