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Trichothecene

This same experimental approach can be used to determine the appHcabiUty of the aDAS—AP to a competitive assay for DAS. As shown in Eigure 6, increasing amounts of free DAS were used to define the 50% inhibition level (ID q) of DAS for binding of two aDAS—AP conjugates to immobilized DAS. This approach was also used to determine the sensitivity of an EIA, as well as the specificity of the assay, as shown in Table 2. Increasing amounts of trichothecene mycotoxins closely related to DAS were added to microtiter plate wells containing a constant amount of prereacted DAS—aDAS—AP. After 30 min, excess toxin and any free toxin—aDAS—AP were washed out, and substrate was added. Quantification of the color produced was directly related to the abihty of the added toxin to displace aDAS—AP from the immobilized DAS, which is an indication that the aDAS also has an avidity for that toxin. [Pg.25]

Reagent for Epoxides e.g. trichothecene-mycotoxins [1 — 6] valepotriates [7,17] Olefins, acetylene derivatives [8] 4-Hydroxycumarin, anthraquinone [8] Alkylating agents [9-12] NOz... [Pg.359]

Note Trichothecenes and valepotriates only react when there is an epoxy group present in the molecule their detection limits are in the range 25—200 ng substance per chromatogram zone [1]. The detection limits for acetylene derivatives are 100— 800 ng substance per chromatogram zone, but not all give a positive reaction [8]. [Pg.362]

Group 2 includes some 80 sesquiterpene trichothecenes, which are particularly associated with fungi belonging to the group Fusarium. Fusarium species are widely known both as plant pathogens and contaminants of stored foods snch as maize. Trichothecenes are strong inhibitors of protein synthesis in mammalian cells. There have been many incidents of poisoning of farm animals cansed by contamination of their food by these componnds. [Pg.13]

However, the most interesting of the Baccharis species is most certainly B. coridifolia. This plant is well-known in Brazil as being one of that country s most toxic plants (49) and is a serious hazard to livestock who graze in pastures populated by B. coridifolia (49). Four separate collections were made of B. coridifolia (48). Three of these collections were "From several miles outside Curitaba and a fourth collection in a pasture near Santa Maria, the site of an earlier collection of 13. coridifolia (47), and several hundred miles away from Curitaba. ThTs latter collection and two of the three former collections contained appreciable quantities of roridins A and E. A third collection from near Curitaba appeared to contain no macrocyclic trichothecenes. From a 20 g sample of one of the collections of B. coridifolia... [Pg.153]

Our most recent work with B megapotamica has been with the isolation of large quantities of baccharinoids from a 1800 Kg collection. The workup of the crude extract (ca. 30 Kg of black tarry material) of this plant material was conducted by Dr. Fred Boettner of Polyscience, Inc. This near Herculean task required tremendous quantities of solvents, column packings and time to complete. An outline of the fractionation scheme is presented in Figure 2. Fractions F6-F11 contain a large number of baccharinoids. To date, we have characterized over twenty macrocyclic trichothecenes found in B mega-... [Pg.155]

Ueno, Y. (ED) "Trichothecenes - Chemical, Biological, and Toxicological Aspects" Kodensha Scientific, Tokyo, 1983. [Pg.158]

Soil microorganisms produce many compounds that are potentially toxic to higher plants. Examples include members of the following antibiotics (1-6), fatty and phenolic acids (7-12), amino compounds (13-15), and trichothecenes (16, 17). "Soil sickness" and "replant problems" have been reported where certain crops or their residues interfere with establishment of a subsequent crop (18, 19). Toxins resulting from microbial activity sometimes are involved, but it is often unclear whether these are synthesized de novo in microbial metabolism or are breakdown products of the litter itself (20). [Pg.337]

Of four basic trichothecene groups (A, B, C and D), types A and B represent the most important mycotoxins. Type A includes the T-2 toxin that can suppress the immune system and can cause damage to bone marrow. The T-2 toxin is about 14 times more toxic than the most widespread Fusarium-based type B mycotoxin, deoxynivalenol (DON), previously called vomitoxin. DON is a... [Pg.355]

Fusarium species Trichothecenes Zearalenone Fumonisins Moniliformin... [Pg.355]

Edwards S G, Pirgozliev S R, Hare M C and Jenkinson P (2001), Quantification of trichothecene-producing Fusarium species in harvested grain by competitive PCR to determine efficacies of fungicides against Fusarium head blight of winter wheat , Appl. Environ. Microbiol., 67, 1575-1580. [Pg.385]

Miller J D, ApSimon J W, Blackwell B A K Greenhalgh R and Taylor A (2001), Deoxynivalenol a 25 year perspective on a trichothecene of agricultural importance , in Summerell B A, Leslie J F, Backhouse D, Bryden W L and Burgess L W, Fusarium Paul E. Nelson Memorial Symposium, The American Phytopathological Society Press, St. Paul, Minnesota, 310-320. [Pg.388]

Nicholson P, Simpson D R, Wilson A H, Chandler E and Thomsett M (2004), Detection and differentiation of trichothecene enniatin-producing Fusarium species on small-grain cereals , Europ. J. Plant Pathol., 110, 503-514. [Pg.389]

WHO (1990), Selected mycotoxins ochratoxins, trichothecenes, ergot , Environ, Health Criteria 105, Geneva, Switzerland, WHO, 1-163. [Pg.391]

Cundliffe, E., Cannon, M., and Davies, J. (1974). Mechanism of inhibition of eukaryotic protein synthesis b trichothecene fungal toxins. Proc. Natl. Acad. Sci. USA 71, 30-34. [Pg.352]

This material is hazardous through inhalation, skin absorption, penetration through broken skin, ingestion, and produces local skin/eye impacts. Trichothecenes are radiomimetic and may cause bone marrow suppression, liver failure, and internal bleeding. [Pg.485]


See other pages where Trichothecene is mentioned: [Pg.24]    [Pg.244]    [Pg.147]    [Pg.195]    [Pg.361]    [Pg.411]    [Pg.496]    [Pg.576]    [Pg.599]    [Pg.683]    [Pg.708]    [Pg.734]    [Pg.149]    [Pg.152]    [Pg.152]    [Pg.153]    [Pg.153]    [Pg.155]    [Pg.160]    [Pg.180]    [Pg.355]    [Pg.355]    [Pg.356]    [Pg.486]    [Pg.486]    [Pg.486]    [Pg.487]    [Pg.487]   
See also in sourсe #XX -- [ Pg.104 ]

See also in sourсe #XX -- [ Pg.67 ]




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Apoptosis trichothecene-induced

Apoptosis trichothecenes

Baccharis cordifolia macrocyclic trichothecenes fro

Bean, trichothecenes

Biological warfare trichothecene mycotoxins

Cytotoxicity trichothecenes

Feed refusal trichothecenes

Fungi trichothecene production

Fusarium trichothecenes, detection

Macrocyclic trichothecene mycotoxins

Macrocyclic trichothecene mycotoxins roridin

Macrocyclic trichothecenes

Macrocyclic trichothecenes in vivo toxicity

Macrocyclic trichothecenes toxicity

Metabolism trichothecenes

Mitogen-activated protein kinases trichothecene activation

Monoclonal antibodies, trichothecenes

Mycotoxins trichothecenes

Non-Macrocyclic Trichothecenes

Protein synthesis inhibition trichothecenes

Sesquiterpenoids trichothecenes

Simple trichothecenes

The Trichothecenes

Trichothecene Biosynthetic Gene Clusters

Trichothecene Poisoning

Trichothecene biosynthesis cluster genes

Trichothecene complex

Trichothecene derivatives

Trichothecene macrolides

Trichothecene my cotoxin

Trichothecene mycotoxins

Trichothecene mycotoxins acute effects

Trichothecene mycotoxins aerosolized

Trichothecene mycotoxins biosynthesis

Trichothecene mycotoxins decontamination

Trichothecene mycotoxins deoxynivalenol

Trichothecene mycotoxins dermal exposure

Trichothecene mycotoxins diacetoxyscirpenol

Trichothecene mycotoxins effect

Trichothecene mycotoxins excretion

Trichothecene mycotoxins fusarenon

Trichothecene mycotoxins inactivation

Trichothecene mycotoxins lethality

Trichothecene mycotoxins metabolism

Trichothecene mycotoxins nivalenol

Trichothecene mycotoxins production

Trichothecene mycotoxins respiratory exposure

Trichothecene mycotoxins structure

Trichothecene mycotoxins toxicology

Trichothecene mycotoxins treatment

Trichothecene mycotoxins, inflammatory

Trichothecene mycotoxins, inflammatory gene expression modulation

Trichothecene mycotoxins, specificity

Trichothecene producers, detection

Trichothecene relatives

Trichothecene ring

Trichothecene toxins

Trichothecene via sulfur ylide reagents

Trichothecene, synthesis

Trichothecenes

Trichothecenes analytical methods

Trichothecenes as mycotoxins

Trichothecenes biosynthesis

Trichothecenes chemical types

Trichothecenes classification

Trichothecenes decontamination

Trichothecenes diseases

Trichothecenes epoxide opening

Trichothecenes food contamination

Trichothecenes fungal toxins

Trichothecenes mechanisms

Trichothecenes mitogen-activated protein kinases

Trichothecenes occurrence

Trichothecenes organisms

Trichothecenes phytotoxicity

Trichothecenes poisoning

Trichothecenes properties

Trichothecenes responses

Trichothecenes risk assessment

Trichothecenes role in mycotoxicoses

Trichothecenes signs/symptoms

Trichothecenes structures

Trichothecenes synthesis

Trichothecenes toxicity

Trichothecenes treatment

Trichothecenes types

Trichothecenes via cyclohexadienyl complexes

Trichothecenes vomiting

Trichoverroids and Macrocyclic Trichothecenes

Wheat trichothecene mycotoxins

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