来自假单胞菌属菌株NCIB 9816-4的萘双加氧酶对（R）-和（S）-1-茚醇的立体特异性氧化作用。
Stereospecific oxidation of (R)- and (S)-1-indanol by naphthalene dioxygenase from Pseudomonas sp. strain NCIB 9816-4.
作者信息
Lee K, Resnick S M, Gibson D T
机构信息
Department of Microbiology, University of Iowa, Iowa City 52242, USA.
出版信息
Appl Environ Microbiol. 1997 May;63(5):2067-70. doi: 10.1128/aem.63.5.2067-2070.1997.
Abstract
A recombinant Escherichia coli strain which expresses naphthalene dioxygenase (NDO) from Pseudomonas sp. strain NCIB 9816-4 oxidized (S)-1-indanol to trans-(1S,3S)-indan-1,3-diol (95.5%) and (R)-3-hydroxy-1-indanone (4.5%). The same cells oxidized (R)-1-indanol to cis-1,3-indandiol (71%), (R)-3-hydroxy-1-indanone (18.2%), and cis-1,2,3-indantriol (10.8%). Purified NDO oxidized (S)-1-indenol to both syn- and anti-2,3-dihydroxy-1-indanol.
摘要
一种表达来自假单胞菌属菌株NCIB 9816 - 4的萘双加氧酶（NDO）的重组大肠杆菌菌株，将（S）-1-茚醇氧化为反式-（1S，3S）-茚-1,3-二醇（95.5%）和（R）-3-羟基-1-茚酮（4.5%）。同样的细胞将（R）-1-茚醇氧化为顺式-1,3-茚二醇（71%）、（R）-3-羟基-1-茚酮（18.2%）和顺式-1,2,3-茚三醇（10.8%）。纯化的NDO将（S）-1-茚醇氧化为顺式和反式-2,3-二羟基-1-茚醇。
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