Hydroxytropane tiglates in the roots of Mandragora species

Roots of Mandragora autumnalis and M. vernalis contain hyoscyamine, hyoscine, cuscohygrine, apoatropine 3α-tigloyloxytropane and 3,6-ditigloyloxytropane. Belladonnine is present in the dried roots but could not be detected in fresh roots. No major differences were found in the alkaloids present in the two species. This is the first time the presence of tiglic acid esters has been reported in Mandragora species and the significance of this in the chemotaxonomy of the genus is indicated.     

Biosynthesis of ticloidine in Physalis peruviana

The aerial parts and roots of Physalis peruviana (Cape Gooseberry) have been shown to contain tigloidine (3β-tigloyloxytropane) and 3α-tigloyloxytropane. The tiglic acid moiety of these alkaloids is derived from l-iSoleucine.     

The biosynthesis of angelic acid in Cynoglossum officinale

Six-month-old Cynoglossum officinale plants were fed via the roots with tiglic acid-[1-¹⁴C]. After a week the plants were harvested, the alkaloid heliosupine was isolated and hydrolysed to heliotridine and angelic acid. The latter contained all the radioactivity of the original heliosupine showing that angelic acid may be formed from tiglic acid by a cis-trans isomerization.     

Biosynthesis of 3α,6β-ditigloyloxytropane and 3α,6β-ditigloyloxytropan-7β-ol in Datura

Datura meteloides; plants were fed with tiglic acid-[-¹⁴C] via the roots and after 2 days the percentage incorporation into the alkaloids 3α-tigloyloxytropane, 3α,6β-ditigloyloxytropane, meteloidine and 3α,6β-ditigloyloxytropan-7β-ol were 15·2, 1·82, 2·2 and 1·8 respectively. 3α,6β-Ditigloyloxytropane was partially hydrolysed to 6β-hydroxy-3α-tigloyloxytropane which contained 58·1% of the radioactivity of the original base, whereas 3α,6β-ditigloyloxytropan-7β-ol gave meteloidine containing only 9·2% of the original activity. The results suggest that the di- and tri-hydroxytropanes may be formed by different routes.     

Non-reversibility of the isoleucine-acetate pathway in Datura

Five-month-old Datura meteloides plants were fed via the roots with 3-hydroxy-2-methylbutanoic acid-[1-¹⁴C] and isoleucine-[U-¹⁴C] as a positive control. After 5 days the plants were collected and in each case the root alkaloids 3α,6β-ditigloyloxytropane, 3α,6β-ditigloyloxytropan-7β-ol, meteloidine, hyoscine and hyoscyamine were isolated. Whereas isoleucine served as a precursor for the tiglic acid moieties 3-hydroxy-2-methylbutanoic acid did not.     

Neue C10-säureamide,furanoeremophilane und andere inhaltsstoffe aus bolivianischen Senecio-arten

The investigation of seven Bolivian Senecio species afforded in addition to known compounds five new furanoeremophilanes, two C₁₀-amides, a new isoeugenol ester and the isomer of pterophorin. The structures are elucidated mainly by spectroscopic methods. While most of the new compounds are closely related to those isolated before from Senecio species, four of them are unusual. Another is a new type of a furanoeremophilane; its biogenesis however, can be explained easily from known types.     

Biotransformation of isoeugenol catalyzed by growing cells of Pseudomonas putida

Abstract

Growing cells of Pseudomonas putida transformed isoeugenol after 5 days of incubation to give mainly vanillin, eugenol, 4-(E)-(3-hydroxyprop-1-enyl)-2-methoxyphenol and the dimeric molecule (+)-4-[2,3-dihydro-7-methoxy-3-methyl-5-(E)-(1-propenyl)-2-benzofuranyl]-2-methoxyphenol (licarin A). The formation of the latter compound from isoeugenol by biotransformation with P. putida is reported here for the first time.     

Biosynthetic conversion of α-methylbutyric acid to tiglic acid in Datura meteloides

The administration of RS-α-methylbutyric-[1-¹⁴C] acid to Datura meteloides plants resulted in the formation of radioactive meteloidine. A systematic degradation indicated that essentially all the activity was located at C-1 of the tiglic acid moiety of the alkaloid.     

Root-shoot ratio in irrigated plants

Relationship between roots and shoots ofPimpinella saxifraga L.,Petroselinum hortense Hoffm.,Lactuca sativa L., andBeta vulgaris subsp.esculenta (Salisbury) Gürke var.altissima Roessig was studied in irrigated and non-irrigated plants. It was found that the irrigation water did not influence distinctly the root-shoot ratio of the experimental plants. From the statical point of view, this relationship could be expressed by the following quantitative ratios for irrigated and non-irrigated plants: 3∶1 forPimpinella saxifraga L., 2∶1 forPetroselinum hortense Hoffm., 9∶1 forLactuca sativa L., and 1∶1 for beetroot. From the dynamic point of view it is possible to state that this ratio changes in the course of individual development. With plants cultivated for their aerial parts, it increased with age, while with plants cultivated for their roots, it decreased with age. The irrigation water produced much greater morphological changes (the shape and the surface area) in the root and shoot system of experimental plants.     

Neue germacranolide aus Calea urticifolia

The investigation of Calea urticifolia afforded eight new germacranolides. While five are heliangolides, three are of a new type and have some unusual structural features. The structures are elucidated by extensive ¹H-NMR studies and some chemical transformations. In addition, a new isoeugenol and an unusual phloroglucinol derivative were isolated; the structure of the latter could only be established after some chemical transformations. Other Calea species contain typical C₁₇ acetylenes only, also present in other species of the subtribe Galinsoginae. So far, the results on Calea indicate that the genus is chemically heterogenous.     

Coumarins and ferulol esters from Cachrys sicula

(−)-Sprengelianin, (−)-prantschimgin and other minor coumarins were isolated from the roots and/or the umbels of Cachrys sicula. The roots also afforded the monoterpene hydroxyaldehyde ferulol esterified to angelic, tiglic and senecioic acids. The (−)-enantiomer of sprengelianin (2′S) had not been reported previously. The coumarins saxalin and pabulenol and the aromatic aldehyde 2,3,4-trimethylbenzaldehyde were also identified but these substances are presumably artefacts.     

Oxiranylphenyl esters from Pimpinella diversifolia

The major components of the essential oil from roots of Pimpinella diversifolia, gathered in the Kumaun Region of India, have been identified as the (+)-Z-2-methyl-2-butenoate (angelate) and (+)-isobutyrate esters of 4-methoxy-2-(E-3-methyloxiranyl)phenol. Aromatic ¹³C NMR resonances of these compounds and their synthetic acetate analog, as well as those of 2-methoxy-4-(E-3-methyloxiranyl)phenyl acetate prepared from isoeugenol, were found to be in excellent agreement with calculated values. Comparison of the EIMS of the natural and synthetic products with those reported for compounds previously identified as 2-methoxy-4-(E-3-methyloxiranyl)phenyl esters indicates that they also have the 4-methoxy-2-(E-3-methyloxiranyl)phenyl structure.     

Inhibition and stimulation of root respiration in pisum and plantago by hydroxamate : its consequences for the assessment of alternative path activity

The contribution of the alternative pathway in root respiration of Pisum sativum L. cv Rondo, Plantago lanceolata L., and Plantago major L. ssp major was determined by titration with salicylhydroxamate (SHAM) in the absence and presence of cyanide. SHAM completely inhibited the cyanide-resistant component of root respiration at 5 to 10 millimolar with an apparent K_i of 600 micromolar. In contrast, SHAM enhanced pea root respiration by 30% at most, at concentrations below 15 millimolar. An unknown oxidase appeared to be responsible for this stimulation. Its maximum activity in the presence of low SHAM concentrations (1-5 millimolar) was 40% of control respiration rate in pea roots, since 25 millimolar SHAM resulted in 10% inhibition. In plantain roots, the maximum activity was found to be 15%. This hydroxamate-activated oxidase was distinct from the cytochrome path by its resistance to antimycin. The results of titrations with cyanide and antimycin indicated that high SHAM concentrations (up to 25 millimolar) block the hydroxamate-activated oxidase, but do not affect the cytochrome path and, therefore, are a reliable tool for estimating the activity of the alternative path in vivo. A considerable fraction of root respiration was mediated by the alternative path in plantain (45%) and pea (15%), in the latter because of the saturation of the cytochrome path.     

Efficiency of Rumex dentatus L. Leaves Extract for Enhancing Phytoremediation of Plantago major L. in Soil Contaminated by Carbosulfan

Carbosulfan and carbofuran induce water pollution and health issues. Such issues may be solved by phytoremediation. Here we tested the potential of adding Rumex dentatus L. leaves extract to Plantago major L. for enhancing phytoremediation of carbosulfan-contaminated soil. The phytoremediation efficiency of P. major L. amended with R. dentatus L. leaves extract was significantly greater than that of P. major only and R. dentatus with respect to the removal of carbosulfan from contaminated soil. The contribution of R. dentatus leaves extract to the degradation of carbosulfan in the soil were 20.95%, 18.85%, 5.2% and 1.85% after 2, 4, 8 and 16 days of treatments, respectively. The presence of P. major amended with R. dentatus leaves extract showed significant effect on uptake of carbosulfan into roots at 2 and 4 days, the uptake ratio was about 2.39 and 1.31 times higher compared to P. major alone, respectively. Carbofuran appeared in the P. major roots amended with R. dentatus leaves extract within 2 days of treatment (5.49 mg/kg) and reached the maximum over 8 days (10.19 mg/kg), while carbofuran appeared in the P. major over 4 days of treatment (4.09 mg/kg) and reached the maximum (6.92 mg/kg) over 8 days of exposure. Carbosulfan taken up into P. major leaves reached 4.36 mg/kg over 4 days, while it reached 2.75 mg/kg in P. major leaves amended with R. dentatus leaves extract over the same time. Carbofuran translocated into the P. major leaves amended with R. dentatus leaves extract and reached the maximum over 16 days of exposure (10.43 mg/kg), followed by P. major (9.47 mg/kg) and R. dentatus leaves (9.5 mg/kg), respectively. This study indicates that R. dentatus leaves extract can improve the efficiency of phytoremediation of carbosulfan.     

Detection, identification and molecular typing of Leishmania major in Phlebotomus papatasi from a focus of zoonotic cutaneous leishmaniasis in central of Iran

Leishmania major is the causative agent and Phlebotomus papatasi is the main vector of rural zoonotic cutaneous leishmaniasis (ZCL) in Iran and elsewhere. Nested PCR protocols were used to amplify a region of the ribosomal RNA amplicon of Leishmania (ITS1-5.8S rRNA gene) in female P. papatasi. In the current investigation, L. major was found in Natanz, Isfahan province in centre of Iran, in a focus of rural ZCL. Ten (1.8%) out of 549 female P. papatasi was found to be infected with L. major based on the PCR detection and sequencing of parasite ITS-rDNA.Nine (1.8%) out of 498 female P. papatasi infected with L. major came from animal shelters, inside houses and yards. And one (1.9%) out of 51 female P. papatasi infected with L. major came from gerbil borrows. Infection rates were higher for females containing red blood meals, large eggs (semi-mature and mature) than for those without either blood meals or eggs. From the 10 infections detected three different haplotypes of L. major were identified. Two haplotypes were found to be novel. The other haplotypes of L. major was found to be identical to that of isolates of L. major from Iran and in elsewhere using GenBank data. Comparisons of infection rates between habitats will be inaccurate when the proportions of blood-fed and gravid flies differ among sandfly samples.     

Validity and Reliability of Enzyme Immunoassays Using Leishmania major or L. infantum Antigens for the Diagnosis of Canine Visceral Leishmaniasis in Brazil

Background

American visceral leishmaniasis is caused by the protozoan Leishmania infantum. Dogs are the main reservoirs in the domestic transmission cycle. The limited accuracy of diagnostic tests for canine leishmaniasis may contribute to the lack of impact of control measures recommended by the Brazilian Ministry of Health. The objective of this study was to estimate the accuracy of two enzyme-linked immunosorbent assays employing L. major or L. infantum antigens and their reliability between three laboratories of different levels of complexity.

Methods

A validation study of ELISA techniques using L. major or L. infantum antigens was conducted. Direct visualization of the parasite in hematoxylin/eosin-stained histopathological sections, immunohistochemistry, and isolation of the parasite in culture.were used as gold standard. An animal that was positive in at least one of the tests was defined as infected with L. infantum. Serum samples collected from 1,425 dogs were analyzed. Samples were separated in three aliquots and tested in three different laboratories. Sensitivity, specificity and the area under de ROC curve were calculated and the reliability was evaluated between the participant laboratories.

Results

The sensitivity was 91.8% and 89.8% for the L. major and L. infantum assays, respectively. The specificity was 83.75% and 82.7% for the L. major and L. infantum assays, respectively. The area under de ROC curve was 0.920 and 0.898 for L. major and L. infantum, respectively. The mean intraclass correlation coefficients between laboratories ranged from 0.890 to 0.948 when L. major was used as antigen, and from 0.818 to 0.879 when L. infantum was used.

Interpretation

ELISA tests using L. major or L. infantum antigens have similar accuracy and reliability. Our results do not support the substitution of the L. major antigen of the ELISA test currently used for the diagnosis of canine visceral leishmaniasis in Brazil.     

Antibacterial isoeugenol coating on stainless steel and polyethylene surfaces prevents biofilm growth

Aims

Pathogenic bacteria can spread between individuals or between food items via the surfaces they share. Limiting the survival of pathogens on surfaces, therefore, presents an opportunity to limit at least one route of how pathogens spread. In this study, we propose that a simple coating with the essential oil isoeugenol can be used to circumvent the problem of bacterial transfer via surfaces.

Methods and Results

Two commonly used materials, stainless steel and polyethylene, were coated by physical adsorption, and the coatings were characterized by Raman spectroscopy, atomic force microscopy and water contact angle measurements. We quantified and visualized the colonization of coated and uncoated surfaces by three bacteria: Staphylococcus aureus, Listeria monocytogenes and Pseudomonas fluorescens. No viable cells were detected on surfaces coated with isoeugenol.

Conclusions

The isoeugenol coating prepared with simple adsorption proved effective in preventing biofilm formation on stainless steel and polyethylene surfaces. The result was caused by the antibacterial effect of isoeugenol, as the coating did not diminish the adhesive properties of the surface.

Significance and Impact of the Study

Our study demonstrates that a simple isoeugenol coating can prevent biofilm formation of S. aureus, L. monocytogenes and P. fluorescens on two commonly used surfaces.     

New sesquiterpene lactones and other constituents from Fitchia speciosa

The investigation of Fitchia speciosa afforded, in addition to known compounds, three new sesquiterpene lactones, iso-β-costal, two p-hydroxyacetophenone derivatives and an isoeugenol derivative. The structures were elucidated by spectroscopic methods. The chemotaxonomic situation in this complicated genus is discussed.     

纺锤芽孢杆菌CGMCC1347发酵生产异丁香酚单加氧酶的条件优化

对从土壤中筛选获得的纺锤芽孢杆菌CGMCCl347生产异丁香酚单加氧酶的发酵条件进行了单因素考察及正交实验优化,确定了最适的发酵摇瓶培养基组成和培养条件。在发酵培养基组成为尿素1g／L,玉米浆55g/L,K2HP042g／L,MgSO4·7H2O1g／L,初始pH7．5,发酵温度37℃,摇床转速180r／min的条件下培养16h获得的细胞,能转化2％的异丁香酚生成2．49g／L香兰素,异丁香酚单加氧酶酶活达3．79U／L。     

Immunity to distinct sand fly salivary proteins primes the anti-Leishmania immune response towards protection or exacerbation of disease

Background

Leishmania parasites are transmitted in the presence of sand fly saliva. Together with the parasite, the sand fly injects biologically active salivary components that favorably change the environment at the feeding site. Exposure to bites or to salivary proteins results in immunity specific to these components. Mice immunized with Phlebotomus papatasi salivary gland homogenate (SGH) or pre-exposed to uninfected bites were protected against Leishmania major infection delivered by needle inoculation with SGH or by infected sand fly bites. Immunization with individual salivary proteins of two sand fly species protected mice from L. major infection. Here, we analyze the immune response to distinct salivary proteins from P. papatasi that produced contrasting outcomes of L. major infection.

Methodology/Principal Findings

DNA immunization with distinct DTH-inducing salivary proteins from P. papatasi modulates L. major infection. PpSP15-immunized mice (PpSP15-mice) show lasting protection while PpSP44-immunized mice (PpSP44-mice) aggravate the infection, suggesting that immunization with these distinct molecules alters the course of anti-Leishmania immunity. Two weeks post-infection, 31.5% of CD4⁺ T cells produced IFN-γ in PpSP15-mice compared to 7.1% in PpSP44-mice. Moreover, IL-4-producing cells were 3-fold higher in PpSP44-mice. At an earlier time point of two hours after challenge with SGH and L. major, the expression profile of PpSP15-mice showed over 3-fold higher IFN-γ and IL-12-Rβ2 and 20-fold lower IL-4 expression relative to PpSP44-mice, suggesting that salivary proteins differentially prime anti-Leishmania immunity. This immune response is inducible by sand fly bites where PpSP15-mice showed a 3-fold higher IFN-γ and a 5-fold lower IL-4 expression compared with PpSP44-mice.

Conclusions/Significance

Immunization with two salivary proteins from P. papatasi, PpSP15 and PpSP44, produced distinct immune profiles that correlated with resistance or susceptibility to Leishmania infection. The demonstration for the first time that immunity to a defined salivary protein (PpSP44) results in disease enhancement stresses the importance of the proper selection of vector-based vaccine candidates.