Literature DB >> 3897217

Photoaffinity labeling of undecaprenyl pyrophosphate synthetase with a farnesyl pyrophosphate analogue.

T Baba, J Muth, C M Allen.   

Abstract

The prenyl transferase undecaprenyl pyrophosphate synthetase was partially purified from the cytosolic fraction of Escherichia coli. Its enzymic products were characterized as a family of cis-polyprenyl phosphates, which ranged in carbon number from C55 to C25. The enzyme is constituted of two subunits of approximately 30,000 molecular weight. A radiolabeled photolabile analogue of t,t-farnesyl pyrophosphate, [3H]2-diazo-3-trifluoropropionyloxy geranyl pyrophosphate, was shown to label Lactobacillus plantarum and E. coli undecaprenyl pyrophosphate synthetase on UV irradiation in the presence of isopentenyl pyrophosphate and divalent cation. The only labeled polypeptide migrated on electrophoresis in a sodium dodecyl sulfate-polyacrylamide gel at a molecular weight of approximately 30,000. No protein was radiolabeled when the natural substrate, t,t-farnesyl pyrophosphate was included in the irradiation mixture. Irradiation in the presence of MgCl2 without isopentenyl pyrophosphate gave less labeling of the polypeptide. Irradiation with only isopentenyl pyrophosphate gave little labeling of the polypeptide. When the enzyme was irradiated with 3H-photoprobe, [14C]isopentenyl pyrophosphate, and MgCl2, the labeled polypeptide gave a ratio of 14C/3H that indicated the product must also bind to the enzyme on irradiation. These results demonstrate the ability to radiolabel the allylic pyrophosphate binding site and possibly product binding site of undecaprenyl pyrophosphate synthetase by a process which is favored when both cosubstrate and divalent cation are present.

Entities:  

Mesh:

Substances:

Year:  1985        PMID: 3897217

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  5 in total

1.  A Defective Undecaprenyl Pyrophosphate Synthase Induces Growth and Morphological Defects That Are Suppressed by Mutations in the Isoprenoid Pathway of Escherichia coli.

Authors:  William J MacCain; Suresh Kannan; Dannah Z Jameel; Jerry M Troutman; Kevin D Young
Journal:  J Bacteriol       Date:  2018-08-24       Impact factor: 3.490

2.  Synthesis of a-factor peptide from Saccharomyces cerevisiae and photoactive analogues via Fmoc solid phase methodology.

Authors:  Daniel G Mullen; Kelly Kyro; Melinda Hauser; Martin Gustavsson; Gianluigi Veglia; Jeffery M Becker; Fred Naider; Mark D Distefano
Journal:  Bioorg Med Chem       Date:  2010-11-12       Impact factor: 3.641

3.  Synthesis, properties, and applications of diazotrifluropropanoyl-containing photoactive analogs of farnesyl diphosphate containing modified linkages for enhanced stability.

Authors:  Marisa L Hovlid; Rebecca L Edelstein; Olivier Henry; Joshua Ochocki; Amanda DeGraw; Stepan Lenevich; Trista Talbot; Victor G Young; Alan W Hruza; Fernando Lopez-Gallego; Nicholas P Labello; Corey L Strickland; Claudia Schmidt-Dannert; Mark D Distefano
Journal:  Chem Biol Drug Des       Date:  2010-01       Impact factor: 2.817

4.  A versatile photoactivatable probe designed to label the diphosphate binding site of farnesyl diphosphate utilizing enzymes.

Authors:  Olivier Henry; Fernando Lopez-Gallego; Sean A Agger; Claudia Schmidt-Dannert; Stephanie Sen; David Shintani; Katrina Cornish; Mark D Distefano
Journal:  Bioorg Med Chem       Date:  2009-04-22       Impact factor: 3.641

5.  Use of genomics to identify bacterial undecaprenyl pyrophosphate synthetase: cloning, expression, and characterization of the essential uppS gene.

Authors:  C M Apfel; B Takács; M Fountoulakis; M Stieger; W Keck
Journal:  J Bacteriol       Date:  1999-01       Impact factor: 3.490

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.