PROCESS FOR THE TRANSFORMATION OF ESSENTIAL OILS COMPRISING LINALOL

Abstract

A process for transforming essential oils comprising linalool and the production of mixtures of linalool derivatives useful as fragrances in cosmetic compositions.

Claims

1. A process for transforming essential oils comprising linalool, which comprises incubating an essential oil comprising linalool in a culture medium of microorganism that expresses a P450 protein.

2. The process according to claim 1, wherein the essential oil is from a plant belonging to the genus selected from the group consisting of Ocimum, Copaifera, Mentha, and Cyperus.

3. The process according to claim 1, wherein the essential oil is from a plant selected from the group consisting hoary basil (Ocimum americanum), copaiba (Copaifera officinalis L., C. guianensis, C. reticulate, C. multijuga, C. confertiflora, C. langsdorffii, C. cariacea and C. cearensis), pudding grass (Mentha pulegium) and priprioca (Cyperus articulatus).

4. The process according to 1, wherein the microorganism is transgenic yeast.

5. The process according to claim 4, wherein the P450 cytochrome protein is farneseno synthase of Artemisia annua L., CYP71AV1.

6. The process according to claim 1, wherein the reaction is carried out in an aerobic medium.

7. The process according to claim 1, wherein the culture medium is kept under stirring during the reaction.

8. The process according to claim 1, wherein the cell density of the culture ranges from about 1.5 to about 20.

9. The process according to claim 1, wherein the incubation is kept between about 30 and about 50 hours.

10. The process according to claim 1, wherein the reaction temperature ranges from about 24 to about 36 C.

11. The process according to claim 1, wherein the reaction pH is between about pH 4.0 and pH 7.0.

12. A mixture of linalool derivatives obtained by a process as defined in claim 1.

13. A cosmetic composition comprising a mixture as defined in claim 12.

Description

DETAILED DESCRIPTION OF THE PRESENT INVENTION

[0013] Linalool is a natural terpene alcohol found in many flowers and spice plants, known also as -linalool, linalyl alcohol, linaloyl oxide, p-linalool, alo-ocimenol, and 3,7-dimethyl-1,6-octadien-3-ol. More than 200 species of plants produce linalool, chiefly those of the Laminaceae family (mint, aromatic herbs), Lauraceae family (laurel tree, cinnamon, rose-wood), and Rutaceae family (citric fruits), Birch, cannabis and other plants from tropical to boreal climatic zones, as well as a few fungi.

[0014] An essential oil is a hydrophobic liquid concentrate containing volatile compounds of plant aroma. Essential oils are also known as volatile oils, ethereal oils or simply as oil from the plant from which they have been extracted, such as clove oil. An oil is essential in the sense that it contains the essence of the plant fragrancethe characteristic fragrance of the plant from which it derives. The term essential as used herein does not mean indispensable, as in the case of essential amino acids or essential fatty acids, which are thus called because they are nutritionally demanded by a determined live organism.

[0015] Essential oils are generally extracted by distillation, often by using vapor. Other processes include expression, extraction with solvent, extraction of absolute petroleum, resining and cold pressing. They are used in perfumes, cosmetics, toilet-soaps and other products, for flavoring foods and beverages, and for imparting aromas to incense and household cleaning products.

[0016] Linalool is a natural terpene alcohol found in many flowers and spice plants with many commercial applications, most of which are based on its pleasant aroma (floral, with a spice touch). It has other names such as -linalool, linalyl alcohol, linaloyl oxide, p-linalool, alo-ocimenol, and 3,7-dimethyl-1,6-octadien-3-ol.

[0017] A few examples of essential oils comprising linalool that can be transformed according to the present invention are essential oils of plants of the genera Ocimum, Copaifera, Mentha, and Cyperus. Preferably, essential oils are of hoary basil (Ocimum americanum), copaiba (Copaifera officinalis L., C. guianensis, C. reticulate, C. multijuga, C. confertiflora, C. langsdorffii, C. cariacea and C. cearensis), pudding grass (Mentha pulegium) and priprioca (Cyperus articulatus).

[0018] According to the present invention, the essential oil comprising linalool is transformed by reaction with a microorganism expressing a P450 cytochrome protein, producing a mixture of linalool derivatives. Preferably, the linalool derivatives are linalool oxides.

[0019] The microorganism expressing a P450 cytochrome protein is a transgenic microorganism. More preferably, the transgenic microorganism is yeast. More preferably, the yeast is Sccharomyces cerevisiae.

[0020] The P45 cytochrome protein expressed in the transgenic microorganism used in the process of the present invention is preferably a farneseno synthase. More preferably, the P450 cytochrom protein is the farneseno synthase of Artemisia annua L., CYP71AV1. A region encoding farneseno synthase of Artemisia annua L., CYP71AV1 useful in the present invention can be obtained, for instance, from the access number GenBank No. AY835398.

[0021] Examples of transgenic microorganisms expressing a P45 cytochrome protein of the farneseno synthase type, as well as its amino acid sequences and encoding sequences and genic constructions useful in the present invention can be found in documents: WO2012106405, WO200614837, WO200705604, WO200839499, WO2012149470, WO201595804, WO2012158466, US7172886, WO200685899, WO200914636, WO2008140492, WO2008133658, WO2009126623, WO2007139924, WO2007136847, WO200942070, WO201371172, WO200727338 and WO2012135591, incorporated herein by reference.

[0022] The process of transforming essential oils comprising linalool of the present invention can be further carried out with yeasts stains available commercially as, for example, the stains Y1979 and Y5056 (Amyris Brasil S.A.).

[0023] The essential oil to be transformed is added to the culture medium of the transgenic microorganism and then incubated, preferably according to the parameters below.

[0024] The biotransformation reaction for transforming essential oil according to the present invention is preferably carried out in an aerobic medium. Besides, the culture medium is kept preferably under stirring during the reaction.

[0025] Preferably, the cell density of the microorganism ranges from 1.5 to about 20. Optionally, the cell density is of about 1.5, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19 or 20. More preferably, the cell density is of about DO=10.

[0026] Preferably, the reaction time if of about 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49 or 50 hours. More preferably, the reaction time is of about 30 and about 40 hours.

[0027] Preferably, the reaction temperature ranges from about 24 to about 37 C. Optionally, the temperature is of about 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36 or 37 C. More preferably, the temperature ranges from about 24 to 30 C. Still more preferably it is of about 30 C.

[0028] Preferably, the pH of the reaction is between about pH 4.0 and pH 7.0. Optionally, the pH of the reaction is of about pH 4.0 4.5, 5.0, 5.5, 6.0, 6, or 7.0. More preferably the pH of the reaction is of about pH 7.0.

[0029] The present invention further provides cosmetic compositions comprising the linalool derivatives obtained according to the process described herein.

EXAMPLE 1

[0030] In reaction tubes of the falcon and erlenmaeyer type, one added volumes of 1, 2, 3, 4 and 5 mL of culture medium (DO=1.5, 3, 10 and 20) of Saccharomyces cerevisiae expressing the P450 cytochrome protein and of hoary basil (Ocimum americanum) essential oil. Reaction times of 37-40 and 48-50 hours, raction times of 24, 30 and 37 C. and pH de 4.0, 5.5 and 7.0 were tested

[0031] In the mixture of linalool derivatives obtained under the above conditions, one detected cis furanoid linalool oxide, cis pyranoid linalool oxide, epoxylinalool, 5-hydroxylinalool, 8-hydroxylinalool, hotrienol, fenchone, fenchol, limonene oxide, among others.

[0032] The results referring to the obtainment of the above compounds are represented in Table 1.

TABLE-US-00001 TABLE 1 Parameter Results Reaction tube Falcon proved to be a superior option to provide Falcon x Erlenmeyer ideal aeration for 2 mL culture and to reduce tube loss of substrate and product by evaporation Cell density 10 OD-mL ensured the highest amount of P450 OD-ml = 1, 5, 3, 10 present, with less loss of material in biomass and 20 Culture Volume: 1 and 2 mL performed in a similar way or 1, 2, 3, 4, 5 mL (to 10 better than the others. OD-mL, proportion- ally stepped substrate) Reaction time: More incubation time led to a few low-intensity 37-40 h vs 48-50 h peaks. Reaction temperature: Conversion tendency: 24 C. > 30 C. > 37 C. 24, 30, 37 C. pH of the reaction 7.0 > 5.5 > 4.0 4.0, 5.5, 7.0