[Gas chromatographic detection of nitrogen-containing drugs in aqueous solutions by means of the nitrogen detector].
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Chemistry, Pharmaceutical↗
Biomedical subjects
L Jaenicke
Publications and source records attributed to L Jaenicke.
[Synthesis of dihydrofolate reductase by synchronized yeast cells. Relationship between DNA replication and the graded time course of enzyme synthesis].
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DNA↗
[A regulating factor of methionine biosynthesis].
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Bacterial Proteins↗
Methionine synthetase. Existence and interconversion of two enzyme species.
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Chromatography, Gel↗
Methionine synthesis: Demonstration of the reversibility of the reaction.
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Journal Article↗
On the role of S-adenoxylmethionine in the vitamin B12 dependent methionine biosynthesis.
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Alcohols↗
[Neopterin and neopterin-3'-phosphate as precursors of folic acid in Mycobacterium smegmatis].
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Biological Assay↗
[Desoxyribonucleic acid polymerase in the human leukocytes. Enzyme activity in leukemia and virus infections].
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Adenosine Triphosphate↗
[Model investigations on the function of tetrahydropterine as cofactor in biologic hydroxylation].
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Models, Chemical↗
Kinetic evidence for an enzyme-bound intermediate in the biosynthesis of a methionine.
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Journal Article↗
[Regulation of dihydrofolic acid reductase synthesis in synchronously growing yeast cells].
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Culture Media↗
[Reaction rate of methionine synthesis in Escherichia coli].
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Binding Sites↗
Biosynthesis of methionine by bacteria.
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Enterococcus faecalis↗
[Synthesis and properties of phosphorylated models of tetrahydrofolic acid].
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Amines↗
[Purification and properties of glutamine synthetase from pig brains].
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Adenosine Triphosphate↗
Formation of methionine methyl groups.
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Autoradiography↗
Enantiospecificity of immobilized horse liver alcohol dehydrogenase.
Horse liver alcohol dehydrogenase (EC 1.1.1.1) accepts a wide structural range of substrates but exhibits a well-defined and predictable stereospecificity. The enzyme was immobilized on CNBr-activated Sepharose 4B. The immobilized preparation was used to oxidize the enantiomeric pair of cis-1,2-bis(hydroxymethyl)-3-cyclopentene enantioselectively to a mixture of two diastereoisomeric chiral lactones. The two diastereoisomeric products are readily separated and each was isolated with an optical yield of greater than 99%.
Alcohol Dehydrogenase↗