Abstract:
PURPOSE: A Lactococcus lactis NK34 for producing bacteriocin lacticin NK34 having antibacterial effect to bovine mastitis bacteria is provided to replace antibiotics and to produce a large amount of lacticin NK34. CONSTITUTION: A Lactococcus lactis NK34 strain is purely cultured in MRS medium and produces bacteriocin lacticin NK34 having an effect of suppressing bovine mastitis causing bacteria. The Lactococcus lactis NK34 KFCC 11458P is cultured in a medium containing sucrose, tryptone, yeast extract, tween 80, sodium acetate, and NaCl. A medium composition for culturing Lactococcus lactis NK34 KFCC 11458P or performing biosynthesis of bacteriocin lactinic NK34 contains sucrose, tryptone, yeast extract, tween 80, sodium acetate, and NaCl.
Abstract:
PURPOSE: A bacteriocin which is derived from Lactococcus lactis NK34 KFCC 11458P and a therapeutic agent for breast cancer using the same are provided to ensure antibacterial activity and to be used as an antibiotic substitute. CONSTITUTION: A Lactcin NK34 enzyme is isolated from Lactococcus lactis NK34 KFCC 11458P and is used for treating breast cancer of dairy cattle. The Lacticin NK34 has an antibacterial effect to S. uberis E290, S. agalactiae ATCC 13813, E. gallinarum E362, E. faecium E363, E. faecium E374 and P. autotrophica KCTC 9455. A method for isolating bacteriocin Lacticin NK34 enzyme comprises: a step of isolating and culturing using a strain; a step of measuring antibacterial activity of the bacteriocin; a step of researching the characteristics of Lactin NK 34 enzyme; and a step of measuring antibacterial effects to a breast cancer pathogenic bacteria.
Abstract:
A bacteriolysis extract of Saccharomyces chevalieri is provided to increase the activation of neutrophil and enhance non-specific defense activity against the pathogenic bacteria. An immune enhancer, vaccine adjuvant, adjuvant treating agent or feed additive comprises bacteriolysis extract of Saccharomyces chevalieri as an active ingredient. A method for manufacturing a bacteriolysis extract of Saccharomyces chevalieri comprises: a step of culturing Saccharomyces chevalieri in media at 26°C for 72 hours; a step of centrifuging media and suspending in PBS; a step of adding dissolution agent and treating at room temperature for 2-3 days; a step of confirming the dissolution status with a microscope; a step of adjusting pH concentration to 6.5-7.2; and a step of drying and maintaining in a refrigerator.
Abstract:
An immune enhancer and vaccine adjuvant additive for animal, which contains Zygosaccharomyces bailii lysates and an auxiliary therapeutic agent are provided to enhance the activation of neutrophil and non-specific protection effect to attack inoculation. An immune enhancer, vaccine adjuvant additive, auxiliary therapeutic agent and feed additive comprises a Zygosaccharomyces bailii lysates. A method for manufacturing the Zygosaccharomyces bailii lysate comprises: a step of culturing the Zygosaccharomyces bailii in the media at 26‹C for 72 hours; a step of centrifuging the cultured media and suspending in phosphate buffered saline (PBS); a step of adding dissolution agent and stirring at room temperature for two to three days; a step of adjusting pH concentration to 6.5-7.2; and a step of drying and maintaining in a thermostatic chamber.
Abstract:
A plate agglutination tester and a method for measuring an immuno-reaction using the same are provided to decrease error of the result analysis in accordance with proficiency of a person performing diagnosis, show the degree of various immuno-reactions in an objective value and perform various statistical analyses, thereby being very useful for measuring the immuno-reaction. A plate agglutination tester consists of a transparent film and is characterized in that a section, which consists of a plurality of circles and where an antigen-antibody agglutination reaction occurs, is arranged and formed in horizontal and vertical directions on an upper side of the film. A method for measuring an immuno-reaction comprises the steps of: (a) mixing an antigen and an antibody specifically bound to the antigen with the plate agglutination tester to induce an agglutination reaction; (b) scanning the agglutination reaction induced plate agglutination tester and converting a scanning result into an image file; and (c) analyzing the obtained image file using a computer program capable of detecting fine agglutination reactants to numberize the intensity of the agglutination reaction. Further, the transparent film is an over head project film.
Abstract:
PURPOSE: Diagnostic methods of foot-and-mouth disease using recombinant 3ABC non-structural protein expressed in insect cells and a monoclonal antibody is provided, thereby more rapidly and accurately diagnosing the foot-and-mouth disease than the prior methods. CONSTITUTION: A gene encoding a recombinant 3ABC non-structural protein derived from Korean foot-and-mouth disease virus O/SKR/2000 has the nucleotide sequence of SEQ ID NO: 1. A recombinant baculovirus to be expressed in insect cells is prepared by co-transfection with a recombinant vector containing the recombinant 3ABC non-structural protein gene of SEQ ID NO: 1. The recombinant 3ABC non-structural protein is expressed by infection of the insect cells with the recombinant baculovirus. A hybridoma cell line 3F-11(KCTC 10138BP) is prepared by introducing the recombinant 3ABC non-structural protein expressed in E. coli into an animal, collecting an immunized cell from the animal and fusing the immunized cell with a cancer cell. A monoclonal antibody is produced from the hybridoma cell line 3F-11(KCTC 10138BP). A diagnostic method of foot-and-mouth disease comprises the steps of: (1) diluting the recombinant 3ABC non-structural protein in a coating buffer solution and pouring the diluate on a plate; (2) reacting the testing serum with the plate; (3) reacting a conjugate, which binds with an antibody for foot-and-mouth disease virus in the testing serum and has an enzyme, a radioactive material or a fluorescent material, with the testing serum; and (4) measuring intensity of the enzyme reaction, fluorescence reaction or radiation reaction with the conjugate.
Abstract translation:目的:提供使用在昆虫细胞和单克隆抗体中表达的重组3ABC非结构蛋白的口蹄疫诊断方法,从而比现有方法更快速和准确地诊断口蹄疫。 构成:编码来源于韩国口蹄疫病毒O / SKR / 2000的重组3ABC非结构蛋白的基因具有SEQ ID NO:1的核苷酸序列。在昆虫细胞中表达的重组杆状病毒由 用含有SEQ ID NO:1的重组3ABC非结构蛋白基因的重组载体共转染。通过用重组杆状病毒感染昆虫细胞表达重组3ABC非结构蛋白。 通过将在大肠杆菌中表达的重组3ABC非结构蛋白导入动物中,从动物中收集免疫的细胞并将免疫的细胞与癌细胞融合来制备杂交瘤细胞系3F-11(KCTC 10138BP)。 从杂交瘤细胞系3F-11(KCTC 10138BP)产生单克隆抗体。 一种口蹄疫诊断方法,包括以下步骤:(1)将重组3ABC非结构蛋白稀释于包被缓冲液中,并将稀释液倒入平板中; (2)使测试血清与平板反应; (3)使与试验血清中的口蹄疫病毒抗体结合的缀合物与测试血清具有酶,放射性物质或荧光物质; 和(4)测量酶反应的强度,荧光反应或与缀合物的辐射反应。
Abstract:
본 발명은 락토바실러스 존슨니( Lactobacillus johnsonnii ) G22-2(KACC91458P), 락토바실러스 루테리( Lactobacillus reuteri ) G8-5(KACC91450P) 및 락토바실러스 살리바리우스( Lactobacillus salivarius ) G1-1(KACC91449P)로 이루어진 유산균 복합 균주를 유효성분으로 함유하는 사료첨가제에 관한 것이다. 본 발명의 유산균 복합 균주는 다양한 병원성 세균에 대한 항균력, 전분 분해능, 내산성, 내담즙성 및 장부착능이 우수하고 항생제 내성이 없어 안전하며 상호 억제 효과가 없어 사료첨가제로 사용하기에 적절하다. 본 발명의 유산균 복합 균주 사료첨가제는 여러 병원성 세균에 의한 감염으로부터 보호하고 사료의 이용 효율을 증대시킬 수 있을 뿐만 아니라 동물용 의약품을 대체할 수 있다.
Abstract:
본 발명은 내산성, 내담즙, 및 장부착능이 있고, 한국농업미생물지원센터(KACC)에 기탁번호 KACC91449P로 기탁된 균주인 락토바실러스 살리바리우스( Lactobacillus salivarius ) G1-1 및 이를 유효성분으로 함유한 사료첨가제 조성물에 관한 것이다. 본 발명에 따르면, 본 발명의 락토바실러스 살리바리우스 G1-1 균주는 다양한 병원성 세균에 대해 우수한 항균활성을 나타냄은 물론 내산성 및 내담즙성 등이 우수하므로, 장내 병원성 세균 억제제, 소화제, 정장제 등의 프로바이오틱 조성물로 제조하여 사료 및 동물용 의약품에 유용하게 활용될 수 있고, 축산 농가의 가축질병으로 인한 경제적 피해를 크게 감소시킬 수 있을 뿐만 아니라 수입 동물용 의약품을 대체할 수 있다. 락토바실러스 살리바리우스, 항균활성, 내담즙성, 내산성
Abstract:
본 발명은 우 결핵균 항체에 특이적으로 반응하는 단백질 및 그 정제 방법에 관한 것으로, 더욱 상세하게는 우 결핵균 단백질 중 우결핵균 감염 혈청에 대한 항체 특이 단백질 및 그 정제 방법에 관한 것이다. 본 발명은 우결핵균의 혈청학적 진단 기술을 향상시킴으로써 우결핵의 확산방지를 도모할 수 있다. 우결핵, 단백질항원, 이온교환크로마토그래피, 항체검사, 면역블롯팅
Abstract:
PURPOSE: Diagnostic methods of foot-and-mouth disease using recombinant 3ABC non-structural protein expressed in insect cells and a monoclonal antibody is provided, thereby more rapidly and accurately diagnosing the foot-and-mouth disease than the prior methods. CONSTITUTION: A gene encoding a recombinant 3ABC non-structural protein derived from Korean foot-and-mouth disease virus O/SKR/2000 has the nucleotide sequence of SEQ ID NO: 1. A recombinant baculovirus to be expressed in insect cells is prepared by co-transfection with a recombinant vector containing the recombinant 3ABC non-structural protein gene of SEQ ID NO: 1. The recombinant 3ABC non-structural protein is expressed by infection of the insect cells with the recombinant baculovirus. A hybridoma cell line 3F-11(KCTC 10138BP) is prepared by introducing the recombinant 3ABC non-structural protein expressed in E. coli into an animal, collecting an immunized cell from the animal and fusing the immunized cell with a cancer cell. A monoclonal antibody is produced from the hybridoma cell line 3F-11(KCTC 10138BP). A diagnostic method of foot-and-mouth disease comprises the steps of: (1) diluting the recombinant 3ABC non-structural protein in a coating buffer solution and pouring the diluate on a plate; (2) reacting the testing serum with the plate; (3) reacting a conjugate, which binds with an antibody for foot-and-mouth disease virus in the testing serum and has an enzyme, a radioactive material or a fluorescent material, with the testing serum; and (4) measuring intensity of the enzyme reaction, fluorescence reaction or radiation reaction with the conjugate.
Abstract translation:目的:提供使用在昆虫细胞中表达的重组3ABC非结构蛋白和单克隆抗体的口蹄疫诊断方法,从而比现有方法更快速,准确地诊断口蹄疫。 构成:编码来自韩国口蹄疫病毒O / SKR / 2000的重组体3ABC非结构蛋白的基因具有SEQ ID NO:1的核苷酸序列。在昆虫细胞中表达的重组杆状病毒通过 用含有SEQ ID NO:1的重组3ABC非结构蛋白基因的重组载体共转染。重组体3ABC非结构蛋白用重组杆状病毒感染昆虫细胞表达。 通过将在大肠杆菌中表达的重组3ABC非结构蛋白质导入动物中,从动物中收集免疫的细胞并将免疫的细胞与癌细胞融合来制备杂交瘤细胞系3F-11(KCTC 10138BP)。 从杂交瘤细胞系3F-11(KCTC 10138BP)产生单克隆抗体。 口蹄疫的诊断方法包括以下步骤:(1)在包被缓冲溶液中稀释重组体3ABC非结构蛋白,将稀释液倒入平板上; (2)使测试血清与板反应; (3)使与测试血清中的口蹄疫病毒抗体结合并具有酶,放射性物质或荧光材料的缀合物与测试血清反应; 和(4)测量酶反应的强度,荧光反应或与缀合物的辐射反应。