CN114158740A - Preparation method of hazelnut meal soluble dietary fiber and application of hazelnut meal soluble dietary fiber in regulating blood fat - Google Patents
Preparation method of hazelnut meal soluble dietary fiber and application of hazelnut meal soluble dietary fiber in regulating blood fat Download PDFInfo
- Publication number
- CN114158740A CN114158740A CN202111308267.3A CN202111308267A CN114158740A CN 114158740 A CN114158740 A CN 114158740A CN 202111308267 A CN202111308267 A CN 202111308267A CN 114158740 A CN114158740 A CN 114158740A
- Authority
- CN
- China
- Prior art keywords
- hazelnut
- dietary fiber
- zymolyte
- enzymolysis
- soluble dietary
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 241000723382 Corylus Species 0.000 title claims abstract description 89
- 235000007466 Corylus avellana Nutrition 0.000 title claims abstract description 89
- 235000001543 Corylus americana Nutrition 0.000 title claims abstract description 84
- 235000012054 meals Nutrition 0.000 title claims abstract description 80
- 235000013325 dietary fiber Nutrition 0.000 title claims abstract description 57
- 238000002360 preparation method Methods 0.000 title claims abstract description 22
- 230000001105 regulatory effect Effects 0.000 title claims abstract description 17
- 210000004369 blood Anatomy 0.000 title claims abstract description 12
- 239000008280 blood Substances 0.000 title claims abstract description 12
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 93
- 102000004190 Enzymes Human genes 0.000 claims abstract description 46
- 108090000790 Enzymes Proteins 0.000 claims abstract description 46
- 229940088598 enzyme Drugs 0.000 claims abstract description 46
- 108090000637 alpha-Amylases Proteins 0.000 claims abstract description 20
- 102000004139 alpha-Amylases Human genes 0.000 claims abstract description 20
- 229940024171 alpha-amylase Drugs 0.000 claims abstract description 20
- 108090000526 Papain Proteins 0.000 claims abstract description 19
- 239000004365 Protease Substances 0.000 claims abstract description 19
- 229940055729 papain Drugs 0.000 claims abstract description 19
- 235000019834 papain Nutrition 0.000 claims abstract description 19
- 239000000126 substance Substances 0.000 claims abstract description 17
- 229920002678 cellulose Polymers 0.000 claims abstract description 15
- 239000001913 cellulose Substances 0.000 claims abstract description 15
- 150000004676 glycans Chemical class 0.000 claims abstract description 15
- 229920001277 pectin Polymers 0.000 claims abstract description 15
- 239000001814 pectin Substances 0.000 claims abstract description 15
- 235000010987 pectin Nutrition 0.000 claims abstract description 15
- 229920001282 polysaccharide Polymers 0.000 claims abstract description 15
- 239000005017 polysaccharide Substances 0.000 claims abstract description 15
- 238000001556 precipitation Methods 0.000 claims abstract description 14
- 108010073178 Glucan 1,4-alpha-Glucosidase Proteins 0.000 claims abstract description 13
- 102100022624 Glucoamylase Human genes 0.000 claims abstract description 13
- 238000001035 drying Methods 0.000 claims abstract description 12
- 239000002244 precipitate Substances 0.000 claims abstract description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 69
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 51
- 239000000706 filtrate Substances 0.000 claims description 44
- 238000001914 filtration Methods 0.000 claims description 28
- 238000010438 heat treatment Methods 0.000 claims description 28
- 230000001376 precipitating effect Effects 0.000 claims description 27
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 26
- 239000012153 distilled water Substances 0.000 claims description 18
- 238000001816 cooling Methods 0.000 claims description 15
- 238000005406 washing Methods 0.000 claims description 13
- 238000000034 method Methods 0.000 claims description 9
- 238000012869 ethanol precipitation Methods 0.000 claims description 7
- 108010059892 Cellulase Proteins 0.000 claims description 6
- 108010059820 Polygalacturonase Proteins 0.000 claims description 6
- 229940106157 cellulase Drugs 0.000 claims description 6
- 108010093305 exopolygalacturonase Proteins 0.000 claims description 6
- 235000013305 food Nutrition 0.000 claims description 6
- 229940059442 hemicellulase Drugs 0.000 claims description 6
- 108010002430 hemicellulase Proteins 0.000 claims description 6
- 238000000227 grinding Methods 0.000 claims description 5
- 238000010298 pulverizing process Methods 0.000 claims description 5
- 230000009849 deactivation Effects 0.000 claims description 4
- 230000003301 hydrolyzing effect Effects 0.000 claims description 4
- 230000000415 inactivating effect Effects 0.000 claims description 4
- 150000002632 lipids Chemical class 0.000 claims description 3
- 239000000825 pharmaceutical preparation Substances 0.000 claims 1
- 229940127557 pharmaceutical product Drugs 0.000 claims 1
- 238000004108 freeze drying Methods 0.000 description 9
- UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 description 9
- 239000000843 powder Substances 0.000 description 8
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 7
- 229910052782 aluminium Inorganic materials 0.000 description 7
- 239000011888 foil Substances 0.000 description 7
- 238000005303 weighing Methods 0.000 description 7
- 230000000052 comparative effect Effects 0.000 description 6
- 230000002779 inactivation Effects 0.000 description 5
- 108010023302 HDL Cholesterol Proteins 0.000 description 4
- 108010028554 LDL Cholesterol Proteins 0.000 description 4
- 210000002966 serum Anatomy 0.000 description 4
- 241000700159 Rattus Species 0.000 description 3
- 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 3
- 238000000605 extraction Methods 0.000 description 3
- 210000005228 liver tissue Anatomy 0.000 description 3
- 108091005658 Basic proteases Proteins 0.000 description 2
- 208000031226 Hyperlipidaemia Diseases 0.000 description 2
- 108010019077 beta-Amylase Proteins 0.000 description 2
- 239000006227 byproduct Substances 0.000 description 2
- 238000005034 decoration Methods 0.000 description 2
- 239000003814 drug Substances 0.000 description 2
- 229940079593 drug Drugs 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000007710 freezing Methods 0.000 description 2
- 230000008014 freezing Effects 0.000 description 2
- 210000004185 liver Anatomy 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 235000015097 nutrients Nutrition 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 235000019198 oils Nutrition 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 238000011160 research Methods 0.000 description 2
- 210000001519 tissue Anatomy 0.000 description 2
- 108090000145 Bacillolysin Proteins 0.000 description 1
- 102000015781 Dietary Proteins Human genes 0.000 description 1
- 108010010256 Dietary Proteins Proteins 0.000 description 1
- 101710121765 Endo-1,4-beta-xylanase Proteins 0.000 description 1
- 108010010234 HDL Lipoproteins Proteins 0.000 description 1
- 102000015779 HDL Lipoproteins Human genes 0.000 description 1
- 235000019487 Hazelnut oil Nutrition 0.000 description 1
- 108010007622 LDL Lipoproteins Proteins 0.000 description 1
- 102000007330 LDL Lipoproteins Human genes 0.000 description 1
- 108091005507 Neutral proteases Proteins 0.000 description 1
- 102000035092 Neutral proteases Human genes 0.000 description 1
- 235000001014 amino acid Nutrition 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- 210000000702 aorta abdominal Anatomy 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 235000012000 cholesterol Nutrition 0.000 description 1
- 235000009508 confectionery Nutrition 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- 239000003337 fertilizer Substances 0.000 description 1
- 230000037406 food intake Effects 0.000 description 1
- 235000012631 food intake Nutrition 0.000 description 1
- 239000010468 hazelnut oil Substances 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 210000000936 intestine Anatomy 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 229930014626 natural product Natural products 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 235000016709 nutrition Nutrition 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000036186 satiety Effects 0.000 description 1
- 235000019627 satiety Nutrition 0.000 description 1
- 210000000582 semen Anatomy 0.000 description 1
- 210000002784 stomach Anatomy 0.000 description 1
- 238000005728 strengthening Methods 0.000 description 1
- 239000006228 supernatant Substances 0.000 description 1
- 239000011573 trace mineral Substances 0.000 description 1
- 235000013619 trace mineral Nutrition 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 239000002699 waste material Substances 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
- A23L33/00—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
- A23L33/20—Reducing nutritive value; Dietetic products with reduced nutritive value
- A23L33/21—Addition of substantially indigestible substances, e.g. dietary fibres
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K36/00—Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
- A61K36/18—Magnoliophyta (angiosperms)
- A61K36/185—Magnoliopsida (dicotyledons)
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/06—Antihyperlipidemics
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
- A23V2002/00—Food compositions, function of food ingredients or processes for food or foodstuffs
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2236/00—Isolation or extraction methods of medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicine
- A61K2236/10—Preparation or pretreatment of starting material
- A61K2236/19—Preparation or pretreatment of starting material involving fermentation using yeast, bacteria or both; enzymatic treatment
Abstract
The invention provides a preparation method of hazelnut meal soluble dietary fiber, which comprises the following steps: sequentially carrying out enzymolysis on the desugarized hazelnut meal by using thermostable alpha-amylase, papain, glucoamylase and enzymes capable of carrying out enzymolysis on cellulose, polysaccharide and pectin substances to obtain an zymolyte; and (3) carrying out alcohol precipitation on the zymolyte, and drying the obtained precipitate to obtain the soluble dietary fiber. The preparation method provided by the invention can obviously improve the yield of the soluble dietary fiber in the hazelnut meal, and the obtained soluble dietary fiber has good function of regulating blood fat.
Description
Technical Field
The invention belongs to the technical field of natural product extraction, and particularly relates to a preparation method of hazelnut meal soluble dietary fiber and application of the hazelnut meal soluble dietary fiber in regulating blood fat.
Background
Hazelnut is called nut king, the content of nutrient substances is very rich, and the history of food application is very long. Hazelnuts have been eaten 3 rd century before yuan to 4 th century before yuan in the coasts of the black sea of gacaogue, northern turkish and italy. The Ming dynasty Li Shizhen Ben Cao gang mu carries it: "Renlun" is sweet, mild and non-toxic. It is mainly used for tonifying qi and strengthening intestines and stomach. Modern researches show that the hazelnuts contain nutrient substances such as protein, dietary fiber, vitamins, amino acid, trace elements and the like, and the hazelnuts have very strong satiety after being eaten, so that the effect of reducing the food intake can be achieved. Hazelnut is not only eaten as a nut, but also made into hazelnut oil by various methods, and widely applied to the fields of light industrial foods such as food, cosmetics and the like. The hazelnut meal is a byproduct of oil extraction of hazelnuts and is traditionally mainly used as feed, fertilizer and the like, and researches show that the hazelnut meal mainly contains dietary fiber, protein, sugar, fat and other nutritional ingredients, wherein the content of the dietary fiber is about more than 50 percent, but the application value of the hazelnut meal is not effectively developed at present. If the hazelnut deep processing agent is reasonably utilized, the requirements of people on healthy products are met, waste is changed into valuable, the added value of products is increased for hazelnut deep processing enterprises, and the income of vast planting farmers is further increased.
Disclosure of Invention
In view of the above, the technical problem to be solved by the present invention is to provide a method for preparing hazelnut meal soluble dietary fiber and an application thereof in blood lipid regulation.
The invention provides a preparation method of hazelnut meal soluble dietary fiber, which comprises the following steps:
sequentially carrying out enzymolysis on the desugarized hazelnut meal by using thermostable alpha-amylase, papain, glucoamylase and enzymes capable of carrying out enzymolysis on cellulose, polysaccharide and pectin substances to obtain an zymolyte;
and (3) carrying out alcohol precipitation on the zymolyte, and drying the obtained precipitate to obtain the soluble dietary fiber.
Preferably, the method comprises the following steps:
A) dispersing the desugarized hazelnut meal into distilled water, adding thermostable alpha-amylase for heating enzymolysis to obtain a first zymolyte;
B) cooling the first zymolyte, adding papain, and heating for enzymolysis to obtain a second zymolyte;
C) adding acetic acid into the second zymolyte, then adjusting the pH value to acidity, adding saccharifying enzyme, and heating for enzymolysis to obtain a third zymolyte;
D) adding enzymes capable of performing enzymolysis on cellulose, polysaccharide and pectin substances into the third zymolyte, and performing heating enzymolysis to obtain a zymolyte;
E) and (3) inactivating the enzyme of the zymolyte, filtering, precipitating the filtrate with ethanol, and drying the precipitate to obtain the soluble dietary fiber.
Preferably, the preparation method of the desugarized hazelnut meal comprises the following steps: pulverizing hazelnut meal, and desugarizing with ethanol;
the hazelnut meal after desugarization is the hazelnut meal after superfine grinding.
Preferably, the mass percentage of the thermostable alpha-amylase in the hazelnut meal after desugarization is 0.3-0.7 wt%;
in the step A), the heating enzymolysis temperature is 90-95 ℃, and the time is 30-40 min.
Preferably, the mass percentage of the papain to the desugarized hazelnut meal is 0.3 wt% -0.7 wt%;
in the step B), the heating enzymolysis temperature is 55-65 ℃, and the time is 0.5-1.5 h.
Preferably, in the step C), the adding amount of the acetic acid accounts for 10-15% of the volume percentage of the distilled water in the step A);
the pH regulator used for regulating the pH is hydrochloric acid, and the pH is regulated to 4-5;
the saccharifying enzyme accounts for 0.3-0.7 wt% of the desugarized hazelnut meal;
the temperature of heating enzymolysis is 55-65 ℃, and the time is 25-35 min.
Preferably, in step D), the enzymes capable of hydrolyzing cellulose, polysaccharide and pectin substances are selected from one or more of cellulase, hemicellulase and pectinase;
the mass percentage of the enzymes capable of hydrolyzing cellulose, polysaccharide and pectin substances in the hazelnut meal after desugarization is 0.5-1.0 wt%;
the temperature of heating enzymolysis is 45-55 ℃, and the time is 0.5-1.5 h.
Preferably, in step E), the enzyme deactivation is: washing twice with hot water at 90-100 ℃ to inactivate enzyme;
the alcohol precipitation is carried out by adopting 95% ethanol precipitation for 1h, filtering, concentrating the filtrate, and then adding absolute ethanol into the concentrated filtrate for alcohol precipitation for 6 h.
The invention also provides the hazelnut meal soluble dietary fiber prepared by the preparation method.
The invention also provides application of the hazelnut meal soluble dietary fiber in preparing foods or medicines for regulating blood fat.
Compared with the prior art, the invention provides a preparation method of hazelnut meal soluble dietary fiber, which comprises the following steps: sequentially carrying out enzymolysis on the desugarized hazelnut meal by using thermostable alpha-amylase, papain, glucoamylase and enzymes capable of carrying out enzymolysis on cellulose, polysaccharide and pectin substances to obtain an zymolyte; and (3) carrying out alcohol precipitation on the zymolyte, and drying the obtained precipitate to obtain the soluble dietary fiber. The preparation method provided by the invention can obviously improve the yield of the soluble dietary fiber in the hazelnut meal, and the obtained soluble dietary fiber has good function of regulating blood fat.
Detailed Description
The invention provides a preparation method of hazelnut meal soluble dietary fiber, which comprises the following steps:
sequentially carrying out enzymolysis on the desugarized hazelnut meal by using thermostable alpha-amylase, papain, glucoamylase and enzymes capable of carrying out enzymolysis on cellulose, polysaccharide and pectin substances to obtain an zymolyte;
and (3) carrying out alcohol precipitation on the zymolyte, and drying the obtained precipitate to obtain the soluble dietary fiber.
The invention takes the desugared hazelnut meal as a raw material to extract soluble dietary fiber, wherein the preparation method of the desugared hazelnut meal comprises the following steps:
pulverizing semen Coryli Heterophyllae dregs, and desugarizing with ethanol. Wherein the hazelnut meal is a byproduct of oil extraction of hazelnuts. The pulverization is preferably through a 50 mesh sieve. The ethanol is an 85% ethanol solution by volume percentage.
After desugarization with ethanol, drying the hazelnut meal, and then carrying out superfine grinding. In the invention, the superfine grinding time is 0-20 min, preferably 10 min. When the hazelnut meal is subjected to superfine grinding for 10min, the yield of the soluble dietary fiber in the hazelnut meal can be obviously improved.
After obtaining the desugarized hazelnut meal, the preparation of the soluble dietary fiber is carried out, and the method specifically comprises the following steps:
A) dispersing the desugarized hazelnut meal into distilled water, adding thermostable alpha-amylase for heating enzymolysis to obtain a first zymolyte;
B) cooling the first zymolyte, adding papain, and heating for enzymolysis to obtain a second zymolyte;
C) adding acetic acid into the second zymolyte, then adjusting the pH value to acidity, adding saccharifying enzyme, and heating for enzymolysis to obtain a third zymolyte;
D) adding enzymes capable of performing enzymolysis on cellulose, polysaccharide and pectin substances into the third zymolyte, and performing heating enzymolysis to obtain a zymolyte;
E) and (3) inactivating the enzyme of the zymolyte, filtering, precipitating the filtrate with ethanol, and drying the precipitate to obtain the soluble dietary fiber.
The hazelnut meal after desugarization is dispersed in distilled water, and the mass-volume ratio of the hazelnut meal to the distilled water is 1 g: 20-40 ml, preferably 1 g: 20ml, 1 g: 25ml, 1 g: 30ml, 1 g: 35ml, 1 g: 40ml, or 1 g: any value between 20 and 40 ml.
Then, adding thermostable alpha-amylase for heating enzymolysis to obtain a first zymolyte. The mass percentage of the thermostable alpha-amylase in the hazelnut meal after desugarization is 0.3 wt% -0.7 wt%, preferably 0.3 wt%, 0.4 wt%, or any value between 0.3 wt% -0.7 wt%;
in the step A), the temperature of heating enzymolysis is 90-95 ℃, preferably 90, 91, 92, 93, 94, 95, or any value between 90-95 ℃, and the time is 30-40 min, preferably 30, 32, 35, 38, 40, or any value between 30-40 min.
Then, cooling the first zymolyte, adding papain, and heating for enzymolysis to obtain a second zymolyte;
wherein the cooling temperature is 55-65 ℃, preferably 55, 60, 65 or any value between 55-65 ℃.
The mass percentage of the papain to the hazelnut meal after desugaring is 0.3 wt% -0.7 wt%, preferably 0.3 wt%, 0.4 wt%, or any value between 0.3 wt% -0.7 wt%;
in the step B), the temperature of heating and enzymolysis is 55-65 ℃, preferably 55, 57, 60, 62, 65, or any value between 55-65 ℃, and the time is 0.5-1.5 h, preferably any value between 0.5, 1.0, 1.5, or 0.5-1.5 h.
Then, adding acetic acid into the second zymolyte, then adjusting the pH value to acidity, adding saccharifying enzyme, and heating for enzymolysis to obtain a third zymolyte;
wherein the adding amount of the acetic acid accounts for 10-15% of the distilled water in the step A), and is preferably any value between 10%, 11%, 12%, 13%, 14%, 15% or 10-15%;
the pH regulator used for regulating the pH is hydrochloric acid, and the pH is regulated to 4-5;
the mass percentage of the saccharifying enzyme in the hazelnut meal after desugarization is 0.3-0.7 wt%, preferably 0.3, 0.4 or 0.3-0.7 wt%;
the temperature of the heating enzymolysis is 55-65 ℃, and is selected to be any value between 55, 57, 60, 62 and 65, or 55-65 ℃, and the time is 25-35 min, preferably any value between 25, 28, 30, 32 and 35, or 25-35 min.
After a third zymolyte is obtained, enzymes capable of carrying out enzymolysis on cellulose, polysaccharide and pectin substances are added into the third zymolyte for heating and enzymolysis, so as to obtain a zymolyte;
the enzymes capable of performing enzymolysis on the cellulose, the polysaccharide and the pectin substances are selected from one or more of hemicellulase and pectinase;
the mass percentage of the enzymes capable of hydrolyzing cellulose, polysaccharide and pectin substances in the desugarized hazelnut meal is 0.5-1.0 wt%, preferably 0.5 wt%, 0.6 wt%, 0.7 wt%, 0.8 wt%, 0.9 wt%, 1.0 wt%, or any value between 0.5-1.0 wt%;
the temperature of the heating enzymolysis is 45-55 ℃, preferably 45, 48, 50, 52, 55, or any value between 45-55 ℃, and the time is 0.5-1.5 h, preferably 0.5, 1.0, 1.5, or any value between 0.5-1.5 h.
And finally, inactivating the enzyme of the zymolyte, filtering, precipitating the filtrate with ethanol, and drying the precipitate to obtain the soluble dietary fiber.
The enzyme deactivation is as follows: washing twice with hot water of 90-100 ℃ for enzyme inactivation, and filtering after enzyme inactivation to obtain filtrate.
And carrying out alcohol precipitation on the filtrate, wherein the alcohol precipitation adopts 95% ethanol precipitation for 1h filtration, the volume ratio of the filtrate to the ethanol is 1:4, carrying out alcohol precipitation to obtain a filtrate, concentrating the filtrate, and then adding absolute ethanol with the volume ratio of 1:4 into the concentrated filtrate to carry out alcohol precipitation for 6 h.
And finally, freeze-drying the precipitate after alcohol precipitation to obtain the soluble dietary fiber.
The invention also provides the hazelnut meal soluble dietary fiber prepared by the preparation method.
The invention also provides application of the hazelnut meal soluble dietary fiber in preparing foods or medicines for regulating blood fat.
According to the preparation method provided by the invention, the hazelnut meal is subjected to enzymolysis through the enzymes of specific types and steps, so that the yield of the soluble dietary fibers in the hazelnut meal can be obviously improved, and the obtained soluble dietary fibers have a good blood fat regulating effect.
In order to further understand the present invention, the following examples are provided to illustrate the preparation method of the hazelnut meal soluble dietary fiber and the application thereof in blood lipid regulation, and the scope of the present invention is not limited by the following examples.
The hazelnut meal is crushed and sieved by a 50-mesh sieve, desugared by 85% ethanol and dried for standby. Placing the desugared hazelnut meal into a superfine pulverizer, pulverizing for 10 minutes to obtain hazelnut meal superfine powder, and extracting soluble dietary fibers by the following examples.
Example 1
Weighing 1.0g of hazelnut meal superfine powder, fully dispersing in 40ml of distilled water, adding 0.5% of thermostable alpha-amylase, covering with an aluminum foil, placing in a 95 ℃ water bath kettle for enzymolysis for 35min, taking out, cooling to 60 ℃, adding 0.8% of papain in 60 ℃ water bath for 1h, adding 5ml of acetic acid, adjusting the pH to 4.5 with hydrochloric acid, adding 0.5% of glucoamylase, then performing 60 ℃ water bath for 30min, adding 0.8% of cellulase in 50 ℃ water bath for 1h, washing with 100 ℃ hot water for two times to inactivate enzyme, filtering, adding 95% of ethanol according to a filtrate ratio of 1:4, precipitating with ethanol for 1h, filtering, concentrating the filtrate, adding absolute ethanol according to a filtrate ratio of 1:4, precipitating with ethanol for 6h, centrifuging, precipitating, and freeze-drying to obtain the soluble dietary fiber.
Example 2
Weighing 1.0g of hazelnut meal superfine powder, fully dispersing in 40ml of distilled water, adding 0.5% of thermostable alpha-amylase, covering with an aluminum foil, placing in a 95 ℃ water bath kettle for enzymolysis for 35min, taking out, cooling to 60 ℃, adding 1.0% of papain in 60 ℃ water bath for 1h, adding 5ml of acetic acid, adjusting the pH to 4.5 with hydrochloric acid, adding 0.5% of glucoamylase, then performing 60 ℃ water bath for 30min, adding 0.8% of cellulase in 50 ℃ water bath for 1h, washing with 100 ℃ hot water for two times to inactivate enzyme, filtering, adding 95% of ethanol according to a filtrate ratio of 1:4, precipitating with ethanol for 1h, filtering, concentrating the filtrate, adding absolute ethanol according to a filtrate ratio of 1:4, precipitating with ethanol for 6h, centrifuging, precipitating, and freeze-drying to obtain the soluble dietary fiber.
Example 3
Weighing 1.0g of hazelnut meal superfine powder, fully dispersing in 40ml of distilled water, adding 0.5% of thermostable alpha-amylase, covering with an aluminum foil, placing in a 95 ℃ water bath kettle for enzymolysis for 35min, taking out, cooling to 60 ℃, adding 1.0% of papain in 60 ℃ water bath for 1h, adding 5ml of acetic acid, adjusting the pH to 4.5 with hydrochloric acid, adding 0.5% of glucoamylase, then performing 60 ℃ water bath for 30min, adding 0.8% of hemicellulase in 50 ℃ water bath for 1h, washing with 100 ℃ hot water for two times to inactivate enzyme, filtering, adding 95% ethanol according to a filtrate ratio of 1:4, precipitating with ethanol for 1h, filtering, concentrating the filtrate, adding absolute ethanol according to a filtrate ratio of 1:4, precipitating with ethanol for 6h, centrifuging, precipitating, and freeze-drying to obtain the soluble dietary fiber.
Example 4
Weighing 1.0g of hazelnut meal superfine powder, fully dispersing in 40ml of distilled water, adding 0.5% of thermostable alpha-amylase, covering an aluminum foil, placing in a 95 ℃ water bath kettle for enzymolysis for 35min, taking out, cooling to 60 ℃, adding 1.0% of papain in 60 ℃ water bath for 1h, adding 5ml of acetic acid, adjusting the pH to 4.5 with hydrochloric acid, adding 0.5% of glucoamylase, then performing 60 ℃ water bath for 30min, adding 1.0% of pectinase in 50 ℃ water bath for 1h, washing with 100 ℃ hot water for two times to inactivate enzyme, filtering, adding 95% of ethanol according to a filtrate ratio of 1:4, precipitating with ethanol for 1h, filtering, concentrating the filtrate, adding absolute ethanol according to a filtrate ratio of 1:4, precipitating with ethanol for 6h, centrifuging, precipitating, and freeze-drying to obtain the soluble dietary fiber.
Example 5
Weighing 1.0g of hazelnut meal superfine powder, fully dispersing in 40ml of distilled water, adding 0.5% of thermostable alpha-amylase, covering with an aluminum foil, placing in a 95 ℃ water bath kettle for enzymolysis for 35min, taking out, cooling to 60 ℃, adding 1.0% of papain in 60 ℃ water bath for 1h, adding 5ml of acetic acid, adjusting the pH to 4.5 with hydrochloric acid, adding 0.5% of glucoamylase, then in 60 ℃ water bath for 30min, adding 0.4% of cellulase and 0.4% of hemicellulase in 50 ℃ water bath for 1h, washing with 100 ℃ hot water for twice for enzyme inactivation, filtering, adding 95% of ethanol according to the ratio of the filtrate to 1:4, precipitating with ethanol for 1h, filtering, concentrating the filtrate, adding absolute ethanol according to the ratio of the filtrate to 1:4, precipitating with ethanol for 6h, centrifuging, precipitating, freezing and drying to obtain the soluble dietary fiber.
Example 6
Weighing 1.0g of hazelnut meal superfine powder, fully dispersing in 40ml of distilled water, adding 0.5% of thermostable alpha-amylase, covering an aluminum foil, placing in a 95 ℃ water bath kettle for enzymolysis for 35min, taking out, cooling to 60 ℃, adding 1.0% of papain in 60 ℃ water bath for 1h, adding 5ml of acetic acid, adjusting the pH to 4.5 with hydrochloric acid, adding 0.5% of glucoamylase, then in 60 ℃ water bath for 30min, adding 0.4% of cellulase and 0.4% of pectinase in 50 ℃ water bath for 1h, washing twice with 100 ℃ hot water for enzyme inactivation, filtering, adding 95% of ethanol according to the ratio of 1:4 of the filtrate to precipitate for 1h, filtering, concentrating the filtrate, adding absolute ethanol according to the ratio of 1:4 of the filtrate to precipitate for 6h, centrifuging, precipitating, and freeze-drying to obtain the soluble dietary fiber.
Example 7
Weighing 1.0g of hazelnut meal superfine powder, fully dispersing in 40ml of distilled water, adding 0.5% of thermostable alpha-amylase, covering an aluminum foil, placing in a 95 ℃ water bath kettle for enzymolysis for 35min, taking out, cooling to 60 ℃, adding 1.0% of papain in 60 ℃ water bath for 1h, adding 5ml of acetic acid, adjusting the pH to 4.5 with hydrochloric acid, adding 0.5% of glucoamylase, then in 60 ℃ water bath for 30min, adding 0.4% of hemicellulase and 0.4% of pectinase in 50 ℃ water bath for 1h, washing twice with 100 ℃ hot water for enzyme inactivation, filtering, adding 95% ethanol according to the ratio of the filtrate to 1:4, precipitating for 1h, filtering, concentrating the filtrate, adding absolute ethanol according to the ratio of the filtrate to 1:4, precipitating for 6h, centrifuging, precipitating, freezing and drying to obtain the soluble dietary fiber.
Comparative example 1
Dispersing 1.0g of desugarized hazelnut meal into 40ml of distilled water, adding 0.5% of thermostable alpha-amylase for enzymolysis for 35min in a water bath at 95 ℃, cooling to 60 ℃, adding 0.8% of neutral protease for 1h in the water bath at 60 ℃, adding 5ml of acetic acid, adjusting the pH to 4.5 with hydrochloric acid, adding 0.5% of saccharifying enzyme, further performing water bath at 60 ℃ for 30min, washing twice with 100 ℃ hot water for enzyme deactivation, filtering, adding 95% ethanol according to the filtrate ratio of 1:4, performing ethanol precipitation for 1h, filtering, concentrating the filtrate, adding absolute ethanol according to the filtrate ratio of 1:4, performing ethanol precipitation for 6h, centrifuging, precipitating, and freeze-drying to obtain the soluble dietary fiber.
Comparative example 2
Dispersing 1.0g of desugarized hazelnut meal into 40ml of distilled water, adding 0.5% of beta-amylase for enzymolysis for 35min in a water bath at 95 ℃, cooling to 50 ℃, adding 0.5% of alkaline protease for 1h in a water bath at 50 ℃, adding 5ml of acetic acid, adjusting the pH value to 4.5 with hydrochloric acid, adding 0.5% of glucoamylase, then performing water bath at 60 ℃ for 30min, washing twice with hot water at 100 ℃ to inactivate the enzyme, filtering, adding 95% of ethanol according to the filtrate ratio of 1:4, performing ethanol precipitation for 1h, filtering, concentrating the filtrate, adding absolute ethanol according to the filtrate ratio of 1:4, performing ethanol precipitation for 6h, centrifuging, precipitating, and freeze-drying to obtain the soluble dietary fiber.
Comparative example 3
Dispersing 1.0g of desugarized hazelnut meal into 40ml of distilled water, adding 0.5% of beta-amylase for enzymolysis for 35min in a water bath at 95 ℃, cooling to 50 ℃, adding 0.5% of alkaline protease for 1h in a water bath at 50 ℃, adding 5ml of acetic acid, adjusting the pH value to 4.5 with hydrochloric acid, adding 0.5% of saccharifying enzyme, further performing water bath at 60 ℃ for 30min, adding 0.8% of xylanase for 1h in a water bath at 50 ℃, washing with hot water at 100 ℃ for two times to inactivate enzyme, filtering, adding 95% of ethanol according to a filtrate ratio of 1:4, precipitating with ethanol for 1h, filtering, concentrating the filtrate, adding absolute ethanol according to a filtrate ratio of 1:4, centrifuging for 6h, precipitating, and freeze-drying to obtain the soluble dietary fiber.
TABLE 1 Effect of soluble dietary fiber yield
Note: each set of samples was replicated three times. In comparison with the example 1, the present inventors have conducted a comparison,aP<0.05 (with significant difference); in comparison with the example 3, the present inventors have conducted a comparison,bP<0.05; in comparison with comparative example 1,cP<0.05,dP<0.01,eP<0.001; in comparison with comparative example 2,fP<0.05,gP<0.01; in comparison with comparative example 3,hP<0.05,iP<0.01。
example 8
Regulating effect of hazelnut meal soluble dietary fiber on hyperlipidemia rats
SD rats fed with high-fat feed are used for creating a hyperlipidemia model, and after 5 weeks of continuous molding, hazelnut meal soluble dietary fiber (0.9g/kg) is given. After 5 weeks of administration, rats were anesthetized, and abdominal aorta was bled and serum was isolated for measuring cholesterol (TC) and Triglyceride (TG), and 0.1g of liver was taken, and the ratio of tissue to tissue was 1: 9, adding precooled PBS buffer, homogenizing, centrifuging, collecting supernatant, and using for measuring TC, TG, low density lipoprotein (LDL-C) and high density lipoprotein (HDL-C).
The results are shown in table 2 and table 3, and compared with the blank group, the serum TC and TG levels of the model group are obviously increased (P < 0.01); the TC, TG and LDL-C levels of liver tissues are obviously increased (P <0.01), and the HDL-C level is obviously reduced (P < 0.01). Compared with a model group, the hazelnut meal soluble dietary fiber can obviously reduce the TC and TG levels of serum (P is less than 0.01); obviously reduce TC, TG and LDL-C levels of liver tissues and obviously increase HDL-C levels of liver tissues. The hazelnut meal soluble dietary fiber extracted by the invention has good function of regulating blood fat.
note: comparison with model group*p<0.05,**p<0.01。
note: p <0.05, P <0.01 to model group.
The foregoing is only a preferred embodiment of the present invention, and it should be noted that, for those skilled in the art, various modifications and decorations can be made without departing from the principle of the present invention, and these modifications and decorations should also be regarded as the protection scope of the present invention.
Claims (10)
1. A preparation method of hazelnut meal soluble dietary fiber is characterized by comprising the following steps:
sequentially carrying out enzymolysis on the desugarized hazelnut meal by using thermostable alpha-amylase, papain, glucoamylase and enzymes capable of carrying out enzymolysis on cellulose, polysaccharide and pectin substances to obtain an zymolyte;
and (3) carrying out alcohol precipitation on the zymolyte, and drying the obtained precipitate to obtain the soluble dietary fiber.
2. The method of claim 1, comprising the steps of:
A) dispersing the desugarized hazelnut meal into distilled water, adding thermostable alpha-amylase for heating enzymolysis to obtain a first zymolyte;
B) cooling the first zymolyte, adding papain, and heating for enzymolysis to obtain a second zymolyte;
C) adding acetic acid into the second zymolyte, then adjusting the pH value to acidity, adding saccharifying enzyme, and heating for enzymolysis to obtain a third zymolyte;
D) adding enzymes capable of performing enzymolysis on cellulose, polysaccharide and pectin substances into the third zymolyte, and performing heating enzymolysis to obtain a zymolyte;
E) and (3) inactivating the enzyme of the zymolyte, filtering, precipitating the filtrate with ethanol, and drying the precipitate to obtain the soluble dietary fiber.
3. The method according to claim 2, wherein the method for preparing the desugarized hazelnut meal comprises: pulverizing hazelnut meal, and desugarizing with ethanol;
the hazelnut meal after desugarization is the hazelnut meal after superfine grinding.
4. The preparation method according to claim 2, wherein the thermostable alpha-amylase accounts for 0.3 wt% to 0.7 wt% of the desugarized hazelnut meal;
in the step A), the heating enzymolysis temperature is 90-95 ℃, and the time is 30-40 min.
5. The preparation method according to claim 2, wherein the mass percentage of the papain to the desugarized hazelnut meal is 0.3-0.7 wt%;
in the step B), the heating enzymolysis temperature is 55-65 ℃, and the time is 0.5-1.5 h.
6. The preparation method according to claim 2, wherein in the step C), the adding amount of the acetic acid is 10-15% of the volume percentage of the distilled water in the step A);
the pH regulator used for regulating the pH is hydrochloric acid, and the pH is regulated to 4-5;
the saccharifying enzyme accounts for 0.3-0.7 wt% of the desugarized hazelnut meal;
the temperature of heating enzymolysis is 55-65 ℃, and the time is 25-35 min.
7. The method according to claim 2, wherein in step D), the enzymes that can hydrolyze cellulose, polysaccharide and pectin substances are selected from one or more of cellulase, hemicellulase and pectinase;
the mass percentage of the enzymes capable of hydrolyzing cellulose, polysaccharide and pectin substances in the hazelnut meal after desugarization is 0.5-1.0 wt%;
the temperature of heating enzymolysis is 45-55 ℃, and the time is 0.5-1.5 h.
8. The method according to claim 2, wherein in step E), the enzyme deactivation is: washing twice with hot water at 90-100 ℃ to inactivate enzyme;
the alcohol precipitation is carried out by adopting 95% ethanol precipitation for 1h, filtering, concentrating the filtrate, and then adding absolute ethanol into the concentrated filtrate for alcohol precipitation for 6 h.
9. The hazelnut meal soluble dietary fiber prepared by the preparation method of any one of claims 1-8.
10. Use of the hazelnut meal soluble dietary fiber of claim 9 in the preparation of a food or a pharmaceutical product for regulating blood lipid.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202111308267.3A CN114158740A (en) | 2021-11-05 | 2021-11-05 | Preparation method of hazelnut meal soluble dietary fiber and application of hazelnut meal soluble dietary fiber in regulating blood fat |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202111308267.3A CN114158740A (en) | 2021-11-05 | 2021-11-05 | Preparation method of hazelnut meal soluble dietary fiber and application of hazelnut meal soluble dietary fiber in regulating blood fat |
Publications (1)
Publication Number | Publication Date |
---|---|
CN114158740A true CN114158740A (en) | 2022-03-11 |
Family
ID=80478143
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN202111308267.3A Pending CN114158740A (en) | 2021-11-05 | 2021-11-05 | Preparation method of hazelnut meal soluble dietary fiber and application of hazelnut meal soluble dietary fiber in regulating blood fat |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN114158740A (en) |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN106923350A (en) * | 2017-02-28 | 2017-07-07 | 天津大学 | Method for preparing water-soluble dietary fiber from corn stigma |
CN107712170A (en) * | 2017-09-30 | 2018-02-23 | 江苏农林职业技术学院 | A kind of preparation method and applications of soluble dietary fiber |
-
2021
- 2021-11-05 CN CN202111308267.3A patent/CN114158740A/en active Pending
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN106923350A (en) * | 2017-02-28 | 2017-07-07 | 天津大学 | Method for preparing water-soluble dietary fiber from corn stigma |
CN107712170A (en) * | 2017-09-30 | 2018-02-23 | 江苏农林职业技术学院 | A kind of preparation method and applications of soluble dietary fiber |
Non-Patent Citations (1)
Title |
---|
张金堂: "长白山野生榛仁膳食纤维制备工艺及理化性质分析", 《食品科技》, pages 232 - 238 * |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN102669423B (en) | Moringa extract as well as preparation method of moringa extract and moringa feed additive | |
CN104172353A (en) | Giant salamander polypeptide beverage and preparation method thereof | |
CN105273934A (en) | Fermented sweet prickly pear wine and production method thereof | |
CN106343410A (en) | Production method of kelp extract | |
CN110403056A (en) | A kind of preparation method and applications of delicate flavour peptide | |
CN109757600B (en) | Preparation method of perilla peptide | |
CN105996028A (en) | Ginger extract, ginger fiber and preparation method of ginger extract and ginger fiber | |
CN111011833A (en) | Processing technology of ash tree pollen and ash tree pollen solid beverage | |
CN107385003A (en) | A kind of preparation technology of soy peptide powder | |
CN103923793A (en) | Sprouted buckwheat and pumpkin wine and brewing method thereof | |
CN105777927A (en) | Separation and purification method for Vaccinium bracteatum Thunb. leaf polysaccharide and blueberry leaf polysaccharide | |
CN102823896A (en) | Puffed food rich in dietary fibers of seaweeds and production method for puffed food | |
CN113349356A (en) | Iceland red-pole ginseng intestine egg nutritional jelly and preparation method thereof | |
CN111387489A (en) | Lactobacillus bird's nest product and preparation method thereof | |
CN106387615A (en) | Method for removing fishy smell of spirulina with quercetin | |
CN114158740A (en) | Preparation method of hazelnut meal soluble dietary fiber and application of hazelnut meal soluble dietary fiber in regulating blood fat | |
CN109043323A (en) | A kind of preparation method of the numb albumen rice flour of fire with health care function | |
CN101940284B (en) | Potato extract and application thereof | |
CN108503722A (en) | A kind of preparation method of bamboo bird's nest mannosan | |
CN111944009B (en) | Preparation method and application of salicornia bigelovii antihypertensive peptide | |
CN111602736A (en) | Preparation method of composite modified dietary fiber soft sweets | |
CN113397094A (en) | Soybean protein powder capable of reducing blood fat and blood sugar and preparation method thereof | |
CN112813125A (en) | Preparation method of walnut peptide | |
CN112956676A (en) | Preparation method of radix puerariae soy sauce | |
CN107801784B (en) | Vegetable protein beverage and preparation method thereof |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PB01 | Publication | ||
PB01 | Publication | ||
SE01 | Entry into force of request for substantive examination | ||
SE01 | Entry into force of request for substantive examination |