KR100500161B1 - The manufacturing method and vinegar mushroom - Google Patents

The manufacturing method and vinegar mushroom Download PDF

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KR100500161B1
KR100500161B1 KR1020040110260A KR20040110260A KR100500161B1 KR 100500161 B1 KR100500161 B1 KR 100500161B1 KR 1020040110260 A KR1020040110260 A KR 1020040110260A KR 20040110260 A KR20040110260 A KR 20040110260A KR 100500161 B1 KR100500161 B1 KR 100500161B1
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fermentation
vinegar
mushroom
situation mushroom
acetic acid
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정재현
김길환
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충청북도
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    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12JVINEGAR; PREPARATION OR PURIFICATION THEREOF
    • C12J1/00Vinegar; Preparation or purification thereof
    • C12J1/04Vinegar; Preparation or purification thereof from alcohol
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12JVINEGAR; PREPARATION OR PURIFICATION THEREOF
    • C12J1/00Vinegar; Preparation or purification thereof
    • C12J1/08Addition of flavouring ingredients
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    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N1/00Microorganisms, e.g. protozoa; Compositions thereof; Processes of propagating, maintaining or preserving microorganisms or compositions thereof; Processes of preparing or isolating a composition containing a microorganism; Culture media therefor
    • C12N1/14Fungi; Culture media therefor
    • C12N1/16Yeasts; Culture media therefor
    • C12N1/18Baker's yeast; Brewer's yeast
    • C12N1/185Saccharomyces isolates
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    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12RINDEXING SCHEME ASSOCIATED WITH SUBCLASSES C12C - C12Q, RELATING TO MICROORGANISMS
    • C12R2001/00Microorganisms ; Processes using microorganisms
    • C12R2001/645Fungi ; Processes using fungi
    • C12R2001/85Saccharomyces
    • C12R2001/865Saccharomyces cerevisiae

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Abstract

본 발명은 현미에 배양한 상황버섯 균사체를 주 재료로 이용한 상황버섯 식초 및 그 제조방법에 관한 것이다.The present invention relates to a situation mushroom vinegar using the situation mushroom mycelium cultured in brown rice as a main material and a manufacturing method thereof.

본 발명은 이를 위해 배양기질로 사용하고자 하는 현미를 쪄서 수분함량을 조절함과 동시에 1차 멸균을 한 다음 배양하고자 하는 양적인 면이나 형태적인 면을 조절하여 배양 용기에 담은 후 2차적으로 멸균하여 현미를 기질로 하여 상황버섯 균사체 고체 배양물을 배양하는 단계; 주모 담금과 1, 2단 담금에 의해 상황버섯 균사체 고체 배양물을 술덧제조에 사용하는 알콜발효단계; 향과 맛을 한층 더 좋게 하기 위한 초산균의 분리 및 종초 제조단계; 알코올 발효단계에서 생성된 발효물을 활용한 초산발효단계; 및 초산발효단계에서 생성된 발효물의 여과 및 숙성단계;가 구비된다.The present invention by controlling the moisture content and steaming the brown rice to be used as a culture substrate for this purpose, and then sterilized by secondary sterilization after controlling the quantitative or morphological aspects to be cultured in the culture vessel Culturing the situation mushroom mycelium solid culture using the substrate as a substrate; Alcohol fermentation step of using the situation mushroom mycelium solid culture by preparation of laxatives by the main hair immersion and the first and second stage immersion; Isolation of acetic acid bacteria and seed production to further enhance the flavor and taste; Acetic acid fermentation step using the fermented product produced in the alcohol fermentation step; And filtration and aging step of the fermentation product produced in the acetic acid fermentation step.

상기와 같이 구성된 본 발명은 곡류에 배양된 상황버섯 균사체를 주재료(10-100%)로 하여 백미 또는 현미(0-90%)와 혼합하여 알코올발효 및 초산발효를 행하여 식초를 생산하는 것이다, 또한 본 발명이 갖는 특징은 기존의 상황버섯을 이용한 식초제조에 있어서, 자실체 추출물을 알코올발효 및 초산발효 시 일정량을 첨가하여 식초를 제조하는 것과는 달리 곡류에 배양시킨 상황버섯 균사체를 알코올발효의 2단 담금 술덧제조에 직접 사용(10-100%)하는 것이 기존의 방법과 다른 점이다. 특히 상황버섯 추출물을 이용한 식초제조에 있어서, 그 유효성분의 용출이 추출방법에 따라 많은 차이가 보이는 것과는 달리 본 발명에서는 직접 상황버섯 균사체를 이용함으로서 항산화효과 및 항균효과 등 다양한 생리활성을 갖는 상황버섯식초를 얻을 수 있도록 한 것이다.The present invention configured as described above is to produce the vinegar by alcohol fermentation and acetic acid fermentation by mixing with white rice or brown rice (0-90%) using the situation mushroom mycelium cultured in cereals as a main ingredient (10-100%), and also Features of the present invention is that in the production of vinegar using conventional mushrooms, immersion of the fruiting body mushroom cultured in cereals, unlike the production of vinegar by adding a certain amount during the fermentation of alcohol and acetic acid fermentation of two stages of alcohol fermentation Direct use (10-100%) in the manufacture of drunk is different from the conventional method. In particular, in the production of vinegar using the situation mushroom extract, unlike the elution of the active ingredient shows a lot of difference according to the extraction method, in the present invention by using the situation mushroom mycelium directly, the situation mushroom having various physiological activities such as antioxidant effect and antibacterial effect It is to get vinegar.

Description

상황버섯 식초 및 그 제조방법{THE MANUFACTURING METHOD AND VINEGAR MUSHROOM} Situation mushroom vinegar and its manufacturing method {THE MANUFACTURING METHOD AND VINEGAR MUSHROOM}

본 발명은 현미에 배양한 상황버섯 균사체를 주재료로 이용한 상황버섯 식초 및 그 제조방법에 관한 것으로서, 보다 상세하게는 현미를 기질로 하여 7-15일정도 배양된 상황버섯 균사체를 알코올발효의 2단 담금 술덧제조에 10-100%를 직접 사용하여 알코올발효를 거친 다음 그 발효물에 초산균을 접종함으로서 다양한 생리활성을 갖는 상황버섯식초를 생산하는 것이다. The present invention relates to a situation mushroom vinegar using the situation mushroom mycelium cultured in brown rice as a main material, and more specifically, to a two-step alcohol fermentation of the situation mushroom mycelium cultured for about 7-15 days using brown rice as a substrate. 10-100% is directly used in the preparation of soaked alcohol, and after fermentation of alcohol, the fermented product is inoculated with acetic acid to produce situational mushroom vinegar having various physiological activities.

주지하다시피 식초는 동서양을 막론하고 오래 전부터 이용되어온 발효식품으로 수세기를 거치는 동안 여러 가지 원료를 사용하여 많은 종류의 식초가 만들어져 왔으며 우리의 식생활과 밀접한 관계를 가져왔다. 예로부터 우리나라의 각 가정에서는 전통적인 병행복발효 방법으로 다양한 식초를 제조하여 음식의 맛을 내는 조리에 이용되거나 때로는 민간 의약품으로 사용되기도 하였다. 일반적으로 알려진 식초의 기능성은 체내에서 젖산을 분해하여 피로와 스트레스를 풀어주므로 피로회복 및 질병예방, 식욕증진 및 소화흡수증진, 그리고 콜레스테롤 저하로 동맥경화 및 고혈압예방, 비만 및 변비예방, 면역기능향상과 치매예방 등의 효과가 있는 것으로 알려져 있다. As is well known, vinegar is a fermented food that has been used for a long time, both east and west, and for many centuries, many kinds of vinegar have been made using various raw materials and have been closely related to our diet. Since ancient times, various households in Korea have been using traditional parallel fermentation methods to produce various kinds of vinegar, which is used for cooking and sometimes as a folk medicine. In general, the function of vinegar is to break down lactic acid in the body to relieve fatigue and stress, thus preventing fatigue and preventing diseases, increasing appetite and digestion, and lowering cholesterol, preventing arteriosclerosis and hypertension, preventing obesity and constipation, and improving immune function. It is known to have an effect of preventing dementia and the like.

현대의 식초는 단순히 조미료로서 사용되고 있기보다는 현미식초, 포도식초, 감식초, 인삼식초, 마늘식초 등과 같이 체내대사 조절기능 등 기능성성분을 함유한 음료로서, 또한 고부가가치성을 가진 건강음료로서 자리를 잡아가고 있는 실정이다. Modern vinegar is not simply used as a seasoning, but as a beverage containing functional ingredients such as brown rice vinegar, grape vinegar, persimmon vinegar, ginseng vinegar, garlic vinegar, etc. There is a situation.

본 발명과 같이 버섯을 이용한 식초제조방법으로는 느타리버섯(특10-0408867)을 이용한 식초제조방법이 있으나, 상황버섯 등 약용버섯을 이용한 식초제조에 대한 연구는 아직 없다. 특히 상황버섯(P. linteus)의 경우에는 항암 활성이 96.7% 수준임이 알려져 있으며(Maeda 등), 상황버섯 균사체의 단백다당체가 sacorma 180 복수암 및 고형암을 효과적으로 억제(Chung 등)한다고 하였다. As a vinegar manufacturing method using the mushroom as in the present invention, there is a vinegar manufacturing method using oyster mushroom (special 10-0408867), but there is no research on the vinegar production using medicinal mushrooms such as situation mushrooms. In the case of P. linteus, anticancer activity is known to be 96.7% (Maeda et al.), And the protein polysaccharide of S. aureus mycelium effectively inhibits sacorma 180 ascites and solid cancer (Chung et al.).

그 이외에도 상황버섯 등 약용버섯이 가지는 다양한 약리적인 효과는 연구 중에 있으며, 식품으로서의 이용성이 다양화되고 있으나 아직 식초로 개발된 사례는 거의 없다. In addition, various pharmacological effects of medicinal mushrooms, such as situation mushrooms, are being studied, and their use as foods is diversified, but there are few examples of vinegar.

또한 알코올발효 단계에서부터 상황버섯 추출물을 첨가하는 방법이 아닌, 곡류에 상황버섯균사체를 배양하여 직접 사용하여 식초를 제조하는 연구는 아직 없었다. In addition, there is no research to prepare vinegar by directly using the mushroom mushroom mycelium in grains, rather than adding the mushroom extract from the alcohol fermentation step.

본 발명은 상기와 같은 종래 기술의 제반 문제점을 해소하기 위하여 안출한 것으로, 현미를 기질로 배양된 상황버섯 균사체를 이용하여 상황버섯 균사체 및 현미의 유용성분이 함유된 상황버섯식초를 제조하는 방법을 제공하는데 있고 또한 현미에 배양시킨 상황버섯 균사체를 이용한 식초제조는 다양한 기능성을 함유하고 있어 현대인의 다양한 기호도를 충족시키는 고부가가치를 가지는 상황버섯식초를 제공한다. The present invention has been made to solve all the problems of the prior art as described above, by using a situation mushroom mycelium cultured with brown rice as a substrate provides a method for producing a situation mushroom vinegar containing the useful components of mushroom mushroom mycelium and brown rice In addition, the vinegar production using the situation mushroom mycelium cultured in brown rice contains a variety of functionalities to provide a situation mushroom vinegar having a high value that satisfies various tastes of modern people.

이러한 목적 달성을 위하여 본 발명은 현미를 기질로 하여 상황버섯 균사체 고체 배양물을 직접 배양하는 단계; 주모 담금과 1, 2단 담금에 의해 상황버섯 균사체 고체 배양물을 술덧제조에 사용하는 알콜발효단계; 향과 맛을 한층 더 좋게 하기 위한 초산균의 분리 및 종초 제조단계; 알코올 발효단계에서 생성된 발효물을 활용한 초산발효단계; 및 초산발효단계에서 생성된 발효물의 여과 및 숙성단계;가 포함됨을 특징으로 하는 상황버섯 식초 제조방법을 제공한다.In order to achieve the above object, the present invention comprises the steps of directly culturing the situation mushroom mycelium solid culture using brown rice as a substrate; Alcohol fermentation step of using the situation mushroom mycelium solid culture by preparation of laxatives by the main hair immersion and the first and second stage immersion; Isolation of acetic acid bacteria and seed production to further enhance the flavor and taste; Acetic acid fermentation step using the fermented product produced in the alcohol fermentation step; And filtration and aging step of the fermentation product produced in the acetic acid fermentation step.

이하에서는 이러한 목적 달성을 위한 본 발명의 바람직한 실시예를 첨부된 도면에 따라 상세히 설명하면 다음과 같다. Hereinafter, described in detail with reference to the accompanying drawings a preferred embodiment of the present invention for achieving this purpose are as follows.

본 발명에 적용된 상황버섯 식초 및 그 제조방법은 도 1 내지 도 5 에 도시된 바와 같이 구성되는 것이다.Situation mushroom vinegar and its manufacturing method applied to the present invention is configured as shown in Figs.

하기에서 본 발명을 설명함에 있어, 관련된 공지 기능 또는 구성에 대한 구체적인 설명이 본 발명의 요지를 불필요하게 흐릴 수 있다고 판단되는 경우에는 그 상세한 설명은 생략할 것이다.In the following description of the present invention, if it is determined that a detailed description of a related known function or configuration may unnecessarily obscure the subject matter of the present invention, the detailed description thereof will be omitted.

그리고 후술되는 용어들은 본 발명에서의 기능을 고려하여 설정된 용어들로서 이는 생산자의 의도 또는 관례에 따라 달라질 수 있으므로 그 정의는 본 명세서 전반에 걸친 내용을 토대로 내려져야 할 것이다.The following terms are terms set in consideration of functions in the present invention, which may vary depending on the intention or custom of the producer, and their definitions should be made based on the contents throughout the specification.

먼저, 본 발명의 상황버섯식초 제조에 있어 특징은, 현미에 배양시킨 상황버섯균사체(10-100%)를 알코올발효 시 2단 담금 초기에 사용하여 알코올발효 및 초산발효를 거치는 것이다.First, in the production of the situation mushroom vinegar of the present invention, the situation mushroom mycelium (10-100%) cultured in brown rice is subjected to alcohol fermentation and acetic acid fermentation using two stages of immersion during alcohol fermentation.

1단계: 상황버섯균사체 고체 배양물 준비단계 Step 1: Preparation of Situation Mushroom Mycelia Solid Culture

본 발명에서 현미를 기질로 하여 균사체를 배양하는 방법은, 기질의 준비 단계에서 기존의 방법인 배양용기에 현미와 물을 넣고 멸균하는 방법으로 배양기질을 준비하는 것이 아니라, 배양기질로 사용하고자 하는 현미를 미리 많은 양을 쪄서 수분함량을 조절함과 동시에 1차 멸균을 한 다음 배양하고자 하는 양적인면이나 형태적(모양)인면을 조절하여 배양 용기에 담은 후 2차적으로 멸균하여 기질을 준비하는 것을 특징으로 한다. 이와 같은 방법으로 상황버섯균사체를 준비할 경우 선행기술로 배양했을 경우보다 균사체의 생육이 용이하며 15-20%정도의 배양기간 단축이 가능하다. In the present invention, the method of culturing mycelium with brown rice as a substrate is not to prepare a culture substrate by sterilizing brown rice and water in a culture vessel, which is a conventional method, in the preparation step of the substrate, and to be used as a culture substrate. The amount of brown rice is preliminarily controlled to control the water content and at the same time as the first sterilization, then the quantitative or morphological (shape) side to be cultured is put in the culture vessel and then sterilized secondly to prepare the substrate. It features. When preparing the situation mushroom mycelium in this way, it is easier to grow mycelium than when cultured by the prior art, it is possible to reduce the culture period of about 15-20%.

2단계: 상황버섯균사체 고체 배양물을 술덧제조에 사용하는 알콜발효단계Step 2: Alcohol Fermentation Step Using Situation Mushroom Mycelia Solid Cultures

주모 담금 : 발효용기에 입국과 물을 4:6(효모 접종량을 1로 기준)의 비율로 혼합한 다음 효모(Sacchromyces cerevisiae)를 접종하여 25℃ 발효실에서 24시간 배양시킨다.Stem immersion: Enter the fermentation vessel and mix water with a ratio of 4: 6 (by yeast inoculation as 1), inoculate yeast (Sacchromyces cerevisiae) and incubate in a fermentation chamber at 25 ℃ for 24 hours.

1단 담금 : 발효용기에 주모담금 한 것 전체를 넣고, 주모담금에서 사용한 입국 및 물의 양을 각각 10배를 넣은 다음 잘 혼합하여 25℃ 발효실에서 다시 24시간 배양시킨다.1-stage immersion: Put the whole fermented coriander into the fermentation vessel, add 10 times the amount of entry and water used in the fermented soybeans, mix well, and incubate for 24 hours in a 25 ℃ fermentation chamber.

2단 담금 : 1단담금을 마친 발효물과 상황버섯균사체 증자한 것(또는 상황버섯균사체와 현미(or 멥쌀)를 증자한 것을 혼합한 것)을 물과 잘 혼합하여 알코올발효를 진행시켜 15-19% 정도의 상황버섯주를 얻는다. 이 상황버섯발효주를 여과장치를 이용 여과하여 초산발효단계에 바로 사용할 수 있도록 준비한다.Two-stage immersion: fermented product after one-stage immersion and the increase of mushroom mushroom mycelium (or a mixture of mushroom mushroom mycelium and brown rice (or non-glutinous rice)) are mixed well with water to proceed alcohol fermentation. You get about 19% mushroom mushrooms. This situation mushroom fermented liquor is filtered using a filtration device to prepare for immediate use in acetic acid fermentation.

3단계: 초산균의 분리 및 종초 제조단계Step 3: Separation of acetic acid bacteria and seed production

본 발명에 사용한 초산균(acetic acid bacteria)으로는 향과 맛을 한층 더 좋게 하기 위하여 전통적인 방법으로 제조된 사과식초로부터 초산균을 분리하여 사용하였다. 초산균의 분리는 충북 충주시의 농업기술센터의 전통적인 발효법을 거친 사과식초 1mL을 취해서 매니톨(Manitol)배지 50mL에 접종한 다음 30℃에서 170rpm으로 3∼4일간 진탕 배양 한 후, 초산균 분리용 평판배지에 1백금이 취해서 스트리킹(streaking)하여 30℃에서 4일간 배양하였다. 이때 배지의 색깔이 자색에서 황색으로, 다시 자색으로 변하는 과정이 확인된 군체(colony)를 1차 분리한다. 평판배양에서 분리된 1차 군체(colony)중 각각 1백금이를 취해서 초산균 분리용 액체배지에 접종한 후 다시 30℃에서 170rpm으로 3∼4일간 진탕 배양한다. 다시 초산분리용 액체 기본배지에 2% 접종한 후 30℃에서 정치 배양한다. 이와 같은 조작을 수회 반복하여 액체배지에서의 초산의 생성능력이 가장 좋은 균주를 선발하여 종초를 제조하는 균주로 사용하였다. 또한 분리한 초산균의 형태를 알아보기 위하여 이미지 분석 시스템(Image analyzer system)(USA, 올림푸스, 1600*1200 PIXEL)을 이용하여 생명공학연구소 유전자은행으로부터 분양 받은 아세토박터 아세티(Acetobacter aceti:KCTC 2335)를 대조균으로 분리균과 형태를 비교 관찰하여 아세토박터(Acetobacter)계열의 초산균(acetic acid bacteria)임을 확인하였다. Acetic acid bacteria used in the present invention (acetic acid bacteria) was used to separate the acetic acid bacteria from apple vinegar prepared by the traditional method in order to further improve the flavor and taste. For isolation of acetic acid bacteria, take 1 mL of apple vinegar, which has undergone the traditional fermentation method of Chungju-si Agricultural Technology Center, inoculate 50 mL of mannitol medium, incubate at 30 rpm for 170 days at 170 ° C, and then culture the acetic acid bacterium. 1 platinum was taken, streaking, and incubated at 30 ° C for 4 days. At this time, the color of the medium is first separated from the colony (colony) is confirmed the process of changing from purple to yellow to purple again. Take one platinum of each colony isolated from the plate culture, inoculate it into the liquid medium for acetic acid bacterium separation, and incubate for 3 to 4 days at 170 rpm at 30 ° C. Inoculate 2% in acetic acid separation liquid medium again and incubate at 30 ℃. This operation was repeated several times to select the best strain for the production of acetic acid in the liquid medium was used as a strain for producing seed. In addition, Acetobacter aceti (KCTC 2335), which was distributed from the Biotechnology Research Institute Genetic Bank using an image analyzer system (USA, Olympus, 1600 * 1200 PIXEL), was used to determine the type of isolated acetic acid bacteria. As a control bacterium, the isolates were compared with the isolates and identified as acetic acid bacteria of Acetobacter family.

사과식초로부터 분리한 초산균(acetic acid bacteria)를 종초로 사용하기 위해 흡광도(660nm)를 이용한 균체의 증식을 검토하여, 그 초산균을 72시간 배양하여 종초균으로 제조 준비한다. In order to use acetic acid bacteria isolated from apple cider vinegar as seed vinegar, the growth of the cells using absorbance (660 nm) is examined, and the acetic acid bacteria are incubated for 72 hours to prepare as seed vinegar.

4단계: 알코올 발효단계에서 생성된 발효물을 활용한 초산발효단계 Step 4: Acetic acid fermentation step using fermented product produced in alcoholic fermentation

2단계의 여과한 알코올발효주의 알코올농도를 7%, 당도는 약 4Brix로 조절한 다음 3%의 종초를 접종하여 30℃에서 초산발효를 실시한다. 그 발효기간은 약10-15일정도 한다. The alcohol concentration of the filtered alcoholic fermentation liquor of the second stage is adjusted to 7%, the sugar content is about 4Brix and then inoculated with 3% of the seed inoculation to perform acetic acid fermentation at 30 ℃. The fermentation period is about 10-15 days.

5단계: 초산발효단계에서 생성된 발효물의 여과 및 숙성단계 Step 5: Filtration and Aging of the Fermentation Product Produced in the Fermentation of Acetic Acid

알코올발효 단계를 거쳐 초산발효가 완료되면 여과장치에서 여과한 다음 5 에서 10-15일정도 숙성시킨 후 다시 여과하여 식초제조를 완성한다.After the fermentation of acetic acid through alcohol fermentation step, it is filtered through a filtration device, and then aged for 5 to 10-15 days, followed by filtration to complete the vinegar production.

상기의 제조방법 중 알코올발효의 2단담금 덧밥 제조에 있어, 현미에 배양된 상황버섯균사체를 증자하여 100%를 사용할 수 있으며, 또는 상황버섯균사체(10-99%)와 현미(or 백미, 1-90%)를 증자하여 일정비율로 혼합하여 사용할 수 있다. In the production method of alcohol fermentation two-dip rice paddy, 100% can be used by increasing the situation mushroom mycelium cultured in brown rice, or situation mushroom mycelium (10-99%) and brown rice (or white rice, 1 -90%) can be added and mixed at a certain ratio.

또한 현미에 배양한 상황버섯균사체 뿐만 아니라 노루궁뎅이 버섯(Hericium erinaceum), 상황버섯(Phellinus linteus), 영지버섯(Ganoderma lucidum), 눈꽃동충하초(Peacylomyces japonica), 밀리타리스 동충하초(Cordyceps militaris) 등을 현미에 배양한 균사체를 이용하여 같은 방법으로 제조가 가능하다. In addition to the brown mushroom mycelium cultured in brown rice, brown rice mushrooms (Hericium erinaceum), green mushroom (Phellinus linteus), Ganoderma lucidum, Peacylomyces japonica, and Militaris cordyceps (Cordyceps militaris) It can be produced in the same manner using mycelium cultured in.

[실시예] 현미에 배양시킨 상황버섯 균사체를 이용한 상황버섯 식초 제조[Example] Preparation of situation mushroom vinegar using situation mushroom mycelium cultured in brown rice

1 알코올발효1 alcohol fermentation

현미에 고체 배양한 상황버섯 균사체 배양물 준비Situation mushroom mycelium culture prepared by solid culture on brown rice

2 알콜발효 (술덧의 제조)2 alcoholic fermentation

① 주모담금 : 발효용기 5개에 입국 120g과 물 180ml를 넣고 혼합한 후 효모(S. cerevisiae) 30mL를 접종하여 25℃ 발효실에서 24시간 발효시켰다.① Main hair immersion: 5 g of fermentation vessels, 120 g of immigration and 180 ml of water were mixed, inoculated with 30 ml of yeast (S. cerevisiae) and fermented in a fermentation chamber at 25 ° C. for 24 hours.

② 1단 담금 : 발효용기 5개에 각각 주모담금한 것 전체를 넣고 입국 1200g과 물 1800mL를 넣고 혼합 한 후 25℃ 발효실에서 24시간 발효시켰다② One-stage immersion: Put the whole fermented base immersed into each of five fermentation vessels, add 1200g of immigration and 1800mL of water, mix and ferment for 24 hours in a fermentation chamber at 25 ℃.

③ 2단 담금 : 현미 10Kg과 현미-상황 균사체 배양물 10Kg을 깨끗이 수세한 후 물을 부어 24시간 침지 시킨 후 121℃에서 15분간 증자하여 1단 담금한 것에 현미 : 현미-상황 균사체 배양물을 각각 Control(5,000g : 0g), A(3,750g : 1,250g), B(2,500g : 2,500g), C(1,250g : 3,750g), D(0g : 5,000g)과 물 8,500mL을 넣고 잘 혼합 한 후 25℃ Incubator에서 14일간 발효시켰다(표 1).③ Two-stage immersion: 10Kg of brown rice and 10Kg of brown rice-situation mycelium culture, washed with water, immersed in water for 24 hours, and then immersed in 1 stage by increasing the temperature for 15 minutes at 121 ℃. Add Control (5,000g: 0g), A (3,750g: 1,250g), B (2,500g: 2,500g), C (1,250g: 3,750g), D (0g: 5,000g) and 8,500mL of water and mix well After fermentation in a 25 ℃ incubator for 14 days (Table 1).

표 1. 상황버섯발효주를 생산하기 위한 단계적 담금 조성 Table 1. Phased Soaking Composition for Production of Strain Mushroom Fermented Wine

1)Control1) Control 2)A2) A 3)B3) B 4)C4) C 5)D5) D YeastCultivationYeastCultivation YipkukYipkuk 120g120 g 120g120 g 120g120 g 120g120 g 120g120 g YeastYeast 30mL30 mL 30mL30 mL 30mL30 mL 30mL30 mL 30mL30 mL WaterWater 180mL180 mL 180mL180 mL 180mL180 mL 180mL180 mL 180mL180 mL 1stStage1stStage YipkukYipkuk 1200g1200 g 1200g1200 g 1200g1200 g 1200g1200 g 1200g1200 g WaterWater 1800mL1800 mL 1800mL1800 mL 1800mL1800 mL 1800mL1800 mL 1800mL1800 mL 2ndStage2ndStage Cooked RiceCooked rice 5000g5000 g 3750g3750 g 2500g2500 g 1250g1250 g 0g0g Culture ProductCulture Product 0g0g 1250g1250 g 2500g2500 g 3750g3750 g 5000g5000 g WaterWater 8500mL8500mL 8500mL8500mL 8500mL8500mL 8500mL8500mL 8500mL8500mL

1)Control: Cooked Rice : Culture product of Phellinus linteus in brown rice = 100% : 0%1) Control: Cooked Rice: Culture product of Phellinus linteus in brown rice = 100%: 0%

2) A : Cooked Rice : Culture product of Phellinus linteus in brown rice = 75% : 25%2) A: Cooked Rice: Culture product of Phellinus linteus in brown rice = 75%: 25%

3) B : Cooked Rice : Culture product of Phellinus linteus in brown rice = 50% : 50%3) B: Cooked Rice: Culture product of Phellinus linteus in brown rice = 50%: 50%

4) C : Cooked Rice : Culture product of Phellinus linteus in brown rice = 25% : 75%4) C: Cooked Rice: Culture product of Phellinus linteus in brown rice = 25%: 75%

5) D : Cooked Rice : Culture product of Phellinus linteus in brown rice = 0% : 100%5) D: Cooked Rice: Culture product of Phellinus linteus in brown rice = 0%: 100%

3. 알코올생성 및 생리활성(항산화효과, 항균효과) 검토3. Review of alcohol production and physiological activity (antioxidant effect, antibacterial effect)

① 알코올생성① Alcohol production

알코올생성은 상황버섯균사체를 많이 넣은 것이 알코올생성이 약간 낮게 나타났으나 16-18%정도로 큰 차이가 없었다. Alcohol production was slightly lower in alcohol production with a lot of situation mushroom mycelium, but there was no significant difference (16-18%).

② 항산화효과② antioxidant effect

* DPPH 프리라디칼(free radical)소거법에 의한 전자공여능 : 알코올발효물(상황버섯 발효주)의 전자공여능(electron donating abilities. EDA)은 Blois의 방법을 변형하여 측정하였다. 각 시료용액 1ml에 4×10-4 M 의 a,a-diphenyl- β-picryl-hydrazyl(DPPH) 1.0ml를 넣고 교반한 후 30분간 실온에 방치한 다음 빛의 투과도 측정장비로 520nm에서 흡광도를 측정하였다. 전자공여능(Electron donating ability.EDA)은 시료욕액의 첨가구와 무첨가구의 흡광도 감소율로 나타내었다.* Electron-donating ability by DPPH free radical scavenging method: The electron donating ability (EDA) of alcohol fermentation products (fermented mushroom fermentation strain) was measured by modifying Blois' method. 1.0 ml of 4 × 10 -4 M a, a-diphenyl-β-picryl-hydrazyl (DPPH) was added to 1 ml of each sample solution, stirred, and allowed to stand at room temperature for 30 minutes. The absorbance at 520 nm was measured using a light transmittance measuring instrument. Measured. Electron donating ability (EDA) was expressed as a decrease in absorbance of the sample bath addition and no addition baths.

* 피로갈롤(Pyrogallol) 자동산화 억제활성 : 알코올발효물(상황버섯 발효주)의 피로갈롤(Pyrogallol) 자동산화 억제활성은 각 시료 용액 0.2 mL에 Tris-HCl 버퍼(buffer)( 50 mM tris + 10 mM EDTA, pH 8.5) 3.0 mL와 12 mM pyrogallol 0.2 mL를 가하여 25 에서 10분간 반응시킨 후 1.0 N HCl 1mL를 가하여 반응을 정지시키고 반응액 중 산화된 pyrogallol의 양을 분광광도계로 420 nm에서 흡광도를 측정하였다.* Pyrogallol autooxidation inhibitory activity: Pyrogallol autooxidation inhibitory activity of alcoholic fermentation (situation mushroom fermentation strain) is Tris-HCl buffer (50 mM tris + 10 mM) in 0.2 mL of each sample solution. EDTA, pH 8.5) 3.0 mL and 0.2 mL of 12 mM pyrogallol were added and reacted for 25 to 10 minutes. Then, 1.0 N HCl 1 mL was added to stop the reaction. The amount of oxidized pyrogallol in the reaction solution was measured at 420 nm using a spectrophotometer. It was.

상황버섯식초 제조하기 위한 1단계인 알코올발효단계의 발효물인 상황버섯발효주가 갖는 생리활성 중 항산화 효과를 검토하여 얻은 결과 도 1, 2 에서 보듯이 순수 현미로 만 발효시킨 콘트롤(control)구와 비교하면 상황버섯균사체를 이용한 상황버섯발효주가 높은 항산화효과를 갖는다. As a result of examining the antioxidant effect of the physiological activity of the ethanol fermentation liquor which is the fermentation product of alcohol fermentation stage, which is the first stage for producing phyto mushroom vinegar, as shown in FIGS. 1 and 2, Situation mushroom fermented liquor using the situation mushroom mycelium has a high antioxidant effect.

4. 초산발효4. Acetic acid fermentation

① 초산생성① Acetic acid production

상황버섯 발효주를 여과한 다음 알코올농도를 7%, 당도를 4birx로 조절한 후에 3%의 종초를 접종하여 30℃에서 초산발효를 실시한다. 초산생성은 모든 발효용기에서 total acid(%) 가 4.2-4.4 정도 생성되었다. After filtering the fermented mushrooms of the situation mushroom, the alcohol concentration was adjusted to 7% and the sugar content to 4birx, and then 3% seed inoculation was inoculated to perform acetic acid fermentation at 30 ° C. Acetic acid production produced about 4.2-4.4 total acid (%) in all fermentation vessels.

② 항산화효과② antioxidant effect

* DPPH 프리라디칼(free radical) 소거법에 의한 전자공여능(위의 측정방법과 같음)* Electron donating ability by DPPH free radical scavenging method (same as the measuring method above)

* 피로갈롤(Pyrogallol) 자동산화 억제활성(위의 측정방법과 같음)* Pyrogallol automatic oxidation inhibitory activity (same as the above measurement method)

상황버섯식초 제조를 위한 초산발효단계를 거친 발효물인 상황버섯식초가 갖는 생리활성 중 항산화 효과를 검토하여 얻은 결과 도 3, 4 에서 보듯이 현미만을 사용하여 발효시킨 control구(현미식초)와 비교하면 상황버섯식초가 우수한 항산화 효과를 갖는 것을 알 수 있다. As a result of examining the antioxidant effect of the physiological activity of the situation mushroom vinegar, which is a fermented acetic acid fermentation step for the production of situation mushroom vinegar, as shown in FIGS. 3 and 4, compared to the control (fermented rice vinegar) fermented using only brown rice It can be seen that the situation mushroom vinegar has an excellent antioxidant effect.

상기 항균효과는 다음과 같다.The antimicrobial effect is as follows.

즉, 현미에 배양한 상황버섯균사체를 이용하여 제조한 상황버섯식초의 항균력을 측정하기 위해 종이원판(paper disc) ( 8 mm, Tyoyo Roshi Kaisha,Ltd. Japan)를 이용한 아가확산(agar diffusion)법으로 측정하였다. That is, the agar diffusion method using a paper disc (8 mm, Tyoyo Roshi Kaisha, Ltd. Japan) to measure the antibacterial activity of the situation mushroom vinegar prepared using the situation mushroom mycelium cultured in brown rice Measured by.

각각의 균주는 계대배양한 후 1백금이취해 10mL 보통배지(nutrient broth)에 접종하고 30 에서 24시간 배양하여 활성 시킨 후 사용하였다. 항균력 시험용 평판배지는 보통아가(nutrient agar)로서 기층용배지(2% agar)를 멸균된 페트리접시(petri dish)에 약 15mL씩 분주하여 응고시킨다. 중층용배지(agar 1%)를 각각 10mL씩 시험관에 분주하여 멸균한 후, 50℃ 중탕남비(water bath)에 보관하면서 각 시험균액 0.1 mL를 접종한 후, 기층용배지 위에 고르게 펴지도록 부어 응고시켰다. 그 다음 멸균된 종이원판(paper disc)을 평판배지 표면에 밀착시킨 후 발효된 각각의 식초액(산도를 3.0으로 조절하여 사용) 60㎕을 첨가하여 배양하면서 종이원판(paper disc) 주변에 생성된 저해환(mm)의 직경을 항균력으로 나타내었다.Each strain was inoculated in 10mL nutrient broth after subculture and incubated at 30 to 24 hours for activating. Plates for testing antimicrobial activity are nutrient agars and coagulated by dispensing the basal medium (2% agar) in a sterile petri dish at about 15 mL. Disinfect 10 ml of agar medium (agar 1%) into test tubes and sterilize them, inoculate 0.1 mL of each test cell solution while keeping it in a water bath at 50 ° C, and pour to spread evenly on the base medium. I was. Then, the sterilized paper disc was brought into close contact with the surface of the plate medium, and 60 µl of each fermented vinegar solution (adjusted to pH 3.0) was added and cultured around the paper disc. The diameter of the inhibitory ring (mm) is represented by antimicrobial activity.

도 2 에는 항균실험에 사용한 균주명, 배지, 생육온도를 나타내었으며, 도 3 에는 상황버섯균사체를 이용하여 제조된 상황버섯식초의 항균활성정도를 나타내었으며, 도 5 에는 항균활성 실험결과 확연히 맑은구역(clear zone)이 나타난 페트리접시(petri-dish)이다. Figure 2 shows the strain name, medium, growth temperature used in the antimicrobial experiment, Figure 3 shows the antimicrobial activity of the situation mushroom vinegar prepared using the situation mushroom mycelium, Figure 5 clearly shows the antimicrobial activity test results It is a petri dish with a clear zone.

표 2. 항균활성에 사용한 미생물 및 그 생육특징Table 2. Microorganisms used for antimicrobial activity and their growth characteristics

StrainsStrains MediaMedia Temp.(℃)Temp. (℃) Bacillus cereus (KCTC1) 1092) Stephylococcus aureus (KCTC 2199) Salmonella typhimurium (KCTC 2053) Pseudomonas aeruginosa (KCTC 1636) Escherichia coli O157:H7 (ATCC2) 0019) Escherichia coli (KCTC 1041) Bacillus cereus (KCTC1) 1092) Stephylococcus aureus (KCTC 2199) Salmonella typhimurium (KCTC 2053) Pseudomonas aeruginosa (KCTC 1636) Escherichia coli O157: H7 (ATCC2) 0019) Escherichia coli (KCTC 1041) Nutrient agarNutrient agarNutrient agarNutrient agarNutrient agarNutrient agarNutrient agarNutrient agarNutrient agarNutrient agarNutrient agarNutrient agar 353737373737353737373737

1)KCTC : Korea Collection for Type Cultures.     1) KCTC: Korea Collection for Type Cultures.

2)ATCC : American Type Culture Collection     2) ATCC: American Type Culture Collection

표 3. 상황버섯균사체를 이용하여 제조된 상황버섯식초의 미생물에 대한 항균활성Table 3. Antimicrobial Activity against Microorganisms of Situation Mushroom Vinegar Prepared by Situation Mushroom Mycelia

StrainsStrains Clear zone on plate (mm)Clear zone on plate (mm) ControlControl AA BB CC DD Bacillus cereus (KCTC1) 1092) Stephylococcus aureus (KCTC 2199) Salmonella typhimurium (KCTC 2053) Pseudomonas aeruginosa (KCTC 1636) Escherichia coli O157:H7 (ATCC2) 0019) Escherichia coli (KCTC 1041) Bacillus cereus (KCTC1) 1092) Stephylococcus aureus (KCTC 2199) Salmonella typhimurium (KCTC 2053) Pseudomonas aeruginosa (KCTC 1636) Escherichia coli O157: H7 (ATCC2) 0019) Escherichia coli (KCTC 1041) 111512141315111512141315 202222221925202222221925 142320242322142320242322 202322232126202322232126 202523232026202523232026

상황버섯식초 제조를 위한 초산발효단계를 거친 발효물인 상황버섯식초가 갖는 생리활성 중 항균 효과를 검토하여 얻은 결과 현미만을 사용하여 발효시킨 control구(현미식초)와 비교하면 상황버섯식초의 항균효과가 우수하게 나타난 것을 알 수 있다. The antimicrobial effect of the physiological activity of the physiological mushroom vinegar, a fermented product of acetic acid fermentation for the preparation of circumferential mushroom vinegar, was obtained. It can be seen that excellent.

한편 본 발명은 상기의 구성부를 적용함에 있어 다양하게 변형될 수 있고 여러 가지 형태를 취할 수 있다.On the other hand, the present invention may be variously modified and may take various forms in applying the above configuration.

그리고 본 발명은 상기의 상세한 설명에서 언급되는 특별한 형태로 한정되는 것이 아닌 것으로 이해되어야 하며, 오히려 첨부된 청구범위에 의해 정의되는 본 발명의 정신과 범위 내에 있는 모든 변형물과 균등물 및 대체물을 포함하는 것으로 이해되어야 한다.And it is to be understood that the invention is not limited to the specific forms referred to in the above description, but rather includes all modifications, equivalents and substitutions within the spirit and scope of the invention as defined by the appended claims. It should be understood that.

상기에서 상세히 살펴본 바와 같이 본 발명은 곡류에 배양된 상황버섯 균사체를 주재료(10-100%)로 하여 백미 또는 현미(0-90%)와 혼합하여 알코올발효 및 초산발효를 행하여 식초를 생산하는 것이다, 또한 본 발명이 갖는 특징은 기존의 상황버섯을 이용한 식초제조에 있어서, 자실체 추출물을 알코올발효 및 초산발효 시 일정량을 첨가하여 식초를 제조하는 것과는 달리 곡류에 배양시킨 상황버섯 균사체를 알코올발효의 2단 담금 술덧제조에 직접 사용(10-100%)하는 것이 기존의 방법과 다른 점이다. 특히 상황버섯 추출물을 이용한 식초제조에 있어서, 그 유효성분의 용출이 추출방법에 따라 많은 차이가 보이는 것과는 달리 본 발명에서는 직접 상황버섯 균사체를 이용함으로서 항산화효과 및 항균효과 등 다양한 생리활성을 갖는 상황버섯식초를 얻을 수 있도록 한 매우 유용한 발명인 것이다.As described in detail above, the present invention is to produce vinegar by alcohol fermentation and acetic acid fermentation by mixing with white rice or brown rice (0-90%) as a main ingredient (10-100%) of the situation mushroom mycelium cultured in cereals In addition, the characteristics of the present invention, in the production of vinegar using conventional situation mushrooms, unlike the fruit fermentation extract alcoholic fermentation and acetic acid fermentation, a certain amount is added to prepare a vinegar, the situation mushroom mycelium cultured in cereals 2 However, the direct use (10-100%) in immersion preparation is different from the conventional method. In particular, in the production of vinegar using the situation mushroom extract, unlike the elution of the active ingredient shows a lot of difference according to the extraction method, in the present invention by using the situation mushroom mycelium directly, the situation mushroom having various physiological activities such as antioxidant effect and antibacterial effect It is a very useful invention to get vinegar.

도 1 은 현미에 배양한 상황버섯 균사체의 사용 양을 달리하여 제조1 is prepared by varying the amount of situation mushroom mycelium cultured in brown rice

한 상황버섯 발효주의 항산화효과(Electron donating         Antioxidant Effect of Situation Mushroom Fermented Wine

ability (EDA)-in vitro)를 나타낸 그래프.        Graph showing ability (EDA) -in vitro.

도 2 는 현미에 배양한 상황버섯균사체의 사용 양을 달리하여 제조한 Figure 2 prepared by varying the amount of situation mushroom mycelium cultured in brown rice

상황버섯발효주의 항산화효과(Pyrogallol 자동산화 억제활성        Antioxidative Effect of Situation Mushroom Fermented Wine

-in vitro)를 나타낸 그래프.        -in vitro).

도 3 은 현미에 배양한 상황버섯균사체의 사용 양을 달리하여 제조한 3 is prepared by varying the amount of situation mushroom mycelium cultured in brown rice

상황버섯식초의 항산화효과(Electron donating ability         Electron donating ability of situation mushroom vinegar

(EDA)-in vitro)를 나타낸 그래프.        (EDA) -in vitro).

도 4 는 현미에 배양한 상황버섯균사체의 사용 양을 달리하여 제조한 Figure 4 prepared by varying the amount of situation mushroom mycelium cultured in brown rice

상황버섯식초의 항산화효과(Pyrogallol 자동산화 억제활성        Antioxidant Effect of Situation Mushroom Vinegar

-in vitro)를 나타낸 그래프.        -in vitro).

도 5 는 현미에 배양한 상황버섯균사체의 사용 양을 달리하여 제조한 5 is prepared by varying the amount of the situation mushroom mycelium cultured in brown rice

상황버섯식초의 항균효과 결과물.        Antimicrobial Effect of Situation Mushroom Vinegar

Claims (11)

배양기질로 사용하고자 하는 현미를 쪄서 수분함량을 조절함과 동시에 1차 멸균을 한 다음 배양하고자 하는 양적인 면이나 형태적인 면을 조절하여 배양 용기에 담은 후 2차적으로 멸균하여 현미를 기질로 하여 상황버섯 균사체 고체 배양물을 배양하는 단계;While controlling the water content by steaming the brown rice to be used as the culture substrate, the first sterilization is carried out, then the quantity or morphological side to be cultured is controlled and put into the culture vessel and sterilized by secondary sterilization. Culturing the mushroom mycelium solid culture; 주모 담금과 1, 2단 담금에 의해 상황버섯 균사체 고체 배양물을 술덧제조에 사용하는 알콜발효단계;Alcohol fermentation step of using the situation mushroom mycelium solid culture by preparation of laxatives by the main hair immersion and the first and second stage immersion; 향과 맛을 한층 더 좋게 하기 위한 초산균의 분리 및 종초 제조단계;Isolation of acetic acid bacteria and seed production to further enhance the flavor and taste; 알코올 발효단계에서 생성된 발효물을 활용한 초산발효단계; 및Acetic acid fermentation step using the fermented product produced in the alcohol fermentation step; And 초산발효단계에서 생성된 발효물의 여과 및 숙성단계;가 포함됨을 특징으로 하는 상황버섯 식초 제조방법.Filtration and aging step of the fermentation product produced in the acetic acid fermentation step; situation mushroom vinegar production method characterized in that it comprises a. 삭제delete 제 1 청구항에 있어서,According to claim 1, 상기 주모 담금은, The primary hair immersion is, 발효용기에 입국과 물을 효모 접종량을 1로 기준으로 4:6의 비율로 혼합한 다음 효모(Sacchromyces cerevisiae)를 접종하여 25℃ 발효실에서 24시간 배양시킴을 특징으로 하는 상황버섯 식초 제조방법.A situation mushroom vinegar production method characterized in that the entry into the fermentation vessel and water is mixed with yeast inoculum in a ratio of 4: 6 and then inoculated with yeast (Sacchromyces cerevisiae) and incubated in a fermentation chamber at 25 ° C. for 24 hours. 제 1 청구항에 있어서,According to claim 1, 상기 1단 담금은, The first stage immersion, 발효용기에 주모담금 한 것 전체를 넣고, 주모담금에서 사용한 입국 및 물의 양을 각각 10배를 넣은 다음 잘 혼합하여 25℃ 발효실에서 다시 24시간 배양시킴을 특징으로 하는 상황버섯 식초 제조방법.Situation mushroom vinegar production method characterized in that the whole fermented simmered fermentation vessel, put 10 times the amount of entry and water used in the main immersion, and then mixed well and incubated again in a fermentation room at 25 ℃ for 24 hours. 제 1 청구항에 있어서,According to claim 1, 상기 2단 담금은,The two-stage immersion, 1단 담금을 마친 발효물과 상황버섯균사체 증자한 것을 물과 잘 혼합하여 알코올 발효를 진행시켜 15-19% 정도의 상황버섯주를 얻고, 이 상황버섯발효주를 여과장치를 이용 여과하여 초산발효단계에 바로 사용할 수 있도록 함을 특징으로 하는 상황버섯 식초 제조방법.The fermented product and the mushroom mushroom mycelium, which have been immersed in 1 stage, are mixed well with water to proceed with alcohol fermentation to obtain 15-19% of mushroom mushrooms. Situation mushroom vinegar manufacturing method characterized in that to be used immediately. 삭제delete 제 1 청구항에 있어서,According to claim 1, 상기 알코올 발효단계에서 생성된 발효물을 활용한 초산발효단계는,Acetic acid fermentation step using the fermented product produced in the alcohol fermentation step, 2단계의 여과한 알코올발효주의 알코올농도를 7%, 당도는 약 4Brix로 조절한 다음 3%의 종초를 접종하여 30℃ 에서 초산발효를 실시하고, 그 발효기간은 약10-15일 정도임을 특징으로 하는 상황버섯 식초 제조방법.The alcohol concentration of the filtered alcohol fermented wine of the second stage was adjusted to 7%, and the sugar content was adjusted to about 4 Brix, and then inoculated with 3% of the vinegar and fermented with acetic acid at 30 ° C. The fermentation period was about 10-15 days. Situation mushroom vinegar manufacturing method. 제 1 청구항에 있어서,According to claim 1, 상기 초산발효단계에서 생성된 발효물의 여과 및 숙성단계는,Filtration and ripening step of the fermentation product produced in the acetic acid fermentation step, 알코올발효 단계를 거쳐 초산발효가 완료되면 여과장치에서 여과한 다음 5℃ 에서 10-15일정도 숙성시킨 후 다시 여과함을 특징으로 하는 상황버섯 식초 제조방법.After the fermentation of acetic acid through the alcohol fermentation step, the filtrate is filtered in a filtration apparatus, and then aged for about 10-15 days at 5 ° C. 제 5 청구항에 있어서,The method of claim 5 wherein 상기 알코올 발효는 술덧 제조 시 현미에 배양한 상황버섯 균사체 100%를 사용하여 상황버섯발효주를 제조하고, 현미에 배양한 상황버섯 균사체를 10-99%와 현미를 1-90%를 혼합 사용하여 14-19%의 상황버섯 발효주를 제조한 후 상기 상황버섯 발효주의 알코올 농도를 4-9%로 조절하여 종초를 접종하여 발효 단계를 거침으로서 4.1-4.5%의 산도를 갖도록 함을 특징으로 하는 상황버섯 식초 제조방법.The alcoholic fermentation is prepared by using 100% of the situation mushroom mycelium cultured in brown rice at the time of preparation of sake mushrooms, 10-99% and 1-90% of brown rice mushroom mycelium cultured in brown rice 14 After preparing -19% of the situation mushroom fermented liquor after adjusting the alcohol concentration of the situation mushroom fermented wine to 4-9% inoculated with the seed to go through the fermentation step of the situation mushroom characterized in that it has a pH of 4.1-4.5% Vinegar manufacturing method. 제 9 청구항에 있어서,The method of claim 9, 상기 상황버섯 균사체 배양물, 현미 및 백미에 영지버섯, 노루궁뎅이버섯, 동충하초, 아가리쿠스버섯, 잎새버섯을 배양시켜 술덧제조 시 사용하여 각각의 알코올발효물 및 초산발효물를 얻도록 함을 특징으로 하는 상황버섯 식초 제조방법.Situary mushroom mycelium culture, brown rice and white rice cultivate Ganoderma lucidum mushroom, roe deer mushroom, Cordyceps sinensis, Agaricus mushroom, leaf mushrooms used in the preparation of sake to obtain the respective alcohol fermentation and acetic acid fermentation Mushroom vinegar production method. 제 1 청구항의 방법으로 제조된 상황버섯 식초.Situation mushroom vinegar prepared by the method of claim 1.
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KR100903848B1 (en) 2007-11-09 2009-06-19 서원대학교산학협력단 Method for concentrated separation of fiber from mushroom
KR101012405B1 (en) * 2007-12-14 2011-02-09 (주)휴럼 The process of a mushroom mycelium fermented and functional food using the same
KR101026856B1 (en) 2008-06-30 2011-04-06 강용수 Grifola frondosa vinegar and preparation method thereof
KR20160095738A (en) 2015-02-04 2016-08-12 정병석 Functional food comprising Dendropanax morbifera Lev. fermentation vinegar and process for preparing the same
KR20160130672A (en) 2015-05-04 2016-11-14 김은경 Culture bottle having cultivated fruit body and hypha therein and liquid composition comprising mushroom extract, and preparation method of the same
KR20190056025A (en) * 2017-11-16 2019-05-24 농업회사법인 한국상황버섯 (주) FUNCTIONAL BEVERAGE COMPRISING Phellinus linteus EXTRACT AND METHOD FOR PREPARING THE SAME
KR102021530B1 (en) * 2017-11-16 2019-09-16 농업회사법인 한국상황버섯(주) FUNCTIONAL BEVERAGE COMPRISING Phellinus linteus EXTRACT AND METHOD FOR PREPARING THE SAME
CN111643417A (en) * 2020-07-07 2020-09-11 广州维创技术开发有限公司 Antiseptic composition for cosmetics and preparation method thereof
KR102571887B1 (en) * 2022-09-14 2023-08-28 조문창 Method for producing functional vinegar using mushroom mycelium grain

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