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公开(公告)号:US20070134771A1
公开(公告)日:2007-06-14
申请号:US11628000
申请日:2007-01-29
CPC分类号: C12P41/006 , C12N9/1096 , C12P13/001
摘要: Thermostable omega-transaminases, particularly thermostable omega-transaminases which have a high reaction rate and which are tolerant to high concentrations of donor amine, can be used to enrich enantiomerically a mixture of chiral amines or to synthesize stereoselectively one of a pair of chiral amines in which the amino group is bound to a non-terminal, chirally substituted, carbon atom.
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公开(公告)号:US20070134772A1
公开(公告)日:2007-06-14
申请号:US11668001
申请日:2007-01-29
CPC分类号: C12P41/006 , C12N9/1096 , C12P13/001
摘要: Thermostable omega-transaminases, particularly thermostable omega-transaminases which have a high reaction rate and which are tolerant to high concentrations of donor amine, can be used to enrich enantiomerically a mixture of chiral amines or to synthesize stereoselectively one of a pair of chiral amines in which the amino group is bound to a non-terminal, chirally substituted, carbon atom.
摘要翻译: 热稳定性ω-转氨酶,特别是具有高反应速率且耐受高浓度供体胺的热稳定性ω-转氨酶,可用于富集对映异构体的手性胺混合物,或合成立体选择性的一对手性胺之一 氨基与非末端,手性取代的碳原子结合。
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公开(公告)号:US20070275444A1
公开(公告)日:2007-11-29
申请号:US11627999
申请日:2007-01-29
CPC分类号: C12P41/006 , C12N9/1096 , C12P13/001
摘要: Thermostable omega-transaminases, particularly thermostable omega-transaminases which have a high reaction rate and which are tolerant to high concentrations of donor amine, can be used to enrich enantiomerically a mixture of chiral amines or to synthesize stereoselectively one of a pair of chiral amines in which the amino group is bound to a non-terminal, chirally substituted, carbon atom.
摘要翻译: 热稳定性ω-转氨酶,特别是具有高反应速率且耐受高浓度供体胺的热稳定性ω-转氨酶,可用于富集对映异构体的手性胺混合物,或合成立体选择性的一对手性胺之一 氨基与非末端,手性取代的碳原子结合。
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公开(公告)号:US20070134770A1
公开(公告)日:2007-06-14
申请号:US11627997
申请日:2007-01-29
CPC分类号: C12P41/006 , C12N9/1096 , C12P13/001
摘要: Thermostable omega-transaminases, particularly thermostable omega-transaminases which have a high reaction rate and which are tolerant to high concentrations of donor amine, can be used to enrich enantiomerically a mixture of chiral amines or to synthesize stereoselectively one of a pair of chiral amines in which the amino group is bound to a non-terminal, chirally substituted, carbon atom.
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