KR100227001B1 - Method for producing fermentation food from grain starch - Google Patents

Method for producing fermentation food from grain starch Download PDF

Info

Publication number
KR100227001B1
KR100227001B1 KR1019950057916A KR19950057916A KR100227001B1 KR 100227001 B1 KR100227001 B1 KR 100227001B1 KR 1019950057916 A KR1019950057916 A KR 1019950057916A KR 19950057916 A KR19950057916 A KR 19950057916A KR 100227001 B1 KR100227001 B1 KR 100227001B1
Authority
KR
South Korea
Prior art keywords
starch
fermentation
raw material
bifidobacterium
producing
Prior art date
Application number
KR1019950057916A
Other languages
Korean (ko)
Other versions
KR970032449A (en
Inventor
지근억
목철균
이세경
Original Assignee
목철균
지근억
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by 목철균, 지근억 filed Critical 목철균
Priority to KR1019950057916A priority Critical patent/KR100227001B1/en
Publication of KR970032449A publication Critical patent/KR970032449A/en
Application granted granted Critical
Publication of KR100227001B1 publication Critical patent/KR100227001B1/en

Links

Classifications

    • 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
    • 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
    • A23V2250/50Polysaccharides, gums
    • A23V2250/51Polysaccharide
    • A23V2250/5118Starch
    • 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
    • A23V2400/00Lactic or propionic acid bacteria
    • A23V2400/51Bifidobacterium

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical & Material Sciences (AREA)
  • Microbiology (AREA)
  • Health & Medical Sciences (AREA)
  • Nutrition Science (AREA)
  • Biotechnology (AREA)
  • Food Science & Technology (AREA)
  • Polymers & Plastics (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Cereal-Derived Products (AREA)
  • Micro-Organisms Or Cultivation Processes Thereof (AREA)
  • Preparation Of Fruits And Vegetables (AREA)

Abstract

본 발명은 전분질 원료를 분쇄하고, 물을 가하여 호화시키고, 상기 호화된 생성물에 아밀라제 생성능이 높은 비피도박테리움을 접종하여 배양하는 것을 특징으로 하는 전분질 발효식품의 제조방법에 관한 것이다. 본 발명에 의한 전분질 발효식품의 제조방법에 의하면, 전분질 원료에 대하여 종래의 이단 발효(당화 및 젖산균 발효)를 거치지 않고 단순한 공정(당화 및 젖산 발효를 동시에 진행)에 의해 양질의 전분질 발효식품을 바로 얻을 수 있다.The present invention relates to a method for producing a starch fermented food, characterized in that the starch raw material is ground, gelatinized by addition of water, and inoculated with bifidobacterium having high amylase-producing ability. According to the production method of starch fermented food according to the present invention, starch fermented food of high quality by a simple process (saccharification and lactic acid fermentation at the same time) without going through conventional two-stage fermentation (glycosylation and lactic acid bacteria fermentation) for starch raw material immediately You can get it.

Description

곡분 전분질 발효식품의 제조방법Manufacturing method of starch fermented food

본 발명은 곡분 전분질 발효식품의 제조방법에 관한 것으로, 특히 비피도박테리움을 이용하여 곡분 전분질 원료를 직접 발효시킴으로써 발효 효율이 높고 향미가 좋은 곡분 전분질 발효식품의 제조방법에 관한 것이다.The present invention relates to a method for producing a starch fermented food starch, and more particularly to a method for producing a starch fermented food with high fermentation efficiency and good flavor by directly fermenting the starch starch raw material using Bifidobacterium.

젖산균을 이용하여 식품을 발효시키는 기술은 오래 전부터 널리 행해져 왔다. 특히, 요구르트 등의 유제품과 김치 등은 젖산 발효를 이용하는 대표적인 식품으로서, 널리 식용되고 있다. 이러한 젖산 발효는 식품의 저장기간을 연장시키거나 영양 및 풍미를 증진시키는 수단으로 여러 식품의 제조에 적용되고 있다.The technique of fermenting food using lactic acid bacteria has been widely used for a long time. In particular, dairy products such as yogurt and kimchi are widely used as representative foods using lactic acid fermentation. Lactic acid fermentation has been applied to the production of various foods as a means to extend the shelf life of food or to enhance nutrition and flavor.

한편, 쌀과 같은 전분질 원료를 사용하여 발효식품을 제조하고자 하는 연구도 꾸준히 이루어지고 있는 실정이다. 한국 특허공고 제93-5199호는 쌀을 호화 및 당화시킨 후 얻어진 살 당화액에 활성화된 락토바실러스 불가리커스와 스트렙토코커스 써모필러스 스타터를 첨가하여 발효시킴으로써 얻어진 쌀 젖산발효물과, 대두를 원료로 하여 동일한 방법으로 얻어진 대두 젖산발효물을 혼합하는 것을 특징으로 하는 풍미가 개선된 쌀-대두 젖산 발효혼합제품을 제조하는 방법을 제시하고 있다. 이 방법은 전분질 원료를 먼저 호화 및 당화시킨 후 발효 균주를 접종하는 것으로서 공정히 복잡하고 전체적인 발효효율이 떨어지는 단점이 있다.On the other hand, research to manufacture fermented foods using starch raw materials such as rice is being steadily made. Korean Patent Publication No. 93-5199 discloses a rice lactic acid fermentation product obtained by fermentation by adding activated Lactobacillus vulgaris and Streptococcus thermophilus starter to the fleshy saccharification liquid obtained after gelatinization and saccharification of rice, and soybean as raw materials. It proposes a method for producing a rice-soybean lactic acid fermentation mixture with improved flavor, characterized in that the fermented soybean lactic acid fermentation product obtained by the same method. This method has a disadvantage in that the starch raw material is first gelatinized and saccharified and then inoculated with the fermentation strain, which is fairly complicated and the overall fermentation efficiency is lowered.

또한 한국 특허공개 제92-16030 호는 쌀을 분쇄하지 않고 곡립상태로 호화시킨 후 액화당화하여 살균하고 락토바실러스 불가리커스와 스트렙토코커스 써모필러스를 1 대 1로 혼합하여 고농도로 발효시키는 쌀 젖산발효식품의 제조방법을 개시하고 있다. 이 방법에 있어서도, 쌀을 먼저 액화 및 당화시키는 공정을 거쳐야 하기 때문에, 공정이 번거롭고 효율이 낮은 문제점이 있다.In addition, Korean Patent Publication No. 92-16030 discloses rice lactic acid fermentation in which the rice is not crushed to be granulated and then liquefied to be liquefied and sterilized. Disclosed is a method for producing food. Also in this method, since the rice must first go through a process of liquefying and saccharifying, there is a problem that the process is cumbersome and low in efficiency.

1999. 11. 27. 자 공개된 일본 특허공개 평 4-341166 은 디카르복시셀룰로스 및/또는 스타치 포스페이트로 구성된 폴리사카라이드 겔에 고정된 젖산균을 이용하여 과일 쥬스를 발효시키는 방법을 보이고 있다. 이렇게 얻어진 과일 쥬스는 향미의 손실이 적다는 장점이 있다.Japanese Patent Laid-Open No. 4-341166, published November 27, 1999, shows a method of fermenting fruit juice using lactic acid bacteria immobilized on a polysaccharide gel composed of dicarboxycellulose and / or starch phosphate. The fruit juice thus obtained has the advantage of little loss of flavor.

본 발명은 상술한 바와 같은 젖산균 발효식품에 관한 종래 기술을 감안하여 안출된 것으로, 그 목적은 전분질을 별도의 당화공정 없이 아밀라제의 생성능이 높은 비피도박테리움(amylolytic Bifidobacterium) 균주를 접종하고 발효시키는 전분질 발효식품의 제조방법을 제공하는 것이다.The present invention has been made in view of the prior art related to the lactic acid bacteria fermented food as described above, the object is to inoculate and ferment the strain of amylolytic Bifidobacterium (amylolytic Bifidobacterium) high amylase production capacity without a separate glycosylation process It is to provide a method for producing a starch fermented food.

본 발명의 다른 목적은 전분질 원료를 비피도박테리움 균주로 발효시켜 얻어진 전분질 발효식품을 제공하는 것이다.Another object of the present invention is to provide a starch fermented food obtained by fermenting the starch raw material to Bifidobacterium strains.

상기 본 발명의 목적은 전분질 원료를 분쇄하고, 물을 가하여 호화시카고, 상기 호화된 생성물에 아밀라제 생성능이 높은 비피도박테리움을 접종하여 배양하는 것을 특징으로 하는 전분질 발효식품의 제조방법에 의해 달성될 수 있다.The object of the present invention is achieved by a method for producing a starch fermented food, characterized in that by crushing the starch raw material, adding water and gelatinization, inoculated Bifidobacterium with high amylase production ability to the luxury product. Can be.

본 발명에 있어서, 발효의 원료로는 전분질 원료를 사용한다. 전분질 원료로서 쌀, 옥수수, 밀 등을 거론할 수 있으나, 쌀을 원료로 사용하는 것이 본 발명의 목적에 가장 적합하다. 얻고자 하는 발효 제품의 필요에 따라 쌀과 다른 전분질 원료를 혼합하여 원료러 사용하는 것도 가능하다.In the present invention, starch raw materials are used as raw materials for fermentation. Rice, corn, wheat, etc. may be mentioned as a starch raw material, but using rice as a raw material is most suitable for the purpose of this invention. Depending on the needs of the fermentation product to be obtained, it is also possible to mix rice and other starch raw materials and use them as raw materials.

본 발명에서 쌀 등 전분질 원료는 적절히 분쇄한 후 물에 담가 호화 시켜야 한다. 따라서 원료를 먼저 분쇄하여야 하며, 원료의 분쇄 정도는 20 내지 80 메시(mesh)가 적당하다. 조쇄된 원료에는 그 중량의 1.5 내지 8 배의 물을 가한 후, 가열하여 호화 시킨다. 원료로서 상술한 바와 같이 전분질 원료를 분쇄하여 사용하지만, 여기에 과일이나 야채 등 과채류를 적당량 첨가하여 발효를 진행시키면, 최종 제품의 향미가 크게 향상된다. 따라서, 사과, 당근, 배, 오이 등의 과채류를 분쇄하여 첨가하여도 좋고 과채류를 액화하여 쥬스 상태로 하여 첨가하여도 무방하다.In the present invention, the starch raw material such as rice should be properly pulverized and soaked in water. Therefore, the raw material must be pulverized first, and the crushing degree of the raw material is suitably 20 to 80 mesh. The pulverized raw material is added with 1.5 to 8 times the weight of water, followed by heating and gelatinization. As a raw material, the starch raw material is pulverized as described above, but when the appropriate amount of fruit and vegetables such as fruits and vegetables is added to the fermentation, the flavor of the final product is greatly improved. Therefore, fruit and vegetables such as apples, carrots, pears and cucumbers may be pulverized and added, or the fruit and fruit may be liquefied and added to juice.

상기와 같은 전분질 원료는 액화 및 당화를 거쳐 발효되기 때문에 종래에는 최종 발효 단계에 들어가기 전에 액화 및 당화를 시키거나, 또는 당화에 관련된 균주와 최종 발효균주를 동시에 투입하였다. 그러나, 본 발명에서는 아밀라제(amylase)의 생성능이 높은 비피도박테리움 균주를 접종하여 발효를 진행하기 때문에, 종래에서와 같은 다단 발효를 거치지 않고 바로 발효 생성능이 높은 발효 생성물을 얻을 수 있으므로 공정이 단순해지고 효율이 높다.Since the starch raw material as described above is fermented through liquefaction and saccharification, conventionally, liquefaction and saccharification are performed before entering the final fermentation stage, or the strains and final fermentation strains related to saccharification are simultaneously introduced. However, in the present invention, since the fermentation proceeds by inoculating the Bifidobacterium strain having high amylase production ability, the fermentation product having high fermentation production ability can be obtained without undergoing the multi-stage fermentation as in the prior art, so the process is simple. And the efficiency is high.

본 발명에 사용하기에 적합한 아밀라제생성능이 높은 비피도박테리움은 시판되는 것을 사용할 수도 있고, 공지의 방법에 따라 선별하는 것도 가능하다. 즉, 비피도박테리움이 포함된 자연물을 트립티케이스 10 중량부, 프로테오스 펩톤 5 중량부, 황산암모늄 3 중량부, K2HPO41 중량부, KH2PO42 중량부, MgSO40.2 중량부, L-시스테인·HCI 0.5 중량부, 아가 15 중량부, 20%(W/V) TOS(transgalactosylated oligosaccharide) 용액 50㎖ 및 30%(W/V) 프로피온산 나트륨 용액 50㎖ 및 증류수를 포함하는 TP배지(지근억 등, 한국식품과학회지 26(5), 526-531, 1994 참조)에서 배양하여 비피도박테리움을 순수분리한 다음 요오드 용액으로 콜로니 주위의 맑아지는 부분을 관찰하여 아밀라제(amylase)의 생산 콜로니를 확인할 수 있다. 또한, 상기 TP 배지 이외에도, BHI-soluble starch 배지를 사용하여 위와 같이 아밀라제 생산 콜로니를 확인할 수 있다(Ji, Geun Eog et al., Journal of Microbiology and Biotechnology 2(2), 85-91, 1992).Suitable for use in the present invention, Bifidobacterium having high amylase-producing ability may be commercially available or may be selected according to a known method. That is, a natural product containing Bifidobacterium is 10 parts by weight of trypticase, 5 parts by weight of proteose peptone, 3 parts by weight of ammonium sulfate, 1 part by weight of K 2 HPO 4, 2 parts by weight of KH 2 PO 4 , MgSO 4 0.2 parts by weight, 0.5 parts by weight of L-cysteine-HCI, 15 parts by weight of agar, 50 ml of 20% (W / V) transgalactosylated oligosaccharide (TOS) solution and 50 ml of 30% (W / V) sodium propionate solution and distilled water The Bifidobacterium was purified by cultivation in a TP medium (see Geun-Eum et al., 26 (5), 526-531, 1994), and then cleared around amylose by iodine solution. Production colonies). In addition to the TP medium, amylase producing colonies can be identified using BHI-soluble starch medium as described above (Ji, Geun Eog et al., Journal of Microbiology and Biotechnology 2 (2), 85-91, 1992).

비피도박테리움은 그램 양성 간균의 굴곡된 모습으로서 글루코즈(glucose)를 발효하여 락토즈(latose)와 아세테이트(acetate)를 주요 산물로 생산하고, 프룩토즈-6-포스포케톨라제(frutose-6-phosphoketolase) 양성임을 확인하여 동정한다(Loure, F. and O. Kandler, Archives in Microbiology 110, 271-277, 1976).Bifidobacterium is a curved form of Gram-positive bacillus, which ferments glucose to produce lactose and acetate as major products, and fructose-6-phosphoketolase (frutose-6). Identify and identify positive phosphoketolase (Loure, F. and O. Kandler, Archives in Microbiology 110, 271-277, 1976).

본 발명에서 발효 균주로 사용되는 것은 상기 (a)비피도박테리움을 단독으로 사용하여도 좋고, (b) 비피도박테리움과 락토바실루스의 혼합균주, (c) 비피도박테리움과 스트렙토코커스의 혼합균주 또는 (d) 비피도박테리움과 락토바실루스와 스트렙토코커스의 혼합균주를 사용하는 것도 가능하다. 이들 혼합균주는 사용되는 원료의 발효에 적합하게 그 종류와 혼합량을 선택, 조절할 수 있음은 물론이다.As the fermentation strain in the present invention, the (a) Bifidobacterium may be used alone, (b) a mixed strain of Bifidobacterium and lactobacillus, (c) Bifidobacterium and Streptococcus It is also possible to use mixed strains or (d) mixed strains of Bifidobacterium, Lactobacillus and Streptococcus. These mixed strains can, of course, be selected and adjusted the type and amount of mixing to suit the fermentation of the raw materials used.

호화된 원료를 발효시키기 위하여, 상기 전분질 원료에 대하여 상기 비피도박테리움을 104CFU/㎖ 내지 106CFU/㎖의 양으로 첨가한다. 이 때, 첨가제로서 원료에 대하여 0.05 중량%의 시스테인을 첨가하는 것이 바람직하다. 특히. 약 0.2%의 효모 추출물(yeast extract)과 0.5%의 soluble starch를 첨가하면, 발효가 촉진되어 균체의 수가 크게 증가되고 발효시간이 단축될 수 있다. 또한, 안정제로서 젤라틴을 첨가하여 발효를 진행시키면, 얻어진 발효 식품의 물성이 좋아진다.To ferment the raw material, the Bifidobacterium is added in an amount of 10 4 CFU / mL to 10 6 CFU / mL with respect to the starch raw material. At this time, it is preferable to add 0.05 weight% of cysteine with respect to a raw material as an additive. Especially. When about 0.2% of yeast extract and 0.5% of soluble starch are added, the fermentation may be promoted, thereby greatly increasing the number of cells and reducing the fermentation time. In addition, when the fermentation proceeds by adding gelatin as a stabilizer, the physical properties of the obtained fermented food are improved.

본 발명에 있어서, 비피도박테리움을 이용한 발효를 원활하게 진행하기 위해서는 혐기조건을 부여하여야 한다. 혐기조건을 조성하기 위해서 발효조 용적의 80 내지 95%를 기질(발효 원료)로 채우고, 스팀 챔버(steam chamber)를 통과시키거나 질소(N2) 가스를 불어넣어 산소를 제거하는 방법을 채용할 수 있다. 또한 스타터의 접종시에도 혐기조건을 유지하기 위하여 혐기 챔버(anaerobic chamber)를 사용하는 것이 바람직하다.In the present invention, in order to proceed with the fermentation using Bifidobacterium smoothly must be given anaerobic conditions. In order to create anaerobic conditions, 80 to 95% of the volume of the fermenter can be filled with a substrate (fermented raw material), and oxygen can be removed by passing a steam chamber or blowing nitrogen (N 2 ) gas. have. In addition, it is preferable to use an anaerobic chamber in order to maintain the anaerobic condition during starter inoculation.

비피도박테리움을 호화된 전분질 원료에 접종하여 발효를 진행시키는 발효공정에서 발효온도는 25 내지 45℃(가장 바람직하게는 37℃)로 제어하고, 발효 8 내지 15 시간 동안 진행한다. 이렇게 발효시킨 전분질 발효식품은 독특한 풍미를 가지는 것으로, 영양이 풍부하며 식용으로서 적합하다.In the fermentation process in which the Bifidobacterium is inoculated on the gelatinized starch raw material and the fermentation proceeds, the fermentation temperature is controlled to 25 to 45 ° C. (most preferably 37 ° C.), and the fermentation is performed for 8 to 15 hours. This fermented starch fermented food has a unique flavor, is rich in nutrition and suitable for food.

이하 본 발명의 바람직한 실시예를 설명한다. 그러나, 본 발명의 범위가 이들 실시예로 한정되는 것은 아니다.Hereinafter, preferred embodiments of the present invention will be described. However, the scope of the present invention is not limited to these Examples.

[실시예 1]Example 1

아밀라제생산능이 높은 비피도박테리움의 분리Isolation of Bifidobacterium with High Amylase Production Capacity

다양한 연령층의 사람으로부터 그들의 동의하에 분변을 채취하고, 비로 4℃의 혐기성 용액에 넣었다. 이어서, 용액을 10 배 순차 희석하고 37℃에서 혐기적 조건하에 평판 배양을 하였다. 분변의 채취에 있어서, 항생제를 복용한 사람과 설사나 변비가 심한 사람은 제외되었다.Feces were taken from people of various ages with their consent and placed in anaerobic solution at 4 ° C. in rain. The solution was then diluted 10-fold serially and plated at 37 ° C. under anaerobic conditions. Fecal samples were excluded from those taking antibiotics and those with diarrhea or constipation.

이와 같이 얻어진 미생물을 0.5% soluble starch가 첨가된 TP-soluble starch배지에서 다시 배양하고, 요오드 용액을 가하였을 때 주위가 맑아지는 부분의 콜로니를 선택하였다.The microorganisms thus obtained were incubated again in a TP-soluble starch medium to which 0.5% soluble starch was added, and colonies were selected to clear the surroundings when iodine solution was added.

상기 선택된 콜로니에 글루코즈를 가하고 생성물을 채취하여 분석하였다. 얻어진 생성물은 락토즈 및 아세테이트로 밝혀졌다. 또한 프룩토즈-6-포스포케톨레이즈 양성임도 확인되었다.Glucose was added to the selected colonies and the product was collected and analyzed. The product obtained was found to be lactose and acetate. It was also confirmed that fructose-6-phosphokeketase was positive.

[실시예 2]Example 2

선발된 비피도박테리움의 아밀라제 활성의 측정Measurement of Amylase Activity of Selected Bifidobacterium

실시예 1에서 분리된 비피도박테리움 균주를 원심분리하여 상징액을 분리하였다. 200 ㎕의 상징액을 200 ㎕의 아세트산나트륨 완충액(pH 5.5)에 첨가하였다. 여기에 1 %의 soluble starch 400 ㎕를 첨가하고, 45℃에서 2 시간 동안 효소반응을 진행시켰다. Somogy Nelson(Journal of Biological Chemistry. 195, 19-23, 1952)에 따라 비피도박테리움에서 분비된 아밀라제에 의해 분해된 환원당을 측정하였다. 1 unit는 45℃에서 1 분간 반응시켰을 때 스타치(starch)로부터 1μ㏖의 말토즈(maltose)를 생성하는데 필요한 효소의 양으로 정의하였다. 그 결과, 효소활성은 상기 반응조건에서 1 ㎖ 배양액당 0.5 내지 2 units으로 나타났다.The Bifidobacterium strain isolated in Example 1 was centrifuged to separate the supernatant. 200 μl of supernatant was added to 200 μl sodium acetate buffer (pH 5.5). 400 μl of 1% soluble starch was added thereto, followed by enzymatic reaction at 45 ° C. for 2 hours. Reducing sugars degraded by amylase secreted from Bifidobacterium were measured according to Somogy Nelson (Journal of Biological Chemistry. 195, 19-23, 1952). One unit was defined as the amount of enzyme required to produce 1 mol of maltose from starch when reacted at 45 ° C. for 1 minute. As a result, the enzyme activity was found to be 0.5 to 2 units per 1 ml culture medium under the reaction conditions.

[실시예 3]Example 3

전분질 원료의 전처리Pretreatment of Starch Raw Material

1 ㎏의 쌀을 20 내지 80 메시가 되도록 조쇄하여 분말을 얻은 후, 7㎏의 물을 가하였다. 이 상태로 30 분 동안 유지시킨 후 100℃로 30 분간 가열하여 쌀분말을 호화시켰다.1 kg of rice was pulverized to 20 to 80 mesh to obtain a powder, and 7 kg of water was added thereto. After maintaining for 30 minutes in this state, the rice powder was gelatinized by heating to 100 ℃ for 30 minutes.

[실시예 4]Example 4

비피도박테리움에 의한 발효Fermentation by Bifidobacterium

실시예 2의 전처리된 전분질 원료를 발효조 용적의 90%가 되도록 넣은 후, 스팀 챔버(steam chamber)를 통과시키고 탈기시켜 배양액의 산소를 제거하였다. 여기에 실시예 1에 따른 본 발명의 비피도박테리움 균주를 106CFU/㎖의 수준으로 혐기 챔버(anaeroboc chamber)내에서 접종하였다. 접종후 37℃의 온도에서 12 시간 배양하였다. 배양액의 균체수를 검수한 결과, 3X107CFU/㎖로 나타났다.The pretreated starch raw material of Example 2 was added to 90% of the volume of the fermenter, and then passed through a steam chamber and degassed to remove oxygen from the culture. Herein, the Bifidobacterium strain of the present invention according to Example 1 was inoculated in an anaeroboc chamber at a level of 10 6 CFU / ml. After inoculation, the cells were incubated for 12 hours at a temperature of 37 ° C. As a result of checking the cell count of the culture solution, it was found to be 3 × 10 7 CFU / ml.

계속 배양을 진행하면서 배양액의 변화를 조사한 결과, 환원당의 농도가 5㎎/㎖ 이상으로 증가하고 산도는 0.5 이상이 되었다. pH를 측정한 결과 4.5 이하로 감소하였다. 이러한 변화는 비피도박테리움의 증식이 효과적으로 이루어짐으로써 발효가 적정하게 일어나고 있음을 뜻하는 것이다.As a result of examining the change in the culture solution while continuing the culture, the concentration of the reducing sugar increased to 5 mg / ml or more and the acidity became 0.5 or more. The pH was measured and decreased to 4.5 or less. This change means that fermentation is taking place properly because the growth of Bifidobacterium is effective.

[실시예 5]Example 5

효모 추출물을 첨가한 전분질 원료의 발효Fermentation of Starch Raw Material with Yeast Extract

실시예 3의 전분질 원료에 0.2%의 효모 추출물을 첨가하고 실시예 4 의 방법에 따라 발효를 진행하였다. 12 시간 반응을 시키고 균체수를 검수한 결과, 1×108CFU/㎖로 나타났다.Yeast extract of 0.2% was added to the starch raw material of Example 3, and the fermentation was performed according to the method of Example 4. The reaction was carried out for 12 hours and the number of cells was checked. As a result, it was 1 × 10 8 CFU / ml.

[실시예 6]Example 6

효모 추출물과 가용성 스타치를 첨가한 전분질 원료의 발효Fermentation of Starch Raw Material Added Yeast Extract and Soluble Starch

실시예 3의 전처리된 전분질 원료에 0.2%의 효모 추출물 및 0.5%의 soluble starch를 첨가하고 실시예 4의 방법에 따라 발효를 진행하였다. 12 시간 반응을 시키고 균체수를 검수한 결과, 1.2×108CFU/㎖로 나타났다.0.2% yeast extract and 0.5% soluble starch were added to the pretreated starch raw material of Example 3, and the fermentation was carried out according to the method of Example 4. The reaction was carried out for 12 hours and the number of cells was checked. As a result, it was 1.2 × 10 8 CFU / ml.

[실시예 7]Example 7

과채류 원료를 첨가한 전분질 원료의 발효Fermentation of Starch Raw Material Added Fruit Vegetables

실시예 3의 전처리된 전분질 원료에 사과, 당근, 배, 오이 등 과채류를 분쇄하여 차례로 혼합한 후 실시예 4의 방법에 따라 발효를 진행하였다. 얻어진 배양물은 첨가된 과채류의 종류에 따라 풍미가 개선되어 제품의 물성 및 관능성이 증진되었다. 이들 과채류의 혼합물을 첨가한 경우에도 같은 결과가 나타났다. 특히, 젤라틴을 첨가하였을 때는 제품의 물성(안정성)이 크게 향상되었다.Apples, carrots, pears, cucumbers, and the like were pulverized and mixed sequentially in the pretreated starch raw material of Example 3, followed by fermentation according to the method of Example 4. The obtained culture was improved in flavor depending on the type of fruit and vegetables added to enhance the physical properties and functionality of the product. The same result was obtained when a mixture of these fruits and vegetables was added. In particular, when the gelatin was added, the physical properties (stability) of the product were greatly improved.

[실시예 8]Example 8

비피도박테리움과 스트렙토코커스의 혼합 균주를 이용한 전분질 원료의 발효Fermentation of Starch Raw Material Using Mixed Strains of Bifidobacterium and Streptococcus

실시예 3의 전처리된 전분질 원료에 비피도박테리움과 시판중인 스트렙토코커스를 5:1 로 혼합하여 실시예 4의 방법에 따라 발효를 진행하였다. 12 시간 반응을 시키고 균체수를 검수한 결과, 1.05X108CFU/㎖로 나타났다.Bifidobacterium and commercial Streptococcus were mixed at 5: 1 in the pretreated starch raw material of Example 3, and the fermentation was carried out according to the method of Example 4. The reaction was carried out for 12 hours and the number of cells was checked. As a result, 1.05 × 10 8 CFU / mL was obtained.

[실시예 9]Example 9

비피도박테리움과 락토바실루스의 혼합 균주를 이용한 전분질 원료의 발효Fermentation of Starch Raw Material Using Mixed Strains of Bifidobacterium and Lactobacillus

실시예 3의 전분질 원료에 비피도박테리움과 시판중인 락토바실루스를 5:1 로 혼합하여 실시예 4 의 방법에 따라 발효를 진행하였다. 12 시간 반응을 시키고 균체수를 검수한 결과, 1.02X108CFU/㎖로 나타났다.Bifidobacterium and commercially available lactobacillus were mixed at 5: 1 in the starch raw material of Example 3, followed by fermentation according to the method of Example 4. The reaction was carried out for 12 hours and the number of the cells was checked, and found to be 1.02X10 8 CFU / mL.

[실시예 10]Example 10

비피도박테리움, 락토바실루스 및 스트렙토코커스의 혼합 균주를 이용한 전분질 원료의 발효Fermentation of Starch Raw Material Using Mixed Strains of Bifidobacterium, Lactobacillus and Streptococcus

실시예 3의 전분질 원료에 비피도박테리움과 시판중인 락토바실루스와 시판중인 스트렙토코커스의 균주를 5:0.5:0.5 의 비율로 혼합하여 실시예 4의 방법에 따라 발효를 진행하였다. 12 시간 반응을 시키고 균체수를 검수한 결과, 9.5×107CFU/㎖로 나타났다.Bifidobacterium, commercially available lactobacillus and commercial Streptococcus strains were mixed in a ratio of 5: 0.5: 0.5 to the starch raw material of Example 3, and the fermentation was carried out according to the method of Example 4. The reaction was carried out for 12 hours and the number of cells was checked, and found to be 9.5 × 10 7 CFU / mL.

이상의 설명에서 명백한 바와 같이, 본 발명에 따라 아밀라제생성능이 강한 비피도박테리움을 전분질 원료에 접종하여 배양한 결과 바로 식용에 적당한 배양물이 얻어졌다. 특히, 전분질 원료에 각종 과채류를 첨가하여 배양하는 경우에 과채류의 독특한 향미가 제품에 가미되어 제품의 물성, 영양 및 관능성이 좋은 제품을 얻을 수 있다. 따라서, 본 발명에 의하면, 전분질 원료에 대하여 종래의 이단 발효(당화 및 젖산균 발효)를 거치지 않고 단순한 공정(당화 및 젖산 발효를 동시에 진행)에 의해 양질의 전분질 발효식품을 바로 얻을 수 있다.As apparent from the above description, according to the present invention, a bifidobacterium having high amylase-producing ability was inoculated into a starch raw material and cultured immediately to obtain a culture suitable for food. In particular, in the case of cultivation by adding various fruit vegetables to the starch raw material, the unique flavor of fruit vegetables is added to the product to obtain a product having good physical properties, nutrition and functionality. Therefore, according to the present invention, high-quality starch fermented foods can be directly obtained by simple processes (simultaneous glycosylation and lactic acid fermentation) without undergoing conventional two-stage fermentation (glycosylation and lactic acid bacteria fermentation).

이상에서 본 발명의 바람직한 실시예에 의거하여 본 발명을 상세히 설명하였으나, 본 발명의 범위내에서 이 분야의 전문가에게 자명한 치환, 변형 및 변경은 본 발명의 범위에 속하는 것을 이해되어야 한다.Although the present invention has been described in detail based on the preferred embodiments of the present invention, it should be understood that substitutions, modifications, and changes apparent to those skilled in the art within the scope of the present invention fall within the scope of the present invention.

Claims (2)

TP 배지에 비피도박테리움이 포함된 자연물을 배양하여 아밀라제 생성능을 갖는 비피도박테리움을 순수분리하고, 곡분 전분질 원료를 20 내지 80 메시의 크기로 분쇄하고, 상기 분쇄된 원료에 대하여 1.5 내지 8배의 물을 가하여 가열함으로써 호화시키고, 상기 호화된 생성물에 상기 분리된 아밀라제 생성능을 갖는 비피도박테리움을 104내지 106CFU/㎖의 양으로 접종하고, 혐기 조건에서 25 내지 45℃의 온도로 8 내지 15시간 동안 배양하는 것을 특징으로 하는 곡분 전분질 발효식품의 제조방법.By cultivating the natural material containing Bifidobacterium in TP medium to purely separate the Bifidobacterium having amylase-producing ability, grinding the starch starch raw material to the size of 20 to 80 mesh, 1.5 to 8 with respect to the pulverized raw material The pear water was gelatinized by heating, and the gelatinized product was inoculated with Bifidobacterium having the ability to produce amylase isolated in an amount of 10 4 to 10 6 CFU / ml, and at a temperature of 25 to 45 ° C. under anaerobic conditions. Method of producing a starch fermented food grains, characterized in that incubated for 8 to 15 hours. 제1항에 있어서, 상기 곡분 전분질 원료가 쌀인 것을 특징으로 하는 방법.The method of claim 1 wherein the starch starch raw material is rice.
KR1019950057916A 1995-12-27 1995-12-27 Method for producing fermentation food from grain starch KR100227001B1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
KR1019950057916A KR100227001B1 (en) 1995-12-27 1995-12-27 Method for producing fermentation food from grain starch

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
KR1019950057916A KR100227001B1 (en) 1995-12-27 1995-12-27 Method for producing fermentation food from grain starch

Publications (2)

Publication Number Publication Date
KR970032449A KR970032449A (en) 1997-07-22
KR100227001B1 true KR100227001B1 (en) 1999-10-15

Family

ID=19444813

Family Applications (1)

Application Number Title Priority Date Filing Date
KR1019950057916A KR100227001B1 (en) 1995-12-27 1995-12-27 Method for producing fermentation food from grain starch

Country Status (1)

Country Link
KR (1) KR100227001B1 (en)

Also Published As

Publication number Publication date
KR970032449A (en) 1997-07-22

Similar Documents

Publication Publication Date Title
Brauman et al. Microbiological and biochemical characterization of cassava retting, a traditional lactic acid fermentation for foo-foo (cassava flour) production
Adegoke et al. Characteristics of micro‐organisms of importance in the fermentation of fufu and ogi—two Nigerian foods
Zvauya et al. Microbial and biochemical changes occurring during production of masvusvu and mangisi, traditional Zimbabwean beverages
Antony et al. Microbial population and biochemical changes in fermenting finger millet (Eleusine coracana)
CN109259188B (en) Preparation method of bran lactic acid fermentation tablet rich in viable bacteria
JP2019193634A (en) Production method of enzyme liquid of low sugar vegetable and/or fruit
US3966555A (en) Alpha-galactosidase production
Rodrigues et al. Effects of inoculum concentration, temperature, and carbon sources on tannase production during solid state fermentation of cashew apple bagasse
KR101753372B1 (en) Method for producing steamed rice cake with improved volume and flavor using functional strain
Pompeyo et al. Comparison of amylolytic properties of Lactobacillus amylovorus and of Lactobacillus amylophilus
US4844911A (en) Quality improvement of alcoholic liquors
Giraud et al. Production of a Lactobacillus plantarum starter with linamarase and amylase activities for cassava fermentation
KR101753374B1 (en) Mixture of Saccharomyces cerevisiae and Lactobacillus brevis strain for making steamed rice-cake having excellent flavor and volume expansion ability
KR100543242B1 (en) Precess of enzyme health food having high activity by microbial fermentation
Tchekessi et al. Isolation and quantification of lactic acid bacteria from traditional fermented products in Benin
KRABI et al. SCREENING OF LACTIC ACID BACTERIA AS POTENTIAL STARTER FOR THE PRODUCTION OF ATTIÉKÉ, A FERMENTED CASSAVA FOOD.
KR100227001B1 (en) Method for producing fermentation food from grain starch
Yuliana et al. Potentially lactic acid bacteria as an EPS producing starter from yellow sweet potato fermentation
Damayanti et al. Fermentation of amylolytic yeast and lactic acid bacteria to improve the quality of modified cassava
KR101945940B1 (en) Novel use of Lactococcus chungangensis having enzyme activity
Giraud et al. Development of a miniaturized selective counting strategy of lactic acid bacteria for evaluation of mixed starter in a model cassava fermentation
RShalinimol Identification and Evaluation of Bacillus Species Bacteria from Sago Industrial Waste
CN112401232A (en) Preparation method and application of Tibetan mushroom fermented plant enzyme
FR2785294A1 (en) PROCESS FOR PRODUCING LACTIC FLOURS AND PRODUCTS OBTAINED
KR101848128B1 (en) Method for fermentation of lactic acid bacteria

Legal Events

Date Code Title Description
A201 Request for examination
E902 Notification of reason for refusal
AMND Amendment
E601 Decision to refuse application
J201 Request for trial against refusal decision
E902 Notification of reason for refusal
B701 Decision to grant
GRNT Written decision to grant
FPAY Annual fee payment

Payment date: 20110711

Year of fee payment: 13

LAPS Lapse due to unpaid annual fee