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  • 11
    Electronic Resource
    Electronic Resource
    Palo Alto, Calif. : Annual Reviews
    Annual Review of Physiology 42 (1980), S. 493-510 
    ISSN: 0066-4278
    Source: Annual Reviews Electronic Back Volume Collection 1932-2001ff
    Topics: Medicine , Biology
    Type of Medium: Electronic Resource
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  • 12
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 285 (1980), S. 669-670 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Establishment of the neurohaemal organ for PTTH required the identification of the cerebral NSC responsible for its synthesis and their axonal distribution, as well as a titre of PTTH in the brain and retrocerebral complex (CC plus CA) during metamorphosis. The PTTH NSC in freshly ecdysed pupae of ...
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  • 13
    Electronic Resource
    Electronic Resource
    Springer
    Cellular and molecular life sciences 50 (1994), S. 159-163 
    ISSN: 1420-9071
    Keywords: Prothoracicotropic hormone ; Manduca sexta ; anti-PTTH monoclonal antibody ; sedimentation coefficient ; frictional ratio ; molecular weight
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract The prothoracicotropic hormones (PTTHs) are cerebral peptides that control insect postembryonic development by stimulating the prothoracic glands to synthesize ecdysteroids. InManduca sexta, the tobacco hornworm, two classes of PTTH are distinguished by their Mr, small (ca. 7 kDa) and big PTTH (ca. 25–30 kDa). Little is known about the physical nature of the PTTHs and this study takes a first step towards defining characteristics of theManduca big PTTH. The neurohormone has a Stokes radius of 2.59 nm and a sedimentation coefficient of 2.76 S. Based on these data, an Mr of 29,443.7 and anf/f 0 of 1.27 were calculated. Combined, the physical data revealManduca big PTTH is an asymmetrical acidic homodimeric peptide with intra- and intermolecular disulfide bonds.
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  • 14
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Fig 1 Stoichiometry of a cytochrome P-450 mixed function oxidase type reaction and the C-20 hydroxylation of α- to β- ecdysone. In vertebrates, steroid hormone hydroxylations are catalysed by hydroxylase systems possessing a terminal cytochrome P-450 (refs 7 and 8). These enzyme ...
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  • 15
    Electronic Resource
    Electronic Resource
    Springer
    Cellular and molecular life sciences 39 (1983), S. 984-988 
    ISSN: 1420-9071
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary The kinetics of prothoracicotropic hormone (PTTH) activation of pupal prothoracic glands (PG) of the cabbage army worm,Mamestra brassicae, and silkworm,Bombyx mori, were determined in vitro. Activation was assessed by comparing the increase in the rate of ecdysone synthesis by one member of a PG pair incubated with a PTTH preparation from pupal brains with the basal rate of synthesis of the other PG incubated without PTTH. A time course of ecdysone synthesis revealed thatBombyx PTTH extract activatedBombyx PG, andMamestra PTTH extract activatedMamestra PG. Dose responses of activation ofBombyx andMamestra PG by their respective PTTH were saturable and were indicative of neurohormonal activation. TheBombyx PG were half-maximally activated (A50) by far less PTTH thanMamestra PG, 0.34 and 0.91 brain equivalents, respectively. Heterologous dose response of activation studies, in which PTTH and PG fromMamestra, Bombyx and the tobacco hornworm,Manduca sexta, were assayed for interspecific PG sensitivity and PTTH specificity, revealed cross-reactivity among the three PTTH-PG axes, withManduca PG being more sensitive to the PTTH of the other species andBombyx PTTH being the most effective in activating the PG of the other two species.
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  • 16
    Electronic Resource
    Electronic Resource
    Springer
    Journal of chemical ecology 5 (1979), S. 335-344 
    ISSN: 1573-1561
    Keywords: Hymenoptera ; Formicidae ; Aphaenogaster rudis ; ant ; behavior ; diglyceride ; elaiosome ; myrmecochory ; Viola odorata
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract The chemical basis of an ant-seed interaction was investigated for the antAphaenogaster rudis and the ant-dispersed violetViola odorata. A laboratory behavioral bioassay was developed to chemically identify the attractant responsible for the interaction. The ant attractant, localized in the elaiosome, was classified as a lipid by both field and laboratory bioassays. Assays of partially purified lipid extracts revealed that the principal attractant may be a diglyceride. Gas-liquid chromatography analysis of the hydrolyzed diglyceride fraction revealed oleic acid as the major fatty acid present, suggesting that either 1,2- or 1,3-diolein may be the attractant. Structure-activity correlations for lipid standards demonstrated a clear preference for the diglyceride 1,2-diolein. The data also suggest that ricinoleic acid is not the lipid eliciting the ant response toViola odorata, as had been previously suggested.
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