Shotgun proteomics suggests involvement of additional enzymes in dioxin degradation by Sphingomonas wittichii RW1
Version of Record online: 30 SEP 2013
© 2013 Society for Applied Microbiology and John Wiley & Sons Ltd
Special Issue: Metabolism & Biodegradation
Volume 16, Issue 1, pages 162–176, January 2014
How to Cite
Hartmann, E. M. and Armengaud, J. (2014), Shotgun proteomics suggests involvement of additional enzymes in dioxin degradation by Sphingomonas wittichii RW1. Environmental Microbiology, 16: 162–176. doi: 10.1111/1462-2920.12264
- Issue online: 6 JAN 2014
- Version of Record online: 30 SEP 2013
- Accepted manuscript online: 30 AUG 2013 04:48AM EST
- Manuscript Accepted: 24 AUG 2013
- Manuscript Revised: 6 AUG 2013
- Manuscript Received: 10 JUN 2013
- Commissariat à l'Energie Atomique et aux Energies Alternatives
Fig. S1. Detection of select proteins encoded on the pSWIT01 plasmid after 72 h.
A. Normalized spectral abundance factors (NSAF) are calculated by dividing by the length of the protein in amino acids and normalized to total signal per run. Data represent the average of three biological replicates; error bars indicate the standard deviation.
B. Gene locations and orientations as annotated in the NCBI RefSeq genome sequence (NC_009511.1).
Table S1. List of peptides from all experiments.
Table S2. List of proteins from 72 h cultures.
Table S3. List of proteins from time series cultures.
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