WO2002066668A2 - Procede de fabrication de proteines par fermentation de micro-organismes de la famille thermus, melange de proteines ainsi obtenu et composition cosmetiques les contenant. - Google Patents
Procede de fabrication de proteines par fermentation de micro-organismes de la famille thermus, melange de proteines ainsi obtenu et composition cosmetiques les contenant. Download PDFInfo
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- WO2002066668A2 WO2002066668A2 PCT/FR2002/000488 FR0200488W WO02066668A2 WO 2002066668 A2 WO2002066668 A2 WO 2002066668A2 FR 0200488 W FR0200488 W FR 0200488W WO 02066668 A2 WO02066668 A2 WO 02066668A2
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- WIPO (PCT)
- Prior art keywords
- cosmetic
- proteins
- microorganisms
- fermentation
- skin
- Prior art date
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- 239000000203 mixture Substances 0.000 title claims abstract description 34
- 239000002537 cosmetic Substances 0.000 title claims abstract description 32
- 238000000855 fermentation Methods 0.000 title claims abstract description 18
- 230000004151 fermentation Effects 0.000 title claims abstract description 18
- 244000005700 microbiome Species 0.000 title claims abstract description 17
- 241000589596 Thermus Species 0.000 title claims abstract description 12
- 102000004169 proteins and genes Human genes 0.000 title claims description 32
- 108090000623 proteins and genes Proteins 0.000 title claims description 32
- 238000004519 manufacturing process Methods 0.000 title claims description 17
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- -1 oxygen peroxide Chemical class 0.000 claims abstract description 11
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- 238000011282 treatment Methods 0.000 claims description 7
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 claims description 6
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- HYPYXGZDOYTYDR-HAJWAVTHSA-N 2-methyl-3-[(2e,6e,10e,14e)-3,7,11,15,19-pentamethylicosa-2,6,10,14,18-pentaenyl]naphthalene-1,4-dione Chemical compound C1=CC=C2C(=O)C(C/C=C(C)/CC/C=C(C)/CC/C=C(C)/CC/C=C(C)/CCC=C(C)C)=C(C)C(=O)C2=C1 HYPYXGZDOYTYDR-HAJWAVTHSA-N 0.000 claims description 3
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- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 claims 2
- 235000019270 ammonium chloride Nutrition 0.000 claims 1
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- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 102000019197 Superoxide Dismutase Human genes 0.000 description 3
- 108010012715 Superoxide dismutase Proteins 0.000 description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
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- 101000867659 Bos taurus Catalase Proteins 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- 241000282414 Homo sapiens Species 0.000 description 2
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 2
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- ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 description 1
- 108020004465 16S ribosomal RNA Proteins 0.000 description 1
- 208000002874 Acne Vulgaris Diseases 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N Acrylic acid Chemical compound OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
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- 108010077805 Bacterial Proteins Proteins 0.000 description 1
- YDNKGFDKKRUKPY-JHOUSYSJSA-N C16 ceramide Natural products CCCCCCCCCCCCCCCC(=O)N[C@@H](CO)[C@H](O)C=CCCCCCCCCCCCCC YDNKGFDKKRUKPY-JHOUSYSJSA-N 0.000 description 1
- 206010015150 Erythema Diseases 0.000 description 1
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- CRJGESKKUOMBCT-VQTJNVASSA-N N-acetylsphinganine Chemical compound CCCCCCCCCCCCCCC[C@@H](O)[C@H](CO)NC(C)=O CRJGESKKUOMBCT-VQTJNVASSA-N 0.000 description 1
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- ZVEQCJWYRWKARO-UHFFFAOYSA-N ceramide Natural products CCCCCCCCCCCCCCC(O)C(=O)NC(CO)C(O)C=CCCC=C(C)CCCCCCCCC ZVEQCJWYRWKARO-UHFFFAOYSA-N 0.000 description 1
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- LWGJTAZLEJHCPA-UHFFFAOYSA-N n-(2-chloroethyl)-n-nitrosomorpholine-4-carboxamide Chemical compound ClCCN(N=O)C(=O)N1CCOCC1 LWGJTAZLEJHCPA-UHFFFAOYSA-N 0.000 description 1
- VVGIYYKRAMHVLU-UHFFFAOYSA-N newbouldiamide Natural products CCCCCCCCCCCCCCCCCCCC(O)C(O)C(O)C(CO)NC(=O)CCCCCCCCCCCCCCCCC VVGIYYKRAMHVLU-UHFFFAOYSA-N 0.000 description 1
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P21/00—Preparation of peptides or proteins
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/64—Proteins; Peptides; Derivatives or degradation products thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/16—Emollients or protectives, e.g. against radiation
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P39/00—General protective or antinoxious agents
- A61P39/06—Free radical scavengers or antioxidants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/80—Process related aspects concerning the preparation of the cosmetic composition or the storage or application thereof
- A61K2800/85—Products or compounds obtained by fermentation, e.g. yoghurt, beer, wine
Definitions
- the invention which is the subject of this present patent lies in the discovery that it is possible to obtain, by biotechnology techniques, active principles having powerful anti-free radical effects from suitably used microorganisms.
- microorganisms concerned are part of new strains of thermophiles discovered at the level of underwater hydrothermal resurgences.
- thermophilic microorganisms have been used in biotechnology to prepare DNA usable in new amplification techniques called "PCR" (Polymerase Chain Reaction) from cell lysates.
- PCR Polymerase Chain Reaction
- thermophiles are therefore probably made up of original and original substances capable of having innovative therapeutic or even cosmetic effects. • Certain metabolites produced by these thermophilic bacteria are thermostable, that is to say that their properties are preserved at high temperature. The lifespan and activity of the molecules could make them stable long-term active ingredients in the finished cosmetic product.
- the process for manufacturing proteins by fermentation of microorganisms which is the subject of this present patent uses a strain of the genus Thermus, in particular Thermus thermophilus, variant GY1211, and have been isolated from an underwater hydrothermal resurgence ( 2000 m deep) from the east- Pacific ridge in the Guaymas basin
- Bacille Gram (Gulf of California). These are Bacille Gram (-), whose size is substantially equal to 0.5 ⁇ m x 10 ⁇ m and which are aerobic, heterotrophic, non-sporulated, thermophilic, barotolerant and which, in culture, give orange, round, regular, smooth, non-convex colonies.
- thermophilic strains are capable of producing or providing molecules which have numerous physiological activities which can be used in the cosmetic and dermopharmaceutical fields.
- composition of nutritional elements in the GY / 01 medium yeast extract and NELCl.
- yeast extract To avoid the classic problems of coloring and odor, it is necessary to limit their concentration to the minimum necessary.
- yeast extract As regards the yeast extract, it has been found that the concentration of 0.25% is the limiting concentration and that at 1%, no more biomass is obtained than at 0.5%. The concentration of yeast extract chosen is therefore 0.5%.
- the optimal concentration of use of the NK Cl chosen is found at 0.3%
- the doubling time of the population is equal to 47 minutes with a growth rate ⁇ m equal to 0.386 (H -1 ).
- any other fermentation and protein extraction process can be used in the context of this patent.
- tangential ultrafiltration on 20kD threshold tangential ultrafiltration on 20kD threshold
- the product obtained after fermentation and filtration can undergo different types of treatment: clarification, concentration or dilution, conservation, purification, fractionation by precipitation, by chromatography, lyophilization or atomization.
- One of the preferred embodiments of the invention consists of the fermented medium of GY1211 after detergent treatment and concentration by Ultrafiltration.
- compositions, powders, crystals, emulsions, ...) can be used in all the usual dosage forms in cosmetics and dermopharmacy.
- the following two compositions are given by way of nonlimiting examples.
- the H 2 O 2 absorbs at 240 nm, therefore the drop in OD at 240 nm is proportional to the degradation of H 2 O 2 which makes it possible, by comparison with a standard range produced from bovine catalase, to measure the enzymatic or pseudoenzymatic activity of the unknown sample.
- the following table summarizes the pseudoenzymatic activities of the catalase type (means ⁇
- Enzymatic activity is observed for all samples fermented by Thermus, while the non-fermented culture media do not. In addition, the relationship between the activities measured is consistent with that of the concentration achieved. It is also possible to note that the treatments used are equivalent in terms of enzymatic activity obtained.
- the fermented medium described above which has peroxidase, catalase-like, anti-radical, glycation inhibiting and modulating collagen synthesis enzymatic activities, may be used for skin care, particularly for combating deleterious effects of free radicals and against all their consequences on skin, physiological or premature aging, during exposure to natural NUs or as well as for skin care, in particular of the face, body, scalp and hair ; to modulate the cutaneous concentration of ceramides, to stimulate the immune system, to obtain a protective effect by chaperone effect and as detoxifier with respect to the various hyper-reactive free radicals including, in particular, oxygen peroxide, by the presence of menaquinone in the culture medium which is the subject of this patent.
- the fermented media are generally used between 0.001% and 2% (w / w) by dry weight for concentrated, lyophilized or atomized media, generally between 0.1 and 10.0% (w / p) for fermented media in liquid form.
- the fermented medium can be used in any dosage form used in cosmetics or dermopharmacy: O / W and W / O emulsions, milks, lotions, ointments, hair lotions, shampoos, soaps, sticks and pencils, sprays, body oils, without this list is exhaustive.
- the fermented medium can be combined in cosmetic compositions with any other ingredient usually used in cosmetics: extraction and / or synthetic lipids, gelling and viscosifying polymers, surfactant and emulsifiers, water-soluble or liposoluble active principles, extracts from other plants. , tissue extracts, other marine extracts.
- the cosmetic or dermopharmaceutical compositions containing the fermented medium can be creams, balms or gels or lotions or sunscreens and after sunscreens, after-shave products, depilatory or post-depilatory creams.
- These cosmetic compositions containing the fermented or dermopharmaceutical medium are intended for skin care, particularly for combating the deleterious effects of free radicals and all their consequences on skin, physiological or premature aging, during exposure to natural or artificial UNs.
- compositions containing the fermented or dermopharmaceutical medium are used for the preparation of medicaments intended for skin care, particularly for combating the deleterious effects of fiber radicals and against all of their consequences on skin, physiological or premature aging, during exposure to natural UN or as well as for skin care, in particular of the face, body, scalp and hair; to modulate the cutaneous concentration in ceramides, to stimulate the immune system, to obtain a protective effect by chaperone effect and as detoxifier and anti-free radical vis-à-vis, in particular, oxygen peroxide.
- the fermented medium can also be used alone, or incorporated in cosmetic or dermopharmaceutical compositions, bound (s) or incorporated (s) or absorbed (s) or adsorbed (s) in the form of macro-, micro- and nanoparticles or in macro-, micro- and nanocapsules for application on or in textiles, synthetic or natural fibers, wools and any material capable of being used to make clothes and underwear for day or night, directly in contact with the skin or hair to allow one continuous topical delivery.
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- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Engineering & Computer Science (AREA)
- Zoology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Wood Science & Technology (AREA)
- Biochemistry (AREA)
- Dermatology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Epidemiology (AREA)
- Birds (AREA)
- Pharmacology & Pharmacy (AREA)
- Molecular Biology (AREA)
- Biotechnology (AREA)
- Microbiology (AREA)
- Medicinal Chemistry (AREA)
- Toxicology (AREA)
- General Engineering & Computer Science (AREA)
- Genetics & Genomics (AREA)
- Cosmetics (AREA)
- Peptides Or Proteins (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Medicinal Preparation (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
Description
Claims
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AU2002235994A AU2002235994A1 (en) | 2001-02-21 | 2002-02-07 | Method for producing proteins by fermentation of microorganisms from the thermus family, the protein mixture thus obtained and cosmetic compositions containing same |
JP2002566372A JP2005501805A (ja) | 2001-02-21 | 2002-02-07 | Thermus科の微生物の発酵によるタンパク質の生成のためのプロセス、このようにして得られたタンパク質の混合物、およびそれらを含有する美容用組成物 |
US10/468,081 US20040115766A1 (en) | 2001-02-21 | 2002-02-07 | Method for producing proteins by fermentation of microorganisms from the thermus family the protein mixture thus obtained and cosmetic compositions containing same |
EP02702466A EP1392840A2 (fr) | 2001-02-21 | 2002-02-07 | Procede de fabrication de proteines par fermentation de micro-organismes de la famille thermus, melange de proteines ainsi obtenu et composition cosmetiques les contenant. |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR01/02442 | 2001-02-21 | ||
FR0102442A FR2821086B1 (fr) | 2001-02-21 | 2001-02-21 | Procede de fabrication de proteines par fermentation de microorganismes de la famille thermus, melange de proteines ainsi obtenu et composition cosmetique les contenant |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2002066668A2 true WO2002066668A2 (fr) | 2002-08-29 |
WO2002066668A3 WO2002066668A3 (fr) | 2003-12-18 |
Family
ID=8860339
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/FR2002/000488 WO2002066668A2 (fr) | 2001-02-21 | 2002-02-07 | Procede de fabrication de proteines par fermentation de micro-organismes de la famille thermus, melange de proteines ainsi obtenu et composition cosmetiques les contenant. |
Country Status (6)
Country | Link |
---|---|
US (1) | US20040115766A1 (fr) |
EP (1) | EP1392840A2 (fr) |
JP (1) | JP2005501805A (fr) |
AU (1) | AU2002235994A1 (fr) |
FR (1) | FR2821086B1 (fr) |
WO (1) | WO2002066668A2 (fr) |
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WO2005074951A1 (fr) * | 2004-01-30 | 2005-08-18 | E-L Management Corporation | Compositions renfermant un antioxydant active de maniere interne |
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WO2010082175A2 (fr) | 2009-01-16 | 2010-07-22 | Sederma | Nouveaux composés, notamment des peptides, compositions comprenant ces derniers et utilisations dans les domaines cosmétique et dermopharmaceutique |
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WO2015181688A1 (fr) | 2014-05-22 | 2015-12-03 | Sederma | Peptides, compositions les comprenant et utilisations, en particulier utilisations cosmétiques |
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FR3004351B1 (fr) * | 2013-04-16 | 2015-03-27 | Sederma Sa | Prevention et traitement des dommages cutanes lies aux infra-rouges |
Family Cites Families (5)
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JP3219792B2 (ja) * | 1991-09-04 | 2001-10-15 | 三省製薬株式会社 | 皮膚老化防止用外用剤 |
US5405767A (en) * | 1992-04-08 | 1995-04-11 | Solvay Enzymes, Inc. | Purified enzyme concentrate and method of preparation |
US5739156A (en) * | 1994-09-21 | 1998-04-14 | The Procter & Gamble Company | Methods of using 2,4-dienoic acid esters of tocopherols to reduce free radical damage in mammalian cells |
US5969121A (en) * | 1996-01-11 | 1999-10-19 | Thermogen, Inc. | Stable biocatalysts for ester hydrolysis |
FR2783169B1 (fr) * | 1998-09-15 | 2001-11-02 | Sederma Sa | Utilisation cosmetique ou dermopharmaceutique de peptides pour la cicatrisation et pour l'amelioration de l'aspect cutane lors du vieillissement naturel ou accelere (heliodermie, pollution) |
-
2001
- 2001-02-21 FR FR0102442A patent/FR2821086B1/fr not_active Expired - Lifetime
-
2002
- 2002-02-07 JP JP2002566372A patent/JP2005501805A/ja active Pending
- 2002-02-07 EP EP02702466A patent/EP1392840A2/fr not_active Ceased
- 2002-02-07 US US10/468,081 patent/US20040115766A1/en not_active Abandoned
- 2002-02-07 AU AU2002235994A patent/AU2002235994A1/en not_active Abandoned
- 2002-02-07 WO PCT/FR2002/000488 patent/WO2002066668A2/fr active Application Filing
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EP2510982A1 (fr) | 2006-05-05 | 2012-10-17 | Sederma | Nouvelles compositions cosmétiques contenant au moins un peptide doté d'au moins un cycle aromatique immobilisé |
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WO2010067327A1 (fr) | 2008-12-11 | 2010-06-17 | Sederma | Composition cosmétique contenant des oligoglucuronanes acétylés |
WO2010082175A2 (fr) | 2009-01-16 | 2010-07-22 | Sederma | Nouveaux composés, notamment des peptides, compositions comprenant ces derniers et utilisations dans les domaines cosmétique et dermopharmaceutique |
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WO2012164488A2 (fr) | 2011-06-01 | 2012-12-06 | Sederma | Nouvelle utilisation topique cosmétique ou dermopharmaceutique d'un mélange d'un tripeptide ghk et d'un tétrapeptide gqpr |
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WO2016003505A1 (fr) | 2014-07-02 | 2016-01-07 | Geoffrey Brooks Consultants, Llc | Compositions à base de peptide et procédés d'utilisation |
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US11071711B2 (en) | 2016-05-13 | 2021-07-27 | Yi-Chun Lin | Compositions for skin application |
US11191712B2 (en) | 2017-01-13 | 2021-12-07 | Galactic Beauty, LLC | Skin treatment compositions, masks, and related methods |
WO2021064173A1 (fr) | 2019-10-04 | 2021-04-08 | Sederma | Utilisation de cellules végétales de leontodium alpinum pour un traitement cutané anti-âge anti-glycation |
FR3101542A1 (fr) | 2019-10-04 | 2021-04-09 | Sederma | UTILISATION DE cellules VÉGÉTALES de LEONTODIUM ALPINUM POUR UN TRAITEMENT cosmÉtique ANTIGLYCATION |
Also Published As
Publication number | Publication date |
---|---|
FR2821086B1 (fr) | 2003-12-12 |
WO2002066668A3 (fr) | 2003-12-18 |
US20040115766A1 (en) | 2004-06-17 |
AU2002235994A1 (en) | 2002-09-04 |
JP2005501805A (ja) | 2005-01-20 |
EP1392840A2 (fr) | 2004-03-03 |
FR2821086A1 (fr) | 2002-08-23 |
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