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首页> 外文期刊>Biotechnology Letters >High throughput solid-phase screening of bacteria with cyclic amino alcohol deamination activity for enantioselective synthesis of chiral cyclic beta-amino alcohols
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High throughput solid-phase screening of bacteria with cyclic amino alcohol deamination activity for enantioselective synthesis of chiral cyclic beta-amino alcohols

机译:细菌的高通量固相筛选循环氨基醇脱氨基活性,用于映选择性合成手性循环β-氨基醇

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摘要

Objectives To screening of bacteria with cyclic amino alcohol deamination activity for enantioselective synthesis of chiral cyclic beta-amino alcohols. Results A new strain named Arthrobacter sp. TYUT010-15 with the (R)-selective deamination activity of cyclic beta-amino alcohol has been isolated from nature via a high throughput solid-phase screening method. The reaction conditions of TYUT010-15 were optimized. Using the resting cell of TYUT010-15 as the catalyst, kinetic resolution of trans-2-aminocyclopentanol, trans-2-aminocyclohexanol and cis-1-amino-2-indanol was carried out to afford (1S, 2S)-trans-2-aminocyclopentanol, (1S, 2S)-trans-2-aminocyclohexanol and (1R, 2S)-cis-1-amino-2-indanol in > 99% ee and 49.6-50% conversion. Four aromatic beta-amino alcohols and two amines were also resolved, (S)-beta-amino alcohols and (R)-amines were obtained in > 99% ee. Preparation experiment was conducted with 200 mM (23.2 g L-1) racemic trans-2-aminocyclohexanol, yielding the desired (1S, 2S)-trans-2-aminocyclohexanol in 40% isolated yield, > 99% ee and 5.8 g L-1 d(-1) space time yields. Conclusions This study provides a high throughput solid-phase method for screening of bacteria with cyclic amino alcohol deamination activity and a first example for practical preparation of chiral cyclic beta-amino alcohol by Arthrobacter sp. TYUT010-15.
机译:筛选细菌的循环氨基醇脱氨基脱氨基对映选择性合成手性循环β-氨基醇的目的。结果一个名为Arthrobacter sp的新菌株。通过高通量固相筛选方法从性质中分离出循环β-氨基醇的(R) - 选择性脱胺活性的Tyut010-15。优化Tyut010-15的反应条件。使用Tyut010-15的静止细胞作为催化剂,进行反式-2-氨基酰氯醇,反式-2-氨基环己醇和顺式-1-氨基-2-茚满醇的动力学分辨率,得到(1s,2s) - 转发-2 - 氨基氰基戊醇,(1S,2S) - 转移-2-氨基酰己醇和(1R,2S)-CIS-1-氨基-2-茚满醇> 99%EE和49.6-50%转化率。还溶解了四种芳族β-氨基醇和两种胺,得到(S) - 氨基醇和(R) - 胺在> 99%EE中获得。用200mM(23.2g L-1)外消旋反式-2-氨基己醇进行制备实验,得到所需的(1S,2S)-Trans-2-氨基环己醇,分离出90%,> 99%EE和5.8g L- 1 d(-1)空间时间收益率。结论本研究提供了一种高通量固相方法,用于筛选具有环状氨基醇脱氨基活性的细菌,以及通过Arthrobacter SP进行手性环状β-氨基醇的第一个实施例。 tyut010-15。

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