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1.发明授权Microorganism producing 5′-inosinic acid and process for producing 5′-inosinic acid using the same 有权产生5'-肌苷酸的微生物和使用其产生5'-肌苷酸的方法公开(公告)号：US07244608B2
公开(公告)日：2007-07-17
申请号：US10227508
申请日：2002-08-23
申请人： Hyun-Soo Kim , Sung-Oh Chung , Jin-Ho Lee , Sung-Goo Kang , Jeong-Hwan Kim , Soo-Youn Hwang , Byung-Chon Lee , Jae-Chul Lee
发明人： Hyun-Soo Kim , Sung-Oh Chung , Jin-Ho Lee , Sung-Goo Kang , Jeong-Hwan Kim , Soo-Youn Hwang , Byung-Chon Lee , Jae-Chul Lee
摘要： The present invention relates to a novel microorganism, Corynebacterium ammoniagenes strain CJIP009 having Accession No. KCCM-10226, which is capable of producing 5′-inosinic acid and a process for producing 5′-inosinic acid using the same.
摘要翻译： 本发明涉及一种能够产生5'-肌苷酸的新型微生物，具有登录号KCCM-10226的产氨杆菌菌株CJIP009和使用该微生物产生5'-肌苷酸的方法。
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公开(公告)号：US07662943B2
公开(公告)日：2010-02-16
申请号：US11721515
申请日：2005-12-16
申请人： Young-Hoon Park , Hyun-Soo Kim , Hye-Jin Choi , Jin-Ho Lee , Soo-Youn Hwang , Jae-Ick Sim , Tae-Sun Kang , Won-Sik Lee
发明人： Young-Hoon Park , Hyun-Soo Kim , Hye-Jin Choi , Jin-Ho Lee , Soo-Youn Hwang , Jae-Ick Sim , Tae-Sun Kang , Won-Sik Lee
CPC分类号： C07K14/34
摘要： Provided are a promoter including at least one polynucleotide selected from the group consisting of SEQ ID NOS: 1 to 7, an expression cassette including the same, a vector including the expression cassette, a host cell including the vector, and a method of expressing a gene using the host cell.
摘要翻译： 提供了包含选自SEQ ID NO：1至7的至少一种多核苷酸的启动子，包含其的表达盒，包含表达盒的载体，包含载体的宿主细胞，以及表达 基因使用宿主细胞。
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3.发明申请Novel Promoter Nucleic Acid Derived From Corynebacterium Genus Bacteria, Expression Cassette Comprising The Promoter And Vector Comprising The Cassette, Host Cell Comprising The Vector And Method For Expressing A Gene Using The Cell 有权由棒状杆菌属细菌衍生的新型启动子核酸，包含包含载体的启动子和载体的表达盒和包含载体的宿主细胞和使用细胞表达基因的方法公开(公告)号：US20080138859A1
公开(公告)日：2008-06-12
申请号：US11721515
申请日：2005-12-16
申请人： Young-Hoon Park , Hyun-Soo Kim , Hye-Jin Choi , Jin-Ho Lee , Soo-Youn Hwang , Jae-Ick Sim , Tae-Sun Kang , Won-Sik Lee
发明人： Young-Hoon Park , Hyun-Soo Kim , Hye-Jin Choi , Jin-Ho Lee , Soo-Youn Hwang , Jae-Ick Sim , Tae-Sun Kang , Won-Sik Lee
CPC分类号： C07K14/34
摘要： Provided are a promoter including at least one polynucleotide selected from the group consisting of SEQ ID NOS: 1 to 7, an expression cassette including the same, a vector including the expression cassette, a host cell including the vector, and a method of expressing a gene using the host cell.
摘要翻译： 提供了包含选自SEQ ID NO：1至7的至少一种多核苷酸的启动子，包含其的表达盒，包含表达盒的载体，包含载体的宿主细胞，以及表达 基因使用宿主细胞。
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公开(公告)号：US20090311757A1
公开(公告)日：2009-12-17
申请号：US12309048
申请日：2007-07-12
申请人： Young Hoon Park , Hye Won Kim , Ji-Hye Lee , Soo-Youn Hwang
发明人： Young Hoon Park , Hye Won Kim , Ji-Hye Lee , Soo-Youn Hwang
摘要： Disclosed herein are a microorganism producing L-arginine and a method of producing L-arginine using the same. The microorganism is a mutant strain of the genus Corynebacterium, Corynebacterium glutamicum CJR0500. The method for L-arginine production comprises activating the mutant strain C. glutamicum CJR0500 in a fermentation medium at 30° C. for 16 hours and then culturing the activated mutant strain for 72 hours with shaking.
摘要翻译： 本文公开了生产L-精氨酸的微生物和使用其的L-精氨酸的生产方法。 微生物是棒状杆菌属（Corynebacterium），谷氨酸棒杆菌（Corynebacterium glutamicum）CJR0500的突变菌株。 L-精氨酸生产方法包括在30℃的发酵培养基中活化突变菌株C.谷氨酸棒杆菌CJR0500 16小时，然后摇动培养活化的突变菌株72小时。
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公开(公告)号：US08034602B2
公开(公告)日：2011-10-11
申请号：US12309048
申请日：2007-07-12
申请人： Young Hoon Park , Hye Won Kim , Ji-Hye Lee , Soo-Youn Hwang
发明人： Young Hoon Park , Hye Won Kim , Ji-Hye Lee , Soo-Youn Hwang
摘要： Disclosed herein are a microorganism producing L-arginine and a method of producing L-arginine using the same. The microorganism is a mutant strain of the genus Corynebacterium, Corynebacterium glutamicum CJR0500. The method for L-arginine production comprises activating the mutant strain C. glutamicum CJR0500 in a fermentation medium at 30° C. for 16 hours and then culturing the activated mutant strain for 72 hours with shaking.
摘要翻译： 本文公开了生产L-精氨酸的微生物和使用其的L-精氨酸的生产方法。 微生物是棒状杆菌属（Corynebacterium），谷氨酸棒杆菌（Corynebacterium glutamicum）CJR0500的突变菌株。 L-精氨酸生产方法包括在30℃的发酵培养基中活化突变菌株C.谷氨酸棒杆菌CJR0500 16小时，然后摇动培养活化的突变菌株72小时。
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