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School of Engineering and Science - Jacobs University

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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

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