A Case of Convergent Evolution: The Bacterial Sesquiterpene Synthase for 1-epi-Cubenol from Nonomuraea coxensis

A terpene synthase from Nonomuraea coxensis was identified as (+)-1-epi-cubenol synthase. The enzyme is phylogenetically unrelated to the known enzyme of the same function that is widespread in streptomycetes. Isotopic labelling experiments were performed to unambiguously assign the NMR data and to investigate hydrogen migrations during terpene cyclisations. Epoxidations of (+)-1-epi-cubenol and of the plant derived compounds (−)-cubenol and (−)-1-epi-cubenol confirmed the structure of a natural product isolated from the brown alga Dictyopteris divaricata and allowed to conclude on its absolute configuration. The crystal structures of the epoxides from (+)- and (−)-1-epi-cubenol and the acid catalysed conversion into an isomeric ketone are reported.     

Revision of the Cyclisation Mechanism for the Diterpene Spiroviolene and Investigations of Its Mass Spectrometric Fragmentation

The diterpene spiroviolene, its diterpene synthase from Streptomyces violens and the experimentally determined terpene cyclisation mechanism were reported in 2017. Recently, the structure of spiroviolene was revised based on a total synthesis, with consequences for the cyclisation mechanism. Herein, a reinvestigation of the terpene cyclisation to spiroviolene and the mass spectrometric fragmentation mechanism investigated by ¹³C-labelling experiments are presented.     

Sesquiterpene Synthase‐Catalysed Formation of a New Medium‐Sized Cyclic Terpenoid Ether from Farnesyl Diphosphate Analogues

Terpene synthases catalyse the first step in the conversion of prenyl diphosphates to terpenoids. They act as templates for their substrates to generate a reactive conformation, from which a Mg²⁺‐dependent reaction creates a carbocation–PP_i ion pair that undergoes a series of rearrangements and (de)protonations to give the final terpene product. This tight conformational control was exploited for the (R)‐germacrene A synthase– and germacradien‐4‐ol synthase–catalysed formation of a medium‐sized cyclic terpenoid ether from substrates containing nucleophilic functional groups. Farnesyl diphosphate analogues with a 10,11‐epoxide or an allylic alcohol were efficiently converted to a 11‐membered cyclic terpenoid ether that was characterised by HRMS and NMR spectroscopic analyses. Further experiments showed that other sesquiterpene synthases, including aristolochene synthase, δ‐cadinene synthase and amorphadiene synthase, yielded this novel terpenoid from the same substrate analogues. This work illustrates the potential of terpene synthases for the efficient generation of structurally and functionally novel medium‐sized terpene ethers.     

Volatile Terpenes from Actinomycetes: A Biosynthetic Study Correlating Chemical Analyses to Genome Data

The volatile terpenes of 24 actinomycetes whose genomes have been sequenced (or are currently being sequenced) were collected by use of a closed‐loop stripping apparatus and identified by GC/MS. The analytical data were compared against a phylogenetic analysis of all 192 currently available sequences of bacterial terpene cyclases (excluding geosmin and 2‐methylisoborneol synthases). In addition to the several groups of terpenes with known biosynthetic origin, selinadienes were identified as a large group of biosynthetically related sesquiterpenes that are produced by several streptomycetes. The detection of a large number of previously unrecognised side products of known terpene cyclases proved to be particularly important for an in depth understanding of biosynthetic pathways to known terpenes in actinomycetes. Interpretation of the chemical analytical data in the context of the phylogenetic tree of bacterial terpene cyclases pointed to the function of three new enzymes: (E)‐β‐caryophyllene synthase, selina‐3,7(11)‐diene synthase and aristolochene synthase.     

Total Syntheses and Chemical Biology Studies of Hymeglusin and Fusarilactone A,Novel Circumventors of β-Lactam Drug Resistance in Methicillin-Resistant Staphylococcus aureus

Hymeglusin, a previously known eukaryotic hydroxymethylglutaryl-CoA (HMG−CoA) synthase inhibitor, was identified as circumventing the β-lactam drug resistance in methicillin-resistant Staphylococcus aureus (MRSA). We describe the concise total syntheses of a series of natural products, which enabled determination of the absolute configuration of fusarilactone A and provided structure-activity relationship information. Based on previous reports, we speculated that the target protein of this circumventing effect may be MRSA bacterial HMG−CoA synthase (mvaS). We found that this enzyme was dose-dependently inhibited by hymeglusin. Furthermore, overexpression of the MRSA mvaS gene and site-directed mutagenesis studies suggested its binding site and the mechanism of action.     

Protonation‐Initiated Cyclization by a Class II Terpene Cyclase Assisted by Tunneling

Terpenes represent one of the most diversified classes of natural products with potent biological activities. The key to the myriad of polycyclic terpene skeletons with crucial functions in organisms from all kingdoms of life are terpene cyclase enzymes. These biocatalysts enable stereospecific cyclization of relatively simple, linear, prefolded polyisoprenes by highly complex, partially concerted, electrophilic cyclization cascades that remain incompletely understood. Herein, additional mechanistic light is shed on terpene biosynthesis by kinetic studies in mixed H₂O/D₂O buffers of a class II bacterial ent‐copalyl diphosphate synthase. Mass spectrometry determination of the extent of deuterium incorporation in the bicyclic product, reminiscent of initial carbocation formation by protonation, resulted in a large kinetic isotope effect of up to seven. Kinetic analysis at different temperatures confirmed that the isotope effect was independent of temperature, which is consistent with hydrogen tunneling.     

Zeolite NaY‐Promoted Monocyclization of Epoxy Polyene Terpenes: A Unique Route for the Direct Synthesis of Incompletely Cyclized Naturally Occurring Terpenols

A variety of epoxy polyene terpenes cyclize readily by confinement within zeolite NaY to form primarily products of monocyclization. The monocyclization pathway is highly predominant, irrespectively of the side chain of the epoxy terpene, while the monocyclic products possess regioselectively an exomethylenic double bond. The selective monocyclization in the case of epoxyfarnesyl acetate, epoxyfarnesylacetone or 2,3‐epoxysqualene, provides a direct route to the synthesis of a variety of natural products, such as elengasidiol, farnesiferols B–D, achilleol A, camelliol C and to four farnesylacetone‐derived metabolites isolated from the brown algae Cystophora monoliformis. The optical rotation of achilleol A derived from the cyclization of (S)‐2,3‐epoxysqualene matches with that of the natural product, thus the absolute configuration of achilleol A was established as 1S,3R. From the mechanistic point of view, the NaY‐promoted cyclization of 9,10‐epoxygeranylacetone, selectively deuterium labelled at the C‐10 methyl group, is >97% stereoselective with respect to the topicity of the gem‐dimethyl group. This result is in agreement with a concerted mechanism. Finally, we have proved through labelling experiments, for the first time, that the biomimetic transformation of epoxy polyene terpenes to 2,3,4‐trimethylcyclohexanones upon acid catalysis is a highly stereoselective process. Thus, the less hindered gem‐methyl group on the epoxide functionality becomes α‐ to the carbonyl in the final isomerized product.     

Production and Diversity of Volatile Terpenes from Plants on Calcareous and Siliceous Soils: Effect of Soil Nutrients

Fertilizer effects on terpene production have been noted in numerous reports. In contrast, only a few studies have studied the response of leaf terpene content to naturally different soil fertility levels. Terpene content, as determined by gas chromatography/mass spectrometry/flame ionization detector, and growth of Pinus halepensis, Rosmarinus officinalis, and Cistus albidus were studied on calcareous and siliceous soils under field conditions. The effect of nitrogen (N) and extractable phosphorus (P_E) from these soils on terpenes was also investigated since calcareous soils mainly differ from siliceous soils in their higher nutrient loadings. Rich terpene mixtures were detected. Twenty-one terpenes appeared in leaf extracts of R. officinalis and C. albidus and 20 in P. halepensis. Growth of all species was enhanced on calcareous soils, while terpene content showed a species-specific response to soil type. The total monoterpene content of P. halepensis and that of some major compounds (e.g., δ-terpinene) were higher on calcareous than on siliceous soils. A significant and positive relationship was found between concentration of N and P_E and leaf terpene content of this species. These findings suggest that P. halepensis may respond to an environment characterized by increasing soil deposition, by allocating carbon resources to the synthesis of terpene defense metabolites without growth reduction. Results obtained for R. officinalis showed high concentrations of numerous major monoterpenes (e.g., myrcene, camphor) in plants growing on calcareous soils, while α-pinene, β-caryophyllene, and the total sesquiterpene content were higher on siliceous soils. Finally, only alloaromadendrene and δ-cadinene of C. albidus showed higher concentrations on siliceous soils. Unlike P. halepensis, soil nutrients were not involved in terpene variation in calcareous and siliceous soils of these two shrub species. Possible ecological explanations on the effect of soil type for these latter two species as well as the ecological explanation of rich terpene mixtures are discussed.     

Terpenes in sponge cell membranes: Cell separation and membrane fractionation studies with the tropical marine spongeAmphimedon sp.

The differing sponge and symbiotic microbial cell types in the tropical marine spongeAmphimedon sp. were fractionated according to density, investigated by electron microscopy, and analyzed by high-performance liquid chromatography and nuclear magnetic resonance for the presence of the terpene metabolite diisocyanoadociane (1) and Δ^5,7-sterols (2–7). A sample of whole sponge was dissected into superficial ectosome and deeper choanosome. The superficial tissue was found to be enriched in sterol relative to choanosome; however, extracts from both tissues contained terpene. Dissociation of whole sponge followed by Ficoll density gradient fractionation showed that there are two chemically distinct types of sponge cells inAmphimedon sp.—small non-nucleolated cells of low density contain terpene 1 together with sterols, while larger nucleolated cells contain significant levels of terpene, but only traces of sterol. Membrane fractionation studies were undertaken to establish whether the terpene components were located specifically in the cell membranes of these two cell types. A membrane vesicle pellet spun down at 100,000×g from small sponge cells contained sterols, but only traces of terpene, whereas the membrane vesicle preparation from heavier cells contained both terpenes and sterols. Subsequently, the presence of terpenes together with sterols was demonstrated in a membrane vesicle preparation of purity >90% prepared from bacteria-free sponge cells. These results provide the first experimental evidence that terpenes are associated with sponge cell membranes, where they may function as structural components. Part of this work has been published in preliminary form (ref. 1)     

A method for determination of the absolute stereochemistry of α,β-epoxy alcohols derived from fatty acid hydroperoxides

A method for the determination of the absolute configuration of the alcohol group of fatty acid α,β-epoxy alcohols was developed. The method consists of:(i) deoxygenation of the saturated epoxy alcohol to an allylic alcohol by treatment with triphenylphosphine selenide and trifluoroacetic acid; (ii) oxidative ozonolysis of the (−)-menthoxycarbonyl derivative of the allylic alcohol; and (iii) steric analysis of the resulting 2-hydroxy acid (methyl ester, (−)-menthoxycarbonyl derivative) by gas-liquid chromatography using appropriate reference compounds. The result obtained, coupled with knowledge of the relative configuration of the epoxy alcohol (erythro/threo) and of the geometrical configuration of the epoxide group (cis/trans), permitted assignment of the absolute configuration of all three asymmetric carbons of the α,β-epoxy alcohol. The method was applied to the determination of the absolute stereochemistry of two hepoxilins recently isolated from the red algaMurrayella perilados.     

CYPArm2 is a CYP450 Monooxygenase with Protoilludene 13-Hydroxylase Activity Involved in the Biosynthesis of Armillyl Orsellinate-Type Sesquiterpenoids

The melleolides are a family of structurally and functionally diverse sesquiterpenoids with potential applications as fungicides, antimicrobials, and cancer therapeutics. The initial and terminal steps of the biosynthesis pathway in Armillaria spp. have been characterized, but the intermediate steps are unclear. Biosynthetic gene clusters in A. mellea and A. gallica were shown to encode a terpene cyclase, a polyketide synthase, and four CYP450 monooxygenases. We have characterized CYPArm3, which is responsible for the hydroxylation of Δ-6-protoilludene, but the functions of the other CYP450s remain to be determined. Here we describe CYPArm2, which accepts Δ-6-protoilludene and 8α-hydroxy-6-protoilludene as substrates. To investigate the products in more detail, we generated recombinant Saccharomyces cerevisiae strains overexpressing CYPArm2 in combination with the previously characterized protoilludene synthase and 8α-hydroxylase. Using this total biosynthesis approach, sufficient quantities of product were obtained for NMR spectroscopy. This allowed the identification of 8α,13-dihydroxy-protoilludene, confirming that CYPArm2 is a protoilludene 13-hydroxylase.     

An Isotopic Labelling Strategy to Study Cytochrome P450 Oxidations of Terpenes

The cytochrome P450 monooxygenase CYP267B1 from Sorangium cellulosum was applied for the enzymatic oxidation of the sesquiterpene alcohols T‐muurolol and isodauc‐8‐en‐11‐ol. Various isotopically labelled geranyl and farnesyl diphosphates were used for product identification from micro‐scale reactions, for the determination of the absolute configurations of unknown compounds, to follow the stereochemical course of a cytochrome P450‐catalysed hydroxylation step, and to investigate kinetic isotope effects. Overall, this study demonstrates that isotopically labelled terpene precursors are highly useful to follow cytochrome P450 dependent oxidations of terpenes.     

Effect of Intraspecific Competition and Substrate Type on Terpene Emissions from Some Mediterranean Plant Species

Competition is an important factor that has been extensively reported in the Mediterranean area. There is evidence that leaf terpene accumulation may vary between plants growing on calcareous and siliceous soils. In the present study, leaf terpene emissions from potted seedlings of Pinus halepensis, Cistus albidus, and Quercus coccifera, growing under natural environmental conditions on calcareous and siliceous substrates, were studied by using a bag enclosure method. In both substrates, seedlings were potted alone and in intraspecific competition, to examine the effect of substrate type and that of intraspecific competition on terpene emissions. The results showed that competition favored: (i) overall monoterpene and sesquiterpene emissions from Q. coccifera; (ii) overall monoterpene emissions from P. halepensis; (iii) overall sesquiterpene emissions from C. albidus. Substrate type affected terpene emissions to a limited extent and in a species-specific way. Whereas for Q. coccifera, the overall monoterpene emissions and that of Allo-aromadendrene were favored on siliceous substrate, no significant changes were found in emissions from P. halepensis. Only the release of AR-curcumene from C. albidus was higher on siliceous substrate. We also found high variability in terpene emission composition from the study species, particularly for P. halepensis and Q. coccifera. These two species released both monoterpenes and sesquiterpenes, instead of monoterpenes only, as shown in previous studies.     

Variation in Growth, Chemical Defense, and Herbivore Resistance in Scots Pine Provenances

Variation in the growth, chemical defense, and susceptibility to monophagous and polyphagous sucking herbivores was assessed for four Scots pine (Pinus sylvestris) provenances in Petri dish and pot experiments. Seed provenances, Muonio (MU), Suomussalmi (SU), Korpilahti (KO), and Saaremaa (SA) represented a 1200-km N–S gradient. Scots pines from SU were least preferred as a host plant by pine-feeding aphids Schizolachnus pineti Fabr. and Eulachnus agilis, and in pot experiments, pines from SA were most preferred. S. pineti also produced the fewest nymphs on pines from SU. Polyphagous Lygus rugulipennis laid significantly fewer eggs on pines from MU provenance, which were smaller than seedlings from other provenances. The total and some individual terpene concentrations increased, while the total resin acid concentration decreased, towards the north. The absolute concentrations of total or individual terpenes and resin acids in the needles of unfavored SU plants did not differ significantly from the other provenances. Only the proportional quantity of dehydroabietic acid was higher in SU plants than in KO plants, and it correlated, together with sandaracopimaric acid, negatively with the number of S. pineti nymphs in the reproduction experiment. Conversely, absolute concentrations of some terpenes correlated negatively and some resin acids positively with the number of S. pineti nymphs. The length and weight of shoots decreased towards the north, adequately explaining the number of Lygus eggs and the final numbers of both aphids. The results suggest that seedling size is a better estimator of susceptibility of pine seedlings to both specialist and generalist sucking insects than relative or absolute concentrations of monoterpenes and resin acids.     

Inhibitory effects of terpene alcohols and aldehydes on growth of green algaChlorella pyrenoidosa

The growth of the green algaChlorella pyrenoidosa was inhibited by terpene alcohols and the terpene aldehyde citral. The strongest activity was shown by citral. Nerol, geraniol, and citronellol also showed pronounced activity. Strong inhibition was linked to acyclic terpenes containing a primary alcohol or aldehyde function. Inhibition appeared to be taking place through the vapor phase rather than by diffusion through the agar medium from the terpene-treated paper disks used in the system. Inhibition through agar diffusion was shown by certain aged samples of terpene hydrocarbons but not by recently purchased samples.     

Attractiveness of Constitutive and Herbivore-Induced Sesquiterpene Blends of Maize to the Parasitic Wasp <Emphasis Type="Italic">Cotesia marginiventris</Emphasis> (Cresson)

Plant volatile compounds induced by herbivore attack have been demonstrated to provide a signal to herbivore enemies such as parasitic wasps that use these volatiles to locate their hosts. However, in addition to herbivore-induced volatiles, plants often release volatiles constitutively. We assessed the interaction between herbivore-induced and constitutively released volatiles of maize in the attraction of the wasp Cotesia marginiventris that parasitizes herbivorous lepidopteran larvae feeding on maize. Experiments were carried out with olfactometers in which the sources of volatiles were transgenic Arabidopsis thaliana plants overexpressing maize sesquiterpene synthases that produce blends of herbivore-induced or constitutive compounds. We found that the constitutive volatiles of maize terpene synthase 8 (TPS8) were attractive to C. marginiventris, just like the herbivore-induced volatiles of TPS10 studied earlier. A mixture of both the TPS8 and TPS10 volatile blends, however, was more effective in parasitoid attraction, indicating that constitutively released sesquiterpenes enhance the attraction of those induced by herbivores. While C. marginiventris did not distinguish among the volatiles of TPS8, TPS10, nor those of another maize sesquiterpene synthase (TPS5), when these blends were combined, their attractiveness to the wasp appeared to increase with the complexity of the blend.     

Seasonal Changes in Foliar Terpenes Indicate Suitability Of Douglas-fir Buds for Western Spruce Budworm

The terpene composition of current-year buds of Douglas-fir, Pseudotsuga menziesii (Mirb.) Franco, was analyzed from before budburst to after buds were fully flushed. Terpene composition was measured at weekly intervals for several seasons at eight different locations in the southern interior of British Columbia, Canada. Discriminant functions relating terpene composition to suitability of buds for newly emerged western spruce budworm, Choristoneura occidentalis Freeman, were developed based on terpene profiles of the buds and bioassays measuring the suitability to budworms of a sister group of buds. Changes in percent composition of bud terpenes before and during budburst were closely associated with changes in the suitability of the buds to utilization by budworms at both the tree and site by date levels. Use of a degree-day scale for bud suitability removed much of the year-to-year variation, but remaining differences among sites suggest additional sources of variation influencing the insect-host plant relationship. The success of correctly classifying bud suitability using terpene profiles demonstrates the value of foliar terpenes as indicators of seasonal changes in suitability of Douglas-fir foliage during the critical spring emergence period of western spruce budworm. This indicator could be used to screen individual trees susceptible to budworm damage and identify sites at high risk of damaging defoliation.     

Herbivore-Induced Volatile Production by Arabidopsis thaliana Leads to Attraction of the Parasitoid Cotesia rubecula: Chemical, Behavioral, and Gene-Expression Analysis

Many plant species defend themselves against herbivorous insects indirectly by producing volatiles in response to herbivory. These volatiles attract carnivorous enemies of the herbivores. Research on the model plant Arabidopsis thaliana (L.) Heynh. has contributed considerably to the unraveling of signal transduction pathways involved in direct plant defense mechanisms against pathogens. Here, we demonstrate that Arabidopsis is also a good candidate for studying signal transduction pathways involved in indirect defense mechanisms by showing that: (1) Adult females of Cotesia rubecula, a specialist parasitic wasp of Pieris rapae caterpillars, are attracted to P. rapae-infested Arabidopsis plants. (2) Arabidopsis infested by P. rapae emits volatiles from several major biosynthetic pathways, including terpenoids and green leaf volatiles. The blends from herbivore-infested and artificially damaged plants are similar. However, differences can be found with respect to a few components of the blend, such as two nitriles and the monoterpene myrcene, that were produced exclusively by caterpillar-infested plants, and methyl salicylate, that was produced in larger amounts by caterpillar-infested plants. (3) Genes from major biosynthetic pathways involved in volatile production are induced by caterpillar feeding. These include AtTPS10, encoding a terpene synthase involved in myrcene production, AtPAL1, encoding phenylalanine ammonia-lyase involved in methyl salicylate production, and AtLOX2 and AtHPL, encoding lipoxygenase and hydroperoxide lyase, respectively, both involved in the production of green leaf volatiles. AtAOS, encoding allene oxide synthase, involved in the production of jasmonic acid, also was induced by herbivory.     

Chimeric Terpene Synthases Possessing both Terpene Cyclization and Prenyltransfer Activities

Prenyltransferase (PT) and terpene synthase (TPS) are key enzymes in the formation of the basic carbon skeletons of terpenoids. The PTs determine the prenyl carbon chain length, whereas TPSs generate the structural complexity of the molecular scaffolds, forming various ring structures. Normally, PTs and TPSs are separate, independent enzymes. However, in 2007, a chimeric enzyme, in which the PT was fused with the TPS, was found in a fungus. Recent studies have revealed that such chimeric TPSs are widely distributed in fungi and function in the biosyntheses of various terpene natural products, including sesterterpenes, which are a relatively rare group of terpenoids. This review summarizes the accumulated knowledge of these recently discovered, unique, chimeric TPSs.     

The Absolute Configuration of the Products of the Enantioselective Rhodium(I)/BINAP‐Catalyzed Enyne Cyclization

The absolute configuration of the product 7 obtained from a rhodium‐catalyzed enyne cyclization of 6 with the (R)‐BINAP ligand was determined by anomalous diffraction in the X‐ray crystal structure analysis.