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 carbon monoxide dissolution device for producing hydrogen using anaerobic microorganisms is provided to help hydrogen-producing anaerobic microorganisms to effectively use carbon monoxides when hydrogen is produced, thereby enhancing hydrogen production efficiency. CONSTITUTION: A carbon monoxide dissolution device (100) for producing hydrogen using anaerobic microorganisms comprises: a main body (110) with an opening (111); tube cassettes (120) which have a tube for allowing a culture medium containing hydrogen-producing anaerobic microorganisms and carbon monoxides to pass; and a fitting member (130) which provides a delayed path for delaying time for dissolving the carbon monoxides. The tubes have supply ports (123) and outlets (124) by connecting the tubes between the tube cassettes. The both ends of the tubes are exposed to the outside to help the tube to be connected to other tubes. [Reference numerals] (230) Carbon monoxide supplying unit; (240) Hydrogen collecting unit; (250) Cooling unit; (260) Culture medium supplying unit
Abstract:
본 발명은 신규한 나이트릴레이즈 및 이의 용도에 관한 것으로, 보다 구체적으로, 본 발명은 서열번호 1, 서열번호 3, 서열번호 5 및 서열번호 7로 이루어진 군에서 선택되는 아미노산 서열로 나타내는 나이트릴레이즈를 나이트릴 기질과 반응시키는 단계를 포함하는 카르복실산을 제조하는 방법, 및 상기 나이트릴레이즈를 포함하는 카르복실산 제조용 생촉매 조성물에 관한 것이다.
Abstract:
PURPOSE: A novel nitrilase and a method for preparing carboxylic acid using the same are provided to enable biosynthesis of carboxylic acid with high efficiency. CONSTITUTION: A method for preapring carboxylic acid comprises: a step of preparing nitrilase VMN1 of sequence number 7 amino acid sequence or a biocatalyst composition containing nitrilase VMN1; and a step of reacting nitrilase VMN1 or the biocatalyst composition with nitrile substrate. The biocatalyst composition contains cells containing nitrilase VMN1 or cell culture or crushed material thereof. The nitrile substrate includes acetonitrile, acrylonitrile, adiponitrile, benzonitrile, butyronitrile, 4-chlorobenzonitrile, or mandelonitrile. A biocatalyst composition for preparing carboxylic acid contains nitrilase VMN1.
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).
Abstract:
PURPOSE: A method for producing hydrogen using hydrogenase isolated from Thermococcus spp. is provided to cheaply and efficiently produce hydrogen even at high temperature. CONSTITUTION: A hydrogenase contains an amino acid sequence of sequence number 7. A gene encoding the hydrogenase contains a base sequence of sequence number 18. A method for producing hydrogen from Thermococcus spp. comprises: a step of preparing a medium; a step of culturing Thermococcus spp. in the medium at 80°C under the anaerobic condition; and a step of isolating hydrogen. The Thermococcus spp. is Thermococcus onnurineus NA1(deposit number: KCTC 10859BP). The medium contains formate.
Abstract:
PURPOSE: A novel hydrogenase isolated from Thermococcus sp. and a method for producing hydrogen using the same are provided to produce a large amount of hydrogen even at high temperature. CONSTITUTION: A hydrogenase has an amino acid sequence selected from sequence numbers 1-8. A gene encoding the hydrogenase contains a base sequence selected from sequence numbers 12-19. A method for producing hydrogen from Thermococcus spp. comprises: a step of preparing a medium; a step of culturing Thermococcus spp. in a culture container; and a step of isolating hydrogen from culture container. The Thermococcus spp. is Thermococcus onnurineus NA1(deposit number: KCTC 10859BP). The medium contains carbon monoxide, alkyl formate, or starch. The culture is performed at 80°C and under anaerobic condition.
Abstract:
PURPOSE: A novel epoxide hydrolase is provided to hydrolyze non-degradable epoxide and to attenuate SO cytotoxicity. CONSTITUTION: An expoxide hydrolase has an amino acid sequence of sequence number 1. A method for preparing the epoxide hydrolase comprises: a step of inserting a gene encoding the epoxide hydrolase to an expression vector to prepare a recombinant vector; a step of introducing the recombinant vector to a host cell for overexpression; and a step of isolating and purifying the overexpressed apoxide hydrolase. The epoxy substrate is non-degradable epoxide substrate, styrene 7,8-oxide.