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Biomedical subjects

S J Ajl

Publications and source records attributed to S J Ajl.

At least 19 recordsLinked to original sources

Birth defects research: 1980 and after.

Very little is known about environmentally-induced birth defects, i.e., those due to exogenous agents acting directly on the fetus or indirectly through the mother. Established teratogens include some viruses, drugs, radiations and one or two industrial chemicals. Much is known about birth defects due to single-gene mutations. Knowledge is scarce, however, concerning faulty regulation of gene expression or additive effects involving multiple-gene causation of disease and defect, and almost nothing is known about the mechanisms of multifactorial (gene plus environment) defects, which probably account for the majority of developmental anomalies known to man. Impressive progress has been made in understanding and control of inborn errors of metabolism. Carrier detection, prenatal diagnosis and effective ameliorative therapy have been worked out for many types of biochemical defects, and the entry of molecular biology into the field adumbrates the coming of more definitive preventive and therapeutic measures for many birth defects. Carrier detection and prenatal diagnosis make possible prevention of important birth defects by means of reproductive control. Ethical, social and psychological problems arising in the wake of this development are not here discussed but will surely be one of the dominating issues of medicine and public health for the coming years.

Abnormalities, Drug-Induced↗

Plague toxin.

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Animals↗

Multiple forms of bacterial NADP-specific isocitrate dehydrogenase.

Electrophoretically distinct forms of nicotinamide adenine dinucleotide phosphate-specific isocritrate dehydrogenase have been observed in extracts of Escherichia coli grown under different culture conditions. In glucose-grown cells, two distinct bands of isocitrate dehydrogenase activity were observed on polyacrylamide gels and have been completely resolved by employing ion-exchange chromatography. These multiple forms of the enzyme have been studied and their possible metabolic role is discussed.

Chromatography, Ion Exchange↗

Noninvolvement of acyl carrier protein with citrate synthase and malate synthase.

Acyl carrier protein (ACP coli) was isolated from commercially grown Escherichia coli B and was acetylated by chemical methods. Biological activity of the synthesized acetyl-ACP coli was checked in an in vitro fatty acid-synthesizing system isolated from E. coli B. Since acetyl-ACP is preferred over acetyl-coenzyme A (CoA) as a substrate in these reactions, the possibility that it may substitute for acetyl-CoA in biosynthetically and oxidatively important cellular pathways (glyoxylate and Krebs cycles, respectively) was examined. Acetyl-ACP was tested for substrate activity with the enzyme of each cycle which has been found to utilize acetyl-CoA. Crystalline citrate synthase (EC 4.1.3.7) of porcine origin (Calbiochem) was found to be inactive with acetyl-ACP coli, which acted neither as a substrate nor as an inhibitor in the presence of acetyl-CoA. Malate synthase (EC 4.1.3.2) of the acetate type was isolated from acetate-grown cells of a mutant of E. coli K-12 (VGD(3)H(5)) and was also found to be inactive with acetyl-ACP coli. The significance of these results and of the recent discovery of another phospho-pantetheine-containing protein are discussed.

Bacterial Proteins↗