Abstract:
Provided is lipase and esterase isolated from deep sea mass-produced by genes coding the lipase and esterase. An esterase gene codes esterase having amino acid sequence of SEQ ID:NO 2, 4, 6, 10, 14, 16, 18, 20, 22, 24, 26, 28, 30, 32 or 34. A method for preparing the esterase comprises the following steps of: cultivating a transformed cell with a recombinant vector; and isolating the esterase from the cultivated cells. The recombinant vector includes sequence number of 1, 3, 5, 9, 13, 15, 17, 19, 21, 23, 25, 27, 29, 31 or 33. The lipase gene codes lipase having amino acid sequence of SEQ ID:NO 8 or 12. The method for preparing the lipase consists of the following steps of: cultivating a transformed cell with a recombinant vector; and isolating the lipase from the cultivated cells. The recombinant vector has sequence number of 7 or 11.
Abstract translation:提供从通过编码脂肪酶和酯酶的基因产生的深海分离的脂肪酶和酯酶。 酯酶基因编码具有SEQ ID NO:2,4,6,10,14,16,18,20,22,24,26,28,30,32或34的氨基酸序列的酯酶。制备酯酶的方法 包括以下步骤:用重组载体培养转化的细胞; 并从培养的细胞中分离酯酶。 重组载体包含序列号1,3,5,9,13,15,17,19,21,23,25,27,29,31或33.脂肪酶基因编码具有SEQ ID NO:1的氨基酸序列的脂肪酶, NO 8或12.制备脂肪酶的方法包括以下步骤:用重组载体培养转化的细胞; 并从培养的细胞中分离脂肪酶。 重组载体的序列号为7或11。
Abstract:
본 발명은 신규의 에스터라제 및 이를 암호화하는 유전자, 및 이를 이용한 에스터라제 생산방법에 관한 것으로, 본 발명에 따른 에스터라제는 고온에서도 높은 활성을 나타내고, 높은 pH에서도 에스터라제 활성이 있다. 따라서 본 발명에 따른 에스터라제는 세제, 식품 및 의약품 생산에 유용하게 활용될 수 있다.
Abstract:
본 발명은 심해 해저에서 분리된 리파제 및 에스터라제 효소 및 이의 제조방법에 관한 것으로서, 서남태평양 해역(남위 3°89′, 동경 152°49′) 깊이 1,400 미터에 이르는 심해 퇴적물, 북극 다산기지 주변 연안 퇴적물, 강화도 갯벌 퇴적물로부터 구축된 메타게놈 라이브러리를 대상으로 분리한 신규 리파제 및 에스터라제 효소, 이들을 암호화 하는 유전자 및 리파제 및 에스터라제 효소 생산방법을 제공한다. 리파제, 에스터라제
Abstract:
The present invention relates to a Thermococcus onnurineus NA1 mutant having improved hydrogen producibility from formate and a method for producing hydrogen using the same. According to the present, the mutated Thermococcus onnurineus NA1 has improved hydrogen producibility in a medium including formate rather than a wild type, and improved growth velocity compared to the wild type. If a strain according to the present invention is used, hydrogen can be produced from formic acid at high efficiency.
Abstract:
The present invention relates to novel amidase, a gene encoding thereof, and a production method of caprolactam by using the amidase and the gene. The amidase of the present invention is capable of producing alpha-amino-epsilon-caprolactam from lysine. The alpha-amino-epsilon-caprolactam is a material for nylon and is internationally mass-produced. Therefore, the present invention provides a novel method of producing the alpha-amino-epsilon-caprolactam which is an environmentally friendly material for nylon.
Abstract:
The present invention relates to novel hydrogenases separated from new hyperthermophilic strains belonging to Thermococcus genus, genes encoding the same, and a method for producing hydrogen using the same. According to a method for producing hydrogen of the present invention, a large amount of hydrogen can be produced by culturing the strains in a specific culture condition and therefore, it is more economical and effective compared to the existing method for producing hydrogen and hydrogen can be produced at a high temperature.
Abstract:
The present invention relates to novel hydrogenases separated from new hyperthermophilic strains belonging to Thermococcus genus, genes encoding the same, and a method for producing hydrogen using the same. According to a method for producing hydrogen of the present invention, a large amount of hydrogen can be produced by culturing the strains in a specific culture condition and therefore, it is more economical and effective compared to the existing method for producing hydrogen and hydrogen can be produced at a high temperature.
Abstract:
PURPOSE: A DNA polymerase F7 and genes thereof are provided to enhance elongation and processivity and to be used in PCR. CONSTITUTION: A DNA polymerase F7 contains an amino acid sequence of sequence number 2. A DNA polymerase F7 gene encoding an amino acid sequence of sequence number 2 contains a base of sequence number 1. A recombinant vector contains the polymerase F7 gene of sequence number 1. A host cell is transformed with the recombinant vector containing the DNA polymerase F7 gene.
Abstract:
PURPOSE: A novel hydrogenase isolated from Thermococcus spp. and a method for producing hydrogen using the same are provided to produce hydrogen without high temperature and pressure. CONSTITUTION: A hydrogenase contains an amino acid sequence of sequence number 5. A gene encoding the hydrogenase contains a base sequence of sequence number 16. A method for producing hydrogen from Thermococcus spp. comprises: a step of preparing a medium; a step of culturing Thermococcus spp. in the medium; and a step of isolating hydrogen. The medium contains carbon monoxide. The Thermococcus spp. is Thermococcus onnurineus NA1(deposit number: KCTC 10859BP).