KR20230069509A - Method for producing steamed rice cake with enhanced GABA content using starter - Google Patents
Method for producing steamed rice cake with enhanced GABA content using starter Download PDFInfo
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- 235000007164 Oryza sativa Nutrition 0.000 title claims abstract description 34
- 235000009566 rice Nutrition 0.000 title claims abstract description 34
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 30
- 239000007858 starting material Substances 0.000 title abstract 3
- 229960003692 gamma aminobutyric acid Drugs 0.000 title description 8
- BTCSSZJGUNDROE-UHFFFAOYSA-N gamma-aminobutyric acid Chemical compound NCCCC(O)=O BTCSSZJGUNDROE-UHFFFAOYSA-N 0.000 title description 8
- 240000007594 Oryza sativa Species 0.000 title 1
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 claims abstract description 98
- 241000894006 Bacteria Species 0.000 claims abstract description 50
- 235000014655 lactic acid Nutrition 0.000 claims abstract description 49
- 239000004310 lactic acid Substances 0.000 claims abstract description 49
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- 230000004151 fermentation Effects 0.000 description 8
- LPUQAYUQRXPFSQ-DFWYDOINSA-M monosodium L-glutamate Chemical compound [Na+].[O-]C(=O)[C@@H](N)CCC(O)=O LPUQAYUQRXPFSQ-DFWYDOINSA-M 0.000 description 6
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- 108010073178 Glucan 1,4-alpha-Glucosidase Proteins 0.000 description 1
- 102100022624 Glucoamylase Human genes 0.000 description 1
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- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 1
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Abstract
Description
본 발명은 (1) MRS 한천 배지에 락토바실러스 브레비스(Lactobacillus brevis) 균주를 배양하여 유산균 균체를 확보하는 단계; (2) YM 배지에 사카로마이세스 세레비지애(Saccharomyces cerevisiae) 균주를 배양하여 효모 균체를 확보하는 단계; (3) 포도당, 효모추출물 및 다시마 추출물이 포함된 배지에 상기 (1)단계의 확보한 유산균 균체를 배양하여 유산균 배양액을 제조하는 단계; (4) 설탕, 효모추출물 및 맥아엑기스 분말이 포함된 배지에 상기 (2)단계의 확보한 효모 균체를 배양하여 효모 배양액을 제조하는 단계; 및 (5) 멥쌀가루에 물, 백국, 효모 추출물, 맥아엑기스 분말 및 정제효소와 상기 (3)단계의 제조한 유산균 배양액 및 상기 (4)단계의 제조한 효모 배양액을 혼합하여 배양하는 단계를 포함하여 제조하는 것을 특징으로 하는 증편 제조용 발효종의 제조방법, 상기 방법으로 제조된 증편 제조용 발효종과 상기 발효종을 이용한 증편의 제조방법에 관한 것이다.The present invention comprises the steps of (1) culturing Lactobacillus brevis strains in MRS agar medium to secure lactic acid bacteria cells; (2) culturing the strain of Saccharomyces cerevisiae in YM medium to obtain yeast cells; (3) culturing the lactic acid bacteria obtained in step (1) in a medium containing glucose, yeast extract and kelp extract to prepare a lactic acid bacteria culture solution; (4) preparing a yeast culture solution by culturing the yeast cells obtained in step (2) in a medium containing sugar, yeast extract and malt extract powder; And (5) mixing and culturing nonglutinous rice flour with water, white koji, yeast extract, malt extract powder and purified enzyme, the lactic acid bacteria culture solution prepared in step (3) and the yeast culture solution prepared in step (4) It relates to a method for producing a fermented species for producing jeungpyeon, characterized in that it is produced, a fermented species for producing jeungpyeon prepared by the above method, and a method for producing jeungpyeon using the fermented species.
증편은 우리의 떡 중 유일하게 발효과정을 거쳐 만들어지는 쌀떡으로 다른 종류의 떡과는 달리 다공성의 조직을 가지며 그로 인한 특유의 식감 때문에 소비자의 선호도가 높은 식품이다. 전 세계적으로 발효 식품에 대한 관심이 커지는 상황에 따라, 외국인들의 전통 음식, 특히 떡에 대한 인지도도 높아지고 있다. 따라서 증편은 국내시장 및 세계 시장에서 경쟁력 있는 식품군으로 각광받을 수 있다.Jeungpyeon is the only rice cake made through a fermentation process among our rice cakes. Unlike other types of rice cakes, it has a porous structure and is highly preferred by consumers because of its unique texture. As interest in fermented foods grows around the world, foreigners' awareness of traditional foods, especially rice cakes, is also increasing. Therefore, Jeungpyeon can be spotlighted as a competitive food group in the domestic and global markets.
증편이 우리나라에서 만들어지기 시작한 정확한 시기는 알 수 없으나 고문헌인 규곤시의방, 규합총서, 주방문, 시의전서 등 문헌들에 다양한 방법으로 제조된 증편이 소개되고 있다. 또한, 지역에 따라 증병, 기주떡, 기지떡, 술떡, 벙거지떡이라고도 하며 강원도에서는 기장떡, 기주떡, 쪽기정, 전남에서는 기정떡, 경북에서는 순흥기주떡, 제주도에서는 기증편이라고도 한다.The exact time when Jeungpyeon began to be made in Korea is unknown, but Jeungpyeon manufactured in various ways is introduced in ancient documents such as Gyugon Sibang, Gyuhapchongseo, Kitchen Gate, and Siuijeonseo. In addition, depending on the region, it is also called Jeungbyeong, Gijutteok, Gijitteok, Sultteok, and Beonggeotteok. In Gangwon-do, it is called Gijangtteok, Gijutteok, and Jjokgijeong.
증편은 쌀가루에 탁주를 넣고 반죽하여 발효시킨 다음 찐 것으로서, 내부구조는 스펀지와 비슷한 다공질 조직을 가지며 서양의 빵과 비슷하다. 원래 밀가루를 주재료로 하는 빵은 제조과정 중 밀단백질인 글루텐을 형성하여 유동성과 점탄성을 갖지만, 쌀을 주재료로 하는 떡은 글루텐이 없기 때문에 빵과 같은 조직을 갖지 못한다. 하지만 증편은 글루텐이 없이 발효 중 변화에 의해 특정물질이 고분자화되어 빵과 비슷한 구조를 가질 수 있다.Jeungpyeon is made by adding takju to rice flour, kneading it, fermenting it, and then steaming it. Originally, wheat flour-based bread forms gluten, a wheat protein, to have fluidity and viscoelasticity during the manufacturing process. However, Jeungpyeon can have a structure similar to bread because certain substances are polymerized by changes during fermentation without gluten.
또한, 증편은 발효에 의해 pH 4~5를 나타내며, 잡균이 번식하기 어려운 환경을 형성하기 때문에 미생물에 의한 변패가 지연되고, 저장성이 우수하다. 이러한 특징으로 인해 쉽게 상하지 않아 예로부터 여름철에 떡으로 많이 애용되어 왔다.In addition, Jeungpyeon exhibits a pH of 4 to 5 by fermentation, and because it forms an environment in which various bacteria are difficult to propagate, deterioration by microorganisms is delayed and storage stability is excellent. Due to these characteristics, it does not spoil easily, so it has been popular as a rice cake in the summer since ancient times.
그러나, 기존의 증편 제조 시 사용하는 막걸리로 인해 제조된 증편에서 술취 및 발효취 등의 이취로 인해 소비자들에게 호불호 갈리는 문제점이 있으며, 획일화된 재료의 사용으로 인해 영양성분이 다양하지 않은 문제점이 있다.However, there is a problem that consumers do not like or dislike due to off-flavors such as drunkenness and fermentation in Jeungpyeon manufactured by makgeolli used in the manufacture of existing Jeungpyeon. there is.
한국등록특허 제1219374호에는 마를 함유한 증편의 제조방법이 개시되어 있고, 한국공개특허 제2021-0068800호에는 포도주가 첨가된 쌀반죽을 이용한 증편의 제조방법이 개시되어 있으나, 본 발명의 GABA 함량이 증진된 증편의 제조방법과는 상이하다.Korean Registered Patent No. 1219374 discloses a method for manufacturing Jeungpyeon containing hemp, and Korean Patent Publication No. 2021-0068800 discloses a method for manufacturing Jeungpyeon using rice dough to which wine is added. However, the GABA content of the present invention It is different from the manufacturing method of this enhanced jeungpyeon.
본 발명은 상기와 같은 요구에 의해 도출된 것으로서, 본 발명의 목적은 증편의 풍미를 개선시키면서 기능성 성분(GABA)을 증진시킬 수 있는 발효종을 제조하기 위한 균주 선정, 배지 선정, 발효조건 등을 최적화하여 증편 제조용 발효종을 제조함으로써, 상기 발효종을 이용하여 증편을 제조할 경우 GABA 함량을 증진시킬 수 있는 증편 제조용 발효종의 제조방법을 제공하는 데 있다.The present invention was derived from the above needs, and an object of the present invention is to select strains, medium selection, fermentation conditions, etc. By optimizing and producing a fermented species for producing jeungpyeon, it is to provide a method for producing a fermented species for producing jeungpyeon that can increase the GABA content when producing jeungpyeon using the fermented species.
상기 과제를 해결하기 위해, 본 발명은 (1) MRS 한천 배지에 락토바실러스 브레비스(Lactobacillus brevis) 균주를 배양하여 유산균 균체를 확보하는 단계; (2) YM 배지에 사카로마이세스 세레비지애(Saccharomyces cerevisiae) 균주를 배양하여 효모 균체를 확보하는 단계; (3) 포도당, 효모추출물 및 다시마 추출물이 포함된 배지에 상기 (1)단계의 확보한 유산균 균체를 배양하여 유산균 배양액을 제조하는 단계; (4) 설탕, 효모추출물 및 맥아엑기스 분말이 포함된 배지에 상기 (2)단계의 확보한 효모 균체를 배양하여 효모 배양액을 제조하는 단계; 및 (5) 멥쌀가루에 물, 백국, 효모 추출물, 맥아엑기스 분말 및 정제효소와 상기 (3)단계의 제조한 유산균 배양액 및 상기 (4)단계의 제조한 효모 배양액을 혼합하여 배양하는 단계를 포함하여 제조하는 것을 특징으로 하는 증편 제조용 발효종의 제조방법을 제공한다.In order to solve the above problems, the present invention (1) culturing the Lactobacillus brevis strain in MRS agar medium to secure lactic acid bacteria cells; (2) culturing the strain of Saccharomyces cerevisiae in YM medium to obtain yeast cells; (3) culturing the lactic acid bacteria obtained in step (1) in a medium containing glucose, yeast extract and kelp extract to prepare a lactic acid bacteria culture solution; (4) preparing a yeast culture solution by culturing the yeast cells obtained in step (2) in a medium containing sugar, yeast extract and malt extract powder; And (5) mixing and culturing nonglutinous rice flour with water, white koji, yeast extract, malt extract powder and purified enzyme, the lactic acid bacteria culture solution prepared in step (3) and the yeast culture solution prepared in step (4) It provides a method for producing a fermented species for producing jeungpyeon, characterized in that it is produced by.
또한, 본 발명은 상기 방법으로 제조된 증편 제조용 발효종을 제공한다.In addition, the present invention provides a fermented species for preparing jeungpyeon prepared by the above method.
또한, 본 발명은 발효종에 습식 멥쌀가루, 설탕 및 물을 혼합한 후 성형하고, 발효한 후 증숙하여 제조하는 것을 특징으로 하는 증편의 제조방법을 제공한다.In addition, the present invention provides a method for producing jeungpyeon, characterized in that it is produced by mixing wet nonglutinous rice flour, sugar and water with fermented species, forming, fermenting and then steaming.
기존의 막걸리를 이용하여 증편을 제조할 경우 발효기간이 오래걸렸으나, 본 발명의 발효종을 사용하여 증편을 제조할 경우 발효기간을 단축시킬 수 있을 뿐만 아니라, GABA 함량을 증진시키고 기호도도 우수한 증편을 제조할 수 있는 이점이 있다.When Jeungpyeon was prepared using conventional makgeolli, the fermentation period took a long time. However, when Jeungpyeon is prepared using the fermented species of the present invention, the fermentation period can be shortened, and the GABA content is increased and the preference is excellent. has the advantage of being able to manufacture
도 1은 포도당(Glucose) 2%, 효모추출물(Y.E) 6%가 포함된 기본 배지(Based Culture medium)에 0.5% MSG(mono-sodium glutamate) 첨가군, 1% 다시마추출물(S.W.E) 첨가군, 1.5% 다시마추출물(S.W.E) 첨가군, 2% 다시마추출물(S.W.E) 첨가군에 따른 배양액 내 GABA 및 글루타메이트(glutamate) 집적량을 TLC(thin layer chromatography)를 통해 확인한 결과이다.Figure 1 is a base culture medium containing 2% glucose and 6% yeast extract (Y.E), 0.5% MSG (mono-sodium glutamate) added group, 1% kelp extract (S.W.E) added group, This is the result of confirming the accumulation of GABA and glutamate in the culture medium according to the 1.5% kelp extract (S.W.E) added group and the 2% kelp extract (S.W.E) added group through TLC (thin layer chromatography).
본 발명의 목적을 달성하기 위하여, 본 발명은In order to achieve the object of the present invention, the present invention
(1) MRS 한천 배지에 락토바실러스 브레비스(Lactobacillus brevis) 균주를 배양하여 유산균 균체를 확보하는 단계;(1) culturing Lactobacillus brevis strains on MRS agar medium to secure lactic acid bacteria cells;
(2) YM 배지에 사카로마이세스 세레비지애(Saccharomyces cerevisiae) 균주를 배양하여 효모 균체를 확보하는 단계;(2) culturing the strain of Saccharomyces cerevisiae in YM medium to obtain yeast cells;
(3) 포도당, 효모추출물 및 다시마 추출물이 포함된 배지에 상기 (1)단계의 확보한 유산균 균체를 배양하여 유산균 배양액을 제조하는 단계;(3) culturing the lactic acid bacteria obtained in step (1) in a medium containing glucose, yeast extract and kelp extract to prepare a lactic acid bacteria culture solution;
(4) 설탕, 효모추출물 및 맥아엑기스 분말이 포함된 배지에 상기 (2)단계의 확보한 효모 균체를 배양하여 효모 배양액을 제조하는 단계; 및(4) preparing a yeast culture solution by culturing the yeast cells obtained in step (2) in a medium containing sugar, yeast extract and malt extract powder; and
(5) 멥쌀가루에 물, 백국, 효모 추출물, 맥아엑기스 분말 및 정제효소와 상기 (3)단계의 제조한 유산균 배양액 및 상기 (4)단계의 제조한 효모 배양액을 혼합하여 배양하는 단계를 포함하여 제조하는 것을 특징으로 하는 증편 제조용 발효종의 제조방법을 제공한다.(5) mixing and culturing nonglutinous rice flour with water, white koji, yeast extract, malt extract powder and purified enzyme, the lactic acid bacteria culture solution prepared in step (3) and the yeast culture solution prepared in step (4) It provides a method for producing fermented species for producing jeungpyeon, characterized in that for producing.
본 발명의 증편 제조용 발효종의 제조방법에서, 상기 (1)단계는 바람직하게는 MRS 한천 배지에 락토바실러스 브레비스(Lactobacillus brevis) 균주를 28~32℃에서 1~2일 동안 배양하여 유산균 균체를 확보할 수 있으며, 더욱 바람직하게는 MRS 한천 배지에 락토바실러스 브레비스(Lactobacillus brevis) 균주를 30℃에서 1일 동안 배양하여 유산균 균체를 확보할 수 있다.In the method for producing fermented species for producing jeungpyeon of the present invention, step (1) is preferably performed by culturing the Lactobacillus brevis strain on MRS agar medium at 28 to 32 ° C. for 1 to 2 days to secure lactic acid bacteria cells It can be done, more preferably, Lactobacillus brevis ( Lactobacillus brevis ) strain is cultured for 1 day at 30 ° C. on an MRS agar medium to secure lactic acid bacteria cells.
또한, 본 발명의 증편 제조용 발효종의 제조방법에서, 상기 (2)단계는 바람직하게는 YM 배지에 사카로마이세스 세레비지애(Saccharomyces cerevisiae) 균주를 28~32℃에서 1~2일 동안 배양하여 효모 균체를 확보할 수 있으며, 더욱 바람직하게는 YM 배지에 사카로마이세스 세레비지애(Saccharomyces cerevisiae) 균주를 30℃에서 1일 동안 배양하여 효모 균체를 확보할 수 있다.In addition, in the method for producing a fermented species for producing jeungpyeon of the present invention, the step (2) is preferably a YM medium in Saccharomyces cerevisiae ( Saccharomyces cerevisiae ) Incubation of the strain at 28 to 32 ° C. for 1 to 2 days Yeast cells can be obtained by doing this, and more preferably, Saccharomyces cerevisiae ( Saccharomyces cerevisiae ) in YM medium can be cultured for one day at 30 ° C. to obtain yeast cells.
또한, 본 발명의 증편 제조용 발효종의 제조방법에서, 상기 (3)단계의 유산균 배양액은 바람직하게는 포도당 1.8~2.2%(v/v), 효모추출물 5.5~6.5%(v/v) 및 다시마 추출물 0.8~1.2%(v/v) 포함된 배지에 유산균 균체를 32~38℃에서 배양하여 유산균 배양액을 제조할 수 있으며, 더욱 바람직하게는 포도당 2%(v/v), 효모추출물 6%(v/v) 및 다시마 추출물 1%(v/v) 포함된 배지에 유산균 균체를 35℃에서 배양하여 유산균 배양액을 제조할 수 있다.In addition, in the method for producing fermented species for producing Jeungpyeon of the present invention, the lactic acid bacteria culture solution in step (3) preferably contains 1.8 to 2.2% (v/v) of glucose, 5.5 to 6.5% (v/v) of yeast extract and kelp. A lactic acid bacteria culture solution can be prepared by culturing lactic acid bacteria cells in a medium containing 0.8 to 1.2% (v/v) of the extract at 32 to 38° C., more preferably 2% of glucose (v/v) and 6% of yeast extract ( v/v) and 1% (v/v) of kelp extract by culturing lactic acid bacteria in a medium at 35° C. to prepare a culture medium of lactic acid bacteria.
또한, 본 발명의 증편 제조용 발효종의 제조방법에서, 상기 (4)단계의 배양은 바람직하게는 32~38℃에서 배양할 수 있으며, 더욱 바람직하게는 35℃에서 배양할 수 있다.In addition, in the method for preparing fermented species for preparing jeungpyeon of the present invention, the culture in step (4) may be preferably cultured at 32 to 38 ° C, more preferably at 35 ° C.
또한, 본 발명의 증편 제조용 발효종의 제조방법에서, 상기 (5)단계는 바람직하게는 멥쌀가루 800~1200 g에 물 2700~3300 mL, 백국 180~220 g, 효모 추출물 8~12 g, 맥아엑기스 분말 4.5~5.5 g, 정제효소 0.4~0.6 g, 유산균 배양액 27~33 g 및 효모 배양액 55~65 g을 혼합하여 32~38℃에서 10~20시간 동안 배양할 수 있으며, 더욱 바람직하게는 멥쌀가루 1000 g에 물 3000 mL, 백국 200 g, 효모 추출물 10 g, 맥아엑기스 분말 5 g, 정제효소 0.5 g, 유산균 배양액 30 g 및 효모 배양액 60 g을 혼합하여 35℃에서 15시간 동안 배양할 수 있다.In addition, in the method for producing fermented species for producing jeungpyeon of the present invention, step (5) is preferably 800 to 1200 g of nonglutinous rice flour, 2700 to 3300 mL of water, 180 to 220 g of white rice, 8 to 12 g of yeast extract, malt 4.5 ~ 5.5 g of extract powder, 0.4 ~ 0.6 g of purified enzyme, 27 ~ 33 g of lactic acid bacteria culture and 55 ~ 65 g of yeast culture can be mixed and cultured at 32 ~ 38 ℃ for 10 ~ 20 hours, more preferably nonglutinous rice 1000 g of powder is mixed with 3000 mL of water, 200 g of white koji, 10 g of yeast extract, 5 g of malt extract powder, 0.5 g of purified enzyme, 30 g of lactic acid bacteria culture medium, and 60 g of yeast culture medium and incubated at 35 ° C for 15 hours. .
본 발명의 증편 제조용 발효종의 제조방법은, 보다 구체적으로는The method for producing fermented species for producing jeungpyeon of the present invention is more specifically
(1) MRS 한천 배지에 락토바실러스 브레비스(Lactobacillus brevis) 균주를 28~32℃에서 1~2일 동안 배양하여 유산균 균체를 확보하는 단계;(1) culturing the Lactobacillus brevis strain on MRS agar medium at 28-32 ° C. for 1-2 days to obtain lactic acid bacteria cells;
(2) YM 배지에 사카로마이세스 세레비지애(Saccharomyces cerevisiae) 균주를 28~32℃에서 1~2일 동안 배양하여 효모 균체를 확보하는 단계;(2) YM medium Saccharomyces cerevisiae ( Saccharomyces cerevisiae ) Step of culturing the strain for 1 to 2 days at 28 ~ 32 ℃ to secure yeast cells;
(3) 포도당 1.8~2.2%(v/v), 효모추출물 5.5~6.5%(v/v) 및 다시마 추출물 0.8~1.2%(v/v) 포함된 배지에 상기 (1)단계의 확보한 유산균 균체를 32~38℃에서 배양하여 유산균 배양액을 제조하는 단계;(3) Lactic acid bacteria obtained in step (1) above in a medium containing 1.8-2.2% (v/v) glucose, 5.5-6.5% (v/v) yeast extract, and 0.8-1.2% (v/v) kelp extract. Preparing a lactic acid bacteria culture solution by culturing the cells at 32 ~ 38 ℃;
(4) 설탕, 효모추출물 및 맥아엑기스 분말이 포함된 배지에 상기 (2)단계의 확보한 효모 균체를 32~38℃에서 배양하여 효모 배양액을 제조하는 단계; 및(4) preparing a yeast culture solution by culturing the yeast cells obtained in step (2) at 32 to 38 ° C. in a medium containing sugar, yeast extract and malt extract powder; and
(5) 멥쌀가루 800~1200 g에 물 2700~3300 mL, 백국 180~220 g, 효모 추출물 8~12 g, 맥아엑기스 분말 4.5~5.5 g 및 정제효소 0.4~0.6 g과 상기 (3)단계의 제조한 유산균 배양액 27~33 g 및 상기 (4)단계의 제조한 효모 배양액 55~65 g을 혼합하여 32~38℃에서 10~20시간 동안 배양하는 단계를 포함할 수 있으며,(5) 800 ~ 1200 g of nonglutinous rice flour, 2700 ~ 3300 mL of water, 180 ~ 220 g of white rice, 8 ~ 12 g of yeast extract, 4.5 ~ 5.5 g of malt extract powder, and 0.4 ~ 0.6 g of purified enzyme and the above step (3) Mixing 27 to 33 g of the prepared lactic acid bacteria culture medium and 55 to 65 g of the yeast culture medium prepared in step (4) and incubating at 32 to 38 ° C. for 10 to 20 hours,
더욱 구체적으로는more specifically
(1) MRS 한천 배지에 락토바실러스 브레비스(Lactobacillus brevis) 균주를 30℃에서 1일 동안 배양하여 유산균 균체를 확보하는 단계;(1) culturing the Lactobacillus brevis strain on an MRS agar medium at 30° C. for 1 day to secure lactic acid bacteria cells;
(2) YM 배지에 사카로마이세스 세레비지애(Saccharomyces cerevisiae) 균주를 30℃에서 1일 동안 배양하여 효모 균체를 확보하는 단계;(2) Saccharomyces cerevisiae in YM medium ( Saccharomyces cerevisiae ) Step of culturing the strain for 1 day at 30 ° C. to obtain yeast cells;
(3) 포도당 2%(v/v), 효모추출물 6%(v/v) 및 다시마 추출물 1%(v/v) 포함된 배지에 상기 (1)단계의 확보한 유산균 균체를 35℃에서 배양하여 유산균 배양액을 제조하는 단계;(3) Cultivate the lactic acid bacteria obtained in step (1) at 35 ° C in a medium containing 2% (v / v) glucose, 6% (v / v) yeast extract and 1% (v / v) kelp extract To prepare a lactic acid bacteria culture solution;
(4) 설탕, 효모추출물 및 맥아엑기스 분말이 포함된 배지에 상기 (2)단계의 확보한 효모 균체를 35℃에서 배양하여 효모 배양액을 제조하는 단계; 및(4) preparing a yeast culture solution by culturing the yeast cells obtained in step (2) at 35 ° C. in a medium containing sugar, yeast extract and malt extract powder; and
(5) 멥쌀가루 1000 g에 물 3000 mL, 백국 200 g, 효모 추출물 10 g, 맥아엑기스 분말 5 g 및 정제효소 0.5 g과 상기 (3)단계의 제조한 유산균 배양액 30 g 및 상기 (4)단계의 제조한 효모 배양액 60 g을 혼합하여 35℃에서 15시간 동안 배양하는 단계를 포함할 수 있다.(5) 1000 g of nonglutinous rice flour, 3000 mL of water, 200 g of white yeast, 10 g of yeast extract, 5 g of malt extract powder, and 0.5 g of purified enzyme, 30 g of the lactic acid bacteria culture solution prepared in step (3) and step (4) It may include mixing 60 g of the prepared yeast culture solution and incubating at 35 ° C. for 15 hours.
본 발명은 또한, 상기 방법으로 제조된 증편 제조용 발효종을 제공한다.The present invention also provides a fermented species for preparing jeungpyeon prepared by the above method.
본 발명은 또한, 상기 발효종에 습식 멥쌀가루, 설탕 및 물을 혼합한 후 성형하고, 발효한 후 증숙하여 제조하는 것을 특징으로 하는 증편의 제조방법을 제공한다.The present invention also provides a method for producing jeungpyeon, characterized in that the fermented species is mixed with wet nonglutinous rice flour, sugar and water, molded, fermented, and then steamed.
본 발명의 증편의 제조방법은, 보다 구체적으로는 발효종 120~150 g, 습식 멥쌀가루 0.8~1.2 kg, 설탕 140~180 g 및 물 140~170 mL를 혼합한 후 성형하고, 32~38℃에서 90~120분 동안 발효한 후, 90~110℃에서 50~70분 동안 증숙하여 제조할 수 있으며, 더욱 구체적으로는 발효종 133.3 g, 습식 멥쌀가루 1 kg, 설탕 158.6 g 및 물 156.5 mL를 혼합한 후 성형하고, 35℃에서 90~120분 동안 발효한 후, 100℃에서 55~60분 동안 증숙하여 제조할 수 있다.More specifically, the method for producing Jeungpyeon of the present invention is molded after mixing 120 to 150 g of fermented species, 0.8 to 1.2 kg of wet nonglutinous rice flour, 140 to 180 g of sugar, and 140 to 170 mL of water, and then molded at 32 to 38 ° C. After fermenting for 90 to 120 minutes, it can be prepared by steaming at 90 to 110 ° C for 50 to 70 minutes. It can be prepared by molding after mixing, fermenting at 35 ° C for 90 to 120 minutes, and then steaming at 100 ° C for 55 to 60 minutes.
이하, 본 발명을 실시예에 의해 상세히 설명한다. 단, 하기 실시예는 본 발명을 예시하는 것일 뿐, 본 발명의 내용이 하기 실시예에 한정되는 것은 아니다.Hereinafter, the present invention will be described in detail by examples. However, the following examples are only to illustrate the present invention, and the content of the present invention is not limited to the following examples.
제조예 1: 발효종 제조Preparation Example 1: Preparation of fermented species
(1) 선정된 유산균(Lactobacillus brevis JCM1059 YDS01/ KCCM11870P) 및 효모(Saccharomyces cerevisiae YJM993 YDS02/ KCCM11871P)의 균주는 5% 글리세롤(glycerol) 멸균액과 균주 배양액을 1:1 부피비율로 섞어 -80℃에서 보관하며 약 1년 주기로 보관균주를 계대 배양하여 균주를 보관하였다.(1) The strains of selected lactic acid bacteria ( Lactobacillus brevis JCM1059 YDS01/ KCCM11870P) and yeast ( Saccharomyces cerevisiae YJM993 YDS02/ KCCM11871P) were mixed with 5% glycerol sterilized solution and strain culture solution at a volume ratio of 1:1 at -80 ° C. The strains were stored by subculturing the stored strains at intervals of about 1 year.
(2) MRS agar 배지에 상기 (1)단계의 보관한 유산균(Lactobacillus brevis JCM1059 YDS01)을 도말하여 30℃에서 1일 이상 배양하여 유산균 단일 균체를 확보하였다.(2) The lactic acid bacteria ( Lactobacillus brevis JCM1059 YDS01) stored in step (1) was smeared on the MRS agar medium and cultured at 30 ° C for one day or more to secure a single lactic acid bacteria cell.
(3) YM(yeast malt) 배지에 상기 (1)단계의 보관한 효모(Saccharomyces cerevisiae YJM993 YDS02)을 도말하여 30℃에서 1일 이상 배양하여 효모 단일 균체를 확보하였다.(3) The yeast ( Saccharomyces cerevisiae YJM993 YDS02) stored in step (1) was spread on YM (yeast malt) medium and cultured at 30 ° C for one day or more to obtain single yeast cells.
(4) 유산균 배지(GY)에 상기 (2)단계의 확보한 유산균 단일 균체를 35℃에서 180 rpm으로 24시간 동안 배양하여 유산균 씨드(seed) 배양액을 제조하였다. 상기 유산균 배지(GY)는 포도당(glucose) 2%, 효모추출물 6%, 다시마 추출물 1%로 물과 혼합하여 121℃에서 20분간 멸균한 것을 사용하였다.(4) A lactic acid bacteria seed culture was prepared by culturing the single lactic acid bacteria obtained in step (2) in a lactic acid bacteria medium (GY) at 35 ° C. at 180 rpm for 24 hours. As the lactic acid bacteria medium (GY), 2% glucose, 6% yeast extract, and 1% kelp extract were mixed with water and sterilized at 121° C. for 20 minutes.
(5) 효모 배지(SYM)에 상기 (3)단계의 확보한 효모 단일 균체를 35℃에서 180 rpm으로 24시간 동안 배양하여 효모 씨드(seed) 배양액을 제조하였다. 상기 효모 배지(SYM)는 설탕(sucrose), 효모추출물, 맥아엑기스 분말을 물과 혼합하여 121℃에서 20분간 멸균한 것을 사용하였다.(5) A yeast seed culture solution was prepared by culturing the single yeast cells obtained in step (3) in a yeast medium (SYM) at 35 ° C. at 180 rpm for 24 hours. As the yeast medium (SYM), sucrose, yeast extract, and malt extract powder were mixed with water and sterilized at 121° C. for 20 minutes.
(6) 유산균 배지(GY) 900 mL에 상기 (4)단계의 제조한 유산균 씨드(seed) 배양액을 1/1000 볼륨으로 접종하고, 35℃에서 36~48시간 동안 배양하였다.(6) The lactic acid bacteria seed culture solution prepared in step (4) was inoculated in 900 mL of lactic acid bacteria medium (GY) at a volume of 1/1000, and cultured at 35 ° C. for 36 to 48 hours.
(7) 효모 배지(SYM) 900 mL에 상기 (4)단계의 제조한 효모 씨드(seed) 배양액을 1/1000 볼륨으로 접종하고, 35℃에서 36~48시간 동안 배양하였다.(7) Yeast medium (SYM) 900 mL was inoculated with the yeast seed culture solution prepared in step (4) at a volume of 1/1000, and cultured at 35 ° C for 36 to 48 hours.
(8) 멥쌀가루를 수침하여 제분하고 온풍건조하여 수분함량 15% 이하로 떨어트린 건조 멥쌀가루 1000 g에 물 3000 mL, 백국 200 g, 효모 추출물 10 g, 맥아엑기스 분말 5 g 및 정제효소(글루코아밀라아제, 당화력역가 15,000 sp) 0.5 g과 상기 (6)단계의 배양한 유산균 배양액 30 g 및 상기 (7)단계의 배양한 효모 배양액 60 g을 혼합하여 35℃에서 필터링된 공기를 넣어주면서 15시간 동안 배양하여 발효종을 제조하였다.(8) 3000 mL of water, 200 g of white rice, 10 g of yeast extract, 5 g of malt extract powder, and purified enzyme (gluco Amylase, glycosylation titer 15,000 sp) 0.5 g, 30 g of cultured lactic acid bacteria cultured in step (6) and 60 g of cultured yeast cultured in step (7) were mixed and stirred at 35°C for 15 hours while introducing filtered air. A fermented species was prepared by culturing.
제조예 2. 증편 제조Manufacturing Example 2. Manufacture of Jeungpyeon
(1) 백미를 12시간 동안 물에 불린 후 30분 동안 물빼기를 실시한 후 수침된 멥쌀의 무게에 대한 소금 128% 첨가 후 롤밀 제분 2회를 통해 습식 멥쌀가루(수분함량 46%)를 제조하였다.(1) After soaking the white rice in water for 12 hours, draining the water for 30 minutes, adding 128% of salt based on the weight of the soaked nonglutinous rice, and then milling the roll mill twice to prepare wet nonglutinous rice flour (moisture content: 46%). .
(2) 상기 (1)단계의 습식 멥쌀가루 1 kg, 상기 제조예 1의 발효종 133.3 g, 설탕 158.6 g 및 물 156.5 mL를 혼합한 후 35 g씩 소분하여 성형하고, 35℃에서 85%의 높은 습도를 유지하면서 1시간 30분에서 2시간 동안 발효한 후, 100℃에서 55~60분 동안 증숙하였다.(2) After mixing 1 kg of wet nonglutinous rice flour in step (1), 133.3 g of the fermented species of Preparation Example 1, 158.6 g of sugar and 156.5 mL of water, it was subdivided into 35 g each and molded, and 85% at 35 ° C. After fermentation for 1 hour and 30 minutes to 2 hours while maintaining high humidity, it was steamed at 100 ° C. for 55 to 60 minutes.
실시예 1. 배양액 내 GABA 및 글루타메이트 분석Example 1. Analysis of GABA and glutamate in culture medium
본 실험에서는 유산균 배양 기본 배지에 MSG(mono-sodium glutamate) 또는 다시마 추출물 첨가에 따른 GABA 및 글루타메이트(glutamate) 집적량을 TLC를 통해 확인하였다. 그 결과, 확연한 GABA 및 글루타메이트 증가는 무첨가 및 0.5% MSG(mono-sodium glutamate) 첨가군보다 1% 이상의 다시마 추출물을 넣었을 때 더빠르게 집적되는 것을 확인하였다(도 1).In this experiment, the accumulation of GABA and glutamate according to the addition of MSG (mono-sodium glutamate) or kelp extract to the lactic acid bacteria culture basal medium was confirmed through TLC. As a result, it was confirmed that the clear increase in GABA and glutamate was accumulated more rapidly when 1% or more kelp extract was added than in the non-added and 0.5% MSG (mono-sodium glutamate) added groups (FIG. 1).
Claims (5)
(2) YM 배지에 사카로마이세스 세레비지애(Saccharomyces cerevisiae) 균주를 배양하여 효모 균체를 확보하는 단계;
(3) 포도당, 효모추출물 및 다시마 추출물이 포함된 배지에 상기 (1)단계의 확보한 유산균 균체를 배양하여 유산균 배양액을 제조하는 단계;
(4) 설탕, 효모추출물 및 맥아엑기스 분말이 포함된 배지에 상기 (2)단계의 확보한 효모 균체를 배양하여 효모 배양액을 제조하는 단계; 및
(5) 멥쌀가루에 물, 백국, 효모 추출물, 맥아엑기스 분말 및 정제효소와 상기 (3)단계의 제조한 유산균 배양액 및 상기 (4)단계의 제조한 효모 배양액을 혼합하여 배양하는 단계를 포함하여 제조하는 것을 특징으로 하는 증편 제조용 발효종의 제조방법.(1) culturing Lactobacillus brevis strains on MRS agar medium to secure lactic acid bacteria cells;
(2) culturing the strain of Saccharomyces cerevisiae in YM medium to obtain yeast cells;
(3) culturing the lactic acid bacteria obtained in step (1) in a medium containing glucose, yeast extract and kelp extract to prepare a lactic acid bacteria culture solution;
(4) preparing a yeast culture solution by culturing the yeast cells obtained in step (2) in a medium containing sugar, yeast extract and malt extract powder; and
(5) mixing and culturing nonglutinous rice flour with water, white koji, yeast extract, malt extract powder and purified enzyme, the lactic acid bacteria culture solution prepared in step (3) and the yeast culture solution prepared in step (4) A method for producing fermented species for producing jeungpyeon, characterized in that for producing.
(1) MRS 한천 배지에 락토바실러스 브레비스(Lactobacillus brevis) 균주를 28~32℃에서 1~2일 동안 배양하여 유산균 균체를 확보하는 단계;
(2) YM 배지에 사카로마이세스 세레비지애(Saccharomyces cerevisiae) 균주를 28~32℃에서 1~2일 동안 배양하여 효모 균체를 확보하는 단계;
(3) 포도당 1.8~2.2%(v/v), 효모추출물 5.5~6.5%(v/v) 및 다시마 추출물 0.8~1.2%(v/v) 포함된 배지에 상기 (1)단계의 확보한 유산균 균체를 32~38℃에서 배양하여 유산균 배양액을 제조하는 단계;
(4) 설탕, 효모추출물 및 맥아엑기스 분말이 포함된 배지에 상기 (2)단계의 확보한 효모 균체를 32~38℃에서 배양하여 효모 배양액을 제조하는 단계; 및
(5) 멥쌀가루 800~1200 g에 물 2700~3300 mL, 백국 180~220 g, 효모 추출물 8~12 g, 맥아엑기스 분말 4.5~5.5 g 및 정제효소 0.4~0.6 g과 상기 (3)단계의 제조한 유산균 배양액 27~33 g 및 상기 (4)단계의 제조한 효모 배양액 55~65 g을 혼합하여 32~38℃에서 10~20시간 동안 배양하는 단계를 포함하여 제조하는 것을 특징으로 하는 증편 제조용 발효종의 제조방법.According to claim 1,
(1) culturing the Lactobacillus brevis strain on MRS agar medium at 28-32 ° C. for 1-2 days to obtain lactic acid bacteria cells;
(2) YM medium Saccharomyces cerevisiae ( Saccharomyces cerevisiae ) Step of culturing the strain for 1 to 2 days at 28 ~ 32 ℃ to secure yeast cells;
(3) Lactic acid bacteria obtained in step (1) above in a medium containing 1.8-2.2% (v/v) glucose, 5.5-6.5% (v/v) yeast extract, and 0.8-1.2% (v/v) kelp extract. Preparing a lactic acid bacteria culture solution by culturing the cells at 32 ~ 38 ℃;
(4) preparing a yeast culture solution by culturing the yeast cells obtained in step (2) at 32 to 38 ° C. in a medium containing sugar, yeast extract and malt extract powder; and
(5) 800 ~ 1200 g of nonglutinous rice flour, 2700 ~ 3300 mL of water, 180 ~ 220 g of white rice, 8 ~ 12 g of yeast extract, 4.5 ~ 5.5 g of malt extract powder, and 0.4 ~ 0.6 g of purified enzyme and the above step (3) For manufacturing jeungpyeon, characterized in that it is prepared by mixing 27 to 33 g of the prepared lactic acid bacteria culture medium and 55 to 65 g of the yeast culture medium prepared in step (4) and incubating at 32 to 38 ° C for 10 to 20 hours. Method for producing fermented species.
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