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At least 217 records · Page 12Linked to original sources
PubMed1974

The influence of substrate concentrations on the rate of insect juvenile hormone biosynthesis by corpora allata of the desert locust in vitro.

The rate at which isolated corpora allata of adult female Schistocerca gregaria incorporate [(3)H]farnesenic acid and [(14)C]methionine into C(16)juvenile hormone in vitro was examined at different concentrations of farnesenic acid, methionine, O(2) and H(+) ions. Maximum juvenile hormone biosynthesis is obtained at a farnesenic acid concentration of 20mum. The range of optimum l-methionine concentrations (0.1-0.4mm) encompasses the physiological concentration of this substrate in the haemolymph. Hormone biosynthesis is dependent on O(2), but is not stimulated by hyperbaric oxygen tension. The glands had a maximum synthetic activity at pH8.0, but their activity was more reproducible in the the physiological range pH7.0-7.5. At pH6.5 and less, the synthetic ability was considerably decreased. The relative incorporations of the labelled substrates into methyl farnesoate and C(16) juvenile hormone indicate that [(3)H]farnesenic acid comes into isotopic equilibrium within the gland more rapidly than [(14)C]methionine. The incorporations into methyl farnesoate become stoicheiometric after 20min incubation and into C(16) juvenile hormone after a further 10min. Labelled juvenile hormone is detectable after 10min incubation and the rate of incorporation is constant for up to 4h. It is proposed that the described method may be usefully employed to assess the physiological changes in the enzymic competence of the glands to effect the last two stages in C(16) juvenile hormone biosynthesis.

Animals↗
PubMed1973

Isolation, Structure, and Absolute Configuration of a New Natural Insect Juvenile Hormone from Manduca sexta.

Two juvenile hormones are isolated from organ cultures of corpora allata of the tobacco hornworm moth, Manduca sexta Johannson, and are purified by high-resolution liquid chromatography. These are identified as methyl (2E, 6E)-(10R)-10,11-epoxy-3,7,11-trimethyl-2,6-dodecadienoate, a new natural hormone, and methyl (2E,6E) - (10R,11S) - 10,11 - epoxy - 3,7,11 - trimethyl-2,6-tridecadienoate. [(14)C]Methionine is incorporated only into their methoxycarbonyl group. Details of the in vitro techniques and the chemical proof of structures are presented. The significance of the occurrence of a new juvenile hormone and the new techniques used for production, isolation, and identification are discussed.

Journal Article↗
PubMed1979

Cellular localization of the insect prothoracicotropic hormone: In vitro assay of a single neurosecretory cell.

The distribution of prothoracicotropic hormone in the pupal brain of Manduca sexta has been determined by an in vitro assay for prothoracic gland activation. Prothoracicotropic activity was observed in both the brain and retrocerebral complex, but predominantly in the dorosolateral regions of the protocerebrum. Of the two groups of neurosecretory cells present in this area of the brain, only the two lateral type III neurosecretory cells exhibited significant prothoracicotropic hormone activity. Further analysis revealed that the neurohormone was localized in only one of the two type III cells, suggesting that a single neurosecretory cell in each hemisphere is the source of the hormone at the stage examined (day 0). Prothoracicotropic hormone activity was detected in both the corpora allata and the corpora cardiaca, but the corpora allata contained 2 to 9 times the activity of the corpora cardiaca, depending on developmental stage. The significantly higher level of activity in the corpora allata suggests that they may be the neurohemal organs through which the prothoracicotropic hormone of Manduca is released.

Journal Article↗
PubMed1987

Sources of propionate for the biogenesis of ethyl-branched insect juvenile hormones: Role of isoleucine and valine.

Corpora allata from adult female Manduca sexta biosynthesize the sesquiterpenoid juvenile hormone (JH) III and the unusual ethyl-branched homologue JH II in vitro. We maintained corpora allata in medium 199 using [methyl-(3)H]methionine as the source of the JH methyl ester moiety and as a mass marker. This allowed measurement of the relative contributions of (14)C-labeled precursors to the biogenesis of JH II and III carbon skeletons. We showed efficient incorporation of a propionate equivalent, from isoleucine or valine catabolism, into the ethyl-branched portion of JH II, using double-label liquid scintillation counting of isolated JHs and gas chromatography/mass spectrometry with selected ion monitoring of JH deuteromethoxyhydrin derivatives. Methionine was a poor source of propionate for JH II biosynthesis, while glucose, succinate, threonine, and beta-alanine did not contribute propionate at all. Leucine, isoleucine, and glucose incorporated into JH III and the acetate-derived portion of JH II.

Journal Article↗
PubMed1966

Properties of bursicon: an insect protein hormone that controls cuticular tanning.

On gel filtration the retention volume of bursicon indicates a molecular weight of about 40,000. On disc electrophoresis bursicon migrates toward the anode and appears at an R(F) (relative to the marker dye) of 0.3 to 0.4. The properties of fractions with bursicon activity in blood, brain, and ganglion of a fly (Sarcophaga bullata), and in blood, ganglion, and corpora cardiaca of a roach (Periplaneta americana) are similar, but not identical. Bursicon in the blood is more heat labile, and the activity in brain and corpora cardiaca shows two peaks in electrophoresis, instead of one as in the other fractions.

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