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Biomedical subjects

G Siebert

Publications and source records attributed to G Siebert.

At least 73 records · Page 4Linked to original sources

A study of acetyl CoA-carboxylase in adipose tissues.

Acetyl-CoA-carboxylase activities were measured in adipose tissues of pigs during a breeding experiment for a low-fat line, and of rats and obese mice under different nutritional conditions. Acetyl-CoA-carboxylase behaves uniformly with the four major NADPH-generating dehydrogenases, like a block of lipogenic enzymes, and is found to be genetically determined in pigs. Correlation with body fat under a variety of experimental conditions confirms the rate-limiting character of acetyl-CoA-carboxylase, not only for the biosynthesis of fatty acids, but obviously also for their esterification and for triglyceride deposition. Activity ratios of this enzyme in different adipose tissues, e.g. outer versus inner layer of subcutaneous adipose tissue in pigs, epididymal versus subcutaneous, or epididymal versus perirenal adipose tissue in rats and obese mice, correlate well with predicted fattening in pigs and with fat deposition in laboratory rodents. Moderate biotin deficiency in obese mice leads to a preferred fat deposition in the epididymal fat pad in comparison with normal biotin supply. The concept of a lipogenic potential in the body is derived from the activity ratios of acetyl-CoA-carboxylase.

Acetyl-CoA Carboxylase↗

Mathematical processes in the evaluation of the dangerous nature of chemicals.

The present study was carried out on the basis of the question of "whether it is possible to use mathematical methods meaningfully for the evaluation of the environmental effects of chemicals." The analysis of the evaluation process showed that this may be considered as a relation between the set of test data and a target set, that of the danger classes. The very general structure of a relation considerably restricts the use of algorithms; in particular it can be shown that algorithms which would map the data directly onto the danger classes like a functional coordination are, in general, excluded. This is partly due to the highly nonhomogeneous parameter set which must be determined for evaluation purposes, and partly to the high degree of randomness or human participation in the selection of the parameters. Moreover, there was no indication whether or to what extent the parameters are interdependent, i.e., whether there are interdisciplinary regularities which could be expressed algebraically and interpreted scientifically. Questions of this kind remain components of interdisciplinary research, and they cannot be explained from a mathematical--i.e., theoretical--point of view. Considerably more empirical material needs to be available for use as the foundation for a reasonable theory.

Animals↗

Enzymatic cleavage of the epsilon-peptide bond in alpha- and epsilon-substituted glycyl- and phenylalanyl-lysine peptides.

Lysine peptides, X-Lys-OH (Formula: see text) were synthesized, following classic or non-classic routes. Some bacterial and mammalian enzymes, endo- and exo-peptide hydrolases of the enzyme nomenclature type EC 3.4., were tested for their ability to split the epsilon-peptide bond in the above substrates. Kinetic constants (Km,kcat) were evaluated with leucine aminopeptidase from hog kidney and eye lens with aminopeptidase I from yeast. Aminopeptidase M (hog pancreas) and hog intestinal aminopeptidase were additionally examined for their Ki values with the above substrates in comparison to the classic protease substrate leucine p-nitroanilide. Especially the intestinal mucosa hydrolases are shown to be efficient in cleaving epsilon-peptide bonds.

Amino Acid Sequence↗

Linkage of Pgm-3 in the house mouse and homologies of three phosphoglucomutase loci in mouse and man.

The discovery of a third phosphoglucomutase locus (Pgm-3) in the house mouse is reported. Three alleles are recognized on the basis of differences in electrophoretic mobility and enzymatic activity. Pgm-3A (fast mobility and high activity) is present in inbred strain C57BL/10J and 24 other strains; Pgm-3b (slow mobility and high activity) is present in LP/Pas and six other strains; and Pgm-3c (no detectable activity in any tissue tested) is present in strain DBA/2J and 14 other strains. Seventy-four recombinant inbred strains derived from progenitors that differed at Pgm-3 were used to study genic linkage. Pgm-3 is on chromosome 9 and is linked to Sep-1, d, Mod-1, and Ltw-3. Gene order and recombination frequencies are estimated as d 3.8 +/- 1.8%. Pgm-3 2.3 +/- 1.2% Mod-1. Substrate specificities and cofactor requirements show that mouse Pgm-1 is homologous with human Pgm-2, mouse Pgm-2 with human Pgm-1, and mouse Pgm-3 with human Pgm-3.

Alleles↗

[Nutrition and cancer. A meeting report].

A meeting report is given (Annual Symposium on Fundamental Cancer Research, Houston, and International Congress of Nutrition, San Diego) which mainly deals with cancerogenesis: The role of retinoids as inhibitors, and the role of pyrolysis products as promoter of cancerogenesis, both essentially active in the tumor promotion range of cancerogenesis, after previous initiation. In the future, enhanced chances may be foreseen for active prevention and for causal elucidation of cancer formation, which until now seems to be a spontaneous disease.

Carcinogens↗

Recent results concerning physiological tooth movement and anterior guidance.

Physiological tooth movements during mandibular excursions with and without occlusion have been considered. Using electronic and pantographic techniques, anterior guidance and tooth movements during simulated mastication (without a bolus) were investigated. Investigations in the absence of occlusion showed that elastic deformation of the mandible gave rise to tooth movements. During occlusion three-dimensional tooth movements of up to 60 micro m in each direction occurred. Pantographic measurements of anterior guidance showed that each type of occlusion (balanced occlusion, group function and canine protected occlusion) has its own characteristic. Only canine protected occlusion gave values which corresponded to physiological data.

Cuspid↗

Galactose-1-phosphate-uridyltransferase (E.C. 2.7.7.11): a simple routine method for detecting individuals heterozygous for the silent allele Gt 0.

A simple routine method for detecting individuals who are heterozygous for the silent gene Gt 0 is presented. This method consists of a combination of electrophoresis and densitometry. The results confirm the theoretical expectation that these individuals would exhibit about 50% of the enzyme activity found in the corresponding normal phenotype.

Alleles↗

Human phosphoglycolate phosphatase (PGP) E.C. 3.1.3.18: linkage analysis.

Linkage data on phosphoglycolate phosphatase (PGP) E.C. 3.1.3.18 and 26 other human genetic markers are presented. One hundred and one families from the southwestern area of Germany were tested. Close linkage between PGP and the following markers could be ruled out: ABO, acP, ADA, GPT, PGM1, GLO, HLA, and PGM3. There is some evidence for possible linkage with MNSs, Rh, Gm and EsD. Family segregation data confirm the hypothesis formerly established by Barker and Hopkinson: three common alleles PG1, PGP2 and PGP3 at an autosomal locus PGP.

Alleles↗

Data on linkage relations between GLO and 21-hydroxylase.

Linkage between GLO and 21-hydroxylase was investigated in 11 families with 24 children. Positive lod score values with a maximum of +1.618 at theta = 0.05 indicate close linkage between these marker loci.

Adrenal Hyperplasia, Congenital↗

Substrate affinity in PGM1, PGM2, and PGM2 isozymes.

An easy method for routine detection of PGM1, PGM2, and PGM3 isozymes is given. Differences in substrate affinity are discussed. Gene products pgm1 can be differentiated from gene products pgm3 by cofactor requirement.

Electrophoresis, Agar Gel↗

Increase of mono(ADP-ribose) protein conjugate levels in rat liver induced by nicotinamide administration.

Protein-bound mono(ADP-ribose) residues were quantitated in the livers of nicotinamide-treated and control rats. Nicotinamide administration led to a rise in NAD+ (2.5-fold) and in protein-bound mono (ADP-ribose) residues (1.5-fold). This increase was higher in the NH2OH-sensitive mono(ADP-ribose) protein conjugates than in the NH2OH-resistant subfraction. NADH, NADP and NADPH levels did not change significantly under these conditions. The findings show that nicotinamide induced an increased ADP ribosylation of new acceptor sites, and not merely an elongation of pre-existing (ADP-ribose)n chains. A correlation of the NAD+ concentration and the extent of post-synthetic modification of nuclear proteins by mono(ADP-ribose) residues was not restricted to nicotinamide-induced changes. It was also seen in various tissues with widely differing NAD+ levels.

Adenosine Diphosphate Ribose↗