CN206089712U - Whole blood peptide powder extraction element - Google Patents

Whole blood peptide powder extraction element Download PDF

Info

Publication number
CN206089712U
CN206089712U CN201620870483.5U CN201620870483U CN206089712U CN 206089712 U CN206089712 U CN 206089712U CN 201620870483 U CN201620870483 U CN 201620870483U CN 206089712 U CN206089712 U CN 206089712U
Authority
CN
China
Prior art keywords
whole blood
gly
lys
liquid
extraction element
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.)
Active
Application number
CN201620870483.5U
Other languages
Chinese (zh)
Inventor
白祖国
彭文博
熊福军
邓唯
丁邦超
杨文银
张建嵩
杨积衡
范克银
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Jiangsu Jiuwu Hi Tech Co Ltd
Original Assignee
Jiangsu Jiuwu Hi Tech Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Jiangsu Jiuwu Hi Tech Co Ltd filed Critical Jiangsu Jiuwu Hi Tech Co Ltd
Priority to CN201620870483.5U priority Critical patent/CN206089712U/en
Application granted granted Critical
Publication of CN206089712U publication Critical patent/CN206089712U/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Landscapes

  • Separation Using Semi-Permeable Membranes (AREA)

Abstract

The utility model relates to a whole blood peptide powder extraction element, especially one kind is drawed the whitewashed method of whole blood peptide with enzyme hydrolysis, ceramic membrane, reverse osmosis method coupling, belongs to biotechnology enzymolysis whole blood albumen and membrane separation technique field. Including: enzymolysis tank (1) for it handles to carry out the enzymolysis to livestock blood, solid -liquid separation equipment (8) for enzymolysis liquid to obtaining among the enzymolysis tank carries out solid -liquid separation disposal, milipore filter (4) for the edulcoration is filtered to feed liquid to behind the solid -liquid separation, reverse osmosis membrane (6) for penetrant to milipore filter (4) carries out the concentration processing. The device can obtain protein in the livestock blood effectively to draw the acid soluble protein content of product, the extraction efficiency is high, can isolate polypeptide and amino acid simultaneously, has realized cleaner production, has reduced area.

Description

A kind of whole blood Gly-His-Lys extraction element
Technical field
The utility model is related to a kind of whole blood Gly-His-Lys extraction element, particularly a kind of by enzyme hydrolysis, ceramic membrane, hyperfiltration The method that whole blood Gly-His-Lys are extracted in coupling, belongs to biotechnology enzymolysis whole blood albumen and technical field of membrane separation.
Background technology
At present, of paramount importance albumen source is fish meal in China's feed.Gly-His-Lys as a kind of good feed addictive, Per kilogram can produce the kilocalorie of digestible energy 41, and rich in protein, fat and various trace elements, nutrient content is comprehensive.Chicken, pig, Add Gly-His-Lys in the animal and fowl fodders such as ox, growth of animals or poultry can be promoted, shorten breeding cycle.Gly-His-Lys animal digestion rate relies ammonia up to 90% Acid is 7%~8%, is, leucine content 8% or so higher than fish meal, digested tankage content first of all natural feeds.In addition, livestock Blood accounts for body weight 8%, and the recovery ratio of blood accounts for the 3%~5% of body weight, for the whole nation, can be used to process profit Livestock blood is a huge numeral.Now some areas, can replacing whole using Gly-His-Lys and the mutual compatibility of feather meal High-quality fish meal.
Chinese patent CN101843289B discloses a kind of use enzymatic isolation method and whole blood polypeptide albumen powder is extracted from livestock blood Method, by selecting suitable substrates concentration, proteolysis complex enzyme and reaction temperature, makes livestock blood pass through enzymolysis, reduction, be dried Whole blood polypeptide albumen powder is obtained with crushing.Patent CN101263861B discloses a kind of method of extraction annimal hydrolyzed protein powder, Annimal hydrolyzed protein powder is obtained after enzyme hydrolysis, filtration, evaporation and concentration, drying.Although the protein one that above-mentioned method is extracted Determine degree and remain its biologically active, but filtering accuracy is not high, therefore product purity is not high, additionally, adopted condensing mode is equal To be concentrated by evaporation, the removal of the salts substances in high energy consumption and product is studied.Therefore a kind of economically feasible is developed, is produced The high easily absorbed method of protein of product purity.
Utility model content
The purpose of this utility model is to provide a kind of whole blood Gly-His-Lys extraction element, needs to improve and extracts purity of protein, increases The content of sour molten albumen in finished product, and it is simple to operate, pollute it is little, can realize clean manufacturing, suitable for large-scale production.Mainly Purified concentration operation is carried out by ceramic membrane ultrafitration+reverse osmosis membrane integrated technology, the concrete technical scheme of employing is as follows:
A kind of whole blood Gly-His-Lys extracting method, comprises the steps:
1st step, in livestock blood add enzyme digested;
2nd step, enzymolysis liquid carry out separation of solid and liquid process;
The feed liquid that 3rd step, separation of solid and liquid are obtained carries out filtering and impurity removing by milipore filter;
4th step, the permeate of milipore filter are again through reverse osmosis membrane concentration.
Described livestock blood is the blood obtained after the butchering of pig, ox, sheep, horse, donkey, chicken, duck, goose etc..
In the 1st described step, it is trypsase, pancreatinum, chymotrypsin, stomach cardia to digest the ferment for using In the protein decomposition enzymes such as enzyme, papain, kallikrein, cathepsin, thermolysin or V8 protease One or several combination;55~70 DEG C of hydrolysis temperature, digests pH7~9, enzymolysis time 2~2.5 hours.
In the 2nd described step, the mode of separation of solid and liquid selected from centrifugation mode, expression separation mode, filter type, on One or several combination in floating separate mode, sedimentation separation mode;It is preferred that first using coarse filter again using centrifugation Separated.
In the 3rd described step, the 1000~200000Da of molecular cut off of described milipore filter, the material of milipore filter is selected from Cellulose, cellulose esters, polysulfones, polyether sulfone, polyvinyl chloride, chloropropene, polyolefin, polyvinyl alcohol, polymethyl methacrylate, One or several combination in polyvinylidene fluoride, polytetrafluoroethylene (PTFE), ceramics.
In the 3rd described step, described milipore filter is ceramic super-filtering film, and the scope of average pore size is 50~200nm, cross-film Pressure differential range is 0.1~0.3MPa, and 2~5m/s of crossflow velocity, ultra-filtration filters temperature is preferably 40~60 DEG C, and multiple is concentrated by ultrafiltration It is 3~4 times.
In the 4th described step, the material of reverse osmosis membrane is sub- selected from birds of the same feather flock together compound, polyamide, polyester, polyamides of cellulose acetate One or several combination in amine or polyvinyl etc.;Reverse osmosis process preferred parameter is:Operating pressure is 2.5 ~3.0MPa, circular flow is 2.0~3.0m3/ h, cycles of concentration is 2~3 times.
In one embodiment, the concentrate drying that reverse osmosis membrane is obtained is processed;Dried process is preferably using spray Mist is dried.
In one embodiment, the permeate of milipore filter is after electrodialysis desalination, be re-fed into reverse osmosis membrane carry out it is dense Contracting.The preferred operational factor of electrodialysis desalination is:Electrodialysis operation voltage is 100~200V, 1~3A of electric current, and feed pressure is 0.05~0.2MPa.
A kind of whole blood Gly-His-Lys extraction element, includes:
Enzymatic vessel, for carrying out enzymolysis processing to livestock blood;
Equipment for separating liquid from solid, for carrying out separation of solid and liquid process to the enzymolysis liquid obtained in enzymatic vessel;
Milipore filter, for carrying out filtering and impurity removing to the feed liquid after separation of solid and liquid;
Reverse osmosis membrane, for carrying out concentration to the penetrating fluid of milipore filter 4.
Described equipment for separating liquid from solid is filled selected from centrifugal separating device, expression separation device, filter, separation of floating Put, one or several the component in settling separation device;It is preferred that first using the combination of centrifugal separating device and coarse filter, Centrifugal separating device is used to carry out enzymolysis liquid centrifugal treating, and the mother liquor that coarse filter is used to obtain centrifugal separating device is carried out Filtering and impurity removing process.
1000~the 200000Da of molecular cut off of described milipore filter, the material of milipore filter is selected from cellulose, cellulose Ester, polysulfones, polyether sulfone, polyvinyl chloride, chloropropene, polyolefin, polyvinyl alcohol, polymethyl methacrylate, polyvinylidene fluoride, One or several combination in polytetrafluoroethylene (PTFE), ceramics.
Described milipore filter is ceramic super-filtering film, and the scope of average pore size is 50~200nm.
The material of reverse osmosis membrane selected from cellulose acetate birds of the same feather flock together compound, polyamide, polyester, polyimides or vinyl gather One or several combination in compound etc..
In one embodiment, drying device is also included, for being dried process to the concentrate of reverse osmosis membrane.
Drying device is spray-drying installation.
In one embodiment, electrodialysis plant is also included in device, for being concentrated into reverse osmosis membrane The penetrating fluid of milipore filter 4 carries out desalting processing.
Enzyme is also included in described device and adds part, for adding enzyme in livestock blood.
Beneficial effect
The utility model provides a kind of method that membrane separation technique extracts whole blood Gly-His-Lys, using enzyme hydrolysis and ceramic membrane+ Hyperfiltration is coupled, and simple to operate, recovery rate is high, and energy consumption is low, realizes clean manufacturing, reduces floor space.Ceramic excessive filtration Process greatly mitigates the pollution of electrodialysis desalination system and counter-infiltration system, and counter-infiltration system substitutes traditional economic benefits and social benefits and is concentrated by evaporation energy Substantially reduce energy consumption, improving product quality, it is adaptable to industrial production.
Description of the drawings
Fig. 1 is installation drawing of the present utility model.
Specific embodiment
The utility model is described in further detail below by specific embodiment.But those skilled in the art will Understand, the following example is merely to illustrate the utility model, and should not be regarded as limiting scope of the present utility model.In embodiment not Dated particular technique or condition person, enter according to the technology or condition described by document in the art or according to product description OK.Agents useful for same or the unreceipted production firm person of instrument, be can pass through city available from conventional products.
Using range format expression value should be interpreted as in a flexible way not only include clearly include as scope The numerical value of limit value, but also including all single numbers or subinterval for covering within the range, just as each numerical value and sub-district Between be expressly recited out.For example, the concentration range of " about 0.1% to about 5% " should be understood to not only include clearly including About 0.1% to about 5% concentration, also including in the range of alluding to single concentration (e.g., 1%, 2%, 3% and 4%) and son Interval (for example, 0.1% to 0.5%, 1% to 2.2%, 3.3% to 4.4%).Percentage described in the utility model is in nothing In the case of special instruction, percentage by weight is referred to.
" one embodiment ", " another embodiment ", " embodiment " for addressing in this manual etc., refer to Specific features, structure with reference to embodiment description are included at least one embodiment of the application generality description. It is not necessarily to refer to same embodiment that in the description statement of the same race occur in multiple places.Furthermore, it is understood that with reference to arbitrary When embodiment describes specific features, structure or a feature, what is advocated is realizing this spy with reference to other embodiment Levy, structure or feature also fall in the application scope of the claimed.
The extracting method first step of the present utility model is that the effect by digesting digests protein macromolecule in livestock blood, Make it be more easy to be separated, purified and be more easy to animal absorption, further, since can produce in enzymolysis process a part of polypeptide and Amino acid, simultaneously containing a large amount of impurity, the polypeptide and amino acid in this part of hydrolysate is sour molten albumen in finished product Gly-His-Lys Main constituents, need to separate it from protein, improve the quality of product, and the utility model to enzymolysis liquid by carrying out Solid-liquid initial gross separation, the detached process of ultrafiltration precision are by Impurity removal, then are extracted by reverse osmosis concentration, drying.Hydrolysis The parameter of technique includes the type of enzyme, enzymolysis pH, hydrolysis temperature and enzymolysis time etc., and the difference of enzymolysis process influences whether egg The Degree of Enzymatic Hydrolysis of white matter, the technological parameter of ultrafiltration, yield of product etc..If Degree of Enzymatic Hydrolysis is higher, protein can be caused excessive Be hydrolyzed and yield is low;If conversely, Degree of Enzymatic Hydrolysis not enough, can cause protein to be unable to complete hydrolysis, more albumen Matter can produce pollution to milipore filter.More preferably digesting parameter is:The ferment that uses of enzymolysis be trypsase, pancreatinum, Chymotrypsin, pepsin, papain, kallikrein, cathepsin, thermolysin and V8 protease Deng protein decomposition enzyme;55~70 DEG C of hydrolysis temperature, digests pH7~9, enzymolysis time 2~2.5 hours.
Livestock blood described in the utility model, is not particularly limited, as long as the blood of the livestock for generally cultivating is all It is achieved that for example:The blood obtained after the butchering of pig, ox, sheep, horse, donkey, chicken, duck, goose etc..
After enzymolysis liquid has been obtained, larger solids therein can be gone by way of separation of solid and liquid Remove, the mode of separation of solid and liquid here is not particularly limited.As the method for specific separation of solid and liquid process, centrifugation can be enumerated Separate mode, expression separation mode, filter type, floating separate mode, sedimentation separation mode.As centrifugation mode, can To illustrate horizontal continuous centrifuge (process of spiral decanter), separate board-like centrifugal separator, filter centrifugal, the general Le in tall building This type UCF ultracentrifuge, as filter type, can illustrate band filter, belt press, flypress, precoat filter, Filter press, as floating separate mode, can illustrate continuous floating separator, as sedimentation separation mode, can illustrate solidifying Collection sedimentation separation machine, rapid sedimentation separation machine etc., but it is not particularly limited in above-mentioned any one.But above-mentioned appointing can be passed through One or its combination are reducing when secondary filter film and/or ultrafiltration membrane treatment to the load of film.More preferably mode is to first pass through Centrifugation goes out solids, then with coarse filter after filtration, is re-fed into carrying out filtering and impurity removing to follow-up milipore filter.Centrifugation Parameter is preferably:2500~3000 revs/min of mair motor, 1000 revs/min of auxiliary motor.In 3rd step, hydrolysate firstly the need of Large granular impurity therein is removed by coarse filter, this is mainly livestock hair, skin etc., the pollution of milipore filter can be mitigated, carried High product purities, coarse filter can be conventional sheet frame, video disc etc..
Milipore filter used in the utility model, be molecular cut off be 1000~200000 film, referred to as ultrafiltration Film, UF films etc..Here, being difficult to determine the aperture on film surface with electron microscope etc. because the aperture of milipore filter is too small, institute To replace average pore size to be used as the index of pore size with the value of referred to as molecular cut off.With regard to molecular cut off, such as at this Described in the handbook of field:" will with molecular weight solute as transverse axis, prevention rate as the longitudinal axis, the curve for carrying out drawing to data Referred to as molecular cut off curve.And the molecular weight that prevention rate is 90% is referred to as into the molecular cut off of film ", molecular cut off is made To represent the index of the film properties of milipore filter, it is well known to those skilled in the art.
As the material of these milipore filters, as long as can realize removing as above-mentioned water soluble polymer and colloid composition The utility model purpose, is not particularly limited, and can enumerate:Cellulose, cellulose esters, polysulfones, polyether sulfone, polychlorostyrene second The organic materials such as alkene, chloropropene, polyolefin, polyvinyl alcohol, polymethyl methacrylate, polyvinylidene fluoride, polytetrafluoroethylene (PTFE), Or the inorganic material such as metal or ceramics such as stainless steel.The material of milipore filter can consider the proterties of zymolyte or operation Into original appropriate selection, consider from the service life of film, the milipore filter of preferably ceramic material.As many of composition ceramic separation film The material of pore membrane, can suitably select from existing known ceramic material.It is, for example possible to use aluminum oxide, zirconium oxide, oxidation The oxide materials such as magnesium, silica, titanium oxide, cerium oxide, yittrium oxide, barium titanate;Cordierite, mullite, magnesium olive The combined oxidation species material such as stone, steatite, sialon, zircon, ferrite;Silicon nitride, aluminum nitride and other nitride class Material;The carbon compound material such as carborundum;The hydroxide composition material such as hydroxyapatite;The element class material such as carbon, silicon;Or contain There are their two or more inorganic composite materials etc..Can also using natural minerals (clay, clay mineral, cry loudly slag, silica sand, Pottery stone, feldspar, white sand) or blast-furnace slag, flying dust etc..Wherein, be preferably selected from aluminum oxide, zirconium dioxide, titanium oxide, magnesia, Ceramic powder that is one kind or two or more in silica, more preferably being constituted as main body using aluminum oxide, zirconium dioxide or titanium oxide End.More than 50 overall mass % of " as main body " wherein, mentioned here expression ceramic powders (more than preferably 75 mass %, More preferably 80 mass %~100 mass %) it is aluminum oxide or silica.For example, in the porous material, aluminum oxide is relatively inexpensive And operability is excellent.Further, it is possible to be readily formed with the loose structure for being suitable for the detached aperture of liquid, therefore, it is possible to hold Manufacture of changing places has the ceramic separation film of excellent liquid permeability.Also, in above-mentioned aluminum oxide, particularly preferably using α-oxygen Change aluminium.Alpha-alumina has the characteristic of stable and fusing point and high mechanical strength in terms of chemistry.Therefore, by using alpha-oxidation Aluminium, can manufacture the ceramic separation film that can be utilized in broad use (such as industrial circle).
In the operating process of ceramic super-filtering film, to grope through lot of experiments, the scope of the average pore size of milipore filter is 50~ 200nm, because aperture is too big, the purity that can cause product declines;Aperture is too little, a part of protein while flux is relatively low Also it is trapped, product yield is reduced.The material of ceramic super-filtering film is preferably the one kind in aluminum oxide, zirconium oxide, titanium oxide.Super During filter, the selection of transmembrane pressure suffers from interactional pass with the average pore size of milipore filter, filtration flux, product purity System, if transmembrane pressure is excessive, per-meate side is reached after a part of protein colloid can be caused pressurized through fenestra, affects product pure Degree, if transmembrane pressure is too small, can cause filtration flux too small, and cost increases.Groping through lot of experiments, preferably across Film pressure differential range is 0.1~0.3MPa.Crossflow velocity influences whether filtration flux, if crossflow velocity is excessive, transmembrane pressure meeting Reduce, filtration flux can be too small, if crossflow velocity is too small, film surface pollution can aggravate, and flux stability can be reduced, preferred model It is 2~5m/s to enclose.Filtration temperature is preferably 40~60 DEG C, and cocnentration factor is preferably material and concentrates 3~4 times.
After the permeate for obtaining ultrafiltration, can concentration by way of feed liquid is processed so that amino acid and Polypeptide is concentrated, and here the mode of preferred concentration is concentrated using counter-infiltration, due to counter-infiltration for salt has one Fixed permeability, passes through can the part inorganic salts in material, so that amino acid and polypeptide are purified.
As the material of reverse osmosis membrane, generally use cellulose acetate and birds of the same feather flock together compound, polyamide, polyester, polyimides, second Alkenyl polymer Polymer material.In addition, as its construction, having and there is compacted zone at least side of film, from the compacted zone There is the anisotropic membrane of the minute aperture in the aperture for slowly becoming big to the surface of film inside or opposite side and in the anisotropic membrane Compacted zone on there is composite membrane of very thin active layer for being formed by other materials etc..Wherein, as the shape of reverse osmosis membrane Formula, there is macaroni yarn, flat film etc..Generally, it is preferred to the thickness of macaroni yarn peace film is 10 μm~1mm, the external diameter of macaroni yarn is 50 μm ~4mm.In addition, as flat film, preferred anisotropic membrane, as composite membrane preferably by substrate supports such as fabric, braid, non-woven fabrics Film.But, method of the present utility model is used in which can not rely on the material of reverse osmosis membrane, film construction or form, It is all effective for any one situation.As representational reverse osmosis membrane, for example, can enumerate cellulose acetate class or polyamide Class anisotropic membrane, with polyamide-based, polyureas active layer composite membrane etc..Wherein, method of the present utility model is for acetic acid Cellulose family anisotropic membrane, polyamide-based composite membrane are especially effective.Reverse osmosis membrane assembly is for actually used above-mentioned counter-infiltration Film and be allowed to the material of shape.In the case that the form of reverse osmosis membrane is flat film, can be incorporated into helical form, tubulose or plate with Used in the component of frame, in addition, in the case of macaroni yarn, component being incorporated on the basis of bundles of and be used. The utility model is suitable in which can not rely on the form of the composition of these reverse osmosis membrane assemblies.Reverse osmosis process preferred parameter is: Operating pressure is 2.5~3.0MPa, and circular flow is 2.0~3.0m3/ h, cycles of concentration is 2~3 times.Reverse osmosis concentration can be with Material liquid volume is substantially reduced, mitigates the load that subsequent spray is dried.Grope through many experiments, the choosing of reverse osmosis membrane molecular cut off 50Da~100Da is selected, because containing small molecule amino acid such as lysine, tryptophans in feed liquid, molecular cut off crosses conference and makes yield Reduce;Molecular cut off is too small to increase can energy consumption.
After reverse osmosis concentrated liquid has been obtained, pressed powder can be obtained by way of other dryings, for example may be used To be processed reverse osmosis concentrated liquid using spray dried form, the operating time is short, it is ensured that protein is in dry mistake Will not be destroyed in journey, obtain the Gly-His-Lys containing polypeptide and amino acid.
In one embodiment, ultrafiltration permeate can be carried out after desalting processing using electrodialysis, is re-fed into reverse osmosis Permeable membrane is concentrated, and electrodialysis with good desalting effect, shows because operating condition is gentle, without phase transformation and the features such as easily amplify Work improves product quality, it is possible to improve the rejection of reverse osmosis membrane, and preferred operational factor is:Electrodialysis operation voltage is 100~200V, 1~3A of electric current, feed pressure is 0.05~0.2MPa.
The device that the utility model is provided is as shown in figure 1, include:
Enzymatic vessel 1, for carrying out enzymolysis processing to livestock blood;
Equipment for separating liquid from solid 8, for carrying out separation of solid and liquid process to the enzymolysis liquid obtained in enzymatic vessel;
Milipore filter 4, for carrying out filtering and impurity removing to the feed liquid after separation of solid and liquid;
Reverse osmosis membrane 6, for carrying out concentration to the penetrating fluid of milipore filter 4;
Drying device 7, for being dried process to the concentrate of reverse osmosis membrane 6.
In one embodiment, centrifugal separating device 2 and coarse filter 3, centrifugation are included in equipment for separating liquid from solid 8 Device 2 is used to carry out enzymolysis liquid centrifugal treating, and coarse filter 3 is used to filter the mother liquor that centrifugal separating device 2 is obtained Removal of impurities is processed.
In one embodiment, electrodialysis plant 5 is also included in device, for concentrating into reverse osmosis membrane 6 The penetrating fluid of milipore filter 4 carry out desalting processing.
In one embodiment, drying device 7 is spray-drying installation.
Embodiment 1
Take the livestock blood 200kg that pig slaughtering factory obtains and pump into enzymatic vessel, be passed through steam and be warming up to 55 DEG C, add tryptose Enzyme 100g is digested, and it is 7 to control pH, digests 2h, 65 DEG C of hydrolysis temperature.Enzymolysis liquid feeding centrifuge is centrifuged, main electricity 2500 revs/min of machine, 1000 revs/min of auxiliary motor.Centrifuge mother liquor sends into sheet frame and carries out entering ceramic super-filtering film, pottery after press filtration It is respectively that using 20nm, 50nm, 200nm, 500nm, material is aluminum oxide, ultra-filtration process cross-film that the average pore size of porcelain milipore filter is Pressure reduction 0.1Mpa, crossflow velocity 2m/s, 40 DEG C of filtration temperature stops after feed liquid is concentrated into 3 times.Ultrafiltration dope is returned into enzymatic vessel Continue to digest, the penetrating fluid of ultrafiltration is sent into reverse osmosis membrane and concentrated, and operating pressure is 2MPa, and circular flow is 3.0m3/h, dense Demagnification number is 3 times, obtains the mixture of polypeptide and amino acid.Result of the test at different conditions is as follows:3
Ceramic membrane average pore size 20nm 50nm 200nm 500nm
Peptide content g/100g 12.4 14.1 13.8 11.4
Sour molten total amino acid content g/100g in Gly-His-Lys 15.4 16.3 16.4 14.2
Reverse osmosis membrane amino acid rejection % 95.4 96.3 96.5 94.2
Gly-His-Lys number-average molecular weight 513 564 789 2432
Gly-His-Lys weight average molecular weight 538 623 884 2682
VBN mg/100g 72 70 84 96
Fatty % 0.9 0.8 1.3 1.5
Embodiment 2
Take the livestock blood 200kg that pig slaughtering factory obtains and pump into enzymatic vessel, be passed through steam and be warming up to 55 DEG C, add tryptose Enzyme 100g is digested, and it is 7 to control pH, digests 2h, 65 DEG C of hydrolysis temperature.Enzymolysis liquid feeding centrifuge is centrifuged, main electricity 2500 revs/min of machine, 1000 revs/min of auxiliary motor.Centrifuge mother liquor sends into sheet frame and carries out entering ceramic super-filtering film, pottery after press filtration The average pore size of porcelain milipore filter is 50nm, and material is aluminum oxide, ultra-filtration process transmembrane pressure is respectively 0.1,0.2,0.3,0.4, 0.5Mpa, crossflow velocity 2m/s, 40 DEG C of filtration temperature stops after feed liquid is concentrated into 3 times.Ultrafiltration dope is returned into enzymatic vessel to continue Enzymolysis, the penetrating fluid of ultrafiltration is sent into reverse osmosis membrane and is concentrated, and operating pressure is 2MPa, and circular flow is 3.0m3/h, concentration times Number is 3 times, obtains the mixture of polypeptide and amino acid.Result of the test at different conditions is as follows:3
Ceramic membrane transmembrane pressure MPa 0.1 0.2 0.3 0.4 0.5
Peptide content g/100g 14.1 14.3 14.5 13.2 13.6
Sour molten total amino acid content g/100g in Gly-His-Lys 16.3 16.4 15.6 15.3 15.1
Reverse osmosis membrane amino acid rejection % 96.3 96.5 95.6 95.7 95.1
Gly-His-Lys number-average molecular weight 564 532 635 754 891
Gly-His-Lys weight average molecular weight 623 565 681 795 962
VBN mg/100g 70 72 86 84 88
Fatty % 0.8 0.7 0.9 1.1 1.1
Embodiment 3
Take the livestock blood 200kg that pig slaughtering factory obtains and pump into enzymatic vessel, be passed through steam and be warming up to 55 DEG C, add tryptose Enzyme 80g is digested, and it is 7 to control pH, digests 3h, 60 DEG C of hydrolysis temperature.Enzymolysis liquid feeding centrifuge is centrifuged, mair motor 2000 revs/min, 1500 revs/min of auxiliary motor.Centrifuge mother liquor sends into sheet frame and carries out entering ceramic super-filtering film, ceramics after press filtration The average pore size of milipore filter is 200nm, and material is aluminum oxide, and ultra-filtration process transmembrane pressure is respectively 0.3Mpa, crossflow velocity 2m/ S, 35 DEG C of filtration temperature stops after feed liquid is concentrated into 4 times.Ultrafiltration dope is returned into enzymatic vessel to continue to digest, the penetrating fluid of ultrafiltration Send into reverse osmosis membrane to be concentrated, operating pressure is respectively 1.5,2.0,2.5,3.0MPa, circular flow is 2.5m3/h, concentration Multiple is 3.5 times, obtains the mixture of polypeptide and amino acid.Result of the test at different conditions is as follows:3
Counter-infiltration operates MPa 1.5 2.0 2.5 3.0
Peptide content g/100g 13.6 12.4 14.1 13.8
Sour molten total amino acid content g/100g in Gly-His-Lys 16.5 15.4 16.3 16.4
Reverse osmosis membrane amino acid rejection % 95.4 96.9 96.8 97.1
Gly-His-Lys number-average molecular weight 768 786 795 826
Gly-His-Lys weight average molecular weight 779 854 815 849
VBN mg/100g 75 83 79 80
Fatty % 1.1 1.2 1.1 1.2
Embodiment 4
Take the livestock blood 200kg that pig slaughtering factory obtains and pump into enzymatic vessel, be passed through steam and be warming up to 55 DEG C, add tryptose Enzyme 100g is digested, and it is 7 to control pH, digests 2h, 65 DEG C of hydrolysis temperature.Enzymolysis liquid feeding centrifuge is centrifuged, main electricity 2500 revs/min of machine, 1000 revs/min of auxiliary motor.Centrifuge mother liquor sends into sheet frame and carries out entering ceramic super-filtering film, pottery after press filtration It is respectively that using 20nm, 50nm, 200nm, 500nm, material is aluminum oxide, ultra-filtration process cross-film that the average pore size of porcelain milipore filter is Pressure reduction 0.1Mpa, crossflow velocity 2m/s, 40 DEG C of filtration temperature stops after feed liquid is concentrated into 3 times.Ultrafiltration dope is returned into enzymatic vessel Continue to digest, the penetrating fluid of ultrafiltration sends into electrodialysis plant desalination, electrodialysis operation voltage is 150V, electric current 2A, feed pressure For 0.1MPa, electrodialytic desalinization liquor is sent into reverse osmosis membrane and is concentrated, and operating pressure is 2MPa, and circular flow is 3.0m3/h, Cycles of concentration is 3 times, obtains the mixture of polypeptide and amino acid.Result of the test at different conditions is as follows:3
Ceramic membrane average pore size 20nm 50nm 200nm 500nm
Peptide content g/100g 13.7 14.5 14.6 12.3
Sour molten total amino acid content g/100g in Gly-His-Lys 16.2 16.5 16.7 14.8
Reverse osmosis membrane amino acid rejection % 97.2 98.7 97.7 96.6
Gly-His-Lys number-average molecular weight 502 534 782 2653
Gly-His-Lys weight average molecular weight 528 603 852 2745
VBN mg/100g 38 37 40 42
Fatty % 0.7 0.7 1.1 1.3
Embodiment 5
Take the livestock blood 200kg that pig slaughtering factory obtains and pump into enzymatic vessel, be passed through steam and be warming up to 55 DEG C, add tryptose Enzyme 80g is digested, and it is 9 to control pH, digests 3h, 60 DEG C of hydrolysis temperature.Enzymolysis liquid feeding centrifuge is centrifuged, mair motor 2000 revs/min, 1500 revs/min of auxiliary motor.Centrifuge mother liquor sends into sheet frame and carries out entering ceramic super-filtering film, ceramics after press filtration The average pore size of milipore filter is 200nm, and material is aluminum oxide, and ultra-filtration process transmembrane pressure is respectively 0.3Mpa, crossflow velocity 2m/ S, 35 DEG C of filtration temperature stops after feed liquid is concentrated into 4 times.Ultrafiltration dope is returned into enzymatic vessel to continue to digest, the penetrating fluid of ultrafiltration Send into reverse osmosis membrane to be concentrated, operating pressure is respectively 1.5,2.0,2.5,3.0MPa, circular flow is 2.5m3/ h, concentration Multiple is 3.5 times, obtains the mixture of polypeptide and amino acid.Result of the test at different conditions is as follows.

Claims (10)

1. a kind of whole blood Gly-His-Lys extraction element, it is characterised in that include:
Enzymatic vessel(1), for carrying out enzymolysis processing to livestock blood;
Equipment for separating liquid from solid(8), for carrying out separation of solid and liquid process to the enzymolysis liquid obtained in enzymatic vessel;
Milipore filter(4), for carrying out filtering and impurity removing to the feed liquid after separation of solid and liquid;
Reverse osmosis membrane(6), for milipore filter(4)Penetrating fluid carry out concentration.
2. whole blood Gly-His-Lys extraction element according to claim 1, it is characterised in that described equipment for separating liquid from solid(8)Choosing It is a kind of or several from centrifugal separating device, expression separation device, filter, floating separator, settling separation device The component planted.
3. whole blood Gly-His-Lys extraction element according to claim 2, it is characterised in that described equipment for separating liquid from solid(8)It is Centrifugal separating device(2)And coarse filter(3)Combination, centrifugal separating device(2)For carrying out centrifugal treating to enzymolysis liquid, slightly Filter(3)For to centrifugal separating device(2)The mother liquor for obtaining carries out filtering and impurity removing process.
4. whole blood Gly-His-Lys extraction element according to claim 1, it is characterised in that described milipore filter(4)Retention point Son 1000~200000Da of amount.
5. whole blood Gly-His-Lys extraction element according to claim 1, it is characterised in that milipore filter(4)Material be selected from fiber It is element, cellulose esters, polysulfones, polyether sulfone, polyvinyl chloride, chloropropene, polyolefin, polyvinyl alcohol, polymethyl methacrylate, poly- inclined One or several combination in difluoroethylene, polytetrafluoroethylene (PTFE), ceramics.
6. whole blood Gly-His-Lys extraction element according to claim 1, it is characterised in that described milipore filter(4)It is that ceramics are super Filter membrane, the scope of average pore size is 50~200nm.
7. whole blood Gly-His-Lys extraction element according to claim 1, it is characterised in that reverse osmosis membrane(6)Material be selected from vinegar Acid cellulose is birdsed of the same feather flock together one or several the group in compound, polyamide, polyester, polyimides or polyvinyl etc. Close.
8. whole blood Gly-His-Lys extraction element according to claim 1, it is characterised in that also include drying device(7), it is used for To reverse osmosis membrane(6)Concentrate be dried process.
9. whole blood Gly-His-Lys extraction element according to claim 8, it is characterised in that drying device(7)It is to be spray-dried dress Put.
10. whole blood Gly-His-Lys extraction element according to claim 1, it is characterised in that electrodialysis dress is also included in device Put(5), for entering reverse osmosis membrane(6)The milipore filter for being concentrated(4)Penetrating fluid carry out desalting processing;Described device In also include enzyme and add part, for adding enzyme in livestock blood.
CN201620870483.5U 2016-08-12 2016-08-12 Whole blood peptide powder extraction element Active CN206089712U (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201620870483.5U CN206089712U (en) 2016-08-12 2016-08-12 Whole blood peptide powder extraction element

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201620870483.5U CN206089712U (en) 2016-08-12 2016-08-12 Whole blood peptide powder extraction element

Publications (1)

Publication Number Publication Date
CN206089712U true CN206089712U (en) 2017-04-12

Family

ID=58468230

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201620870483.5U Active CN206089712U (en) 2016-08-12 2016-08-12 Whole blood peptide powder extraction element

Country Status (1)

Country Link
CN (1) CN206089712U (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106086142A (en) * 2016-08-12 2016-11-09 江苏久吾高科技股份有限公司 A kind of whole blood Gly-His-Lys extracting method and device

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106086142A (en) * 2016-08-12 2016-11-09 江苏久吾高科技股份有限公司 A kind of whole blood Gly-His-Lys extracting method and device

Similar Documents

Publication Publication Date Title
CN101041486B (en) Method for treatment and comprehensive utilization of silk production waste water
AU2012210671B2 (en) Method for processing thin stillage and apparatus for producing a protein-containing product
CN103555798B (en) A kind of method adopting ceramic membrane to extract fly maggot protein
BRPI0709693A2 (en) tangential flow filtration apparatus, systems, and processes for the separation of compounds
CN104119456B (en) Method for separation and purification of edible (medicinal) mushroom active components by multistage membrane process
CN103205480A (en) Method for producing high-quality collagen oligopeptide by using fish skin or fishbone
JP2013537541A (en) Method to obtain high purity lactic acid from fermentation broth
CN106086142A (en) A kind of whole blood Gly-His-Lys extracting method and device
CN106319014A (en) Extracting method for micro-molecule deep-sea fish polypeptides
CN102978250B (en) Method for producing Gamma-aminobutyric acid through centrifugal mother liquid of glutamic acid
CN106417667A (en) Production method of desalted sheep whey powder
CN101195652A (en) Method for recycling protein and lactose from milk product wastewater
CN100399930C (en) Method for production of peptides/amino acids, peptides/amino acids produced by said method and use of the same
CN104194927A (en) Method for extracting egg yolk oil, lecithin and egg yolk protein polypeptide powder from egg yolk powder
CN105495658B (en) A kind of fish meal production system based on membrane technology
CN104262230B (en) The extracting method of a kind of L-Trp and device
CN207619299U (en) A kind of purifying plant of oligosaccharide
CN106348429B (en) A kind of pueraria lobata resource utilization method of separating-purifying flavonol, starch and amino acid
CN206089712U (en) Whole blood peptide powder extraction element
CN109928566B (en) Method and device for treating animal extraction industrial wastewater
CN1329103A (en) Method for extracting protein, short peptide, nucleic acid, isoflavone, saponin and oligosaccharide by using high and low temperature soybean cake
CN212713178U (en) Treatment device for wastewater generated in vitamin B2 fermentation process
CN108148100A (en) The method of purification and device of a kind of oligosaccharide
CN111808185A (en) Method for extracting elastin peptide from bovine cartilage
CN206051627U (en) A kind of bean cake recycling treatment system

Legal Events

Date Code Title Description
GR01 Patent grant
GR01 Patent grant