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  • AUXILIARY SYSTEMS
  • Life and Medical Sciences
  • Organic Chemistry
  • 1
    Digitale Medien
    Digitale Medien
    Electrofusion for the pronuclear transplantation of mouse eggs (1987)
    New York, NY : Wiley-Blackwell
    Gamete Research 17 (1987), S. 15-20 
    Details
    ISSN: 0148-7280
    Schlagwort(e): nuclear transplantation ; electrofusion ; Life and Medical Sciences ; Cell & Developmental Biology
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Biologie
    Notizen: The present study was undertaken to determine the efficiency of HVJ treatment and electrofusion for pronuclear transplantation in the mouse. The output voltage and duration of the pulses were fixed to 200 μsec at 10 V or to 150 μsec at 15 V for electrofusion, because the maximum rates of blastomere fusion of 2-cell embryos and development of fused embryos in vitro were obtained under these conditions. Although the proportion of eggs with fused karyoplast (78%) and the fused eggs developed to morulae or blastocysts (67%) was significantly lower than those obtained after HVJ treatment (94% and 94%), the proportion of pregnant recipients and young obtained after treatment of fused eggs was not significantly different between these two procedures.It is advised that electrofusion can be used as a fusogenic procedure for pronuclear transplantation in the mouse in some cases where HVJ cannot be applied.
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
    URL: http://dx.doi.org/10.1002/mrd.1120170103
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  • 2
    Digitale Medien
    Digitale Medien
    Crystalline luciferin from live CypridinaThis study has been aided in part by Contract Nonr-1353(00) between the Office of Naval Research and Princeton University, by grants NSF-G-4578 and NSF-G-4266, by the Eugene Higgins Fund allocated to Princeton University and by the Japanese Commission for UNESCO. Publication in whole or in part by or for any purpose of the United States Government is permitted.Contribution number 121 from the Shimoda Marine Biological Station. (1961)
    Philadelphia : Wiley-Blackwell
    Journal of Cellular and Comparative Physiology 57 (1961), S. 55-62 
    Details
    ISSN: 0095-9898
    Schlagwort(e): Life and Medical Sciences ; Cell & Developmental Biology
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Biologie , Medizin
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
    URL: http://dx.doi.org/10.1002/jcp.1030570108
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  • 3
    Digitale Medien
    Digitale Medien
    Untersuchungen zur Spin-Trapping-Kinetik in Systemen von Radikalen unterschiedlicher Reaktivität. Die Photolyse von α-Phenylbenzoin in Gegenwart von Benzyliden-tert.-butylamin-N-oxid (1985)
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 327 (1985), S. 749-758 
    Details
    ISSN: 0021-8383
    Schlagwort(e): Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Investigations on Spin-Trapping Kineties in Radical Systems with Different Reactivity. Photolyses of α-Phenylbenzoine in the Presence of Benzylideneter. -butylamine N-oxideAs a model system to study the spin-trapping kinetics of systems forming two radicals of different reactivity α-phenylbenzoine (PhB) was chosen. The photolysis of PhB forms benzoyl (B·) and diphenylketylradikals (K·), respectively, which can be trapped by benzylidene-tert-butyl-amine N-oxide (PBN), as a spin trap. The rate constants of radical addition to PBN and their reactions with the spin adducts were determined by means of flash photolysis and kinetic calculations of the PBN concentration dependence. For B· and K· addtion rate constants to PBN of k1 = 8,1 × 105 M-1s-1, and k2 = 5,8 · 104 M-1s-1, respectively, were found. The rate constants for the reactions of B· and K· with the spin adducts are in the order of 109…1010 M-1s-1.
    Zusätzliches Material: 6 Ill.
    Materialart: Digitale Medien
    URL: http://dx.doi.org/10.1002/prac.19853270507
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  • 4
    Digitale Medien
    Digitale Medien
    Morphogenesis and ductal development of the prostatic complex of the guinea pig (1993)
    New York, NY : Wiley-Blackwell
    Journal of Morphology 217 (1993), S. 219-227 
    Details
    ISSN: 0362-2525
    Schlagwort(e): Life and Medical Sciences ; Cell & Developmental Biology
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Biologie , Medizin
    Notizen: The morphogenesis of glandular architecture of the three lobes of prostate gland of the guinea pig, lateral, dorsal, and coagulating gland was studied from 35 days gestation to 90 postnatal days. Epithelial ductal tubules of various lobes of the gland were microdissected after treatment by collagenase and displayed two dimensionally. The number of ductal tips was counted, and the volume of the ductal network was quantified using a graphic tablet. The results show that the growth and ductal morphogenesis fall into two phases: prenatal and postnatal. The first outgrowth of prostatic buds begins at 35 days gestation (gestational length is 65 days). Ductal growth and branching continues over the next 15-20 days and by 55 days gestation, approximately 60%, 79%, and 71% of the adult number of ductal tips of the lateral and dorsal lobes and coagulating gland respectively, are formed. The figures increase to 89%, 84%, and 106%, respectively, by birth. There is little increase in number of ductal tips thereafter. Postnatal growth is accomplished mainly by elongation of existing ductal network with a little additional branching but with an increase in size (volume) of the tubules. Canalization of ductal tubules occurs prenatally in all lobes but postnatal functional cytodifferentiation takes a slightly different pace among them. Ductal morphogenesis of the guinea pig prostate gland differs significantly in time-course from that of the mouse in which ductal development occurs mainly postnatally. © 1993 Wiley-Liss, Inc.
    Zusätzliches Material: 14 Ill.
    Materialart: Digitale Medien
    URL: http://dx.doi.org/10.1002/jmor.1052170209
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  • 5
    Digitale Medien
    Digitale Medien
    A histological study of the “stomach” and caecum in the genus Pheretima (Oligochaeta) (1941)
    New York, NY : Wiley-Blackwell
    Journal of Morphology 68 (1941), S. 507-517 
    Details
    ISSN: 0362-2525
    Schlagwort(e): Life and Medical Sciences ; Cell & Developmental Biology
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Biologie , Medizin
    Materialart: Digitale Medien
    URL: http://dx.doi.org/10.1002/jmor.1050680305
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  • 6
    Digitale Medien
    Digitale Medien
    2,3:5,6-bis(ethylenedithio)- and bis(trimethylenedithio)-N,N′- dicyanoquinonediimines as new electron acceptors (1988)
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 1 (1988), S. 275-280 
    Details
    ISSN: 0894-3230
    Schlagwort(e): Organic Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: In order to examine the substituent effect of ethylenedithio and trimethylenedithio groups on electron acceptors, the two title compounds were prepared in one step from the corresponding quinones. These species behave as weak π-electron acceptors owing to the electronic and sterical effects of the fused groups. Only the bis(ethylenedithio) derivative formed a charge-transfer complex with tetrathiotetracene, which showed a moderate electric conductivity of 2·0 × 10-2 S cm-1. In addition, both species oxidized copper, sodium, and potassium iodides to give the corresponding deeply colored metal salts, most of which were semiconductive. The naphtho analogs were similarly studied, but hardly served as electron acceptors.
    Zusätzliches Material: 2 Tab.
    Materialart: Digitale Medien
    URL: http://dx.doi.org/10.1002/poc.610010505
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  • 7
    Digitale Medien
    Digitale Medien
    Formation of glycine conjugate and (-)-(R)-enantiomer from (+)-(S)-2-phenylpropionic acid suggesting the formation of the coa thioester intermediate of (+)-(S)-enantiomer in dogs (1992)
    New York, NY [u.a.] : Wiley-Blackwell
    Chirality 4 (1992), S. 342-348 
    Details
    ISSN: 0899-0042
    Schlagwort(e): arylpropionic acid ; 2-phenylpropionic acid ; glycine conjugation ; stereoselectivity ; chiral inversion ; reverse chiral inversion ; glycine N-acyl transferase ; dog hepatocytes ; chiral HPLC ; Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: It has been proposed that the chiral inversion of the 2-arylpropionic acids is due to the stereospecific formation of the (-)-R-profenyl-CoA thioesters which are putative intermediates in the inversion. Accordingly, amino acid conjugation, for which the CoA thioesters are obligate intermediates, should be restricted to those optical forms which give rise to the (-)-R-profenyl-CoA, i.e., the racemates and the (-)-(R)-isomers. We have examined this problem in dogs with respect to 2-phenylpropionic acid(2-PPA). Regardless of the optical configuration of 2-phenylpropionic acid administered, the glycine conjugate was the major urinary metabolite and this was shown to be exclusively the (+)-(S)-enantiomer by chiral HPLC. Both (-)-(R)- and (+)-(S)-2-phenylpropionic acid were present in plasma after the administration of either antipode, and further evidence of the chiral inversion of both enantiomers was provided by the presence of some 25% of the opposite enantiomer in the free 2-phenylpropionic acid and its glucuronide excreted in urine after administration of (-)-(R)- and (+)-(S)-2-phenylpropionic acid. The (+)-(S)-enantiomer underwent chiral inversion to the (-)-(R)-antipode when incubated with dog hepatocytes. These data suggests that both enantiomers of 2-phenylpropionic acid are substrates for canine hepatic acyl CoA ligase(s) and thus undergo chiral inversion, but that the CoA thioester of only (+)-(S)-2-phenylpropionic acid is a substrate for the glycine N-acyl transferase. These studies are presently being extended to the structure and species specificity of the reverse inversion and amino acid conjugation of profen NSAIDs. © 1992 Wiley-Liss, Inc.
    Zusätzliches Material: 7 Ill.
    Materialart: Digitale Medien
    URL: http://dx.doi.org/10.1002/chir.530040603
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  • 8
    Digitale Medien
    Digitale Medien
    Siderophore-Mediated microbial iron(III) uptake: An exercise in chiral recognition (1993)
    New York, NY [u.a.] : Wiley-Blackwell
    Chirality 5 (1993), S. 359-365 
    Details
    ISSN: 0899-0042
    Schlagwort(e): synthetic siderophore analogs ; hydroxamates ; ferrichrome ; ferrioxamine ; coprogen ; Pseudomonas putida ; membrane receptors ; transport proteins ; growth promotion ; growth inhibition ; Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Molecular recognition by microbial receptors for siderophores [natural iron(III) carriers] is examined with synthetic iron(III) carriers as structural probes. The iron(III) carriers have been designed to reproduce the two essential features of the natural siderophores: the capability to form octahedral iron(III) binding cavities and to fit specific membrane receptors. Specifically, analogs of tripodal ferrichrome and linear ferrioxamines have been prepared and examined. The ferrichrome analogs rely on C3-symmetric binders that are assembled from triscarboxylates as anchors, amino acids as bridges, and terminal hydroxamate groups as binding sites. The ferrioxamine analogs are based on linear assemblies of three identical monomers, each derived from a chiral amino acid. The deliberate use of animo acid residues as variable building blocks enables us to systematically modify the molecules' envelopes and the preferred absolute configuration of the iron(III) complexes until optimal performance is reached. Examination of the synthetic analogs in Pseudomonas putida demonstrates that the domains around the iron(III) center and their chiral sense dictate the extent of recognition by the membrane receptors. It is also shown that the synthetic siderophore analogs may be designed to either exert a broader, or a more narrow range of microbial activity than the natural siderophores. The implications of these findings are discussed in relation to the possible design of species-specific antimicrobial agents. © 1993 Wiley-Liss, Inc.
    Zusätzliches Material: 9 Ill.
    Materialart: Digitale Medien
    URL: http://dx.doi.org/10.1002/chir.530050516
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  • 9
    Digitale Medien
    Digitale Medien
    Spectrophotometric Study of Some Arylidene Derivatives of Benzoic and Salicylic Acid Hydrazides in Buffer Solutions (1978)
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 320 (1978), S. 1029-1035 
    Details
    ISSN: 0021-8383
    Schlagwort(e): Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Spektrophotometrische Untersuchungen einiger Arylidenderivate von Benzoe- und Salicylsäurehydraziden in Pufferlösungen
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
    URL: http://dx.doi.org/10.1002/prac.19783200620
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  • 10
    Digitale Medien
    Digitale Medien
    Association of vanadate-sensitive Mg2+-ATPase and shape change in intact red blood cells (1991)
    New York, N.Y. : Wiley-Blackwell
    Journal of Cellular Biochemistry 46 (1991), S. 284-290 
    Details
    ISSN: 0730-2312
    Schlagwort(e): erythrocytes ; magnesium ; echinocyte ; calcium ; plasma membrane ; Life and Medical Sciences ; Cell & Developmental Biology
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Biologie , Chemie und Pharmazie , Medizin
    Notizen: Intact human erythrocytes, initially depleted of Mg2+ by EDTA incubation in the presence of A23187, exhibit Mg2+-dependent phosphate production of around 1.5 mmol per liter cells · h, half-maximally activated at around 0.4 mM added free Mg2+. This appears to correspond to Mg2+-stimulated adenosine triphosphatase (Mg2+-ATPase) activity found in isolated membranes, which is known to have a similar activity and affinity for Mg2+. Vanadate (up to 100 μM) inhibited Mg2+-dependent phosphate production and ATP breakdown in intact cells. Over a similar concentration range vanadate (3-100 μM) transformed intact cells from normal discocytes to echinocytes within 4-8 h at 37°C, and more rapidly in Mg2+-depleted cells. The rate of Ca2+-induced echinocytosis was also enhanced in Mg2+-depleted cells. These results support previous studies in erythrocyte ghosts suggesting that vanadate-induced shape change is associated with inhibition of Mg2+-ATPase activity localized in the plasma membrane of the red blood cell.
    Zusätzliches Material: 6 Ill.
    Materialart: Digitale Medien
    URL: http://dx.doi.org/10.1002/jcb.240460403
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