Abstract:
The present invention relates to a vector. More specifically, the vector is replicated by using a corynebacterium or colon bacterium and used in various cloning process. The vector according to an embodiment of the present invention can be used to observe the transcription induction activation process of promoters in the corynebacterium or produce a product of a target gene. The vector includes a nucleotide sequence of SEQ ID NO. 1 and a multiple cloning site (MCS) of SEQ ID NO. 2.
Abstract translation:本发明涉及载体。 更具体地,通过使用棒状杆菌或结肠细菌复制载体并用于各种克隆过程。 根据本发明实施方案的载体可用于观察棒状杆菌中启动子的转录诱导活化过程或产生靶基因的产物。 载体包含SEQ ID NO:1的核苷酸序列。 1和SEQ ID NO:1的多克隆位点(MCS)。 2。
Abstract:
The present invention relates to: a promoter specific homologous part which is homologous with a part of the promoter of a target gene; a marker gene which is connected with the promoter specific homologous part in order to be able to operate; a cassette, for causing a defect of the target gene, which is connected to the downstream of the marker gene and includes a gene specific homologous part which is homologous with at least one target gene; and a gene manipulation method which uses the cassette. The efficient gene manipulation and selection of a cell are possible by using the cassette and the gene manipulation method using the cassette.
Abstract:
An embodiment relates to a metabolic network model for analyzing metabolic characteristics of Kluyveromyces marxianus microorganisms for producing 3HP and to metabolic characteristic analysis of Kluyveromyces marxianus using the same. More specifically, the present invention relates to building metabolic network model of the Kluyveromyces marxianus using gene-protein-biochemistry reaction relationship, to analysis of metabolic characteristics of metabolic flux using the model, and to a method for predicting a novel metabolic path which enhances production capacity of the 3HP using simulation based on metabolic flux. The method of an embodiment can efficiently predict cell growth speed and production of microorganisms, save time and costs for optimizing the novel path, and provide variant microorganisms which can produce specific metabolites with high efficiency.
Abstract:
The present invention relates to a modified microorganism for the highly efficient production of 1,4-butanediol, and a production method of 1,4-butanediol using the modified microorganism. The modified microorganism has improved tolerance against 1,4-butanediol by the loss or destruction of a gene encoding more than one selected from the group consisting of a transcriptional regulatory factor NCgl2886, GCN5-related N-acetyl transferase NCgl2090, hypothetical protein NCgl0224, and sugar phosphate isomerase/epimerase NCgl2956; and enables users to produce 1,4-butanediol in high efficiency even under the presence of the high concentration of 1,4-butanediol.
Abstract:
PURPOSE: A solid lipid nanoparticle is provided to offer an effective method for transferring an active ingredient to the target site of body. CONSTITUTION: A solid lipid nanoparticle comprises an elastin-like polypeptide in which the moiety having hydrophobic group is bound and lipid molecule. The moiety having hydrophobic group is the saturated or unsaturated hydrocarbon group, the saturated or unsaturated acyl group, the saturated or unsaturated amide group, or the saturated or unsaturated alkoxy group. The lipid molecule is neutral lipid molecule or amphiphilic lipid molecule. The elastic-like polypeptide includes more than one repeat unit selected from among VPGXG, PGXGV, GXGVP, XGVPG, GVPGX, and a group comprised of combination thoseof more than once. The V, P, G, and X is respectively means valine, proline, glycine, and an amino acid which is not proline. [Reference numerals] (AA) Coefficient
Abstract:
PURPOSE: A liposome containing elastin-like polypeptide and cancer cell targeting material is provided to offer an effective method for transferring an active ingredient to the target site of body. CONSTITUTION: A liposome comprises: a lipid bilayer; an elastin-like polypeptide in which the moiety having hydrophobic group is bound; and a lipid bilayer stabilizer. The moiety having hydrophobic group is filled in the lipid bilayer. A first lipid molecule combining with cancer cell targeting material is included in the lipid bilayer. [Reference numerals] (AA) DOX discharge (%); (BB) Temperature (°C)
Abstract:
본발명에따른피부임피던스측정센서는, 사용자피부에접촉되는 R 전극(Reference Electrode)과 C 전극(Current Carrying Electrode); 및상기 R 전극및 상기 C 전극사이에흐르는전류의임피던스(Impedance)를측정하는 M 전극(Measuring Electrode)을포함하고, 상기 M 전극은상기 R 전극및 상기 C 전극에대해단차를갖는것을특징으로한다.
Abstract:
PURPOSE: An isolated protein and a composition containing the same for enhancing polysaccharide hydrolase activity are provided to enhance hydrolysis ability and to reduce the use of hydrolase. CONSTITUTION: An isolated protein enhances polysaccharide hydrolase activity and has polysaccharide binding ability. The protein contains GH45(glycoside hydrolase 45) or pollen-allergen domain. The polysaccharide hydrolase is cellulase, hemicellulase, alpha-amylase, glycoamylase, pectinase, xylanase, or cellobiase. The GH45 domain or pollen allergen domain is isolated from expansin, expansin-like protein, or bacterial protein.
Abstract:
PURPOSE: A pretreatment method of a biomass using internal heat is provided to induce heating reaction and to enhance pretreatment efficiency. CONSTITUTION: A pretreatment method of a biomass using internal heat comprises a step of adding water-reactive anhydride to the biomass for internal heat reaction. The biomass is lignocellulose biomass or macroalgae biomass. The water-reactive anhydride is alkaline gas and acidic gas. The water-reactive anhydride is anhyudrous ammonia, hydrogen sulfide(H_2S), anhydrous hydrochloride(HCl), phosphorus pentoxide (P_2O_5), the carbon dioxide (CO_2), or mixture thereof.
Abstract:
PURPOSE: A wave sensor with a gas removing unit, and a method for detecting a target material in a liquid sample are provided to effectively detect a target material within a liquid sample. CONSTITUTION: A method for detecting a target material in a liquid sample is as follows: A wave signal is offered to a standard liquid sample which not comprises a target material. And the wave signal is measured from the standard liquid sample. The measured signal is a base value, and offered to a target liquid sample which comprises the target material. A wave signal is measured from the target liquid sample. The target material is detected from the measured wave signal.