KR20190082179A - Enzyme food composite manufacture method using Isolated Soy Protein and brown rice - Google Patents

Enzyme food composite manufacture method using Isolated Soy Protein and brown rice Download PDF

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KR20190082179A
KR20190082179A KR1020190078372A KR20190078372A KR20190082179A KR 20190082179 A KR20190082179 A KR 20190082179A KR 1020190078372 A KR1020190078372 A KR 1020190078372A KR 20190078372 A KR20190078372 A KR 20190078372A KR 20190082179 A KR20190082179 A KR 20190082179A
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김두상
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푸른솔푸드 주식회사
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    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23LFOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
    • A23L7/00Cereal-derived products; Malt products; Preparation or treatment thereof
    • A23L7/10Cereal-derived products
    • A23L7/104Fermentation of farinaceous cereal or cereal material; Addition of enzymes or microorganisms
    • A23L7/107Addition or treatment with enzymes not combined with fermentation with microorganisms
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23LFOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
    • A23L29/00Foods or foodstuffs containing additives; Preparation or treatment thereof
    • A23L29/065Microorganisms
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23LFOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
    • A23L33/00Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
    • A23L33/10Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
    • A23L33/105Plant extracts, their artificial duplicates or their derivatives
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23VINDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
    • A23V2002/00Food compositions, function of food ingredients or processes for food or foodstuffs
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23VINDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
    • A23V2250/00Food ingredients
    • A23V2250/54Proteins
    • A23V2250/548Vegetable protein
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23VINDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
    • A23V2250/00Food ingredients
    • A23V2250/54Proteins
    • A23V2250/55Peptide, protein hydrolysate
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23VINDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
    • A23V2300/00Processes
    • A23V2300/10Drying, dehydrating

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Abstract

The present invention relates to a method for producing an enzyme food composition using isolated soy protein and brown rice. The present invention includes: a step of generating a decomposition material by increasing a mixture made by mixing 95 to 105 parts by weight of brown rice with 100 parts by weight of isolated soy bean protein and then decomposing the mixture with proteolytic enzymes; a step of performing the enzymatic deactivation of the decomposition material for 30 to 40 minutes at 75 to 85°C,and cooling and sterilizing the same at 5 to 15°C; a step of inoculating microorganisms in the sterilized decomposition material and fermenting the same at the temperature of 30 to 35°Cand a humidity of 95 to 97% for 70 to 80 hours; a step of adding 3 to 7 parts by weight of additive to 100 parts by weight of the fermented decomposition material; a step of making a dried product by drying the additive-added decomposition material with wind at 50 to 70°Cfor 20 to 28 hours to prevent the deactivation of enzymes on the additive-added decomposition material; and a step of molding the dried product in granules, pills, or powder and packing the molded product. The present invention is able to shorten fermentation time and increase enzyme activities.

Description

분리대두단백 및 현미를 이용한 효소 식품 조성물의 제조방법{Enzyme food composite manufacture method using Isolated Soy Protein and brown rice}TECHNICAL FIELD The present invention relates to a method for producing an enzyme food composition using isolated soybean protein and brown rice,

본 발명은 분리대두단백 및 현미를 이용한 효소식품 조성물의 제조방법에 관한 것으로 더욱 자세하게는, 미생물을 접종하여 발효하여 제조하는 고활성 효소식품의 제조방법에 관한 것이다. The present invention relates to a method for producing an enzyme food composition using isolated soybean protein and brown rice, and more particularly, to a method for producing a highly active enzyme food by fermenting microorganisms inoculated.

분리대두단백은 필수 아미노산을 풍부하게 제공하는 양질의 식물성 단백으로써 동물성 단백과 비교하여 가격이 저렴하므로 동물성 단백의 대체식품으로 사용되고 있다. 분리대두단백은 특유의 콩 비린내로 인해 그 이용이 제한받고 있으나 동물성 단백이 가지고 있는 여러 기능적 특성을 나타내고 있으므로 식품산업에 이용되고 있다. Soybean protein isolate is a high quality vegetable protein that is rich in essential amino acids. It is used as an alternative food for animal protein because it is cheaper than animal protein. Soybean protein isolate is limited in its use due to its unique soybean malt, but it is used in the food industry because it exhibits various functional properties of animal proteins.

또한, 식품영양 측면에서 뿐만 아니라 생리활성도 우수하여 혈청 콜레스테롤의 함량을 낮추는 역할을 하며 항암효과, 골다공증의 예방을 비롯하여 신장기능 이상증상을 개선하는 등의 작용을 한다.In addition, it has excellent physiological activity not only in terms of food nutrition, but also serves to lower the serum cholesterol content and to improve anti-cancer effect, prevention of osteoporosis, and improvement of abnormal kidney function.

분리대두단백은 단백질을 90% 이상 함유하고 있어 식품에 첨가하였을 경우 단백질의 기능적 성질인 수분결합력, 유화성, 기포성 등을 부여한다. 즉, 식품산업에서 분리대두단백은 제품의 물리적 성질을 향상시켜 주고 조직감 개선 및 냉동식품의 결착력 등을 증가시키기 위해 사용되고 있을 뿐만 아니라 분리대두단백을 첨가한 요구르트, 영양음료, 치즈, 아이스크림 등의 가공품에도 이용될 수 있으므로 유제품 대체식품으로서 대두의 이용에 관한 연구가 보고되고 있다.Separated soybean protein contains more than 90% of protein, and when added to food, it imparts the functional properties of proteins such as water-binding ability, emulsifying ability and bubble. In other words, the soy protein isolate in the food industry is used not only to improve the physical properties of the product but also to improve the texture and increase the binding power of frozen foods, as well as processed products such as yogurt, nutritional drinks, cheese, ice cream , Research on the use of soybean as a dairy alternative food has been reported.

현미는 유기농 곡류의 일종으로서, 인체에 필요한 효소를 풍부하게 생성하여 건강에 효과를 가져다주며 특히, 현미의 쌀겨를 유산균 등에 의하여 발효시키면 현미에 함유된 영양소와 유성분이 쌀겨 효소에 더욱 응축될 수 있으며, 발효군 효소에 의하여 고분자가 저분자로 쉽게 분해되어 소화 및 흡수가 용이하게 되는 특징이 있어 효소식품의 재료로서 많이 사용되는 것이다. Brown rice is a kind of organic cereal, it produces the enriched enzymes necessary for the human body to bring about health effects. Especially, when rice bran of brown rice is fermented by lactic acid bacteria, the nutrients and oil components contained in brown rice can be further condensed into rice bran enzyme , And the polymer is easily decomposed by the fermentation group enzyme into small molecules, which facilitates digestion and absorption, and is widely used as a material for enzyme foods.

효소는 생리 활성 물질인데, 신체 내의 분해대사 과정이 보다 원활하게 이루어지도록 촉매작용을 하는 단백질의 일종으로 우리 몸의 필수적인 조효소라고 불리우는 비타민과 미네랄도 효소가 없으면 사실상 아무 필요가 없을 정도로 매우 가치가 높은 것이다. Enzyme is a physiologically active substance, a kind of protein that catalyzes the degradation metabolism in the body more smoothly. Vitamins and minerals, which are called essential coenzymes of our body, are highly valuable will be.

그러므로, 체내 효소가 부족하게 되지 않도록 효소가 충분하게 함유된 식품을 섭취하는 것이 건강에 좋은 것은 당연한 것이다. 이러한 효소를 이용하는 효소 식품들이 많이 개발되었으나 종래 효소 식품은 발효시간이 길어지게 되어 효소 활성도가 낮다는 단점이 있었다. Therefore, it is natural that it is healthful to consume foods containing sufficient enzymes so that the enzyme in the body does not become insufficient. Although many enzyme foods using such enzymes have been developed, conventional enzyme foods have a disadvantage in that the fermentation time is prolonged and the enzyme activity is low.

대한민국 공개특허 제2001-0091737호Korea Patent Publication No. 2001-0091737 대한민국 공개특허 제2009-0037085호Korea Patent Publication No. 2009-0037085

본 발명은 원료 중의 단백질을 가수분해하여 미생물의 성장 및 효소 분비를 촉진하여 미처리군에 대비하여 발효시간을 단축시키고 효소활성이 높은 효소 식품 조성물의 제조방법을 제공하고자 하는 데 있는 것이다. The present invention is to provide a method for producing an enzyme food composition having a high enzymatic activity by shortening the fermentation time in comparison with the untreated group by promoting microbial growth and enzyme secretion by hydrolyzing the protein in the raw material.

이러한 목적을 달성하기 위하여 본 발명은 분리대두단백 및 현미를 이용한 효소식품 조성물의 제조방법에 있어서, 상기 효소식품 조성물의 제조방법은 분리대두단백 100중량부에 현미 95~ 105중량부를 혼합한 혼합물을 증자한 후, 단백질 가수분해 효소로 분해하여 분해물질을 생성하는 단계와 상기 분해물질을 75~ 85℃에 30~40분 동안 효소 실활 처리하여 5~ 15℃로 냉각하고 살균하는 단계와 상기 살균된 분해물질에 미생물을 접종하여 발효시키는 단계와 상기 발효된 분해물질 100중량부에 첨가제 3~ 7중량부를 추가하는 단계와 상기 첨가제가 추가된 분해물질을 효소의 실활을 방지하도록 하기 위하여 50~ 70℃에서 20~ 28시간 동안 통풍 건조하여 건조물을 만드는 단계와 상기 건조물을 과립 또는 환, 분말 형태로 성형하여 포장하는 단계를 포함하는 것을 특징으로 한다. In order to achieve the above object, the present invention provides a method of preparing an enzyme food composition using isolated soybean protein and brown rice, wherein the enzyme food composition comprises a mixture of 100 parts by weight of isolated soybean protein and 95 to 105 parts by weight of brown rice A step of decomposing the protein with a proteolytic enzyme to produce a decomposition material, and a step of sterilizing the decomposition material at a temperature of from 5 to 15 ° C by inactivating the enzyme at 75 to 85 ° C for 30 to 40 minutes, Adding 3 to 7 parts by weight of an additive to 100 parts by weight of the fermented decomposition product and adding the additive to the decomposition material to prevent deactivation of the enzyme, For 20 to 28 hours to form a dried material, and molding the dried material in a granular, ring, or powder form and packaging It shall be.

또한, 상기 단백질 가수분해효소는 뉴트라제(Neutrase), 알칼라제(alcalase) 및 플로보자임(flavourzyme) 중에서 적어도 하나 이상을 포함하는 것을 특징으로 하는 것이다.In addition, the protein hydrolyzing enzyme comprises at least one of Neutrase, Alcalase, and flavorzyme.

또한, 상기 미생물은 바실러스 서브틸리스(Bacillus subtilis), 아스퍼질러스 오리재(Aspergillus oryzae) 및 복합 유산균을 사용하는 것을 특징으로 한다.In addition, the microorganism is characterized by using Bacillus subtilis, Aspergillus oryzae and a complex lactic acid bacterium.

또한, 상기 첨가제는 알긴산, 산탄검, 카르복시메틸셀루로즈 중에서 최소 1개 이상 선택하여 추가하는 것을 특징으로 한다.Further, the additive is characterized in that at least one of alginic acid, xanthan gum, and carboxymethylcellulose is selected and added.

또한, 상기 건조물의 수분함량은 7~ 10%인 것을 특징으로 한다.Also, the moisture content of the dried material is 7 to 10%.

따라서, 본 발명에 의한 제조방법으로 제조된 효소 식품 조성물은 발효시간을 더욱 단축시키고, 효소 활성이 높은 효소 식품 조성물의 제조를 할 수 있는 효과가 있는 것이다. Accordingly, the enzyme food composition prepared by the method of the present invention can further shorten the fermentation time and produce an enzyme food composition having a high enzyme activity.

도 1은 본 발명에 의한 효소 식품 조성물의 제조방법을 나타내는 흐름도. BRIEF DESCRIPTION OF THE DRAWINGS FIG. 1 is a flow chart showing a method for producing an enzyme food composition according to the present invention. FIG.

이하에서는 도면을 첨부하여 본 발명의 바람직한 실시예를 설명한다.Hereinafter, preferred embodiments of the present invention will be described with reference to the drawings.

또한, 본 발명을 설명함에 있어서 관련된 공지 구성 또는 기능에 대한 구체적인 설명이 본 발명의 요지를 흐릴 수가 있다고 판단되는 경우에는 그 상세한 설명은 생략하기로 한다. 도 1은 본 발명에 의한 효소식품 조성물의 제조방법의 순서를 나타내는 흐름도이다. In the following description of the present invention, a detailed description of known functions and configurations incorporated herein will be omitted when it may make the subject matter of the present invention rather unclear. 1 is a flow chart showing a procedure of a method for producing an enzyme food composition according to the present invention.

분리 대두 단백 및 현미를 단백질 가수분해 효소로 가수분해하여 가수분해물질을 생성하는 단계Hydrolyzing hydrolyzed soybean protein and brown rice with protein hydrolyzate to produce hydrolyzate

먼저, 본 발명의 주재료에 해당하는 상기 분리대두단백과 상기 현미에 관하여 설명하기로 한다. First, the separated soybean protein and the brown rice corresponding to the main ingredient of the present invention will be described.

상기 분리대두단백이란 일종의 콩 고기로서 대두에서 추출한 단백질로서, 콩에서 유기용매 헥산을 이용하여 콩기름을 추출한 후 남은 건더기를 탈지대두라 하는데, 상기 탈지대두에는 지방이 모두 빠져 나가 단백질과 탄수화물 등이 남아 있다. 이러한 탈지대두에서 수용성 및 비수용성 탄수화물과 같은 비 단백질을 제거한 것을 대두단백이라 하는데, 다르게 표현하면 콩에서 기름과 탄수화물 등을 제거한 것으로 순수한 식물성 콩 단백질을 응축한 것을 의미한다. 참고로, 상기 분리대두단백은 A.D.M(Decatun, IL, USA)사의 Proten 972를 사용하였다. The separated soybean protein is a kind of soybean protein extracted from soybean, and soybean oil is extracted from organic soybean soybean using soybean oil. The remaining soybean oil is called defatted soybean. The defatted soybean leaves fat, and protein and carbohydrate remain have. These defatted soybeans remove soybean protein, such as water-soluble and non-water-soluble carbohydrates. In other words, oil and carbohydrates are removed from soybean, which means that pure vegetable soybean protein is condensed. For reference, the isolated soybean protein was Protein 972 from A.D.M (Decatun, IL, USA).

본 발명의 주재료 중의 하나로 사용되는 상기 분리대두단백의 제조방법은 이하와 같다. The method for producing the isolated soybean protein used as one of the main ingredients of the present invention is as follows.

단백질 함량이 높은 대두(大豆) 또는 검은 콩을 준비하여 8시간~ 16시간 동안 불린다. 상기 대두 또는 콩을 탈피(脫皮)하여 30~ 50메쉬(mesh)의 크기로 분말 형태로 분쇄한다. 상기와 같이 분쇄한 콩 100중량부에 글루텐 45~ 60중량부를 혼합한 혼합재료 100중량부에 정제수 70~ 80중량부를 투입하여 반죽한 반죽물을 호모믹서에서 교반하여 분리 대두 단백을 완성한다. 반죽 방식은 상기 정제수의 온도가 60~ 70℃이고, 교반시간은 5~ 10분이며, 상기 호모믹서의 회전속도는 2,500~ 3,500 rpm인 것이 바람직하다. 보관은 랩 등으로 싸서 냉장 보관하는 것이 바람직하다. High protein soybeans or black beans are prepared for 8 to 16 hours. The soybean or soybean is cut off and pulverized into a powder having a size of 30 to 50 mesh. 70 to 80 parts by weight of purified water is added to 100 parts by weight of a mixed material obtained by mixing 100 parts by weight of pulverized soybean with 45 to 60 parts by weight of gluten, and the kneaded mixture is stirred in a homomixer to complete isolated soybean protein. The kneading method is preferably such that the temperature of the purified water is 60 to 70 DEG C, the stirring time is 5 to 10 minutes, and the rotational speed of the homomixer is 2,500 to 3,500 rpm. It is preferable that the storage is wrapped in a wrap or the like and stored in the refrigerator.

상기 현미(玄米)는 수확한 벼에서 왕겨만 제거한 상태의 쌀을 의미한다, 상기 현미는 겨층, 배아(쌀눈) 및 배유(배젖)로 구성되어 있는 것이 특징이며 영양분은 배아(쌀눈)에 66%, 겨층 및 내피에 29%, 배유에 5% 정도로 분포된다. The brown rice is characterized in that it is composed of a bottom layer, an embryo (rice grain) and an endosperm (endosperm), and the nutrients are 66% or more in the embryo (rice grain) , 29% in the shell and endothelium, and 5% in the endosperm.

이러한 과정으로 채취한 상기 분리대두단백 100중량부에 거의 비슷한 중량비인 현미 95~ 105중량부를 혼합시켜 혼합물을 만든 후, 상기 혼합물을 100~ 150℃의 온도로 30~ 45분 동안 스팀 증자(cooking)하였다. 상기 증자로 인하여 가공에 따른 영양소 파괴를 최소화하는 것이다. 증자시킨 다음에 혼합물을 냉각하는 과정을 거치는데 냉각시키고 난 후의 혼합물 온도는 10~ 20℃가 바람직하다. 95 to 105 parts by weight of brown rice, which is almost the same weight ratio, is mixed with 100 parts by weight of the isolated soybean protein thus obtained, and the mixture is steamed at 100 to 150 ° C. for 30 to 45 minutes, Respectively. Minimization of nutrient destruction due to processing due to the above mentioned capital increase. The mixture is cooled and then cooled. The temperature of the mixture is preferably 10 to 20 ° C.

상기 증자시킨 혼합물을 단백질 가수분해 효소를 혼합물 100중량부 기준 0.5~ 2중량부 분사하여 40~ 55℃의 온도로 3시간~ 5시간 동안 처리하여 단백질을 가수분해하여 가수분해 물질을 생성하는 것이다. The thus-prepared mixture is treated with a protein hydrolyzing enzyme in an amount of 0.5 to 2 parts by weight based on 100 parts by weight of the mixture and treated at 40 to 55 ° C. for 3 hours to 5 hours to hydrolyze the protein to produce a hydrolyzate.

참고로, 상기 가수분해 물질을 생성하는 데에 사용하는 단백질 가수분해 효소는 뉴트라제(Neutrase), 알칼라제(alcalase) 및 플라보자임(flavourzyme) 중에서 적어도 하나 이상을 포함하는 것이다. 여기서, 상기 효소를 이용하여 가수분해 물질을 생성하는 기술에 대하여는 널리 공지된 기술이므로 자세한 설명은 생략하기로 한다. For reference, the protein hydrolyzing enzyme used for producing the hydrolyzate includes at least one of Neutrase, Alcalase, and flavorzyme. Here, the technology for producing the hydrolyzed substance using the enzyme is a well-known technology, and a detailed description thereof will be omitted.

상기 분해물질을 75~ 85℃에 30~ 40분 동안 효소 실활 처리하여 5~ 15℃로 냉각하여 살균하는 단계Sterilizing the decomposing substance at 75 to 85 ° C for 30 to 40 minutes, inactivating the enzyme, cooling to 5 to 15 ° C

상기 단계에서 가수분해된 물질을 75~ 85℃의 온도로 30분~ 40분간 효소 실활(효소 활성이 이루어지지 않도록 하는 것) 처리를 하여 살균처리를 한 다음, 5~ 15℃가 되도록 상기 가수분해된 물질을 냉각시킨다. In the above step, the hydrolyzed substance is sterilized by treating the enzyme at a temperature of 75 to 85 ° C for 30 minutes to 40 minutes (in order to prevent enzymatic activity), and then hydrolyzed at 5 to 15 ° C Cool the resulting material.

상기 살균 분해물질에 미생물을 접종하여 70~ 80시간 동안 30 ~ 35℃, 습도 95~ 97%의 조건에서 발효시키는 단계 Microbes are inoculated in the sterilizing and decomposing material and fermented at a temperature of 30 to 35 DEG C and a humidity of 95 to 97% for 70 to 80 hours

상기와 같은 과정을 거쳐 냉각된 가수분해된 물질에 균주를 접종시키게 되는데, 상기 균주는 유용 미생물로서 바실러스 서브틸리스(Bacillus subtilis), 아스퍼질러스 오리재(Aspergillus oryzae) 및 복합 유산균을 상기 냉각된 물질 100중량부에 0.1~ 0.3중량부를 접종한다. 상기 미생물의 각 중량비는 거의 동일한 중량부이며, 구체적으로는 바실러스 서브틸리스 100중량부에 아스퍼질러스 및 복합 유산균 95~ 105중량부가 바람직하다. 미생물 접종이 끝나면 30~ 35℃의 온도에 90~ 97%의 습도로 70~ 80시간 동안 배양하여 발효한다. 상기 냉각된 물질에 미생물 접종작업을 실행한 후, 85~ 95℃로 8~ 12분간 열처리하여 멸균 과정을 행한다. 상기 열처리는 멸균과 함께 대두의 비린내를 줄이기 위한 것이다. 더욱 효과적인 감소를 위하여 상기 분해물질 100중량부에 베타사이클로덱스트린을 1~ 2중량부 첨가하는 것이 바람직하다. The strain is inoculated with the hydrolyzate which has been cooled through the above process, wherein the strain is a useful microorganism, such as Bacillus subtilis, Aspergillus oryzae, and a complex lactic acid bacterium, 0.1 to 0.3 parts by weight are inoculated to 100 parts by weight of the substance. Each weight ratio of the microorganisms is approximately the same parts by weight. Specifically, 100 parts by weight of Bacillus subtilis is preferably 95 to 105 parts by weight of aspergillus and complex lactic acid bacteria. After the inoculation of the microorganism is completed, it is fermented by incubation at a temperature of 30 to 35 ° C and a humidity of 90 to 97% for 70 to 80 hours. After the microorganism inoculation work is performed on the cooled material, the microorganism is sterilized by heat treatment at 85 to 95 ° C for 8 to 12 minutes. The heat treatment is intended to sterilize soybean and reduce the fishy smell of soybean. It is preferable to add 1 to 2 parts by weight of betacyclodextrin to 100 parts by weight of the decomposition material for more effective reduction.

상기 단계에서 배양된 분해물질에 첨가제를 추가하는 단계Adding the additive to the degraded material cultured in the step

상기 단계에서와 같이 배양하여 발효된 가수분해 물질에 첨가제를 추가하여 혼합물을 만드는 것인데, 상기 첨가제는 다시마나 감태, 대황 따위와 같이 녹갈색이나 담갈색을 띠는 바닷말의 세포막을 구성하는 알긴산(alginic acid), 식품의 점착성 및 점도를 증가시키고 유화 안정성을 증진하며 식품의 물성 및 촉감을 향상시키는 산탄검(Xantham Gum), 알칼리 셀룰로오스에 클로로 초산염을 반응시켜 제조하며 접착제, 아이스크림과 쨈의 안정제로 사용되는 카르복시메틸 셀루로오즈(carboxymethyl cellulose) 중에서 최소 1개 이상 선택하여 추가하는 것이다. The additive is added to the fermented hydrolyzate by culturing as in the above step. The additive is an alginic acid which constitutes the cell membrane of green brown or pale brown, Xantham Gum, which improves the tackiness and viscosity of food, improves emulsification stability, improves the physical properties and texture of food, is made by reacting chlorosaccharide with alkali cellulose, and used as a glue, carboxy At least one of carboxymethyl cellulose is selected and added.

상기 첨가제의 중량비는 가수분해 물질 100중량부에 3~ 7중량부가 바람직할 것이다. 3중량부 미만이면 첨가 효과가 거의 없고, 7중량부를 초과하면 첨가제의 향이 너무 진해져서 바람직하지 못하다. The weight ratio of the additive is preferably 3 to 7 parts by weight per 100 parts by weight of the hydrolysis material. If the amount is less than 3 parts by weight, the effect of addition is scarcely produced. If the amount is more than 7 parts by weight, the additive is undesirably smelled.

상기 첨가제가 추가된 분해물질을 효소의 실활을 방지하도록 하기 위하여 50~ 70℃에서 수분함량이 7~ 10%가 되도록 20~ 28시간 동안 통풍 건조하여 건조물을 만드는 단계To prevent the enzyme from being deactivated, the decomposable substance added with the additive is blown dried at 50 to 70 ° C for 20 to 28 hours so as to have a moisture content of 7 to 10%

상기 단계에서와 같이 첨가제가 혼합된 분해물질을 건조하게 되는데, 상기 건조하는 방식은 분해물질 내의 효소의 실활을 방지하도록 하기 위하여 50~ 70℃에서 20~ 28시간 동안 통풍 건조하여 건조물을 만드는 것이다.  The decomposition material mixed with the additive is dried as in the above step. In order to prevent deactivation of the enzyme in the decomposition material, the drying method is to blow dry at 50-70 ° C for 20-28 hours to make the dried material.

여기서, 상기 건조물의 수분 함량은 7~ 10%가 바람직한데 7% 미만이면 지나친 건조함으로 인하여 효소의 유효성분의 추출이 제대로 이루어지지 않게 되고, 10%를 초과하면 수분이 너무 많아져서 변질의 가능성이 있기 때문이다. Here, the moisture content of the dried material is preferably 7 to 10%. If it is less than 7%, the effective ingredient of the enzyme is not properly extracted due to excessive drying. If the moisture content is more than 10%, the possibility of deterioration It is because.

상기 건조물을 과립 또는 환, 분말형태로 성형하여 조성물로 만들어 포장하는 단계Molding the dried material into a granule, a ring or powder form,

상기와 같은 과정으로 생성된 건조물을 과립이나 환(丸) 형태 또는 분말 형태로 성형하여 성형물을 만드는 것이다. 만일, 분말 형태로 성형할 경우에는 입자 크기는 40~ 60메쉬(mesh)가 바람직할 것이다. 상기와 같이 성형물을 출고를 위한 포장 작업을 하는 것이다. The dried product produced in the above process is molded into a granule, a round shape or a powder to form a molded product. In case of molding in the form of a powder, the particle size is preferably 40 to 60 mesh. The packaging operation for delivering the molded article as described above is performed.

[실험예]       [Experimental Example]

분리대두단백 및 현미의 단백질 가수분해 효소에 의한 분해조성물의 제조Preparation of degradation products by proteolytic enzymes of isolated soybean protein and brown rice

분리대두 단백 및 현미를 1 : 1의 중량비로 혼합한 후, 스팀으로 증자 후 냉각하여 가수분해 효소를 기질대비 1% 분사하고 45℃에서 4시간 동안 처리하였다. 이때, 사용한 효소는 단백질 분해 효소인 뉴트라제(Neutrase) 및 플라보자임(flavourzyme)을 1 : 1의 중량비로 혼합한 후에 사용하였다. 이후 80℃에서 30분간 효소 실활 처리 후, 15℃의 온도가 되도록 냉각하고, 바실러스 서브틸리스(Bacillus subtilis), 아스퍼질러스 오리재(Aspergillus oryzae) 및 복합 유산균을 접종하여 72시간 동안 30~ 35℃, 습도 95% 조건으로 배양, 발효하였다. 배양 후, 배양물에 첨가제인 산탄검을 5중량부 첨가하여 출국 및 건조(24시간, 50℃, 수분 8% 이하)하여 건조물을 만들고, 건조물(배양물)을 40~ 60메쉬(mesh)로 분쇄하여 분말 형태의 발효 조성물(즉, 성형물)을 수득하였다.The separated soybean protein and brown rice were mixed at a weight ratio of 1: 1, steamed, and cooled. The hydrolytic enzyme was sprayed with 1% of the substrate and treated at 45 ° C for 4 hours. At this time, the used enzyme was used after mixing protease enzymes Neutrase and flavorzyme at a weight ratio of 1: 1. Then, the enzyme was inactivated at 80 ° C for 30 minutes, cooled to a temperature of 15 ° C, inoculated with Bacillus subtilis, Aspergillus oryzae and complex lactic acid bacteria, Lt; 0 > C and 95% humidity. After culturing, 5 parts by weight of an additive, xanthan gum, was added to the culture, and the mixture was allowed to leave the host and dried (24 hours at 50 DEG C, moisture content of 8% or less) to obtain a dried material. The dried material was pulverized to 40 to 60 mesh To obtain a fermented composition in the form of a powder (i.e., a molded product).

[현미 대두 효소의 효소역가 분석] [Enzyme potency analysis of brown rice soybean enzyme]

효소 역가란 당화력(糖化力)이라고도 부르며, 즉 효소 활성도를 의미하며, 분해력이라는 말과 유사하다. 따라서, 효소 역가가 낮은 것은 분해력이 낮은 것으로 효소의 효능이 적다는 것을 나타내는 것이다. The enzyme is called saccharifying power, meaning enzyme activity, similar to the word decomposition. Therefore, a low enzyme activity indicates that the enzymatic activity is low due to its low decomposition ability.

현미 대두 효소의 효소 역가의 측정은 식품의약품안전평가원 건강기능식품공전시험법에 따라 시험용액 중에 효소 활성이 있는 검액과 효소 활성을 잃은 검액을 분광 광도계로 흡광도의 차이를 측정함으로서 조성물의 α- 아밀라아제와 프로테아제(protease)의 활성을 측정하는 방법을 사용하였다.Measurement of the enzyme activity of brown rice soybean enzyme was carried out by measuring the difference between the absorbance of the test solution having the enzyme activity in the test solution and the test solution having the enzyme activity lost by the spectrophotometer according to the Test of the Functional Food of the Food and Drug Administration, And protease activity were used for the measurement.

1) α- 아밀라아제 역가(activity) 측정1) Measurement of α-amylase activity

*먼저, 현미 대두 효소 분말 25그램을 1,000ml 삼각 플라스크에 취하여 0.5% 염화나트륨 용액 500ml를 가하여 30±0.1℃에서 20분에 32cm의 와트만 No.1 또는 동종의 여지로 지름 20cm의 깔때기를 사용하여 여과한 후, 시험용액으로 하였다. α- 아밀라아제 역가(activity) 측정은 비세균성 측정방식으로 바실러스 서브틸러스, 아스퍼질루스 오리재 및 복합 유산균에서 얻어진 효소제의 α- 아밀라아제 역가를 측정하는 방법이다(Unit/g로 표시). 역가 시험은 온도 30±0.1℃에서 일정 농도의 전분용액의 표준 가수분해 정도를 얻는데 요하는 시간에 근거를 두고 가수분해 정도는 표준색과 가수분해물의 요오드 색과 비교하여 측정해서 계산식에 따라 효소의 역가를 측정하였다. First, 25 grams of brown rice soybean enzyme powder was taken in a 1,000 ml Erlenmeyer flask, and 500 ml of 0.5% sodium chloride solution was added thereto. The resulting mixture was subjected to a heat treatment at 30 ± 0.1 ° C. for 20 minutes using a 32 cm Wattman No. 1 or a 20 cm diameter funnel After filtration, a test solution was prepared. The α-amylase activity measurement is a non-bacteriological measurement method to measure the α-amylase activity of an enzyme obtained from Bacillus subtilis, Aspergillus oryzae and complex lactic acid bacteria (expressed as Unit / g). The potency test was based on the time required to obtain the standard hydrolysis degree of the starch solution at a temperature of 30 ± 0.1 ° C and the degree of hydrolysis was measured in comparison with the standard color and the iodine color of the hydrolyzate, Were measured.

2) 프로테아제 역가(activity) 측정 2) Measurement of protease activity

프로테아제의 역가(activity) 측정은 pH 7.0, 온도 37℃에서 casein(카세인: 젖 단백질의 주성분으로 미량의 당을 포함하는 인 단백질의 일종)기질의 30분 동안의 단백질 가수분해에 근거를 두고 있으며, 시료는 트리스 완충액을 사용하며 최종 희석액 2mL가 10~ 44PC 단위를 함유하도록 시험용액을 조제하였다. 가수분해되지 않은 casein은 여과로 제거되고 용해된 casein을 흡광도 측정법으로 측정하여 효소의 역가를 구하였다. Protease activity measurement is based on protein hydrolysis of casein (casein: a major protein of phospholipids containing a small amount of sugar as a major component of milk protein) for 30 minutes at pH 7.0 and 37 ° C, Tris buffer was used as a sample, and a test solution was prepared so that 2 mL of the final dilution contained 10 to 44PC units. The casein, which was not hydrolyzed, was removed by filtration and the enzyme activity was determined by measuring the dissolved casein by absorbance measurement.

역가 측정은 아스페르질루스 니게르 및 그 변종, 아스페르질루스 오리재 및 그 변종의 배양물에서 얻어진 것의 Unit/g 단위로 표시된 프로테아제 역가를 티로신을 기준물질로 하여 측정하는 방법이다. 시료를 0.5M, pH 4.7의 초산염 완충액에 녹여 최종 희석액 1mL가 9~ 22Unit를 함유하도록 시험 용액을 조제하였다.Titration is a method of measuring the protease activity expressed in units / g of a product obtained from cultures of Aspergillus niger and its variants, Aspergillus oryzae and its variants with tyrosine as a reference substance. The sample was dissolved in a 0.5 M acetate buffer solution, pH 4.7, and a test solution was prepared so that 1 mL of the final dilution contained 9 to 22 Units.

역가 시험은 pH 4.7, 온도 40℃에서 헤모글로빈 기질의 30분간 가수분해에 근거를 두고 있으며 가수분해되지 않은 기질은 삼염화초산으로 침전시켜 여과로 제거되고 여액에 있는 용해된 헤모글로빈의 양을 흡광도 측정법으로 측정하여 효소제의 역가를 구하였다. The potency test was based on hydrolysis of the hemoglobin substrate for 30 minutes at pH 4.7 and temperature 40 ° C. The hydrolyzed substrate was precipitated with trichloroacetic acid and removed by filtration. The amount of dissolved hemoglobin in the filtrate was measured by absorbance measurement And the activity of the enzyme was determined.

현미 대두 효소   Brown rice soy enzyme Activity (역가)  Activity
α- 아밀라아제

alpha -amylase

4,775 Unit/g

4,775 Units / g

프로테아제

Protease

3,969 Unit/g

3,969 Units / g

따라서, 상기 [표 1]에 나타난 바와 같이 효소 역가(효소 활성도)가 높으므로 본 발명에 의한 제조방법으로 제조된 효소식품 조성물은 매우 영양분이 풍부한 식품 조성물인 것으로 사료된다. Therefore, as shown in Table 1, since the enzyme activity (enzyme activity) is high, the enzyme food composition prepared by the method of the present invention is considered to be a nutrient rich food composition.

[비교예][Comparative Example]

현미는 포함시키되, 분리대두단백 대신에 미강(米糠: 쌀을 찧을 때 나오는 고운 속겨)으로 대체하여 효소식품 조성물을 제조하였다. The enzyme food composition was prepared by replacing brown rice with rice bran (rice bran: rice bran), instead of isolated soybean protein.

그 제조방식을 설명하면, 현미 및 상기 미강을 혼합한 혼합물을 100℃에서 1시간 동안 증숙하는 단계와 상기 증숙된 혼합물에 황국균 및 유산균을 접종한다. 상기 황국균 및 유산균은 혼합물 총 100중량부에 대하여 각각 0.1~ 1.0 중량부로 접종되는 것이다.Describing the preparation method, the mixture of the brown rice and the rice bran are mixed at 100 ° C for 1 hour, and the mixture is inoculated with the Hwang Gukguk and the lactic acid bacteria. The Hwang guk gyun and the lactic acid bacteria are inoculated at 0.1 to 1.0 part by weight with respect to 100 parts by weight of the mixture.

다음으로, 접종된 상기 혼합물을 30~ 35℃에서 48~ 72시간 동안 발효시켜 발효물을 만드는 단계와 상기 발효물을 40 내지 50℃에서 5 내지 10시간 동안 건조를 실시하는 단계 및 상기 건조된 발효물을 분쇄한 후 과립, 분말, 환, 캡슐 중의 어느 하나의 형태로 만들어 효소식품 조성물을 제조하였다.  Next, the inoculated mixture is fermented at 30-35 ° C for 48-72 hours to produce a fermented product, the fermented product is dried at 40-50 ° C for 5-10 hours, and the dried fermentation After pulverizing the water, the enzyme food composition was prepared in the form of granules, powder, ring or capsules.

[관능 검사][Sensory Test]

상기 실시예에 의하여 제조된 식품과 상기 비교예에 의하여 제조된 조성물을 투입한 효소식품에 대하여 관능 검사를 실시하였다. 관능검사는 20~ 40대 성인남녀 각각 10명의 평가단이 실시예로 제조한 조성물을 투입한 식품과 비교예로 제조한 조성물을 투입한 식품의 냄새, 맛, 향을 평가하였다. 각 평가항목을 5점 표시법으로 채택하였고, 각 항목에 대한 평균점수를 하기의 [표 2]에 나타내었다.The sensory evaluation was performed on the food prepared according to the above example and the enzyme food containing the composition prepared according to the comparative example. The sensory evaluation was carried out by evaluating the odor, taste, and flavor of the foods into which the composition prepared in the Example and the composition prepared in the Comparative Example were added. Each evaluation item was adopted as a five-point notation, and the average score for each item is shown in [Table 2].

실 시 예    Example 비 교 예   Comparative example 냄 새  smell 2.8    2.8 2.2    2.2    flavor 2.4    2.4 1.8    1.8    incense 2.5    2.5 2.1    2.1

상기 [표 2]와 같이 배양과정과 발효과정을 거친 본 발명의 효소식품 조성물을 함유한 실시예의 식품이 비교예 식품과 비교하여 볼 때 냄새, 맛 및 향에서 우수한 평가를 받은 것으로 나타났다.As shown in Table 2, the food of the examples containing the enzyme food composition of the present invention which had undergone the culturing process and the fermentation process showed excellent evaluation in odor, taste and flavor as compared with the food of the comparative example.

Claims (2)

분리대두단백 및 현미를 이용한 효소식품 조성물의 제조방법에 있어서,
상기 효소식품 조성물의 제조방법은 대두(大豆) 또는 검은 콩을 8시간~ 16시간 동안 불린 다음 탈피(脫皮)한 후 30~ 50메쉬(mesh)의 크기의 분말로 분쇄하고, 분쇄한 콩 100중량부에 글루텐 45~ 60중량부를 혼합한 혼합재료 100중량부에 정제수 70~ 80중량부를 투입하여 반죽하여 분리대두단백을 제조하고, 상기 분리대두단백 100중량부에 현미 95~105중량부를 혼합한 혼합물을 증자한 후 상기 증자시킨 혼합물 100중량부에 뉴트라제(Neutrase), 알칼라제(alcalase) 또는 플라보자임(flavourzyme) 중 하나 이상의 단백질 가수분해 효소 0.5~2중량부를 분사한 다음 40~ 55℃의 온도로 3시간~ 5시간 동안 처리하여 분해물질을 생성하는 단계; 및
상기 분해물질을 75~ 85℃에 30~ 40분 동안 효소 실활 처리하여 5~ 15℃로 냉각하고 살균하는 단계; 및
상기 냉각 살균된 분해물질 100중량부에 바실러스 서브틸리스(Bacillus subtilis), 아스퍼질러스 오리재(Aspergillus oryzae) 및 복합 유산균으로 구성되는 유용 미생물 0.1~ 0.3중량부를 접종하되, 접종되는 유용 미생물의 중량비는 바실러스 서브틸리스 100중량부에 아스퍼질러스 및 복합 유산균 95~ 105중량부의 비율로 혼합된 미생물을 접종한 다음 30~ 35℃의 온도 및 90~ 97%의 습도로 70~ 80시간 동안 배양하여 발효시키는 단계; 및
상기 발효된 분해물질 100중량부에 첨가제 3~ 7중량부를 추가하되, 상기 첨가제는 녹갈색이나 담갈색을 띠는 바닷말의 세포막을 구성하는 알긴산(alginic acid), 식품의 점착성 및 점도를 증가시키고 유화 안정성을 증진시키는 산탄검(Xantham Gum), 알칼리 셀룰로오스에 클로로 초산염을 반응시켜 제조하는 카르복시메틸 셀루로오즈(carboxymethyl cellulose) 중에서 1개 이상 선택하여 추가하는 단계;
상기 첨가제가 추가된 분해물질을 효소의 실활을 방지하도록 하기 위하여 50~ 70℃에서 20~ 28시간 동안 통풍 건조하여 건조물을 만드는 단계; 및
상기 건조물을 과립 또는 환, 분말 형태로 성형하여 포장하는 단계를 포함하는 것을 특징으로 하는 분리대두단백 및 현미를 이용한 효소 식품 조성물의 제조방법.
A method for preparing an enzyme food composition using isolated soybean protein and brown rice,
The enzyme food composition is prepared by soaking soybeans or black beans for 8 to 16 hours and then crushing them into powder having a size of 30 to 50 mesh, 70 to 80 parts by weight of purified water is added to 100 parts by weight of a mixed material obtained by mixing 45 to 60 parts by weight of gluten with a mixture of 95 to 105 parts by weight of brown rice with 100 parts by weight of the isolated soybean protein, 0.5 to 2 parts by weight of at least one proteinase of Neutrase, alcalase or flavorzyme is sprayed on 100 parts by weight of the mixture, Deg.] C for 3 hours to 5 hours to produce a decomposition material; And
Deactivating the decomposition material at 75 to 85 ° C for 30 to 40 minutes, cooling to 5 to 15 ° C and sterilizing the decomposition material; And
Wherein 0.1 to 0.3 parts by weight of a useful microorganism consisting of Bacillus subtilis, Aspergillus oryzae and a complex lactic acid bacterium are inoculated on 100 parts by weight of the thermally decomposed substance, Is prepared by inoculating microorganisms mixed with 100 parts by weight of Bacillus subtilis at a ratio of 95-105 parts by weight of aspergillus and complex lactic acid bacteria and culturing at 30-35 ° C and 90-97% humidity for 70-80 hours Fermenting step; And
3 to 7 parts by weight of an additive is added to 100 parts by weight of the fermented decomposition product, wherein the additive is an alginic acid which forms a cellulosic membrane of a greenish brown or pale brown color, an increase in stickiness and viscosity of a food, (Xantham Gum), carboxymethyl cellulose prepared by reacting chloroplatinic acid with an alkali cellulose, and adding the selected one or more;
Drying the resulting decomposition material by air blowing at 50 to 70 ° C for 20 to 28 hours to prevent deactivation of the enzyme; And
And molding and drying the dried product in the form of a granule, a ring, or a powder, and packaging the enzyme food composition using the isolated soybean protein and brown rice.
제1항에 있어서,
상기 건조물의 수분함량은 7~ 10%인 것을 특징으로 하는 분리대두단백 및 현미를 이용한 효소 식품 조성물의 제조방법.
The method according to claim 1,
Wherein the water content of the dried product is 7 to 10%.
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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20210020321A (en) 2019-08-14 2021-02-24 지디앤와이 주식회사 Gluten free snack using cereals and rice, manufacturing method therof
WO2022145793A1 (en) * 2020-12-28 2022-07-07 어업회사법인 월드푸드서비시즈 주식회사 Method for preparing glycine max extract having effect of improving bone metabolic functions

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR102388920B1 (en) * 2021-04-29 2022-04-25 종근당건강 주식회사 Method of producing the fermented low molecular weight protein with enhanced digestibility and Functional food including the fermented protein produced by the same
KR102665526B1 (en) 2021-05-25 2024-05-13 (주)리턴라이프 Manufacturing method of natural amino acid powder

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH11113513A (en) * 1997-10-21 1999-04-27 Sooi:Kk Fermented brown rice
KR20010091737A (en) 2000-03-17 2001-10-23 이숙영 soy yogurt and process for preparation thereof
KR20090037085A (en) 2007-10-11 2009-04-15 대한민국(관리부서:농촌진흥청) Method of preparing whey protein hydrolysates using protease and its usage
KR101405372B1 (en) * 2013-05-21 2014-06-13 한독화장품 주식회사 Composition for diet containing soybean peptide
KR20160063659A (en) * 2014-11-27 2016-06-07 (주)해나눔 The producing method of lactic acid fermented cereal grains that increase the availability and preservation of lactic acid using a enzyme pretreatment cereal grains
KR20160092327A (en) * 2015-01-27 2016-08-04 대구가톨릭대학교산학협력단 Method for producing fermented powder of white rice and amaranth mixture for improving constipation

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH11113513A (en) * 1997-10-21 1999-04-27 Sooi:Kk Fermented brown rice
KR20010091737A (en) 2000-03-17 2001-10-23 이숙영 soy yogurt and process for preparation thereof
KR20090037085A (en) 2007-10-11 2009-04-15 대한민국(관리부서:농촌진흥청) Method of preparing whey protein hydrolysates using protease and its usage
KR101405372B1 (en) * 2013-05-21 2014-06-13 한독화장품 주식회사 Composition for diet containing soybean peptide
KR20160063659A (en) * 2014-11-27 2016-06-07 (주)해나눔 The producing method of lactic acid fermented cereal grains that increase the availability and preservation of lactic acid using a enzyme pretreatment cereal grains
KR20160092327A (en) * 2015-01-27 2016-08-04 대구가톨릭대학교산학협력단 Method for producing fermented powder of white rice and amaranth mixture for improving constipation

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20210020321A (en) 2019-08-14 2021-02-24 지디앤와이 주식회사 Gluten free snack using cereals and rice, manufacturing method therof
WO2022145793A1 (en) * 2020-12-28 2022-07-07 어업회사법인 월드푸드서비시즈 주식회사 Method for preparing glycine max extract having effect of improving bone metabolic functions

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