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Purification, crystallization and preliminary X-ray crystallographic analysis of the receiver and stalk domains (PA3346RS) of the response regulator PA3346 from Pseudomonas aeruginosa PAO1

  • Pei Hsiu Wu
  • , Jye Jin Hsu
  • , Ting Wei Chiang
  • , Yin Cheng Hsieh
  • , Hwan You Chang
  • , Shou Lin Chang*
  • , Chun Jung Chen
  • *Corresponding author for this work
  • National Synchrotron Radiation Research Center Taiwan
  • National Tsing Hua University
  • National Cheng Kung University

Research output: Contribution to journalJournal Article peer-review

1 Scopus citations

Abstract

The regulatory domain (PA3346RS), comprising the receiver and stalk domains, of the response regulator PA3346 requires phosphorylation for activation with magnesium ions as cofactors in order to modulate the downstream protein phosphatase activity for the regulation of swarming motility in Pseudomonas aeruginosa PAO1. Fusion-tagged recombinant PA3346RS of total molecular mass 25.3 kDa has been overexpressed in Escherichia coli, purified using Ni 2+-NTA and Q - Sepharose ion-exchange columns and crystallized using the hanging-drop vapour-diffusion method. X-ray diffraction data were collected from PA3346RS crystals to 2.0 Å resolution. The crystal belonged to space group P4 1 or P4 3, with unit-cell parameters a = 82.38, c = 73.34 Å. Preliminary analysis indicated the presence of a dimer of PA3346RS in the asymmetric unit, with a solvent content of 48.6%.

Original languageEnglish
Pages (from-to)937-940
Number of pages4
JournalActa Crystallographica Section F: Structural Biology and Crystallization Communications
Volume67
Issue number8
DOIs
StatePublished - 08 2011
Externally publishedYes

Keywords

  • Pseudomonas aeruginosa
  • receiver domain
  • response regulator
  • stalk domain

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