Proteome Science
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ResearchProteomic profiling of L-cysteine induced selenite resistance in Enterobacter sp. YSUAshley Jasenec , Nathaniel Barasa , Samatha Kulkarni , Nabeel Shaik , Swarnalatha Moparthi , Venkataramana Konda and Jonathan Caguiat  Department of Biological Sciences, Proteomics/Genomics Research Group, Youngstown State University, One University Plaza, Youngstown, OH 44555, USA author email corresponding author email
Proteome Science 2009,
7:30doi:10.1186/1477-5956-7-30
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| Published: |
28 August 2009 |
Abstract
Background
Enterobacter sp. YSU is resistant to several different heavy metal salts, including selenite. A previous study using M-9 minimal medium showed that when the selenite concentration was 100,000 times higher than the sulfate concentration, selenite entered Escherichia coli cells using two pathways: a specific and a non-specific pathway. In the specific pathway, selenite entered the cells through a yet to be characterized channel dedicated for selenite. In the non-specific pathway, selenite entered the cells through a sulfate permease channel. Addition of L-cystine, an L-cysteine dimer, appeared to indirectly decrease selenite import into the cell through the non-specific pathway. However, it did not affect the level of selenite transport into the cell through the specific pathway.
Results
Growth curves using M-9 minimal medium containing 40 mM selenite and 1 mM sulfate showed that Enterobacter sp. YSU grew when L-cysteine was present but died when it was absent. Differential protein expression analysis by two dimensional gel electrophoresis showed that CysK was present in cultures containing selenite and lacking L-cysteine but absent in cultures containing both selenite and L-cysteine. Additional RT-PCR studies demonstrated that transcripts for the sulfate permease genes, cysA, cysT and cysW, were down-regulated in the presence of L-cysteine.
Conclusion
L-cysteine appeared to confer selenite resistance upon Enterobacter sp. YSU by decreasing the level of selenite transport into the cell through the non-specific pathway. |