The metabolic fate of [35S]-diallyl disulphide in mice

Summary Diallyl disulphide (DADS) is a major constituent of garlic oil. Uptake of [³⁵S]-labelled diallyl disulphide by mouse liver is highest at 90 min after treatment. 2h after treatment with [³⁵S]-DADS, 70% of the radioactivity is present in the liver cytosol of which 80% is metabolized to sulphate.     

Fractal symmetry of protein interior: what have we learned?

The application of fractal dimension-based constructs to probe the protein interior dates back to the development of the concept of fractal dimension itself. Numerous approaches have been tried and tested over a course of (almost) 30 years with the aim of elucidating the various facets of symmetry of self-similarity prevalent in the protein interior. In the last 5 years especially, there has been a startling upsurge of research that innovatively stretches the limits of fractal-based studies to present an array of unexpected results on the biophysical properties of protein interior. In this article, we introduce readers to the fundamentals of fractals, reviewing the commonality (and the lack of it) between these approaches before exploring the patterns in the results that they produced. Clustering the approaches in major schools of protein self-similarity studies, we describe the evolution of fractal dimension-based methodologies. The genealogy of approaches (and results) presented here portrays a clear picture of the contemporary state of fractal-based studies in the context of the protein interior. To underline the utility of fractal dimension-based measures further, we have performed a correlation dimension analysis on all of the available non-redundant protein structures, both at the level of an individual protein and at the level of structural domains. In this investigation, we were able to separately quantify the self-similar symmetries in spatial correlation patterns amongst peptide–dipole units, charged amino acids, residues with the π-electron cloud and hydrophobic amino acids. The results revealed that electrostatic environments in the interiors of proteins belonging to ‘α/α toroid’ (all-α class) and ‘PLP-dependent transferase-like’ domains (α/β class) are highly conducive. In contrast, the interiors of ‘zinc finger design’ (‘designed proteins’) and ‘knottins’ (‘small proteins’) were identified as folds with the least conducive electrostatic environments. The fold ‘conotoxins’ (peptides) could be unambiguously identified as one type with the least stability. The same analyses revealed that peptide–dipoles in the α/β class of proteins, in general, are more correlated to each other than are the peptide–dipoles in proteins belonging to the all-α class. Highly favorable electrostatic milieu in the interiors of TIM-barrel, α/β-hydrolase structures could explain their remarkably conserved (evolutionary) stability from a new light. Finally, we point out certain inherent limitations of fractal constructs before attempting to identify the areas and problems where the implementation of fractal dimension-based constructs can be of paramount help to unearth latent information on protein structural properties.     

Effect of chloramphenicol on the expansion of isolated cotyledons ofCucurbita pepo in light and in presence of kinetin

Zusammenfassung Kotyledonen von Cucurbita-Keimlingen zeigen im Licht in Wasser eine deutliche Zunahme der Blattfläche. Durch Chloramphenicol kann dieses Flächenwachstum gehemmt werden. Die Hemmung wird durch Kinetin aufgehoben, wobei die durch Kinetin bewirkte prozentuale Zunahme der Fläche in Wasser und in Chloramphenicol enthaltenden Lösungen ungefähr gleich gross ist.     

Adrenal dopamine-β-hydroxylase activity: 24-hour rhythmicity and evidence for pineal control

Summary Adrenal medullary dopamine--hydroxylase activity was found in male rats to have a 24-hour rhythm, with an approximately 6-fold increase at about the time of the onset of darkness. This nocturnal rise in enzyme activity did not occur when lights were kept on, nor did it occur in animals that had been pinealectomized.Supported in part by grants from the Ford Foundation (No. 630-05050A), National Institutes of Health (No. HD-03352) and National Institute of Mental Health (No. MH-25019) USPHS.