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Appl. Environ. Microbiol., Jan 1997, 156-161, Vol 63, No. 1
H Weingart and B Volksch
Significant amounts of ethylene were produced by Pseudomonas syringae pv.
glycinea, pv. phaseolicola (which had been isolated from viny weed Pueraria
lobata [Willd.] Ohwi [common name, kudzu]), and pv. pisi in synthetic
medium. On the other hand, the bean strains of P. syringae pv. phaseolicola
and strains of 17 other pathovars did not produce ethylene. P. syringae pv.
glycinea and P. syringae pv. phaseolicola produced nearly identical levels
of ethylene (about 5 x 10(sup-7) nl h(sup-1) cell(sup-1)), which were about
10 times higher than the ethylene level of P. syringae pv. pisi. Two 22-bp
oligonucleotide primers derived from the ethylene-forming enzyme (efe) gene
of P. syringae pv. phaseolicola PK2 were investigated for their ability to
detect ethylene-producing P. syringae strains by PCR analysis. PCR
amplification with this primer set resulted in a specific 0.99-kb fragment
in all ethylene-producing strains with the exception of the P. syringae pv.
pisi strains. Therefore, P. syringae pv. pisi may use a different
biosynthetic pathway for ethylene production or the sequence of the efe
gene is less conserved in this bacterium. P. syringae pv. phaseolicola
isolated from kudzu and P. syringae pv. glycinea also produced ethylene in
planta. It could be shown that the enhanced ethylene production in diseased
tissue was due to the production of ethylene by the inoculated bacteria.
Ethylene production in vitro and in planta was strictly growth associated.
Copyright © 1997, American Society for Microbiology
Ethylene Production by Pseudomonas syringae Pathovars In Vitro and In Planta
Institut fur Mikrobiologie, Friedrich-Schiller-Universitat, D-07743 Jena, Germany
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