리파아제를 생산하는 신규 포토박테리움 갯버리코라 Gung47
    21.
    发明公开
    리파아제를 생산하는 신규 포토박테리움 갯버리코라 Gung47 有权
    新型光合智珠菌GUNG47生产脂蛋白的菌株

    公开(公告)号:KR1020110048746A

    公开(公告)日:2011-05-12

    申请号:KR1020090105447

    申请日:2009-11-03

    Abstract: PURPOSE: A novel Photobacterium gaetbulicola Gung47 which produces lipase is provided to be used as a detergent, bleaching agent, food, and feed additive. CONSTITUTION: A novel Photobacterium gaetbulicola Gung47 which produces lipase is deposited by deposit number KACC 91494P. The Photobacterium gaetbulicola strain has 16S rRNA of sequence number 3. The molecular weight of the lipase is 100 kDa. The Photobacterium gaetbulicola strain grows at 10°C-40°C and pH 5.0 to pH 9.5 and under anaerobic condition. A feed additive contains the Photobacterium gaetbulicola Gung47, culture liquid, and lipase as an active ingredient.

    Abstract translation: 目的:提供生产脂肪酶的新型光杆菌Gung47,用作洗涤剂,漂白剂,食品和饲料添加剂。 构成:产生脂肪酶的新型光杆菌Gung47由保藏号KACC 91494P保藏。 光杆菌菌株具有序列号3的16S rRNA。脂肪酶的分子量为100kDa。 光杆菌菌株在10℃-40℃,pH5.0至pH9.5和无氧条件下生长。 饲料添加剂含有光杆菌Gung47,培养液和脂肪酶作为活性成分。

    신규 바실러스 속 균주 및 그의 용도
    28.
    发明授权
    신규 바실러스 속 균주 및 그의 용도 有权
    一种新型芽孢杆菌 应变和使用

    公开(公告)号:KR101618220B1

    公开(公告)日:2016-05-18

    申请号:KR1020140020365

    申请日:2014-02-21

    Abstract: 항균활성및 프로바이오틱스활성을갖는신규바실러스속균주가제공된다. 본발명의균주는다양한어류병원성세균뿐만아니라, 화장품표준균주및 치아우식균에대한광범위한항균활성을가지고있을뿐만아니라, 프로테아제, 아밀라제, 셀룰라제, 자일라제등 사료의소화흡수에도움을주는유용한효소를분비하는등 프로바이오틱스로서기능을하기때문에, 어류및 갑각류의사료첨가제는물론, 항균제와식품및 화장품분야의보존용첨가제로유용하게사용될수 있다.

    넙치 유래의 새로운 항미생물성 펩타이드 및 그의 용도
    29.
    发明授权
    넙치 유래의 새로운 항미생물성 펩타이드 및 그의 용도 有权
    来自OLIVE FLOUNDER的新型抗微生物肽及其用途

    公开(公告)号:KR101395942B1

    公开(公告)日:2014-05-15

    申请号:KR1020130030496

    申请日:2013-03-21

    CPC classification number: Y02A50/473

    Abstract: The present invention relates to antimicrobial peptides, and provides an antibiotic peptide having a length of more than 12 amino acids selected from the amino acid sequence of SEQ ID: 3 and comprising the amino acid sequences of SEQ ID: 21 and uses thereof. According to an aspect of the present invention, a polynucleotide encoding an antimicrobial peptide according to an embodiment of the present invention is provided. In addition, a vector comprising a polynucleotide according to an embodiment of the present invention is provided.

    Abstract translation: 本发明涉及抗微生物肽,并提供长度多于12个氨基酸的抗生素肽,其选自SEQ ID:3的氨基酸序列并且包含SEQ ID:21的氨基酸序列及其用途。 根据本发明的一个方面,提供了编码本发明实施方案的抗微生物肽的多核苷酸。 此外,提供了包含根据本发明实施方案的多核苷酸的载体。

    N-말단 pI 값 조절에 의한 수용성 재조합 단백질 생산방법
    30.
    发明公开
    N-말단 pI 값 조절에 의한 수용성 재조합 단백질 생산방법 有权
    通过PI端控制N-末端生产可溶性重组蛋白

    公开(公告)号:KR1020090055457A

    公开(公告)日:2009-06-02

    申请号:KR1020080035162

    申请日:2008-04-16

    CPC classification number: C12N15/62 C12N15/625

    Abstract: A method for producing a water soluble recombinant fusion protein from an exogenous gene and collecting a protein having an original amino terminal is provided to prevent insoluble precipitation of the recombinant protein and improve the secretion efficiency of the recombinant protein to cytoplasm outside or periplasm. A method for improving the secretion efficiency of a foreign protein comprises: a step of constructing a leader sequence containing N-region of the signal sequence and/or leader sequence of foreign protein, of which pI value is 9.90-11.28; a step of adjusting the distance of amino acid which makes an impact on pI value in the leader sequence; a step of constructing the leaser sequence, distance adjusting site, restriction enzyme recognition site and a polynucleotide coding fusion protein containing foreign protein; a step of inserting the constructed gene into an expression vector to produce a recombinant expression vector; a step of transforming a host cell with the recombinant expression vector; and a step of screening a transformant having high water-soluble expression.

    Abstract translation: 提供从外源基因产生水溶性重组融合蛋白并收集具有原始氨基末端的蛋白质的方法,以防止重组蛋白的不溶性沉淀,并提高重组蛋白在细胞质外周或周质中的分泌效率。 提高外源蛋白质分泌效率的方法包括:构建含有pI值为9.90-11.28的信号序列的N-区和/或外来蛋白的前导序列的前导序列的步骤; 调整导致序列中对pI值产生影响的氨基酸的距离的步骤; 构建leaser序列,距离调整位点,限制酶识别位点和含有外源蛋白的多核苷酸编码融合蛋白的步骤; 将构建的基因插入表达载体以产生重组表达载体的步骤; 用重组表达载体转化宿主细胞的步骤; 以及筛选具有高水溶性表达的转化体的步骤。

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