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公开(公告)号：KR1019940000888B1
公开(公告)日：1994-02-03
申请号：KR1019910014105
申请日：1991-08-14
Applicant: 삼성전자주식회사
IPC: G11B15/02
Abstract: The device enables the long time recording by controlling the recording time of image signal. The device comprises an input means (1), an image signal processing part (2), a recording head (REC-CH), a recording amplifier (AMP1), a capstan motor (10), a record control signal generating part for controlling the output state of the recording amplifier (AMP1) and a control part for controlling the capstan motor to rotate during the complex image signal is recorded.
Abstract translation: 该装置通过控制图像信号的记录时间来实现长时间记录。 该装置包括输入装置（1），图像信号处理部分（2），记录头（REC-CH），记录放大器（AMP1），主导轴马达（10），用于控制的记录控制信号产生部分 记录放大器（AMP1）的输出状态和用于控制主导马达在复合图像信号期间旋转的控制部。
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55.发明授权알코올 발효저해물에 대한 저항성을 증대시키는 단리된 폴리뉴클레오티드, 이를 포함하는 재조합 벡터, 알코올 생산성 형질전환 균주 및 이를 이용한 알코올의 제조방법 有权分离的多核苷酸增加酒精发酵抑制性化合物重组载体和酒精生产转化细胞的耐受性及其使用方法
公开(公告)号：KR101690289B1
公开(公告)日：2016-12-28
申请号：KR1020100025395
申请日：2010-03-22
Applicant: 삼성전자주식회사 , 서울대학교산학협력단
CPC classification number: Y02E50/17
Abstract: 알코올발효저해물에대한저항성을증대시키는단리된폴리뉴클레오티드, 이를포함하는벡터, 알코올생산성균주및 이를이용한알코올의생산방법에관한기술로서, 특정한단리된폴리뉴클레오티드가호스트셀내에서과발현됨으로써호스트셀의알코올발효저해물에대한저항성이증대되므로알코올발효시생산성이증대될수 있다.
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Patent Agency Ranking56.发明授权
公开(公告)号：KR101657095B1
公开(公告)日：2016-09-19
申请号：KR1020100005576
申请日：2010-01-21
Applicant: 삼성전자주식회사 , 고려대학교 산학협력단
IPC: C07K14/195 , C07K14/32 , C12P19/04 , C12N9/14
CPC classification number: C12P7/10 , C07K14/195 , C07K14/32 , C07K14/37 , C12N9/2437 , C12N9/248 , C12P19/02 , C12P19/14 , Y02E50/16 , Y02E50/343
Abstract: 셀룰라아제등 다당류가수분해효소의가수분해능을증진하고, 다당류에부착될수 있으며효소활성이결핍된단리된단백질에관한기술로서, 상기단리된단백질을첨가하는경우다당류또는그 가수분해물의분해를촉진할수 있어서다당류분해를위한가수분해효소사용량을줄일수 있다.
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57.发明公开전사 인자 조작을 통하여 재프로그래밍된 유전자를 발현하는 내산성이 증가된 클루베로마이세스 마르시아누스 审中-实审耐药性增强的KLUYVEROMYCES MARXIANUS通过工程化转录因子表达遗传基因
公开(公告)号：KR1020150051081A
公开(公告)日：2015-05-11
申请号：KR1020130132526
申请日：2013-11-01
Applicant: 삼성전자주식회사
CPC classification number: C12P7/42 , C07K14/39 , C07K14/4705 , C12N9/1247 , C12P7/18 , C12P7/46 , C12P7/56 , Y02P20/52
Abstract: 클루베로마이세스마르시아누스에서산업적으로유용한형질을유도하기위해전사인자변이를이용한시스템및 이를이용하여제작한변형된클루베로마이세스마르시아누스를제공하기위한것이다. 이를위해유전자발현을조절하는전사인자복합체의조절인자에속하는각각의주요인자를이용하여변이라이브러리이를구축하였다. 구축된변이벡터라이브러리를균주에도입및 발현하여내산성이향상된변이주를개발하였다. 또한, 이를이용하여 3-HP를효율적으로생산할수 있는균주를개발하였고, 이러한균주는산업적으로매우유용하다.
Abstract translation: 本发明提供一种使用转录因子突变诱导马克斯克鲁维酵母的工业上有用的性状的系统，以及由其制备的改良的马克斯克鲁维酵母（Kluyveromyces marxianus）。 为此，通过使用属于调节基因表达的转录因子复合物的调节元件的各个关键因子构建了突变文库。 通过引入和表达在菌株中构建的突变体载体文库，开发了具有较高耐酸性的突变菌株。 此外，已经开发了能够有效地产生3-HP的菌株，并且该菌株在工业上非常有用。
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公开(公告)号：KR1020150023175A
公开(公告)日：2015-03-05
申请号：KR1020130100567
申请日：2013-08-23
Applicant: 삼성전자주식회사
CPC classification number: C12P7/18 , C07K14/34 , C12N9/0006 , C12N9/1025 , C12Q1/48 , C12Y101/01027 , C12Y203/03001 , G01N2333/91045
Abstract: The present invention relates to a method for screening genes used for increasing 1,4-butanediol (BDO) production by using proteomics data. In the present invention, 1,4-BDO productivity is increased when a Ncgl0630 (citrate synthase) protein and a Ncgl2145 (hypothetical protein) protein are overly expressed wherein the Ncgl0630 (citrate synthase) protein and the Ncgl2145 (hypothetical protein) protein are screened via the method which is used to find proteins related to 1,4-BDO productivity and accordingly increases productivity, thereby being widely applicable industrially.
Abstract translation: 本发明涉及通过使用蛋白质组学数据筛选用于增加1,4-丁二醇（BDO）生产的基因的方法。 在本发明中，当Ncgl0630（柠檬酸合成酶）蛋白和Ncgl2145（假想蛋白））蛋白被过度表达时，其中筛选出Ncgl0630（柠檬酸合成酶）蛋白和Ncgl2145（假想蛋白））蛋白质时，1,4-BDO生产力增加 通过用于发现与1,4-BDO生产率相关的蛋白质的方法，从而提高生产率，从而在工业上广泛应用。
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公开(公告)号：KR1020150022530A
公开(公告)日：2015-03-04
申请号：KR1020130100568
申请日：2013-08-23
Applicant: 삼성전자주식회사
CPC classification number: C12P7/42 , C12N9/0008 , C12N9/93 , C12P7/46 , C12P17/04 , C12Y101/01027 , C12Y101/01061 , C12Y102/01002 , C12Y102/01024 , C12Y102/07003 , C12Y103/05 , C12Y108/01004 , C12Y203/01012 , C12Y208/03 , C12Y401/01 , C12Y604/01001 , Y02P20/52
Abstract: The present invention relates to a strain that produces 4-hydroxybutyrate (4HB) wherein the activity of malate quinone oxidoreductase or phosphoenolpyruvate carboxykinase is reduced or removed; or introduces a polynucleotide that codes alpha-ketoglutarate synthase or mutants thereof, or pyruvate carboxykinase or mutants thereof, thereby improving the productivity of 4HB. Also, the strain has an additonally improved function of producing 4HB by introducing polynucleotide that codes pyruvate dehydrogenase and formate dehydrogenase. In the present invention, the transgenic strain in an anaerobic fermentation is used for producing 4HB in a high yield rate, thus being very useful in industrial application.
Abstract translation: 本发明涉及产生4-羟基丁酸（4HB）的菌株，其中苹果酸醌氧化还原酶或磷酸烯醇丙酮酸羧激酶的活性被降低或去除; 或引入编码α-酮戊二酸合酶或其突变体或丙酮酸羧激酶或其突变体的多核苷酸，从而提高4HB的生产率。 此外，通过引入编码丙酮酸脱氢酶和甲酸脱氢酶的多核苷酸，该菌株具有产生4HB的附加功能。 在本发明中，厌氧发酵中的转基因菌株以高产率用于生产4HB，因此在工业应用中非常有用。
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公开(公告)号：KR1020150018227A
公开(公告)日：2015-02-23
申请号：KR1020130094885
申请日：2013-08-09
Applicant: 삼성전자주식회사
CPC classification number: C12P7/46 , C12N9/88 , C12Y402/01002
Abstract: 외인성 푸마라아제 유전자를 포함하는 코리네박테리움 속 미생물 및 이를 이용한 C4 디카르복실산의 혐기적 생산 방법을 제공한다. 상기 코리네박테리움을 이용하여 혐기 조건에서 환원성 대사물질의 생산을 증가시키는 것이 가능하다.
Abstract translation: 本发明提供了一种棒状杆菌属 包含异源延胡索酸酶基因的微生物和使用其的厌氧生产C4二羧酸的方法。 通过使用棒状杆菌，可以在厌氧条件下生产还原性代谢物。 此外，根据本发明的C4二羧酸的制造方法，可以有效地制造C4二羧酸。
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