RESUMO
The ability of methyl jasmonate (MeJa) to induce sesquiterpene production in root cultures of Hyoscyamus muticus has been studied. Although MeJa alone could not induce sesquiterpene in unwounded culture, MeJa added in the presence of wounding displayed a dose-dependent response, saturating at 50 µM. The ability to respond to MeJa declined with an increase in time between MeJa contact and wounding; however, responsiveness could be recovered by re-wounding of tissue prior to MeJa contact, suggesting that additional signaling related to wounding is required for sesquiterpene pathway induction. The saturation level of sesquiterpene induction with fungal elicitor was four times higher than the saturation level achieved by MeJa, with clear differences in sesquiterpene composition. Fungal elicitation results in a higher level of lubimin and a lower level of solavetivone production; whereas, methyl jasmonate induces predominantly solavetivone and little or no lubimin production. This suggests that fungal elicitation induces enzymes further down the sesquiterpene pathway which are not affected by MeJa. The induction of roots in contact with subsaturated levels of elicitor can be enhanced to saturation production levels by the addition of small amounts of MeJa (5-10 µmoles/l). In these studies, MeJa was consistently found to favor the earlier metabolite (solavetivone), while fungal elicitation promoted conversion to subsequent metabolites in the pathway (lubimin). The interactive role of MeJa in signal transduction for secondary metabolic production is discussed.
RESUMO
Cleared lysates of a proteolytic (Prt) strain and a naturally occurring non-proteolytic (Prt) variant of Streptococcus cremoris Wg2 contain equal amounts of covalently closed circular plasmid DNA. An analysis of this plasmid DNA by agarose gel electrophoresis revealed the presence of at least five different plasmid species in the Prt strain and only three plasmid species in the Prt variant. Curing studies with acriflavine indicated that a 16-megadalton plasmid determined proteolytic activity in the Prt strain. In energy-limited chemostats inoculated with both strains it was observed that the Prt strain was replaced by the Prt variant. This effect was most apparent when the pH of the culture was fixed at a value above 6.3. No selection for the Prt variant was observed at pH 5.9. Since the two types of organisms contain equal amounts of plasmid DNA, it was concluded that the energy gain of the Prt variants at pH values above 6.0 probably has to be found in protein synthesis rather than in plasmid DNA synthesis.
