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. 1999 May;65(5):1904–1909. doi: 10.1128/aem.65.5.1904-1909.1999

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Copyright © 1999, American Society for Microbiology

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FIG. 1 — PCR products amplified with syrD primers from 1-ng portions of DNA from various phytobacteria. Program 1 was used with an annealing temperature of 64°C. Lanes 1 and 12, HaeIII-digested φX174 replicative-form DNA; lane 2, P. syringae pv. syringae B301D; lane 3, P. syringae pv. syringae P268; lane 4, P. syringae pv. syringae HS191; lane 5, P. syringae pv. atrofaciens LMG 5095; lane 6, P. syringae pv. aptata LMG 5059; lane 7, P. syringae pv. tabaci LMG 5393; lane 8, P. syringae pv. pisi LMG 5079; lane 9, P. syringae pv. morsprunorum LMG 2222; lane 10, P. syringae pv. papulans LMG 5076; lane 11, P. viridiflava LMG 2352. Products were separated on a 0.8% agarose gel.