ARTIFICIAL METALLOPHOSPHOESTERASES BUILT ON POLY(ETHYLENIMINE)

被引:33
作者
KIM, N [1 ]
SUH, J [1 ]
机构
[1] SEOUL NATL UNIV,DEPT CHEM,SEOUL 151742,SOUTH KOREA
关键词
D O I
10.1021/jo00085a050
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Various derivatives of poly(ethylenimine) (PEI)-containing macrocyclic metal centers were prepared by condensation of PEI with several dicarbonyl compounds in the presence of a series of metal ions involved as templates. In view of the biological functions of transphosphorylation reactions, the PEI-based macrocyclic complexes were tested for their activity as artificial metallophosphoesterases. Hydrolysis of bis(p-nitrophenyl) phosphate (BNPP) and p-nitrophenyl phosphate (NPP) was catalyzed by the PEI-based macrocyclic complexes. Kinetic data for the hydrolysis of BNPP or NPP revealed complex formation between the substrate and the catalysts, followed by efficient dephoephorylation of the complexed substrate. Depending upon the structure of the catalyst and the reaction conditions, the degree of acceleration observed for BNPP and NPP hydrolysis was up to 6 orders of magnitude. The most effective catalyis was achieved by the macrocyclic complex prepared by condensation of PEI with glyoxal in the presence of Co(II) ion. The PEI-based macrocycles containing divalent metal ions such as Fe(III), Ni(II), Cu(II), or Zn(II) ion were also quite effective catalysts for the hydrolysis of BNPP or NPP. The catalytic activity of the PEI-based macrocyclic complexes containing divalent metal ions was much greater than that of other synthetic catalysts containing divalent metal ions ever reported. Possible origins of the effective catalysis are discussed, in view of the mechanisms proposed for analogous enzymatic and nonenzymatic hydrolysis of phosphate esters. Characteristics of actions of metalloenzymes such as essential involvement of metal ions, complex formation with the substrates, and efficient catalysis in the conversion of bound substrates were reproduced by the artificial metallophosphoesterases. The metal centers of the artificial metallophosphoesterases are involved both in substrate binding and in catalytic transformation. Catalytic repertoires played by the metal ions are discussed.
引用
收藏
页码:1561 / 1571
页数:11
相关论文
共 57 条
[51]   COBALT(III)-PROMOTED HYDROLYSIS OF AMINO-ACID ESTERS AND PEPTIDES AND THE SYNTHESIS OF SMALL PEPTIDES [J].
SUTTON, PA ;
BUCKINGHAM, DA .
ACCOUNTS OF CHEMICAL RESEARCH, 1987, 20 (10) :357-364
[52]   EFFECTS OF METAL-IONS ON THE HYDROLYSIS OF P-NITROPHENYL CAPROATE BY MODIFIED POLY(ETHYLENIMINE)S [J].
TAKAGISHI, T ;
KLOTZ, IM .
BIOPOLYMERS, 1979, 18 (10) :2497-2505
[53]   AMINOPEPTIDASES - STRUCTURE AND FUNCTION [J].
TAYLOR, A .
FASEB JOURNAL, 1993, 7 (02) :290-298
[54]  
VALLEE BL, 1986, ZINC ENZYMES, pCH1
[55]   HYDROLYSIS OF PHOSPHATE MONOESTERS - A BIOLOGICAL PROBLEM WITH MULTIPLE CHEMICAL SOLUTIONS [J].
VINCENT, JB ;
CROWDER, MW ;
AVERILL, BA .
TRENDS IN BIOCHEMICAL SCIENCES, 1992, 17 (03) :105-110
[56]   CRYSTAL-STRUCTURE OF PENICILLIUM-CITRINUM P1 NUCLEASE AT 2.8-A RESOLUTION [J].
VOLBEDA, A ;
LAHM, A ;
SAKIYAMA, F ;
SUCK, D .
EMBO JOURNAL, 1991, 10 (07) :1607-1618
[57]   SELECTIVE HYDROLYSIS OF PEPTIDES, PROMOTED BY PALLADIUM AQUA COMPLEXES - KINETIC EFFECTS OF THE LEAVING GROUP, PH, AND INHIBITORS [J].
ZHU, LG ;
KOSTIC, NM .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1993, 115 (11) :4566-4570