NOVEL VIOLAXANTHIN-OVERPRODUCING STRAIN OF CHLORELLA VULGARIS AND THE METHOD FOR PRODUCING VIOLAXANTHIN USING THE SAME

Abstract

The present invention relates to a novel violaxanthin-overproducing strain of Chlorella vulgaris and a method of producing violaxanthin therefrom. The inventors have developed a strain that produces violaxanthin at a significantly higher level than a wild-type strain by inducing a random chemical mutation in a Chlorella vulgaris strain to, and then as a result of analysis, confirmed that the strain produces violaxanthin up to 0.41% based on dry weight, which reaches the highest level that is possible to be produced in microalgae. Furthermore, as a method of effectively extracting a carotenoid pigment containing violaxanthin from the strain was established, since the strain and the developed pigment extraction method according to the present invention allow effective production and separation of violaxanthin, the strain is expected to increase commercial applications such as cosmetics, health functional foods and feed.

Claims

1. A violaxanthin-overproducing Chlorella vulgaris CvLD-01 strain (Accession No. KCTC 14091BP).

2. The strain of claim 1, wherein the strain is derived from a Chlorella vulgaris UTEX395 strain (Accession No. KCTC 14091BP).

3. The strain of claim 1, wherein the strain has alanine (A), which is amino acid 336 of the lycopene epsilon cyclase (CvLCYE) gene, substituted with valine (V) (Accession No. KCTC 14091BP).

4. A method of extracting carotenoid pigment from the Chlorella vulgaris strain of claim 1 using glass bead-added sonication.

5. The method of claim 4, wherein the extraction method uses methanol as a solvent.

6. The method of claim 4, wherein the glass bead has a diameter of 0.4 to 0.7 mm.

7. A method of producing violaxanthin on a large scale, which comprises culturing the Chlorella vulgaris CvLD-01 strain of claim 1.

8. The method of claim 7, wherein the culturing is performed for 72 to 96 hours in a medium containing acetic acid as a carbon source under 100 μmol photon m.sup.−2s.sup.−1.

9. A composition for food or a food additive, comprising one or more selected from the group consisting of the Chlorella vulgaris CvLD-01 strain of claim 1, a dry product thereof, a culture broth thereof and an extract thereof.

10. An antioxidant method, comprising: injecting a composition comprising one or more selected from the group consisting of the Chlorella vulgaris CvLD-01 strain of claim 1, a dry product thereof, a culture broth thereof and an extract thereof into a subject.

11. A cosmetic composition, comprising one or more selected from the group consisting of the Chlorella vulgaris CvLD-01 strain of claim 1, a dry product thereof, a culture broth thereof and an extract thereof.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0024] The above and other objects, features and advantages of the present invention will become more apparent to those of ordinary skill in the art by describing in detail exemplary embodiments thereof with reference to the accompanying drawings, in which:

[0025] FIG. 1A shows the results of comparing methods of extracting carotenoid pigment from Chlorella vulgaris, shows vortexing with a vortex, sonication and glass bead-added sonication (Bead+Sonication) improved in the present invention, and FIG. 1B shows the result of comparatively analyzing pigment extraction efficiency by extracting each of chlorophyll-a (Chl-a) and chlorophyll-b (Chl-b) from a Chlorella vulgaris strain by each of the three extraction methods;

[0026] FIG. 2A shows the result of fluorescence analysis using IMAGING-PAM of observing and analyzing the phenotypes of the wild type and mutant strains of Chlorella vulgaris which are cultured in TAP media, and FIG. 2B shows the result of profiling various pigments produced in the strains through HPLC (WT: wild type strain, CvLD: mutant strain);

[0027] FIG. 3A shows a carotenoid biosynthesis pathway for the comparison results obtained by sequencing of lycopene epsilon cyclase (CvLCYE) and the analysis of a three-dimensional structure, FIG. 3B shows the result of aligning CvLCYE amino acid sequences of wild-type Chlorella vulgaris (C. vulgaris), other species including Arabidopsis thaliana and a mutant strain (C. vulgaris LD) according to the present invention (A. thaliana: SEQ ID NO: 5, C. reinhardtii: SEQ ID NO: 6, C. variabilis: SEQ ID NO: 7, C. vulgaris: SEQ ID NO: 8, C. vulgaris LD: SEQ ID NO. 9), FIG. 3C shows the result of comparatively analyzing expected 3D structures of CvLCYE using a SWISS-mode, and FIG. 3D shows the result of comparing CvLCYE mRNA expression levels in wild-type Chlorella vulgaris and the mutant strain (CvLD) according to the present invention;

[0028] FIG. 4A shows the results of analyzing the growth rates of wild-type Chlorella vulgaris and a mutant strain according to the present invention in flask culture, which shows the result of comparing a cell growth rate over time for each strain having a cell density of 1×10.sup.4 cells/mL, FIG. 4B shows the result of comparing cell growth rates between the strains by measuring optical densities (OD.sub.750), FIG. 4C shows the result of comparing a dry cell weight of each strain, and FIG. 4D shows the result of comparing an oxygen evolution rate according to light intensity in each strain;

[0029] FIG. 5A shows the result of culturing a mutant strain according to the present invention under various light intensity conditions, and analyzing a growth rate and carotenoid production, which shows a result of measuring an optical density (OD.sub.750) and comparing a cell growth rate, and FIG. 5B shows production amounts of various pigments; and

[0030] FIG. 6A shows the results of culturing mutant strains according to the present invention in media containing three different types of carbon sources and analyzing growth rates and carotenoid production, which shows a result of measuring optical densities and comparing growth rates of mutant strains cultured in media containing different carbon sources, and FIG. 6B shows a pigment production amount in each strain.

DETAILED DESCRIPTION OF EXEMPLARY EMBODIMENTS

[0031] The inventors have developed a Chlorella vulgaris mutant significantly improved in violaxanthin content by a random chemical mutation to improve the major limitations, such as low intracellular content and low intracellular pigment extraction yield, in violaxanthin production, and the strain was deposited with the Biological Resource Center of the Korea Research Institute of Bioscience and Biotechnology under Accession No. KCTC 14091BP. In addition, the inventors have established a method of effectively extracting a pigment containing violaxanthin in the strain and optimal culture conditions that can maximize violaxanthin production from the strain, and thus the present invention was completed.

[0032] Therefore, the present invention provides a violaxanthin overproducing Chlorella vulgaris CvLD-01 strain (Accession No. KCTC 14091BP).

[0033] In the present invention, Chlorella vulgaris, which is a strain used as a host strain for pigment production, is generally recognized as safe (GRAS) by US Food and Drug Administration and widely used as a component of health food and nutrient supplements.

[0034] In the present invention, a novel mutant strain that is able to accumulate violaxanthin was isolated using the Chlorella vulgaris strain, and a method of producing and isolating violaxanthin from the strain with the maximum efficiency was established.

[0035] In one embodiment of the present invention, mutations were randomly generated by treating a Chlorella vulgaris UTEX395 strain with EMS, a mutant exhibiting low fluorescence was selected first, and then a lutein-deficient mutant strain (CvLD) having excessive violaxanthin was finally selected through HPLC. As a result of HPLC, it was confirmed that antheraxanthin and zeaxanthin as well as violaxanthin also increased approximately 3 to 6-fold, and β-carotene increased 1.64-fold in the strain (see Example 3).

[0036] In another embodiment of the present invention, as a result of analyzing a gene mutated in the CvLD strain according to the present invention, it was confirmed that a CvLCYE gene involved in a carotenoid biosynthesis pathway is mutated (A336V). In addition, it was confirmed that a decrease in lutein in the CvLD strain is caused by the structural change of a protein of the gene by analyzing the 3D structure of the protein in the wild-type and CvLD strains (see Example 4).

[0037] In still another embodiment of the present invention, as a result of analyzing the growth rates of the wild type and CvLD in flask culture by various methods, it was confirmed that, overall, the cell growth of CvLD increases 1.2 to 1.4-fold, compared with the wild type. In addition, it was confirmed that the photosynthesis and respiration rates of the mutant strain are significantly higher than the wild type by an oxygen evolution rate, determining that such a difference affects the improvement in growth rate (see Example 5).

[0038] The results from the embodiments of the present invention through specific experiments prove that a violaxanthin-overproducing strain of Chlorella vulgaris according to the present invention is able to be used as a novel natural source for violaxanthin.

[0039] As described above, the Chlorella vulgaris strain according to the present invention has a property of excessively producing violaxanthin and lacks the ability to produce lutein. In addition, the production of one or more selected from the group consisting of antheraxanthin, zeaxanthin and β-carotene may be increased.

[0040] In addition, the growth rate of the Chlorella vulgaris strain according to the present invention may be increased 1.2 to 2-fold, preferably, 1.2 to 1.7-fold, more preferably, 1.2 to 1.5-fold, and still more preferably, 1.2 to 1.4-fold, compared to the wild-type strain.

[0041] In the present invention, the CvLCYE gene in which a mutation occurs in the Chlorella vulgaris strain is called a carotenoid psi-end group lyase (decyclizing), and is one of the enzymes involved in lycopene cyclization that coverts the carotenoid biosynthesis pathway into two metabolic branches, resulting in production of lutein by LCYE.

[0042] In another aspect of the present invention, the present invention provides a method of extracting a carotenoid pigment from the Chlorella vulgaris strain using glass bead-added sonication.

[0043] Specifically, in one embodiment of the present invention, an improved extraction method that can extract a carotenoid pigment from the Chlorella vulgaris strain with high efficiency was invented and its efficiency was analyzed, confirming that, when the glass bead-added sonication according to the present invention was used, the highest extraction efficiency is exhibited compared to when using vortexing and simple sonication (see Example 2).

[0044] In the present invention, sonication is one of the methods of disrupting cells to release an intracellular product, and a mechanical method of disrupting the cell wall and cell membrane of a cell due to a pressure change caused by generating a sound wave of 16 kHz or more. Here, the extraction efficiency of the carotenoid pigment from the strain may be further improved using a method improved by adding a 0.4 to 0.7, and preferably, 0.5 to 0.6-mm glass bead to apply a high shearing force and a high impact force may be further improved.

[0045] Here, as a solvent, methanol may be used, but the present invention is not limited thereto.

[0046] In still another aspect of the present invention, the present invention provides a method of producing violaxanthin on a large scale, which includes culturing the Chlorella vulgaris CvLD-01 strain.

[0047] In one embodiment of the present invention, to establish the optimal conditions of flask culture of a CvLD strain according to the present invention, the effect of light intensity and a carbon source was analyzed. First, it was confirmed that cell growth and violaxanthin production are not proportional to light intensity by measuring cell growth and carotenoid production of the mutant strain under various light intensity conditions, and the light intensity exhibiting the highest efficiency was confirmed (see Example 6). In addition, as a result of culturing the CvLD strain in a medium having different carbon sources and measuring cell growth and a carotenoid production rate, it can be seen that the strain uses acetic acid more effectively than glucose used. Further, after the CvLD strain was cultured under the optimal culture conditions deduced from the analysis, the production yield of violaxanthin was measured, resulting in reaching the highest yield of 0.41% (see Example 7).

[0048] Therefore, the culture for the mass production of violaxanthin may be performed for 72 to 96 hours in a medium containing acetic acid as a carbon source under 100 μmol photon m.sup.−2s.sup.−1, but the present invention is not limited thereto.

[0049] In yet another aspect of the present invention, the present invention provides a composition for food or a food additive, which includes one or more selected form the group consisting of the Chlorella vulgaris CvLD-01 strain, a dry product thereof, a culture broth thereof and an extract thereof.

[0050] In yet another aspect of the present invention, the present invention provides a composition for health functional food, which includes one or more selected from the group consisting of the Chlorella vulgaris CvLD-01 strain, a dry product thereof, a culture broth thereof and an extract thereof.

[0051] The health functional food may exhibit an anticancer, antioxidant or anti-inflammatory effect, and preferably, an antioxidant effect, and may be used to improve a related disease or symptom.

[0052] The term “improvement” used herein refers to all types of actions that at least reduce parameters related to a condition to be treated, for example, a degree of a symptom, and the health functional food can be used before or after the onset of the corresponding disease, or simultaneously with or separately from a drug for treatment.

[0053] The term “health functional food composition” used herein includes one or more of a carrier, a diluent, an excipient and an additive, and is formulated into one selected from the group consisting of a tablet, a pill, a powder, a granule, a capsule and a liquid. Foods that can be added to the extract of the present invention may include various foods, powders, granules, tablets, capsules, syrups, beverages, gums, teas, vitamin complexes, and health functional foods. As an additive further included in the present invention, one or more types of ingredients selected from the group consisting of natural carbohydrates, sweeteners, nutrients, vitamins, minerals (electrolytes), flavoring agents (synthetic flavoring agents, natural flavoring agents, etc.), coloring agents, fillers, pectic acid and a salt thereof, alginic acid and a salt thereof, organic acids, protective colloid thickening agents, pH modifiers, stabilizers, preservatives, antioxidants, glycerin, alcohols, carbonating agents, and fruit flesh may be used. Examples of the above-mentioned natural carbohydrates include conventional sugars, for example, monosaccharides such as glucose, fructose, etc.; disaccharides such as maltose, sucrose, etc.; and polysaccharides such as dextrin, cyclodextrin, etc., and sugar alcohols such as xylitol, sorbitol, erythritol, etc. As the sweeteners, natural sweeteners [thaumatin, Stevia extract (e.g., rebaudioside A, glycyrrhizin, etc.)] and synthetic sweeteners (saccharin, aspartame, etc.) may be advantageously used. In addition to the above ingredients, the composition according to the present invention may contain a variety of nutrients, vitamins, minerals (electrolytes), flavoring agents including synthetic and natural flavoring agents, coloring agents and fillers (cheese, chocolate, etc.), pectic acid and a salt thereof, alginic acid and a salt thereof, an organic acid, protective colloid thickening agents, pH modifiers, stabilizers, preservatives, glycerin, alcohols, or carbonating agents used in carbonated beverages. In addition, the composition according to the present invention may contain flesh for preparing natural fruit juices and vegetable juices. Such an ingredient may be used independently or in combination. Specific examples of the carriers, excipients, diluents and additives may include, but are not limited to, one or more selected from the group consisting of lactose, dextrose, sucrose, sorbitol, mannitol, erythritol, starch, acacia gum, calcium phosphate, alginate, gelatin, calcium phosphate, calcium silicate, microcrystalline cellulose, polyvinylpyrrolidone, cellulose, methyl cellulose, water, sugar syrup, methyl hydroxybenzoate, propyl hydroxybenzoate, talc, magnesium stearate, and mineral oil.

[0054] In a yet another aspect of the present invention, the present invention provides a cosmetic composition, which includes one or more selected from the group consisting of the Chlorella vulgaris CvLD-01 strain, a dry product thereof, a culture broth thereof and an extract thereof.

[0055] The cosmetic composition may have antioxidative, antiaging or anti-inflammatory activity.

[0056] The cosmetic composition of the present invention may include the Chlorella vulgaris CvLD-01 strain, a dry product thereof, a culture broth thereof and an extract thereof, as well as components conventionally used in a cosmetic composition, for example, conventional adjuvants such as an antioxidant, a stabilizing agent, a solubilizer, vitamins, pigments and flavors, and a carrier.

[0057] In addition, the cosmetic composition of the present invention may include the Chlorella vulgaris CvLD-01 strain, a dry product thereof, a culture broth thereof and an extract thereof, and may be mixed with an organic UV blocking agent that has been conventionally used as long as it does not impair the skin protection effect. The organic sunscreen may be one or more selected from the group consisting of glyceryl PABA, drometrizole trisiloxane, drometrizole, digalloyl trioleate, disodium phenyl dibenzimidazole tetrasulfonate, diethylhexyl butamidotriazone, diethylamino hydroxybenzoyl hexylbenzoate, DEA-methoxycinnamate, a Lawson/dihydroxyacetone mixture, methylenebis-benzotriazolyltetramethylbutylphenol, 4-methylbenzylidene camphor, methyl anthranilate, benzophenone-3(oxybenzone), benzophenone-4, benzophenone-8(dioxyphebenzone), butyl methoxydibenzoylmethane, bisethylhexyloxyphenol methoxyphenyl triazine, cinoxate, ethyl dihydroxypropyl PABA, octocrylene, ethylhexyldimethyl PABA, ethylhexyl methoxycinnamate, ethylhexyl salicylate, ethylhexyl triazone, isoamyl-p-methoxycinnamate, polysilicon-15 (dimethicodiethylbenzal malonate), terephthalylidene dicamphor sulfonic acid and a salt thereof, TEA-salicylate and aminobenzoic acid (PABA).

[0058] Products that can contain the cosmetic composition of the present invention include, for example, cosmetics such as an astringent, a skin toner, a nourishing toner, various types of creams, essences, packs and foundations, cleansers, face washes, soaps, treatments, and tonics. Specific formulations of the cosmetic composition of the present invention include a skin lotion, a skin softener, a skin toner, an astringent, a lotion, a milk lotion, a moisturizing lotion, a nourishing lotion, a massage cream, a nourishing cream, a moisturizing cream, a hand cream, an essence, a nourishing essence, a pack, a soap, a shampoo, a cleansing foam, a cleansing lotion, a cleansing cream, a body lotion, a body cleanser, an emulsion, a lipstick, a makeup base, a foundation, a pressed powder, a loose powder, and an eyeshadow.

[0059] According to an exemplary embodiment of the present invention, the content of the Chlorella vulgaris CvLD-01 strain, a dry product thereof, a culture broth thereof or an extract thereof may be 0.00001 to 30 wt %, preferably 0.5 to 20 wt %, and more preferably, 1.0 to 10 wt %, with respect to the total weight of the composition.

[0060] Hereinafter, to help in understanding the present invention, exemplary examples will be suggested. However, the following examples are merely provided to more easily understand the present invention, and not to limit the present invention.

EXAMPLES

Example 1. Experimental Materials and Methods

[0061] 1-1. Strain Culture and Measurement of Growth Rate

[0062] Chlorella vulgaris UTEX395 (Culture Collection of the University of Texas at Austin, USA) was cultured in a Tris-acetate-phosphate (TAP) medium, and grown mixotrophically. To maintain wild-type and mutant strains, the strains were cultured in a filter-capped flask at 25° C. under 80 to 100 μmol photon m.sup.−2s.sup.−1 (continuous) while shaking at 100 rpm. Afterward, an initial experiment for pigment and growth analyses was performed under the same conditions. The number of cells of the wild-type or mutant strain was counted using a Neubauer hemocytometer, and an optical density (OD) was measured through spectrophotometry at a wavelength of 750 nm. Meanwhile, to measure a biomass, 1 to 5 mL of cells were recovered by centrifugation at 3,200 rpm for 5 minutes, and a cell pellet was dried using a centrifugal vacuum concentrator (Biotron Inc., Bucheon-si, Gyeonggi-do, Korea). In addition, to compare growth rates, the initial cell concentration was 100×10.sup.4 cells mL.sup.−1, and initial OD.sub.750=0.2 or 0.05 gL.sup.−1. Specific cell growth was measured during the exponential phase, and the OD and biomass per cell were measured and calculated during the late log-stationary phase.

[0063] 1-2. Optimization of Culture Conditions

[0064] 1-2-1. Light Intensity

[0065] To determine the optimal light intensity for cell growth, cells were grown under four different irradiances: low light (45-50 μmol photon m.sup.−2s.sup.−1); normal light (80-100 μmol photon m.sup.−2s.sup.−1); medium light (200-250 μmol photon m.sup.−2s.sup.−1); and high light (380-430 μmol photon m.sup.−2s.sup.−1). Afterward, the cells were inoculated at OD.sub.750=0.2, and grown for 5 days, followed by analyzing a pigment through high-performance liquid chromatography (HPLC).

[0066] 1-2-2. Carbon Source

[0067] To verify the effect of a carbon source on pigment production, cells were incubated in each of three different media, that is, a TAP, Tris-bicarbonate-phosphate (TBP), medium and a Tris-glucose-phosphate (TGP) medium. An acetate medium (TAP) was used as a basal medium, and bicarbonate and glucose were cultured in TBP and TGP media at the same molar concentration (18.1 mM), respectively. Afterward, the cells were inoculated at OD.sub.750=0.2, and incubated for 5 days, followed by analyzing a pigment through HPLC.

[0068] 1-3. Preparation of Mutant Strain

[0069] Cells in the exponential phase were recovered and a mutation was induced using ethyl methanesulfonate (EMS). Specifically, approximately 1-2×10.sup.7 cells were recovered in a 2 mL tube, and treated with 0.2-0.4 M EMS. The treated cells were cultured in a dark room for 2 hours, and washed with fresh TAP three times. Subsequently, the cells were resuspended in 500 μL of fresh TAP, and cultured overnight (6 to 18 hours) in the dark room using an orbital shaker. Afterward, the cells were plated in 5 solid TAP media, and when colonies were formed, a single colony was transferred to a fresh solid medium using a sterile toothpick for an additional experiment. Since a mutant strain having a high xanthophyll pigment level exhibited low fluorescence compared to the wild type, the mutant strain was screened based on the low fluorescence emission value using a fluorescence imaging system (IMAGING-PAM, Heinz-Walz, Effeltrich, Germany). Mutants exhibiting low fluorescence were additionally analyzed by HPLC, thereby selecting a xanthophyll-accumulated mutant strain.

[0070] 1-4. In Vivo Fluorescence Analysis

[0071] Photosynthetic parameters of mixotrophically grown cells were measured in vivo in a TAP medium using a fluorescence imaging system (IMAGING-PAM, Heinz-Walz, Effeltrich, Germany). The cells in the exponential phase were filtered (2.5×10.sup.7 cells), transferred to a solid agar plate, and cultured in a dark room for 20 minutes. The cells were adapted to the dark, and a fluorescence dynamic curve was plotted with a saturated light pulse at 2,200 μmol photon m.sup.−2s.sup.−1 and actinic light at 120 μmol photon m.sup.−2s.sup.−1 by a 450-nm light-emitting diodes (LED) having a step width of 20 seconds.

[0072] 1-5. Quantification of Xanthophyll Pigment and Chlorophyll

[0073] To quantify a pigment of a Chlorella strain, a modified extraction method was used. The xanthophyll pigment and chlorophyll of C. vulgaris were more effectively extracted using 100% ethanol than 90% acetone. In addition, pigment extraction efficiency was improved using ultrasonic extraction (Vibra-Cell, 130 Watts, 20 kHz) (Sonics, Newtown, Conn., USA). Finally, sonication (30 sec “on” and 5 sec “off”, 5 min×60% amplitude) using 0.1 g of glass beads (0.5-0.6 mm) was additionally applied to the extraction method.

[0074] Subsequently, for pigment analysis, 0.2 mL of cells were recovered and centrifuged at 13,000 rpm for 1 minute, followed by extracting the xanthophyll pigment and chlorophyll through the above-described new extraction method; and sonication was performed by repeating “on” for 5 seconds and “off” for 5 seconds using a 6-mm probe at a 60% amplitude for 5 minutes. Afterward, the extracted xanthophyll pigment was analyzed using an HPLC system (LC-20AD, Shimadzu, Japan, Japan) equipped with a Waters Spherisorb S5 ODS1 column (4.6×250 mm; Waters, Milford, USA). Chlorophyll was analyzed by spectrophotometry. Chlorophyll a was measured at 665 nm, and chlorophyll b was measured at 652 nm. The concentrations of the xanthophyll pigment and chlorophylls were calibrated with a cell count or culture volume.

[0075] 1-6. mRNA Expression of Lycopene Epsilon Cyclase and Proteomic Analysis of Amino Acid

[0076] The inventors investigated a DNA sequence using an mRNA sequence (not shown) and aligned it with the entire genomic sequence (Accession No. PRJNA278897) to confirm a CvLCYE sequence. Additionally, mRNA expression of CvLCYE was confirmed by quantitative real-time polymerase chain reaction using TaKaRa PCR Thermal Cycler Dice (Takara, Shiga, Japan). More specifically, total RNA was extracted using a hybrid-R RNA prep kit with Trizol (GeneAll, Seoul, Korea), and cDNA was synthesized by reverse transcription using a random hexamer (EBT-1511, E1PIS BIO, Daejeon, Korea). To evaluate a CvLCYE mRNA expression level of in wild type and CvLD, CvLCYE was amplified with specific primers (forward: 5′-GTG TTT GGC ATG GAG CTG TTG TG-3 ‘ (SEQ ID NO: 1), reverse: 5’-CCA CGT GAG CAT CGC AAA GGT G-3 ‘ (SEQ ID NO: 2)), and 18s ribosome RNA was used as an internal control (forward: 5’-TAT GGG TGG TGG TGC ATG GC-3′ (SEQ ID NO: 3), reverse: 5′-TGC CTC ATG CTT CCA TTG GCT-3′ (SEQ ID NO: 4)). Raw data was analyzed by the AACt method using the software provided by the manufacturer.

[0077] The amino acid sequence of CvLCYE was determined by Sanger sequencing for cDNA (Macrogen, Seoul, Korea). To predict the CvLCYE structures of the wild-type and CvLCYE mutant strains, homology (comparative) modeling was performed, and to this end, a SWISS-model server was used. Conserved Archaeal protein (PDB: AOPI.1) was used as a template for constructing new CvLCYE. Finally, a predicted CvLCYE model was analyzed, and visualized using PyMOL 2.0 (http://www.pymol.org).

[0078] 1-7. Measurement of Photosynthetic Activity

[0079] Cells were cultured in a TAP medium according to the method of Example 1-1, and the generation of oxygen in the wild-type and mutant strains was measured using a Clark-type oxygen electrode S1 (Hansatech, Norfolk, UK) illuminated by red LED (660 nm) at 25° C. The aliquot (1 mL) of a cell suspension (4-5×10.sup.6 cell mL.sup.−1) was loaded in an electrode chamber, and to check whether oxygen evolution is not limited by the supply of carbon, 40 μL of 0.5 M NaHCO.sub.3 was added before measurement. After the dark cycle, while increasing the light intensity (20, 40, 80, 160, 300, 500, 800, 1,000 and 1,200 μmol photon m.sup.−2s.sup.−1), an oxygen evolution rate was measured and recorded for 2 minutes at each light intensity. In addition, after the oxygen evolution rate was measured at 1,200 μmol photon m.sup.−2s.sup.−1, the cells were placed in a dark room for 5 minutes to measure oxygen respiration. The oxygen evolution rate was calibrated with a chlorophyll amount (mg) and time (h).

[0080] 1-8. Statistical Analysis

[0081] Measurement of all growth rates and quantification of pigment analysis were performed at least three times, and statistical significance was verified by the Student's t-test, and when p<0.05, it is considered statistically significant.

Example 2. Improvement of Extraction Method for Extracting Carotenoid from Chlorella vulgaris and its Efficiency Analysis

[0082] The inventors first tried to verify whether the improved extraction method described in Example 1-5 can more effectively extract the carotenoid pigment from Chlorella vulgaris. To this end, as shown in FIG. 1A, a methanol solvent was commonly used, and chlorophyll-a and chlorophyll-b were extracted by applying each of vortexing using a vortex, sonication and glass bead-added sonication (Bead+Sonication) improved in the present invention.

[0083] As a result, sonication showed higher pigment extraction efficiency than vortexing, and when the glass bead-added sonication according to the present invention was used, it can be seen that the highest extraction efficiency was exhibited, and as a result of quantification, the extraction efficiency was improved by 12%.

Example 3. Isolation of Vioxanthin-Accumulated Mutant Strain

[0084] A chemical mutagenic agent such as ethyl methanesulfonic acid (EMS) is known to be effective to produce algae mutants having high carotenoid contents. In addition, a xanthophyll mutant is able to be simply confirmed through fluorescence analysis. Therefore, in this example, a C. vulgaris UTEX395 strain in which a mutation was caused by EMS was screened through fluorescence analysis by IMAGING-PAM, and a mutant strain producing violaxanthin at a high level was confirmed through HPLC. Briefly, after EMS treatment, 1,600 colonies were randomly selected for phenotypic analysis, and then fluorescent analysis was performed to select mutants showing low fluorescence. HPLC was performed additionally on the 27 selected mutants, confirming one lutein-deficient mutant strain (hereinafter, CvLD) in which violaxanthin is abundantly present.

[0085] As shown in FIG. 2A, in the CvLD strain, fluorescence was reduced by approximately 50% in the same number of cells, compared to the wild-type strain (WT). However, unlike the obvious decrease in fluorescence, it was confirmed that the chlorophyll content was slightly reduced (wild type: 12.7±0.6 μg-Chl/10.sup.7 cells, and CvLD: 11.1±0.8 μg-Chl/10.sup.7 cells). In addition, according to HPLC, as shown in FIG. 2B and Table 1 below, compared to the wild-type strain, in CvLD, lutein (Lut) and α-carotene (α-car) were significantly reduced, but a β-branch pool of violaxanthin (Vio), antheraxanthin (Ant) and zeaxanthin (Zea) included in xanthophyll increased. More specifically, compared to the wild-type strain, in CvLD, lutein was reduced by 15.2%, whereas violaxanthin, antheraxanthin and zeaxanthin were increased 3.18-, 5.75- and 3.66-fold, respectively. In addition, α-carotene was reduced, whereas β-carotene was increased 1.64-fold.

TABLE-US-00001 TABLE 1 Carotenoid Pigments (μg/10.sup.7 Cells) Genotype Neo Vio Ant Lut Zea α-Car β-Car WT 0.45 ± 0.04 0.44 ± 0.04 0.04 ± 0.01 1.71 ± 0.03 0.06 ± 0.00 0.06 ± 0.00 0.17 ± 0.01 CvLD 0.45 ± 0.02 1.40 ± 0.08 0.23 ± 0.02 0.26 ± 0.01 0.22 ± 0.01 N.D. 0.28 ± 0.01

Example 4. Confirmation of Gene Mutated in Carotenoid Biosynthesis Pathway

[0086] The inventors speculated that the increased accumulation of violaxanthin in CvLD is caused by a decrease in the α-branch of xanthophyll. According to the conventionally reported result, as shown in FIG. 3A, when CvLCYE was mutated in the genera Chlamydomonas, Ipomoea and Arabidopsis, the inhibition of α-branch synthesis and an increase in β-branch synthesis occurred simultaneously. Accordingly, to investigate the mutation of a carotenogenic gene in CvLD, the CvLCYE gene of C. vulgaris was intended to be identified.

[0087] To this end, first, the encoded DNA sequence of CvLCYE of C. vulgaris was determined, confirming that, as shown in FIG. 3B, a single amino acid mutation (A336V) occurring in a highly-conserved region in LCYE of C. vulgaris, C. reinhardtii and A. thaliana. Subsequently, a homology model structure was formed using a SWISS-model server. As a result of structure analysis, as shown in FIG. 3C, compared to the wild-type strain, it was found that there is a structural difference around the mutant site, and structural changes in surrounding amino acids (indicated by a white arrow at a of FIG. 3C) were predicted. The structural change in this region seemed to be associated with the interaction of side chains between 336A and amino acids highlighted in b and c of FIG. 3C. As shown in FIG. 3D, since there is no significant difference in gene expression between the wild-type and CvLD, it was determined that a decrease in lutein in the CvLD mutant strain may be caused by the structural change in CvLCYE.

Example 5. Analysis of Growth Rates of Wild-Type and CvLD Strains in Flask Culture

[0088] To compare the growth rates of the wild-type and CvLD strains, the number of cells, an optical density (OD750 nm) and a dry cell weight were simultaneously measured. As shown in FIG. 4A, as a result of analyzing cell density, the maximum cell density of the wild-type (WT) strain was 3.17±0.14×10.sup.7 cells mL.sup.−1, whereas the maximum cell density of CvLD was 4.58±0.16×10.sup.7 cells mL.sup.−1, confirming that the maximum cell density of CvLD was 1.44-fold higher than that of the wild-type strain. In the WT strain and CvLD, the growth rates (day.sup.−1) based on the number of cells were 1.03±0.10 and 1.31±0.11, respectively. In addition, as a result of measurement of OD in FIG. 4B and a dry biomass (g/L) in FIG. 4C, similar results were also shown to the cell density results. Specifically, the OD difference between the wild-type and CvLD was shown to be 1.7 to 2.0-fold in the exponential phase, and 1.2-fold in the lag phase, and based on the dry weight of cells, it was confirmed that, in the exponential phase (24 to 72 hr), productivity was 0.38±0.03 gL.sup.−1day.sup.−1 in the case of the wild-type strain, and 0.49±0.02 gL.sup.−1day.sup.−1 in CvLD. Overall, it was found that the cell growth of CvLD was 1.2 to 1.4-fold higher than that of the wild-type strain.

[0089] Meanwhile, a change in photosynthesis efficiency is considered as the main cause frequently affecting microalgae growth. The inventors found that, through fluorescence analysis, the photosynthesis efficiency of CvLD can be higher than the wild-type strain. For more accurate comparison of photosynthesis efficiency, the oxygen evolution rates of the wild-type and CvLD were analyzed. As a result, as shown in FIG. 4D, as the light intensity increased in the range of 0 to 900 μmol photon m.sup.−2s.sup.−1, the oxygen evolution rates increased. In addition, the half-saturation light intensities in the wild-type and CvLD were 308±71.3 and 322±36.4 μmol photon m.sup.−2s.sup.−1, respectively.

[0090] As a result of analysis, since the oxygen evolution yield did not increase any more at 1,000 μmol photon m.sup.−2s.sup.−1, the maximum oxygen evolution rate was measured at 1,000-1,200 μmol photon m.sup.−2s.sup.−1. The maximum oxygen evolution rates were 59±9.8 μmol-O.sub.2 mg-Chl.sup.−1h.sup.−1 (0.57±0.01 μmol-O.sub.2 cell.sup.−7 h.sup.−1) and 115±33.7 μmol-O.sub.2 mg-Chl.sup.−1h.sup.−1 (1.03±0.30 μmol-O.sub.2 cell.sup.−7 h.sup.−1) in the wild-type and CvLD, respectively. In addition, as a result of measurement of respirations of the wild-type and CvLD in the dark, oxygen consumption rates after lights-out were 33±15.4 μmol-O.sub.2 mg-Chl.sup.−1h.sup.−1 and 56±3.3 μmol-O.sub.2 mg-Chl.sup.−1h.sup.−1 in the wild-type and CvLD, respectively. The oxygen evolution and consumption rates were calibrated with a chlorophyll content in a sample, and comprehensively, through the analysis results, it was confirmed that the photosynthesis and respiration rates of CvLD are significantly higher than those of the wild-type strain (p<0.05), and it was determined that such a difference probably causes the improved growth rate of CvLD.

Example 6. Analysis of Effect of Light Intensity on Cell Growth and Carotenoid Production

[0091] The inventors measured cell growth and carotenoid production of the CvLD strain under four different light conditions (50, 100, 200 and 400 μmol photon m.sup.−2s.sup.−1) to investigate the optimal culture conditions for violaxanthin production. As shown in FIG. 4D, oxygen evolution increased as the light intensity increased, the inventors assumed that the growth rate of CvLD increases with light intensity.

[0092] Therefore, as a result of the cell growth analysis of the CvLD strain, unexpectedly, as shown in FIG. 5A, the growth rate of CvLD in the range of 50 to 400 μmol photon m.sup.−2s.sup.−1 was not proportional to light intensity. The maximum growth was 4.02 (OD.sub.750) at 100 μmol photon m.sup.−2s.sup.−1, and the cell growth was reduced at 200 μmol photon m.sup.−2s.sup.−1. At 400 μmol photon m.sup.−2s.sup.−1, the cell growth was reduced to the level shown at 50 μmol photon m.sup.−2s.sup.−1. This result may be due to the light suppression effect caused by high light intensity. Accordingly, under the four light conditions which are the same as used above, various carotenoid concentrations produced by the CvLD strain were measured. As a result, as shown in FIG. 5B, it was confirmed that violaxanthin was abundantly present under the light condition, and its amount was dependent on light intensity.

[0093] As a result, it can be seen that carotenoid production shows a similar pattern to cell growth. The total carotenoid production in the CvLD strain reached the maximum level at 100 μmol photon m.sup.−2s.sup.−1, and all carotenoid pigments were dramatically reduced at 400 μmol photon m.sup.−2s.sup.−1. In addition, in terms of cell growth and carotenoid production, responses to various light intensities were similar to those in the wild-type strain.

Example 7. Analysis of Effect of Carbon Source on Cell Growth and Carotenoid Production

[0094] Further, the inventors measured the cell growth and violaxanthin production of CvLD in various culture media according to the method described in Example 1-2-2 to analyze the effect of a carbon source on the violaxanthin production and investigate optimal conditions. Generally, C. vulgaris is known to well grow using glucose as a carbon source under heterotrophic and mixotrophic conditions. In this experiment, a common carbon source of green microalgae, acetic acid, was used, and a comparative culture experiment was performed to examine growth using acetic acid (TAP medium) and glucose (TGP medium) and pigment production. In addition, as an alternative to organic carbon, bicarbonate (HCO.sub.3.sup.−) was used (TBP medium) to simulate autotrophic culture.

[0095] As a result of culturing the CvLD strain in each medium and analyzing cell growth, as shown in FIG. 6A, the maximum cell density of CvLD was similar to that in the TAP and TGP media, the maximum growth reached 4.2 (OD.sub.750) in the TAP medium, and 4.3 (OD.sub.750) in the TGP medium. However, the initial cell growth period of CvLD extended in the TGP medium, and the growth was then drastically reduced after the lag phase. Therefore, from the result, it was confirmed that CvLD uses acetic acid more effectively than glucose. In addition, when the bicarbonate (inorganic carbon) is a carbon source, the cell growth of CvLD was remarkably low. Moreover, in an air injection experiment using a TAP medium, additional air supply seemed to inhibit cell growth (data is not shown).

[0096] As a result of carotenoid production analysis, as shown in FIG. 6B, acetic acid was shown to be most effectively used by CvLD. When glucose is supplied as a carbon source, carotenoid pigment and chlorophyll were reduced by less than 30%, compared to the TAP medium.

[0097] Finally, the inventors examined a violaxanthin production yield of the CVLD strain under the optimal conditions for the highest growth and pigment production as described above. As a result, as shown in Table 2 below, in flask culture, violaxanthin production reached 0.41% (3.7±0.45 mg/g-DCW) in the TAP medium at 100 μmol photon m.sup.−2s.sup.−1. Accordingly, it was experimentally confirmed that CvLD can be effectively used by substituting a conventional source as a source that produces natural violaxanthin in a high yield.

TABLE-US-00002 TABLE 2 Pigment Pigment amount in CvLD production Neo Vio Ant Lut Zea α-Car β-Car mg/L- 1.05 ± 0.22 5.23 ± 0.64 0.64 ± 0.04 0.76 ± 0.06 0.63 ± 0.03 N.D. 1.24 ± 0.13 culture mg/g- 0.74 ± 0.16 3.70 ± 0.45 0.45 ± 0.03 0.54 ± 0.04 0.44 ± 0.02 N.D. 0.88 ± 0.09 DCW

[0098] It should be understood by those of ordinary skill in the art that the above description of the present invention is exemplary, and the exemplary embodiments disclosed herein can be easily modified into other specific forms without departing from the technical spirit or essential features of the present invention. Therefore, the exemplary embodiments described above should be interpreted as illustrative and not limited in any aspect.

[0099] [Accession Number]

[0100] Name of Depository Authority: Biological Resource Center of Korea Research Institute of Bioscience and Biotechnology

[0101] Accession No.: KCTC14091BP

[0102] Deposition Date: Dec. 20, 2019