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1.
J Chem Ecol ; 31(3): 461-80, 2005 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-15898495

RESUMO

Differences in allelochemistry of plants may influence their ability to attract parasitoids. We studied responses of Diadegma semiclausum (Hellén), a parasitoid of the diamondback moth (Plutella xylostella L.), to inter- and intraspecific variation in odor blends of crucifers and a non-crucifer species. Uninfested Brussels sprout (Brassica oleracea L. gemmifera), white mustard (Sinapis alba L.), a feral Brassica oleracea, and malting barley (Hordeum vulgare L.) were compared for their attractivity to D. semiclausum in a Y-tube bioassay. Odors from all plants were more attractive to the parasitoid than clean air. However, tested against each other, parasitoids preferred the volatile blend from the three cruciferous species over that of malting barley. Wasps also discriminated between uninfested crucifers: mustard was as attractive as feral B. oleracea, and both were more attractive than Brussels sprout. Attractivity of uninfested plants was compared with that of plants infested by larvae of the host P. xylostella. Host-infested mustard and Brussels sprout were more attractive than uninfested conspecifics. Interestingly, the volatile blends of uninfested white mustard and infested Brussels sprout were equally attractive. We also compared the volatile composition of different plant sources by collecting headspace samples and analysing them with GC-MS. Similarities of volatile profiles were determined by hierarchic clustering and non-metric scaling based on the Horn-index. Due to the absence of several compounds in its blend, the volatile profile of barley showed dissimilarities from blends of crucifers. The odor profile of white mustard was distinctly different from the two Brassicaceae. Feral Brassica oleracea odor profile was different from infested Brussels sprout, but showed overlap with uninfested Brussels sprout. Odor blends from infested and uninfested Brussels sprout were similar, and mainly quantitative differences were found. D. semiclausum appears to discriminate based on subtle differences in volatile composition of odor blends from infested and uninfested plants.


Assuntos
Brassicaceae/metabolismo , Hordeum/metabolismo , Himenópteros/fisiologia , Óleos Voláteis/metabolismo , Animais , Comportamento Animal/efeitos dos fármacos , Brassicaceae/parasitologia , Feminino , Hordeum/parasitologia , Interações Hospedeiro-Parasita , Larva/parasitologia , Larva/fisiologia , Mariposas/parasitologia , Mariposas/fisiologia , Óleos Voláteis/farmacologia , Especificidade da Espécie
2.
Planta Med ; 71(1): 40-7, 2005 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-15678372

RESUMO

An important group of antimalarial drugs consists of the endoperoxide sesquiterpene lactone artemisinin and its derivatives. Only little is known about the biosynthesis of artemisinin in Artemisia annua L., particularly about the early enzymatic steps between amorpha-4,11-diene and dihydroartemisinic acid. Analyses of the terpenoids from A. annua leaves and gland secretory cells revealed the presence of the oxygenated amorpha-4,11-diene derivatives artemisinic alcohol, dihydroartemisinic alcohol, artemisinic aldehyde, dihydroartemisinic aldehyde and dihydroartemisinic acid. We also demonstrated the presence of a number of biosynthetic enzymes such as the amorpha-4,11-diene synthase and the--so far unknown--amorpha-4,11-diene hydroxylase as well as artemisinic alcohol and dihydroartemisinic aldehyde dehydrogenase activities in both leaves and glandular trichomes. From these results, we hypothesise that the early steps in artemisinin biosynthesis involve amorpha-4,11-diene hydroxylation to artemisinic alcohol, followed by oxidation to artemisinic aldehyde, reduction of the C11-C13 double bond to dihydroartemisinic aldehyde and oxidation to dihydroartemisinic acid.


Assuntos
Antimaláricos/metabolismo , Artemisia annua/metabolismo , Artemisininas/metabolismo , Fitoterapia , Artemisia annua/enzimologia , Cromatografia Gasosa-Espectrometria de Massas , Humanos , Folhas de Planta/enzimologia , Folhas de Planta/metabolismo
3.
J Chem Ecol ; 27(10): 1911-28, 2001 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-11710601

RESUMO

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.


Assuntos
Arabidopsis/fisiologia , Comportamento Alimentar , Fixadores/farmacologia , Regulação da Expressão Gênica , Himenópteros , Lepidópteros/fisiologia , Terpenos/farmacologia , Adaptação Fisiológica , Animais , Arabidopsis/genética , Fixadores/análise , Larva , Lepidópteros/parasitologia , Folhas de Planta/química , Plantas Comestíveis , Salicilatos/análise , Salicilatos/farmacologia , Terpenos/análise , Volatilização
4.
J Chem Ecol ; 27(7): 1355-72, 2001 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-11504033

RESUMO

We investigated whether volatiles produced by spider mite-damaged plants of four gerbera cultivars differ in attractiveness to Phytoseiulus persimilis, a specialist predator of spider mites, and how the mite-induced odor blends differ in chemical composition. The gerbera cultivars differed in resistance, as expressed in terms of spider mite intrinsic rate of population increase (rm). In order of increasing resistance these were Sirtaki, Rondena, Fame, and Bianca. To correct for differences in damage inflicted on the cultivars, we developed a method to compare the attractiveness of the blends, based on the assumption that a larger amount of spider mite damage leads to higher attraction of P persimilis. Spider mite-induced volatiles of cultivars Rondena and Bianca were preferred over those of cultivar Sirtaki. Spider mite-induced volatiles of cultivars Sirtaki and Fame did not differ in attractiveness to P. persimilis. Sirtaki plants had a lower relative production of terpenes than the other three cultivars. This was attributed to a low production of cis-alpha-bergamotene, trans-alpha-bergamotene, trans-beta-bergamotene, and (E)-beta-farnesene. The emission of (E)-beta-ocimene and linalool was lower in Sirtaki and Fame leaves than in Bianca and Rondena. The importance of these chemical differences in the differential attraction of predatory mites is discussed.


Assuntos
Asteraceae/química , Quimiotaxia , Ácaros , Odorantes , Comportamento Predatório , Animais , Dinâmica Populacional , Volatilização
5.
Arch Biochem Biophys ; 381(2): 173-80, 2000 Sep 15.
Artigo em Inglês | MEDLINE | ID: mdl-11032404

RESUMO

In plants, sesquiterpenes of different structural types are biosynthesized from the isoprenoid intermediate farnesyl diphosphate. The initial reaction of the biosynthesis is catalyzed by sesquiterpene cyclases (synthases). In Artemisia annua L. (annual wormwood), a number of such sesquiterpene cyclases are active. We have isolated a cDNA clone encoding one of these, amorpha-4,11-diene synthase, a putative key enzyme of artemisinin biosynthesis. This clone contains a 1641-bp open reading frame coding for 546 amino acids (63.9 kDa), a 12-bp 5'-untranslated end, and a 427-bp 3'-untranslated sequence. The deduced amino acid sequence is 32 to 51% identical with the sequence of other known sesquiterpene cyclases from angiosperms. When expressed in Escherichia coli, the recombinant enzyme catalyzed the formation of both olefinic (97.5%) and oxygenated (2.5%) sesquiterpenes from farnesyl diphosphate. GC-MS analysis identified the olefins as (E)-beta-farnesene (0.8%), amorpha-4,11diene (91.2%), amorpha-4,7(11)-diene (3.7%), gamma-humulene (1.0%), beta-sesquiphellandrene (0.5%), and an unknown olefin (0.2%) and the oxygenated sesquiterpenes as amorpha-4-en-11-ol (0.2%) (tentatively), amorpha-4-en-7-ol (2.1%), and alpha-bisabolol (0.3%) (tentatively). Using geranyl diphosphate as substrate, amorpha-4,11-diene synthase did not produce any monoterpenes. The recombinant enzyme has a broad pH optimum between 7.5 and 9.0 and the Km values for farnesyl diphosphate, Mg2+, and Mn2+ are 0.9, 70, and 13 microM, respectively, at pH 7.5. A putative reaction mechanism for amorpha-4,11-diene synthase is suggested.


Assuntos
Alquil e Aril Transferases/genética , Alquil e Aril Transferases/metabolismo , Artemisia/enzimologia , Artemisia/genética , Artemisininas , Plantas Medicinais , Sesquiterpenos/metabolismo , Alquil e Aril Transferases/química , Sequência de Aminoácidos , Sequência de Bases , Clonagem Molecular , Primers do DNA/genética , DNA Complementar/genética , DNA Complementar/isolamento & purificação , DNA de Plantas/genética , DNA de Plantas/isolamento & purificação , Escherichia coli/genética , Expressão Gênica , Genes de Plantas , Cinética , Modelos Químicos , Dados de Sequência Molecular , Fosfatos de Poli-Isoprenil/metabolismo , Homologia de Sequência de Aminoácidos , Sesquiterpenos/química
6.
J Agric Food Chem ; 48(6): 2409-14, 2000 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-10888559

RESUMO

The essential oils from leaves and flowers of costmary, Balsamita major (L.) Desf. (syn. Chrysanthemum balsamita L.), were analyzed at various phases of plant growth. The highest contents of oil both in leaves and in flowers were determined before full blooming, 1.15 and 1.34% (w/w), respectively. Seventy-eight volatile compounds have been identified in the oils of Balsamita major, of which 58 (19 tentatively, 39 positively) have not been reported in this plant previously. Carvone and alpha-thujone were found to be dominating compounds constituting from 51.8 to 68.0% and from 9.0 to 16.1% in the total oil, respectively. Seasonal variations in the oil compositions were not considerable except for the starting phase (May 25, 1995), when the content of carvone was lower and the content of alpha-thujone and sesquiterpenes higher. The content of sesquiterpenes was approximately 2 times higher in flowers than in the leaves. Absolute amount of most components was highest at the bud formation period.


Assuntos
Aditivos Alimentares , Óleos Voláteis/análise , Desenvolvimento Vegetal , Óleos de Plantas/análise , Folhas de Planta/química , Folhas de Planta/crescimento & desenvolvimento , Caules de Planta/química , Caules de Planta/crescimento & desenvolvimento , Plantas/química
7.
J Agric Food Chem ; 48(12): 6183-90, 2000 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-11312790

RESUMO

Volatiles of five different parts of lovage (leaves, stems, flowers, seeds, and roots) were isolated by dynamic headspace (DHS) method and analyzed by GC-FID and GC-olfactometry (GC-O) techniques. In total, 98 compounds were identified in the samples, of which 41 are reported as lovage volatiles for the first time. Qualitative differences in the composition of DHS constituents of various anatomical parts of the plants were not significant, whereas the amounts of a number of identified volatile compounds were different in leaves, stems, flowers, seeds, and roots. Seasonal variations in the composition of headspace volatiles were also determined. Except for roots, beta-phellandrene was found to be the most abundant headspace component in all anatomical parts of lovage constituting from 36.50% to 79.28% of the total GC peak area. The sniffing panel characterized effluents from the GC column, and odor descriptors were attributed to the recognized constituents. alpha-Pinene and alpha-phellandrene/myrcene were the most frequently recognized constituents among 11 GC effluents constituting 12 identified compounds and 1 unknown compound, which were detected by the members of the sniffing panel. None of the detected constituents was recognized as a lovage character impact aroma compound.


Assuntos
Cromatografia Gasosa-Espectrometria de Massas/métodos , Plantas/química , Odorantes/análise , Plantas/anatomia & histologia , Plantas/classificação , Volatilização
8.
J Agric Food Chem ; 47(10): 4365-9, 1999 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-10552817

RESUMO

The formation of odor active compounds resulting from initial lipid oxidation in sunflower oil-in-water emulsions was examined during storage at 60 degrees C. The emulsions differed in initial pH, that is, pH 3 and 6. The volatile compounds were isolated under mouth conditions and were analyzed by gas chromatography/sniffing port analysis. The lipid oxidation rate was followed by the formation of conjugated hydroperoxide dienes and headspace hexanal. The initial pH affected the lipid oxidation rate in the emulsions: the formation of conjugated diene hydroperoxides and the hexanal concentration in the static headspace were increased at pH 6. Pentanal, hexanal, 3-pentanol, and 1-octen-3-one showed odor activity in the emulsions after 6 days of storage, for both pH 3 and 6. Larger amounts of odor active compounds were released from the pH 6 emulsion with extended storage. It was shown that this increased release at pH 6 was not due to increased volatility because an increase in pH diminished the static headspace concentrations of added compounds in emulsions.


Assuntos
Gorduras Insaturadas/química , Conservação de Alimentos , Odorantes/análise , Óleos de Plantas/química , Água/química , Emulsões , Humanos , Concentração de Íons de Hidrogênio , Oxirredução , Óleo de Girassol , Volatilização
9.
Plant Physiol ; 121(1): 173-80, 1999 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-10482672

RESUMO

Many plant species respond to herbivory with de novo production of a mixture of volatiles that attracts carnivorous enemies of the herbivores. One of the major components in the blend of volatiles produced by many different plant species in response to herbivory by insects and spider mites is the homoterpene 4,8-dimethyl-1,3(E), 7-nonatriene. One study (J. Donath, W. Boland [1995] Phytochemistry 39: 785-790) demonstrated that a number of plant species can convert the acyclic sesquiterpene alcohol (3S)-(E)-nerolidol to this homoterpene. Cucumber (Cucumis sativus L.) and lima bean (Phaseolus lunatus L.) both produce 4,8-dimethyl-1,3(E),7-nonatriene in response to herbivory. We report the presence in cucumber and lima bean of a sesquiterpene synthase catalyzing the formation of (3S)-(E)-nerolidol from farnesyl diphosphate. The enzyme is inactive in uninfested cucumber leaves, slightly active in uninfested lima bean leaves, and strongly induced by feeding of the two-spotted spider mite (Tetranychus urticae Koch) on both plant species, but not by mechanical wounding. The activities of the (3S)-(E)-nerolidol synthase correlated well with the levels of release of 4, 8-dimethyl-1,3(E),7-nonatriene from the leaves of the different treatments. Thus, (3S)-(E)-nerolidol synthase is a good candidate for a regulatory role in the release of the important signaling molecule 4,8-dimethyl-1,3(E),7-nonatriene.


Assuntos
Carbono-Carbono Liases/metabolismo , Cucumis sativus/enzimologia , Fabaceae/enzimologia , Ácaros/fisiologia , Plantas Medicinais , Sesquiterpenos/metabolismo , Terpenos/metabolismo , Ar , Animais , Carbono-Carbono Liases/biossíntese , Cucumis sativus/metabolismo , Cucumis sativus/parasitologia , Ingestão de Alimentos , Indução Enzimática , Fabaceae/metabolismo , Fabaceae/parasitologia , Cinética , Modelos Químicos , Óleos Voláteis/metabolismo , Monoéster Fosfórico Hidrolases/metabolismo , Estimulação Física , Folhas de Planta/enzimologia , Folhas de Planta/metabolismo , Folhas de Planta/parasitologia , Fosfatos de Poli-Isoprenil/metabolismo , Transdução de Sinais
10.
Phytochemistry ; 52(5): 843-54, 1999 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-10626375

RESUMO

The endoperoxide sesquiterpene lactone artemisinin and its derivatives are a promising new group of drugs against malaria. Artemisinin is a constituent of the annual herb Artemisia annua L. So far only the later steps in artemisinin biosynthesis--from artemisinic acid--have been elucidated and the expected olefinic sesquiterpene intermediate has never been demonstrated. In pentane extracts of A. annua leaves we detected a sesquiterpene with the mass spectrum of amorpha-4,11-diene. Synthesis of amorpha-4,11-diene from artemisinic acid confirmed the identity. In addition we identified several sesquiterpene synthases of which one of the major activities catalysed the formation of amorpha-4,11-diene from farnesyl diphosphate. This enzyme was partially purified and shows the typical characteristics of sesquiterpene synthases, such as a broad pH optimum around 6.5-7.0, a molecular mass of 56 kDa, and a K(m) of 0.6 microM. The structure and configuration of amorpha-4,11-diene, its low content in A. annua and the high activity of amorpha-4,11-diene synthase all support that amorpha-4,11-diene is the likely olefinic sesquiterpene intermediate in the biosynthesis of artemisinin.


Assuntos
Alquil e Aril Transferases/metabolismo , Antimaláricos/metabolismo , Artemisininas , Ligases/metabolismo , Sesquiterpenos/metabolismo , Artemisia/enzimologia , Artemisia/metabolismo , Catálise , Medicamentos de Ervas Chinesas/metabolismo , Concentração de Íons de Hidrogênio , Peso Molecular , Folhas de Planta/enzimologia , Folhas de Planta/metabolismo , Plantas Medicinais , Fosfatos de Poli-Isoprenil/metabolismo
11.
Chem Res Toxicol ; 11(11): 1319-25, 1998 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-9815192

RESUMO

This study reports the microperoxidase-8 (MP8)/H2O2-catalyzed dehalogenation of pentafluorophenol and pentachlorophenol, compounds whose toxic effects and persistence in the environment are well documented. The primary products of this dehalogenation reaction appear to be the corresponding tetrahalo-p-benzoquinones. Under the conditions used, the fluorinated phenol and its intermediate products are more susceptible to degradation than the corresponding chlorinated analogue and its products. The main degradation products of tetrachloro-p-benzoquinone and tetrafluoro-p-benzoquinone were identified as trichlorohydroxy-p-benzoquinone and trifluorohydroxy-p-benzoquinone, respectively. This secondary conversion of tetrafluoro-p-benzoquinone and tetrachloro-p-benzoquinone was not mediated by MP8, but was driven by H2O2. Evidence is presented for a mechanism where H2O2 molecules and not hydroxide anions are the reactive nucleophilic species attacking the tetrahalo-p-benzoquinones. In addition to the formation of the trihalohydroxy-p-benzoquinones, the formation of adducts of the tetrahalo-p-benzoquinone products with ethanol, present in the incubation medium, was observed. The adduct from the reaction of tetrachloro-p-benzoquinone with ethanol was isolated and identified as trichloroethoxyquinone. Thus, the present paper describes a system in which the formation of tetrahalo-p-benzoquinone-type products by an oxidative heme-based catalyst could be unequivocally demonstrated.


Assuntos
Benzoquinonas/síntese química , Peróxido de Hidrogênio/química , Peroxidases/química , Fenóis/química , Ácido Ascórbico/química , Catálise , Cromatografia Líquida de Alta Pressão , Sistema Enzimático do Citocromo P-450/metabolismo , Cromatografia Gasosa-Espectrometria de Massas , Conformação Molecular , Ligação Proteica
12.
Eur J Biochem ; 253(3): 659-68, 1998 May 01.
Artigo em Inglês | MEDLINE | ID: mdl-9654063

RESUMO

The present paper describes the oxygen incorporation into naphthalene and anthracene by H2O2-driven microperoxidase-8, forming alpha-naphthol and anthraquinone, respectively. Microperoxidase-8 is a minienzyme containing a histidinyl-coordinated Fe3+-protoporphyrin IX cofactor covalently attached to an eight-amino-acid peptide. Additional experiments were performed to investigate whether the reaction mechanism involved is like that of peroxidase and/or cytochrome P-450. A reaction pathway like that of cytochrome P-450 implies oxygen transfer to the substrate from the as yet uncharacterized iron-oxo species formed in the reaction of the heine cofactor with H2O2. In contrast, a peroxidase-type reaction chemistry involves reaction pathways proceeding by initial one-electron oxidation of, or H-abstraction from, the substrate, followed by incorporation of oxygen from sources other than the iron-oxo species, i.e. from other than H2O2. The results of the present study exclude Fenton-type chemistry and prove that the minicatalyst is able to catalyze the oxygen incorporation by both peroxidase and cytochrome P-450 types of reaction pathways, while exchange occurs between the high-valency iron-oxo species and H2O. The mechanistic implications of this exchange for cytochrome P-450 are discussed.


Assuntos
Antracenos/metabolismo , Benzeno/metabolismo , Sistema Enzimático do Citocromo P-450/metabolismo , Peróxido de Hidrogênio/metabolismo , Microssomos Hepáticos/enzimologia , Naftalenos/metabolismo , Oxigênio/metabolismo , Peroxidases/metabolismo , Animais , Catálise , Grupo dos Citocromos c/química , Grupo dos Citocromos c/metabolismo , Cavalos , Cinética , Masculino , Modelos Químicos , Ratos , Ratos Wistar , Especificidade por Substrato , Água
13.
Nucl Med Biol ; 25(4): 411-21, 1998 May.
Artigo em Inglês | MEDLINE | ID: mdl-9639304

RESUMO

We have synthesized and evaluated E-11beta-nitrato-17alpha-iodovinylestradiol (E-NIVE; E-3c) and its 123I-labelled form, as a new potential radioligand for imaging of estrogen receptor (ER)-positive human breast tumors. E-[123I]NIVE was prepared by stereospecific iododestannylation of the E-tri-n-butylstannylvinyl precursor (E-2c), obtained from reaction of 11beta-nitrato-estrone (8) with E-tributylstannylvinyllithium. In competitive binding studies, E-NIVE proved to have high binding affinity for both the rat and the human ER (Ki 280-730 pM), without significant binding to human sex hormone binding globulin. Distribution studies in normal and mammary tumor-bearing rats showed specific ER-mediated uptake of E-[123I]NIVE in the estrogen target tissues, i.e., uterus, ovaries, pituitary, and hypothalamus, but not in the mammary tumors. Selective retention in these target tissues, including tumor tissue, resulted in significant increases over time for the target tissue-to-muscle uptake ratios, but not for the target tissue-to-fat uptake ratios. The tumor-to-fat uptake ratio even appeared constantly below 1. In the primary estrogen target tissues, E-[123I]NIVE displayed high specific ER-mediated uptake and retention, which resulted in moderate target-to-nontarget tissue uptake ratios. In contrast, in tumor tissue, E-[123I]NIVE uptake appeared to be rather low and not ER-specific. As a consequence, E-[123I]NIVE appears to be a less favorable radioligand for ER imaging in breast cancer than the previously studied stereoisomers of 11beta-methoxy-17alpha-[123I]iodovinylestradiol (E- and Z-[123I]MIVE; [123I]E- and [123I]Z-3b).


Assuntos
Estradiol/análogos & derivados , Neoplasias Mamárias Experimentais/metabolismo , Receptores de Estrogênio/metabolismo , Animais , Ligação Competitiva , Neoplasias da Mama/diagnóstico por imagem , Estradiol/síntese química , Estradiol/metabolismo , Estradiol/farmacocinética , Feminino , Humanos , Injeções Intravenosas , Radioisótopos do Iodo , Neoplasias Mamárias Experimentais/diagnóstico por imagem , Ensaio Radioligante , Ratos , Ratos Sprague-Dawley , Globulina de Ligação a Hormônio Sexual/metabolismo , Distribuição Tecidual , Tomografia Computadorizada de Emissão de Fóton Único , Células Tumorais Cultivadas
14.
Z Lebensm Unters Forsch ; 203(1): 1-6, 1996 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-8765985

RESUMO

Influence of saliva composition and volume on flavour release from rehydrated French beans (Phaseolus vulgaris) was studied in three types of mouth model systems; dynamic headspace (DH), dynamic headspace and mastication (DHM) and a purge-and-trap (PT) model system. Volatile compounds were analysed by gas chromatography, using flame ionization detection (FID), mass spectrometry and sniffing port detection. Areas of FID peaks were largest in the PT system, followed by those of the DHM and DH systems, respectively. Saliva composition as well as volume influenced the release of volatile compounds from rehydrated French beans. Generally, FID data showed a decrease in release by the saliva component mucin, because of interactions between volatile compounds and protein, and in increase in release by its alpha-amylase, probably due to degradation of inclusion complexes of starch. The decrease in flavour release by the enlarged saliva volume was evaluated by a model study. Sniffing patterns of odour active compounds were barely influenced by either saliva composition or volume.


Assuntos
Fabaceae , Conservação de Alimentos , Plantas Medicinais , Saliva Artificial , Paladar , Cromatografia Gasosa , Liofilização , Humanos , Mastigação , Modelos Biológicos , Amido
15.
Proc Natl Acad Sci U S A ; 92(6): 2036-40, 1995 Mar 14.
Artigo em Inglês | MEDLINE | ID: mdl-11607516

RESUMO

Cabbage plants respond to caterpillar (Pieris brassicae) herbivory by releasing a mixture of volatiles that makes them highly attractive to parasitic wasps (Cotesia glomerata) that attack the herbivores. Cabbage leaves that are artificially damaged and subsequently treated with gut regurgitant of P. brassicae caterpillars release a volatile blend similar to that of herbivore-damaged plants. We demonstrate the presence of beta-glucosidase in P. brassicae regurgitant. Leaves treated with commercial beta-glucosidase (from almonds) release a volatile blend similar to that of leaves treated with P. brassicae regurgitant. In a flight bioassay, leaves treated with almond beta-glucosidase are highly attractive to the parasitic wasp C. glomerata. Furthermore, the wasps do not discriminate between cabbage leaves treated with almond beta-glucosidase and leaves treated with larval regurgitant. beta-Glucosidase was also recorded in cabbage leaf extract, but this is not as effective as caterpillar beta-glucosidase in eliciting the volatile production. Caterpillars that feed on a beta-glucosidase-free diet secrete the enzyme, and their regurgitant is an effective elicitor of the plant response. These findings show that beta-glucosidase is a P. brassicae-secreted elicitor of the defense response of cabbage plants to herbivore injury, inducing the emission of volatiles that are used by parasitoids of the herbivore to locate their victims.

16.
J Chem Ecol ; 21(11): 1789-811, 1995 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-24233830

RESUMO

The role of volatile infochemicals emitted by feces of larvae in the host-searching behavior of the parasitoidCotesia rubecula was evaluated during single- and dual-choice tests inside a wind tunnel. The following treatments were tested: feces produced by second and fourth instars ofPieris rapae (preferred host), second instars ofP. brassicae (inferior host), second instars ofP. napi (nonhost), and wet feces of second instars ofP. rapae. During a single-choice situation females ofC. rubecula oriented to all types of feces tested. When a preference was to be made,C. rubecula preferred feces of second instars ofP. rapae over that of fourth, feces ofP. rapae over that ofP. brassicae, feces ofP. napi over that ofP. brassicae, and wet over normal host feces. No preference was exhibited between feces of second instars ofP. napi and that of second instars ofP. rapae. The relative importance of infochemicals from host feces versus plant damage caused by host larvae to the searching behavior ofC. rubecula was also evaluated. Plant damage was more important to the searching females than host feces when feces were present in specific concentrations in relation to damage. The volatiles released by normal and wet feces of second instars ofP. rapae, wet feces of fourth instars ofP. rapae, and normal and wet feces ofP. brassicae were collected and identified. Overall, 85 chemical compounds were recorded belonging to the following chemical groups: alcohols, ketones, aldehydes, esters, isothiocyanates, sulfides, nitriles, furanoids, terpenoids and pyridines. The blend of chemicals emitted by feces of different instars ofP. rapae and different species ofPieris exhibited an instar and species specificity in both quantity and quality. Wetting of normal feces increased the amount of volatile chemicals released, and it was also responsible for the appearance of new compounds. The role of feces of larvae in the host-seeking behavior ofC. rubecula is discussed.

17.
J Chem Ecol ; 21(3): 273-87, 1995 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-24234060

RESUMO

The female parasitic waspCotesia kariyai discriminated between the volatiles of corn leaves infested by younger host larvaePseudaletia separata (first to fourth instar) and uninfested leaves in a Y-tube olfactometer; the wasps were attracted to the infested leaves. In contrast, when corn plants were infested by the later stages (fifth and sixth instar) of the armyworm, the wasps did not distinguish between infested corn leaves and uninfested corn leaves in the olfactometer. Mechanically damaged leaves were no more attractive than undamaged leaves, and host larvae or their feces were not attractive to the parasitoid. Through chemical analysis, the herbivore-induced plant volatiles were identified in the headspace of infested corn leaves. The herbivore-induced volatiles (HIVs) constituted a larger proportion of the headspace of corn leaves infested by early instar armyworms than of corn leaves infested by late instar armyworms. Application of third-instar larval regurgitant onto artificially damaged sites of leaves resulted in emission of parasitoid attractants from the leaf, whereas leaves treated with sixth-instar regurgitant did not. The function of this herbivore-stage related specificity of herbivore-induced synomones is discussed in a tritrophic context.

19.
J Chem Ecol ; 20(2): 373-86, 1994 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-24242061

RESUMO

We investigated the olfactory response of the predatory mitePhytoseiulus persimilis to cucumber leaves infested with prey, the herbivorous spider miteTetranychus urticae. The predators responded to volatiles from young rather than old infested cucumber leaves. GC-MS analysis of the head-space of spider mite-infested, artificially damaged and undamaged cucumber plants showed that herbivore-induced plant volatiles were present among the volatiles of both old and young infested cucumber leaves. The major components of the herbivore-induced plant volatiles were (3E)-4,8-dimethyl-1,3,7-nonatriene and (E)-ß-ocimene: these compounds are known to attract the predatory mites. In addition, we found three oximes (2-methylbutanalO-methyloxime, 3-methylbutanalO-methyloxime, and an unknown oxime) in the headspace of both old and young infested cucumber leaves. 3-MethylbutanalO-methyloxime and the unknown oxime were much more abundant in the headspace of infested old cucumber leaves. The potential adaptive value of differential attractiveness of cucumber plant leaves of different age is discussed.

20.
J Chem Ecol ; 20(6): 1329-54, 1994 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-24242342

RESUMO

Plants may defend themselves against herbivores by enhancing the effectiveness of natural enemies of herbivores. This is termed "indirect defense," which may be induced by herbivore damage. An important aspect of induced indirect defense is the attraction of the herbivore's natural enemies to infested plants by the plant emitting so-called "herbivore-induced synomone" (HIS) in response to herbivore damage. In this paper, we review the role of terpenoids in the induced indirect defense of plants against herbivorous mites. HIS are emitted from both damaged and undamaged areas of infested plants, and the composition of HIS varies among different plant species. The emission of HIS may also vary within a plant species, depending upon: (1) plant cultivar, (2) leaf growth stage, (3) the herbivore species that is attacking, and (4) abiotic conditions (light intensity, time of year, and water stress). Predatory mites cope with this variation of HIS by innate recognition as well as temporary specialization to a certain HIS via learning.

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