WO2006056585A1 - Method for the preparation of a carminic acid lake - Google Patents

Method for the preparation of a carminic acid lake Download PDF

Info

Publication number
WO2006056585A1
WO2006056585A1 PCT/EP2005/056195 EP2005056195W WO2006056585A1 WO 2006056585 A1 WO2006056585 A1 WO 2006056585A1 EP 2005056195 W EP2005056195 W EP 2005056195W WO 2006056585 A1 WO2006056585 A1 WO 2006056585A1
Authority
WO
WIPO (PCT)
Prior art keywords
carminic acid
lake
proteins
aluminum
calcium
Prior art date
Application number
PCT/EP2005/056195
Other languages
French (fr)
Inventor
Julie Faust Schmidt-Jacobsen
Rikke Sakstrup Frandsen
Original Assignee
Chr. Hansen A/S
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 Chr. Hansen A/S filed Critical Chr. Hansen A/S
Priority to CN2005800394464A priority Critical patent/CN101061185B/en
Priority to US11/577,751 priority patent/US7641704B2/en
Priority to BRPI0518294-8A priority patent/BRPI0518294A2/en
Publication of WO2006056585A1 publication Critical patent/WO2006056585A1/en
Priority to US12/621,769 priority patent/US8021440B2/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09BORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B61/00Dyes of natural origin prepared from natural sources, e.g. vegetable sources
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/60Sugars; Derivatives thereof
    • A61K8/602Glycosides, e.g. rutin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/64Proteins; Peptides; Derivatives or degradation products thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q1/00Make-up preparations; Body powders; Preparations for removing make-up
    • A61Q1/02Preparations containing skin colorants, e.g. pigments
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09BORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B63/00Lakes
    • C09B63/005Metal lakes of dyes
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/40Chemical, physico-chemical or functional or structural properties of particular ingredients
    • A61K2800/42Colour properties
    • A61K2800/43Pigments; Dyes

Definitions

  • TITLE METHOD FOR THE PREPARATION OF A CARMINIC ACID LAKE
  • the present invention relates to a method for the preparation of carminic acid lakes, novel carminic acid lake compositions and their uses in foods, such as yogurt, fruit preparations, beverages, other miscellaneous food products that may need a stable red color, and in cosmet ⁇ ics.
  • Carminic acid is a colorant, which can be extracted from the female insect bodies of Dacty- lopius coccus costa (alternative name Coccus cacti L.).
  • the insects live on Nopalea coccinel- lifera, Opuntiafidus indica andcAhsr plants of the family Cactaceae cultivated for instance in the desert areas of Mexico and Central and South America.
  • the colorant may be a color in a spectrum from orange over red to purple and is generally known as cochi ⁇ neal or cochineal color.
  • Carmine colorant is widely used in foods and beverages.
  • Carminic acid is harvested by extraction from said insects' dried bodies with water or alcohol. During the aqueous based extraction of carminic acid from the insect, an amount of insect pro ⁇ tein is also released from the insect and will be contained in the color extract. The level of in ⁇ sect protein is typically less than 0.5%.
  • the aqueous based extract of cochineal is primarily containing carminic acid plus some cochineal protein and other minor extractable substances from the insect. Hereinafter this extract is referred to as cochineal extract solution.
  • a carminic acid lake denotes herein a type of coloring composition consisting essentially of carminic acid combined more or less definitely with aluminum and calcium. This is termed carminic acid calcium-aluminum lake.
  • the lake is prepared by reacting carminic acid with aluminum and/or calcium under aqueous conditions. The conditions are adjusted in a way that favors precipitation of the aluminum/calcium - carminic acid lake complex composition. This complex composition is termed carmine.
  • US2002/0058016 (SAN-EI GEN (Japan) describes preparation of a carminic acid calcium-aluminum lake based on a pure carminic acid solution made in example 1.
  • Example 2 section [0085] then explains that "when a carminic acid aluminum lake or cal ⁇ cium lake (Carmine) is caused to form a polymer, there is the tendency that when a low mo ⁇ lecular protein is allowed to be present, a more neat lake can be obtained with an increased intensity of red color.
  • a cochineal color (carmine) with a higher intensity of redness and an increase market value may be prepared by adding a protein of comparatively low mo ⁇ lecular weight, which does not become an allergen to the above allergen- free solution.” Besides this speculative statement, no further relevant details with respect to a possible addi ⁇ tion of low molecular weight protein to the carminic acid lake are described.
  • the aim of the present invention is to provide an improved carminic acid lake, which is free of potentially allergenic cochineal insect proteins.
  • the solution is based on several relevant parameters important for the preparation of an opti ⁇ mal lake that has been identified by the present inventors by starting from a pure carminic acid product substantially free of Dactylopius coccus costa insect proteins. These parameters are described in further details below and include details regarding added non cochineal insect proteins and carminic acid percentage.
  • a first aspect of the invention relates to a process for making a carminic acid lake comprising the steps of:
  • a commercially produced cochineal extract solution normally comprises around 0.6% car- minic acid and relatively low amounts Dactylopius coccus costa insect proteins, generally around 0.1 to 0.25% of proteins. In the art this has been regarded as a sufficient amount of proteins to produce a lake. Contrary to the art, the present inventors identified that improved lakes may be obtained by including higher amounts of proteins as described herein.
  • An advan ⁇ tage of using significantly higher amounts of proteins, as described in step (i) above, is that the yield of carminic acid is improved. The yield relates to the amount of carminic acid in the lake of step (ii) as compared to the initial amount in the aqueous solution of step (i).
  • a second aspect relates to a carminic acid calcium-aluminum lake obtainable by a process of the first aspect and embodiments thereof as described herein, wherein the lake comprises
  • the word "obtainable” shall be understood in the normal English sense of the word, i.e. as the lake may be obtained by the specified process but could in theory be obtained in a different manner.
  • the lake of the second aspect is obtained by a process of the first aspect and embodiments thereof as described herein.
  • a third aspect of the invention relates to use of a carminic acid aluminum lake, a carminic acid calcium lake or a carminic acid calcium-aluminum lake of the second aspect and em ⁇ bodiments thereof as described herein for making a color composition to be added to food products, sweets, confectionary, beverages, pharmaceuticals or cosmetics.
  • This third aspect may alternatively be described as a method for colouring food products, sweets, confectionary, beverages, pharmaceuticals or cosmetics comprising use of a color composition made from a carminic acid aluminum lake, a carminic acid calcium lake or a carminic acid calcium-aluminum lake of the second aspect and embodiments thereof as de ⁇ scribed herein.
  • the carminic acid to be used to make the aqueous solution of step (i) shall preferably be from a pure carminic acid composition.
  • a "pure carminic acid composition” denotes herein a highly purified cochineal extract solution. Preferably it comprises from 90 to 99% carminic acid (dry weight) and is preferably substantially free of Dactylopius coccus costa insect proteins.
  • a pure carminic acid composition may be made in a number of routine ways e.g. based on methods that generally use suitable adsorption treatments, ion exchange treatments, acid treatments and/or membrane treatments.
  • Commercially available pure carminic acid composi ⁇ tions include a water-soluble Cochineal powder from Chr. Hansen, A/S (Denmark) or similar commercially available products from e.g. the companies Pronex (Peru) or Sensient.
  • a pure carminic acid composition may be made by the proteolysis-based method described in US2002/0058016.
  • the not Dactylopius coccus costa insect proteins used to make the aqueous solution of step (i) shall preferably be from a protein composition obtained from a source that is acceptable for the food industry and/or pharmaceutically acceptable.
  • the proteins should pref- erably not be based on a composition of proteins obtained from e.g. a snake known to be toxic for e.g. humans. It should furthermore preferably be from a source known to cause no or only acceptable allergy related problems.
  • step (i) used to make the aqueous solution of step (i) globally denotes herein peptides, amino acids, proteins or mixtures thereof.
  • suitable protein compositions are based on plant proteins such as soya proteins and potato proteins.
  • the proteins are milk proteins such a cow milk proteins.
  • the milk pro ⁇ teins are obtained from a milk-based hydro lysate such as a whey hydro lysate.
  • Suitable com ⁇ soirally available whey hydrolysate may be obtained from commercial dairy companies. This is particularly relevant when the carminic acid color is to be used in a milk based food product.
  • substantially all of the not Dactylopius coccus costa insect proteins have a molecu ⁇ lar weight (MW) below 6,000 Da, more preferably below 4,000 Da and even more preferably below 3,000 Da.
  • step (i) when the proteins of step (i) have a certain MW then the resulting lake of step (ii) will also get a corresponding protein MW composition. For instance, if substantially all of the proteins of step (i) have a molecular weight (MW) be ⁇ low 6,000 Da then substantially all of the proteins in the lake, of step (ii) will have a molecu- lar weight (MW) below 6,000 Da.
  • MW molecular weight
  • An aqueous solution may preferably be prepared simply by adding a suitable protein composi ⁇ tion (e.g. in powder form) to a pure carminic acid solution or simply by adding e.g. pure car ⁇ minic acid (e.g. in powder form) to a solution comprising a suitable protein composition. In other words, simply by mixing a suitable protein composition with a suitable pure carminic acid composition.
  • a suitable protein composi ⁇ tion e.g. in powder form
  • e.g. pure car ⁇ minic acid e.g. in powder form
  • the ratio Carminic acid/not Dactylopius coccus costa insect proteins (g/1) is less than 1.
  • the present inventors have identified that if the ratio is greater than 1 the solution has a tendency to gel. See table of working example 1 herein.
  • the ratio Carminic acid/not Dactylopius coccus costa insect proteins (g/1) is from 0.4 to 0.9, more preferably from 0.5 to 0.8 and most preferably from 0.5 to 0.7.
  • the pH of the solution shall preferably be adjusted to a pH from 5 to 7, more preferably around pH 6.
  • the aqueous media is water, preferably distilled water.
  • the aqueous solution is substantially free of Dactylopius coccus costa insect pro ⁇ teins.
  • the aqueous solution comprises from 1 to 10% carminic acid and from 1.5 to 10% not Dactylopius coccus costa insect proteins, more preferably the aqueous solution comprises from 2 to 7% carminic acid and from 3 to 8% not Dactylopius coccus costa insect proteins, even more preferably the aqueous solution comprises from 3 to 5% carminic acid and from 4 to 6% not Dactylopius coccus costa insect proteins.
  • the carminic acid/protein aqueous solution is treated with the aluminum and calcium com- pound under suitable conditions to produce the carminic acid lake.
  • suitable conditions to make a lake are known. However, the present inventors have analyzed this in detail and the preferred conditions are explained below.
  • Treatment of the aqueous solution with an aluminum and calcium compound may be per- formed in different ways. It may e.g. be performed by adding the aluminum and calcium to a solution only comprising the proteins and then thereafter by adding the carminic acids to the solution.
  • aqueous solution comprising both the carminic acid and the proteins and then add the aluminum and calcium compound to this solution.
  • the present inventors have identified that if calcium is added to the carminic acid/protein solution first, then there is a risk of unwanted "black spots” developing in the fi ⁇ nal lake.
  • the black spots are believed to be calcium carminate.
  • the aqueous solution is treated with from 1 g aluminum/1 solution to 20 g alumi ⁇ num/1 solution and from 1 g calcium/1 solution to 20 g calcium/1 solution.
  • the skilled person knows how to optimize this in relation to the desired color of interest.
  • a suitable aluminum compound is aluminum sulphate.
  • the aluminum compound is A1K(SO 4 )2*12 H 2 O.
  • a suitable calcium compound is calcium carbonate or Calcium chloride.
  • the calcium compound is (CH3COO)2Ca*H2 ⁇ .
  • the pH is adjusted to a value from 3 to 7 in order to produce the carminic acid lake.
  • the pH is adjusted to a value from 4 to 6 and more prefera ⁇ bly adjusted to a pH value from 4.5 to 5.5.
  • the adjustment of the pH may be done after the carminic acid/proteins has been combined with the salts. However, preferably the adjustment is done before addition of salts.
  • the carminic acid/protein aqueous solution is treated with the aluminum and cal ⁇ cium compound under following suitable conditions to produce the carminic acid lake: time period: 15 minutes to 2 hours, more preferably from 30 minutes to 60 minutes temperature: from 80°C to 99°C, more preferably from 92°C to 97°C
  • the final composition of the produced carminic acid lake of step (ii) relates to the initial com ⁇ position of the aqueous solution of step (i).
  • the preferred carminic acid/protein contents of the aqueous solution are given above.
  • Corresponding preferred compositions of the produced carminic acid lake of step (ii) are wherein the lake comprises from 55 to 75% carminic acid (dry weight) and from 15 to 25% proteins (dry weight), more preferably wherein the lake comprises from 62 to 72% carminic acid (dry weight) and from 18 to 22% proteins (dry weight).
  • the amount of carminic acid and proteins in the lake cannot be more than 100%. Actually, the sum will generally be around 90% since the lake will comprise other material such as the salts used to produce the lake. Accordingly, if the lake comprises 75% carminic acid (dry weight) then it would normally not have more than 15% proteins (dry weight).
  • a preferred method to determine the amounts of carminic acid is a known standard method described by FAOAVHO: Document from 44 th session of the JECFA committee in 1995 and Food Chemical Codex, second edition (FCCII). In Commission Directive 94/45/EC from July 1995, Official journal of the European Communities No. L 226, p. 9, it is described that the proper diluted color product E- 120 has a maximum at 494 nm.
  • a preferred method to determine the amount of proteins is the known Kjeldahl method and/or by amino acid analysis.
  • step (ii) After the carminic acid lake of step (ii) is produced it is routine to include adequate subse ⁇ quent steps. These may include a step of filtering the carminic acid lake and/or a step of dry ⁇ ing the carminic acid lake to get a dried carminic acid lake. These steps are routine for the skilled persons and reference is made to the reference textbook given above.
  • the carminic acid lake In order to use the carminic acid lake, as described herein, it should be converted into a suit ⁇ able color composition.
  • the term color composition should be understood broadly. Depending on the final needs it may be the carminic acid lake as such or maybe the lake after filtering and/or drying. Alternatively, the lake may be converted into a suitable carmine solution or wa ⁇ ter-soluble carmine (powder). However, it may also be a color composition where a suitable carrier or additive which is food sanitation- wise or pharmaceutically acceptable has been added. The specific choice of carrier or additive will depend on the final use, e.g. in food or pharmaceuticals, and the skilled person may routinely select adequate carriers or additives. For further details, see US2002/0058016.
  • the color composition may be added to food products, sweets, confectionary, beverages, pharmaceuticals or cosmetics.
  • food product denotes herein both food and feed products. Preferably it is food prod- ucts. Preferred food products include dairy products such as yogurt or meat.
  • a further relevant feature of the color composition is the strength of the color.
  • the color of the carminic acid may e.g. be red and the color composition may be made with different strength of e.g. red in order to get an adequate color in the final e.g. food product.
  • the color composition may be encapsulated, using conventional micro encapsulation tech- niques suitable for food products, for example, as described in WO97/26803 (Chr. Hansen AJS), by encapsulation in gum arabic.
  • Carminic acid Commercially available carminic Acid obtained from purified cochineal extract (Dactylopius coccus Costa). Minimum around 90% Carminic Acid.
  • Protein composition Commercial whey protein hydrolysate suitable as protein source in in- fant formulas with reduced allergen content. Substantially all of the proteins have a molecular weight (MW) below 6,000 Da.
  • the lakes of carmine were added buffer solution so that all samples contained the same amount Carminic Acid/ml corresponding to 1.5 g/1 of a 46.56% CA. lake.
  • NUPAGE Novex high performance pre-cast gel 4-12% BIS-TRIS are stained by cromassie blue and/or silver
  • This example discloses examples of preparation of Al-Ca carmine lake with carminic acid and whey hydrolysate.
  • the resulting carmine lakes had a carminic acid content of 65-75% and a protein content of 18-22%. None of the proteins in the lakes, detectable in the SDS-PAGE analysis, were bigger than 3,000 Da.
  • the resulting carmine lakes have bright red color shades and were applicable as cochineal protein based carmine lakes for making carmine solutions and water-soluble carmine powders.
  • the ratio carminic acid/added proteins shall be less than 1 to avoid gelling and thereby impossible processing. Furthermore, the preferred ratio is from 0.5 to 0.8 and most preferably around 0.6.
  • This example discloses examples of Al-Ca carmine lake preparation with carminic acid and whey hydrolysate.
  • example 2 demonstrates that it is important to first add the aluminum, wait for a period and then add the calcium in order to get less "black spots”.

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Epidemiology (AREA)
  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Birds (AREA)
  • Coloring Foods And Improving Nutritive Qualities (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Peptides Or Proteins (AREA)
  • Non-Alcoholic Beverages (AREA)
  • Cosmetics (AREA)
  • Dairy Products (AREA)
  • Medicinal Preparation (AREA)

Abstract

A method for the preparation of carminic acid lakes, novel carminic acid lake compositions and their uses in foods, such as yogurt, fruit preparations, beverages, other miscellaneous food products that may need a stable red color, and in cosmetics.

Description

TITLE: METHOD FOR THE PREPARATION OF A CARMINIC ACID LAKE
FIELD OF THE INVENTION
The present invention relates to a method for the preparation of carminic acid lakes, novel carminic acid lake compositions and their uses in foods, such as yogurt, fruit preparations, beverages, other miscellaneous food products that may need a stable red color, and in cosmet¬ ics.
BACKGROUND OF THE INVENTION
Carminic acid is a colorant, which can be extracted from the female insect bodies of Dacty- lopius coccus costa (alternative name Coccus cacti L.). The insects live on Nopalea coccinel- lifera, Opuntiafidus indica andcAhsr plants of the family Cactaceae cultivated for instance in the desert areas of Mexico and Central and South America. Depending on the pH the colorant may be a color in a spectrum from orange over red to purple and is generally known as cochi¬ neal or cochineal color. Carmine colorant is widely used in foods and beverages.
Carminic acid is harvested by extraction from said insects' dried bodies with water or alcohol. During the aqueous based extraction of carminic acid from the insect, an amount of insect pro¬ tein is also released from the insect and will be contained in the color extract. The level of in¬ sect protein is typically less than 0.5%. The aqueous based extract of cochineal is primarily containing carminic acid plus some cochineal protein and other minor extractable substances from the insect. Hereinafter this extract is referred to as cochineal extract solution.
It has been reported that the cochineal insect proteins could create some allergy related prob¬ lems. In order to solve this allergy problem, US2002/0058016; EP1318178 (SAN-EI GEN (Japan)) describes a process wherein the cochineal extract solution is subjected to enzymatic proteolysis and Dactylopius coccus costa insect proteins with a molecular weight greater than 6,000 is subsequently removed.
The art describes numerous other not proteolysis based standard methods to make a pure car¬ minic acid product substantially free of Dactylopius coccus costa insect proteins. Such meth- ods generally use suitable adsorption treatments, ion exchange treatments, acid treatments and/or membrane treatments. Commercially available carminic acid products substantially free of Dactylopius coccus costa insect proteins include a water-soluble Cochineal powder from Chr. Hansen, A/S (Denmark) or similar commercially available products from e.g. the companies Pronex (Peru) or Sensient.
A carminic acid lake denotes herein a type of coloring composition consisting essentially of carminic acid combined more or less definitely with aluminum and calcium. This is termed carminic acid calcium-aluminum lake. The lake is prepared by reacting carminic acid with aluminum and/or calcium under aqueous conditions. The conditions are adjusted in a way that favors precipitation of the aluminum/calcium - carminic acid lake complex composition. This complex composition is termed carmine.
The working example 2, US2002/0058016 (SAN-EI GEN (Japan) describes preparation of a carminic acid calcium-aluminum lake based on a pure carminic acid solution made in example 1. Example 2 section [0085] then explains that "when a carminic acid aluminum lake or cal¬ cium lake (Carmine) is caused to form a polymer, there is the tendency that when a low mo¬ lecular protein is allowed to be present, a more neat lake can be obtained with an increased intensity of red color. Therefore, a cochineal color (carmine) with a higher intensity of redness and an increase market value may be prepared by adding a protein of comparatively low mo¬ lecular weight, which does not become an allergen to the above allergen- free solution." Besides this speculative statement, no further relevant details with respect to a possible addi¬ tion of low molecular weight protein to the carminic acid lake are described.
SUMMARY OF THE INVENTION
The aim of the present invention is to provide an improved carminic acid lake, which is free of potentially allergenic cochineal insect proteins.
The solution is based on several relevant parameters important for the preparation of an opti¬ mal lake that has been identified by the present inventors by starting from a pure carminic acid product substantially free of Dactylopius coccus costa insect proteins. These parameters are described in further details below and include details regarding added non cochineal insect proteins and carminic acid percentage.
Accordingly, a first aspect of the invention relates to a process for making a carminic acid lake comprising the steps of:
(i) treating an aqueous solution, comprising
(a) 0.5 to 15% (g/1) carminic acid and
(b) from 0.75 to 15% (g/1) not Dactylopius coccus costa insect proteins, where sub- stantially all of the not Dactylopius coccus costa insect proteins have a molecular weight (MW) below 10,000 Da, wherein the aqueous solution is substantially free of Dactylopius coccus costa insect proteins with a molecular weight (MW) above 6,000 Da; with an aluminum and calcium compound, (ii) adjusting the conditions to get suitable conditions to produce a calcium-aluminum carminic acid lake, wherein the lake comprises
(a) from 40 to 80% carminic acid (dry weight) and
(b) from 10 to 30% not Dactylopius coccus costa insect proteins (dry weight), where substantially all of the not Dactylopius coccus costa insect proteins have a molecular weight (MW) below 10,000 Da and wherein the lake is substantially free of Dactylopius coccus costa insect proteins with a molecular weight (MW) above 6,000 Da.
A commercially produced cochineal extract solution normally comprises around 0.6% car- minic acid and relatively low amounts Dactylopius coccus costa insect proteins, generally around 0.1 to 0.25% of proteins. In the art this has been regarded as a sufficient amount of proteins to produce a lake. Contrary to the art, the present inventors identified that improved lakes may be obtained by including higher amounts of proteins as described herein. An advan¬ tage of using significantly higher amounts of proteins, as described in step (i) above, is that the yield of carminic acid is improved. The yield relates to the amount of carminic acid in the lake of step (ii) as compared to the initial amount in the aqueous solution of step (i). See work¬ ing examples herein for further details, where yields up to 98.2% have been obtained. At the filing date of the present application, the present inventors were not aware of any prior art (for instance commercial lake products) that describes carminic acid lake with the amounts of carminic acid and non insect proteins as described herein.
Accordingly, a second aspect relates to a carminic acid calcium-aluminum lake obtainable by a process of the first aspect and embodiments thereof as described herein, wherein the lake comprises
(a) from 40 to 80% of carminic acid (dry weight) and
(b) from 10 to 30% of not Dactylopius coccus costa insect proteins (dry weight), where substantially all of the not Dactylopius coccus costa insect proteins have a mo¬ lecular weight (MW) below 10,000 Da and wherein the lake is substantially free of Dactylopius coccus costa insect proteins with a molecular weight (MW) above 6,000 Da.
The word "obtainable" shall be understood in the normal English sense of the word, i.e. as the lake may be obtained by the specified process but could in theory be obtained in a different manner. Preferably, the lake of the second aspect is obtained by a process of the first aspect and embodiments thereof as described herein.
A third aspect of the invention relates to use of a carminic acid aluminum lake, a carminic acid calcium lake or a carminic acid calcium-aluminum lake of the second aspect and em¬ bodiments thereof as described herein for making a color composition to be added to food products, sweets, confectionary, beverages, pharmaceuticals or cosmetics.
This third aspect may alternatively be described as a method for colouring food products, sweets, confectionary, beverages, pharmaceuticals or cosmetics comprising use of a color composition made from a carminic acid aluminum lake, a carminic acid calcium lake or a carminic acid calcium-aluminum lake of the second aspect and embodiments thereof as de¬ scribed herein. DETAILED DESCRIPTION OF THE INVENTION
A process for making a carminic acid lake
The carminic acid to be used to make the aqueous solution of step (i) shall preferably be from a pure carminic acid composition. A "pure carminic acid composition" denotes herein a highly purified cochineal extract solution. Preferably it comprises from 90 to 99% carminic acid (dry weight) and is preferably substantially free of Dactylopius coccus costa insect proteins.
The term "substantially free of Dactylopius coccus costa insect proteins" denotes herein that it is not detectable by a SDS-PAGE analysis. A suitable SDS-PAGE analysis is given in Exam¬ ple 1.
A pure carminic acid composition may be made in a number of routine ways e.g. based on methods that generally use suitable adsorption treatments, ion exchange treatments, acid treatments and/or membrane treatments. Commercially available pure carminic acid composi¬ tions include a water-soluble Cochineal powder from Chr. Hansen, A/S (Denmark) or similar commercially available products from e.g. the companies Pronex (Peru) or Sensient. A pure carminic acid composition may be made by the proteolysis-based method described in US2002/0058016.
The not Dactylopius coccus costa insect proteins used to make the aqueous solution of step (i) shall preferably be from a protein composition obtained from a source that is acceptable for the food industry and/or pharmaceutically acceptable. For example, the proteins should pref- erably not be based on a composition of proteins obtained from e.g. a snake known to be toxic for e.g. humans. It should furthermore preferably be from a source known to cause no or only acceptable allergy related problems.
The term "not Dactylopius coccus costa insect proteins" used to make the aqueous solution of step (i) globally denotes herein peptides, amino acids, proteins or mixtures thereof.
Examples of suitable protein compositions are based on plant proteins such as soya proteins and potato proteins. Preferably, the proteins are milk proteins such a cow milk proteins. Preferably, the milk pro¬ teins are obtained from a milk-based hydro lysate such as a whey hydro lysate. Suitable com¬ mercially available whey hydrolysate may be obtained from commercial dairy companies. This is particularly relevant when the carminic acid color is to be used in a milk based food product.
Preferably, substantially all of the not Dactylopius coccus costa insect proteins have a molecu¬ lar weight (MW) below 6,000 Da, more preferably below 4,000 Da and even more preferably below 3,000 Da.
It is implicit in the process as described herein that when the proteins of step (i) have a certain MW then the resulting lake of step (ii) will also get a corresponding protein MW composition. For instance, if substantially all of the proteins of step (i) have a molecular weight (MW) be¬ low 6,000 Da then substantially all of the proteins in the lake, of step (ii) will have a molecu- lar weight (MW) below 6,000 Da.
The term "substantially all of the proteins have a molecular weight (MW) below [a number] Da" denotes herein that proteins with a greater MW than indicated are not detectable by a SDS-PAGE analysis. A suitable SDS-PAGE analysis is given in Example 1.
An aqueous solution may preferably be prepared simply by adding a suitable protein composi¬ tion (e.g. in powder form) to a pure carminic acid solution or simply by adding e.g. pure car¬ minic acid (e.g. in powder form) to a solution comprising a suitable protein composition. In other words, simply by mixing a suitable protein composition with a suitable pure carminic acid composition.
In the aqueous solution of step (i) of the first aspect it is preferred that the ratio Carminic acid/not Dactylopius coccus costa insect proteins (g/1) is less than 1. The present inventors have identified that if the ratio is greater than 1 the solution has a tendency to gel. See table of working example 1 herein.
Preferably, the ratio Carminic acid/not Dactylopius coccus costa insect proteins (g/1) is from 0.4 to 0.9, more preferably from 0.5 to 0.8 and most preferably from 0.5 to 0.7. Before the proteins are added to the aqueous solution, the pH of the solution shall preferably be adjusted to a pH from 5 to 7, more preferably around pH 6. Preferably, the aqueous media is water, preferably distilled water.
Preferably, the aqueous solution is substantially free of Dactylopius coccus costa insect pro¬ teins.
Preferably, the aqueous solution comprises from 1 to 10% carminic acid and from 1.5 to 10% not Dactylopius coccus costa insect proteins, more preferably the aqueous solution comprises from 2 to 7% carminic acid and from 3 to 8% not Dactylopius coccus costa insect proteins, even more preferably the aqueous solution comprises from 3 to 5% carminic acid and from 4 to 6% not Dactylopius coccus costa insect proteins.
The carminic acid/protein aqueous solution is treated with the aluminum and calcium com- pound under suitable conditions to produce the carminic acid lake. The skilled person gener¬ ally knows suitable conditions to make a lake. However, the present inventors have analyzed this in detail and the preferred conditions are explained below.
Treatment of the aqueous solution with an aluminum and calcium compound may be per- formed in different ways. It may e.g. be performed by adding the aluminum and calcium to a solution only comprising the proteins and then thereafter by adding the carminic acids to the solution.
However, it is preferred to first make an aqueous solution comprising both the carminic acid and the proteins and then add the aluminum and calcium compound to this solution.
Without being limited by theory, it is believed to be important for optimal lake formation that the aluminum and calcium are added to a solution already comprising both the carminic acid and the proteins.
In fact this is different to the suggestion in working example 2 of US2002/0058016, where a carminic acid aluminum solution is first made and it is then suggested to add low MW pro¬ teins to this solution. It is preferred to first add the aluminum and then wait for a suitable time before the calcium is added to the aqueous solution. A suitable time is around from 30 seconds to 1 hour, preferably from 1 minute to 15 minutes.
Surprisingly, the present inventors have identified that if calcium is added to the carminic acid/protein solution first, then there is a risk of unwanted "black spots" developing in the fi¬ nal lake. The black spots are believed to be calcium carminate. There are created far less "black spots" when aluminum is added first to the carminic acid/protein aqueous solution. See working example 2 herein for further details.
Preferably, the aqueous solution is treated with from 1 g aluminum/1 solution to 20 g alumi¬ num/1 solution and from 1 g calcium/1 solution to 20 g calcium/1 solution. The skilled person knows how to optimize this in relation to the desired color of interest.
A suitable aluminum compound is aluminum sulphate. Preferably the aluminum compound is A1K(SO4)2*12 H2O. A suitable calcium compound is calcium carbonate or Calcium chloride. Preferably the calcium compound is (CH3COO)2Ca*H2θ.
During the treatment of the carminic acid/protein aqueous solution with the aluminum and/or calcium compound it is preferred to adjust the pH to a value from 3 to 7 in order to produce the carminic acid lake. Preferably, the pH is adjusted to a value from 4 to 6 and more prefera¬ bly adjusted to a pH value from 4.5 to 5.5.
The adjustment of the pH may be done after the carminic acid/proteins has been combined with the salts. However, preferably the adjustment is done before addition of salts.
Preferably the carminic acid/protein aqueous solution is treated with the aluminum and cal¬ cium compound under following suitable conditions to produce the carminic acid lake: time period: 15 minutes to 2 hours, more preferably from 30 minutes to 60 minutes temperature: from 80°C to 99°C, more preferably from 92°C to 97°C
The final composition of the produced carminic acid lake of step (ii) relates to the initial com¬ position of the aqueous solution of step (i). The preferred carminic acid/protein contents of the aqueous solution are given above. Corresponding preferred compositions of the produced carminic acid lake of step (ii) are wherein the lake comprises from 55 to 75% carminic acid (dry weight) and from 15 to 25% proteins (dry weight), more preferably wherein the lake comprises from 62 to 72% carminic acid (dry weight) and from 18 to 22% proteins (dry weight).
Of course the amount of carminic acid and proteins in the lake cannot be more than 100%. Actually, the sum will generally be around 90% since the lake will comprise other material such as the salts used to produce the lake. Accordingly, if the lake comprises 75% carminic acid (dry weight) then it would normally not have more than 15% proteins (dry weight).
A preferred method to determine the amounts of carminic acid is a known standard method described by FAOAVHO: Document from 44th session of the JECFA committee in 1995 and Food Chemical Codex, second edition (FCCII). In Commission Directive 94/45/EC from July 1995, Official journal of the European Communities No. L 226, p. 9, it is described that the proper diluted color product E- 120 has a maximum at 494 nm.
A preferred method to determine the amount of proteins is the known Kjeldahl method and/or by amino acid analysis.
After the carminic acid lake of step (ii) is produced it is routine to include adequate subse¬ quent steps. These may include a step of filtering the carminic acid lake and/or a step of dry¬ ing the carminic acid lake to get a dried carminic acid lake. These steps are routine for the skilled persons and reference is made to the reference textbook given above.
Use of a carminic acid lake in different products
In order to use the carminic acid lake, as described herein, it should be converted into a suit¬ able color composition. The term color composition should be understood broadly. Depending on the final needs it may be the carminic acid lake as such or maybe the lake after filtering and/or drying. Alternatively, the lake may be converted into a suitable carmine solution or wa¬ ter-soluble carmine (powder). However, it may also be a color composition where a suitable carrier or additive which is food sanitation- wise or pharmaceutically acceptable has been added. The specific choice of carrier or additive will depend on the final use, e.g. in food or pharmaceuticals, and the skilled person may routinely select adequate carriers or additives. For further details, see US2002/0058016.
As said above, the color composition may be added to food products, sweets, confectionary, beverages, pharmaceuticals or cosmetics.
The term food product denotes herein both food and feed products. Preferably it is food prod- ucts. Preferred food products include dairy products such as yogurt or meat.
A further relevant feature of the color composition is the strength of the color. The color of the carminic acid may e.g. be red and the color composition may be made with different strength of e.g. red in order to get an adequate color in the final e.g. food product.
Starting from the carminic acid lake, as described herein, it is routine work to make adequate steps to get a color composition with required color strength.
The color composition may be encapsulated, using conventional micro encapsulation tech- niques suitable for food products, for example, as described in WO97/26803 (Chr. Hansen AJS), by encapsulation in gum arabic.
EXAMPLES
Materials and analytical methods:
Pure carminic acid: Commercially available carminic Acid obtained from purified cochineal extract (Dactylopius coccus Costa). Minimum around 90% Carminic Acid. Protein composition: Commercial whey protein hydrolysate suitable as protein source in in- fant formulas with reduced allergen content. Substantially all of the proteins have a molecular weight (MW) below 6,000 Da.
ELISA analysis: Antigenecity tested by one site immunometic assay ELISA with polyclonal antibodies raised on whey protein concentrate μg protein eqv./g protein max 85 Aluminum salt: A1K(SO4)2*12H2O Calcium salt: (CH3COO)2Ca*H2O Acetic Acid: CH3COOH Sodium Hydroxide: NaOH-pellets SDS-PAGE Analysis Solvent Tris buffer pH 8 (20 g Tris/1,000 ml demi water, pH adjusted with cone. HCl)
The lakes of carmine were added buffer solution so that all samples contained the same amount Carminic Acid/ml corresponding to 1.5 g/1 of a 46.56% CA. lake.
Marker 12 or Sea Blue is applied as the protein size indicator (MW)
IM DL-Dithiothreitol (DTT): 20 mg DTT solution in 130 μl MQW
Volume added to the gel: Mark 12 5 μl, Sea Blue 7 μl, Carmine samples 10 μl
NUPAGE Novex high performance pre-cast gel 4-12% BIS-TRIS are stained by cromassie blue and/or silver
Example 1: Production of carminic acid lake
This example discloses examples of preparation of Al-Ca carmine lake with carminic acid and whey hydrolysate.
An amount of 21 g Carminic acid was dissolved in 500 ml water and in this carmine solution 33 g peptide was dissolved. pH was adjusted to 5 and the temperature was raised to 85-95°C. Then 8 g A1K(SO4)2*12H2O was dissolved in 50 ml water and added to the solution and then 8.2 g (CH3COO)2Ca*H2O was dissolved in 50 ml water and added to the solution. After 45 minutes 70-98% of the carminic acid in the solution was converted to carmine lake, which precipitated from the solution. The carmine lake was separated from the solution, dried and analyzed.
Figure imgf000012_0001
Figure imgf000013_0001
The resulting carmine lakes had a carminic acid content of 65-75% and a protein content of 18-22%. None of the proteins in the lakes, detectable in the SDS-PAGE analysis, were bigger than 3,000 Da.
The resulting carmine lakes have bright red color shades and were applicable as cochineal protein based carmine lakes for making carmine solutions and water-soluble carmine powders.
Conclusions:
The results shown in the table in example 1 demonstrates the following:
(1) that optimal carminic acid yields are obtained when the aqueous solution comprises from 3% to 5% carminic acid and from 4% to 7% of whey protein hydrolysate;
(2) when the amount of protein is increased, within the ranges as described herein, the yield is improved;
(3) that the ratio carminic acid/added proteins shall be less than 1 to avoid gelling and thereby impossible processing. Furthermore, the preferred ratio is from 0.5 to 0.8 and most preferably around 0.6.
Example 2:
This example discloses examples of Al-Ca carmine lake preparation with carminic acid and whey hydrolysate.
An amount of 21 g Carminic acid was dissolved in 500 ml water and in this carmine solution 33 g peptide was dissolved. pH was adjusted to 5 and the temperature was raised to 85-95°C.
Then 8 g (CH3COO)2Ca*H2θ was dissolved in 50 ml water and added to the solution and then 8.2 g AlK(SO4)2*12H2θ was dissolved in 50 ml water and added to the solution. After 45 minutes 70-98% of the carminic acid in the solution had been converted to carmine lake, which precipitated from the solution. The carmine lake was separated from the solution, dried and analyzed.
Visible black spots in the lake were identified. The black spots were most likely calcium car- minate, which had not undergone the change from calcium carminate to aluminum-calcium carmine lake.
By adding the AlK(SO4)2*12H2θ solution first, it is believed, that the aluminum and peptide attach to the carminic acid and makes it difficult/impossible for the calcium to form calcium carminate before it forms aluminum-calcium carmine lake.
Conclusions:
The result in example 2 demonstrates that it is important to first add the aluminum, wait for a period and then add the calcium in order to get less "black spots".

Claims

1. A process for making a carminic acid lake comprising the steps of
(i) treating an aqueous solution, comprising
(a) 0.5 to 15% (g/1) of carminic acid and
(b) from 0.75 to 15% (g/1) of not Dactylopius coccus costa insect proteins, where substantially all of the not Dactylopius coccus costa insect proteins have a molecular weight (MW) below 10,000 Da, wherein the aqueous solution is substantially free of Dactylopius coccus costa insect proteins with a molecular weight (MW) above 6,000 Da; with an aluminum and calcium compound,
(ii) adjusting the conditions to get suitable conditions to produce a calcium-aluminum carminic acid lake, wherein the lake comprises (b) from 40 to 80% carminic acid (dry weight) and
(b) from 10 to 30% not Dactylopius coccus costa insect proteins (dry weight), where substantially all of the not Dactylopius coccus costa insect proteins have a molecular weight (MW) below 10,000 Da and wherein the lake is substantially free of Dactylopius coccus costa insect proteins with a molecular weight (MW) above 6,000 Da.
2. The process of claim 1, wherein the aqueous solution is prepared by mixing a suitable pro¬ tein composition with a suitable pure carminic acid composition.
3. The process of claim 2, wherein the protein composition is a milk-based hydrolysate, in particular a whey hydrolysate.
4. The process of any of the preceding claims, wherein substantially all of the proteins have a molecular weight (MW) below 6,000 Da, more preferably below 4,000 Da and even more preferably below 3,000 Da.
5. The process of any of the preceding claims, wherein the aqueous solution comprises from 2 to 7% carminic acid and from 3 to 8% of proteins, more preferably the aqueous solution com- prises from 3 to 5% of carminic acid and from 4 to 6% of proteins; and wherein the produced carminic acid lake of step (ii) comprises from 55 to 75% of carminic acid (dry weight) and from 15 to 25% of proteins (dry weight), more preferably wherein lake comprises from 62 to 72% carminic acid (dry weight) and from 18 to 22% proteins (dry weight).
6. The process of any of the preceding claims, where in the aqueous solution of step (i) of claim 1 the ratio Carminic acid/not Dactylopius coccus costa insect proteins (g/1) is less than 1, more preferably from 0.5 to 0.8 and most preferably from 0.5 to 0.7.
7. The process of claim 6, wherein there, in step (i), the aluminum is first added and then after a suitable time the calcium is added to the aqueous solution; a suitable time being from 2 min¬ utes to 3 days.
8. The process of any of the preceding claims, wherein during the treatment of the carminic acid/protein aqueous solution with the aluminum and/or calcium compound the pH is adjusted to a value from 2 to 8 in order to produce the carminic acid lake, preferably the pH is adjusted to a value from 3 to 7 and more preferably adjusted to a pH value from 4 to 6.
9. A carminic acid aluminum lake, a carminic acid calcium lake or a carminic acid calcium- aluminum lake obtainable by a process of any of the claims 1 to 8, wherein the lake comprises from 40 to 80% carminic acid (dry weight) and from 10 to 30% proteins (dry weight) and wherein the lake is substantially free of Dactylopius coccus costa insect proteins and substan¬ tially all of the proteins in the lake have a molecular weight (MW) below 10,000 Da.
10. Use of a carminic acid aluminum lake, a carminic acid calcium lake or a carminic acid calcium-aluminum lake of claim 9 for making a color composition to be added to food prod¬ ucts, sweets, confectionary, beverages, pharmaceuticals or cosmetics.
PCT/EP2005/056195 2004-11-25 2005-11-24 Method for the preparation of a carminic acid lake WO2006056585A1 (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
CN2005800394464A CN101061185B (en) 2004-11-25 2005-11-24 Method for the preparation of a carminic acid lake
US11/577,751 US7641704B2 (en) 2004-11-25 2005-11-24 Method for the preparation of a carminic acid lake
BRPI0518294-8A BRPI0518294A2 (en) 2004-11-25 2005-11-24 Method for the preparation of a carminic acid pigment
US12/621,769 US8021440B2 (en) 2004-11-25 2009-11-19 Method for the preparation of a carminic acid lake

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP04106069A EP1669414B1 (en) 2004-11-25 2004-11-25 Method for the preparation of a carminic acid lake
EP04106069.0 2004-11-25

Related Child Applications (2)

Application Number Title Priority Date Filing Date
US11/577,751 A-371-Of-International US7641704B2 (en) 2004-11-25 2005-11-24 Method for the preparation of a carminic acid lake
US12/621,769 Continuation US8021440B2 (en) 2004-11-25 2009-11-19 Method for the preparation of a carminic acid lake

Publications (1)

Publication Number Publication Date
WO2006056585A1 true WO2006056585A1 (en) 2006-06-01

Family

ID=34929935

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/EP2005/056195 WO2006056585A1 (en) 2004-11-25 2005-11-24 Method for the preparation of a carminic acid lake

Country Status (9)

Country Link
US (2) US7641704B2 (en)
EP (1) EP1669414B1 (en)
CN (1) CN101061185B (en)
AT (1) ATE469191T1 (en)
BR (1) BRPI0518294A2 (en)
DE (1) DE602004027396D1 (en)
ES (1) ES2346212T3 (en)
RU (1) RU2398801C2 (en)
WO (1) WO2006056585A1 (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7641704B2 (en) 2004-11-25 2010-01-05 Chr-Hansen A/S Method for the preparation of a carminic acid lake
WO2012131057A2 (en) 2011-03-30 2012-10-04 Chr. Hansen A/S Carmine food coloring composition with high stability
US10415066B2 (en) 2015-06-10 2019-09-17 Danmarks Tekniske Universitet Use of octaketide synthases to produce kermesic acid and flavokermesic acid
WO2020200550A1 (en) 2019-03-29 2020-10-08 Chr. Hansen Natural Colors A/S Formulation for coloring surimi products

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US10188085B2 (en) * 2007-08-31 2019-01-29 Sciconsult, Inc. System and methodology for culturing cochineal insects on an artificial medium
WO2009032085A1 (en) * 2007-08-31 2009-03-12 Badderloch Woad, Inc. Means to culture cochineal insects in an artificial medium
US9497946B2 (en) 2007-08-31 2016-11-22 Badderloch Woad, Inc. System and methodology for culturing cochineal insects on an artificial medium
US20140364512A9 (en) * 2012-04-19 2014-12-11 Epc (Beijing) Natural Products Co., Ltd. Compositions comprising a combination of at least one colorant and at least one polysaccharide
WO2015004275A1 (en) 2013-07-11 2015-01-15 Chr. Hansen A/S Color composition comprising carmine pigment and ferrous ions
CA2923844C (en) 2013-09-11 2022-07-26 Arsia Therapeutics, Inc. Liquid protein formulations containing organophosphates
WO2016054259A1 (en) 2014-10-01 2016-04-07 Arsia Therapeutics, Inc. Polysaccharide and nucleic acid formulations containing viscosity-lowering agents
CN111454588B (en) * 2020-04-10 2021-12-07 江南大学 Method for preparing cochineal red aluminum-free lake pigment by using protein, product and application thereof
MX2020007632A (en) * 2020-07-16 2022-01-17 Carinlab S A P I De C V Process for obtaining carminic acid.

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20020058016A1 (en) * 2000-09-11 2002-05-16 San-Ei Gen F.F.I., Inc. Purified cochineal and method for its production

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ATE469191T1 (en) 2004-11-25 2010-06-15 Chr Hansen As METHOD FOR PRODUCING A CARMINAL ACID LACQUER

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20020058016A1 (en) * 2000-09-11 2002-05-16 San-Ei Gen F.F.I., Inc. Purified cochineal and method for its production

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
LIZASO M T ET AL: "IDENTIFICATION OF ALLERGENS INVOLVED IN OCCUPATIONAL ASTHMA DUE TO CARMINE DYE", ANNALS OF ALLERGY, ASTHMA & IMMUNOLOGY, ARLINGTON HEIGHTS, IL, US, vol. 84, May 2000 (2000-05-01), pages 549 - 552, XP002942166, ISSN: 1081-1206 *

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7641704B2 (en) 2004-11-25 2010-01-05 Chr-Hansen A/S Method for the preparation of a carminic acid lake
US8021440B2 (en) 2004-11-25 2011-09-20 Chr-Hansen A/S Method for the preparation of a carminic acid lake
WO2012131057A2 (en) 2011-03-30 2012-10-04 Chr. Hansen A/S Carmine food coloring composition with high stability
US9192183B2 (en) 2011-03-30 2015-11-24 Chr. Hansen Natural Colors A/S Carmine food coloring composition with high stability
US10415066B2 (en) 2015-06-10 2019-09-17 Danmarks Tekniske Universitet Use of octaketide synthases to produce kermesic acid and flavokermesic acid
US10900056B2 (en) 2015-06-10 2021-01-26 Danmarks Tekniske Universitet Use of octaketide synthases to produce kermesic acid and flavokermesic acid
WO2020200550A1 (en) 2019-03-29 2020-10-08 Chr. Hansen Natural Colors A/S Formulation for coloring surimi products
EP4209133A1 (en) 2019-03-29 2023-07-12 Oterra A/S Formulation for coloring surimi products

Also Published As

Publication number Publication date
CN101061185A (en) 2007-10-24
DE602004027396D1 (en) 2010-07-08
US20100061949A1 (en) 2010-03-11
EP1669414B1 (en) 2010-05-26
RU2007123561A (en) 2008-12-27
US7641704B2 (en) 2010-01-05
CN101061185B (en) 2011-12-07
ES2346212T3 (en) 2010-10-13
US8021440B2 (en) 2011-09-20
EP1669414A1 (en) 2006-06-14
ATE469191T1 (en) 2010-06-15
BRPI0518294A2 (en) 2008-11-11
RU2398801C2 (en) 2010-09-10
US20090025153A1 (en) 2009-01-29

Similar Documents

Publication Publication Date Title
US7641704B2 (en) Method for the preparation of a carminic acid lake
EP3238550A1 (en) Genipin-rich material and its use
WO2010074552A1 (en) Collagen extraction from aquatic animals
CA2491241A1 (en) Process for cross-linking proteins using a ketose with three to five carbon atoms
CA3026642C (en) Rapeseed protein isolate, food comprising the isolate and use as foaming or emulsifying agent
Li et al. Structural and functional properties of soluble Antarctic krill proteins covalently modified by rutin
CN115916992A (en) Dark rose pigment as food pigment
WO1997048288A1 (en) Method of encapsulation and product produced thereby
JP2005187401A (en) Protein-chitosan complex and method for producing the same
WO2017121859A1 (en) Composition containing amino acids
CN114605490B (en) Bamboo shoot protein with high oxidation resistance and functional characteristics, and preparation method and application thereof
US7264839B2 (en) Protein beverage
JPH01249709A (en) Cosmetic containing hen's egg polypeptide derivative
KR20220015657A (en) Functional low molecular peptide from the Mytilus coruscus with enhanced antioxidative activity and method for making the same
DE2909854A1 (en) L-Aminoacid-substd. polypeptide food additive prepn. - by reacting protein, aminoacid alkyl ester hydrochloride and proteolytic enzyme
KR102694251B1 (en) Method for food extract collagen from golden hibiscus leaves
JP4750693B2 (en) Method for producing kusunohagashi dye composition and composition thereof
JP2649361B2 (en) Blood cell-derived water-soluble protein hydrolyzate that does not exhibit bitterness and raw odor
JPH09111140A (en) Red pigment
JP2022146119A (en) Edible composition and method for producing the same
JPH1077208A (en) Composition for cosmetic, its production and cosmetic obtained by blending the same
WO2023152262A1 (en) Process of obtaining a protein preparation
RU2191195C1 (en) Method of preparing iodine-modified pectin
AXELSSON Protein isolation from brown seaweed, Saccharina latissima, as part of an integrated bio-refinery
NZ624662B2 (en) Genipin-rich material and its use

Legal Events

Date Code Title Description
AK Designated states

Kind code of ref document: A1

Designated state(s): AE AG AL AM AT AU AZ BA BB BG BR BW BY BZ CA CH CN CO CR CU CZ DE DK DM DZ EC EE EG ES FI GB GD GE GH GM HR HU ID IL IN IS JP KE KG KM KN KP KR KZ LC LK LR LS LT LU LV LY MA MD MG MK MN MW MX MZ NA NG NI NO NZ OM PG PH PL PT RO RU SC SD SE SG SK SL SM SY TJ TM TN TR TT TZ UA UG US UZ VC VN YU ZA ZM ZW

AL Designated countries for regional patents

Kind code of ref document: A1

Designated state(s): GM KE LS MW MZ NA SD SL SZ TZ UG ZM ZW AM AZ BY KG KZ MD RU TJ TM AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IS IT LT LU LV MC NL PL PT RO SE SI SK TR BF BJ CF CG CI CM GA GN GQ GW ML MR NE SN TD TG

121 Ep: the epo has been informed by wipo that ep was designated in this application
WWE Wipo information: entry into national phase

Ref document number: 200580039446.4

Country of ref document: CN

NENP Non-entry into the national phase

Ref country code: DE

WWE Wipo information: entry into national phase

Ref document number: 11577751

Country of ref document: US

ENP Entry into the national phase

Ref document number: 2007123561

Country of ref document: RU

Kind code of ref document: A

122 Ep: pct application non-entry in european phase

Ref document number: 05826359

Country of ref document: EP

Kind code of ref document: A1

WWW Wipo information: withdrawn in national office

Ref document number: 5826359

Country of ref document: EP

ENP Entry into the national phase

Ref document number: PI0518294

Country of ref document: BR