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Kinetics of Malonyl-CoA Synthetase from Rhizobium trifolii and Evidences for Malonyl-AMP Formation as a Reaction Intermediate

  • Kang, Sang-Won (Department of Biochemistry, College of Sciences, Yonsei University) ;
  • Hong, Sung-Yu (Department of Biochemistry, College of Sciences, Yonsei University) ;
  • Ryoo, Hyung-Don (Department of Biochemistry, College of Sciences, Yonsei University) ;
  • Rhyu, Gyung-Ihm (National Industrial Technology Institute) ;
  • Kim Yu-Sam (Department of Biochemistry, College of Sciences, Yonsei University)
  • Published : 1994.05.20

Abstract

The catalytic mechanism of malonyl-CoA synthetase from Rhizobium trifolii was investigated by the steady state kinetics and intermediate identification. Initial velocity studies and the product inhibition studies with AMP and PPi strongly suggested ordered Bi Uni Uni Bi Ping-Pong Ter Ter system as the most probable steady state kinetic mechanism of malonyl-CoA synthetase. Michaelis constants were $0.17{\pm}0.04 {\mu}M,\;0.24{\pm}0.18 {\mu}M\;and\;0.045{\pm}0.26 {\mu}$M for ATP, malonate and CoA, respectively. The TLC analysis of the $^{32}P-labelled$ products in reaction mixture containing $[{\gamma}-^{32}P]$ ATP in the absence of CoA showed that PPi was produced after the sequential addition of ATP and malonate. Formation of malonyl-AMP, suggested as an intermediate in the kinetically deduced mechanism, was confirmed by the analysis of $^{31}P-NMR$ spectra of AMP product isolated from the $^{18}O$ transfer experiment using $[^{18}O]$malonate. Two resonances were observed, corresponding to AMP labelled with zero and one atom of $^{18}O$, indicating that one atom of $^{18}O$ transferred from $[^{18}O]$malonate to AMP through the formation of malonyl-AMP. Formation of malonyl-AMP was also confirmed through the TLC analysis of reaction mixture containing $[{\alpha}-^{32}P]$ATP. These results strongly support the ordered Bi Uni Uni Bi Ping-Pong Ter Ter mechanism deduced from the initial velocity and product inhibition studies.

Keywords

References

  1. Kor. Biochem. J. v.26 no.2 Kim, Y. S.;Kwon, S. J.;Kang, S. W.
  2. Kor. Biochem. J. v.26 no.3 Lee, S. C.;Kim, Y. S.
  3. Kor. Biochem. J. v.26 no.3 Lee, S. C.;Kim, Y. S.
  4. Kor. Biochem. J. v.26 no.4 Lee, S. C.;Kim, Y. S.
  5. Kor. Biochem. J. v.25 no.8 Kim, Y. S.;Park, J. W.;Kang, S. W.
  6. Kor. J. Microbiol. v.29 no.1 Kim, Y. S.;Chae, H. Z.;Lee, E.;Kim, Y. S.
  7. Anal. Biochem. v.170 Kim, Y. S.;Bang, S. K.
  8. J. Biol. Chem. v.234 Frieden, C.
  9. Methods Enzymol v.63 Cleland, W. W.
  10. Enzyme Kinetics; Behavior and Analysis of Rapid Equilibrium and Steady State Systems Segal, I. H.
  11. Proc. Natl. Acad. Sci. U. S. A. v.75 Cohn, M.;Hu, A.
  12. Eur. J. Biochem. v.5 Waldenstrom, J.
  13. J. Biol. Chem. v.243 Hirsh, D. I.
  14. J. Biol. Chem. v.250 Lovgren, T. N.;Heinonen, J.;Loftfield, R. B.

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  2. Identification of Active-Site Residues in Bradyrhizobium japonicum Malonyl-Coenzyme A Synthetase vol.378, pp.1, 1994, https://doi.org/10.1006/abbi.2000.1813
  3. Transcriptomic Studies of the Effect of nod Gene-Inducing Molecules in Rhizobia: Different Weapons, One Purpose vol.9, pp.1, 2018, https://doi.org/10.3390/genes9010001