KR20110107971A - Water-soluble fermented turmeric extract powder with excellent palatability and preparation method thereof - Google Patents
Water-soluble fermented turmeric extract powder with excellent palatability and preparation method thereof Download PDFInfo
- Publication number
- KR20110107971A KR20110107971A KR1020100027192A KR20100027192A KR20110107971A KR 20110107971 A KR20110107971 A KR 20110107971A KR 1020100027192 A KR1020100027192 A KR 1020100027192A KR 20100027192 A KR20100027192 A KR 20100027192A KR 20110107971 A KR20110107971 A KR 20110107971A
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- KR
- South Korea
- Prior art keywords
- turmeric
- lactobacillus
- fermented
- curcumin
- turmeric extract
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
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Abstract
본 발명은 기호성이 우수한 수용성 발효 울금 추출분말 및 이의 제조하는 방법에 관한 것으로서, 보다 구체적으로 본 발명은 울금을 배지로 하여 락토바실러스 카세이 (Lactobacillus casei)를 배양하여 유산균에 의한 울금의 쓴 맛을 차폐시키고, 0.1M 아세트산 나트륨 용액과 에탄올의 혼합용매를 추출용매로 하여 커큐민이 고함량으로 함유된 발효 울금을 추출하고, 이 발효 울금 추출물에 계면활성제 및 시클로덱스트린을 첨가하여 울금의 지용성 성분을 포접함으로서 커큐민 성분이 안정한 수가용성 발효 울금 추출분말 및 이의 제조방법에 관한 것이다.The present invention relates to a water-soluble fermented turmeric extract powder having excellent palatability and a method for preparing the same. More specifically, the present invention cultivates Lactobacillus casei using turmeric as a medium to shield the bitter taste of turmeric by lactic acid bacteria. By using a mixed solvent of 0.1 M sodium acetate solution and ethanol as an extraction solvent, fermented turmeric containing a high content of curcumin is extracted, and by adding a surfactant and cyclodextrin to the fermented turmeric extract to encapsulate the fat-soluble component of turmeric The present invention relates to a water-soluble fermented turmeric extract powder having a stable curcumin component and a preparation method thereof.
Description
본 발명은 울금을 배지로 하여 커큐민을 안정한 상태로 유지한 채 락토바실러스 카세이 (Lactobacillus casei)를 배양하여 유산균에 의한 울금의 쓴 맛을 차폐시키고, 상기 발효물에 계면활성제 및 시클로덱스트린으로 울금의 지용성 성분을 포접함으로서 기호성이 우수한 수가용성의 발효 울금 추출분말 및 이의 제조방법을 제조하는 방법에 관한 것이다.
The present invention is Lactobacillus Casei ( Lactobacillus) while keeping the curcumin in a stable state with a turmeric medium casei ) was cultured to mask the bitter taste of turmeric by lactic acid bacteria, and the fermented turmeric extract powder having excellent palatability by preparing a fat-soluble component of turmeric with a surfactant and a cyclodextrin in the fermented product and a method for preparing the same. It is about a method.
[문헌 1] Trends in Food Sci . & Technol., 16, pp.533-548, 2005.Document 1 Trends in Food Sci . & Technol ., 16 , pp.533-548, 2005.
[문헌 2] Life Sci., 78, pp.2081-2087, 2006.2 Sci ., 78 , pp.2081-2087, 2006.
[문헌 3] J. Pharma . Biomed . Anal., 15, pp.1867-1876, 1997. [Reference 3] J. Pharma . Biomed . Anal ., 15, pp. 1867-1876, 1997.
[문헌 4] 노장숙외, 식품용유화제 제 2판, 수서원, pp.59-83, 2005.[Document 4] Noh Jang Sook et al., Food Emulsifier 2nd Edition, Suseowon, pp.59-83, 2005.
[문헌 5] Pro . Biochem., 39, pp.1033-1046, 2003.
[문헌 6] Chem . Rev., 98, pp.1743-1753, 1998.
[문헌 7] J. Inclusion Phenomena & Macrocyclic Chem., 36, pp.355-370, 2000.[Reference 7] J. Inclusion Phenomena & Macrocyclic Chem ., 36 , pp. 355-370, 2000.
[문헌 8] 한국특허공개 10-2006-0092585.Document 8 Korean Patent Laid-Open No. 10-2006-0092585.
[문헌 9] 한국특허공개 10-2009-0011872.Document 9 Korean Patent Publication 10-2009-0011872.
[문헌 10] 한국특허공개 10-2008-0054634.[Patent 10] Korean Patent Publication 10-2008-0054634.
[문헌 11] 한국특허공개 10-2005-0040223.
Document 11 Korean Patent Publication 10-2005-0040223.
울금(Curcuma longa L.)은 생강과에 속하는 다년생 초목으로, 마술(馬述), 마술, 황울(黃鬱), 을금(乙金), 걸금(乞金), 옥금(玉金), 왕금(王金)또는 심황(深黃) 등으로 불리우기도 한다.Curcuma longa L. is a perennial vegetation belonging to the family of Ginger, which is magic, horse, magic, yellow wool, eulgeum, gumgeum, jadeumum, and kingumum王 金) or turmeric (深 黄) is also called.
울금은 기원전부터 기록되어 있으며 우리나라에서는 생강과의 식물인 울금(Curcuma longa Linn)의 덩이뿌리를 그대로 또는 주피를 제거하고 쪄서 말린 것을 말하고, 일본에서는 뿌리줄기를 말하며, 중국에서는 울금 및 생강과의 동속식물인 광서아출(Curcuma kwangsiensis SG Lee & CF Liang:廣西莪朮), 온욱금(Curcuma wenyujin YH Chen & C. Ling:溫郁金), 봉아출(Curcuma phaeocaulis Valeton:蓬莪朮)의 뿌리줄기를 말한다. 주로 한약재, 염료, 식품착색제 및 인도 카레의 원료 등으로 사용되어 왔으며, 인도를 중심으로 중국 및 일본 등 아시아 지역에서 오랜 기간 동안 사용되어 왔다. 특징은 특이한 냄새가 있고 씹으면 침을 누렇게 물들이며 자극성이 있는 편이고, 맛은 맵고 쓰며 성질은 서늘하다. 울금의 뿌리, 줄기의 성분은 항산화 및 세포보호 효과가 있으며, 주성분은 커큐민(curcumin)과 커큐민 유도체로 알려져 있다(Trends in Food Sci . Technol., 16, pp.533-548,2005) Turmeric has been recorded since BC, and in Korea, the root of Curcuma longa Linn, a plant of ginger family, is dried or steamed after removing the bark, and in Japan, it is root stem, and in China, the same as that of turmeric and ginger It refers to the root stems of plants Cucurma kwangsiensis SG Lee & CF Liang (廣西 莪 朮), Curcuma wenyujin YH Chen & C. Ling (溫 郁金), and Cucuma phaeocaulis Valeton (蓬 莪 朮). It has been used mainly as a herbal medicine, dye, food coloring agent and raw material of Indian curry, and has been used for a long time in Asia, such as China and Japan, mainly in India. It has a peculiar smell, and when chewed, the saliva is yellowed and irritating. The taste is spicy, bitter, and cool. The root and stem components of turmeric have antioxidant and cytoprotective effects, and the main components are known as curcumin and curcumin derivatives (Trends in Food Sci . Technol ., 16 , pp.533-548,2005)
울금의 주요성분인 커큐민은 항염증효과, 항산화 효과, 돌연변이 억제효과, 항암효과, 항균효과, 혈중 콜레스테롤의 저하, 혈소판 활성, 혈액응고활성의 억제 및 혈관 평활근 세포의 증식억제 효과 등의 다양한 생리활성을 나타낸다(Life Sci., 78, pp.2081-2087, 2006). 하지만, 커큐민은 불안정하여 빛과 pH, 산소 등에 의해 산화되어 바닐린(vanillin), 바닐산(vanillic acid), 페룰알데히드(ferulic aldehyde), 페룰산(ferulic acid)등으로 전환된다. 수용화시에는 pH 7.2의 phosphate buffer에 용해할 경우 37℃에서 30분만에 약 90%정도가 분해되고. pH가 4.0~5.0 사이에서는 비교적 안정성을 유지할 수 있다. (J. Pharma . Biomed . Anal., 15, pp.1867-1876, 1997). Curcumin, the main component of turmeric, has various physiological activities such as anti-inflammatory effect, antioxidant effect, mutation suppression effect, anticancer effect, antibacterial effect, lowering of blood cholesterol, platelet activity, inhibition of blood coagulation activity, and inhibition of proliferation of vascular smooth muscle cells. (Life Sci ., 78 , pp.2081-2087, 2006). However, curcumin is unstable and is oxidized by light, pH, oxygen, etc. and converted into vanillin, vanillic acid, ferulic aldehyde, and ferulic acid. At the time of solubilization, when dissolved in phosphate buffer of pH 7.2, about 90% is decomposed in 30 minutes at 37 ℃. When the pH is between 4.0 and 5.0, relatively stable can be maintained. ( J. Pharma . Biomed . Anal ., 15, pp. 1867-1876, 1997).
계면활성제는 두 개의 상을 분산시킬 경우에 사용되는 매체로서 에멀젼을 만들기 위해 식품, 화장품등에 사용되고 있으며, 식품용으로는 모노글리세라이드 에스테르(monoglyceride ester), 폴리글리세라이드 에스테르(polyglyceride ester), 슈크로즈 에스테르(sucrose ester)등을 사용할 수 있다. 계면활성제는 그 성질에 따라 친수성과 친유성으로 나눌 수 있는데, 에이치엘비(hydrophile lipophile balance) 수치가 높을수록 친수성의 성질을 나타내고, 수치가 낮을수록 친유성의 성질을 나타낸다. 먼저 친수성 계면활성제는 에이치엘비 수치가 10 이하인 모노글리세라이드, 락트산 모노글리세라이드, 소르비탄에스테르, PG에스테르, 레시틴 등이 있으며, 친유성 계면활성제는 폴리소르베트, 에톡시화모노글리세라이드, SSL, 지방산염등이 있고, 계면활성제중에는 에이치엘비의 범위가 넓은 설탕 에스테르, 폴리글리세린에스테르등도 존재한다(노장숙외, 식품용유화제 제 2판, 수서원, pp.59-83, 2005). 수용성 성분으로 만들기 위해서는 친수성의 계면활성제를 사용하는 것이 유리하다. Surfactant is a medium used to disperse two phases. It is used in food, cosmetics, etc. to make emulsion. For food, monoglyceride ester, polyglyceride ester, sucrose Sucrose esters can be used. Surfactants can be divided into hydrophilic and lipophilic according to their properties. The higher the hydrophile lipophile balance, the lower the hydrophilic property, and the lower the hydrophilic property. Hydrophilic surfactants include monoglycerides, lactic acid monoglycerides, sorbitan esters, PG esters, lecithin, etc., which have HLB values of 10 or less, and lipophilic surfactants include polysorbet, ethoxylated monoglycerides, SSL, and fats. There are acid salts and the like, and sugar esters and polyglycerol esters with a wide range of HLBI are also present in the surfactants (outside the elderly, Food Emulsifier 2nd Edition, Suseowon, pp.59-83, 2005). In order to make it a water-soluble component, it is advantageous to use a hydrophilic surfactant.
계면활성제는 추출물을 20~30%(w/v)의 농도로 농축을 하는 과정에서 커큐민등의 지용성 성분이 분리되는 것을 막고 서로 균질화하기 위해 첨가하여 리포좀(liposome), 미셀(micelle)등을 형성함으로써 지용성성분을 수용화시킬 수 있다. Surfactants are added to prevent the separation of fat-soluble components such as curcumin and to homogenize each other in the process of concentrating the extract to a concentration of 20-30% (w / v) to form liposomes and micelles. The fat-soluble component can be solubilized by doing so.
시클로덱스트린류, 즉 시클로덱스트린 알파, 베타 또는 감마 또는 이들의 복합체는 샤르딩거 덱스트린 (Schardinger dextrins), 시클로아밀로오스 (Cycloamyloses) 및 시클로글루칸 (Cycloglucans) 등의 다른 명칭으로 합성의약품 분야에 도입되어 프로스타글란딘류, 스테로이드류 및 바르비탈류 등의 용해 보조제, 아스피린, 에피네프린 및 비타민류 등의 화학적 안정화제, 프로스타글란딘류, 알킬파라벤류 등의 맛과 냄새개선제 등으로 응용되고 있다. Cyclodextrins, ie, cyclodextrin alpha, beta, or gamma, or complexes thereof, have been introduced into the field of synthetic pharmaceuticals under other names, such as Shardinger dextrins, Cycloamyloses, and Cyclologcans, to prostaglandins, It is applied to dissolution aids such as steroids and barbitals, chemical stabilizers such as aspirin, epinephrine and vitamins, and taste and odor improving agents such as prostaglandins and alkyl parabens.
시클로덱스트린은 6~8개의 글루코즈(glucose) 분자가 고리모양의 a-1,4 결합의 형태로 이루어진 비환원성 말토올리고당(malto-oligos accharide)으로, 환산형의 도우넛 구조로 이루어져 있고, 2번과 3번의 탄소에 결합된 수산화기(-OH)가 수소결합을 함으로써 공동하는 소수성의 성질을 띄고, 반대로 극성이 높은 수산화기에 의해 외부는 친수성의 성질을 갖는데, 이런 성질로 인해 시클로덱스트린은 소수성 물질과 포접화합물을 형성하여 소수성 물질의 용해도를 증가시키고, 불안정한 물질의 안정성을 높일 수 있다. 또한, 맛과 향을 나타내는 유기 분자의 일부분 내지 전체를 공동내에 포접함으로써 고미나 이취를 제거하는 데 사용할 수 있다(Pro . Biochem., 39, pp.1033-1046, 2003; Chem . Rev., 98, pp.1743-1753, 1998; J. Inclusion Phenomena and Macrocyclic Chem., 36, pp.355-370, 2000). Cyclodextrins are non-reducing malto-oligos accharides in which 6 to 8 glucose molecules are in the form of cyclic a-1,4 bonds. Hydroxyl group (-OH) bonded to 3 carbons has the property of hydrophobicity which is shared by hydrogen bonding, and on the contrary, it has hydrophilicity on the outside by highly polar hydroxyl group, and cyclodextrin is enclosed with hydrophobic material due to this property. Compounds can be formed to increase the solubility of hydrophobic materials and increase the stability of unstable materials. It can also be used to remove odors by enveloping some or all of the organic molecules exhibiting taste and aroma in the cavity ( Pro . Biochem ., 39 , pp. 1033-1046, 2003; Chem . Rev. , 98 , pp.1743-1753, 1998; J. Inclusion Phenomena and Macrocyclic Chem ., 36 , pp. 355-370, 2000).
일반적으로 사용되고 있는 시클로덱스트린액은 시클로덱스트린 알파, 베타 및 감마형의 복합체로서 전분을 함유한 배지에 사이클로 덱스트린 트란스 글리코시다제라는 효소의 작용으로 생성되면, 쥐에게 경구 투여시에 LD50값이 10 g/kg이상의 높은 수치인 것으로 보고되어 있으며, 위장관에서는 단지 미량만이 흡수되기 때문에 독성이 거의 없는 안정성이 확보된 물질이다. 이 중 베타-시클로덱스트린은 일반적으로 의약품 및 식품 분야에 가장 널리 사용되는 물질로 그 안전성 등이 인정되어 미국약전 (USP)에 수재되어 있는 물질로 랫트와 마우스에 경구투여시 LD50값이 각각 12, 12.5 g/kg 이상으로 안전한 물질이다.Typically, when a cyclodextrin solution in use on the cyclodextrin alpha, beta, and a medium containing starch as a complex of a gamma-cyclodextrin trans-glycosidase produced by the action of an enzyme agent, a LD 50 value of 10 rats in oral administration It is reported to have a high value of g / kg or more, and because only a small amount is absorbed in the gastrointestinal tract, it is a material that has almost no toxicity. Among these, beta-cyclodextrin is generally the most widely used substance in the pharmaceutical and food fields, and has been recognized in the US Pharmacopeia (USP) because of its safety, etc., and the LD 50 value of oral administration to rats and mice is 12 It is a safe substance above 12.5 g / kg.
기능이 우수한 울금을 제품화하려는 다양한 시도들이 행해지고 있는데, 수용성 쿠르쿠민 및 그의 제조방법(한국특허공개 10-2006-0092585)에서 커큐민에 당을 결합시켜서 수용화하는 방법이 연구되었고, 분산성 및 침전안전성이 우수한 커큐민 함유 울금 음료 및 이의 제조방법(한국특허공개 10-2009-0011872)에서 커큐민을 수 분산시키는 방법이 연구되었으며, 울금 발효 추출물의 제조방법(한국특허공개 10-2008-0054634)에서 울금추출물에 흑설탕과 흑국균을 혼합하여 유기산의 함량을 증가시키는 방법이 연구되었고, 울금 발효방법 및 울금을 주재료로 하는 식품조성물제조방법(한국특허공개 10-2005-0040223)에서 황국균을 이용하여 울금을 배양하는 방법이 연구되었으나, 먼저, 수용성 쿠르쿠민을 제조하는 방법은 고순도 쿠르쿠민의 경우에만 적용이 가능하고, 쿠르쿠민 이외의 성분들이 혼합되어 있는 추출물의 상태를 수용화 시키는 것과는 목적이 다르며, 분산성 및 침전안전성이 우수한 커큐민 함유 음료의 제조방법은 커큐민 함량이 60~72%의 울금파우더를 안정제를 사용하여 고속호모믹서로 분산을 고르게 시키는 방법인데, 본 발명은 수용화가 가능한 울금 추출 분말을 제조하는 것이라서 제형의 상태가 상이하고, 울금 추출물에 흑설탕과 흑국균을 혼합하여 발효하는 방법은 울금 추출물 이외에 배지인 흑설탕이 과량 첨가되어 배양 기간이 50일로 장기간이 소요되는 점 등 산업적으로 이용하기 어렵다는 단점이 있다. Various attempts have been made to commercialize turmeric with excellent function. In water-soluble curcumin and its preparation method (Korean Patent Laid-Open No. 10-2006-0092585), a method of incorporating sugar into curcumin was studied. Excellent curcumin-containing turmeric drink and its preparation method (Korean Patent Publication No. 10-2009-0011872) has been studied how to disperse curcumin, and the turmeric extract in the manufacturing method of turmeric fermentation extract (Korean Patent Publication No. 10-2008-0054634) The method of increasing the content of organic acid by mixing brown sugar and black yeast bacteria was studied.The method of cultivating turmeric using sulfur bacterium in the method of fermentation of fermented rice and the method of manufacturing food composition mainly using turmeric (Korean Patent Publication No. 10-2005-0040223) Although the method has been studied, first, the method of preparing water-soluble curcumin is applicable only to high-purity curcumin. The purpose of preparing a curcumin-containing beverage with superior dispersibility and sedimentation safety is to use a turmeric powder with curcumin content of 60-72% using a stabilizer. How to evenly disperse with a homomixer, the present invention is to prepare a turmeric extract powder that can be solubilized, the state of the formulation is different, and the method of fermenting by mixing black sugar and black yeast bacteria in turmeric extract is a medium other than turmeric extract There is a disadvantage in that it is difficult to use industrially, such that it is added in excess and the culture period is 50 days.
울금의 주 기능성을 나타내는 성분은 커큐민이기 때문에 커큐민의 고함량으로 추출하기 위해서는 고순도의 에탄올로 추출해야 하지만, 울금 특유의 쓴 맛에 의해 사용성에 제약이 있고, 울금의 주요 성분은 지용성 성분으로 수불용성인 천연물로 바꾸기 위해 에탄올로 추출하여 농축할 경우 지용성 성분에 의해 농축과정에서 층 분리가 일어나기 때문에, 이를 균질화하여 분말화하기가 어려우며, 분말화를 하기 위한 보조제로 당류를 과량 첨가하더라도 분말상태가 양호하지 못하고, 이러한 상태로 분말화를 할 경우 일정시간이 지나면 굳어버리는 현상이 발생한다. 이렇게 제조한 분말은 물에 다시 용해할 경우 층 분리가 일어나는 현상이 발생하므로, 현재 이런 문제를 해결하기 위해서 주요성분을 덜 추출하더라도 분말화가 용이하게 추출용매를 물로 한정하여 개발하는 경우가 대부분이고, 물이 아닌 에탄올(에탄올)로 추출한다고 해도 울금에 함유되어 있는 지용성 성분이 다량 추출되어서 쉽게 분말화하기는 어렵다(Trends in Food Sci. & Technol., 16, pp.533-548, 2005). Curcumin's main functional ingredient is curcumin, so it must be extracted with high-purity ethanol in order to extract it with high content of curcumin. However, the turmeric's unique bitter taste restricts usability, and the main component of turmeric is water-soluble and water-insoluble. When ethanol is extracted and concentrated to change to natural phosphorus, it is difficult to powder it by homogenizing it, so it is difficult to make it homogeneous and powdered, and the powder state is good even if excess saccharides are added as an adjuvant for powdering. If it is not possible to powder in such a state, a phenomenon occurs that after a certain time is hardened. The powder thus prepared is a phenomenon that layer separation occurs when dissolved again in water, so in order to solve this problem, even if less extract the main components, it is most often developed to limit the extraction solvent to water for easy powdering, Even if it is extracted with ethanol (ethanol), not water, it is difficult to easily powder the fat-soluble components contained in turmeric (Trends in Food Sci. & Technol., 16 , pp.533-548, 2005).
울금에 특이적으로 잘 자라고 울금의 쓴 맛을 개선할 수 있는 유산균을 선별하여 배양을 하는 과정에서 커큐민의 구조적인 불안정성에 의해 멸균, 배양등의 과정에서 커큐민의 함량은 급격히 떨어진다. pH를 보정하지 않은 채 멸균시에 커큐민의 약 70%가 손실된다. pH를 보정할 경우에 100℃에서 30분까지는 커큐민의 함량이 100% 유지된다. 이에 울금을 배양시에 0.1M 아세트산 나트륨 완충액을 이용하여 안정성을 유지한 채로 살균조건에서 오염균을 제거한 후에 배양을 하였다. 수불용성인 커큐민을 추출하기 위해서 70% 에탄올(에탄올)을 사용하여 추출한 후에 커큐민 등의 지용성 성분을 계면활성제로 균질화한 후에 시클로덱스트린으로 포접하여 커큐민 성분의 안정성이 증가시킨 수가용화된 발효 울금 추출분말을 제조하는 방법을 개발하게 되었다. The curcumin content rapidly decreases during sterilization and cultivation due to the structural instability of curcumin in the process of selecting and culturing lactic acid bacteria that grow well specifically in turmeric and improve the bitter taste of turmeric. About 70% of curcumin is lost during sterilization without pH correction. When the pH is corrected, the curcumin content is maintained at 100% for up to 30 minutes at 100 ° C. Thus, turmeric was cultured after removing contaminants under sterilization conditions while maintaining stability using 0.1 M sodium acetate buffer. Solubilized fermented turmeric extract powder that was extracted with 70% ethanol (ethanol) to extract water-insoluble curcumin, and then homogenized fat-soluble components such as curcumin with a surfactant, followed by inclusion of cyclodextrin to increase the stability of curcumin components. It was developed a method for manufacturing a.
이에 본 발명자들은 울금 추출물의 쓴 맛을 완화하기 위해 유산균을 이용하여 젖산 발효를 하고, 분말화를 용이하게 하고 재용해시에 수가용화하기 위해서 계면활성제 및 시클로덱스트린(CD)을 혼합 사용하는 방법을 개발하여 울금 추출분말의 쓴 맛을 개선하고 수용화함으로써 기호성을 향상시키고, 커큐민이 다량 함유되어 기능성 식품, 건강기능식품의 소재로 다양하게 사용할 수 있는 수가용성 발효 울금 추출분말의 제조방법을 개발하게 되어 본 발명을 완성하게 되었다.
Therefore, the present inventors have used a method of lactic acid fermentation using lactic acid bacteria to alleviate the bitter taste of turmeric extract, and using a mixture of a surfactant and a cyclodextrin (CD) to facilitate powdering and solubilization upon re-dissolution. Develop and improve the palatability by improving and accepting the bitter taste of turmeric extract powder, and develop a manufacturing method of water-soluble fermented turmeric extract powder that can be used as a material for functional foods and health functional foods by containing large amount of curcumin. Thus, the present invention has been completed.
상기 목적을 달성하기 위하여, 본 발명은 수가용성 발효 울금 추출분말을 제조하는 방법 및 이 제법으로 제조된 커큐민이 다량 함유된 수가용성 발효 울금 추출분말을 제공한다.In order to achieve the above object, the present invention provides a method for producing a water-soluble fermented turmeric extract powder and a water-soluble fermented turmeric extract powder containing a large amount of curcumin prepared by the method.
구체적으로, 이에 본 발명은 울금을 마쇄, pH 보정, 살균 및 울금을 배지로 하여 유산균, 바람직하게는 페디오코커스 펜토사세우스 (Pediococcus pentosaceus), 락토바실러스 아시도필루스(Lactobacillus acidophillus), 락토바실러스 카세이(Lactobacillus casei), 락토바실러스 헤베티쿠스(Lactobacillus heveticus), 락토바실러스 레우테리(Lacto bacillus reuteri), 락토바실러스 플란타럼(Lactobacillus plan tarum), 락토바실러스 퍼멘텀(Lactobacillus fermentum), 리우코너스톡 메센테로이드(Leuconostoc mesenteroides), 및 락토코커스 락티스 (Lactococcus lactis)로 구성되는 군으로부터 선택된 하나 이상의 균주를 배양함으로서 유산균에 의한 울금의 쓴 맛을 완화하여 울금 발효물을 수득하는 제 1단계; 상기 울금 발효물을 추출용매로 추출 및 농축하여 고형분의 함량으로 20 내지 30 %(w/v)로 농축하여 발효 울금 추출 농축물을 수득하는 제 2단계; 상기 추출 농축물에 계면활성제를 가하여 유화물을 수득하는 제 3단계: 이 유화물에 사이클로 덱스트린을 첨가하여 울금의 지용성 성분을 포접하여 발효 울금 추출 포접물을 수득하는 제 4단계; 및 이 포접물을 건조하는 제 5단계를 포함하는 수가용성 발효 울금 추출분말을 제조하는 제조 방법을 제공한다. Specifically, according to the present invention, the lactobacillus, pH correction, sterilization and turmeric as a medium, lactobacillus, preferably Pediococcus pentosaceus , Lactobacillus acidophillus , Lactobacillus acidophillus , Lactobacillus Lactobacillus casei , Lactobacillus heveticus , Lacto bacillus reuteri , Lactobacillus plan tarum , Lactobacillus fermentum , Lactobacillus fermentus mesen steroid (Leuconostoc mesenteroides ), and Lactococcus lactis culturing at least one strain selected from the group consisting of the first step of relieving the bitter taste of turmeric by lactic acid bacteria to obtain turmeric fermentation products; A second step of extracting and concentrating the turmeric fermentation product with an extraction solvent and concentrating the content of solids to 20 to 30% (w / v) to obtain a fermentation turmeric extract concentrate; A third step of obtaining an emulsion by adding a surfactant to the extract concentrate: a fourth step of adding cyclodextrin to the emulsion to include fat-soluble components of turmeric to obtain a fermented turmeric extract clath; And it provides a manufacturing method for producing a water-soluble fermented turmeric extract powder comprising a fifth step of drying the inclusions.
보다 구체적으로, 상기 제조방법 제 1단계에서, 울금을 마쇄한 후 울금 중량의 약 5 내지 15배(W/W), 바람직하게는 약 8 내지 12배(W/W) 달하는 아세트산 나트륨 완충액, 바람직하게는 0.01M 내지 1M 아세트산 나트륨을 첨가하여 pH 3-7, 바람직하게는 pH 4.0 내지 6.0, 보다 바람직하게는 pH 4.5 내지 5.0으로 조정한 후, 약 80~150℃, 바람직하게는 약 90~120℃, 보다 바람직하게는 약 100~110℃,에서, 약 10분 내지 2시간, 바람직하게는 약 30분간 동안 살균한 후에 유산균, 바람직하게는 페디오코커스 펜토사세우스(Pediococcus pentosaceus), 락토바실러스 아시도필루스(Lactobacillus acidophillus), 락토바실러스 카세이(Lactobacillus casei), 락토바실러스 헤베티쿠스(Lactobacillus heveticus), 락토바실러스 레우테리(Lacto bacillus reuteri), 락토바실러스 플란타럼(Lactobacillus plantarum), 락토바실러스 퍼멘텀(Lactobacillus fermentum), 리우코너스톡 메센테로이드(Leuconostoc mesenteroides), 및 락토코커스 락티스(Lactococcus lactis)로 구성되는 군으로부터 선택된 하나 이상의 균주, 보다 바람직하게는 페디오코커스 펜토사세우스 KCCM11004P(Pediococcus pentosaceus KCCM11004P), 락토바실러스 아시도필루스 KCCM40265(Lactobacillus acidophillus KCCM40265), 락토바실러스 카세이 KCCM12452(Lactobacillus casei KCCM1 2452), 락토바실러스 헤베티쿠스 KCCM112 23(Lactobacillus heveticus KCCM 11223), 락토바실러스 레우테리 KCCM407 17(Lactobacillus reuteri KC CM40717)또는 락토바실러스 플란타럼 KCCM121 16(Lactobacillus plantarum KCCM12116), 락토바실러스 퍼멘텀 BLJH10 1(Lactobacillus fermentum), 리우코너스톡 메센테로이드 KCTC3505(Leuconostoc mesenteroides), 및 락토코커스 락티스 KCTC 2013(Lactococcus lactis)로 구성되는 군으로부터 선택된 하나 이상의 균주, 보다 더 바람직하게는 락토바실러스 카세이(Lactobacillus casei) 또는 페디오코커스 펜토사세우스(Pediococcus pentos aceus), 더 보다 더 바람직하게는 락토바실러스 카세이 KCC M12452(Lactobacillus casei KCCM12452) 또는 페디오코커스 펜토사세우스(Pediococcus pentosaceus) KCCM11004P 균주를 접종하여 약 12시간 내지 일주일, 바람직하게는, 약 24시간 내지 48시간 동안 정치배양하여 울금 발효물을 수득함을 특징으로 한다.More specifically, in the first step of the manufacturing method, sodium acetate buffer solution of about 5 to 15 times (W / W), preferably about 8 to 12 times (W / W) of the turmeric weight after grinding the turmeric Preferably, 0.01 M to 1 M sodium acetate is added to adjust pH to 3-7, preferably pH 4.0 to 6.0, more preferably pH 4.5 to 5.0, and then about 80 to 150 ° C, preferably about 90 to 120 Lactic acid bacteria, preferably Pediococcus pentosaceus , Lactobacillus, after sterilization at about 100 to 110 ° C. for about 10 minutes to 2 hours, preferably about 30 minutes Lactobacillus acidophillus ), Lactobacillus casei ), Lactobacillus heveticus), Lactobacillus Terry Leu (Lacto bacillus reuteri), Lactobacillus Planta Rum (Lactobacillus plantarum ), Lactobacillus fermentum ), Leuconostoc mesenteroides ), and one or more strains selected from the group consisting of Lactococcus lactis , more preferably Pediococcus pentosaceus KCCM11004P, Lactobacillus asidophilus KCCM40265 ( Lactobacillus acidophillus) KCCM40265), Lactobacillus casei KCCM12452 ( Lactobacillus casei KCCM1 2452), Lactobacillus heveticus KCCM 11223), Lactobacillus reuteri KCCM407 17 ( Lactobacillus reuteri KC CM40717) or Lactobacillus plantarum KCCM121 16 ( Lactobacillus plantarum KCCM12116), Lactobacillus Fermentum BLJH10 1 ( Lactobacillus fermentum ), Rioconstock stock centenoid KCTC3505 ( Leuconostoc mesenteroides ), and one or more strains selected from the group consisting of Lactococcus lactis , more preferably Lactobacillus casei ) or Pediococcus pentos aceus , even more preferably Lactobacillus casei KCC M12452 ( Lactobacillus casei KCCM12452) or Pediococcus pentosaceus pentosaceus ) is inoculated with the KCCM11004P strain is characterized in that the culture culture for about 12 hours to a week, preferably, about 24 to 48 hours to obtain turmeric fermentation.
상기 제조방법 제 2단계에서, 추출용매로는 울금 중량의 약 20 내지 40배(V/W)에 달하는 추출용매, 바람직하게는 아세트산 및 에탄올 혼합용매, 더 바람직하게는, 0.01M 내지 1M 아세트산 나트륨 및 에탄올 혼합용매, 더욱 더 바람직하게는 0.05 내지 0.2M 아세트산 나트륨 (pH 4.5) 및 에탄올 혼합용매, 보다 더욱 더 바람직하게는 60~90% (v/v), 보다 바람직하게는 에탄올 순도가 70~80 % (v/v) 0.1M 아세트산 나트륨(pH 4.5) 및 에탄올 혼합용매를 사용하여 약 1 내지 10시간, 바람직하게는 약 4 내지 5시간 동안 환류냉각 추출방법, 열수추출, 초음파 추출, 환류냉각추출 등의 추출방법, 바람직하게는 환류냉각 추출방법을 이용하여 추출한 추출액을 감압 여과하여 얻은 추출물을 약 40 내지 80℃, 바람직하게는 약 50 내지 60℃에서 감압 농축하여 발효 울금 농축물을 수득함을 특징으로 한다.In the second step of the preparation method, the extraction solvent is about 20 to 40 times the weight of turmeric (V / W) extraction solvent, preferably a mixture of acetic acid and ethanol, more preferably 0.01M to 1M sodium acetate And ethanol mixed solvent, even more preferably 0.05 to 0.2M sodium acetate (pH 4.5) and ethanol mixed solvent, even more preferably 60 to 90% (v / v), more preferably ethanol purity 70 to Reflux cooling extraction method, hot water extraction, ultrasonic extraction, reflux cooling using 80% (v / v) 0.1 M sodium acetate (pH 4.5) and ethanol mixed solvent for about 1 to 10 hours, preferably about 4 to 5 hours. Extraction obtained by extraction method such as extraction, preferably by reflux cooling extraction method, the extract obtained by filtration under reduced pressure is concentrated under reduced pressure at about 40 to 80 ℃, preferably about 50 to 60 ℃ to obtain a fermented turmeric concentrate Features .
상기 제조방법 제 3단계에서, 계면활성제, 바람직하게는 상기 추출 농축액 고형분 중량 대비 0.1 내지 20 %(w/w), 보다 바람직하게는 3 내지 8 %(w/w)의 레시틴, 설탕에스테르, 포스포리피드, 소르비탄 지방산 에스테르, 폴리글리세린 에스테르인 MS-5S 등의 계면활성제, 바람직하게는, MS-5S 계 계면활성제를 첨가하여 30 내지 80℃, 바람직하게는 약 60 내지 70℃에서 약 0.5 내지 4시간, 바람직하게는 약 1 내지 2 시간 동안 교반하여 균일하게 균질화하여 유화물을 수득함을 특징으로 한다.In the third step of the preparation method, a surfactant, preferably 0.1 to 20% (w / w), more preferably 3 to 8% (w / w) of lecithin, sugar ester, phos to weight of the extract concentrate solids Surfactant such as MS-5S, which is a lipid feed, sorbitan fatty acid ester, and polyglycerol ester, and preferably, MS-5S-based surfactant is added at 30-80 ° C, preferably about 0.5-70 ° C It is characterized by stirring for 4 hours, preferably about 1 to 2 hours, to homogenize homogeneously to obtain an emulsion.
상기 제조방법 제 4단계에서, 상기 시클로덱스트린은 상기 유화물에 울금 추출물 고형분 중량 대비 30 내지 200 % (w/w), 바람직하게는 60 내지 100 % (w/w) 배합양의 베타-시클로덱스트린 및 감마-시클로덱스트린 혼합물, 바람직하게는 0.1~2: 2~0.1(w/w), 보다 바람직하게는 1: 1.5~0.5(w/w)의 혼합비를 갖는 시클로덱스트린 혼합물을 혼합 첨가하여 약 30 내지 80℃, 바람직하게는 약 60 내지 70℃에서 약 0.5 내지 4시간, 바람직하게는 약 1 내지 2 시간 동안 교반하여 포접 반응을 수행하여 포접물을 제조함을 특징으로 한다.In the fourth step of the preparation method, the cyclodextrin is 30 to 200% (w / w), preferably 60 to 100% (w / w) of beta-cyclodextrin in the emulsion, based on the weight of the turmeric extract solids and Gamma-cyclodextrin mixture, preferably from 0.1 to 2: 2 to 0.1 (w / w), more preferably from about 30 to about 30 to about by adding a cyclodextrin mixture having a mixing ratio of 1.5 to 0.5 (w / w) A clathrate is prepared by carrying out a clathrate reaction by stirring at 80 ° C., preferably about 60 to 70 ° C. for about 0.5 to 4 hours, preferably about 1 to 2 hours.
상기 제조방법 제 5단계에서, 건조는 분무건조, 동결건조, 또는 열풍건조, 바람직하게는 분무건조방법으로, 보다 바람직하게는, 주입구 온도 160 내지 180 ℃, 출구 온도는 60 내지 80℃에서 건조하는 것을 특징으로 한다. In the fifth step of the production method, the drying is spray drying, freeze drying, or hot air drying, preferably spray drying, more preferably, the inlet temperature is 160 to 180 ℃, the outlet temperature is dried at 60 to 80 ℃ It is characterized by.
또한 본 발명은 상기 3단계와 4단계를 연속적으로 수행하는 것을 특징으로 한다.
In another aspect, the present invention is characterized in that the three and four steps are carried out continuously.
이하, 본 발명의 수용성 발효 울금 추출분말을 수득하는 방법을 상세히 설명한다. Hereinafter, a method of obtaining the water-soluble fermented turmeric extract powder of the present invention will be described in detail.
예를 들어, 울금에 적합한 유산균을 선별하기 위해 유산균을 배지에 30 내지 40℃, 1 내지 7일간 정치 배양하여 소량의 유산균을 제조하고, 울금을 분쇄하여 울금의 약 8 내지 12배(W/W)에 달하는 아세트산 나트륨 완충액, 바람직하게는 0.01M 내지 1M 아세트산 나트륨을 첨가하여 pH 3.0 내지 7.0, 바람직하게는 pH 4.0 내지 5.0으로 조정한 후, 약 100~150℃, 바람직하게는 약 100℃에서, 약 10분 내지 2시간, 바람직하게는 약 30분간 동안 살균한 후에 냉각한 후 미리 준비한 균주를 각각 접종하여 20 내지 50℃, 바람직하게는 30 내지 40℃, 약 12시간 내지 일주일, 바람직하게는, 약 24시간 내지 48시간 동안 정치배양하여 유산균을 선별한다.For example, to select lactic acid bacteria suitable for turmeric, lactic acid bacteria are cultured in a medium for 30 to 40 ° C. for 1 to 7 days to prepare a small amount of lactic acid bacteria, and the turmeric is pulverized by about 8 to 12 times (W / W). ) Is adjusted to pH 3.0 to 7.0, preferably pH 4.0 to 5.0 by addition of sodium acetate buffer, preferably 0.01 M to 1 M sodium acetate, at about 100 to 150 ° C, preferably at about 100 ° C, After sterilization for about 10 minutes to 2 hours, preferably about 30 minutes, after cooling, the prepared strains are respectively inoculated to obtain 20 to 50 ° C., preferably 30 to 40 ° C., about 12 hours to 1 week, preferably, The lactic acid bacteria are selected by static culture for about 24 to 48 hours.
울금을 그 중량의 약 8 내지 12배(W/W)에 달하는 0.1M 아세트산 나트륨 완충액을 첨가한 후에 약 100℃에서 30분내지 1시간동안 살균한 후 유산균, 바람직하게는 페디오코커스 펜토사세우스 (Pediococcus pentosaceus)(Pediococcus pento saceus), 락토바실러스 아시도필루스(Lactobacillus acidophillus), 락토바실러스 카세이(Lactobacillus casei), 락토바실러스 헤베티쿠스(Lactobacillus heve ticus), 락토바실러스 레우테리(Lactobacillus reuteri), 락토바실러스 플란타럼(Lactobacillus plantarum), 락토바실러스 퍼멘텀(Lactobacillus fermentum), 리우코너스톡 메센테로이드(Leuconostoc mesenteroides), 및 락토코커스 락티스 (Lactococcus lactis)로 구성되는 군으로부터 선택된 하나 이상의 균주를 접종하여 24 내지 72시간, 바람직하게는 24내지 48시간 동안 배양하는 제 1단계; The turmeric is sterilized at about 100 ° C. for 30 minutes to 1 hour after addition of 0.1 M sodium acetate buffer of about 8 to 12 times the weight (W / W), followed by lactic acid bacteria, preferably Pediococcus pentosase. Us ( Pediococcus pentosaceus ) ( Pediococcus pento saceus ), Lactobacillus acidophillus ), Lactobacillus casei), Lactobacillus H. Betty kusu (Lactobacillus heve ticus), Lactobacillus Leu Terry (Lactobacillus reuteri ), Lactobacillus plantarum ), Lactobacillus fermentum ), Leuconostoc mesenteroides ), and the first step of inoculating one or more strains selected from the group consisting of Lactococcus lactis and incubating for 24 to 72 hours, preferably 24 to 48 hours;
상기 제 1단계의 배양액에 에탄올을 배양액의 약 2 내지 5배(v/v)에 달하는, 바람직하게는 3 내지 4배(v/v)에 달하는 에탄올을 첨가하여 아세트산 나트륨 및 에탄올 혼합용매, 더 바람직하게는, 0.01M 내지 1M 아세트산 나트륨 및 에탄올 혼합용매, 더욱 더 바람직하게는 0.05 내지 0.2M 아세트산 나트륨 (pH 4.5) 및 에탄올 혼합용매, 보다 더욱 더 바람직하게는 에탄올 순도가 60~90% (v/v), 보다 바람직하게는 70~80% (v/v)가 되게 에탄올을 첨가한 후에, 약 1 내지 10시간, 바람직하게는 약 4 내지 5시간 동안 열수추출, 초음파 추출, 환류냉각추출 등의 추출방법, 바람직하게는 환류냉각 추출방법을 이용하여 추출한 추출액을 감압 여과하여 얻은 추출물을 약 40 내지 80℃, 바람직하게는 약 50 내지 60℃에서 감압 농축하여 농축물을 수득하는 제 2 단계; The ethanol is added to the culture medium of the first step to add about 2 to 5 times (v / v) of ethanol, preferably 3 to 4 times (v / v) of ethanol, and a mixed solvent of sodium acetate and ethanol, more Preferably, 0.01 M to 1 M sodium acetate and ethanol mixed solvent, even more preferably 0.05 to 0.2 M sodium acetate (pH 4.5) and ethanol mixed solvent, even more preferably 60 to 90% ethanol purity (v / v), more preferably 70 to 80% (v / v) after adding ethanol, hydrothermal extraction, ultrasonic extraction, reflux cooling extraction for about 1 to 10 hours, preferably about 4 to 5 hours A second step of obtaining a concentrate by concentrating the extract obtained by filtration under reduced pressure at an extraction method of the extraction method, preferably using a reflux cooling extraction method at about 40 to 80 ° C., preferably at about 50 to 60 ° C .;
상기 제 2 단계의 울금 농축물에 계면활성제, 바람직하게는 상기 추출 농축액 고형분 중량 대비 0.1 내지 20%(w/w), 보다 바람직하게는 3 내지 8%(w/w)의 레시틴, 설탕에스테르, 포스포리피드, 소르비탄 지방산 에스테르, 폴리글리세린 에스테르 등의 계면활성제, 바람직하게는, 폴리글리세린 에스테르계 계면활성제, 보다 더 바람직하게는, MS-5S(hexaglycerol monoesterate, Sakamoto Yakuhin Kogyo, Japan) 등의 계면활성제를 첨가하여 30 내지 80℃, 바람직하게는 약 60 내지 70℃에서 약 0.5 내지 4시간, 바람직하게는 약 1 내지 2 시간 동안 교반하여 균질화하는 제 3 단계; Surfactant in the second step turmeric concentrate, preferably 0.1 to 20% (w / w), more preferably 3 to 8% (w / w) of lecithin, sugar esters, based on the weight of the extract concentrate solids, Surfactants, such as phospholipid, sorbitan fatty acid ester, and polyglycerol ester, Preferably, polyglycerol ester type surfactant, More preferably, interface of MS-5S (hexaglycerol monoesterate, Sakamoto Yakuhin Kogyo, Japan) etc. A third step of homogenization by adding the active agent, stirring at 30 to 80 ° C., preferably at about 60 to 70 ° C., for about 0.5 to 4 hours, preferably about 1 to 2 hours;
상기 제 3 단계의 유화물에 시클로덱스트린은 상기 유화물에 울금 추출물 고형분 중량 대비 30 내지 100% (w/w), 바람직하게는 40 내지 60% (w/w) 배합양의 베타-시클로덱스트린 및 감마-시클로덱스트린 혼합물, 바람직하게는 0.1~2: 2~0.1(w/w), 보다 바람직하게는 1: 1.5~0.5(w/w)의 혼합비를 갖는 시클로덱스트린 혼합물을 울금 추출물 고형분 중량 대비 30 내지 200 w/w%, 바람직하게는 60 내지 100 w/w%를 각각 혼합 첨가하여 30 내지 80℃, 바람직하게는 약 60 내지 70℃에서 약 0.5 내지 4시간, 바람직하게는 약 1 내지 2 시간 동안 교반하여 포접 반응함을 특징으로 하는 제 4 단계; Cyclodextrin in the emulsion of the third step is 30 to 100% (w / w), preferably 40 to 60% (w / w) blended amount of beta-cyclodextrin and gamma- relative to the weight of the turmeric extract solids in the emulsion Cyclodextrin mixture, preferably cyclodextrin mixture having a mixing ratio of 0.1 to 2: 2 to 0.1 (w / w), more preferably 1: 1.5 to 0.5 (w / w) is 30 to 200 by weight of turmeric extract solids Add w / w%, preferably 60-100 w / w%, respectively, and stir at 30-80 ° C, preferably about 60-70 ° C for about 0.5-4 hours, preferably about 1-2 hours A fourth step characterized in that the reaction is included;
제 4단계의 포접물을 분무건조, 동결건조, 열풍건조, 바람직하게는 분무건조를 통하여 수용성 울금 추출분말을 제조하는 방법을 제공한다. Provided is a method for preparing a water-soluble turmeric extract powder by spray drying, freeze drying, hot air drying, and preferably spray drying of the clathrate of the fourth step.
보다 구체적으로는, 예를 들어, 상기 제 1단계에서 울금에 특이적으로 잘 자라는 유산균을 선별하기 위하여, 울금을 미세하게 마쇄한 다음에 배양기에 약 8 내지 12배(v/w)에 달하는 아세트산 나트륨 용액, 바람직하게는 0.01M 내지 1M 아세트산 나트륨 (pH 4.5)을 첨가하여 약 10 %(w/v)의 농도로 0.1M 아세트산 나트륨 (pH4.5)에 현탁한 후 살균한다. 살균 종료 후 락토바실러스 (lactobacillus ) 속, 페디오코커스(pediocuccus ) 속 등의 여러 종의 유산균을 접종하여 24시간동안 배양한 후 생균수와 배양물의 쓴 맛이 경감되는 정도를 평가하여 선별한다.More specifically, for example, in order to screen for lactic acid bacteria that grows specifically to turmeric in the first step, acetic acid of about 8 to 12 times (v / w) is finely crushed and then incubated in the incubator. A sodium solution, preferably 0.01 M to 1 M sodium acetate (pH 4.5) is added to suspend and sterilized in 0.1 M sodium acetate (pH 4.5) at a concentration of about 10% (w / v). After sterilization end Lactobacillus bacteria (lactobacillus), A Phedi O Rhodococcus (pediocuccus) and incubated for 24 hours was inoculated to different species of lactic acid bacteria such as genus are selected by evaluating the degree to which the viable cell count and the culture bitter taste of water to be reduced.
상기 제조방법으로 얻은 발효 울금 추출분말은 현재 시공품으로 판매되고 있는 제품상의 문제점들 즉, 울금의 쓴 맛을 제거하고, 주성분 원료인 커큐민의 용해도가 좋지 않아 재석출되어 생기는 침전의 문제와 이 침전으로 인한 시공품의 탁해짐, 제품 바닥에 쌓이는 침전물로 인한 소비자의 클레임과 이로 인한 제조사의 이미지 손상 등의 기존 제품상의 문제점을 유화제로 균질화한 후 시클로덱스트린의 포접화합물을 생성하여 용해도를 증가시킴으로서 해결하였으며 따라서 시공품의 탁해짐 현상이나 바닥의 침전물 생성 등이 방지되어 제품의 질을 높일 뿐만 아니라 커큐민의 재석출로 인한 미감의 저하 문제도 해결할 수 있는 장점을 갖는다.
The fermented turmeric extract powder obtained by the above manufacturing method is a problem of the product currently being sold as a construction product, that is, removing the bitter taste of turmeric, and the problem of precipitation caused by reprecipitation due to poor solubility of curcumin, the main ingredient, and this precipitation We solved the problems of existing products such as turbidity of construction products, consumer claims due to sediment accumulated on the bottom of the product, and consequent damage to the manufacturer's image. The turbidity of the construction products and the formation of deposits on the floor are prevented to improve the quality of the product as well as to solve the problem of deterioration of aesthetics due to the re-precipitation of curcumin.
따라서, 본 발명은 상기 제조방법에 의해 제조된 수가용성 발효 울금 추출분말을 제공한다. 상기 제조방법으로 제조된 발효 울금 추출분말은 커큐민 함량이 2% 이상임을 특징으로 한다.
Accordingly, the present invention provides a water-soluble fermented turmeric extract powder prepared by the above production method. Fermented turmeric extract powder prepared by the manufacturing method is characterized in that the curcumin content of 2% or more.
또한, 본 발명은 상기 수가용성 발효 울금 추출분말을 함유한 식품, 식품첨가물 및/또는 건강기능식품을 제공한다.The present invention also provides a food, food additive and / or health functional food containing the water-soluble fermented turmeric extract powder.
본 발명의 건강기능식품은 울금의 쓴 맛을 제거하고, 이와 동시에 울금 추출물의 용해도와 안정성을 높이고, 액상제형화시에 투명성을 높여 제품의 전반적인 품질을 향상시킴을 특징으로 한다.
Health functional food of the present invention is characterized by removing the bitter taste of turmeric, at the same time to improve the solubility and stability of turmeric extract, increase the transparency during liquid formulation to improve the overall quality of the product.
또한 본 발명의 계면활성제에 의해 균질화된 울금 추출물의 지용성 성분은 액상 상태에서는 균질화가 되지만, 분말화하기 위해 베타-시클로덱스트린은 지용성 성분과 안정적인 포접화합물을 형성하여 용해도 증가 효과가 있고, 감마-시클로덱스트린은 쓴 맛을 제거하는 효과가 있어서 이 두가지 성분을 혼합하여 사용하는 것이 단일 성분을 사용하였을 때 보다 효율적이다. In addition, although the fat-soluble component of the turmeric extract homogenized by the surfactant of the present invention is homogenized in the liquid state, in order to powder, beta-cyclodextrin forms a stable clathrate compound with the fat-soluble component and has an effect of increasing solubility, and gamma-cyclo Dextrin has the effect of eliminating bitter taste, so it is more efficient to mix these two components when using a single component.
본 발명은 상기 제조방법에 의해 제조된 수가용성 발효 울금 추출분말을 함유하는 식품 및 식품첨가제를 제공한다.The present invention provides a food and food additive containing a water-soluble fermented turmeric extract powder prepared by the above method.
본 발명의 수가용성 발효 울금 추출분말을 함유하는 식품첨가제에는 구연산, 후말산, 아디픽산, 젖산, 사과산 등의 유기산이나 인산나트륨, 인산칼륨, 산성피로인산염, 폴리인산염 (중합인산염) 등의 인산염이나 폴리페놀, 카테킨 (catechin), 알파-토코페롤, 로즈마리 추출물 (rosemary extract), 비타민 C, 녹차 추출물, 감초 추출물, 키토산, 탄닌산, 피틴산 등의 천연 항산화제 중 어느 하나 또는 하나 이상을 추가로 포함할 수 있다.Food additives containing the water-soluble fermented turmeric extract powder of the present invention include organic acids such as citric acid, fumaric acid, adipic acid, lactic acid, malic acid, phosphates such as sodium phosphate, potassium phosphate, acid pyrophosphate and polyphosphate (polymeric phosphate); It may further include any one or more of natural antioxidants such as polyphenols, catechin, alpha-tocopherol, rosemary extract, vitamin C, green tea extract, licorice extract, chitosan, tannic acid, phytic acid, and the like. have.
상기의 식품첨가제용 수가용성 발효 울금 추출분말은 분말 또는 과립형태일 수 있다.The water-soluble fermented turmeric extract powder for food additives may be in powder or granule form.
마찬가지로, 본 발명의 수가용성 발효 울금 추출분말을 함유하는 식품첨가제는 유당 카제인, 덱스트린, 포도당, 설탕, 솔비톨 중 어느 하나 또는 하나 이상을 추가로 포함할 수 있다.Similarly, the food additive containing the water-soluble fermented turmeric extract powder of the present invention may further include any one or more of lactose casein, dextrin, glucose, sugar, sorbitol.
또한, 본 발명은 상기 수가용성 발효 울금 추출분말을 함유하는 식품첨가제를 식품에 보존료, 살균제, 산화 방지제, 향신료, 조미료, 감미료, 착향료, 팽창제, 강화제, 개량제, 유화제, 여러 가지 영양제, 합성 풍미제 및 천연 풍미제 등의 풍미제, 착색료, 발색제, 중진제(치즈, 초콜렛 등), 펙트산 및 그의 염, 알긴산 및 그의 염, 유기산, 보호성 콜로이드 증점제, pH 조절제, 안정화제, 소포제, 용제, 이형제, 방부제, 품질 개량제, 글리세린, 알콜, 탄산 음료에 사용되는 탄산화제 등 또는 기타 식품제조용 첨가제 및 식품소재(부원료)의 필수원료로 사용하는 것을 특징으로 하는 식품첨가제의 이용방법을 제공한다. 이때 식품첨가제는 식품에 침지, 분무 또는 혼합하여 상기 식품에 첨가할 수 있으며, 이러한 첨가제의 비율은 그렇게 중요하진 않지만 본 발명의 조성물 100 중량부 당 0.01 내지 약 90 중량부의 범위에서 선택되는 것이 일반적이다.In addition, the present invention is a food additive containing the water-soluble fermented turmeric extract powder in food preservatives, fungicides, antioxidants, spices, seasonings, sweeteners, flavoring agents, swelling agents, reinforcing agents, modifiers, emulsifiers, various nutrients, synthetic flavors And flavoring agents such as natural flavoring agents, coloring agents, coloring agents, neutralizing agents (such as cheese and chocolate), pectic acid and salts thereof, alginic acid and salts thereof, organic acids, protective colloid thickeners, pH adjusting agents, stabilizers, antifoaming agents, solvents, It provides a method of using a food additive, characterized in that it is used as a release agent, preservatives, quality improvers, glycerin, alcohol, carbonation agent used in carbonated beverages, or the like as an essential raw material of food additives (food additives). In this case, the food additive may be added to the food by immersing, spraying or mixing the food, and the ratio of such additive is not so important, but it is generally selected in the range of 0.01 to about 90 parts by weight per 100 parts by weight of the composition of the present invention. .
본 발명에서 적용가능한 식품으로는 과일, 야채, 과일이나 야채의 건조제품이나 절단제품, 과일쥬스, 야채쥬스, 이들의 혼합쥬스이거나 칩류, 면류, 축산가공식품, 수산가공식품, 유가공식품, 발효유식품, 두류식품, 곡류식품, 미생물발효식품, 제과제빵, 양념류, 육가공류, 산성음료수, 감초류, 허브류 중 어느 하나 또는 하나 이상이고, 보다 구체적으로 껌, 캔디, 비스켓, 아이스크림, 초콜렛 중 어느 하나 또는 하나 이상이다. Foods applicable in the present invention are fruits, vegetables, dried or cut products of fruit or vegetables, fruit juices, vegetable juices, mixed juices or chips, noodles, livestock processed foods, fish processed foods, dairy products, fermented milk foods , Legumes, cereals, microbial fermented foods, bakery, condiments, processed meats, acidic beverages, licorice, herbs or any one or more of, more specifically, any of gum, candy, biscuits, ice cream, chocolate or More than one.
이들을 각각 구체적으로 설명하면 하기와 같다.Each of these is explained in detail as follows.
껌 제조시, 본 발명의 식품첨가제 0.5 중량%, 껌베이스 25 중량%, 솔비톨 72 중량%를 60 내지 70℃로 예비 가열한 믹서에 넣어 혼합한 후, 믹서내부 온도를 55 ℃로 유지시키면서 페퍼민트 향료를 2.5 중량% 첨가한 다음 30분 혼합한 다음 추출하여 압연하고, 24-48시간 숙성시킨 후 재단하고 포장하여 껌을 제조할 수 있다. In the preparation of gum, 0.5% by weight of the food additive of the present invention, 25% by weight of gum base, 72% by weight of sorbitol were mixed in a preheated mixer at 60 to 70 ° C, and then mixed with peppermint while maintaining the temperature inside the mixer at 55 ° C. 2.5% by weight of the mixture is then mixed for 30 minutes, then extracted and rolled, aged for 24-48 hours and then cut and packaged to prepare a gum.
또한 제과제빵 제조과정에서 반죽할 때 첨가 사용하며, 소스, 양념장에도 첨가 사용하고, 또한 발효유 또는 요구르트 등에 분말이나 액상을 첨가하여 기능성 또는 기호성 식품으로 사용할 수 있다. 생약 추출분말을 김치, 젓갈, 야채 가공에 직접 투입하여 맛 보존성, 항산화, 변색 방지의 목적으로 사용할 수도 있다. 육가공에서 햄, 소세지 등에 침지 또는 분무 살포하여 사용하며, 분말 또는 과립 형태의 본 발명에 따른 식품첨가제를 마늘, 파, 생강, 허브(herb), 감초 등을 섞어 향신료를 만들어 사용할 수 있고, 수산가공식품인 어묵, 생선, 조미어포, 젓갈 등에도 침지, 분무 및 첨가 방법으로 사용하며, 김치, 단무지, 깍두기, 야채 절임 등에도 침지, 분무 및 첨가할 수 있다.In addition, it is used when kneading in the manufacturing process of confectionery baking, it is added to the sauce, seasoning sauce, and can be used as a functional or palatable food by adding powder or liquid to fermented milk or yogurt. The herbal extract powder can be directly added to kimchi, salted fish, or vegetable processing to be used for the purpose of preserving taste, anti-oxidation and discoloration. It is used by immersing or spraying in ham, sausage, etc. in meat processing, and the food additive according to the present invention in the form of powder or granule can be used to make spices by mixing garlic, green onion, ginger, herb, licorice, etc. Food, fish paste, fish, seasoned fish, salted fish, etc. are used as a dipping, spraying and addition method, can also be immersed, sprayed and added to kimchi, pickled radish, pickled radish, pickled vegetables.
또한, 본 발명은 울금 추출분말을 유효성분으로 함유하는 건강기능식품을 제공한다.The present invention also provides a health functional food containing turmeric extract powder as an active ingredient.
상기 건강기능식품은 울금의 쓴 맛을 제거하고, 이와 동시에 울금 추출물의 용해도와 안정성을 높이고, 액상제형화시에 투명성을 높여 제품의 전반적인 품질을 향상시킴을 특징으로 한다.The health functional food is characterized by removing the bitter taste of turmeric, and at the same time to improve the solubility and stability of turmeric extract, increase the transparency during the liquid formulation to improve the overall quality of the product.
본 발명의 울금 추출분말을 첨가할 수 있는 식품으로는, 예를 들어, 각종 식품류, 음료, 껌, 차, 비타민 복합제, 건강 기능성 식품류 등이 있다.Examples of the food to which the turmeric extract powder of the present invention can be added include various foods, beverages, gums, teas, vitamin complexes, and health functional foods.
본 발명의 건강기능식품은 정제(tablet), 캡슐제(capsule), 분말제(powder), 과립제(granule), 환제(pill), 액제(liquid) 등의 형태를 포함한다.The dietary supplement of the present invention includes tablets, capsules, powders, granules, pills, liquids and the like.
본 발명의 건강 기능성 음료 조성물은 지시된 비율로 필수 성분으로서 상기 추출물을 함유하는 외에는 다른 성분에는 특별한 제한이 없으며 통상의 음료와 같이 여러 가지 향미제 또는 천연 탄수화물 등을 추가 성분으로서 함유할 수 있다. 상술한 천연 탄수화물의 예는 모노사카라이드, 예를 들어, 포도당, 과당 등; 디사카라이드, 예를 들어 말토스, 슈크로스 등; 및 폴리사카라이드, 예를 들어 덱스트린, 시클로덱스트린 등과 같은 통상적인 당, 및 자일리톨, 소르비톨, 에리트리톨 등의 당알콜이다. 상술한 것 이외의 향미제로서 천연 향미제(타우마틴, 스테비아 추출물(예를 들어 레바우디오시드 A, 글리시르히진등) 및 합성 향미제(사카린, 아스파르탐 등)를 유리하게 사용할 수 있다. 상기 천연 탄수화물의 비율은 본 발명의 조성물 100 ㎖당 일반적으로 약 1 내지 20 g, 바람직하게는 약 5 내지 12 g이다.The health functional beverage composition of the present invention has no particular limitation on the other ingredients other than the above-mentioned extract as an essential ingredient in the indicated ratio, and may contain various flavors or natural carbohydrates as an additional ingredient such as ordinary beverages. Examples of the above-mentioned natural carbohydrates include monosaccharides such as glucose, fructose and the like; Disaccharides such as maltose, sucrose and the like; And conventional sugars such as polysaccharides such as dextrin, cyclodextrin, and sugar alcohols such as xylitol, sorbitol, and erythritol. As flavoring agents other than those mentioned above, natural flavoring agents (tauumatin, stevia extract (for example, rebaudioside A, glycyrrhizin, etc.) and synthetic flavoring agents (saccharin, aspartame, etc.) can be advantageously used. The proportion of said natural carbohydrates is generally about 1-20 g, preferably about 5-12 g per 100 ml of the composition of the present invention.
상기 외에 본 발명의 조성물은 여러 가지 영양제, 비타민, 광물(전해질), 합성 풍미제 및 천연 풍미제 등의 풍미제, 착색제 및 중진제(치즈, 초콜릿 등), 펙트산 및 그의 염, 알긴산 및 그의 염, 유기산, 보호성 콜로이드 증점제, pH 조절제, 안정화제, 방부제, 글리세린, 알코올, 탄산음료에 사용되는 탄산화제 등을 함유할 수 있다. 그밖에 본 발명의 조성물은 천연 과일 쥬스 및 과일 쥬스 음료 및 야채 음료의 제조를 위한 과육을 함유할 수 있다. 이러한 성분은 독립적으로 또는 조합하여 사용할 수 있다. 이러한 첨가제의 비율은 그렇게 중요하진 않지만 본 발명의 조성물 100 중량부 당 0 내지 약 20 중량부의 범위에서 선택되는 것이 일반적이다.In addition to the above, the composition of the present invention includes various nutrients, vitamins, minerals (electrolytes), flavors such as synthetic flavors and natural flavors, coloring and neutralizing agents (such as cheese and chocolate), pectic acid and salts thereof, alginic acid and its Salts, organic acids, protective colloidal thickeners, pH adjusters, stabilizers, preservatives, glycerin, alcohols, carbonation agents used in carbonated drinks, and the like. In addition, the composition of the present invention may contain a natural fruit juice and a pulp for the production of fruit juice drinks and vegetable drinks. These components can be used independently or in combination. The proportion of such additives is not so critical, but is generally selected in the range of 0 to about 20 parts by weight per 100 parts by weight of the composition of the present invention.
또한 본 발명은 발효 울금 엑스 함유 액상제제를 제조함에 있어 추가의 장비가 필요 없으며 또한 포접체 형성 방법이 간단하여 생산에 적용하기 용이하고 바로 적용이 가능하다는 장점이 제공된다.
In addition, the present invention does not require additional equipment in preparing the fermented turmeric extract-containing liquid formulation and also provides an advantage that the method of forming a clathrate is easy to apply to production and can be directly applied.
본 발명은 울금을 배지로 하여 락토바실러스 카세이 (Lactobacillus casei)를 배양 및 발효하여 쓴 맛을 완화시킨 후, 0.1 M 아세트산 나트륨 용액과 에탄올의 혼합용매를 추출용매로 하여 커큐민이 고함량으로 함유된 발효 울금을 추출하 고, 이 발효 울금 추출물에 계면활성제 및 시클로덱스트린을 첨가하여 제조되는 기호성이 우수한 수가용성 발효 울금 추출분말 및 이의 제조방법은 비용과 시간의 절감 효과뿐만 아니라, 고함량 및 고순도 효과를 확인함으로서, 상기의 제조방법은 식품, 약학조성물, 건강기능식품 및 화장료 조성물의 원료로 사용할 수 있으며, 특히, 액상제형화시에도 유용하게 이용할 수 있다.
The present invention is cultured and fermented Lactobacillus casei with turmeric as a medium to alleviate the bitter taste, fermentation containing a high content of curcumin using a mixed solvent of 0.1 M sodium acetate solution and ethanol as an extraction solvent A water-soluble fermented turmeric extract powder having excellent palatability, prepared by adding turmeric and adding a surfactant and cyclodextrin to the fermented turmeric extract, and a method of preparing the same, not only reduce cost and time, but also have high content and high purity effect. By confirming, the above production method can be used as a raw material for food, pharmaceutical compositions, health functional foods and cosmetic compositions, and in particular, it can be usefully used for liquid formulation.
도 1은 울금을 온도별로 처리한 후에 커큐민의 함량을 분석한 결과를 나타낸 도이고,
도 2는 울금을 pH별로 처리한 후에 커큐민의 함량을 분석한 결과를 나타낸 도이고,
도 3은 울금을 0.1 M 아세트산 나트륨 용액(pH 4.5)에 용해하여 온도별로 처리한 후에 커큐민의 함량을 분석한 결과를 나타낸 도이고,
도 4은 본 발명의 발효 울금 추출분말의 제조 공정을 도시한 순서도이고,
도 5는 발효 울금 추출분말 중에 커큐민의 분석한 결과를 나타낸 도이며,
도 6은 발효 울금 추출분말과 1% 용해액을 나타낸 도이고,
도 7은 발효 울금 추출분말과 울금 추출분말의 3개월 경시변화를 측정한 도이다.1 is a view showing the results of analyzing the content of curcumin after treatment of turmeric by temperature,
2 is a view showing the results of analyzing the content of curcumin after treatment of turmeric by pH,
3 is a diagram showing the results of analyzing curcumin content after dissolving turmeric in 0.1 M sodium acetate solution (pH 4.5) and treating it by temperature.
Figure 4 is a flow chart showing the manufacturing process of the fermented turmeric extract powder of the present invention,
5 is a view showing the results of the analysis of curcumin in fermented turmeric extract powder,
6 is a view showing the fermented turmeric extract powder and 1% solution,
7 is a view measuring the three-month change of the fermented turmeric extract powder and turmeric extract powder.
이하, 본 발명을 하기 실시예 및 실험예에 의해 자세히 설명한다. Hereinafter, the present invention will be described in detail by the following Examples and Experimental Examples.
하기 실시예 및 실험예는 본 발명을 예시하는 것일 뿐, 본 발명의 내용이 하기 실시예 및 실험예에 한정되는 것은 아니다.
The following Examples and Experimental Examples are only illustrative of the present invention, and the content of the present invention is not limited to the following Examples and Experimental Examples.
참고예Reference Example 1. 재료의 준비 1. Preparation of materials
울금은 경동시장에서 구입하였고, 글리세린 지방산 에스테르(SY Glyster MS-5S; 80922)는 사카모토 야쿠힌 쿄교사(Sakamoto Yakuhin Kogyo)에서 구입하였고, 베타-시클로덱스트린(CAVAMAXR W7 Food), 감마-시클로덱스트린(CAVAMAXR W8 Food)을 바커 케미컬사(Wacker Chemical Corporation)에서 구입하여 준비하였다.
Turmeric was purchased from Kyungdong Market, Glycerin fatty acid ester (SY Glyster MS-5S; 80922) was purchased from Sakamoto Yakuhin Kogyo, CAVAMAX R W7 Food, Gamma-cyclodextrin (CAVAMAX R W8 Food) was purchased from Wacker Chemical Corporation and prepared.
실시예Example 1. One. 커큐민의Curcumin 열처리 Heat treatment
울금 10 g에 정제수 100 ml를 첨가하여 100℃에서 30분간, 121℃ 30분간 autoclave(DA-AC, 동아과학)에서 열처리한 후에 에탄올 300ml를 첨가하여 70℃ 에서 2시간동안 환류추출한 후에 커큐민의 함량을 분석하였다. 대조군의 커큐민 함량을 100%로 한 후 상대적인 함량으로 환산했을 때 도 1에서와 같이 100℃, 30분 열처리시 약 24%, 121℃ 30분은 약 70%정도 분해되었다.
Curcumin content after adding 100 ml of purified water to 100 g of turmeric and heat-treating at 100 ° C for 30 minutes and 121 ° C for 30 minutes in autoclave (DA-AC), followed by reflux extraction at 70 ° C for 2 hours with 300 ml of ethanol. Was analyzed. When the curcumin content of the control group was set to 100% and then converted to relative content, as shown in FIG. 1, 100 ° C and 30 minutes of heat treatment were decomposed about 24% and 121 ° C for 30 minutes to about 70%.
실시예Example 2. 2. pHpH 별 star 커큐민의Curcumin 안정성 stability
울금 10 g에 0.1 M 아세트산 나트륨 (pH 4, 5, 6)과 0.1 M 인산 칼륨(pH 7) 100 ml와 에탄올 300 ml를 각각 첨가하여 70℃에서 2시간 동안 환류추출한 후에 커큐민의 함량을 분석하였다. 대조군의 커큐민 함량을 100%로 한 후 상대적인 함량으로 환산했을 때 도 2에서와 같이 pH 6에서는 약 44%, pH 7에서는 약 80% 정도 분해되었다.100 g of 0.1 M sodium acetate (
실시예Example 3. 3. pHpH 4.5에서의 열처리 Heat treatment at 4.5
울금 10 g에 0.1M 아세트산 나트륨 (pH 4.5)를 100 ml 첨가하여 100℃에서 30분간, 121℃ 30분간 autoclave(DA-AC, 동아과학)에서 열처리한 후에 에탄올 300 ml를 첨가하여 70℃에서 2시간 동안 환류추출한 후에 커큐민의 함량을 분석하였다. 대조군의 커큐민 함량을 100%로 한 후 상대적인 함량으로 환산했을 때 도 3에서와 같이 100℃, 30분 열처리시 그대로 유지되었고, 121℃ 30분은 약 27%정도 분해되었다.
100 ml of 0.1 M sodium acetate (pH 4.5) was added to 10 g of turmeric, and heat-treated in autoclave (DA-AC) for 30 minutes at 100 ° C and 30 minutes at 121 ° C, followed by 300 ml of ethanol. Curcumin content was analyzed after refluxing for a period of time. When the curcumin content of the control group was 100% and converted to a relative content, the curcumin content was maintained at 100 ° C. and 30 minutes of heat treatment as shown in FIG.
실시예Example 4. 유산균의 선별 4. Screening of Lactic Acid Bacteria
울금 1 kg을 분쇄기(KM-LS-2K, KM tech, Korea)를 이용하여 5분 동안 분쇄한 후에 배양기(MSJ-U3, Marubishi사, Tokyo, Japan)에 상기 분쇄한 울금 100 g을 넣고, 0.1M 아세트산 나트륨 (pH4.5)을 1 L 첨가하였다. 100℃에서 30분간 살균한 후에 미리 준비한 유산균들 즉, Pediococcus pentosaceus KCCM11004P, Lactobacillus acidophillus KCCM40265, Lactobacillus casei KCCM12452, Lactobacillus hevet icus KCCM11223, Lactobacillus reuteri KCCM40717, Lactobacillus plantarum KCCM12116, Lactobacillus fermentum BLJH101, Leuconostoc mesenteroides KC TC3505, 및 Lactococcus lactis KCTC2013 각각 20 ml 접종하였다. 24시간 동안 정치 배양하여 하기 실험에 사용하여 유산균 선별에 사용하였다.
After grinding 1 kg of turmeric using a grinder (KM-LS-2K, KM tech, Korea) for 5 minutes, put 100 g of the ground turmeric into an incubator (MSJ-U 3 , Marubishi, Tokyo, Japan), 1 L of 0.1 M sodium acetate (pH4.5) was added. Lactobacillus, Pediococcus , prepared in advance after sterilization at 100 ° C for 30 minutes pentosaceus KCCM11004P, Lactobacillus acidophillus KCCM40265, Lactobacillus casei KCCM12452, Lactobacillus hevet icus KCCM11223, Lactobacillus reuteri KCCM40717, Lactobacillus plantarum KCCM12116, Lactobacillus fermentum BLJH101, Leuconostoc mesenteroides KC TC3505, and
실시예Example 5. 발효 5. Fermentation 울금Turmeric 추출분말의 제조 Preparation of Extract Powder
도 4에 나타낸 바와 같이 상기 실시예 1에서 준비한 분쇄한 울금 1 kg을 넣고, 0.1 M 아세트산 나트륨을 10 L를 첨가하였다. 100℃에서 30분간 살균한 후에 락토바실러스 카세이 KCCM12452(Lactobacillus casei KCCM12452)를 200 ml 접종하였다. 24시간 동안 정치배양을 한 후에 에탄올 30 L를 첨가하여 4시간 동안 환류냉각 추출하였다. 여기에서 얻어진 추출물에 여과보조제(perlite) 200 g을 넣고, 압착 여과한 후 45~50℃에서 농축하여 고형분 함량이 15%인 농축액 100g을 얻었다. 이 발효물 농축액에 MS-5S(80922, Sakamoto Yakuhin Kogyo, Osaka, Japan)를 고형분량의 5%(w/w)(농축액의 고형분)인 0.75 g을 넣고 60℃에서 1시간 동안 교반하였다. 베타-시클로덱스트린 6.75 g과 감마-시클로덱스트린 7.5 g을 첨가한 후에 70℃에서 1시간 동안 교반한 후에 생성된 포접물을 분무 건조하여 발효 울금 추출 포접 분말 28.5 g을 수득하였다(도 4 참조).
As shown in Fig. 4, 1 kg of the ground turmeric prepared in Example 1 was added, and 10 L of 0.1 M sodium acetate was added thereto. Lactobacillus casei Lactobacillus casei KCCM12452 after sterilization at 100 ° C for 30 minutes KCCM12452) was inoculated in 200 ml. After incubation for 24 hours, 30 L of ethanol was added and reflux-cooled for 4 hours. 200 g of a filtration aid (perlite) was added to the extract obtained, compressed and filtered, and then concentrated at 45 to 50 ° C. to obtain 100 g of a concentrate having a solid content of 15%. MS-5S (80922, Sakamoto Yakuhin Kogyo, Osaka, Japan) was added 0.75 g of 5% (w / w) of solids (solids of concentrate) in the fermentation broth and stirred at 60 ° C for 1 hour. 6.75 g of beta-cyclodextrin and 7.5 g of gamma-cyclodextrin were added, followed by stirring at 70 ° C. for 1 hour, and then the resulting clathrate was spray dried to obtain 28.5 g of fermented turmeric extract clathrate powder (see FIG. 4).
실시예Example 6. 6. 울금추출분말의Of turmeric extract powder 제조 Produce
커큐민의 안정성을 비교하기 위해서 상기 특허에서 제시한 방법이 아닌 단순 추출방법에 의해서 제조하였다. 울금 1 kg을 넣고, 70% (v/v) 에탄올을 넣고, 4시간 동안 환류냉각 추출하였다. 여기에서 얻어진 추출물에 여과보조제(perlite) 200 g을 넣고, 압착 여과한 후 45~50℃에서 농축하여 고형분 함량이 14%인 농축액 100g을 얻었다. 이 농축액에 고형분과 동량인 말토덱스트린을 14 g 첨가한 후에 동결건조하여 울금추출분말 26.8 g을 얻었다.
In order to compare the stability of curcumin was prepared by a simple extraction method, not the method proposed in the patent. 1 kg turmeric was added, 70% (v / v) ethanol was added, and the mixture was reflux cooled for 4 hours. 200 g of a filtration aid (perlite) was added to the extract obtained, compressed and filtered, and then concentrated at 45 to 50 ° C. to obtain 100 g of a concentrate having a solid content of 14%. 14 g of maltodextrin, which is the same amount as solid, was added to the concentrate, followed by lyophilization to obtain 26.8 g of turmeric extract powder.
실험예Experimental Example 1. 유산균 배양물의 관능평가 및 1. Sensory Evaluation of Lactic Acid Bacteria Culture and 생균수Viable count
울금 특유의 쓴 맛을 제거하고 울금을 배지로 잘 자라는 효과가 있는 유산균을 선별하기 위해서 상기 실시예 4에서 제조한 유산균 배양물을 고형분 0.1 w/v%의 농도로 각각 정제수에 희석한 후 쓴 맛의 차이 및 생균수를 측정하였다. 향기, 맛, 색, 조직감에 잘 훈련된 15명의 관능검사 요원을 대상으로 울금의 맛을 대조군(유산균을 접종하지 않은 추출물)을 기준으로, 대조군을 10의 수치로 정하고, 9단계 평점법(매우 좋다: 1점, 매우 나쁘다: 9점)으로 상대 평가하여 이를 평균치 또는 평균치± 표준편차로 나타내었고, 3회 이상 반복 분석하여, 던칸의 다중범위 검증법(Duncan's multiple range test)으로 그 유의성을 검증하였다. In order to remove the unique bitterness of turmeric and to select lactic acid bacteria that are effective in growing turmeric with medium, the lactic acid bacteria cultured in Example 4 was diluted in purified water at a concentration of 0.1 w / v% of solids, respectively, and then bitter taste. Difference and viable cell count were measured. For 15 sensory test personnel who were well trained in fragrance, taste, color, and texture, the taste of turmeric was based on the control group (extract without lactobacillus), and the control group was determined as 10. Good: 1 point, very bad: 9 points) Relative evaluation, expressed as mean or mean ± standard deviation, repeated analysis three or more times, and verified its significance by Duncan's multiple range test It was.
실험결과, 상기 표 1에 나타난 바와 같이, 대조군과 비교하여 유산균 종류별로 각각 쓴 맛과 생균수를 비교하였을 때, 락토바실러스 카세이(Lactobacillus ca sei)와 페디오코커스 펜토사세우스(Pediococcus pento saceus)의 쓴 맛 개선효과와 생균수에서 우수한 효과를 확인 할 수 있었다. 따라서, 유산균에 의한 쓴 맛 개선효과를 확인 및 유산균으로 배양함으로써 정장작용과 같은 우수한 생리활성 효과가 있음을 알 수 있었다(표 1 참조).
Experimental results, as shown in Table 1, Lactobacillus casei ( Lactobacillus) when comparing the bitter taste and the number of live bacteria for each type of lactic acid bacteria compared to the control group ca sei ) and Pediococcus pentosaceus pento saceus ) was able to improve the bitter taste and excellent effect on the number of viable cells. Therefore, by confirming the effect of improving the bitter taste by lactic acid bacteria and cultured with lactic acid bacteria it was found that there is an excellent physiological activity effect such as intestinal action (see Table 1).
실험예Experimental Example 2. 2. 커큐민의Curcumin 함량 분석 Content analysis
실시예 2에서 제조한 발효 울금 추출분말의 유효성분인 커큐민의 함량을 측정하기 위해 고성능액체크로마토그래피(Acquity UPLC, Waters, USA)를 사용하여 그 함량을 측정하였고, 컬럼은 Acquity UPLC BEH C18(10cm * 2.1mm, 1.7um, Waters, USA)를 사용하였으며, 검출 스펙트럼은 UV 400 nm를 사용하여 측정하였다. 이동상은 0.1% acetate와 acetonitrile을 40:60(v/v)으로 혼합하여 사용하였고, 유속은 0.3 ml/min 로 하였다. 표준품으로는 curcumin(sigma, St-Louis, Mo, USA)를 1 mg/ml의 농도로 메탄올에 녹여 스톡(stock)용액으로하여 도 2에서 나타낸 바와 같이 대조군으로는 발효하지 않은 울금 추출분말을 사용하였고, 1, 0.1, 0.01 ml/min의 검액을 만들어 검량선용 표준용액으로 사용하여 검량선을 작성하여 커큐민의 함량을 측정하였다. In order to determine the content of curcumin, the active ingredient of the fermented turmeric extract powder prepared in Example 2, the content was measured using high performance liquid chromatography (Acquity UPLC, Waters, USA), and the column was Acquity UPLC BEH C 18 ( 10 cm * 2.1 mm, 1.7 um, Waters, USA) and the detection spectrum was measured using UV 400 nm. The mobile phase was mixed with 0.1% acetate and acetonitrile at 40:60 (v / v), and the flow rate was 0.3 ml / min. As a standard product, curcumin (sigma, St-Louis, Mo, USA) was dissolved in methanol at a concentration of 1 mg / ml and used as a stock solution. As shown in FIG. 1, 0.1, 0.01 ml / min of the test solution was prepared using the standard solution for the calibration curve to prepare a calibration curve to determine the content of curcumin.
실험결과, 표 2 에 나타낸 바와 같이 발효 울금 추출분말의 커큐민 함량은 각각 2.44, 2.52, 2.29 %(w/w)로 측정되었다.
As a result, as shown in Table 2, the curcumin content of the fermented turmeric extract powder was measured to be 2.44, 2.52, and 2.29% (w / w), respectively.
실험예Experimental Example 3. 3. 커큐민의Curcumin 안정성 분석 Stability analysis
실시예 5에서 제조한 발효울금 추출분말과 실시예6에서 제조한 울금추출분말을 불투명한 용기에 담아 45℃, 습도 75% 항온항습기(TH-150, 제이오텍사)에 넣고, 3개월 동안 커큐민의 함량을 분석하였다. 발효울금 추출분말은 3개월 후에도 커큐민의 함량이 90% 이상 유지되었다.
The fermented turmeric extract powder prepared in Example 5 and the turmeric extract powder prepared in Example 6 were placed in an opaque container and placed in an oven at 45 ° C. and 75% humidity (TH-150, Jeiotech Co., Ltd.) for 3 months. The content of was analyzed. The fermented turmeric extract powder maintained more than 90% of curcumin after 3 months.
Claims (9)
A first step of culturing lactic acid bacteria with grinding turmeric, pH correction, sterilization and turmeric as a medium to obtain turmeric fermented product; A second step of extracting and concentrating the turmeric fermentation product with an extraction solvent and concentrating the content of solids to 20 to 30% (w / v) to obtain a fermentation turmeric extract concentrate; A third step of obtaining an emulsion by adding a surfactant to the extract concentrate: a fourth step of adding cyclodextrin to the emulsion to encapsulate the fat-soluble component of turmeric to obtain a fermented turmeric extract clath; And a fifth step of drying the clathrate to prepare a water-soluble fermented turmeric extract powder.
상기 제 1단계에서, 울금 중량의 약 5 내지 15배(W/W)에 달하는 0.1M 아세트산 나트륨을 첨가하여 pH 3-7으로 조정한 후, 약 100~150℃에서, 약 10분 내지 2시간 동안 살균함을 특징으로 하는 방법.
The method of claim 1,
In the first step, after adjusting the pH to 3-7 by adding 0.1M sodium acetate amount of about 5 to 15 times (W / W) of turmeric weight, at about 100 ~ 150 ℃, about 10 minutes to 2 hours Sterilizing during the process.
상기 제 1단계에서, 상기 유산균은 페디오코커스 펜토사세우스(Pediococcus pentosaceus), 락토바실러스 아시도필루스(Lactobacillus acidophillus), 락토바실러스 카세이(Lactobacillus casei), 락토바실러스 헤베티쿠스(Lactobacillus heveticus), 락토바실러스 레우테리(Lacto bacillus reuteri), 락토바실러스 플란타럼(Lactobacillus plantarum), 락토바실러스 퍼멘텀(Lactobacillus fermentum), 리우코너스톡 메센테로이드(Leuconostoc mesenteroides), 및 락토코커스 락티스(Lactococcus lactis)로 구성되는 군으로부터 선택된 하나 이상의 균주임을 특징으로 하는 방법.
The method of claim 1,
In the first step, the lactic acid bacteria are Pediococcus pentosaceus , Lactobacillus Lactobacillus acidophillus ), Lactobacillus casei , Lactobacillus heveticus , Lactobacillus reuteri , Lactobacillus plantarum , Lactobacillus plantarum , Lactobacillus fermentum fermentation Leuconostoc ( Leuconostoc) mesenteroides ), and Lactococcus lactis .
상기 제 1단계에서, 상기 유산균은 락토바실러스 카세이(Lactobacillus casei) 또는 페디오코커스 펜토사세우스(Pediococcus pentosaceus)임을 특징으로 하는 방법.
The method of claim 3,
In the first step, the lactic acid bacteria is Lactobacillus casei or Pediococcus pentosaceus ( Pediococcus pentosaceus ).
상기 제 2단계에서, 상기 추출용매로는 0.01M 내지 1M 아세트산 나트륨 및 에탄올 혼합용매를 사용함을 특징으로 하는 방법.
The method of claim 1,
In the second step, the extraction solvent is characterized in that using a mixed solvent of 0.01M to 1M sodium acetate and ethanol.
상기 제 3단계에서, 상기 계면활성제는 레시틴, 설탕에스테르, 포스포리피드, 소르비탄 지방산 에스테르, 또는 폴리글리세린 에스테르 계면활성제을 사용함을 특징으로 하는 방법.
The method of claim 1,
In the third step, the surfactant is characterized in that using a lecithin, sugar ester, phospholipid, sorbitan fatty acid ester, or polyglycerol ester surfactant.
상기 제 4단계에서, 상기 시클로덱스트린은 울금 추출물 고형분 중량 대비 30 내지 200 % (w/w) 배합양의 베타-시클로덱스트린 및 감마-시클로덱스트린 혼합물을 사용함을 특징으로 하는 방법.
The method of claim 1,
In the fourth step, the cyclodextrin is characterized in that using a beta-cyclodextrin and gamma-cyclodextrin mixture in the amount of 30 to 200% (w / w) relative to the weight of turmeric extract solids.
Manufacturing method characterized in that the steps 3 and 4 are carried out continuously
Water-soluble turmeric extract powder having a curcumin content of 2% or more prepared by the method of claim 1.
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Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
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KR101293926B1 (en) * | 2010-12-30 | 2013-08-07 | 조선대학교산학협력단 | Curcumin-containing solid dispersion and composition comprising the same |
KR101418058B1 (en) * | 2011-11-30 | 2014-07-11 | 한국과학기술연구원 | Melted tumeric extract and curcumin with high solubility in biocompatible solvents |
KR102030560B1 (en) * | 2019-09-02 | 2019-10-10 | 권오직 | Liquefied type health supplement food using curcuma domestica and preparation method thereof |
WO2020122646A1 (en) * | 2018-12-12 | 2020-06-18 | 경희대학교 산학협력단 | Microbial formulation having biologically active material accumulated within cell thereof and preparation method therefor |
KR20210024759A (en) | 2019-08-26 | 2021-03-08 | (주)정농바이오 | Manufacturing method for fermented product of Curcuma longa |
KR20230172944A (en) * | 2022-06-16 | 2023-12-26 | (주)세준에프앤비 | Method for producing rice and nurungji containing curcumin using curcumin aqueous solution |
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Publication number | Priority date | Publication date | Assignee | Title |
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KR101293926B1 (en) * | 2010-12-30 | 2013-08-07 | 조선대학교산학협력단 | Curcumin-containing solid dispersion and composition comprising the same |
KR101418058B1 (en) * | 2011-11-30 | 2014-07-11 | 한국과학기술연구원 | Melted tumeric extract and curcumin with high solubility in biocompatible solvents |
WO2020122646A1 (en) * | 2018-12-12 | 2020-06-18 | 경희대학교 산학협력단 | Microbial formulation having biologically active material accumulated within cell thereof and preparation method therefor |
KR20210024759A (en) | 2019-08-26 | 2021-03-08 | (주)정농바이오 | Manufacturing method for fermented product of Curcuma longa |
KR102030560B1 (en) * | 2019-09-02 | 2019-10-10 | 권오직 | Liquefied type health supplement food using curcuma domestica and preparation method thereof |
KR20230172944A (en) * | 2022-06-16 | 2023-12-26 | (주)세준에프앤비 | Method for producing rice and nurungji containing curcumin using curcumin aqueous solution |
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