Enrichment and analysis of desmosine and isodesmosine in biological fluids

A method has been developed for the enrichment and analysis of the elastin crosslinks, desmosine and isodesmosine, in biological fluids and tissues. It is adapted from published methods, offering improved recovery, sensitivity, resolution, and speed of analysis. Samples were hydrolyzed in 6 M HCl, after which the desmosines were enriched by CF1 cellulose chromatography and analyzed by HPLC with a C₁₈ column. Isodesmosine and desmosine were quantitated based on absorbance at 275 nm, with a limit of detection of approximately 30 pmol and recovery of approximately 66% in urine. Their t_R values on our HPLC system were approximately 9 and 12 min, respectively. This method was used to evaluate the daily and weekly variation in the concentrations of desmosine and isodesmosine in human urine. The results suggest that this method can be used to process large numbers of biological samples for analysis of desmosine and isodesmosine.     

Metabolic enhancement due to plasmid maintenance

Summary Plasmid maintenance allows the strain JM109 of Escherichia coli to grow in a minimal defined medium (M9). JM109 carrying no plasmid can hardly grow in M9 whereas JM109 carrying one, two and three plasmids have a clear metabolic advantage over the untransformed strain. In a complex medium like LB (Luria-Bertani Broth) all strains grow well and despite the number of plasmids carried by the host maximum specific growth rates are not severely affected. Our results suggest that the glucose metabolism is an essential factor contributing to this behavior.     

Preliminary studies on the reproduction and population dynamics of Monodonta lineata and Gibbula umbilicalis (Mollusca,Gastropoda) on the central coast of Asturias (N. Spain)

Summary Populations of Monodonta lineata and Gibbula umbilicalis were studied at Aramar beach (Luanco, Asturias) from October 1982 to November 1983. Both species show a sexual ratio of 1: 1 but differ in their gonadal cycle patterns. M. lineata gonadal development stages are found from November to May–June in a significant part of the population. Breeding stages occur from June–July to September, and in some individuals to November, with complete discharge of all spawn at the end of the reproductive season. Some degree of inter-annual variation is detected. Spawning stages of mature G. umbilicalis are found through the year but the higher frequencies occur in summer and autumn samples, with development phases predominating in January to May. Animals over 10 mm in shell diameter maintain their gonads close to spawning stages, completely spawned individuals being less than 10 percent. In both species variability in gonad stages for a given month reduces as size increases, indicating a certain synchrony.The new recruits of M. lineata are detected on the bare rock by September to November and are recognizable through their first year. Due to the amplitude of the breeding period and differing growth rates size distribution within an age class is wide. Size class frequencies rapidly decrease after the second year of life. The data for G. umbilicalis are difficult to interpret given the scarce number of juveniles and size overlapping.     

Continuous conversion of neuron phenotype in hydra.

All neurons in adult hydra are constantly changing their location. This poses interesting problems for the maintenance of the organization of the hydra nervous system. The solutions provide a different perspective on the development of nervous systems.     

1H-NMR studies on poly(oxyethylene)-bound oligopeptides

Conformational studies on poly(oxyethylene)-bound homo-, oligo-, guest-host, and sequential peptides synthesized according to the liquid-phase method were carried out by means of ¹H-nmr spectroscopy. The solubilizing effect of the C-terminal polymeric support allowed a thorough investigation of the secondary structure in solution.