CN106615597A - Method for preparing red snapper fish scale collagen protein - Google Patents
Method for preparing red snapper fish scale collagen protein Download PDFInfo
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- 102000008186 Collagen Human genes 0.000 title claims abstract description 56
- 108010035532 Collagen Proteins 0.000 title claims abstract description 56
- 241000123826 Lutjanus campechanus Species 0.000 title claims abstract description 46
- 238000000034 method Methods 0.000 title claims abstract description 8
- 241000251468 Actinopterygii Species 0.000 claims abstract description 51
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims abstract description 23
- 239000000843 powder Substances 0.000 claims abstract description 21
- 238000004140 cleaning Methods 0.000 claims abstract description 16
- 238000001914 filtration Methods 0.000 claims abstract description 14
- 238000000605 extraction Methods 0.000 claims abstract description 13
- 238000002242 deionisation method Methods 0.000 claims abstract description 8
- 239000012535 impurity Substances 0.000 claims abstract description 8
- 239000008399 tap water Substances 0.000 claims abstract description 7
- 235000020679 tap water Nutrition 0.000 claims abstract description 7
- 239000002994 raw material Substances 0.000 claims abstract description 3
- 229920001436 collagen Polymers 0.000 claims description 50
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 16
- 238000002360 preparation method Methods 0.000 claims description 10
- 238000003756 stirring Methods 0.000 claims description 10
- 239000003292 glue Substances 0.000 claims description 9
- 229920002678 cellulose Polymers 0.000 claims description 5
- 239000001913 cellulose Substances 0.000 claims description 5
- 238000005119 centrifugation Methods 0.000 claims description 5
- 239000012141 concentrate Substances 0.000 claims description 5
- 239000011347 resin Substances 0.000 claims description 5
- 229920005989 resin Polymers 0.000 claims description 5
- 239000007787 solid Substances 0.000 claims description 5
- 239000007921 spray Substances 0.000 claims description 5
- 238000010410 dusting Methods 0.000 claims description 2
- 239000007788 liquid Substances 0.000 claims description 2
- 239000004833 fish glue Substances 0.000 claims 2
- 239000000428 dust Substances 0.000 claims 1
- 238000010438 heat treatment Methods 0.000 claims 1
- 238000007654 immersion Methods 0.000 claims 1
- 230000008676 import Effects 0.000 claims 1
- 238000002156 mixing Methods 0.000 claims 1
- 239000000203 mixture Substances 0.000 claims 1
- 238000003828 vacuum filtration Methods 0.000 claims 1
- 102000004169 proteins and genes Human genes 0.000 abstract description 9
- 108090000623 proteins and genes Proteins 0.000 abstract description 9
- 238000005507 spraying Methods 0.000 abstract description 9
- 235000013305 food Nutrition 0.000 abstract description 6
- 239000002537 cosmetic Substances 0.000 abstract description 3
- 238000004806 packaging method and process Methods 0.000 abstract description 3
- 238000004519 manufacturing process Methods 0.000 abstract description 2
- 108010010803 Gelatin Proteins 0.000 abstract 1
- 238000004380 ashing Methods 0.000 abstract 1
- 229920000159 gelatin Polymers 0.000 abstract 1
- 239000008273 gelatin Substances 0.000 abstract 1
- 235000019322 gelatine Nutrition 0.000 abstract 1
- 235000011852 gelatine desserts Nutrition 0.000 abstract 1
- 150000001450 anions Chemical class 0.000 description 14
- 150000001768 cations Chemical class 0.000 description 8
- 239000012982 microporous membrane Substances 0.000 description 8
- 235000018102 proteins Nutrition 0.000 description 8
- 238000002791 soaking Methods 0.000 description 8
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 4
- 239000012528 membrane Substances 0.000 description 4
- 239000011148 porous material Substances 0.000 description 4
- PMMYEEVYMWASQN-DMTCNVIQSA-N Hydroxyproline Chemical compound O[C@H]1CN[C@H](C(O)=O)C1 PMMYEEVYMWASQN-DMTCNVIQSA-N 0.000 description 3
- PMMYEEVYMWASQN-UHFFFAOYSA-N dl-hydroxyproline Natural products OC1C[NH2+]C(C([O-])=O)C1 PMMYEEVYMWASQN-UHFFFAOYSA-N 0.000 description 3
- 239000000706 filtrate Substances 0.000 description 3
- 229960002591 hydroxyproline Drugs 0.000 description 3
- FGMPLJWBKKVCDB-UHFFFAOYSA-N trans-L-hydroxy-proline Natural products ON1CCCC1C(O)=O FGMPLJWBKKVCDB-UHFFFAOYSA-N 0.000 description 3
- 208000007212 Foot-and-Mouth Disease Diseases 0.000 description 2
- 241000710198 Foot-and-mouth disease virus Species 0.000 description 2
- 239000004471 Glycine Substances 0.000 description 2
- 241001465754 Metazoa Species 0.000 description 2
- 235000015278 beef Nutrition 0.000 description 2
- 201000010099 disease Diseases 0.000 description 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000010088 rubber extraction Methods 0.000 description 2
- QNAYBMKLOCPYGJ-REOHCLBHSA-N L-alanine Chemical compound C[C@H](N)C(O)=O QNAYBMKLOCPYGJ-REOHCLBHSA-N 0.000 description 1
- QIVBCDIJIAJPQS-VIFPVBQESA-N L-tryptophane Chemical compound C1=CC=C2C(C[C@H](N)C(O)=O)=CNC2=C1 QIVBCDIJIAJPQS-VIFPVBQESA-N 0.000 description 1
- 241000124008 Mammalia Species 0.000 description 1
- 206010028980 Neoplasm Diseases 0.000 description 1
- QIVBCDIJIAJPQS-UHFFFAOYSA-N Tryptophan Natural products C1=CC=C2C(CC(N)C(O)=O)=CNC2=C1 QIVBCDIJIAJPQS-UHFFFAOYSA-N 0.000 description 1
- 210000001361 achilles tendon Anatomy 0.000 description 1
- 235000004279 alanine Nutrition 0.000 description 1
- 235000001014 amino acid Nutrition 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 210000000988 bone and bone Anatomy 0.000 description 1
- 210000002808 connective tissue Anatomy 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 210000002435 tendon Anatomy 0.000 description 1
Classifications
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23J—PROTEIN COMPOSITIONS FOR FOODSTUFFS; WORKING-UP PROTEINS FOR FOODSTUFFS; PHOSPHATIDE COMPOSITIONS FOR FOODSTUFFS
- A23J1/00—Obtaining protein compositions for foodstuffs; Bulk opening of eggs and separation of yolks from whites
- A23J1/10—Obtaining protein compositions for foodstuffs; Bulk opening of eggs and separation of yolks from whites from hair, feathers, horn, skins, leather, bones, or the like
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23J—PROTEIN COMPOSITIONS FOR FOODSTUFFS; WORKING-UP PROTEINS FOR FOODSTUFFS; PHOSPHATIDE COMPOSITIONS FOR FOODSTUFFS
- A23J3/00—Working-up of proteins for foodstuffs
- A23J3/04—Animal proteins
- A23J3/06—Gelatine
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- Life Sciences & Earth Sciences (AREA)
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- Engineering & Computer Science (AREA)
- Food Science & Technology (AREA)
- Polymers & Plastics (AREA)
- Health & Medical Sciences (AREA)
- Nutrition Science (AREA)
- Peptides Or Proteins (AREA)
- Meat, Egg Or Seafood Products (AREA)
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Abstract
Description
技术领域technical field
本发明涉及一种红鲷鱼鱼鳞胶原蛋白粉的制备方法,属于食品加工技术领域。The invention relates to a preparation method of red snapper scale collagen powder, which belongs to the technical field of food processing.
背景技术Background technique
胶原蛋白是动物体中普遍存在的一种大分子蛋白,主要存在于动物的结缔组织中,如猪皮、猪跟腱、牛骨、牛筋中含有大量的胶原蛋白。胶原蛋白具有良好的生物相容性、生物可降解性、低抗原性,因此在食品、医药、化妆品、包装行业得到广泛的应用。目前市场上的胶原蛋源主要为哺乳动物,近些年爆发的疯牛病、口蹄疫等限制了哺乳动物胶原的使用。因此人们开始探寻新的蛋白源,如从鱼鳞、鱼皮等中提取胶原蛋白。从鱼鳞中提取胶原蛋白,既可解决由口蹄疫、疯牛病等可能带来的胶原蛋白的食品安全问题,又可打破宗教信仰和习俗文化的限制,满足不同种族人群的需求。Collagen is a macromolecular protein ubiquitous in animals, mainly in the connective tissue of animals, such as pigskin, pig Achilles tendon, beef bone, and beef tendon contain a large amount of collagen. Collagen has good biocompatibility, biodegradability, and low antigenicity, so it is widely used in food, medicine, cosmetics, and packaging industries. At present, the source of collagen on the market is mainly mammals. The outbreaks of mad cow disease and foot-and-mouth disease in recent years have restricted the use of mammalian collagen. Therefore, people began to search for new protein sources, such as extracting collagen from fish scales and fish skins. Extracting collagen from fish scales can not only solve the food safety problems of collagen that may be caused by foot-and-mouth disease and mad cow disease, but also break the restrictions of religious beliefs and customs and cultures to meet the needs of different ethnic groups.
红鲷鱼是一种生活在大概200米的深海鱼种,主要分布在中国的渤海、黄海、东海、南海等地。红鲷鱼鱼鳞中含有大量的胶原蛋白,蛋白由羟脯氨酸、甘氨酸、丙氨酸、色氨酸等近二十种氨基酸组成,其中的羟脯氨酸对皮肤的作用很好,而甘氨酸有抑制肿瘤扩散的作用。与其他鱼类鱼鳞相比,红鲷鱼鱼鳞中羟脯氨酸的含量其他鱼种的几倍,此外红鲷鱼的生活环境温度相对较低,使其胶原的热量较低,在补充营养的同时不会增加脂肪。另外鱼鳞中提取的胶原蛋白在一些方面明显优于哺乳动物胶原蛋白,比如低抗原性、低过敏性等。因此水产胶原蛋白具有替代哺乳动物胶原蛋白的趋势。Red snapper is a deep-sea fish that lives at about 200 meters, and is mainly distributed in China's Bohai Sea, Yellow Sea, East China Sea, and South China Sea. Red snapper scales contain a large amount of collagen, which is composed of nearly 20 kinds of amino acids such as hydroxyproline, glycine, alanine, tryptophan, etc. Among them, hydroxyproline has a good effect on the skin, while glycine It has the effect of inhibiting tumor spread. Compared with other fish scales, the content of hydroxyproline in red snapper scales is several times that of other fish species. In addition, the living environment temperature of red snapper is relatively low, so that the calories of collagen are low. At the same time will not add fat. In addition, the collagen extracted from fish scales is obviously superior to mammalian collagen in some aspects, such as low antigenicity and hypoallergenicity. Therefore, aquatic collagen has a tendency to replace mammalian collagen.
发明内容Contents of the invention
本发明的目的在于提供一种红鲷鱼鱼鳞胶原蛋白粉的制备方法,其提高红鲷鱼鱼鳞的综合利用率,改善鱼鳞蛋白的提取工艺。The object of the present invention is to provide a preparation method of red snapper fish scale collagen powder, which improves the comprehensive utilization rate of red snapper fish scales and improves the extraction process of fish scale protein.
按照本发明提供的技术方案,一种红鲷鱼鱼鳞胶原蛋白粉的制备方法,其以红鲷鱼干鱼鳞为原料,用自来水对干鱼鳞进行清洗,去掉鱼鳞表面的杂质,晾干,再经过盐酸脱灰、清洗、提胶、过滤、去离子、浓缩和喷粉后制备得到红鲷鱼鱼鳞胶原蛋白粉;具体步骤如下:According to the technical scheme provided by the present invention, a preparation method of red snapper fish scale collagen powder, it uses dried red snapper fish scales as raw material, cleans the dried fish scales with tap water, removes impurities on the surface of the fish scales, dries them, and then passes through Red snapper scale collagen powder is prepared after hydrochloric acid deliming, cleaning, gel extraction, filtration, deionization, concentration and dusting; the specific steps are as follows:
(1)干鱼鳞清洗:用清水对红鲷鱼干鱼鳞进行清洗,去掉表面的杂质,常温晾干;(1) Cleaning of dried fish scales: Clean the dried fish scales of red snapper with clean water, remove surface impurities, and dry at room temperature;
(2)脱灰处理:用0.2-0.5mol/L的盐酸在浸泡罐中对步骤(1)所得的红鲷鱼鱼鳞进行浸泡脱灰处理10-16h,其中红鲷鱼鱼鳞和盐酸固液比为1g鱼鳞:10-14mL盐酸,边浸泡边搅拌,搅拌转速为20-60r/min;(2) Deliming treatment: use 0.2-0.5mol/L hydrochloric acid to soak and deash the red snapper scales obtained in step (1) in a soaking tank for 10-16 hours, wherein the red snapper scales and hydrochloric acid have a solid-to-liquid ratio of For 1g fish scale: 10-14mL hydrochloric acid, stir while soaking, the stirring speed is 20-60r/min;
(3)清洗:用清水对步骤(2)处理所得的红鲷鱼干鱼鳞进行清洗3-5遍,准备提胶;(3) Cleaning: Clean the dried red snapper fish scales obtained in step (2) with clean water for 3-5 times, and prepare for gel extraction;
(4)提胶:在步骤(3)清洗后的红鲷鱼鱼鳞中加入10-14倍体积自来水后,将提胶罐加热至70-100℃,搅拌速度为40-80r/min,保持3-5h后过滤掉固体鱼鳞制得红鲷鱼鱼鳞胶原液;(4) Glue extraction: After adding 10-14 times the volume of tap water to the cleaned red snapper scales in step (3), heat the rubber extraction tank to 70-100°C, stir at 40-80r/min, and keep for 3 After -5h, the solid scales were filtered out to obtain the red snapper scale collagen solution;
(5)离心过滤:用离心机对步骤(4)提取的红鲷鱼鱼鳞胶原液进行离心,用微孔滤膜和真空泵对胶原液进行真空抽滤;(5) Centrifugal filtration: centrifuge the red snapper scale collagen solution extracted in step (4) with a centrifuge, and vacuum filter the collagen solution with a microporous filter membrane and a vacuum pump;
(6)去离子:将处理过的阴阳树脂分别装在两个柱子中,将步骤(5)所得离心过滤后的胶原液通过阴阳离子柱去离子;(6) Deionization: Pack the treated anion and cation resins into two columns respectively, and deionize the collagen solution after centrifugal filtration obtained in step (5) through anion and cation columns;
(7)浓缩:将步骤(6)制得的胶原液在浓缩装置中浓缩至28%-40%;(7) Concentration: Concentrate the collagen solution prepared in step (6) to 28%-40% in the concentration device;
(8)喷粉:采用喷雾干燥机进行喷粉,进口热风温度为 160-200℃,出口热风温度 60-100℃,即制得红鲷鱼鱼鳞胶原蛋白粉。(8) Powder spraying: use a spray dryer for powder spraying, the inlet hot air temperature is 160-200°C, and the outlet hot air temperature is 60-100°C, and the red snapper scale collagen powder is obtained.
步骤(5)中离心过滤时的离心机转速为4000-6000r/min,离心时间为15-20min;所述微孔滤膜为孔径为20-50μm的混合纤维素微孔滤膜;真空泵为-0.1MPa的循环水式真空泵。The centrifuge speed during centrifugal filtration in step (5) is 4000-6000r/min, and the centrifugation time is 15-20min; the microporous membrane is a mixed cellulose microporous membrane with a pore size of 20-50 μm; the vacuum pump is - 0.1MPa circulating water vacuum pump.
本发明的有益效果:本发明制备的红鲷鱼鱼鳞蛋白具有一般蛋白所具有的特性,可应用于食品、包装、化妆品等行业,且本发明采用的鱼鳞胶原蛋白的制备工艺生产成本低,周期短。Beneficial effects of the present invention: the red snapper fish scale protein prepared by the present invention has the characteristics of general protein, and can be applied to industries such as food, packaging, cosmetics, etc., and the preparation process of fish scale collagen adopted by the present invention has low production cost and short cycle time. short.
具体实施方式detailed description
下面将结合具体实施例对本发明作进一步的说明。The present invention will be further described below in conjunction with specific embodiments.
本发明中采用的仪器有上海精密科学仪器公司制造的FC104 电子分析天平;上海雷磁仪器厂制造的PHS-25型酸度计;上海浦东荣丰科学仪器有限公司制造的876A-S2真空干燥箱;无锡市瑞江分析仪器有限公司制造的RJ-TDL-50A 离心机 ;HN-15-0510反应釜;爱拓公司的master-53α浓度仪。The instrument that adopts in the present invention has the FC104 electronic analytical balance that Shanghai Precision Scientific Instrument Company manufactures; The PHS-25 type acidity meter that Shanghai Lei Magnetic Instrument Factory manufactures; The 876A-S2 vacuum oven that Shanghai Pudong Rongfeng Scientific Instrument Co., Ltd. manufactures; RJ-TDL-50A centrifuge manufactured by Wuxi Ruijiang Analytical Instrument Co., Ltd.; HN-15-0510 reaction kettle; master-53α concentration meter of Aituo Company.
实施例1 红鲷鱼鱼鳞蛋白的制备方法,包括如下步骤:The preparation method of embodiment 1 red snapper fish scale protein, comprises the steps:
(1)干鱼鳞清洗:秤取600g干鱼鳞,对干鱼鳞用清水进行清洗,去掉表面的杂质后,晾干。(1) Cleaning of dried fish scales: Weigh 600g of dried fish scales, wash the dried fish scales with clean water, remove surface impurities, and dry them in the air.
(2)脱灰处理:秤取500g清洗晾干后的鱼鳞,将鱼鳞放入浸泡罐中,再加入5L0.2mol/L的盐酸,对红鲷鱼鱼鳞进行浸泡脱灰处理10h,边浸泡边搅拌,转速为20r/min。(2) Deliming treatment: Weigh 500g of fish scales after cleaning and drying, put the scales into a soaking tank, then add 5L0.2mol/L hydrochloric acid, soak and deash the red snapper scales for 10 hours, and soak them while soaking. Stir at a speed of 20r/min.
(3)清洗:用清水对(2)中处理后的鱼鳞进行清洗3遍后,准备提胶。(3) Cleaning: Wash the fish scales treated in (2) three times with clean water, and prepare for gel extraction.
(4)提胶:在清洗后的鱼鳞中加入10倍体积自来水后,将提胶罐加热至70℃,搅拌速度为40r/min,保持3h后过滤掉固体鱼鳞制得胶原液。(4) Gel extraction: Add 10 times the volume of tap water to the cleaned fish scales, heat the gel tank to 70°C, stir at 40r/min, keep for 3 hours, and filter out the solid fish scales to obtain a collagen solution.
(5)离心过滤:用离心机对提取的鱼鳞胶原液进行离心,用微孔滤膜和真空泵对胶原液进行真空抽滤,收取滤液。过滤时的离心机转速为4000r/min,离心时间为20min;所述微孔滤膜为孔径为20μm的混合纤维素微孔滤膜;真空泵为-0.1MPa的循环水式真空泵。(5) Centrifugal filtration: Centrifuge the extracted fish scale collagen solution with a centrifuge, vacuum filter the collagen solution with a microporous filter membrane and a vacuum pump, and collect the filtrate. The rotating speed of the centrifuge during filtration is 4000r/min, and the centrifugation time is 20min; the microporous membrane is a mixed cellulose microporous membrane with a pore size of 20 μm; the vacuum pump is a circulating water vacuum pump of -0.1MPa.
(6)去离子:将处理过的阴阳树脂分别装在两个柱子中,胶液依次通过阳阴离子柱,去掉胶原液中的阴阳杂离子。(6) Deionization: The treated anion and cation resins are respectively installed in two columns, and the glue solution passes through the anion and anion columns in turn to remove the anion and cation heteroions in the collagen solution.
(7)浓缩:用三效浓缩装置将制得的胶原液进行浓缩至28%。(7) Concentration: Concentrate the prepared collagen solution to 28% with a three-effect concentration device.
(8)喷粉:采用喷雾干燥机进行喷粉,进口热风温度为 160℃,出口热风温度 80℃,制得红鲷鱼鱼鳞胶原蛋白粉。(8) Powder spraying: use a spray dryer for powder spraying, the inlet hot air temperature is 160°C, and the outlet hot air temperature is 80°C to prepare red snapper scale collagen powder.
实施例2 红鲷鱼鱼鳞蛋白的制备方法,包括如下步骤:The preparation method of embodiment 2 red snapper fish scale protein, comprises the steps:
(1)干鱼鳞清洗:秤取600g干鱼鳞,对干鱼鳞用清水进行清洗,去掉表面的杂质后,晾干。(1) Cleaning of dried fish scales: Weigh 600g of dried fish scales, wash the dried fish scales with clean water, remove surface impurities, and dry them in the air.
(2)脱灰处理:秤取500g晾干后的鱼鳞,将鱼鳞放入浸泡罐中,再加入5L 0.5mol/L的盐酸,对红鲷鱼鱼鳞进行浸泡脱灰处理16h,边浸泡边搅拌,转速为60r/min。(2) Deliming treatment: Weigh 500g of dried fish scales, put the fish scales into a soaking tank, then add 5L of 0.5mol/L hydrochloric acid, soak and deash the red snapper scales for 16 hours, and stir while soaking , the speed is 60r/min.
(3)清洗:用清水对(2)中处理后的鱼鳞进行清洗5遍后,准备提胶。(3) Cleaning: After cleaning the fish scales treated in (2) 5 times with clean water, prepare for gel extraction.
(4)提胶:在清洗后的鱼鳞中加入14倍体积自来水后,将提胶罐加热至100℃,搅拌速度为60r/min,保持5h后过滤掉固体鱼鳞制得胶原液。(4) Glue extraction: After adding 14 times the volume of tap water to the cleaned fish scales, heat the rubber extraction tank to 100°C with a stirring speed of 60r/min, keep for 5 hours, and then filter out the solid fish scales to obtain a collagen solution.
(5)离心过滤:用离心机对提取的鱼鳞胶原液进行离心,用微孔滤膜和真空泵对胶原液进行真空抽滤,收取滤液。过滤时的离心机转速为6000r/min,离心时间为15min;所述微孔滤膜为孔径为50μm的混合纤维素微孔滤膜;真空泵为-0.1MPa的循环水式真空泵。(5) Centrifugal filtration: Centrifuge the extracted fish scale collagen solution with a centrifuge, vacuum filter the collagen solution with a microporous filter membrane and a vacuum pump, and collect the filtrate. The rotating speed of the centrifuge during filtration is 6000r/min, and the centrifugation time is 15min; the microporous membrane is a mixed cellulose microporous membrane with a pore size of 50 μm; the vacuum pump is a circulating water vacuum pump of -0.1MPa.
(6)去离子:将处理过的阴阳树脂分别装在两个柱子中,胶液依次通过阳阴离子柱,去掉胶原液中的阴阳杂离子。(6) Deionization: The treated anion and cation resins are respectively installed in two columns, and the glue solution passes through the anion and anion columns in turn to remove the anion and cation heteroions in the collagen solution.
(7)浓缩:用三效浓缩装置将制得的胶原液进行浓缩至40%。(7) Concentration: Concentrate the prepared collagen solution to 40% with a three-effect concentration device.
(8)喷粉:采用喷雾干燥机进行喷粉,进口热风温度为 200℃,出口热风温度 100℃,制得红鲷鱼鱼鳞胶原蛋白粉。(8) Powder spraying: use a spray dryer for powder spraying, the inlet hot air temperature is 200°C, and the outlet hot air temperature is 100°C to prepare red snapper scale collagen powder.
实施例3 红鲷鱼鱼鳞蛋白的制备方法,包括如下步骤:The preparation method of embodiment 3 red snapper fish scale protein, comprises the steps:
(1)干鱼鳞清洗:秤取600g干鱼鳞,对干鱼鳞用清水进行清洗,去掉表面的杂质后,晾干。(1) Cleaning of dried fish scales: Weigh 600g of dried fish scales, wash the dried fish scales with clean water, remove surface impurities, and dry them in the air.
(2)脱灰处理:秤取500g晾干后的鱼鳞,将鱼鳞放入浸泡罐中,再加入5L 0.4mol/L的盐酸,对红鲷鱼鱼鳞进行浸泡脱灰处理10h,边浸泡边搅拌,转速为50r/min。(2) Deliming treatment: weigh 500g of dried fish scales, put the fish scales into a soaking tank, then add 5L of 0.4mol/L hydrochloric acid, soak and deash the red snapper scales for 10 hours, and stir while soaking , the speed is 50r/min.
(3)清洗:用清水对(2)中处理后的鱼鳞进行清洗4遍后,准备提胶。(3) Cleaning: After cleaning the fish scales treated in (2) 4 times with clean water, prepare for gel extraction.
(4)提胶:在清洗后的鱼鳞中加入12倍体积自来水后,将提胶罐加热至80℃,搅拌速度为50r/min,保持4h后过滤掉固体鱼鳞制得胶原液。(4) Gel extraction: After adding 12 times the volume of tap water to the cleaned fish scales, heat the gel extraction tank to 80°C with a stirring speed of 50r/min, keep for 4 hours, and then filter out the solid fish scales to obtain a collagen solution.
(5)离心过滤:用离心机对提取的鱼鳞胶原液进行离心,用微孔滤膜和真空泵对胶原液进行真空抽滤,收取滤液。过滤时的离心机转速为5000r/min,离心时间为18min;所述微孔滤膜为孔径为30μm的混合纤维素微孔滤膜;真空泵为-0.1MPa的循环水式真空泵。(5) Centrifugal filtration: Centrifuge the extracted fish scale collagen solution with a centrifuge, vacuum filter the collagen solution with a microporous filter membrane and a vacuum pump, and collect the filtrate. The rotating speed of the centrifuge during filtration is 5000r/min, and the centrifugation time is 18min; the microporous membrane is a mixed cellulose microporous membrane with a pore size of 30 μm; the vacuum pump is a circulating water vacuum pump of -0.1MPa.
(6)去离子:将处理过的阴阳树脂分别装在两个柱子中,胶液依次通过阳阴离子柱,去掉胶原液中的阴阳杂离子。(6) Deionization: The treated anion and cation resins are respectively installed in two columns, and the glue solution passes through the anion and anion columns in turn to remove the anion and cation heteroions in the collagen solution.
(7)浓缩:用三效浓缩装置将制得的胶原液进行浓缩至35%。(7) Concentration: Concentrate the prepared collagen solution to 35% with a three-effect concentration device.
(8)喷粉:采用喷雾干燥机进行喷粉,进口热风温度为 180℃,出口热风温度 80℃,制得红鲷鱼鱼鳞胶原蛋白粉。(8) Powder spraying: use a spray dryer for powder spraying, the inlet hot air temperature is 180°C, and the outlet hot air temperature is 80°C to prepare red snapper scale collagen powder.
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Publication number | Priority date | Publication date | Assignee | Title |
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CN109777126A (en) * | 2019-03-20 | 2019-05-21 | 江南大学 | A kind of fish scale collagen/curly grass polysaccharide blend film and preparation method thereof |
CN109769920A (en) * | 2019-03-20 | 2019-05-21 | 江南大学 | A kind of fish scale protein-celestial glue-asparagus powder nutritious edible film and preparation method thereof |
CN114947111A (en) * | 2022-07-16 | 2022-08-30 | 广东欧帝玛生物工程有限公司 | Method for preparing food gum by mixing soybean hulls and fish scales |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20070231878A1 (en) * | 2004-10-27 | 2007-10-04 | Fisheries Research Institute | Collagen of fish scale and method of making thereof |
CN102952837A (en) * | 2011-08-19 | 2013-03-06 | 上海华睿生物科技有限公司 | Medical fish collagen polypeptide raw material and its preparation technology |
CN103540635A (en) * | 2013-09-23 | 2014-01-29 | 石狮海星食品有限公司 | Preparation process of fish scale collagen protein |
-
2016
- 2016-11-15 CN CN201611002904.3A patent/CN106615597A/en active Pending
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20070231878A1 (en) * | 2004-10-27 | 2007-10-04 | Fisheries Research Institute | Collagen of fish scale and method of making thereof |
CN102952837A (en) * | 2011-08-19 | 2013-03-06 | 上海华睿生物科技有限公司 | Medical fish collagen polypeptide raw material and its preparation technology |
CN103540635A (en) * | 2013-09-23 | 2014-01-29 | 石狮海星食品有限公司 | Preparation process of fish scale collagen protein |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN109777126A (en) * | 2019-03-20 | 2019-05-21 | 江南大学 | A kind of fish scale collagen/curly grass polysaccharide blend film and preparation method thereof |
CN109769920A (en) * | 2019-03-20 | 2019-05-21 | 江南大学 | A kind of fish scale protein-celestial glue-asparagus powder nutritious edible film and preparation method thereof |
CN114947111A (en) * | 2022-07-16 | 2022-08-30 | 广东欧帝玛生物工程有限公司 | Method for preparing food gum by mixing soybean hulls and fish scales |
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