• Publications
  • Influence
Metabolic function and properties of 4-hydroxyphenylacetic acid 1-hydroxylase from Pseudomonas acidovorans
TLDR
An observation suggests that, during its shift from C-1 to C-2 of the nucleus, the side chain of the substrate remains bound to a site on the enzyme while a conformational change of the protein permits the necessary movement of the benzene ring. Expand
THE BACTERIAL DEGRADATION OF CATECHOL.
TLDR
Two strains of Pseudomonas were grown with phenol and used to prepare cell extracts that metabolized catechol with the transient formation of 2-hydroxymuconic semialdehyde and aldolase, which appeared to attack only one enantiomer of synthetic 4-hydroxy-2-oxovalerate. Expand
The Bacterial Cell
Synthesis and Organisation in the Bacterial CellBy E. F. Gale. (Ciba Lectures in Microbial Biochemistry, 1959). Pp. vii + 110. (New York and London: John Wiley and Sons, Inc., 1959.) 3.50 dollars,Expand
The metabolism of cresols by species of Pseudomonas.
TLDR
A comparison of rates of oxidation of various compounds by whole cells indicated that protocatechuate was a reaction intermediate when a non-fluorescent species of Pseudomonas oxidized p-cresol, and that cell extracts appeared to attack only one enantiomer of synthetic 4-hydroxy-2-oxohexanoate. Expand
Catabolism of aromatic acids in Trichosporon cutaneum
TLDR
All the reactions of these catabolic sequences were catalyzed by cell extracts, supplemented with reduced pyridine nucleotide coenzymes where necessary, except for the hydroxylations of benzoic and phenylacetic acids which were demonstrated with cell suspensions and isotopically labeled substrates. Expand
THE METABOLISM OF GALACTARATE, D-GLUCARATE AND VARIOUS PENTOSES BY SPECIES OF PSEUDOMONAS.
TLDR
This compound was isolated as its bis-2,4-dinitrophenylhydrazone, and several properties of the derivative were compared with those of the chemically synthesized material. Expand
Stereospecific Enzymes in the Degradation of Aromatic Compounds by Pseudomonas putida
TLDR
It was demonstrated that l-(S)-4-hydroxy-2-oxohexanoate is the biologically active enantiomer of this hydroxy acid, and a mechanism is proposed which closely resembles that for 4-Hydroxy- 2-oxopentanoate aldolase. Expand
Purification and Some Properties of Maleylpyruvate Hydrolase and Fumarylpyruvate Hydrolase from Pseudomonas alcaligenes
Hydrolysis of the gentisate ring-cleavage product, maleylpyruvate (cis-2,4-diketohept-5-enedioic acid), was shown to be catalyzed by an enzyme, maleylpyruvate hydrolase 11, in Pseudomonas alcaligenesExpand
...
1
2
3
4
5
...