KR20030005452A - The manufacturing method of bread using saccharomyces cerevisiae previously treated with starch syrup - Google Patents

The manufacturing method of bread using saccharomyces cerevisiae previously treated with starch syrup Download PDF

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KR20030005452A
KR20030005452A KR1020010040742A KR20010040742A KR20030005452A KR 20030005452 A KR20030005452 A KR 20030005452A KR 1020010040742 A KR1020010040742 A KR 1020010040742A KR 20010040742 A KR20010040742 A KR 20010040742A KR 20030005452 A KR20030005452 A KR 20030005452A
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yeast
bread
maltose
fermentation
myp
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KR100430040B1 (en
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이기평
윤강섭
강원진
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이기평
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    • AHUMAN NECESSITIES
    • A21BAKING; EDIBLE DOUGHS
    • A21DTREATMENT, e.g. PRESERVATION, OF FLOUR OR DOUGH, e.g. BY ADDITION OF MATERIALS; BAKING; BAKERY PRODUCTS; PRESERVATION THEREOF
    • A21D2/00Treatment of flour or dough by adding materials thereto before or during baking
    • A21D2/08Treatment of flour or dough by adding materials thereto before or during baking by adding organic substances
    • A21D2/36Vegetable material
    • A21D2/38Seed germs; Germinated cereals; Extracts thereof
    • AHUMAN NECESSITIES
    • A21BAKING; EDIBLE DOUGHS
    • A21DTREATMENT, e.g. PRESERVATION, OF FLOUR OR DOUGH, e.g. BY ADDITION OF MATERIALS; BAKING; BAKERY PRODUCTS; PRESERVATION THEREOF
    • A21D15/00Preserving finished, partly finished or par-baked bakery products; Improving
    • A21D15/02Preserving finished, partly finished or par-baked bakery products; Improving by cooling, e.g. refrigeration, freezing
    • AHUMAN NECESSITIES
    • A21BAKING; EDIBLE DOUGHS
    • A21DTREATMENT, e.g. PRESERVATION, OF FLOUR OR DOUGH, e.g. BY ADDITION OF MATERIALS; BAKING; BAKERY PRODUCTS; PRESERVATION THEREOF
    • A21D2/00Treatment of flour or dough by adding materials thereto before or during baking
    • A21D2/08Treatment of flour or dough by adding materials thereto before or during baking by adding organic substances
    • A21D2/14Organic oxygen compounds
    • A21D2/18Carbohydrates
    • A21D2/181Sugars or sugar alcohols
    • AHUMAN NECESSITIES
    • A21BAKING; EDIBLE DOUGHS
    • A21DTREATMENT, e.g. PRESERVATION, OF FLOUR OR DOUGH, e.g. BY ADDITION OF MATERIALS; BAKING; BAKERY PRODUCTS; PRESERVATION THEREOF
    • A21D8/00Methods for preparing or baking dough
    • A21D8/02Methods for preparing dough; Treating dough prior to baking
    • AHUMAN NECESSITIES
    • A21BAKING; EDIBLE DOUGHS
    • A21DTREATMENT, e.g. PRESERVATION, OF FLOUR OR DOUGH, e.g. BY ADDITION OF MATERIALS; BAKING; BAKERY PRODUCTS; PRESERVATION THEREOF
    • A21D8/00Methods for preparing or baking dough
    • A21D8/02Methods for preparing dough; Treating dough prior to baking
    • A21D8/04Methods for preparing dough; Treating dough prior to baking treating dough with microorganisms or enzymes
    • A21D8/047Methods for preparing dough; Treating dough prior to baking treating dough with microorganisms or enzymes with yeasts
    • AHUMAN NECESSITIES
    • A21BAKING; EDIBLE DOUGHS
    • A21DTREATMENT, e.g. PRESERVATION, OF FLOUR OR DOUGH, e.g. BY ADDITION OF MATERIALS; BAKING; BAKERY PRODUCTS; PRESERVATION THEREOF
    • A21D8/00Methods for preparing or baking dough
    • A21D8/06Baking processes
    • 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
    • A23L5/00Preparation or treatment of foods or foodstuffs, in general; Food or foodstuffs obtained thereby; Materials therefor
    • A23L5/10General methods of cooking foods, e.g. by roasting or frying
    • A23L5/15General methods of cooking foods, e.g. by roasting or frying using wave energy, irradiation, electrical means or magnetic fields, e.g. oven cooking or roasting using radiant dry heat
    • CCHEMISTRY; METALLURGY
    • 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

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  • General Engineering & Computer Science (AREA)
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  • Bakery Products And Manufacturing Methods Therefor (AREA)
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Abstract

PURPOSE: A method for preparing bread is provided to obtain high quality of bread by using Saccharomyces cerevisiae as one of common yeast to be treated into grain syrup state and adding the grain syrup yeast. CONSTITUTION: The method comprises treating the common yeast of Saccharomyces cerevisiae in a medium containing 2-5% MYP (consisting of 2-5% maltose, 0.5% yeast extract, 1% peptone, 0.3% KH2PO4) for 1.5-2.5 hours to preliminarily derive expression of a specified yeast gene concerning fermentation of the maltose; then adding the pre-treated yeast in the first kneading flour for baking the bread to ferment the kneading; alternatively forming a second kneading flour and adding it to the first kneading then secondly fermenting the kneading; and baking the kneading. The 2.5% MYP medium may be formed into the grain syrup state.

Description

물엿 전처리 효모를 이용한 빵의 제조방법{THE MANUFACTURING METHOD OF BREAD USING SACCHAROMYCES CEREVISIAE PREVIOUSLY TREATED WITH STARCH SYRUP }The manufacturing method of bread using syrup pretreatment yeast {THE MANUFACTURING METHOD OF BREAD USING SACCHAROMYCES CEREVISIAE PREVIOUSLY TREATED WITH STARCH SYRUP}

본 발명은 물엿 전처리 효모를 이용한 빵의 제조방법에 관한 것이다.The present invention relates to a method for producing bread using starch pretreated yeast.

빵의 제조과정 중에서 효모의 반죽 내 당분 발효 활성은 제품의 품질을 결정하는 가장 중요한 요소 가운데 하나이다.The sugar fermentation activity of the yeast dough during the manufacturing process of bread is one of the most important factors that determine the quality of the product.

효모 세포의 당분 발효대사에 관여하는 효소계 및 관련 유전자발현 조절계의 생화학적인 특성상, 밀가루 반죽 속의 조건에서는 일정 기간 당분 발효작용이 진행된 후, 잔존하는 포도당 분자에 의해 주된 탄소원인 맥아당의 발효가 억제되며, 이로인해 생성되는 탄산가스의 양이 제한되어 성형화 된 반죽 내에서의 충분한 팽창이 이루어질 수 없다.Due to the biochemical characteristics of the enzyme system involved in sugar fermentation metabolism of yeast cells and related gene expression control system, after fermentation of sugar for a certain period of time under the conditions of the dough, the remaining glucose molecules inhibit fermentation of maltose, a major carbon source, This limits the amount of carbon dioxide produced so that sufficient expansion cannot be achieved in the molded dough.

이러한 효모의 발효특성은 발효 빵의 품질을 고급화하며 동시에 빵의 제조원가를 낮추고자하는 노력에 결정적인 걸림돌이 되고 있다.Such fermentation characteristics of yeast have become a decisive obstacle to efforts to improve the quality of fermented bread and at the same time lower the manufacturing cost of bread.

한편, 한국특허출원 10-1999-0002680 (엿기름 추출액의 용도)에서는 제빵 또는 제과 공정에서 엿기름 추출액을 사용하여 맥아 특유의 향취와 발아시에 생성되는 알파-아밀레이즈, 베타-아밀레이즈, 글루코아밀레이즈 등의 효소활성을 이용하여 제품의 식감 개선과 , 향취 증진, 녹말의 노화 억제 등의 효과를 위해서 첨가제로 사용한 것이 있으나, 이것은 엿기름을 첨가제로 사용한 것으로 본 발명과는 그 목적과 기술구성이 다른 것이다.Meanwhile, Korean Patent Application No. 10-1999-0002680 (Use of malt extract) uses alpha-amylase, beta-amylase, and glucoamylase produced by malt odor and germination by using malt extract in the baking or confectionery process. It is used as an additive to improve the texture of the product by using the enzymatic activity such as, enhance the odor, suppress the aging of starch, etc., but this is malt as an additive and its purpose and technical configuration is different from the present invention. .

또한, 한국특허출원 10-1999-0050363(엿밥을 이용한 효모의 배양)에는, 가축사료 첨가용 효모 배양물을 엿밥을 기본 배양배지로 하여 효모를 배양하는 방법이 공지되어 있으나, 본원 발명과는 그 목적과 기술 구성이 본원 발명과는 다른 것이다.In addition, Korean Patent Application No. 10-1999-0050363 (cultivation of yeast using a rice cake), a method for cultivating yeast using a yeast culture for adding livestock feed as a basic culture medium is known, but with the present invention The object and the technical configuration are different from the present invention.

현재까지 물엿으로 전처리한 효모를 이용한 빵의 제조방법에 대해서는 알려진 것이 없다.To date, there is no known method for producing bread using yeast pretreated with starch syrup.

본 발명은 제빵용 효모를 본 반죽에 첨가하기 전에, 순수 맥아당 또는 물엿으로 만든 MYP배지에서 효모를 전처리함으로써 고농도의 맥아당 분자에 미리 노출시켜, 맥아당 발효에 관여하는 효소 유전자의 발현을 충분히 유도하여, 제빵시 밀가루 반죽 속에 있는 맥아당의 발효를 촉진하여 고품질의 빵을 제조하고, 또한 가격이 저렴한 물엿을 이용함으로써 제조원가를 절감하는데 있다.The present invention pretreatment of yeast in MYP medium made of pure maltose or starch syrup before adding the baker's yeast to the dough, exposing it to high concentrations of maltose molecules in advance to sufficiently induce the expression of the enzyme gene involved in maltose fermentation, It promotes fermentation of maltose in flour dough during baking to produce high quality bread, and also to reduce manufacturing cost by using cheap starch syrup.

본 발명은 물엿으로 전처리한 효모를 이용하여 빵을 제조하는 방법에 관한것이다.The present invention relates to a method for preparing bread using yeast pretreated with starch syrup.

본 발명은 고농도의 맥아당 분자에 효모를 미리 노출시키는 전처리를 하여, 맥아당 발효에 관여하는 효소 유전자의 발현을 사전에 충분히 유도 합성하여 상대적으로 포도당에 의한 억제작용을 약화시켜 발효 효율을 높임으로써 품질이 좋은 빵을 제조하는 방법에 관한 것이다.The present invention is a pre-treatment to expose the yeast to a high concentration of maltose molecules in advance, sufficiently inducing and synthesizing the expression of the enzyme gene involved in the maltose fermentation in advance to relatively weaken the inhibitory action by glucose to improve fermentation efficiency It is about how to make good bread.

본 발명에 의한 빵의 제조과정은 제빵용으로 사용되고 있는 통상의 효모(Saccahromyces cerevisiae)를 순수 맥아당 또는 물엿으로 만든 맥아당 2~5 % MYP( 2 ~ 5 % maltose, 0.5 % yeast extract, 1 % peptone, 0.3 % KH2PO4)배지에서 1.5 ~ 2.5 시간 전처리한 후, 1차 반죽에 첨가하여 발효시키고, 여기에 2 차 반죽을 별도로 만들어 1차 발효된 것에 추가하여 2 차 발효시킨 다음 , 굽는 과정으로 수행된다.In the manufacturing process of the bread according to the present invention, malt sugar 2-5% MYP (2-5% maltose, 0.5% yeast extract, 1% peptone, made from pure malt sugar or starch syrup, which is a conventional yeast (Saccahromyces cerevisiae) used for baking 0.3% KH 2 PO 4 ) After pre-treatment for 1.5 to 2.5 hours in a medium, it is added to the primary dough and fermented. Is performed.

이하 실시예에 의하여 본 발명을 상세히 설명한다.Hereinafter, the present invention will be described in detail with reference to Examples.

단, 하기 실시예들은 본 발명을 예시하는 것으로, 본 발명의 내용이 실시예에 의하여 한정되는 것은 아니다.However, the following examples are illustrative of the present invention, and the content of the present invention is not limited by the examples.

<실시예 1> 맥아당 전처리에 의한 효모의 발효 활성 최적조건 조사Example 1 Investigation of Optimal Conditions for Fermentation Activity of Yeast by Maltose Pretreatment

제빵에 통상적으로 이용되고 있는 효모(Saccharomyces cerevisiae)를 사용하여 실험을 하였다.Experiments were performed using yeast ( Saccharomyces cerevisiae) commonly used in baking.

효모의 단일 균주 분리 및 증식 배양에는 2% GYP(2% glucose, 0.5% yeastextract, 1% peptone, 0.3% KH2PO4) 배지를 사용하였다.2% GYP (2% glucose, 0.5% yeastextract, 1% peptone, 0.3% KH 2 PO 4 ) medium was used for isolation and growth of a single strain of yeast.

고체배지 제조에는 2% agar를 첨가하였다.2% agar was added to the solid medium.

맥아당 전처리 과정에는 0∼5% MYP(0∼5% maltose, 0.5% yeast extract, 1% peptone, 0.3% KH2PO4) 배지를 사용하였다.Maltose pretreatment was performed with 0-5% MYP (0-5% maltose, 0.5% yeast extract, 1% peptone, 0.3% KH 2 PO 4 ) medium.

전처리에 대한 대조실험을 위해서는 GlyEtYP(3% glycerol, 2% ethanol, 0.5% yeast extract, 1% peptone, 0.3% KH2PO4) 배지를 사용하였다.GlyEtYP (3% glycerol, 2% ethanol, 0.5% yeast extract, 1% peptone, 0.3% KH 2 PO 4 ) medium was used for control.

효모의 발효 활성 측정에는 빵의 반죽과 유사한 당 성분의 조성을 가진 FMGYP(0.33% fructose, 4.3% maltose, 0.38% glucose, 0.5% yeast extract, 1% peptone, 0.28% KH2PO4) 배지를 사용하였다.FMGYP (0.33% fructose, 4.3% maltose, 0.38% glucose, 0.5% yeast extract, 1% peptone, 0.28% KH 2 PO 4 ) medium was used to determine the fermentation activity of yeast. .

모든 배양 및 전처리 온도는 30℃를 이용하였다.All incubation and pretreatment temperatures used 30 ° C.

발효 활성의 측정은, 맥아당(maltose)농도가 0∼5%로 첨가된 MYP(Maltose-Yeast extract-Peptone) 배지에서 1∼3시간 동안 30℃로 전처리 한 효모를 사용하였다.The fermentation activity was measured using yeast pretreated at 30 ° C. for 1-3 hours in a Malose-Yeast extract-Peptone (MYP) medium containing maltose concentration of 0-5%.

이때, 빵의 반죽과 유사한 당 성분의 조성을 가진 30℃의 FMGYP(Fructose-Maltose-Glucose-Yeast extract-Peptone) 발효배지에서, 효모량이 1∼5%(w/v) 범위의 동일한 양의 효모가 포함된 10ml 배양용액에 대해 발효활성을 0∼3시간 동안 CO2기체 발생량을 이용하여 측정하였다.At this time, in the fermentation medium of FMGYP (Fructose-Maltose-Glucose-Yeast extract-Peptone) having a composition of sugar similar to the dough of bread, the same amount of yeast in the range of 1-5% (w / v) The fermentation activity of the contained 10ml culture solution was measured using CO 2 gas generation amount for 0 to 3 hours.

효모 5 %(w/v) 사용한 결과를 표1에 효모 1 %(w/v)를 사용한 결과를 표2에 나타냈다.Table 1 shows the results of using the yeast 5% (w / v) Table 1 shows the results of using the yeast 1% (w / v).

<표 1> 맥아당 전처리 조건에 따른 효모(5%)의 CO2발생량.Table 1 CO 2 generation of yeast (5%) according to maltose pretreatment conditions.

"-"는 0.1 이하, 단위는 ml"-" Is 0.1 or less, unit is ml

전처리 시간Pretreatment time 1시간1 hours 2시간2 hours 3시간3 hours 전처리 발효 배지시간(분)Pretreatment Fermentation Medium Time (min) 3%MYP3% MYP 5%MYP5% MYP GlyEtYPGlyEtYP 3%MYP3% MYP 5%MYP5% MYP GlyEtYPGlyEtYP 3%MYP3% MYP 5%MYP5% MYP GlyEtYPGlyEtYP 33 -- -- -- -- -- -- -- -- -- 66 -- -- -- -- 0.40.4 -- -- -- -- 99 -- -- -- -- 0.50.5 -- -- -- -- 1212 -- -- -- -- 0.90.9 -- -- -- -- 1515 0.20.2 0.30.3 -- 0.30.3 1.31.3 -- 0.20.2 -- -- 1818 0.20.2 0.50.5 -- 0.40.4 1.91.9 -- 0.20.2 -- -- 2121 0.30.3 0.70.7 -- 0.70.7 2.42.4 -- 0.30.3 0.30.3 0.30.3 2424 0.40.4 1.11.1 -- 1.21.2 3.33.3 -- 0.40.4 0.40.4 0.30.3 2727 0.70.7 1.51.5 -- 1.61.6 4.54.5 0.40.4 0.50.5 0.70.7 0.40.4 3030 1.01.0 2.02.0 -- 2.02.0 5.95.9 0.50.5 0.70.7 1.01.0 0.50.5

<표 2> 맥아당 전처리 조건에 따른 효모(1%)의 CO2발생량.Table 2 CO 2 generation of yeast (1%) according to maltose pretreatment conditions.

"-"는 0.1 이하, 단위는 ml"-" Is 0.1 or less, unit is ml

전처리 시간Pretreatment time 1시간1 hours 2시간2 hours 3시간3 hours 전처리 발효 배지 시간(분)Pretreatment Fermentation Medium Time (min) 3%MYP3% MYP 5%MYP5% MYP GlyEtYPGlyEtYP 3%MYP3% MYP 5%MYP5% MYP GlyEtYPGlyEtYP 3%MYP3% MYP 5%MYP5% MYP GlyEtYPGlyEtYP 2020 -- -- -- -- -- -- -- -- -- 4040 -- 0.40.4 -- 0.40.4 -- -- 0.40.4 0.40.4 -- 6060 -- 0.40.4 0.30.3 1.01.0 0.40.4 0.30.3 0.80.8 0.90.9 0.30.3 7575 -- 0.40.4 0.30.3 1.61.6 0.70.7 0.40.4 1.41.4 1.61.6 0.40.4 9090 0.30.3 0.40.4 0.50.5 2.62.6 1.41.4 0.70.7 2.02.0 2.52.5 0.70.7 105105 0.40.4 0.70.7 0.80.8 3.53.5 2.12.1 1.11.1 2.72.7 3.13.1 1.11.1 120120 0.80.8 1.01.0 1.41.4 4.84.8 2.92.9 1.61.6 3.53.5 4.04.0 1.61.6 135135 1.41.4 1.51.5 2.02.0 6.46.4 3.73.7 2.22.2 4.44.4 4.94.9 2.22.2 150150 2.02.0 2.12.1 2.72.7 8.18.1 4.74.7 2.82.8 5.35.3 5.65.6 2.82.8

표1의 5%(w/v) 효모 농도가 발효실험에 사용된 경우에서 뚜렷한 발효율의 차이가 나타나는 0∼30분 동안의 측정결과를 볼 때, 전처리에 사용된 맥아당의 농도가 높을수록 발효율이 높았으며 농도에 관계없이 2시간의 전처리에서 가장 좋은 결과를 보였다.When the 5% (w / v) yeast concentration in Table 1 was used in the fermentation experiment, and the result of the measurement for 0 to 30 minutes showing the difference in the remarkable efficiency, the higher the concentration of maltose used for the pretreatment The efficiency was high and the best results were obtained after 2 hours of pretreatment regardless of the concentration.

표2의 1%(w/v) 효모 농도가 사용된 경우에서도 발효시간이 진행됨에 따라 비슷한 결과가 관찰됨으로써 맥아당 전처리가 효모의 발효율을 명확히 증가시키는 것으로 확인되었다.Similar results were observed as the fermentation time progressed even when the 1% (w / v) yeast concentration in Table 2 was used, and it was confirmed that maltose pretreatment significantly increased yeast efficiency.

그 조건은 효모 농도를 비롯한 여러 요인에 따라 변화는 있지만 3-5% 의 맥아당 조건에서 2시간 정도가 적정한 것으로 나타났다.The conditions varied depending on several factors including yeast concentration, but 2 hours were adequate at 3-5% maltose condition.

<실시예 2> 물엿 전처리에 의한 효모의 발효 활성 최적조건 조사Example 2 Investigation of Optimal Conditions for Fermentation Activity of Yeast by Syrup Preparation

정제된 맥아당 대신 실제 빵 생산에 이용이 가능한 저렴한 물엿을 사용하여 맥아당에서와 같이 효모의 발효 활성 증가 효과가 나타내는지를 조사하였다.It was investigated whether yeast fermentation activity was increased as in maltose by using inexpensive starch which can be used for actual bread production instead of purified maltose.

기본적으로 효모의 배양, 전처리 및 발효활성 측정 등은 실시예1에서 사용한 실험 방법과 동일하나, 시약용으로 정제된 맥아당을 효모의 전처리에 사용하는 대신 시중에서 판매되고 있는 식용 물엿(맥아당 55% 함유)을 구매하여 맥아당 원료로 사용하였다.Basically, yeast culture, pretreatment and fermentation activity measurement are the same as the experimental method used in Example 1, but instead of using malt sugar purified for reagents for pretreatment of yeast, commercially available starch syrup (containing 55% malt sugar) ) Was used as a maltose raw material.

고가의 정제된 맥아당 대신에 실제 발효빵 제품 생산에 이용되고 있으며 원료 수급이 용이한 물엿(맥아당 55% 함유)을 사용하여도 정제된 맥아당에서와 같이 효모의 발효 활성 증가 효과가 나타나는지를 조사하였다.Instead of expensive refined maltose, it was used to produce fermented bread products, and it was investigated whether yeast fermentation activity increased as in refined maltose even when starch syrup (containing 55% maltose), which is easy to obtain raw materials, was investigated.

효모를 물엿 YMP 배지로 1.5 시간 전처리 한 다음의 효모 3 %(w/v)의 1 시간 발효에 따른 CO2발생량을 표 3에 나타냈다.Yeast was pretreated with starch syrup YMP medium for 1.5 hours, and the amount of CO 2 generated by fermentation of 3% (w / v) of yeast for 1 hour is shown in Table 3.

<표 3> 물엿 전처리(1.5시간) 후 효모(3%)의 1시간 발효에 따른 CO2발생량. 단위는 ml<Table 3> The amount of CO 2 generated after 1 hour fermentation of yeast (3%) after starch syrup pretreatment (1.5 hours). Unit is ml

실험차수Experiment order 1차Primary 2차Secondary 3차3rd 전처리배지Pretreatment medium 3%MYP3% MYP 물엿(3%맥아당)Starch syrup (3% maltose) GlyEtYPGlyEtYP 3%MYP3% MYP 물엿(3%맥아당)Starch syrup (3% maltose) GlyEtYPGlyEtYP 3%MYP3% MYP 물엿(3%맥아당)Starch syrup (3% maltose) GlyEtYPGlyEtYP CO2발생량CO 2 generation amount 3.53.5 5.75.7 2.22.2 3.83.8 8.28.2 2.62.6 3.83.8 7.07.0 2.52.5

표3에서 볼 수 있듯이 정제된 맥아당보다 더 큰 활성 증가 효과를 보임으로써 정제된 맥아당보다 경제성이 높은 물엿을 효모의 전처리에 효과적으로 사용할 수 있음을 확인하였다.As shown in Table 3, it was confirmed that the economical starch syrup having higher economic efficiency than the purified maltose could be effectively used for pretreatment of yeast by showing a greater activity increase effect than the purified maltose.

<실시예 3> 실제 반죽 조건에서 물엿 전처리 효모의 발효활성Example 3 Fermentation Activity of Starch Pretreated Yeast under Actual Dough Conditions

물엿(맥아당 55%함유) 전처리에 의한 효모의 발효활성 변화가 실제 빵 생산을 위한 반죽조건에서는 어떻게 나타나는지를 분석하기 위하여 빵 제조의 전 과정을 거치며 그 발효활성을 분석하였다.In order to analyze how the change of fermentation activity of yeast by starch syrup (containing 55% malt sugar) pretreatment appears in the kneading conditions for the actual bread production, the fermentation activity was analyzed throughout the whole bread manufacturing process.

물엿 전처리 실험군과 대조군의 두 시료 효모에 대한 발효활성의 비교는 반죽 발효과정에 가스제거 단계가 포함되기 때문에 CO2기체 발생량으로는 비교가 어려우므로, 이와 비례적으로 나타나는 결과로 볼 수 있는 굽기 과정을 거쳐 완성된 빵의 부피 변화를 측정함으로써 발효활성을 평가하였다.The comparison of fermentation activity of the two yeasts of the syrup pretreatment experimental group and the control group is difficult to compare with the amount of CO 2 gas generated since the dough fermentation process involves the degassing step. Fermentation activity was evaluated by measuring the volume change of the finished bread through.

빵의 제조과정은 효모의 물엿 전처리 → 1차 반죽 → 1차 발효 → 2차 반죽→ 2차 발효 → 굽기 단계로 수행되었으며 각 단계의 실험조건은 다음과 같았다.The manufacturing process of bread was carried out in the yeast syrup pretreatment → primary dough → primary fermentation → secondary dough → secondary fermentation → baking step, and the experimental conditions of each step were as follows.

(1) 효모의 물엿 전처리(1) Yeast syrup pretreatment

효모 전처리 과정은 실제 생산공정의 물리적인 효율을 감안하여 최종적으로 2% 맥아당의 농도가 되도록 하였고 전처리 조건은 실시예1에서 확인된 조건과 동일하게 30℃에서 1.5∼2.5 시간 처리방법을 이용하였다.The yeast pretreatment process was finally made to have a concentration of 2% maltose in consideration of the physical efficiency of the actual production process and the pretreatment conditions were used for 1.5 to 2.5 hours at 30 ℃ the same conditions as confirmed in Example 1.

실험 대조군으로는 4℃에 보관된 효모를 그대로 사용하였으며 이와 조건을 맞추기 위해 전처리 된 효모 역시 반죽에 투입되기 전에 2시간 이상 4℃로 유지시킨 후 사용하였다.As the experimental control, the yeast stored at 4 ° C. was used as it was, and the pretreated yeast was also used after maintaining at 4 ° C. for 2 hours or more before being put into dough.

(2) 1차 반죽 및 발효(2) primary dough and fermentation

표 4에 나타낸 대로 1차 반죽 재료를 모두 섞은 후 온도를 26℃로 유지하며 저속으로 3분, 고속으로 2분 혼합하여 반죽을 제조하였다. 1차 발효는 27℃, 77% 습도로 유지시킨 발효기에서 2시간 동안 발효시켰다.After mixing all the primary dough material as shown in Table 4, the temperature was maintained at 26 ℃ to prepare a dough by mixing for 3 minutes at low speed, 2 minutes at high speed. The primary fermentation was fermented for 2 hours in a fermentor maintained at 27 ° C., 77% humidity.

(3) 2차 반죽 및 발효(3) secondary dough and fermentation

표 4에 나타낸 대로 2차 반죽 재료를 발효된 1차 반죽에 모두 추가한 후 온도를 28℃로 유지하며 저속으로 3분, 고속으로 7분 혼합하여 반죽을 완료하고, 20분 동안 상온에 방치한 다음 밀대를 이용하여 가스를 제거해 준 후 알루미늄 용기에 옮겨 성형하였다.After adding all of the secondary dough material to the fermented primary dough as shown in Table 4, the temperature is maintained at 28 ℃ and mixed for 3 minutes at low speed, 7 minutes at high speed to complete the dough, and left at room temperature for 20 minutes Next, the gas was removed using a rod and then transferred to an aluminum container for molding.

2차 발효는 39℃, 80% 습도로 유지시킨 발효기에서 40분 동안 발효시켰다.Secondary fermentation was fermented for 40 minutes in a fermentor maintained at 39 ° C., 80% humidity.

(4) 굽기(4) burning

알루미늄 용기에 성형된 채로 2차 발효가 끝난 반죽을 190℃ 오븐에서 20분 동안 구워낸 후 상온에서 냉각시켜 빵 제조를 완료하였다.Baking the secondary fermented dough in an aluminum container after baking for 20 minutes in an oven at 190 ℃ and cooled to room temperature to complete the bread production.

<표 4> 반죽 재료의 조성비.TABLE 4 Composition ratios of dough materials.

재료반죽Dough 강력분Strong 설탕Sugar YeastYeast YeastFoodYeastfood 유지maintain 물엿corn syrup 소금Salt water 1차 반죽Primary dough 660660 150150 3030 1.321.32 -- -- -- 440440 2차 반죽Secondary dough 220220 2626 -- -- 114.4114.4 4.44.4 11.4411.44 4444

반죽공정을 완료한 후 굽기 과정을 거쳐 완성된 빵의 부피를 측정하는 방법은 상당히 재현성이 있는 결과를 제시하는 것으로 나타났다.The method of measuring the volume of the finished bread after the completion of the kneading process has been shown to give fairly reproducible results.

그 결과를 표5에 나타냈다.The results are shown in Table 5.

<표 5> 물엿 전처리에 따른 완성된 빵의 부피 변화<Table 5> Volume change of finished bread according to syrup pretreatment

실험차수Experiment order 1차Primary 2차Secondary 3차3rd 시료번호Sample Number 1One 22 33 평균Average 1One 22 33 평균Average 1One 22 33 평균Average 물엿 전처리군(a) 시료 부피(ml)Starch pretreatment group (a) Sample volume (ml) 425425 430430 445445 433433 375375 375375 415415 388388 380380 400400 410410 397397 대조군(b)시료 부피(ml)Control (b) Sample Volume (ml) 370370 405405 390390 388388 340340 355355 355355 350350 350350 360360 370370 360360 부피 증가율(a/b)Volume increase rate (a / b) 112%112% 111%111% 110%110%

표 5에서 볼 수 있듯이 3중 실험으로 3회에 걸쳐 수행한 부피 측정의 결과는 물엿으로 전처리한 효모의 발효에 의해 11% 정도의 부피 증가가 일정하게 나타나는 것을 확인할 수 있었다.As can be seen in Table 5, the results of the volume measurement performed three times in a triple experiment showed that the volume increase of about 11% was constant by fermentation of yeast pretreated with syrup.

이 같은 결과는 시중에서 저렴하게 판매되고 있는 물엿으로 효모를 전처리하여 빵 반죽의 발효를 향상시키는 것을 보여준다.These results show that pretreatment of yeast with starch syrup sold at low cost improves the fermentation of bread dough.

또한, 물엿으로 전처리한 효모는 수 일 동안은 저장하여 사용하는 것이 가능하므로 기존의 제품 생산 체제에서와 같이 효모의 사전 비축 및 적기 공급에 문제가 없다.In addition, yeast pretreated with starch syrup can be stored and used for several days, so there is no problem in pre-stocking and timely supply of yeast as in the existing product production system.

통상의 효모를 고농도 맥아당 배지에서 전처리하여 맥아당 발효 효소의 유전자 발현을 향상시키고, 이 효모를 사용하여 빵을 만들므로써, 발효율을 향상시키고, 좋은 품질의 빵을 만들며, 물엿을 이용한 배지로 처리시 원가를 절감하는 효과도 가져다 준다.The conventional yeast is pretreated in a high concentration of maltose medium to improve the gene expression of the maltose fermentation enzyme, and the bread is made using this yeast to improve the efficiency of the paw, to make a good quality bread, and to treat with medium using starch syrup. It also reduces the cost.

Claims (2)

제빵용으로 사용하고 있는 통상의 효모(Saccharomyces cerevisiae)를 2 ~ 5 % 맥아당 MYP( 2~5 % maltose, 0.5 % yeast extract, 1 % peptone, 0.3 % KH2PO4) 배지에서 1.5 ~ 2.5 시간 처리하여, 맥아당 발효에 관여하는 효소 유전자의 발현을 사전에 유도한 다음, 이 전처리 효모를 빵 제조용 반죽에 첨가하여 빵을 제조하는 방법.Conventional yeast ( Saccharomyces cerevisiae ) used for baking is treated for 2-5% malt in MYP (2-5% maltose, 0.5% yeast extract, 1% peptone, 0.3% KH 2 PO 4 ) medium for 1.5-2.5 hours By inducing expression of an enzyme gene involved in maltose fermentation in advance, and then adding this pre-treated yeast to bread dough to make bread. 제1항에 있어서, 2 ~ 5 % 맥아당 MYP 배지는 물엿으로 만든 것이 특징인 빵을 제조하는 방법.The method of claim 1, wherein the 2-5% maltose MYP medium is made of starch syrup.
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WO2009147154A1 (en) * 2008-06-03 2009-12-10 Ernst Böcker Gmbh & Co. Kg Single-stage baked goods production
KR102492177B1 (en) 2022-07-29 2023-01-27 임성철 Method for producing natural fermented species
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