EP0239575A1 - Verfahren zur extraktion von caroteen aus rüben und das erhaltene konzentrat von caroteen - Google Patents

Verfahren zur extraktion von caroteen aus rüben und das erhaltene konzentrat von caroteen

Info

Publication number
EP0239575A1
EP0239575A1 EP86900602A EP86900602A EP0239575A1 EP 0239575 A1 EP0239575 A1 EP 0239575A1 EP 86900602 A EP86900602 A EP 86900602A EP 86900602 A EP86900602 A EP 86900602A EP 0239575 A1 EP0239575 A1 EP 0239575A1
Authority
EP
European Patent Office
Prior art keywords
carotene
juice
temperature
carrots
order
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.)
Pending
Application number
EP86900602A
Other languages
English (en)
French (fr)
Inventor
Jacques Dikansky
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.)
AROMES DE BRETAGNE SA
GEOVITAL Sarl
Original Assignee
AROMES DE BRETAGNE SA
GEOVITAL Sarl
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 AROMES DE BRETAGNE SA, GEOVITAL Sarl filed Critical AROMES DE BRETAGNE SA
Publication of EP0239575A1 publication Critical patent/EP0239575A1/de
Pending legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C403/00Derivatives of cyclohexane or of a cyclohexene or of cyclohexadiene, having a side-chain containing an acyclic unsaturated part of at least four carbon atoms, this part being directly attached to the cyclohexane or cyclohexene or cyclohexadiene rings, e.g. vitamin A, beta-carotene, beta-ionone
    • C07C403/24Derivatives of cyclohexane or of a cyclohexene or of cyclohexadiene, having a side-chain containing an acyclic unsaturated part of at least four carbon atoms, this part being directly attached to the cyclohexane or cyclohexene or cyclohexadiene rings, e.g. vitamin A, beta-carotene, beta-ionone having side-chains substituted by six-membered non-aromatic rings, e.g. beta-carotene
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23LFOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
    • A23L2/00Non-alcoholic beverages; Dry compositions or concentrates therefor; Their preparation
    • A23L2/70Clarifying or fining of non-alcoholic beverages; Removing unwanted matter
    • A23L2/84Clarifying or fining of non-alcoholic beverages; Removing unwanted matter using microorganisms or biological material, e.g. enzymes
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23LFOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
    • A23L5/00Preparation or treatment of foods or foodstuffs, in general; Food or foodstuffs obtained thereby; Materials therefor
    • A23L5/40Colouring or decolouring of foods
    • A23L5/42Addition of dyes or pigments, e.g. in combination with optical brighteners
    • A23L5/43Addition of dyes or pigments, e.g. in combination with optical brighteners using naturally occurring organic dyes or pigments, their artificial duplicates or their derivatives
    • A23L5/44Addition of dyes or pigments, e.g. in combination with optical brighteners using naturally occurring organic dyes or pigments, their artificial duplicates or their derivatives using carotenoids or xanthophylls
    • 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

Definitions

  • the present invention relates to a process for extracting carotene from carrots as well as to the carotene concentrate obtained by the implementation of this process.
  • Carotene is a product sought after by the food, pharmaceutical and dietetic industries, on the one hand as a colorant (red-orange), on the other hand because of its provitamin A properties.
  • carotene is generally produced by synthetic processes.
  • the invention aims to solve this problem, by proposing a process for extracting natural carotene, which is efficient and profitable, making it possible to obtain a final product rich in carotene and free of undesirable chemical substances.
  • the carrots are ground, b) the crushed product is pressed in order to extract a juice therefrom, c) this juice is subjected to an enzymation by a pectolytic enzyme, d) an ultrafiltration of the depectinized juice is carried out, e) the retentate is recovered , rich in carotene.
  • the ultrafiltration is preferably carried out by means of a membrane whose cut-off point is between 10,000 and 100,000, for example 20,000.
  • the ultrafiltration is advantageously carried out at a temperature of the order of ⁇ to 50 ° C and under a differential pressure of 2.5. 10 Pa.
  • the enzymation is also carried out at a temperature of the order of 5 to 50 ° C., for a period of 1 hour 30 minutes to approximately 2 hours.
  • the yield of the process can be further improved by subjecting, before pressing, the ground product to an enzymation with a pectolytic enzyme with cellulosic activity, at a temperature in the region of 5 ° C., for 1 hour 30 minutes to approximately 2 hours.
  • the carrots are first washed with water and sorted, so that the defective carrots are eliminated.
  • the retained carrots are then subjected to a blanching operation. This operation, which is carried out in water brought to a temperature between 90 and 10 ° C., for approximately 5 minutes, causes a softening of the carrots, and a destruction of the enzymes and the contaminants (molds and bacteria ) possibly present.
  • the carrots are then subjected to grinding; the characteristics of the crusher (of any type) are such that, at the output thereof, the pieces of crushed carrots have an average diameter of between 1 millimeter and 5 millimeters.
  • the ground materials are subjected to pressing, for example by means of an endless screw with decreasing pitch housed in a perforated cage the diameter of the perforations is of the order of 0.5 to 1 millimeter.
  • This operation separates the pulp from a juice.
  • the weight percentage of juice obtained is of the order of 60 to 70% of the ground product.
  • the juice is pasteurized at a temperature of about 85 ° C, for 10 to 15 seconds, which causes the destruction of a large part of the contaminants.
  • This pasteurized juice is then decanted, sieved, or centrifuged, so as to separate the grains of relatively large size still present; a clarified juice is thus obtained.
  • a pectolytic enzyme is then added to the juice, the role of which will be to completely degrade the pectin in order to prevent the juice from having too high a viscosity which would harm subsequent ultrafiltration.
  • This enzymation operation is carried out at a temperature comprised between 5 and 50 ° C, for a period of I hour 30 minutes to 2 hours approximately.
  • the juice obtained contains a content of 2 to 10 milligrams of carotene per 100 grams.
  • the juice is introduced into an ultrafiltration cartridge, provided with mineral membranes having a cut point of between 10,000 and 100,000, for example 20,000.
  • a cut point of 20 000 corresponds to a membrane, the pores of which have a diameter of the order of 500 micrometers. Only molecules with a molar mass of less than 20,000 grams can pass through it.
  • the ultrafiltration operation separates a permeate (which passes through the membranes) from a retentate (which does not pass through the membranes).
  • Carotene has a molecular weight greater than the cut-off point of the membranes, so it is contained in the retentate.
  • To increase the concentration of the carotene retentate several ultrafiltration cycles are carried out, by reintroducing the retentate several times into the filter.
  • the retentate obtained has a carotene content of the order of 500 to 600 milligrams per 100 grams.
  • the total ultrafiltration operation lasts approximately 16 to 18 hours. It is carried out at a temperature of the order of 45 to 50 ° C, under a differential pressure of 2.5. 10 Pa approximately.
  • Permeate is a liquid made up of water, sugar, organic nitrogen and mineral salts; it can advantageously be used, optionally after concentration, for animal feed.
  • the retentate includes proteins, starch, lipids, cellulose.
  • the concentrate obtained with the consistency of a paste, of an orange-red color.
  • the concentrate Before packaging, it is advantageous to pasteurize the concentrate, exposing it to a temperature of 85 ° C., for a time of the order of 10 to 15 seconds.
  • the product is then optionally atomized so as to be transformed into a powder. It is then packaged, under vacuum or under an inert atmosphere (devoid of oxygen) and in the dark; it is finally cooled and stored at a temperature below 5 °.
  • a pectolytic enzyme with cellulosic activity is used which facilitates the bursting of the carrot cells. This enzymation is carried out at a temperature in the region of 45 ° C., for a period of the order of 1 hour 30 minutes to 2 hours.
  • the process which is the subject of the invention is an entirely natural process, relatively easy to implement, while making it possible to obtain a product very rich in carotene.
  • the process which is the subject of the invention relates only to the extraction of carotene from carrots, it goes without saying that this same process could also be used for the extraction of carotene from other vegetables or fruit containing it.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Food Science & Technology (AREA)
  • Nutrition Science (AREA)
  • Engineering & Computer Science (AREA)
  • Polymers & Plastics (AREA)
  • Molecular Biology (AREA)
  • Zoology (AREA)
  • Microbiology (AREA)
  • Coloring Foods And Improving Nutritive Qualities (AREA)
  • Preparation Of Fruits And Vegetables (AREA)
  • Non-Alcoholic Beverages (AREA)
  • Jellies, Jams, And Syrups (AREA)
EP86900602A 1985-01-08 1986-01-07 Verfahren zur extraktion von caroteen aus rüben und das erhaltene konzentrat von caroteen Pending EP0239575A1 (de)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
FR8500280A FR2575748B1 (fr) 1985-01-08 1985-01-08 Procede d'extraction du carotene des carottes et concentre de carotene obtenu
FR8500280 1985-01-08

Publications (1)

Publication Number Publication Date
EP0239575A1 true EP0239575A1 (de) 1987-10-07

Family

ID=9315135

Family Applications (1)

Application Number Title Priority Date Filing Date
EP86900602A Pending EP0239575A1 (de) 1985-01-08 1986-01-07 Verfahren zur extraktion von caroteen aus rüben und das erhaltene konzentrat von caroteen

Country Status (4)

Country Link
EP (1) EP0239575A1 (de)
JP (1) JPS62501840A (de)
FR (1) FR2575748B1 (de)
WO (1) WO1986004059A1 (de)

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CH671322A5 (de) * 1986-09-29 1989-08-31 Bucher Guyer Ag Masch
CH673375A5 (de) * 1987-02-14 1990-03-15 Bucher Guyer Ag Masch
ES2032701B1 (es) * 1990-08-30 1993-12-16 Indulerida S A Procedimiento para la produccion de concentrado/clarificado de melocoton o nectarina.
US5245095A (en) * 1991-04-12 1993-09-14 Humanetics Corporation Extraction of carotenoids from natural sources
AU9497198A (en) * 1998-09-21 2000-04-10 Ajanta Pharma Limited Isolation of nutrient-rich carotenoids and their formulations
EP1051918A1 (de) * 1999-05-12 2000-11-15 Société des Produits Nestlé S.A. Verfahren zum Extrahieren von Carotenoiden und anderen Anti-Oxidantien; durch dieses Verfahren erhaltene Extrakte; diese Extrakte enthaltende Nahrungsmittel und Haustierfutter
FR2818992B1 (fr) * 2000-12-29 2003-10-24 Le Pot Au Pin Procede de concentration et de stabilisation de carotenoides a partir de legumes ou de fruits
BR102012009761A2 (pt) * 2012-04-26 2015-01-20 Embrapa Pesquisa Agropecuaria Processo de concentracao e purificacao de extrato obtido a partir de residuos de pseudofruto de caju e produto de elevado teor de carotenoides
EP3320784A1 (de) * 2016-11-10 2018-05-16 GNT Group B.V. Konzentrierte permeate aus gelben karotten
FR3101757B1 (fr) 2019-10-14 2023-09-22 Baumaniere Procédé de préparation aromatique d’ingrédients issus de tout composant alimentaire naturel contenus dans une capsule individuelle pour appareil de percolation standard

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3229345A1 (de) * 1982-08-06 1984-02-09 Henkel KGaA, 4000 Düsseldorf Herstellung eines rote bete-saftkonzentrats mit besserer geschmacksneutralitaet und haltbarkeit

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See references of WO8604059A1 *

Also Published As

Publication number Publication date
WO1986004059A1 (fr) 1986-07-17
JPS62501840A (ja) 1987-07-23
FR2575748A1 (fr) 1986-07-11
FR2575748B1 (fr) 1987-07-17

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Inventor name: DIKANSKY, JACQUES