CN113493489A - 具有醒酒功能的多肽scgh及其用途 - Google Patents
具有醒酒功能的多肽scgh及其用途 Download PDFInfo
- Publication number
- CN113493489A CN113493489A CN202110781160.4A CN202110781160A CN113493489A CN 113493489 A CN113493489 A CN 113493489A CN 202110781160 A CN202110781160 A CN 202110781160A CN 113493489 A CN113493489 A CN 113493489A
- Authority
- CN
- China
- Prior art keywords
- polypeptide
- scgh
- dehydrogenase
- activity
- sobering
- 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
- 108090000765 processed proteins & peptides Proteins 0.000 title claims abstract description 39
- 102000004196 processed proteins & peptides Human genes 0.000 title claims abstract description 33
- 229920001184 polypeptide Polymers 0.000 title claims abstract description 31
- 230000000694 effects Effects 0.000 claims abstract description 31
- 102000007698 Alcohol dehydrogenase Human genes 0.000 claims abstract description 18
- 108010021809 Alcohol dehydrogenase Proteins 0.000 claims abstract description 18
- 108010081577 aldehyde dehydrogenase (NAD(P)+) Proteins 0.000 claims abstract description 18
- 125000003275 alpha amino acid group Chemical group 0.000 claims abstract description 3
- 230000004913 activation Effects 0.000 claims description 20
- 230000003213 activating effect Effects 0.000 abstract description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 18
- 102000004190 Enzymes Human genes 0.000 description 11
- 108090000790 Enzymes Proteins 0.000 description 11
- 238000001514 detection method Methods 0.000 description 10
- IKHGUXGNUITLKF-UHFFFAOYSA-N Acetaldehyde Chemical compound CC=O IKHGUXGNUITLKF-UHFFFAOYSA-N 0.000 description 6
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- BAWFJGJZGIEFAR-NNYOXOHSSA-N NAD zwitterion Chemical compound NC(=O)C1=CC=C[N+]([C@H]2[C@@H]([C@H](O)[C@@H](COP([O-])(=O)OP(O)(=O)OC[C@@H]3[C@H]([C@@H](O)[C@@H](O3)N3C4=NC=NC(N)=C4N=C3)O)O2)O)=C1 BAWFJGJZGIEFAR-NNYOXOHSSA-N 0.000 description 4
- 238000002835 absorbance Methods 0.000 description 4
- 210000004185 liver Anatomy 0.000 description 4
- 229950006238 nadide Drugs 0.000 description 4
- 238000003786 synthesis reaction Methods 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 235000013361 beverage Nutrition 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 231100000331 toxic Toxicity 0.000 description 3
- 230000002588 toxic effect Effects 0.000 description 3
- 235000001674 Agaricus brunnescens Nutrition 0.000 description 2
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- 101710088194 Dehydrogenase Proteins 0.000 description 2
- 206010019133 Hangover Diseases 0.000 description 2
- 239000007853 buffer solution Substances 0.000 description 2
- 230000015556 catabolic process Effects 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 239000012153 distilled water Substances 0.000 description 2
- 230000004783 oxidative metabolism Effects 0.000 description 2
- 102000004169 proteins and genes Human genes 0.000 description 2
- 108090000623 proteins and genes Proteins 0.000 description 2
- FQENQNTWSFEDLI-UHFFFAOYSA-J sodium diphosphate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]P([O-])(=O)OP([O-])([O-])=O FQENQNTWSFEDLI-UHFFFAOYSA-J 0.000 description 2
- 229940048086 sodium pyrophosphate Drugs 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 235000019818 tetrasodium diphosphate Nutrition 0.000 description 2
- 239000001577 tetrasodium phosphonato phosphate Substances 0.000 description 2
- 108020002663 Aldehyde Dehydrogenase Proteins 0.000 description 1
- OBMZMSLWNNWEJA-XNCRXQDQSA-N C1=CC=2C(C[C@@H]3NC(=O)[C@@H](NC(=O)[C@H](NC(=O)N(CC#CCN(CCCC[C@H](NC(=O)[C@@H](CC4=CC=CC=C4)NC3=O)C(=O)N)CC=C)NC(=O)[C@@H](N)C)CC3=CNC4=C3C=CC=C4)C)=CNC=2C=C1 Chemical compound C1=CC=2C(C[C@@H]3NC(=O)[C@@H](NC(=O)[C@H](NC(=O)N(CC#CCN(CCCC[C@H](NC(=O)[C@@H](CC4=CC=CC=C4)NC3=O)C(=O)N)CC=C)NC(=O)[C@@H](N)C)CC3=CNC4=C3C=CC=C4)C)=CNC=2C=C1 OBMZMSLWNNWEJA-XNCRXQDQSA-N 0.000 description 1
- 101000744390 Catharanthus roseus 8-hydroxygeraniol oxidoreductase Proteins 0.000 description 1
- 208000015879 Cerebellar disease Diseases 0.000 description 1
- 208000018522 Gastrointestinal disease Diseases 0.000 description 1
- 244000068988 Glycine max Species 0.000 description 1
- 235000010469 Glycine max Nutrition 0.000 description 1
- GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 1
- 229920001491 Lentinan Polymers 0.000 description 1
- 229920000168 Microcrystalline cellulose Polymers 0.000 description 1
- 206010033799 Paralysis Diseases 0.000 description 1
- 101710176384 Peptide 1 Proteins 0.000 description 1
- WTKZEGDFNFYCGP-UHFFFAOYSA-N Pyrazole Chemical compound C=1C=NNC=1 WTKZEGDFNFYCGP-UHFFFAOYSA-N 0.000 description 1
- RNFKSBPHLTZHLU-WHFBIAKZSA-N Ser-Cys-Gly Chemical compound C([C@@H](C(=O)N[C@@H](CS)C(=O)NCC(=O)O)N)O RNFKSBPHLTZHLU-WHFBIAKZSA-N 0.000 description 1
- 240000008042 Zea mays Species 0.000 description 1
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- IKHGUXGNUITLKF-XPULMUKRSA-N acetaldehyde Chemical compound [14CH]([14CH3])=O IKHGUXGNUITLKF-XPULMUKRSA-N 0.000 description 1
- 229960005070 ascorbic acid Drugs 0.000 description 1
- 235000010323 ascorbic acid Nutrition 0.000 description 1
- 239000011668 ascorbic acid Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 230000017531 blood circulation Effects 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 235000005822 corn Nutrition 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 230000035622 drinking Effects 0.000 description 1
- 210000003238 esophagus Anatomy 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 230000037406 food intake Effects 0.000 description 1
- 210000001156 gastric mucosa Anatomy 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- 235000012907 honey Nutrition 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 239000008101 lactose Substances 0.000 description 1
- 229940115286 lentinan Drugs 0.000 description 1
- 208000019423 liver disease Diseases 0.000 description 1
- 230000005976 liver dysfunction Effects 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- VUZPPFZMUPKLLV-UHFFFAOYSA-N methane;hydrate Chemical compound C.O VUZPPFZMUPKLLV-UHFFFAOYSA-N 0.000 description 1
- 235000019813 microcrystalline cellulose Nutrition 0.000 description 1
- 239000008108 microcrystalline cellulose Substances 0.000 description 1
- 229940016286 microcrystalline cellulose Drugs 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 229930014626 natural product Natural products 0.000 description 1
- 210000005036 nerve Anatomy 0.000 description 1
- 210000000653 nervous system Anatomy 0.000 description 1
- 208000020911 optic nerve disease Diseases 0.000 description 1
- 208000021090 palsy Diseases 0.000 description 1
- 231100000915 pathological change Toxicity 0.000 description 1
- 230000036285 pathological change Effects 0.000 description 1
- 206010036067 polydipsia Diseases 0.000 description 1
- 210000004896 polypeptide structure Anatomy 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 230000001953 sensory effect Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 150000003628 tricarboxylic acids Chemical class 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/10—Tetrapeptides
- C07K5/1002—Tetrapeptides with the first amino acid being neutral
- C07K5/1005—Tetrapeptides with the first amino acid being neutral and aliphatic
- C07K5/1013—Tetrapeptides with the first amino acid being neutral and aliphatic the side chain containing O or S as heteroatoms, e.g. Cys, Ser
-
- 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
- A23L33/10—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
- A23L33/17—Amino acids, peptides or proteins
- A23L33/18—Peptides; Protein hydrolysates
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
- C12N9/0004—Oxidoreductases (1.)
- C12N9/0006—Oxidoreductases (1.) acting on CH-OH groups as donors (1.1)
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
- C12N9/0004—Oxidoreductases (1.)
- C12N9/0008—Oxidoreductases (1.) acting on the aldehyde or oxo group of donors (1.2)
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Y—ENZYMES
- C12Y101/00—Oxidoreductases acting on the CH-OH group of donors (1.1)
- C12Y101/01—Oxidoreductases acting on the CH-OH group of donors (1.1) with NAD+ or NADP+ as acceptor (1.1.1)
- C12Y101/01001—Alcohol dehydrogenase (1.1.1.1)
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Y—ENZYMES
- C12Y102/00—Oxidoreductases acting on the aldehyde or oxo group of donors (1.2)
- C12Y102/01—Oxidoreductases acting on the aldehyde or oxo group of donors (1.2) with NAD+ or NADP+ as acceptor (1.2.1)
- C12Y102/0101—Acetaldehyde dehydrogenase (acetylating) (1.2.1.10)
-
- 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
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Genetics & Genomics (AREA)
- Engineering & Computer Science (AREA)
- Zoology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Wood Science & Technology (AREA)
- General Health & Medical Sciences (AREA)
- Biochemistry (AREA)
- Molecular Biology (AREA)
- General Engineering & Computer Science (AREA)
- Medicinal Chemistry (AREA)
- Biomedical Technology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Microbiology (AREA)
- Biotechnology (AREA)
- Biophysics (AREA)
- Polymers & Plastics (AREA)
- Food Science & Technology (AREA)
- Nutrition Science (AREA)
- Mycology (AREA)
- Enzymes And Modification Thereof (AREA)
Abstract
本发明属于生物技术领域,特别涉及一个具有激活乙醇脱氢酶和乙醛脱氢酶活性的多肽SCGH,该多肽的氨基酸序列为:Ser‑Cys‑Gly‑His。多肽SCGH能用于制备醒酒产品。
Description
技术领域
本发明属于生物技术领域,特别涉及一个具有激活乙醇脱氢酶和乙醛脱氢酶活性的多肽。
背景技术
酒在我国已经有近千年的历史,也形成了独具特色的酒文化。但饮酒过量或者是经常饮酒则可对人体健康造成一定影响,大量的酒精摄入能刺激食道与胃粘膜,导致胃肠疾病,肝功能代谢障碍,导致肝病变等。过量的酒精进入人体血液循环系统后,还会影响人体神经系统,造成感觉神经麻搏、小脑功能障碍及视神经障碍等。酒精在人体内的分解代谢主要通过肝脏的酶系统进行氧化代谢,酒精进入肝脏通过乙醇脱氢酶脱掉乙醇两个氢原子,使乙醇分解变成乙醛,乙醛进一步通过乙醛脱氧酶氧化为乙酸,最终进入三羧酸循环分解为二氧化碳和水。因此加快肝脏中乙醇的氧化代谢对于醒酒具有重要作用。
目前,市场上很多解酒产品大多是化学制品,具有一定的毒副作用。近几年有研究发现大豆肽、玉米肽等多肽产品可激活乙醇脱氢酶的活性,具有醒酒的作用。由于多肽属天然产品,吸收迅速发挥效果快、无毒副作用,具有较广阔的应用前景。
发明内容
本发明要解决的技术问题是提供一种具有醒酒功能的多肽及其用途。
为了解决上述技术问题,本发明提供一种从香菇蛋白酶解液中鉴定出的多肽SCGH,该多肽的氨基酸序列为:Ser-Cys-Gly-His。
本发明的多肽SCGH可通过香菇蛋白酶解液分离制备,也可由多肽合成公司通过化学合成制备。
本发明提供的多肽具有较强的乙醇脱氢酶和乙醛脱氢酶激活作用,且具有安全无毒副作用、易于吸收等优点,可用于醒酒食品中,服用方式为口服,用量可参照现有的醒酒肽。
本发明的多肽针对乙醇脱氢酶和乙醛脱氢酶具有激活活性,从而表现出具有醒酒功能的特性。
本发明中所涉及的乙醇脱氢酶激活活性的检测方法:
向96孔酶标板中依次加入pH 8.8的焦磷酸钠缓冲液120μL,加入27mmol/L氧化型辅酶I(NAD+)80μL,体积分数为11.5%的乙醇40μL,一定浓度的样品(对照组加入同体积蒸馏水)50μL。混匀,在25℃条件下温育5min,取出立即加入0.5U/mL的乙醇脱氢酶10μL,混匀后于340nm波长处测定吸光度,每10s读数1次,连续测定5min。以A340nm对时间作图。计算△A340nm/min的增加值,以吸光度每分钟的变化率衡量酶活力。
激活率(%)=(样品组酶活力-对照组酶活力)/对照组酶活力×100%
本发明中所涉及的乙醛脱氢酶激活活性的检测方法:
向96孔酶标板加入100mmol/L pH9.5的焦磷酸钠缓冲液120μL,加入27mmol/L氧化型辅酶I(NAD+)100μL;加入1mmol/L乙醛10μL;10mM吡唑20μL,加入一定浓度的样品(对照组加入同体积蒸馏水)30μL;混匀,在30℃条件下温育5min;取出立即加入1.5U/mL ALDH 15μL摇匀,于340nm波长处测定吸光度,每1min读数1次,连续测定10min。以吸光度每分钟的变化率衡量酶活力。
激活率(%)=(样品组酶活力-对照组酶活力)/对照组酶活力×100%
本发明从香菇酶解液中分鉴定得到具有乙醇脱氢酶和乙醛脱氢酶激活作用的多肽,可在醒酒产品中应用。
附图说明
下面结合附图对本发明的具体实施方式作进一步详细说明。
图1为本发明的乙醇脱氢酶和乙醛脱氢酶的激活率对比图。
具体实施方式
下面对本发明的实施例作详细说明:本实施例在以本发明技术方案为前提下进行实施,给出了详细的实施方式和具体的操作过程,但本发明的保护范围不限于下述的实施例。
实施例1
多肽SCGH在3.0mg/mL的浓度下的乙醇脱氢酶和乙醛脱氢酶激活活性:
检测方法:将通过化学合成法获得的此多肽SCGH,进行活性检测(检测方法同上)。此时多肽SCGH浓度为3.0mg/mL。
结果:多肽SCGH在3.0mg/mL时的乙醇脱氢酶激活率为76.8%,乙醛脱氢酶激活率为43.8%。对应图1中的“untreated”。
将3mg/mL四肽SCGH溶液于80℃和100℃放置1h后,再进行活性检测(检测方法同上),测得的乙醇脱氢酶和乙醛脱氢酶激活率如图1,在高温处理下,活性肽的乙醇脱氢酶和乙醛脱氢酶激活率相对比较稳定,具有较好的稳定性。
实施例2
多肽SCGH在1.5mg/mL的浓度下的乙醇脱氢酶和乙醛脱氢酶激活活性:
检测方法:将通过化学合成法获得的此多肽SCGH,进行活性检测(检测方法同上)。此时多肽SCGH浓度为1.5mg/mL。
结果:多肽SCGH在1.5mg/mL时的乙醇脱氢酶激活率为40.6%,乙醛脱氢酶激活率为24.2%。
通过上述实施例中的活性数据可知,此多肽结构具有乙醇脱氢酶和乙醛脱氢酶激活活性,且该活性未见报道,活性效应与剂量具有相关性,属于新的具有乙醇脱氢酶和乙醛脱氢酶激活活性功能肽,该肽还具有较好的热稳定性。
对比例、将表1所述的多肽,按照上述实验方法进行乙醇脱氢酶和乙醛脱氢酶激活活性测定;所得结果与本发明实施例1所得结果的对比如表1所述。
表1、3.0mg/mL浓度下的乙醇脱氢酶和乙醛脱氢酶激活活性
实施例3、醒酒肽的应用
1、按50%的醒酒肽,25%的乳糖,25%微晶纤维素充分混合后,通过压片机进行压片,制造成具有醒酒作用的片剂。
2、饮料:将饮料各成分按以下比例进行混合:蜂蜜6%,醒酒肽为1%,柠檬酸0.1%,抗坏血酸0.02%,水92.88%,制成具有醒酒功能的饮料。
最后,还需要注意的是,以上列举的仅是本发明的若干个具体实施例。显然,本发明不限于以上实施例,还可以有许多变形,比如不同蛋白质来源降解分离所得的SCGH结构及其衍生化结构。本领域的普通技术人员能从本发明公开的内容直接导出或联想到的所有变形,均应认为是本发明的保护范围。
序列表
<110> 浙江省农业科学院
<120> 具有醒酒功能的多肽SCGH及其用途
<160> 1
<170> SIPOSequenceListing 1.0
<210> 1
<211> 4
<212> PRT
<213> 人工序列(Artificial Sequence)
<400> 1
Ser Cys Gly His
1
Claims (3)
1.具有醒酒功能的多肽SCGH,其特征是:该多肽的氨基酸序列为:Ser-Cys-Gly-His。
2.如权利要求1所述的多肽SCGH的用途,其特征是:制备醒酒产品。
3.根据权利要求2所述的多肽SCGH的用途,其特征是:同时具有乙醇脱氢酶激活活性和乙醛脱氢酶激活活性。
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202110781160.4A CN113493489B (zh) | 2021-07-10 | 2021-07-10 | 具有醒酒功能的多肽scgh及其用途 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202110781160.4A CN113493489B (zh) | 2021-07-10 | 2021-07-10 | 具有醒酒功能的多肽scgh及其用途 |
Publications (2)
Publication Number | Publication Date |
---|---|
CN113493489A true CN113493489A (zh) | 2021-10-12 |
CN113493489B CN113493489B (zh) | 2024-02-13 |
Family
ID=77996111
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN202110781160.4A Active CN113493489B (zh) | 2021-07-10 | 2021-07-10 | 具有醒酒功能的多肽scgh及其用途 |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN113493489B (zh) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN114409731A (zh) * | 2022-01-05 | 2022-04-29 | 浙江省农业科学院 | 同时具有激活乙醇脱氢酶和乙醛脱氢酶活性的两种多肽 |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH07285881A (ja) * | 1994-04-18 | 1995-10-31 | Nippon Shokuhin Kako Co Ltd | アルコール代謝促進剤 |
CN104004813A (zh) * | 2014-06-12 | 2014-08-27 | 北京林业大学 | 一种香菇生物活性肽的制备 |
CN105063139A (zh) * | 2015-07-17 | 2015-11-18 | 山西大学 | 一种用于醒酒的沙棘籽多肽的制备方法 |
CN105238837A (zh) * | 2015-11-05 | 2016-01-13 | 山西大学 | 一种花生粕醒酒肽的制备方法 |
CN106866787A (zh) * | 2016-10-27 | 2017-06-20 | 北京林业大学 | 一种香菇醒酒肽及其制备方法与应用 |
-
2021
- 2021-07-10 CN CN202110781160.4A patent/CN113493489B/zh active Active
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH07285881A (ja) * | 1994-04-18 | 1995-10-31 | Nippon Shokuhin Kako Co Ltd | アルコール代謝促進剤 |
CN104004813A (zh) * | 2014-06-12 | 2014-08-27 | 北京林业大学 | 一种香菇生物活性肽的制备 |
CN105063139A (zh) * | 2015-07-17 | 2015-11-18 | 山西大学 | 一种用于醒酒的沙棘籽多肽的制备方法 |
CN105238837A (zh) * | 2015-11-05 | 2016-01-13 | 山西大学 | 一种花生粕醒酒肽的制备方法 |
CN106866787A (zh) * | 2016-10-27 | 2017-06-20 | 北京林业大学 | 一种香菇醒酒肽及其制备方法与应用 |
Non-Patent Citations (1)
Title |
---|
程湛等: "香菇肽提取优化及其体外抗氧化醒酒活性", 《中国食品学报》, vol. 15, no. 4, pages 93 - 102 * |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN114409731A (zh) * | 2022-01-05 | 2022-04-29 | 浙江省农业科学院 | 同时具有激活乙醇脱氢酶和乙醛脱氢酶活性的两种多肽 |
CN114409731B (zh) * | 2022-01-05 | 2023-08-11 | 浙江省农业科学院 | 同时具有激活乙醇脱氢酶和乙醛脱氢酶活性的两种多肽 |
Also Published As
Publication number | Publication date |
---|---|
CN113493489B (zh) | 2024-02-13 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN109400678B (zh) | 一种刺参来源的抗氧化和dpp-iv抑制活性肽 | |
CN108998488B (zh) | 一种活性蜂王浆oco多肽冻干粉及其制备方法 | |
CN105324483B (zh) | 工程化苯丙氨酸解氨酶多肽 | |
EP2444480B1 (en) | Method for fermentation and cultivation, fermented plant extract, fermented plant extract powder, and composition containing the extract of fermented plant | |
EP2380901B1 (en) | Angiotensin converting enzyme inhibitory peptide | |
YU et al. | Ultrafiltration preparation of potent bioactive corn peptide as alcohol metabolism stimulator in vivo and study on its mechanism of action | |
Liu et al. | Production, bioactivities and bioavailability of bioactive peptides derived from walnut origin by-products: a review | |
KR100787633B1 (ko) | 간 기능 개선과 숙취해소용 차 및 그 제조방법 | |
CN113151386A (zh) | 具有dpp-iv抑制功能的牡蛎肽及其制备方法和应用 | |
CN114891065B (zh) | 一种具有α-淀粉酶抑制活性的降血糖海参肽及其制备方法和应用 | |
CN114032273B (zh) | 一种多功能西洋参水解肽及其制备方法和应用 | |
CN117820431B (zh) | 一种具有降尿酸功效的青稞酒糟肽及其制备方法与应用 | |
CN113493489B (zh) | 具有醒酒功能的多肽scgh及其用途 | |
KR101548340B1 (ko) | 콩나물을 이용한 숙취해소음료 및 이의 제조방법 | |
CN108178782B (zh) | 一种鲻鱼鱼鳞铁螯合肽的用途 | |
CN104758925A (zh) | 带鱼鱼骨铁螯合胶原肽的铁螯合用途 | |
KR101632262B1 (ko) | DagA 효소반응으로 조제한 항비만 및 항당뇨 효능을 갖는 한천 유래 네오아가로올리고당 복합 조성물 | |
KR101539820B1 (ko) | 혈전성 질환 예방 식품 | |
KR102111969B1 (ko) | 비스코자임 엘을 처리하여 뽕나무 잎 추출물 내 퀘르세틴을 수득하는 방법 | |
CN113087773B (zh) | 一种具有降血糖和抗氧化功能的牦牛骨肽及其制备方法 | |
Wang et al. | The effects of Monascus purpureus fermentation on metabolic profile, α-glucosidase inhibitory action, and in vitro digestion of mulberry leaves flavonoids | |
CN114409731B (zh) | 同时具有激活乙醇脱氢酶和乙醛脱氢酶活性的两种多肽 | |
WO2021082310A1 (zh) | 一种具有美白功能的大米肽及其制备方法 | |
JPH07285881A (ja) | アルコール代謝促進剤 | |
KR101082598B1 (ko) | 노루궁뎅이버섯을 이용한 숙취해소음료 |
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 | ||
GR01 | Patent grant | ||
GR01 | Patent grant |