Dinuclear zinc(II) complex of a new acyclic phenol-based dinucleating ligand with four methoxyethyl chelating arms: first dizinc model with aminopeptidase function

(Note: The full text of this document is currently only available in the PDF Version )

Hiroshi Sakiyama, Rieko Mochizuki, Akihiko Sugawara, Masatomi Sakamoto, Yuzo Nishida and Mikio Yamasaki


Abstract

A new end-off type acyclic ligand with four methoxyethyl chelating arms, 2,6-bis[bis(2-methoxyethyl)aminomethyl]-4-methylphenol (Hbomp), formed a dinuclear zinc(II) complex [Zn2(bomp)(MeCO2)2]BPh4 1. X-Ray analysis revealed that the complex 1·CHCl3 contains two zinc ions bridged by the phenolic oxygen and two acetate groups, forming a µ-phenoxo-bis(µ-acetato)dizinc(II) core. The aminopeptidase function of complex 1 was estimated using N-p-nitrophenyl-L-leucine as substrate. The release of p-nitroaniline as the result of the substrate hydrolysis is first order in both complex and substrate concentrations with k = 2.3(1) × 10–3 dm3 mol–1 s–1.


References

  1. C. G. Dealwis, L. Chen, C. Brennan, W. Mandecki and C. Abad-Zapatero, Protein Eng., 1995, 8, 865 CAS.
  2. Y. Zhang, J. Y. Liang, S. Huang, H. Ke and W. N. Lipscomb, Biochemistry, 1993, 32, 1844 CrossRef CAS.
  3. S. K. Burley, P. R. David, A. Taylor and W. N. Lipscomb, Proc. Natl. Acad. Sci. USA, 1990, 87, 6878 CAS.
  4. S. L. Roderick and B. W. Matthews, Biochemistry, 1993, 32, 3907 CrossRef CAS.
  5. B. Chevrier, C. Schalk, H. D'orchymont, J. M. Rondeau, D. Moras and C. Tarnus, Structure, 1994, 2, 283 CrossRef CAS.
  6. A. Ishikubo, M. Yashiro and M. Komiyama, Nucleic Acids Symp. Ser., 1995, 34, 85 Search PubMed.
  7. C. Bazzicalupi, A. Bencini, A. Bianchi, V. Fusi, C. Giorgi, P. Paoletti, B. Valtancoli and D. Zanchi, Inorg. Chem., 1997, 36, 2784 CrossRef CAS.
  8. M. Suzuki, H. Kanatomi and I. Murase, Chem. Lett., 1981, 1745 CAS.
  9. M. Suzuki, M. Mikuriya, S. Murata, A. Uehara, H. Oshio, S. Kida and K. Saito, Bull. Chem. Soc. Jpn., 1987, 60, 4305 CAS; A. S. Borovik and L. Que, Jr., J. Am. Chem. Soc., 1988, 110, 2345 CrossRef CAS; H. Diril, H.-R. Chang, M. J. Nilges, X. Zhang, J. A. Potenza, H. J. Schugar, S. S. Isied and D. H. Hendrickson, J. Am. Chem. Soc., 1989, 111, 5102 CrossRef CAS; A. S. Borovik, V. Papaefthymiou, L. F. Taylor, O. P. Anderson and L. Que, Jr., J. Am. Chem. Soc., 1989, 111, 6183 CrossRef CAS; T. R. Holman, C. Juarez-Garcia, M. P. Hendrich, L. Que, Jr. and E. Münck, J. Am. Chem. Soc., 1990, 112, 7611 CrossRef CAS; M. Ghiladi, C. J. McKenzie, A. Meier, A. K. Powell, J. Ulstrup and K. Wocadlo, J. Chem. Soc., Dalton Trans., 1997, 4011 RSC.
  10. B. P. Murch, P. D. Boyle and L. Que, Jr., J. Am. Chem. Soc., 1985, 107, 6728 CrossRef CAS; B. P. Murch, F. C. Bradley, P. D. Boyle, V. Papaefthymiou and L. Que, Jr., J. Am. Chem. Soc., 1987, 109, 7993 CrossRef CAS.
  11. N. Sträter and W. N. Lipscomb, Biochemistry, 1995, 34, 14792 CrossRef CAS.
  12. G. Chen, T. Edwards, V. M. D'souza and R. C. Holz, Biochemistry, 1997, 36, 4278 CrossRef CAS.
  13. A. Altomare, M. C. Burla, M. Camalli, M. Cascarano, C. Giacovazzo, A. Guagliardi and G. Polidori, J. Appl. Crystallogr., 1994, 27, 435 CrossRef.
  14. P. T. Beurskens, G. Admiraal, G. Beurskens, W. P. Bosman, R. de Geder, R. Israel and J. M. M. Smits, The DIRDIF 94 program system, Technical Report of the Crystallography Laboratory, University of Nijmegen, 1994.
  15. D. T. Cromer and J. T. Waber, International Tables for X-Ray Crystallography, Kynoch Press, Birmingham, 1974, vol. IV, Table 2.2 A Search PubMed.
  16. TEXSAN, Crystal Structure Analysis Package, Molecular Structure Corporation, Houston, TX, 1985 and 1992.
  17. C. K. Johnson, ORTEP, Report ORNL 5138, Oak Ridge National Laboratory, Oak Ridge, TN, 1976.
  18. G. B. Deacon and R. J. Phillips, Coord. Chem. Rev., 1980, 32, 227 CrossRef.
Click here to see how this site uses Cookies. View our privacy policy here.