Structural studies of Escherichia coli UDP-N-acetylmuramate:L-alanine ligase
| Autor: | Paul Falk, Haiyong Jin, Robert Fairman, Hsu-Tso Ho, James G. Robertson, John J. Emanuele, Mark E. Hail, Joseph J. Villafranca |
|---|---|
| Rok vydání: | 1996 |
| Předmět: |
chemistry.chemical_classification
Alanine Circular dichroism DNA ligase Chemistry Electrospray ionization Centrifugation Isopycnic Biochemistry Mass Spectrometry Protein Structure Secondary Recombinant Proteins Dissociation constant Molecular Weight chemistry.chemical_compound Uridine diphosphate Sedimentation equilibrium Escherichia coli Peptidoglycan Peptide Synthases |
| Zdroj: | Biochemistry. 35(5) |
| ISSN: | 0006-2960 |
| Popis: | Uridine diphosphate N-acetylmuramate:L-alanine ligase (EC 6.3.2.8, UNAM:L-Ala ligase or MurC gene product) adds the first amino acid to the sugar moiety of the peptidoglycan precursor, catalyzing one of the essential steps in cell wall biosynthesis for both gram-positive and gram-negative bacteria. Here, we report our studies on the secondary and quaternary structures of UNAM:L-Ala ligase from Escherichia coli. The molecular weight of the purified recombinant enzyme determined by electrospray ionization mass spectrometry agreed well with the molecular weight deduced from the DNA sequence. Through sedimentation equilibrium analysis, we show that the enzyme exists in equilibrium between monomeric and dimeric forms and that the dissociation constant of the dimer, Kd, was determined to be 1.1 +/- 0.4 microM at 37 degrees C and 0.58 +/- 0.30 microM at 4 degrees C. A very similar Kd value was also obtained at 37 degrees C by gel filtration chromatography. The secondary structure of the enzyme was characterized by circular dichroism spectroscopy. No change in the secondary structure was observed between the monomeric and dimeric forms of the enzyme. The activity assays at enzyme concentrations both below and above the determined Kd value lead to the conclusion that the enzyme is active both as dimers and as monomers and that the specific activity is independent of the oligomerization state. |
| Databáze: | OpenAIRE |
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