캘빈회로 유전자가 도입된 이산화탄소 저감용 재조합 미생물 및 이를 활용한 이산화탄소 저감 방법
    12.
    发明授权
    캘빈회로 유전자가 도입된 이산화탄소 저감용 재조합 미생물 및 이를 활용한 이산화탄소 저감 방법 有权
    包含用于还原二氧化碳和二氧化碳还原方法的卡尔文循环的重组微生物

    公开(公告)号:KR101639031B1

    公开(公告)日:2016-07-12

    申请号:KR1020150120520

    申请日:2015-08-26

    Abstract: 본발명은캘빈회로(Calvin Cycle) 유전자가도입된재조합미생물및 이를활용한방법에관한것으로, 보다상세하게는로도박터스페로이드() 유래의캘빈회로의캘빈-벤슨-배스햄순환(CalvinBensonBassham cycle; cbb)를코딩하는유전자를포함하는재조합벡터, 상기재조합벡터로형질전환된재조합미생물및 상기재조합미생물을이용한이산화탄소저감방법또는유용유기물생산방법에관한것이다. 본발명의캘빈회로유전자가도입된재조합미생물은상기캘빈회로유전자도입으로인해생성된이산화탄소고정능에의해이산화탄소저감기능이있을뿐만아니라, 광합성효율증가로인한유용유기물의생성을증가시키는방법을제공할수 있으므로, 종래의미세조류보다배양속도가빠르고, 이산화탄소저감효과보다현저히우수한재조합미생물을이용하여생물학적환경문제해결이가능할뿐만아니라, 이산화탄소고정을통한고부가가치물질의생산을향상시킬수 있다.

    미생물 분리배양 장치 및 미생물 배양 폐배지 재사용 방법
    13.
    发明公开
    미생물 분리배양 장치 및 미생물 배양 폐배지 재사용 방법 审中-实审
    微生物分离培养装置及废弃微生物培养基再利用方法

    公开(公告)号:KR1020160073953A

    公开(公告)日:2016-06-27

    申请号:KR1020160074078

    申请日:2016-06-14

    CPC classification number: C12M29/24 C12M21/02 C12M41/34

    Abstract: 본발명은미생물분리배양장치및 미생물배양폐배지재사용방법에관한것으로서, 보다상세하게는미생물배양후 버려지는폐배지의재사용을통한이산화탄소의저감뿐만아니라여러유용한생리활성물질을생산할수 있기때문에친환경적이며, 까다로운폐배지의처리과정에있어비용절감효과가우수한매우경제적인미생물배양폐배지재사용방법및 이에사용할수 있는미생물분리배양장치에관한것이다.

    Abstract translation: 本发明涉及一种微生物分离培养装置和一种再循环废微生物培养基的方法。 更具体地说,本发明涉及一种循环利用废旧微生物培养基的方法,其是环保的,因为可以生产各种有用的生物活性物质,并且通过再循环培养微生物后废弃的废弃物来减少二氧化碳的量。 此外,该方法还可以通过降低难以处理的废料处理过程中的成本来确保经济可行性。 本发明还涉及用于其的微生物分离培养装置。

    대칭용량 달성을 위한 극 퀀텀 채널 코딩 방법 및 이를 적용한 통신기기
    14.
    发明公开
    대칭용량 달성을 위한 극 퀀텀 채널 코딩 방법 및 이를 적용한 통신기기 有权
    极数量子信道编码方法和对称能力实现的装置

    公开(公告)号:KR1020150002085A

    公开(公告)日:2015-01-07

    申请号:KR1020130075434

    申请日:2013-06-28

    Inventor: 이문호 박주용

    Abstract: The present invention relates to a method for combining and dividing a quantum channel which is refer to a polar quantum channel for generating a quantum bit (qubit) which achieves symmetric capacity even if some binary input discrete quantum channels are given. Current capacity is determined according to qubit input having the same probability. The polarization of the quantum channel is transmitted to rate 1 if a symmetric channel is close to one. Or if not, the polarization of the quantum channel is transmitted to rate 0. The polarization of the quantum channel is suitable for coding quantum error correction for partially transmitting quantum data through the channel.

    Abstract translation: 本发明涉及一种用于组合和划分量子信道的方法,该量子信道是指产生量子比特(量子比特)的极性量子信道,即使给出一些二进制输入的离散量子信道也能实现对称容量。 电流容量根据具有相同概率的量子位输入确定。 如果对称信道接近1,则量子信道的极化被传送到速率1。 否则,量子信道的极化被传输到速率0.量子信道的极化适用于通过信道部分地传输量子数据的量子纠错的编码。

    Toeplitz Jacket 행렬을 이용한 신호 처리 방법
    16.
    发明授权
    Toeplitz Jacket 행렬을 이용한 신호 처리 방법 有权
    用TOEPLITZ JACKET MATRICES信号处理的方法

    公开(公告)号:KR101401388B1

    公开(公告)日:2014-06-19

    申请号:KR1020130035566

    申请日:2013-04-02

    Inventor: 이문호 박주용

    CPC classification number: H04B7/0413 H04L1/0014

    Abstract: Provided is a signal processing method using a Toeplitz Jacket (TJ) matrix. The communications method according to an embodiment of the present invention converts an input signal by using the TJ matrix. The TJ matrix is generated by pre-multiplying a left side of a circulant Jacket matrix by a reverse matrix of a diagonal matrix and post-multiplying a right side of the circulant Jacket matrix by the diagonal matrix. Accordingly, the present invention can process various signals more effectively, and enhance the system performance ultimately.

    Abstract translation: 提供了使用Toeplitz Jacket(TJ)矩阵的信号处理方法。 根据本发明的实施例的通信方法通过使用TJ矩阵来转换输入信号。 通过将循环夹套矩阵的左侧预先乘以对角矩阵的反向矩阵并将循环夹层矩阵的右侧乘以对角矩阵来生成TJ矩阵。 因此,本发明可以更有效地处理各种信号,并最终提高系统性能。

    유전자 RNA 코드 기반 재킷 행렬을 이용한 신호 처리 방법 및 장치
    17.
    发明公开
    유전자 RNA 코드 기반 재킷 행렬을 이용한 신호 처리 방법 및 장치 有权
    RNA信号处理方法和装置,使用基于遗传RNA编码的夹克矩阵

    公开(公告)号:KR20180034873A

    公开(公告)日:2018-04-05

    申请号:KR20160124621

    申请日:2016-09-28

    CPC classification number: G06F19/10 G06N3/126 H03M13/61

    Abstract: 유전자 RNA 코드기반재킷행렬을이용한신호처리방법및 장치가제공된다. 본발명의실시예에따른방법및 장치는, 유전자 RNA Code의 C(Cytosine), U(Uracil), G(Guanine), A(Adenine) 유전자코드가 Circulant 행렬을갖고있음을이용하여, Element (Block)-wise Inverse인 Jacket 행렬로적용하여신호처리하는방법을제시하였다.

    Abstract translation: 提供了使用基于遗传RNA编码的夹克矩阵的信号处理方法和装置。 根据本发明的实施例中,C基因RNA代码,U的(胞嘧啶)(尿嘧啶),G(鸟嘌呤),A(腺嘌呤)的遗传密码,使用具有循环矩阵,元素(块的方法和装置 )信号处理的逆向夹套矩阵。

    광합성 세균을 이용한 테르펜 계열 화합물 또는 이소프렌의 제조방법
    18.
    发明公开
    광합성 세균을 이용한 테르펜 계열 화합물 또는 이소프렌의 제조방법 有权
    用光合细菌制备萜烯化合物或异戊二烯的方法

    公开(公告)号:KR1020170050666A

    公开(公告)日:2017-05-11

    申请号:KR1020150152501

    申请日:2015-10-30

    Abstract: 본발명은광합성세균을이용한테르펜계열화합물또는이소프렌의제조방법에관한것으로, 보다상세하게는 (a) 배지에아르곤(Ar) 가스를퍼징(purging)하고밀봉하여혐기성상태를유지하는단계; (b) 광합성세균을접종하는단계; 및 (c) 배지에접종된광합성세균을형광등을통한빛 조건에서혐기상태로배양하는단계를포함하는테르펜계열화합물또는이소프렌의제조방법및 이로부터제조된테르펜계열화합물또는이소프렌을함유하는항균제품에관한것이다.

    Abstract translation: 本发明包括涉及一种方法,用于使用光合细菌,更具体地,涉及保持在培养基中在厌氧条件并密封的(a)吹扫(清洗)和氩(Ar)气的萜烯系化合物或异戊二烯的制备; (b)接种光合细菌; 和(c)萜烯基化合物或用于生产异戊二烯,包括培养在厌氧状态下过荧光灯和包含由其制备的萜烯系化合物或异戊二烯抗菌产物接种到在光条件下的培养基中的光合细菌的方法 它涉及。

    재조합 발현벡터, 이를 포함하는 숙주세포 및 그 용도
    19.
    发明授权
    재조합 발현벡터, 이를 포함하는 숙주세포 및 그 용도 有权
    重组表达载体,含有相同的宿主细胞及其用途

    公开(公告)号:KR101524926B1

    公开(公告)日:2015-06-01

    申请号:KR1020130096182

    申请日:2013-08-13

    Abstract: 본발명은이산화탄소저감효과및 생리활성물질생산을향상시키기위한재조합발현벡터에관한것으로서, 보다상세하게는세포외막단백질을이용한탄산무수화효소의세포표면발현을통해탄산무수화효소가효소로서의안정성을보다쉽고오랫동안유지할수 있도록하고, 이를통해이산화탄소를기반으로다양한유기물질을생산할수 있는광합성세균인로도박터스페로이드를통한최적의이산화탄소저감효율및 고부가가치물질의생산을향상시킬수 있는재조합발현벡터에관한것이다.

    로도박터 스페로이드의 변이균주 추출물을 포함하는 성장촉진용 배지조성물 및 그 제조방법
    20.
    发明公开
    로도박터 스페로이드의 변이균주 추출물을 포함하는 성장촉진용 배지조성물 및 그 제조방법 有权
    用于加速光合微生物和动物细胞生长的中间组合物和制造方法

    公开(公告)号:KR1020130044534A

    公开(公告)日:2013-05-03

    申请号:KR1020110108641

    申请日:2011-10-24

    Abstract: PURPOSE: A culture composition for promoting photosynthetic microorganism and animal cell growth and a manufacturing method thereof are provided to accelerate the production of photosynthetic microorganisms and promote growth by promoting the animal cells and reducing the stress in the cells. CONSTITUTION: A culture composition for promoting photosynthetic microorganism and animal cell growth includes a mutant strain of Rhodobacter sphaeroides, MBTLJ- 8(accession number: KACC91572P) as an active ingredient. The generation process of the mutant strain comprises the following steps: adding N-Methyl-N'-nitro-Nnitrosoguanidine to a rhodobacter sphaeroides culture medium; and culturing the same at 15 Watts for 48 hours. The culture composition for promoting photosynthetic microorganism and animal cell growth includes a mutant strain of Rhodobacter sphaeroides, photosynthetic activating(or alternative) compound as an active ingredient. A manufacturing method of culture composition for promoting photosynthetic microorganism and animal cell growth comprises the following steps: a first step of manufacturing culture medium 1 by shake culturing the Rhodobacter sphaeroides at 30°C for 48 hours; a second step of manufacturing culture medium 2 by mainly culturing the culture medium 1 at 30°C for 48 hours; and a third step of manufacturing a culture composition containing Rhodobacter sphaeroides mutant strain, MBTLJ-8 by cultivating at 15 Watts for 48 hours after adding N-Methyl-N'-nitro-N-nitrosoguanidine to the culture medium 2. [Reference numerals] (AA) Inoculate Rhodobacter sphaeroides into 5ml of sistrom's minimal medium and shake culture at 30°C and 140rpm for 24 hours; (BB) Add 1ml of the culture medium into 100ml of the sistrom's minimal medium and main culture at 30°C and 150rpm for 24 hours under the dark state; (CC) Add 1ml of the culture medium into 100ml of the sistrom's minimal medium and main culture at 30°C and 150rpm for 24 hours under the light state; (DD) Add 1ml of the culture medium into 100ml of the sistrom's minimal medium, main culture at 30°C and 150rpm for 12 hours under the 15W light state and for 12 hours under the dark state; (EE) Arrange the cultured cells and medium in a tube, centrifuge at 4 °C and 5000rpm for 30 minutes, and collect precipitated cells; (FF) Adjust volume by adding sterilized water into the cells which are collected to be as much as 1/20 of the culture medium and sonicate using an ultra sonicator under a refrigerating state for 30 minutes based on the condition of 20 seconds pulse and 10 seconds recess; (GG) Name a solution obtained by filtering supernatant, which is centrifuged at 4°C and 13000rpm for 30 minutes, using 0.2um filter as PACs

    Abstract translation: 目的:提供一种用于促进光合微生物和动物细胞生长的培养组合物及其制备方法,其通过促进动物细胞并减少细胞中的应激来加速光合微生物的产生并促进生长。 构成:用于促进光合微生物和动物细胞生长的培养组合物包括作为活性成分的球形红细菌的突变株,MBTLJ-8(登录号:KACC91572P)。 突变菌株的产生过程包括以下步骤:将N-甲基-N'-硝基 - 硝基胍胍加入到球形罗汉字菌培养基中; 并在15瓦下培养48小时。 用于促进光合微生物和动物细胞生长的培养组合物包括球形红细菌(Rhodobacter sphaeroides)的突变菌株,光合活化(或替代)化合物作为活性成分。 用于促进光合微生物和动物细胞生长的培养组合物的制造方法包括以下步骤:通过在30℃下摇动培养球形红细菌48小时来制造培养基1的第一步骤; 通过主要在30℃下培养培养基1 48小时来制造培养基2的第二步骤; 以及在向培养基2中加入N-甲基-N'-硝基-N-亚硝基胍后,通过在15瓦下培养48小时,制造含有球菌属球菌突变菌株MBTLJ-8的培养组合物的第三步骤。 (AA)将球形罗霍球菌接种到5ml的sistrom的基本培养基中,并在30℃和140rpm振摇培养24小时; (BB)在黑暗状态下,将30ml和150rpm的培养基加入100ml的主要培养基和主培养物中24小时; (CC)在轻度状态下,将1ml培养基加入到100ml的sistrom的基本培养基和主培养物中,在30℃和150rpm下培养24小时; (DD)将1ml培养基加入100ml的sistrom's基本培养基中,在15W光照条件下在30℃和150rpm下主培养12小时,在黑暗状态下培养12小时; (EE)将培养的细胞和培养基置于管中,在4℃和5000rpm离心30分钟,收集沉淀的细胞; (FF)通过向收集的细胞中加入灭菌水至培养基的1/20,调节体积,并使用基于20秒脉冲条件的制冷状态下的超声波处理器超声处理30分钟,10 秒钟; (GG)命名通过过滤上清液获得的溶液,将上清液在4℃和13000rpm离心30分钟,使用0.2um过滤器作为PAC

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