Investigating the role of protein UnkG from the pseudomonas putida UW4 in the ability of the bacterium to facilitate plant growth

Wei Jiang, Zhenyu Cheng, Brendan J. McConkey, Bernard R. Glick

Producción científica: Contribución a una revistaArtículorevisión exhaustiva

2 Citas (Scopus)

Resumen

A previous study showed that overexpressing protein UnkG decreased the ability of the plant growth-promoting bacterium Pseudomonas putida UW4 to facilitate plant growth and an unkG knockout mutant of P. putida UW4 displayed increased plant growth promotion. When activities of wild-type and the UnkG overexpressing strain, including growth rates, carbon utilization, cell size, 3-indoleacetic acid production, and 1-aminocyclopropane-1-carboxylate deaminase activity, were measured, there were no apparent differences between the strains. Monitoring proteome-level changes to the wild-type and overexpressing transformant by means of two-dimensional difference in-gel electrophoresis followed by mass spectrometry identification of the altered proteins, 1839 protein spots were detected and 16 of the 84 protein spots with changed expression levels were identified. Proteins with increased expression included arginine deiminase, dihydrodipicolinate synthase, azurin, flavoprotein (α-subunit), ferredoxin-NADP reductase, ATP-dependent Hs1 protease (ATP-binding subunit), UDP-N-acetyl muramate-l-alanine ligase, biotin carboxyl carrier protein subunit of acetyl-CoA carboxylase, and Fis two-component transcriptional regulator. Proteins with decreased expression included glutaminase-asparaginase, arginine/ornithine ABC transporter, cell division protein FtsZ and glutamyl-tRNA synthetase. The functions of three of the 16 proteins could not be identified. The results are consistent with UnkG being detrimental to plant growth because it acts as a regulatory protein that negatively affects several key cellular functions related to the energy balance of the bacterium.

Idioma originalEnglish
Páginas (desde-hasta)331-336
Número de páginas6
PublicaciónCurrent Microbiology
Volumen66
N.º4
DOI
EstadoPublished - abr. 2013
Publicado de forma externa

Nota bibliográfica

Funding Information:
This work was supported by the Natural Science and Engineering Research Council of Canada Grant to B.R.G. We thank Mr. Dale Weber, Department of Biology, University of Waterloo, for help with electron microscopy.

ASJC Scopus Subject Areas

  • Microbiology
  • Applied Microbiology and Biotechnology

PubMed: MeSH publication types

  • Journal Article
  • Research Support, Non-U.S. Gov't

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