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  • Food Science, Agricultural, Medicinal and Pharmaceutical Chemistry  (10)
  • Wiley-Blackwell  (10)
  • Cambridge University Press
  • Institute of Physics
  • International Union of Crystallography
  • Nature Publishing Group
  • Oxford University Press
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  • Wiley-Blackwell  (10)
  • Cambridge University Press
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  • International Union of Crystallography
  • Nature Publishing Group
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  • 1
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Archives of Insect Biochemistry and Physiology 7 (1988), S. 75-89 
    ISSN: 0739-4462
    Schlagwort(e): natriuresis ; diuretic hormone ; Malpighian tubules ; diuretic assay ; Chemistry ; Food Science, Agricultural, Medicinal and Pharmaceutical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Biologie
    Notizen: In previous studies we have presented evidence for the role of peptides, isolated from heads of the mosquito Aedes aegypti, in stimulating fluid secretion by isolated Malpighian tubules. In the present study we conducted experiments to investigate whether these peptides are involved in hormone-mediated diuresis after a blood meal. In vivo experiments showed that the head was required to maintain diuresis after the blood meal. Whereas feeding on blood triggered a prompt diuresis in the intact mosquito, subsequent decapitation caused a gradual, not an abrupt, decline in urine excretion rate. Hemolymph collected from mosquitoes fed blood significantly stimulated fluid secretion in vitro by isolated Malpighian tubules, whereas hemolymph from unfed or blood-fed decapitated mosquitoes did not. These results indicate that a diuretic factor was released into the hemolymph after a blood meal. This factor was not present in the hemolymph of decapitated females. We identified the head as a source of diuretic factors. Peptides isolated from a head extract by high-performance liquid chromatography, when injected into the hemocoel of blood-fed decapitated mosquitoes, triggered diuresis in vivo and also stimulated fluid secretion in isolated Malpighian tubules. These studies support the hypothesis that the head is a storage site for diuretic peptides that may be released after a blood meal to control diuresis.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Archives of Insect Biochemistry and Physiology 8 (1988), S. 25-37 
    ISSN: 0739-4462
    Schlagwort(e): juvenile hormone ; epoxide hydrolase ; JH esterase ; Chemistry ; Food Science, Agricultural, Medicinal and Pharmaceutical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Biologie
    Notizen: A thin-layer chromatographic assay was developed for the resolution of hydrolytic and conjugative catabolites of juvenile hormone (JH). A single-dimension, dual-development thin-layer system allowed complete resolution of the catabolites. Thus, this system provided a means for the rapid and economic analysis of JH hydrolysis even when different hydrolytic activities were present concurrently. Purified hydrolytic enzymes were found to be superior to chemical methods for the generation of small amounts of standards of JH catabolites. The relative levels of activities of an epoxide hydrolase and an esterase toward JH III were found to be similar in microsomal preparations from three lines of adult Drosophila melanogaster isolated from a field population. However, selection of flies by exposure to cut orange resulted in the elevation of levels of epoxide hydrolase activities, whereas esterase levels were not affected to the same extent. The formation of the JH acid-diol was not detected under the conditions of this study, suggesting that the JH acid and diol were not good substrates for epoxide hydrolase and juvenile hormone esterase, respectively.
    Zusätzliches Material: 6 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Archives of Insect Biochemistry and Physiology 9 (1988), S. 81-90 
    ISSN: 0739-4462
    Schlagwort(e): Manduca sexta ; hemolymph ; postlarval ; protein ; Chemistry ; Food Science, Agricultural, Medicinal and Pharmaceutical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Biologie
    Notizen: The identification, purification and characterization of a new postlarval specific hemolymph protein from Manduca sexta is described. Incorporation of [35S]methionine into Manduca sexta hemolymph proteins in vivo was investigated as a function of development. A major protein band of Mr ≈ 50,000 was highly labeled during the prepupal and adult stage but not in feeding larvae. This postlarval protein (PLP) was isolated from adult male hemolymph and its chemical and immunological properties determined. PLP is a basic protein (pI ∼8.6). Electrophoresis under denaturing conditions reveals a subunit Mr ≈ 50,000 while the native protein has an apparent Mr ∼ 85,000 by gel permeation chromatography. Anti-PLP serum recognized PLP but not other hemolymph proteins on immunoblots. In vitro translation of fat body mRNA followed by immunoprecipitation revealed that fat body is the site of PLP synthesis. Quantitation of PLP levels in hemolymph throughout development was performed and suggests PLP may play a role in adult development of M. sexta.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 4
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Archives of Insect Biochemistry and Physiology 9 (1988), S. 47-65 
    ISSN: 0739-4462
    Schlagwort(e): tobacco hornworm ; Manduca sexta ; hemolymph proteins ; developmental disruption ; insect ecdysis inhibitors ; Chemistry ; Food Science, Agricultural, Medicinal and Pharmaceutical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Biologie
    Notizen: Injection of the insect growth regulator (IGR) azadirachtin into Manduca sexta larvae that were parasitized by Cotesia congregata adversely affected subsequent endoparasite development when the compound was administered prior to the first larval ecdysis of the wasps. Injection of 2.5-10 μg of azadirachtin into newly ecdysed fourth or fifth instar hosts partially inhibited or totally suppressed the first larval ecdysis of the parasites. Instead of initiating rapid growth similar to parasites developing in hosts injected with the solvent carrier (ethanol) only, parasites in azadirachtin-treated hosts never grew beyond the size normally attained in early terminal stage hosts. The host larvae survived for 2 weeks or longer following injection of azadirachtin, but their parasites never recovered and died encased within one or two exuvial cuticles. The parasitism-specific hemolymph polypeptides previously shown to be characteristic of terminal stage hosts were undetectable in larvae in which the parasites failed to ecdyse to the second instar. The observed effects of azadirachtin on development of C. congregata differ significantly from those induced by other IGRs in parasitized M. sexta, suggesting azadirachtin has a unique, though as yet undefined, mode of action. Compared to other IGRs, this compound is extremely potent in terms of the minimum doses required to prevent emergence, but affects only the L1-L2 ecdysis and not the L2-L3 transition. In contrast, other compounds such as juvenoids and the JH esterase inhibitor BEPAT (S-benzyl-0-ethyl phosphoramidothiolate) permit the parasite to grow and develop normally until the wasps become pharate third instar larvae, then inhibit the second larval ecdysis and emergence from the host.
    Zusätzliches Material: 6 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 5
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Archives of Insect Biochemistry and Physiology 7 (1988), S. 105-118 
    ISSN: 0739-4462
    Schlagwort(e): JH binding ; lipoprotein ; migratory locust ; Chemistry ; Food Science, Agricultural, Medicinal and Pharmaceutical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Biologie
    Notizen: The juvenile hormone binding protein in Locusta migratoria is a very high density lipoprotein of Mr ∼ 566,000. It contains 15% lipid and is composed of six seemingly identical subunits of Mr ∼ 77,000. It is a minor protein, constituting 1-2% of the total hemolymph proteins. Its concentration fluctuates with total protein content and follows a cyclic pattern related to the molting cycles.The binding protein has a high affinity for (10R)-juvenile hormone III. The dissociation constant for the hormone is 3.7 ∼ 0.6 nM, and one binding molecule contains six hormone-specific binding sites. The concentration of binding sites in the hemolymph is therefore very high, reaching a value of 26 μM in the last larval instar and 11 μM in the adult male.
    Zusätzliches Material: 7 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 6
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Archives of Insect Biochemistry and Physiology 8 (1988), S. 113-126 
    ISSN: 0739-4462
    Schlagwort(e): insect viruses ; parasitoid ; prothoracic glands ; Chemistry ; Food Science, Agricultural, Medicinal and Pharmaceutical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Biologie
    Notizen: Campoletis sonorensis calyx fluid arrests the development of last-instar Heliothis virescens larvae and is associated with the gross degeneration of the host's prothoracic glands. Through manipulations of ovary supernatant, Campoletis sonorensis polydnavirus (CsV) was found to be the only component of calyx fluid responsible for causing host developmental arrest. Venom from C. sonorensis had no effect on host development. Suspensions of CsV were quantified, and various doses were injected into last-instar hosts. The percentage of larvae developmentally arrested was dose dependent. In addition, larvae not arrested by injection with CsV suspensions were developmentally delayed in a dose-dependent manner. Hosts were delayed in the stage in which they were injected and, after recovery, developed at normal rates. Measurements by radioimmunoassay indicated that developmental delay was due to a suppression of ecdysteroid titers. After a dose-dependent period of suppression, hemolymph ecdysteroid titers recovered and reached titers comparable to those observed in saline-injected controls. Examination of prothoracic glands from developmentally delayed larvae revealed that partial degeneration occurred. Comparisons of the number and mean size of surviving gland cells and the length of developmental delay suggested that surviving gland cells may compensate for degenerated cells by increasing their ecdysone production.
    Zusätzliches Material: 7 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 7
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Archives of Insect Biochemistry and Physiology 8 (1988), S. 59-72 
    ISSN: 0739-4462
    Schlagwort(e): cereal pests ; polysaccharases ; feeding ; wheat damage ; Chemistry ; Food Science, Agricultural, Medicinal and Pharmaceutical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Biologie
    Notizen: Several carbohydrases and glycosidases from the alimentary cancal and/or salivary glands of feeding larvae of mayetiola destructor have been identified. Pectinase activity was identified in the midgut and may be present in the salivary glands. No endocellulase activity was found in larvae; however, hemicellulase activity was detected in extract of larvae. Amylase activity was present in midguts from feeding larvae and at a low level in extract of salivary glands. Amylases detected in the midgut showed mobilities during polyacrylamide gel electrophoresis similar to the two major amylases in tissues of the insect's host plant. The possibility exists that Hessian fly larvae utilize amylases obtained from their host plant in the digestion of starch. The major glycosidases detected in the midgut lumen of larve were: α-D-glucosidase and α-D-and β-D-galactosidase. The role of these enzymes in the feeding process of Hessian fly larvae is discussed as well as their potential role in feeding damage to wheat.
    Zusätzliches Material: 6 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 8
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Archives of Insect Biochemistry and Physiology 9 (1988), S. 91-106 
    ISSN: 0739-4462
    Schlagwort(e): yolk protein ; vitellogenesis ; tephritids ; Chemistry ; Food Science, Agricultural, Medicinal and Pharmaceutical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Biologie
    Notizen: A single major yolk polypeptide (YP) having a molecular mass of approximately 48,000 daltons (Da), was identified in the ovaries and oviposited eggs of the Caribbean fruit fly, Anastrepha suspensa. The polypeptide was partially purified from oviposited eggs using gel permeation and ion-exchange chromatography. Analysis of YP synthesis in vivo and in tissues cultured in vitro indicated that the ovary was the major site of synthesis with very low levels of YP derived from the adult fat body. Using a monospecific polyclonal antiserum to 48 kDa YP in an immunoblot assay, low levels of vitellogenin were found in female hemolymph; slightly lower levels of an immunoreactive 48-kDa polypeptide were detectable in male hemolymph. Although YP synthesis was detectable within 12 h after eclosion, the major increase in YP accumulation occurred at 3-4 days posteclosion coincident with the initiation of observable yolk deposition. The physical characteristics of YP from A. suspensa were similar to YPs from other dipterans in terms of molecular mass and antigenicity, yet the tissue- and sex-specific regulation of the YP differed from other dipterans as well as most other insects.
    Zusätzliches Material: 8 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 9
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Archives of Insect Biochemistry and Physiology 9 (1988), S. 135-156 
    ISSN: 0739-4462
    Schlagwort(e): ecdysis (control of) ; JH esterase (inhibition of titer of) ; JH epoxide hydrolase ; molting (control of) ; JH acid (effects of) ; Chemistry ; Food Science, Agricultural, Medicinal and Pharmaceutical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Biologie
    Notizen: Extensive juvenile hormone (JH) hydrolysis was detected and characterized in whole-body homogenates of larvae and tissues of Trichoplusia ni during periods of early larval development. The capacity to hydrolyze JH that exists in homogenates of penultimate-instar larvae is far in excess of the measured hormone levels. The major initial metabolites of JH found in diluted homogenates of early-instar larvae and larval tissues were JH acid and JH diol as shown by thin-layer chromatography and microchemical derivatization. Experiments using subcellular fractionation or immunoprecipitation and inhibition studies showed the two hydrolytic activities to be roughly equivalent but located in different subcellular compartments. JH epoxide hydrolase activity was present in the large particle and microsomal fractions, whereas most JH esterase activity was present in the cytosol. Subsequent studies concentrated on JH esterolysis. A titer of JH esterase activity throughout larval development showed this enzyme to be present continuously inside tissues, with periodic manifestations in the hemolymph during each larval molt. Partial purification by affinity chromatography and analysis with sodium dodecyl sulfate-polyacrylamide gel electrophoresis, Western blotting, and isoelectric focusing showed JH esterase from earlyinstar larvae to be indistinguishable from the enzyme from the last instar. Application of JH II or a juvenoid, Ro 10-3108, during any time of early larval development caused no apparent abnormalities, suggesting that the action of JH esterase is not involved with elimination of JH during this period. However, application of a JH esterase inhibitor during a critical period of the third to fourth larval molt caused failure of ecdysis, suggesting that JH acid or at least some esterase or protease may be a factor required for the molt.
    Zusätzliches Material: 7 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 10
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Archives of Insect Biochemistry and Physiology 7 (1988), S. 13-28 
    ISSN: 0739-4462
    Schlagwort(e): catecholamine ; dopamine ; sclerotization ; dopamine sulfate ; catechol ; Chemistry ; Food Science, Agricultural, Medicinal and Pharmaceutical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Biologie
    Notizen: Diphenolic compounds in cockroach hemolymph and cuticle were extracted with 1.2 N HCI, partially purified by alumina adsorption, and analyzed by liquid chromatography. Dopamine (DA) is the major catecholamine in hemolymph of Periplaneta americana, Blatta orientalis, Blattella germanica, Gromphadorhina portentosa, and Blaberus craniifer at adult ecdysis, while N-acetyldopamine (NADA) predominates in hemolymph of Leucophaea maderae. In P. americana, NADA is the second most abundant catecholamine, while N-β-alanyldopamine (NBAD), norepinephrine (NE), 3,4-dihydroxyphenylalanine, 3,4-dihydroxyphenylethanol, 3,4-dihydroxyphenylacetic acid, and 3,4-dihydroxybenzoic acid occur in lesser quantities. Catecholamines occur mainly as acid labile conjugates in hemolymph. Dopamine, conjugated primarily as the 3-sulfate ester, increases in hemolymph from 0.1 to 0.8 mM during the last instar. Concentrations decrease by 75% in pharate adults, partially because of an increase in hemolymph volume. A second smaller peak of DA sulfate occurs after ecdysis followed by a rapid disappearance as the cuticle tans. A conjugate of catechol (o-dihydroxybenzene) is also present in relatively high concentrations at all ages examined. In cuticle, N-β-alanylnorepinephrine accumulates during the early period of adult tanning, while NBAD, NADA, N-acetylnorepinephrine, and DA increase more slowly. The N-β-alanyl and N-acetyl derivatives of DA and NE occure in relatively high concentrations in tanned cutical of P. americana and probably play an important role in the stablization process.
    Zusätzliches Material: 7 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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