KR100227001B1 - Method for producing fermentation food from grain starch - Google Patents
Method for producing fermentation food from grain starch Download PDFInfo
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- 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
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- starch
- fermentation
- raw material
- bifidobacterium
- producing
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- 229920002472 Starch Polymers 0.000 title claims abstract description 58
- 239000008107 starch Substances 0.000 title claims abstract description 58
- 235000019698 starch Nutrition 0.000 title claims abstract description 58
- 238000000855 fermentation Methods 0.000 title abstract description 50
- 230000004151 fermentation Effects 0.000 title abstract description 50
- 238000004519 manufacturing process Methods 0.000 title abstract description 17
- 235000013305 food Nutrition 0.000 title description 8
- 239000002994 raw material Substances 0.000 claims abstract description 46
- 241000186000 Bifidobacterium Species 0.000 claims abstract description 35
- 238000000034 method Methods 0.000 claims abstract description 20
- 235000021107 fermented food Nutrition 0.000 claims abstract description 14
- 239000004382 Amylase Substances 0.000 claims abstract description 12
- 102000013142 Amylases Human genes 0.000 claims abstract description 12
- 108010065511 Amylases Proteins 0.000 claims abstract description 12
- 235000019418 amylase Nutrition 0.000 claims abstract description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 7
- 240000007594 Oryza sativa Species 0.000 claims description 12
- 235000007164 Oryza sativa Nutrition 0.000 claims description 12
- 235000009566 rice Nutrition 0.000 claims description 12
- 238000010438 heat treatment Methods 0.000 claims description 3
- 235000014443 Pyrus communis Nutrition 0.000 claims 1
- 235000013339 cereals Nutrition 0.000 claims 1
- 239000005445 natural material Substances 0.000 claims 1
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 abstract description 26
- 239000004310 lactic acid Substances 0.000 abstract description 13
- 235000014655 lactic acid Nutrition 0.000 abstract description 13
- 230000008569 process Effects 0.000 abstract description 6
- 241000894006 Bacteria Species 0.000 abstract description 5
- 230000013595 glycosylation Effects 0.000 abstract description 4
- 238000006206 glycosylation reaction Methods 0.000 abstract description 4
- 239000000047 product Substances 0.000 description 12
- 239000000796 flavoring agent Substances 0.000 description 8
- 235000019634 flavors Nutrition 0.000 description 8
- 239000000243 solution Substances 0.000 description 8
- 241000186660 Lactobacillus Species 0.000 description 7
- 229940039696 lactobacillus Drugs 0.000 description 7
- 241000194017 Streptococcus Species 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 6
- 229940041514 candida albicans extract Drugs 0.000 description 5
- 235000013399 edible fruits Nutrition 0.000 description 5
- 235000012055 fruits and vegetables Nutrition 0.000 description 5
- 239000012138 yeast extract Substances 0.000 description 5
- 239000002609 medium Substances 0.000 description 4
- 230000000704 physical effect Effects 0.000 description 4
- 235000016709 nutrition Nutrition 0.000 description 3
- 230000035764 nutrition Effects 0.000 description 3
- 235000013311 vegetables Nutrition 0.000 description 3
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 2
- GUBGYTABKSRVRQ-XLOQQCSPSA-N Alpha-Lactose Chemical compound O[C@@H]1[C@@H](O)[C@@H](O)[C@@H](CO)O[C@H]1O[C@@H]1[C@@H](CO)O[C@H](O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-XLOQQCSPSA-N 0.000 description 2
- 240000008067 Cucumis sativus Species 0.000 description 2
- 235000009849 Cucumis sativus Nutrition 0.000 description 2
- 244000000626 Daucus carota Species 0.000 description 2
- 235000002767 Daucus carota Nutrition 0.000 description 2
- 108090000790 Enzymes Proteins 0.000 description 2
- 102000004190 Enzymes Human genes 0.000 description 2
- 108010010803 Gelatin Proteins 0.000 description 2
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 2
- 244000068988 Glycine max Species 0.000 description 2
- 235000010469 Glycine max Nutrition 0.000 description 2
- GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 2
- 244000070406 Malus silvestris Species 0.000 description 2
- 241000220324 Pyrus Species 0.000 description 2
- 230000003625 amylolytic effect Effects 0.000 description 2
- 235000021016 apples Nutrition 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 235000015203 fruit juice Nutrition 0.000 description 2
- 239000008273 gelatin Substances 0.000 description 2
- 229920000159 gelatin Polymers 0.000 description 2
- 235000019322 gelatine Nutrition 0.000 description 2
- 235000011852 gelatine desserts Nutrition 0.000 description 2
- 239000008103 glucose Substances 0.000 description 2
- 238000011081 inoculation Methods 0.000 description 2
- 229910052740 iodine Inorganic materials 0.000 description 2
- 239000011630 iodine Substances 0.000 description 2
- 239000008101 lactose Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 235000021017 pears Nutrition 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 235000000346 sugar Nutrition 0.000 description 2
- 239000006228 supernatant Substances 0.000 description 2
- OWEGMIWEEQEYGQ-UHFFFAOYSA-N 100676-05-9 Natural products OC1C(O)C(O)C(CO)OC1OCC1C(O)C(O)C(O)C(OC2C(OC(O)C(O)C2O)CO)O1 OWEGMIWEEQEYGQ-UHFFFAOYSA-N 0.000 description 1
- 229920001817 Agar Polymers 0.000 description 1
- 229920000856 Amylose Polymers 0.000 description 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- 241000193830 Bacillus <bacterium> Species 0.000 description 1
- 206010010774 Constipation Diseases 0.000 description 1
- 206010012735 Diarrhoea Diseases 0.000 description 1
- GUBGYTABKSRVRQ-PICCSMPSSA-N Maltose Natural products O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1O[C@@H]1[C@@H](CO)OC(O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-PICCSMPSSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 241000194020 Streptococcus thermophilus Species 0.000 description 1
- 235000021307 Triticum Nutrition 0.000 description 1
- 244000098338 Triticum aestivum Species 0.000 description 1
- 235000010716 Vigna mungo Nutrition 0.000 description 1
- 240000001417 Vigna umbellata Species 0.000 description 1
- 235000011453 Vigna umbellata Nutrition 0.000 description 1
- 240000008042 Zea mays Species 0.000 description 1
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 239000008272 agar Substances 0.000 description 1
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 1
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 1
- 235000011130 ammonium sulphate Nutrition 0.000 description 1
- 239000003242 anti bacterial agent Substances 0.000 description 1
- 229940088710 antibiotic agent Drugs 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 235000005822 corn Nutrition 0.000 description 1
- XUJNEKJLAYXESH-UHFFFAOYSA-N cysteine Natural products SCC(N)C(O)=O XUJNEKJLAYXESH-UHFFFAOYSA-N 0.000 description 1
- 235000018417 cysteine Nutrition 0.000 description 1
- 235000013365 dairy product Nutrition 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 238000006911 enzymatic reaction Methods 0.000 description 1
- 230000002550 fecal effect Effects 0.000 description 1
- 210000003608 fece Anatomy 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 235000011389 fruit/vegetable juice Nutrition 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- 150000004676 glycans Chemical class 0.000 description 1
- 239000001963 growth medium Substances 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 235000021109 kimchi Nutrition 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 229930014626 natural product Natural products 0.000 description 1
- 229920001542 oligosaccharide Polymers 0.000 description 1
- 150000002482 oligosaccharides Chemical class 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 108010004621 phosphoketolase Proteins 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 108010009004 proteose-peptone Proteins 0.000 description 1
- 239000007974 sodium acetate buffer Substances 0.000 description 1
- JXKPEJDQGNYQSM-UHFFFAOYSA-M sodium propionate Chemical compound [Na+].CCC([O-])=O JXKPEJDQGNYQSM-UHFFFAOYSA-M 0.000 description 1
- 239000004324 sodium propionate Substances 0.000 description 1
- 235000010334 sodium propionate Nutrition 0.000 description 1
- 229960003212 sodium propionate Drugs 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 150000008163 sugars Chemical class 0.000 description 1
- 108010050327 trypticase-soy broth Proteins 0.000 description 1
- 235000013618 yogurt Nutrition 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, 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
- A23L7/00—Cereal-derived products; Malt products; Preparation or treatment thereof
- A23L7/10—Cereal-derived products
- A23L7/104—Fermentation of farinaceous cereal or cereal material; Addition of enzymes or microorganisms
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
- A23V2002/00—Food compositions, function of food ingredients or processes for food or foodstuffs
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
- A23V2250/00—Food ingredients
- A23V2250/50—Polysaccharides, gums
- A23V2250/51—Polysaccharide
- A23V2250/5118—Starch
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
- A23V2400/00—Lactic or propionic acid bacteria
- A23V2400/51—Bifidobacterium
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
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.
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