@misc{Peter1980, author = {Peter, Martin G.}, title = {Products of in vitro oxidation of N-acetyldopamine as possible components in the sclerotization of insect cuticle}, url = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-16759}, year = {1980}, abstract = {[1-14C]-N-Acetyldopamine (NADA) was oxidized in the presence of methyl [3-3H]-β-alanate with mushroom tyrosinase. The complex mixture of reaction products was partly resolved by chromatographic procedures and analyzed by spectroscopic methods. Methyl-β-alanate is incorporated to only a small extent into oxidation products of NADA which inter alia are presumed to be oligomeric hydroxyquinones. After oxidation of [1-14C, 2-3H]-NADA with preparations from tanning Manduca sexta pupal cuticle, N-acetylnoradrenalin was identified as one of the products. Binding of radioactivity to melanin-like material was also observed. These results suggest that oxidation products different from those formulated usually for the crosslinkages between protein amino groups and N-acetyldopaquinone are deposited in darkly brown coloured insect cuticles during sclerotization.}, language = {en} } @misc{FerenzPeterBerg1983, author = {Ferenz, Hans-J{\"u}rgen and Peter, Martin G. and Berg, Dieter}, title = {Inhibition of farnesoic acid methyltransferase by sinefungin}, url = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-17016}, year = {1983}, abstract = {Sinefungin inhibited the S-adenosylmethionine-dependent farnesoic acid methyltransferase in a cell-free system containing a homogenate of corpora allata from female locusts, Locusta migratoria. The enzyme catalyzed the penultimate step of juvenile hormone biosynthesis in the insects. Culturing corpora allata in the presence of sinefungin greatly suppressed juvenile hormone production. The following in vivo effects were visible after injection of the inhibitor: increase in mortality and reduction of total haemolymph protein liter and ovary fresh weight, as well as length of terminal oocytes. Attempts to reverse these effects by topical application of the juvenile hormone analog ZR-515 (methoprene) were only partly successful. Therefore, the in vivo effects may be due to a general inhibition of methyltransferase enzymes in the insect. Sinefungin appeared to be of potential interest as the first representative of a new class of insect growth regulators.}, language = {en} } @misc{KortPeterKoopmanschap1983, author = {Kort, C. A. D. de and Peter, Martin G. and Koopmanschap, A. B.}, title = {Binding and degradation of juvenile hormone III by haemolymph proteins of the Colorado potato beetle: a re-examination}, url = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-16777}, year = {1983}, abstract = {The haemolymph of the adult Colorado potato beetle, Lepinotarsa decemlineata Say, contains a high molecular weight (MW > 200,000) JH-III specific binding protein. The Kd value of the protein for racemic JH-III is 1.3 ± 0.2 × 10-7 M. It has a lower affinity for racemic JH-I and it does not bind JH-III-diol or JH-III-acid. The binding protein does discriminate between the enantiomers of synthetic, racemic JH-III as was determined by stereochemical anaysis of the bound and the free JH-III. Incubation of racemic JH-III with crude haemolymph results in preferential formation of (10S)-JH-III-acid, the unnatural configuration. The JH-esterase present in L. decemlineata haemolymph is not enantioselective. It is concluded that the most important function of the binding protein is that of a specific carrier, protecting the natural hormone against degradation by esterases. The carrier does not protect JH-I as efficiently as the lower homologue.}, language = {en} } @misc{PeterStuppLentes1983, author = {Peter, Martin G. and Stupp, Hans-Peter and Lentes, Klaus-Ulrich}, title = {Umkehr der Enantioselektivit{\"a}t bei der enzymatischen Hydrolyse von Juvenilhormon als Ergebnis einer Proteinfraktionierung}, url = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-17001}, year = {1983}, abstract = {Aus dem Inhalt: Die Juvenilhormone 1a-c werden im Blut von Insekten enzymatisch zu den biologisch inaktiven Sluren hydrolysiert. Bei der Hydrolyse von racemischem 1c im Blut der Wanderheuschrecke Locusta migratoria wird ein Umsatz von 40-60\% erreicht. Das unumgesetzte Edukt enth{\"a}llt einen {\"U}berschuß an nat{\"u}rlich konfiguriertem (10R)-1c (e.e. 47.2\%). Wir konnten zeigen, daß das in der H{\"a}molymphe vorhandene Hormon-Bindungsprotein bevorzugt mit (10R)- 1c assoziiert.}, language = {de} } @misc{LaschewskyRingsdorfSchmidt1985, author = {Laschewsky, Andr{\´e} and Ringsdorf, H. and Schmidt, G.}, title = {Polymerization of hydrocarbon and fluorocarbon amphiphiles in Langmuir-Blodgett multilayers}, url = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-17096}, year = {1985}, abstract = {Langmuir-Blodgett multilayers of polymerizable carboxylic acids with hydrocarbon or fluorocarbon chains were prepared. The multilayers were polymerized by UV light and the reactions were studied by UV/visible spectroscopy. The polyreactions strongly influence the multilayer structures which were investigated by X-ray small-angle scattering and scanning electron microscopy. The spreading behaviour of the monomers, the preparation of multilayers, their reactivities in multilayers and structural effects caused by the polyreactions are discussed with regard to the hydrophilic head groups, the polymerizable groups and the hydrophobic chains.}, language = {en} } @misc{ElbertLaschewskyRingsdorf1985, author = {Elbert, R. and Laschewsky, Andr{\´e} and Ringsdorf, H.}, title = {Hydrophilic spacer groups in polymerizable lipids: formation of biomembrane models from bulk polymerized lipids}, url = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-17361}, year = {1985}, abstract = {A variety of polymerizable lipids containing a hydrophilic spacer group between the reactive group and the main amphiphilic structure have been synthesized. They were investigated in monolayers, liposomes, and multilayers. When the spacer concept was used, efficient decoupling of the motions of the polymeric chain and the amphiphilic side groups is achieved. Thus, the often found loss of the important fluid phases by polymerization is avoided. Polymeric monolayers of the spacer lipid, prepared either by polymerization in the monolayer or by spreading of prepolymerized lipid, exhibit nearly identical surface pressure-area diagrams. Most distinctly, the successful decoupling of the motions of the polymer main chain and the membrane forming amphiphilic side groups is demonstrated by the self-organization of bulk polymerized spacer lipids to polymeric liposomes. In addition, spacer lipids are able to build polymeric Langmuir-Blodgett multilayers. The decoupling of the polymer main chain and the membrane-forming amphiphilic side groups enables the deposition of already polymeric monolayers onto supports to form defined multilayers. If, alternatively, monomeric monolayers are deposited and polymerized on the support, defects in the layers due to structural changes during the polymerization are avoided by the flexible spacer group.}, language = {en} } @misc{KochLaschewskyRingsdorfetal.1986, author = {Koch, Horst and Laschewsky, Andr{\´e} and Ringsdorf, Helmut and Teng, Kang}, title = {Photodimerization and photopolymerization of amphiphilic cinnamic acid derivatives in oriented monolayers, vesicles and solution}, url = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-17111}, year = {1986}, abstract = {Cinnamic acid moieties were incorporated into amphiphilic compounds containing one and two alkyl chains. These lipid-like compounds with photoreactive units undergo self-organization to form monolayers at the gas-water interface and bilayer structures (vesicles) in aqueous solutions. The photoreaction of the cinnamic acid moiety induced by 254 nm UV light was investigated in the crystalline state, in monolayers, in vesicles and in solution in organic solvents. The single-chain amphiphiles undergo dimerization to yield photoproducts with twice the molecular weight of the corresponding monomers in organized systems. The photoreaction of amphiphiles containing two cinnamic acid groups occurs via two mechanisms: The intramolecular dimerization produces bicycles, with retention of the molecular weight of the corresponding monomer. The intermolecular reaction leads to oligomeric and polymeric photoproducts. In contrast to the single-chain amphiphiles, photodimerization processes of lipoids containing two cinnamic acid moieties also occur in solution in organic solvents.}, language = {en} } @misc{AlbrechtCummingKreuderetal.1986, author = {Albrecht, O. and Cumming, W. and Kreuder, W. and Laschewsky, Andr{\´e} and Ringsdorf, Helmut}, title = {Monolayers of rod-shaped and disc-shaped liquid crystalline compounds at the air-water interface}, url = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-17124}, year = {1986}, abstract = {Calamitic (rod-shaped) and discotic (disc-shaped) thermotropic liquid crystalline (LC) compounds were spread at the air-water interface, and their ability to form monolayers was studied. The calamitic LCs investigated were found to form monolayers which behave analogously to conventional amphiphiles such as fatty acids. The spreading of the discotic LCs produced monolayers as well, but with a behaviour different from classical amphiphiles. The areas occupied per molecule are too small to allow the contact of all hydrophilic groups with the water surface and the packing of all hydrophobic chains. Various molecular arrangements of the discotics at the water surface to fit the spreading data are discussed.}, language = {en} } @misc{LaschewskyRingsdorfSchneider1986, author = {Laschewsky, Andr{\´e} and Ringsdorf, H. and Schneider, J.}, title = {Oriented supramolecular systems-polymeric monolayers and multilayers from prepolymerized amphiphiles}, url = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-17131}, year = {1986}, abstract = {Oriented polymeric membranes were originally prepared by polymerization or polycondensation of preoriented monomers. The introduction of hydrophilic spacer groups into the polymeric amphiphiles allowed the formation of highly ordered systems (monolayers, liposomes, multilayers) from prepolymerized amphiphiles: due to the partial decoupling of the different mobilities and orientation tendencies of the polymer chain and the amphiphilic side groups, these polymers are able to self-organize. In monolayer experiments the high order of these membranes could be demonstrated by their surface pressure area-diagrams. In addition the combination of order and mobility of these spacer groups containing polymeric amphiphiles allowed the formation of Langmuir-Blodgett-multilyers with a high layer correlation. Thus, disturbancies in highly oriented layers can be avoided normally taking place during the polymerization reaction (e.g. contractions) or oriented monomeric layers.}, language = {en} } @misc{LaschewskyRingsdorfSchmidtetal.1987, author = {Laschewsky, Andr{\´e} and Ringsdorf, H. and Schmidt, G. and Schneider, J.}, title = {Self-organization of polymeric lipids with hydrophilic spacers in side groups and main chain : investigation in monolayers and multilayers}, url = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-17147}, year = {1987}, abstract = {Several polymerizable lipids were synthesized and polymerized to amphiphilic homopolymers and to copolymers with the help of hydrophilic comonomers. The self-organization of these polymeric lipids was investigated in monolayers and Langmuir-Blodgett multilayers. The self-organization of these polymers in model membranes is due to hydrophilic spacer groups in the amphiphilic side groups as well as to hydrophilic spacer groups in the polymer backbone. Thus, highly ordered monolayers and LB-multilayers are easily obtained.}, language = {en} } @misc{FerenzPeter1987, author = {Ferenz, Hans-J{\"o}rg and Peter, Martin G.}, title = {The inhibitory effect of sinefungin on juvenile hormone biosynthesis and development in locusts}, url = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-16811}, year = {1987}, abstract = {The antibiotic fungal metabolite sinefungin is a potent inhibitor of S-adenosylmethionine-acceptor methyltransferases. Its effect on insect metabolism and especially on corpora allata farnesoic acid methyltransferase, which catalyzes the penultimate step of juvenile hormone biosynthesis, was investigated in Locusta migratoria. Injection of sinefungin results in a delay of imaginal molt and in suppression of ovary development. Isolated corpora allata are unable to synthesize juvenile hormone III in the presence of more than 1.0 mM sinefungin. In a cell-free system containing the S-adenosylmethionine-dependent farnesoic acid methyltransferase from corpora allata sinefungin is a competitive inhibitor of the synthesis of methylfarnesoate with Ki of 1 μM.}, language = {en} } @misc{LaschewskyRingsdorf1988, author = {Laschewsky, Andr{\´e} and Ringsdorf, H.}, title = {Polymerization of amphiphilic dienes in Langmuir-Blodgett multilayers}, url = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-17176}, year = {1988}, abstract = {Amphiphilic derivatives of octadiene and docosadiene were investigated in monolayers and Langmuir-Blodgett multilayers, with respect to their self-organization and their polymerization behavior. All amphiphiles investigated form monolayers. However, only acid and alcohol derivatives were able to build up multilayers. Those multilayers are rapidly photopolymerized in the layers via a two-step process: Irradiation with long-wavelength UV light yields soluble polymers, whereas additional irradiation with sfiort-wavelength UV light produces insoluble and presumably cross-linked polymers. The reaction meclianism is discussed according to the polymer characterization by UV spectroscopy, small-angle X-ray scattering, NMR spectroscopy, and gel permeation chromatography. All multilayers undergo structural changes during the polymerization; substantial changes result in defects in the polymerized layers as observed by scanning electron microscopy. In contrast to the acids and alcohols, the deposition of monolayers of the aldehyde derivatives did not yield well-ordered multilayers, but rather amorphous films. In this different film structure, the photopolymerization process differs from the one observed in multilayers.}, language = {en} } @misc{LupoPrassScheunemannetal.1988, author = {Lupo, Donald and Prass, Werner and Scheunemann, Ude and Laschewsky, Andr{\´e} and Ringsdorf, Helmut and Ledoux, Isabelle}, title = {Second-harmonic generation in Langmuir-Blodgett monolayers of stilbazium salt and phenylhydrazone dyes}, url = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-17401}, year = {1988}, abstract = {Contents: 1. INTRODUCTION 2. SYNTHESIS OF THE COMPOUNDS 3. PREPARATION AND CHARACTERIZATION OF MONOLAYERS A. Monolayer Isotherms B. Langmuir-Blodgett Monolayer Films 4. EXPERIMENTAL SETUP FOR NONLINEAR MEASUREMENTS 5. NONLINEAR OPTICAL PROPERTIES 6. DISCUSSION 7. CONCLUSION}, language = {en} } @misc{PeterFoerster1989, author = {Peter, Martin G. and F{\"o}rster, Hans}, title = {On the structure of Eumelanins : identification of constitutional patterns by solid-state NMR spectroscopy}, url = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-17027}, year = {1989}, abstract = {Aus dem Inhalt: Melanins are complex polyphenolic polymers. They are usually formed in nature by enzyme-catalyzed oxidative polymerization of o-diphenols. The deep black eumelanins, derived from Dopa 1 or dopamine 3, are distinguished from the yellow to brown phaeomelanins obtained from Dopa in the presence of cysteine. Characteristic of eumelanins are the indole units, which are formed from catecholamines by intramolecular addition of the amino groups to the oxidatively generated o-quinones. [...]}, language = {en} } @misc{ErdelenLaschewskyRingsdorfetal.1989, author = {Erdelen, C. and Laschewsky, Andr{\´e} and Ringsdorf, H. and Schneider, J. and Schuster, A.}, title = {Thermal behaviour of polymeric Langmuir-Blodgett multilayers}, url = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-17378}, year = {1989}, abstract = {Langmuir-Blodgett multilayers of hydrocarbon and fluorocarbon polymers with hydrophilic spacer, lipid-polyelectrolyte complexes and mesogenic polymers have been prepared. The thermal behaviour of the multilayers was studied by small angle X-ray scattering, IR and UV—visible spectroscopy. Good thermal stabilities were found for the various classes of polymers. In addition, for both complexed multilayers and mesogenic polymer films, reorientation processes were observed.}, language = {en} } @misc{Peter1989, author = {Peter, Martin G.}, title = {Chemische Modifikation von Biopolymeren durch Chinone und Chinonmethide}, url = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-16802}, year = {1989}, abstract = {Chinone und Vorstufen, die oxidativ in Chinone und/oder Chinonmethide umgewandelt werden k{\"o}nnen, sind in der Natur weit verbreitet. Als sekund{\"a}re Naturstoffe wirken sie h{\"a}ufig antibiotisch, cytotoxisch, aber auch pathogen, und eine Reihe von Pflanzen und Tieren benutzt chinoide Substanzen als Abwehrstoffe, oft mit spektakul{\"a}rem Erfolg. Auf makromolekularer Ebene spielen Chinonmethide im Pflanzenreich eine Schl{\"u}sselrolle bei der Biosynthese von Lignin, w{\"a}hrend die Bildung von Melanoproteinen ein Beispiel f{\"u}r Reaktionen von o-Chinonen im Tierreich ist. Bei den Insekten dienen Chinone und Chinonmethide zur Bildung des lebensnotwendigen Exoskeletts. Die Reaktivit{\"a}t von Chinonen in biologischen Systemen hat auch f{\"u}r den Menschen unmittelbare Bedeutung in pharmazeutischer, toxikologischer und technologischer Hinsicht. Den Beispielen in diesem Aufsatz liegt ein gemeinsames Prinzip zugrunde, n{\"a}mlich die chemische Modifikation von Biopolymeren durch Chinone und Chinonmethide. Wie sich besonders bei einer detaillierteren Betrachtung der Reaktionen zeigt, die zur Sklerotisierung der Insektencuticula f{\"u}hren, sind in den letzten Jahren wichtige neue Erkenntnisse hinzugekommen, die vor allem durch die modernen Methoden der Stofftrennung und der Festk{\"o}rper-NMR-Spektroskopie erm{\"o}glicht worden sind.}, language = {de} } @misc{Laschewsky1989, author = {Laschewsky, Andr{\´e}}, title = {Monolayers and Langmuir-Blodgett multilayers of discotic liquid crystals?}, url = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-17396}, year = {1989}, abstract = {Contents: 1. Discotic Liquid Crystals 2. Monolayers and Langmuir-Blodgett Multilayers 3. Theoretical Considerations on the Molecular Packing of Discotic LCs in Monolayers and Multilayers 4. Spreading Experiments with Discotic LCs 5. LB-Multilayers of Discotic LCs 6. Polymeric Discotic LCs 7. Summary}, language = {en} } @misc{BiddleRickertLandoetal.1989, author = {Biddle, M. B. and Rickert, S. E. and Lando, J. B. and Laschewsky, Andr{\´e}}, title = {The use of the Langmuir-Blodgett technique to obtain ultra-thin polar films}, url = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-17185}, year = {1989}, abstract = {The piezoelectric and pyroelectric properties of oriented films possessing dipole moments are increasingly being used in pressure, acoustic, thermal and optical devices. The performance of these devices in many applications may be enhanced by thin-film technology.The developing Langmuir-Blodgett thin-film deposition technique offers the opportunity to obtain highly oriented and uniform organic-based films in the 10-5000 nm thickness range. Special techniques must be used, however, to assemble these molecules in such a way as to result in polar multilayer films. Several possible deposition techniques are investigated, with one resulting in a polar and pyroelectric film about 50 nm thick.}, language = {en} } @misc{PeterFoerster1989, author = {Peter, Martin G. and F{\"o}rster, Hans}, title = {Zur Struktur von Eumelaninen : Identifizierung von Konstitutionsmustern durch Festk{\"o}rper-NMR-Spektroskopie}, url = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-17038}, year = {1989}, abstract = {Aus dem Inhalt: Melanine sind komplexe polyphenolische Polymere. In der Natur entstehen sie durch meist enzymkatalysierte oxidative Polymerisation von o-Diphenolen. Man unterscheidet die aus Dopa 1 oder Dopamin 3 hervorgehenden, tiefschwarzen Eumelanine von den aus Dopa in Gegenwart von Cystein entstehenden, gelben bis braunen Phaomelaninen. [...]}, language = {de} } @misc{PeterBoldtNiedersteinetal.1990, author = {Peter, Martin G. and Boldt, Peter C. and Niederstein, Yvonne and Peter-Katalinić, Jasna}, title = {Synthesen von Galactose-Cluster-haltigen Steroid-Derivaten}, url = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-16783}, year = {1990}, abstract = {The synthesis of galactose clusters that are linked to a steroid moiety by a peptide-like spacer unit is described. The galactose cluster is obtained by Koenigs-Knorr glycosylation of TRIS-Gly-Fmoc (2b) under Helferich conditions. Peptide and ester bonds are formed after activation of carboxylic acids as diphenylthiophene dioxide (TDO) esters. 6a is synthesized in a convergent way by coupling of (Ac4Gal)3-TRIS-Gly (3e) with cholesteryl TDO succinate (5b). Coupling of (Ac4Gal)3-TRIS-Gly hydrogen succinate (3f) with Gly-O-Chol (5d) by means of EEDQ yields 6d. Reaction of (Ac4Gal)3-TRIS-Gly-SUCC-O-TDO (3g) with 25-hydroxycholesterol leads in a linear sequence to the oxysterol derivative 6f. Selective cleavage of the acetyl groups from galactose units yields the known compound 6b and the new derivatives 6e and 6g.}, language = {de} }