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81.
Zusammenfassung Die hier kurz geschilderten Versuche konnten natürlich keine erschöpfende Klärung des gestellten Problems ergeben und sollten lediglich orientierend auf etwaige Möglichkeiten hinweisen. Trotzdem zeigten sie bereits, daß die hier künstlich erzeugten elektrischen Felder, die den in der Natur vorkommenden nachgebildet sind, einen Einfluß auf das Wachstum pflanzlicher Organismen ausüben. Sie bewirken eine Steigerung der Vermehrungsgeschwindigkeit bei Mikroorganismen und ein erhöhtes Streckungswachstum der Sprosse von keimendem Weizen. Es konnte im speziellen hier gezeigt werden, daß Milchsäurebakterien nicht nur, wie bekannt, auf eine Temperaturerhöhung (in bestimmten Grenzen) mit einer Wachstumszunahme reagieren, sondern auch auf die vor Gewittern auftretenden, hier künstlich nachgeahmten elektrischen Wechselfelder in der Atmosphäre. 相似文献
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83.
Little MH Brennan J Georgas K Davies JA Davidson DR Baldock RA Beverdam A Bertram JF Capel B Chiu HS Clements D Cullen-McEwen L Fleming J Gilbert T Herzlinger D Houghton D Kaufman MH Kleymenova E Koopman PA Lewis AG McMahon AP Mendelsohn CL Mitchell EK Rumballe BA Sweeney DE Valerius MT Yamada G Yang Y Yu J 《Gene expression patterns : GEP》2007,7(6):680-699
Cataloguing gene expression during development of the genitourinary tract will increase our understanding not only of this process but also of congenital defects and disease affecting this organ system. We have developed a high-resolution ontology with which to describe the subcompartments of the developing murine genitourinary tract. This ontology incorporates what can be defined histologically and begins to encompass other structures and cell types already identified at the molecular level. The ontology is being used to annotate in situ hybridisation data generated as part of the Genitourinary Development Molecular Anatomy Project (GUDMAP), a publicly available data resource on gene and protein expression during genitourinary development. The GUDMAP ontology encompasses Theiler stage (TS) 17-27 of development as well as the sexually mature adult. It has been written as a partonomic, text-based, hierarchical ontology that, for the embryological stages, has been developed as a high-resolution expansion of the existing Edinburgh Mouse Atlas Project (EMAP) ontology. It also includes group terms for well-characterised structural and/or functional units comprising several sub-structures, such as the nephron and juxtaglomerular complex. Each term has been assigned a unique identification number. Synonyms have been used to improve the success of query searching and maintain wherever possible existing EMAP terms relating to this organ system. We describe here the principles and structure of the ontology and provide representative diagrammatic, histological, and whole mount and section RNA in situ hybridisation images to clarify the terms used within the ontology. Visual examples of how terms appear in different specimen types are also provided. 相似文献
84.
Huwiler A Döll F Ren S Klawitter S Greening A Römer I Bubnova S Reinsberg L Pfeilschifter J 《Biochimica et biophysica acta》2006,1761(3):367-376
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Licata L Haase W Eckhardt-Strelau L Parcej DN 《Protein expression and purification》2006,47(1):171-178
Mammalian SK proteins are Ca2+-activated K+ channels, which show a sub-20 pS conductance. We have expressed the SK2 variant gene in Pichia pastoris and found protein to be produced at considerably higher levels than in brain tissue. The channel was correctly folded as evidenced by its high affinity interaction with apamin, a specific ligand from bee venom. However, the protein was largely unable to reach the plasma membrane, its normal destination, instead remaining in the endoplasmic reticulum. Adding a putative translocation sequence altered the intracellular distribution significantly with enhanced trafficking out of the endoplamic reticulum. Fusion of SK2 with the associated protein calmodulin also altered the channel localisation but in a different manner with channels now found mainly in transit between endoplasmic reticulum and Golgi compartments. 相似文献
88.
The glyoxalase system is a ubiquitous pathway catalyzing the glutathione-dependent detoxication of ketoaldehydes such as methylglyoxal, which is mainly formed as a by-product of glycolysis. The gene encoding a glyoxalase II has been cloned from Trypanosoma brucei, the causative agent of African sleeping sickness. The deduced protein sequence contains the highly conserved metal binding motif THXHXDH but lacks three basic residues shown to fix the glutathione-thioester substrate in the crystal structure of human glyoxalase II. Recombinant T. brucei glyoxalase II hydrolyzes lactoylglutathione, but does not show saturation kinetics up to 5 mm with the classical substrate of glyoxalases II. Instead, the parasite enzyme strongly prefers thioesters of trypanothione (bis(glutathionyl)spermidine), which were prepared from methylglyoxal and trypanothione and analyzed by high performance liquid chromatography and mass spectrometry. Mono-(lactoyl)trypanothione and bis-(lactoyl)trypanothione are hydrolyzed by T. brucei glyoxalase II with k(cat)/K(m) values of 5 x 10(5) m(-1) s(-1) and 7 x 10(5) m(-1) s(-1), respectively, yielding d-lactate and regenerating trypanothione. Glyoxalase II occurs in the mammalian bloodstream and insect procyclic form of T. brucei and is the first glyoxalase II of the order of Kinetoplastida characterized so far. Our results show that the glyoxalase system is another pathway in which the nearly ubiquitous glutathione is replaced by the unique trypanothione in trypanosomatids. 相似文献
89.
Trypanosoma brucei, the causative agent of African sleeping sickness, has three nearly identical genes encoding cysteine homologues of classical selenocysteine-containing glutathione peroxidases. The proteins are expressed in the mammalian and insect stages of the parasite. One of the genes, which contains a mitochondrial as well as a glycosomal targeting signal has been overexpressed. The recombinant T. brucei peroxidase has a high preference for the trypanothione/tryparedoxin couple as electron donor for the reduction of different hydroperoxides but accepts also T. brucei thioredoxin. The apparent rate constants k(2)' for the regeneration of the reduced enzyme are 2 x 10(5) m(-1) s(-1) with tryparedoxin and 5 x 10(3) m(-1) s(-1) with thioredoxin. No saturation kinetics was observed and the rate-limiting step of the overall reaction is reduction of the hydroperoxide. With glutathione, the peroxidase has marginal activity and reduction of the enzymes becomes limiting with a k(2)' value of 3 m (-1) s(-1). The T. brucei peroxidase, in contrast to the related Trypanosoma cruzi enzyme, also accepts hydrogen peroxide as substrate. The catalytic efficiency of the peroxidase studied here is comparable with that of the peroxiredoxin-like tryparedoxin peroxidases, which shows that trypanosomes possess two distinct peroxidase systems both dependent on the unique dithiol trypanothione. 相似文献
90.
Tsikas D Schwedhelm E Suchy MT Niemann J Gutzki FM Erpenbeck VJ Hohlfeld JM Surdacki A Frölich JC 《Journal of chromatography. B, Analytical technologies in the biomedical and life sciences》2003,794(2):237-255
Free radical-catalysed oxidation of arachidonic acid esterified to lipids leads to the formation of the F(2)-isoprostane family which may theoretically comprise up to 64 isomers. We have previously shown that the combination of TLC and GC-tandem MS (referred to as method A) allows for the accurate and highly specific quantification of 8-iso-PGF(2alpha) (iPF(2alpha)-III, 15-F(2t)-IsoP) in human urine. Immunoaffinity column chromatography (IAC) with immobilized antibodies raised against 8-iso-PGF(2alpha) (i.e. 15(S)-8-iso-PGF(2alpha)) has been shown by others to be highly selective and specific for this 8-iso-PGF(2alpha) isomer when quantified by GC-MS. In the present study we established IAC for urinary 8-iso-PGF(2alpha) for subsequent quantification by GC-tandem MS (referred to as method B). This method was fully validated and found to be highly accurate and precise for urinary 15(S)-8-iso-PGF(2alpha). 8-iso-PGF(2alpha) was measured in urine of 10 young healthy humans by both methods. 8-iso-PGF(2alpha) was determined to be 291+/-102 pg/mg creatinine by method A and 141+/-41 pg/mg creatinine by method B. Analysis of the combined through and wash phases of the IAC step, i.e. of the unretained compounds, by method A showed the presence of non-immunoreactive 8-iso-PGF(2alpha) at 128+/-55 pg/mg creatinine. This finding suggests that urinary 8-iso-PGF(2alpha) is heterogenous, with 15(S)-8-iso-PGF(2alpha) contributing by approximately 50%. PGF(2alpha) and other 8-iso-PGF(2alpha) isomers including 15(R)-8-iso-PGF(2alpha) are not IAC-immunoreactive and are chromatographically separated from 15(S)-8-iso-PGF(2alpha). We assume that ent-15(S)-8-iso-PGF(2alpha) is also contributing by approximately 50% to urinary 8-iso-PGF(2alpha). This finding may have methodological, mechanistic and clinical implications. 相似文献