School of Engineering and Science - Jacobs University
School of Engineering and Science - Jacobs University
School of Engineering and Science - Jacobs University
Create successful ePaper yourself
Turn your PDF publications into a flip-book with our unique Google optimized e-Paper software.
Material <strong>and</strong> Methods<br />
PCR-Screening for achromobactin-like siderophore production:<br />
iuc1-fwd:<br />
TGCTGGACTGGTTCGATG<br />
iuc1-rev:<br />
GATCAGCAGGCAATAGG<br />
iuc2-fwd:<br />
AAATCGAGCAGACCCAGC<br />
iuc2-rev:<br />
TGTTGGTCATGCTCATCG<br />
4 Methods<br />
4.1 Bacterial growth conditions<br />
4.1.1 Escherichia coli<br />
E. coli cells were grown overnight at 37°C on LB agar plates containing the<br />
appropriate antibiotics. Subsequently, E. coli cells were cultured overnight at<br />
37°C by shaking at 250 rpm in LB medium containing the appropriate<br />
antibiotics. 2 ml plastic reaction tubes <strong>and</strong> test tubes were used for growth <strong>of</strong><br />
small volumes <strong>of</strong> E. coli cultures (1-5 ml), <strong>and</strong> Erlenmeyer flasks were used for<br />
growth <strong>of</strong> big volumes <strong>of</strong> E. coli cultures (50-500 ml).<br />
4.1.2 Pseudomonas syringae<br />
P. syringae cells were grown for 2-5 days at 28°C on MG agar plates<br />
containing appropriate antibiotics. Subsequently, P. syringae cells were<br />
inoculated in liquid media (KB, 5b or Pipes) <strong>and</strong> grown at 28°C by shaking at<br />
280 rpm. Test tubes were used for growth <strong>of</strong> small volumes <strong>of</strong> P. syringae<br />
cultures (5 ml) <strong>and</strong> Erlenmeyer flasks were used for growth <strong>of</strong> big volumes <strong>of</strong><br />
P. syringae cultures (20-250 ml).<br />
28