CN103238723B - Preparation method of low-fluorine euphausia superb hydrolyzed protein powder - Google Patents

Preparation method of low-fluorine euphausia superb hydrolyzed protein powder Download PDF

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CN103238723B
CN103238723B CN201210029946.1A CN201210029946A CN103238723B CN 103238723 B CN103238723 B CN 103238723B CN 201210029946 A CN201210029946 A CN 201210029946A CN 103238723 B CN103238723 B CN 103238723B
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protein
active charcoal
cocoanut active
feed liquid
content
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CN103238723A (en
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何兰
王南平
曹俊
郭休玉
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Shanghai Fisheries Research Institute Shanghai Fisheries Technical Extension Station
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Shanghai Fisheries Research Institute
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Abstract

A preparation method of a low-fluorine euphausia superb hydrolyzed protein powder relates to processing of a euphausia superb protein powder. The preparation method provided by invention is characterized by comprising the following steps: rubbing fresh euphausia superb, adding 2 times of water, mixing, heating to 100-105 DEG C, stirring for 30 min, cooling to an enzymolysis temperature, adding protease and carrying out enzymatic hydrolysis for 2 hours, heating to 90-95 DEG C, keeping for 20 min and killing enzyme, filtering to remove shrimp shell and impurities, letting a feed liquid pass through nanofiltration membrane to be dehydrated until the protein content is 20%+/-2%, adding 4% of cocoanut active charcoal, heating to 70-80 DEG C, stirring for 15-30 min, filtering to remove cocoanut active charcoal, adding 5-7 times of deionized water to dilute a hydrolyzed protein fluid, dehydrating by the use of the nanofiltration membrane until the content of protein in the feed liquid is greater than or equal to 20%, adding 4% of cocoanut active charcoal, heating to 70-80 DEG C, stirring for 15-30 min, filtering to remove cocoanut active charcoal, carrying out vacuum concentration until the protein concentration is 35%-40%, and carrying out spray drying to prepare the dry protein powder.

Description

A kind of preparation method of low fluorine krill aminosal powder
Technical field
The present invention relates to the processing method of krill protein powder, especially a kind of method of preparing low fluorine krill aminosal powder.
Background technology
Krill is that a kind of reserves are huge, has the protein resource of potential value of exploiting and utilizing.Its appreciable reserves are hundred million tons of 4-6.Krill protein content is high, and in muscle, protein content accounts for 64%(in dry), its amino acid content is abundant, and 8 kinds of essential amino acid proportions 45.28%, are a kind of high-quality marine animal property protein.In the marine eco-environment of krill in high latitude low temperature, in its crust transformation process, absorbing the calcium ions and magnesium ions of fluorine ion excessive in seawater in crust is combined, a large amount of fluorine is deposited among crust, after the dried up death of krill under the effect of shrimp body endoenzyme, fluorine ion penetrates among muscle, makes the fluorine content in krill muscle higher.Result of study shows krill fluorine content distribution: crust mean value 4028 μ g/g, and head (connecting feeler) mean value is 2724 μ g/g, and uropodium mean value is 2828 μ g/g, and muscle mean value is 226 μ g/g, ensemble average value is 1232 μ g/g(butts).Because the fluorine content of krill is far above China GB2762-2005 food contaminant fluorine Limited Doses, fish (fresh water) are less than the regulation of 2.0mg/kg, make the krill can not be direct edible as other marine products shrimp.Because fluorine content is higher than edible scope, the essential method of biotechnology defluorinate of passing through of utilization that makes krill, changes into water-solubility protein by the albumen of krill, removes the fluorine ion in the aqueous solution, and then be dried into protein powder, become edible albumen.Because fluorine ion is mainly present in trade effluent, carry out ion exchange with calcium chloride, with aluminium electrode enrichment fluorine ion etc. be to derive from sewage disposal to go fluorine method, among being applied to food production, can cause protein powder salt content high, the problems such as ash, content of beary metal exceed standard, do not meet requirement and the specification of food production.
Summary of the invention
The problem that the present invention need to solve is to provide one and meets food production specification, and production technology is simple and safe, is applicable to the preparation method of the krill protein powder of the low fluorine content of large-scale production.
Technical scheme of the present invention is that complete fresh krill shrimp or shrimp are rubbed and add the water of 2 times of full shrimp or shrimp weight to be uniformly mixed, be warmed to 100~105 DEG C, stir 30 minutes, cool to after 45 DEG C ± 2 DEG C protease hydrolyzed temperature, add 0.2~0.5% trypsase or papain, constant temperature enzymolysis 2 hours, then be warmed up to 20 minutes enzymes that go out of 90~95 DEG C of maintenances, filter and remove shrimp shell and impurity, feed liquid is crossed to NF membrane dewaters to protein content 20% ± 2%, add the cocoanut active charcoal of protein content 20% feed liquid weight 4%, being heated to 70~80 DEG C stirs 15~30 minutes, filter and remove cocoanut active charcoal, add the deionized water of 5 to 7 times of material liquid volumes, dilution hydrolyzed protein liquid, again dewater by NF membrane, until protein in feed liquid content >=20%, add again the cocoanut active charcoal of protein content 20% feed liquid weight 4%, being heated to 70~80 DEG C stirs 15~30 minutes, filter and remove cocoanut active charcoal, Vacuum Concentration is to protein concentration 35%-40% again, be made into protein dry powder with spray dryer.
The present invention's cocoanut active charcoal is fluorine ion adsorption aid, has safe and effective free from extraneous odour, meets the effect of food sanitation safe requirement, can't produce new salt, heavy metal and objectionable impurities.Utilize biological Nanofiltration-membrane technique that the fluorine ion in liquid is got rid of, safe and reliable, technique is simple, easy to operate, meets the krill protein Process requirement of producing low fluorine content in enormous quantities.Can obtain ash content below 5%, the krill protein powder below fluorine content 10ppm, the rate of recovery of krill muscle protein can reach 45~55%.
Brief description of the drawings
What Fig. 1 represented is process flow diagram of the present invention.
Detailed description of the invention
Get fresh krill meat, add 2 times of water 1:2 (w/v), be warmed to 100~105 DEG C, stir and keep temperature 30 minutes, be cooled to 45 DEG C ± 2 DEG C of the applicable operating temperatures of protease, add 0.2~0.5% trypsase (papain) to stir hydrolysis 2 hours, be warmed up to 90~95 DEG C of 20 minutes enzymes that go out, with plate-frame filtering removal shell and impurity, feed liquid is crossed NF membrane dehydration, reach 20% ± 2% to protein content, add 4% (W/V) cocoanut active charcoal, keep 70~80 DEG C of feed temperatures, stir 15~30 minutes, plate-frame filtering is removed cocoanut active charcoal, add the deionized water of 5 to 7 times, washing protein hydrolysate, again with biological NF membrane dehydration, until feed liquid protein content reaches 20% ± 2%, add again 4% (W/V) cocoanut active charcoal, being heated to 70~80 DEG C stirs 15~30 minutes, plate-frame filtering is removed cocoanut active charcoal, Vacuum Concentration, to protein content 35~40%, the dry protein dry powder that is made into of spraying.
Embodiment 1
(1) get fresh krill meat 1000g and be placed in reactor, the 2000g that adds water is heated with stirring to 100~105 DEG C in reactor, keeps 30 minutes.
(2) fluid temperature is down to after 45 DEG C ± 2 DEG C, adds trypsase 0.2%, constant temperature hydrolysis is stirred 2 hours, is warming up to 95 DEG C ± 2 DEG C, keeps 20min, and the enzyme that goes out is lived.
(3) emit feed liquid, with flame filter press separation slag liquid, elimination impurity and insoluble matter.
(4) feed liquid after filtering is dewatered with NF membrane GE rolling Ro film 1812, reaches 20% ± 2% to protein in feed liquid concentration.
(5) add 4%(w/v) cocoanut active charcoal, be warming up to 75 DEG C ± 2 DEG C, stir 15 minutes.
(6) feed liquid is filtered through plate filter, separates cocoanut active charcoal.
(7) in the feed liquid after filtering, slowly add 5-7 deionized water doubly. dewater to protein concentration 18-20% with NF membrane GE rolling Ro film 1812.
(8) again add 4%(w/v) cocoanut active charcoal, be warming up to 75 DEG C ± 2 DEG C, stir 15 minutes.
(9) feed liquid is filtered through plate filter, separates cocoanut active charcoal.
(10) feed liquid Vacuum Concentration, more than vacuum 0.08Mpa, 80 DEG C ± 2 DEG C of temperature, boiling is concentrated in solution protein content and stops 35~40% time.
(11) the krill albumen feed liquid after above-mentioned concentrating is sprayed and is dried, can obtain ash content below 5%, the krill protein powder below fluorine content 10ppm.
Embodiment 2
(1) get fresh krill 1000g, water 2000g, is placed on and in reactor, stirs and be heated to 105 DEG C ± 2 DEG C, and keep 30 minutes.
(2) feed liquid temperature is down to 45 DEG C ± 2 DEG C, adds the 0.2%-0.5% papain that fresh krill is heavy, constant temperature hydrolysis is stirred 2 hours.
(3) hydrolyzate is warming up to 95 DEG C ± 2 DEG C.Keep 15 minutes enzymes that go out.
(4) emit feed liquid, with centrifuge separation, the residue of getting rid of shrimp shell and not being hydrolyzed.
(5) feed liquid is dewatered once with reverse osmosis membrane, with NF membrane GE rolling Ro film 1812, is concentrated into feed liquid protein concentration 20% ± 2%.
(6) add cocoanut active charcoal 4%(w/v), be warming up to 75 DEG C ± 2 DEG C, stir 15 minutes.
(7) feed liquid is filtered with plate frame filter.
(8) in feed liquid, add the deionized water of 5~7 times to cross film, with NF membrane GE rolling Ro film 1812, be concentrated into protein concentration 20% ± 2%, get rid of waste water.
(9) in feed liquid, add 4%(w/v) cocoanut active charcoal, be warming up to 75 DEG C ± 2 DEG C, stir 15 minutes.
(10) feed liquid, through flame filter press, is got rid of cocoanut active charcoal, leaches clear liquid.
(11) Vacuum Concentration, by feed liquid more than vacuum 0.08MPa, 80 DEG C ± 2 DEG C of temperature, boiling is concentrated into protein content in feed liquid and stops in the time of 35-40%.
(12) feed liquid after concentrated is spray-dried, can obtain ash content below 5%, the krill protein powder below fluorine content 10ppm.

Claims (2)

1. the preparation method of one kind low fluorine krill aminosal powder, it is characterized in that complete fresh krill shrimp or shrimp to rub and add the water of 2 times of full shrimp or shrimp weight to be uniformly mixed, be warmed to 100~105 DEG C, stir 30 minutes, cool to after 45 DEG C ± 2 DEG C protease hydrolyzed temperature, add 0.2~0.5% trypsase or papain, constant temperature enzymolysis 2 hours, be warmed up to again 90~95 DEG C and keep 20 minutes enzymes that go out, filter and remove shrimp shell and impurity, feed liquid is crossed to NF membrane dewaters to protein content 20% ± 2%, add the cocoanut active charcoal of protein content 20% feed liquid weight 4%, being heated to 70~80 DEG C stirs 15~30 minutes, filter and remove cocoanut active charcoal, add the deionized water of 5 to 7 times of material liquid volumes, dilution hydrolyzed protein liquid, again dewater by NF membrane, until protein in feed liquid content >=20%, add again the cocoanut active charcoal of protein content 20% feed liquid weight 4%, being heated to 70~80 DEG C stirs 15~30 minutes, filter and remove cocoanut active charcoal, Vacuum Concentration is to protein concentration 35%~40% again, be made into protein dry powder with spray dryer.
2. the preparation method of a kind of low fluorine krill aminosal powder according to claim 1, is characterized in that spray-dired protein dry powder ash content is below 5%, below fluorine content 10ppm.
CN201210029946.1A 2012-02-10 2012-02-10 Preparation method of low-fluorine euphausia superb hydrolyzed protein powder Active CN103238723B (en)

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP4091620A1 (en) * 2018-01-30 2022-11-23 Aker Biomarine Antarctic As Krill protein hydrolysate with low fluoride and trimethylamin content

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CN104232717A (en) * 2014-09-12 2014-12-24 中国海洋大学 Method for reducing fluorine content in water soluble active peptides from Antarctic krill
CN105248833A (en) * 2015-10-23 2016-01-20 天津核生科技生物工程有限公司 Method for extracting shrimp protein nutrients used for enhancing immunity and relieving fatigue
CN105639044A (en) * 2016-01-22 2016-06-08 中国海洋大学 Edible euphausia superba proteolipid compound and processing method thereof
CN107114605A (en) * 2017-04-28 2017-09-01 广东越群海洋生物研究开发有限公司 Application of the euphausia superba powder in terms of blood parrot opening material is prepared
CN110452946A (en) * 2019-08-06 2019-11-15 大连工业大学 A kind of preparation method of the krill antioxidant peptide powder of low fluorine hypoallergenic
CN114181988A (en) * 2021-12-23 2022-03-15 武汉梁子湖水产品加工有限公司 Euphausia superba meat protein peptide and preparation method thereof

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0667307B2 (en) * 1990-02-13 1994-08-31 財団法人韓国食品開発研究院 Antarctic shrimp weight loss method
CN1644073A (en) * 2005-01-25 2005-07-27 江南大学 Method for processing fent by comprehensive utilizing shrimp by enzyme method
CN1648064A (en) * 2004-12-25 2005-08-03 李玉堂 Water purifier for removing fluorine and arsenic and preparing method
CN101756147A (en) * 2010-01-29 2010-06-30 天津商业大学 Method for preparing low allergen shrimp base material by enzyme method
CN102059093A (en) * 2009-11-18 2011-05-18 中国科学院生态环境研究中心 Arsenic and fluorine removing nano-composite adsorbent
CN102170795A (en) * 2008-09-12 2011-08-31 翡翠渔业公司 Process for reducing the fluoride content when producing proteinaceous concentrates from krill
CN102342541A (en) * 2011-09-02 2012-02-08 中国水产科学研究院东海水产研究所 Method for reducing content of fluorine in enzymatic hydrolysate of Euphausia superb by using calcined lime

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0667307B2 (en) * 1990-02-13 1994-08-31 財団法人韓国食品開発研究院 Antarctic shrimp weight loss method
CN1648064A (en) * 2004-12-25 2005-08-03 李玉堂 Water purifier for removing fluorine and arsenic and preparing method
CN1644073A (en) * 2005-01-25 2005-07-27 江南大学 Method for processing fent by comprehensive utilizing shrimp by enzyme method
CN102170795A (en) * 2008-09-12 2011-08-31 翡翠渔业公司 Process for reducing the fluoride content when producing proteinaceous concentrates from krill
CN102059093A (en) * 2009-11-18 2011-05-18 中国科学院生态环境研究中心 Arsenic and fluorine removing nano-composite adsorbent
CN101756147A (en) * 2010-01-29 2010-06-30 天津商业大学 Method for preparing low allergen shrimp base material by enzyme method
CN102342541A (en) * 2011-09-02 2012-02-08 中国水产科学研究院东海水产研究所 Method for reducing content of fluorine in enzymatic hydrolysate of Euphausia superb by using calcined lime

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
祁鲁梁等.纳滤膜的应用.《水处理药剂及材料使用手册》.中国石化出版社,2000,(第1版),第494-495页. *

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP4091620A1 (en) * 2018-01-30 2022-11-23 Aker Biomarine Antarctic As Krill protein hydrolysate with low fluoride and trimethylamin content

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