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    그람양성 식중독 유발 세균 검출용 올리고뉴클레오타이드 및 이의 용도
    2.
    发明公开
    그람양성 식중독 유발 세균 검출용 올리고뉴클레오타이드 및 이의 용도 有权
    用于检测正常食物病原微生物的寡核苷酸及其用途

    公开(公告)号：KR1020120007562A

    公开(公告)日：2012-01-20

    申请号：KR1020120001468

    申请日：2012-01-05

    Applicant: 한국외국어대학교 연구산학협력단 ,  국민대학교산학협력단

    Inventor： 이규호 ,  성문희 ,  조재창 ,  이현정 ,  김한석 ,  이미애 ,  이경조 ,  김정아 ,  김한신

    IPC: C12N15/11 ,  C12Q1/68

    CPC classification number: C12Q1/689 ,  C12Q1/686

    Abstract: PURPOSE: An oligonucleotide for detecting gram positive bacteria causing food poisoning is provided to ensure quick and accuratel detection at once. CONSTITUTION: An oligonucleotide for detecting gram positive bacteria causing food poisoning is used for detect Bacillus cereus, Stapylococcus aureus, or Listeria monocytogenesis. The oligonucleotide for detecting Bacillus cereus contains a sequence of sequence number 1, 2, 3, 4, 5, or 6. The oligonucleotide for Stapylococcus aureus contains a sequence of sequence number 7, 8, 9, 10, 11, or 12. The oligonucleotide for detecting Listeria monocytogenesis contains a sequence of sequence number 13, 14, 15, or 16.

    Abstract translation: 目的：提供用于检测引起食物中毒的革兰氏阳性菌的寡核苷酸，以确保快速和准确地检测。 构成：用于检测引起食物中毒的革兰氏阳性菌的寡核苷酸用于检测蜡状芽孢杆菌，金黄色葡萄球菌或单核细胞增生性李斯特菌。 用于检测蜡状芽孢杆菌的寡核苷酸含有序列号1,2,3,4,5或6的序列。金黄色金黄色葡萄球菌的寡核苷酸含有序列号7,8,9,10,11或12的序列。 用于检测李斯特菌单核细胞增生的寡核苷酸含有序列号为13,14,15或16的序列。

    ＦｒｓＡ를 발현하는 균주 및 이를 이용한 에탄올 생산방법
    5.
    发明公开
    ＦｒｓＡ를 발현하는 균주 및 이를 이용한 에탄올 생산방법 无效
    表达FrsA蛋白的菌株及使用其生产乙醇的方法

    公开(公告)号：KR1020120126827A

    公开(公告)日：2012-11-21

    申请号：KR1020110044903

    申请日：2011-05-13

    Applicant: 한국외국어대학교 연구산학협력단 ,  한국해양과학기술원

    Inventor： 차선신 ,  정창숙 ,  이정현 ,  이경조 ,  이규호

    IPC: C12N1/21 ,  C12N1/19 ,  C12P7/06

    CPC classification number: Y02E50/17 ,  C12N15/63 ,  C07K14/28 ,  C12N9/0006 ,  C12N9/88 ,  C12P7/06 ,  C12Y101/01001 ,  C12Y401/01001

    Abstract: PURPOSE: A method for producing ethanol using a strain which expresses FrsA proteins is provided to reduce use of a biomass and to effectively produce bioethanol. CONSTITUTION: A transformed strain expresses frsA gene derived from V. vulnificus. frsA is denoted by sequence number 1. The strain is bacteria or yeast including E.coli, Erwinia chrysanthemi, Zymomonas mobilis, Klebsiella spp, Bacillus stearothrermophilus, Kluveromyces spp., Pachysolen tanophilus, Lactic acid bacteria, Clostridium spp., Thermococcus spp., Thermococcus onnurineus, Candida shehatae, Saccharomyces eravisiae, or Pichia stipitis. The strain expresses alcohol dehydrogenase gene and IIAGIc gene. A method for producing bioethanol comprises: a step of providing the transformed strain; a step of contacting the microorganism with a carbon source; and a step of culturing the microorganism under an optimal condition for fermentation.

    Abstract translation: 目的：提供使用表达FrsA蛋白的菌株生产乙醇的方法，以减少生物质的使用并有效生产生物乙醇。 构成：转化菌株表达源自创伤弧菌的frsA基因。 菌株是细菌或酵母，包括大肠杆菌，欧文氏菌，运动发酵单胞菌，克雷伯杆菌，嗜热脂肪芽孢杆菌，克鲁维酵母属，苦参素，乳酸菌，梭菌属，Thermococcus spp。， 嗜热热球菌，念珠菌，黑曲霉或树干毕赤酵母。 该菌株表达醇脱氢酶基因和IIAGIc基因。 一种生产生物乙醇的方法包括：提供转化菌株的步骤; 将微生物与碳源接触的步骤; 以及在最佳发酵条件下培养微生物的步骤。

    ＦｒｓＡ 단백질 결정 및 그 용도
    6.
    发明公开
    ＦｒｓＡ 단백질 결정 및 그 용도 有权
    FrsA蛋白晶体及其用途

    公开(公告)号：KR1020120120723A

    公开(公告)日：2012-11-02

    申请号：KR1020110038464

    申请日：2011-04-25

    Applicant: 한국해양과학기술원 ,  한국외국어대학교 연구산학협력단

    Inventor： 차선신 ,  이경조 ,  이규호 ,  정창숙 ,  이정현

    IPC: C07K14/195 ,  C07K1/02 ,  G01N33/68 ,  C12P7/06

    CPC classification number: Y02E50/17 ,  C07K14/28 ,  C07K2299/00 ,  C12P7/06

    Abstract: PURPOSE: A method for preparing vibrio-derived FrsA protein and protein crystalline structure IIAGIc complex and FrsA protein is provided to manufacture bio ethanol. CONSTITUTION: A FrsA protein contains V.vulnificus-derived amino acid of sequence number 1. The FrsA protein comprises N-terminal helix region containing 1-165th residues of sequence number 1, C-terminal alpha/beta region containing 166-415th of sequence number 1, and a space of interface of the region. The N-terminal helix reagion contains 7 alpha-helix. The C-terminal alpha/beta region contains parallel beta-sheets of 8 strands. An alpha-helix is inserted between the beta-sheets.

    Abstract translation: 目的：提供一种制备弧菌衍生的FrsA蛋白和蛋白质晶体结构IIAGIc复合物和FrsA蛋白的方法，用于制造生物乙醇。 构成：FrsA蛋白含有序列号1的V.vulnificus衍生的氨基酸.FsSA蛋白包含含有序列号1的第1-165个残基的N-末端螺旋区，C末端的α/β区含有序列的第4-6-415个 数字1，以及该区域的接口空间。 N-末端螺旋重组含有7个α-螺旋。 C端α/β区包含8条平行的β片。 在β-折叠板之间插入α-螺旋。

    마이크로코커스 알카노보라 SL-010 균주를 이용하여 음식물 쓰레기를 처리하는 방법
    9.
    发明公开
    마이크로코커스 알카노보라 SL-010 균주를 이용하여 음식물 쓰레기를 처리하는 방법 有权
    抗菌脂肪细菌，微藻ALKANOVORA SL-010

    公开(公告)号：KR1020090123272A

    公开(公告)日：2009-12-02

    申请号：KR1020080049258

    申请日：2008-05-27

    Applicant: 한국외국어대학교 연구산학협력단

    Inventor： 김한석 ,  김성민 ,  이상훈 ,  이경조 ,  조재창 ,  이규호

    IPC: C12N1/20 ,  C12N1/00

    Abstract: PURPOSE: A novel Micrococcus alkanovora SL-010 with lipid lysis ability is provided to live even at high temperature, acid, and salinity. CONSTITUTION: A Micrococcus alkanovora SL-010(deposite number: KCTC 18130P) has stress resistance and high lipid lysis ability. The Micrococcus alkanovora SL-010(deposite number: KCTC 18130P) is isolated from insect(scolopendra subspinipes). A gene(DNA) which encodes lipid lysis enzyme is derived from Micrococcus alkanovora SL-010(deposite number: KCTC 18130P).

    Abstract translation: 目的：提供一种具有脂质裂解能力的新型微链球菌​​SL-010，即使在高温，酸和盐度下也能生存。 构成：链霉菌微球菌SL-010（保藏号：KCTC 18130P）具有抗应激性和高脂质裂解能力。 从昆虫（scolopendra subspinipes）中分离出链球菌Micrococcus SL-010（保藏号：KCTC 18130P）。 编码脂质裂解酶的基因（DNA）源自链霉菌Micrococcus SL-010（保藏号：KCTC 18130P）。

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