Abstract:
separating chromosome DNA from Corynebacterium glutamicum KCTC 1445; partly cutting it into constrained enzyme; obtaining gene library of the Corynebacterium glutamicum by adopting colitis germs as a host; and cloning into plasmid pCTS3(KCTC 85729) among the library. It is useful for amino acid fermentation.
Abstract:
본 발명은 신균주 바실러스 속 (Bacillus sp.) NS-70(KCTC 8555P)와 이를 이용하여 발효 소요시간이 짧고, 특히 물에 친화력이 낮은 단백질 기질에서 잘 작용하여 식품 및 제약산업등에 유용하게 사용할 수 있는 신규한 단백질 가수분해효소를 제조하는 방법에 관한 것이다.
Abstract:
A method for culturing lactobacillus spp. TSC-66 comprises: (a) culturing lactobacillus spp. TSC-66 (KCTC 8447P) in the culture medium at 30 deg.C for 6-24hrs to obtain the starter; (b) innoculating the obtd. starter the medium, and culturing at 30-40 deg.C with shaking (60-250 rpm) and pouring into air or N2 gas (0.3-0.5 vvm) for 10-48hrs; (c) centrifuging or ultra filtrating the culture broth to obtain the cell. The cell, culture broth, etc is useful as fermenting agent for fermented milk, fermented cream, or pordn. of Kimchi, and additive for feed.
Abstract:
PURPOSE: A novel catabolism control protein(CcpA) and DNA encoding the same are provided which induce a mutation discharging a catabolism repression phenotype, so it can be useful to construct the mutant which produces a hydrolysis enzyme regardless of a sugar composite ion in a fermentative medium. CONSTITUTION: Provided are a CcpA, DNA sequence encoding the same and a strong promoter thereof which is an inhibitory factor of enzyme production. DNA encoding the CcpA is described by SEQ ID NO. 1 and purified from Thermoactinomyces sp.. The CcpA is concerned in a catabolism repression as an inhibitory factor of enzyme production and regulates the synthesis of protein hydrolysis enzyme.
Abstract translation:目的:提供一种新型的分解代谢控制蛋白(CcpA)和编码该DNA的DNA,其诱导排斥分解代谢阻遏表型的突变体,因此构建不产生糖复合离子的水解酶的突变体是有用的 中。 构成:提供了编码该酶的CcpA,DNA序列和作为酶生产的抑制因子的强启动子。 编码CcpA的DNA由SEQ ID NO: 1并从Thermoactinomyces sp。中纯化.CcpA涉及分解代谢抑制作为酶生产的抑制因子并调节蛋白质水解酶的合成。
Abstract:
본 발명은 고온균 유래의 내열성 β-타이로시네이즈 유전자를 포함하는 발현벡터로 형질전환된 재조합 대장균 JM105/pHLT1(KCTC 0158BP)을 배양하여 수득한 내열성 β-타이로시네이즈를 이용하여 페놀 함유 폐수 중의 페놀을 타이로신으로 전환시켜 침전시키는 단계를 포함하는, 페놀 함유 폐수로부터 페놀을 제거하는 방법에 관한 것으로, 본 발명의 방법에 따르면 10,000ppm 이상의 고농도의 페놀을 함유한 폐수 중의 페놀 농도를 1,000ppm 이하로 저하시킬 수 있다.
Abstract:
PSEUDOMONAS SP. NS-83(KCTC 8600P) AND production of novel protein hydrolysis enzyme is disclosed in this invention. PSEUDOMONAS SP. NS-83(KCTC 8600P) is injected in PH6-8 of medium made by polypepton, extract of enzyme, extract of cow meat, glycol, KH2PO4, K2HPO4, MgSO4.7H2O and NaCl, cultivated for 6 hours at 35-40 degree Celsius. Thereafter, above-cultivated liquid is fermented in medium made by aqueous starch, phytonpepton, KH2PO4, K2HPO4, MgSO4.7H2O and NaCl, for 15 hours at 50 degree Celsius to produce protein hydrolysis enzyme having characteristics below; molecular weight : 32,000 dalton, optimum pH : 8.0, optimum temperature : 60deg.C.