ABSTRACT
The hygrophorones, a class of cyclopentenones isolated from fruiting bodies of the genus Hygrophorus (basidiomycetes), show promising antifungal activity. While the constitution of 4,6-diacetylhygrophorone A(12) (3) and the relative configuration of the stereogenic centers in the cyclopentenone ring were elucidated using standard NMR and MS techniques, the relative configuration of the exocyclic stereogenic center could not be assigned. By introducing a sample of 3 into an alignment medium and measuring anisotropic NMR parameters, namely, residual dipolar couplings, we were able to unambiguously determine the relative configuration of all three stereogenic centers in 4,6-diacetylhygrophorone A(12) simultaneously by fitting several structure proposals to the experimental data.
Subject(s)
Basidiomycota/chemistry , Cyclopentanes/isolation & purification , Cyclopentanes/pharmacology , Fungicides, Industrial/isolation & purification , Fungicides, Industrial/pharmacology , Cyclopentanes/chemistry , Cyclopentanes/classification , Fungicides, Industrial/chemistry , Fungicides, Industrial/classification , Molecular Structure , Nuclear Magnetic Resonance, BiomolecularABSTRACT
Detailed measurements of long-range heteronuclear spin-spin coupling constants, especially (2, 3)J(CH) spin-spin couplings for various cyclopentane derivatives, are reported. The measurements are based on a 2D heteronuclear correlation experiment named G-BIRD(R, X)-CPMG-HSQMBC.
Subject(s)
Cyclopentanes/chemistry , Magnetic Resonance Spectroscopy , Cyclopentanes/classification , Cyclopentanes/standards , Molecular Structure , Reference StandardsABSTRACT
Suspension cultures of Taxus chinensis were used as a model plant cell system to evaluate novel synthetic jasmonates as elicitors for stimulating the biosynthesis of secondary metabolites. Significant increases in accumulation of taxuyunnanine C (Tc) were observed in the presence of newly synthesized 2-hydroxyethyl jasmonate (HEJA) and trifluoroethyl jasmonate (TFEJA) without their inhibition on cell growth. Addition of 100 microM HEJA or TFEJA on day 7 led to a high Tc content of 44.3 +/- 1.1mg/g or 39.7 +/- 1.1 mg/g (at day 21), while the Tc content was 14.0 +/- 0.1 mg/g and 32.4 +/- 1.6 mg/g for the control and that with addition of 100 microM methyl jasmonate (MJA), respectively. The superior stimulating ability of HEJA and TFEJA over MJA, which was generally considered as the best chemical for eliciting taxoid biosynthesis, suggests that the novel jasmonate analogues may have great potential in application to other cell culture systems for effcient elicitation of plant secondary metabolites.
Subject(s)
Cell Culture Techniques/methods , Cyclopentanes/pharmacology , Taxoids/chemical synthesis , Taxus/drug effects , Taxus/metabolism , Cell Division/drug effects , Cells, Cultured , Cyclopentanes/classification , Dose-Response Relationship, Drug , Oxylipins , Taxoids/metabolism , Taxus/cytology , Taxus/growth & developmentABSTRACT
Coronalon, a synthetic 6-ethyl indanoyl isoleucine conjugate, has been designed as a highly active mimic of octadecanoid phytohormones that are involved in insect and disease resistance. The spectrum of biological activities that is affected by coronalon was investigated in nine different plant systems specifically responding to jasmonates and/or 12-oxo-phytodienoic acid. In all bioassays analyzed, coronalon demonstrated a general strong activity at low micromolar concentrations. The results obtained showed the induction of (i) defense-related secondary metabolite accumulation in both cell cultures and plant tissues, (ii) specific abiotic and biotic stress-related gene expression, and (iii) root growth retardation. The general activity of coronalon in the induction of plant stress responses together with its simple and efficient synthesis suggests that this compound might serve as a valuable tool in the examination of various aspects in plant stress physiology. Moreover, coronalon might become employed in agriculture to elicit plant resistance against various aggressors.
Subject(s)
Isoleucine/analogs & derivatives , Isoleucine/pharmacology , Plant Physiological Phenomena , Plants/drug effects , Cells, Cultured , Cyclopentanes/classification , Cyclopentanes/pharmacology , Dose-Response Relationship, Drug , Fatty Acids, Unsaturated/pharmacology , Gene Expression/drug effects , Gene Expression Regulation, Plant/drug effects , Genes, Plant , Isoleucine/chemistry , Kinetics , Molecular Structure , Oxylipins , Plant Development , Plant Growth Regulators/pharmacology , Plant Roots/drug effects , Plant Roots/physiology , Structure-Activity RelationshipABSTRACT
The genomes of most Nicotiana species contain three different subfamilies of the Tnt1 retrotransposon, which differ completely in their U3 sequence, whereas the rest of the sequence is relatively constant. The results presented here show that all three Tnt1 subfamilies are expressed in tobacco (Nicotiana tabacum) and that the U3 sequence variability correlates with differences in the pattern of expression of the Tnt1 elements. Each of the three Tnt1 subfamilies is induced by stress, but their promoters have a different response to different stress-associated signaling molecules. The Tnt1A subfamily is particularly strongly induced by elicitors and methyl jasmonate, whereas expression of the Tnt1C subfamily is more sensitive to salicylic acid and auxins. The direct relationship between U3 sequence variability and differences in the stress-associated expression of the Tnt1 elements present in a single host species gives support to our model that postulates that retrotransposons have adapted to their host genomes through the evolution of highly regulated promoters that mimic those of the stress-induced plant genes. Moreover, here we show that the analysis of the transcriptional control of a retrotransposon population such as Tnt1 provides new insights into the study of the complex and still poorly understood network of defense- and stress-induced plant signal transduction pathways.