0000000000542168

AUTHOR

R. K. Zahn

Gas-chromatographische Bestimmung des DNS-Gehaltes biologischen Materials über den Thymingehalt

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Purification of a nuclease from human serum.

The purification procedure for a nuclease from human serum is described. It includes ammonium sulfate precipitation, chromatography on DEAE-Sephadex and on Sephacryl-S 200, and preparative electrophoresis. The enzyme, purified about 2000-fold, is homogeneous in a sodium dodecyl sulfate electrophoretic system, where it has a mol. wt of 78,000. The pH optimum lies around pH 6.5; it is a sugar-nonspecific endonuclease.

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Genotoxicity of the fungicide dichlofluanid in seven assays

Seven different endpoints for detection of genotoxicity have been used to demonstrate the DNA-altering properties of Dichlofluanid, a fungicide commonly used in viticulture pest control. Each endpoint (DNA synthesis inhibition test, alkaline viscosimetry, umu-test, alkaline filter elution, FADU-test, 32P-postlabeling, and electron microscopy) shows clear evidence of genotoxicity. These data indicate that application of the fungicide dichlofluanid may be mutagenic and/or carcinogenic for exposed humans.

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Desoxyribonuclease-Aktivität im Seminalplasma von normalem und pathologischem Sperma1

Zusammenfassung Das Verteilungsmuster der DNase-Aktivitaten im Seminalplasma von 9 Normalpersonen und 18 Patienten mit einem pathologischen Spermabefund wurde mit dem mikro-disc-elektrophoretischen Verfahren untersucht. Dabei ergaben die Aktivitatsbestimmungen der DNase bei Patienten mit einer Oligoasthenoteratozoospermie als auch bei alien Probanden, die einen pathologischen Spermabefund aufwiesen, in der 1. und 2. Bande deutliche Aktivitatsminderungen im Vergleich zum Seminalplasma von Normalpersonen. Nach den vorliegenden Untersuchungsbefunden stellt sich die Frage, ob den DNasen im Seminalplasma die Aufgabe zukommt, geschadigte und uberalterte Spermatozoen, deren Membran permeabler gewo…

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A Headful of T4 Coliphage DNA Packaged to Fasces-Like Globules in Fractal Models

We present a new model for T4 DNA packaging based on fractal considerations. The proposed model is based on electron microscopic observations of spread and packaged DNA. The model takes into account enzymatically and unidirectionally driven packaging, and quick release of the DNA during infection. We also consider the different biochemical reactions of the packaging process.

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Determination of radioactivity-labelled derivatives of [8-14C]-6-mercaptopurine in homogenates of L5178Y mouse lymphoma cells using high-pressure liquid cation-exchange chromatography

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