Chiral separation of phenylalanine by ultrafiltration through immobilized DNA membranes

被引:70
作者
Higuchi, A [1 ]
Higuchi, Y
Furuta, K
Yoon, BO
Hara, M
Maniwa, S
Saitoh, M
Sanui, K
机构
[1] Seikei Univ, Dept Appl Chem, Musashino, Tokyo 1808633, Japan
[2] Asahi Chem Ind Co Ltd, Cent Lab, Miyazaki 8820847, Japan
[3] Sophia Univ, Dept Chem, Chiyoda Ku, Tokyo 1028554, Japan
关键词
ultrafiltration; optical resolution; DNA; recognition; chiral separation;
D O I
10.1016/S0376-7388(03)00263-1
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
In the current studies, we investigated the use of immobilized DNA membranes for chiral separation. D-Phenylalanine preferentially permeated through immobilized DNA membranes with a pore size <2.0 nm (molecular weight cut-off (MWCO) < 5000) while L-phenylalanine preferentially permeated through immobilized DNA membranes with a pore size >2.0 nm (MWCO > 5000). The pore size of the immobilized DNA membranes regulated preferential permeation of the enantiomer through the membranes. The immobilized DNA membranes are categorized as channel-type membranes and not as affinity membranes. We further propose a multi-stage cascade for chiral separation by ultrafiltration. When the two types of the membranes were used in a cascade filtration system, there was no change of concentration ratio between L-enantiomer and D-enantiomer in the feed solution at each stage. Only two membranes were necessary in a multi-stage processes if both membrane types were used. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:207 / 218
页数:12
相关论文
共 43 条
[1]  
ALBERTS B, MOL BIOL CELL, pCH3
[2]   Enantioselective permeation of racemates through a solid (+)-poly{2-[dimethyl(10-pinanyl)silyl]norbornadiene} membrane [J].
Aoki, T ;
Ohshima, M ;
Shinohara, KI ;
Kaneko, T ;
Oikawa, E .
POLYMER, 1997, 38 (01) :235-238
[3]   ENANTIOSELECTIVE PERMEATION THROUGH POLY(GAMMA-[3-(PENTAMETHYLDISILOXANYL)PROPYL]-L-GLUTAMATE) MEMBRANES [J].
AOKI, T ;
TOMIZAWA, S ;
OIKAWA, E .
JOURNAL OF MEMBRANE SCIENCE, 1995, 99 (02) :117-125
[4]   Fluorescent dye assay for detection of DNA in recombinant protein products [J].
Bolger, R ;
Lenoch, F ;
Allen, E ;
Meiklejohn, B ;
Burke, T .
BIOTECHNIQUES, 1997, 23 (03) :532-&
[5]  
BRANDT K, 1991, NACHR CHEM TECH LAB, V39, pM1
[6]  
Denizli A, 1999, J APPL POLYM SCI, V74, P655, DOI 10.1002/(SICI)1097-4628(19991017)74:3<655::AID-APP19>3.0.CO
[7]  
2-N
[8]   Enantiomeric separation by ultrafiltration: complexation mechanism of tryptophan analogs to bovine serum albumin [J].
Garnier, F ;
Randon, J ;
Rocca, JL .
SEPARATION AND PURIFICATION TECHNOLOGY, 1999, 16 (03) :243-250
[9]  
Hesse G., 1973, CHROMATOGRAPHIA, V6, P277
[10]   Oscillation of membrane potential in immobilized DNA membranes [J].
Higuchi, A ;
Adachi, S ;
Imizu, T ;
Ok, YB ;
Tsubomura, T ;
Hara, M ;
Sakai, K .
JOURNAL OF PHYSICAL CHEMISTRY B, 2000, 104 (42) :9864-9872