This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Chen, L.
Right arrow Articles by Roberts, M. F.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Chen, L.
Right arrow Articles by Roberts, M. F.
Agricola
Right arrow Articles by Chen, L.
Right arrow Articles by Roberts, M. F.

 Previous Article  |  Next Article 

Appl Environ Microbiol, July 1998, p. 2609-2615, Vol. 64, No. 7
0099-2240/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.

Cloning and Expression of the Inositol Monophosphatase Gene from Methanococcus jannaschii and Characterization of the Enzyme

Liangjing Chen and Mary F. Roberts*

Merkert Chemistry Center, Boston College, Chestnut Hill, Massachusetts 02167

Received 16 March 1998/Accepted 4 May 1998

Inositol monophosphatase (EC 3.1.3.25) plays a pivotal role in the biosynthesis of di-myo-inositol-1,1'-phosphate, an osmolyte found in hyperthermophilic archaea. Given the sequence homology between the MJ109 gene product of Methanococcus jannaschii and human inositol monophosphatase, the MJ109 gene was cloned and expressed in Escherichia coli and examined for inositol monophosphatase activity. The purified MJ109 gene product showed inositol monophosphatase activity with kinetic parameters (Km = 0.091 ± 0.016 mM; Vmax = 9.3 ± 0.45 µmol of Pi min-1 mg of protein-1) comparable to those of mammalian and E. coli enzymes. Its substrate specificity, Mg2+ requirement, Li+ inhibition, subunit association (dimerization), and heat stability were studied and compared to those of other inositol monophosphatases. The lack of inhibition by low concentrations of Li+ and high concentrations of Mg2+ and the high rates of hydrolysis of glucose-1-phosphate and p-nitrophenylphosphate are the most pronounced differences between the archaeal inositol monophosphatase and those from other sources. The possible causes of these kinetic differences are discussed, based on the active site sequence alignment between M. jannaschii and human inositol monophosphatase and the crystal structure of the mammalian enzyme.


* Corresponding author. Mailing address: Department of Chemistry, Merkert Chemistry Center, Boston College, Chestnut Hill, MA 02167. Phone: (617) 552-3616. Fax: (617) 552-2705. E-mail: mary.roberts{at}bc.edu.


Appl Environ Microbiol, July 1998, p. 2609-2615, Vol. 64, No. 7
0099-2240/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.



This article has been cited by other articles:

  • Fukuda, C., Kawai, S., Murata, K. (2007). NADP(H) Phosphatase Activities of Archaeal Inositol Monophosphatase and Eubacterial 3'-Phosphoadenosine 5'-Phosphate Phosphatase. Appl. Environ. Microbiol. 73: 5447-5452 [Abstract] [Full Text]  
  • Rodionov, D. A., Kurnasov, O. V., Stec, B., Wang, Y., Roberts, M. F., Osterman, A. L. (2007). Genomic identification and in vitro reconstitution of a complete biosynthetic pathway for the osmolyte di-myo-inositol-phosphate. Proc. Natl. Acad. Sci. USA 104: 4279-4284 [Abstract] [Full Text]  
  • Kawai, S., Fukuda, C., Mukai, T., Murata, K. (2005). MJ0917 in Archaeon Methanococcus jannaschii Is a Novel NADP Phosphatase/NAD Kinase. J. Biol. Chem. 280: 39200-39207 [Abstract] [Full Text]  
  • Movahedzadeh, F., Rison, S. C. G., Wheeler, P. R., Kendall, S. L., Larson, T. J., Stoker, N. G. (2004). The Mycobacterium tuberculosis Rv1099c gene encodes a GlpX-like class II fructose 1,6-bisphosphatase. Microbiology 150: 3499-3505 [Abstract] [Full Text]  
  • Stieglitz, K. A., Johnson, K. A., Yang, H., Roberts, M. F., Seaton, B. A., Head, J. F., Stec, B. (2002). Crystal Structure of a Dual Activity IMPase/FBPase (AF2372) from Archaeoglobus fulgidus. THE STORY OF A MOBILE LOOP. J. Biol. Chem. 277: 22863-22874 [Abstract] [Full Text]  
  • Chen, L., Roberts, M. F. (1999). Characterization of a Tetrameric Inositol Monophosphatase from the Hyperthermophilic Bacterium Thermotoga maritima. Appl. Environ. Microbiol. 65: 4559-4567 [Abstract] [Full Text]  
  • Chen, L., Spiliotis, E. T., Roberts, M. F. (1998). Biosynthesis of Di-myo-Inositol-1,1'-Phosphate, a Novel Osmolyte in Hyperthermophilic Archaea. J. Bacteriol. 180: 3785-3792 [Abstract] [Full Text]